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Sample records for polycrystalline ce-doped y3al5o12

  1. Luminescent and scintillation properties of the Ce3+ doped Y3−xLuxAl5O12:Ce single crystalline films

    International Nuclear Information System (INIS)

    Zorenko, Yu.; Gorbenko, V.; Zorenko, T.; Popielarski, P.; Mosińska, L.; Fedorov, A.

    2016-01-01

    The work is related to the investigation of scintillation and luminescent properties of single crystalline films (SCF) of solid solutions of Ce 3+ doped Y 3−x Lu x Al 5 O 12 :Ce garnets with x value in the 0–3 range. We have shown a possibility of realization of high-energy shift of the Ce 3+ ion emission spectrum in these garnets up to 22 nm. We have also found that the light yield of the radioluminescence under α-particle excitation of LuAG:Ce SCF can exceed by 1.3 times the corresponding values for the YAG:Ce SCF counterpart. For investigation of the luminescent properties of Y 3−x Lu x Al 5 O 12 :Ce SCF at different x values the luminescent spectroscopy of these SCFs under excitation by synchrotron radiation in the VUV range was performed. - Highlights: • Single crystalline films of Y 3−x Lu x Al 5 O 12 garnets at x=0–3.0 were grown by LPE method onto YAG substrates. • Lattice constant of Y 3−x Lu x Al 5 O 12 :Ce film and the film/substrate misfit changed linearly with increasing of Lu content in the x=0–3.0 range. • High-energy shift of the Ce 3+ emission up to 22 nm in Y 3−x Lu x Al 5 O 12 film with increasing of Lu content in the x=0–3.0 range. • Light yield of Y 3−x Lu x Al 5 O 12 :Ce film decreases in the x=0–1.8 range and increases in the x=1.8–3.0 range. • Scintillation LY of Lu 3 Al 5 O 12 :Ce film can exceed by 1.3 times the LY for YAG:Ce film counterpart.

  2. Luminescent properties of Y3Al5−xGaxO12:Ce crystals

    International Nuclear Information System (INIS)

    Zorenko, Yu.; Zorenko, T.; Malinowski, P.; Sidletskiy, O.; Neicheva, S.

    2014-01-01

    Absorption, luminescent and scintillation properties of Ce 3+ doped Y 3 Al 5−x Ga x O 12 crystals with Ga content in the x=1–5 range were investigated in this work and compared with the properties of YAG:Ce crystals. Apart from the traditional spectral methods (absorption, cathodoluminescence and light yield measurements), the intrinsic and Ce 3+ related luminescence of Y 3 Al 5−x Ga x O 12 :Ce solid-solution were also investigated using the luminescent spectroscopy under excitation by synchrotron radiation in the 3.7–25 eV range. We show that the optical properties Y 3 Al 5−x Ga x O 12 :Ce garnets monotonically change with increasing the Ga content in the x=0–3 range due to preferable localization of Ga ions in the tetrahedral position of the garnet lattice. At the highest Ga concentration (x>3) the deviation of the optical properties of Y 3 Al 5−x Ga x O 12 :Ce garnets is observed from the respective properties of these crystals with Ga content in the x=0–3 range due to occupation by Ga ions of the octahedral position in the garnet host. - Highlights: • Different dependence of optical properties of Y 3 Al 5−x Ga x O 12 :Ce crystals on Ga content in x=0–3 and 35 ranges. • Elimination of the luminescence of Y Al antisite defects in Y 3 Al 5−x Ga x O 12 :Ce crystals at x>2. • Significant improvement of the scintillation properties of Y 3 Al 5−x Ga x O 12 :Ce crystals at x=2 and 3 in comparison with YAG:Ce

  3. Synthesis and luminescence properties of Ce{sup 3+}-doped Y{sub 3}Al{sub 3.5}Ga{sub 1.5}O{sub 12} green phosphor for white LEDs

    Energy Technology Data Exchange (ETDEWEB)

    Qiang, Yaochun [Fujian Key Laboratory of Advanced Materials, Department of Materials Science and Engineering, College of Materials, Xiamen University, Xiamen 361005 (China); Yu, Yuxi, E-mail: yu_heart@xmu.edu.cn [Fujian Key Laboratory of Advanced Materials, Department of Materials Science and Engineering, College of Materials, Xiamen University, Xiamen 361005 (China); Chen, Guolong [Fujian Engineering Research Center for Solid-state Lighting, Department of Electronic Science, Xiamen University, Xiamen 361005 (China); Fang, Jiyu [Advanced Materials Processing and Analysis Center, Department of Materials Science and Engineering, University of Central Florida, Orlando, FL 32816 (United States)

    2016-04-15

    A series of Ce{sup 3+}-doped Y{sub 3}Al{sub 3.5}Ga{sub 1.5}O{sub 12} green phosphors were successfully synthesized by a solid-state reaction method. The microstructure, morphology, luminescence spectra, luminescence quantum yield (QY) and thermal stability of the phosphor were investigated. The critical concentration of Ce{sup 3+} ions in Y{sub 3−m}Al{sub 3.5}Ga{sub 1.5}O{sub 12}:mCe{sup 3+} is m=0.06. The QY of Y{sub 2.94}Al{sub 3.5}Ga{sub 1.5}O{sub 12}:0.06Ce{sup 3+} phosphor is as high as 94% under excitation at 450 nm and its luminescence intensity at 150 °C still maintains 90% of that measured at 25 °C, which are just a little worse than those of commercial Lu{sub 3}Al{sub 5}O{sub 12}:Ce{sup 3+} green phosphor but much better than those of commercial (Sr,Ba){sub 2}SiO{sub 4}:Eu{sup 2+} green phosphor. A white LED lamp was fabricated by employing Y{sub 2.94}Al{sub 3.5}Ga{sub 1.5}O{sub 12}:0.06Ce{sup 3+} as a green phosphor and commercial (Ca,Sr)AlSiN{sub 3}:Eu{sup 2+} as a red phosphor (628 nm), its Ra value, correlated color temperature (CCT), CIE1931 chromaticity coordinates and luminous efficiency is 84, 3081 K, (x=0.4369, y=0.4142) and 102 lm/W, respectively. The experimental results demonstrate that Y{sub 2.94}Al{sub 3.5}Ga{sub 1.5}O{sub 12}:0.06Ce{sup 3+} is a promising green phosphor not only can be used for high color rendering index white LEDs but also for high-power white LEDs.

  4. Luminescent properties of Y{sub 3}Al{sub 5−x}Ga{sub x}O{sub 12}:Ce crystals

    Energy Technology Data Exchange (ETDEWEB)

    Zorenko, Yu., E-mail: zorenko@ukw.edu.pl [Institute of Physics, Kazimierz Wielki University in Bydgoszcz, Powstańców Wielkopolskich No 2, 85-090 Bydgoszcz (Poland); Zorenko, T. [Institute of Physics, Kazimierz Wielki University in Bydgoszcz, Powstańców Wielkopolskich No 2, 85-090 Bydgoszcz (Poland); Department of Electronics, Ivan Franko National University of Lviv, Gen. Tarnavskyj str. 107, 70017 Lviv (Ukraine); Malinowski, P. [Institute of Physics, Kazimierz Wielki University in Bydgoszcz, Powstańców Wielkopolskich No 2, 85-090 Bydgoszcz (Poland); Sidletskiy, O.; Neicheva, S. [Institute for Scintillation Materials, National Academy of Sciences of Ukraine, Lenina pr. 60, 61001 Kharkiv (Ukraine)

    2014-12-15

    Absorption, luminescent and scintillation properties of Ce{sup 3+} doped Y{sub 3}Al{sub 5−x}Ga{sub x}O{sub 12} crystals with Ga content in the x=1–5 range were investigated in this work and compared with the properties of YAG:Ce crystals. Apart from the traditional spectral methods (absorption, cathodoluminescence and light yield measurements), the intrinsic and Ce{sup 3+} related luminescence of Y{sub 3}Al{sub 5−x}Ga{sub x}O{sub 12}:Ce solid-solution were also investigated using the luminescent spectroscopy under excitation by synchrotron radiation in the 3.7–25 eV range. We show that the optical properties Y{sub 3}Al{sub 5−x}Ga{sub x}O{sub 12}:Ce garnets monotonically change with increasing the Ga content in the x=0–3 range due to preferable localization of Ga ions in the tetrahedral position of the garnet lattice. At the highest Ga concentration (x>3) the deviation of the optical properties of Y{sub 3}Al{sub 5−x}Ga{sub x}O{sub 12}:Ce garnets is observed from the respective properties of these crystals with Ga content in the x=0–3 range due to occupation by Ga ions of the octahedral position in the garnet host. - Highlights: • Different dependence of optical properties of Y{sub 3}Al{sub 5−x}Ga{sub x}O{sub 12}:Ce crystals on Ga content in x=0–3 and 35 ranges. • Elimination of the luminescence of Y{sub Al} antisite defects in Y{sub 3}Al{sub 5−x}Ga{sub x}O{sub 12}:Ce crystals at x>2. • Significant improvement of the scintillation properties of Y{sub 3}Al{sub 5−x}Ga{sub x}O{sub 12}:Ce crystals at x=2 and 3 in comparison with YAG:Ce.

  5. Luminescence of Ce3+ ions in Y3Al5O12 - Y3Ga5O12 solid solution

    International Nuclear Information System (INIS)

    Zorenko, Yu.V.; Nazar, I.V.; Limarenko, L.N.; Pashkovskij, M.V.

    1996-01-01

    Regularities of changes in spectral and energetic characteristics of the Ce 3+ ions radiation in the Y 3 Al 5-x Ga x O 12 solid solutions, related to change in the matrix crystal field force and dissipation of the luminescence excitation energy because of transfers between the valency zone ceiling and the Ce 3+ excited ion basis state are obtained. 9 refs., 3 figs., 1 tab

  6. Multi-component Ce doped (Gd,Y,La,Lu)3(AlGaSc)5O12 garnets – A new story in the development of scintillating single crystalline film screens

    International Nuclear Information System (INIS)

    Zorenko, Yu.; Gorbenko, V.; Savchyn, V.; Zorenko, T.; Fedorov, A.; Wrzesinski, H.; Vasylkiv, Ya.

    2013-01-01

    The paper is dedicated to development of the scintillators based on single crystalline films of Ce doped (GdLaYLu) 3 (AlGaSc) 5 O 12 multi-component garnets onto Gd 3 Ga 5 O 12 substrates using the liquid phase epitaxy method. -- Highlights: •Growth of Ce doped (GdYLaLu) 3 (AlGaSc) 5 O 12 garnets films by LPE method. •Luminescent and scintillation properties of Ce doped (GdYLaLu) 3 (AlGaSc) 5 O 12 films. •Influence of Pb 2+ flux related impurity on the light yield of Ce 3+ emission

  7. Luminescence properties of Y3Al5O12:Ce nanoceramics

    International Nuclear Information System (INIS)

    Zorenko, Yu.; Voznyak, T.; Gorbenko, V.; Zych, E.; Nizankovski, S.; Dan'ko, A.; Puzikov, V.

    2011-01-01

    Comparative analysis of the luminescent properties of Y 3 Al 5 O 12 :Ce (YAG:Ce) transparent optical ceramics (OS) with those of single crystal (SC) and single crystalline film (SCF) analogues has been performed under excitation by pulsed synchrotron radiation in the fundamental absorption range of YAG host. It has been shown that the properties of YAG:Ce OC are closer to the properties of the SCF counterpart, where Y Al antisite defects are completely absent, rather than to the properties of SC of this garnet with large concentration of Y Al antisite defects. At the same time, the luminescence spectra of YAG:Ce OC show weak emission bands in the 200-470 nm range related to Y Al antisite defects and charged oxygen vacancies (F + and F centers). YAG:Ce OS also possesses significantly larger contribution of slow components in the Ce 3+ luminescence decay under high-energy excitation in comparison with SC and SCF of this garnet due to the involvement of antisite defects, charged oxygen vacancies as well as boundaries of grains in the energy transfer processes from the host to the Ce 3+ ions.

  8. Improvement of photoluminescence intensity of Ce-doped Y{sub 3}Al{sub 5}O{sub 12} phosphor by Si{sub 3}N{sub 4} addition

    Energy Technology Data Exchange (ETDEWEB)

    Shyu, Jiin-Jyh, E-mail: jjshyu@ttu.edu.tw; Yang, Chia-Wei

    2017-06-01

    Yttrium aluminum garnet (Y{sub 3}Al{sub 5}O{sub 12}, YAG) has been widely used as a host for luminescent ions. The present paper describes the effects of Si{sub 3}N{sub 4} addition on the formation and photoluminescence properties of the Ce-doped YAG yellow phosphors. Phosphor powders with the nominal compositions of Y{sub 2.95}Ce{sub 0.05}Al{sub 5-m}Si{sub m}O{sub 12-m}N{sub m} (m = 0–0.6) were prepared by calcining the mixed raw materials at 1500 °C in nitrogen atmosphere. X-ray diffraction, x-ray photoelectron spectroscopy, scanning electron microscope, and transmission electron microscopy equipped with an energy dispersive x-ray spectrometer were used to characterize the structure of the calcined powders. The photoluminescence properties were measured with fluorescence spectrophotometry. It was found that in the range of m = 0–0.27, single phase YAG solid solution (s.s.) in which the Y, Al, and O sites are partially occupied by Ce, Si, and N ions, respectively. The nitrogen ions do not distribute homogeneously over the YAG lattice. The tendency to bond with nitrogen ion for the cations is (Y, Ce) > Si > Al. With the increase in the Si{sub 3}N{sub 4} content, the increase in both the Ce{sup 3+}/(Ce{sup 3+} + Ce{sup 4+}) ratio and the Ce-N bonds improve the intensity of the photoluminescent emission. At m = 0.27, the emission intensity reaches a maximum which is about 2.5 and 1.6 times of that for the Si{sub 3}N{sub 4}-free composition (m = 0) calcined in air and nitrogen, respectively. When the Si{sub 3}N{sub 4} content (m) is higher than 0.27, the emission intensity decreases due to the existence of residual Si{sub 3}N{sub 4} phase. - Highlights: • Addition of Si{sub 3}N{sub 4} can increase the emission intensity of YAG:Ce up to 2.5 times. • Increase in the Ce{sup 3+}/Ce{sup 4+} ratio and the number of Ce-N bonds improve the emission. • The tendency to bond with nitrogen ion for cations in YAG:Ce is (Y, Ce) > Si > Al. • The incomplete dissolution

  9. Scintillation properties of Er-doped Y3Al5O12 single crystals

    International Nuclear Information System (INIS)

    Yamaji, Akihiro; Ogino, Hiraku; Fujimoto, Yutaka; Suzuki, Akira; Yanagida, Takayuki; Yokota, Yuui; Kurosawa, Shunsuke; Yoshikawa, Akira

    2013-01-01

    Er-doped Y 3 Al 5 O 12 single crystals with different Er concentrations of 0.1, 1.0, 10, 30, and 50% were grown by the micro-pulling down method. There were several absorption lines due to the Er 3+ 4f-4f transitions in the transmittance spectra and these lines correspond to the transitions from the ground state of 4 I 15/2 to the excited states. The photo- and radio-luminescence spectra showed Er 3+ 4f-4f emissions. Relative light yield under 5.5 MeV alpha-ray irradiation of Er 0.1%:Y 3 Al 5 O 12 was estimated to be 63% of that of Bi 4 Ge 3 O 12 . -- Highlights: •Er doped Y 3 Al 5 O 12 single crystal scintillators were grown with different Er concentrations. •Optical properties associated with 4f-4f transition were evaluated. •Radio luminescence spectra measurements were performed under 5.5 MeV alpha-ray irradiation. •The highest light yield was estimated to be 63% of that of Bi 4 Ge 3 O 12 under 5.5 MeV alpha-ray irradiation

  10. Growth and scintillation properties of Ce{sup 3+}-doped (Y{sub 1-x}Gd{sub x})AlO{sub 3} crystals

    Energy Technology Data Exchange (ETDEWEB)

    Fujimoto, Yutaka; Wakahara, Shingo; Suzuki, Shotaro; Kurosawa, Shunsuke [Institute of Materials Research, Tohoku University, 2-1-1 Katahira, Aoba-ku, Sendai, Miyagi 980-8577 (Japan); Yanagida, Takayuki [New Industry Creation Hatchery Center, Tohoku University, 6-6-10 Aramaki, Aoba-ku, Sendai 980-8579 (Japan); Yoshikawa, Akira [Institute of Materials Research, Tohoku University, 2-1-1 Katahira, Aoba-ku, Sendai, Miyagi 980-8577 (Japan); New Industry Creation Hatchery Center, Tohoku University, 6-6-10 Aramaki, Aoba-ku, Sendai 980-8579 (Japan)

    2012-12-15

    The optical and scintillation properties of 0.5% fixed Ce-doped (Y{sub 1-x}Gd{sub x})AlO{sub 3} single crystals have been investigated at three different levels of Gd doping: x = 0.2, 0.4 and 0.6. Single crystal of the Ce{sup 3+}-doped (Y{sub 0.8}Gd{sub 0.2})AlO{sub 3}, (Y{sub 0.6}Gd{sub 0.4})AlO{sub 3} and (Y{sub 0.4}Gd{sub 0.6})AlO{sub 3} were successfully grown by {mu}-PD technique in nitrogen atmosphere. From X-ray diffraction analysis, no impurity phase was detected for the grown Ce-doped crystals. Ce-doped (Y{sub 0.6}Gd{sub 0.4})AlO{sub 3} crystal demonstrated highest fluorescence quantum efficiency ({proportional_to} 25%) with improvement of excitation efficiency due to the Gd-doping. When irradiated by the alpha-rays from a {sup 241}Am source, all the Ce-doped crystals showed luminescence band that corresponding to 5d (t{sub 2g})-4f transition of Ce{sup 3+}. The scintillation decay time was characterized by two components; the fast component (5-15 ns) is ascribed to 5d-4f transition of Ce{sup 3+}, while the slow one (100-200 ns) may be related to energy transfer between Ce{sup 3+} and Gd{sup 3+} ion. According to the result of {sup 137}Cs gamma-ray irradiated pulse height spectra compared with BGO scintillator, the relative scintillation light output was found to be about 12200 {+-} 1220 (Gd 20%) and 16000 {+-} 1600 (Gd 40%) ph/MeV. (copyright 2012 WILEY-VCH Verlag GmbH and Co. KGaA, Weinheim) (orig.)

  11. Optical properties of white organic light-emitting devices fabricated utilizing a mixed CaAl12O19:Mn4+ and Y3Al5O12:Ce3+ color conversion layer.

    Science.gov (United States)

    Jeong, H S; Kim, S H; Lee, K S; Jeong, J M; Yoo, T W; Kwon, M S; Yoo, K H; Kim, T W

    2013-06-01

    White organic light-emitting devices (OLEDs) were fabricated by combining a blue OLED with a color conversion layer made of mixed Y3Al5O12:Ce3+ green and Ca2AlO19:Mn4+ red phosphors. The X-ray diffraction patterns showed that Ce3+ ions in the Y3Al5O12:Ce3+ phosphors completely substituted for the Y3+ ions and the Mn4+ ions in the CaAl12O19:Mn4+ phosphors completely substituted for the Ca2+ ions. Electroluminescence spectra at 11 V for the OLEDs fabricated utilizing a color conversion layer showed that the Commission Internationale de l'Eclairage coordinates for the Y3Al5O12:Ce3+ and CaAl12O19:Mn4+ phosphors mixed at the ratio of 1:5 and 1:10 were (0.31, 0.34) and (0.32, 0.37), respectively, indicative of a good white color.

  12. Luminescence and energy transfer in Lu3Al5O12 scintillators co-doped with Ce3+ and Pr3+

    NARCIS (Netherlands)

    Ogiegło, J.M.; Zych, A.K.; Jüstel, T.; Meijerink, A.; Ronda, R.C.

    2013-01-01

    Lu3Al5O12:Ce3+ (LuAG:Ce) is a scintillator with a fast response time. The light yield is lower than theoretically expected and to increase the light yield co-doping with Pr3+ is investigated. To better understand the energy flow to the Ce3+ ion, first low temperature emission and excitation spectra

  13. On the response of Y 3Al 5O 12: Ce (YAG: Ce) powder scintillating screens to medical imaging X-rays

    Science.gov (United States)

    Kandarakis, I.; Cavouras, D.; Sianoudis, I.; Nikolopoulos, D.; Episkopakis, A.; Linardatos, D.; Margetis, D.; Nirgianaki, E.; Roussou, M.; Melissaropoulos, P.; Kalivas, N.; Kalatzis, I.; Kourkoutas, K.; Dimitropoulos, N.; Louizi, A.; Nomicos, C.; Panayiotakis, G.

    2005-02-01

    The aim of this study was to examine Y 3Al 5O 12:Ce (also known as YAG:Ce) powder scintillator under X-ray imaging conditions. This material shows a very fast scintillation decay time and it has never been used in X-ray medical imaging. In the present study various scintillator layers (screens) with coating thickness ranging from 13 to 166 mg/cm 2 were prepared in our laboratory by sedimentation of Y 3Al 5O 12: Ce powder. Optical emission spectra and light emission efficiency (spectrum area over X-ray exposure) of the layers were measured under X-ray excitation using X-ray tube voltages (80-120 kVp) often employed in general medical radiography and fluoroscopy. Spectral compatibility with various optical photon detectors (photodiodes, photocathodes, charge coupled devices, films) and intrinsic conversion efficiency values were determined using emission spectrum data. In addition, parameters related to X-ray detection, energy absorption efficiency and K-fluorescence characteristic emission were calculated. A theoretical model describing radiation and light transfer through scattering media was used to fit experimental data. Intrinsic conversion efficiency (η≈0.03-0.05) and light attenuation coefficients (σ≈26.5 cm/g) were derived through this fitting. Y 3Al 5O 12:Ce showed peak emission in the wavelength range 530-550 nm. The light emission efficiency was found to be maximum for the 107 mg/cm 2 layer. Due to its "green" emission spectrum, Y 3Al 5O 12:Ce showed excellent compatibility (of the order of 0.9) with the sensitivity of many currently used photodetectors. Taking into account its very fast response Y 3Al 5O 12:Ce could be considered for application in X-ray imaging especially in various digital detectors.

  14. On the response of Y3Al5O12: Ce (YAG: Ce) powder scintillating screens to medical imaging X-rays

    International Nuclear Information System (INIS)

    Kandarakis, I.; Cavouras, D.; Sianoudis, I.; Nikolopoulos, D.; Episkopakis, A.; Linardatos, D.; Margetis, D.; Nirgianaki, E.; Roussou, M.; Melissaropoulos, P.; Kalivas, N.; Kalatzis, I.; Kourkoutas, K.; Dimitropoulos, N.; Louizi, A.; Nomicos, C.; Panayiotakis, G.

    2005-01-01

    The aim of this study was to examine Y 3 Al 5 O 12 :Ce (also known as YAG:Ce) powder scintillator under X-ray imaging conditions. This material shows a very fast scintillation decay time and it has never been used in X-ray medical imaging. In the present study various scintillator layers (screens) with coating thickness ranging from 13 to 166mg/cm 2 were prepared in our laboratory by sedimentation of Y 3 Al 5 O 12 : Ce powder. Optical emission spectra and light emission efficiency (spectrum area over X-ray exposure) of the layers were measured under X-ray excitation using X-ray tube voltages (80-120kVp) often employed in general medical radiography and fluoroscopy. Spectral compatibility with various optical photon detectors (photodiodes, photocathodes, charge coupled devices, films) and intrinsic conversion efficiency values were determined using emission spectrum data. In addition, parameters related to X-ray detection, energy absorption efficiency and K-fluorescence characteristic emission were calculated. A theoretical model describing radiation and light transfer through scattering media was used to fit experimental data. Intrinsic conversion efficiency (ηC ∼0.03-0.05) and light attenuation coefficients (σ∼26.5cm 2 /g) were derived through this fitting. Y 3 Al 5 O 12 :Ce showed peak emission in the wavelength range 530-550nm. The light emission efficiency was found to be maximum for the 107mg/cm 2 layer. Due to its 'green' emission spectrum, Y 3 Al 5 O 12 :Ce showed excellent compatibility (of the order of 0.9) with the sensitivity of many currently used photodetectors. Taking into account its very fast response Y 3 Al 5 O 12 :Ce could be considered for application in X-ray imaging especially in various digital detectors

  15. Co-doping effects on luminescence and scintillation properties of Ce doped Lu3Al5O12 scintillator

    International Nuclear Information System (INIS)

    Kamada, Kei; Nikl, Martin; Kurosawa, Shunsuke; Beitlerova, Alena; Nagura, Aya; Shoji, Yasuhiro; Pejchal, Jan; Ohashi, Yuji; Yokota, Yuui; Yoshikawa, Akira

    2015-01-01

    The Mg, Ca, Sr and Ba 200 ppm co-doped Ce:Lu 3 Al 5 O 12 single crystals were prepared by micro pulling down method. Absorption and luminescence spectra were measured together with several other scintillation characteristics, namely the scintillation decay and light yield to reveal the effect of the co-doping. The scintillation decays were accelerated by both Mg and Ca co-dopants. The Mg co-doped samples showed the fastest decay and the highest light yield among the co-doped samples

  16. Y/Gd-free yellow Lu{sub 3}Al{sub 5}O{sub 12}:Ce{sup 3+} phosphor for white LEDs

    Energy Technology Data Exchange (ETDEWEB)

    Park, Kwangwon [Department of Display Science and Engineering, Pukyong National University, Busan 608-737 (Korea, Republic of); Kim, Taehoon; Yu, Youngmoon [LED-Marine Convergence Technology R& BD Center, Pukyong National University, Busan 608−739 (Korea, Republic of); Seo, Kwangil [L-Stone Co. Ltd., Bucheon 421−807 (Korea, Republic of); Kim, Jongsu, E-mail: jsukim@pknu.ac.kr [Department of Display Science and Engineering, Pukyong National University, Busan 608-737 (Korea, Republic of)

    2016-05-15

    Solid solubility limit of Ce{sup 3+} ions into Lu-based garnet, Lu{sub 3(1−x)}Ce{sub 3x}Al{sub 5}O{sub 12}, was determined as below 6.7 mol% (3x<0.2 mol) through Raman spectra and X−ray diffraction patterns. Above the solid solubility limit (3x≥0.2 mol), Lu{sub 3(1−x)}Ce{sub 3x}Al{sub 5}O{sub 12} phosphors showed the significant redshift to the yellow spectral region without Y{sup 3+} and Gd{sup 3+} ions. The redshift was explained in terms of the local compressive strain at the Ce{sup 3+} sites. The optimized sample (3x=0.4 mol) had a dominant emission wavelength of 548 nm, color coordinate of CIEx=0.421, CIEy=0.548, quantum efficiency of 80%, absorbance of 91%, lumen maintenance of 90% and high color stability at 473 K under 450 nm excitation wavelength, suggesting substitutability for the commercial yellow (Y, Gd){sub 3}(Al, Ga){sub 5}O{sub 12}:Ce{sup 3+} phosphor. The measured decay times at higher Ce{sup 3+} concentration are significantly shortened at higher temperature than that of those at lower Ce{sup 3+} concentration. The yellow Lu{sub 2.6}Ce{sub 0.4}Al{sub 5}O{sub 12} and a commercial red (Sr, Ca)AlSiN{sub 3}:Eu{sup 2+} phosphor were applied to the pc-WLED, it gave an excellent luminous efficiency (138 lm/W) with a slightly lower color rendering index (Ra=76.4) under correlated color temperature of 6500 K compared to those of the (Y, Gd){sub 3}(Al, Ga){sub 5}O{sub 12}:Ce{sup 3+}-based one (136 lm/W, Ra=78.7). Especially, the quantities of the used phosphors were significantly decreased by 20% for the yellow LuAG:Ce and by 40% for the red (Sr, Ca)AlSiN{sub 3}:Eu{sup 2+}. Thus, the Y/Gd−free pure LuAG:Ce yellow phosphors can be used as alternative to the commercial yellow YAG:Ce phosphor.

  17. Effect of Al/Ga substitution on the structural and luminescence properties of Y3(Al1-xGax)5O12: Ce3+ phosphors

    Science.gov (United States)

    Fu, Sheng; Tan, Jin; Bai, Xin; Yang, Shanjie; You, Lei; Du, Zhengkang

    2018-01-01

    As candidates for display and lighting materials, a series of gallium-substituted cerium-doped yttrium aluminum garnet (Y3(GaxAl1-x)5O12: Ce3+) phosphors were synthesized by high temperature solid-state reaction. The phases, morphology, luminescence spectra and thermal stability of the phosphors were investigated. The volatilization of Ga2O3 induces the constituents out of stoichiometric ratio and different impurities in the system. The excitation and emission spectra occur red shift (339 nm - 351 nm) and blue shift (465 nm - 437 nm), and blue shift (541 nm - 517 nm), respectively. The spectra have no further blue shift and the luminescence intensity decrease with x over 0.4. Combining crystal structure with PL spectrum, the distortion of dodecahedron and crystal field splitting of 5d level of Ce3+ are influenced by Ga3+ in octahedral coordination polyhedron rather than tetrahedron. The crystalline perfection and Ga3+ occupying the tetrahedron induce less garnet phase formation, more impurities and the 5d level located in the conductive bands, thus accounting for the x = 0.4 turning points of the PL and PLE intensity. Based on the thermal quenching and CIE, the Y3(GaxAl1-x)5O12: Ce3+0.06 phosphors have great potential for use on the w-LED.

  18. Improvement of photoluminescence properties and thermal stability of Y2.9Ce0.1Al5−xSixO12 phosphors with Si3N4 addition

    International Nuclear Information System (INIS)

    Zhang, Fangfang; Song, Kaixin; Jiang, Jun; Wu, Song; Zheng, Peng; Huang, Qingming; Xu, Junming; Qin, Huibin

    2014-01-01

    Highlights: • Y 2.9 Ce 0.1 Al 5−x Si x O 12 phosphors were prepared by solid-state reaction in reduced air ambience. • Si 4+ could be incorporated into the host lattice of Y 3 Al 5 O 12 through partial occupation of the Al 3+ sites. • Si 3 N 4 addition can improve photoluminescence efficiency and thermal stability of Y 3 Al 5 O 12 :Ce. - Abstract: A series of Si 3 N 4 doping Y 2.9 Ce 0.1 Al 5−x Si x O 123x/2 N 4x/3 phosphors were prepared by solid-state reaction in 95%N 2 –5%H 2 reduced air ambience. The XRD characteristics plus Rietveld refinement results shows that the as-sintered powders are unique crystal phase with the same crystal structure of Y 3 Al 5 O 12 (PDF No. 79-1891). The N element was not detected by the analysis of X-ray photoelectron spectroscopy (XPS) and energy dispersive X-ray spectrum (EDS). The photoluminescence spectra (PL and PLE) tests show that the exciting and emitting intensity of PLE and PL gradually increase due to the increase of Si 3 N 4 concentration. Meanwhile, the phosphorescence decay times are prolonged from 45 ns (x = 0) to 78 ns (x = 0.3), under the monitor of 530 nm wavelength. The thermoluminescence tests (TL) confirm the thermal stability of as-phosphors with Si 3 N 4 addition is much better than that of the pristine Y 2.9 Ce 0.1 Al 5 O 12 phosphors

  19. Luminescence and Energy Transfer in Lu3Al5O12 Scintillators Co-Doped with Ce3+ and Tb3+

    NARCIS (Netherlands)

    Ogiegło, J.M.; Zych, A.K.; Ivanovskikh, K.; Jüstel, T.; Ronda, R.C.; Meijerink, A.

    2012-01-01

    Lu3Al5O12 (LuAG) doped with Ce3+ is a promising scintillator material with a high density and a fast response time. The light output under X-ray or γ-ray excitation is, however, well below the theoretical limit. In this paper the influence of codoping with Tb3+ is investigated with the aim to

  20. Luminescence and defects creation in Ce3+-doped YAlO3 and Lu0.3Y0.7AlO3 crystals

    International Nuclear Information System (INIS)

    Blazek, K.; Nejezchleb, K.; Krasnikov, A.; Savikhina, T.; Zazubovich, S.; Nikl, M.

    2005-01-01

    Luminescence, energy transfer and defects creation processes were studied for the Ce 3+ -doped YAlO 3 and Lu x Y 1-x AlO 3 (x=0.3) crystals in the temperature range 4.2-300 K under selective photoexcitation in the energy range 3.5-11.5 eV. For the first time, defects creation spectra were measured and analyzed. Influence of the charge and ionic radii of co-doping ions on the luminescence and defects creation efficiency was considered. The origin of the defects created and possible mechanisms of their formation were discussed. (copyright 2005 WILEY-VCH Verlag GmbH and Co. KGaA, Weinheim) (orig.)

  1. Blue and green emission from Ce3+ and Tb3+ co-doped Y2O3 nanoparticles

    International Nuclear Information System (INIS)

    Loitongbam, Romeo Singh; Singh, W. Rameshwor; Phaomei, Ganngam; Singh, N. Shanta

    2013-01-01

    Tb 3+ doped Y 2 O 3 nanoparticles of 4–10 nm size were synthesized from nitrate precursors by the urea hydrolysis method in ethylene glycol medium at a low temperature of 140 °C. Characteristic green emission of Tb 3+ corresponding to 5 D 4 → 7 F J is observed to be very strong, which is further enhanced with heat treatment temperature. Characteristic blue color emission of Ce 3+ ion originating from 5d→ 2 F 7/2 (424 nm) and 2 F 5/2 (486 nm) transitions are found to be very strong in as-synthesized Ce 0.02 Tb 0.06 Y 1.92 O 3 nanoparticles. However, its luminescence intensity decreases with increase in heating temperature or increase in the particle size/crystallinity, whereas a weak emission peak of Tb 3+ ion at 545 nm is witnessed. The polycrystalline nature of the as-prepared sample changed to highly crystalline state when heated at an elevated temperature (1200 °C). -- Highlights: • Y 2 O 3 nanoparticles doped with Tb 3+ and Ce 3+ of 4–10 nm are synthesized. • Strong green emission of Tb 3+ from 5 D 4 → 7 F J transition is observed. • Strong blue emission of Ce 3+ from 5d→ 2 F 7/2 and 2 F 5/2 transitions is observed. • Ce 3+ emission decreases with annealing or increase in particle size. • Such nanoparticles can be used in LEDs and bio-labeling

  2. Study on preparation of orange-emitting phosphor Y3Mg2AlSi2O12: Ce3+ for wLED

    Directory of Open Access Journals (Sweden)

    Yan Shirun

    2017-12-01

    Full Text Available Ce3+-doped garnet-structured orange-emitting phosphor Y3Mg2AlSi2O12:Ce3+ was prepared by sol-gel combustion using urea as a fuel.Effects of the reduction temperature,Ce3+ doping concentration on the structure,morphology,and photoluminescence property of the as-prepared phosphor were investigated by X-ray diffraction(XRD,scaning electron microscope(SEM,photoluminescence spectroscopy and UV-Vis reflection spectroscopy.The crystallinities,morphologies,and photoluminescence properties of the phosphors prepared by sol-gel combustion and solid-state reaction were compared.The reasons causing different performance of the phosphors were discussed.

  3. Ethanol Sensor of CdO/Al2O3/CeO2 Obtained from Ce-DOPED Layered Double Hydroxides with High Response and Selectivity

    Science.gov (United States)

    Xu, Dongmei; Guan, Meiyu; Xu, Qinghong; Guo, Ying; Wang, Yao

    2013-04-01

    In this paper, Ce-doped CdAl layered double hydroxide (LDH) was first synthesized and the derivative CdO/Al2O3/CeO2 composite oxide was prepared by calcining Ce-doped CdAl LDH. The structure, morphology and chemical state of the Ce doped CdAl LDH and CdO/Al2O3/CeO2 were also investigated by X-ray diffraction (XRD), Fourier transform infrared (FT-IR), solid state nuclear magnetic resonance (SSNMR), scanning electron microscope (SEM) and X-ray photoelectron spectroscopy (XPS). The gas sensing properties of CdO/Al2O3/CeO2 to ethanol were further studied and compared with CdO/Al2O3 prepared from CdAl LDH, CeO2 powder as well as the calcined Ce salt. It turns out that CdO/Al2O3/CeO2 sensor shows best performance in ethanol response. Besides, CdO/Al2O3/CeO2 possesses short response/recovery time (12/72 s) as well as remarkable selectivity in ethanol sensing, which means composite oxides prepared from LDH are very promising in gas sensing application.

  4. Photostimulated luminescence and defects creation processes in Ce{sup 3+}-doped epitaxial films of multicomponent Lu{sub 3−x}Gd{sub x}Ga{sub y}Al{sub 5y}O{sub 12} garnets

    Energy Technology Data Exchange (ETDEWEB)

    Babin, V. [Institute of Physics AS CR, Cukrovarnicka 10, 16253 Prague (Czech Republic); Chernenko, K. [Peter the Great Saint-Petersburg Polytechnic University, Polytekhnicheskaya 29, 195251 St. Petersburg (Russian Federation); Kučera, M. [Charles University, Faculty of Mathematics and Physics, Ke Karlovu 5, 12116 Prague (Czech Republic); Nikl, M. [Institute of Physics AS CR, Cukrovarnicka 10, 16253 Prague (Czech Republic); Zazubovich, S., E-mail: svea@ut.ee [Institute of Physics, University of Tartu, Ravila 14c, 50411 Tartu (Estonia)

    2016-11-15

    Luminescence characteristics of epitaxial films of Ce{sup 3+}-doped multicomponent garnets of the type of Lu{sub 3−x}Gd{sub x}Ga{sub y}Al{sub 5y}O{sub 12}, where x varies from 0.14 to 3 and y varies from 0 to 3.54, are investigated in the 4.2–400 K temperature range by the steady-state and time-resolved spectroscopy methods. Their dependence on the film composition is clarified. The presence in the same film of different Ce{sup 3+}-related luminescence centers is revealed, and a possible structure of these centers is discussed. The processes of the electron and hole centers creation under irradiation of the films in the Ce{sup 3+}-related absorption bands are studied by thermally stimulated luminescence method. The location of the excited 5d{sub 1} level of Ce{sup 3+} with respect to the bottom of the conduction band and the origin and thermal stability parameters of electron traps in the epitaxial films and in the single crystals of the same composition are found to be different.

  5. Effects of flux additives on the characteristics of Y2.95Al5O12:0.05Ce3+ phosphor: Particle growth mechanism and luminescence

    International Nuclear Information System (INIS)

    Chiang, Chung-Hao; Liu, Te-Hsing; Lin, Han-Yu; Kuo, Hung-Yi; Chu, Sheng-Yuan

    2013-01-01

    The dependence of the amount of the BaF 2 flux additive on the luminescence of Y 2.95 Al 5 O 12 :0.05Ce 3+ phosphors was investigated. The integrated emission intensity of Y 2.95 Al 5 O 12 :0.05Ce 3+ prepared without the flux was enhanced by 29% with the addition of BaF 2 flux at the optimum amount of 6 wt. %. Such an enhancement can be attributed to the purer phase of Y 3 Al 5 O 12 and the morphology change from the irregular shape to spherical shape with the smoother surface due to the flux. The morphology and luminescence of Y 2.95 Al 5 O 12 :0.05Ce 3+ prepared with the 6 wt. % BaF 2 flux additive (Sample II) were further compared with those of Y 2.95 Al 5 O 12 :0.05Ce 3+ prepared with the 7 wt. % H 3 BO 3 flux additive (Sample I). The particle size, particle shape, and integrated emission intensity (λ ex  = 450 nm) of the former were found to be larger, more regular, and 6% higher than those of the latter. The difference in the morphology of Samples I and II, which led to the difference in the emission intensity and the external quantum efficiency, were well explained by the particle growth mechanism

  6. Luminescence of Eu:Y3Al5O12, Eu:Lu3Al5O12, and Eu:GdAlO3 Nanocrystals Synthesized by Solution Combustion

    Science.gov (United States)

    Vilejshikova, E. V.; Khort, A. A.; Podbolotov, K. B.; Loiko, P. A.; Shimanski, V. I.; Shashkov, S. N.; Yumashev, K. V.

    2017-11-01

    Nanocrystals of rare-earth garnets Y3Al5O12 and Lu3Al5O12 and perovskite GdAlO3 highly doped (10-20 at%) with Eu3+ are synthesized by the solution combustion technique and subsequent annealing in air at 800 and 1300oC. Their structure, morphology, and phase composition are studied. These materials exhibit intense red luminescence under UV excitation. Eu:GdAlO3 luminescence has CIE 1931 color coordinates (0.632, 0.368); dominant wavelength, 599.6 nm; and color purity, >99%. Judd-Ofelt parameters, luminescence branching ratios, and lifetimes of the Eu3+ 5D0 state are determined. The luminescence quantum yield for Eu:GdAlO3 (10 at%) reaches 74% with a lifetime of 1.4 ms for the 5D0 state. The synthesized materials are promising for red ceramic phosphors.

  7. Improvement of photoluminescence properties and thermal stability of Y{sub 2.9}Ce{sub 0.1}Al{sub 5−x}Si{sub x}O{sub 12} phosphors with Si{sub 3}N{sub 4} addition

    Energy Technology Data Exchange (ETDEWEB)

    Zhang, Fangfang [College of Electronic Information and Engineering, Hangzhou Dianzi University, Hangzhou 310018 (China); Song, Kaixin, E-mail: kxsong@hdu.edu.cn [College of Electronic Information and Engineering, Hangzhou Dianzi University, Hangzhou 310018 (China); Jiang, Jun [Ningbo Institute of Materials Technologies and Engineering, Chinese Academy of Sciences, Ningbo 315201 (China); Wu, Song; Zheng, Peng [College of Electronic Information and Engineering, Hangzhou Dianzi University, Hangzhou 310018 (China); Huang, Qingming [Instrument Analysis and Testing Center, Fuzhou University, Fuzhou 350002 (China); Xu, Junming; Qin, Huibin [College of Electronic Information and Engineering, Hangzhou Dianzi University, Hangzhou 310018 (China)

    2014-12-05

    Highlights: • Y{sub 2.9}Ce{sub 0.1}Al{sub 5−x}Si{sub x}O{sub 12} phosphors were prepared by solid-state reaction in reduced air ambience. • Si{sup 4+} could be incorporated into the host lattice of Y{sub 3}Al{sub 5}O{sub 12} through partial occupation of the Al{sup 3+} sites. • Si{sub 3}N{sub 4} addition can improve photoluminescence efficiency and thermal stability of Y{sub 3}Al{sub 5}O{sub 12}:Ce. - Abstract: A series of Si{sub 3}N{sub 4} doping Y{sub 2.9}Ce{sub 0.1}Al{sub 5−x}Si{sub x}O{sub 123x/2}N{sub 4x/3} phosphors were prepared by solid-state reaction in 95%N{sub 2}–5%H{sub 2} reduced air ambience. The XRD characteristics plus Rietveld refinement results shows that the as-sintered powders are unique crystal phase with the same crystal structure of Y{sub 3}Al{sub 5}O{sub 12} (PDF No. 79-1891). The N element was not detected by the analysis of X-ray photoelectron spectroscopy (XPS) and energy dispersive X-ray spectrum (EDS). The photoluminescence spectra (PL and PLE) tests show that the exciting and emitting intensity of PLE and PL gradually increase due to the increase of Si{sub 3}N{sub 4} concentration. Meanwhile, the phosphorescence decay times are prolonged from 45 ns (x = 0) to 78 ns (x = 0.3), under the monitor of 530 nm wavelength. The thermoluminescence tests (TL) confirm the thermal stability of as-phosphors with Si{sub 3}N{sub 4} addition is much better than that of the pristine Y{sub 2.9}Ce{sub 0.1}Al{sub 5}O{sub 12} phosphors.

  8. Thermoluminescence and optically stimulated luminescence properties of nanocrystalline Er3+ and Yb3+ doped Y3Al5O12 exposed to β-rays

    International Nuclear Information System (INIS)

    RodrIguez, R A; Rosa, E de la; Salas, P; Melendrez, R; Barboza-Flores, M

    2005-01-01

    The thermoluminescence (TL) and optically stimulated luminescence (OSL) characterization of Er 3+ and Yb 3+ doped Y 3 Al 5 O 12 nanocrystalline samples prepared by the precipitation process and exposed to β-rays are discussed. The TL as well as the OSL were two orders of magnitude higher in Er 3+ doped than in Yb 3+ specimens. The charge trapping and the radiative thermally stimulated recombination processes in Y 3 Al 5 O 12 : Er 3+ involve four trapping states at 166, 243, 342 and 424 deg. C, but just two trapping levels at 219 and 413 deg. C for Y 3 Al 5 O 12 : Yb 3+ at a heating rate of 10 deg. C s -1 . The photostimulation with 470 nm light causes in both phosphors a radiative recombination of the optically free charge carriers belonging to the same trapping states. The TL and the OSL as a function of radiation dose behaviour were linear in the 10-100 Gy dose range. The results provide evidence of the potential uses of these materials in radiation storage and dosimeter devices

  9. Site occupancy and magnetic study of Al3+ and Cr3+ co-substituted Y3Fe5O12

    International Nuclear Information System (INIS)

    Bouziane, K.; Yousif, A.; Widatallah, H.M.; Amighian, J.

    2008-01-01

    Single-phased polycrystalline Y 3 Fe 5-2x Al x Cr x O 12 garnet samples (x=0, 0.2, 0.4 and 0.6) have been prepared by the conventional ceramic technique. Rietveld refinement of X-ray diffraction patterns of the samples shows them to crystallize in the Ia3d space group and the corresponding lattice constant to decrease with increasing Al 3+ and Cr 3+ contents (x). Moessbauer results indicate that Cr 3+ substitutes for Fe 3+ at the octahedral sites whilst Al 3+ essentially replaces Fe 3+ at the tetrahedral sites. This result indicates that co-doping of Y 3 Fe 5 O 12 does not affect the preferential site occupancy for separate individual substitution of either Cr 3+ or Al 3+ . The magnetization measurements reveal that the Curie temperature (T c ) monotonically decreases with increasing x while the magnetic moment per unit formula decreases up to x=0.4 and then slightly increases for x=0.6. This reflects a progressive weakening of the ferrimagnetic exchange interaction between the Fe 3+ ions at octahedral and tetrahedral sites due to co-substitution. The magnetic moment was calculated using the cations distribution inferred from the Moessbauer data and the collinear ferrimagnetic model, and was found to agree reasonably with the experimentally measured value. The phenomenological amplitude crossover, characterized by the temperature T*, has also been observed in the doped YIG and briefly discussed

  10. Luminescence characteristics of Pb2+ centres in undoped and Ce3+-doped Lu3Al5O12 single-crystalline films and Pb2+→Ce3+ energy transfer processes

    International Nuclear Information System (INIS)

    Babin, V.; Gorbenko, V.; Makhov, A.; Mares, J.A.; Nikl, M.; Zazubovich, S.; Zorenko, Yu.

    2007-01-01

    At 4.2-350 K, the steady-state and time-resolved emission and excitation spectra and luminescence decay kinetics were studied under excitation in the 2.5-15 eV energy range for the undoped and Ce 3+ -doped Lu 3 Al 5 O 12 (LuAG) single-crystalline films grown by liquid phase epitaxy method from the PbO-based flux. The spectral bands arising from the single Pb 2+ -based centres were identified. The processes of energy transfer from the host lattice to Pb 2+ and Ce 3+ ions and from Pb 2+ to Ce 3+ ions were investigated. Competition between Pb 2+ and Ce 3+ ions in the processes of energy transfer from the LuAG crystal lattice was evidenced especially in the exciton absorption region. Due to overlap of the 3.61 eV emission band of Pb 2+ centres with the 3.6 eV absorption band of Ce 3+ centres, an effective nonradiative energy transfer from Pb 2+ ions to Ce 3+ ions takes place, resulting in the appearance of slower component in the luminescence decay kinetics of Ce 3+ centres and decrease of the Ce 3+ -related luminescence intensity

  11. Color-tunable and luminescence properties of phosphors of Ce{sup 3+} and Tb{sup 3+} co-doped La{sub 5}Si{sub 3}O{sub 12}N for UV w-LEDs

    Energy Technology Data Exchange (ETDEWEB)

    Deng, Junru; Chen, Jian; Liu, Yangai, E-mail: liuyang@cugb.edu.cn

    2016-02-15

    A series of Ce{sup 3+}, Tb{sup 3+} and Ce{sup 3+}/Tb{sup 3+} co-doped in La{sub 5}Si{sub 3}O{sub 12}N phosphors were synthesized by conventional high temperature solid state reaction method. With the increase of Tb{sup 3+}, the green emission was realized in (La{sub 0.94−y}Ce{sub 0.06}Tb{sub y}){sub 5}Si{sub 3}O{sub 12}N phosphors on the basis of the efficient energy transfer from Ce{sup 3+} to Tb{sup 3+} with an efficiency (η{sub T}) over 58.72%. The room temperature PL decay curves of the Ce{sup 3+} ions in (La{sub 0.94−y}Ce{sub 0.06}Tb{sub y}){sub 5}Si{sub 3}O{sub 12}N phosphors monitored at 460 nm with an excitation at 365 nm indicated that the energy transfer process between Ce{sup 3+} and Tb{sup 3+} indeed took place. The CIE chromaticity diagrams for (La{sub 0.94−y}Ce{sub 0.06}Tb{sub y}){sub 5}Si{sub 3}O{sub 12}N phosphors were also observed, which shows the color tuned from blue to blue-greenish to green with the increase of Tb{sup 3+} concentration from 0.01 to 0.08. These results demonstrated that Tb{sup 3+} ion with low 4f–4f absorption efficiency in near UV region can play the role of an activator in narrow green-emitting phosphor through efficient energy feeding by allowing 4f–5d absorption of Ce{sup 3+} with high oscillator strength. All the results indicated that the Ce{sup 3+} and Tb{sup 3+} activated La{sub 5}Si{sub 3}O{sub 12}N phosphor may be good candidates for blue-green components in n-UV white LEDs. - Highlights: • A series of Ce{sup 3+}, Tb{sup 3+} and Ce{sup 3+}/Tb{sup 3+} co-doped in La{sub 5}Si{sub 3}O{sub 12}N phosphors were synthesized by high temperature solid state reaction method. • The green emission was realized in (La{sub 0.94−y}Ce{sub 0.06}Tb{sub y})Si{sub 3}O{sub 12}N phosphors on the basis of the highly efficient energy transfer. • The Ce{sup 3+} and Tb{sup 3+} activated La{sub 5}Si{sub 3}O{sub 12}N phosphor may be good candidates for blue-green components in n-UV white LEDs.

  12. Luminescence and color center distributions in K3YB6O12:Ce3+ phosphor

    International Nuclear Information System (INIS)

    Yang, Li; Wan, Yingpeng; Weng, Honggen; Huang, Yanlin; Chen, Cuili; Seo, Hyo Jin

    2016-01-01

    Polycrystalline Ce 3+ -doped K 3 YB 6 O 12 (1–14 mol%) phosphors were prepared by facile chemical sol–gel synthesis. The phase formation of the phosphors was confirmed by x-ray powder diffraction (XRD) analysis. The photoluminescence excitation spectra (PLE), emission spectra (PL) and the luminescence decay curves were tested. Under the near-UV light, the phosphors present the emission from blue color to yellowish green due to the allowed 4 f  –5 d transitions of Ce 3+ ions. The absolute quantum efficiency (QE) of K 3 YB 6 O 12 :Ce 3+ can reach 53% under the excitation of near-UV light. The luminescence thermal quenching of the phosphor was investigated by the temperature-dependent spectra. The crystallographic site of Ce 3+ ions in the lattice was identified and discussed on the basis of luminescence characteristics and structural data. There is only one isolated Ce 3+ center occupying the Y(II) sites in the lightly doped samples presenting a typical doublet emission profile. While the Ce 3+ multi-centers could be created with the enhancement of the doping levels, which could induce the distinct red-shift of the spectra due to the dipole–dipole interactions. The result in this work could be useful for the further investigation of other rare earth ions in this host. (paper)

  13. Towards Bright and Fast Lu3Al5O12:Ce,Mg Optical Ceramics Scintillators

    CERN Document Server

    Liu, Shuping; Feng, Xiqi; Vedda, Anna; Fasoli, Mauro; Shi, Yun; Kou, Huamin; Beitlerova, Alena; Wu, Lexiang; D'Ambrosio, Carmelo; Pan, Yubai; Nikl, Martin

    2016-01-01

    The recent advent of Lu 3 Al 5 O 12 :Ce optical ceramics marks a turning point in scintillator material technology. Because of their lower preparation tem-perature, brightness, and robustness such materials can now compete with single crystals. Their further scintillation effi ciency optimization includes the thorough control of the defects responsible for optical and scintillation losses. The choice of sintering agent appears critical to achieve both high optical transparency and scintillation performance. In this work, the optical investi-gations coupled with X-ray absorption near-edge spectroscopy evidence the benefi cial role of MgO sintering agent. Mg 2+ co-dopants in ceramics drive the partial conversion of Ce 3+ to Ce 4+ . The Ce 4+ center, however, does not impair the scintillation performance due to its capability to positively infl uence the scintillation process. The importance of simultaneous application of such co-doping and annealing treatment is also demonstrated. With 0.3 at% Mg, our cer...

  14. Absorption intensities and emission cross sections of principal intermanifold and inter-Stark transitions of Er3+(4f 11) in polycrystalline ceramic garnet Y3Al5O12

    International Nuclear Information System (INIS)

    Sardar, Dhiraj K.; Russell, Charles C. III; Gruber, John B.; Allik, Toomas H.

    2005-01-01

    A comparative spectroscopic study is performed on Er 3+ (4f 11 ) ions doped in polycrystalline ceramic garnet Y 3 Al 5 O 12 (YAG) and single-crystal laser rod, both containing nominal 50 at. % of Er 3+ . The standard Judd-Ofelt (JO) model is applied to the room-temperature absorption intensities of Er 3+ (4f 11 ) transitions in both hosts to obtain the phenomenological intensity parameters. These parameters are subsequently used to determine the radiative decay rates, radiative lifetimes, and branching ratios of the Er 3+ transitions from the upper multiplet manifolds to the corresponding lower-lying multiplet manifolds 2S+1 L J of Er 3+ (4f 11 ) in these garnet hosts. The emission cross sections of the intermanifold Er 3+ 4 I 13/2 → 4 I 15/2 (1.5 μm) transition as well as the principal inter-Stark transition Y 1 →Z 4 (1550 nm) within the corresponding multiplet manifolds have been determined. The room-temperature fluorescence lifetimes of the 4 I 13/2 → 4 I 15/2 (1.5 μm) transition in both polycrystalline ceramic and single-crystal YAG samples were measured. From the radiative lifetimes determined from the JO model and the measured fluorescence lifetimes, the quantum efficiencies for both samples were determined. The comparative study of Er 3+ (4f 11 ) ions performed suggests that polycrystalline ceramic YAG is an excellent alternative to single-crystal YAG rod for certain applications

  15. Synthesis and luminescent study of Ce3+-doped terbium–yttrium aluminum garnet

    International Nuclear Information System (INIS)

    Dotsenko, V.P.; Berezovskaya, I.V.; Zubar, E.V.; Efryushina, N.P.; Poletaev, N.I.; Doroshenko, Yu.A.; Stryganyuk, G.B.; Voloshinovskii, A.S.

    2013-01-01

    Highlights: ► Ce 3+ -doped garnets (TYAG) were prepared using nanostructured reagents. ► The Ce 3+ ions cause a very efficient yellow emission of the samples. ► The reasons for the long wavelength position of this emission are discussed. ► Contribution from Al atoms to the conduction band of TYAG is quite essential. - Abstract: Terbium–yttrium aluminum garnets (TYAG) doped with Ce 3+ ions have been prepared by solid state reactions between nanostructured oxides of aluminum and rare earths. The luminescent properties of Ce 3+ ions in (Tb 0.8 Y 0.2 ) 3(1−x) Ce 3x Al 5 O 12 (x = 0.03) have been studied upon excitation in the 2–20 eV region. The substitution of Tb 3+ for Y 3+ in the garnet structure results in broadening the emission band and shifting its maximum towards the longer wavelengths. It was found that in addition to the 4f n → 4f n−1 5d excitation bands of Ce 3+ and Tb 3+ ions, the excitation spectra for the Ce 3+ emission contain broad bands at 6.73 and ∼9.5 eV. These bands are attributed to the Ce 3+ -bound exciton formation and O 2p → Al 3s, 3p transitions, respectively. In contrast to the predictions based on the results of electronic structure calculations on Y 3 Al 5 O 12 and Tb 4 Al 2 O 9 , the threshold of interband transitions in TYAG is at high energies (⩾7.3 eV), and contributions from Al tetr and Al oct atoms to the conduction-band density of states are evaluated as quite essential.

  16. Doping of Czochralski-grown bulk β-Ga2O3 single crystals with Cr, Ce and Al

    Science.gov (United States)

    Galazka, Zbigniew; Ganschow, Steffen; Fiedler, Andreas; Bertram, Rainer; Klimm, Detlef; Irmscher, Klaus; Schewski, Robert; Pietsch, Mike; Albrecht, Martin; Bickermann, Matthias

    2018-03-01

    We experimentally evaluated segregation of Cr, Ce and Al in bulk β-Ga2O3 single crystals grown by the Czochralski method, as well as the impact of these dopants on optical properties. The segregation of Cr and Ce and their incorporation into the β-Ga2O3 crystal structure strongly depends on O2 concentration in the growth atmosphere which has a noticeable impact on decomposition of Ga2O3 and Cr2O3, as well as on the charge state of Cr and Ce. Effective segregation coefficients for Cr are in the range of 3.1-1.5 at 7-24 vol% O2, while for Ce they are roughly below 0.01 at 1.5-34 vol% O2. The effective segregation coefficient for Al is 1.1 at 1.5-21 vol% O2. Both dopants Ce and Al have a thermodynamically stabilizing effect on β-Ga2O3 crystal growth by supressing decomposition. While Ce has no impact on the optical transmittance in the ultraviolet and visible regions, in Cr doped crystals we observe three absorption bands due to Cr3+ on octahedral Ga sites, one in the ultraviolet merging with the band edge absorption of β-Ga2O3 and two in the visible spectrum, for which we estimate the absorption cross sections. Al doping also does not induce dopant related absorption bands but clearly shifts the absorption edge as one expects for a solid-solution crystal Ga2(1-x)Al2xO3 still in the monoclinic phase. For the highest doping concentration (Ga1.9Al0.1O3) we estimate an increase of the energy gap by 0.11 eV.

  17. Site occupancy and magnetic study of Al{sup 3+} and Cr{sup 3+} co-substituted Y{sub 3}Fe{sub 5}O{sub 12}

    Energy Technology Data Exchange (ETDEWEB)

    Bouziane, K. [Department of Physics, College of Science, Sultan Qaboos University, P.O. Box 36, PC 123, Muscat, Sultanate of Oman (Oman)], E-mail: bouzi@squ.edu.om; Yousif, A.; Widatallah, H.M. [Department of Physics, College of Science, Sultan Qaboos University, P.O. Box 36, PC 123, Muscat, Sultanate of Oman (Oman); Amighian, J. [Department of Physics, University of Isfahan, Isfahan (Iran, Islamic Republic of)

    2008-10-15

    Single-phased polycrystalline Y{sub 3}Fe{sub 5-2x}Al{sub x}Cr{sub x}O{sub 12} garnet samples (x=0, 0.2, 0.4 and 0.6) have been prepared by the conventional ceramic technique. Rietveld refinement of X-ray diffraction patterns of the samples shows them to crystallize in the Ia3d space group and the corresponding lattice constant to decrease with increasing Al{sup 3+} and Cr{sup 3+} contents (x). Moessbauer results indicate that Cr{sup 3+} substitutes for Fe{sup 3+} at the octahedral sites whilst Al{sup 3+} essentially replaces Fe{sup 3+} at the tetrahedral sites. This result indicates that co-doping of Y{sub 3}Fe{sub 5}O{sub 12} does not affect the preferential site occupancy for separate individual substitution of either Cr{sup 3+} or Al{sup 3+}. The magnetization measurements reveal that the Curie temperature (T{sub c}) monotonically decreases with increasing x while the magnetic moment per unit formula decreases up to x=0.4 and then slightly increases for x=0.6. This reflects a progressive weakening of the ferrimagnetic exchange interaction between the Fe{sup 3+} ions at octahedral and tetrahedral sites due to co-substitution. The magnetic moment was calculated using the cations distribution inferred from the Moessbauer data and the collinear ferrimagnetic model, and was found to agree reasonably with the experimentally measured value. The phenomenological amplitude crossover, characterized by the temperature T*, has also been observed in the doped YIG and briefly discussed.

  18. Synthesis, Characterization and Sonocatalytic Activity of Co/N/Er3+ : Y3Al5O12 /TiO2 Film for the Degradation of Organic Dyes

    Directory of Open Access Journals (Sweden)

    Wang L.

    2015-07-01

    Full Text Available The sonocatalytic degradation of organic dyes (C.I. 50040, C.I. Reactive Red 1, C.I. Acid Orange 7 catalysed by Co/N/Er3+ : Y3Al5O12/TiO2 films was studied. For the preparation of Co/N/Er3+ : Y3Al5O12/TiO2 films, the sol-gel coating process was used. The phase composition, morphology, precursor at different temperatures and emitting light properties of the calcined powders were analysed by X-ray diffraction (XRD, absorption spectra and upconversion emission spectra. The X-ray diffraction of powder samples of Co/N/Er3+ : Y3Al5O12/TiO2 took on anatase mine peaks and upconversion luminous agent, respectively. Analysis of absorption spectra of amorphous Co/N/Er3+ : Y3Al5O12/TiO2 showed that doping N stretching vibration peak of water or hydroxyl adsorption, Co2+ ion had very strong absorption in 1.0–1.7 μm wavelength range, the transition luminescence of Er3+ ions was just on Co2+ ions absorption band. The emission spectrum indicated that Co/N/Er3+ : Y3Al5O12/TiO2 could launch green 500–560 nm and red 650–700 nm, 525, 550 and 660 nm peaks corresponding to 2H11/2, 4S3/2 → 4I15/2 and 4H9/2 → 4I15/2 transition of Er3+. Doping Co and N enhanced the upconversion luminescence and absorption effect. Sonocatalytic degradation effect of organic dyes loading Co/N/Er3+ : Y3Al5O12/TiO2 was better when ultrasonic intensity was equal to 15 W cm–2. The degradation ratios of aqueous solutions of these three kinds of organic dyes by ultrasonic irradiation were obviously lower than by ultrasonic irradiation together with Co/N/Er3+ : Y3Al5O12/TiO2 films in the same conditions. Degradation kinetics of organic dyes by ultrasonic irradiation and by ultrasonic irradiation cooperating with Co/N/Er3+ : Y3Al5O12/TiO2 films followed the first-order reaction.

  19. Synthesis and effect of Ce and Mn co-doping on photoluminescence characteristics of Ca6AlP5O20:Eu novel phosphors.

    Science.gov (United States)

    Shinde, K N; Dhoble, S J

    2013-01-01

    A series of Ca6AlP5O20 doped with rare earths (Eu and Ce) and co-doped (Eu, Ce and Eu,Mn) were prepared by combustion synthesis. Under Hg-free excitation, Ca6AlP5O20:Eu exhibited Eu(2+) (486 nm) emission in the blue region of the spectrum and under near Hg excitation (245 nm), Ca6AlP5O20:Ce phosphor exhibited Ce(3+) emission (357 nm) in the UV range. Photoluminescence (PL) peak intensity increased in Ca6AlP5O20:Eu,Ce and Ca6AlP5O20:Eu, Mn phosphors due to co-activators of Ce(3+) and Mn(2+) ions. As a result, these ions played an important role in PL emission in the present matrix. Ca6AlP5O20:Eu, Ce and Ca6AlP5O20:Eu, Mn phosphors provided energy transfer mechanisms via Ce(3+) → Eu(2+) and Eu(2+) → Mn(2+), respectively. Eu ions acted as activators and Ce ions acted as sensitizers. Ce emission energy was well matched with Eu excitation energy in the case of Ca6AlP5O20:Eu, Ce and Eu ions acted as activators and Mn ions acted as sensitizers in Ca6AlP5O20:Eu, Mn. This study included synthesis of new and efficient phosphate phosphors. The impact of doping and co-doping on photoluminescence properties and energy transfer mechanisms were investigated and we propose a feasible interpretation. Copyright © 2012 John Wiley & Sons, Ltd.

  20. Luminescence and defects creation in Ce3+-doped aluminium and lutetium perovskites and garnets

    International Nuclear Information System (INIS)

    Krasnikov, A.; Savikhina, T.; Zazubovich, S.; Nikl, M.; Mares, J.A.; Blazek, K.; Nejezchleb, K.

    2005-01-01

    Luminescence, scintillation response, energy transfer and defect creation processes were studied at 4.2-300K for Ce 3+ -doped YAlO 3 , Lu x Y 1-x AlO 3 (x=0.3) and Lu 3 Al 5 O 12 crystals under excitation in the 2.5-11.5eV energy range. Influence of the charge and ionic radius of co-doping ions on the efficiency of these processes, the origin of the defects created and possible mechanisms of their formation were discussed

  1. Relaxation electron excitations in Al2O3, Y3Al5O12 and YAlO3

    International Nuclear Information System (INIS)

    Kuznetsov, A.I.; Namozov, B.R.; Myurk, V.V.

    1985-01-01

    Excitation spectra of short-wave Al 2 O 3 , YAlO 3 and Y 3 Al 5 O 12 crystal luminescence, cathodoluminescence (including time resolution) and lay-temperature thermoluminescence are investigated. Analysis of experimental data permits to distingnish among these objects pairs of bands of supposedly characteristic luminescences: 7.5 and 3.8 eV (Al 2 O 3 ), 5.9 and 4.2 eV (YAlO 3 ), and 4.9 and 4.2 eV (Y 3 Al 5 O 12 ), where recombination luminescence is characteristic for long-wave ones, at that time exciton-like luminescence - for short-wave ones. A hypothesis about strong difference between states of an autolocalized exciton and ''autolocalized hole + electron'' (responsible for short-wave and long-wave bands of characteristic luminescence) is expressed; the difference is based on their genetic origin from different regions of a valent zone (in particular, long-wave bands - from the subzone of heavy holes of a valent zone ceiling, originating from nonbinding 2p-orbitals of oxygen)

  2. [Synthesis and characterization of chromium doped Y3Al5O12 compound pigment].

    Science.gov (United States)

    Yue, Shi-Juan; Su, Xiao; Jiang, Han-Jie; Liu, Shao-Xuan; Hong, You-Li; Zhang, Kai; Huang, Wan-Xias; Xiong, Zu-Jiang; Zhao, Ying; Liu, Cui-Ge; Wei, Yong-Ju; Meng, Tao; Xu, Yi-Zhuang; Wu, Jin-Guang

    2012-09-01

    The authors synthesized a new kind of green pigment via co-precipitation method by doping Y3Al5O12 with Cr+. The size of the pigment particles is around 200 nm as observed under scanning electron microscope. XRD results demonstrate that the pigment crystalline form of the pigment is yttrium alluminium garnet. UV-Vis spectra were used to investigate the coordination states and transition behavior of the doping ions. In addition, the colour feature was measured by CIE L* a* b* chroma value. The pigment was blended with polypropylene and then polypropylene fiber was produced using the polypropelene-pigment composite via molten spinning process. The distribution of the pigment particles in the polypropylene fibers was characterized by Xray computed tomography (CT) technique on the Beijing synchrotron radiation facility. The result states that the composite oxide pigment particles are homogeneously dispersed in the polypropylene fibers. The pigments are stable, non-toxic to the environment, and may be applied in non-aqueous dyeing to reduce waste water emitted by textile dyeing and printing industry.

  3. Tunable emission in Ln3+ (Ce3+/Dy3+, Ce3+/Tb3+) doped KNa3Al4Si4O16 phosphor synthesized by combustion method

    Science.gov (United States)

    Kolte, M. M.; Pawade, V. B.; Bhattacharya, A. B.; Dhoble, S. J.

    2018-05-01

    Ln3+ (Ln = Ce3+/Dy3+, Ce3+/Tb3+) doped KNa3Al4Si4O16 phosphor has been synthesized by Combustion method (CS) at 550° C successfully. Ln3+ (Ln = Ce3+, Dy3+, Tb3+) ions when doped in KNa3Al4Si4O16 host lattice, it shows blue and green emission band under the near Ultraviolet (NUV) excitation wavelength. The Photoluminescence excitation (PLE) and emission spectra are observed due to f-f and d-f transition of rare earth ions. Also, an effective energy transfer (ET) study from Ce3+ → Dy3+ and Ce3+ → Tb3+ ions has been studied and confirmed on the basis of Dexter-Foster theory. Further synthesized phosphor is well characterized by XRD, SEM, TEM and decay time measurement. However, the analysis of crystallite size, lattice strain has been studied by using theoretical as well as experimental techniques. Hence, the observed tunable emission in Ln3+ doped KNa3Al4Si4O16 phosphor may be applicable for solid state lighting technology.

  4. Aerosol synthesis and characterization of nanostructured particles of Y3Al5O12:Ce3+ and Y2O3:Eu3+

    Directory of Open Access Journals (Sweden)

    Marinković Katarina R.

    2007-01-01

    Full Text Available Nanostructured YAG:Ce3+ and Y2O3:Eu3+ were synthesized by low temperature (320°C aerosol synthesis-LTAS and high temperature (900°C aerosol synthesis-HTAS, respectively. The synthesis included aerosol generation from a nitrate precursor solution by an ultrasonic atomizer (1.3 MHz. The obtained aerosol was introduced into a tubular flow reactor, using air as the carrier gas, where successively, on a droplet level, evaporation/drying, precipitation and thermolysis occurred. The obtained powders were collected and thermally treated at different temperatures (900-1200°C. The phase development and the morphology were investigated by the X-ray powder diffraction method (XRPD and scanning electron microscopy combined with energy dispersive spectrometry (SEM/EDS. Structural refinement was performed using the Rietveld method with the Fullprof and Koalariet programs. The average crystallite size for the Y2O3:Eu system was calculated using the Profit program. It was shown that 89 wt.% of Y3Ai5Oi2:Ce was obtained by annealing (1000°C/6 h the as prepared, amorphous powder, synthesized by the low temperature aerosol method (LTAS. High temperature spray pyrolysis (HTAS at 900°C led to the formation of the targeted cubic phase of Y2O3:Eu3+. The microstructural parameters of the asprepared samples of the Y2O3:Eu3+ system indicate the formation of nanostructures with crystallite size smallest than 20 nm. The substitution of luminescent centers (Ce3+, Eu3+ into a host lattice (YAG, Y2O3, respectively was confirmed by changes in the crystal lattice parameters. Also, it was shown in both systems that good morphological characteristics (non-a­gglomerated, spherical, submicron particles were obtained enabling improved luminescent characteristics.

  5. Lu{sub 3}(Al,Si){sub 5}(O,N){sub 12}:Ce{sup 3+} phosphors with broad emission band and high thermal stability for white LEDs

    Energy Technology Data Exchange (ETDEWEB)

    Liu, Jiaqing; Wang, Xiaojun; Xuan, Tongtong; Wang, Chunbo; Li, Huili, E-mail: hlli@phy.ecnu.edu.cn; Sun, Zhuo

    2015-02-15

    A yellow-orange emitting Lu{sub 3}Al{sub 5−x}Si{sub x}O{sub 12−x}N{sub x}:Ce{sup 3+} phosphor with excellent color rendering, high luminescent efficiency and high thermal stability was reported in this paper. It was synthesized by a conventional solid-state reaction method. The effect of Si{sup 4+}–N{sup 3−} incorporation on the optical properties of Lu{sub 3}Al{sub 5}O{sub 12}:Ce{sup 3+} phosphor was investigated and compared to YAG:Ce{sup 3+} with the same compositions. Similarly, the addition of α-Si{sub 3}N{sub 4} leads to a distinct redshift and broadening of photoluminescent spectrum, which is assigned to the increased covalency and crystal field strength caused by N{sup 3−}. Nevertheless, an excellent thermal stability and a higher integrated intensity presented by α-Si{sub 3}N{sub 4}-doped LuAG:Ce{sup 3+} are distinctive. Further, the emission intensity can be greatly enhanced by adding NaF flux. Finally, the white LED flat lamp with a CRI as high as 83 and a luminous efficiency of 85 lm/W is successfully realized by using a single LuAG-based oxynitride phosphor combined with a blue LED chip, which is completely feasible for general indoor illuminations to replace the traditional fluorescent or incandescent lamps. - Highlights: • Si{sub 3}N{sub 4}-doped LuAG:Ce{sup 3+} oxynitride phosphors were synthesized by a solid-state reaction. • The effect of Si{sup 4+}–N{sup 3−} incorporation on the optical properties was investigated. • The addition of Si{sub 3}N{sub 4} leads to an obvious redshift of the emission spectra. • Lu{sub 3}Al{sub 5−x}Si{sub x}O{sub 12−x}N{sub x}:Ce{sup 3+} shows an excellent thermal stability and a higher intensity. • A warm white LED with CRI=83 is achieved by a single oxynitride phosphor.

  6. RBS characterization of Al2O3 films doped with Ce and Mn

    International Nuclear Information System (INIS)

    Martinez-Martinez, R.; Rickards, J.; Garcia-Hipolito, M.; Trejo-Luna, R.; Martinez-Sanchez, E.; Alvarez-Fregoso, O.; Ramos-Brito, F.; Falcony, C.

    2005-01-01

    Rutherford backscattering (RBS) with 4 He energies from 2 to 6 MeV has been used to study the properties of thin amorphous photoluminescent Al 2 O 3 :Ce,Mn films grown by spray pyrolysis on Corning 7059 glass substrates. The source solutions were AlCl 3 , CeCl 3 and MnCl 2 dissolved in deionized water. Different molar concentrations (Ce 10%; Mn 1%, 3%, 5%, 7% and 10%) were investigated under the same deposition conditions at a substrate temperature of 300 deg. C. The RBS spectra show a homogeneous depth profile of both Ce and Mn within the films, and the measured quantities are consistent with the original solution concentrations. An important amount of Cl, which plays a significant role in luminescent properties, was detected, in both the doped and undoped samples

  7. Densification and mechanical properties of sintered Al{sub 2}O{sub 3}-Y{sub 3}Al{sub 5}O{sub 12} ceramic composite

    Energy Technology Data Exchange (ETDEWEB)

    Paneto, Flavio Jose; Pereira, Joaquim Lopes; Oliveira, Jean de Lima; Jesus Filho, Edson de; Silva, Leandro Anselmo da; Cabral, Ricardo de Freitas; Santos, Claudinei dos [Centro Universitario de Volta Redonda (UNIFOA), Volta Redonda, RJ (Brazil); Lima, Eduardo de Sousa [Institutlo Militar de Engenharia (IME), Rio de Janeiro, RJ (Brazil)

    2014-06-15

    In this work, Al{sub 2}O{sub 3}-Y{sub 3}Al{sub 5}O{sub 12} ceramic composites were developed with different proportions of Al{sub 2}O{sub 3}-Y{sub 3}Al{sub 5}O{sub 12}, which were mixed and compacted at different pressures of 40MPa to 100MPa, being consequently sintered at 1600 deg C-2h. The sintered samples were characterized by X-ray diffraction presenting α-Al{sub 2}O{sub 3} and Y{sub 3}Al{sub 5}O{sub 12} as crystalline phases. Samples with relative densities ranging from 78 to 80% and 87 to 91% were obtained depending on the composition and the compaction pressure used. The hardness values obtained were of 1010 to 1080HV and 370- 470HV, for mixes Al{sub 2}O{sub 3}-Y{sub 3}Al{sub 5}O{sub 12} having the composition with levels of 20 and 36.5wt.%, respectively. (author)

  8. Effect of Mg$^{2+}$ ions co-doping on timing performance and radiation tolerance of Cerium doped Gd$_{3}$Al$_{2}$Ga$_{3}$O$_{12}$ crystals

    CERN Document Server

    Lucchini, M.T.; Bohacek, P.; Gundacker, S.; Kamada, K.; Nikl, M.; Petrosyan, A.; Yoshikawa, A.; Auffray, E.

    2016-01-01

    Inorganic scintillators with high density and high light yield are of major interest for applications in medical imaging and high energy physics detectors. In this work, the optical and scintillation properties of Mg co-doped Ce:Gd3Al2Ga3O12 crystals, grown using Czochralski technique, have been investigated and compared with Ce:Gd3Al2Ga3O12 ones prepared with identical technology. Improvements in the timing performance of the Mg co-doped samples with respect to Ce:Gd3Al2Ga3O12 ones have been measured, namely a substantial shortening of the rise time and scintillation decay components and lower afterglow were achieved. In particular, a significantly better coincidence time resolution of 233 ps FWHM, being a fundamental parameter for TOF-PET devices, has been observed in Mg co-doped crystals. The samples have also shown a good radiation tolerance under high doses of γ-rays, making them suitable candidates for applications in harsh radiation environments, such as detectors at future collider experiments.

  9. Annealed Ce{sup 3+}-doped ZnO flower-like morphology synthesized by chemical bath deposition method

    Energy Technology Data Exchange (ETDEWEB)

    Koao, Lehlohonolo F., E-mail: koaolf@ufs.ac.za [Department of Physics, University of the Free State (Qwa Qwa campus), Private Bag X13, Phuthaditjhaba 9866 (South Africa); Dejene, Francis B.; Tsega, Moges [Department of Physics, University of the Free State (Qwa Qwa campus), Private Bag X13, Phuthaditjhaba 9866 (South Africa); Swart, Hendrik C. [Department of Physics, University of the Free State, P.O. Box 339, Bloemfontein 9300 (South Africa)

    2016-01-01

    We have successfully synthesized ZnO:xmol% Ce{sup 3+} (0≤x≤10 mol%) doped nanopowders via the chemical bath deposition method (CBD) technique at low temperature (80 °C) and annealed in air at 700 °C. The X-ray diffraction patterns showed that all the undoped and Ce-doped ZnO nanopowders have a hexagonal wurtzite polycrystalline structure with an average crystallite size of about 46 nm. Weak diffraction peaks related mainly to cerium oxide were also detected at higher concentrations of Ce{sup 3+} (x=5–10 mol%). The scanning electron microscopy study revealed that the nanopowder samples were assembled in flower-shaped undoped ZnO and pyramid-shaped Ce{sup 3+}-doped ZnO nanostructures. The UV–vis spectra showed that the absorption edges shifted slightly to the longer wavelengths with the increase in the Ce{sup 3+} ions concentration. Moreover, the photoluminescence (PL) results showed a relative weak visible emission for the Ce{sup 3+}-doped ZnO nanoparticles compared to the undoped ZnO. The effects of Ce{sup 3+}-doping on the structure and PL of ZnO nanopowders are discussed in detail.

  10. Thermoluminescence of LaAlO3 crystals doped with Eu and Ce - Dy ions exposed to ultraviolet and gamma radiation

    International Nuclear Information System (INIS)

    Oliveira, Vitor H.; Faria, Luiz O.; Silva, Edna S.

    2011-01-01

    Due to environmental problems such as degradation of the ozone layer and control of radiation levels in units of radiation, new dosimetric materials with high sensitivity for ultraviolet (UV) and gamma radiation are of great interest for applications in environmental dosimetry. In this context, this paper presents the results of a systematic investigation of the thermoluminescent (TL) response of LaAlO 3 crystals doped with different concentrations of trivalent optically active ions exposed to UV and gamma radiation doses. The work has been performed under a direct cooperation between the Institute of Inorganic Chemistry in Moscow (IGIC), responsible for crystal growth, and the Center for Development of Nuclear Technology (CDTN), responsible for the study of its luminescent properties. In this context, samples doped with 1% of Eu 3+ , 1% Ce 3+ , 5% of Ce 3+ and also co-doped with 5% Ce 3+ and 1% Dy 3+ were grown under hydrothermal conditions. The investigation was divided into two fronts, one for gamma radiation and the other for UV radiation. In the investigation with gamma radiation the best TL response has been obtained from LaAlO 3 :Eu. This crystal has shown good sensitivity and excellent linearity between TL output and the delivered gamma doses ranging from 0.1 to 10.0 mGy. In addition, its TL curve is quite similar to the Al 2 O 3 :C, a commercial TL phosphor with high sensitivity to gamma radiation. In the investigation with UV radiation the best response has been achieved for co-doped LaAlO 3 :Ce,Dy. They have excellent sensitivity and good linearity for spectral irradiances ranging from 0.042 to 1.2 mJ.cm -2 . (author)

  11. Ce-doping effects on electronic structures of Ba0.5Sr0.5TiO3 thin film

    International Nuclear Information System (INIS)

    Wang, S Y; Cheng, B L; Wang, Can; Button, T W; Dai, S Y; Jin, K J; Lu, H B; Zhou, Y L; Chen, Z H; Yang, G Z

    2006-01-01

    In order to clarify the basic reason why Ce doping can dramatically decrease the leakage current in Ba 0.5 Sr 0.5 TiO 3 (BST) as reported in our previous work (Wang et al 2005 J. Phys. D: Appl. Phys. 38 2253), we have employed x-ray photoelectron spectroscopy (XPS) and the optical transmittance technique to study the electronic structure of undoped and 1.0 at% Ce-doped BST (CeBST) films fabricated by pulsed laser deposition. XPS results show that Ce doping has a strong influence on the valence band and core levels of BST films, and that the Fermi level is lowered by about 0.35 eV by Ce doping. Optical transmittance measurements demonstrate that the energy gap is expanded with Ce doping. These Ce-doping effects can induce an increase in the barrier height for the thermionic emission and eventually reduce leakage current in CeBST thin films

  12. Satellite line mapping in Eu3+–Ce3+ and Pr3+–Ce3+ codoped Y2SiO5

    International Nuclear Information System (INIS)

    Serrano, D.; Karlsson, J.; Zheng, L.; Dong, Y.; Ferrier, A.; Goldner, P.; Walther, A.; Rippe, L.; Kröll, S.

    2016-01-01

    In this work we perform a high-resolution spectroscopic investigation of Eu 3+ –Ce 3+ and Pr 3+ –Ce 3+ codoped Y 2 SiO 5 crystals. Satellite line spectra were recorded at low temperatures around the Eu 3+ : 7 F 0 → 5 D 0 and the Pr 3+ : 3 H 4 → 1 D 2 transitions. It is observed that the incorporation of Ce 3+ as a codopant notably changes the Eu 3+ and Pr 3+ satellite line patterns. Satellite lines measured in singly doped Eu 3+ :Y 2 SiO 5 were found at the same spectral positions in Eu 3+ –Ce 3+ codoped crystals. These coincident lines were concluded to be due to pairs of Eu 3+ ions. Extra satellite lines appeared in the codoped crystals, which were assigned to Ce 3+ related structures such as Ce 3+ –Eu 3+ pairs. The analysis of the Pr 3+ satellite line spectra presents further challenges. Satellite lines associated to Pr 3+ pairs show weaker intensity, presumably due to the efficient quenching of the Pr 3+1 D 2 emission through cross-relaxation paths ( 1 D 2 → 1 G 4 ; 3 H 4 → 3 F 4 ). The investigation of the Eu 3+ and Pr 3+ satellite line patterns in Y 2 SiO 5 is particularly interesting for their exploitation in rare-earth based quantum computation schemes. - Highlights: • We recorded Eu and Pr satellite lines in Y 2 SiO 5 with and without Ce as a codopant. • The presence of Ce leads to the appearance of extra satellite lines in the spectra. • The satellite lines are associated to minor crystal sites such as ion pairs. • Less than 100 ion pairs were detected per satellite line. • The exploitation of the satellite line structure is proposed for quantum computing.

  13. Tunable Luminescence of CeAl11O18 Based Phosphors by Replacement of (AlO)+ by (SiN)+ and Co-Doping with Eu

    NARCIS (Netherlands)

    Yin, L.J.; Chen, G.Z; Wang, C.; Xu, X.; Hao, L.Y.; Hintzen, H.T.J.M.

    2014-01-01

    A series of Si-N or Eu-Li doped CeAl11O18 and CeAl12O18N phosphors are prepared by solid–state reaction. Their structure and luminescence are researched carefully. Si-N doping with the concentration less than 8% can be successfully dissolved into CeAl11O18 crystal lattice and doesn't change the

  14. Effect of Mg"2"+ ions co-doping on timing performance and radiation tolerance of Cerium doped Gd_3Al_2Ga_3O_1_2 crystals

    International Nuclear Information System (INIS)

    Lucchini, M.T.; Babin, V.; Bohacek, P.; Gundacker, S.; Kamada, K.; Nikl, M.; Petrosyan, A.; Yoshikawa, A.; Auffray, E.

    2016-01-01

    Inorganic scintillators with high density and high light yield are of major interest for applications in medical imaging and high energy physics detectors. In this work, the optical and scintillation properties of Mg co-doped Ce:Gd_3Al_2Ga_3O_1_2 crystals, grown using Czochralski technique, have been investigated and compared with Ce:Gd_3Al_2Ga_3O_1_2 ones prepared with identical technology. Improvements in the timing performance of the Mg co-doped samples with respect to Ce:Gd_3Al_2Ga_3O_1_2 ones have been measured, namely a substantial shortening of the rise time and scintillation decay components and lower afterglow were achieved. In particular, a significantly better coincidence time resolution of 233 ps FWHM, being a fundamental parameter for TOF-PET devices, has been observed in Mg co-doped crystals. The samples have also shown a good radiation tolerance under high doses of γ-rays, making them suitable candidates for applications in harsh radiation environments, such as detectors at future collider experiments.

  15. Structure and scintillation yield of Ce-doped Al–Ga substituted yttrium garnet

    International Nuclear Information System (INIS)

    Sidletskiy, Oleg; Kononets, Valerii; Lebbou, Kheirreddine; Neicheva, Svetlana; Voloshina, Olesya; Bondar, Valerii; Baumer, Vyacheslav; Belikov, Konstantin; Gektin, Alexander; Grinyov, Boris; Joubert, Marie-France

    2012-01-01

    Highlights: ► Range of Y 3 (Al 1−x Ga x ) 5 O 12 :Ce solid solution crystals are grown from melt by the Czochralski method. ► Light yield of mixed crystals reaches 130% of the YAG:Ce value at x ∼ 0.4. ► ∼1% of antisite defects is formed in YGG:Ce, but no evidence of this is obtained for the rest of crystals. -- Abstract: Structure and scintillation yield of Y 3 (Al 1−x Ga x ) 5 O 12 :Ce solid solution crystals are studied. Crystals are grown from melt by the Czochralski method. Distribution of host cations in crystal lattice is determined. Quantity of antisite defects in crystals is evaluated using XRD and atomic emission spectroscopy data. Trend of light output at Al/Ga substitution in Y 3 (Al 1−x Ga x ) 5 O 12 :Ce is determined for the first time. Light output in mixed crystals reaches 130% comparative to Ce-doped yttrium–aluminum garnet. Luminescence properties at Al/Ga substitution are evaluated.

  16. Thermoluminescence of LaAlO{sub 3} crystals doped with Eu and Ce - Dy ions exposed to ultraviolet and gamma radiation

    Energy Technology Data Exchange (ETDEWEB)

    Oliveira, Vitor H.; Faria, Luiz O., E-mail: farialo@cdtn.b [Centro de Desenvolvimento da Tecnologia Nuclear (CDTN/CNEN-MG), Belo Horizonte, MG (Brazil); Silva, Edna S. [Universidade Federal de Minas Gerais (DEN/UFMG), Belo Horizonte, MG (Brazil). Dept. de Energia Nuclear; Khaidukov, Nicholas M. [Kurnakov Institute of General and Inorganic Chemistry, IGIC, Moscow (Russian Federation)

    2011-07-01

    Due to environmental problems such as degradation of the ozone layer and control of radiation levels in units of radiation, new dosimetric materials with high sensitivity for ultraviolet (UV) and gamma radiation are of great interest for applications in environmental dosimetry. In this context, this paper presents the results of a systematic investigation of the thermoluminescent (TL) response of LaAlO{sub 3} crystals doped with different concentrations of trivalent optically active ions exposed to UV and gamma radiation doses. The work has been performed under a direct cooperation between the Institute of Inorganic Chemistry in Moscow (IGIC), responsible for crystal growth, and the Center for Development of Nuclear Technology (CDTN), responsible for the study of its luminescent properties. In this context, samples doped with 1% of Eu{sup 3+}, 1% Ce{sup 3+}, 5% of Ce{sup 3+} and also co-doped with 5% Ce{sup 3+} and 1% Dy{sup 3+} were grown under hydrothermal conditions. The investigation was divided into two fronts, one for gamma radiation and the other for UV radiation. In the investigation with gamma radiation the best TL response has been obtained from LaAlO{sub 3}:Eu. This crystal has shown good sensitivity and excellent linearity between TL output and the delivered gamma doses ranging from 0.1 to 10.0 mGy. In addition, its TL curve is quite similar to the Al{sub 2}O{sub 3}:C, a commercial TL phosphor with high sensitivity to gamma radiation. In the investigation with UV radiation the best response has been achieved for co-doped LaAlO{sub 3}:Ce,Dy. They have excellent sensitivity and good linearity for spectral irradiances ranging from 0.042 to 1.2 mJ.cm{sup -2}. (author)

  17. Aluminum-doped Zn O polycrystalline films prepared by co-sputtering of a Zn O-Al target

    Energy Technology Data Exchange (ETDEWEB)

    Becerril, M.; Silva L, H.; Guillen C, A.; Zelaya A, O. [Instituto Politecnico Nacional, Centro de Investigacion y de Estudios Avanzados, Departamento de Fisica, Apdo. Postal 14-740, 07000 Mexico D. F. (Mexico)

    2014-07-01

    Aluminum-doped Zinc oxide polycrystalline thin films (Azo) were grown on 7059 Corning glass substrates at room temperature by co-sputtering from a Zn O-Al target. The target was designed as follows, high purity elemental Aluminum was evaporated onto a Zn O target covering small areas. The structural, optical and electrical properties were analyzed as a function of Al content. The Al doped Zn O polycrystalline films showed an n-type conductivity. It was found that the electrical resistivity drops and the carrier concentration increases as a consequence of Al incorporation within the Zn O lattice. In both cases, the changes are of several orders of magnitude. From the results, we conclude that, using these Zn O-Al targets, n-type Al doped Zn O polycrystalline films with high transmittance and low resistivity can be obtained. The crystalline structure of the films was determined by X-ray diffraction. Atomic Force Microscopy images were obtained with an Auto probe C P (Veeco Metrology Group) Microscope. (Author)

  18. Optical spectroscopy of the Ce-doped multicomponent garnets

    International Nuclear Information System (INIS)

    Canimoglu, A.; Karabulut, Y.; Ayvacikli, M.; Muresan, L.E.; Perhaita, I.; Barbu-Tudoran, L.; Garcia Guinea, J.; Karali, T.; Can, N.

    2016-01-01

    Here, we report our results referring to the preparation of Ce doped Y 2.22 MgGa 2 Al 2 SiO 12 , Y 1.93 MgAl 4 SiO 12 and Y 2.22 Gd 0.75 Ga 2 Al 3 O 12 using solid state reaction at high temperature. Several complementary methods (i.e. powder x-ray diffraction (XRPD), energy dispersive analysis of X-rays (EDX), scanning electron microscopy (SEM) and Fourier transforms infrared spectroscopy (FTIR)) were studied to examine the effects of the synthesis procedure on the morphology and structure. XRD analyses revealed that all compounds include yttrium aluminate phase with garnet structure. Cathodoluminescence (CL), radioluminescence (RL) and photoluminescence (PL) measurements were carried out for clarification of relationship between host lattice defects and the spectral luminescence emissions. Luminescence emission of phosphors is peaked at 530 nm assigned to 5d-4f transitions of the dopant Ce 3+ ions with a broad emission band in 400–700 nm range. Under electron irradiation, the emission spectrum of Ce doped (YGd) 3 Ga 2 Al 3 O 12 is well defined and has a characteristic fairly narrow and sharp emission band peaking at 312 nm and 624 nm corresponding to transition of 6 P 7/2 → 8 S 7/2 and 6 G J → 6 P J (Gd 3+ ), respectively. We suggest some of phosphors might be excellent phototherapy phosphor materials under electron excitation. - Highlights: • Ce-doped Multicomponent Garnets were prepared solid state reaction method. • The shape and size of phosphor particles were examined. • The narrow band UV B emission due to Gd 3+ ions were observed.

  19. Low-temperature synthesis, phonon and luminescence properties of Eu doped Y{sub 3}Al{sub 5}O{sub 12} (YAG) nanopowders

    Energy Technology Data Exchange (ETDEWEB)

    Mączka, M., E-mail: m.maczka@int.pan.wroc.pl [Institute of Low Temperature and Structure Research, Polish Academy of Sciences, P.O. Box 1410, 50-950 Wrocław 2 (Poland); Bednarkiewicz, A. [Institute of Low Temperature and Structure Research, Polish Academy of Sciences, P.O. Box 1410, 50-950 Wrocław 2 (Poland); Mendoza-Mendoza, E.; Fuentes, A.F. [Cinvestav Unidad Saltillo, Apartado Postal 663, 25000 Saltillo, Coahuila (Mexico); Kępiński, L. [Institute of Low Temperature and Structure Research, Polish Academy of Sciences, P.O. Box 1410, 50-950 Wrocław 2 (Poland)

    2014-02-14

    This contribution presents two simple and cost-effective routes for the low-temperature and large-scale production of pure and Eu-doped Y{sub 3}Al{sub 5}O{sub 12} (yttrium aluminum garnet YAG) nanopowders. The proposed methodologies combine a mechanically assisted metathesis reaction or coprecipitation from solution followed by crystallization of the obtained precursors from molten sodium nitrate/nitrite. Both procedures allow obtaining pure and/or doped YAG nanopowders at remarkably low temperatures, i.e. already at 350 °C although firing at 500 °C is needed in order to get single phase and fully crystalline materials. As-obtained samples were characterized by XRD, TEM, Raman, IR and luminescence methods. These methods showed that the mean crystallite size is near 23–31 and 51 nm, when crystallization is performed from the amorphous precursor obtained by a mechanically assisted metathesis reaction and coprecipitation, respectively. Raman and IR spectra indicated better crystallinity of the powders prepared at 500 °C. The emission study showed that the intensity ratio between hypersensitive {sup 5}D{sub 0} → {sup 7}F{sub 2} and magnetic-dipole {sup 5}D{sub 0} → {sup 7}F{sub 1} transitions of Eu{sup 3+} is significantly larger than expected for well-crystallized YAG. Origin of this behavior is discussed. - Highlights: • Nanoparticles of Y{sub 3}Al{sub 5}O{sub 12} (YAG) and YAG:Eu{sup 3+} have been prepared at remarkable 350 °C. • Metathesis/molten salts and coprecipitation/molten salts methods were used. • Metathesis/molten salts method is suitable for preparation of rare-earth doped YAG. • Emission properties of YAG:Eu{sup 3+} are significantly different from bulk YAG.

  20. Thermoluminescence studies of γ-irradiated Al{sub 2}O{sub 3}:Ce{sup 3+} phosphor

    Energy Technology Data Exchange (ETDEWEB)

    Reddy, S. Satyanarayana [Physics R & D Center, PES Institute of Technology, BSK 3rd Stage, Bangalore 560085 (India); Nagabhushana, K.R., E-mail: bhushankr@gmail.com [Physics R & D Center, PES Institute of Technology, BSK 3rd Stage, Bangalore 560085 (India); Department of Physics, PES University, BSK 3rd Stage, Bangalore 560085 (India); Singh, Fouran [Inter University Accelerator Centre, Aruna Asaf Ali Marg, New Delhi 110 067 (India)

    2016-07-15

    Pure and Ce{sup 3+} doped Al{sub 2}O{sub 3} phosphors were synthesized by solution combustion method. The synthesized samples were characterized by X-ray diffraction (XRD) and its shows α-phase of Al{sub 2}O{sub 3}. Crystallite size was estimated by Williamson–Hall (W–H) method and found to be 49, 59 and 84 nm for pure, 0.1 mol% and 1 mol% Ce{sup 3+} doped Al{sub 2}O{sub 3} respectively. Trace elemental analysis of undoped Al{sub 2}O{sub 3} shows impurities viz. Fe, Cr, Mn, Mg, Ti, etc. Photoluminescence (PL) spectra of Al{sub 2}O{sub 3}:Ce{sup 3+} shows emission at 367 nm and excitation peak at 273 nm, which are corresponding to {sup 5}D → {sup 4}F and {sup 4}F → {sup 5}D transitions respectively. PL intensity decreases with concentration up to 0.4 mol%, beyond this mol% PL intensity increases with doping concentration up to 2 mol%. Thermoluminescence (TL) studies of γ-rayed pure and Ce{sup 3+} doped Al{sub 2}O{sub 3} have been studied. Two well resolved TL glow peaks at 457.5 K and 622 K were observed in pure Al{sub 2}O{sub 3}. Additional glow peak at 566 K was observed in Al{sub 2}O{sub 3}:Ce{sup 3+}. Maximum TL intensity was observed for Al{sub 2}O{sub 3}:Ce{sup 3+} (0.1 mol%) beyond this TL intensity decreases with increasing Ce{sup 3+} concentration. Computerized glow curve deconvolution (CGCD) method was used to resolve the multiple peaks and to calculate TL kinetic parameters. Thermoluminescence emission (TLE) spectra of pure Al{sub 2}O{sub 3} glow peaks (457.5 K and 622 K) shows sharp emission at 694 nm and two small humps at 672 nm and 709 nm. The sharp peak at 696 nm corresponds to Cr{sup 3+} impurity of {sup 2}E{sub g} → {sup 4}A{sub 2g} transition of R lines and 713 nm hump is undoubtedly belongs to Cr{sup 3+} emission of near neighbor pairs. The emission at 672 nm is characteristic of Mn{sup 4+} impurity ions of {sup 2}E → {sup 4}A{sub 2} transition. TLE of Al{sub 2}O{sub 3}:Ce{sup 3+} (0.1 mol%) shows additional broad emission at 412 nm

  1. Luminescence rise time in self-activated PbWO4 and Ce-doped Gd3Al2Ga3O12 scintillation crystals

    CERN Document Server

    E. Auffray; A. Borisevich; V. Gulbinas; A. Fedorov; M. Korjik; M.T. Lucchini; V. Mechinsky; S. Nargelas; E. Songaila; G. Tamulaitis; A. Vaitkevičius; S. Zazubovich

    2016-01-01

    The time resolution of scintillation detectors of ionizing radiation is one of the key parameters sought for in the current and future high-energy physics experiments. This study is encouraged by the necessity to find novel detection methods enabling a sub-10-ps time resolution in scintillation detectors and is focused on the exploitation of fast luminescence rise front. Time-resolved photoluminescence (PL) spectroscopy and thermally stimulated luminescence techniques have been used to study two promising scintillators: self-activated lead tungstate (PWO, PbWO4) and Ce-doped gadolinium aluminum gallium garnet (GAGG, Gd3Al2Ga3O12). A sub-picosecond PL rise time is observed in PWO, while longer processes in the PL response in GAGG:Ce are detected and studied. The mechanisms responsible for the PL rise time in self-activated and doped scintillators are under discussion.

  2. Luminescence and Tb3+-Ce3+-Eu3+ ion energy transfer in single-crystalline films of Tb3Al5O12:Ce,Eu garnet

    International Nuclear Information System (INIS)

    Zorenko, Y.; Gorbenko, V.; Voznyak, T.; Batentschuk, M.; Osvet, A.; Winnacker, A.

    2008-01-01

    The paper is devoted to investigation of the processes of excitation energy transfer between the host cations (Tb 3+ ions) and the activators (Ce 3+ and Eu 3+ ions) in single-crystalline films of Tb 3 Al 5 O 12 :Ce,Eu (TbAG:Ce,Eu) garnet which is considered as a promising luminescent material for the conversion of LED's radiation. The cascade process of excitation energy transfer is shown to be realized in TbAG:Ce,Eu: (i) from Tb 3+ ions to Ce 3+ and Eu 3+ ions; (ii) from Ce 3+ ions to Eu 3+ ions by means of dipole-dipole interaction and through Tb 3+ ion sublattice

  3. Thermally stable green Ba(3)Y(PO(4))3:Ce(3+),Tb(3+) and red Ca(3)Y(AlO)(3)(BO(3))4:Eu(3+) phosphors for white-light fluorescent lamps.

    Science.gov (United States)

    Huang, Chien-Hao; Kuo, Te-Wen; Chen, Teng-Ming

    2011-01-03

    A class of thermal stable of green-emitting phosphors Ba(3)Y(PO(4))(3):Ce(3+),Tb(3+) (BYP:Ce(3+),Tb(3+)) and red-emitting phosphors Ca(3)Y(AlO)(3)(BO(3))(4):Eu(3+) (CYAB:Eu(3+)) for white-light fluorescent lamps were synthesized by high temperature solid-state reaction. We observed a decay of only 3% at 150 °C for BYP:0.25Ce3+,0.25Tb3+ (3% for LaPO4:Ce(3+),Tb(3+)), and a decay of 4% for CYAB:0.5Eu(3+) (7% for Y(2)O(3):Eu(3+), 24% for Y(2)O(2)S:Eu(3+)). The emission intensity of composition-optimized Ba(3)(Y(0.5)Ce(0.25)Tb(0.25))(PO(4))(3) is 70% of that of commercial LaPO(4):Ce(3+),Tb(3+) phosphors, and the CIE chromaticity coordinates are found to be (0.323, 0.534). The emission intensity of Ca(3)(Y(0.5)Eu(0.5))(AlO)(3)(BO(3))(4) is 70% and 83% of those of Y(2)O(3):Eu(3+) and Y(2)O(2)S:Eu(3+) phosphors, respectively, and the CIE chromaticity coordinates are redder (0.652, 0.342) than those of Y(2)O(3):Eu(3+) (0.645, 0.347) and Y(2)O(2)S:Eu(3+) (0.647, 0.343). A white-light fluorescent lamp is fabricated using composition-optimized Ba(3)(Y(0.5)Ce(0.25)Tb(0.25))(PO(4))(3) and Ca(3)(Y(0.5)Eu(0.5))(AlO)(3)(BO(3))(4) phosphors and matching blue-emitting phosphors. The results indicate that the quality of the brightness and color reproduction is suitable for application in shortwave UV fluorescent lamps. The white-light fluorescent lamp displays CIE chromaticity coordinates of x = 0.33, y = 0.35, a warm white light with a correlated color temperature of 5646 K, and a color-rendering index of Ra = 70.

  4. Scintillation and optical properties of Ce{sup 3+}-doped CaGdAl{sub 3}O{sub 7} single crystals

    Energy Technology Data Exchange (ETDEWEB)

    Mori, Masaki, E-mail: masaki.mori.mz4@ms.naist.jp [Graduate School of Materials Science, Nara Institute of Science and Technology (NAIST), 8916-5 Takayama-cho, Ikoma-shi, Nara 630-0192 (Japan); Nakauchi, Daisuke; Okada, Go [Graduate School of Materials Science, Nara Institute of Science and Technology (NAIST), 8916-5 Takayama-cho, Ikoma-shi, Nara 630-0192 (Japan); Fujimoto, Yutaka [Department of Applied Chemistry, Graduate School of Engineering, Tohoku University, 6-6-07 Aoba, Aramaki, Aoba-ku, Sendai, 980-8579 (Japan); Kawaguchi, Noriaki [Graduate School of Materials Science, Nara Institute of Science and Technology (NAIST), 8916-5 Takayama-cho, Ikoma-shi, Nara 630-0192 (Japan); Koshimizu, Masanori [Department of Applied Chemistry, Graduate School of Engineering, Tohoku University, 6-6-07 Aoba, Aramaki, Aoba-ku, Sendai, 980-8579 (Japan); Yanagida, Takayuki [Graduate School of Materials Science, Nara Institute of Science and Technology (NAIST), 8916-5 Takayama-cho, Ikoma-shi, Nara 630-0192 (Japan)

    2017-06-15

    The single crystals of 0, 0.6, 1, 1.6 and 2 mol% Ce doped CaGdAl{sub 3}O{sub 7} (Ce:CGAM) were grown by the Floating Zone method, and investigated on photoluminescence (PL) and scintillation properties. In the PL spectra, a broad emission appeared over 380–500 nm under 280 and 360 nm excitations with the quantum yield of 33.8–38.8%. Under a vacuum ultraviolet excitation (90 nm) using a synchrotron source, non-doped CGAM single crystal showed broad emissions over 250–650 nm. The PL decay time profiles followed a monotonic exponential decay with a decay time constant of around 33 ns. The scintillation spectra were similar to those of PL. All of the samples exhibited a clear photoabsorption peak and Compton edge in the pulse height spectra measured under {sup 137}Cs γ-ray irradiation, and the absolute scintillation light yield (LY) was highest for the 2% Ce-doped sample with the value of 3300±300 ph/MeV. The scintillation decay profiles were approximated by a third order exponential decay function, and the extracted decay time of Ce{sup 3+} emission component was around 36–44 ns. Among all the samples, 2%Ce:CGAM single crystal sample showed the best afterglow level as a scintillator under X-ray irradiation. - Highlights: •Ce{sup 3+}-doped CaGdAl{sub 3}O{sub 7} single crystals were synthesized by the FZ method. •Optical and scintillation properties of Ce{sup 3+}-doped CaGdAl{sub 3}O{sub 7} were investigated. •Photoabsorption peak in a pulse height spectrum was clearly observed under γ-rays.

  5. Growth and characterization of ceria thin films and Ce-doped {gamma}-Al{sub 2}O{sub 3} nanowires using sol-gel techniques

    Energy Technology Data Exchange (ETDEWEB)

    Gravani, S; Polychronopoulou, K; Doumanidis, C C; Rebholz, C [Mechanical and Manufacturing Engineering Department, Engineering School, University of Cyprus, 1678, Nicosia (Cyprus); Stolojan, V; Hinder, S J; Baker, M A [Faculty of Engineering and Physical Sciences, University of Surrey, Guildford GU2 7XH (United Kingdom); Cui, Q; Gu, Z [Department of Chemical Engineering and CHN/NCOE Nanomanufacturing Center, University of Massachusetts Lowell, Lowell, MA 01854 (United States); Gibson, P N, E-mail: M.Baker@surrey.ac.uk [Institute for Health and Consumer Protection, Joint Research Centre of the European Commission, 21027 Ispra (Italy)

    2010-11-19

    {gamma}-Al{sub 2}O{sub 3} is a well known catalyst support. The addition of Ce to {gamma}-Al{sub 2}O{sub 3} is known to beneficially retard the phase transformation of {gamma}-Al{sub 2}O{sub 3} to {alpha}-Al{sub 2}O{sub 3} and stabilize the {gamma}-pore structure. In this work, Ce-doped {gamma}-Al{sub 2}O{sub 3} nanowires have been prepared by a novel method employing an anodic aluminium oxide (AAO) template in a 0.01 M cerium nitrate solution, assisted by urea hydrolysis. Calcination at 500 deg. C for 6 h resulted in the crystallization of the Ce-doped AlOOH gel to form Ce-doped {gamma}-Al{sub 2}O{sub 3} nanowires. Ce{sup 3+} ions within the nanowires were present at a concentration of < 1 at.%. On the template surface, a nanocrystalline CeO{sub 2} thin film was deposited with a cubic fluorite structure and a crystallite size of 6-7 nm. Characterization of the nanowires and thin films was performed using scanning electron microscopy, transmission electron microscopy, electron energy loss spectroscopy, x-ray photoelectron spectroscopy and x-ray diffraction. The nanowire formation mechanism and urea hydrolysis kinetics are discussed in terms of the pH evolution during the reaction. The Ce-doped {gamma}-Al{sub 2}O{sub 3} nanowires are likely to find useful applications in catalysis and this novel method can be exploited further for doping alumina nanowires with other rare earth elements.

  6. Stark components of lower-lying manifolds and emission cross-sections of intermanifold and inter-stark transitions of Nd3+(4f3) in polycrystalline ceramic garnet Y3Al5O12

    International Nuclear Information System (INIS)

    Sardar, Dhiraj K.; Yow, Raylon M.; Gruber, John B.; Allik, Toomas H.; Zandi, Bahram

    2006-01-01

    Stark energy levels of the 4 F 3/2 , 4 I 9/2 , and 4 I 11/2 manifolds have been characterized using the room temperature fluorescence spectra for the 4 F 3/2 → 4 I 9/2 and 4 F 3/2 → 4 I 11/2 transitions of Nd 3+ (4f 3 ) in polycrystalline ceramic garnet Y 3 Al 5 O 12 (YAG). The emission cross-sections of the intermanifold transitions, 4 F 3/2 → 4 I 9/2 and 4 F 3/2 → 4 I 11/2 , as well as the principal inter-Stark transitions, R 1 →Z 5 (945.3 nm) and R 1 →Y 2 (1063.5 nm), have also been determined. These results are finally compared with those of Nd 3+ :YAG single crystal

  7. Faraday effect in Gd3Al5O12 and Gd3Ga5O12 rare earth garnets

    International Nuclear Information System (INIS)

    Valiev, U.V.; Klochkov, A.A.; Popov, A.I.; Sokolov, Y.B.

    1989-01-01

    The dispersion of the Faraday rotation of the garnets Gd 3 Ga 5 O 12 and Gd 3 Al 5 O 12 in the 440--700-nm region in the 85--295-K temperature interval and the spectral dependence of the Faraday effect in the garnets Y 3 Ga 5 O 12 and Y 3 Al 5 O 12 for wavelengths from 250 to 700 nm are investigated. The contributions to the Faraday rotation caused by the Gd 3+ ions and the diamagnetic lattice of the garnets are separated

  8. Synthesis design of Y3Al5O12: Ce3+ phosphor for fabrication of ceramic converter in automotive application

    Science.gov (United States)

    Kwon, Seok Bin; Choi, Seung Hee; Yoo, Jung Hyeon; Jeong, Seong Guk; Song, Young Hyun; Yoon, Dae Ho

    2018-06-01

    A cellulose-assisted, liquid-phase precursor (LPP) was used to synthesize a YAG phosphor radiating near 530 nm with a particle size of 400 nm, which may be implemented in many applications. The mixture of the materials was homogeneous, and the cellulose-assisted LPP method involved a liquid-phase reaction at a lower temperature compared to a solid-state reaction (SSR). The reaction was performed at 1200, 1300 and 1400 °C, and the composition ratio of the samples was controlled based on yttrium (L1: 2.7, L2: 2.8, L3: 2.9, L4: 2.95, and L5: 3.1 M). ∼400 nm particles were obtained at 1200 °C and ∼1 μm at 1300 °C. At 1200 °C, the PL intensity was the highest in the Y3.1Al5O12 sample. At 1300 and 1400 °C, the strongest intensity was evident in the Y2.9Al5O12 sample. The XRD patterns for all temperatures showed a YAG phase in JCPDS.

  9. Yb and Er co-doped Y2Ce2O7 nanoparticles: synthesis and ...

    Indian Academy of Sciences (India)

    much attention due to their potential applications in display .... Figure 1. XRD patterns of Yb3+ and Er3+ co-doped Y2Ce2O7 nanoparticles prepared for 4 h at different sintering .... vels relax to the ground 4I15/2 level (You et al 2012). For.

  10. Preparation and characterization of Yttrium-Aluminium garnet (Y3Al5O12)

    International Nuclear Information System (INIS)

    Ruzicka, J.; Niznansky, D.; Houzvicka, J.; Nikl, M.; Cerny, R.

    2009-01-01

    This work deals with the preparation of powders and transparent yttrium aluminium garnet (Y 3 Al 5 O 12 - YAG) from nanopowders. Stoichiometric amounts of nanocrystalline Al 2 O 3 and Y 2 O 3 were mixed and chemically pretreated using different basic agents and using ultrasonic bath. Resulting mixture was dried, pressed and heated up to 1750°C. Final material was characterized by X-ray diffraction, DTA and optical and electron microscopy

  11. Luminescence properties of Sr{sub 3-x-3y/2}M{sub x}Ce{sub y}AlO{sub 4}F (M=Ca, Ba, 0{<=}x{<=}0.9, 0.001{<=}y{<=}0.05) phosphors

    Energy Technology Data Exchange (ETDEWEB)

    Choi, Hye-Min [Department of Engineering in Energy and Applied Chemistry, Silla University, Busan 617-736 (Korea, Republic of); Park, Sangmoon, E-mail: spark@silla.ac.kr [Department of Engineering in Energy and Applied Chemistry, Silla University, Busan 617-736 (Korea, Republic of)

    2012-09-15

    Luminescent materials composed of Sr{sub 3-x-3y/2}M{sub x}Ce{sub y}AlO{sub 4}F (M=Ca, Ba, 0{<=}x{<=}0.9, 0.001{<=}y{<=}0.05) were prepared by the solid-state reaction method. X-ray diffraction (XRD) patterns of the obtained oxyfluorides are exhibited for indexing peak positions. Dynamic excitation and emission spectra of the Ce{sup 3+}-activated oxyfluoride phosphors are clearly monitored. The critical emission quenching as a function of Ce{sup 3+} contents in Sr{sub 2.5-3y/2}M{sub 0.5}Ce{sub y}AlO{sub 4}F phosphors is revealed at quite low concentrations of the activator. CIE coordinates of blue and green Sr{sub 2.5-3y/2}M{sub 0.5}Ce{sub y}AlO{sub 4}F phosphors are clearly measured. The relative quantum efficiency of Sr{sub 2.4985}Ca{sub 0.5}Ce{sub 0.005}AlO{sub 4}F based on the integrated emission is determined. The Sr{sub 3-x-3y/2}M{sub x}Ce{sub y}AlO{sub 4}F phosphors excited near 410 nm light could be prominent phosphors in applications of NUV-LED. - Highlights: Black-Right-Pointing-Pointer Blue and green emitting oxyfluoride phosphors are excitated near 410 nm Black-Right-Pointing-Pointer Ce{sup 3+}-activated oxyfluoride phosphors are quite effective to prepare white light for near-UV LED applications. Black-Right-Pointing-Pointer Gradual substitution of Ce{sup 3+} content in the oxyfluoride hosts changes CIE values.

  12. Preparation of Er3+:Y3Al5O12/WO3-KNbO3 composite and application in treatment of methamphetamine under ultrasonic irradiation.

    Science.gov (United States)

    Zhang, Hongbo; Huang, Yingying; Li, Guanshu; Wang, Guowei; Fang, Dawei; Song, Youtao; Wang, Jun

    2017-03-01

    Er 3+ :Y 3 Al 5 O 12 /WO 3 -KNbO 3 composite powder as an effective sonocatalyst was prepared via collosol-gelling-hydrothermal and high-temperature calcination methods. The textures of materials were observed by X-ray diffractometer (XRD), scanning electron microscopy (SEM) and X-ray photoelectron spectroscopy (XPS). In order to estimate the sonocatalytic activity of Er 3+ :Y 3 Al 5 O 12 /WO 3 -KNbO 3 composite powder, the sonocatalytic degradation of methamphetamine (MAPA) was performed. Furthermore, the influences of mass ratio of WO 3 and KNbO 3 , ultrasonic irradiation time, catalyst addition amount, initial methamphetamine (MAPA) concentration and used times on the sonocatalytic degradation of methamphetamine (MAPA) caused by Er 3+ :Y 3 Al 5 O 12 /WO 3 -KNbO 3 composite powder were investigated by using gas chromatography. Under optimal conditions of 1.00g/L Er 3+ :Y 3 Al 5 O 12 /WO 3 -KNbO 3 addition amount and 10.00mg/L methamphetamine (MAPA) initial concentration, 68% of methamphetamine (MAPA) could be removed after 150min ultrasonic irradiation. The experimental results showed that the Er 3+ :Y 3 Al 5 O 12 /WO 3 -KNbO 3 as sonocatalyst displayed an excellent sonocatalytic activity in degradation of methamphetamine (MAPA) under ultrasonic irradiation. Copyright © 2016 Elsevier B.V. All rights reserved.

  13. Magnetic spectra and Richter aftereffect relaxation in Ce{sub x}Y{sub 3−x}Fe{sub 5}O{sub 12} ferrites

    Energy Technology Data Exchange (ETDEWEB)

    Chen, Fu; Wang, Xian; Feng, Zekun, E-mail: fengzekun@mail.hust.edu.cn [School of Optical and Electric Information, Huazhong University of Science and Technology, Wuhan, 430074 (China); Chen, Yajie; Harris, Vincent G. [Center for Microwave Magnetic Materials and Integrated Circuits, and Department of Electrical and Computer Engineering, Northeastern University, Boston, MA 02115 (United States)

    2016-05-15

    The static and dynamic magnetic properties of cerium (Ce) doped yttrium iron garnet Ce{sub x}Y{sub 3−x}Fe{sub 5}O{sub 12} (x=0, 0.05, 0.1, 0.15, 0.2) ferrites (YIG) have been reported in this work. The ferrites were fabricated by the traditional solid-state reaction method. All ferrite samples reveal pure garnet structure identified by x-ray diffraction (XRD). The substitution of cerium not only enhances the saturation magnetization of the samples, but also regulates the magnetocrystalline anisotropy constant K{sub 1}. Obvious differences in permeability spectra over a frequency of 1 MHz - 1 GHz can be observed. It is verified that the permeability dispersion and magnetic losses of Ce-doped YIG ferrite contain the contribution of Richter aftereffect relaxation due to the existence of Fe{sup 2+} ions. The fitting results of the permeability spectra applied three-mechanism model is in good agreement with experimental data, which successfully explains the mechanisms of magnetic losses observed at 1 MHz to 1 GHz for Ce-doped YIG ferrite. In addition, the frequency shift of Richter aftereffect has also been discussed.

  14. Passive mode locking of 2.09 microm Cr,Tm,Ho:Y3Sc2Al3O12 laser using PbS quantum-dot-doped glass.

    Science.gov (United States)

    Denisov, Igor A; Skoptsov, Nikolai A; Gaponenko, Maxim S; Malyarevich, Alexander M; Yumashev, Konstantin V; Lipovskii, Andrei A

    2009-11-01

    Passive Q-switched mode locking of a 2.09 microm flashlamp-pumped Cr(3+),Tm(3+),Ho(3+):Y(3)Sc(2)Al(3)O(12) laser by use of a phosphate glass doped with PbS quantum dots of 5 nm in radius was demonstrated. Mode-locked pulses of 290 ps in duration and up to 0.5 mJ in energy were registered.

  15. Transition of Emission Colours as a Consequence of Heat-Treatment of Carbon Coated Ce3+-Doped YAG Phosphors

    NARCIS (Netherlands)

    Yin, L.J.; Dierre, B.F.P.R.; Sekiguchi, Takashi; van Ommen, J.R.; Hintzen, H.T.J.M.; Cho, Yujin

    2017-01-01

    To modify the luminescence properties of Ce3+-doped Y3Al5O12 (YAG) phosphors, they have been coated with a carbon layer by chemical vapor deposition and subsequently heat-treated at high temperature under N2 atmosphere. Luminescence of the

  16. Tunable colorimetric performance of Al{sub 2}O{sub 3}-YAG:Ce{sup 3+} eutectic crystal by Ce{sup 3+} concentration

    Energy Technology Data Exchange (ETDEWEB)

    Sai, Qinglin, E-mail: saiql@siom.ac.cn; Xia, Changtai, E-mail: xia_ct@siom.ac.cn

    2017-06-15

    Ce-doped Al{sub 2}O{sub 3}-YAG eutectics with different percentage of Ce were successfully grown by the optical floating zone technique. X-ray diffraction (XRD) and scanning electron microscopy (SEM) were used to investigate the structure. The results show that they have typical eutectic structure of interpenetrating sapphire and garnet phases with the tens of microns lamella spacing. The photoluminescence spectra of the eutectics showed that they have wide excitation band, and samples with 1.6 mol% Ce-doped has the highest emission intensity. The eutectic-packaged LED has high luminous efficiency and its color can be modulated by changing Ce concentration. The results reveal that Ce-doped Al{sub 2}O{sub 3}-YAG eutectic is a promising phosphor for white LED applications.

  17. Hydrothermal-precipitation preparation of CdS@(Er3+:Y3Al5O12/ZrO2) coated composite and sonocatalytic degradation of caffeine.

    Science.gov (United States)

    Huang, Yingying; Wang, Guowei; Zhang, Hongbo; Li, Guanshu; Fang, Dawei; Wang, Jun; Song, Youtao

    2017-07-01

    Here, we reported a novel method to dispose caffeine by means of ultrasound irradiation combinated with CdS@(Er 3+ :Y 3 Al 5 O 12 /ZrO 2 ) coated composite as sonocatalyst. The CdS@(Er 3+ :Y 3 Al 5 O 12 /ZrO 2 ) was synthesized via hydrothermal-precipitation method and then characterized by X-ray diffractometer (XRD), scanning electron microscopy (SEM), transmission electron microscopy (TEM), energy dispersive X-ray analysis (EDX) and UV-vis diffuse reflectance spectra (DRS). After that, the sonocatalytic degradation of caffeine in aqueous solution was conducted adopting CdS@(Er 3+ :Y 3 Al 5 O 12 /ZrO 2 ) and CdS@ZrO 2 coated composites as sonocatalysts. In addition, some influencing factors such as CdS and ZrO 2 molar proportion, caffeine concentration, ultrasonic irradiation time, sonocatalyst dosage and addition of several inorganic oxidants on sonocatalytic degradation of caffeine were investigated by using UV-vis spectra and gas chromatograph. The experimental results showed that the presence of Er 3+ :Y 3 Al 5 O 12 could effectively improve the sonocatalytic degradation activity of CdS@ZrO 2 . To a certain extent some inorganic oxidants can also enhance sonocatalytic degradation of caffeine in the presence of CdS@(Er 3+ :Y 3 Al 5 O 12 /ZrO 2 ). The best sonocatalytic degradation ratio (94.00%) of caffeine could be obtained when the conditions of 5.00mg/L caffeine, 1.00g/L prepared CdS@(Er 3+ :Y 3 Al 5 O 12 /ZrO 2 ), 10.00mmol/LK 2 S 2 O 8 , 180min ultrasonic irradiation (40kHz frequency and 50W output power), 100mL total volume and 25-28°C temperature were adopted. It seems that the method of sonocatalytic degradation caused by CdS@(Er 3+ :Y 3 Al 5 O 12 /ZrO 2 ) displayspotentialadvantages in disposing caffeine. Copyright © 2017 Elsevier B.V. All rights reserved.

  18. Effect of Ga2O3 addition on the properties of Y2O3-doped AlN ceramics

    Directory of Open Access Journals (Sweden)

    Shin H.

    2015-01-01

    Full Text Available Effect Ga2O3 addition on the densification and properties of Y2O3-doped AlN ceramics was investigated under the constraint of total sintering additives (Y2O3 and Ga2O3 of 4.5 wt%. Ga was detected in the AlN grain as well as the grain boundary phases. YAlO3 and Y4Al2O9 were observed as the secondary crystalline phases in all of the investigated compositions. As the substitution of Ga2O3 for Y2O3 increased, the quantity of the Y4Al2O9 phase decreased while that of YAlO3 was more or less similar. Neither additional secondary phases was identified, nor was the sinterability inhibited by the Ga2O3 addition; the linear shrinkage and apparent density were above 20 percent and 3.34-3.37 g/cm3, respectively. However, the optical reflectance and the elastic modulus generally decreased whereas the Poisson ratio increased significantly. The dielectric constant and the loss tangent of 4.0Y2O3-0.5Ga2O3-95.5Y2O3 at the resonant frequency of 8.22 GHz were 8.63 and 0.003, respectively.

  19. Preparation of Ce- and La-Doped Li4Ti5O12 Nanosheets and Their Electrochemical Performance in Li Half Cell and Li4Ti5O12/LiFePO4 Full Cell Batteries

    Directory of Open Access Journals (Sweden)

    Meng Qin

    2017-06-01

    Full Text Available This work reports on the synthesis of rare earth-doped Li4Ti5O12 nanosheets with high electrochemical performance as anode material both in Li half and Li4Ti5O12/LiFePO4 full cell batteries. Through the combination of decreasing the particle size and doping by rare earth atoms (Ce and La, Ce and La doped Li4Ti5O12 nanosheets show the excellent electrochemical performance in terms of high specific capacity, good cycling stability and excellent rate performance in half cells. Notably, the Ce-doped Li4Ti5O12 shows good electrochemical performance as anode in a full cell which LiFePO4 was used as cathode. The superior electrochemical performance can be attributed to doping as well as the nanosized particle, which facilitates transportation of the lithium ion and electron transportation. This research shows that the rare earth doped Li4Ti5O12 nanosheets can be suitable as a high rate performance anode material in lithium-ion batteries.

  20. Preparation of Ce- and La-Doped Li4Ti5O12 Nanosheets and Their Electrochemical Performance in Li Half Cell and Li4Ti5O12/LiFePO4 Full Cell Batteries

    Science.gov (United States)

    Qin, Meng; Li, Yueming; Lv, Xiao-Jun

    2017-01-01

    This work reports on the synthesis of rare earth-doped Li4Ti5O12 nanosheets with high electrochemical performance as anode material both in Li half and Li4Ti5O12/LiFePO4 full cell batteries. Through the combination of decreasing the particle size and doping by rare earth atoms (Ce and La), Ce and La doped Li4Ti5O12 nanosheets show the excellent electrochemical performance in terms of high specific capacity, good cycling stability and excellent rate performance in half cells. Notably, the Ce-doped Li4Ti5O12 shows good electrochemical performance as anode in a full cell which LiFePO4 was used as cathode. The superior electrochemical performance can be attributed to doping as well as the nanosized particle, which facilitates transportation of the lithium ion and electron transportation. This research shows that the rare earth doped Li4Ti5O12 nanosheets can be suitable as a high rate performance anode material in lithium-ion batteries. PMID:28632167

  1. Comparative study of Tm-doped and Tm-Sc co-doped Lu3Al5O12 scintillator

    International Nuclear Information System (INIS)

    Sugiyama, Makoto; Yanagida, Takayuki; Fujimoto, Yutaka

    2014-01-01

    The crystals of Tm doped and Tm-Sc co-doped Lu 3 Al 5 O 12 (LuAG) grown by the floating zone (FZ) method were examined for their optical and scintillation properties. In transmittance spectra, strong absorption lines due to Tm 3+ 4f–4f transitions were observed. X-ray excited radioluminescence spectra were measured and broad and sharp emission peaks were detected. The former one was attributed to Sc 3+ and the latter one was due to Tm 3+ 4f–4f transitions. Scintillation yield enhancement due to Sc co-doping was observed by means of 137 Cs pulse height spectra. Scintillation decay times were several tens of μs under pulse X-ray excitation. - Highlights: • LuAG:Tm and LuAG:Tm, Sc single crystals have been grown by the FZ method. • Tm 3+ 4f–4f absorption has been observed in transmittance spectra. • Scintillation yield of Tm-doped LuAG has been enhanced by Sc co-doping

  2. Al2O3 doped TiO2 ceramic waste forms

    International Nuclear Information System (INIS)

    Uno, Masayoshi; Kinoshita, Hajime; Sakai, Etsuro; Ikeda, Akira; Matsumoto, Y.; Yamanaka, Shinsuke

    1999-01-01

    Melting of the mixture of Nd 2 O 3 , CeO 2 , SrO, TiO 2 and Al 2 O 3 at 1673 K for 1 hour produced one RE 2 Ti 3 O 9 phase compound. Differential Scanning Calorimetry (DSC) measurement showed that the melting temperature of this compound was 1646 K. Density of the alumina doped oxide was higher than that of the oxide obtained by the pressing and sintering without alumina. Vickers hardness of the oxide obtained by the pressing and sintering was 5.3 GPa and nearly same as that of glass waste. That of the alumina doped oxide was around 7 GPa. 7 days Soxhlet leach test (MCC-5) followed by Inductively Coupled Plasma Spectrometry (ICP) showed that normalized leaching rate of Ti for the oxide obtained by the pressing and sintering was 5.54 x 10 -3 kg/m 2 and that for the alumina doped oxide was 2.24 x 10 -3 kg/m 2 . The value of Sr for the pressed and sintered sample was 0.034 x 10 -3 kg/m 2 but that for alumina doped sample was below the detection limit (0.01 x 10 -3 kg/m 2 ). Al was not detected from the leachate of the alumina doped sample. (author)

  3. Effects of Y{sub 2}O{sub 3}/CeO{sub 2} co-doping on microwave dielectric properties of Ba(Co{sub 0.6}Zn{sub 38}){sub 1/3}Nb{sub 2/3}O{sub 3} ceramics

    Energy Technology Data Exchange (ETDEWEB)

    Zhang, Yuqin; Zhou, Xiaohua, E-mail: 1250590698@qq.com; Yang, Xinshi; Sun, Chengli; Yang, Fan; Chen, Hetuo

    2016-09-15

    The effects of CeO{sub 2}/Y{sub 2}O{sub 3} co-doping on the microstructure and microwave dielectric properties of Ba(Co{sub 0.6}Zn{sub 0.38}){sub 1/3}Nb{sub 2/3}O{sub 3}-xA-xB (x = 0,1,2,3,4,6; A = 0.1204 wt%Y{sub 2}O{sub 3}; B = 0.1 wt%CeO{sub 2}) ceramics prepared by the conventional solid-state route technique were investigated. The X-ray diffraction (XRD) results presented that all the well sintered samples exhibited the main phase BaZn{sub 0.33}Nb{sub 0.67}O{sub 3}−Ba{sub 3}CoNb{sub 2}O{sub 9}. A certain amount of Ba{sub 8}CoNb{sub 6}O{sub 24} surface secondary phase and minority phase of Ba{sub 5}Nb{sub 4}O{sub 15} were also observed in all sintered ceramics. The 1:2 B-site cation ordering degree was found to influenced by the substitution of Y{sup 3+} and Ce{sup 4+} in the crystal lattice, especially for x = 0.02. Then the scanning electron microscopy (SEM) picture of the optimally well-sintered (1350 °C for 20 h) ceramic has shown a dense microstructure. Although the ε{sub r} almost kept unchanged, appropriate doping content would greatly improve the Q × f value. Meanwhile, the τ{sub f} value first declined and then increased with increasing x. At last, the excellent microwave dielectric properties of ε{sub r} = 36.09, Q × f = 72006 GHz, τ{sub f} = 3.35 ppm/ºC were obtained for the ceramic with x = 0.02 sintered in air at 1350 °C for 20 h. - Graphical abstract: Fig. SEM images of as-sintered Ba(Co{sub 0.6}Zn{sub 0.38}){sub 1/3}Nb{sub 2/3}O{sub 3}-xA-Xb (A = 0.1204 wt%Y{sub 2}O{sub 3}; B = 0.1 wt%CeO{sub 2)}ceramics: (a) x = 0,(b) x = 0.01,(c) x = 0.02,(d) x = 0.03, (e) x = 0.04,(f) x = 0.06. The images confirmed the presences of two phases on the surface of the ceramics, plate-shaped grains (Ba{sub 8}(C{sub O},Zn){sub 1}Nb{sub 6}O{sub 24}phase) and needle-shaped grains (Ba{sub 3}(Co{sub 0.6}Zn{sub 0.38}){sub 1}Nb{sub 2}O{sub 9} phase). As a small content of CeO{sub 2}/Y{sub 2}O{sub 3} (x = 0.01–0.04) was codoped into the BCZN ceramics, the

  4. Hydrocracking of cumene over Ni/Al 2O 3 as influenced by CeO 2 doping and γ-irradiation

    Science.gov (United States)

    El-Shobaky, G. A.; Doheim, M. M.; Ghozza, A. M.

    2004-01-01

    Cumene hydrocracking was carried out over pure and doped Ni/Al 2O 3 solids and also, on these solids after exposure to different doses of γ-rays between 0.4 and 1.6 MGy. The dopant concentration was varied between 1 and 4 mol% CeO 2. Pure and doped samples were subjected to heat treatment at 400°C and cumene hydrocracking reaction was carried out using various solids at temperatures between 250°C and 400°C by means of micropulse technique. The results showed that both CeO 2 doping and γ-irradiation of the investigated system brought about an increase in its specific surface area. γ-irradiation of pure samples increased their catalytic activities effectively. However, the doping caused a decrease in the catalytic activity. γ-irradiation of the doped samples brought about a net decrease in the catalytic activity. The catalytic reaction products over different investigated solids were ethylbenzene as a major product together with different amounts of toluene, benzene and C 1-C 3 gaseous hydrocarbons. The selectivity towards the formation of various reaction products varies with the reaction temperature, doping and γ-irradiation.

  5. Bright green phosphor, Y/sub 3/Al/sub 5-x/Ga/sub x/O/sub 12/:Tb, for projection CRT

    International Nuclear Information System (INIS)

    Ohno, K.; Abe, T.

    1987-01-01

    A remarkably improved high brightness phosphor, Y/sub 3/Al/sub 5-x/Ga/sub x/O/sub 12/:Tb (x = 0 -- 5) was developed and has been adopted for the projection CRT. The replacement of a portion of Al with Ga in YAG improved the brightness and the saturation characteristics. While the brightness of Y/sub 3/Al/sub 3/Ga/sub 2/O/sub 12/:Tb is almost the same as that of Y/sub 3/Al/sub 5/O/sub 12/:Tb at low cathode current densities, the former becomes about two times greater than the latter at high cathode current densities. The brightness of the Y/sub 3/Al/sub 5-x/Ga/sub x/O/sub 12/:Tb phosphor and its saturation characteristics are presented and compared with other green phosphors which have been used for the projection CRT

  6. Long annealing effect on spin Seebeck devices fabricated using Ce x Y3- x Fe5O12 deposited by metal-organic decomposition

    Science.gov (United States)

    Ono, Tatsuyoshi; Hirata, Satoshi; Amemiya, Yoshiteru; Tabei, Tetsuo; Yokoyama, Shin

    2018-04-01

    The effects of Ce content and annealing temperature on the electromotive force produced by spin Seebeck devices fabricated using Ce x Y3- x Fe5O12 deposited by metal-organic decomposition was investigated. The Ce content was first varied (x = 0,1,2,3) for a fixed annealing condition of 3 h at 900 °C. It was found that increasing the Ce content led to a decrease in electromotive force, which meant that x = 0 was the optimum Ce content. Next, the effect of annealing temperature was investigated for a Ce1Y2Fe5O12 film for an annealing time of 14 h. The highest electromotive force of 24.0 µV/50 °C was obtained for a sample annealed for 14 h at 800 °C, although the X-ray diffraction peaks were weaker than those for a sample annealed for 14 h at 950 °C.

  7. Luminescence rise time in self-activated PbWO{sub 4} and Ce-doped Gd{sub 3}Al{sub 2}Ga{sub 3}O{sub 12} scintillation crystals

    Energy Technology Data Exchange (ETDEWEB)

    Auffray, E. [CERN, Geneva (Switzerland); Augulis, R. [Center for Physical Sciences and Technology, Savanorių av. 231, Vilnius (Lithuania); Borisevich, A. [Research Institute for Nuclear Problems, Bobruiskaya str. 11, Minsk (Belarus); Gulbinas, V. [Center for Physical Sciences and Technology, Savanorių av. 231, Vilnius (Lithuania); Fedorov, A.; Korjik, M. [Research Institute for Nuclear Problems, Bobruiskaya str. 11, Minsk (Belarus); Lucchini, M.T. [CERN, Geneva (Switzerland); Mechinsky, V. [Research Institute for Nuclear Problems, Bobruiskaya str. 11, Minsk (Belarus); Nargelas, S. [Vilnius University, Universiteto str. 3, Vilnius (Lithuania); Songaila, E. [Center for Physical Sciences and Technology, Savanorių av. 231, Vilnius (Lithuania); Tamulaitis, G. [Vilnius University, Universiteto str. 3, Vilnius (Lithuania); Vaitkevičius, A., E-mail: augustas.vaitkevicius@ff.vu.lt [Vilnius University, Universiteto str. 3, Vilnius (Lithuania); Zazubovich, S. [Institute of Physics, University of Tartu, W. Ostwaldi Str. 1, Tartu (Estonia)

    2016-10-15

    The time resolution of scintillation detectors of ionizing radiation is one of the key parameters sought for in the current and future high-energy physics experiments. This study is encouraged by the necessity to find novel detection methods enabling a sub-10-ps time resolution in scintillation detectors and is focused on the exploitation of fast luminescence rise front. Time-resolved photoluminescence (PL) spectroscopy and thermally stimulated luminescence techniques have been used to study two promising scintillators: self-activated lead tungstate (PWO, PbWO{sub 4}) and Ce-doped gadolinium aluminum gallium garnet (GAGG, Gd{sub 3}Al{sub 2}Ga{sub 3}O{sub 12}). A sub-picosecond PL rise time is observed in PWO, while longer processes in the PL response in GAGG:Ce are detected and studied. The mechanisms responsible for the PL rise time in self-activated and doped scintillators are under discussion. - Highlights: • Photoluminescence rise time is studied in two scintillators: PWO and GAGG:Ce. • Sub-picosecond photoluminescence rise time in PWO is observed for the first time. • A multicomponent luminescence rise edge is observed in GAGG:Ce. • The mechanisms behind luminescence kinetics in the crystals are under discussion.

  8. Electronic structure and luminescence properties of self-activated and Eu{sup 2+}/Ce{sup 3+} doped Ca{sub 3}Li{sub 4-y}Si{sub 2}N{sub 6-y}O{sub y} red-emitting phosphors

    Energy Technology Data Exchange (ETDEWEB)

    Wu, Quansheng; Ding, Jianyan; Li, Yanyan; Wang, Xicheng [Key Laboratory for Special Function Materials and Structural Design of the Ministry of the Education (China); Department of Material Science, School of Physical Science and Technology, Lanzhou University, Lanzhou 730000 (China); Wang, Yuhua, E-mail: wyh@lzu.edu.cn [Key Laboratory for Special Function Materials and Structural Design of the Ministry of the Education (China); Department of Material Science, School of Physical Science and Technology, Lanzhou University, Lanzhou 730000 (China)

    2017-06-15

    The undoped and Eu{sup 2+}/Ce{sup 3+} doped Ca{sub 3}Li{sub 4-y}Si{sub 2}N{sub 6-y}O{sub y} (0≤y≤1.5) (CLSN) were successfully prepared by solid-state reaction and their luminescence properties were studied. The undoped CLSN shows red defect-related luminescence with maximum emission intensity at 710 nm, Eu{sup 2+} and Ce{sup 3+} doped CLSN also show red emission centered at 702 nm and 673 nm, respectively. The electronic structure and the thermal stability of CLSN were investigated in this work. The results indicate that CLSN:Eu{sup 2+}/Ce{sup 3+} could be conducive to the development of phosphor-converted light-emitting diodes.

  9. Crystalline and magnetooptical characteristics of (Tb,Bi)3(Fe,Ga)5O12 deposited on (Y,Nd)3Al5O12

    Science.gov (United States)

    Morimoto, Ryohei; Goto, Taichi; Nakamura, Yuichi; Boey Lim, Pang; Uchida, Hironaga; Inoue, Mitsuteru

    2018-06-01

    We prepared Bi- and Ga-substituted Tb3Fe5O12 (BiGa:TIG) films on a Nd-substituted Y3Al5O12 (Nd:YAG) single crystal substrate by pulsed laser deposition, and investigated their magnetic, optical, and magnetooptical properties. A BiGa:TIG film deposited with a substrate temperature of 700 °C shows the easy axis of magnetization along the out-of-plane direction of the film and the Faraday rotation angle of 900°/cm at a wavelength of 1064 nm. The epitaxial growth of the film is confirmed by X-ray diffraction analysis.

  10. Preparation of Er"3"+:Y_3Al_5O_1_2/KNbO_3 composite and application in innocent treatment of ketamine by using sonocatalytic decomposition method

    International Nuclear Information System (INIS)

    Zhang, Hongbo; Wei, Chunsheng; Huang, Yingying; Li, Guanshu; Wu, Qiong; Wang, Jun; Song, Youtao

    2016-01-01

    Highlights: • Upconversion luminescence agent Er:YAG can enhance sonocatalytic activity of KNbO_3. • Harmless of narcotic drugs was achieved through sonocatalytic destruction. • Possible sonocatalytic destruction mechanism on narcotic drugs was proposed. - Abstract: A novel sonocatalyst, Er"3"+:Y_3Al_5O_1_2/KNbO_3 composite, was synthesized, and then, characterized by X-ray diffractometer (XRD), scanning electron microscopy (SEM) and energy dispersive X-ray spectroscopy (EDX). In order to evaluate the sonocatalytic activity of prepared Er"3"+:Y_3Al_5O_1_2/KNbO_3 composite, the sonocatalytic degradation of ketamine, a kind of narcotic drug, was studied. In addition, some influencing factors such as mass ratio, heat-treated temperature and heat-treated time on the sonocatalytic activity of prepared Er"3"+:Y_3Al_5O_1_2/KNbO_3 powders and ultrasonic irradiation time on the sonocatalytic degradation of ketamine were examined by using GC–MS machine. The experimental results showed that the Er"3"+:Y_3Al_5O_1_2/KNbO_3 composite is a good sonocatalyst in the field of ultrasonic chemistry and the sonocatalytic degradation was an effective method for the innocent treatment of ketamine.

  11. Photodynamic Processes in Fluoride Crystals Doped with Ce3+

    Directory of Open Access Journals (Sweden)

    Pavlov V.V.

    2015-01-01

    Full Text Available Integrated studies of photoelectric phenomena and their associated photodynamic processes in LiCaAlF6, LiLuF4, LiYF4, LiY0,5Lu0,5F4, SrAlF5 crystals doped with Ce3+ ions have been carried out using the combination of the methods of optical and dielectric spectroscopy. The numerical values of the basic parameters of photodynamic processes and their spectral dependence in 240 – 310 nm spectral range are evaluated. It has been shown that the most probable process, which leads to the photoionization of Ce3+ ions in LiYxLu1-xF4:Ce3+ (x=0; 0,5; 1 and LiCaAlF6:Ce3+ crystals, is excited-state absorption to the states of mixed configurations of Ce3+ ions localized near/in the conduction band of crystal.

  12. Structural, morphological and optical properties of spray deposited Mn-doped CeO2 thin films

    International Nuclear Information System (INIS)

    Pavan Kumar, CH.S.S.; Pandeeswari, R.; Jeyaprakash, B.G.

    2014-01-01

    Highlights: • Spray deposited undoped and Mn-doped CeO 2 thin films were polycrystalline. • Complete changeover of surface morphology upon 4 wt% Mn doping. • 4 wt% Mn-doped CeO 2 thin film exhibited a hydrophobic nature. • Optical band-gap decreases beyond 2 wt% Mn doping. - Abstract: Cerium oxide and manganese (Mn) doped cerium oxide thin films on glass substrates were prepared by home built spray pyrolysis system. The effect of Mn doping on the structural, morphological and optical properties of CeO 2 films were studied. It was found that both the undoped and doped CeO 2 films were polycrystalline in nature but the preferential orientation and grain size changed upon doping. Atomic force micrograph showed a complete changeover of surface morphology from spherical to flake upon doping. A water contact angle result displayed the hydrophobic nature of the doped CeO 2 film. Optical properties indicated an increase in band-gap and a decrease in transmittance upon doping owing to Moss–Burstein effect and inverse Moss–Burstein effects. Other optical properties such as refractive index, extinction coefficient and dielectric constant as a function of doping were analysed and reported

  13. Influence of the sintering temperature on the Sr content in a Ca_(_1_−_x_−_y_)Ce_xSr_yAl_zTi_(_1_−_z_)O_3 perovskite (x = 0.04–0.16) co-doped with Ce

    International Nuclear Information System (INIS)

    Kamel, Nour-el-hayet; Mouheb, Yasmina; Kamel, Ziane; Moudir, Dalila; Aouchiche, Fairouz; Arabi, Azeddine

    2016-01-01

    A Sr-Ce co-doped perovskite, with the chemical formula: Ca_(_1_−_x_−_y_)Ce_xSr_yAl_zTi_(_1_−_z_)O_3 (y = 0.04, 0.08, 0.12 and 0.16, x = 0.05) is synthesized by sol–gel process. The influence of the sintering temperature, Ts, on the rate of inserted Sr was investigated at 1223, 1373 and 1473 K. The Sr amount sequestered in the perovskite reaches 85% (y = 0.16, 9.50 wt%) for Ts = 1373 K, giving sintering densities between 3.520 and 4.400. XRD analysis reveals an orthorhombic CaTiO_3 structure. The lattice parameters obey to Vegard’s law for Ts = 1373 and 1473 K. SEM analysis shows orthorhombic grains of 0.514 μm × 1 μm mean dimensions. MCC1 and MCC2 tests, performed on minerals sintered at 1373 K, indicate that the most durable one is that containing 9.50 wt% Sr. MCC1 test gave 6.998·10"−"6 g/cm"2 d of Sr, and MCC2 2.143·10"−"4 g/cm"2 d of Ce. The temperature favors the Sr dissolution to the detriment of Ce. The Ca dissolution rate reaches 1.002·10"−"6 to 2.005·10"−"6 g/cm"2 d. - Highlights: • Ca_(_1_−_x_−_y_)Ce_xSr_yAl_zTi_(_1_−_z_)O_3 perovskite is synthesized by sol–gel. • The influence of the sintering temperature, Ts, on the rate of inserted Sr was investigated at 1223, 1373 and 1473 K. • 85% of total Sr was sequestered in the perovskite for Ts = 1373 K. • MCC1 and MCC2 leach tests indicate that the most durable mineral is that containing 9.50 wt.% Sr. • MCC1 test gave 8.10 10"−"1"0 kg/m"2.d Sr. The lower is the leaching temperature the higher is the mineral durability.

  14. Dosimeter properties of Ce and Eu doped LiCaAlF6

    International Nuclear Information System (INIS)

    Yanagida, Takayuki; Fujimoto, Yutaka; Watanabe, Kenichi; Fukuda, Kentaro

    2014-01-01

    Optical, scintillation properties, optical stimulated luminescence, and thermally stimulated luminescence of Ce 1, 3, and 5% doped and Eu 1, 1.5, and 2% doped LiCaAlF 6 crystals fabricated by Tokuyama Corp. were investigated. In transmittance, absorption was proportional to dopant concentrations and typical optical quantum yield of Ce and Eu-doped LiCaAlF 6 were 40 and 100%, respectively. Scintillation wavelength and decay time profiles were investigated under X-ray irradiation. Ce 3+ and Eu 2+ 5d-4f luminescence appeared around 300 nm and 370 nm with typical decay time of 40 ns and 1.5 μs, respectively. Optically stimulated luminescence of Ce-doped ones appeared under 405 nm stimulation with detectable intensity while those of Eu doped ones were quite weak. Thermally stimulated luminescence of Ce- and Eu-doped LiCaAlF 6 were enough strong and they exhibited good response function from 1 to 1000 mGy exposure. - Highlights: • Optical, scintillation, OSL, and TSL properties of Ce or Eu differently doped LiCaAlF6 were studied. • PL quantum yield of Ce and Eu doped LiCaAlF6 showed 40% and 100%, respectively. • OSL was observed in Ce-doped LiCaAlF6. • TSL was observed in both material systems and exhibited a good dose response from 1 to 1000 mGy

  15. Site Occupancies, Luminescence, and Thermometric Properties of LiY9(SiO4)6O2:Ce3+ Phosphors.

    Science.gov (United States)

    Zhou, Weijie; Pan, Fengjuan; Zhou, Lei; Hou, Dejian; Huang, Yan; Tao, Ye; Liang, Hongbin

    2016-10-04

    In this work, we report the tunable emission properties of Ce 3+ in an apatite-type LiY 9 (SiO 4 ) 6 O 2 compound via adjusting the doping concentration or temperature. The occupancies of Ce 3+ ions at two different sites (Wyckoff 6h and 4f sites) in LiY 9 (SiO 4 ) 6 O 2 have been determined by Rietveld refinements. Two kinds of Ce 3+ f-d transitions have been studied in detail and then assigned to certain sites. The effects of temperature and doping concentration on Ce 3+ luminescence properties have been systematically investigated. It is found that the Ce 3+ ions prefer occupying Wyckoff 6h sites and the energy transfer between Ce 3+ at two sites becomes more efficient with an increase in doping concentration. In addition, the charge-transfer vibronic exciton (CTVE) induced by the existence of free oxygen ion plays an important role in the thermal quenching of Ce 3+ at 6h sites. Because of the tunable emissions from cyan to blue with increasing temperature, the phosphors LiY 9 (SiO 4 ) 6 O 2 :Ce 3+ are endowed with possible thermometric applications.

  16. Chrystal structure properties of Al-doped Li{sub 4}Ti{sub 5}O{sub 12} synthesized by solid state reaction method

    Energy Technology Data Exchange (ETDEWEB)

    Sandi, Dianisa Khoirum, E-mail: dianisa875@gmail.com; Suryana, Risa, E-mail: rsuryana@staff.uns.ac.id [Department of Physics, Faculty of Mathematics and Natural Sciences, Sebelas Maret University (Indonesia); Priyono, Slamet, E-mail: slam013@lipi.go.id [Physics Research Center (P2F)-LIPI, Puspiptek Area, Serpong, Tangerang (Indonesia)

    2016-02-08

    This research aim is to analyze the effect of Aluminum (Al) doping in the structural properties of Al-doped Li{sub 4}Ti{sub 5}O{sub 12} as anode in lithium ion battery. Al-doped Li{sub 4}Ti{sub 5}O{sub 12} powders were synthesized by solid state reaction method. LiOH.H{sub 2}O, TiO{sub 2}, and Al{sub 2}O{sub 3} were raw materials. These materials were milled for 15 h, calcined at temperature of 750{sup o}C and sintered at temperature of 800{sup o}C. Mole percentage of doping Al (x) was varied at x=0; x=0.025; and x =0.05. Al-doped Li{sub 4}Ti{sub 5}O{sub 12} powders were synthesized by solid state reaction method. X-ray diffraction was employed to determine the structure of Li{sub 4}Ti{sub 5}O{sub 12}. The PDXL software was performed on the x-ray diffraction data to estimate the phase percentage, the lattice parameter, the unit cell volume, and the crystal density. Al-doped Li{sub 4}Ti{sub 5}O{sub 12} has cubic crystal structure. Al-doping at x=0 and x=0.025 does not change the phase as Li{sub 4}Ti{sub 5}O{sub 12} while at x=0.050 the phase changes to the LiTiAlO{sub 4}. The diffraction patterns show that the angle shifted to the right as the increase of x which indicated that Al substitute Ti site. Percentage of Li{sub 4}Ti{sub 5}O{sub 12} phase at x=0 and x=0.025 was 97.8% and 96.8%, respectively. However, the lattice parameters, the unit cell volume, and the crystal density does not change significantly at x=0; x=0.025; and x=0.050. Based on the percentage of Li{sub 4}Ti{sub 5}O{sub 12} phase, the Al-doped Li at x=0 and x=0.025 is promising as a lithium battery anode.

  17. Photoluminescence properties of Tb3Al5O12:Ce3+ garnet synthesized by the metal organic decomposition method

    Science.gov (United States)

    Onishi, Yuya; Nakamura, Toshihiro; Adachi, Sadao

    2017-02-01

    Tb3Al5O12:Ce3+ garnet (TAG:Ce3+) phosphor was synthesized by the metal organic decomposition (MOD) method and subsequent calcination at Tc = 800-1200°C for 1 h in air. The effects of Ce3+ concentration on the phosphor properties were investigated in detail using X-ray diffraction (XRD) analysis, photoluminescence (PL) analysis, PL excitation (PLE) spectroscopy, and PL decay measurements. The maximum intensity in the Ce3+ yellow emission was observed at the Ce3+ concentration of ∼0.20%. PLE and PL decay measurements suggested an evidence of the energy transfer from Tb3+ to Ce3+. Calcination temperature dependence of the XRD and PL intensities yielded an energy of ∼1.5 eV both for the TAG formation in the MOD process and for the optical activation of Ce3+ in its lattice sites. Temperature dependences of the PL intensity for the TAG:Ce3+ yellow-emitting and K2SiF6:Mn4+ red-emitting phosphors were also examined for the future solid-state lighting applications at T = 20-500 K in 10-K steps. The data of TAG:Ce3+ were analyzed using a theoretical model with considering a reservoir level of Et ∼9 meV, yielding a quenching energy of Eq ∼0.35 eV, whereas the K2SiF6:Mn4+ red-emitting phosphor data yielded a value of Eq ∼1.0 eV. The schematic energy-level diagrams for Tb3+ and Ce3+ were proposed for the sake of a better understanding of these ions in the TAG host.

  18. Effect of thermal annealing on scintillation properties of Ce:Gd{sub 2}Y{sub 1}Ga{sub 2.7}Al{sub 2.3}O{sub 12} under different atmosphere

    Energy Technology Data Exchange (ETDEWEB)

    Wang, Chao; Ding, Dongzhou; Wu, Yuntao; Li, Huanying; Chen, Xiaofeng; Shi, Jian; Wang, Qingqing; Ye, Le; Ren, Guohao [Chinese Academy of Sciences, Shanghai Institute of Ceramics, Shanghai (China)

    2017-05-15

    Cerium-doped 1% Ce:Gd{sub 2}Y{sub 1}Ga{sub 2.7}Al{sub 2.3}O{sub 12}(GYGAG) single crystal samples grown via Czochralski method were annealed under air, O{sub 2} and N{sub 2} atmospheres from 350 to 1400 C. The X-ray excited luminescence spectra, energy spectra and UV as well as thermally stimulated luminescence (TSL) spectra were performed comparatively on ''as-grown'' and thermally annealed samples. It was found that the luminescence efficiency after annealing in air and O{sub 2} was significantly enhanced compared to the non-annealed samples and this phenomenon was suggested to be caused by the existence of some oxygen vacancies in the Ce:GYGAG crystals. And the oxygen vacancies in the as-grown GYGAG crystals can be effectively eliminated by means of annealing in O{sub 2} containing atmosphere without changing the luminescence mechanism. From the TSL curves before and after annealing, three traps within 77-650 K were found to be related to oxygen vacancies. (orig.)

  19. Synthesis and Luminescence Characteristics of Cr3+ doped Y3Al5O12 Phosphors

    Energy Technology Data Exchange (ETDEWEB)

    Smith, Brenda A. [Oak Ridge National Lab. (ORNL), Oak Ridge, TN (United States); Dabestani, Reza T. [Oak Ridge National Lab. (ORNL), Oak Ridge, TN (United States); Lewis, Linda A. [Oak Ridge National Lab. (ORNL), Oak Ridge, TN (United States); Thompson, Cyril V. [Oak Ridge National Lab. (ORNL), Oak Ridge, TN (United States); Collins, Case T. [Oak Ridge National Lab. (ORNL), Oak Ridge, TN (United States); Aytug, Tolga [Oak Ridge National Lab. (ORNL), Oak Ridge, TN (United States)

    2015-10-01

    Luminescence performance of yttrium aluminum garnet (Y3Al5O12) phosphors as a function of Cr3+ concentration has been investigated via two different wet-chemical synthesis techniques, direct- (DP) and hydrothermal-precipitation (HP). Using either of these methods, the red-emitting phosphor [Y3Al5-xCrxO12 (YAG: Cr3+)] showed similar photoluminescence (PL) intensities once the dopant concentration was optimized. Specifically, the YAG: Cr3+ PL emission intensity reached a maximum at Cr3+ concentrations of x = 0.02 (0.4 at.%) and x = 0.13 (2.6 at.%) for DP and HP processed samples, respectively. The results indicated the strong influence of the processing method on the optimized YAG: Cr3+ performance, where a more effective energy transfer rate between a pair of Cr3+ activators at low concentration levels was observed by using the DP synthesis technique. Development of a highly efficient phosphor, using a facile synthesis approach, could significantly benefit consumer and industrial applications by improving the operational efficiency of a wide range of practical devices.

  20. Effects of calcium doping on the superconducting properties of top-seeded melt growth processed Y1.5Ba2-xCaxCu3Oy superconductors

    International Nuclear Information System (INIS)

    Park, S.D.; Kim, H.J.; Park, B.J.; Han, Y.H.; Jun, B.-H.; Lee, J.S.; Kim, C.-J.

    2011-01-01

    We study effects of calcium doping in melt processed Y123 superconductors. We examine a superconducting transition temperature and current density. A transition temperature and current density decreases by calcium doping. Calcium doping leads to coarseing of Y211 particles. Y211 refining effect by CeO 2 is disappreared by calcium doping. The effect of calcium doping on the superconducting properties of top seeded melt growth (TSMG) processed Y 1.5 Ba 2-x Ca x Cu 3 O y superconductors was studied in terms of calcium content (X ca ). YBa 2-x Ca x Cu 3 O 7-δ (X ca = 0, 0.005, 0.01, 0.02, 0.04, 0.1, 0.3) powders were synthesized by the powder calcination method. YBa 2-x Ca x Cu 3 O 7-δ powders were mixed with 0.25 mole Y 2 O 3 powder and 1 wt.% CeO 2 as Y 2 BaCuO 5 (Y211) refiner, and finally made into Y 1 . 5 Ba 2-x Ca x Cu 3 O y (Y1.5) + 1 wt.% CeO 2 composition. The single Y123 growth on the top surface was observed up to X ca = 0.1, while the multiple Y123 growth was observed at X ca ≥ 0.1. The superconducting transition temperature (T c ) and critical current density (J c ) of TSMG processed Y1.5 samples were inversely proportional to X ca . The Y211 size increased with increasing X ca due to the enhancement of Y211 coarsening by calcium doping. No Y211 refining effect by CeO 2 was observed in the calcium doped samples. The T c and J c decrease by calcium doping are likely to be due to the calcium incorporation with the Y123 lattice and formation of coarse Y211 particles.

  1. Structural, morphological and optical properties of spray deposited Mn-doped CeO{sub 2} thin films

    Energy Technology Data Exchange (ETDEWEB)

    Pavan Kumar, CH.S.S.; Pandeeswari, R.; Jeyaprakash, B.G., E-mail: jp@ece.sastra.edu

    2014-07-25

    Highlights: • Spray deposited undoped and Mn-doped CeO{sub 2} thin films were polycrystalline. • Complete changeover of surface morphology upon 4 wt% Mn doping. • 4 wt% Mn-doped CeO{sub 2} thin film exhibited a hydrophobic nature. • Optical band-gap decreases beyond 2 wt% Mn doping. - Abstract: Cerium oxide and manganese (Mn) doped cerium oxide thin films on glass substrates were prepared by home built spray pyrolysis system. The effect of Mn doping on the structural, morphological and optical properties of CeO{sub 2} films were studied. It was found that both the undoped and doped CeO{sub 2} films were polycrystalline in nature but the preferential orientation and grain size changed upon doping. Atomic force micrograph showed a complete changeover of surface morphology from spherical to flake upon doping. A water contact angle result displayed the hydrophobic nature of the doped CeO{sub 2} film. Optical properties indicated an increase in band-gap and a decrease in transmittance upon doping owing to Moss–Burstein effect and inverse Moss–Burstein effects. Other optical properties such as refractive index, extinction coefficient and dielectric constant as a function of doping were analysed and reported.

  2. Formation of qualified BaHfO3 doped Y0.5Gd0.5Ba2Cu3O7-δ film on CeO2 buffered IBAD-MgO tape by self-seeding pulsed laser deposition

    Science.gov (United States)

    Liu, Linfei; Wang, Wei; Yao, Yanjie; Wu, Xiang; Lu, Saidan; Li, Yijie

    2018-05-01

    Improvement in the in-filed transport properties of REBa2Cu3O7-δ (RE = rare earth elements, REBCO) coated conductor is needed to meet the performance requirements for various practical applications, which can be accomplished by introducing artificial pinning centers (APCs), such as second phase dopant. However, with increasing dopant level the critical current density Jc at 77 K in zero applied magnetic field decreases. In this paper, in order to improve Jc we propose a seed layer technique. 5 mol% BaHfO3 (BHO) doped Y0.5Gd0.5Ba2Cu3O7-δ (YGBCO) epilayer with an inserted seed layer was grown on CeO2 buffered ion beam assisted deposition MgO (IBAD-MgO) tape by pulsed laser deposition. The effect of the conditions employed to prepare the seed layer, including tape moving speed and chemical composition, on the quality of 5 mol% BHO doped YGBCO epilayer was systematically investigated by X-ray diffraction (XRD) measurements and scanning electron microscopy (SEM) observations. It was found that all the samples with seed layer have higher Jc (77 K, self-field) than the 5 mol% BHO doped YGBCO film without seed layer. The seed layer could inhibit deterioration of the Jc at 77 K and self-filed. Especially, the self-seed layer (5 mol% BHO doped YGBCO seed layer) was more effective in improving the crystal quality, surface morphology and superconducting performance. At 4.2 K, the 5 mol% BHO doped YGBCO film with 4 nm thick self-seed layer had a very high flux pinning force density Fp of 860 GN/m3 for B//c under a 9 T field, and more importantly, the peak of the Fp curve was not observed.

  3. Study of effect of co-doping on CIE coordinates of strontium cerium oxide phosphor (Sr_2CeO_4)

    International Nuclear Information System (INIS)

    Zambare, Pradip Z.; Ahirrao, P.B.; Chaudhari, D.B.; Zambare, A.P.; Mahajan, O.H.

    2016-01-01

    The phosphors Sr_2CeO_4 doped europium and gadolinium were synthesized by modified solid state diffusion method. From emission spectra, the CIE coordinates (x, y) of x% Eu"3"+ and 0.5 %Gd"3"+ doped Sr_2CeO_4 phosphors was calculated. In present paper, we investigate luminescence properties and colorimetric study of Sr_2CeO_4 doped 0.5% Gd"3"+, x% Eu"3"+. The phosphors Sr_2CeO_4 doped europium and gadolinium were successfully synthesized by modified solid state diffusion method. X-ray diffraction (XRD) profile confirms the orthorhombic nature of Eu"3"+ and 0.5% Gd"3"+ doped Sr_2CeO_4 phosphors. In addition, scanning electron Microscopy (SEM), Fourier-Transformation IR spectroscopy (FTIR), was also used to study the synthesized phosphors

  4. Study of the defect structure of ''pure'' and doped nonstoichiometric CeO2

    International Nuclear Information System (INIS)

    Blumenthal, R.N.

    1975-09-01

    Electrical conductivity and thermogravimetric measurements were made on Ta 2 O 5 -doped nonstoichiometric CeO 2 (i.e. Ce/sub 1-y/Ta/sub y/O/sub 2-x/ ) as a function of temperature and oxygen partial pressure. Over a limited range of temperature and nonstoichiometry, the isothermal dependence of the electrical conductivity on nonstoichiometry may be described by the equation sigma = A + Bx, where A is the electronic conductivity associated with the electronic defects produced by doping CeO 2 with Ta 2 O 5 . The electronic conductivity resulting from the nonstoichiometric defect reaction O/sup x/ + 2Ce/sub Ce//sup x/ = V 0 + 2Ce'sub Ce/ + 1 / 2 O 2 (g) is equal to Bx. The ionic conductivity may be described by the relation sigma/sub i/ = B[y+x]eμ'/sub V 0 / exp (--E/sub i//kT), and the electronic conductivity by the isothermal expressions sigma/sub e/ proportional to P/sub O 2 //sup -1/4/ and sigma/sub e/ proportional to x; x less than 3 x 10 -2 . These results are consistent with defect models involving doubly ionized oxygen vacancies. An empirical expression (i.e. Δ anti H/sub O 2 / proportional to y/2 or z/4) was obtained relating the dependence of Δ anti H/sub O 2 / on the dopant concentration of lower valent foreign cations (e.g. y/2 for Ce/sub 1-y/M/sub y/O/sub 2-y-x/ and z/4 for Ce/sub 1-z/M/sub z/O/sub 2-z/2-x/ where M = Ca, Sr and M' = Y, La). (auth)

  5. Characterizations of Pr-doped Yb3Al5O12 single crystals for scintillator applications

    Science.gov (United States)

    Yoshida, Yasuki; Shinozaki, Kenji; Igashira, Takuya; Kawano, Naoki; Okada, Go; Kawaguchi, Noriaki; Yanagida, Takayuki

    2018-04-01

    Yb3Al5O12 (YbAG) single crystals doped with different concentrations of Pr were synthesized by the Floating Zone (FZ) method. Then, we evaluated their basic optical and scintillation properties. All the samples showed photoluminescence (PL) with two emission bands appeared approximately 300-500 nm and 550-600 nm due to the charge transfer luminescence of Yb3+ and intrinsic luminescence of the garnet structure, respectively. A PL decay profile of each sample was approximated by a sum of two exponential decay functions, and the obtained decay times were 1 ns and 3-4 ns. In the scintillation spectra, we observed emission peaks in the ranges from 300 to 400 nm and from 450 to 550 nm for all the samples. The origins of these emissions were attributed to charge transfer luminescence of Yb3+ and intrinsic luminescence of the garnet structure, respectively. The scintillation decay times became longer with increasing the Pr concentrations. Among the present samples, the 0.1% Pr-doped sample showed the lowest scintillation afterglow level. In addition, pulse height spectrum of 5.5 MeV α-rays was demonstrated using the Pr-doped YbAG, and we confirmed that all the samples showed a full energy deposited peak. Above all, the 0.1% Pr-doped sample showed the highest light yield with a value of 14 ph/MeV under α-rays excitation.

  6. Evaluation of Ce3+ and alkali metal ions Co-doped LiSrAlF6 crystalline scintillators

    International Nuclear Information System (INIS)

    Wakahara, Shingo; Yanagida, Takayuki; Fujimoto, Yutaka; Yokota, Yuui; Pejchal, Jan; Kurosawa, Shunsuke; Suzuki, Shotaro; Kawaguchi, Noriaki; Fukuda, Kentaro; Yoshikawa, Akira

    2013-01-01

    High scintillation efficiency of Eu-doped LiSrAlF 6 (LiSAF) and LiCaAlF 6 (LiCAF) codoped with alkali metal ions has been reported in our recent studies. Thus in this paper, we demonstrated the scintillation properties of 1% Ce-doped LiSAF crystals with 1% alkali metal ions co-doping to increase the light yield and understand the scintillation mechanism. The crystals showed intense emission band corresponding to the 5d-4f transition of Ce 3+ , and their light yields under thermal neutron excitation were higher than that of the Ce only doped crystal. Especially, the light yield of Ce–Na co-doped crystal exceeded about two times that of Ce only doped one. -- Highlights: ► Ce-doped and alkali metal co-doped LiSAF crystals were grown by μ-PD method. ► Alkali metal co-doped crystals showed higher light yield than Ce only doped crystal. ► Decay time of alkali metal co-doped LiSAF were longer than that of Ce only doped one

  7. Luminescence properties and gamma-ray response of the Ce and Ca co-doped (Gd,Y)F3 single crystals

    International Nuclear Information System (INIS)

    Kamada, Kei; Yanagida, Takayuki; Fujimoto, Yutaka; Fukabori, Akihiro; Yoshikawa, Akira; Nikl, Martin

    2011-01-01

    The Ca0.5% and Ce1%, 3%, 7%, 10% co-doped Gd 0.5 Y 0.5 F 3 single crystals were grown by the μ-PD method. In the Ca0.5% and Ce3% co-doped sample, Ce 3+ -perturbed luminescence at 380 nm was observed with 32.4 ns photoluminescence decay time. The energy transfer in the sequence of the regular Ce 3+ → (Gd 3+ ) n → the perturbed Ce 3+ sites was evidenced through observation of decay time shortening of the regular Ce 3+ and Gd 3+ centers and the change between the Gd 3+ and Ce 3+ -perturbed emission intensity. The gamma-ray excited scintillation response of the Ca0.5%, Ce7% co-doped Gd 0.5 Y 0.5 F 3 sample was investigated with the help of the pulse height spectra and the light yield, energy resolution and non-proportionality was evaluated in the interval of energies of 59.4-1274 keV.

  8. Thermoluminescence properties of undoped and Tb3+ and Ce3+ doped YAG nanophosphor under UV-, X- and β-ray irradiation

    International Nuclear Information System (INIS)

    Rosa, E. de la; Rodriguez, R.A.; Melendrez, R.; Salas, P.; Diaz-Torres, L.A.; Barboza-Flores, M.

    2007-01-01

    The thermoluminescence (TL) properties of undoped, Ce 3+ and Tb 3+ doped Y 3 Al 5 O 12 (YAG) nanocrystals under UV-, X- and β-rays irradiation is reported. The TL signal of undoped and doped samples indicates a high sensitivity to UV-, X- and β-ray irradiation. The introduction of the doping ions induces changes in the trapping processes and the TL efficiency. The results show that both undoped and doped YAG nanocrystalline phosphor present good TL efficiency as well as good dose response which qualify them as a potential UV-, X- and β-ray dosimeter. A linear response under X-ray irradiation is observed for low doses level in the 0.02-1.02 μGy range and for relatively high doses level of β-ray irradiation in the range from 10 to 600 Gy

  9. Energy transfer efficiency from Cr(3+) to Nd(3+) in solar-pumped laser using transparent Nd/Cr:Y(3)Al(5)O(12) ceramics.

    Science.gov (United States)

    Hasegawa, Kazuo; Ichikawa, Tadashi; Mizuno, Shintaro; Takeda, Yasuhiko; Ito, Hiroshi; Ikesue, Akio; Motohiro, Tomoyoshi; Yamaga, Mitsuo

    2015-06-01

    We report energy transfer efficiency from Cr3+ to Nd3+ in Nd (1.0 at.%)/Cr (0.4 at.%) co-doped Y3Al5O12 (YAG) transparent ceramics in the laser oscillation states. The laser oscillation has performed using two pumping lasers operating at 808 nm and 561 nm; the former pumps Nd3+ directly to create the 1064 nm laser oscillation, whereas the latter assists the performance via Cr3+ absorption and sequential energy transfer to Nd3+. From the laser output power properties and laser mode analysis, the energy transfer efficiency was determined to be around 65%, which is close to that obtained from the spontaneous Nd3+ emission.

  10. Luminescent properties and energy transfer in the green phosphors LaBSiO5:Tb3+, Ce3+.

    Science.gov (United States)

    Wang, Zhengliang; Cheng, Ping; He, Pei; Liu, Yong; Zhou, Yayun; Zhou, Qiang

    2015-09-01

    LaBSiO5 phosphors doped with Ce(3+) and Tb(3+) were synthesized using the conventional solid-state method at 1100 °C. The phase purity and luminescent properties of these phosphors are investigated. LaBSiO5:Tb(3+) phosphors show intense green emission, and LaBSiO5 phosphors doped with Ce(3+) show blue-violet emission under UV light excitation. LaBSiO5 phosphors co-doped with Ce(3+) and Tb(3+) exhibit blue-violet and green emission under excitation by UV light. The blue-violet emission is due to the 5d-4f transition of Ce(3+) and the green emission is ascribed to the (5) D4 → (7) F5 transition of Tb(3+). The spectral overlap between the excitation band of Tb(3+) and the emission band of Ce(3+) supports the occurrence of energy transfer from Ce(3+) to Tb(3+), and the energy transfer process was investigated. Copyright © 2014 John Wiley & Sons, Ltd.

  11. Space growth studies of Ce-doped Bi12SiO20 single crystal

    International Nuclear Information System (INIS)

    Zhou, Y.F.; Wang, J.C.; Tang, L.A.; Pan, Z.L.; Chen, N.F.; Chen, W.C.; Huang, Y.Y.; He, W.

    2004-01-01

    Ce-doped Bi 12 SiO 20 (BSO) single crystal was grown on board of the Chinese Spacecraft-Shenzhou No. 3. A cylindrical crystal, 10 mm in diameter and 40 mm in length, was obtained. The morphology of crystals is significantly different for ground- and space-grown portions. The space- and ground-grown crystals have been characterized by Ce concentration distribution, X-ray rocking curve absorption spectrum and micro-Raman spectrum. The results show that the quality of Ce-doped BSO crystal grown in space is more homogeneous and more perfect than that of ground grown one

  12. Interaction of Ce{sub 1−x}Er{sub x}O{sub 2−y} nanoparticles with Al{sub 2}O{sub 3}

    Energy Technology Data Exchange (ETDEWEB)

    Krajczyk, L.; Kraszkiewicz, P.; Kepinski, L., E-mail: L.Kepinski@int.pan.wroc.pl

    2015-02-01

    The interaction of nanocrystalline Ce{sub 0.5}Er{sub 0.5}O{sub 1.75} mixed oxide with an amorphous Al{sub 2}O{sub 3} in oxidizing and reducing atmosphere up to 1100 °C was studied by XRD, TEM, SEM-EDS and BET. Uniform, chemically homogeneous Ce{sub 0.5}Er{sub 0.5}O{sub 1.75} nanoparticles (2 nm in size) were prepared by microemulsion method and deposited on a high surface γ-alumina support. The nanoparticles were structurally and chemically stable in the oxidizing atmosphere up to 1100 °C, exhibiting only an increase of the mean crystallite size to 9 nm after 3 h treatment. Prolonged heating (24 h) at 1100 °C caused partial decomposition of the mixed oxide and reaction of the extracted erbium with the support with formation of hexagonal (P6{sub 3}/mmc) ErAlO{sub 3} aluminate. The same hexagonal ErAlO{sub 3} occurred also in Er/Al{sub 2}O{sub 3} sample prepared by impregnation of Al{sub 2}O{sub 3} support with an aqueous solution of Er nitrate and subjected to heating in air or hydrogen at 1100 °C. In the reducing atmosphere the Ce{sub 0.5}Er{sub 0.5}O{sub 1.75} reacted with Al{sub 2}O{sub 3} already at 800 °C, to form an amorphous surface phase. At 900 °C monoclinic (P2{sub 1}/c) (Er,Ce){sub 4}Al{sub 2}O{sub 9} mixed aluminate was formed with the unit cell volume 4.5% bigger than that of pure Er{sub 4}Al{sub 2}O{sub 9} phase. After 3 h treatment at 1000 °C more than half of the (Er,Ce){sub 4}Al{sub 2}O{sub 9} aluminate decomposed into two nanocrystalline mixed monoaluminates: tetragonal (I4/mcm) (Ce,Er)AlO{sub 3} and hexagonal (P6{sub 3}/mmc) (Er,Ce)AlO{sub 3}. Nanocrystalline mixed aluminate particles with Er{sup 3+} ions placed in well-defined lattice sites and supported at the surface of Al{sub 2}O{sub 3} support, may be interesting as highly efficient active components of optical waveguides amplifiers. - Graphical abstract: Structure evolution of Ce{sub 0.5}Er{sub 0.5}O{sub 1.75} on Al{sub 2}O{sub 3} in air and in H{sub 2}. - Highlights:

  13. Ca2 Al2 SiO7 :Ce3+ phosphors for mechanoluminescence dosimetry.

    Science.gov (United States)

    Tiwari, Geetanjali; Brahme, Nameeta; Sharma, Ravi; Bisen, D P; Sao, Sanjay Kumar; Sahu, Ishwar Prasad

    2016-12-01

    A series of Ce 3+ ion single-doped Ca 2 Al 2 SiO 7 phosphors was synthesized by a combustion-assisted method at an initiating temperature of 600 °C. The samples were annealed at 1100 °C for 3 h and their X-ray diffraction patterns confirmed a tetragonal structure. The phase structure, particle size, surface morphology and elemental analysis were analyzed using X-ray diffraction (XRD), transmission electron microscope (TEM), scanning electron microscopy (SEM) and energy dispersive X-ray (EDX) spectroscopy techniques. Thermoluminescence (TL) intensity increased with increase in ultraviolet (UV) light exposure time up to 15 min. With further increase in the UV irradiation time the TL intensity decreases. The increase in TL intensity indicates that trap concentration increased with UV exposure time. A broad peak at 121 °C suggested the existence of a trapping level. The peak of mechanoluminescence (ML) intensity versus time curve increased linearly with increasing impact velocity of the moving piston. Mechanoluminescence intensity increased with increase in UV irradiation time up to 15 min. Under UV-irradiation excitation, the TL and ML emission spectra of Ca 2 Al 2 SiO 7 :Ce 3+ phosphor showed the characteristic emission of Ce 3+ peaking at 400 nm (UV-violet) and originating from the Ce 3+ transitions of 5d-4f ( 2 F 5/2 and 2 F 7/2 ). The photoluminescence (PL) emission spectra for Ca 2 Al 2 SiO 7 :Ce 3+ were similar to the ML/TL emission spectra. The mechanism of ML excitation and the suitability of the Ca 2 Al 2 SiO 7 :Ce 3+ phosphor for radiation dosimetry are discussed. Copyright © 2016 John Wiley & Sons, Ltd. Copyright © 2016 John Wiley & Sons, Ltd.

  14. Enhanced Ce{sup 3+} photoluminescence by Li{sup +} co-doping in CaO phosphor and its use in blue-pumped white LEDs

    Energy Technology Data Exchange (ETDEWEB)

    Hao, Zhendong, E-mail: haozd@ciomp.ac.cn; Zhang, Xia; Luo, Yongshi; Zhang, Ligong; Zhao, Haifeng; Zhang, Jiahua, E-mail: zhangjh@ciomp.ac.cn

    2013-08-15

    In this paper, we demonstrate a method to improve the photoluminescence of CaO: Ce{sup 3+} phosphor and delineate its first use in blue-pumped white LEDs. The results show that the yellow emission of Ce{sup 3+} is enhanced by a factor of 1.88 by adding Li{sup +} into CaO host at 474 nm blue light excitation. On analyzing the diffuse reflection spectra and fluorescence decay curves, we reveal that the photoluminescence enhancement is originated from the rise of absorbance to the excitation photons but not from the improvement of the luminescent efficiency. Li{sup +}-improved CaO: Ce{sup 3+} exhibits more red component when it is compared with the commercial Y{sub 3}Al{sub 5}O{sub 12}: Ce{sup 3+} (YAG: Ce{sup 3+}) phosphor, indicating its potential application for high color rendering white LEDs. Thus, a white LED is fabricated by combining blue InGaN LED chip with CaO: Ce{sup 3+}, Li{sup +} phosphor and a warm white light with high color rendering index (R{sub a}) of 80, low correlated color temperature (T{sub c}) of 4524 K, and sufficient luminous efficiency of 50 lm W{sup −1} is obtained. -- Highlights: • The photoluminescence of Ce{sup 3+} in CaO host was enhanced by Li{sup +} co-doping. • A CaO: Ce{sup 3+}, Li{sup +} based white LED was fabricated for the first time. • An efficient warm white light was obtained. • CaO: Ce{sup 3+}, Li{sup +} is expected to be used as a yellow phosphor for blue-pumped white LEDs.

  15. Ferroelectric relaxor Ba(TiCe)O3

    International Nuclear Information System (INIS)

    Chen Ang; Zhi Jing; Yu Zhi

    2002-01-01

    The dielectric behaviour of Ba(Ti 1-y Ce y )O 3 solid solutions (y=0-0.3) has been studied. A small amount of Ce doping (y=0.02) has weak influence on the dielectric behaviour of Ba(Ti 1-y Ce y )O 3 . With increasing Ce concentration, three phase transitions of pure BaTiO 3 are pinched into one rounded dielectric peak with frequency dispersion, and the relaxation time follows the Vogel-Fulcher relation. The evolution from a normal ferroelectric to a ferroelectric relaxor is emphasized. High strains (S=∼0.1-0.19%) with a small hysteresis under ac fields are obtained in ferroelectric relaxors Ba(Ti 1-y Ce y )O 3 . The physical mechanism of the relaxation process, the pinching effect of the phase transitions and their influence on the ferroelectric and electrostrictive behaviour are discussed. (author)

  16. Preparation of Er{sup 3+}:Y{sub 3}Al{sub 5}O{sub 12}/KNbO{sub 3} composite and application in innocent treatment of ketamine by using sonocatalytic decomposition method

    Energy Technology Data Exchange (ETDEWEB)

    Zhang, Hongbo [College of Chemistry, Liaoning University, Shenyang 110036 (China); Wei, Chunsheng [College of Chemistry, Liaoning University, Shenyang 110036 (China); National Police University of China, Shenyang 110854 (China); Huang, Yingying [College of Chemistry, Liaoning University, Shenyang 110036 (China); Li, Guanshu [College of Environment, Liaoning University, Shenyang 110036 (China); Wu, Qiong [College of Chemistry, Liaoning University, Shenyang 110036 (China); Wang, Jun, E-mail: wangjun888tg@126.com [College of Chemistry, Liaoning University, Shenyang 110036 (China); Song, Youtao [College of Environment, Liaoning University, Shenyang 110036 (China)

    2016-11-05

    Highlights: • Upconversion luminescence agent Er:YAG can enhance sonocatalytic activity of KNbO{sub 3}. • Harmless of narcotic drugs was achieved through sonocatalytic destruction. • Possible sonocatalytic destruction mechanism on narcotic drugs was proposed. - Abstract: A novel sonocatalyst, Er{sup 3+}:Y{sub 3}Al{sub 5}O{sub 12}/KNbO{sub 3} composite, was synthesized, and then, characterized by X-ray diffractometer (XRD), scanning electron microscopy (SEM) and energy dispersive X-ray spectroscopy (EDX). In order to evaluate the sonocatalytic activity of prepared Er{sup 3+}:Y{sub 3}Al{sub 5}O{sub 12}/KNbO{sub 3} composite, the sonocatalytic degradation of ketamine, a kind of narcotic drug, was studied. In addition, some influencing factors such as mass ratio, heat-treated temperature and heat-treated time on the sonocatalytic activity of prepared Er{sup 3+}:Y{sub 3}Al{sub 5}O{sub 12}/KNbO{sub 3} powders and ultrasonic irradiation time on the sonocatalytic degradation of ketamine were examined by using GC–MS machine. The experimental results showed that the Er{sup 3+}:Y{sub 3}Al{sub 5}O{sub 12}/KNbO{sub 3} composite is a good sonocatalyst in the field of ultrasonic chemistry and the sonocatalytic degradation was an effective method for the innocent treatment of ketamine.

  17. Rare earths (Ce, Eu, Tb) doped Y2Si2O7 phosphors for white LED

    International Nuclear Information System (INIS)

    Sokolnicki, Jerzy

    2013-01-01

    Nanocrystalline yttrium pyrosilicate Y 2 Si 2 O 7 (YPS) singly, doubly or triply doped with Ce 3+ , Eu 3+ , Tb 3+ was obtained by the reaction of nanostructured Y 2 O 3 :Ln 3+ and colloidal SiO 2 at high temperatures. X-ray diffraction analysis confirmed the formation of a single phase of α-YPS at 1200 °C. Two series of YPS samples doped with Eu 3+ or Eu 3+ /Tb 3+ were obtained by applying the reducing atmosphere (75%N 2 +25%H 2 ) at different temperatures. The luminescence and excitation spectra are reported. The singly Eu 3+ doped YPS emit from both Eu 3+ and Eu 2+ ions, with the spectral position and width of the Eu 2+ emission different in both series. The presence of Eu 2+ in the samples was confirmed by electron paramagnetic resonance (EPR) spectra. A broadband emission of Eu 2+ (380–650 nm), combined with the red emission of Eu 3+ is perceived by the naked eye as white light. Co-doping of YPS:Eu 3+ with Tb 3+ results in enhancement of the green component of the emission, and well-balanced white luminescence. The colour of this emission is tunable, and it is possible to get Commission International de I'Eclairage (CIE) chromaticity coordinates of (0.327, 0.327), colour-rendering index (CRI) of 85, and quantum efficiency (QE) of 71%. These phosphors are efficiently excited in the wavelength range of 300–420 nm, which perfectly matches a near UV-emitting InGaN chip. It was shown that for triply (Ce 3+ , Eu 3+ and Tb 3+ ) doped samples the three emissions from the particular activators can be generated using one excitation wavelength. The white light resulting from the superposition of the blue (Ce 3+ ), green (Tb 3+ ) and red (Eu 3+ ) emissions can be obtained by varying the concentration of the active ions and the treating atmosphere, i.e. reducing or oxidising. Eu 2+ was not detected in the triply doped samples, and hence line emissions mostly exhibit CRI values equal to or below 30. - Highlights: ► Nanocrystalline Y 2 Si 2 O 7 was obtained by the

  18. New Ce{sup 3+} doped Ca{sub 2}YMgScSi{sub 3}O{sub 12} garnet ceramic phosphor for white LED converters

    Energy Technology Data Exchange (ETDEWEB)

    Khaidukov, N. [Kurnakov Institute of General and Inorganic Chemistry, Russian Academy of Sciences, Moscow (Russian Federation); Zorenko, Yu.; Zorenko, T.; Iskaliyeva, A.; Paprocki, K. [Institute of Physics, Kazimierz Wielki University Bydgoszcz (Poland); Zhydachevskii, Y.; Suchocki, A. [Institute of Physics, Polish Academy of Sciences, Warsaw (Poland); Deun, R. van [L3 - Luminescent Lanthanide Lab, Department of Inorganic and Physical Chemistry, Ghent University (Belgium); Batentschuk, M. [Department of Materials Science and Engineering VI, Institute of Materials for Energy and Electronic Technology (i-IMEET), University of Erlangen-Nuremberg, Erlangen (Germany)

    2017-05-15

    The results on crystallization and investigation of the luminescent properties of a new prospective ceramic phosphor based on the Ce{sup 3+} doped Ca{sub 2}YMgScSi{sub 3}O{sub 12} silicate garnet are presented for the first time in this work. The luminescent properties of Ca{sub 2}YMgScSi{sub 3}O{sub 12}:Ce were compared with the properties of the reference Ca{sub 3}Sc{sub 2}Si{sub 3}O{sub 12}:Ce ceramic sample. Without any doubt, the results of this research can be suitable for the development of a new generation of white converters based on the Ca{sup 2+}-Si{sup 4+} garnet compounds. (copyright 2017 WILEY-VCH Verlag GmbH and Co. KGaA, Weinheim)

  19. Timing characteristics of Ce doped Gd{sub 3}Ga{sub 3}Al{sub 2}O{sub 12} single crystals in comparison with CsI(Tl) scintillators

    Energy Technology Data Exchange (ETDEWEB)

    Tyagi, M.; Singh, A.K.; Singh, S.G.; Sen, S.; Gadkari, S.C. [Technical Physics Division, Bhabha Atomic Research Centre, Mumbai, 400085 (India); Desai, V.V.; Nayak, B.K. [Nuclear Physics Division, Bhabha Atomic Research Centre, Mumbai, 400085 (India)

    2015-10-15

    Single crystals of Gd{sub 3}Ga{sub 3}Al{sub 2}O{sub 12}:Ce with B codopants were successfully grown using the Czochralski technique. The timing characteristics of the crystal was measured by coupling the crystal to photomultiplier tubes (PMT) or silicon photodiodes [Si(PIN)]. The two prompt γ-rays emitted in a cascade from {sup 60}Co or {sup 22}Na source were detected in coincidence using Gd{sub 3}Ga{sub 3}Al{sub 2}O{sub 12}:Ce,B crystal detectors and a BaF{sub 2} detector. The time resolution of these crystals are observed to be better than that measured for CsI:Tl crystal coupled to PMT or Si(PIN) in an identical measurement setup. (copyright 2015 WILEY-VCH Verlag GmbH and Co. KGaA, Weinheim)

  20. The development of new phosphors of Tb3+/Eu3+ co-doped Gd3Al5O12 with tunable emission

    Science.gov (United States)

    Teng, Xin; Wang, Wenzhi; Cao, Zhentao; Li, Jinkai; Duan, Guangbin; Liu, Zongming

    2017-07-01

    The gadolinium aluminum garnets Gd3Al5O12 (GdAG) activated with Tb3+/Eu3+ were successfully prepared via co-precipitation method at 1500 °C in this work. The crystal structure stabilization, elements analysis, microphotograph, PL/PLE spectra, decay behavior and quantum efficiency were discussed in detail. The metastable GdAG compounds been effectively stabilized by doping with smaller 10 at.% Tb3+, which then allows the development of new phosphors of (Gd0.9-xTb0.1Eux)3Al5O12 (GdAG:Tb3+/Eu3+, x = 0-0.03) for opto-functionality explorations. The PLE/PL spectra displays that the strongest PLE peak was located at ∼276 nm, which overlaps the 8S7/2 → 6IJ transition of Gd3+. Under 276 nm excitation, the phosphors exhibited both Tb3+ and Eu3+ emissions at 548 nm (green, 5D4 → 7F5 transition of Tb3+) and 592 nm (orange-red, 5D0 → 7F1 transition of Eu3+), respectively. The emission intensities of Tb3+ and Eu3+ remarkably varied with the Eu3+ incorporation. As a consequence, the emission color can be readily tuned from approximately green to orange-red. Fluorescence decay analysis found that the lifetime for the Tb3+ emission rapidly decreased conforming to the Tb3+ → Eu3+ energy transfer, and the energy transfer efficiency was calculated. Owing to the Gd3+ → Eu3+ and Gd3+ → Tb3+ energy transfer, the emission intensities of Tb3+ and Eu3+ in (Gd0.9-xTb0.1Eux)AG phosphor were higher than (Y0.87Tb0.1Eu0.03)AG and (Lu0.87Tb0.1Eu0.03)AG system. The (Gd0.9-xTb0.1Eux)AG garnet phosphors developed in this work may serve as a new type of phosphor which hopefully meets the requirements of various lighting and optical display applications.

  1. Influence of the sintering temperature on the Sr content in a Ca{sub (1−x−y)}Ce{sub x}Sr{sub y}Al{sub z}Ti{sub (1−z)}O{sub 3} perovskite (x = 0.04–0.16) co-doped with Ce

    Energy Technology Data Exchange (ETDEWEB)

    Kamel, Nour-el-hayet; Mouheb, Yasmina, E-mail: mouhebyascrna@hotmail.com; Kamel, Ziane; Moudir, Dalila; Aouchiche, Fairouz; Arabi, Azeddine

    2016-08-15

    A Sr-Ce co-doped perovskite, with the chemical formula: Ca{sub (1−x−y)}Ce{sub x}Sr{sub y}Al{sub z}Ti{sub (1−z)}O{sub 3} (y = 0.04, 0.08, 0.12 and 0.16, x = 0.05) is synthesized by sol–gel process. The influence of the sintering temperature, Ts, on the rate of inserted Sr was investigated at 1223, 1373 and 1473 K. The Sr amount sequestered in the perovskite reaches 85% (y = 0.16, 9.50 wt%) for Ts = 1373 K, giving sintering densities between 3.520 and 4.400. XRD analysis reveals an orthorhombic CaTiO{sub 3} structure. The lattice parameters obey to Vegard’s law for Ts = 1373 and 1473 K. SEM analysis shows orthorhombic grains of 0.514 μm × 1 μm mean dimensions. MCC1 and MCC2 tests, performed on minerals sintered at 1373 K, indicate that the most durable one is that containing 9.50 wt% Sr. MCC1 test gave 6.998·10{sup −6} g/cm{sup 2} d of Sr, and MCC2 2.143·10{sup −4} g/cm{sup 2} d of Ce. The temperature favors the Sr dissolution to the detriment of Ce. The Ca dissolution rate reaches 1.002·10{sup −6} to 2.005·10{sup −6} g/cm{sup 2} d. - Highlights: • Ca{sub (1−x−y)}Ce{sub x}Sr{sub y}Al{sub z}Ti{sub (1−z)}O{sub 3} perovskite is synthesized by sol–gel. • The influence of the sintering temperature, Ts, on the rate of inserted Sr was investigated at 1223, 1373 and 1473 K. • 85% of total Sr was sequestered in the perovskite for Ts = 1373 K. • MCC1 and MCC2 leach tests indicate that the most durable mineral is that containing 9.50 wt.% Sr. • MCC1 test gave 8.10 10{sup −10} kg/m{sup 2}.d Sr. The lower is the leaching temperature the higher is the mineral durability.

  2. Luminescence and scintillation response of YGd.sub.2./sub.Al.sub.2./sub.Ga.sub.3./sub.O.sub.12./sub.:Ce and LuGd.sub.2./sub.Al.sub.2./sub.Ga.sub.3./sub.O.sub.12./sub.:Ce scintillators

    Czech Academy of Sciences Publication Activity Database

    Chewpraditkul, Wa.; Pattanaboonmee, N.; Chewpraditkul, W.; Kamada, K.; Yoshikawa, A.; Nikl, Martin

    2016-01-01

    Roč. 90, Jul (2016), s. 153-156 ISSN 1350-4487. [International Conference on Luminescent Detectors and Transformers of Ionizing Radiation (LUMDETR). Tartu (Estonsko), 20.09.2015-25.09.2015] R&D Projects: GA ČR GAP204/12/0805 Institutional support: RVO:68378271 Keywords : YGd 2 Al 2 Ga 3 O 12 :Ce * LuGd 2 Al 2 Ga 3 O 12 :Ce * light yield * luminescence * scintillation Subject RIV: BM - Solid Matter Physics ; Magnetism Impact factor: 1.442, year: 2016

  3. Effect of Surface Treatment on Shear Bond Strength between Resin Cement and Ce-TZP/Al2O3

    Directory of Open Access Journals (Sweden)

    Jong-Eun Kim

    2016-01-01

    Full Text Available Purpose. Although several studies evaluating the mechanical properties of Ce-TZP/Al2O3 have been published, to date, no study has been published investigating the bonding protocol between Ce-TZP/Al2O3 and resin cement. The aim of this study was to evaluate the shear bond strength to air-abraded Ce-TZP/Al2O3 when primers and two different cement types were used. Materials and Methods. Two types of zirconia (Y-TZP and Ce-TZP/Al2O3 specimens were further divided into four subgroups according to primer application and the cement used. Shear bond strength was measured after water storage for 3 days or 5,000 times thermocycling for artificial aging. Results. The Y-TZP block showed significantly higher shear bond strength than the Ce-TZP/Al2O3 block generally. Primer application promoted high bond strength and less effect on bond strength reduction after thermocycling, regardless of the type of cement, zirconia block, or aging time. Conclusions. Depending on the type of the primer or resin cement used after air-abrasion, different wettability of the zirconia surface can be observed. Application of primer affected the values of shear bond strength after the thermocycling procedure. In the case of using the same bonding protocol, Y-TZP could obtain significantly higher bond strength compared with Ce-TZP/Al2O3.

  4. Luminescence properties and gamma-ray response of the Ce and Ca co-doped (Gd,Y)F{sub 3} single crystals

    Energy Technology Data Exchange (ETDEWEB)

    Kamada, Kei, E-mail: k-kamada@furukawakk.co.jp [Institute of Multidisciplinary Research for Advanced Materials, Tohoku University, Sendai (Japan); Furukawa Co. Ltd. (Japan); Yanagida, Takayuki; Fujimoto, Yutaka; Fukabori, Akihiro [Institute of Multidisciplinary Research for Advanced Materials, Tohoku University, Sendai (Japan); Yoshikawa, Akira [Institute of Multidisciplinary Research for Advanced Materials, Tohoku University, Sendai (Japan); New Industry Creation Hatchery Center, Tohoku University, Sendai (Japan); Nikl, Martin [Institute of Physics AS CR (Czech Republic)

    2011-12-11

    The Ca0.5% and Ce1%, 3%, 7%, 10% co-doped Gd{sub 0.5}Y{sub 0.5}F{sub 3} single crystals were grown by the {mu}-PD method. In the Ca0.5% and Ce3% co-doped sample, Ce{sup 3+}-perturbed luminescence at 380 nm was observed with 32.4 ns photoluminescence decay time. The energy transfer in the sequence of the regular Ce{sup 3+}{yields} (Gd{sup 3+}){sub n}{yields} the perturbed Ce{sup 3+} sites was evidenced through observation of decay time shortening of the regular Ce{sup 3+} and Gd{sup 3+} centers and the change between the Gd{sup 3+} and Ce{sup 3+}-perturbed emission intensity. The gamma-ray excited scintillation response of the Ca0.5%, Ce7% co-doped Gd{sub 0.5}Y{sub 0.5}F{sub 3} sample was investigated with the help of the pulse height spectra and the light yield, energy resolution and non-proportionality was evaluated in the interval of energies of 59.4-1274 keV.

  5. Experimental evaluation of Gd3Al2Ga3O12:Ce (GAGG:Ce) single crystals coupled to a silicon photomultiplier (SiPM) under high gamma ray irradiation conditions

    Science.gov (United States)

    Metallinos, A.; Kefalidis, E.; Kandarakis, I.; David, S.

    2017-11-01

    Cerium (Ce) ion doped scintillators are of high interest in Medical Imaging systems and radiation monitoring devices, due to their very fast response and very good emission characteristics. In this study, a series of measurements regarding the energy resolution, photofraction, sensitivity, as well as the figure of merit, of Gd3Al2Ga3O12:Ce (GAGG:Ce) scintillator crystals, is presented. All GAGG:Ce crystals have a surface area of 3x3 mm2 with varying thicknesses, from 4 up to 20 mm (4, 5, 6, 8, 10, 15 and 20 mm). These crystals were exposed to γ radiation, using two different radioactive sources: 137Cs (0.662 MeV) and 60Co (1.173 MeV and 1.332 MeV). Each crystal was measured individually and was optically coupled to a KETEK PM3350 SiPM, an optical sensor with high gain, suitable to operate in room temperature. The digitization of the pulses was accomplished using CAEN DT5720 desktop digitizer and its corresponding digital pulse processing (DPP) firmware. Each measurement was performed in a light-tight box and had duration of 30 min. The best energy resolution value was measured for the GAGG:Ce crystal with dimensions 3x3x15mm3, equal to 3.9% at 1.332 MeV. Results were evaluated and compared to previous published data.

  6. Effect of CeO2 and Y2O3 on microstructure, bioactivity and degradability of laser cladding CaO-SiO2 coating on titanium alloy.

    Science.gov (United States)

    Li, H C; Wang, D G; Chen, C Z; Weng, F

    2015-03-01

    To solve the lack of strength of bulk biomaterials for load-bearing applications and improve the bioactivity of titanium alloy (Ti-6Al-4V), CaO-SiO2 coatings on titanium alloy were fabricated by laser cladding technique. The effect of CeO2 and Y2O3 on microstructure and properties of laser cladding coating was analyzed. The cross-section microstructure of ceramic layer from top to bottom gradually changes from cellular-dendrite structure to compact cellular crystal. The addition of CeO2 or Y2O3 refines the microstructure of the ceramic layer in the upper and middle regions. The refining effect on the grain is related to the kinds of additives and their content. The coating is mainly composed of CaTiO3, CaO, α-Ca2(SiO4), SiO2 and TiO2. Y2O3 inhibits the formation of CaO. After soaking in simulated body fluid (SBF), the calcium phosphate layer is formed on the coating surface, indicating the coating has bioactivity. After soaking in Tris-HCl solution, the samples doped with CeO2 or Y2O3 present a lower weight loss, indicating the addition of CeO2 or Y2O3 improves the degradability of laser cladding sample. Copyright © 2015 Elsevier B.V. All rights reserved.

  7. Luminescent and scintillation properties of Sc3+and La3+doped Y2SiO5 powders and single crystalline films

    International Nuclear Information System (INIS)

    Zorenko, Yu.; Gorbenko, V.; Zorenko, T.; Voznyak, T.; Voloshynovskii, A.; Vistovskiy, V.; Paprocki, K.; Mosińska, L.; Bilski, P.; Twardak, A.; Fedorov, A.; Nikl, M.; Mares, J.A.

    2016-01-01

    The paper is dedicated to the investigation of the luminescence of Sc 3+ and La 3+ isoelectronic impurities in Y 2 SiO 5 (YSO) single crystalline films (SCF), grown by the liquid phase epitaxy (LPE) method, and in the powder analogs of these compounds prepared using the ceramic technology. The Sc 3+ and La 3+ dopants replacing the Y 3+ cations in Y1and Y2 positions of YSO host introduce the strong complex emission bands in the UV range peaked at 330 and 345 nm, respectively. The Sc 3+ and La 3+ dopant in YSO matrix yields also the strong TSL peaks at 400 and 405 K related to the ScY and ScLa centers formation, respectively. The luminescence and scintillation properties of YSO SCFs doped with Sc 3+ and La 3+ ions and co-doped with Ce 3+ ions on the trace impurity level have been also studied in our work. We have found that the light yield (LY) of these YSO:Sc and YSO:La SCFs can reach 50–65% of LY in reference YSO:Ce SCF due to strong quenching influence of Pb 2+ ions. Finally, the potential of Sc 3+ and La 3+ doped SCF of orthosilicates for creation of heavy scintillation screens, emitting in the UV range, is discussed.

  8. Crystal growth and scintillation properties of Er-doped Lu3Al5O12 single crystals

    International Nuclear Information System (INIS)

    Sugiyama, Makoto; Fujimoto, Yutaka; Yanagida, Takayuki; Totsuka, Daisuke; Kurosawa, Shunsuke; Futami, Yoshisuke; Yokota, Yuui; Chani, Valery; Yoshikawa, Akira

    2012-01-01

    Er-doped Lu 3 Al 5 O 12 (Er:LuAG) single crystalline scintillators with different Er concentrations of 0.1, 0.5, 1, and 3% were grown by the micro-pulling-down (μ-PD) method. The grown crystals were composed of single-phase material, as demonstrated by powder X-ray diffraction (XRD). The radioluminescence spectra measured under 241 Am α-ray excitation indicated host emission at approximately 350 nm and Er 3+ 4f-4f emissions. According to the pulse height spectra recorded under γ-ray irradiation, the 0.5% Er:LuAG exhibited the highest peak channel among the samples. The γ-ray excited decay time profiles were well fitted by the two-component exponential approximation (0.8 μs and 6-10 μs).

  9. Luminescence properties of the Mg co–doped Ce:SrHfO_3 ceramics prepared by the Spark Plasma Sintering Method

    International Nuclear Information System (INIS)

    Chiba, Hiroyuki; Kurosawa, Shunsuke; Harata, Koichi; Murakami, Rikito; Yamaji, Akihiro; Ohashi, Yuji; Pejchal, Jan; Kamada, Kei; Yokota, Yuui; Yoshikawa, Akira

    2016-01-01

    1300 or 1400 °C pre–sintered Al/Ce/Mg:SrHfO_3 and Al/Ce:SrHfO_3 ceramics were prepared by the Spark Plasma Sintering (SPS) in order to search for a new scintillation material with a high–effective atomic number(Z_e_f_f) and good light output. The SrHfO_3 has a high Z_e_f_f of 60, and high gamma–ray detection efficiency is expected. Meanwhile it has a high melting point of over 2500 °C, and single crystal is hard to be grown. On the other hand, high melting materials can be prepared as ceramics, and the SPS method is a simple process to fabricate the ceramics within a few hours. Thus, we prepared the samples using the SPS method, and their optical and scintillation properties were investigated. We found that Al/Ce/Mg:SrHfO_3 and Al/Ce:SrHfO_3 ceramics had an emission wavelength at around 400 nm originating from 5d–4f transition of Ce"3"+. Moreover, Al/Ce/Mg:SrHfO_3 pre-sintered at a temperature of 1400 °C had a light output of approximately 5,000 ph/MeV. In this paper, the light output of Mg-co-doped samples was improved compared with the Mg-free ones. The light output also depends on the pre-sintering temperature. - Highlights: • Luminescence Properties of Al/Ce/Mg:SrHfO_3 ceramics scintillator was investigated. • These ceramics were prepared by the Spark Plasma Sintering Method. • Light output of the Al/Ce/Mg:SrHfO_3 ceramics was approximately 5,000 ph/MeV.

  10. Luminescence and energy transfer of Ce{sup 3+} and Pr{sup 3+} in LaBSiO{sub 5}

    Energy Technology Data Exchange (ETDEWEB)

    Zhou, Lei; Zhou, Weijie; Shi, Rui; Liu, Chunmeng [MOE Key Laboratory of Bioinorganic and Synthetic Chemistry, KLGHEI of Environment and Energy Chemistry, School of Chemistry and Chemical Engineering, Sun Yat-sen University, Guangzhou 510275 (China); Huang, Yan; Tao, Ye [Beijing Synchrotron Radiation Facility, Institute of High Energy Physics, Chinese Academy of Sciences, Beijing 100039 (China); Liang, Hongbin, E-mail: cesbin@mail.sysu.edu.cn [MOE Key Laboratory of Bioinorganic and Synthetic Chemistry, KLGHEI of Environment and Energy Chemistry, School of Chemistry and Chemical Engineering, Sun Yat-sen University, Guangzhou 510275 (China)

    2016-09-15

    Ce{sup 3+}, Pr{sup 3+} singly doped and Ce{sup 3+}–Pr{sup 3+} doubly doped LaBSiO{sub 5} phosphors were prepared by a high-temperature solid state reaction route. The synchrotron radiation VUV–UV excitation spectra of Ce{sup 3+} and Pr{sup 3+} were measured and the luminescence properties were discussed. The band gap of host compound LaBSiO{sub 5} was estimated from the VUV excitation spectrum of sample activated with Gd{sup 3+}. Furthermore, the influence of temperature on luminescence of Ce{sup 3+} was discussed and the activation energy for thermal quenching was evaluated. The occurrence of energy transfer from excited 5d states of Pr{sup 3+} to Ce{sup 3+} was confirmed by the emission spectra of co-doped samples La{sub 0.99−x}Pr{sub x}Ce{sub 0.01}BSiO{sub 5} and La{sub 0.995−x}Pr{sub 0.005}Ce{sub x}BSiO{sub 5} with different x values.

  11. Phosphor thermometry: On the synthesis and characterisation of Y{sub 3}Al{sub 5}O{sub 12}:Eu (YAG:Eu) and YAlO{sub 3}:Eu (YAP:Eu)

    Energy Technology Data Exchange (ETDEWEB)

    Kissel, T. [Fachgebiet Reaktive Strömungen und Messtechnik (RSM), Center of Smart Interfaces (CSI), Technische Universität Darmstadt, Petersenstraße 32, 64287 Darmstadt (Germany); Brübach, J., E-mail: bruebach@ekt.tu-darmstadt.de [Fachgebiet Reaktive Strömungen und Messtechnik (RSM), Center of Smart Interfaces (CSI), Technische Universität Darmstadt, Petersenstraße 32, 64287 Darmstadt (Germany); Euler, M. [Fachgebiet Reaktive Strömungen und Messtechnik (RSM), Center of Smart Interfaces (CSI), Technische Universität Darmstadt, Petersenstraße 32, 64287 Darmstadt (Germany); Frotscher, M.; Litterscheid, C.; Albert, B. [Eduard-Zintl-Institut für Anorganische und Physikalische Chemie, Technische Universität Darmstadt, Petersenstraße 18, 64287 Darmstadt (Germany); Dreizler, A. [Fachgebiet Reaktive Strömungen und Messtechnik (RSM), Center of Smart Interfaces (CSI), Technische Universität Darmstadt, Petersenstraße 32, 64287 Darmstadt (Germany)

    2013-07-15

    With regard to phosphor thermometry, the materials Y{sub 3}Al{sub 5}O{sub 12}:Eu (YAG:Eu) and YAlO{sub 3}:Eu (YAP:Eu) were synthesised and characterised in order to substitute the commonly used thermographic phosphor Y{sub 2}O{sub 3}:Eu, whose temperature sensitive luminescence lifetime exhibits a strong and most often undesirable cross-sensitivity to the oxygen concentration of the surrounding gas phase. The synthesis is outlined in detail and the crystallographic structure was characterised by X-ray diffraction. In a second step, the luminescence properties following pulsed UV laser excitation were determined. In this context, the emission spectra and the temperature lifetime characteristics were monitored. For Y{sub 3}Al{sub 5}O{sub 12}:Eu and YAlO{sub 3}:Eu, temperature sensitive ranges of 1000 K–1470 K and 850 K–1300 K were identified. Contrary to Y{sub 2}O{sub 3}:Eu, both materials do show much lower cross-sensitivities to the oxygen concentration of the surrounding gas phase. - Highlights: ► Y{sub 3}Al{sub 5}O{sub 12}:Eu and YAlO{sub 3}:Eu were synthesised and characterised. ► The synthesis is outlined and the crystallographic structure was characterised. ► Emission spectra and the temperature lifetime characteristics were monitored. ► Compared to Y{sub 2}O{sub 3}:Eu lower sensitivities to the oxyg. conc. of the gas phase emerged.

  12. Development of La3+ Doped CeO2 Thick Film Humidity Sensors

    Directory of Open Access Journals (Sweden)

    Chunjie Wang

    2014-01-01

    Full Text Available The humidity sensitive characteristics of the sensor fabricated from 10 mol% La2O3 doped CeO2 nanopowders with particle size 17.26 nm synthesized via hydrothermal method were investigated at different frequencies. It was found that the sensor shows high humidity sensitivity, rapid response-recovery characteristics, and narrow hysteresis loop at 100 Hz in the relative humidity range from 11% to 95%. The impedance of the sensor decreases by about five orders of magnitude as relative humidity increases. The maximum humidity hysteresis is about 6% RH, and the response and recovery time is 12 and 13 s, respectively. These results indicate that the nanosized La2O3 doped CeO2 powder has potential application as high-performance humidity sensor.

  13. Optical properties and radiation response of Ce3+-doped GdScO3 crystals

    International Nuclear Information System (INIS)

    Yamaji, Akihiro; Fujimoto, Yutaka; Futami, Yoshisuke; Yokota, Yuui; Kurosawa, Shunsuke; Kochurikhin, Vladimir; Yanagida, Takayuki; Yoshikawa, Akira

    2012-01-01

    10%-Ce doped GdScO 3 perovskite type single crystal was grown by the Czochralski process. The Ce concentration in the crystal was measured. No impurity phases were observed by powder X-ray diffraction analysis. We evaluated the optical and radiation properties of the grown crystal. Ce:GdScO 3 crystal showed photo- and radio-luminescence peaks due to Ce 3+ of 5d-4f transition and colour centre. The photoluminescence decay time was sub-ns order. The relative light yield under 5.5 MeV alpha-ray excitation was calculated to be approximately 9% of BGO. (copyright 2012 WILEY-VCH Verlag GmbH and Co. KGaA, Weinheim) (orig.)

  14. Magnetic ordering and charge transport in electron-doped La1-yCeyMnO3 (0.1 ≤ y ≤ 0.3) films

    International Nuclear Information System (INIS)

    Prokhorov, V.G.; Kaminsky, G.G.; Flis, V.S.; Hyun, Y.H.; Park, S.Y.; Lee, Y.P.; Svetchnikov, V.L.

    2009-01-01

    The microstructure and the magnetic and transport properties of as-deposited La 10-y Ce y MnO 3 (0.1≤ y≤ 0.3) films prepared by pulsed laser deposition are investigated in a wide region of temperature and magnetic field. The microstructure analysis reveals that all films have a high c-oriented texture, an orthorhombic crystal lattice, and a negligible quantity of CeO 2 inclusions. The observed strip-domain phase with a periodic spacing of about 3c, the crystal lattice of which is the same as for the basic film phase, exhibits magnetic behavior typical for the Griffiths phase. Regions of the double-period modulated phase are found at room temperature in the y=0.1 film, which is interpreted as Mn 3+ /Mn 2+ ordering with a partial ferromagnetic → antiferromagnetic transition at T N ≤ 80 K. At the same time, the investigation reveals that the magnetic and transport properties of the electron-doped La 1-y Ce y MnO 3 films, driven by cation doping, are similar to those for the hole-doped La/Ca manganites. Therefore, one can conclude that there is no fundamental difference between the mechanisms of spin ordering and charge transport in the hole-doped and electron-doped manganites

  15. Influence of lead-related centers on luminescence of Ce3+ and Pr3+ centers in single crystalline films of aluminium perovskites and garnets

    International Nuclear Information System (INIS)

    Babin, V.; Gorbenko, V.; Krasnikov, A.; Makhov, A.; Nikl, M.; Zazubovich, S.; Zorenko, Yu.

    2010-01-01

    Luminescence characteristics of Ce 3+ - and Pr 3+ -doped aluminium perovskite (LuAlO 3 , YAlO 3 ) and garnet (Lu 3 Al 5 O 12 , Y 3 Al 5 O 12 ) single crystalline films, prepared by the liquid phase epitaxy method with the use of the PbO-based flux, were investigated by the time-resolved spectroscopy methods in the 80-300 K temperature range. The influence of various lead-related centers on the characteristics of the Ce 3+ - and Pr 3+ -related luminescence centers was studied. It was found that the presence of lead-related centers in the single crystalline films results in a decrease of the quantum efficiency and appearance of undesirable slow components in the luminescence decay kinetics. The possibilities of improving the scintillation characteristics of the single crystalline films were considered.

  16. Effect of 10Ce-TZP/Al2O3 nanocomposite particle amount and sintering temperature on the microstructure and mechanical properties of Al/(10Ce-TZP/Al2O3) nanocomposites

    International Nuclear Information System (INIS)

    Soltani, N.; Pech-Canul, M.I.; Bahrami, A.

    2013-01-01

    Highlights: • Increasing the 10Ce-TZP/Al 2 O 3 content up to 7 wt.%, enhanced composites’ hardness. • Significant enhancement in compressive strength is obtained with 7% 10Ce-TZP/Al 2 O 3 . • Sintering at 450 °C, hardness and compressive strength are higher than at 400 °C. - Abstract: A zirconia/alumina nanocomposite stabilized with cerium oxide (Ce-TZP/Al 2 O 3 nanocomposite) can be a good substitute as reinforcement in metal matrix composites. In the present study, the effect of the amount of 10Ce-TZP/Al 2 O 3 particles on the microstructure and properties of Al/(10Ce-TZP/Al 2 O 3 ) nanocomposites was investigated. For this purpose, aluminum powders with average size of 30 μm were ball-milled with 10Ce-TZP/Al 2 O 3 nanocomposite powders (synthesized by aqueous combustion) in varying amounts of 1, 3, 5, 7, and 10 wt.%. Cylindrical-shape samples were prepared by pressing the powders at 600 MPa for 60 min while heating at 400–450 °C. The specimens were then characterized by scanning and transmission electron microscopy (SEM and TEM) in addition to different physical and mechanical testing methods in order to establish the optimal processing conditions. The highest compression strength was obtained in the composite with 7 wt.% (10Ce-TZP/Al 2 O 3 ) sintered at 450 °C

  17. On the origin of the ultraviolet photoluminescence in the Ce.sup.3+./sup.-doped epitaxial films of multicomponent (Lu,Gd).sub.3./sub.(Ga,Al).sub.5./sub.O.sub.12./sub. garnets

    Czech Academy of Sciences Publication Activity Database

    Babin, Vladimir; Chernenko, K.; Hanus, M.; Krasnikov, A.; Kučera, M.; Nikl, Martin; Zazubovich, S.

    2017-01-01

    Roč. 254, č. 4 (2017), 1-6, č. článku 1600570. ISSN 0370-1972 R&D Projects: GA ČR GA16-15569S Institutional support: RVO:68378271 Keywords : antisite Ce 3+ centers * fast ultraviolet photoluminescence * (Lu,Gd) sub >3 sub >(Ga,Al) sub >5 sub >O sub >12 sub > garnets Sub ject RIV: BM - Solid Matter Physics ; Magnetism OBOR OECD: Condensed matter physics (including formerly solid state physics, supercond.) Impact factor: 1.674, year: 2016

  18. Study of Pt–Rh/CeO2–ZrO2–MxOy (M = Y, La)/Al2O3 three-way catalysts

    International Nuclear Information System (INIS)

    Jiaxiu, Guo; Zhonghua, Shi; Dongdong, Wu; Huaqiang, Yin; Maochu, Gong; Yaoqiang, Chen

    2013-01-01

    CeO 2 –ZrO 2 –M x O y (M = Y; La) mixed oxides, prepared by co-precipitation method and characterized by Brunauer-Emmett-Teller (BET), X-ray diffraction (XRD), Raman spectra (RM) and oxygen pulse reaction, were comparatively investigated to elucidate the combinational effects of Y and/or La oxide promoters on the catalytic activity and anti-aging performance of monolithic cordierite honeycomb catalysts with low Pt and Rh content. The catalytic activities, water-gas shift (WGS) and steam reforming reaction (SR) were studied under a simulated gas mixture. The catalysts were also characterized by H 2 -temperature-programmed reduction (H 2 -TPR) and O 2 -temperature-programmed desorption (O 2 -TPD). The results showed that the prepared CeO 2 –ZrO 2 –M x O y oxides have a face-centered cubic fluorite structure and are nanosize. La 3+ ions can significantly improve thermal stability and efficiently retard CeO 2 –ZrO 2 crystal sintering and growth. Doped CeO 2 –ZrO 2 with Y 3+ and La 3+ has 105 and 60 m 2 /g surface area and 460 and 390 μmol/g OSC before and after aging. The T 50 of fresh Pt–Rh/CZYL/LA is 170 °C for CO, 222 °C for C 3 H 8 and 189 °C for NO, and shift to 205, 262 and 228 °C after hydrothermal aging, which are better than those of Pt–Rh/CZY/LA or Pt–Rh/CZL/LA. WGS and SR are relate to the OSC of oxygen storage materials and absorbed oxygen species on the catalyst surface and affect the three-way catalytic activities of catalysts. The reductive property of noble metals and the dissociatively adsorbed O 2 on the surface of catalysts are closely related to the catalytic activities.

  19. Y{sub 3}Fe{sub 5}O{sub 12}/Na,Bi,Sr-doped PZT particulate magnetoelectric composites

    Energy Technology Data Exchange (ETDEWEB)

    Lisnevskaya, I.V., E-mail: liv@sfedu.ru; Bobrova, I.A.; Lupeiko, T.G.; Agamirzoeva, M.R.; Myagkaya, K.V.

    2016-05-01

    Magnetoelectric (ME) composites of Na, Bi, Sr substituted lead zirconate titanate (PZT) and yttrium iron garnet having representative formula (100−x) wt% Na,Bi,Sr-doped PZT (PZTNB-1)+x wt% Y{sub 3}Fe{sub 5}O{sub 12} (YIG) with x=10–90 were manufactured using powdered components obtained through sol–gel processes. It is shown that the decrease in sintering temperature provided by the use of finely dispersed PZTNB-1 and YIG powders allows to significantly reduce content of fluorite-like foreign phase based on zirconium oxide, which forms due to the interfacial interaction during heat treatment and becomes stabilized by yttrium oxide. Connectivity has considerable effect on the value of ME coefficient of composite ceramics. With the same x value, ΔE/ΔH characteristic decreases when changing from 0–3-type structured composites (PZT grains embedded in ferrite matrix) to 3-3-(interpenetrating network of two phases) and especially 3-0-type samples (YIG grains embedded in PZT matrix); in the last case this can be attributed to the substrate clamping effect when ferrite grains are clamped with piezoelectric matrix. ΔE/ΔH value of 0–3 composites with x=40–60 wt% was found to be ∼1.6 mV/(cm Oe). - Highlights: • Y{sub 3}Fe{sub 5}O{sub 12}/Na,Bi,Sr-doped PZT particulate magnetoelectric composites were prepared. • The decrease in sintering temperature reduces the content of foreign phase of ZrO{sub 2}. • Connectivity pattern is important factor for magnetoelectric response. • The value of ME coefficient reaches ~1,6 mV/(cm Oe) in 0–3 composites.

  20. Sol-gel syntheses of pentaborate β-LaB5O9 and the photoluminescence by doping with Eu3+, Tb3+, Ce3+, Sm3+, and Dy3+

    Science.gov (United States)

    Yang, Ruirui; Sun, Xiaorui; Jiang, Pengfei; Gao, Wenliang; Cong, Rihong; Yang, Tao

    2018-02-01

    Rare earth (RE) borates have been extensively studied as good photoluminescent materials, however, the target hosts were limited to "RE3BO6", REBO3, and REB3O6 in the RE2O3-B2O3 phase diagram until the recent discovery of rare earth pentaborate. For the first time, the sol-gel method was employed to synthesize β-LaB5O9 doped with Eu3+, Tb3+, Ce3+, Sm3+, Dy3+. In comparison to the previous synthetic methods, the sol-gel method possesses superiorities including easily-controllable doping concentration, high yield and emission efficiency. Solid solutions of phosphors were prepared and carefully analyzed by powder X-ray diffraction. Concentration quenching or saturation was observed in Eu3+, Tb3+ and Ce3+ doped phosphors at round 10 at%. Eu3+, Tb3+, Sm3+, and Dy3+ emit red, green, orange, and close-to-white light, respectively. The absolute emission efficiency of Ce3+ is high and in the UV range, suggesting the function of being sensitizer once combined with other activators.

  1. Photocatalytic performance of TiO2 catalysts modified by H3PW12O40, ZrO2 and CeO2

    Institute of Scientific and Technical Information of China (English)

    CAI Tiejun; LIAO Yuchao; PENG Zhenshan; LONG Yunfei; WEI Zongyuan; DENG Qian

    2009-01-01

    The binary composite photo-catalysts CeO2/TiO2, ZrO2/TiO2 and the ternary composite photo-catalysts H3PW12O40-CeO2/TiO2,H2PW12O40-ZrO2/TiO2 were prepared by sol-gel method. The catalysts were characterized by thermogravimetric-differential thermal analysis (TG-DTA), scanning electron microscopy (SEM) and X-ray diffraction (XRD). The photocatalyfic elimination of methanol was used as model reaction to evaluate the photocatalytic activity of the composite catalysts under ultraviolet light irradiation. The effects of doped content, activation temperature, time, initial concentration of methanol and gas flow rate on the catalytic activity were investigated. The results showed that after doping a certain amount of CeO2 and ZrO2, crystaniTation process of TiO2 was restrained, particles of catalysts are smaller and more uniform. Doping ZrO2 not only significantly improved the catalytic activity, but also increased thermal stability. Doping H3PW12O40 also enhanced the catalytic activity. The catalytic activities of binary and ternary composite photocatalysts were significantly higher than tin-doped TiO2. The dynamics law of photocatalytic reaction over the binary CeO2/TiO2 and ZrO2/TiO2 catalysts has been studied. The activation energy 15.627 and 15.631 kJ/mol and pre-exponential factors 0.5176 and 0.9899 s-1 over each corresponding catalyst were obtained. This reaction accords to the first order dynamics law.

  2. Directed laser processing of compacted powder mixtures Al2O3-TiO2-Y2O3

    Directory of Open Access Journals (Sweden)

    Vlasova M.

    2013-01-01

    Full Text Available The phase formation, microstructure and surface texture of laser treated ternary powder mixtures of Al2O3-TiO2-Y2O3 had been studied. Rapid high temperature heating and subsequent rapid cooling due to the directed movement of the laser beam forms concave ceramic tracks. Phase composition and microstructure of the tracks depends on the Al2O3 content and the TiO2/Y2O3 ratio of the initial mixtures. The main phases observed are Y3Al5O12, Y2Ti2O7, Al2O3 and Al2TiO5. Due to the temperature gradient in the heating zone, complex layered structures are formed. The tracks consist of three main layers: a thin surface layer, a layer of crystallization products of eutectic alloys, and a lower sintered layer. The thickness of the crystallization layer and the shrinkage of the irradiation zone depend on the amount of Y3Al5O12 and Al2O3 crystallized from the melt.

  3. Realizing luminescent downshifting in ZnO thin films by Ce doping with enhancement of photocatalytic activity

    Science.gov (United States)

    Narayanan, Nripasree; Deepak, N. K.

    2018-04-01

    ZnO thin films doped with Ce at different concentration were deposited on glass substrates by spray pyrolysis technique. XRD analysis revealed the phase purity and polycrystalline nature of the films with hexagonal wurtzite geometry and the composition analysis confirmed the incorporation of Ce in the ZnO lattice in the case of doped films. Crystalline quality and optical transmittance diminished while electrical conductivity enhanced with Ce doping. Ce doping resulted in a red-shift of optical energy gap due to the downshift of the conduction band minimum after merging with Ce related impurity bands formed below the conduction band in the forbidden gap. In the room temperature photoluminescence spectra, UV emission intensity of the doped films decreased while the intensity of the visible emission band increased drastically implying the degradation in crystallinity as well as the incorporation of defect levels capable of luminescence downshifting. Ce doping showed improvement in photocatalytic efficiency by effectively trapping the free carriers and then transferring for dye degradation. Thus Ce doped ZnO thin films are capable of acting as luminescent downshifters as well as efficient photocatalysts.

  4. Properties of Ce-doped ITO films deposited on polymer substrate by DC magnetron sputtering

    International Nuclear Information System (INIS)

    Kang, Y.M.; Kwon, S.H.; Choi, J.H.; Cho, Y.J.; Song, P.K.

    2010-01-01

    Ce-doped indium tin oxide (ITO:Ce) films were deposited on flexible polyimide substrates by DC magnetron sputtering using ITO targets containing various CeO 2 contents (CeO 2 : 0, 0.5, 3.0, 4.0, 6.0 wt.%) at room temperature and post-annealed at 200 o C. The crystallinity of the ITO films decreased with increasing Ce content, and it led to a decrease in surface roughness. In addition, a relatively small change in resistance in dynamic stress mode was obtained for ITO:Ce films even after the annealing at high temperature (200 o C). The minimum resistivity of the amorphous ITO:Ce films was 3.96 x 10 -4 Ωcm, which was deposited using a 3.0 wt.% CeO 2 doped ITO target. The amorphous ITO:Ce films not only have comparable electrical properties to the polycrystalline films but also have a crystallization temperature > 200 o C. In addition, the amorphous ITO:Ce film showed stable mechanical properties in the bended state.

  5. Preparation and luminescence properties of Ce3+ and Ce3+/Tb(3+)-activated Y4Si2O7N2 phosphors.

    Science.gov (United States)

    Xia, Zhiguo; Wu, Weiwei

    2013-09-28

    Ce(3+) and Ce(3+)/Tb(3+)-activated Y4Si2O7N2 phosphors are synthesized by the solid-state method, which can be efficiently excited by near ultraviolet (UV) light emitting diode (LED) chips. The PL spectrum of Y4Si2O7N2:Ce(3+) shows a broad hump between 380 and 650 nm, assigned to the electron transition from the 4f energy level to different 5d sub levels of the Ce(3+) ions at different Y(3+) sites. The color of the Y4Si2O7N2:Ce(3+) phosphor can shift from blue to green by introducing Tb(3+). In addition, the energy transfer process from Ce(3+) to Tb(3+) in the Y4Si2O7N2 host was investigated and discussed in terms of both the luminescence spectra and decay curves. The energy transfer critical distance has been calculated and evaluated by the concentration quenching method. Therefore, the Ce(3+) and Ce(3+)/Tb(3+)-activated Y4Si2O7N2 phosphors can serve as key materials for phosphor-converted white-light UV-LEDs.

  6. Ho3+/Yb3+ co-doped TeO2-BaF2-Y2O3 glasses for ∼1.2 μm laser applications

    Science.gov (United States)

    Wang, Shunbin; Li, Chengzhi; Yao, Chuanfei; Jia, Shijie; Jia, Zhixu; Qin, Guanshi; Qin, Weiping

    2017-02-01

    Intense ∼1.2 μm fluorescence is observed in Ho3+/Yb3+ co-doped TeO2-BaF2-Y2O3 glasses under 915 nm laser diode excitation. The 1.2 μm emission can be ascribed to the transition 5I6→5I8 of Ho3+. With the introducing of BaF2, the content of OH in the glasses drops markedly, and the 1.2 μm emission intensity increases gradually as increasing the concentration percentage of BaF2. Furthermore, microstructured fibers based on the TeO2-BaF2-Y2O3 glasses are fabricated by using a rod-in-tube method, and a relative positive gain of ∼9.42 dB at 1175.3 nm is obtained in a 5 cm long fiber.

  7. Ce doped NiO nanoparticles as selective NO2 gas sensor

    Science.gov (United States)

    Gawali, Swati R.; Patil, Vithoba L.; Deonikar, Virendrakumar G.; Patil, Santosh S.; Patil, Deepak R.; Patil, Pramod S.; Pant, Jayashree

    2018-03-01

    Metal oxide gas sensors are promising portable gas detection devices because of their advantages such as low cost, easy production and compact size. The performance of such sensors is strongly dependent on material properties such as morphology, structure and doping. In the present study, we report the effect of cerium (Ce) doping on nickel oxide (NiO) nano-structured thin film sensors towards various gases. Bare NiO and Ce doped NiO nanoparticles (Ce:NiO) were synthesized by sol-gel method. To understand the effect of Ce doping in nickel oxide, various molar percentages of Ce with respect to nickel were incorporated. The structure, phase, morphology and band-gap energy of as-synthesized nanoparticles were studied by XRD, SEM, EDAX and UV-vis spectroscopy. Thin film gas sensors of all the samples were prepared and subjected to various gases such as LPG, NH3, CH3COCH3 and NO2. A systematic and comparative study reveals an enhanced gas sensing performance of Ce:NiO sensors towards NO2 gas. The maximum sensitivity for NO2 gas is around 0.719% per ppm at moderate operating temperature of 150 °C for 0.5% Ce:NiO thin film gas sensor. The enhanced gas sensing performance for Ce:NiO is attributed to the distortion of crystal lattice caused by doping of Ce into NiO.

  8. Luminescence properties of Ce3+ doped gadolinium-calcium-silicaborate glass scintillator

    International Nuclear Information System (INIS)

    Park, J.M.; Ha, D.H.; Kaewjeang, S.; Maghanemi, U.; Kothan, S.; Kaewkhao, J.; Kim, H.J.

    2016-01-01

    In this work, the Ce 3+ doped gadolinium-calcium-silicaborate glass scintillators of the composition ratio 25Gd 2 O 3 :10CaO:10SiO 2 :(55−x)B 2 O 3 :xCeF 3 , have been fabricated by using the melt-quenching technique. The doping concentration of the Ce 3+ was varied from 0.05 mol% to 2.5 mol%. The 4f-5d transition of the Ce 3+ allowed scintillation with a fast decay time. The absorption spectrum, X-ray induced emission spectrum, photo luminescence spectrum, laser luminescence spectrum and decay time of the scintillators were measured for studying the luminescence properties. From the X-ray induced emission spectrum result, we checked the trend between doping concentration and light yield. The laser induced luminescence spectrum was measured while changing the temperature from 300 K to 10 K. We also measured the decay time by using the laser excitation of the 0.15 mol% Ce 3+ doped glass scintillator. - Highlights: • Ce 3+ doped gadolinium-calcium-silicaborate glass scintillators were developed. • Glass is easily fabricated with large sizes and various doping materials. • The luminescence properties are studied by using various radiation sources. • The light yield and decay time were measured at low temperature. • One decay time component is found.

  9. Radio- and photoluminescence properties of Ce/Tb co-doped glasses with huntite-like composition

    Science.gov (United States)

    Lorenzi, Roberto; Golubev, Nikita V.; Ziaytdinova, Mariyam Z.; Jarý, Vítězslav; Babin, Vladimir; Malashkevich, Georgii E.; Paleari, Alberto; Sigaev, Vladimir N.; Fasoli, Mauro; Nikl, Martin

    2018-04-01

    Optical properties of yttria-aluminoborate (YAB) glasses with general composition 10(CexTbyY(1-x-y))-30Al2O3-60B2O3 are investigated and compared with data available on YAB crystals with huntite-like structure. Ce doped samples show optical features ascribable to preferential location of rare earth ions in sites with specific geometry similar to that observed in crystalline structures. Samples prepared with Tb ions as emission activator and Ce ions as sensitizer have been studied within the framework of non-radiative energy transfer. The resulting Förster radius is of 4.6 ± 0.5 Å comparable with that observed in Ce/Tb co-doped YAl3(BO3)4 crystals. The investigated materials possess radio- and photoluminescence emission efficiencies and performances comparable to that of crystalline counterparts with the advantage of having easiness of preparation and workability typical of glassy systems.

  10. High performance LiNi0.5Mn1.5O4 cathode by Al-coating and Al3+-doping through a physical vapor deposition method

    International Nuclear Information System (INIS)

    Sun, Peng; Ma, Ying; Zhai, Tianyou; Li, Huiqiao

    2016-01-01

    Highlights: • Metal Al was used as an electrical conductive coating material for LiNi 0.5 Mn 1.5 O 4 . • The uniform surface coating layer of metal Al was successfully achieved with adjusted thickness through a physical vapor deposition technology. • Al 3+ -doped LiNi 0.5 Mn 1.5 O 4 can be easily obtained by further directly annealing of Al-coated LiNi 0.5 Mn 1.5 O 4 in air. • The conductive Al-coating layer can greatly improve the rate performance and cycle stability of LiNi 0.5 Mn 1.5 O 4 . - Abstract: In this work, spinel LiNi 0.5 Mn 1.5 O 4 (LNMO) hollow microspheres are synthesized by an impregnation method using microsphere MnO 2 as both the precursor and template. To enhance the electrical conductivity of LNMO, metal Al was employed for the first time as a coating material for LNMO. Though an Electron-beam Vapor Deposition approach, the surface of LNMO can be easily coated by a tight layer of Al nanoparticles with adjusted thickness. Further annealing the Al-coated sample at 800 °C in air, the Al 3+ -doped LNMO can be obtained. The effects of Al-coating and Al 3+ -doping on the sample morphology and structure are investigated by SEM, TEM, XRD and FT-IR. The electrochemical properties of Al-coated LNMO and Al 3+ -doped LNMO are measured with comparison of bare LNMO by charge/discharge tests and electrochemical impedance spectroscopy (EIS). The results show that both Al-coating and Al 3+ -doping can greatly enhance the cycle performance and rate capability of LNMO. Especially for Al-coated LNMO, it shows the lowest battery impedance due to the existence of conductive Al coating layer, thus delivers the best rate performance among the three. The physical coating procedure used in this work may provide a new facile modification approach for other cathode materials.

  11. Optical properties and radiation response of Ce{sup 3+}-doped GdScO{sub 3} crystals

    Energy Technology Data Exchange (ETDEWEB)

    Yamaji, Akihiro; Fujimoto, Yutaka; Futami, Yoshisuke; Yokota, Yuui; Kurosawa, Shunsuke [Institute of Materials Research, Tohoku University, 2-1-1 Katahira, Aoba-ku, Sendai, Miyagi 980-8577 (Japan); Kochurikhin, Vladimir [General Physics Institute, 38 Vavilov Str., 119991 Moscow (Russian Federation); Yanagida, Takayuki [New Industry Creation Hatchery Center, Tohoku University, 6-6-10 Aramaki, Aoba-ku, Sendai 980-8579 (Japan); Yoshikawa, Akira [Institute of Materials Research, Tohoku University, 2-1-1 Katahira, Aoba-ku, Sendai, Miyagi 980-8577 (Japan); New Industry Creation Hatchery Center, Tohoku University, 6-6-10 Aramaki, Aoba-ku, Sendai 980-8579 (Japan)

    2012-12-15

    10%-Ce doped GdScO{sub 3} perovskite type single crystal was grown by the Czochralski process. The Ce concentration in the crystal was measured. No impurity phases were observed by powder X-ray diffraction analysis. We evaluated the optical and radiation properties of the grown crystal. Ce:GdScO{sub 3} crystal showed photo- and radio-luminescence peaks due to Ce{sup 3+} of 5d-4f transition and colour centre. The photoluminescence decay time was sub-ns order. The relative light yield under 5.5 MeV alpha-ray excitation was calculated to be approximately 9% of BGO. (copyright 2012 WILEY-VCH Verlag GmbH and Co. KGaA, Weinheim) (orig.)

  12. Magnetostriction of the polycrystalline Fe80Al20 alloy doped with boron

    International Nuclear Information System (INIS)

    Bormio-Nunes, Cristina; Teodoro dos Santos, Claudio; Botani de Souza Dias, Mateus; Doerr, Mathias; Granovsky, Sergey; Loewenhaupt, Michael

    2012-01-01

    Highlights: ► Fe 80 Al 20 polycrystalline alloy magnetostriction 40 ppm increased to 80 ppm due to 2% of B doping. ► B stabilizes α-FeAl phase and a coexistence of α-FeAl + Fe 3 Al improves magnetostriction. ► Presence of Fe 2 B phase causes domain rearrangement revealed by the decrease of the volume magnetostriction. - Abstract: The doping of Fe 80 Al 20 polycrystalline alloy with 2% of boron increased the total magnetostriction twofold compared to a sample without boron. A value close to 80 ppm was achieved at 300 K. The microstructures of the boron-doped alloys show a dendritically solidified matrix with interdendritic α-FeAl and/or Fe 3 Al and Fe 2 B eutectic between the grains. The XRD analysis reveals an increase in the volume fraction of α-FeAl and a correspondent decrease of the Fe 3 Al phase volume fraction as the boron content increases. The increase of the volume fraction of this tetragonal Fe 2 B phase in the samples doped with boron causes the decrease of the strong volume magnetostriction that was observed in the alloy without boron. There is some evidence that the improvement of the magnetostriction magnitude due to the addition of boron to the Fe 80 Al 20 alloy could reach the maximal magnetostriction if the 1:1 optimal ratio of the volume fractions of the α-FeAl and Fe 3 Al phases could be reached.

  13. Role of CeO2 promoter in NiO/α-Al2O3 catalyst for dry reforming of methane

    Science.gov (United States)

    Loc, Luu Cam; Phuong, Phan Hong; Tri, Nguyen

    2017-09-01

    A series of Ni/α-Al2O3 (NiAl) catalysts promoted by CeO2 was prepared by co-impregnation methods with content of (NiO+CeO2) being in the range of 10-30 wt%. The NiO:CeO2 weight ratio was fluctuated at 1:1, 1:2 and 1:3. Several techniques, including X-ray powder diffraction (XRD), Hydrogen temperature-programmed reduction (H2-TPR), and transmission electron microscopy (TEM) were used to investigate catalysts' physico-chemical properties. The activity of these catalysts in dry reforming of CH4 was investigated at temperature range of 550-800 °C. The results revealed that the most suitable CeO2 promoted Ni catalyst contained 20 wt% of (NiO+CeO2) and NiO:CeO2 weight ratio of 1:2. The best catalytic performance of catalyst [20(1Ni2Ce)Al] due to a better reducibility resulted in a higher amount of free small particle NiO. At 700 °C and CH4:CO2 molar ratio of 1:1, the conversion of CH4 and CO2 on the most suitable CeO2 promoted Ni catalyst reached 86% and 67%, respectively; H2 and CO selectivity of 90% and H2:CO molar ratio of 1.15 were obtained. Being similar to MgO [1], promoter CeO2 could improve catalytic activity of Ni/α-Al2O3 catalyst at a lower range of temperature. Besides, both MgO and CeO2 had a great impact on improving coke resistance of Ni catalysts. At higher temperature, the role of CeO2 as well as MgO in preventing coke formation on catalyst was clarified by temperature-programmed oxidation (TPO) technique. Coke amount formed after 30-h TOS on 20(1Ni2Ce) catalyst was found to be 22.18 mgC/gcat, being less than on non-promoted catalyst (36.75 mgC/gcat), but more than on 20(1Ni2Mg)Al one (5.25 mgC/gcat).

  14. Surface damages of polycrystalline W and La2O3-doped W induced by high-flux He plasma irradiation

    Science.gov (United States)

    Liu, Lu; Li, Shouzhe; Liu, Dongping; Benstetter, Günther; Zhang, Yang; Hong, Yi; Fan, Hongyu; Ni, Weiyuan; Yang, Qi; Wu, Yunfeng; Bi, Zhenhua

    2018-04-01

    In this study, polycrystalline tungsten (W) and three oxide dispersed strengthened W with 0.1 vol %, 1.0 vol % and 5.0 vol % lanthanum trioxide (La2O3) were irradiated with low-energy (200 eV) and high-flux (5.8 × 1021 or 1.4 × 1022 ions/m2ṡs) He+ ions at elevated temperature. After He+ irradiation at a fluence of 3.0 × 1025/m2, their surface damages were observed by scanning electron microscopy, energy dispersive spectroscopy, scanning electron microscopy-electron backscatter diffraction, and conductive atomic force microscopy. Micron-sized holes were formed on the surface of W alloys after He+ irradiation at 1100 K. Analysis shows that the La2O3 grains doped in W were sputtered preferentially by the high-flux He+ ions when compared with the W grains. For irradiation at 1550 K, W nano-fuzz was formed at the surfaces of both polycrystalline W and La2O3-doped W. The thickness of the fuzz layers formed at the surface of La2O3-doped W is 40% lower than the one of polycrystalline W. The presence of La2O3 could suppress the diffusion and coalescence of He atoms inside W, which plays an important role in the growth of nanostructures fuzz.

  15. Cold white light generation through the simultaneous emission from Ce{sup 3+}, Dy{sup 3+} and Mn{sup 2+} in 90Al{sub 2}O{sub 3}{center_dot}2CeCl{sub 3}{center_dot}3DyCl{sub 3}{center_dot}5MnCl{sub 2} thin film

    Energy Technology Data Exchange (ETDEWEB)

    Gonzalez, W. [Departamento de Fisica, Universidad Autonoma Metropolitana-Iztapalapa, P.O. Box 55-534, Mexico, D.F. 09340 (Mexico); Alvarez, E. [Departamento de Fisica, Universidad de Sonora (UNISON), Boulevard Luis Encinas y Rosales s/n, Hermosillo, Sonora 83000 (Mexico); Martinez-Martinez, R.; Yescas-Mendoza, E. [Instituto de Fisica y Matematicas, Universidad Tecnologica de la Mixteca, Carretera a Acatlima Km. 2.5, Huajuapan de Leon, Oaxaca 69000 (Mexico); Camarillo, I. [Departamento de Fisica, Universidad Autonoma Metropolitana-Iztapalapa, P.O. Box 55-534, Mexico, D.F. 09340 (Mexico); Caldino, U., E-mail: cald@xanum.uam.mx [Departamento de Fisica, Universidad Autonoma Metropolitana-Iztapalapa, P.O. Box 55-534, Mexico, D.F. 09340 (Mexico)

    2012-08-15

    The photoluminescence of a CeCl{sub 3}, DyCl{sub 3} and MnCl{sub 2} doped aluminum oxide film deposited by ultrasonic spray pyrolysis was characterized by excitation, emission and decay time spectroscopy. A nonradiative energy transfer from Ce{sup 3+} to Dy{sup 3+} and Mn{sup 2+} is observed upon UV excitation at 278 nm (peak emission wavelength of AlGaN-based LEDs). Such energy transfer leads to a simultaneous emission of these ions in the blue, green, yellow and red regions, resulting in white light emission with CIE1931 chromaticity coordinates, x=0.34 and y=0.23, which correspond to cold white light with a color temperature of 4900 K. - Highlights: Black-Right-Pointing-Pointer 90Al{sub 2}O{sub 3}{center_dot}2CeCl{sub 3}{center_dot}3DyCl{sub 3}{center_dot}5MnCl{sub 2} thin film (AOCDM) could be prepared by spray pyrolysis. Black-Right-Pointing-Pointer Non-radiative energy transfer from Ce{sup 3+} to Dy{sup 3+} and Mn{sup 2+} takes place in AOCDM. Black-Right-Pointing-Pointer AOCDM (pumped with 278 nm-UV light) can generate 4900 K cold white light.

  16. Al-, Y-, and La-doping effects favoring intrinsic and field induced ferroelectricity in HfO2: A first principles study

    Science.gov (United States)

    Materlik, Robin; Künneth, Christopher; Falkowski, Max; Mikolajick, Thomas; Kersch, Alfred

    2018-04-01

    III-valent dopants have shown to be most effective in stabilizing the ferroelectric, crystalline phase in atomic layer deposited, polycrystalline HfO2 thin films. On the other hand, such dopants are commonly used for tetragonal and cubic phase stabilization in ceramic HfO2. This difference in the impact has not been elucidated so far. The prospect is a suitable doping to produce ferroelectric HfO2 ceramics with a technological impact. In this paper, we investigate the impact of Al, Y, and La doping, which have experimentally proven to stabilize the ferroelectric Pca21 phase in HfO2, in a comprehensive first-principles study. Density functional theory calculations reveal the structure, formation energy, and total energy of various defects in HfO2. Most relevant are substitutional electronically compensated defects without oxygen vacancy, substitutional mixed compensated defects paired with a vacancy, and ionically compensated defect complexes containing two substitutional dopants paired with a vacancy. The ferroelectric phase is strongly favored with La and Y in the substitutional defect. The mixed compensated defect favors the ferroelectric phase as well, but the strongly favored cubic phase limits the concentration range for ferroelectricity. We conclude that a reduction of oxygen vacancies should significantly enhance this range in Y doped HfO2 thin films. With Al, the substitutional defect hardly favors the ferroelectric phase before the tetragonal phase becomes strongly favored with the increasing concentration. This could explain the observed field induced ferroelectricity in Al-doped HfO2. Further Al defects are investigated, but do not favor the f-phase such that the current explanation remains incomplete for Al doping. According to the simulation, doping alone shows clear trends, but is insufficient to replace the monoclinic phase as the ground state. To explain this fact, some other mechanism is needed.

  17. Combined mode I-mode II fracture of 12-mol%-ceria-doped tetragonal zirconia polycrystalline ceramic

    International Nuclear Information System (INIS)

    Tikare, V.; Choi, S.R.

    1997-01-01

    The mode I, mode II, and combined mode I-mode II fracture behavior of ceria-doped tetragonal zirconia polycrystalline (Ce-TZP) ceramic was studied. The single-edge-precracked-beam (SEPB) samples were fractured using the asymmetric four-point-bend geometry. The ratio of mode I to mode II loading was varied by varying the degree of asymmetry in the four-point-bend geometry. The minimum strain energy density theory best described the mixed-mode fracture behavior of Ce-TZP with the mode I fracture toughness, K IC = 8.2 ± 0.6 MPa·m 1/2 , and the mode II fracture toughness, K IIC = 8.6 ± 1.3 MPa·m 1/2

  18. Blue and green emitting Ce3+ and Tb3+ codoped Gd2O3 nanophosphors

    International Nuclear Information System (INIS)

    Loitongbam, Romeo Singh; Singh, W. Rameshwor

    2013-01-01

    Tb 3+ doped Gd 2 O 3 nanoparticles of 4-10 nm in size were synthesized from nitrate precursors by urea hydrolysis method in ethylene glycol medium at low temperature of 140 ℃. Characteristic Tb 3+ ion green emission corresponding to 5 D 4 ’! 7 F J was observed to be very strong, which further increases with heat treatment temperature. Characteristic blue color emission of Ce 3+ ion transitions for 5 d’! 2 F 7/2 and 2 F 5/2 (at 422 nm and 485 nm respectively) was found to be very strong in as-synthesized Ce 0.06 Tb 0.14 Gd 0.8 O 3 nanoparticles. However, its luminescence intensity decreases with increase in heating temperature or increase in the particle size/crystallinity, whereas there was a weak emission peak of Tb 3+ ion at 545 nm. The polycrystalline nature of as-prepared sample change to highly crystalline state when heated at elevated temperature (900 ℃). (author)

  19. The investigation of Ce doped ZnO crystal: The electronic, optical and magnetic properties

    Science.gov (United States)

    Wen, Jun-Qing; Zhang, Jian-Min; Qiu, Ze-Gang; Yang, Xu; Li, Zhi-Qin

    2018-04-01

    The electronic, optical and magnetic properties of Ce doped ZnO crystal have been studied by using first principles method. The research of formation energies show that Ce doped ZnO is energetically stable, and the formation energies reduce from 6.25% to 12.5% for Ce molar percentage. The energy band is still direct band gap after Ce doped, and band gap increases with the increase of Cesbnd Ce distance. The Fermi level moves upward into conduction band and the DOS moves to lower energy with the increase of Ce concentration, which showing the properties of n-type semiconductor. The calculated optical properties imply that Ce doped causes a red-shift of absorption peaks, and enhances the absorption of the visible light. The transition from ferromagnetic to antiferromagnetic has been found in Ce doped ZnO.

  20. Formation of Deep Electron Trap by Yb3+ Codoping Leads into Super-Long Persistent Luminescence in Ce3+-doped Yttrium Aluminum Gallium Garnet Phosphors.

    Science.gov (United States)

    Ueda, Jumpei; Miyano, Shun; Tanabe, Setsuhisa

    2018-05-23

    The Y 3 Al 2 Ga 3 O 12 :Ce 3+ -Cr 3+ compound is one of the brightest persistent phosphors, but its persistent luminescence (PersL) duration is not so long due to the relatively shallow Cr 3+ electron trap. Comparing the vacuum referred binding energy of the electron trapping state by Cr 3+ and those by lanthanide ions, we selected Yb 3+ as a deeper electron trapping center. The Y 3 Al 2 Ga 3 O 12 :Ce 3+ -Yb 3+ phosphors show Ce 3+ :5d→4f green persistent luminescence after ceasing blue light excitation. The formation of Yb 2+ was confirmed by the increased intensity of absorption at 585 nm during the charging process. This result indicates that the Yb 3+ ions act as electron traps by capturing an electron. From the thermoluminescence glow curves, it was found the Yb 3+ trap makes much deeper electron trap with 1.01 eV depth than the Cr 3+ electron trap with 0.81 eV depth. This deeper Yb 3+ trap provides much slower detrapping rate of filled electron traps than the Cr 3+ -codoped persistent phosphor. In addition, by preparing transparent ceramics and optimizing Ce 3+ and Yb 3+ concentrations, the Y 3 Al 2 Ga 3 O 12 :Ce 3+ (0.2%)-Yb 3+ (0.1%) as-made transparent ceramic phosphor showed super long persistent luminescence for over 138.8 hours after ceasing blue light charging.

  1. Luminescence of Bi3+ ions in Y3Al5O12:Bi single crystalline films

    International Nuclear Information System (INIS)

    Zorenko, Yu.; Gorbenko, V.; Voznyak, T.; Vistovsky, V.; Nedilko, S.; Nikl, M.

    2007-01-01

    The absorption and cathodoluminescence spectra of single crystalline films (SCF) of Y 3 Al 5 O 12 :Bi garnet depending on Bi concentration were analyzed. For consideration of the nature of the UV and visible Bi-related emission bands the time-resolved luminescence of Bi 3+ (ns 2 ) ions in YAG:Bi SCF was studied at 10 K under excitation by synchrotron radiation. The difference in the excitation spectra and emission decay of the UV and visible bands has been explained via radiative relaxation from the 3 P 1,0 excited states to the 1 S 0 ground state of the isolated and pair/clustered Bi 3+ emission centers in the garnet lattice, respectively

  2. Optical and scintillation properties of Ce.sup.3+./sup.-doped YGd.sub.2./sub.Al.sub.5-x./sub.Ga.sub.x./sub.O.sub.12./sub. (x=2,3,4) single crystal scintillators

    Czech Academy of Sciences Publication Activity Database

    Chewpraditkul, Wa.; Brůža, P.; Pánek, D.; Pattanaboonmee, N.; Wantong, K.; Chewpraditkul, W.; Babin, Vladimir; Bartosiewicz, Karol; Kamada, K.; Yoshikawa, A.; Nikl, Martin

    2016-01-01

    Roč. 169, Jan (2016), s. 43-50 ISSN 0022-2313 R&D Projects: GA ČR GAP204/12/0805; GA MŠk(CZ) LH14266 EU Projects: European Commission(XE) 316906 - LUMINET Institutional support: RVO:68378271 Keywords : YGd 2 Al 5-x Ga x O 12 :Ce * light yield * luminescence * scintillation Subject RIV: BH - Optics, Masers, Lasers Impact factor: 2.686, year: 2016

  3. Influence of thermal treatment and γ-radiation on absorption, luminescence and scintillation properties of Lu3Al5O12:Ce single crystalline films

    International Nuclear Information System (INIS)

    Zorenko, Yu.; Pavlyk, B.; Turchak, R.; Zorenko, T.; Gorbenko, V.; Konstankevych, I.; Savchyn, V.; Voznyak, T.

    2007-01-01

    The influence of thermal treatment (TT) and irradiation by γ-quanta ( 60 Co, 1.25 MeV) in the range of absorbed doses 10 6 -10 8 R on the absorption, luminescence and light yield (LY) of scintillators based on Lu 3 Al 5 O 12 :Ce (LuAG:Ce) single crystalline films (SCF) grown by LPE from the Pb-based flux is studied. It has been shown that transformation of the Fe 3+ ↔Fe 2+ and Pb 2+ ↔Pb 4+ valent states of iron and lead trace impurities cause the change in the optical absorption of SCF induced by the TT in air and vacuum in the range of annealing temperatures of 800-1200 0 C. Possible types of radiation defects in LuAG:Ce SCF induced by γ-radiation are analyzed

  4. Synthesis of Ce(III)-doped Fe3O4 magnetic particles for efficient removal of antimony from aqueous solution

    International Nuclear Information System (INIS)

    Qi, Zenglu; Joshi, Tista Prasai; Liu, Ruiping; Liu, Huijuan; Qu, Jiuhui

    2017-01-01

    Highlights: • Doping of Ce into Fe 3 O 4 was achieved based on a facile solvothermal method. • After doping, the removal capacity was increased by 5 times for “Sb(V)” and 2 times for “Sb(III)”. • Decreasing pH improved adsorption of Sb(V) but decreased adsorption of Sb(III). • Antimony sorption mechanisms on Ce-doped Fe 3 O 4 were illustrated. - Abstract: Aqueous antimony (Sb) pollution from human activity is of great concern in drinking water due to its adverse health effect. Magnetic Fe 3 O 4 particles, with high separation ability from solution, have been considered as a low-cost Sb adsorbent for contaminants. However, the limited adsorption capacity has restricted its practical application. In this study, a solvothermal approach was developed for doping Ce(III) into Fe 3 O 4 , thereby increasing the adsorption efficacy for both Sb(III) and Sb(V). In contrast to un-doped Fe 3 O 4 , the adsorption capacity towards Sb(III) and Sb(V) in Ce-doped materials increased from 111.4 to 224.2 mg/g and from 37.2 to 188.1 mg/g at neutral pH, respectively. Based on the combined results of XPS, XRD, and FTIR, it confirmed that Ce atom successfully doped into the Fe 3 O 4 structure, resulting in the decreased particle size, increased the surface area, and isoelectric point. Furthermore, the vibrating sample magnetometer (VSM) results showed that the Ce doping process had some side effects on the primitive magnetic property, but remaining the high separation potential during water treatment. According to the high removal efficiency and magnetic property, the Ce-doped Fe 3 O 4 of great simplicity should be a promising adsorbent for aqueous Sb removal.

  5. Towards the development of new phosphors with reduced content of rare earth elements: Structural and optical characterization of Ce:Tb: Al{sub 2}SiO{sub 5}

    Energy Technology Data Exchange (ETDEWEB)

    Chiriu, D.; Stagi, L.; Carbonaro, C.M.; Corpino, R. [Dipartimento di Fisica, Università degli Studi di Cagliari, S.P.n°8 Km 0, 700, I-09042 Monserrato (Italy); Casula, M.F. [Dipartimento di Scienze Chimiche e Geologiche and INSTM, Università di Cagliari, S.P.n°8 Km 0, 700, I-09042 Monserrato (Italy); Ricci, P.C., E-mail: carlo.ricci@dsf.unica.it [Dipartimento di Fisica, Università degli Studi di Cagliari, S.P.n°8 Km 0, 700, I-09042 Monserrato (Italy)

    2016-05-15

    Highlights: • A new promising inert matrix as host of luminescent ions is proposed. • Al2SiO5 matrix is free from Rare earths (critical raw materials). • Doping the matrix with Ce and Tb we obtain an efficient green emitter. • Cerium acts as sensitizer for Terbium emission. - Abstract: A new promising inert matrix as host of luminescent ions is proposed. Al2SiO5 samples, doped with rare earths (Ce, Tb single doped and co-doped) are proposed as good prospect for the development of new UV–vis converter with reduced content of rare earths elements. Structural characterization by Raman, XRD spectroscopy and TEM imaging reveals the sillimanite phase and nano sized dimension of the investigated powders. Optical characterization by steady time and time resolved emission spectroscopy for the single doped and co-doped samples allows to identify an efficient energy transfer from Ce to Tb ions under near UV excitation wavelength. The intense green emission observed in the Ce:Tb co-doped Al2SiO5 system suggests its potential application as efficient blue pumped green emitter phosphor to be exploited for white LED: to this purpose we tested the compound in combination with a red emitting doping ion recording for Ce:Tb:Cr:ASO system a correlated color temperature of 6720 K.

  6. Microstructure, optical, and scintillation characteristics of Pr.sup.3+./sup. doped Lu.sub.3./sub.Al.sub.5./sub.O.sub.12./sub. optical ceramics

    Czech Academy of Sciences Publication Activity Database

    Shi, Y.; Nikl, Martin; Feng, X.; Mareš, Jiří A.; Shen, Y.; Beitlerová, Alena; Kučerková, Romana; Pan, Y.; Liu, Q.

    2011-01-01

    Roč. 109, č. 1 (2011), "013522-1"-"013522-7" ISSN 0021-8979 R&D Projects: GA AV ČR KAN300100802; GA MŠk(CZ) ME10084 Institutional research plan: CEZ:AV0Z10100521 Keywords : Pr 3+ doped Lu 3 Al 5 O 12 , * optical ceramics * microstructure * radio-luminescence * scintillation Subject RIV: BM - Solid Matter Physics ; Magnetism Impact factor: 2.168, year: 2011 http://link.aip.org/link/?JAP/109/013522

  7. Investigating the Effect of Glass Ion Release on the Cytocompatibility, Antibacterial Eflcacy and Antioxidant Activity of Y2O3 / CeO2 doped SiO2-SrO-Na2O glasses

    Directory of Open Access Journals (Sweden)

    Placek L. M.

    2018-02-01

    Full Text Available The effect on ion release and cytocompatibility of Yttrium (Y and Cerium (Ce are investigated when substituted for Sodium (Na in a 0.52SiO2-0.24SrO-0.24-Na2OMOglass series (where MO= Y2O3 or CeO2. Glass leaching was evaluated through pH measurements and Inductive Coupled Plasma-Optical Emission Spectrometry (ICP-OES analysiswhere the extract pH increased during incubation (11.2 - 12.5. Ion release of Silicon (Si, Na and Strontium (Sr from the Con glass was at higher than that of glasses containing Y or Ce, and reached a limit after 1 day. Ion release from Y and Ce containing glasses reached a maximum of 1800 μg/mL, 1800 μg/mL, and 10 μg/mL for Si, Na, and Sr, respectively. Release of Y and Cewas below the ICP- OES detection limit 75% of bacteria at a 9% extract concentration. Antioxidant capacity (mechanism for neuroprotection was evaluated using the ABTS assay. All glasses had inherent radical oxygen species (ROS scavenging capability with Con reaching 9.5 mMTE.

  8. Phase Composition and Long-Term Conductivity of Acceptor Doped Ce(PO3)4 and CeP2O7 with Variable P/Metal Ratio and of CeP2O7-KH2PO4 Composite

    DEFF Research Database (Denmark)

    Chatzichristodoulou, Christodoulos; Hallinder, Jonathan; Lapina, Alberto

    2013-01-01

    The thermal evolution of the phase composition of CeP2O7 and Ce(PO3)4 with 10 mol% Y and Gd doping, respectively, was examined by in-situ powder X-ray diffraction and thermogravimetry with in-line mass spectroscopy. The phase composition depends critically on the P to metal ratio, the annealing...... temperature, humidity and time. CeP2O7 and Ce(PO3)4 were completely decomposed to CePO4 following a 1100 h long conductivity test at 155°C. The conductivity of 10 mol% Gd doped Ce(PO3)4 (synthesized with P:(Ce + Gd) = 5.0) reaches a value of 6.4·10−2 S·cm−1 at 150°C under wet conditions (pH2O = 0.2 atm...

  9. Crystal growth and scintillation properties of Er-doped Lu{sub 3}Al{sub 5}O{sub 12} single crystals

    Energy Technology Data Exchange (ETDEWEB)

    Sugiyama, Makoto, E-mail: makoto.sugiyama@imr.tohoku.ac.jp [Institute for Materials Research, Tohoku University, 2-1-1 Katahira, Aoba-ku, Sendai, Miyagi 980-8577 (Japan); Fujimoto, Yutaka [Institute for Materials Research, Tohoku University, 2-1-1 Katahira, Aoba-ku, Sendai, Miyagi 980-8577 (Japan); Yanagida, Takayuki [New Industry Creation Hatchery Center (NICHe), Tohoku University, 6-6-10 Aoba, Aramaki, Aoba-ku, Sendai, Miyagi 980-8579 (Japan); Totsuka, Daisuke [Institute for Materials Research, Tohoku University, 2-1-1 Katahira, Aoba-ku, Sendai, Miyagi 980-8577 (Japan); Nihon Kessho Kogaku Co. Ltd., 810-5 Nobe-cho Tatebayashi Gunma (Japan); Kurosawa, Shunsuke; Futami, Yoshisuke; Yokota, Yuui; Chani, Valery [Institute for Materials Research, Tohoku University, 2-1-1 Katahira, Aoba-ku, Sendai, Miyagi 980-8577 (Japan); Yoshikawa, Akira [Institute for Materials Research, Tohoku University, 2-1-1 Katahira, Aoba-ku, Sendai, Miyagi 980-8577 (Japan); New Industry Creation Hatchery Center (NICHe), Tohoku University, 6-6-10 Aoba, Aramaki, Aoba-ku, Sendai, Miyagi 980-8579 (Japan)

    2012-02-01

    Er-doped Lu{sub 3}Al{sub 5}O{sub 12} (Er:LuAG) single crystalline scintillators with different Er concentrations of 0.1, 0.5, 1, and 3% were grown by the micro-pulling-down ({mu}-PD) method. The grown crystals were composed of single-phase material, as demonstrated by powder X-ray diffraction (XRD). The radioluminescence spectra measured under {sup 241}Am {alpha}-ray excitation indicated host emission at approximately 350 nm and Er{sup 3+} 4f-4f emissions. According to the pulse height spectra recorded under {gamma}-ray irradiation, the 0.5% Er:LuAG exhibited the highest peak channel among the samples. The {gamma}-ray excited decay time profiles were well fitted by the two-component exponential approximation (0.8 {mu}s and 6-10 {mu}s).

  10. Dependence of glass-forming ability on starting compositions in Y2O3Al2O3–SiO2 system

    Directory of Open Access Journals (Sweden)

    Yixiang Chen

    2011-09-01

    Full Text Available The dependence of glass-forming ability on starting compositions in Y2O3Al2O3–SiO2 (YAS system has been investigated by melting experiment. Transparent YAS glasses have been prepared under the condition of furnace cooling instead of quenching. It is found that, in the YAS ternary phase diagram, the compositions on the Y3Al5O12–SiO2 line and with 52-68 mol% SiO2 have a higher glass-forming ability to produce pure glass. For the compositions with too much or less SiO2 or with Y/Al = 5/3, 1/1, or 1/3, crystallization occurs with the formation of Y3Al5O12, Y2Si2O7, Al6Si2O13, or SiO2. The densities of the YAS glasses increase with decreasing SiO2 contents and increasing Y/Al ratios, and for the samples with Y/Al = 3/5 there is a good linear relationship between the density and SiO2 content.

  11. Simultaneous synthesis and densification of transparent, photoluminescent polycrystalline YAG by current activated pressure assisted densification (CAPAD)

    International Nuclear Information System (INIS)

    Penilla, E.H.; Kodera, Y.; Garay, J.E.

    2012-01-01

    Highlights: ► We report a method for the synthesis of transparent and PL bulk polycrystalline Ce:YAG using CAPAD. ► The process uses γ-Al 2 O 3 , Y 2 O 3 , and CeO 2 nanopowders, reacted and densified simultaneously. ► The synthesis/densification kinetics are faster than those reported previously. ► Optical measurements show good transparency in the visible and photoluminescence (PL) in the Ce:YAG. ► The PL peak is broad and appears white when excited using blue light. - Abstract: We report a method for the synthesis and processing of transparent bulk polycrystalline yttrium aluminum garnet (YAG) and photoluminescent Ce-doped YAG ceramics via solid-state reactive-current activated pressure assisted densification (CAPAD). The process uses commercially available γ-Al 2 O 3 , Y 2 O 3 , and CeO 2 nanopowders. The nanopowders were reacted and densified simultaneously at temperatures between 850 °C and 1550 °C and at a maximum pressure of 105 MPa. The solid-state reaction to phase pure YAG occurs in under 4 min at processing temperatures 1100 °C which is significantly faster (on the order of tens of hours) and occurs at much lower temperatures (∼600 °C) compared to conventional reaction sintering. We found that the reaction significantly improves densification – the shrinkage rate of reaction-produced YAG was three times higher than that of YAG using pre-reacted powder. The Ce additions were found to retard the reaction driven shrinkage kinetics by a factor ∼3, but are still faster (by a factor ∼1.6) than those associated with direct densification (no synthesis). Densities >99% were achieved in both pure YAG and Ce doped YAG (Ce:YAG). Results of optical measurements show good transparency in the visible and photoluminescence (PL) in the Ce:YAG. The PL peak is broad and appears white when excited using blue light confirming that the ceramics can be used in solid state lighting to produce white light.

  12. Application of nanostructured Ca doped CeO2 for ultraviolet filtration

    International Nuclear Information System (INIS)

    Truffault, Laurianne; Ta, Minh-Tri; Devers, Thierry; Konstantinov, Konstantin; Harel, Valerie; Simmonard, Cyriaque; Andreazza, Caroline; Nevirkovets, Ivan P.; Pineau, Alain; Veron, Olivier; Blondeau, Jean-Philippe

    2010-01-01

    Calcium doped CeO 2 nanoparticles with doping concentrations between 0 and 50 mol% were synthesized by a co-precipitation method for ultraviolet filtration application. Below 20 mol% doping concentration, the samples were single-phase. From 30 mol%, CaCO 3 appears as a secondary phase. The calculated CeO 2 mean crystallite size was 9.3 nm for the pure and 5.7 nm for the 50 mol% Ca-doped sample. Between 250 and 330 nm, the absorbance increased for the 10, 30, and 40 mol% Ca-doped samples compared to the pure one. The band-gap was found to be 3.20 eV for the undoped, and between 3.36 and 3.51 eV for the doped samples. The blue shifts are attributed to the quantum confinement effect. X-ray photoelectron spectroscopy showed that the Ce 3+ atomic concentration in the pure sample was higher than that of the 20 mol% Ca-doped sample.

  13. High-resolution structural characterization and magnetic properties of epitaxial Ce-doped yttrium iron garnet thin films

    Science.gov (United States)

    Li, Zhong; Vikram Singh, Amit; Rastogi, Ankur; Gazquez, Jaume; Borisevich, Albina Y.; Mishra, Rohan; Gupta, Arunava

    2017-07-01

    Thin films of magnetic garnet materials, e.g. yttrium iron garnet (Y3Fe5O12, YIG), are useful for a variety of applications including microwave integrated circuits and spintronics. Substitution of rare earth ions, such as cerium, is known to enhance the magneto-optic Kerr effect (MOKE) as compared to pure YIG. Thin films of Ce0.75Y2.25Fe5O12 (Ce:YIG) have been grown using the pulsed laser deposition (PLD) technique and their crystal structure examined using high resolution scanning transmission electron microscopy. Homogeneous substitution of Ce in YIG, without oxidation to form a separate CeO2 phase, can be realized in a narrow process window with resulting enhancement of the MOKE signal. The thermally generated signal due to spin Seebeck effect for the optimally doped Ce:YIG films has also been investigated.

  14. Effect of cerium substitution on microstructure and Faraday rotation of Ce{sub x}Y{sub 3-x}Fe{sub 5}O{sub 12} thin films

    Energy Technology Data Exchange (ETDEWEB)

    Shahrokhvand, S.M.; Mozaffari, M.; Rozatian, A.S.H. [University of Isfahan, Department of Physics, Faculty of Science, Isfahan (Iran, Islamic Republic of); Hamidi, S.M. [Shahid Beheshti University, Laser and Plasma Research Institute, Evin, Tehran (Iran, Islamic Republic of); Tehranchi, M.M. [Shahid Beheshti University, Laser and Plasma Research Institute, Evin, Tehran (Iran, Islamic Republic of); Shahid Beheshti University, Department of Physics, Evin, Tehran (Iran, Islamic Republic of)

    2016-01-15

    In this work, cerium-substituted yttrium iron garnet (Ce{sub x}Y{sub 3-x}Fe{sub 5}O{sub 12}, x = 0.25-1) targets were fabricated by conventional ceramic method at different temperatures, and their crystal structures were investigated by X-ray diffraction method. The results showed that the minimum calcining temperature required to get single-phase targets depends on x value and decreased by increasing x value. Then, thin films of the targets were deposited on GGG (444) single-crystal substrates by pulsed laser deposition technique. Based on the previous studies, preferred (444) oriented Ce{sub x}Y{sub 3-x}Fe{sub 5}O{sub 12} thin films were fabricated under optimum conditions. Faraday rotation of the thin films was measured at 635 nm wavelength, and the results showed that Faraday rotation and sensitivity constant increased by increasing x value. Scanning electron microscope images showed that by increasing x value, cracks on the thin films' surface increased. Atomic force microscopy images showed that the films have smooth surfaces and the surface roughness decreased by increasing the x value. (orig.)

  15. Nd-doped Lu3Al5O12 single-crystal scintillator for X-ray imaging

    International Nuclear Information System (INIS)

    Sugiyama, Makoto; Fujimoto, Yutaka; Yanagida, Takayuki; Totsuka, Daisuke; Chani, Valery; Yokota, Yuui; Yoshikawa, Akira

    2013-01-01

    The optical and scintillation properties of Nd-doped Lu 3 Al 5 O 12 (Nd:LuAG) crystals grown by the Czochralski (Cz) method were examined under X-ray excitation. Their applicability for X-ray imaging was also inspected. The radioluminescence spectrum induced by X-rays showed a broad host emission and sharp Nd 3+ 4f–4f emission peaks in the UV to visible wavelengths. The light output current of the Nd:LuAG was 85% of that of a standard CdWO 4 X-ray scintillator. The afterglow value measured 20 ms after X-ray irradiation was 1.5%. An X-ray radiographic image was successfully obtained using the Nd:LuAG scintillator coupled with the charge coupled device (CCD) photodetector. -- Highlights: ► The Nd:LuAG single crystal was produced to perform X-ray imaging test. ► The sample exhibited the 85% light output current of the standard CdWO 4 . ► The afterglow intensity of the sample was very high compared with the CdWO 4 . ► The X-ray radiographic image was obtained from the Nd:LuAG single crystal

  16. Spectral response of REE3+ doped LaAlO3

    International Nuclear Information System (INIS)

    Boronat, C.; Correcher, V.; Garcia G, J.; Morales, A.; Zarate, J.; Rivera, T.

    2016-10-01

    This paper reports on the preliminary results obtained from the cathodoluminescence (Cl) and thermoluminescence (Tl) properties of undoped LaAlO 3 (LAO) and LaAlO 3 : REE (REE=Dy 3+ , Pr 3+ and Eu 3+ ) to be potentially employed for dosimetric purposes. The samples were synthesized by a sol-gel process based on the Pechini 's method with a spray-drying technique and, subsequently, characterized by environmental scanning electron microscopy and energy dispersive X-ray analysis spectrometry. Cl spectra display sharp and narrow wavebands that could specifically be associated with structural (in the range of 300-450 nm) and point defects (from 450 to 800 nm). The observed wavebands could be assigned as follows: (i) 480 and 570 from the Dy-doped LAO should corresponding respectively to 4 F 9/2 → 6 H 15/2 and 4 F 9/2 → 6 H 13/2 transitions, (II) 490-638 from the Pr-doped LAO is linked to 3 P 0 → 3 H 4 , 1 D 2 → 3 H 4 transitions and (III) 590 and 620 where the dopant Eu 3+ gives rise to 5 D 0 → 7 F 1 and 5 D 0 → 7 F 2 transitions and (IV) a UV-blue broad band is associated with NBOHC in undoped LAO. Such emissions are due to the presence of the 4f electrons of rare earth ions that are shielded by the outer 5s and 5p electrons, the intra-4f emission spectra of REE. Furthermore, the study performed on the Tl emission of LaAlO 3 :Dy 3+ displays (i) two maxima centred at 150 and 240 degrees Celsius (ratio 1:2) similarly to the Pr 3+ doped sample but with 7:5 of ratio. And (II) the highest radiation sensitivity, allowing us to think on the potential use of this material for dosimetric purposes, however further works are necessary to confirm such assertion. (Author)

  17. Luminescence and light yield of (Gd2Y)(Ga3Al2)O12:Pr3+ single crystal scintillators

    Science.gov (United States)

    Lertloypanyachai, Prapon; Pathumrangsan, Nichakorn; Sreebunpeng, Krittiya; Pattanaboonmee, Nakarin; Chewpraditkul, Weerapong; Yoshikawa, Akira; Kamada, Kei; Nikl, Martin

    2017-06-01

    Praseodymium-doped (Gd2Y)(Ga3Al2)O12 (GYGAG: Pr) single crystals are grown by the micro-pulling down method with different Pr concentrations. The energy transfer process between Pr3+ and Gd3+ is investigated by photoluminescence excitation (PLE) and emission (PL) spectra measurements. Photoelectron yield measurements are carried out using photomultiplier. At 662 keV γ-rays, photoelectron yield of 2520 phe/MeV obtained for the GYGAG: Pr (0.01%) sample is larger than that of 1810 phe/MeV obtained for BGO crystal. Light yield degradation for the GYGAG: Pr scintillators is presumably due to the energy transfer from 5d state of Pr3+ to 4f state of Gd3+ together with the concentration quenching in the Gd3+-sublattice.

  18. Preparation and characterization of Ce-doped HfO2 nanoparticles

    International Nuclear Information System (INIS)

    Gálvez-Barboza, S.; González, L.A.; Puente-Urbina, B.A.; Saucedo-Salazar, E.M.; García-Cerda, L.A.

    2015-01-01

    Highlights: • Ce-doped HfO 2 nanoparticles were prepared by a modified solgel method. • Ce-doped HfO 2 nanoparticles have a semispherical shape with sizes between 6 and 11.5 nm. • The samples doped with 10% in weight of Ce directly crystallized in a cubic structure. • A quick, straightforward and effective route for the preparation of Ce-doped nanoparticles. - Abstract: A modified solgel method to synthesize Ce-doped HfO 2 nanoparticles was carried out using a precursor material prepared with cerium nitrate, hafnium chloride, citric acid and ethylene glycol. The obtained precursor material was calcined at 500 and 700 °C for 2 h in air. The influence of the concentration of Ce and the calcination temperature was studied to observe the structural and morphological changes of the obtained materials. For the characterization, X-ray diffraction (XRD), transmission electron microscopy (TEM) and Raman scattering (RS) were employed. The XRD patterns shown that the Ce-doped HfO 2 undergoes a structural transformation from monoclinic to cubic phase, which is significantly dependent on the Ce content and calcination temperature. TEM images have also confirmed the existence of semispherical nanoparticles with sizes between 6 and 11.5 nm

  19. Design of high quality doped CeO2 solid electrolytes with nanohetero structure

    International Nuclear Information System (INIS)

    Mori, T.; Ou, D.R.; Ye, F.; Drennan, J.

    2006-01-01

    Doped cerium (CeO 2 ) compounds are fluorite related oxides which show oxide ionic conductivity higher than yttria-stabilized zirconia in oxidizing atmosphere. As a consequence of this, a considerable interest has been shown in application of these materials for low (400-650 o C) temperature operation of solid oxide fuel cells (SOFCs). In this paper, our experimental data about the influence of microstructure at the atomic level on electrochemical properties were reviewed in order to develop high quality doped CeO 2 electrolytes in fuel cell applications. Using this data in the present paper, our original idea for a design of nanodomain structure in doped CeO 2 electrolytes was suggested. The nanosized powders and dense sintered bodies of M doped CeO 2 (M:Sm,Gd,La,Y,Yb, and Dy) compounds were fabricated. Also nanostructural features in these specimens were introduced for conclusion of relationship between electrolytic properties and domain structure in doped CeO 2 . It is essential that the electrolytic properties in doped CeO 2 solid electrolytes reflect in changes of microstructure even down to the atomic scale. Accordingly, a combined approach of nanostructure fabrication, electrical measurement and structure characterization was required to develop superior quality doped CeO 2 electrolytes in the fuel cells. (author)

  20. Room temperature ferromagnetism in Fe-doped CeO2 nanoparticles.

    Science.gov (United States)

    Maensiri, Santi; Phokha, Sumalin; Laokul, Paveena; Seraphin, Supapan

    2009-11-01

    RT ferromagnetism was observed in nanoparticles of Fe-doped CeO2 (i.e., Ce(0.97)Fe(0.03)O2) synthesized by a sol-gel method. The undoped and Fe-doped CeO2 were characterized by XRD, Raman spectroscopy, TEM, and VSM. The undoped samples and Ce(0.97)Fe(0.03)O2 precursor exhibit a diamagnetic behavior. The 673 K-calcined Ce(0.97)Fe(0.03)O2 sample is paramagnetic whereas 773 and 873 K-calcined Ce(0.97)Fe(0.03)O2 samples are ferromagnetism having the magnetizations of 4.65 x 10(-3) emu/g and 6.20 x 10(-3) emu/g at 10 kOe, respectively. Our results indicate that the ferromagnetic property is intrinsic to the Fe-doped CeO2 system and is not a result of any secondary magnetic phase or cluster formation.

  1. A novel yellow-emitting SrAlSi4N7:Ce3+ phosphor for solid state lighting: Synthesis, electronic structure and photoluminescence properties

    Science.gov (United States)

    Ruan, Jian; Xie, Rong-Jun; Funahashi, Shiro; Tanaka, Yoshinori; Takeda, Takashi; Suehiro, Takayuki; Hirosaki, Naoto; Li, Yuan-Qiang

    2013-12-01

    Ce3+-doped and Ce3+/Li+-codoped SrAlSi4N7 phosphors were synthesized by gas pressure sintering of powder mixtures of Sr3N2, AlN, α-Si3N4, CeN and Li3N. The phase purity, electronic crystal structure, photoluminescence properties of SrAlSi4N7:Ce3+(Ce3+/Li+) were investigated in this work. The band structure calculated by the DMol3 code shows that SrAlSi4N7 has a direct band gap of 3.87 eV. The single crystal analysis of Ce3+-doped SrAlSi4N7 indicates a disordered Si/Al distribution and nitrogen vacnacy defects. SrAlSi4N7 was identified as a major phase of the fired powders, and Sr5Al5Si21N35O2 and AlN as minor phases. Both Ce3+ and Ce3+/Li+ doped SrAlSi4N7 phosphors can be efficiently excited by near-UV or blue light and show a broadband yellow emission peaking around 565 nm. A highest external quantum efficiency of 38.3% under the 450 nm excitation was observed for the Ce3+/Li+-doped SrAlSi4N7 (5 mol%). A white light LED lamp with color temperature of 6300 K and color rendering index of Ra=78 was achieved by combining Sr0.97Al1.03Si3.997N\\94\\maccounttest14=t0005_18193 7:Ce3+0.03 with a commercial blue InGaN chip. It indicates that SrAlSi4N7:Ce3+ is a promising yellow emitting down-conversion phosphor for white LEDs.

  2. Direct observation of multivalent states and 4 f →3 d charge transfer in Ce-doped yttrium iron garnet thin films

    Science.gov (United States)

    Vasili, H. B.; Casals, B.; Cichelero, R.; Macià, F.; Geshev, J.; Gargiani, P.; Valvidares, M.; Herrero-Martin, J.; Pellegrin, E.; Fontcuberta, J.; Herranz, G.

    2017-07-01

    Due to their large magneto-optic responses, rare-earth-doped yttrium iron garnets, Y3F e5O12 (YIG), are highly regarded for their potential in photonics and magnonics. Here, we consider the case of Ce-doped YIG (Ce-YIG) thin films, in which substitutional C e3 + ions are magnetic because of their 4 f1 ground state. In order to elucidate the impact of Ce substitution on the magnetization of YIG, we have carried out soft x-ray spectroscopy measurements on Ce-YIG films. In particular, we have used the element specificity of x-ray magnetic circular dichroism to extract the individual magnetization curves linked to Ce and Fe ions. Our results show that Ce doping triggers a selective charge transfer from Ce to the Fe tetrahedral sites in the YIG structure. This, in turn, causes a disruption of the electronic and magnetic properties of the parent compound, reducing the exchange coupling between the Ce and Fe magnetic moments and causing atypical magnetic behavior. Our work is relevant for understanding magnetism in rare-earth-doped YIG and, eventually, may enable a quantitative evaluation of the magneto-optical properties of rare-earth incorporation into YIG.

  3. Y3Fe5O12/Na,Bi,Sr-doped PZT particulate magnetoelectric composites

    Science.gov (United States)

    Lisnevskaya, I. V.; Bobrova, I. A.; Lupeiko, T. G.; Agamirzoeva, M. R.; Myagkaya, K. V.

    2016-05-01

    Magnetoelectric (ME) composites of Na, Bi, Sr substituted lead zirconate titanate (PZT) and yttrium iron garnet having representative formula (100-x) wt% Na,Bi,Sr-doped PZT (PZTNB-1)+x wt% Y3Fe5O12 (YIG) with x=10-90 were manufactured using powdered components obtained through sol-gel processes. It is shown that the decrease in sintering temperature provided by the use of finely dispersed PZTNB-1 and YIG powders allows to significantly reduce content of fluorite-like foreign phase based on zirconium oxide, which forms due to the interfacial interaction during heat treatment and becomes stabilized by yttrium oxide. Connectivity has considerable effect on the value of ME coefficient of composite ceramics. With the same x value, ΔE/ΔH characteristic decreases when changing from 0-3-type structured composites (PZT grains embedded in ferrite matrix) to 3-3-(interpenetrating network of two phases) and especially 3-0-type samples (YIG grains embedded in PZT matrix); in the last case this can be attributed to the substrate clamping effect when ferrite grains are clamped with piezoelectric matrix. ΔE/ΔH value of 0-3 composites with x=40-60 wt% was found to be ∼1.6 mV/(cm Oe).

  4. On possibility of BaCeO3 production when depositing YBa2Cu3O7-χ films on a cerium oxide surface

    International Nuclear Information System (INIS)

    Mashtakov, A.D.; Kotelyanskij, I.M.; Luzanov, V.A.; Mozhaev, P.B.; Ovsyannikov, G.A.; Bdikin, I.D.

    1997-01-01

    Consideration is given to experimental results of investigation into crystallographic parameters of hetero-structural (1102)Al 2 O 3 /(001)CeO 2 (001)YBa 2 Cu 3 O 7-χ films, prepared by the method of cathode sputtering at substrate temperature, equal to 600-800 deg C. It is shown that main limitation for precipitation temperature of YBa 2 Cu 3 O 7-χ film on CeO 2 surface is caused by chemical interaction of YBa 2 Cu 3 O 7-χ with CeO 2 with formation of polycrystalline BaCeO 3 layer

  5. Development and characterization of nickel catalysts supported in CeO2-ZrO2-Al2O3, CeO2-La2O3-Al2O3 e ZrO2-La2O3-Al2O3 matrixes evaluated for methane reforming reactions

    International Nuclear Information System (INIS)

    Abreu, Amanda Jordão de

    2012-01-01

    Nowadays, the methane reforming is large interest industrial for the take advantage of these gas in production the hydrogen and synthesis gas (syngas). Among in the reactions of methane stand of the reactions steam reforming and carbon dioxide reforming of methane. The main catalysts uses in the methane reforming is Ni/Al 2 O 3 . However, the supported-nickel catalyst is susceptible to the deactivation or the destruction by coke deposition. The carbon dissolves in the nickel crystallite and its diffuses through the nickel, leading for formation of the carbon whiskers, which results in fragmentation of the catalyst. Modification of such catalysts, like incorporation of suitable promoters, is desirable to achieve reduction of the methane hydrogenolysis and/or promotion of the carbon gasification. Catalysts 5%Ni/Al 2 O 3 supported on solid solutions formed by ZrO 2 -CeO 2 , La 2 O 3 and CeO 2 -ZrO 2 -La 2 O 3 were prepared, characterized and evaluated in reactions steam and carbon dioxide reforming and partial oxidation of methane with objective the value effect loading solution solid in support. The supports were prepared by co-precipitation method and catalysts were prepared by impregnation method and calcined at 500 deg C. The supports and catalysts were characterized by Nitrogen Adsorption, method -rays diffraction (XRD), X-rays dispersive spectroscopy (XDS), spectroscopy in the region of the ultraviolet and the visible (UV-vis NIR) to and temperature programmed reduction (TPR), Raman Spectroscopy, X-ray absorption spectroscopy and Thermogravimetric Analysis. After all the catalytic reactions check which the addition of solid solution is beneficial for Ni/Al 2 O 3 catalysts and the best catalysts are Ni/CeO 2 -La 2 O 3 -Al 2 O 3 . (author)

  6. Optical and scintillation characteristics of Gd.sub.2./sub.YAl.sub.2./sub.Ga.sub.3./sub.O.sub.12./sub.:Ce and Lu.sub.2./sub.YAl.sub.2./sub.Ga.sub.3./sub.O.sub.12./sub.:Ce single crystals

    Czech Academy of Sciences Publication Activity Database

    Chewpraditkul, W.; Sakthong, O.; Pattanaboonmee, N.; Chewpraditkul, We.; Szczesniak, T.; Swiderski, L.; Moszynski, M.; Kamada, K.; Yoshikawa, A.; Nikl, Martin

    2017-01-01

    Roč. 468, Jun (2017), 395–398 ISSN 0022-0248 R&D Projects: GA ČR GA16-15569S Institutional support: RVO:68378271 Keywords : Ce-doping * Czochralski method * Gd 2 YAl 2 Ga 3 O 12 :Ce * Lu 2 YAl 2 Ga 3 O 12 :Ce * luminescence * scintillator materials Subject RIV: BM - Solid Matter Physics ; Magnetism OBOR OECD: Condensed matter physics (including formerly solid state physics, supercond.) Impact factor: 1.751, year: 2016

  7. Transport and magnetic properties of Ce-doped LaMnO3 thin films

    International Nuclear Information System (INIS)

    Yanagida, Takeshi; Kanki, Teruo; Vilquin, Bertrand; Tanaka, Hidekazu; Kawai, Tomoji

    2005-01-01

    Ce-doped LaMnO 3 epitaxial thin films were fabricated by a pulsed laser deposition method in consideration of thermodynamics. Oxygen- or argon-atmosphere post-annealed films showed a metal-insulator transition and ferromagnetic property, and the transition temperature T c was found to be significantly influenced by the post-annealing conditions at the T c ranging from 200 to 300 K. Moreover, the majority carriers within Ce-doped LaMnO 3 films were identified to be holes from Hall effect measurements

  8. Synthesis of Ce(III)-doped Fe{sub 3}O{sub 4} magnetic particles for efficient removal of antimony from aqueous solution

    Energy Technology Data Exchange (ETDEWEB)

    Qi, Zenglu; Joshi, Tista Prasai [Key Laboratory of Drinking Water Science and Technology, Research Center for Eco-Environmental Sciences, Chinese Academy of Sciences, Beijing 100085 (China); University of Chinese Academy of Sciences, Beijing 100049 (China); Liu, Ruiping, E-mail: liuruiping@rcees.ac.cn [Key Laboratory of Drinking Water Science and Technology, Research Center for Eco-Environmental Sciences, Chinese Academy of Sciences, Beijing 100085 (China); University of Chinese Academy of Sciences, Beijing 100049 (China); Liu, Huijuan [University of Chinese Academy of Sciences, Beijing 100049 (China); State Key Laboratory of Environmental Aquatic Chemistry, Research Center for Eco-Environmental Sciences, Chinese Academy of Sciences, Beijing, 100085 (China); Qu, Jiuhui [Key Laboratory of Drinking Water Science and Technology, Research Center for Eco-Environmental Sciences, Chinese Academy of Sciences, Beijing 100085 (China); University of Chinese Academy of Sciences, Beijing 100049 (China)

    2017-05-05

    Highlights: • Doping of Ce into Fe{sub 3}O{sub 4} was achieved based on a facile solvothermal method. • After doping, the removal capacity was increased by 5 times for “Sb(V)” and 2 times for “Sb(III)”. • Decreasing pH improved adsorption of Sb(V) but decreased adsorption of Sb(III). • Antimony sorption mechanisms on Ce-doped Fe{sub 3}O{sub 4} were illustrated. - Abstract: Aqueous antimony (Sb) pollution from human activity is of great concern in drinking water due to its adverse health effect. Magnetic Fe{sub 3}O{sub 4} particles, with high separation ability from solution, have been considered as a low-cost Sb adsorbent for contaminants. However, the limited adsorption capacity has restricted its practical application. In this study, a solvothermal approach was developed for doping Ce(III) into Fe{sub 3}O{sub 4}, thereby increasing the adsorption efficacy for both Sb(III) and Sb(V). In contrast to un-doped Fe{sub 3}O{sub 4}, the adsorption capacity towards Sb(III) and Sb(V) in Ce-doped materials increased from 111.4 to 224.2 mg/g and from 37.2 to 188.1 mg/g at neutral pH, respectively. Based on the combined results of XPS, XRD, and FTIR, it confirmed that Ce atom successfully doped into the Fe{sub 3}O{sub 4} structure, resulting in the decreased particle size, increased the surface area, and isoelectric point. Furthermore, the vibrating sample magnetometer (VSM) results showed that the Ce doping process had some side effects on the primitive magnetic property, but remaining the high separation potential during water treatment. According to the high removal efficiency and magnetic property, the Ce-doped Fe{sub 3}O{sub 4} of great simplicity should be a promising adsorbent for aqueous Sb removal.

  9. Study of directionally solidified eutectic Al2O3-ZrO2(3%Y2O3 doped with TiO2

    Directory of Open Access Journals (Sweden)

    Peña, J. I.

    2007-06-01

    Full Text Available An study of directionally grown samples of the eutectic composition in the Al2O3-ZrO2 (3 mol% Y2O3 system, with small TiO2 additions (1 wt%, is presented. The microstructural changes induced by this addition are analysed using SEM (EDX techniques. The mechanical changes, when TiO2 is added, are studied by measuring the flexural strength by three point bending. Also, the toughness is determined by Vickers indentation method. When slow growth rates (10 mm/h are used, interpenetratred and homogeneous microstructure is obtained, independently of the TiO2 doping. When growth rates are higher (300 and 1000 mm/h the structure changes and the phases are organized in form of colonies or cells, which have smaller size when TiO2 is present. This size reduction is accompanied with an increase of the toughness.Este trabajo presenta un estudio de muestras crecidas direccionalmente del sistema Al2O3-ZrO2 (3 mol% Y2O3 en su composición eutéctica con pequeñas adiciones de óxido de titanio (1% de TiO2 en peso. Se analizan los cambios microestructurales inducidos por esta adición mediante SEM (EDX y se estudian los cambios en su comportamiento mecánico medido por flexión en tres puntos, así como la tenacidad de fractura mediante indentación Vickers. Con velocidades lentas de solidificación (10 mm/h se obtiene en ambos casos una microestructura homogénea e interpenetrada, mientras que a velocidades mayores, 300 y 1000 mm/h, se forma una estructura en las que las fases se organizan en forma de colonias o células, siendo éstas de menor tamaño en las muestras dopadas. Esta disminución en el tamaño viene acompañada de un aumento de la tenacidad de fractura medida por indentación.

  10. Preparation and characterization of Ce-doped HfO{sub 2} nanoparticles

    Energy Technology Data Exchange (ETDEWEB)

    Gálvez-Barboza, S. [Centro de Investigación en Química Aplicada, Departamento de Materiales Avanzados, Blvd. Enrique Reyna Hermosillo #140, C.P. 25294 Saltillo, Coahuila (Mexico); Centro de Investigación y de Estudios Avanzados del Instituto Politécnico Nacional, Av. Industria Metalúrgica # 1062 Parque Industrial, C.P. 25900 Ramos Arizpe, Coahuila (Mexico); González, L.A. [Centro de Investigación y de Estudios Avanzados del Instituto Politécnico Nacional, Av. Industria Metalúrgica # 1062 Parque Industrial, C.P. 25900 Ramos Arizpe, Coahuila (Mexico); Puente-Urbina, B.A.; Saucedo-Salazar, E.M. [Centro de Investigación en Química Aplicada, Departamento de Materiales Avanzados, Blvd. Enrique Reyna Hermosillo #140, C.P. 25294 Saltillo, Coahuila (Mexico); García-Cerda, L.A., E-mail: luis.garcia@ciqa.edu.mx [Centro de Investigación en Química Aplicada, Departamento de Materiales Avanzados, Blvd. Enrique Reyna Hermosillo #140, C.P. 25294 Saltillo, Coahuila (Mexico)

    2015-09-15

    Highlights: • Ce-doped HfO{sub 2} nanoparticles were prepared by a modified solgel method. • Ce-doped HfO{sub 2} nanoparticles have a semispherical shape with sizes between 6 and 11.5 nm. • The samples doped with 10% in weight of Ce directly crystallized in a cubic structure. • A quick, straightforward and effective route for the preparation of Ce-doped nanoparticles. - Abstract: A modified solgel method to synthesize Ce-doped HfO{sub 2} nanoparticles was carried out using a precursor material prepared with cerium nitrate, hafnium chloride, citric acid and ethylene glycol. The obtained precursor material was calcined at 500 and 700 °C for 2 h in air. The influence of the concentration of Ce and the calcination temperature was studied to observe the structural and morphological changes of the obtained materials. For the characterization, X-ray diffraction (XRD), transmission electron microscopy (TEM) and Raman scattering (RS) were employed. The XRD patterns shown that the Ce-doped HfO{sub 2} undergoes a structural transformation from monoclinic to cubic phase, which is significantly dependent on the Ce content and calcination temperature. TEM images have also confirmed the existence of semispherical nanoparticles with sizes between 6 and 11.5 nm.

  11. Preparation and studies of Eu3+ and Tb3+ co-doped Gd2O3 and Y2O3 sol-gel scintillating films

    International Nuclear Information System (INIS)

    Morales Ramirez, A. de J; Garcia Murillo, A.; Carrillo Romo, F. de J; Ramirez Salgado, J.; Le Luyer, C.; Chadeyron, G.; Boyer, D.; Moreno Palmerin, J.

    2009-01-01

    Eu 3+ (2.5 at.%) and Tb 3+ (0.005-0.01 at.%) co-doped gadolinium and yttrium oxide (Gd 2 O 3 and Y 2 O 3 ) powders and films have been prepared using the sol-gel process. High density and optical quality thin films were prepared with the dip-coating technique. Gadolinium (III) 2,4-pentadionate and yttrium (III) 2,4-pentadionate were used as precursors, and europium and terbium in their nitrate forms were used as doping agents. Chemical and structural analyses (infrared spectroscopy, X-ray diffraction and high-resolution transmission electron microscopy) were conducted on both sol-gel precursor powders and dip-coated films. The morphology of thin films heat-treated at 700 o C was studied by means of atomic force microscopy. It was shown that the highly dense and very smooth films had a root mean roughness (RMS) of 2 nm ± 0.2 (A = 0.0075 Tb 3+ ) and 24 nm ± 3.0 (B = 0.01 Tb 3+ ). After treatment at 700 o C, the crystallized films were in the cubic phase and presented a polycrystalline structure made up of randomly oriented crystallites with grain sizes varying from 20 to 60 nm. The X-ray induced emission spectra of Eu 3+ - and Tb 3+ -doped Gd 2 O 3 and Y 2 O 3 powders showed that Tb 3+ contents of 0.005, 0.0075 and 0.01 at.% affected their optical properties. Lower Tb 3+ concentrations (down to 0.005 at.%) in both systems enhanced the light yield.

  12. Thermopower studies of doped CeAl sub 2 and UAl sub 2

    CERN Document Server

    Park, J G

    1997-01-01

    We have studied the thermopower of U doped CeAl sub 2 and Ce and La doped UAl sub 2. Despite different ground state properties of CeAl sub 2 and UAl sub 2 , the former being an antiferromagnetic heavy-fermion compound and the latter non-magnetic, we have found that not only thermopower data for pure CeAl sub 2 and UAl sub 2 are similar but also the thermopower results of doped samples behave similarly. Although the similarity seen in pure systems is yet to be understood, we interpret the doping effects as the results of changes in energy dependent relaxation time with doping. (author)

  13. Electron traps and scintillation mechanism in YAlO3:Ce and LuAlO3:Ce scintillators

    International Nuclear Information System (INIS)

    Wojtowicz, A.J.; Glodo, J.; Drozdowski, W.; Przegietka, K.R.

    1998-01-01

    In this paper we present the results of thermoluminescence, isothermal decay and scintillation light yield measurements on two isostructural scintillator materials, YAlO 3 :Ce and LuAlO 3 :Ce. In addition to the variety of deep traps identified by thermoluminescence and isothermal decays, scintillation light yield experiments demonstrate the presence in both materials of a number of relatively shallow traps. While the deep traps may reduce the scintillation light yield, they do not influence the kinetics of the process. The shallow traps, on the other hand, by interfering with the process of radiative recombination of charge carriers via Ce 3+ ions, can strongly affect not only the yield of the scintillation process but its kinetics as well. The presence of shallow traps provides a consistent explanation for a number of poorly understood relationships between the two scintillator materials, including a higher room temperature scintillation light yield and longer scintillation decay time in YAlO 3 :Ce, and a longer scintillation rise time in LuAlO 3 :Ce. Theoretical analysis indicates that elimination of these traps would make the two materials nearly identical in scintillator performance. Although the specific identity of all traps remains elusive, the performance of both scintillator materials is now, in practical terms, fully understood. (Copyright (c) 1998 Elsevier Science B.V., Amsterdam. All rights reserved.)

  14. Scintillation properties of transparent Lu{sub 3}Al{sub 5}O{sub 12} (LuAG) ceramics doped with different concentrations of Pr{sup 3+}

    Energy Technology Data Exchange (ETDEWEB)

    Yanagida, Takayuki; Fukabori, Akihiro; Fujimoto, Yutaka; Kamada, Kei; Yokota, Yuui; Yoshikawa, Akira; Chani, Valery [IMRAM, Tohoku University, 2-1-1 Katahira Aoba-ku, 980-8577 Sendai (Japan); Ikesue, Akio [World Labo, Co. Ltd., Mutsuno 2-4-1, Atsuta, 456-0023 Nagoya (Japan); Kataoka, Jun [School of Advanced Science and Engineering,Waseda University, Ohkubo 3-4-1, Shinjuku, 169-0072 Tokyo (Japan)

    2011-01-15

    Transparent ceramics of Pr-doped (0.2 mol%, 0.6 mol%, 1 mol%, and 2 mol%) Lu{sub 3}Al{sub 5}O{sub 12} (LuAG) scintillators produced by the sintering method are discussed. These materials were cut to the specimens with physical dimensions of 5 x 5 x 2 mm{sup 3}. Similar size specimens were also prepared from Czochralski grown Pr:LuAG single crystals to compare scintillation properties. Their transmittance and radio luminescence spectra were evaluated. All specimens were highly transparent in wavelength range above 300 nm, and intense Pr{sup 3+} 5d-4f emission was detected around 310 and 370 nm under excitation with X-ray. Under {sup 137}Cs {gamma}-ray is irradiation, 2 keV photo-absorption peaks were also clearly observed in each sample. The Pr 0.6 mol% doped LuAG ceramics demonstrated highest light yield achievable among the ceramics, and it was half of that observed in the single crystals. Under pulse X-ray excitation, the decay time constants became faster when Pr concentration increased, and. the fastest decay ({proportional_to}5.7 ns time constant) was noticed in the 2 mol% doped ceramic. (copyright 2011 WILEY-VCH Verlag GmbH and Co. KGaA, Weinheim) (orig.)

  15. Surface and catalytic properties of MoO3/Al2O3 system doped with Co3O4

    International Nuclear Information System (INIS)

    Zahran, A.A.; Shaheen, W.M.; El-Shobaky, G.A.

    2005-01-01

    Thermal solid-solid interactions in cobalt treated MoO 3 /Al 2 O 3 system were investigated using X-ray powder diffraction. The solids were prepared by wet impregnation method using Al(OH) 3 , ammonium molybdate and cobalt nitrate solutions, drying at 100 deg. C then calcination at 300, 500, 750 and 1000 deg. C. The amount of MoO 3 , was fixed at 16.67 mol% and those of cobalt oxide were varied between 2.04 and 14.29 mol% Co 3 O 4 . Surface and catalytic properties of various solid samples precalcined at 300 and 500 deg. C were studied using nitrogen adsorption at -196 deg. C, conversion of isopropanol at 200-500 deg. C and decomposition of H 2 O 2 at 30-50 deg. C. The results obtained revealed that pure mixed solids precalcined at 300 deg. C consisted of AlOOH and MoO 3 phases. Cobalt oxide-doped samples calcined at the same temperature consisted also of AlOOH, MoO 3 and CoMoO 4 compounds. The rise in calcination temperature to 500 deg. C resulted in complete conversion of AlOOH into very poorly crystalline γ-Al 2 O 3 . The further increase in precalcination temperature to 750 deg. C led to the formation of Al 2 (MoO 4 ) 3 , κ-Al 2 O 3 besides CoMoO 4 and un-reacted portion of Co 3 O 4 in the samples rich in cobalt oxide. Pure MoO 3 /Al 2 O 3 preheated at 1000 deg. C composed of MoO 3Al 2 O 3 solid solution (acquired grey colour). The doped samples consisted of the same solid solution together with CoMoO 4 and CoAl 2 O 4 compounds. The increase in calcination temperature of pure and variously doped solids from 300 to 500 deg. C increased their specific surface areas and total pore volume which suffered a drastic decrease upon heating at 750 deg. C. Doping the investigated system with small amounts of cobalt oxide (2.04 and 4 mol%) followed by heating at 300 and 500 deg. C increased its catalytic activity in H 2 O 2 decomposition. This increase, measured at 300 deg. C, attained 25.4- and 12.9-fold for the solids precalcined at 300 and 500 deg. C, respectively

  16. Synthesis of Ce-doped SnO{sub 2} nanoparticles and their acetone gas sensing properties

    Energy Technology Data Exchange (ETDEWEB)

    Lian, Xiaoxue, E-mail: lianxiaoxues@163.com; Li, Yan; Tong, Xiaoqiang; Zou, Yunling; Liu, Xiulin; An, Dongmin; Wang, Qiong

    2017-06-15

    Highlights: • The Ce-doped SnO{sub 2} nanoparticles were fabricated via a simple hydrothermal method. • Ce ions were successfully doped into the SnO{sub 2} lattice, and 5 wt% SnO{sub 2}:Ce had a higher specific surface area. • The Ce-doped SnO{sub 2} nanoparticles exhibited the highest response values and a well selectivity to acetone. - Abstract: Hydrothermal method was generally used to synthesis nanoparticles, which was used to fabricate pure and Ce-doped (3 wt%, 5 wt%, 7 wt%) SnO{sub 2} nanoparticles in this experiment. The as-prepared products were characterized by X-ray diffraction (XRD), energy dispersive spectrum (EDS), scanning electron microscopy (SEM), transmission electron microscopy (TEM) and Brunauer–Emmett–Teller (BET). The results clearly indicated that the nanoparticles were composed of SnO{sub 2} nanoparticles and Ce ions were successfully doped into the SnO{sub 2} lattice, and 5 wt% SnO{sub 2}:Ce has a higher specific surface area (173.53 m{sup 2}/g). Importantly, SnO{sub 2}:Ce sensor had obviously improved performance compared to pure SnO{sub 2} and exhibited the highest response values (50.5 for 50 ppm) and a well selectivity to acetone at 270 °C. It could detect acetone gas in a wide concentration range with very high response, good long-term stability and repeatability of response. The possible sensing mechanism was discussed in this paper.

  17. Electronic structure study of Co doped CeO2 nanoparticles using X-ray absorption fine structure spectroscopy

    International Nuclear Information System (INIS)

    Kumar, Shalendra; Gautam, Sanjeev; Song, T.K.; Chae, Keun Hwa; Jang, K.W.; Kim, S.S.

    2014-01-01

    Highlights: • The electronic structural of Co–CeO 2 nanoparticles is investigated using XAFS. • Ce M 5,4 , Ce L 3 and O K edge NEXAFS reveal that the Ce-ions are in +4 valence state. • The NEXAFS spectrum performed at Co L3,2-edge confirms Co-ion in 2+ state. • The EXAFS analysis also show that Co ions are occupying Ce position in doped CeO 2 . • The distances between Ce–O and Ce–Ce/Co in all shells decreases with Co doping. - Abstract: We investigated the electronic structure of well characterized Co doped CeO 2 nanoparticles using X-ray absorption fine structure (XAFS) spectroscopy. Near edge X-ray absorption fine structure (NEXAFS) spectra at Ce M 5,4 , Ce L 3 and O K-edge conclude that the Ce-ions are in +4 valence state in pure as well as in Co doped CeO 2 nanoparticles. The local structure around Ce-atom in Co doped CeO 2 nanoparticles was also determined using extended X-ray absorption fine structure (EXAFS) spectroscopy at Ce L 3 edge. The EXAFS analysis suggest that the inter-atomic distance of Ce–O, Ce–Ce/Co decreases with Co doping, which indicate a contraction of the lattice. The decease in Ce–O distance also reflect that there is a formation of oxygen vacancies in CeO 2 matrix. The Debye–Waller factor also shows the consistent behaviour for all the coordination shells. The atomic multiplet calculations for Co L 3,2 -edge was performed to determine the valence state, symmetry and field splitting, which reflect that Co-ions are in 2+ state and substituted at Ce-site with crystal field splitting of 10Dq=-0.57eV. The XAFS measurements reveal that the Co-ions occupy the Ce position in the CeO 2 host matrix and create a oxygen vacancy

  18. Electron paramagnetic resonance investigation of polycrystalline CaCu3Ti4O12

    International Nuclear Information System (INIS)

    Mozzati, Maria Cristina; Azzoni, Carlo Bruno; Capsoni, Doretta; Bini, Marcella; Massarotti, Vincenzo

    2003-01-01

    Electron paramagnetic resonance (EPR) measurements on pure polycrystalline CaCu 3 Ti 4 O 12 have been performed and are discussed within a crystal-field approach. A symmetric signal centred at g = 2.15 is observed for T>25 K, with no evidence of hyperfine structure. At this temperature an antiferromagnetic transition is observed as confirmed by static magnetization data. Cu defective and 2% doped (V, Cr, Mn, La) samples were also prepared and considered, mainly to understand the nature of the observed paramagnetic centre. Substitutions in the octahedral sites, causing variations of the configuration in CuO 4 -TiO 6 -CuO 4 complexes, change the magnetic and EPR features. To justify the EPR response a strong copper-hole delocalization is suggested

  19. Catalytic Oxidation of Propene over Pd Catalysts Supported on CeO2, TiO2, Al2O3 and M/Al2O3 Oxides (M = Ce, Ti, Fe, Mn

    Directory of Open Access Journals (Sweden)

    Sonia Gil

    2015-04-01

    Full Text Available In the following work, the catalytic behavior of Pd catalysts prepared using different oxides as support (Al2O3, CeO2 and TiO2 in the catalytic combustion of propene, in low concentration in excess of oxygen, to mimic the conditions of catalytic decomposition of a volatile organic compound of hydrocarbon-type is reported. In addition, the influence of different promoters (Ce, Ti, Fe and Mn when added to a Pd/Al2O3 catalyst was analyzed. Catalysts were prepared by the impregnation method and were characterized by ICP-OES, N2 adsorption, temperature-programmed reduction, temperature-programmed oxidation, X-ray diffraction, X-ray photoelectron spectroscopy and transmission electron microscopy. Catalyst prepared using CeO2 as the support was less easily reducible, due to the stabilization effect of CeO2 over the palladium oxides. Small PdO particles and, therefore, high Pd dispersion were observed for all of the catalysts, as confirmed by XRD and TEM. The addition of Ce to the Pd/Al2O3 catalysts increased the metal-support interaction and the formation of highly-dispersed Pd species. The addition of Ce and Fe improved the catalytic behavior of the Pd/Al2O3 catalyst; however, the addition of Mn and Ti decreased the catalytic activity in the propene oxidation. Pd/TiO2 showed the highest catalytic activity, probably due to the high capacity of this catalyst to reoxidize Pd into PdO, as has been found in the temperature-programmed oxidation (TPO experiments.

  20. Simultaneous synthesis and densification of transparent, photoluminescent polycrystalline YAG by current activated pressure assisted densification (CAPAD)

    Energy Technology Data Exchange (ETDEWEB)

    Penilla, E.H.; Kodera, Y. [Mechanical Engineering Dept., Materials Science and Engineering Program, University of California, Riverside (United States); Garay, J.E., E-mail: jegaray@engr.ucr.edu [Mechanical Engineering Dept., Materials Science and Engineering Program, University of California, Riverside (United States)

    2012-08-20

    Highlights: Black-Right-Pointing-Pointer We report a method for the synthesis of transparent and PL bulk polycrystalline Ce:YAG using CAPAD. Black-Right-Pointing-Pointer The process uses {gamma}-Al{sub 2}O{sub 3}, Y{sub 2}O{sub 3}, and CeO{sub 2} nanopowders, reacted and densified simultaneously. Black-Right-Pointing-Pointer The synthesis/densification kinetics are faster than those reported previously. Black-Right-Pointing-Pointer Optical measurements show good transparency in the visible and photoluminescence (PL) in the Ce:YAG. Black-Right-Pointing-Pointer The PL peak is broad and appears white when excited using blue light. - Abstract: We report a method for the synthesis and processing of transparent bulk polycrystalline yttrium aluminum garnet (YAG) and photoluminescent Ce-doped YAG ceramics via solid-state reactive-current activated pressure assisted densification (CAPAD). The process uses commercially available {gamma}-Al{sub 2}O{sub 3}, Y{sub 2}O{sub 3}, and CeO{sub 2} nanopowders. The nanopowders were reacted and densified simultaneously at temperatures between 850 Degree-Sign C and 1550 Degree-Sign C and at a maximum pressure of 105 MPa. The solid-state reaction to phase pure YAG occurs in under 4 min at processing temperatures 1100 Degree-Sign C which is significantly faster (on the order of tens of hours) and occurs at much lower temperatures ({approx}600 Degree-Sign C) compared to conventional reaction sintering. We found that the reaction significantly improves densification - the shrinkage rate of reaction-produced YAG was three times higher than that of YAG using pre-reacted powder. The Ce additions were found to retard the reaction driven shrinkage kinetics by a factor {approx}3, but are still faster (by a factor {approx}1.6) than those associated with direct densification (no synthesis). Densities >99% were achieved in both pure YAG and Ce doped YAG (Ce:YAG). Results of optical measurements show good transparency in the visible and

  1. Influence of Zr and Ce doping on electromagnetic properties of (Gd,Y)-Ba-Cu-O superconducting tapes fabricated by metal organic chemical vapor deposition

    International Nuclear Information System (INIS)

    Selvamanickam, V.; Chen, Y.; Xie, J.; Zhang, Y.; Guevara, A.; Kesgin, I.; Majkic, G.; Martchevsky, M.

    2009-01-01

    (Gd,Y)Ba 2 Cu 3 O x tapes have been fabricated by metal organic chemical vapor deposition (MOCVD) with Zr-doping levels of 0-15 mol.% and Ce doping levels of 0-10 mol.% in 0.4 μm thick films. The critical current density (J c ) of Zr-doped samples at 77 K, 1 T applied in the orientation of H -parallel c is found to increase with Zr content and shows a maximum at 7.5% Zr doping. The 7.5% Zr-doped sample exhibits a critical current density (J c ) of 0.95 MA/cm 2 at H -parallel c which is more than 70% higher than the J c of the undoped sample. The peak in J c at H -parallel c is 83% of that at H -parallel a-b in the 7.5% Zr-doped sample which is more than twice as that in the undoped sample. Superconducting transition temperature (T c ) values as high as about 89 K have been achieved in samples even with 15% Zr and 10% Ce. Ce-doped samples with and without Ba compensation are found to exhibit substantially different J c values as well as angular dependence characteristics.

  2. Influence of Zr and Ce doping on electromagnetic properties of (Gd,Y)-Ba-Cu-O superconducting tapes fabricated by metal organic chemical vapor deposition

    Energy Technology Data Exchange (ETDEWEB)

    Selvamanickam, V., E-mail: selva@uh.ed [Department of Mechanical Engineering and Texas Center for Superconductivity, University of Houston, 4800 Calhoun Rd., Houston, TX 77204-4006 (United States); Chen, Y.; Xie, J. [SuperPower Inc., 450 Duane Ave., Schenectady, NY 12304 (United States); Zhang, Y.; Guevara, A.; Kesgin, I.; Majkic, G. [Department of Mechanical Engineering and Texas Center for Superconductivity, University of Houston, 4800 Calhoun Rd., Houston, TX 77204-4006 (United States); Martchevsky, M. [SuperPower Inc., 450 Duane Ave., Schenectady, NY 12304 (United States)

    2009-12-01

    (Gd,Y)Ba{sub 2}Cu{sub 3}O{sub x} tapes have been fabricated by metal organic chemical vapor deposition (MOCVD) with Zr-doping levels of 0-15 mol.% and Ce doping levels of 0-10 mol.% in 0.4 mum thick films. The critical current density (J{sub c}) of Zr-doped samples at 77 K, 1 T applied in the orientation of H -parallel c is found to increase with Zr content and shows a maximum at 7.5% Zr doping. The 7.5% Zr-doped sample exhibits a critical current density (J{sub c}) of 0.95 MA/cm{sup 2} at H -parallel c which is more than 70% higher than the J{sub c} of the undoped sample. The peak in J{sub c} at H -parallel c is 83% of that at H -parallel a-b in the 7.5% Zr-doped sample which is more than twice as that in the undoped sample. Superconducting transition temperature (T{sub c}) values as high as about 89 K have been achieved in samples even with 15% Zr and 10% Ce. Ce-doped samples with and without Ba compensation are found to exhibit substantially different J{sub c} values as well as angular dependence characteristics.

  3. Synthesis and characterization of (Lu{sub 1−x−y}Y{sub x}Ce{sub y}){sub 2}SiO{sub 5} luminescent powders with fast decay time

    Energy Technology Data Exchange (ETDEWEB)

    Aburto-Crespo, M. [Programa de Posgrado en Física de Materiales CICESE-UNAM, Km. 107 Carretera Tij-Ens, Ensenada, B. C. 22860, México (Mexico); Hirata, G.A., E-mail: hirata@cnyn.unam.mx [Centro de Nanociencias y Nanotecnología-Universidad Nacional Autónoma de México, Km. 107 Carretera Tijuana-Ensenada, Ensenada, B. C. 22860, México (Mexico); McKittrick, J. [University of California at San Diego, La Jolla, CA 92093-0411 (United States)

    2013-04-15

    The structural and luminescent properties of blue-emitting (Lu{sub 1−x−y}Y{sub x}Ce{sub y}){sub 2}SiO{sub 5} (0.1≤x≤0.4, y=0.05, 0.005) phosphors prepared by combustion synthesis and post-annealed at 1200 °C for different annealing times are reported. X-ray diffraction analysis revealed the formation of a (Lu,Y){sub 2}SiO{sub 5} solid solution as a majority phase with small traces of a residual phase that was identified as Lu{sub 2}SiO{sub 7}. Under long-UV excitation, the powders yield a very bright blue-emission consisting of two bands with maximum emissions located at λ=405 nm and λ=440 nm, both corresponding to the Ce{sup 3+} allowed transitions {sup 2}D{sub 3/2}→{sup 2}F{sub 5/2} and {sup 2}D{sub 5/2}→{sup 2}F{sub 7/2}, respectively. Moreover, luminescence decay times of 38–45 ns were measured, which depend on the composition, making these powders excellent candidates for application as scintillators in medical imaging. -- Highlights: ► A facile technique to fabricate (Lu,Y)-oxyorthosilicate nanophosphors is presented. ► The structural and excellent luminescent properties including excitation, emission and short decay times are reported. ► The Ce-doped oxyorthosilicates nanophosphors present a fast decay time of the order of 38–45 ns.

  4. Improved dielectric properties and grain boundary response in neodymium-doped Y_2_/_3Cu_3Ti_4O_1_2 ceramics

    International Nuclear Information System (INIS)

    Liang, Pengfei; Yang, Zupei; Chao, Xiaolian

    2016-01-01

    Rare earth element neodymium was adopted to refine grain and in turn increase the volume of grain boundary of Y_2_/_3Cu_3Ti_4O_1_2 ceramics, which could strongly increase the resistance of grain boundary. Proper amount of Nd substitution in Y_2_/_3_−_xNd_xCu_3Ti_4O_1_2 ceramics could significantly depress the low-frequency dielectric loss. When the doping level is 0.06 and 0.09, the samples exhibited a relatively low dielectric loss (below 0.050 between 0.3 and 50 kHz) and high dielectric constant above 11000 over a wide frequency range from 40 Hz to 100 kHz. Based on the ε′-T plots, dielectric relaxation intensity was substantially weakened by Nd doping so that the temperature stability of dielectric constant was improved obviously. The correlations between low-frequency dielectric loss and the resistance of grain boundary were revealed. After Nd doping, the activation energies for the conduction behavior in grain boundaries were significantly enhanced, and the activation energies for the dielectric relaxation process in grain boundaries were slightly influenced. - Highlights: • Significant decrease in dielectric loss of Y_2_/_3_−_xNd_xCu_3Ti_4O_1_2 ceramics was realized. • The enhanced grain boundary density is responsible for the lowered dielectric loss. • Nd doping could improve the temperature stability of dielectric constant. • Oxygen vacancies contribute to conduction and relaxation process of grain boundaries.

  5. Magnetostriction of the polycrystalline Fe{sub 80}Al{sub 20} alloy doped with boron

    Energy Technology Data Exchange (ETDEWEB)

    Bormio-Nunes, Cristina, E-mail: cristina@demar.eel.usp.br [Escola de Engenharia de Lorena, Dep. de Eng. de Materiais, Universidade de S.Paulo, Lorena, SP (Brazil); Teodoro dos Santos, Claudio; Botani de Souza Dias, Mateus [Escola de Engenharia de Lorena, Dep. de Eng. de Materiais, Universidade de S.Paulo, Lorena, SP (Brazil); Doerr, Mathias; Granovsky, Sergey; Loewenhaupt, Michael [Institut fuer Festkoerperphysik, TU Dresden, D-01062 Dresden (Germany)

    2012-10-25

    Highlights: Black-Right-Pointing-Pointer Fe{sub 80}Al{sub 20} polycrystalline alloy magnetostriction 40 ppm increased to 80 ppm due to 2% of B doping. Black-Right-Pointing-Pointer B stabilizes {alpha}-FeAl phase and a coexistence of {alpha}-FeAl + Fe{sub 3}Al improves magnetostriction. Black-Right-Pointing-Pointer Presence of Fe{sub 2}B phase causes domain rearrangement revealed by the decrease of the volume magnetostriction. - Abstract: The doping of Fe{sub 80}Al{sub 20} polycrystalline alloy with 2% of boron increased the total magnetostriction twofold compared to a sample without boron. A value close to 80 ppm was achieved at 300 K. The microstructures of the boron-doped alloys show a dendritically solidified matrix with interdendritic {alpha}-FeAl and/or Fe{sub 3}Al and Fe{sub 2}B eutectic between the grains. The XRD analysis reveals an increase in the volume fraction of {alpha}-FeAl and a correspondent decrease of the Fe{sub 3}Al phase volume fraction as the boron content increases. The increase of the volume fraction of this tetragonal Fe{sub 2}B phase in the samples doped with boron causes the decrease of the strong volume magnetostriction that was observed in the alloy without boron. There is some evidence that the improvement of the magnetostriction magnitude due to the addition of boron to the Fe{sub 80}Al{sub 20} alloy could reach the maximal magnetostriction if the 1:1 optimal ratio of the volume fractions of the {alpha}-FeAl and Fe{sub 3}Al phases could be reached.

  6. New insights on the synthesis and electronic transport in bulk polycrystalline Pr-doped SrTiO3−δ

    International Nuclear Information System (INIS)

    Dehkordi, Arash Mehdizadeh; Bhattacharya, Sriparna; Darroudi, Taghi; Alshareef, Husam N.; Tritt, Terry M.

    2015-01-01

    Recently, we have reported a significant enhancement in the electronic and thermoelectric properties of bulk polycrystalline SrTiO 3 ceramics via praseodymium doping. This improvement was originated from the simultaneous enhancement in the thermoelectric power factor and reduction in thermal conductivity, which was contributed to the non-uniform distribution of Pr dopants. In order to further understand the underlying mechanism, we herein investigate the role of praseodymium doping source (Pr 2 O 3 versus Pr 6 O 11 ) on the synthesis and electronic transport in Pr-doped SrTiO 3 ceramics. It was observed that the high-temperature electronic transport properties are independent of the choice of praseodymium doping source for samples prepared following our synthesis strategy. Theoretical calculations were also performed in order to estimate the maximum achievable power factor and the corresponding optimal carrier concentration. The result suggests the possibility of further improvement of the power factor. This study should shed some light on the superior electronic transport in bulk polycrystalline Pr-doped SrTiO 3 ceramics and provide new insight on further improvement of the thermoelectric power factor

  7. New insights on the synthesis and electronic transport in bulk polycrystalline Pr-doped SrTiO3−δ

    KAUST Repository

    Dehkordi, Arash Mehdizadeh

    2015-02-07

    Recently, we have reported a significant enhancement in the electronic and thermoelectric properties of bulk polycrystalline SrTiO3 ceramics via praseodymium doping. This improvement was originated from the simultaneous enhancement in the thermoelectric power factor and reduction in thermal conductivity, which was contributed to the non-uniform distribution of Pr dopants. In order to further understand the underlying mechanism, we herein investigate the role of praseodymium doping source (Pr2O3 versus Pr6O11) on the synthesis and electronic transport in Pr-doped SrTiO3 ceramics. It was observed that the high-temperature electronic transport properties are independent of the choice of praseodymium doping source for samples prepared following our synthesis strategy. Theoretical calculations were also performed in order to estimate the maximum achievable power factor and the corresponding optimal carrier concentration. The result suggests the possibility of further improvement of the power factor. This study should shed some light on the superior electronic transport in bulk polycrystalline Pr-doped SrTiO3 ceramics and provide new insight on further improvement of the thermoelectric power factor.

  8. Remarkable changes in the photoluminescent properties of Y2Ce2O7:Eu(3+) red phosphors through modification of the cerium oxidation states and oxygen vacancy ordering.

    Science.gov (United States)

    Raj, Athira K V; Prabhakar Rao, P; Sreena, T S; Sameera, S; James, Vineetha; Renju, U A

    2014-11-21

    A new series of red phosphors based on Eu(3+)-doped yttrium cerate [Y1.9Ce2O7:0.1Eu(3+), Y2Ce1.9O7:0.1Eu(3+) and Y2Ce2-xO7:xEu(3+) (x = 0.05, 0.10, 0.15, 0.20, 0.25 and 0.50)] was prepared via a conventional solid-state method. The influence of the substitution of Eu(3+) at the aliovalent site on the photoluminescent properties was determined by powder X-ray diffraction, FT Raman spectroscopy, X-ray photoelectron spectroscopy, transmission electron microscopy, scanning electron microscopy with energy-dispersive spectroscopy, UV-visible absorption spectroscopy, photoluminescence spectroscopy and lifetime measurements. The substitution of Eu(3+) at the Ce(4+) site induces a structural transition from a defect fluorite to a C-type structure, which increases the oxygen vacancy ordering and the distortion of the Eu(3+) environment, and decreases the formation of Ce(3+) states. In contrast, phosphors with isovalent substitution at the Y(3+) site exhibit the biphasic nature of defect fluorite and a C-type structure, thereby increasing the number of Ce(3+) oxidation states. These modifications resulted in remarkable changes in the photoluminescent properties of Y2Ce1.9O7:0.1Eu(3+) red phosphors, with emission intensities 3.8 times greater than those of the Ce0.9O2:0.1Eu(3+) and Y1.9Ce2O7:0.1Eu(3+). The photoluminescent properties of Y2Ce2-xO7:xEu(3+) were studied at different Eu(3+) concentrations under excitation with blue light. These phosphors emit intense red light due to the (5)D0-(7)F2 transition under excitation at 466 nm and no concentration quenching is observed with up to 50 mol% Eu(3+). They show increased lifetimes in the range 0.62-0.72 ms at Eu(3+) concentrations. The cation ordering linked to the oxygen vacancy ordering led to the uniform distribution of Eu(3+) ions in the lattice, thus allowing higher doping concentrations without quenching and consequently increasing the lifetime of the (5)D0 states. Our results demonstrate that significant improvements in

  9. Comparison of Efficiencies and Mechanisms of Catalytic Ozonation of Recalcitrant Petroleum Refinery Wastewater by Ce, Mg, and Ce-Mg Oxides Loaded Al2O3

    Directory of Open Access Journals (Sweden)

    Chunmao Chen

    2017-02-01

    Full Text Available The use of catalytic ozonation processes (COPs for the advanced treatment of recalcitrant petroleum refinery wastewater (RPRW is rapidly expanding. In this study, magnesium (Mg, cerium (Ce, and Mg-Ce oxide-loaded alumina (Al2O3 were developed as cost efficient catalysts for ozonation treatment of RPRW, having performance metrics that meet new discharge standards. Interactions between the metal oxides and the Al2O3 support influence the catalytic properties, as well as the efficiency and mechanism. Mg-Ce/Al2O3 (Mg-Ce/Al2O3-COP reduced the chemical oxygen demand by 4.7%, 4.1%, 6.0%, and 17.5% relative to Mg/Al2O3-COP, Ce/Al2O3-COP, Al2O3-COP, and single ozonation, respectively. The loaded composite metal oxides significantly increased the hydroxyl radical-mediated oxidation. Surface hydroxyl groups (–OHs are the dominant catalytic active sites on Al2O3. These active surface –OHs along with the deposited metal oxides (Mg2+ and/or Ce4+ increased the catalytic activity. The Mg-Ce/Al2O3 catalyst can be economically produced, has high efficiency, and is stable under acidic and alkaline conditions.

  10. Preparation and characterization of Ce-doped ZnO nanofibers by an electrospinning method

    Directory of Open Access Journals (Sweden)

    Jong-Pil Kim

    2011-02-01

    Full Text Available ZnO and Ce-doped ZnO Nanofibers on (111 Pt/SiO2/Si substrates were produced using an electrospinning technique. The as-prepared composite fibres were subjected to high-temperature calcination to produce inorganic fibers. After calcining at a temperature of 500 °C, the average diameter of the ZnO and Ce-doped ZnO nanofibers were determined to be 170 nm and 225 nm, respectively. The average grain size of the ZnO and Ce-doped ZnO nanofibers were about 50 nm and 57 nm, respectively. The microstructure, chemical bonding state and photoluminescence of the produced ZnO and Ce-doped ZnO nanofibers were investigated. The Ce-doped ZnO nanofiber can be assigned to the presence of Ce ions on substitutional sites of Zn ions and the Ce3+ state from X-ray photoelectron spectra. Compared with PL spectra of ZnO nanofibers, the peak position of the UV emission of the Ce-doped ZnO nanofibers is sharply suppressed while the green emission band is highly enhanced.

  11. Luminescent and scintillation properties of the Pr"3"+ doped single crystalline films of Lu_3Al_5_−_xGa_xO_1_2 garnet

    International Nuclear Information System (INIS)

    Gorbenko, V.; Zorenko, Yu; Zorenko, T.; Voznyak, T.; Paprocki, K.; Fabisiak, K.; Fedorov, A.; Bilski, P.; Twardak, A.; Zhusupkalieva, G.

    2016-01-01

    The Pr"3"+ d–f luminescence was investigated in the single crystalline films (SCF) of Lu_3Al_5_−_xGa_xO_1_2:Pr garnet solid solution at x = 1–3, grown by the liquid phase epitaxy (LPE) method from the melt-solution based on the PbO–B_2O_3 flux. The shape of CL spectra and decay kinetics of Pr"3"+ ions in Lu_3Al_5_−_xGa_xO_1_2 SCFs strongly depend on the total gallium concentration x and distribution of Ga"3"+ ions between the tetrahedral and octahedral position of the garnet host. The best scintillation properties of Lu_3Al_5_−_xGa_xO_1_2:Pr SCF are achieved at the nominal Ga content in melt-solution in the x = 2–2.5 range. - Highlights: • Single crystalline films of Lu_3Al_5_−_x Ga_xO_1_2:Pr garnet at x = 1–3 were grown by the LPE method. • Pr"3"+ emission spectra, light yield and decay time of films show strong dependence on Ga content. • The maximal light yield of Lu_3Al_5_−_x Ga_xO_1_2:Pr film is observed at Ga content x = 2.0–2.5.

  12. Ce3+ doping into 0.6Li2MnO3·0.4LiNi0.5Co0.2Mn0.3O2 as cathode material for Li-ion batteries applied in new energy vehicle

    Science.gov (United States)

    Peng, Han; Yao, Linxiao; Zhang, Ming

    2018-06-01

    The pristine Li1.20[Mn0.52Ni0.20Co0.08]O2 and Ce3+-doped Li1.20[Mn0.50Ni0.20Co0.08Ce0.02]O2 cathode materials have been synthesized by using the typical sol-gel method. The XRD, SEM, ICP-OES and galvanostatic charge-discharge tests were carried out to study the influence of Ce3+ doping on the crystal structural, morphology and electrochemical properties of Li1.20Mn0.54Ni0.13Co0.13O2. The XRD result revealed the Ce3+ doping modification could decrease the cation mixing degree. The galvanostatic charge-discharge tests results showed that the sample after Ce3+ doping demonstrated the smaller irreversible capacity loss, more stable cyclic performance and better rate capacity than those of the pristine one.

  13. Isolated centres versus defect associates in Sm3+-doped CeO2: a spectroscopic investigation

    International Nuclear Information System (INIS)

    Tiseanu, Carmen; Avram, Daniel; Cojocaru, Bogdan; Parvulescu, Vasile I; Vela-Gonzalez, Andrea V; Sanchez-Dominguez, Margarita

    2013-01-01

    The interactions between Sm 3+ and oxygen vacancies in CeO 2 are probed by the use of tuneable laser excited time-resolved photoluminescence and Raman spectroscopies. It is found that Sm 3+ (with doping concentrations of 0.1, 0.3, 1 and 5 wt%) substitutes largely for Ce 4+ in sites with cubic symmetry and the corresponding emission is sensitized via the Ce 4+ –O 2− charge-transfer band of CeO 2 . It is established from the photoluminescence spectra measured at long delay after the laser pulse that the local environment around cubic Sm 3+ centres is not changed with concentration and ceria size. In addition to cubic symmetry Sm 3+ centres, low-symmetry Sm 3+ centres tentatively assigned to the Sm 3+ –oxygen vacancy associates of nearest-neighbour type are also observed. Their emission is preferentially excited via the weak f–f absorption transitions of Sm 3+ . A relatively strong concentration-induced quenching of Sm 3+ emission was inferred from the decrease in the average emission lifetimes from 2.1 ms (0.1 wt%) to 0.87 ms (5 wt%). The local environments of Sm 3+ and Eu 3+ in CeO 2 are also compared on the basis of their emission spectra and decays. (paper)

  14. Towards understanding the electronic structure of Fe-doped CeO2 nanoparticles with X-ray spectroscopy.

    Science.gov (United States)

    Wang, Wei-Cheng; Chen, Shih-Yun; Glans, Per-Anders; Guo, Jinghua; Chen, Ren-Jie; Fong, Kang-Wei; Chen, Chi-Liang; Gloter, Alexandre; Chang, Ching-Lin; Chan, Ting-Shan; Chen, Jin-Ming; Lee, Jyh-Fu; Dong, Chung-Li

    2013-09-21

    This study reports on the electronic structure of Fe-doped CeO2 nanoparticles (NPs), determined by coupled X-ray absorption spectroscopy and X-ray emission spectroscopy. A comparison of the local electronic structure around the Ce site with that around the Fe site indicates that the Fe substitutes for the Ce. The oxygen K-edge spectra that originated from the hybridization between cerium 4f and oxygen 2p states are sensitive to the oxidation state and depend strongly on the concentration of Fe doping. The Ce M(4,5)-edges and the Fe L(2,3)-edges reveal the variations of the charge states of Ce and Fe upon doping, respectively. The band gap is further obtained from the combined absorption-emission spectrum and decreased upon Fe doping, implying Fe doping introduces vacancies. The oxygen vacancies are induced by Fe doping and the spectrum reveals the charge transfer between Fe and Ce. Fe(3+) doping has two major effects on the formation of ferromagnetism in CeO2 nanoparticles. The first, at an Fe content of below 5%, is that the formation of Fe(3+)-Vo-Ce(3+) introduces oxygen deficiencies favoring ferromagnetism. The other, at an Fe content of over 5%, is the formation of Fe(3+)-Vo-Fe(3+), which favors antiferromagnetism, reducing the Ms. The defect structures Fe(3+)-Vo-Ce(3+) and Fe(3+)-Vo-Fe(3+) are crucial to the magnetism in these NPs and the change in Ms can be described as the effect of competitive interactions of magnetic polarons and paired ions.

  15. Carbon doped lanthanum aluminate (LaAlO3:C) synthesized by solid state reaction for application in UV thermoluminescent dosimetry

    International Nuclear Information System (INIS)

    Alves, N.

    2015-01-01

    In this work we discuss the TL output for LaAlO 3 :C crystals grown by using three different combinations of Al 2 O 3 , La 2 O 3 and carbon atoms during the synthesis process. Recently, LaAlO 3 single crystals, co-doped with Ce 3+ and Dy 3+ rare earth trivalent ions and grown under hydrothermal conditions, have been reported to show high thermoluminescent response (TL) when exposed to low levels of ultraviolet radiation (UVR). However, undoped LaAlO 3 synthesized by solid state reaction method from the 1:1 mixture of aluminum and lanthanum oxide under reducing atmosphere revealed to have still higher thermoluminescent sensitivity to UV photon fields than the co-doped with Ce 3+ and Dy 3+ . It is well known that carbon doped aluminum oxide monocrystals have excellent TL and photoluminescent response properties for X-rays, UV and gamma radiation fields. Thus, we conducted three different syntheses of LaAlO 3 by this solid state reaction method, doping the mixture with carbon. The lanthanum aluminate polycrystals were synthesized from the 1:1 mixture of aluminum and lanthanum oxide, adding 0.1wt.% carbon and annealed at 1700°C for two hours in hydrogen atmosphere. The X-ray diffraction analysis revealed the formation of rhombohedral LaAlO 3 crystallographic phase, however a small percentage (15%) of Al 2 O 3 has been also identified. The UV-Vis absorbance spectra were obtained and F and F + - center were ascribed. The UV irradiations were carried out using a commercial 8W UV lamp. Thermoluminescence measurements were performed at a Harshaw 4500 TL reader. All compositions investigated have shown high TL sensitivity to UVR. (author)

  16. Giant Faraday rotation in Bi(x)Ce(3-x)Fe5O12 epitaxial garnet films.

    Science.gov (United States)

    Chandra Sekhar, M; Singh, Mahi R; Basu, Shantanu; Pinnepalli, Sai

    2012-04-23

    Thin films of Bi(x)Ce(3-x)Fe(5)O(12) with x = 0.7 and 0.8 compositions were prepared by using pulsed laser deposition. We investigated the effects of processing parameters used to fabricate these films by measuring various physical properties such as X-ray diffraction, transmittance, magnetization and Faraday rotation. In this study, we propose a phase diagram which provides a suitable window for the deposition of Bi(x)Ce(3-x)Fe(5)O(12) epitaxial films. We have also observed a giant Faraday rotation of 1-1.10 degree/µm in our optimized films. The measured Faraday rotation value is 1.6 and 50 times larger than that of CeYIG and YIG respectively. A theoretical model has been proposed for Faraday rotation based on density matrix method and an excellent agreement between experiment and theory is found. © 2012 Optical Society of America

  17. Strain induced atomic structure at the Ir-doped LaAlO3/SrTiO3 interface.

    Science.gov (United States)

    Lee, M; Arras, R; Warot-Fonrose, B; Hungria, T; Lippmaa, M; Daimon, H; Casanove, M J

    2017-11-01

    The structure of Ir-doped LaAlO 3 /SrTiO 3 (001) interfaces was investigated on the atomic scale using probe-corrected transmission electron microscopy in high-angle annular dark-field scanning mode (HAADF-STEM) and electron energy loss spectroscopy (EELS), combined with first-principles calculations. We report the evolution of the strain state experimentally measured in a 5 unit-cell thick LaAlO 3 film as a function of the Ir concentration in the topmost SrTiO 3 layer. It is shown that the LaAlO 3 layers remain fully elastically strained up to 3% of Ir doping, whereas a higher doping level seems to promote strain relaxation through enhanced cationic interdiffusion. The observed differences between the energy loss near edge structure (ELNES) of Ti-L 2,3 and O-K edges at non-doped and Ir-doped interfaces are consistent with the location of the Ir dopants at the interface, up to 3% of Ir doping. These findings, supported by the results of density functional theory (DFT) calculations, provide strong evidence that the effect of dopant concentrations on the properties of this kind of interface should not be analyzed without obtaining essential information from the fine structural and chemical analysis of the grown structures.

  18. Mixed conductivity, structural and microstructural characterization of titania-doped yttria tetragonal zirconia polycrystalline/titania-doped yttria stabilized zirconia composite anode matrices

    International Nuclear Information System (INIS)

    Colomer, M.T.; Maczka, M.

    2011-01-01

    Taking advantage of the fact that TiO 2 additions to 8YSZ cause not only the formation of a titania-doped YSZ solid solution but also a titania-doped YTZP solid solution, composite materials based on both solutions were prepared by solid state reaction. In particular, additions of 15 mol% of TiO 2 give rise to composite materials constituted by 0.51 mol fraction titania-doped yttria tetragonal zirconia polycrystalline and 0.49 mol fraction titania-doped yttria stabilized zirconia (0.51TiYTZP/0.49TiYSZ). Furthermore, Y 2 (Ti 1-y Zr y ) 2 O 7 pyrochlore is present as an impurity phase with y close to 1, according to FT-Raman results. Lower and higher additions of titania than that of 15 mol%, i.e., x=0, 5, 10, 20, 25 and 30 mol% were considered to study the evolution of 8YSZ phase as a function of the TiO 2 content. Furthermore, zirconium titanate phase (ZrTiO 4 ) is detected when the titania content is equal or higher than 20 mol% and this phase admits Y 2 O 3 in solid solution according to FE-SEM-EDX. The 0.51TiYTZP/0.49TiYSZ duplex material was selected in this study to establish the mechanism of its electronic conduction under low oxygen partial pressures. In the pO 2 range from 0.21 to 10 -7.5 atm. the conductivity is predominantly ionic and constant over the range and its value is 0.01 S/cm. The ionic plus electronic conductivity is 0.02 S/cm at 1000 o C and 10 -12.3 atm. Furthermore, the onset of electronic conductivity under reducing conditions exhibits a -1/4 pO 2 dependence. Therefore, it is concluded that the n-type electronic conduction in the duplex material can be due to a small polaron-hopping between Ti 3+ and Ti 4+ . -- Graphical abstract: FE-SEM micrograph of a polished and thermal etched surface of a Ti-doped YTZP/Ti-doped YSZ composite material. Display Omitted Research highlights: → Ti-doped YTZP/Ti-doped YSZ composite materials are mixed conductors under low partial pressures. → From 5 mol% of TiO 2 , Y 2 (Ti 1-y ,Zr y ) 2 O 7 pyrochlore is

  19. Comparative study of transparent ceramic and single crystal Ce doped LuAG scintillators

    International Nuclear Information System (INIS)

    Yanagida, Takayuki; Fujimoto, Yutaka; Yokota, Yuui; Kamada, Kei; Yanagida, Satoko; Yoshikawa, Akira; Yagi, Hideki; Yanagitani, Takagimi

    2011-01-01

    Transparent ceramic Ce 0.5% doped Lu 3 Al 5 O 12 (LuAG) scintillator grown by the sintering method and single crystalline Ce doped LuAG grown by the Czochralski method are prepared. They are cut to the physical dimensions 4 × 4 × 2 mm 3 . Their transmittance and radio luminescence spectra are evaluated. They are both transmissive in wavelength longer than 500 nm and intense Ce 3+ 5d–4f emission appears around 520 nm. When 137 Cs γ-ray is irradiated, 662 keV photo-absorption peaks are clearly observed in each sample. The transparent ceramic one shows higher light yield than that of the single crystalline one. The absolute light yield of the ceramic sample is turned out to be 14800 ± 1500 ph/MeV. The decay time constants are evaluated under pulse X-ray excitation. The main component of the decay time of ceramic and single crystalline one are determined as 37 and 46 ns, respectively.

  20. Evaluation of critical distances for energy transfer between Pr{sup 3+} and Ce{sup 3+} in yttrium aluminium garnet

    Energy Technology Data Exchange (ETDEWEB)

    Zeng, Peng; Wei, Xiantao; Yin, Min; Chen, Yonghu, E-mail: yhuchen@ustc.edu.cn [Key Laboratory of Strongly-Coupled Quantum Matter Physics, Chinese Academy of Sciences, School of Physical Sciences, University of Science and Technology of China, No. 96 Jinzhai Road, Hefei, Anhui 230026 (China); Zhou, Shaoshuai [Key Laboratory of Strongly-Coupled Quantum Matter Physics, Chinese Academy of Sciences, School of Physical Sciences, University of Science and Technology of China, No. 96 Jinzhai Road, Hefei, Anhui 230026 (China); Department of Physics, Qufu Normal University, Qufu, Shandong 273165 (China)

    2016-09-07

    A series of Pr{sup 3+}/Ce{sup 3+} doped yttrium aluminium garnet (Y{sub 3}Al{sub 5}O{sub 12} or simply YAG) phosphors were synthesized to investigate the energy transfer between Pr{sup 3+} and Ce{sup 3+} for their potential application in a white light-emitting diode and quantum information storage and processing. The excitation and emission spectra of YAG:Pr{sup 3+}/Ce{sup 3+} were measured and analyzed, and it revealed that the reabsorption between Pr{sup 3+} and Ce{sup 3+} was so weak that it can be ignored, and the energy transfer from Pr{sup 3+} (5d) to Ce{sup 3+} (5d) and Ce{sup 3+} (5d) to Pr{sup 3+} ({sup 1}D{sub 2}) did occur. By analyzing the excitation and the emission spectra, the energy transfer from Pr{sup 3+} (5d) to Ce{sup 3+} (5d) and Ce{sup 3+} (5d) to Pr{sup 3+} ({sup 1}D{sub 2}) was examined in detail with an original strategy deduced from fluorescence dynamics and the Dexter energy transfer theory, and the critical distances of energy transfer were derived to be 7.9 Å and 4.0 Å for Pr{sup 3+} (5d) to Ce{sup 3+} (5d) and Ce{sup 3+} (5d) to Pr{sup 3+} ({sup 1}D{sub 2}), respectively. The energy transfer rates of the two processes of various concentrations were discussed and evaluated. Furthermore, for the purpose of sensing a single Pr{sup 3+} state with a Ce{sup 3+} ion, the optimal distance of Ce{sup 3+} from Pr{sup 3+} was evaluated as 5.60 Å, where the probability of success reaches its maximum value of 78.66%, and meanwhile the probabilities were evaluated for a series of Y{sup 3+} sites in a YAG lattice. These results will be of valuable reference for achievement of the optimal energy transfer efficiency in Pr{sup 3+}/Ce{sup 3+} doped YAG and other similar systems.

  1. Thermodynamic properties of Y/sub 3/Fe/sub 5/O/sub 12/ and TbFeO/sub 3/

    Energy Technology Data Exchange (ETDEWEB)

    Shchelkotunov, V A; Danilov, V N; Reznitskii, L A; Korobeinikova, A V [Moskovskij Gosudarstvennyj Univ. (USSR)

    1975-01-01

    Two types of chemical compounds-garnets and perovskites - exist in Fe/sub 2/O/sub 3/-Y/sub 2/O/sub 3/ and Fe/sub 2/O/sub 3/-Tb/sub 2/..omega../sub 3/ systems. Both of them are noncompensated antiferromagnetics. Thermal-physical properties of TbFeO/sub 3/ were determined. Values of Csub(p),(Hsub(t)-Hsub(o)) and Ssub(T) in the temperature range 298 to 700 deg K for Y/sub 3/Fe/sub 5/O/sub 12/ and in the range 298 to 600 deg K for TbFeO/sub 3/ were calculated using the experimental data on TbFeO/sub 3/ and Y/sub 3/Fe/sub 5/O/sub 12/ thermal capacity. Magnetic contribution for Y/sub 3/Fe/sub 5/O/sub 12/ Usub(mag)=1617 cal/mol and ..delta..S=3.44 cal/mol.deg. was determined.

  2. Microcolumnar and polycrystalline growth of LaBr3:Ce scintillator

    Science.gov (United States)

    Nagarkar, V. V.; Miller, S.; Sia, R.; Gaysinskiy, V.

    2011-05-01

    While a wide variety of new scintillators are now available, cerium-doped lanthanide halide scintillators have shown a strong potential toward fulfilling the needs of highly demanding applications such as radioisotope identification at room temperature, homeland security, quantitative molecular imaging for medical diagnostics, and disease staging and research. Despite their extraordinary advantages in terms of light yield and response uniformity over a wide energy range, issues related to reliable, large volume manufacturing of these high-light-yield materials in a rapid and economic manner has not been resolved or purposefully addressed. Here we report on synthesizing LaBr3:Ce scintillator using a thermal evaporation technique, which offers the potential to synthesize large quantities of small-to-large volume, high-quality material in a time-efficient and cost-effective manner. To date we have successfully applied this method to form both microcolumnar films and thick polycrystalline slabs of LaBr3:Ce, and have characterized their light yield, response linearity, decay time and afterglow.

  3. Er3+-Al2O3 nanoparticles doping of borosilicate glass

    International Nuclear Information System (INIS)

    Massera, Jonathan; Petit, Laeticia; Hupa, Leena; Hupa, Mikko; Koponen, Joona; Glorieux, Benoit

    2015-01-01

    Novel borosilicate glasses were developed by adding in the glass batch Er 3+ -Al 2 O 3 nanoparticles synthetized by using a soft chemical method. A similar nanoparticle doping with modified chemical vapour deposition (MCVD) process was developed to increase the efficiency of the amplifying silica fibre in comparison to using MCVD and solution doping. It was shown that with the melt quench technique, a Er 3+ -Al 2 O 3 nanoparticle doping neither leads to an increase in the Er 3+ luminescence properties nor allows one to control the rare-earth chemical environment in a borosilicate glass. The site of Er 3+ in the Er 3+ -Al 2 O 3 nanoparticle containing glass seems to be similar as in glasses with the same composition prepared using standard raw materials. We suspect the Er 3+ ions to diffuse from the nanoparticles into the glass matrix. There was no clear evidence of the presence of Al 2 O 3 nanoparticles in the glasses after melting. (author)

  4. Facile synthesis of ferromagnetic Ni doped CeO{sub 2} nanoparticles with enhanced anticancer activity

    Energy Technology Data Exchange (ETDEWEB)

    Abbas, Fazal; Jan, Tariq [Laboratory of Nanoscience and Technology, Department of Physics, International Islamic University Islamabad (Pakistan); Iqbal, Javed, E-mail: javed.saggu@iiu.edu.pk [Laboratory of Nanoscience and Technology, Department of Physics, International Islamic University Islamabad (Pakistan); Ahmad, Ishaq [Experimental Physics Labs, National Center for Physics, Islamabad (Pakistan); Naqvi, M. Sajjad H. [Department of Biochemistry, University of Karachi, Karachi (Pakistan); Malik, Maaza [UNESCO-UNISA Africa Chair in Nanosciences/Nanotechnology, College of Graduate Studies, University of South Africa, Muckleneuk Ridge, PO Box 392, Pretoria (South Africa); Nanosciences African Network (NANOAFNET), iThemba LABS-National Research Foundation, 1 Old Faure Road, Somerset West 7129, PO Box 722, Somerset West, Western Cape Province (South Africa)

    2015-12-01

    Highlights: • The synthesized undoped and Ni doped CeO{sub 2} nanoparticles exhibited RTFM. • Oxygen vacancies and magnetic ions both were believed to be responsible for RTFM. • The prepared nanoparticles exhibited selective cytotoxicity. • Ni doping enhanced the anticancer activity of CeO{sub 2} nanoparticles. • Differential ROS generation was observed to control their cytotoxicity. - Abstract: Ni{sub x}Ce{sub 1−x}O{sub 2} (where x = 0, 0.01, 0.03, 0.05 and 0.07) nanoparticles were synthesized by soft chemical method and were characterized using X-ray diffraction (XRD), scanning electron microscopy (SEM), Raman, UV–vis absorption spectroscopy and vibrating sample magnetometer (VSM). XRD and Raman results indicated the formation of single phase cubic fluorite structure for the synthesized nanoparticles. Ni dopant induced excessive structural changes such as decrease in crystallite size as well as lattice constants and enhancement in oxygen vacancies in CeO{sub 2} crystal structure. These structural variations significantly influenced the optical and magnetic properties of CeO{sub 2} nanoparticles. The synthesized Ni{sub x}Ce{sub 1−x}O{sub 2} nanoparticles exhibited room temperature ferromagnetic behavior. Ni doping induced effects on the cytotoxicity of CeO{sub 2} nanoparticles were examined against HEK-293 healthy cell line and SH-SY5Y neuroblastoma cancer cell line. The prepared Ni{sub x}Ce{sub 1−x}O{sub 2} nanoparticles demonstrated differential cytotoxicity. Furthermore, anticancer activity of CeO{sub 2} nanoparticles observed to be significantly enhanced with Ni doping which was found to be strongly correlated with the level of reactive oxygen species (ROS) production. The prepared ferromagnetic Ni{sub x}Ce{sub 1−x}O{sub 2} nanoparticles with differential cytotoxic nature may be potential for future targeted cancer therapy.

  5. Pulse shape discrimination properties of Gd{sub 3}Ga{sub 3}Al{sub 2}O{sub 12}:Ce,B single crystal in comparison with CsI:Tl

    Energy Technology Data Exchange (ETDEWEB)

    Rawat, S. [Technical Physics Division, Bhabha Atomic Research Centre, Mumbai 400085 (India); Department of Physics, Indian Institute of Technology, Roorkee 247667 (India); Tyagi, Mohit [Technical Physics Division, Bhabha Atomic Research Centre, Mumbai 400085 (India); Netrakanti, P.K.; Kashyap, V.K.S.; Mitra, A. [Nuclear Physics Division, Bhabha Atomic Research Centre, Mumbai 400085 (India); Singh, A.K.; Desai, D.G. [Technical Physics Division, Bhabha Atomic Research Centre, Mumbai 400085 (India); Kumar, G. Anil [Department of Physics, Indian Institute of Technology, Roorkee 247667 (India); Gadkari, S.C. [Technical Physics Division, Bhabha Atomic Research Centre, Mumbai 400085 (India)

    2016-12-21

    Single crystals of Gd{sub 3}Ga{sub 3}Al{sub 2}O{sub 12}:Ce,B and CsI:Tl were grown by Czochralski and Bridgman techniques, respectively. While both the crystals exhibited similar emission at about 550 nm, their scintillation decay times showed significantly different characteristics. The average scintillation decay time of Gd{sub 3}Ga{sub 3}Al{sub 2}O{sub 12}:Ce,B crystal was found to be about 284 ns for alpha excitation compared to 108 ns measured for a gamma source. On the other hand in CsI:Tl crystals, the alpha excitation resulted in a lower average decay time of 600 ns compared to 1200 ns with gamma excitation. Their pulse shape discrimination (PSD) for gamma and alpha radiations were studied by coupling the scintillators with photomultiplier tube or SiPM and employing an advanced digitizer as well as a conventional zero-crossing setup. In spite of having a poor α/γ light yield ratio, the PSD figure of merit and the difference of zero-crossing time in Gd{sub 3}Ga{sub 3}Al{sub 2}O{sub 12}:Ce,B crystals were found to be superior in comparison to CsI:Tl crystals.

  6. A novel yellow-emitting SrAlSi4N7:Ce3+ phosphor for solid state lighting: Synthesis, electronic structure and photoluminescence properties

    International Nuclear Information System (INIS)

    Ruan, Jian; Xie, Rong-Jun; Funahashi, Shiro; Tanaka, Yoshinori; Takeda, Takashi; Suehiro, Takayuki; Hirosaki, Naoto; Li, Yuan-Qiang

    2013-01-01

    Ce 3+ -doped and Ce 3+ /Li + -codoped SrAlSi 4 N 7 phosphors were synthesized by gas pressure sintering of powder mixtures of Sr 3 N 2 , AlN, α-Si 3 N 4 , CeN and Li 3 N. The phase purity, electronic crystal structure, photoluminescence properties of SrAlSi 4 N 7 :Ce 3+ (Ce 3+ /Li + ) were investigated in this work. The band structure calculated by the DMol 3 code shows that SrAlSi 4 N 7 has a direct band gap of 3.87 eV. The single crystal analysis of Ce 3+ -doped SrAlSi 4 N 7 indicates a disordered Si/Al distribution and nitrogen vacnacy defects. SrAlSi 4 N 7 was identified as a major phase of the fired powders, and Sr 5 Al 5 Si 21 N 35 O 2 and AlN as minor phases. Both Ce 3+ and Ce 3+ /Li + doped SrAlSi 4 N 7 phosphors can be efficiently excited by near-UV or blue light and show a broadband yellow emission peaking around 565 nm. A highest external quantum efficiency of 38.3% under the 450 nm excitation was observed for the Ce 3+ /Li + -doped SrAlSi 4 N 7 (5 mol%). A white light LED lamp with color temperature of 6300 K and color rendering index of Ra=78 was achieved by combining Sr 0.97 Al 1.03 Si 3.997 N/94/maccounttest14=t0005 1 8193 7 :Ce 3+ 0.03 with a commercial blue InGaN chip. It indicates that SrAlSi 4 N 7 :Ce 3+ is a promising yellow emitting down-conversion phosphor for white LEDs. - Graphical abstract: One-phosphor converted white light-emitting diode (LED) was fabricated by combining a blue LED chip and a yellow-emitting SrAlSi4N7:Ce 3+ phosphor (see inset), which has the color rendering index of 78 and color temperature of 6300 K. - Highlights: • We reported a new yellow nitride phosphor suitable for solid state lighting. • We solved the crystal structure and evidenced a disordered Si/Al distribution. • We fabricated a high color rendering white LEDs by using a single SrAlSi4N7:Ce

  7. Sol-gel syntheses, luminescence, and energy transfer properties of α-GdB5O9:Ce(3+)/Tb(3+) phosphors.

    Science.gov (United States)

    Sun, Xiaorui; Gao, Wenliang; Yang, Tao; Cong, Rihong

    2015-02-07

    Sol-gel method was applied to prepare homogenous and highly crystalline phosphors with the formulas α-GdB5O9:xTb(3+) (0 ≤ x ≤ 1), α-Gd1-xCexB5O9 (0 ≤ x ≤ 0.40), α-GdB5O9:xCe(3+), 0.30Tb(3+) (0 ≤ x ≤ 0.15) and α-GdB5O9:0.20Ce(3+), xTb(3+) (0 ≤ x ≤ 0.10). The success of the syntheses was proved by the linear shrinkage or expansion of the cell volumes against the substitution contents. In α-GdB5O9:xTb(3+), an efficient energy transfer from Gd(3+) to Tb(3+) was observed and there was no luminescence quenching. The exceptionally high efficiency of the f-f excitations of Tb(3+) implies that these phosphors may be good green-emitting UV-LED phosphors. For α-Gd1-xCexB5O9, Ce(3+) absorbs the majority of the energy and transfers it to Gd(3+). Therefore, the co-doping of Ce(3+) and Tb(3+) leads to a significant enhancement in the green emission of Tb(3+). Our current results together with the study on α-GdB5O9:xEu(3+) in the literature indicate that α-GdB5O9 is a good phosphor host with advantages including controllable preparation, diverse cationic doping, the absence of concentration quenching, and effective energy transfer.

  8. Photoluminescence and scintillation properties of Ce-doped Sr2(Gd1-xLux)8(SiO4)6O2 (x = 0.1, 0.2, 0.4, 0.5, 0.6) crystals

    Science.gov (United States)

    Igashira, Takuya; Kawano, Naoki; Okada, Go; Kawaguchi, Noriaki; Yanagida, Takayuki

    2018-05-01

    Apatite crystals with chemical compositions of 0.5% Ce-doped Sr2(Gd1-xLux)8(SiO4)6O2 (x = 0.1, 0.2, 0.4, 0.5, 0.6) were synthesized by the Floating Zone method, and then we evaluated their photoluminescence (PL) and scintillation properties. All the Ce-doped samples exhibited PL and scintillation with an intense broad emission in 400-550 nm in which the origin was attributed to the 5d-4f transition of Ce3+, and the emission peak became broader with increasing the concentration of Lu3+. Both PL and scintillation decay time profiles were best-approximated by a sum of two exponential decay functions, and the origin of slower component was attributed to the 5d-4f transition of Ce3+. In the X-ray induced afterglow measurements, the Ce-doped Sr2(Gd0.4Lu0.6)8(SiO4)6O2 sample exhibited the lowest afterglow level. Furthermore, the Ce-doped Sr2(Gd0.5Lu0.5)8(SiO4)6O2 and Sr2(Gd0.4Lu0.6)8(SiO4)6O2 samples showed a clear full energy deposited peak under 5.5 MeV 241Am α-ray irradiation, and the estimated absolute scintillation light yields were around 290 and 1300 ph/5.5 MeV-α, respectively.

  9. Comment on “Synthesis of ceria (CeO_2 and CeO_2_−_x) nanoparticles via decarbonation and Ce(III) oxidation of synthetic bastnaesite (CeCO_3F)” by Montes-Hernandez et al

    International Nuclear Information System (INIS)

    Gysi, Alexander P.; Williams-Jones, Anthony E.

    2016-01-01

    Montes-Hernandez et al. [5] recently reported results of a study of the decarbonation of fine-grained synthetic bastnäsite-(Ce) precipitates involving the oxidation of Ce(III) to Ce(IV) and the formation of ceria (CeO_2 and CeO_2_-_x with oxygen vacancies) nano-particles. The purpose of their study was to show that oxidation of Ce(III) to Ce(IV) occurs spontaneously during heating of bastnäsite-(Ce) in air, a vacuum, N_2 or Ar gas. However, their interpretation of the formation of CeO_2 is not supported by the findings of Gysi and Williams-Jones [3], who showed that natural bastnäsite-(Ce) decomposes to form rare earth element (REE) oxyfluorides (REEOF). The latter was documented using differential scanning calorimetric (DSC) and thermogravimetric (TGA) experiments under a deoxygenated N_2 atmosphere. In their experiments, Gysi and Williams-Jones [3] found no evidence for the oxidation of Ce(III) to Ce(IV). This raises the question of whether the experiments of Montes-Hernandez et al. [5] in a N_2 atmosphere (and by extension in an Ar atmosphere) were compromised because of contamination by O_2 and that, as a result, they reached the erroneous conclusion that Ce(III) oxidizes spontaneously to Ce(IV) during heating of bastnäsite-(Ce) under these conditions. In order to explain the disagreement between their findings and those of Gysi and Williams-Jones [3], Montes-Hernandez et al. [5], proposed that the X-ray diffraction data of the former study were incorrectly interpreted. Here, we provide further evidence that the natural bastnäsite-(Ce) employed in the study by Gysi and Williams-Jones [3] decomposed to form REE oxyfluorides (i.e., CeOF, LaOF, PrOF and NdOF) and not CeO_2, and supply explanations for why Montes-Hernandez et al. [5] erroneously concluded that CeO_2 is produced during decomposition of this mineral under N_2 and Ar atmospheres. In so doing, we hope to provide new insights into the decomposition of bastnäsite-(Ce) that will help guide future

  10. Solid-state reaction synthesis and aqueous durability of Ce-doped zirconolite-rich ceramics

    Energy Technology Data Exchange (ETDEWEB)

    Wen, Guanjun [State Key Laboratory Cultivation Base for Nonmetal Composite and Functional Materials, Southwest University of Science and Technology, Mianyang, Sichuan 621010 (China); Zhang, Kuibao, E-mail: xiaobao320@163.com [State Key Laboratory Cultivation Base for Nonmetal Composite and Functional Materials, Southwest University of Science and Technology, Mianyang, Sichuan 621010 (China); Yin, Dan [State Key Laboratory Cultivation Base for Nonmetal Composite and Functional Materials, Southwest University of Science and Technology, Mianyang, Sichuan 621010 (China); Zhang, Haibin, E-mail: hbzhang@imr.ac.cn [Institute of Nuclear Physics and Chemistry, China Academy of Engineering Physics, Mianyang 621900 (China)

    2015-11-15

    In this study, Ce-doped zirconolite-rich ceramics were prepared by solid-state reaction process using cerium as the surrogate of tetravalence actinide nuclide. The occupancy of Ce in the waste forms was investigated. The aqueous durability of Ce-doped zirconolite-rich ceramic was examined as well. The results show that zirconolite and pseudobrookite coexisted after being sintered at 1200 °C for 6 h. Meanwhile, perovskite is inevitable generated during the process. CeO{sub 2} can be successfully incorporated into the lattice structure of the zirconolite-rich ceramics. The maximum containing capacity of CeO{sub 2} is up to 14.95 wt% or y = 0.4. The normalized elemental leaching rates of Ce and Ca are fairly constant in low values of 1.2 × 10{sup −6} and 2.3 × 10{sup −2} g m{sup −2} d{sup −1} after 28 days. The normalized leaching rate of Fe is also in a low value of 2.9 × 10{sup −4} g m{sup −2} d{sup −1} after 7 days. - Highlights: • Ce-doped zirconolite-rich ceramic was produced at 1200 °C. • Pseudobrookite-type Fe{sub 2}TiO{sub 5} was employed to incorporate Fe element. • Ce{sup 3+} and Ce{sup 4+} coexisted in the Ce-doped zirconolite-rich waste form after being sintered at 1200 °C for 6 h. • The leaching rate of Ca was relatively higher than that of borosilicate glasses.

  11. Preparation of high magneto-optical performance and crystalline quality Ce{sub 1}Gd{sub 2}Fe{sub 5−x}Ga{sub x}O{sub 12} films on CLNGG substrate crystal

    Energy Technology Data Exchange (ETDEWEB)

    Fu, Qiu-ping; Zheng, Ze-yuan; Lin, Nan-xi; Liu, Xiao-feng; Hong, Can-huang; Hu, Xiao-lin, E-mail: linamethyst@fzu.edu.cn; Zhuang, Nai-feng; Chen, Jian-zhong, E-mail: j.z.chen@fzu.edu.cn

    2016-11-01

    Thin films of Ce{sub 1}Gd{sub 2}Fe{sub 5−x}Ga{sub x}O{sub 12} (Ce,Ga:GIG) were prepared on Gd{sub 3}Ga{sub 5}O{sub 12} (GGG) and Ca{sub 2.90}Li{sub 0.30}Nb{sub 1.93}Ga{sub 2.76}O{sub 12} (CLNGG) substrates by using radio frequency magnetron sputtering technique. The phase, grain orientation, surface morphology, transmittance, magnetism and magnetic circular dichroism (MCD) properties of films were analyzed. And the effects of lattice mismatch and non-magnetic Ga{sup 3+}-doping were discussed. The results show that the films with higher crystallized quality and lower stress can be obtained by growing on CLNGG than on GGG. Moreover, the coercive force, magnetization, magneto-optical effect intensity and orientation of film can be effectively regulated by adjusting Ga{sup 3+}-doped concentration. - Highlights: • With excellent magneto-optical performance, Ce,Ga:GIG film has a good application prospect. • Ce,Ga:GIG film with high quality were prepared on CLNGG by RF magnetron sputtering. • Crystalline quality and morphology of films are intently related to the substrate. • Ga{sup 3+} doping obviously affect on magnetism and magneto-optical property of Ce:GIG film.

  12. Ca doping of TSMTG-YBa2Cu3O7-δ/Y2BaCuO5 composites

    International Nuclear Information System (INIS)

    Delorme, F.; Harnois, C.; Monot-Laffez, I.; Marinel, S.

    2002-01-01

    Calcium doped YBa 2 Cu 3 O 7-δ /Y 2 BaCuO 5 bulk samples have been synthesised by the top-seeding-melt-texture growth (TSMTG) process up to 1 wt.% of CaCO 3 . Calcium additions up to 0.25 wt.% of CaCO 3 do not change the decomposition temperature whereas additions of 1 wt.% of CaCO 3 lead to an increase of the decomposition temperature of about 10 deg. C. This difference is not important enough to change the thermal cycle used to process YBa 2 Cu 3 O 7-δ undoped bulk samples. Microstructure studies show that no precursor or secondary phases containing calcium are present in the samples. Energy dispersive spectroscopy analyses have shown that Ca is present both in the YBa 2 Cu 3 O 7-δ matrix and the Y 2 BaCuO 5 particles. The position of the calcium atoms in the superconducting matrix is discussed. The calcium doped samples present slightly depressed critical temperatures but drastically depressed critical current densities

  13. Influence of Mn site doping on electrical resistivity of polycrystalline La1-yAyMn1-xBxO3 (A=Ba, Sr; B=Cu, Cr, Co Manganites

    Directory of Open Access Journals (Sweden)

    Paunović N.

    2008-01-01

    Full Text Available We have the measured electrical resistivity of La1-yBayMn1-xCuxO3 (0.17≤y≤0.30; 0.04≤x≤0.10, La1-ySryMn1-xCrxO3 and La1-ySryMn1-xCoxO3 (0.270≤y≤0.294; 0.02≤x≤0.10 polycrystalline samples in the 25-325 K temperature range. The increase of Mn site doping concentration leads to an increase of the electrical resistivity of the samples and the appearance of a “double-peak” structure in the electrical resistivity versus temperature graphs. The first peak represents the insulator-metal transition in vicinity of the paramagnetic-ferromagnetic transition (TC. We have found that the intensity of the second peak increases with an increase of concentration of Mn substituents, due to the hole scattering by the random potential of the Mn site impurities.

  14. Characterization and Luminescence Properties of Color-Tunable Dy3+-Doped BaY2ZnO5 Nanophosphors

    Science.gov (United States)

    Sonika; Khatkar, S. P.; Khatkar, Avni; Kumar, Rajesh; Taxak, V. B.

    2015-01-01

    Dy3+-doped BaY2ZnO5 nanophosphors were successfully synthesized by use of a solution combustion process. The effects of sintering temperature and dysprosium concentration on the structural and luminescence characteristics of the phosphors were investigated. X-ray diffraction (XRD) analysis confirmed the formation of pure orthorhombic BaY2ZnO5 with the space group Pbnm at 1100°C. Morphological investigation revealed spherical nanoparticles with smooth surfaces. The luminescence features of the nanophosphor were studied by use of photoluminescence excitation (PLE) and photoluminescence emission (PL), with luminescence decay curves and color ( x, y) coordinates. On excitation at 355 nm, BaY2ZnO5 nanophosphor doped with trivalent dysprosium ion emits white light as a mixture of blue (4F9/2 → 6H15/2) and yellow (4F9/2 → 6H13/2) emission. Concentration quenching is explained on the basis of cross-relaxation between intermediate Dy3+ states. Thus, BaY2ZnO5:Dy3+ nanophosphor may be suitable for producing efficient white light for ultraviolet-light-emitting diodes (UV-LEDs), fluorescent lamps, and a variety of optical display panels.

  15. Thermoluminescent response of Y2O3:Ce,Eu irradiated with X-rays

    International Nuclear Information System (INIS)

    Sanchez J, F. del R.; Sosa A, M. A.

    2017-10-01

    The thermoluminescent response of various materials has been studied when irradiated with X-rays, and the parameters that characterize the order of the kinetics of the material, depth of traps and frequency have been determined. The objective of this project was to characterize the thermoluminescent response of dosimeters based on yttrium oxide (Y 2 O 3 ) irradiated with X-rays. To do this, the thermoluminescent response of the Y 2 O 3 :Ce,Eu dosimeter was measured and exposed to an X-ray radiation field; five levels of radiation were used: in the first, a potential of 53.5 kv was used and a working load of 5.6 m As, in the second: 70.0 kv, 12.5 m As; in the third: 81.0 kv, 20.0 m As; in the fourth: 109 kv, 32 m As, in the fifth: 121 kv, 80.0 m As, applying an exposure range between 17.7 and 40 R. The irradiation was performed exposing the sample at 104 cm from the focus of the X-ray tube. To obtain the readings of the thermoluminescent response, a Harshaw TLD 3500 reader was used. The data captured by the reader was processed using the WinREMS software. The deletion protocol was as follows: the dosimeters already read were placed, one hour in the Terlab MA12D muffle at a temperature of (400 ± 1) degrees centigrade, the dosimeters were removed and left at room temperature of 20 degrees centigrade for 20 minutes. Then they were placed in the Binder high temperature oven ED23 at 100 ± 1 centigrade degrees for 2 hours. The brightness curves were de convolved using the WebPlotDigitizer v 3.8 software and the individual peaks of the brightness curves were obtained. We found that: the synthesized materials presented a good thermoluminescent response when irradiated with X-rays. However, only one of the dosimeters, of Yttrium oxide doped with 0.5% Cerium, showed a relatively linear response in the applied dose range. The analysis made to the brightness curve of the Yttrium oxide doped with Cerium at 0.5%, applying the method of the three points for the parameters

  16. Synthesis by Sol-gel and characterization of catalysts Ag/Al{sub 2}O{sub 3}-CeO{sub 2}; Sintesis por Sol-gel y caracterizacion de catalizadores Ag/Al{sub 2}O{sub 3}-CeO{sub 2}

    Energy Technology Data Exchange (ETDEWEB)

    Zayas, M.L.; Perez H, R. [ININ, 52045 Ocoyoacac, Estado de Mexico (Mexico); Rubio, E. [BUAP, Centro de Vinculacion, 72000 Puebla (Mexico); Velasco, A. [BUAP, Facultad de Quimica, 72000 Puebla (Mexico)

    2004-07-01

    Aluminia, cerium and mixed oxides Al{sub 2}O{sub 3}-CeO{sub 2} with different relationship Al/Ce (0.75, 0.50 and 0.25) were prepared by sol-gel and used as support for the Ag. The samples were characterized by XRD, DRIFT, TPR and adsorption of N{sub 2} to temperature of liquid nitrogen. The surface area BET showed that the materials that contain aluminia present near values among them. XRD allowed to identify to the cerianite in the oxides that whose support contains cerium and to the {alpha}-aluminia. A mixture of phases was observed in the aluminia. Vibration bands attributed to the bond Al-O and Ce-O were observed by DRIFT in the catalytic materials. TPR showed differences in the reducibility of the Ag precursor in the indicative catalysts of a different interaction with the support. (Author)

  17. Transition of Emission Colours as a Consequence of Heat-Treatment of Carbon Coated Ce3+-Doped YAG Phosphors

    Directory of Open Access Journals (Sweden)

    Liang-Jun Yin

    2017-10-01

    Full Text Available To modify the luminescence properties of Ce3+-doped Y3Al5O12 (YAG phosphors, they have been coated with a carbon layer by chemical vapor deposition and subsequently heat-treated at high temperature under N2 atmosphere. Luminescence of the carbon coated YAG:Ce3+ phosphors has been investigated as a function of heat-treatment at 1500 and 1650 °C. The 540 nm emission intensity of C@YAG:Ce3+ is the highest when heated at 1650 °C, while a blue emission at 400–420 nm is observed when heated at 1500 °C but not at 1650 °C. It is verified by X-ray diffraction (XRD that the intriguing luminescence changes are induced by the formation of new phases in C@YAG:Ce3+-1500 °C, which disappear in C@YAG:Ce3+-1650 °C. In order to understand the mechanisms responsible for the enhancement of YAG:Ce3+ emission and the presence of the blue emission observed for C@YAG:Ce3+-1500 °C, the samples have been investigated by a combination of several electron microscopy techniques, such as HRTEM, SEM-CL, and SEM-EDS. This local and cross-sectional analysis clearly reveals a gradual transformation of phase and morphology in heated C@YAG:Ce3+ phosphors, which is related to a reaction between C and YAG:Ce3+ in N2 atmosphere. Through reaction between the carbon layer and YAG host materials, the emission colour of the phosphors can be modified from yellow, white, and then back to yellow under UV excitation as a function of heat-treatment in N2 atmosphere.

  18. Radiation-induced transmission spectral variations of Ce3+-doped heavy germanate glasses

    International Nuclear Information System (INIS)

    Yang Yunxia; Baccaro, S.; Cecilia, A.; Rao Jinhua; Zhang Junbiao; Xia Fang; Chen Guorong

    2005-01-01

    Radiation-induced transmission spectral variations of Ce 3+ -doped heavy germanate glasses used as scintillating materials are presented. Glass matrix contains mainly GeO 2 , BaO and Gd 2 O 3 with a density higher than 5 g/cm 3 . Glasses are melted in the different atmosphere. The transmission spectra of glasses before and after radiation treatments are measured and compared. Unlike exhibiting the monotonous deterioration effect on the glass matrix, radiation plays the radiation protection role, even making enhanced transmission of Ce 3+ -doped glasses, depending upon glass melting atmosphere and radiation dose. Radiation-induced reducing and oxidizing mechanism is proposed to explain phenomena

  19. Synthesis of Y{sub 1-x}Al{sub x}Ba{sub 2}Cu{sub 3}O{sub 7-δ} via combustion route: Effects of Al{sub 2}O{sub 3} nanoparticles on superconducting properties

    Energy Technology Data Exchange (ETDEWEB)

    Mohd Suan, Mohd Shahadan, E-mail: mohdshahadan@utem.edu.my [Department of Engineering Materials, Faculty of Manufacturing Engineering, Universiti Teknikal Malaysia Melaka, 76100 Durian Tunggal, Melaka (Malaysia); Johan, Mohd Rafie [Nanomaterial Engineering Research Group, Advanced Materials Research Laboratory, Department of Mechanical Engineering, University of Malaya, 50603 Kuala Lumpur (Malaysia)

    2017-02-01

    Combustion reaction was used to synthesis Al{sub 2}O{sub 3} nanoparticles embedded Y{sub 1-x}Al{sub x}Ba{sub 2}Cu{sub 3}O{sub 7-δ} simultaneously. The effects of Al{sub 2}O{sub 3} nanoparticles with nominal molar mass (x{sub mol}) of 0.02, 0.04, 0.06, 0.08 and 0.10 towards the critical current density J{sub C} of Y{sub 1-x}Al{sub x}Ba{sub 2}Cu{sub 3}O{sub 7-δ} were verified by magnetic measurement. Resulted XRD patterns revealed that the calcined samples consist of pure Al{sub 2}O{sub 3} and Y{sub 1-x}Al{sub x}Ba{sub 2}Cu{sub 3}O{sub 7-δ} phases which had been confirmed by EDX results. The SEM images showed that Al{sub 2}O{sub 3} nanoparticles (~10 nm) were distributed in polycrystalline YBa{sub 2}Cu{sub 3}O{sub 7-δ} grains and grain boundaries. The presence of higher concentration of Al{sub 2}O{sub 3} nanoparticles has developed Al{sup 3+} rich spots which diffused within the YBa{sub 2}Cu{sub 3}O{sub 7-δ} superconducting matrix to form Y{sub 1-x}Al{sub x}Ba{sub 2}Cu{sub 3}O{sub 7-δ} and was confirmed by EDX analysis. The samples were electrically superconducting at temperature above 85 K as measured by using standard four-probe technique. The magnetic field (H) dependent magnetization (M), M-H hysteresis loops measured at 77 K for x{sub mol}≤0.06 samples are significantly improved attributed to the increase of trapped fluxes in the samples. Remarkable increase of magnetic J{sub C} (H) in Al{sub 2}O{sub 3} nanoparticles added samples compared to the as prepared polycrystalline YBa{sub 2}Cu{sub 3}O{sub 7-δ} sample indicating strong pinning effect. It is suggested that well-distributed Al{sub 2}O{sub 3} nanoparticles in the polycrystalline YBa{sub 2}Cu{sub 3}O{sub 7-δ} matrix achieved via auto-combustion reaction has efficiently pin the magnetic vortex. The magnetic J{sub C} was optimized to ~6 kAcm{sup -2} in x{sub mol}=0.06 sample. On the other hand, insignificant magnetic J{sub C} improvement in x{sub mol}≥0.08 samples is probably resulted from the

  20. Photo- and radio-excited luminescence properties of Eu-doped La2O3Al2O3 based eutectics

    International Nuclear Information System (INIS)

    Fujimoto, Yutaka; Kamada, Kei; Yanagida, Takayuki; Wakahara, Shingo; Suzuki, Shotaro; Kurosawa, Shunsuke; Yoshikawa, Akira

    2013-01-01

    Eutectic crystal of 0.5% Eu-doped 30LaAlO 3 –70Al 2 O 3 (vol %) was prepared by micro-pulling down (μ-PD) technique under nitrogen atmosphere. Being excited at a wavelength of 320 nm, the crystal exhibited intense emission band with a maximum at 450 nm which is corresponding to 4f 6 5d-4f 7 ( 8 S 7/2 ) transitions of Eu 2+ . The decay time and fluorescence quantum efficiency (QE) were determined to be about 475 ns and 60%, respectively. When alpha-ray excited the crystal, both Eu 2+ 4f 6 5d-4f 7 ( 8 S 7/2 ) and Eu 3+ 4f 6 -4f 6 ( 5 D 0 - 7 F 1,2 ) emission peaks were observed at 435 nm and 600 nm. By the pulse height spectra, the relative scintillation light yield of the crystal was about 4% compared with that of BGO commercial scintillator. -- Highlights: •0.5% Eu-doped 30LaAlO 3 –70Al 2 O 3 eutectic crystal was grown by μ-PD technique. •The crystal showed intense Eu 2+ 5d-4f emission at 450 nm under excited at 320 nm. •The fluorescence quantum efficiency was calculated to be about 60%. •The scintillation light yield was about 4% compared with that of BGO scintillator

  1. Photoluminescence analysis of Ce3+:Zn2SiO4 & Li++ Ce3+:Zn2SiO4: phosphors by a sol-gel method

    Science.gov (United States)

    Babu, B. Chandra; Vandana, C. Sai; Guravamma, J.; Rudramadevi, B. Hemalatha; Buddhudu, S.

    2015-06-01

    Here, we report on the development and photoluminescence analysis of Zn2SiO4, Ce3+:Zn2SiO4 & Li+ + Ce3+: Zn2SiO4 novel powder phosphors prepared by a sol-gel technique. The total amount of Ce3+ ions was kept constant in this experiment at 0.05 mol% total doping. The excitation and emission spectra of undoped (Zn2SiO4) and Ce3+ doped Zn2SiO4 and 0.05 mol% Li+ co-doped samples have been investigated. Cerium doped Zn2SiO4 powder phosphors had broad blue emission corresponding to the 2D3/2→2FJ transition at 443nm. Stable green-yellow-red emission has been observed from Zn2SiO4 host matrix and also we have been observed the enhanced luminescence of Li+ co-doped Zn2SiO4:Ce3+. Excitation and emission spectra of these blue luminescent phosphors have been analyzed in evaluating their potential as luminescent screen coating phosphors.

  2. The Influence of α- and γ-Al2O3 Phases on the Thermoelectric Properties of Al-doped ZnO

    DEFF Research Database (Denmark)

    Han, Li; Van Nong, Ngo; Le, Thanh Hung

    2013-01-01

    A systematic investigation on the microstructure and thermoelectric properties of Al-doped ZnO using α- and γ-Al2O3 as dopants was conducted in order to understand the doping effect and its mechanism. The samples were prepared by the spark plasma sintering technique from precursors calcined...... at various temperatures. Clear differences in microstructure and thermoelectric properties were observed between the samples doped with α- and γ-Al2O3. At any given calcination temperature, γ-Al2O3 resulted in the formation of a larger amount of the ZnAl2O4 phase in the Al-doped ZnO samples. The average...... grain size was found to be smaller for the γ-Al2O3-doped samples than that for the α-Al2O3-doped ones under the same sintering condition. It is proposed that the ZnAl2O4 phase is the reason for the observed suppression of grain growth and also for the slightly reduced lattice thermal conductivity...

  3. Effect of microstructure on the high temperature mechanical properties of (CeO{sub 2}){sub 0.8}(GdO{sub 1.5}){sub 0.2} electrolytes

    Energy Technology Data Exchange (ETDEWEB)

    Sammes, N.M.; Zhang, Y. [Univ. of Waikato, Hamilton (New Zealand)

    1996-12-31

    CeO{sub 2}-based oxides have recently been shown to have great potential as electrolytes in medium temperature solid oxide fuel cell applications, primarily due to their high ionic conductivity. Steele et al., for example, have examined a cell of the type: O{sub 2}, La{sub 0.6}Sr{sub 0.4}Fe{sub 0.8}Co{sub 0.2}O{sub 3}{vert_bar}Ce{sub 0.9}Gd{sub 0.1}O{sub 1.95}{vert_bar}Ni-ZrO{sub 2}, H{sub 2}/H{sub 2}O at 715{degrees}C. Gd{sub 2}O{sub 3} doped CeO{sub 2} has been reported as having one of the highest oxygen ion conductivities of the ceria-based materials. An ionic conductivity of 8.3 x 10{sup -2} s/cm has been reported for (CeO{sub 2}){sub 0.8}(GdO{sub 1.5}){sub 0.2} at 800{degrees}C, which is approximately four times that of Y{sub 2}O{sub 3}-doped ZrO{sub 2}, at the same temperature. Although the electrical properties of the material have been examined in detail, very little work has considered the microstructural/property relationships, particularly in relation to the mechanical properties. It is well know that CeO{sub 2}-based materials are difficult to density and attempts have been performed to examine this. Preliminary studies have also been undertaken to examine the effect of sintering on the mechanical properties of the material. In this paper we examine the effect of microstructure on the high temperature mechanical properties of (CeO{sub 2}){sub 0.8}(GdO{sub 1.5}){sub 0.2}.

  4. Structural and dielectric studies of Ce doped BaSnO3 perovskite nanostructures

    Science.gov (United States)

    Angel, S. Lilly; Deepa, K.; Rajamanickam, N.; Jayakumar, K.; Ramachandran, K.

    2018-04-01

    Undoped and Cerium (Ce) doped BaSnO3(BSO) nanostructures were synthesized by co-precipitation method. The cubic structure and perovskite phase were confirmed by X-ray diffraction (XRD). The crystallite size of BSO is 41nm and when Ce ion concentration is increased, the crystallite sizesdecreased. The nanocube, nanocuboids and nanorods are observed from SEM analysis. The purity of the undoped and doped samples are confirmed by EDS spectrum. For larger defects, wide band gap was obtained from UV-Vis and PL spectrum. The dielectric constants are increased at low frequencies when Ce impurities are introduced in the BSO matrix at Sn site.

  5. Dependence of glass-forming ability on starting compositions in Y2O3Al2O3–SiO2 system

    OpenAIRE

    Yixiang Chen; Zengchao Yang; Bin He; Guanghua Liu; Jiangtao Li; Liang Wu

    2011-01-01

    The dependence of glass-forming ability on starting compositions in Y2O3Al2O3–SiO2 (YAS) system has been investigated by melting experiment. Transparent YAS glasses have been prepared under the condition of furnace cooling instead of quenching. It is found that, in the YAS ternary phase diagram, the compositions on the Y3Al5O12–SiO2 line and with 52-68 mol% SiO2 have a higher glass-forming ability to produce pure glass. For the compositions with too much or less SiO2 or with Y/Al = 5/3, 1/1,...

  6. Spectral response of REE{sup 3+} doped LaAlO{sub 3}

    Energy Technology Data Exchange (ETDEWEB)

    Boronat, C.; Correcher, V. [CIEMAT, Av. Complutense 40, 28040 Madrid (Spain); Garcia G, J. [Museo Nacional de Ciencias Naturales - Consejo Superior de Investigaciones Cientificas, 28006 Madrid (Spain); Morales, A.; Zarate, J. [Universidad Michoacana de San Nicolas de Hidaldo, Instituto de Investigacion en Metalurgia y Materiales, Ciudad Universitaria, Morelia, Michoacan (Mexico); Rivera, T., E-mail: Cecilia.Boronat@ciemat.es [IPN, Ciudad de Mexico (Mexico)

    2016-10-15

    This paper reports on the preliminary results obtained from the cathodoluminescence (Cl) and thermoluminescence (Tl) properties of undoped LaAlO{sub 3} (LAO) and LaAlO{sub 3}: REE (REE=Dy{sup 3+}, Pr{sup 3+} and Eu{sup 3+}) to be potentially employed for dosimetric purposes. The samples were synthesized by a sol-gel process based on the Pechini 's method with a spray-drying technique and, subsequently, characterized by environmental scanning electron microscopy and energy dispersive X-ray analysis spectrometry. Cl spectra display sharp and narrow wavebands that could specifically be associated with structural (in the range of 300-450 nm) and point defects (from 450 to 800 nm). The observed wavebands could be assigned as follows: (i) 480 and 570 from the Dy-doped LAO should corresponding respectively to {sup 4}F{sub 9/2}→{sup 6}H{sub 15/2} and {sup 4}F{sub 9/2}→{sup 6}H{sub 13/2} transitions, (II) 490-638 from the Pr-doped LAO is linked to {sup 3}P{sub 0}→{sup 3}H{sub 4}, {sup 1}D{sub 2}→{sup 3}H{sub 4} transitions and (III) 590 and 620 where the dopant Eu{sup 3+} gives rise to {sup 5}D{sub 0}→{sup 7}F{sub 1} and {sup 5}D{sub 0}→{sup 7}F{sub 2} transitions and (IV) a UV-blue broad band is associated with NBOHC in undoped LAO. Such emissions are due to the presence of the 4f electrons of rare earth ions that are shielded by the outer 5s and 5p electrons, the intra-4f emission spectra of REE. Furthermore, the study performed on the Tl emission of LaAlO{sub 3}:Dy{sup 3+} displays (i) two maxima centred at 150 and 240 degrees Celsius (ratio 1:2) similarly to the Pr{sup 3+} doped sample but with 7:5 of ratio. And (II) the highest radiation sensitivity, allowing us to think on the potential use of this material for dosimetric purposes, however further works are necessary to confirm such assertion. (Author)

  7. Eu3+-doped (Y0.5La0.5)2O3: new nanophosphor with the bixbyite cubic structure

    Science.gov (United States)

    Đorđević, Vesna; Nikolić, Marko G.; Bartova, Barbora; Krsmanović, Radenka M.; Antić, Željka; Dramićanin, Miroslav D.

    2013-01-01

    New red sesquioxide phosphor, Eu3+-doped (Y0.5La0.5)2O3, was synthesized in the form of nanocrystalline powder with excellent structural ordering in cubic bixbyite-type, and with nanoparticle sizes ranging between 10 and 20 nm. Photoluminescence measurements show strong, Eu3+ characteristic, red emission ( x = 0.66 and y = 0.34 CIE color coordinates) with an average 5D0 emission lifetime of about 1.3 ms. Maximum splitting of the 7F1 manifold of the Eu3+ ion emission behaves in a way directly proportional to the crystal field strength parameter, and experimental results show perfect agreement with theoretical values for pure cubic sesquioxides. This could be used as an indicator of complete dissolution of Y2O3 and La2O3, showing that (Y0.5La0.5)2O3:Eu3+ behaves as a new bixbyite structure oxide, M2O3, where M acts as an ion having average ionic radius of constituting Y3+ and La3+. Emission properties of this new phosphor were documented with detailed assignments of Eu3+ energy levels at 10 K and at room temperature. Second order crystal field parameters were found to be B 20 = -66 cm-1 and B 22 = -665 cm-1 at 10 K and B 20 = -78 cm-1 and B 22 = -602 cm-1 at room temperature, while for the crystal field strength the value of 1495 cm-1 was calculated at 10 K and 1355 cm-1 at room temperature.

  8. Al{sub 2}O{sub 3} reinforced nanoparticle ZrO{sub 2} (3at%?Y{sub 2}O{sub 3}); Al{sub 2}O{sub 3} reforcado com nanoparticulas de ZrO{sub 2}(3%mol Y{sub 2}O{sub 3})

    Energy Technology Data Exchange (ETDEWEB)

    Cossu, C.M.F.A.; Alves, M.F.R.P.; Campos, L.Q.B.; Magnago, R.O.; Santos, C., E-mail: caio.cossu@usp.br [Universidade do Estado do Rio de Janeiro (UERJ), Resende, RJ (Brazil). Faculdade de Tecnologia; Simba, B.G. [Universidade Estadual Paulista Julio de Mesquita Filho (UNESP), Guaratingueta, SP (Brazil). Faculdade de Engenharia

    2016-07-01

    This work developed a composite Al{sub 2}O{sub 3}-based reinforced with nanoparticles of ZrO{sub 2} (Y{sub 2}O{sub 3}), to evaluate the effect of the content of ZrO{sub 2} nanoparticles (Y{sub 2}O{sub 3}) on the mechanical properties. Mixtures containing a matrix of Al{sub 2}O{sub 3} with fractions in weight of 3%, 5%, 10% and 15%, ZrO{sub 2} (Y{sub 2}O{sub 3}), and were mixed in mortar mill. Mixtures received 5% polymeric binder (PVA); and after adding the binder, the material was pressed uniaxially to 50MPa, and then sintered at a temperature of 1600 ° C - 2h. The sintered products were characterized by X-ray diffraction, scanning electron microscopy (SEM), relative density, hardness and fracture toughness. The results of X-ray diffraction showed that Al{sub 2}O{sub 3} and tetragonal ZrO{sub 2} as crystal phases found after sintering. Furthermore, the relative green density of 55% was predominant in the compact; and after sintering, varied depending on the ZrO{sub 2} content, reaching 97% in sintered compositions with 3% ZrO{sub 2} nanoparticles (Y{sub 2O}3). The hardness of the samples showed values of 1670HV and the maximum toughness of 3.2 MPa × m{sup 1/2}, directly influenced by the presence of nanoparticles ZrO{sub 2} uniformly dispersed in the matrix Al{sub 2}O{sub 3}, which results in at least two main mechanisms tenacifiers: transformation of tetragonal-monoclinic phase of zirconia, and compressive residual strain between the two phases present, Al{sub 2}O{sub 3} and tetragonal ZrO{sub 2}. (author)

  9. Structure and properties of the Mn doped CeO{sub 2} thin film grown on LaAlO{sub 3} (0 0 1) via a modified sol–gel spin-coating technique

    Energy Technology Data Exchange (ETDEWEB)

    Mahmoud, Waleed E., E-mail: w_e_mahmoud@yahoo.com [King Abdulaziz University, Faculty of Science, Department of Physics, Jeddah (Saudi Arabia); Suez Canal University, Faculty of Science, Department of Physics, Ismailia (Egypt); Al-Ghamdi, A.A. [King Abdulaziz University, Faculty of Science, Department of Physics, Jeddah (Saudi Arabia); Al-Agel, F.A. [Hail University, College of Science, Department of Physics, Hail (Saudi Arabia); Al-Arfaj, E. [Umm Alqura University, Department of Physics, Makkah (Saudi Arabia); Qaseem University, Physics Department, Qaseem (Saudi Arabia); Shokr, F.S. [King Abdulaziz University, Faculty of Science & Arts, Department of Physics, Rabigh (Saudi Arabia); Al-Gahtany, S.A. [King Abdulaziz University, Faculty of Science for Girls, Department of Physics, Jeddah (Saudi Arabia); Alshahrie, Ahmed [King Abdulaziz University, Faculty of Science, Department of Physics, Jeddah (Saudi Arabia); Hafez, M. [King Abdulaziz University, Faculty of Science, Department of Physics, Jeddah (Saudi Arabia); Suez Canal University, Faculty of Science, Department of Physics, Ismailia (Egypt); Bronstein, L.M. [King Abdulaziz University, Faculty of Science, Department of Physics, Jeddah (Saudi Arabia); Indiana University, Department of Chemistry, Bloomington, IN 47405 (United States); Beall, Gary W. [King Abdulaziz University, Faculty of Science, Department of Physics, Jeddah (Saudi Arabia); Texas State University-San Marcos, Department of Chemistry and Biochemistry, 601 University Dr., San Marcos, TX 78666 (United States)

    2015-08-15

    Highlights: • Mn doped CeO{sub 2} was grown on LaAlO{sub 3} (0 0 1) via sol–gel technique. • The concentration of the Mn ions was varied from 1 to 13 at.%. • The incorporation of 7 at.% of Mn ions was found to provide formation of exceptionally smooth films. • This amount demonstrated the highest saturation magnetization of 1.75 μ{sub B}/Mn and coercive field of 487 Gauss. - Abstract: Here we report Mn doped cerium oxide films prepared on the LaAlO{sub 3} (0 0 1) substrate via an ethylene glycol modified sol–gel spin coating technique and evaluation of their properties as diluted magnetic semiconductors. Cerium oxide was selected because of its high dielectric constant and fluorite cubic structure, matching the silicon and lanthanum aluminate based electronic devices. The concentration of the Mn ions was varied from 1 to 13 at.% and the influence of this concentration on the structure, surface morphology, optical and magnetic properties of these films was studied using scanning electron microscopy, energy dispersive spectroscopy, atomic force microscopy, ellipsometric spectroscopy, X-ray powder diffraction, X-ray photoelectron spectroscopy, and magnetic measurements. The incorporation of 7 at.% of Mn ions was found to provide formation of exceptionally smooth films, demonstrating the highest saturation magnetization of 1.75 μ{sub B}/Mn and the coercive field of 487 Gauss. These properties are assigned to the conversion of Ce{sup 4+} to Ce{sup 3+} upon incorporation of Mn ions into the CeO{sub 2} structure and the oxidation of Mn{sup 2+} to Mn{sup 4+}, creating two oxygen vacancies to preserve the cubic structure of cerium oxide and promoting ferromagnetism.

  10. Ce3+-Doped garnet phosphors : Composition modification, luminescence properties and applications

    NARCIS (Netherlands)

    Xia, Zhiguo; Meijerink, Andries

    2017-01-01

    Garnets have the general formula of A3B2C3O12 and form a wide range of inorganic compounds, occurring both naturally (gemstones) and synthetically. Their physical and chemical properties are closely related to the structure and composition. In particular, Ce3+-doped garnet phosphors have a long

  11. Photoluminescence properties of the Eu-doped alpha-Al2O3 microspheres

    International Nuclear Information System (INIS)

    Liu, Dianguang; Zhu, Zhenfeng

    2014-01-01

    Highlights: • Al 2 O 3 :Eu 3+ phosphors were prepared via a microwave solvothermal route. • The particles were hierarchically nanostructured microspheres packaged by nanosheets. • The powders presented excellent orange–red emission when excited at 393 nm. • Critical concentration and distance of Eu 3+ in Al 2 O 3 is 0.007, 18 Å, respectively. -- Abstract: Al 2 O 3 :Eu 3+ samples were synthesized via microwave solvothermal method and thermal decomposition of Eu 3+ doped precursors. The sample characterizations were carried out by means of X-ray diffraction (XRD), scanning electron microscope (SEM) and photoluminescence (PL) spectra. XRD results indicated that Eu 3+ doped samples were most of α-Al 2 O 3 phase after being calcined at 1473 K. SEM results showed that the obtained α-Al 2 O 3 based powders via microwave solvothermal method were microspheres with an average diameter about 1.6 μm. PL spectra showed that upon excitation at 393 nm, the orange–red emission bands at the wavelength longer than 560 nm were from 5 D 0 → 7 F J (J = 1, 2) transitions. The asymmetry ratio of ( 5 D 0 → 7 F 2 )/( 5 D 0 → 7 F 1 ) intensity is about 1 and this value suggests that Eu 3+ ions occupy the same ratio of symmetry and asymmetry sites. It is shown that the 0.7 mol% of doping concentration of Eu 3+ ions in α-Al 2 O 3 :Eu 3+ is optimum. According to Dexter’s theory, the critical distance between Eu 3+ ions for energy transfer was determined to be 18 Å

  12. Luminescence and energy transfer of Tb3+-doped BaO-Gd2O3-Al2O3-B2O3-SiO2 glasses.

    Science.gov (United States)

    Zuo, Chenggang; Huang, Jinze; Liu, Shaoyou; Xiao, Anguo; Shen, Youming; Zhang, Xiangyang; Zhou, Zhihua; Zhu, Ligang

    2017-12-05

    Transparent Tb 3+ -doped BaO-Gd 2 O 3 -Al 2 O 3 -B 2 O 3 -SiO 2 glasses with the greater than 4g/cm 3 were prepared by high temperature melting method and its luminescent properties have been investigated by measured UV-vis transmission, excitation, emission and luminescence decay spectra. The transmission spectrum shows there are three weak absorption bands locate at about 312, 378 and 484nm in the glasses and it has good transmittance in the visible spectrum region. Intense green emission can be observed under UV excitation. The effective energy transfer from Gd 3+ ion to Tb 3+ ion could occur and sensitize the luminescence of Tb 3+ ion. The green emission intensity of Tb 3+ ion could change with the increasing SiO 2 /B 2 O 3 ratio in the borosilicate glass matrix. With the increasing concentration of Tb 3+ ion, 5 D 4 → 7 F J transitions could be enhanced through the cross relaxation between the two nearby Tb 3+ ions. Luminescence decay time of 2.12ms from 546nm emission is obtained. The results indicate that Tb 3+ -doped BaO-Gd 2 O 3 -Al 2 O 3 -B 2 O 3 -SiO 2 glasses would be potential scintillating material for applications in X-ray imaging. Copyright © 2017 Elsevier B.V. All rights reserved.

  13. Carbon doped lanthanum aluminate (LaAlO3:C) UV thermoluminescent properties synthesized by solid state reaction with three different mixing methodologies

    International Nuclear Information System (INIS)

    Alves, N.

    2017-01-01

    In this work we discuss the thermoluminescent (TL) response for LaAlO 3 :C crystals grown by using three different combinations of Al 2 O 3 , La 2 O 3 and carbon atoms during the synthesis process. Recently, LaAlO 3 single crystals, co-doped with Ce 3+ and Dy 3+ rare earth trivalent ions and grown under hydrothermal conditions, have been reported to show high thermoluminescent response (TL) when exposed to low levels of ultraviolet radiation (UVR). However, undoped LaAlO 3 synthesized by solid state reaction method from the 1:1 mixture of aluminum and lanthanum oxide under reducing atmosphere revealed to have still higher thermoluminescent sensitivity to UV photon fields than the co-doped with Ce 3+ and Dy 3+ . It is well known that carbon doped aluminum oxide monocrystals have excellent TL and photoluminescent response properties for X-rays, UV and gamma radiation fields. Thus, we conducted three different syntheses of LaAlO 3 by the solid state reaction method, doping the mixture with carbon. The lanthanum aluminate polycrystals were synthesized from the 1:1 mixture of aluminum and lanthanum oxide, adding 0.1wt.% carbon and annealed at 1700°C for two hours in hydrogen atmosphere. The X-ray diffraction analysis revealed the formation of rhombohedral LaAlO 3 crystallographic phase, however a small percentage (15%) of Al 2 O 3 has been also identified. The UV-Vis absorbance spectra were obtained and F and F + - center were ascribed. The UV irradiations were carried out using a commercial 8W UV lamp. Thermoluminescence measurements were performed at a Harshaw 4500 TL reader. All compositions investigated have shown high TL sensitivity to UVR. (author)

  14. Effect of yttrium doping on the dielectric properties of CaCu{sub 3}Ti{sub 4}O{sub 12} thin film produced by chemical solution deposition

    Energy Technology Data Exchange (ETDEWEB)

    Saji, Viswanathan S., E-mail: vssaji@chosun.ac.k [Chosun University, College of Dentistry and 2nd Stage of Brain Korea 21 for College of Dentistry, Gwangju-501-759 (Korea, Republic of); Choe, Han Cheol [Chosun University, College of Dentistry and 2nd Stage of Brain Korea 21 for College of Dentistry, Gwangju-501-759 (Korea, Republic of)

    2009-05-29

    Pure and yttrium substituted CaCu{sub 3}Ti{sub 4-x}Y{sub x}O{sub 12-x/} {sub 2} (x = 0, 0.02, 0.1) thin films were prepared on boron doped silica substrate employing chemical solution deposition, spin coating and rapid thermal annealing. The phase and microstructure of the sintered films were examined using X-ray diffraction and scanning electron microscopy. Dielectric properties of the films were measured at room temperature using electrochemical impedance spectroscopy. Highly ordered polycrystalline CCTO thin film with bimodal grain size distribution was achieved at a sintering temperature of 800 {sup o}C. Yttrium doping was found to have beneficial effects on the dielectric properties of CCTO thin film. Dielectric parameters obtained for a CaCu{sub 3}Ti{sub 4-x}Y{sub x}O{sub 12-x} {sub /2} (x = 0.02) film at 1 KHz were k {approx} 2700 and tan {delta} {approx} 0.07.

  15. Magnetotransport of CaCu3Mn4O12 complex perovskite derivatives

    International Nuclear Information System (INIS)

    Sanchez-Benitez, J.; Andres, A. de; Garcia-Hernandez, M.; Alonso, J.A.; Martinez-Lope, M.J.

    2006-01-01

    Neutron powder diffraction, magnetic and magnetotransport studies were carried out on new derivatives of the CaCu 3 Mn 4 O 12 (A'A 3 B 4 O 12 ) complex perovskite. The samples were prepared in polycrystalline form under moderate pressure conditions. Substitutions at A and A' sites of CaCu 3 Mn 4 O 12 , with only Mn 4+ and insulating behavior, imply electron doping that affects the magnetic and transport properties. X-ray Absorption Spectroscopy showed that Mn 3+ /Mn 4+ valence mixing occurs only at B site, progressively filling the e g band and providing the metallic character in these compounds, as we observe in most of these samples. A semiconducting behavior is observed in samples with 50% Mn 3+ at B site. This can be understood by the opening of a gap in the conduction band corresponding to the half filling of the e g states. This is the case of the tetravalent rare earth doped samples (Ce and Th at A' site) and of the appropriate A site doped Ca(CuMn 2 )Mn 4 O 12 sample. At the strongly distorted A positions, Mn 3+ , with localized e g electrons, act as magnetic impurities at very low temperatures (<40 K) giving rise to the observed upturn in the resistivity. The magnetic origin of this scattering is evidenced by its drastic reduction under a magnetic field

  16. Synthesis and characterization of molybdenum catalysts supported on γ-Al2O3-CeO2 composite oxides

    International Nuclear Information System (INIS)

    Farooq, Muhammad; Ramli, Anita; Subbarao, Duvvuri

    2012-01-01

    The physical and chemical properties of a catalyst play a vital role in various industrial applications. Molybdenum catalysts supported on γ-Al 2 O 3 and γ-Al 2 O 3 -CeO 2 mixed oxides with varying loading of CeO 2 (5, 10, 15, 20 wt% with respect to γ-Al 2 O 3 ) were prepared by wet impregnation method. The physiochemical properties of these synthesized Mo catalysts were studied with various characterization techniques such as X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS), temperature-programmed reduction (TPR), field emission scanning electron microscopy-energy dispersive analysis (FESEM-EDX) and X-ray fluorescence spectrometer (XRF). The results showed that the addition of CeO 2 into the support affected the binding energies of the elements and reducibility of the metal oxides formed after calcination of catalyst samples due to the change in metal-support interaction. Further, the characterization techniques showed that the active metal was well dispersed on the surface of support material.

  17. Effect of Al2O3 on the sintering of garnet-type Li6.5La3Zr1.5Ta0.5O12

    Energy Technology Data Exchange (ETDEWEB)

    Wang, Yuxing; Yan, Pengfei; Xiao, Jie; Lu, Xiaochuan; Zhang, Ji-Guang; Sprenkle, Vincent L.

    2016-10-01

    It is widely recognized that Al plays a dual role in the fabrication of garnet-type solid electrolytes, i.e., as a dopant that stabilizes the cubic structure and a sintering aid that facilitates the densification. However, the sintering effect of Al2O3 has not been well understood so far because Al is typically “unintentionally” introduced into the sample from the crucible during the fabrication process. In this study, we have investigated the sintering effect of Al on the phase composition, microstructure, and ionic conductivity of Li6.5La3Zr1.5Ta0.5O12 by using an Al-free crucible and intentionally adding various amounts of γ-Al2O3. It was found that the densification of Li6.5La3Zr1.5Ta0.5O12 occurred via liquid-phase sintering, with evidence of morphology change among different compositions. Among all of the compositions, samples with 0.05 mol of Al per unit formula of garnet oxide (i.e., 0.3 wt% Al2O3) exhibited the optimal microstructure and the highest total ionic conductivity of 5 10-4 S cm-1 at room temperature.

  18. Unclonable Security Codes Designed from Multicolor Luminescent Lanthanide-Doped Y2O3 Nanorods for Anticounterfeiting.

    Science.gov (United States)

    Kumar, Pawan; Nagpal, Kanika; Gupta, Bipin Kumar

    2017-04-26

    The duplicity of important documents has emerged as a serious problem worldwide. Therefore, many efforts have been devoted to developing easy and fast anticounterfeiting techniques with multicolor emission. Herein, we report the synthesis of multicolor luminescent lanthanide-doped Y 2 O 3 nanorods by hydrothermal method and their usability in designing of unclonable security codes for anticounterfeiting applications. The spectroscopic features of nanorods are probed by photoluminescence spectroscopy. The Y 2 O 3 :Eu 3+ , Y 2 O 3 :Tb 3+ , and Y 2 O 3 :Ce 3+ nanorods emit hypersensitive red (at 611 nm), strong green (at 541 nm), and bright blue (at 438 nm) emissions at 254, 305, and 381 nm, respectively. The SEM and TEM/HRTEM results reveal that these nanorods have diameter and length in the range of 80-120 nm and ∼2-5 μm, respectively. The two-dimensional spatially resolved photoluminescence intensity distribution in nanorods is also investigated by using confocal photoluminescence microscopic technique. Further, highly luminescent unclonable security codes are printed by a simple screen printing technique using luminescent ink fabricated from admixing of lanthanide doped multicolor nanorods in PVC medium. The prospective use of these multicolor luminescent nanorods provide a new opportunity for easily printable, highly stable, and unclonable multicolor luminescent security codes for anti-counterfeiting applications.

  19. Scintillation properties of Zr co-doped Ce:(Gd, La)_2Si_2O_7 grown by the Czochralski process

    International Nuclear Information System (INIS)

    Murakami, Rikito; Kurosawa, Shunsuke; Shoji, Yasuhiro; Jary, Vitezslav; Ohashi, Yuji; Pejchal, Jan; Yokota, Yuui; Kamada, Kei; Nikl, Martin; Yoshikawa, Akira

    2016-01-01

    (Gd_0_._7_5,Ce_0_._0_1_5,La_0_._2_3_5)_2Si_2O_7 (Ce:La-GPS) single crystals co-doped with 0, 100, 200, 500 and 1000 ppm Zr were grown by the Czochralski process, and their scintillation properties were investigated. We investigated the co-doping effect of a stable tetravalent ion in Ce:La-GPS for the first time. The scintillation decay times in the faster component were shortened with increasing the Zr concentration. While the non-co-doped sample showed ∼63 ns day time, the Zr 100, 200, 500 and 1000 ppm co-doped samples showed ∼61, ∼59, ∼57, ∼54 ns, respectively. Additionally, light output, photon nonproportional response (PNR) and other optical properties were investigated. - Highlights: • Czochralski growth of Ce:(Gd,La)_2Si_2O_7 single crystals. • Co-doping effect of a stable tetravalent ion in Ce:(Gd,La)_2Si_2O_7 system. • Photon nonproportional response of Zr co-doped Ce:(Gd,La)_2Si_2O_7.

  20. A high performance BaZr0.1Ce0.7Y0.2O3-δ-based solid oxide fuel cell with a cobalt-free Ba0.5Sr0.5FeO3-δ–Ce0.8Sm0.2O2-δ composite cathode

    NARCIS (Netherlands)

    Sun, Wenping; Shi, Zhen; Fang, S.; Yan, Litao; Zhu, Zhiwen; Liu, Wei

    2010-01-01

    A cobalt-free Ba0.5Sr0.5FeO3-δ–Ce0.8Sm0.2O2-δ (BSF–SDC) composite is employed as a cathode for an anode-supported proton-conducting solid oxide fuel cells (H-SOFCs) using BaZr0.1Ce0.7Y0.2O3-δ (BZCY) as the electrolyte. The chemical compatibility between BSF and SDC is evaluated. The XRD results show

  1. Plasma-catalyst hybrid reactor with CeO2/γ-Al2O3 for benzene decomposition with synergetic effect and nano particle by-product reduction.

    Science.gov (United States)

    Mao, Lingai; Chen, Zhizong; Wu, Xinyue; Tang, Xiujuan; Yao, Shuiliang; Zhang, Xuming; Jiang, Boqiong; Han, Jingyi; Wu, Zuliang; Lu, Hao; Nozaki, Tomohiro

    2018-04-05

    A dielectric barrier discharge (DBD) catalyst hybrid reactor with CeO 2 /γ-Al 2 O 3 catalyst balls was investigated for benzene decomposition at atmospheric pressure and 30 °C. At an energy density of 37-40 J/L, benzene decomposition was as high as 92.5% when using the hybrid reactor with 5.0wt%CeO 2 /γ-Al 2 O 3 ; while it was 10%-20% when using a normal DBD reactor without a catalyst. Benzene decomposition using the hybrid reactor was almost the same as that using an O 3 catalyst reactor with the same CeO 2 /γ-Al 2 O 3 catalyst, indicating that O 3 plays a key role in the benzene decomposition. Fourier transform infrared spectroscopy analysis showed that O 3 adsorption on CeO 2 /γ-Al 2 O 3 promotes the production of adsorbed O 2 - and O 2 2‒ , which contribute benzene decomposition over heterogeneous catalysts. Nano particles as by-products (phenol and 1,4-benzoquinone) from benzene decomposition can be significantly reduced using the CeO 2 /γ-Al 2 O 3 catalyst. H 2 O inhibits benzene decomposition; however, it improves CO 2 selectivity. The deactivated CeO 2 /γ-Al 2 O 3 catalyst can be regenerated by performing discharges at 100 °C and 192-204 J/L. The decomposition mechanism of benzene over CeO 2 /γ-Al 2 O 3 catalyst was proposed. Copyright © 2017 Elsevier B.V. All rights reserved.

  2. The effect of Ce doping on the structure, surface morphology and magnetic properties of Dy doped-yttrium iron garnet films prepared by a sol–gel method

    Energy Technology Data Exchange (ETDEWEB)

    Arsad, A.Z.; Ibrahim, N.B., E-mail: baayah@ukm.edu.my

    2016-07-15

    Cerium substitute Y{sub 2.8−x}Dy{sub 0.2}Ce{sub x}Fe{sub 5}O{sub 12} (x=0, 0.2, 0.25, 0.3, 0.35) films have been prepared on quartz substrates by a simple sol–gel method and followed by a spin-coating technique. The crystalline structures, surface and magnetic properties of the films has been investigated by an X-ray diffractometer (XRD), a field emission scanning electron microscope (FESEM), an atomic force microscope (AFM) and a vibrating sample magnetometer (VSM). The XRD analysis revealed that the films have garnet structure. The lattice parameter increased as Ce content was increased up to 0.25 due to the Ce{sup 3+} ions completely substituted for Y{sup 3+} ions. For films x≥0.3, the lattice parameter decreased. The FESEM results showed that the average grains were small, ranging from 11 to 14 nm and the thickness of films increased with the increment of Ce contents. VSM results for both in and out-plane magnetic measurement showed the film with x=0 has the highest saturation magnetization (M{sub s}) values. With the increment of Ce contents, the M{sub s} of films decreased due to the substitution of Ce{sup 3+}, Dy{sup 3+} ions in the c-site. For films x≥0.3 the reduction of M{sub s} values was due to the presence of CeO{sub 2} in the film. The films with x=0–0.25 exhibited increases in H{sub c} values. The improvement of coercivity value, small grain size and high crystalline structure of film with x=0.25 has a potential to be used in magneto optical (MO) memory storage applications. - Highlights: • Ce-doped Y{sub 2.8−x}Dy{sub 0.2}Ce{sub x}Fe{sub 5}O{sub 12} films were prepared by the sol–gel method. • The solubility limit of Ce{sup 3+} ions in the film was x=0.25. • The average grain size ranging from 11 to 14 nm with the increment of Ce doping. • Increasing Ce contents degrades the saturation of magnetization of films. • Increasing Ce contents improve the coercivity of films.

  3. Comment on “Synthesis of ceria (CeO{sub 2} and CeO{sub 2−x}) nanoparticles via decarbonation and Ce(III) oxidation of synthetic bastnaesite (CeCO{sub 3}F)” by Montes-Hernandez et al

    Energy Technology Data Exchange (ETDEWEB)

    Gysi, Alexander P., E-mail: agysi@mines.edu [Department of Geology and Geological Engineering, Colorado School of Mines, 1516 Illinois Street, Golden, CO, 80401 (United States); Williams-Jones, Anthony E. [Department of Earth and Planetary Sciences, McGill University, 3450 University Street, Montreal, QC, Canada, H3A 2A7 (Canada)

    2016-11-01

    Montes-Hernandez et al. [5] recently reported results of a study of the decarbonation of fine-grained synthetic bastnäsite-(Ce) precipitates involving the oxidation of Ce(III) to Ce(IV) and the formation of ceria (CeO{sub 2} and CeO{sub 2-x} with oxygen vacancies) nano-particles. The purpose of their study was to show that oxidation of Ce(III) to Ce(IV) occurs spontaneously during heating of bastnäsite-(Ce) in air, a vacuum, N{sub 2} or Ar gas. However, their interpretation of the formation of CeO{sub 2} is not supported by the findings of Gysi and Williams-Jones [3], who showed that natural bastnäsite-(Ce) decomposes to form rare earth element (REE) oxyfluorides (REEOF). The latter was documented using differential scanning calorimetric (DSC) and thermogravimetric (TGA) experiments under a deoxygenated N{sub 2} atmosphere. In their experiments, Gysi and Williams-Jones [3] found no evidence for the oxidation of Ce(III) to Ce(IV). This raises the question of whether the experiments of Montes-Hernandez et al. [5] in a N{sub 2} atmosphere (and by extension in an Ar atmosphere) were compromised because of contamination by O{sub 2} and that, as a result, they reached the erroneous conclusion that Ce(III) oxidizes spontaneously to Ce(IV) during heating of bastnäsite-(Ce) under these conditions. In order to explain the disagreement between their findings and those of Gysi and Williams-Jones [3], Montes-Hernandez et al. [5], proposed that the X-ray diffraction data of the former study were incorrectly interpreted. Here, we provide further evidence that the natural bastnäsite-(Ce) employed in the study by Gysi and Williams-Jones [3] decomposed to form REE oxyfluorides (i.e., CeOF, LaOF, PrOF and NdOF) and not CeO{sub 2}, and supply explanations for why Montes-Hernandez et al. [5] erroneously concluded that CeO{sub 2} is produced during decomposition of this mineral under N{sub 2} and Ar atmospheres. In so doing, we hope to provide new insights into the decomposition of

  4. Luminescence in Eu2+ and Ce3+ doped SrCaP2O7 phosphors

    Directory of Open Access Journals (Sweden)

    K.N. Shinde

    Full Text Available Eu2+ and Ce3+ doped SrCaP2O7 has been achieved by modified solid state diffusion in reducing atmosphere. The prepared phosphor powders have been identified by their characteristic X-ray diffraction patterns. The mixed phases of α-Sr2P2O7 type with orthorhombic and α-Ca2P2O7 type with monoclinic form were investigated. Its excitation wavelength ranging from 250 to 430 nm fits well with the characteristic emission of UV light-emitting diode (LED. The excitation and emission spectra indicate that these phosphors can be effectively excited by the near-UV light, and emits blue (visible range due to 4f7 → 4f65d1 transition of Eu2+ particularly, SrCaP2O7: Eu2+ whereas, photoluminescence excitation spectrum measurements of Ce3+ activated SrCaP2O7 shows that the phosphor can be efficiently excited by UV–Vis light from 280 to 310 nm to realize emission in the near visible range due to the 5d–4f transition of Ce3+ ions which is applicable for scintillation purpose. The impacts of doping of divalent europium and trivalent cerium on photoluminescence properties on SrCaP2O7 pyrophosphate phosphors were investigated and I propose a feasible interpretation. Keywords: Phosphor, Luminescence, XRD, LED, FTIR

  5. Thermoluminescent response of Y{sub 2}O{sub 3}:Ce,Eu irradiated with X-rays; Respuesta termoluminiscente del Y{sub 2}O{sub 3}:Ce,Eu irradiado con rayos X

    Energy Technology Data Exchange (ETDEWEB)

    Sanchez J, F. del R. [Universidad APEC, Escuela de Ingenieria, Apdo. Postal No. 2867, 10107 Santo Domingo (Dominican Republic); Sosa A, M. A., E-mail: sanchezjaquez@gmail.com [Universidad de Guanajuato, Division de Ciencias e Ingenierias, Campus Leon, 37670 Leon, Guanajuato (Mexico)

    2017-10-15

    The thermoluminescent response of various materials has been studied when irradiated with X-rays, and the parameters that characterize the order of the kinetics of the material, depth of traps and frequency have been determined. The objective of this project was to characterize the thermoluminescent response of dosimeters based on yttrium oxide (Y{sub 2}O{sub 3}) irradiated with X-rays. To do this, the thermoluminescent response of the Y{sub 2}O{sub 3}:Ce,Eu dosimeter was measured and exposed to an X-ray radiation field; five levels of radiation were used: in the first, a potential of 53.5 kv was used and a working load of 5.6 m As, in the second: 70.0 kv, 12.5 m As; in the third: 81.0 kv, 20.0 m As; in the fourth: 109 kv, 32 m As, in the fifth: 121 kv, 80.0 m As, applying an exposure range between 17.7 and 40 R. The irradiation was performed exposing the sample at 104 cm from the focus of the X-ray tube. To obtain the readings of the thermoluminescent response, a Harshaw TLD 3500 reader was used. The data captured by the reader was processed using the WinREMS software. The deletion protocol was as follows: the dosimeters already read were placed, one hour in the Terlab MA12D muffle at a temperature of (400 ± 1) degrees centigrade, the dosimeters were removed and left at room temperature of 20 degrees centigrade for 20 minutes. Then they were placed in the Binder high temperature oven ED23 at 100 ± 1 centigrade degrees for 2 hours. The brightness curves were de convolved using the WebPlotDigitizer v 3.8 software and the individual peaks of the brightness curves were obtained. We found that: the synthesized materials presented a good thermoluminescent response when irradiated with X-rays. However, only one of the dosimeters, of Yttrium oxide doped with 0.5% Cerium, showed a relatively linear response in the applied dose range. The analysis made to the brightness curve of the Yttrium oxide doped with Cerium at 0.5%, applying the method of the three points for the

  6. Optimizing white light luminescence in Dy3+-doped Lu3Ga5O12 nano-garnets

    International Nuclear Information System (INIS)

    Haritha, P.; Linganna, K.; Venkatramu, V.; Martín, I. R.; Monteseguro, V.; Rodríguez-Mendoza, U. R.; Babu, P.; León-Luis, S. F.; Jayasankar, C. K.; Lavín, V.

    2014-01-01

    Trivalent dysprosium-doped Lu 3 Ga 5 O 12 nano-garnets have been prepared by sol-gel method and characterized by X-ray powder diffraction, high-resolution transmission electron microscopy, dynamic light scattering, and laser excited spectroscopy. Under a cw 457 nm laser excitation, the white luminescence properties of Lu 3 Ga 5 O 12 nano-garnets have been studied as a function of the optically active Dy 3+ ion concentration and at low temperature. Decay curves for the 4 F 9/2 level of Dy 3+ ion exhibit non-exponential nature for all the Dy 3+ concentrations, which have been well-fitted to a generalized energy transfer model for a quadrupole-quadrupole interaction between Dy 3+ ions without diffusion. From these data, a simple rate-equations model can be applied to predict that intense white luminescence could be obtained from 1.8 mol% Dy 3+ ions-doped nano-garnets, which is in good agreement with experimental results. Chromaticity color coordinates and correlated color temperatures have been determined as a function of temperature and are found to be within the white light region for all Dy 3+ concentrations. These results indicate that 2.0 mol% Dy 3+ ions doped nano-garnet could be useful for white light emitting device applications

  7. Luminescence of Ce3+ doped LaPO4 nanophosphors upon Ce3+ 4f-5d and band-to-band excitation

    International Nuclear Information System (INIS)

    Stryganyuk, G.; Trots, D.M.; Voloshinovskii, A.; Shalapska, T.; Zakordonskiy, V.; Vistovskyy, V.; Pidzyrailo, M.; Zimmerer, G.

    2008-01-01

    Luminescence spectral-kinetic studies have been performed for pure and Ce-doped LaPO 4 micro- and nanosized phosphates using synchrotron radiation for the excitation within 5-20 eV energy range at T=8-300 K. Mechanisms for the excitation of Ce 3+ 5d-4f emission as well as the quenching processes are discussed. The influence of surface defects has been considered to modify considerably the luminescent properties of nanosized phosphors upon the excitation in the energy range of Ce 3+ 4f-5d transitions and LaPO 4 host absorption

  8. Nanocrystalline Ce 1- xY xO 2- x/2 (0≤ x≤0.35) Oxides via Carbonate Precipitation: Synthesis and Characterization

    Science.gov (United States)

    Li, Ji-Guang; Ikegami, Takayasu; Wang, Yarong; Mori, Toshiyuki

    2002-10-01

    A novel carbonate (co)precipitation method, employing nitrates as the starting salts and ammonium carbonate as the precipitant, has been used to synthesize nanocrystalline CeO 2 and Ce 1- xY xO 2- x/2 ( x≤0.35) solid-solutions. The resultant powders are characterized by elemental analysis, differential thermal analysis/thermogravimetry (DTA/TG), X-ray diffractometry (XRD), Brunauer-Emmett-Teller (BET) analysis, and high-resolution scanning electron microscopy (HRSEM). Due to the direct formation of carbonate solid-solutions during precipitation, Ce 1- xY xO 2- x/2 solid-solution oxides are formed directly during calcination at a very low temperature of ˜300°C for 2 h. The thus-produced oxide nanopowders are essentially non-agglomerated, as revealed by BET in conjunction with XRD analysis. The solubility of YO 1.5 in CeO 2 is determined via XRD to be somewhere in the range from 27 to 35 mol%, from which a Y 2O 3-related type-C phase appears in the final product. Y 3+-doping promotes the formation of spherical nanoparticles, retards thermal decomposition of the precursors, and suppresses significantly crystallite coarsening of the oxides during calcination. The activation energy for crystallite coarsening increases gradually from 68.7 kJ mol -1 for pure CeO 2 to 138.6 kJ mol -1 for CeO 2 doped with 35 mol% YO 1.5. The dopant effects on crystallite coarsening is elaborated from the view point of solid-state chemistry.

  9. Carbon doped lanthanum aluminate (LaAlO{sub 3}:C) UV thermoluminescent properties synthesized by solid state reaction with three different mixing methodologies

    Energy Technology Data Exchange (ETDEWEB)

    Alves, N., E-mail: neire.radiologia@yahoo.com.br, E-mail: farialo@cdtn.br [Universidade Federal do Estado de Minas Gerais (UFMG), Belo Horizonte, MG (Brazil). Departamento de Engenharia Nuclear; Ferraz, W.B.; Faria, L.O., E-mail: ferrazw@cdtn.br [Centro de Desenvolvimento da Tecnologia Nuclear (CDTN/CNEN-MG), Belo Horizonte, MG (Brazil)

    2017-07-01

    In this work we discuss the thermoluminescent (TL) response for LaAlO{sub 3}:C crystals grown by using three different combinations of Al{sub 2}O{sub 3}, La{sub 2}O{sub 3} and carbon atoms during the synthesis process. Recently, LaAlO{sub 3} single crystals, co-doped with Ce{sup 3+} and Dy{sup 3+} rare earth trivalent ions and grown under hydrothermal conditions, have been reported to show high thermoluminescent response (TL) when exposed to low levels of ultraviolet radiation (UVR). However, undoped LaAlO{sub 3} synthesized by solid state reaction method from the 1:1 mixture of aluminum and lanthanum oxide under reducing atmosphere revealed to have still higher thermoluminescent sensitivity to UV photon fields than the co-doped with Ce{sup 3+} and Dy{sup 3+}. It is well known that carbon doped aluminum oxide monocrystals have excellent TL and photoluminescent response properties for X-rays, UV and gamma radiation fields. Thus, we conducted three different syntheses of LaAlO{sub 3} by the solid state reaction method, doping the mixture with carbon. The lanthanum aluminate polycrystals were synthesized from the 1:1 mixture of aluminum and lanthanum oxide, adding 0.1wt.% carbon and annealed at 1700°C for two hours in hydrogen atmosphere. The X-ray diffraction analysis revealed the formation of rhombohedral LaAlO{sub 3} crystallographic phase, however a small percentage (15%) of Al{sub 2}O{sub 3} has been also identified. The UV-Vis absorbance spectra were obtained and F and F{sup +}- center were ascribed. The UV irradiations were carried out using a commercial 8W UV lamp. Thermoluminescence measurements were performed at a Harshaw 4500 TL reader. All compositions investigated have shown high TL sensitivity to UVR. (author)

  10. Estudo da viabilidade de obtenção de cerâmicas de SiC por infiltração espontânea de misturas eutéticas de Y2O3-AlN, Y2O3-Al2O3, R2O3-AlN Study of the viability to produce SiC ceramics by Y2O3-AlN, Y2O3-Al2O3, R2O3-AlN spontaneous infiltration

    Directory of Open Access Journals (Sweden)

    G. C. R. Garcia

    2008-06-01

    Full Text Available As cerâmicas de carbeto de silício, SiC, apresentam excelentes propriedades quando obtidas por infiltração de determinados líquidos. Na infiltração o tempo de contato entre o líquido e o SiC a temperaturas elevadas é muito curto, diminuindo a probabilidade de formação dos produtos gasosos que interferem negativamente na resistência da peça final, como ocorre na sinterização via fase líquida. O objetivo deste trabalho é mostrar uma correlação entre molhabilidade e capacidade de infiltração de alguns aditivos em compactos de SiC. Foram preparados compactos de SiC por prensagem isostática a frio e posterior pré-sinterização via fase sólida. Nesses compactos foram infiltradas misturas de Y2O3-AlN, Y2O3-Al2O3, R2O3-AlN, nas composições eutéticas, 10 ºC acima da temperatura de fusão das respectivas misturas por 4, 8 e 12 min. Após infiltração, as amostras foram analisadas quanto à densidade aparente e real, fases cristalinas, microestrutura e grau de infiltração, sendo que as amostras infiltradas com Y2O3-AlN apresentaram melhores resultados.Silicon carbide ceramics, SiC, obtained by liquid infiltration have shown excellent properties. In infiltration process the contact time of the liquid with SiC at elevated temperature is short, decreasing the probability to form gaseous products that contribute negatively in the final product properties. This phenomenon occurs during SiC liquid phase sintering. The purpose of the present study was to investigate the correlation between wettability and infiltration tendency of some additives in SiC compacts. SiC compacts were prepared by cold isostatic pressing followed by solid phase pre-sintering. Into the compacts were introduced Y2O3-AlN, Y2O3-Al2O3, R2O3-AlN liquids with eutectic compositions at a temperature 10 ºC higher than the melting point of each mixture for 4, 8 and 12 min. Before infiltration, the samples were analyzed by determining densities, crystalline phases

  11. Ce and Eu-doped LiSrAlF6 scintillators for neutron detectors

    International Nuclear Information System (INIS)

    Yanagida, Takayuki; Kawaguchi, Noriaki; Fujimoto, Yutaka; Yokota, Yuui; Yamazaki, Atsushi; Watanabe, Kenichi; Kamada, Kei; Yoshikawa, Akira; Chani, Valery

    2011-01-01

    Ce 1%, Eu 1%, and Eu 2%-doped LiSrAlF 6 (LiSAF) single crystals were grown by the micro-pulling-down method for thermal neutron applications. The crystals were transparent, 2.0 mm in diameter and 20–40 mm in length. Neither visible inclusions nor cracks were observed. Their transmittance spectra were measured. The strong absorption lines were observed at 200, 240, and 300 nm for Ce:LiSAF due to Ce 3+ 4f–5d transition. In Eu:LiSAF, 200 (4f–5d) and 300 (4f–4f) nm absorption lines were detected. The samples demonstrated strong emission peaks at 300 nm (Ce:LiSAF) and 370 nm (Eu:LiSAFs) when they were irradiated with 241 Am α-rays simulating the α-particles from the 6 Li(n, α) reaction. Thermal neutron responses were examined under 252 Cf irradiation. The absolute light yield of Ce, Eu 1%, and Eu 2% crystals were 3400, 18000, and 30000 ph/n, respectively. Main components of the scintillation decay time of Ce, Eu 1%, and Eu 2%-doped LiSAFs were 63, 1293, and 1205 ns.

  12. Redox behavior of a low-doped Pr-CeO_2(111) surface. A DFT+U study

    International Nuclear Information System (INIS)

    Milberg, Brian; Juan, Alfredo; Irigoyen, Beatriz

    2017-01-01

    Highlights: • Pr doping facilitates oxygen donation due to the easy formation of Pr"3"+/Pr"4"+ and Ce"3"+/Ce"4"+ redox couples. • Pr doping also favors the formation of superoxide (O_2"−) radicals on surface O-holes. • CO can be oxidized by superoxide radical forming a CO_2 molecule floating on the surface. • CO can also interact on the (O_2"−)/Pr"3"+ interphase and forms weakly adsorbed carbonate-type intermediates. - Abstract: In this work, we investigated the redox behavior (donation and replenishing of oxygen) of a low praseodymium (Pr)-doped CeO_2(111) surface. We considered a 3.7 at.% Pr doping and performed density functional calculations using the GGA formalism with the ‘U’ correction on Ce(4f) and Pr(4f) orbitals. Our results indicate that Pr doping promotes oxygen donation by lowering the energy necessary to form surface anionic vacancies. When the Ce_0_._9_6_3Pr_0_._0_3_7O_2(111) surface donates one oxygen, the two excess electrons locate on Pr and Ce cations and reduce them to Pr"3"+ and Ce"3"+ ones. Praseodymium doping also favors the activation of O_2 molecule on surface O-holes, leading to formation of a superoxide (O_2"−) radical as well as to reoxidation of the Ce"3"+ cation to Ce"4"+ one. Additionally, we used the CO molecular adsorption for testing the reactivity of those superoxide species. The calculations expose the ability of these radicals to oxidize CO forming a CO_2 molecule floating on the surface. However, when the superoxide is in the immediate vicinity of Pr dopant a carbonate-type species is formed. Our theoretical results may help to gain insight into redox properties and improved catalytic performance of low-doped Pr-CeO_2 solids.

  13. Characterization of the alteration products formed at the surface of LaYSiAlO and CeYSiAlO glasses using ERDA and RBS techniques

    International Nuclear Information System (INIS)

    Gavarini, S.; Trocellier, P.; Matzen, G.

    2004-01-01

    Leaching tests have been performed on LnYSiAlO glasses (Ln = La or Ce) that are considered as potential matrices for the specific immobilization of minor actinides. Elastic recoil detection analysis (ERDA) performed on leached samples indicated a superficial hydration of LaYSiAlO glass of about 100-150 nm. This hydrated layer is (Al, Y)-enriched according to SEM-EDS analysis, suggesting the formation of hydroxide (or hydroxycarbonates) compounds including these two elements. This process leads to a very efficient passivation of the material due to the low solubility of Al and Y hydroxides (and hydroxycarbonates) species in near neutral media, even when the solution is rapidly replenished is dynamic leaching experiments. Rutherford Backscattering Spectrometry elemental mapping revealed very localized and significantly Y-enriched deposits at the surface of the sample after leaching. This could be the sign of heterogeneities already present on the pristine glass. These may be correlated with the weak solubility of yttrium (and rare earth) elements in silicate matrices (Y + Ln initial content in the glass ∼11 at.%). In the case of CeYSiAlO glass, a thin layer was formed on the solid after leaching. The simulation of the corresponding RBS spectra showed a surface (Y, Ce)-enrichment and (Al, Si)-depletion in both cases. This could be explained by the oxidation of trivalent cerium initially present in the glass structure during leaching. This might be explained by the low solubility of Ce(IV)-compounds (CeO 2 and/or Ce(OH) 4 ) in solution leading to an enrichment of this element at the glass/solution interface, to form a mixture of amorphous CeO 2 and Y(OH) 3 , as confirmed by XPS and XRD experiments

  14. Phase evolution and aqueous durability of Zr{sub 1−x−y}Ce{sub x}Nd{sub y}O{sub 2−y/2} ceramics designed to immobilize actinides with multi-valences

    Energy Technology Data Exchange (ETDEWEB)

    Ding, Yi, E-mail: dingyi2279@126.com [Institute of Nuclear Physics and Chemistry, China Academy of Engineering Physics, Mianyang, Sichuan, 621900 (China); Key Subject Laboratory of National Defense for Radioactive Waste and Environmental Security, Southwest University of Science and Technology, Mianyang 621010 (China); Long, Xinggui, E-mail: xingguil@caep.cn [Institute of Nuclear Physics and Chemistry, China Academy of Engineering Physics, Mianyang, Sichuan, 621900 (China); Peng, Shuming [Institute of Nuclear Physics and Chemistry, China Academy of Engineering Physics, Mianyang, Sichuan, 621900 (China); Zhang, Dong, E-mail: zd0823@sina.com [Institute of Nuclear Physics and Chemistry, China Academy of Engineering Physics, Mianyang, Sichuan, 621900 (China); Tan, Zhaoyi [Institute of Nuclear Physics and Chemistry, China Academy of Engineering Physics, Mianyang, Sichuan, 621900 (China); Lu, Xirui [Key Subject Laboratory of National Defense for Radioactive Waste and Environmental Security, Southwest University of Science and Technology, Mianyang 621010 (China)

    2017-04-15

    Zr{sub 1−x−y}Ce{sub x}Nd{sub y}O{sub 2−y/2} ceramics, which were designed as waste form materials, were obtained by simultaneous substitution of Ce{sup 4+} and Nd{sup 3+} for Zr{sup 4+} in ZrO{sub 2}. The influences of the simultaneous substitution of Ce and Nd on phase transformation of ZrO{sub 2} were investigated systematically. Also, the aqueous durability of the ceramics was evaluated. The results show that the phase transformation caused by the simultaneous substitution mainly relates to the total content of Ce and Nd. The ZrO{sub 2} ceramics containing Ce + Nd < 30 mol% exhibit both monoclinic and cubic phases, while the ceramics containing Ce + Nd ≥ 30 mol% are cubic phase. And the cubic phase can be stabilized by incorporating 30 mol% Ce + Nd. Moreover, LR{sub i} are modified by the incorporation of Ce and Nd, because of the presence of oxygen vacancies. The Nd and Ce co-doped zirconia waste form exhibit excellent aqueous durability (∼10{sup −5} g m{sup −2} d{sup −1}). - Highlights: •Zr{sub 1−x−y}Ce{sub x}Nd{sub y}O{sub 2−y/2} were obtained by substitution of Ce and Nd for Zr in ZrO{sub 2}. •Phase transformation mainly relates to the total content of Ce and Nd. •Samples with Ce + Nd < 30 mol% show monoclinic and cubic phases, while ≥30 mol% are cubic. •Stabilized cubic zirconia can be obtained by doping with 30 mol% Ce and Nd. •LR{sub Ce} and LR{sub Nd} (42 d) are ∼ 10{sup −5} g m{sup −2} d{sup −1}, exhibiting excellent aqueous durability.

  15. Preparation and properties of visible light responsive Y3+ doped Bi5Nb3O15 photocatalysts for Ornidazole decomposition

    International Nuclear Information System (INIS)

    Zhao, Jie; Yao, Binghua; He, Qiang; Zhang, Ting

    2012-01-01

    Highlights: ► A novel Y 3+ -Bi 5 Nb 3 O 15 material was prepared. ► Y 3+ -Bi 5 Nb 3 O 15 is firstly used for the photocatalytic degradation of Ornidazole. ► Possible pathway of Ornidazole degradation in aqueous solution is proposed. - Abstract: Nanoparticle of Bi 5 Nb 3 O 15 doped with Y 3+ was prepared for the first time by the sol–gel method combined with impregnation. The degradation of Ornidazole reacting with Y 3+ -Bi 5 Nb 3 O 15 was investigated to explore the feasibility of using Y 3+ -Bi 5 Nb 3 O 15 to treat antibiotics in wastewater. The products were characterized by X-ray diffraction, field emission scanning electron microscopy, transmission electron microscopy, high-resolution transmission electron microscopy, UV–vis diffuse reflectance spectrum and X-ray photoelectron spectroscopy. The results showed that the Y 3+ -Bi 5 Nb 3 O 15 exhibited single-crystalline orthorhombic structure with small particle size (20–100 nm); additionally, its UV–vis absorbance edges significantly shift to the visible-light region. The as-prepared nanoparticles exhibited a high photocatalytic activity in the decomposition of Ornidazole and several possible pathways of degradation of Ornidazole were proposed according to the results of ultra-performance liquid chromatography tandem mass spectrometry.

  16. Fabrication of highly conductive Ta-doped SnO2 polycrystalline films on glass using seed-layer technique by pulse laser deposition

    International Nuclear Information System (INIS)

    Nakao, Shoichiro; Yamada, Naoomi; Hitosugi, Taro; Hirose, Yasushi; Shimada, Toshihiro; Hasegawa, Tetsuya

    2010-01-01

    We discuss the fabrication of highly conductive Ta-doped SnO 2 (Sn 1-x Ta x O 2 ; TTO) thin films on glass by pulse laser deposition. On the basis of the comparison of X-ray diffraction patterns and resistivity (ρ) values between epitaxial films and polycrystalline films deposited on bare glass, we proposed the use of seed-layers for improving the conductivity of the TTO polycrystalline films. We investigated the use of rutile TiO 2 and NbO 2 as seed-layers; these are isostructural materials of SnO 2, which are expected to promote epitaxial-like growth of the TTO films. The films prepared on the 10-nm-thick seed-layers exhibited preferential growth of the TTO (110) plane. The TTO film with x = 0.05 on rutile TiO 2 exhibited ρ = 3.5 x 10 -4 Ω cm, which is similar to those of the epitaxial films grown on Al 2 O 3 (0001).

  17. [Structure and luminescence properties of Ga2O3 : Cr3+ by Al doping].

    Science.gov (United States)

    Wang, Xian-Sheng; Wan, Min-Hua; Wang, Yin-Hai; Zhao, Hui; Hu, Zheng-Fa; Li, Hai-Ling

    2013-11-01

    The Al doping gallate phosphor (Ga(1-x)Al(x))2O3 : Cr3+ (x = 0, 0.1, 0.2, 0.3, 0.4, 0.5) was synthesized by a high temperature solid-state reaction method. The X-ray diffractions show that the phase of the phosphors remains to be Ga2 O3 structure with increase in the contents of Al3+ ion. Beside, the fact that the X-ray diffraction peak shifts towards big angles with increasing Al3+ ions content shows that Al3+ ions entered the Ga2 O3 lattice. The peaks of the excitation spectra located at 258, 300, 410 and 550 nm are attributed to the band to band transition of the matrix, charge transfer band transition, and 4A2 --> 4T1 and 4A2 --> 4T2 transition of Cr3+ ions, respectively. Those excitation spectrum peak positions show different degrees of blue shift with the increase in the Al3+ ions content. The blue shift of the first two peaks are due to the band gap energy of substrate and the electronegativity between Cr3+ ions and ligands increasing, respectively. The blue shift of the energy level transition of Cr3+ ion is attributed to crystal field strength increasing. The Cr3+ ion luminescence changes from a broadband emission to a narrow-band emission with Al3+ doping, because the emission of Cr3+ ion changed from 4 T2 --> 4A2 to 2E --> 4A2 transition with the crystal field change after Al3+ ions doping. The Al3+ ions doping improved the long afterglow luminescence properties of samples, and the sample showed a longer visible near infrared when Al3+ ions content reaches 0.5. The thermoluminescence curve shows the sample with suitable trap energy level, and this is also the cause of the long afterglow luminescence materials.

  18. Low-temperature magnetic susceptibility of the solid solutions (ErxY1-x)3Al5O12

    International Nuclear Information System (INIS)

    Bagdasarov, Kh.S.; Dodokin, A.P.; Sorokin, A.A.

    1988-01-01

    Measurements of magnetic susceptibility of erbium-yttrium alumogarnets in the 0.04-4.2 K temperature range are carried out. (Er x I 1-x ) 3 Al 5 O 12 monocrystals were grown by the method of vertical directed crystallization. The specimens were produced as 5 cm high cylinders 0.63 cm in diameter; the axis of the cylinders coincided with the (100) direction of the crystals. Magnetic susceptibility was measured by the Harsthorn bridge method at the frequency of 33 Hz. The analysis of measurement results shows that susceptibility of the investigated crystals at T >or approx. 2T N is well described by the Curie-Weiss law. Existence of threshold concentration of the magnetic component testifies to an essential role of exchange interactions in establishment of the magnetic order in Er 3 Al 5 O 12

  19. Superconducting properties of Zn and Al double-doped Mg1-x(Zn0.5Al0.5)xB2

    DEFF Research Database (Denmark)

    Xu, G.J.; Grivel, Jean-Claude; Abrahamsen, A.B.

    2004-01-01

    (XRD), ac susceptibility, magnetization and resistivity. The double doping leads to decreases in both the lattice parameters a and c, and the T-c decreases with increasing dopant content. A systematical comparison with Al doped- and Li, Al double doped MgB2 of structure, superconducting transition......A series of polycrystalline samples of Mg1-x(Zn0.5Al0.5)(x)B-2 (0less than or equal toxless than or equal to0.8) were prepared by solid state reaction method and their structure, superconducting transition temperature (T-c) and transport properties were investigated by means of X-ray diffraction...

  20. Enhanced photorefractive properties in Hf, Ce and Cu co-doped LiNbO{sub 3} crystals for holographic application

    Energy Technology Data Exchange (ETDEWEB)

    Zhang, Tao, E-mail: tzhang_hit02@yahoo.com [Key Laboratory of In-fiber Integrated Optics, Ministry of Education of China, Harbin Engineering University, Harbin 150001 (China); College of Science, Harbin Engineering University, Harbin 150001 (China); Postdoctoral Research Station of Mechanical Engineering, College of Mechanical and Electrical Engineering, Harbin Engineering University, Harbin 150001 (China); Wang, Xin; Geng, Tao; Tong, Chengguo [Key Laboratory of In-fiber Integrated Optics, Ministry of Education of China, Harbin Engineering University, Harbin 150001 (China); College of Science, Harbin Engineering University, Harbin 150001 (China); Kang, Chong [Key Laboratory of In-fiber Integrated Optics, Ministry of Education of China, Harbin Engineering University, Harbin 150001 (China); College of Science, Harbin Engineering University, Harbin 150001 (China); Postdoctoral Research Station of Mechanical Engineering, College of Mechanical and Electrical Engineering, Harbin Engineering University, Harbin 150001 (China)

    2015-04-25

    Graphical abstract: Correlation spots of 200 holograms in a Hf, Ce and Cu co-doped LiNbO{sub 3}. - Highlights: • Several doped LiNbO{sub 3} crystals with various level of Hf doping were grown by Cz method. • IR peak shift is attributed to the complex defect change at different level of Hf. • Enhanced photorefractive properties have been got with higher Hf-doping level. • Reduced defect and increased photoconductivity are responsible for optical properties. • 200 holograms’ experiment is realized in a coherent volume 0.073 cm{sup 3}. - Abstract: Hf, Ce and Cu co-doped LiNbO{sub 3} crystals with various level of Hf doping were grown in air by a conventional Cz method. The infrared spectra were measured to discuss the defect structures and the mechanism of the absorption peak shift in these crystals. The light-induced scattering of the crystals was evaluated by the transmitted light method. The influence of the Hf-doping level on the photorefractive properties of Hf, Ce and Cu co-doped LiNbO{sub 3} crystals was studied via two-beam coupling. It is found that proper doping Hf is an efficient method to enhance the comprehensive photorefractive properties of the LiNbO{sub 3}. Using one of these crystals as medium, 200 holograms storage and correlation experiments based on angle fractal multiplexing have been realized in a coherent volume 0.073 cm{sup 3}. Moreover the diffraction efficiency is uniform and the storage density has reached 2.2 Gb/cm{sup 3}.

  1. Crystal growth and scintillation properties of Ce and Eu doped LiSrAlF{sub 6}

    Energy Technology Data Exchange (ETDEWEB)

    Yamaji, Akihiro, E-mail: yamaji-a@imr.tohoku.ac.jp [Institute of Materials Research, Tohoku University, 2-1-1 Katahira, Aoba-ku, Sendai 980-8577 (Japan); Yanagida, Takayuki [New Industry Creation Hatchery Center (NICHe), Tohoku University, 6-6-10 Aoba, Aramaki, Aoba-ku, Sendai 980-8579 (Japan); Kawaguchi, Noriaki [Tokuyama Corporation, Shibuya 3-chome, Shibuya, Tokyo 150-8383 (Japan); Fujimoto, Yutaka; Yokota, Yuui [Institute of Materials Research, Tohoku University, 2-1-1 Katahira, Aoba-ku, Sendai 980-8577 (Japan); Watanabe, Kenichi; Yamazaki, Atsushi [Department of Material, Physics and Energy Engineering, Nagoya University, Furo-cho, Chikusa-ku, Nagoya, 464-8603 (Japan); Yoshikawa, Akira [Institute of Materials Research, Tohoku University, 2-1-1 Katahira, Aoba-ku, Sendai 980-8577 (Japan); New Industry Creation Hatchery Center (NICHe), Tohoku University, 6-6-10 Aoba, Aramaki, Aoba-ku, Sendai 980-8579 (Japan); Pejchal, Jan [Institute of Physics AS CR, Cukrovarnicka 10, 16200 Prague 6 (Czech Republic)

    2011-12-11

    Ce and Eu doped LiSrAlF{sub 6} (LiSAF) single crystals for the neutron detection with different dopant concentrations were grown by the micro-pulling-down method ({mu}-PD). In Ce:LiSAF, intense emission peaks due to Ce{sup 3+} 5d-4f transitions were observed at approximately 315 and 335 nm in photo- and {alpha}-ray induced radio-luminescence spectra. In case of Eu:LiSAFs, an intense emission peak at 375 nm due to Eu{sup 2+} 5d-4f transition was observed in the radio-luminescence spectra. The pulse height spectra and decay time profiles were measured under {sup 252}Cf neutron irradiation to examine the neutron response. The Ce 3% and Eu 2% doped LiSAF showed the highest light yield of 2860 ph/n with 19 ns main decay time component and 24,000 ph/n with 1610 ns.

  2. Preparation and characterization of carbonate terminated polycrystalline Al2O3/Al films

    International Nuclear Information System (INIS)

    Tornow, C.; Noeske, P.-L.M.; Dieckhoff, S.; Wilken, R.; Gaertner, K.

    2005-01-01

    X-ray photoelectron spectroscopy (XPS) was applied to investigate the surface reactivity of polycrystalline Al films in contact with a gas mixture of carbon dioxide and oxygen at room temperature. Based on the characterization of interactions between these substrates and the individual gases at selected exposures, various surface functionalities were identified. Simultaneously dosing both carbon dioxide and oxygen is shown to create surface-terminating carbonate species, which contribute to inhibiting the formation of an Al 2 O 3 layer. Finally, a reaction scheme is suggested to account for the observed dependence of surface group formation on the dosing conditions

  3. Preparation and studies of Eu{sup 3+} and Tb{sup 3+} co-doped Gd{sub 2}O{sub 3} and Y{sub 2}O{sub 3} sol-gel scintillating films

    Energy Technology Data Exchange (ETDEWEB)

    Morales Ramirez, A. de J, E-mail: amoralesra@ipn.m [Centro de Investigacion en Ciencia Aplicada y Tecnologia Avanzada (CICATA) Unidad Altamira Instituto Politecnico Nacional Km. 14.5 Carr. Tampico-Puerto Industrial, C.P. 89600, Altamira, Tamaulipas (Mexico); Depto. de Ingenieria Metalurgica, ESIQIE-Instituto Politecnico Nacional UPALM C.P. 07738, Mexico D.F. (Mexico); Garcia Murillo, A.; Carrillo Romo, F. de J [Depto. de Ingenieria Metalurgica, ESIQIE-Instituto Politecnico Nacional UPALM C.P. 07738, Mexico D.F. (Mexico); Ramirez Salgado, J. [Programa de Ingenieria Molecular, Instituto Mexicano del Petroleo, Eje Lazaro Cardenas No. 152, CP 07730, Mexico D.F. (Mexico); Le Luyer, C. [LPCML, CNRS-UMR 5620/Universite Claude Bernard Lyon 1/69622 Villeurbanne Cedex (France); Chadeyron, G.; Boyer, D. [Laboratoire des Materiaux Inorganiques, CNRS-UMR 6002, Universite Blaise Pascal, 24 Ave des Landais F 63177 Aubiere Cedex (France); Moreno Palmerin, J. [Depto. de Ingenieria Metalurgica, ESIQIE-Instituto Politecnico Nacional UPALM C.P. 07738, Mexico D.F. (Mexico)

    2009-10-30

    Eu{sup 3+} (2.5 at.%) and Tb{sup 3+} (0.005-0.01 at.%) co-doped gadolinium and yttrium oxide (Gd{sub 2}O{sub 3} and Y{sub 2}O{sub 3}) powders and films have been prepared using the sol-gel process. High density and optical quality thin films were prepared with the dip-coating technique. Gadolinium (III) 2,4-pentadionate and yttrium (III) 2,4-pentadionate were used as precursors, and europium and terbium in their nitrate forms were used as doping agents. Chemical and structural analyses (infrared spectroscopy, X-ray diffraction and high-resolution transmission electron microscopy) were conducted on both sol-gel precursor powders and dip-coated films. The morphology of thin films heat-treated at 700 {sup o}C was studied by means of atomic force microscopy. It was shown that the highly dense and very smooth films had a root mean roughness (RMS) of 2 nm {+-} 0.2 (A = 0.0075 Tb{sup 3+}) and 24 nm {+-} 3.0 (B = 0.01 Tb{sup 3+}). After treatment at 700 {sup o}C, the crystallized films were in the cubic phase and presented a polycrystalline structure made up of randomly oriented crystallites with grain sizes varying from 20 to 60 nm. The X-ray induced emission spectra of Eu{sup 3+}- and Tb{sup 3+}-doped Gd{sub 2}O{sub 3} and Y{sub 2}O{sub 3} powders showed that Tb{sup 3+} contents of 0.005, 0.0075 and 0.01 at.% affected their optical properties. Lower Tb{sup 3+} concentrations (down to 0.005 at.%) in both systems enhanced the light yield.

  4. Atomic layer deposition of Al-doped ZnO thin films

    Energy Technology Data Exchange (ETDEWEB)

    Tynell, Tommi; Yamauchi, Hisao; Karppinen, Maarit; Okazaki, Ryuji; Terasaki, Ichiro [Department of Chemistry, Aalto University, FI-00076 Aalto (Finland); Department of Physics, Nagoya University, Nagoya 464-8602 (Japan)

    2013-01-15

    Atomic layer deposition has been used to fabricate thin films of aluminum-doped ZnO by depositing interspersed layers of ZnO and Al{sub 2}O{sub 3} on borosilicate glass substrates. The growth characteristics of the films have been investigated through x-ray diffraction, x-ray reflection, and x-ray fluorescence measurements, and the efficacy of the Al doping has been evaluated through optical reflectivity and Seebeck coefficient measurements. The Al doping is found to affect the carrier density of ZnO up to a nominal Al dopant content of 5 at. %. At nominal Al doping levels of 10 at. % and higher, the structure of the films is found to be strongly affected by the Al{sub 2}O{sub 3} phase and no further carrier doping of ZnO is observed.

  5. Luminescence, scintillation, and energy transfer in SiO{sub 2}-Al{sub 2}O{sub 3}-B{sub 2}O{sub 3}-Gd{sub 2}O{sub 3}:Ce{sup 3+},Pr{sup 3+} glasses

    Energy Technology Data Exchange (ETDEWEB)

    Lertloypanyachai, Prapon; Chewpraditkul, Weerapong; Pattanaboonmee, Nakarin [Department of Physics, King Mongkut' s University of Technology Thonburi, Bangkok (Thailand); Chen, Danping [Shanghai Institute of Optics and Fine Mechanics, Chinese Academy of Sciences, Shanghai (China); Babin, Vladimir; Beitlerova, Alena; Nikl, Martin [Institute of Physics, AS CR, Prague (Czech Republic)

    2017-09-15

    Ce{sup 3+},Pr{sup 3+}-codoped SiO{sub 2}-Al{sub 2}O{sub 3}-B{sub 2}O{sub 3}-Gd{sub 2}O{sub 3} glasses (SABG:Ce,Pr) were prepared by melt quenching under a CO reducing atmosphere. Luminescence properties were investigated under UV and X-ray excitations. A dominant emission band at 430 nm belonging to the Ce{sup 3+}:5d{sub 1} → 4f transition was observed in the photo- and radio-luminescence spectra. The energy transfer occurs from this Ce{sup 3+} band toward the {sup 3}P{sub J} levels of Pr{sup 3+} with an efficiency of up to 24%, followed by the reduction of integrated luminescence intensity with an increasing Pr{sup 3+} concentration. This result is attributed to the increase in the reabsorption of Ce{sup 3+} luminescence and the non-radiative energy transfer toward the {sup 3}P{sub J} levels of Pr{sup 3+}. The cross-relaxation process within the Pr{sup 3+} pairs can further diminish the total luminescence yield at high Pr{sup 3+} concentrations. The integral scintillation efficiency and light yield measurements were carried out and compared to the reference Bi{sub 4}Ge{sub 3}O{sub 12} (BGO) crystal. (copyright 2017 WILEY-VCH Verlag GmbH and Co. KGaA, Weinheim)

  6. Microestructura de Al2O3/TZP codopado con Fe2O3 y TiO2 fabricado por reacción (RBAO

    Directory of Open Access Journals (Sweden)

    Jiménez, M.

    2003-02-01

    Full Text Available Reaction-bonded 80 vol% Al2O3/TZP (2 mol% Y2O3-stabilized tetragonal zirconia polycrystals composites co-doped with 1 vol% Fe2O3 and 1 vol% TiO2 have been produced, and then presureless sintered (1450 ºC, 60 min or sinter-forged (20 MPa, 1200 ºC, 60 min. The resulting microstructures have been characterized using scanning electron microscopy. Both types of materials are dense, with a fine and homogeneous dual microstructure consisting of Al2O3 and TZP grains without intermediate grain boundary phases. Sinter-forged composites exhibit a very narrow pore size distribution, essentially smaller than the grain size of the alumina and zirconia phases. Co-doping promotes the sintering of alumina at lower temperatures, while still retains a fine grain size due to the presence of the dispersed zirconia phase. First results on presureless sintered RBAO materials show a fracture strength higher than in conventionally sintered and sinter-forged composites.Se han fabricado compuestos de 80% vol. Al2O3/TZP (ZrO2 estabilizada con 2% mol Y2O3 codopados con 1% vol. Fe2O3 y 1% vol. TiO2 mediante la tecnología RBAO (“Reaction Bonding of Aluminum Oxide”, que se han sinterizado libremente (1450 ºC, 60 min y bajo carga uniaxial (20 MPa, 1200 ºC, 60 min. Se ha caracterizado la microestructura mediante microscopía electrónica de barrido. Ambos materiales son densos con una microestructura homogénea formada por granos de alúmina y de circona, sin fases en juntas de grano. En el caso de la sinterización bajo carga, la distribución del tamaño de los poros es muy estrecha, y esencialmente menor que las correspondientes a los granos de Al2O3 y TZP. El codopado promueve la sinterización de la alúmina, mientras que los granos dispersos de circona inhiben su crecimiento de grano. Los ensayos preliminares de flexión en cuatro puntos realizados sobre los materiales sinterizados sin carga indican una resistencia a la fractura superior a la que presentan los

  7. Eu3+-doped Y2O3 hexagonal prisms: Shape-controlled synthesis and tailored luminescence properties

    International Nuclear Information System (INIS)

    Yang, Errui; Li, Guangshe; Fu, Chaochao; Zheng, Jing; Huang, Xinsong; Xu, Wen; Li, Liping

    2015-01-01

    In this work, Eu 3+ doped Y 2 O 3 hexagonal prisms were synthesized by a novel two-phase approach, which involves water at the bottom as aqueous phase and oleylamine in the above as oil phase. With this unique reaction system, precursors of hexagonal prisms Y 4 O(OH) 9 (NO 3 ) were first obtained by simply varying the volume ratio of water to oleylamine. Time-dependent experiments were systematically performed to reveal the growth mechanism of the precursor. After subsequent heat treatment, these precursors transformed to Y 2 O 3 hexagonal prisms with controlled diameters and aspect ratios varying from 4 to 19. Such a transformation is preceded via a topotactic process, as indicated by TG-DTA and mass spectra. Eventually, all Eu 3+ doped Y 2 O 3 hexagonal prisms were found to exhibit an intensive red emission at 611 nm, which corresponds to 5 D 0 → 7 F 2 transition of Eu 3+ . With varying the aspect ratio of hexagonal prisms and increasing Eu 3+ concentration in Y 2 O 3 , an optimum external quantum efficiency was achieved. - Graphical abstract: In this work, Eu 3+ doped Y 2 O 3 hexagonal prisms with controlled aspect ratio from 4.4 to 19.3 were synthesized by transformation of the precursor Y 4 O(OH) 9 (NO 3 ) hexagonal prisms from a novel two-phase reaction system. The growth mechanism of the precursor has been systematically investigated, and a topotactic phase transformation from precursors to cubic Y 2 O 3 is for the first time put forward. By the size controlling and aspect ratio adjusting, the luminescence emission intensity as well as external quantum efficiency of Eu 3+ doped Y 2 O 3 hexagonal prisms is further tailored to show an optimum. - Highlights: • Eu 3+ doped Y 2 O 3 hexagonal prisms were synthesized by a novel two-phase approach. • Inheriting mechanism of prisms morphology from Y 4 O(OH) 9 (NO 3 ) to Y 2 O 3 was discussed. • Aspect ratio of prisms was tailored by the volume ratio of water to oleylamine. • Luminescence properties were

  8. Room-temperature ferromagnetism in pure and Co doped CeO2 powders

    International Nuclear Information System (INIS)

    Wen Qiye; Zhang Huaiwu; Song Yuanqiang; Yang Qinghui; Zhu Hao; Xiao, John Q

    2007-01-01

    We report the room-temperature (RT) ferromagnetism (FM) observed in pure and Co doped CeO 2 powder. An insulating nonmagnetic CeO 2 single crystal, after grinding into fine powder, shows an RT-FM with a small magnetization of 0.0045 emu g -1 . However, the CeO 2 powder became paramagnetic after oxygen annealing, which strongly suggests an oxygen vacancy meditated FM ordering. Furthermore, by doping Co into CeO 2 powder the FM can significantly enhance through a F-centre exchange (FCE) coupling mechanism, in which both oxygen vacancies and magnetic ions are involved. As the Co content increases, the FM of Co doped CeO 2 initially increases to a maximum 0.47 emu g -1 , and then degrades very quickly. The complex correlation between the Co content and saturation magnetization was well interpreted by supposing the coexistence of three subsets of Co ions in CeO 2 . Our results reveal that the large RT-FM observed in Co doped CeO 2 powder originates from a combination effect of oxygen vacancies and transition metal doping

  9. Investigating the effect of Mn-doped CeO2 nanoparticles by co-precipitation method

    International Nuclear Information System (INIS)

    Prabaharan, D.D.M.; Sadaiyandi, K.; Mahendran, M.; Sagadevan, Suresh

    2018-01-01

    The paper exhibits a detailed study about the synthesis and characterization in analysis of structural, morphological, optical and electrical investigations of pure and Mn-doped Cerium oxide (CeO 2 ) nanoparticles which were synthesized by co-precipitation technique. Phase formation of the prepared sample was analyzed with powder X-ray diffraction (PXRD) examines, scanning electron microscopy (SEM) examination. The PXRD comes about affirmed partial crystallinity having cubic phases and the crystallite sizes of the pure and Mn-doped Cerium oxide (CeO 2 ) were estimated by utilizing Debye-Scherrer's formula and they were calculated to be 12 and 14 nm individually. SEM pictures revealed that the particles were profoundly accumulated and were of permeable nature. The optical properties of pure and Mn-doped CeO 2 were ascertained by using UV-visible absorption spectrum. The estimated band gap values for the pure and the Mn-doped CeO 2 nanoparticles were observed to be 2.7 and 2.6 eV, respectively, utilizing UV-Vis spectroscopy. At different frequencies and temperatures the dielectric properties of the Mn-doped Cerium oxide (CeO 2 ) nanoparticles, for example, the dielectric consistent, the dielectric loss and the AC conductivity, were studied. (orig.)

  10. Electron paramagnetic resonance investigation of polycrystalline CaCu{sub 3}Ti{sub 4}O{sub 12}

    Energy Technology Data Exchange (ETDEWEB)

    Mozzati, Maria Cristina [INFM-Dipartimento di Fisica ' Alessandro Volta' , Universita di Pavia, via Bassi 6, I-27100 Pavia (Italy); Azzoni, Carlo Bruno [INFM-Dipartimento di Fisica ' Alessandro Volta' , Universita di Pavia, via Bassi 6, I-27100 Pavia (Italy); Capsoni, Doretta [Dipartimento di Chimica Fisica ' Mario Rolla' , Universita di Pavia and IENI-CNR, Sezione di Pavia, viale Taramelli 16, I-27100 Pavia (Italy); Bini, Marcella [Dipartimento di Chimica Fisica ' Mario Rolla' , Universita di Pavia and IENI-CNR, Sezione di Pavia, viale Taramelli 16, I-27100 Pavia (Italy); Massarotti, Vincenzo [Dipartimento di Chimica Fisica ' Mario Rolla' , Universita di Pavia and IENI-CNR, Sezione di Pavia, viale Taramelli 16, I-27100 Pavia (Italy)

    2003-11-05

    Electron paramagnetic resonance (EPR) measurements on pure polycrystalline CaCu{sub 3}Ti{sub 4}O{sub 12} have been performed and are discussed within a crystal-field approach. A symmetric signal centred at g = 2.15 is observed for T>25 K, with no evidence of hyperfine structure. At this temperature an antiferromagnetic transition is observed as confirmed by static magnetization data. Cu defective and 2% doped (V, Cr, Mn, La) samples were also prepared and considered, mainly to understand the nature of the observed paramagnetic centre. Substitutions in the octahedral sites, causing variations of the configuration in CuO{sub 4}-TiO{sub 6}-CuO{sub 4} complexes, change the magnetic and EPR features. To justify the EPR response a strong copper-hole delocalization is suggested.

  11. Development and characterization of nickel catalysts supported in CeO{sub 2}-ZrO{sub 2}-Al{sub 2}O{sub 3}, CeO{sub 2}-La{sub 2}O{sub 3}-Al{sub 2}O{sub 3} e ZrO{sub 2}-La{sub 2}O{sub 3}-Al{sub 2}O{sub 3} matrixes evaluated for methane reforming reactions; Desenvolvimento e caracterização de catalisadores de níquel suportados em matrizes CeO{sub 2}-ZrO{sub 2}-Al{sub 2}O{sub 3}, CeO{sub 2}-La{sub 2}O{sub 3}-Al{sub 2}O{sub 3} e ZrO{sub 2}-La{sub 2}O{sub 3}-Al{sub 2}O{sub 3} avaliados para as reações de reforma do metano

    Energy Technology Data Exchange (ETDEWEB)

    Abreu, Amanda Jordão de

    2012-07-01

    Nowadays, the methane reforming is large interest industrial for the take advantage of these gas in production the hydrogen and synthesis gas (syngas). Among in the reactions of methane stand of the reactions steam reforming and carbon dioxide reforming of methane. The main catalysts uses in the methane reforming is Ni/Al{sub 2}O{sub 3}. However, the supported-nickel catalyst is susceptible to the deactivation or the destruction by coke deposition. The carbon dissolves in the nickel crystallite and its diffuses through the nickel, leading for formation of the carbon whiskers, which results in fragmentation of the catalyst. Modification of such catalysts, like incorporation of suitable promoters, is desirable to achieve reduction of the methane hydrogenolysis and/or promotion of the carbon gasification. Catalysts 5%Ni/Al{sub 2}O{sub 3} supported on solid solutions formed by ZrO{sub 2}-CeO{sub 2}, La{sub 2}O{sub 3} and CeO{sub 2}-ZrO{sub 2}-La{sub 2}O{sub 3} were prepared, characterized and evaluated in reactions steam and carbon dioxide reforming and partial oxidation of methane with objective the value effect loading solution solid in support. The supports were prepared by co-precipitation method and catalysts were prepared by impregnation method and calcined at 500 deg C. The supports and catalysts were characterized by Nitrogen Adsorption, method -rays diffraction (XRD), X-rays dispersive spectroscopy (XDS), spectroscopy in the region of the ultraviolet and the visible (UV-vis NIR) to and temperature programmed reduction (TPR), Raman Spectroscopy, X-ray absorption spectroscopy and Thermogravimetric Analysis. After all the catalytic reactions check which the addition of solid solution is beneficial for Ni/Al{sub 2}O{sub 3} catalysts and the best catalysts are Ni/CeO{sub 2}-La{sub 2}O{sub 3}-Al{sub 2}O{sub 3}. (author)

  12. Effect of Annealing Time of YAG:Ce3+ Phosphor on White Light Chromaticity Values

    Science.gov (United States)

    Abd, Husnen R.; Hassan, Z.; Ahmed, Naser M.; Almessiere, Munirah Abdullah; Omar, A. F.; Alsultany, Forat H.; Sabah, Fayroz A.; Osman, Ummu Shuhada

    2018-02-01

    Yttrium and aluminium nitrate phosphors doped with cerium nitrate and mixed with urea (fuel) are prepared by using microwave-induced combustion synthesis according to the formula Y(3-0.06)Al5O12:0.06Ce3+ (YAG:Ce3+) to produce white light emitting diodes by conversion from blue indium gallium nitride-light emitting diode chips. The sintering time with fixed temperature (1050°C) for phosphor powder was optimized and found to be 5 h. The crystallinity, structure, chemical composition, luminescent properties with varying currents densities and chromaticity were characterized by x-ray diffraction, field emission-scanning electron microscopy, transmission electron microscopy, energy dispersive spectroscopy, photoluminescence emission, electroluminescence and standard CIE 1931 chromaticity diagram, respectively. The energy levels of Ce3+ in YAG were discussed based on its absorption and excitation spectra. The results show that the obtained YAG:Ce3+ phosphor sintered for 5 h has good crystallinity with pure phase, low agglomerate with spherical shaped particles and strong yellow emission, offering cool-white LED with tuneable correlated color temperature and a good color rendering index compared to those prepared by sintering for 2 h and as-prepared phosphor powders.

  13. Photoluminescence and excited state structure in Bi3+-doped Y2SiO5 single crystalline films

    International Nuclear Information System (INIS)

    Babin, V.; Gorbenko, V.; Krasnikov, A.; Mihokova, E.; Nikl, M.; Zazubovich, S.; Zorenko, Yu.

    2013-01-01

    Single crystalline films of Bi-doped Y 2 SiO 5 are studied at 4.2–350 K by the time-resolved luminescence methods under excitation in the 3.8–6.2 eV energy range. Ultraviolet luminescence of Y 2 SiO 5 :Bi (≈3.6 eV) is shown to arise from the radiative decay of the metastable and radiative minima of the triplet relaxed excited state (RES) of Bi 3+ centers which are related to the 3 P 0 and 3 P 1 levels of a free Bi 3+ ion, respectively. The lowest-energy excitation band of this emission, located at ≈4.5 eV, is assigned to the 1 S 0 → 3 P 1 transitions of a free Bi 3+ ion. The phenomenological model is proposed to describe the excited-state dynamics of Bi 3+ centers in Y 2 SiO 5 :Bi, and parameters of the triplet RES are determined. -- Highlights: •Luminescence of Y 2 SiO 5 :Bi is investigated for the first time. •Ultraviolet emission arises from Bi 3+ ions located in Y lattice sites. •The triplet relaxed excited states parameters of Bi 3+ centers are determined

  14. Luminescence and scintillation properties of YAG:Ce single crystal and optical ceramics

    CERN Document Server

    Mihóková, E; Mareš, J A; Beitlerová, A; Vedda, A; Nejezchleb, K; Blažek, K; D’Ambrosio, C

    2007-01-01

    We use various techniques to study optical and scintillation properties of Ce-doped yttrium aluminum garnet, Y3Al5O12 (YAG:Ce), in the form of a high-quality industrial single crystal. This was compared to optical ceramics prepared from YAG:Ce nanopowders. We present experimental data in the areas of optical absorption, radioluminescence, scintillation decay, photoelectron yield, thermally stimulated luminescence and radiation-induced absorption. The results point to an interesting feature—the absence of antisite (YAl, i.e. Y at the Al site) defects in optical ceramics. The scintillation decay of the ceramics is faster than that of the single crystal, but its photoelectron yield (measured with 1 μs integration time) is about 30–40% lower. Apart from the photoelectron yield value the YAG:Ce optical ceramic is fully comparable to a high quality industrial YAG:Ce single crystal and can become a competitive scintillator material.

  15. Structure and superconductivity of double-doped Mg1-x(Al0.5Li0.5)xB2

    DEFF Research Database (Denmark)

    Xu, G.J.; Grivel, Jean-Claude; Abrahamsen, A.B.

    2003-01-01

    A series of polycrystalline samples of Mg1-x(Al0.5Li0.5)(x)B-2 (0less than or equal toxless than or equal to0.6) were prepared by a solid state reaction method and their structure, superconducting transition temperature and magneto-transport properties were investigated by means of X-ray diffract......A series of polycrystalline samples of Mg1-x(Al0.5Li0.5)(x)B-2 (0less than or equal toxless than or equal to0.6) were prepared by a solid state reaction method and their structure, superconducting transition temperature and magneto-transport properties were investigated by means of X......-ray diffraction (XRD), ac-susceptibility and resistance in varied magnetic fields. The double doping leads to decreases in both the lattice parameters a and c. The superconducting transition temperature (T-c) decreases with double doping, but the T-c is systematically higher than that of the single Al......-doped samples. It is suggested that the hole band filling has little effect on T-c at high doping level, while the disorder induced by doping plays an important role in suppressing T-c. A systematic comparison with Al-doped MgB2 of the structure, superconducting transition and irreversibility field is made. (C...

  16. Free carrier absorption in self-activated PbWO_4 and Ce-doped Y_3(Al_0.25Ga_0.75)_3O_12 and Gd_3Al_2Ga_3O_12 garnet scintillators

    CERN Document Server

    Auffray, E.; M.T. Lucchini; S. Nargelas; O. Sidletskiy; G. Tamulaitis; Y. Tratsiak; A. Vaitkevičius

    2016-01-01

    tungstate (PbWO_4, PWO) ant two garnet crystals, GAGG:Ce and YAGG:Ce. It was shown that free electrons appear in the conduction band of PWO and YAGG:Ce crystals within a sub-picosecond time scale, while the free holes in GAGG:Ce appear due to delocalization from Gd^3+ ground states to the valence band within a few picoseconds after short-pulse excitation. The influence of Gd ions on the nonequilibrium carrier dynamics is discussed on the base of comparison the results of the free carrier absorption in GAGG:Ce containing gadolinium and in YAGG without Gd in the host lattice.

  17. Influence of microgravity on Ce-doped Bi12 SiO20 crystal defect

    Indian Academy of Sciences (India)

    TECS

    studied by comparing space grown BSO crystal with ground grown one. These results show ... fractive properties (Aldrich et al 1971; Peltier and. Micheron ... The shape of interface changes from concave to convex by suppressing ... cations. Figure 1. Parts of Ce doped BSO crystals: (a) space growth and (b) ground growth.

  18. Sensitization by UV light of α-Al2O3:C polycrystalline detectors

    International Nuclear Information System (INIS)

    Meira B, L. C.; Rubio F, H.; Neres de A, E.; Santos, A.

    2014-08-01

    This paper describes an increase in sensitivity to gamma and beta radiation on α-Al 2 O 3 :C polycrystalline detector, which has been produced by a sol-gel process, following previous exposure to ultraviolet light. The increased sensitivity of the detector as a function of the exposure time and ultraviolet wavelength was studied. Since the main luminescent centers have emission peaks at different wavelengths, selective measurements of thermoluminescent emission intensity were done, in order to investigate the possible conversion of centers as a result of the exposition to ultraviolet light. Experimental results indicate that the nature and parameters of the luminescent centers in α-Al 2 O 3 :C sol-gel material can be very different of those in α-Al 2 O 3 :C single crystal. (author)

  19. Synthesis of Cu and Ce co-doped ZnO nanoparticles: crystallographic, optical, molecular, morphological and magnetic studies

    Directory of Open Access Journals (Sweden)

    Rawat Mohit

    2017-07-01

    Full Text Available In the present research work, crystallographic, optical, molecular, morphological and magnetic properties of Zn1-xCuxO (ZnCu and Zn1-x-yCeyCuxO (ZnCeCu nanoparticles have been investigated. Polyvinyl alcohol (PVA coated ZnCu and ZnCeCu nanoparticles have been synthesized by chemical sol-gel method and thoroughly studied using various characterization techniques. X-ray diffraction pattern indicates the wurtzite structure of the synthesized ZnCu and ZnCeCu particles. Transmission electron microscopy analysis shows that the synthesized ZnCu and ZnCeCu particles are of spherical shape, having average sizes of 27 nm and 23 nm, respectively. The incorporation of Cu and Ce in the ZnO lattice has been confirmed through Fourier transform infrared spectroscopy. Room temperature photoluminescence spectra of the ZnO doped with Cu and co-doped Ce display two emission bands, predominant ultra-violet near-band edge emission at 409.9 nm (3 eV and a weak green-yellow emission at 432.65 nm (2.27 eV. Room temperature magnetic study confirms the diamagnetic behavior of ZnCu and ferromagnetic behavior of ZnCeCu.

  20. A computational study of magnetic exchange interactions of 3d and 4f electrons in Ti-Ce co-doped AlN

    Energy Technology Data Exchange (ETDEWEB)

    Majid, Abdul, E-mail: abdulmajid40@yahoo.com [Department of Physics, University of Gujrat, Gujrat (Pakistan); Department of Adaptive Machine Systems, Osaka University, Osaka (Japan); Azmat, Mian [Department of Physics, University of Gujrat, Gujrat (Pakistan); Rana, Usman Ali; Khan, Salah Ud-Din [Sustainable Energy Technologies Center, College of Engineering, King Saud University, PO-Box 800, Riyadh 11421 (Saudi Arabia); Alzahrani, Eman [Department of Chemistry, Faculty of Science, Taif University, 888 Taif (Saudi Arabia)

    2016-08-15

    To investigate the nature of 3d-4f exchange interactions in III-Nitride semiconductors, Ti-Ce co-doped AlN were studied using first principles calculations. The calculations were performed using supercell approach with varying dopant concentration and different inter-dopant separation. The configuration with dopant located as nearest neighbor distance and diluted concentration of 3.125% was found most stable. The results exhibited prominent evidence of 3d-4f-5d strong hybridization suggesting 3d-4f direct exchange interactions which may play valuable role to exploit the system as high Curie temperature ferromagnetic semiconductors for use in spintronics. Moreover, metal to metal charge transfer was also observed in the materials which may be exploited for their use in electrochemical applications. The 4f-5d and 3d-5d hybridizations were observed that predicts excellent luminescence phenomena in the materials. The presence of impurity related deep intermediate bands suggest applications of the materials in opto-electronic and spintronics devices. - Highlights: • Double exchange interaction in Ti:AlN. • Impurity induced narrowing of band gap. • Superexchange interaction in Ce:AlN. • 3d-4f exchange interaction between Ti-3d and Ce-4f states. • High Curie temperature n-type ferromagnetic semiconductors.

  1. A computational study of magnetic exchange interactions of 3d and 4f electrons in Ti-Ce co-doped AlN

    International Nuclear Information System (INIS)

    Majid, Abdul; Azmat, Mian; Rana, Usman Ali; Khan, Salah Ud-Din; Alzahrani, Eman

    2016-01-01

    To investigate the nature of 3d-4f exchange interactions in III-Nitride semiconductors, Ti-Ce co-doped AlN were studied using first principles calculations. The calculations were performed using supercell approach with varying dopant concentration and different inter-dopant separation. The configuration with dopant located as nearest neighbor distance and diluted concentration of 3.125% was found most stable. The results exhibited prominent evidence of 3d-4f-5d strong hybridization suggesting 3d-4f direct exchange interactions which may play valuable role to exploit the system as high Curie temperature ferromagnetic semiconductors for use in spintronics. Moreover, metal to metal charge transfer was also observed in the materials which may be exploited for their use in electrochemical applications. The 4f-5d and 3d-5d hybridizations were observed that predicts excellent luminescence phenomena in the materials. The presence of impurity related deep intermediate bands suggest applications of the materials in opto-electronic and spintronics devices. - Highlights: • Double exchange interaction in Ti:AlN. • Impurity induced narrowing of band gap. • Superexchange interaction in Ce:AlN. • 3d-4f exchange interaction between Ti-3d and Ce-4f states. • High Curie temperature n-type ferromagnetic semiconductors.

  2. Physicochemical compatibility of SrCeO3 with potential SOFC cathodes

    International Nuclear Information System (INIS)

    Tolchard, J.; Grande, T.

    2007-01-01

    The chemical and physical compatibility of SrCeO 3 is investigated with respect to LaMO 3 (M=Mn, Fe, Co) and La 2-x Sr x NiO 4 (x=0, 0.8), via the reaction of fine-grained powder compacts and solid-state diffusion couples. Compositions were chosen so as to give predictive insight into possible candidate materials for all-oxide electrochemical devices. Results show the primary reaction in these systems to be the dissolution of SrO from SrCeO 3 into the LaMO 3 /La 2-x Sr x NiO 4 , and corresponding formation of La-doped CeO 2 . Reaction kinetics are observed to be relatively fast, with element profiles suggesting the diffusion of Sr 2+ in ceria to be surprisingly rapid. It is demonstrated that perovskite starting materials represent poor candidates for use with SrCeO 3 , reacting completely to form Ruddlesden-Popper/K 2 NiF 4 type oxides. Reaction with La 2 NiO 4 is less pronounced, and formation of secondary phases suppressed for the composition La 1.2 Sr 0.8 NiO 4 . It is thus concluded that Ruddlesden-Popper type oxides represent good candidate materials for use with a SrCeO 3 -based electrolytes when doped with appropriate levels of Sr. - Graphical abstract: Assessment of the SrCeO 3 proton conductor shows this material to have poor chemical compatibility with LaMO 3 perovskite systems, but predicts coexistence with Ruddlesden-Popper type oxides

  3. Positive and negative exchange bias effects from magnetization reversal in Ho{sup 3+} doped YFe{sub 0.5}Cr{sub 0.5}O{sub 3}

    Energy Technology Data Exchange (ETDEWEB)

    Shi, L.R., E-mail: shiliran1127@126.com [College of Physics and Electrical Engineering, Anyang Normal University, Anyang 455000 (China); Wei, C.X.; Wang, Z.; Ju, L.; Xu, T.S.; Li, T.X.; Yan, X.W. [College of Physics and Electrical Engineering, Anyang Normal University, Anyang 455000 (China); Xia, Z.C. [Wuhan National High Magnetic Field Center, Huazhong University of Science and Technology, Wuhan 430074 (China)

    2017-07-01

    Highlights: • The dual magnetization reversal is observed in Y{sub 1−x}Ho{sub x}Fe{sub 0.5}Cr{sub 0.5}O{sub 3}. • The EB field transforms from negative to positive and then to negative. • A large exchange bias effect induced by Ho{sup 3+} doping is obtained in Y{sub 1−x}Ho{sub x}Fe{sub 0.5}Cr{sub 0.5}O{sub 3}. - Abstract: The polycrystalline ceramics of Y{sub 1−x}Ho{sub x}Fe{sub 0.5}Cr{sub 0.5}O{sub 3} (x = 0, 0.05 and 0.1) are synthesized by a sol-gel method. The magnetization reversal and exchange bias effect are investigated in single phase bulk Y{sub 1−x}Ho{sub x}Fe{sub 0.5}Cr{sub 0.5}O{sub 3}. Magnetic Ho{sup 3+} ion as a dopant is introduced into the system to confirm the influence of A-site ion on the magnetic interactions. The dual reversal of exchange bias field for x = 0.05 is observed, and its characteristic temperatures are corresponding to the compensation temperatures of magnetization reversal. The exchange bias field of x = 0.1 is found to be ∼10.03 kOe at 4 K, revealing a large value compared with that of x = 0. A schematic diagram based on the competition between the single ion anisotropy and Dzyaloshinsky-Moriya interaction, and the antiparallel coupling between the Ho{sup 3+} moments and the canted Cr{sup 3+}/Fe{sup 3+} moments, is used to understand the dual reversal phenomenon of magnetization and exchange bias effect.

  4. Effects of deposition temperatures and annealing conditions on the microstructural, electrical and optical properties of polycrystalline Al-doped ZnO thin films

    Energy Technology Data Exchange (ETDEWEB)

    Oh, Joon-Ho [Department of Materials Science and Engineering, Korea University, Seoul 136-713 (Korea, Republic of); Kim, Kyoung-Kook [Department of Nano-Optical Engineering, Korea Polytechnic University, Gyeonggi 429-793 (Korea, Republic of); Seong, Tae-Yeon, E-mail: tyseong@korea.ac.kr [Department of Materials Science and Engineering, Korea University, Seoul 136-713 (Korea, Republic of)

    2011-01-15

    Al-doped ZnO (AZO, ZnO:Al{sub 2}O{sub 3} = 98:2 wt%) films are deposited on different substrates by an RF magnetron sputtering and subsequently annealed at three different conditions to investigate the microstructural, electrical, and optical properties. X-ray diffraction and scanning electron microscope results show that all the samples are polycrystalline and the samples rapid-thermal-annealed at 900 deg. C in an N{sub 2} ambient contain larger grains compared to the furnace-annealed samples. It is shown that the sample deposited at room temperature on the sapphire gives a resistivity of 5.57 x 10{sup -4} {Omega} cm when furnace-annealed at 500 deg. C in a mixture of N{sub 2}:H{sub 2} (9:1). It is also shown that the Hall mobility vs. carrier concentration ({mu}-n) relation is divided into two groups, depending on the annealing conditions, namely, either rapid-thermal annealing or furnace annealing. The relations are described in terms of either grain boundary scattering or ionized impurity scattering mechanism. In addition, the samples produce fairly high transmittance of 91-96.99% across the wavelength region of 400-1100 nm. The optical bandgaps of the samples increase with increasing carrier concentration.

  5. Ultrafine Nanocrystalline CeO2@C-Containing NaAlH4 with Fast Kinetics and Good Reversibility for Hydrogen Storage.

    Science.gov (United States)

    Zhang, Xin; Liu, Yongfeng; Wang, Ke; Li, You; Gao, Mingxia; Pan, Hongge

    2015-12-21

    A nanocrystalline CeO2@C-containing NaAlH4 composite is successfully synthesized in situ by hydrogenating a NaH-Al mixture doped with CeO2@C. Compared with NaAlH4 , the as-prepared CeO2@C-containing NaAlH4 composite, with a minor amount of excess Al, exhibits significantly improved hydrogen storage properties. The dehydrogenation onset temperature of the hydrogenated [NaH-Al-7 wt % CeO2@C]-0.04Al sample is 77 °C lower than that of the pristine sample because of a reduced kinetic barrier. More importantly, the dehydrogenated sample absorbs ∼4.7 wt % hydrogen within 35 min at 100°C and 10 MPa of hydrogen. Compositional and structural analyses reveal that CeO2 is converted to CeH2 during ball milling and that the newly formed CeH2 works with the excess of Al to synergistically improve the hydrogen storage properties of NaAlH4. Our findings will aid in the rational design of novel catalyst-doped complex hydride systems with low operating temperatures, fast kinetics, and long-term cyclability. © 2015 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

  6. Structure and photocatalytic activity studies of TiO2-supported over Ce-modified Al-MCM-41

    International Nuclear Information System (INIS)

    Krishna Reddy, Jakkidi; Durgakumari, Valluri; Subrahmanyam, Machiraju; Sreedhar, Bojja

    2009-01-01

    Ce-Al-MCM-41, TiO 2 /Al-MCM-41 and TiO 2 /Ce-Al-MCM-41 materials with varying contents of Ce (by impregnation) and TiO 2 loaded (by solid-state dispersion) on Al-MCM-41 support are prepared. The Ce modified and TiO 2 loaded composite systems are characterized by X-ray diffraction (XRD), transmission electron microscopy (TEM), UV-vis diffuse reflectance spectra (DRS) and X-ray photoelectron spectroscopy (XPS) techniques. The DRS and XPS of low Ce content (0.2-0.5 wt.%) modified Al-MCM-41 samples are showing more characteristic of Ce 3+ species wherein cerium in interaction with Al-MCM-41 and that of high Ce (0.8, 3.0 wt.%) content modified samples are showing the characteristic of both Ce 4+ and Ce 3+ species. A series of Ce-modified Al-MCM-41 and TiO 2 loaded composite catalysts are evaluated for photocatalytic degradation of phenol under UV irradiation. Low Ce content in Ce 3+ state on Al-MCM-41 is showing good photoactivity in comparison with high Ce content samples and pure ceria. The composite TiO 2 /Ce-Al-MCM-41 is showing enhanced degradation activity due decreased rate of electron-hole recombination on TiO 2 surface by the redox properties of cerium. The photocatalyst TiO 2 /Ce-Al-MCM-41 with an optimum of 10 wt.% TiO 2 and 0.3 wt.% Ce is showing maximum phenol degradation activity. The possible mechanism of phenol degradation on the composite photocatalyst is proposed.

  7. Mechanoluminescence, photoluminescence and thermoluminescence studies of SrZrO3:Ce phosphor

    Directory of Open Access Journals (Sweden)

    Neha Tiwari

    2015-01-01

    Full Text Available The present paper reports the synthesis and characterization, photoluminescence thermoluminescence and mechanoluminescence studies of Ce3+ doped SrZrO3 phosphors. The effects of variable concentration of Cerium on meachanoluminescence (ML and photoluminescence behavior were studied. The samples were prepared by combustion a synthesis technique which is suitable for less time taking techniques also for large scale production for phosphors. The starting material used for sample preparation are Sr(NO33, Zr(NO33 XH2O and Ce(NO33 6H2O and urea used as a fuel. The prepared sample was characterized by X-ray diffraction technique (XRD with variable concentration of Ce (0.05–0.5 mol%. There is no any phase change found with increase the concentration of Ce. Sample shows orthorhombic structure and the particle size calculated by Scherer's formula. The surface morphology of prepared phosphor was determined by field emission gun scanning electron microscopy (FEGSEM technique. Mechanoluminescence studies on SrZrO3phosphors doped with Ce and underwent an impulsive deformation with an impact of a piston for Mechanoluminescence (ML investigations. Temporal characteristics in order to investigate about the luminescence centre responsible for ML peak, increasing impact velocity causes more number of electrons will be ionized to reach to the conduction band so there will be more number of electrons available to be recombined at recombination or luminescence centre. In photoluminescence study PL emission spectra show the isolated peak position observed at 388 nm near UV region of spectrum due to 5d–4f transition of Ce3+ion.Thermoluminescence study shows doping of Ce3+ ions reduced the TL intensity TL glow curve shows the high fading and less stability when it doped with cerium. The activation energy high for the doped SrZrO3 phosphor means that the trapped electron is highly trapped in trap level. The present study gives the advance application for fracture

  8. Modulation-doped β-(Al0.2Ga0.8)2O3/Ga2O3 field-effect transistor

    Science.gov (United States)

    Krishnamoorthy, Sriram; Xia, Zhanbo; Joishi, Chandan; Zhang, Yuewei; McGlone, Joe; Johnson, Jared; Brenner, Mark; Arehart, Aaron R.; Hwang, Jinwoo; Lodha, Saurabh; Rajan, Siddharth

    2017-07-01

    Modulation-doped heterostructures are a key enabler for realizing high mobility and better scaling properties for high performance transistors. We report the realization of a modulation-doped two-dimensional electron gas (2DEG) at the β-(Al0.2Ga0.8)2O3/Ga2O3 heterojunction by silicon delta doping. The formation of a 2DEG was confirmed using capacitance voltage measurements. A modulation-doped 2DEG channel was used to realize a modulation-doped field-effect transistor. The demonstration of modulation doping in the β-(Al0.2Ga0.8)2O3/Ga2O3 material system could enable heterojunction devices for high performance electronics.

  9. Redox behavior of a low-doped Pr-CeO{sub 2}(111) surface. A DFT+U study

    Energy Technology Data Exchange (ETDEWEB)

    Milberg, Brian [ITHES, UBA-CONICET, Departamento de Ingeniería Química, Pabellón de Industrias, Ciudad Universitaria, 1428 Buenos Aires (Argentina); Juan, Alfredo [Departamento de Física & IFISUR, UNS-CONICET, Avda. Alem 1253, 8000 Bahía Blanca (Argentina); Irigoyen, Beatriz, E-mail: beatriz@di.fcen.uba.ar [ITHES, UBA-CONICET, Departamento de Ingeniería Química, Pabellón de Industrias, Ciudad Universitaria, 1428 Buenos Aires (Argentina)

    2017-04-15

    Highlights: • Pr doping facilitates oxygen donation due to the easy formation of Pr{sup 3+}/Pr{sup 4+} and Ce{sup 3+}/Ce{sup 4+} redox couples. • Pr doping also favors the formation of superoxide (O{sub 2}{sup −}) radicals on surface O-holes. • CO can be oxidized by superoxide radical forming a CO{sub 2} molecule floating on the surface. • CO can also interact on the (O{sub 2}{sup −})/Pr{sup 3+} interphase and forms weakly adsorbed carbonate-type intermediates. - Abstract: In this work, we investigated the redox behavior (donation and replenishing of oxygen) of a low praseodymium (Pr)-doped CeO{sub 2}(111) surface. We considered a 3.7 at.% Pr doping and performed density functional calculations using the GGA formalism with the ‘U’ correction on Ce(4f) and Pr(4f) orbitals. Our results indicate that Pr doping promotes oxygen donation by lowering the energy necessary to form surface anionic vacancies. When the Ce{sub 0.963}Pr{sub 0.037}O{sub 2}(111) surface donates one oxygen, the two excess electrons locate on Pr and Ce cations and reduce them to Pr{sup 3+} and Ce{sup 3+} ones. Praseodymium doping also favors the activation of O{sub 2} molecule on surface O-holes, leading to formation of a superoxide (O{sub 2}{sup −}) radical as well as to reoxidation of the Ce{sup 3+} cation to Ce{sup 4+} one. Additionally, we used the CO molecular adsorption for testing the reactivity of those superoxide species. The calculations expose the ability of these radicals to oxidize CO forming a CO{sub 2} molecule floating on the surface. However, when the superoxide is in the immediate vicinity of Pr dopant a carbonate-type species is formed. Our theoretical results may help to gain insight into redox properties and improved catalytic performance of low-doped Pr-CeO{sub 2} solids.

  10. Study of cerium doped magnetite (Fe 3O 4:Ce)/PMMA nanocomposites

    Science.gov (United States)

    Padalia, Diwakar; Johri, U. C.; Zaidi, M. G. H.

    2012-03-01

    The paper presents the synthesis and properties of polymer nanocomposite material based on cerium doped magnetite (Fe 3O 4) as filler material and poly methyl methacrylate (PMMA) as host matrix. The magnetite (Fe 3O 4) particles were synthesized by co-precipitation route using stable ferrous and ferric salts with ammonium hydroxide as precipitating agent. Further, they doped by cerium oxide (CeO 2) non-stoichiometrically. The composite material was fabricated by solvent evaporation method. Here 2.4 GHz microwaves were used to study the effect of microwaves heating on polymerization. The phase and crystal structure is determined by X-ray diffraction (XRD). The average crystallite size of the composites varies from 28 to 35 nm. The chemical structure is confirmed by Fourier transform infrared (FTIR) spectroscopy. The magnetic and thermal properties are investigated by vibrating sample magnetometer (VSM) and differential scanning calorimetry (DSC). The thermal study shows that the microwave heated samples possess higher glass transition temperature ( Tg). The magnetic results suggest that coercivity ( HC) and squareness ( Mr/ Ms) of the loop increases with increasing doping percent of cerium.

  11. Photoluminescence properties of the Eu-doped alpha-Al{sub 2}O{sub 3} microspheres

    Energy Technology Data Exchange (ETDEWEB)

    Liu, Dianguang, E-mail: dianguang12@gmail.com [State Key Laboratory of Solidification Processing, Northwestern Polytechnical University, West Youyi Rd., No. 127, Xi’an, Shaanxi 710072 (China); Science and Technology on Thermostructure Composite Materials Laboratory, Northwestern Polytechnical University, West Youyi Rd., No. 127, Xi’an, Shaanxi 710072 (China); Zhu, Zhenfeng [School of Materials Science and Engineering, Shaanxi University of Science and Technology, Xi’an 710021 (China)

    2014-01-15

    Highlights: • Al{sub 2}O{sub 3}:Eu{sup 3+} phosphors were prepared via a microwave solvothermal route. • The particles were hierarchically nanostructured microspheres packaged by nanosheets. • The powders presented excellent orange–red emission when excited at 393 nm. • Critical concentration and distance of Eu{sup 3+} in Al{sub 2}O{sub 3} is 0.007, 18 Å, respectively. -- Abstract: Al{sub 2}O{sub 3}:Eu{sup 3+} samples were synthesized via microwave solvothermal method and thermal decomposition of Eu{sup 3+} doped precursors. The sample characterizations were carried out by means of X-ray diffraction (XRD), scanning electron microscope (SEM) and photoluminescence (PL) spectra. XRD results indicated that Eu{sup 3+} doped samples were most of α-Al{sub 2}O{sub 3} phase after being calcined at 1473 K. SEM results showed that the obtained α-Al{sub 2}O{sub 3} based powders via microwave solvothermal method were microspheres with an average diameter about 1.6 μm. PL spectra showed that upon excitation at 393 nm, the orange–red emission bands at the wavelength longer than 560 nm were from {sup 5}D{sub 0} → {sup 7}F{sub J} (J = 1, 2) transitions. The asymmetry ratio of ({sup 5}D{sub 0} → {sup 7}F{sub 2})/({sup 5}D{sub 0} → {sup 7}F{sub 1}) intensity is about 1 and this value suggests that Eu{sup 3+} ions occupy the same ratio of symmetry and asymmetry sites. It is shown that the 0.7 mol% of doping concentration of Eu{sup 3+} ions in α-Al{sub 2}O{sub 3}:Eu{sup 3+} is optimum. According to Dexter’s theory, the critical distance between Eu{sup 3+} ions for energy transfer was determined to be 18 Å.

  12. Preparation of Mn doped CeO_2 nanoparticles with enhanced ferromagnetism

    International Nuclear Information System (INIS)

    Ravi, S.; Winfred Shashikanth, F.

    2017-01-01

    Spherical-like CeO_2 and Mn-doped CeO_2 using 6-aminohexanoic acid as surfactant exhibit enhanced ferromagnetism. The optical absorption spectra reveal a red shift with a band gap of 2.51 eV. The mechanics of ferromagnetism and the red shift were analyzed. These results provide a promising platform for developing a dilute magnetic semiconductor in spintronics. - Highlights: • Pure and Mn-doped CeO_2 is prepared with aminohexanoic acid as capping. • They exhibit wide optical absorption with red-shift in their band gap. • Mn-doped CeO_2 nanoparticle exhibit hysteresis at room temperature. • Results were promising to use in spintronics and opto-electronics field.

  13. Structural, optical and photo thermal properties of Er3+:Y2O3 doped PMMA nanocomposite

    Science.gov (United States)

    Tabanli, Sevcan; Eryurek, Gonul

    2018-02-01

    Thermal decomposition technique was employed to synthesize of phosphors of yttria (Y2O3) doped with erbium (Er3+) ions. After the synthesized procedure, the nano-sized crystalline powders were annealed at 800oC for 24 h. Annealed powders were embedded in poly(methyl methacrylate) (PMMA) by free radical polymerization to fabricate nanocomposite polymer materials. The crystalline structure of the powder and doped PMMA nanocomposite samples were determined using X-ray diffraction technique. Scherrer's equation and the FW1/5/4/5M method were used to determine average crystalline size and grain size distributions, respectively. The spectroscopic properties of the powders and doped PMMA nanocomposites were studied by measuring the upconversion emission spectra under near-infrared laser excitation at room temperature. The laser-induced photo thermal behaviors of Er3+:Y2O3 nano-powders and doped PMMA nanocomposite were investigated using the fluorescence intensity ratio (FIR) technique.

  14. Luminescence properties of Ce3+ and Tb3+ co-activated ZnAl2O4 phosphor

    International Nuclear Information System (INIS)

    Tshabalala, K.G.; Cho, S.-H.; Park, J.-K.; Pitale, Shreyas S.; Nagpure, I.M.; Kroon, R.E.; Swart, H.C.; Ntwaeaborwa, O.M.

    2012-01-01

    In this study, a solution combustion method was used to prepare green emitting Ce 3+ –Tb 3+ co-activated ZnAl 2 O 4 phosphor. The samples were annealed at 700 °C in air or hydrogen atmosphere to improve their crystallinity and optical properties. X-ray diffraction study confirmed that both as-prepared and post-preparation annealed samples crystallized in the well known cubic spinel structure of ZnAl 2 O 4 . An agglomeration of irregular platelet-like particles whose surfaces were encrusted with smaller spheroidal particles was confirmed by scanning electron microscopy (SEM). The fluorescence data collected from the annealed samples with different concentrations of Ce 3+ and Tb 3+ show the enhanced green emission at 543 nm associated with 5 D 4 → 7 F 5 transitions of Tb 3+ . The enhancement was attributed to energy transfer from Ce 3+ to Tb 3+ . Possible mechanism of energy transfer via a down conversion process is discussed. Furthermore, cathodoluminescence (CL) intensity degradation of this phosphor was also investigated and the degradation data suggest that the material was chemically stable and the CL intensity was also stable after 10 h of irradiation by a beam of high energy electrons.

  15. Photoluminescence and Energy Transfer Properties with Y+SiO4 Substituting Ba+PO4 in Ba3Y(PO4)3:Ce(3+)/Tb(3+), Tb(3+)/Eu(3+) Phosphors for w-LEDs.

    Science.gov (United States)

    Li, Kai; Liang, Sisi; Shang, Mengmeng; Lian, Hongzhou; Lin, Jun

    2016-08-01

    A series of Ce(3+), Tb(3+), Eu(3+) doped Ba2Y2(PO4)2(SiO4) (BYSPO) phosphors were synthesized via the high-temperature solid-state reaction route. X-ray diffraction, high-resolution transmission electron microscopy, Fourier transform infrared, solid-state NMR, photoluminescence (PL) including temperature-dependent PL, and fluorescent decay measurements were conducted to characterize and analyze as-prepared samples. BYSPO was obtained by the substitution of Y+SiO4 for Ba+PO4 in Ba3Y(PO4)3 (BYPO). The red shift of PL emission from 375 to 401 nm occurs by comparing BYSPO:0.14Ce(3+) with BYPO:0.14Ce(3+) under 323 nm UV excitation. More importantly, the excitation edge can be extended from 350 to 400 nm, which makes it be excited by UV/n-UV chips (330-410 nm). Tunable emission color from blue to green can be observed under 365 nm UV excitation based on the energy transfer from Ce(3+) to Tb(3+) ions after codoping Tb(3+) into BYSPO:0.14Ce(3+). Moreover, energy transfer from Tb(3+) to Eu(3+) ions also can be found in BYSPO:Tb(3+),Eu(3+) phosphors, resulting in the tunable color from green to orange red upon 377 nm UV excitation. Energy transfer properties were demonstrated by overlap of excitation spectra, variations of emission spectra, and decay times. In addition, energy transfer mechanisms from Ce(3+) to Tb(3+) and Tb(3+) to Eu(3+) in BYSPO were also discussed in detail. Quantum yields and CIE chromatic coordinates were also presented. Generally, the results suggest their potential applications in UV/n-UV pumped LEDs.

  16. Significant enhancement in thermoelectric properties of polycrystalline Pr-doped SrTiO3−δ ceramics originating from nonuniform distribution of Pr dopants

    KAUST Repository

    Dehkordi, Arash Mehdizadeh

    2014-05-12

    Recently, we have reported a significant enhancement ( >70% at 500 °C) in the thermoelectric power factor (PF) of bulk polycrystalline Pr-doped SrTiO3 ceramics employing a novel synthesis strategy which led to the highest ever reported values of PF among doped polycrystalline SrTiO3. It was found that the formation of Pr-rich grain boundary regions gives rise to an enhancement in carrier mobility. In this Letter, we investigate the electronic and thermal transport in Sr1− x Pr x TiO3 ceramics in order to determine the optimum doping concentration and to evaluate the overall thermoelectric performance. Simultaneous enhancement in the thermoelectric power factor and reduction in thermal conductivity in these samples resulted in more than 30% improvement in the dimensionless thermoelectric figure of merit (ZT) for the whole temperature range over all previously reported maximum values. Maximum ZT value of 0.35 was obtained at 500 °C.

  17. Significant enhancement in thermoelectric properties of polycrystalline Pr-doped SrTiO3−δ ceramics originating from nonuniform distribution of Pr dopants

    KAUST Repository

    Dehkordi, Arash Mehdizadeh; Bhattacharya, Sriparna; He, Jian; Alshareef, Husam N.; Tritt, Terry M.

    2014-01-01

    Recently, we have reported a significant enhancement ( >70% at 500 °C) in the thermoelectric power factor (PF) of bulk polycrystalline Pr-doped SrTiO3 ceramics employing a novel synthesis strategy which led to the highest ever reported values of PF among doped polycrystalline SrTiO3. It was found that the formation of Pr-rich grain boundary regions gives rise to an enhancement in carrier mobility. In this Letter, we investigate the electronic and thermal transport in Sr1− x Pr x TiO3 ceramics in order to determine the optimum doping concentration and to evaluate the overall thermoelectric performance. Simultaneous enhancement in the thermoelectric power factor and reduction in thermal conductivity in these samples resulted in more than 30% improvement in the dimensionless thermoelectric figure of merit (ZT) for the whole temperature range over all previously reported maximum values. Maximum ZT value of 0.35 was obtained at 500 °C.

  18. Polar phase transitions in heteroepitaxial stabilized La0.5Y0.5AlO3 thin films

    Science.gov (United States)

    Liu, Shenghua; Zhang, Chunfeng; Zhu, Mengya; He, Qian; Chakhalian, Jak; Liu, Xiaoran; Borisevich, Albina; Wang, Xiaoyong; Xiao, Min

    2017-10-01

    We report on the fabrication of epitaxial La0.5Y0.5AlO3 ultrathin films on (001) LaAlO3 substrates. Structural characterizations by scanning transmission electron microscopy and x-ray diffraction confirm the high quality of the film with a - b + c - AlO6 octahedral tilt pattern. Unlike either of the nonpolar parent compound, LaAlO3 and YAlO3, second harmonic generation measurements on the thin films suggest a nonpolar-polar phase transition at T c near 500 K, and a polar-polar phase transition at T a near 160 K. By fitting the angular dependence of the second harmonic intensities, we further propose that the two polar structures can be assigned to the Pmc2 1 and Pmn2 1 space group, while the high temperature nonpolar structure belongs to the Pbnm space group.

  19. Synthesis and Characterization of Yttria-Stabilized Zirconia Nanoparticles Doped with Ytterbium and Gadolinium: ZrO2 9.5Y2O3 5.6Yb2O3 5.2Gd2O3

    Science.gov (United States)

    Bahamirian, M.; Hadavi, S. M. M.; Rahimipour, M. R.; Farvizi, M.; Keyvani, A.

    2018-06-01

    Defect cluster thermal barrier coatings (TBCs) are attractive alternatives to Yttria-stabilized zirconia (YSZ) in advanced applications. In this study, YSZ nanoparticles doped with ytterbium and gadolinium (ZrO2 9.5Y2O3 5.6Yb2O3 5.2Gd2O3 (ZGYbY)) were synthesized through a chemical co-precipitation and calcination method, and characterized by in situ high-temperature X-ray diffraction analysis in the temperature range of 25 °C to 1000 °C (HTK-XRD), thermogravimetric analysis, differential thermal analysis, Fourier transform infrared spectroscopy, Raman spectroscopy, and field emission scanning electron microscopy (FE-SEM). Precise cell parameters of t-prime phase and the best zirconia phase for TBC applications were calculated by Cohen's and Rietveld refinement methods. Optimum crystallization temperature of the precursor powder was found to be 1000 °C. Furthermore, FE-SEM results for the calcined ZGYbY powders indicated orderly particles of uniform shape and size with a small tendency toward agglomeration. Average lattice thermal expansion coefficient in the temperature range of 25 °C to 1000 °C was determined to be 31.71 × 10-6 K-1.

  20. Synthesis and Characterization of Yttria-Stabilized Zirconia Nanoparticles Doped with Ytterbium and Gadolinium: ZrO2 9.5Y2O3 5.6Yb2O3 5.2Gd2O3

    Science.gov (United States)

    Bahamirian, M.; Hadavi, S. M. M.; Rahimipour, M. R.; Farvizi, M.; Keyvani, A.

    2018-03-01

    Defect cluster thermal barrier coatings (TBCs) are attractive alternatives to Yttria-stabilized zirconia (YSZ) in advanced applications. In this study, YSZ nanoparticles doped with ytterbium and gadolinium (ZrO2 9.5Y2O3 5.6Yb2O3 5.2Gd2O3 (ZGYbY)) were synthesized through a chemical co-precipitation and calcination method, and characterized by in situ high-temperature X-ray diffraction analysis in the temperature range of 25 °C to 1000 °C (HTK-XRD), thermogravimetric analysis, differential thermal analysis, Fourier transform infrared spectroscopy, Raman spectroscopy, and field emission scanning electron microscopy (FE-SEM). Precise cell parameters of t-prime phase and the best zirconia phase for TBC applications were calculated by Cohen's and Rietveld refinement methods. Optimum crystallization temperature of the precursor powder was found to be 1000 °C. Furthermore, FE-SEM results for the calcined ZGYbY powders indicated orderly particles of uniform shape and size with a small tendency toward agglomeration. Average lattice thermal expansion coefficient in the temperature range of 25 °C to 1000 °C was determined to be 31.71 × 10-6 K-1.

  1. High energy transmission of Al2O3 doped with light transition metals

    KAUST Repository

    Schuster, Cosima

    2012-01-31

    The transmission of transparent colored ceramics based on Al2O3doped with light transition metals is measured in the visible and infrared range. To clarify the role of the dopands we perform ab initiocalculations. We discuss the electronic structure and present optical spectra obtained in the independent particle approximation. We argue that the gross spectral features of Co- and Ni-doped Al2O3 samples are described by our model, while the validity of the approach is limited for Cr-doped Al2O3.

  2. High energy transmission of Al2O3 doped with light transition metals

    KAUST Repository

    Schuster, Cosima; Klimke, J.; Schwingenschlö gl, Udo

    2012-01-01

    The transmission of transparent colored ceramics based on Al2O3doped with light transition metals is measured in the visible and infrared range. To clarify the role of the dopands we perform ab initiocalculations. We discuss the electronic structure and present optical spectra obtained in the independent particle approximation. We argue that the gross spectral features of Co- and Ni-doped Al2O3 samples are described by our model, while the validity of the approach is limited for Cr-doped Al2O3.

  3. Neutron investigation of Ru-doped Nd1/2Ca1/2MnO3. Comparison with Cr-doped Nd1/2Ca1/2MnO3

    International Nuclear Information System (INIS)

    Moritomo, Yutaka; Nonobe, Toshihiko; Machida, Akihiko; Ohoyama, Kenji

    2002-01-01

    Lattice and magnetic properties are investigated for 3% Ru- and Cr-doped Nd 1/2 Ca 1/2 MnO 3 . The parent Nd 1/2 Ca 1/2 MnO 3 is a charge-ordered insulator (T CO =250K). With decreasing temperature below ≅210K, these compounds are separated into two perovskite phases, that is, the long-c and short-c phases. The long-c region shows a ferromagnetic transition at T C ≅210K for the Ru-doped compound and ≅130K for the Cr-doped compound, while the short-c region shows antiferromagnetic transition at T N ≅150K for Ru and ≅110K for Cr. We discuss the origin of the enhanced T C for the Ru-doped compound in terms of the effective one-electron bandwidth W of the e g -band. (author)

  4. Investigation of spectroscopic properties and energy transfer between Ce and Dy in (Lu{sub 0.2}Gd{sub 0.8−x−y}Ce{sub x}Dy{sub y}){sub 2}SiO{sub 5} single crystals

    Energy Technology Data Exchange (ETDEWEB)

    Strzęp, A. [Institute of Low Temperature and Structure Research PAS, Wroclaw (Poland); Martin, I.R. [Faculty of Physics, Universidad de La Laguna, S/C de Tenerife (Spain); Malta Consolider Team and Instituto de Materiales y Nanotecnología (IMN), Universidad de La Laguna, S/C de Tenerife (Spain); Głowacki, M. [Institute of Physics PAS, Warsaw (Poland); Ryba-Romanowski, W. [Institute of Low Temperature and Structure Research PAS, Wroclaw (Poland); Berkowski, M. [Institute of Physics PAS, Warsaw (Poland); Pérez-Rodríguez, C. [Faculty of Physics, Universidad de La Laguna, S/C de Tenerife (Spain); Malta Consolider Team and Instituto de Materiales y Nanotecnología (IMN), Universidad de La Laguna, S/C de Tenerife (Spain)

    2015-10-15

    In this paper we present results of spectroscopic investigations of single crystals with general formula (Lu{sub 0.2}Gd{sub 0.8−x−y}){sub 2}SiO{sub 5} codoped with x% of Ce{sup {sub 3}{sub +}} and y% of Dy{sup {sub 3}{sub +}} ions. Investigated materials exhibit strong optical anisotropy what can be easily observed in polarized absorption and emission spectra. Based on room temperature polarized absorption spectra calculations in framework of phenomenological Judd–Ofelt model was carried out. Intensity parameters Ω{sub t} were evaluated to be Ω{sub 2}=7.08 (±0.39), Ω{sub 4}=2.76 (±0.44), and Ω{sub 6}=3.36 (±0.21) [10{sup −20} cm{sup 2}] for sample doped with 1% of cerium and Ω{sub 2}=10.72 (±0.33), Ω{sub 4}=1.98 (±0.37), and Ω{sub 6}=2.11 (±0.18) [10{sup −20} cm{sup 2}] for sample doped with 3% of cerium. Influence of cerium admixture on Judd Ofelt intensity parameters is discussed. Value of experimental lifetime of {sub 4}F{sub 9/2} multiplet of Dy{sup 3+} ion in sample doped with 1 at% Ce is 0.5 ms (τ{sub rad}=0.45 ms), while for sample doped with 3 at% of Ce, experimental lifetime is 0.45 ms (τ{sub rad}=0.43 ms). Absorption bands located between 440 and 460 nm, can be utilized for optical pumping of material by GaN laser diodes. Intense and broad emission bands at 465–495 and 560–590 nm, with experimental branching ratio strongly depending on polarization, give high chance for obtaining white luminophore, due to appropiate mixing of blue and yellow luminescence. By means of a pump and probe experiment optical amplification was demonstrated in the codoped sample with 1 at% of Ce and 1 at% Dy at 575 nm corresponding to the emission of Dy{sup 3+} with a high net gain coefficient of 34 cm{sup −1}. Such high amplification was obtained under 359 nm excitation (at the maximum of intense absorption band of Ce{sup 3+} ions). - Highlights: • Influence of anisotropy on properties of LGSO: Ce, Dy crystals was investigated. • ET between Ce

  5. Fabrication of highly conductive Ta-doped SnO{sub 2} polycrystalline films on glass using seed-layer technique by pulse laser deposition

    Energy Technology Data Exchange (ETDEWEB)

    Nakao, Shoichiro, E-mail: tg-s-nakao@newkast.or.j [Kanagawa Academy of Science and Technology (KAST), Kawasaki 213-0012 (Japan); Department of Chemistry, University of Tokyo, Tokyo 113-0033 (Japan); Yamada, Naoomi [Kanagawa Academy of Science and Technology (KAST), Kawasaki 213-0012 (Japan); Hitosugi, Taro [Kanagawa Academy of Science and Technology (KAST), Kawasaki 213-0012 (Japan); Advanced Institute for Materials Research, Tohoku University, Sendai 980-8577 (Japan); Hirose, Yasushi; Shimada, Toshihiro; Hasegawa, Tetsuya [Kanagawa Academy of Science and Technology (KAST), Kawasaki 213-0012 (Japan); Department of Chemistry, University of Tokyo, Tokyo 113-0033 (Japan)

    2010-03-31

    We discuss the fabrication of highly conductive Ta-doped SnO{sub 2} (Sn{sub 1-x}Ta{sub x}O{sub 2}; TTO) thin films on glass by pulse laser deposition. On the basis of the comparison of X-ray diffraction patterns and resistivity ({rho}) values between epitaxial films and polycrystalline films deposited on bare glass, we proposed the use of seed-layers for improving the conductivity of the TTO polycrystalline films. We investigated the use of rutile TiO{sub 2} and NbO{sub 2} as seed-layers; these are isostructural materials of SnO{sub 2,} which are expected to promote epitaxial-like growth of the TTO films. The films prepared on the 10-nm-thick seed-layers exhibited preferential growth of the TTO (110) plane. The TTO film with x = 0.05 on rutile TiO{sub 2} exhibited {rho} = 3.5 x 10{sup -4} {Omega} cm, which is similar to those of the epitaxial films grown on Al{sub 2}O{sub 3} (0001).

  6. Novel tunable green-red-emitting oxynitride phosphors co-activated with Ce3+, Tb3+, and Eu3+: photoluminescence and energy transfer.

    Science.gov (United States)

    Huo, Jiansheng; Dong, Langping; Lü, Wei; Shao, Baiqi; You, Hongpeng

    2017-07-14

    A series of novel Ce 3+ , Tb 3+ and Eu 3+ ion doped Y 4 SiAlO 8 N-based oxynitride phosphors were synthesized by the solid-state method and characterized by X-ray powder diffraction, scanning electron microscopy, photoluminescence, lifetimes and thermo-luminescence. The excitation of the Ce 3+ /Tb 3+ co-doped and Ce 3+ /Tb 3+ /Eu 3+ tri-doped phosphor with near-UV radiation results in strong linear Tb 3+ green and Eu 3+ red emission. The occurrence of Ce 3+ -Tb 3+ and Ce 3+ -Tb 3+ -Eu 3+ energy transfer processes is responsible for the bright green or red luminescence. The Tb 3+ ion acting as an energy transfer bridge can alleviate MMCT quenching between the Ce 3+ -Eu 3+ ion pairs. The lifetime measurements demonstrated that the energy-transfer mechanisms of Ce 3+ → Tb 3+ and Tb 3+ → Eu 3+ are dipole-quadrupole and quadrupole-quadrupole interactions, respectively. The temperature dependent luminescence measurements showed that as-prepared green/red phosphors have good thermal stability against temperature quenching. The obtained results indicate that these phosphors might serve as promising candidates for n-UV LEDs.

  7. Luminescence properties of Eu2+- and Ce3+-doped CaAl2S4 and application in white LEDs

    International Nuclear Information System (INIS)

    Yu Ruijin; Wang Jing; Zhang Jianhui; Yuan Haibin; Su Qiang

    2008-01-01

    The Eu 2+ - and Ce 3+ -doped CaAl 2 S 4 phosphors were comparatively synthesized by conventional solid-state reaction and the evacuated sealed quartz ampoule. The X-ray diffraction (XRD) patterns show that the sample with better crystalline quality was prepared by the evacuated sealed quartz ampoule, resulting in the enhancement of the emission intensity of Eu 2+ ion by a factor of 1.7. The intensive green LEDs were also fabricated by combining CaAl 2 S 4 :Eu 2+ with near-ultraviolet InGaN chips (λ em =395 nm). The dependence of as-fabricated green LEDs on forward-bias currents shows that it presents good chromaticity stability and luminance saturation, indicating that CaAl 2 S 4 :Eu 2+ is a promising green-emitting phosphor for a near-UV InGaN-based LED. In addition, the optical properties of CaAl 2 S 4 :Ce 3+ were systematically investigated by means of diffuse reflectance, photoluminescence excitation and emission, concentrating quenching and the decay curve. - Graphical abstract: The Eu 2+ - and Ce 3+ -doped CaAl 2 S 4 phosphors were comparatively synthesized by two methods. The emission intensity of Eu 2+ ion in sample synthesized by the evacuated sealed quartz ampoule method is by a factor of 1.7 as strong as that of Eu 2+ ion in sample prepared by the conventional solid-state reaction method

  8. Structural, magnetic and optical properties of a dilute magnetic semiconductor based on Ce{sub 1−x}Co{sub x}O{sub 2} thin film grown on LaAlO{sub 3}

    Energy Technology Data Exchange (ETDEWEB)

    Mahmoud, Waleed E., E-mail: w_e_mahmoud@yahoo.com [King Abdulaziz University, Faculty of Science, Department of Physics, Jeddah (Saudi Arabia); Suez Canal University, Faculty of Science, Department of Physics, Ismailia (Egypt); Al-Ghamdi, A.A. [King Abdulaziz University, Faculty of Science, Department of Physics, Jeddah (Saudi Arabia); Al-Agel, F.A. [Hail University, College of Science, Department of Physics, Hail (Saudi Arabia); Al-Arfaj, E. [Umm Alqura University, Department of Physics, Makkah (Saudi Arabia); Qassim University, College of Science, Physics Department, Buraidah 5145 (Saudi Arabia); Shokr, F.S. [King Abdulaziz University, Faculty of Science & Arts, Department of Physics, Rabigh (Saudi Arabia); Al-Gahtany, S.A. [King Abdulaziz University, Faculty of Science for Girls, Department of Physics, Jeddah (Saudi Arabia); Alshahrie, Ahmed [King Abdulaziz University, Faculty of Science, Department of Physics, Jeddah (Saudi Arabia); Jalled, Ouissem [King Abdulaziz University, Faculty of Science, Department of Physics, Jeddah (Saudi Arabia); Laboratory of Applied Mineral Chemistry, Department of Chemistry, University Tunis ElManar, Faculty of Sciences, Campus 2092, Tunis (Tunisia); Bronstein, L.M. [King Abdulaziz University, Faculty of Science, Department of Physics, Jeddah (Saudi Arabia); Texas State University-San Marcos, Department of Chemistry and Biochemistry, 601 University Dr., San Marcos, TX 78666 (United States); Beall, Gary W. [King Abdulaziz University, Faculty of Science, Department of Physics, Jeddah (Saudi Arabia); Indiana University, Department of Chemistry, Bloomington, IN 47405 (United States)

    2015-12-15

    Highlights: • Co doped CeO{sub 2} was grown on LaAlO{sub 3} (0 0 1) via a modified sol–gel spin-coating technique. • The concentration of the Co ions was varied from 1 to 15 at.%. • The incorporation of 5 at.% of Mn ions was found to provide formation of exceptionally magnetic moment. • This amount demonstrated a giant magnetic moment of 1.09 μ{sub B}/Co. • This amount reduced the optical band gap and enhanced the optical performance. - Abstract: The enhancement of the room temperature ferromagnetism and optical properties of the dilute magnetic metal oxides is a crucial clue to construct spin-based optoelectronic devices. In this work, Ce{sub 1−x}Co{sub x}O{sub 2} (0.01 ≤ x ≤0.15) thin films were prepared via ethylene glycol modified sol–gel spin coating technique on the LaAlO{sub 3} (0 0 1) substrate to enhance their room temperature ferromagnetism and optical properties. The structures, magnetic and optical properties of the prepared films were characterized by X-ray diffraction, atomic force microscopy, scanning electron microscopy, energy dispersive X-ray spectroscopy, SQUID magnetometer, X-ray photoelectron spectroscopy and UV–vis spectrophotometer. The results demonstrated that a single phase cubic structure was formed, implying the substitution of Co ions into the Ce ions sites. The prepared films showed room temperature ferromagnetism with saturation magnetic moment of 1.09 μ{sub B}/Co was achieved for 5 at.% Co-doped CeO{sub 2}. This film exhibited high optical transparency of 85% and low optical band energy gap of 3.39 eV. The improved magnetic and optical properties are argued to the increase of the density of the oxygen vacancies into the cerium oxide crystal structure due to the incorporation of Co ions.

  9. QUANTUM-MECHANICAL MODELING OF SPATIAL AND BAND STRUCTURE OF Y3AL5O12 SCINTILLATION CRYSTAL

    Directory of Open Access Journals (Sweden)

    I. I. Vrubel

    2016-05-01

    Full Text Available Spatial and electronic structures of a unit cell of yttrium-aluminum garnet have been studied. Quantum-mechanical model have been presented. Semi-empirical methods PM6 and PM7 have been used for geometry optimization of the crystal unit cell. Band structure has been calculated within density functional theory with the use of PBE exchange-correlation functional. Histograms of metal-oxygen distances for equilibrium geometry have been constructed. Comparison of the used methods has been carried out and recommendation about their applicability for such problems was given. The single-particle wave functions and energies have been calculated. The bandgap was estimated. The band structure was plotted. It was shown that the method gives reliable results for spatial and band structure of Y3Al5O12 scintillation crystal. The results of this work can be used for improvement of characteristics of garnet scintillation crystals.

  10. Synthesis, characterization and visible light photocatalytic activity of Cr 3+ , Ce 3+ and N co-doped TiO 2 for the degradation of humic acid

    KAUST Repository

    Rashid, S. G.; Gondal, M. A.; Hameed, A.; Aslam, M.; Dastageer, M. A.; Yamani, Z. H.; Anjum, Dalaver H.

    2015-01-01

    The synthesis, characterization and photocatalytic activity of Cr3+ and Ce3+ co-doped TiON (N-doped TiO2) for the degradation of humic acid with exposure to visible light is reported. The synthesized bimetal (Cr3+ + Ce3+) modified TiON (Cr-Ce/TiON), with an evaluated bandgap of 2.1 eV, exhibited an enhanced spectral response in the visible region as compared to pure and Ce3+ doped TiON (Ce/TiON). The XRD analysis revealed the insertion of Cr3+ and Ce3+ in the crystal lattice along with Ti4+ and N that resulted in the formation of a strained TiON anatase structure with an average crystallite size of ∼10 nm. Raman analysis also supported the formation of stressed rigid structures after bimetal doping. HRTEM confirmed the homogeneous distribution of both the doped metallic components in the crystal lattice of TiON without the formation of surface oxides of either Cr3+ or Ce3+. Electron energy loss spectroscopy (EELS) analysis revealed no change in the oxidation of either Cr or Ce during the synthesis. The synthesized Cr-Ce/TiON catalyst exhibited appreciable photocatalytic activity for the degradation of humic acid on exposure to visible light. Additionally, a noticeable mineralization of carbon rich humic acid was also witnessed. The photocatalytic activity of the synthesized catalyst was compared with pristine and Ce3+ doped TiON. © The Royal Society of Chemistry 2015.

  11. Structural and photoluminescence investigations of Sm{sup 3+} doped BaY{sub 2}ZnO{sub 5} nanophosphors

    Energy Technology Data Exchange (ETDEWEB)

    Chahar, Sangeeta; Taxak, V.B.; Dalal, Mandeep; Singh, Sonika; Khatkar, S.P., E-mail: s_khatkar@rediffmail.com

    2016-05-15

    Highlights: • BaY{sub 2(1−x)}Sm{sub 2x}ZnO{sub 5} nanophosphors have been synthesized via solution combustion. • The nanophosphors have been characterized by XRD, TEM and PL spectroscopy. • The crystal structure reveals influence of doping on lattice parameters. • This nanophosphor executes orange–red emission under near UV excitation. - Abstract: BaY{sub 2}ZnO{sub 5}:Sm{sup 3+} nanophosphor was successfully synthesized using solution combustion process. XRD and photoluminescence (PL) techniques were used to analyze the structural and photoluminescence properties. Morphological study of the thermally stable powder was carried out using transmission electron microscope (TEM). Rietveld refinement technique has been used to analyze the samples qualitatively as well as quantitatively. X-Ray diffraction analysis confirms that the highly crystalline single phased Sm{sup 3+} doped BaY{sub 2}ZnO{sub 5} nanophosphor crystallizes in orthorhombic lattice with Pbnm space group. The average particle size lies in the range 80–90 nm with spherical morphology. The photoluminescence excitation at 411 nm yields an intense orange–red emission centered at 610 nm due to {sup 4}G{sub 5/2}–{sup 6}H{sub 7/2} transition. The concentration dependent luminescent behavior of BaY{sub 2(1−x)}Sm{sub 2x}ZnO{sub 5} nanophosphor shows that the optimum concentration for best luminescence is 3 mol%. These results indicate that these nanophosphors find potential applications in the field of phosphor-converted white LED systems.

  12. Synthesis by Sol-gel and characterization of catalysts Ag/Al2O3-CeO2

    International Nuclear Information System (INIS)

    Zayas, M.L.; Perez H, R.; Rubio, E.; Velasco, A.

    2004-01-01

    Aluminia, cerium and mixed oxides Al 2 O 3 -CeO 2 with different relationship Al/Ce (0.75, 0.50 and 0.25) were prepared by sol-gel and used as support for the Ag. The samples were characterized by XRD, DRIFT, TPR and adsorption of N 2 to temperature of liquid nitrogen. The surface area BET showed that the materials that contain aluminia present near values among them. XRD allowed to identify to the cerianite in the oxides that whose support contains cerium and to the α-aluminia. A mixture of phases was observed in the aluminia. Vibration bands attributed to the bond Al-O and Ce-O were observed by DRIFT in the catalytic materials. TPR showed differences in the reducibility of the Ag precursor in the indicative catalysts of a different interaction with the support. (Author)

  13. Scintillation properties of polycrystalline LaxY1-xO3 ceramic

    Science.gov (United States)

    Sahi, Sunil; Chen, Wei; Kenarangui, Rasool

    2015-03-01

    Scintillators are the material that absorbs the high-energy photons and emits visible photons. Scintillators are commonly used in radiation detector for security, medical imaging, industrial applications and high energy physics research. Two main types of scintillators are inorganic single crystals and organic (plastic or liquid) scintillators. Inorganic single crystals are expensive and difficult to grow in desire shape and size. Also, some efficient inorganic scintillator such as NaI and CsI are not environmental friendly. But on the other hand, organic scintillators have low density and hence poor energy resolution which limits their use in gamma spectroscopy. Polycrystalline ceramic can be a cost effective alternative to expensive inorganic single crystal scintillators. Here we have fabricated La0.2Y1.8O3 ceramic scintillator and studied their luminescence and scintillation properties. Ceramic scintillators were fabricated by vacuum sintering of La0.2Y1.8O3 nanoparticles at temperature below the melting point. La0.2Y1.8O3 ceramic were characterized structurally using XRD and TEM. Photoluminescence and radioluminescence studies were done using UV and X-ray as an excitation source. We have used gamma isotopes with different energy to studies the scintillation properties of La0.2Y1.8O3 scintillator. Preliminary studies of La0.2Y1.8O3 scintillator shows promising result with energy resolution comparable to that of NaI and CsI.

  14. XAFS Analysis of Local Structure around Ce in Ca3Sc2Si3O12:Ce Phosphor for White LEDs

    International Nuclear Information System (INIS)

    Akai, Toshio; Shigeiwa, Motoyuki; Okamoto, Kaoru; Shimomura, Yasuo; Kijima, Naoto; Honma, Tetsuo

    2007-01-01

    We have studied the local structure around Ce atom in Ca3Sc2Si3O12 host crystal, which has been developed as a new green phosphor for white light emitting diodes (LEDs). As the local structure and chemical environment of the dopant atom are very important to improve the performance of the phosphor, we have used XAFS to get chemical and structural information around the Ce dopant. The XANES spectrum of the Ce LIII-edge reveals that the Ce atom is trivalent in Ca3Sc2Si3O12. There are two kinds of possible Ce substitution sites, Ca site and Sc site, in garnet type Ca3Sc2Si3O12 crystal structure. The Ce atom is found to be at the Ca site in the host crystal by the comparison of the Fourier transform of Ce K-edge EXAFS spectrum with those of Ca and Sc K-edge EXAFS spectra. The theoretical analysis with FEFF also clarified the Ce substitution at the Ca site. Furthermore, the result of the analysis indicates the structural disorder around Ca and Si atoms at 3.75 A. It is possible that there are some defects around the Ca and Si atoms at 3.75 A to compensate the excess positive charge by introduced Ce3+ at the Ca2+ site

  15. Structural and luminescence effects of Ga co-doping on Ce-doped yttrium aluminate based phosphors

    Energy Technology Data Exchange (ETDEWEB)

    Ayvacikli, M. [Celal Bayar University, Faculty of Arts and Sciences, Department of Physics, Muradiye, Manisa (Turkey); Canimoglu, A. [Nigde University, Faculty of Arts and Sciences, Physics Department, Nigde (Turkey); Muresan, L.E., E-mail: laura_muresan2003@yahoo.com [Babes Bolyai University, Raluca Ripan Institute for Research in Chemistry, Fantanele 30, 400294 Cluj-Napoca (Romania); Barbu Tudoran, L. [Babes Bolyai University, Electronic Microscopy Centre, Clinicilor 37, 400006 Cluj Napoca (Romania); Garcia Guinea, J. [Museo Nacional Ciencias Naturales, Jose Gutierrez Abascal 2, Madrid 28006 (Spain); Karabulut, Y. [Celal Bayar University, Faculty of Arts and Sciences, Department of Physics, Muradiye, Manisa (Turkey); Jorge, A. [Museo Nacional Ciencias Naturales, Jose Gutierrez Abascal 2, Madrid 28006 (Spain); Karali, T. [Ege University, Institute of Nuclear Sciences, 35100 Bornova, İzmir (Turkey); Can, N., E-mail: cannurdogan@yahoo.com [Celal Bayar University, Faculty of Arts and Sciences, Department of Physics, Muradiye, Manisa (Turkey); Jazan University, Physics Department, P.O. Box 114, 45142 Jazan (Saudi Arabia)

    2016-05-05

    Herein, we primarily focus on luminescence spectrum measurements of various types of green emitting yttrium aluminate phosphors modified with gallium (Y{sub 3}Al{sub 5-x}Ga{sub x}O{sub 12}) synthesised by solid state reaction. The luminescent emission of samples depends on sample temperature and excitation radiation such as incident X-ray, electron and laser beam. Here, we measured radioluminescence (RL), cathodoluminescence (CL), photoluminescence (PL) along with XRD in order to clarify relationship between lattice defects and the spectral luminescence emissions. The RL and CL spectra of YAG:Ce exhibit an emission band ranging from 300 to 450 nm related to Y{sub Al} antisite defects. The broad emission band of garnet phosphors is shifted from 526 nm to 498 nm with increasing of Ga{sup 3+} content, while full width at half maximum (FWHM) of the band tends to be greater than the width of unmodified YAG:Ce garnet. Deconvolution of the spectrum reveals that three emission bands centred at 139, 234 and 294 °C occur in aluminate host garnets. - Highlights: • We present preparation of YAG:Ce{sup 3+}, Ga{sup 3+} phosphors by a solid state reaction method. • The shape and size of phosphor particles were investigated. • The luminescence properties were studied by different excitation sources.

  16. Study of cerium doped magnetite (Fe3O4:Ce)/PMMA nanocomposites

    International Nuclear Information System (INIS)

    Padalia, Diwakar; Johri, U.C.; Zaidi, M.G.H.

    2012-01-01

    The paper presents the synthesis and properties of polymer nanocomposite material based on cerium doped magnetite (Fe 3 O 4 ) as filler material and poly methyl methacrylate (PMMA) as host matrix. The magnetite (Fe 3 O 4 ) particles were synthesized by co-precipitation route using stable ferrous and ferric salts with ammonium hydroxide as precipitating agent. Further, they doped by cerium oxide (CeO 2 ) non-stoichiometrically. The composite material was fabricated by solvent evaporation method. Here 2.4 GHz microwaves were used to study the effect of microwaves heating on polymerization. The phase and crystal structure is determined by X-ray diffraction (XRD). The average crystallite size of the composites varies from 28 to 35 nm. The chemical structure is confirmed by Fourier transform infrared (FTIR) spectroscopy. The magnetic and thermal properties are investigated by vibrating sample magnetometer (VSM) and differential scanning calorimetry (DSC). The thermal study shows that the microwave heated samples possess higher glass transition temperature (T g ). The magnetic results suggest that coercivity (H C ) and squareness (M r /M s ) of the loop increases with increasing doping percent of cerium.

  17. Synthesis and characterization of molybdenum catalysts supported on {gamma}-Al{sub 2}O{sub 3}-CeO{sub 2} composite oxides

    Energy Technology Data Exchange (ETDEWEB)

    Farooq, Muhammad; Ramli, Anita; Subbarao, Duvvuri [Department of Chemical EngineeringUniversiti Teknologi PETRONAS Bandar Seri Iskandar, 31750 Tronoh, Perak (Malaysia); Fundamental and Applied Sciences Department, Universiti Teknologi PETRONAS Bandar Seri Iskandar, 31750 Tronoh, Perak (Malaysia); Department of Chemical EngineeringUniversiti Teknologi PETRONAS Bandar Seri Iskandar, 31750 Tronoh, Perak (Malaysia)

    2012-09-26

    The physical and chemical properties of a catalyst play a vital role in various industrial applications. Molybdenum catalysts supported on {gamma}-Al{sub 2}O{sub 3} and {gamma}-Al{sub 2}O{sub 3}-CeO{sub 2} mixed oxides with varying loading of CeO{sub 2} (5, 10, 15, 20 wt% with respect to {gamma}-Al{sub 2}O{sub 3}) were prepared by wet impregnation method. The physiochemical properties of these synthesized Mo catalysts were studied with various characterization techniques such as X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS), temperature-programmed reduction (TPR), field emission scanning electron microscopy-energy dispersive analysis (FESEM-EDX) and X-ray fluorescence spectrometer (XRF). The results showed that the addition of CeO{sub 2} into the support affected the binding energies of the elements and reducibility of the metal oxides formed after calcination of catalyst samples due to the change in metal-support interaction. Further, the characterization techniques showed that the active metal was well dispersed on the surface of support material.

  18. Preparation and characterization of carbonate terminated polycrystalline Al{sub 2}O{sub 3}/Al films

    Energy Technology Data Exchange (ETDEWEB)

    Tornow, C. [Fraunhofer-Institute for Manufacturing Technology and Applied Materials Research (IFAM), Adhesive Bonding Technology and Surfaces, Wiener Str. 12, D-28359 Bremen (Germany); Fachhochschule Oldenburg/Ostfriesland/Wilhelmshaven, University of Applied Sciences, Faculty of Technology, Department of Applied Natural Sciences, Engineering Physics, Constantiaplatz 4, D-26723 Emden (Germany); Noeske, P.-L.M. [Fraunhofer-Institute for Manufacturing Technology and Applied Materials Research (IFAM), Adhesive Bonding Technology and Surfaces, Wiener Str. 12, D-28359 Bremen (Germany); Dieckhoff, S. [Fraunhofer-Institute for Manufacturing Technology and Applied Materials Research (IFAM), Adhesive Bonding Technology and Surfaces, Wiener Str. 12, D-28359 Bremen (Germany); Wilken, R. [Fraunhofer-Institute for Manufacturing Technology and Applied Materials Research (IFAM), Adhesive Bonding Technology and Surfaces, Wiener Str. 12, D-28359 Bremen (Germany)]. E-mail: rw@ifam.fraunhofer.de; Gaertner, K. [Fachhochschule Oldenburg/Ostfriesland/Wilhelmshaven, University of Applied Sciences, Faculty of Technology, Department of Applied Natural Sciences, Engineering Physics, Constantiaplatz 4, D-26723 Emden (Germany)

    2005-12-15

    X-ray photoelectron spectroscopy (XPS) was applied to investigate the surface reactivity of polycrystalline Al films in contact with a gas mixture of carbon dioxide and oxygen at room temperature. Based on the characterization of interactions between these substrates and the individual gases at selected exposures, various surface functionalities were identified. Simultaneously dosing both carbon dioxide and oxygen is shown to create surface-terminating carbonate species, which contribute to inhibiting the formation of an Al{sub 2}O{sub 3} layer. Finally, a reaction scheme is suggested to account for the observed dependence of surface group formation on the dosing conditions.

  19. Inducing self-assembly of Y2BaCuO5 nanoparticles via Ca-doping for improved pinning in YBa2Cu3O7-x

    International Nuclear Information System (INIS)

    Barnes, P.N.; Haugan, T.J.; Baca, F.J.; Varanasi, C.V.; Wheeler, R.; Meisenkothen, F.; Sathiraju, S.

    2009-01-01

    Different mechanisms may exists as a means to provide additional or specialized enhancement of existing nanoparticulate pinning in YBa 2 Cu 3 O 7-x (YBCO) thin films. In the particular case of Y 2 BaCuO 5 (Y211) nanoparticles, Ca-doping of these nanoparticles via addition to the Y211 target material provides an additional increase to the J c (H). YBCO + Y211 samples were created by pulsed laser deposition with alternating targets of YBCO with Y211 and Y211 doped with Ca. Initial indications suggest that this improvement in pinning results from some scattered short-ranged self-assembly of the nanoparticles into short nanocolumns.

  20. Bond-versus-site doping models for off-chain-doped Haldane-gap system Y2BaNiO5

    International Nuclear Information System (INIS)

    Lou Jizhong; Qin Shaojin; Su Zhaobin; Yu Lu

    1998-09-01

    Using the density matrix renormalization-group technique, we calculate the impurity energy levels for two different effective models of off-chain doping for quasi-one-dimensional Heisenberg chain compound Y 2 BaNiO 5 : ferromagnetic bond doping and antiferromagnetic site spin-1/2 doping. Thresholds of the impurity strength for the appearance of localized states are found for both models. However, the ground-state and low-energy excitations for weak impurity strength are different for these two models and the difference can be detected by experiments. (author)

  1. Preparation of Mn doped CeO{sub 2} nanoparticles with enhanced ferromagnetism

    Energy Technology Data Exchange (ETDEWEB)

    Ravi, S., E-mail: sravi@mepcoeng.ac.in; Winfred Shashikanth, F.

    2017-06-15

    Spherical-like CeO{sub 2} and Mn-doped CeO{sub 2} using 6-aminohexanoic acid as surfactant exhibit enhanced ferromagnetism. The optical absorption spectra reveal a red shift with a band gap of 2.51 eV. The mechanics of ferromagnetism and the red shift were analyzed. These results provide a promising platform for developing a dilute magnetic semiconductor in spintronics. - Highlights: • Pure and Mn-doped CeO{sub 2} is prepared with aminohexanoic acid as capping. • They exhibit wide optical absorption with red-shift in their band gap. • Mn-doped CeO{sub 2} nanoparticle exhibit hysteresis at room temperature. • Results were promising to use in spintronics and opto-electronics field.

  2. Dependence of the up-conversion emission of Li+ co-doped Y2O3:Er3+ films with dopant concentration

    International Nuclear Information System (INIS)

    Meza-Rocha, A.N.; Huerta, E.F.; Caldiño, U.; Carmona-Téllez, S.; Bettinelli, M.; Speghini, A.; Pelli, S.; Righini, G.C.

    2015-01-01

    The effect of dopant concentration on the up-conversion emission, and in particular on the Er 3+ related green and red emissions of spray pyrolysis deposited films of Y 2 O 3 :Er 3+ co-doped with Li + , is reported. Er 3+ concentrations in the films in the range of 1.1–5.6 at% (1.5–14 at% Er 3+ in the spraying solution) were studied, as well as the effect of co-doping them with Li + . Large concentrations of Er 3+ favor the red emission, especially for contents higher than 10 at% in the spraying solution. Li + co-doping improves the green and red emissions up to 365 and 171 times, respectively, depending on the Er 3+ and Li + concentrations. - Highlights: Up-converting Y 2 O 3 :Er 3+ and Y 2 O 3 :Er 3+ , Li + films were deposited by spray pyrolysis. The effect of Li + co-doping on the green and red UC Er 3+ emission is reported. Li + co-doping improves the green and red emission up to 365 and 171 times

  3. Electron paramagnetic resonance study of Ce doped partially stabilized ZrO2 crystals

    Directory of Open Access Journals (Sweden)

    Mikhail А. Borik

    2017-09-01

    Full Text Available ZrO2 (PSZ solid solutions crystals stabilized with yttrium and cerium oxides have been studied using electron paramagnetic resonance (EPR in the X and Q ranges. Zr3+ have been observed centers in the as-annealed ZrO2 crystals stabilized only by yttrium oxide (2.8 mol% Y2O3. Another type of paramagnetic-O-centers appear as a result of CeO2 addition to ZrO2 crystals along with yttrium oxide. To estimate the concentration of Ce3+ ions in PZS crystals, we recorded the EPR spectra in the presence of a reference at 7 K. Paramagnetic Ce3+ ions have been identified and their relative amount in the PSZ crystals before and after high-temperature heat treatment has been assessed. Annealing in air leads decreases the concentration of Ce3+ ions for all the test compositions and changes the color of the crystals from red to white. After annealing of the sample 2.0Y0.8Ce3Zr, the amount of paramagnetic Ce3+ ions decreased approximately twofold. Paramagnetic centers from Ce3+ have not been detected in the specimen with a low cerium content of 0.1 mol% after annealing which indicates the complete transition of Ce3+ to the Ce4+ state. We show that the forming cerium paramagnetic centers are bound by strong exchange interactions. No angular dependence of the EPR lines of the paramagnetic Ce3+ cations on the applied external magnetic field has been observed. Probable origin of the absence of angular dependence is that the impurity rare-earth ions are located close to one another, forming impurity clusters with an effective spin of Seff=1/2.

  4. The effect of grain size and phosphorous-doping of polycrystalline 3C–SiC on infrared reflectance spectra

    International Nuclear Information System (INIS)

    Rooyen, I.J. van; Engelbrecht, J.A.A.; Henry, A.; Janzén, E.; Neethling, J.H.; Rooyen, P.M. van

    2012-01-01

    Highlights: ► IR is investigated as a technique to measure grain size and P-doping of polycrystalline SiC. ► Infrared plasma minima can be used to determine doping levels in 3C–SiC for doping levels greater than 5 × 10 17 cm −3 . ► A linear relationship is found between FWHM and the inverse of grain size of 3C–SiC irrespective of P-doping level. ► It is further found that ω p is not influenced by the grain size. ► P-doping level has no significant effect on the linear relationship between grain size and surface roughness. - Abstract: The effect of P-doping and grain size of polycrystalline 3C–SiC on the infrared reflectance spectra is reported. The relationship between grain size and full width at half maximum (FWHM) suggest that the behavior of the 3C–SiC with the highest phosphorous doping level (of 1.2 × 10 19 at. cm −3 ) is different from those with lower doping levels ( 18 at. cm −3 ). It is also further demonstrated that the plasma resonance frequency (ω p ) is not influenced by the grain size.

  5. Photophysical and energy transfer processes in Ce{sup 3+} co-doped ZrO{sub 2}: Eu{sup 3+} nanorods

    Energy Technology Data Exchange (ETDEWEB)

    Ahemen, I.; Dejene, F.B. [University of the Free State-Qwaqwa Campus, Department of Physics, Phuthaditjhaba (South Africa)

    2017-02-15

    Cerium (III) ion co-doped ZrO{sub 2}: Eu{sup 3+} nanorods at varying Ce{sup 3+} ion concentrations were synthesized by a simple chemical dehydration route. Their structural, morphological and optical properties were investigated. Structural studies revealed a tetragonal phase with CeO{sub 2} phase grafted onto its surface. Field emission scanning electron microscopy images show nanorods of different dimensions. Diffraction peaks shifted towards smaller angles indicating the incorporation of the rare earth ions. Both Ce{sup 3+} (donor) and Eu{sup 3+} (activator) emission peaks were obtained when the samples were excited via the Ce{sup 3+} excitation band indicating energy transfer from the donor to activator. The process of energy transfer is both multipolar and exchange interactions. However, no significant enhancement of the activator's emission intensity, because concentration quenching process dominated the energy transfer process. The internal quantum efficiency, though low (20-25%), increased with increasing Ce{sup 3+} concentration. (orig.)

  6. Conductivity of A- and B-site doped LaAlO3, LaGaO3, LaScO3 and LaInO3 perovskites

    DEFF Research Database (Denmark)

    Lybye, D.; Poulsen, F.W.; Mogensen, Mogens Bjerg

    2000-01-01

    The conductivity of the materials LaAlO3, LaGaO3, LaScO3 and LaInO3 all doped with 10% strontium on the A-site and 10% magnesium at the B-site has been measured at different temperatures and oxygen partial pressures. The doped LaGaO3 is found to be an almost pure ionic conductor with a conductivi...

  7. Electric-field control of electronic transport properties and enhanced magnetoresistance in La0.7Sr0.3MnO3/0.5BaZr0.2Ti0.8O3-0.5Ba0.7Ca0.3TiO3 lead-free multiferroic structures

    Science.gov (United States)

    Yan, Jian-Min; Gao, Guan-Yin; Liu, Yu-Kuai; Wang, Fei-Fei; Zheng, Ren-Kui

    2017-10-01

    We report the fabrication of lead-free multiferroic structures by depositing ferromagnetic La0.7Sr0.3MnO3 (LSMO) polycrystalline films on polished 0.5BaZr0.2Ti0.8O3-0.5Ba0.7Ca0.3TiO3 (BZT-BCT) piezoelectric ceramic substrates. By applying electric fields to the BZT-BCT along the thickness direction, the resistivity of LSMO films can be effectively manipulated via the piezoelectric strain of the BZT-BCT. Moreover, the LSMO polycrystalline films exhibit almost temperature independent and significantly enhanced magnetoresistance (MR) below TC. At T = 2 K and H = 8 T, the MR of polycrystalline films is approximately two orders of magnitude higher than that of LSMO epitaxial films grown on (LaAlO3)0.3(SrAl1/2Ta1/2O3)0.7 single-crystal substrates. The enhanced MR mainly results from the spin-polarized tunneling of charge carriers across grain boundaries. The LSMO/BZT-BCT structures with electric-field controllable modulation of resistivity and enhanced MR effect may have potential applications in low-energy consumption and environmentally friendly electronic devices.

  8. Specific heat measurements of CePt{sub 3}Si and Ce{sub 1+x}Pt{sub 3+y}Si{sub 1+z}

    Energy Technology Data Exchange (ETDEWEB)

    Motoyama, G. [Graduate School of Material Science, University of Hyogo, Kamigori-cho, Ako-gun, Hyogo 678-1297 (Japan)]. E-mail: motoyama@sci.u-hyogo.ac.jp; Watanabe, M. [Graduate School of Material Science, University of Hyogo, Kamigori-cho, Ako-gun, Hyogo 678-1297 (Japan); Maeda, K. [Graduate School of Material Science, University of Hyogo, Kamigori-cho, Ako-gun, Hyogo 678-1297 (Japan); Oda, Y. [Graduate School of Material Science, University of Hyogo, Kamigori-cho, Ako-gun, Hyogo 678-1297 (Japan); Ueda, K. [Graduate School of Material Science, University of Hyogo, Kamigori-cho, Ako-gun, Hyogo 678-1297 (Japan); Kohara, T. [Graduate School of Material Science, University of Hyogo, Kamigori-cho, Ako-gun, Hyogo 678-1297 (Japan)

    2007-03-15

    We have measured the specific heat of a series of polycrystalline CePt{sub 3}Si and Ce{sub 1+x}Pt{sub 3+y}Si{sub 1+z} samples whose compositions vary slightly from the stoichiometric composition. We observed two peaks derived from magnetic anomalies on the specific heat measurements of the Ce{sub 1+x}Pt{sub 3+y}Si{sub 1+z} samples. One of the peaks relates to the antiferromagnetic phase transition at T{sub N}=2.2K. The other is a large peak at 2.7K observed for the sample that showed a ferromagnetic anomaly at 3.0K on the temperature dependence of the magnetization. Heat treatment had different effects between these anomalies.

  9. Luminescence properties of LiPrxCe1-xP4O12

    International Nuclear Information System (INIS)

    Shalapska, T.; Stryganyuka, G.; Trotsc, D.; Demkiv, T.; Gektin, A.; Voloshinovskii, A.; Dorenbos, P.

    2010-01-01

    LiPr 1-x Ce x P 4 O 12 (x=0, 0.002, 0.02; 0.1) powder samples were prepared using the melt solution technique. Luminescent parameters of LiPr 1-x Ce x P 4 O 12 phosphors have been investigated under ultraviolet-vacuum ultraviolet (3-12 eV) synchrotron radiation and X-rays excitation at room and near liquid He temperatures. Excitation luminescence spectra of Ce 3+ emission, luminescent spectra and decay curves from the lower excited state levels of the 4f 1 5d 1 and 5d 1 electronic configuration of the Pr 3+ and Ce 3+ , respectively, clearly indicate energy transfer from Pr 3+ to Ce 3+ . Energy migration proceeds via the Pr-sublattice followed by nonradiation transfer from Pr 3+ to Ce 3+ ions.

  10. Cube textured CeO2, BaZrO3 and LaAlO3 buffer layers on Ni based Substrates

    International Nuclear Information System (INIS)

    Deinhofer, C; Gritzner, G

    2006-01-01

    CeO 2 , BaZrO 3 as well as LaAlO 3 buffer layers were deposited on {100} Ni + 5 weight-% W substrates by a wet chemical technique. The solutions were prepared by dissolving the metal nitrates or acetates and zirconiumacetylacetonate, respectively, in mixtures of acetic acid, methanol and water. The solutions were applied by dip- or spincoating, dried at 135 deg. C and annealed at temperatures between 900 and 1 400 deg. C depending on the buffer layer for 15 min. under Ar-5% H 2 gas flow. Pole-figure measurements proved the exact texture of each buffer layer. Electron microscopy showed dense and smooth buffer layers

  11. Infrared to visible upconversion luminescence in Er3+/Yb3+ co-doped CeO2 inverse opal

    International Nuclear Information System (INIS)

    Yang, Zhengwen; Wu, Hangjun; Liao, Jiayan; Li, Wucai; Song, Zhiguo; Yang, Yong; Zhou, Dacheng; Wang, Rongfei; Qiu, Jianbei

    2013-01-01

    Highlights: • UC emission of Er 3+ was modified by introducing the structure of inverse opal. • Color tuning of CeO 2 :Yb, Er inverse opal was realized by inhibition of UC emission. • Two-photon excitation processes were observed in CeO 2 :Yb, Er inverse opal. -- Abstract: Infrared to visible upconversion luminescence has been investigated in Er 3+ /Yb 3+ co-doped CeO 2 inverse opal. Under the excitation of 980 nm diode lasers, visible emissions centered at 525, 547, 561, 660 and 680 nm are observed, which are assigned to the Er 3+ transitions of 2 H 11/2 → 4 I 15/2 (525 nm), 4 S 3/2 → 4 I 15/2 (547, 561 nm), 4 F 9/2 → 4 I 15/2 (660 and 680 nm), respectively. The effect of photonic band gap on the upconversion luminescence intensity was also obtained. Additionally, the upconversion luminescence mechanism was studied. The dependence of Er 3+ upconversion emission intensity on pump power reveals that it is a two-photon excitation process

  12. Beta radiation induced luminescence of polycrystalline Cu-doped Li{sub 2}B{sub 4}O{sub 7}

    Energy Technology Data Exchange (ETDEWEB)

    Cruz-Zaragoza, E., E-mail: ecruz@nucleares.unam.mx [Instituto de Ciencias Nucleares, Universidad Nacional Autónoma de México, A.P. 70543, México D.F. 04510, México (Mexico); Furetta, C. [Instituto de Ciencias Nucleares, Universidad Nacional Autónoma de México, A.P. 70543, México D.F. 04510, México (Mexico); Marcazzó, J.; Santiago, M. [Instituto de Física Arroyo Seco (UNCPBA) and CIFICEN (UNCPBA – CICPBA – CONICET), Pinto 399, 7000 Tandil (Argentina); Guarneros, C. [Centro de Investigación en Ciencia y Tecnología Avanzada- IPN, Carretera Puerto Industrial Altamira Km 14.5, 896000 Altamira, Tamaulipas, México (Mexico); Consejo Nacional de Ciencia y Tecnología, Av. Insurgentes Sur 1582, 03940 México D.F., México (Mexico); Pacio, M. [Centro de Investigación en Dispositivos Semiconductores, Instituto de Ciencias Universidad Autónoma de Puebla, Av. 14 Sur, 72570 Puebla, México (Mexico); Palomino, R. [Facultad de Ciencias Físico-Matemáticas, Benemérita Universidad Autónoma de Puebla, Av. San Claudio y 18 Sur, 72570 Puebla, México (Mexico)

    2016-11-15

    Thermoluminescence (TL) and radioluminescence (RL) properties of polycrystalline lithium tetraborate (Li{sub 2}B{sub 4}O{sub 7}) doped with different concentrations of copper (0.25, 0.5, 1 wt %) under beta irradiation have been investigated. The feasibility of using this borate in radiation dosimetry at low doses has been evaluated. Tissue equivalent Li{sub 2}B{sub 4}O{sub 7} was prepared by solid state reaction using mixing stoichiometric compositions of lithium carbonate (Li{sub 2}CO{sub 3}) and boric acid (H{sub 3}BO{sub 3}) and a solution of CuCl{sub 2} as dopant. The glow curve of the most efficient copper doped borate (Li{sub 2}B{sub 4}O{sub 7}:Cu 0.5 wt %) shows a main stable peak centered at 225 °C and a second low temperature peak centered at 80 °C. The low temperature peak fades completely after 24 h of storage in darkness and at room temperature or after an annealing at 120 °C for 10 s. The main peak of the Li{sub 2}B{sub 4}O{sub 7}:Cu remains constant. The TL response of Li{sub 2}B{sub 4}O{sub 7}:Cu shows good linearity in the analyzed dose range. The stability and repeatability of RL signals of the borate have been studied and the Li{sub 2}B{sub 4}O{sub 7}:Cu (0.5 wt %) shows the higher RL emission and a stable and repetitive response. Results show that polycrystalline Li{sub 2}B{sub 4}O{sub 7}:Cu has prospects to be used in beta radiation dosimetry. - Highlights: • Polycrystalline Cu-doped lithium tetraborate (LTB) was obtained by high temperature solid state reaction. • Beta-irradiated LTB:Cu (0.5 wt %) showed to have the highest TL and RL response. • A very good TL linearity in the dose range from 0.01 up to 100 Gy was obtained. • No fading is observed when an annealing at 120 °C for 10 s is carried out. • Results show that LTB:Cu has good prospects to be used in beta radiation dosimetry.

  13. Promoting Effect of CeO2 Addition on Activity and Catalytic Stability in Steam Reforming of Methane over Ni/Al2O3

    International Nuclear Information System (INIS)

    Rakib, A.; Gennequin, C.; Ringot, S.; Aboukais, A.; Abi-Aad, E.; Dhainaut, T.

    2011-01-01

    Hydrogen production by steam reforming of methane was studied over Ni catalysts supported on CeO 2 , Al 2 O 3 and CeO 2 -Al 2 O 3 . These catalysts were prepared using the impregnation method and characterized by XRD. The effect of CeO2 promoter on the catalytic performance of Ni/Al 2 O 3 catalyst for methane steam reforming reaction was investigated. In fact, CeO 2 had a positive effect on the catalytic activity in this reaction. Experimental results demonstrated that Ni/CeO 2 -Al 2 O 3 catalyst showed excellent catalytic activity and high reaction performance. In addition, the effects of reaction temperature and metal content on the conversion of CH 4 and H 2 /CO ratio were also investigated. Results indicated that CH4 conversion increased significantly with the increase of the reaction temperature and metal content. (author)

  14. Effect of Al-doped on physical properties of ZnO Thin films grown by spray pyrolysis on SnO2: F/glass

    Directory of Open Access Journals (Sweden)

    Castagné M.

    2012-06-01

    Full Text Available Transparent conducting thin films of aluminum-doped zinc oxide (ZnO:Al have been deposited on SnO2:F/glass by the chemical spray technique, starting from zinc acetate (CH3CO22Zn.2H2O and aluminum chloride AlCl3. The effect of changing the aluminum-to-zinc ratio y from 0 to 3 at.%, has been thoroughly investigated. It was found that the optical and electrical properties of Al doped ZnO films improved with the addition of aluminum in the spray solution until y=2%. At this Al doping percentage, the thin layers have a resistivity equal to 4.1 × 10−4 Ω.cm and a transmittance of about 90 % in the region [600-1000] nm. XRD patterns confirm that the films have polycristalline nature and a wurtzite (hexagonal structure which characterized with (100, (002 and (101 principal orientations. The undoped films have (002 as the preferred orientation but Al doped ones have (101 as the preferred orientation. Beyond y= 1%, peak intensities decrease considerably.

  15. Enhanced stability of Zr-doped Ba(CeTb)O(3-δ)-Ni cermet membrane for hydrogen separation.

    Science.gov (United States)

    Wei, Yanying; Xue, Jian; Fang, Wei; Chen, Yan; Wang, Haihui; Caro, Jürgen

    2015-07-25

    A mixed protonic and electronic conductor material BaCe(0.85)Tb(0.05)Zr(0.1)O(3-δ) (BCTZ) is prepared and a Ni-BCTZ cermet membrane is synthesized for hydrogen separation. Stable hydrogen permeation fluxes can be obtained for over 100 h through the Ni-BCTZ membrane in both dry and humid conditions, which exhibits an excellent stability compared with Ni-BaCe(0.95)Tb(0.05)O(3-δ) membrane due to the Zr doping.

  16. Different magnetic behaviour of the Kondo compounds Al3Ce and Al11Ce3

    International Nuclear Information System (INIS)

    Benoit, A.; Flouquet, J.; Palleau, J.; Buevoz, J.L.

    1979-08-01

    Neutron diffraction experiments on the Al 3 Ce and Al 11 Ce 3 compounds have been performed on the multidetector of the I.L.L. high flux reactor. No magnetic structure has been detected on the Al 3 Ce compound down to 20 mK. This confirms the non magnetic ground state of Al 3 Ce. For Al 11 Ce 3 , two magnetic structures have been observed: a ferromagnetic one at 4.2 K and an antiferromagnetic one at 2 K. The antiferromagnetic structure, which corresponds to a propagation vector (0,0,1/3), implies a strong reduction of the magnetic moment of determined sites; this reflects the Kondo character of the compounds

  17. Spectroscopic and structural properties of polycrystalline Y{sub 2}Si{sub 2}O{sub 7} doped with Er{sup 3+}

    Energy Technology Data Exchange (ETDEWEB)

    Marciniak, L., E-mail: L.Marciniak@int.pan.wroc.pl [Institute for Low Temperature and Structure Research, Polish Academy of Sciences, Wroclaw (Poland); Hreniak, D.; Strek, W. [Institute for Low Temperature and Structure Research, Polish Academy of Sciences, Wroclaw (Poland); Piccinelli, F., E-mail: fabio.piccinelli@univr.it [Laboratorio di Chimica dello Stato Solido, DB, Università di Verona and INSTM, UdR Verona, Strada Le Grazie 15, 37134 Verona (Italy); Speghini, A.; Bettinelli, M. [Laboratorio di Chimica dello Stato Solido, DB, Università di Verona and INSTM, UdR Verona, Strada Le Grazie 15, 37134 Verona (Italy); Miritello, M., E-mail: maria.miritello@ct.infn.it [CNR-IMM MATIS and Dipartimento di Fisica e Astronomia, Università di Catania, Via S. Sofia 64, 95123 Catania (Italy); Lo Savio, R.; Cardile, P.; Priolo, F. [CNR-IMM MATIS and Dipartimento di Fisica e Astronomia, Università di Catania, Via S. Sofia 64, 95123 Catania (Italy)

    2016-02-15

    Powders of yttrium disilicate (Y{sub 2}Si{sub 2}O{sub 7}) doped with Er{sup 3+} have been prepared by the sol–gel method. The structure of the obtained powders has been determined. Room temperature emission spectra have been recorded and excited state decay profiles have been analyzed. Differences between the spectroscopic properties of Er{sup 3+} in monoclinic α-Y{sub 2}Si{sub 2}O{sub 7} (space group P-1) and β-Y{sub 2}Si{sub 2}O{sub 7} (space group C2/m) polymorphs have been investigated and shown. The significant broadening of the emission spectra recorded for the α phase compared to the one for the β phase was discussed in terms of higher number of Y{sup 3+} sites (4) present in the α phase with respect to only one Y{sup 3+} site in the case of β phase. The higher value of the luminescence decay time of β phase (11.2 ms) compared to the α phase (8.5 ms) is associated with the higher site symmetry of β-Y{sub 2}Si{sub 2}O{sub 7}. Moreover it was found that Er{sup 3+} concentration affects the shape of the {sup 4}I{sub 13/2}→{sup 4}I{sub 15/2} emission band. It results in changes of the relative emission intensities of peaks localized at 1527 nm and 1532 nm; this indicates changes of the Y{sup 3+} sites occupation on increasing the Er{sup 3+} concentration. The luminescence lifetime was observed to decrease with the increase of Er{sup 3+} concentration. The spectroscopic results have been compared with the ones relative to thin films of Y{sub 2}Si{sub 2}O{sub 7}:Er{sup 3+} with a similar composition. The lower value of the luminescence decay time observed for thin films compared to the powder of α phase was explained with the changes of the particles packing resulting in the change of the effective refractive index.

  18. VUV-UV–vis photoluminescence of Ce{sup 3+} and Ce{sup 3+}-Eu{sup 2+} energy transfer in Ba{sub 2}MgSi{sub 2}O{sub 7}

    Energy Technology Data Exchange (ETDEWEB)

    Yan, Jing; Liu, Chunmeng; Zhou, Weijie [MOE Key Laboratory of Bioinorganic and Synthetic Chemistry, KLGHEI of Environment and Energy Chemistry, School of Chemistry, Sun Yat-sen University, Guangzhou 510275 (China); Huang, Yan; Tao, Ye [Beijing Synchrotron Radiation Facility, Institute of High Energy Physics, Chinese Academy of Sciences, Beijing 100039 (China); Liang, Hongbin, E-mail: cesbin@mail.sysu.edu.cn [MOE Key Laboratory of Bioinorganic and Synthetic Chemistry, KLGHEI of Environment and Energy Chemistry, School of Chemistry, Sun Yat-sen University, Guangzhou 510275 (China)

    2017-05-15

    A series of Ce{sup 3+} doped and Ce{sup 3+}-Eu{sup 2+} co-doped Ba{sub 2}MgSi{sub 2}O{sub 7} phosphors was prepared via a high-temperature solid-state reaction technique. The photoluminescence properties, which include synchrotron radiation VUV-UV excitation spectra, emission spectra and concentration effect, thermal stability of Ce{sup 3+} are investigated. Hence the energies of the crystal field split 5d excited states of Ce{sup 3+} are determined. Due to spectral overlap, the energy transfer from sensitizer Ce{sup 3+} to activator Eu{sup 2+} in Ba{sub 2}MgSi{sub 2}O{sub 7}:Ce{sup 3+}, Eu{sup 2+} occurs, and the mechanism is demonstrated to be an electric dipole−dipole interaction. - Highlights: •The energies of five crystal field split 5d states of Ce{sup 3+} in Ba{sub 2}MgSi{sub 2}O{sub 7} were determined by synchrotron radiation VUV-UV excitation spectrum. •The concentration effect, thermal stability of Ce{sup 3+} were investigated. •The energy transfer from Ce{sup 3+} to Eu{sup 2+} and its influence on luminescence decays of Ce{sup 3+} and Eu{sup 2+} were studied.

  19. Combustion synthesis as a novel approach in preparation of polycrystalline Y{sub 2}Cu{sub 2}O{sub 5}

    Energy Technology Data Exchange (ETDEWEB)

    Gebrel, Z., E-mail: z_gebrel@yahoo.com; Blanusa, J.; Spasojevic, V.; Kusigerski, V.; Mrakovic, A.; Alqat, A.; Perovic, M.

    2013-08-15

    Highlights: •Y{sub 2}Cu{sub 2}O{sub 5} was successfully synthesized by both the glycine–nitrate and SHS method. •The reduction of synthesis duration down to 12 h has been achieved. •The detailed crystal structure and magnetic analyses of obtained material are provided. -- Abstract: Polycrystalline samples of Y{sub 2}Cu{sub 2}O{sub 5} were for the first time sintered from precursors obtained by two combustion routes – the glycine–nitrate method (sample S1) and a modified self-propagating high-temperature synthesis (sample S2). The detailed X-ray diffraction analysis has confirmed that both samples are well crystallized and single phase, with the high crystallization degree and cation ordering within a Cu sublattice. Magnetic characterization has shown magnetic behavior typical of pure Y{sub 2}Cu{sub 2}O{sub 5}. The distinctive advantages of these new synthesis routes in comparison to the ceramic sintering are in simplification of the overall procedure as well as in a significant reduction of synthesis duration from several days down to 31 h (S1) or 12 h (S2)

  20. Microstructure and Mechanical Properties of Al2O3/Er3Al5O12 Binary Eutectic Ceramic Prepared by Bridgman Method

    Science.gov (United States)

    Song, Caiyu; Wang, Shunheng; Liu, Juncheng; Zhai, Shuoyan

    2018-01-01

    Directionally solidified Al2O3/Er3Al5O12 (EAG) eutectic ceramic was prepared via vertical Bridgman method with high-frequency induction heating. The effects of the growth rate on the microstructure and mechanical properties of the solidified ceramic were investigated. The experimental results showed that there were no pores or amorphous phases in the directionally solidified Al2O3/EAG eutectic ceramic. Al2O3 phase was embedded in the EAG matrix phase, and the two phases were intertwined with each other to form a typical binary eutectic “hieroglyphic” structure. With the increase of growth rate, the phase size and spacing of the solidified Al2O3/EAG ceramic both decreased, and the growth rate and phase spacing satisfied the λ2v ≈ 60 formula of Jackson-Hunt theory. The cross section microstructure of the solidified ceramic always exhibited an irregular eutectic growth, while the longitudinal section microstructure presented a directional growth. The mechanical properties of the solidified ceramic gradually increased with the increase of growth rate, and the maximum hardness and fracture toughness could reach 21.57 GPa and 2.98 MPa·m1/2 respectively. It was considered that the crack deflection and branching could enhance the toughness of the solidified ceramic effectively. PMID:29601545

  1. Effect of yttrium on electron–phonon coupling strength of 5d state of Ce3+ ion in LYSO:Ce crystals

    International Nuclear Information System (INIS)

    Ding, Dongzhou; Liu, Bo; Wu, Yuntao; Yang, Jianhua; Ren, Guohao; Chen, Junfeng

    2014-01-01

    This paper aims at an improved understanding of luminescence properties of (Lu 1−x Y x ) 2 SiO 5 :Ce (x=0 at%, 26 at%, 45 at%, 66 at% and 100 at%). Photoluminescence emission and excitation spectra as well as Raman spectra of (Lu 1−x Y x ) 2 SiO 5 :Ce were investigated as a function of yttrium (shortened as Y) content in it. Obtained Huang–Rhys factor S indicates that the coupling between Ce1 (7-oxygen-coordinated), Ce2 (6-oxygen-coordinated) and LYSO lattice is intermediate and strong, respectively. Besides, it was found that: with the increase of Y content, crystal field strength around Ce1 and Ce2 decreases, Stokes shift of Ce1 and Ce2 presents an increase trend, and S of Ce2 tends to decrease. These phenomena were explained by geometrical influence of Y 3+ /Lu 3+ on the crystal field splitting of the 5d levels of Ce 3+ and coupling strength. With the increase of Y content, the evolution of S and coupling energy ħω of Ce1 present a slight increase and decrease trend respectively, while S and coupling energy ħω of Ce2 present an obvious decrease and increase trend, respectively. - Highlights: • Crystal field strength around Ce1 decreases with increase of Y content in LYSO:Ce. • A diagram of Huang–Rhys factor S against Y content in LYSO:Ce was constructed. • A diagram of coupling energy ħω against Y content in LYSO:Ce was constructed. • A diagram of Stokes shift against Y content in LYSO:Ce was constructed

  2. Color tunable emission in Ce3+ and Tb3+ co-doped Ba2Ln(BO3)2Cl (Ln=Gd and Y) phosphors for white light-emitting diodes.

    Science.gov (United States)

    Zhang, Niumiao; Guo, Chongfeng; Jing, Heng; Jeong, Jung Hyun

    2013-12-01

    Ce(3+) and Tb(3+) co-doped Ba2Ln(BO3)2Cl (Ln=Y and Gd) green emitting phosphors were prepared by solid state reaction in reductive atmosphere. The emission and excitation spectra as well as luminescence decays were investigated, showing the occurrence of efficient energy transfer from Ce(3+) to Tb(3+) in this system. The phosphors exhibit both a blue emission from Ce(3+) and a green emission from Tb(3+) under near ultraviolet light excitation with 325-375 nm wavelength. Emission colors of phosphors could be tuned from deep blue through cyan to green by adjusting the Tb(3+) concentrations. The energy transfer efficiency and emission intensity of Ba2Y(BO3)2Cl:Ce(3+), Tb(3+) precede those of Ba2Gd(BO3)2Cl:Ce(3+), Tb(3+), and the sample Ba2Y(BO3)2Cl:0.03Ce(3+), 0.10Tb(3+) is the best candidate for n-UV LEDs. Copyright © 2013 Elsevier B.V. All rights reserved.

  3. Study of the defect structure of ''pure'' and doped nonstoichiometric CeO2. Final report, January 1, 1965--May 31, 1977

    International Nuclear Information System (INIS)

    Blumenthal, R.N.

    1977-11-01

    The defect structure and transport properties of defects in nonstoichiometric oxides was studied based on their electrical and thermodynamic behavior. Similar studies were also made on doped-nonstoichiometric oxides to determine the effect of the ionic radii, valence and concentration of the dopant cation on the nonstoichiometric defect structure and the transport properties of these defects. The thermodynamic and electrical property study on ''pure'' and doped-nonstoichiometric CeO 2 /sub -x/ is reviewed. The combined study of the electrical conductivity, ionic transference, and thermodynamic measurements initiated on CaO-doped CeO 2 as a function of temperature, oxygen pressure and CaO content is discussed. The results of similar measurements on CeO 2 doped with other oxides (e.g., ThO 2 , Ta 2 O 5 , etc.) which have cations with different valences and ionic radii are also discussed. The primary objective of these studies was to determine the effect of ionic radii, valence and concentration of the dopant cation on (1) the nonstoichiometric behavior, (2) the thermodynamic quantities ΔantiH/sub O 2 / and ΔantiS/sub O 2 /, (3) the nonstoichiometric defect structure, (4) the electronic and ionic conductivities, and (5) the mobility of electrons and oxygen vacancies in doped CeO 2 /sub -x/

  4. Synthesis, structure, and characterization of a new sandwich-type arsenotungstocerate, [As 2W 18Ce 3O 71(H 2O) 3] 12-

    Science.gov (United States)

    Alizadeh, M. H.; Eshtiagh-Hosseini, H.; Khoshnavazi, R.

    2004-01-01

    The rational synthesis of the new sandwich-type arsenotungstocerate [As 2W 18Ce 3O 71(H 2O) 3] 12- is reported for the first time by reaction of the trivacant lacunary species A-α-[AsW 9O 34] 9- with appropriate Ce IV. The single crystal structure analysis was carried out on K 7(H 3O) 5[As 2W 18Ce 3O 71(H 2O) 3]·9H 2O; H 39As 2Ce 3K 7O 88W 18; ( 2) which crystallizes in triclinic system, space group P overline1 with a=11.615(5) Å, b=17.638(7) Å, c=19.448(8) Å, α=73.643(7)°, β=88.799(7)°, γ=88.078(7)° and Z=2. The anion consists on two lacunary A-α-[AsW 9O 34] 9- Keggin moieties linked via a (H 2OCeO) 3 belt leading to a sandwich-type structure. Each cerium atom adopts tri-capped trigonal-prismatic coordination achieved by two terminal oxygen of an edge shared paired of WO 6 octahedra to each A-α-AsW 9O 349- moiety and two oxygen from the belt and the cap by one μ 3-O (As, W 2) to each A-α-AsW 9O 349- moiety and one external water ligand. The Ce-O bond lengths average in CeO 6 group, Ce-O(As, W 2) and Ce-O(nW) are 2.300(9), 2.887(3) and 2.682(5) Å, respectively. The acid/base titration curve reveals that the anion has two different titrable protons.

  5. The Complete Oxidation of Ethanol at Low Temperature over a Novel Pd-Ce/γ-Al2O3-TiO2 Catalyst

    International Nuclear Information System (INIS)

    Wang, Yanping; Zhao, Jinshuang; Wang, Xiaoli; Li, Zhe; Liu, Pengfei

    2013-01-01

    Pd-Ce/γ-Al 2 O 3 -TiO 2 catalysts were prepared by combined sol.gel and impregnation methods. Transmission electron microscopy, X-ray diffraction, H 2 -temperature-programmed reduction, O 2 -temperature-programmed desorption, and ethanol oxidation experiments were conducted to determine the properties of the catalysts. Addition of an optimal amount of Ce improved the performance of the Pd/γ-Al 2 O 3 -TiO 2 catalyst in promoting the complete oxidation of ethanol. The catalyst with 1% Ce exhibited the highest activity, and catalyzed complete oxidation of ethanol at 175 .deg. C; its selectivity to CO 2 reached 87%. Characterization results show that addition of appropriate amount of Ce could enrich the PdO species, and weaken the Pd-O bonds, thus enhancing oxidation ability of the catalyst. Meanwhile, the introduction of CeO 2 could make PdO better dispersed on γ-Al 2 O 3 -TiO 2 , which is beneficial for the improvement of the catalytic oxidation activity

  6. Highly conductive homoepitaxial Si-doped Ga2O3 films on (010) β-Ga2O3 by pulsed laser deposition

    Science.gov (United States)

    Leedy, Kevin D.; Chabak, Kelson D.; Vasilyev, Vladimir; Look, David C.; Boeckl, John J.; Brown, Jeff L.; Tetlak, Stephen E.; Green, Andrew J.; Moser, Neil A.; Crespo, Antonio; Thomson, Darren B.; Fitch, Robert C.; McCandless, Jonathan P.; Jessen, Gregg H.

    2017-07-01

    Si-doped Ga2O3 thin films were fabricated by pulsed laser deposition on semi-insulating (010) β-Ga2O3 and (0001) Al2O3 substrates. Films deposited on β-Ga2O3 showed single crystal, homoepitaxial growth as determined by high resolution transmission electron microscopy and x-ray diffraction. Corresponding films deposited on Al2O3 were mostly single phase, polycrystalline β-Ga2O3 with a preferred (20 1 ¯ ) orientation. An average conductivity of 732 S cm-1 with a mobility of 26.5 cm2 V-1 s-1 and a carrier concentration of 1.74 × 1020 cm-3 was achieved for films deposited at 550 °C on β-Ga2O3 substrates as determined by Hall-Effect measurements. Two orders of magnitude improvement in conductivity were measured using native substrates versus Al2O3. A high activation efficiency was obtained in the as-deposited condition. The high carrier concentration Ga2O3 thin films achieved by pulsed laser deposition enable application as a low resistance ohmic contact layer in β-Ga2O3 devices.

  7. Al-Doped ZnO Monolayer as a Promising Transparent Electrode Material: A First-Principles Study

    Directory of Open Access Journals (Sweden)

    Mingyang Wu

    2017-03-01

    Full Text Available Al-doped ZnO has attracted much attention as a transparent electrode. The graphene-like ZnO monolayer as a two-dimensional nanostructure material shows exceptional properties compared to bulk ZnO. Here, through first-principle calculations, we found that the transparency in the visible light region of Al-doped ZnO monolayer is significantly enhanced compared to the bulk counterpart. In particular, the 12.5 at% Al-doped ZnO monolayer exhibits the highest visible transmittance of above 99%. Further, the electrical conductivity of the ZnO monolayer is enhanced as a result of Al doping, which also occurred in the bulk system. Our results suggest that Al-doped ZnO monolayer is a promising transparent conducting electrode for nanoscale optoelectronic device applications.

  8. Thermoluminescence and optically stimulated luminescence properties of Dy3+-doped CaO-Al2O3-B2O3-based glasses

    Science.gov (United States)

    Yahaba, T.; Fujimoto, Y.; Yanagida, T.; Koshimizu, M.; Tanaka, H.; Saeki, K.; Asai, K.

    2017-02-01

    We developed Dy3+-doped CaO-Al2O3-B2O3 based glasses with Dy concentrations of 0.5, 1.0, and 2.0 mol% using a melt-quenching technique. The as-synthesized glasses were applicable as materials exhibiting thermoluminescence (TL) and optically stimulated luminescence (OSL). The optical and radiation response properties of the glasses were characterized. In the photoluminescence (PL) spectra, two emission bands due to the 4F9/2 → 6H15/2 and 4F9/2 → 6H13/2 transitions of Dy3+ were observed at 480 and 580 nm. In the OSL spectra, the emission band due to the 4F9/2 → 6H15/2 transition of Dy3+ was observed. Excellent TL and OSL responses were observed for dose ranges of 0.1-90 Gy. In addition, TL fading behavior was better than that of OSL in term of the long-time storage. These results indicate that the Dy3+-doped CaO-Al2O3-B2O3-based glasses are applicable as TL materials.

  9. Growth and characterization of air annealing Tb-doped YAG:Ce single crystal for white-light-emitting diode

    International Nuclear Information System (INIS)

    Gong, Maogao; Xiang, Weidong; Liang, Xiaojuan; Zhong, Jiasong; Chen, Daqin; Huang, Jun; Gu, Guorui; Yang, Cheng; Xiang, Run

    2015-01-01

    Highlights: • We report preparation of transparent Ce,Tb:YAG single crystal by Czochralski method. • The effect of annealing on Ce,Tb:YAG single crystal had been investigated. • The Ce,Tb:YAG single crystal after annealing exhibited better optical performance. • The Ce,Tb:YAG single crystal could be used as an ideal candidate for WLED. - Abstract: We report the preparation of transparent Ce and Tb co-doped Y 3 Al 5 O 12 single crystal by the Czochralski method. The characterization of the resulting single crystal was accomplished by using X-ray powder diffractometer, scanning electron microscopy and energy dispersive X-ray spectroscopy. Absorption peak of the single crystal at about 460 nm has been obtained from ultraviolet–visible absorption spectrometer and their intensity is changed with different annealing condition. Its optical properties also have been investigated using fluorescence spectrometer. What’s more, its photoelectric parameters were studied by LED fast spectrometer. The constructed single crystal based white-light-emitting diode exhibits a high luminous efficiency of 140.89 lm/W, and a correlated color temperature of 4176 K as well as a color rendering index of 56.7, which reveal the prominent feasibility of the present single crystal material in white-light-emitting diode application

  10. Growth and characterization of air annealing Tb-doped YAG:Ce single crystal for white-light-emitting diode

    Energy Technology Data Exchange (ETDEWEB)

    Gong, Maogao [College of Chemistry and Materials Engineering, Wenzhou University, Wenzhou 325035 (China); Xiang, Weidong, E-mail: xiangweidong001@126.com [College of Chemistry and Materials Engineering, Wenzhou University, Wenzhou 325035 (China); Liang, Xiaojuan [College of Chemistry and Materials Engineering, Wenzhou University, Wenzhou 325035 (China); Zhong, Jiasong; Chen, Daqin [College of Materials & Environmental Engineering, Hangzhou Dianzi University, Hangzhou 310018 (China); Huang, Jun; Gu, Guorui; Yang, Cheng; Xiang, Run [College of Chemistry and Materials Engineering, Wenzhou University, Wenzhou 325035 (China)

    2015-08-05

    Highlights: • We report preparation of transparent Ce,Tb:YAG single crystal by Czochralski method. • The effect of annealing on Ce,Tb:YAG single crystal had been investigated. • The Ce,Tb:YAG single crystal after annealing exhibited better optical performance. • The Ce,Tb:YAG single crystal could be used as an ideal candidate for WLED. - Abstract: We report the preparation of transparent Ce and Tb co-doped Y{sub 3}Al{sub 5}O{sub 12} single crystal by the Czochralski method. The characterization of the resulting single crystal was accomplished by using X-ray powder diffractometer, scanning electron microscopy and energy dispersive X-ray spectroscopy. Absorption peak of the single crystal at about 460 nm has been obtained from ultraviolet–visible absorption spectrometer and their intensity is changed with different annealing condition. Its optical properties also have been investigated using fluorescence spectrometer. What’s more, its photoelectric parameters were studied by LED fast spectrometer. The constructed single crystal based white-light-emitting diode exhibits a high luminous efficiency of 140.89 lm/W, and a correlated color temperature of 4176 K as well as a color rendering index of 56.7, which reveal the prominent feasibility of the present single crystal material in white-light-emitting diode application.

  11. Sensitization by UV light of α-Al{sub 2}O{sub 3}:C polycrystalline detectors

    Energy Technology Data Exchange (ETDEWEB)

    Meira B, L. C.; Rubio F, H.; Neres de A, E. [Centro de Desenvolvimento da Tecnologia Nuclear - CNEN, Laboratorio de Dosimetria Termoluminicente, Av. Antonio Carlos 6627, Campus UFMG, CEP 31270-901, Belo Horizonte (Brazil); Santos, A., E-mail: hrf@cdtn.br [Centro de Desenvolvimento da Tecnologia Nuclear - CNEN, Laboratorio de Microesferas Gel, Av. Antonio Carlos 6627, Campus UFMG, CEP 31270-901, Belo Horizonte (Brazil)

    2014-08-15

    This paper describes an increase in sensitivity to gamma and beta radiation on α-Al{sub 2}O{sub 3}:C polycrystalline detector, which has been produced by a sol-gel process, following previous exposure to ultraviolet light. The increased sensitivity of the detector as a function of the exposure time and ultraviolet wavelength was studied. Since the main luminescent centers have emission peaks at different wavelengths, selective measurements of thermoluminescent emission intensity were done, in order to investigate the possible conversion of centers as a result of the exposition to ultraviolet light. Experimental results indicate that the nature and parameters of the luminescent centers in α-Al{sub 2}O{sub 3}:C sol-gel material can be very different of those in α-Al{sub 2}O{sub 3}:C single crystal. (author)

  12. Improving the fast discharge performance of high-voltage LiNi{sub 0.5}Mn{sub 1.5}O{sub 4} spinel by Cu{sup 2+}, Al{sup 3+}, Ti{sup 4+} tri-doping

    Energy Technology Data Exchange (ETDEWEB)

    Deng, Jicheng [Electronic Materials Research Laboratory, Key Laboratory of the Ministry of Education & International Center for Dielectric Research, Xi' an Jiaotong University, Xi' an (China); Shaanxi Engineering Research Center of Advanced Energy Materials & Devices, Xi' an Jiaotong University, Xi' an (China); Xu, Youlong, E-mail: ylxuxjtu@mail.xjtu.edu.cn [Electronic Materials Research Laboratory, Key Laboratory of the Ministry of Education & International Center for Dielectric Research, Xi' an Jiaotong University, Xi' an (China); Shaanxi Engineering Research Center of Advanced Energy Materials & Devices, Xi' an Jiaotong University, Xi' an (China); Xiong, Lilong; Li, Liang [Electronic Materials Research Laboratory, Key Laboratory of the Ministry of Education & International Center for Dielectric Research, Xi' an Jiaotong University, Xi' an (China); Sun, Xiaofei [Shaanxi Engineering Research Center of Advanced Energy Materials & Devices, Xi' an Jiaotong University, Xi' an (China); Zhang, Yuan [Electronic Materials Research Laboratory, Key Laboratory of the Ministry of Education & International Center for Dielectric Research, Xi' an Jiaotong University, Xi' an (China)

    2016-08-25

    The sluggish Li{sup +} ion diffusion coefficient at ∼4.7 V (vs. Li{sup +}/Li) greatly impairs the fast discharge performance of LiMn{sub 1.5}Ni{sub 0.5}O{sub 4} cathode material. Herein, a tri-doping strategy is proposed where Cu{sup 2+}, Al{sup 3+}, Ti{sup 4+} ions are partially substituted for Ni{sup 2+} and Mn{sup 4+}. Cu{sup 2+}, Al{sup 3+}, Ti{sup 4+} tri-doping effectively suppresses the Li{sub x}Ni{sub 1−x}O impurity phase, increases the cation mixing in the octahedral B-site in the spinel, enlarges the electronic conductivity, and enhances the structural stability. Most importantly, the Li{sup +} diffusion coefficients show a peculiar boost at 4.7 V by two orders of magnitude after tri-doping. Compared to the pristine LiMn{sub 1.5}Ni{sub 0.5}O{sub 4} (denoted P-LNM), the tri-doped Li[Ni{sub 0.455}Cu{sub 0.03}Al{sub 0.03}Mn{sub 1.455}Ti{sub 0.03}]O{sub 4} (denoted TD-LNM) exhibits much better fast discharge performance, delivering a specific capacity of ∼101 mAh g{sup −1} at 100 C discharge rate. - Graphical abstract: For the LiMn{sub 1.5}Ni{sub 0.5}O{sub 4} cathode material, the sluggish Li{sup +} ion diffusion coefficient around the ∼4.7 V (vs. Li{sup +}/Li) plateau greatly impair its fast discharge performance, which therefore limit its application in electric vehicles. Herein, a tri-doping strategy is proposed where Cu{sup 2+}, Al{sup 3+}, Ti{sup 4+} ions are partially substituted for Ni{sup 2+} and Mn{sup 4+}. After tri-doping, the Li{sup +} diffusion coefficient at 4.7 V (vs. Li{sup +}/Li) is boosted by two orders of magnitude. Compared to the pristine LiMn{sub 1.5}Ni{sub 0.5}O{sub 4} (denoted P-LNM), the tri-doped Li[Ni{sub 0.455}Cu{sub 0.03}Al{sub 0.03}Mn{sub 1.455}Ti{sub 0.03}]O{sub 4} (denoted TD-LNM) exhibits much better fast discharge performance, delivering a capacity of ∼101 mAh·g{sup −1} at 100 C discharge rate. - Highlights: • Cu, Al, Ti Tri-doping improves electronic conductivity of LiNi{sub 0.5}Mn{sub 1.5}O{sub 4}. • Cu

  13. Synthesis by sol-gel and characterization of catalysts Ag/Al{sub 2}O{sub 3}- CeO{sub 2} for the elimination of nitric oxide; Sintesis por sol-gel y caracterizacion de catalizadores Ag/Al{sub 2}O{sub 3}- CeO{sub 2} para la eliminacion del oxido nitrico

    Energy Technology Data Exchange (ETDEWEB)

    Zayas R, M.L

    2005-07-01

    The environmental pollution is one from the big problems to solve at the present time, because the quality of the alive beings life is affected. For such reason, more clean and economic technologies are required, that it conduces to develop new catalytic alternatives to diminish the nitrogen oxides that due to its chemical processes in the environment contribute considerably in the air pollution. The main objective of the present work, is the preparation and characterization of catalytic materials with base of silver supported in simple and mixed aluminium oxides (Al{sub 2}O{sub 3}) and Cerium oxide (CeO{sub 2}), and its catalytic evaluation that through of the reduction of nitric oxide (NO) using hydrogen (H{sub 2}) as reducer agent. It was synthesized alumina (Al{sub 2}O{sub 3}) and Cerium oxide (CeO{sub 2}) and mixed oxides (Al{sub 2}O{sub 3}- CeO{sub 2}), by the sol-gel method and the cerium oxide (CeO{sub 2}) by precipitation of the cerium nitrate (III) hexa hydrated. The oxides were stabilized thermally at 900 C by 5 hr. The catalysts were prepared by impregnation using silver nitrate (AgNO{sub 3}), the nominal concentration of Ag was of 5% in weight. The catalysts were reduced at 400 C by 2 hr, in hydrogen flow of 60 cc/min. The characterization of the catalytic materials was carried out through different techniques as: nitrogen adsorption to determine the surface area BET, scanning electron microscopy (SEM) to observe the final morphology of the catalysts, X-ray diffraction (XRD) to identify the crystalline phases of the catalytic materials, Infrared spectroscopy (DRIFT) to know the structural characterization of the catalysts, reduction to programmed temperature (TPR) to evidence the interaction metal-support. The catalytic properties of the catalysts were evaluated in the model reaction NO + H{sub 2}, to determine the activity and selectivity. The results indicate that the preparation technique, the precursors and the thermal treatments that underwent

  14. Positron Annihilation Lifetime Study of Pure and Doped Polyvinyl Chloride with Al2O3

    International Nuclear Information System (INIS)

    Abdel-Hady, E.E.; Hamdy, F. M. M.; Alaa, H.B.

    2005-01-01

    Positron annihilation lifetime of pure and doped polyvinyl chloride (PVC) with Al 2 O 3 reflect the effect of concentration as well as temperature on free volume. Therefore, variations of the ortho-positronium (o-Ps) lifetime and its intensity have been correlated with changes in the dielectric properties of the pure and doped PVC. The o-Ps lifetime and its intensity show a linear dependence with a discontinuity at 20 % concentration of Al 2 O 3 . The size and the fractional of the o-Ps hole volume were estimated from the positron annihilation parameters. Therefore, the temperature dependence of the electrical conductivity and the positron annihilation parameters on pure and doped PVC with 20 % Al 2 O 3 were studied in the range from 20 to 140 degree C. The shift of the glass transition temperature to lower temperature for the 20 % Al 2 O 3 doped PVC might explain the increase in the electrical conductivity with the concentration of the additive

  15. Chemical interaction between Ba{sub 2}YCu{sub 3}O{sub 6+x} and CeO{sub 2} at pO{sub 2}=100 Pa

    Energy Technology Data Exchange (ETDEWEB)

    Wong-Ng, W.; Yang, Z.; Cook, L.P.; Huang, Q.; Frank, J. [Materials Science and Engineering Laboratory, National Institute of Standards and Technology, Gaithersburg, MD (United States); Kaduk, J.A. [BP-Amoco Research, Naperville, IL (United States)

    2005-07-01

    Chemical interaction between the Ba{sub 2}YCu{sub 3}O{sub 6+x} superconductor and the CeO{sub 2} buffer layers employed in coated conductor architectures has been modeled experimentally by investigating phase equilibria on the Ba{sub 2}YCu{sub 3}O{sub 6+x}-CeO{sub 2} join at pO{sub 2}=100 Pa. This join is actually a non-binary join within the BaOY{sub 2}O{sub 3}CeO{sub 2}CuO{sub x} quaternary system. At an approximate mole ratio of Ba{sub 2}YCu{sub 3}O{sub 6+x}:CeO{sub 2} = 40:60, a phase boundary was found to separate two four-phase regions. At the Ba{sub 2}YCu{sub 3}O{sub 6+x}-rich side of the join, the four-phase region consists of Ba{sub 2}YCu{sub 3}O{sub 6+x}, Ba(Ce{sub 1-z}Y{sub z})O{sub 3-x}, BaY{sub 2}CuO{sub 5}, and Cu{sub 2}O; at the CeO{sub 2} rich side, the four phases were determined to be Ba(Ce{sub 1-z}Y{sub z})O{sub 3-x}, BaY{sub 2}CuO{sub 5}, Cu{sub 2}O and CeO{sub 2}. At 810 C and pO{sub 2}=100 Pa, there appears to be negligible solid solution formation of the types Y{sub 1-z}Ce{sub z}O{sub 3-x} and Ce{sub 1-z}Y{sub z}O{sub 2-x}. The minimum melting temperature along the Ba{sub 2}YCu{sub 3}O{sub 6+x}-CeO{sub 2} join was determined to be {approx} 860 C. As part of this study, phase diagrams of the subsystems CeO{sub 2}-Y{sub 2}O{sub 3}-CuO{sub x}, BaO-CeO{sub 2}-CuO{sub x}, and BaO-Y{sub 2}O{sub 3}-CeO{sub 2} were also determined at 810 C under 100 Pa pO{sub 2}. The Y{sub 2}O{sub 3}-CeO{sub 2}-CuO{sub x} diagram does not contain ternary phases and shows a tie-line from Y{sub 2}O{sub 3} to the binary phase Y{sub 2}Cu{sub 2}O{sub 5-x}. Similarly, the BaO-CeO{sub 2}-CuO{sub x} diagram contains no ternary phases, but has four tie-lines originating from BaCeO{sub 3} to Ba{sub 2}CuO{sub 3+x}, BaCuO{sub 2+x}, BaCu{sub 2}O{sub 2+x} and CuO{sub x}. The BaO-Y{sub 2}O{sub 3}-CeO{sub 2} system contains one ternary phase, the solid solution Ba(Ce{sub 1-z}Y{sub z})O{sub 3-x} (0{<=}z{<=}0.13), which crystallizes with the orthorhombic space group Pmcn (No. 62

  16. Development of accident tolerant FeCrAl-ODS steels utilizing Ce-oxide particles dispersion

    Science.gov (United States)

    Shibata, Hiroki; Ukai, Shigeharu; Oono, Naoko H.; Sakamoto, Kan; Hirai, Mutsumi

    2018-04-01

    FeCrAl-ODS ferritic steels with Ce-oxide dispersion instead of Y-oxide were produced for the accident tolerant fuel cladding of the light water reactor. Excess oxygen (Ex.O) was added to improve the mechanical property. The tensile strength at Ex.O = 0 is around 200 MPa at 700 °C, mainly owing to dispersed Ce2O3 particles in less than 10 nm size. The formation of the fine Ce2O3 particles is dominated by a coherent interface with ferritic matrix. With increasing Ex.O, an increased of number density of coarser Ce-Al type oxide particles over 10 nm size is responsible for the improvement of the tensile strength. Change of the type of oxide particle, CeO2, Ce2O3, CeAlO3, Al2O3, in FeCrAl-ODS steel was thermodynamically analyzed as a parameter of Ex.O.

  17. Investigation of the physical, optical, and photocatalytic properties of CeO2/Fe-doped InVO4 composite

    Science.gov (United States)

    Chaison, Jindaporn; Wetchakun, Khatcharin; Wetchakun, Natda

    2017-12-01

    The CeO2/Fe-doped InVO4 composites with various Fe concentrations (0.5, 1.0, 2.0, 5.0 and 6.0 mol%) was synthesized by homogeneous precipitation and hydrothermal methods. The as-synthesized samples were characterized by powder X-ray diffraction (XRD), Brunauer Emmett and Teller (BET)-specific surface area, field emission scanning electron microscopy (FE-SEM), transmission electron microscopy (TEM), energy-dispersive X-ray spectroscopy (EDS), X-ray photoelectron spectroscopy (XPS), and UV-visible diffuse reflectance spectroscopy (DRS). Fe-doping into InVO4 crystal induces the distortion of the crystalline structure, the transformation of InVO4 morphology, and the new energy subband level generation of Fe between the CB and VB edge of InVO4. The electron excitation from the VB to Fe orbitals results in the decreased band gap and the extended absorption of visible-light, and thus enhances its photocatalytic performance. Visible-light-driven photocatalytic degradation of Rhodamine B (RhB) dye in water was used to evaluate the photocatalytic performance of CeO2/Fe-doped InVO4 composites. The results revealed that there is an optimum Fe (5.0 mol %) doping level. The composite with the optimum doping level obtains high photocatalytic activity of CeO2/Fe-doped InVO4 composite compared to pure CeO2 and pure InVO4 host. The increase of photocatalytic activity of CeO2/Fe-doped InVO4 composite was ascribed to the surface area, crystal defect, and band gap energy. Moreover, the photocatalytic enhancement is also because iron ions act as a trapping site, which results in the higher separation efficiency of photogenerated electrons and holes pairs in the CeO2/InVO4 composite. The evaluation of radical scavengers confirmed that hydroxyl radical was the main active species during the photodegradation of RhB. These synergistic effects are responsible for the enhanced photocatalytic activity of CeO2/Fe-doped InVO4 composite. Furthermore, the possible enhanced photocatalytic mechanism

  18. Photoluminescence properties and energy transfer in Ce(3+) /Dy(3+) co-doped Sr(3) MgSi(2) O(8) phosphors for potential application in ultraviolet white light-emitting diodes.

    Science.gov (United States)

    Yu, Hong; Zi, Wenwen; Lan, Shi; Gan, Shucai; Zou, Haifeng; Xu, Xuechun; Hong, Guangyan

    2013-01-01

    Sr(3) MgSi(2) O(8) :Ce(3+) , Dy(3+) phosphors were prepared by a solid-state reaction technique and the photoluminescence properties were investigated. The emission spectra show not only a band due to Ce(3+) ions (403 nm) but also as a band due to Dy(3+) ions (480, 575 nm) (UV light excitation). The photoluminescence properties reveal that effective energy transfer occurs in Ce(3+) /Dy(3+) co-doped Sr(3) MgSi(2) O(8)phosphors, and the co-doping of Ce(3+) could enhance the emission intensity of Dy(3+) to a certain extent by transferring its energy to Dy(3+) . The Ce(3+) /Dy(3+) energy transfer was investigated by emission/excitation spectra, and photoluminescence decay behaviors. In Sr2.94 MgSi2 O8 :0.01Ce(3+) , 0.05Dy(3+) phosphors, the fluorescence lifetime of Dy(3+) (from 3.35 to 27.59 ns) is increased whereas that of Ce(3+) is greatly decreased (from 43.59 to 13.55 ns), and this provides indirect evidence of the Ce(3+) to Dy(3+) energy transfer. The varied emitted color of Sr(3) MgSi(2) O(8):Ce(3+) , Dy(3+) phosphors from blue to white were achieved by altering the concentration ratio of Ce(3+) and Dy(3+) . These results indicate Sr(3) MgSi(2) O(8):Ce(3+) , Dy(3+) may be as a candidate phosphor for white light-emitting diodes. Copyright © 2012 John Wiley & Sons, Ltd.

  19. Integrated chemical process for exothermic wave synthesis of high luminance YAG:Ce phosphors

    International Nuclear Information System (INIS)

    Won, C.W.; Nersisyan, H.H.; Won, H.I.; Youn, J.W.

    2011-01-01

    In this paper, high-luminance yellow-emitting Y 3 Al 5 O 12 :Ce 3+ phosphor (YAG:Ce) microparticles were prepared in a solid flame using a 1.425Y 2 O 3 +2.5Al 2 O 3 +0.15CeO 2 +k(KClO 3 +urea)+mNH 4 F precursor mixture (here k is the number of moles of the KClO 3 +urea red-ox mixture, and m is the number of moles of NH 4 F). The self-sustaining combustion process for the entire reaction sample was provided by the heat generated from the KClO 3 +urea mixture. Parametric studies demonstrated that the maximum temperature in the combustion wave varied from 885 to 1200 deg. C for k=2.0-3.0 mole and m=0-1.5 mole. X-ray analysis results showed that the product obtained in the solid flame consisted of Y 3 Al 5 O 12 :Ce 3+ and KCl phases. Therefore, after dissolving potassium chloride in distillated water, pure-phase YAG:Ce phosphor powder was obtained. The as-prepared YAG:Ce phosphor particles had diameters of 10-25 μm and good dispersity and exhibited luminescence properties comparable to those of YAG:Ce phosphor powders prepared by conventional high-temperature processing. - Highlights: → A new solid-flame strategy was developed for synthesizing high-luminance YAG:Ce phosphor. → Adding KClO 3 +CO(NH 2 ) 2 +NH 4 F mixture to oxide powders provides a low-temperature combustion process. → YAG:Ce phosphor particles 10-25 μm in diameter were obtained at 1000-1100 deg. C within tens of seconds. → As-prepared YAG:Ce emission intensity was 90.1-103.2% compared to that of the reference sample.

  20. The effect of grain size and phosphorous-doping of polycrystalline 3C-SiC on infrared reflectance spectra

    Energy Technology Data Exchange (ETDEWEB)

    Rooyen, I.J. van, E-mail: Isabella.vanRooyen@inl.gov [Fuel Performance and Design Department, Idaho National Laboratory, Idaho Falls, ID 83415-6188 (United States); Department of Physics, Nelson Mandela Metropolitan University, Port Elizabeth (South Africa); Engelbrecht, J.A.A. [Department of Physics, Nelson Mandela Metropolitan University, Port Elizabeth (South Africa); Henry, A.; Janzen, E. [Department of Physics, Chemistry and Biology, Semiconductor Materials, Linkoeping University, Linkoeping 58183 (Sweden); Neethling, J.H. [Department of Physics, Nelson Mandela Metropolitan University, Port Elizabeth (South Africa); Rooyen, P.M. van [Philip M van Rooyen Network Consultants, Midlands Estates (South Africa)

    2012-03-15

    Highlights: Black-Right-Pointing-Pointer IR is investigated as a technique to measure grain size and P-doping of polycrystalline SiC. Black-Right-Pointing-Pointer Infrared plasma minima can be used to determine doping levels in 3C-SiC for doping levels greater than 5 Multiplication-Sign 10{sup 17} cm{sup -3}. Black-Right-Pointing-Pointer A linear relationship is found between FWHM and the inverse of grain size of 3C-SiC irrespective of P-doping level. Black-Right-Pointing-Pointer It is further found that {omega}{sub p} is not influenced by the grain size. Black-Right-Pointing-Pointer P-doping level has no significant effect on the linear relationship between grain size and surface roughness. - Abstract: The effect of P-doping and grain size of polycrystalline 3C-SiC on the infrared reflectance spectra is reported. The relationship between grain size and full width at half maximum (FWHM) suggest that the behavior of the 3C-SiC with the highest phosphorous doping level (of 1.2 Multiplication-Sign 10{sup 19} at. cm{sup -3}) is different from those with lower doping levels (<6.6 Multiplication-Sign 10{sup 18} at. cm{sup -3}). It is also further demonstrated that the plasma resonance frequency ({omega}{sub p}) is not influenced by the grain size.

  1. Hydrothermal synthesis and characterization of polycrystalline gadolinium aluminum perovskite (GdAlO3, GAP

    Directory of Open Access Journals (Sweden)

    N. Girish H.

    2015-06-01

    Full Text Available Gadolinium aluminum perovskite (GdAlO3, GAP is a promising high temperature ceramic material, known for its wide applications in phosphors. Polycrystalline gadolinium aluminum perovskites were synthesized using a precursor of co-precipitate gel of GdAlO3 by employing hydrothermal supercritical fluid technique under pressure and temperature ranging from 150 to 200 MPa and 600 to 700 °C, respectively. The resulted products of GAP were studied using the characterization techniques, such as powder X-ray diffraction analysis (XRD, infrared spectroscopy (IR, scanning electron microscopy (SEM and energy dispersive analysis of X-ray (EDX. The X-ray diffraction pattern matched well with the reported orthorhombic GAP pattern (JCPDS-46-0395.

  2. Structural and magnetotransport properties of the Y doped A-site deficient double layered manganites La{sub 1.2−x}□{sub 0.2}Y{sub x}Ca{sub 1.6}Mn{sub 2}O{sub 7}

    Energy Technology Data Exchange (ETDEWEB)

    Mahamdioua, N., E-mail: mahamdioua.nabil@gmail.com [LEND, Faculty of Science and Technology, Jijel University, Jijel 18000 (Algeria); Amira, A. [LEND, Faculty of Science and Technology, Jijel University, Jijel 18000 (Algeria); Altintas, S.P. [Department of Physics, Faculty of Arts and Sciences, AIB University, Bolu 14280 (Turkey); Koc University, Surface Science and Technology Center (KUYTAM), 34450-Sariyer, Istanbul (Turkey); Varilci, A.; Terzioglu, C. [Department of Physics, Faculty of Arts and Sciences, AIB University, Bolu 14280 (Turkey)

    2016-08-15

    We present structural, magnetic and electrical properties of the polycrystalline A-site-deficient yttrium doped double layered manganites La{sub 1.2−x}□{sub 0.2}Y{sub x}Ca{sub 1.6}Mn{sub 2}O{sub 7} (x=0.2, 0.3 and 0.4) prepared by a solid state reaction method. The samples crystallize in the tetragonal structure with the space group I4/mmm. Doping with Y decreases the cell parameters and causes a decrease of the metal-insulator transition temperature. The same evolution with doping is also seen for the deduced Curie temperature from susceptibility curves which present a clear paramagnetic-ferromagnetic transition. The significant positive intrinsic magnetoresistance, shown in all samples, reaches 85% at 122 K under 7 T for 0.3 doped sample and can be attributed to the suppression of spin fluctuations via aligning the spins under external magnetic field, while the extrinsic one is attributed to the inter-grain spin-polarized tunneling across the grain boundaries. The simulation of the resistivity curves in the entire temperature range show that the percolation model is suitable to fit our results. The applied magnetic field increases the density of states near the Fermi level, which is in accordance with the observed decrease of resistivity. - Graphical abstract: Resistivity and magnetoresistance of La{sub 1.2−x}□{sub 0.2}Y{sub x}Ca{sub 1.6}Mn{sub 2}O{sub 7} (x=0.2, 0.3, 0.4). Solid lines correspond to the fitting results. Display Omitted.

  3. Eu{sup 3+}-doped Y{sub 2}O{sub 3} hexagonal prisms: Shape-controlled synthesis and tailored luminescence properties

    Energy Technology Data Exchange (ETDEWEB)

    Yang, Errui [Key Laboratory of Design and Assembly of Functional Nanostructures, Fujian Institute of Research on the Structure of Matter, Chinese Academy of Sciences, Fuzhou, Fujian 350002 (China); Li, Guangshe [Fujian Provincial Key Laboratory of Nanomaterials, Fujian Institute of Research on the Structure of Matter, Chinese Academy of Sciences, Fuzhou, Fujian 350002 (China); Fu, Chaochao; Zheng, Jing [Key Laboratory of Design and Assembly of Functional Nanostructures, Fujian Institute of Research on the Structure of Matter, Chinese Academy of Sciences, Fuzhou, Fujian 350002 (China); Huang, Xinsong [Fujian Provincial Key Laboratory of Nanomaterials, Fujian Institute of Research on the Structure of Matter, Chinese Academy of Sciences, Fuzhou, Fujian 350002 (China); Xu, Wen [State Key Laboratory on Integrated Optoelectronics, College of Electronic Science and Engineering, Jilin University, 2699 Qianjin Street, Changchun 130012 (China); Li, Liping, E-mail: lipingli@fjirsm.ac.cn [Key Laboratory of Design and Assembly of Functional Nanostructures, Fujian Institute of Research on the Structure of Matter, Chinese Academy of Sciences, Fuzhou, Fujian 350002 (China)

    2015-10-25

    In this work, Eu{sup 3+} doped Y{sub 2}O{sub 3} hexagonal prisms were synthesized by a novel two-phase approach, which involves water at the bottom as aqueous phase and oleylamine in the above as oil phase. With this unique reaction system, precursors of hexagonal prisms Y{sub 4}O(OH){sub 9}(NO{sub 3}) were first obtained by simply varying the volume ratio of water to oleylamine. Time-dependent experiments were systematically performed to reveal the growth mechanism of the precursor. After subsequent heat treatment, these precursors transformed to Y{sub 2}O{sub 3} hexagonal prisms with controlled diameters and aspect ratios varying from 4 to 19. Such a transformation is preceded via a topotactic process, as indicated by TG-DTA and mass spectra. Eventually, all Eu{sup 3+} doped Y{sub 2}O{sub 3} hexagonal prisms were found to exhibit an intensive red emission at 611 nm, which corresponds to {sup 5}D{sub 0}→{sup 7}F{sub 2} transition of Eu{sup 3+}. With varying the aspect ratio of hexagonal prisms and increasing Eu{sup 3+} concentration in Y{sub 2}O{sub 3}, an optimum external quantum efficiency was achieved. - Graphical abstract: In this work, Eu{sup 3+} doped Y{sub 2}O{sub 3} hexagonal prisms with controlled aspect ratio from 4.4 to 19.3 were synthesized by transformation of the precursor Y{sub 4}O(OH){sub 9}(NO{sub 3}) hexagonal prisms from a novel two-phase reaction system. The growth mechanism of the precursor has been systematically investigated, and a topotactic phase transformation from precursors to cubic Y{sub 2}O{sub 3} is for the first time put forward. By the size controlling and aspect ratio adjusting, the luminescence emission intensity as well as external quantum efficiency of Eu{sup 3+} doped Y{sub 2}O{sub 3} hexagonal prisms is further tailored to show an optimum. - Highlights: • Eu{sup 3+} doped Y{sub 2}O{sub 3} hexagonal prisms were synthesized by a novel two-phase approach. • Inheriting mechanism of prisms morphology from Y{sub 4}O(OH){sub 9

  4. Influence of Ce Doping on the Electrical and Optical Properties of TiO2 and Its Photocatalytic Activity for the Degradation of Remazol Brilliant Blue R

    Directory of Open Access Journals (Sweden)

    Aisha Malik

    2013-01-01

    Full Text Available Nanocrystalline TiO2 particles doped with different concentrations of Cerium (Ce, 1–10% have been synthesized using sol-gel method. The prepared particles were characterized by standard analytical techniques such as X-ray diffraction (XRD, FTIR and Scanning Electron Microscopy (SEM, and Transmission Electron Microscopy (TEM. The XRD analysis shows no change in crystal structure of TiO2 after doping with different concentrations of Ce, which indicates the single-phase polycrystalline material. The SEM analysis shows the partial crystalline nature of undoped, and doped TiO2 and TEM analysis shows the particle sizes were in the range of 9–14 nm in size. The a.c. analysis shows that the dielectric constant ε and dielectric loss tan δ decrease with the increase in frequency. The dielectric property decreases with the increase in dopant concentration. It is also observed that the impedance increases with an increase in dopant concentration. The photocatalytic activity of the synthesized particles (Ce-doped TiO2 with dopant concentration of 9% (Ce showed the highest photocatalytic activity for the degradation of the dye derivative Remazol Brilliant Blue R in an immersion well photochemical reactor with 500 W halogen linear lamp in the presence of atmospheric oxygen.

  5. Effect of shallow donors on Curie–Weiss temperature of Co-doped ZnO

    Energy Technology Data Exchange (ETDEWEB)

    Guo, Shuxia, E-mail: gsx0391@sina.com [Department of Physics, Jiaozuo Teachers College, Jiaozuo 454001 (China); Key Laboratory for Special Functional Materials of Ministry of Education, Henan University, Kaifeng 475004 (China); Li, Jiwu [Department of Physics, Jiaozuo Teachers College, Jiaozuo 454001 (China); Du, Zuliang [Key Laboratory for Special Functional Materials of Ministry of Education, Henan University, Kaifeng 475004 (China)

    2014-12-15

    Co-doped ZnO and Al, Co co-doped ZnO polycrystalline powders were synthesized by co-precipitation method. The magnetization curves measured at 2 K show no hysteresis neither remanence for all samples. ZnO:Co grown at low temperature has a positive Curie–Weiss temperature Θ, and ZnO:Co grown at high temperature has a negative Θ. But Al-doped ZnO:Co grown at high temperature has a positive Θ. Positive Curie–Weiss temperature Θ was considered to have relation to the presence of shallow donors in the samples. - Highlights: • Co-doped ZnO and Al, Co co-doped ZnO polycrystalline powders were synthesized. • No hysteresis is observed for all samples. • The Curie–Weiss temperature Θ changes its sign by Al doping. • Positive Θ should be related to shallow donors.

  6. Significant improvement in performances of LiNi0.5Mn1.5O4 through surface modification with high ordered Al-doped ZnO electro-conductive layer

    International Nuclear Information System (INIS)

    Sun, Hongdan; Xia, Bingbo; Liu, Weiwei; Fang, Guoqing; Wu, Jingjing; Wang, Haibo; Zhang, Ruixue; Kaneko, Shingo; Zheng, Junwei; Wang, Hongyu; Li, Decheng

    2015-01-01

    Graphical abstract: Al-doped ZnO (AZO)-coated LiNi 0.5 Mn 1.5 O 4 (LNMO) was prepared by sol–gel method. AZO-coated LNMO electrode shows excellent rate capability and a remarkable improvement in the cyclic performance at a high rate at elevated temperature. - Highlights: • Al-doped ZnO (AZO)-coated LiNi 0.5 Mn 1.5 O 4 (LNMO) was prepared by a traditional sol–gel method. • Al-doped ZnO (AZO) layer grown on the surface of LNMO is high ordered. • At a high rate of 10 C, the discharge capacity of the AZO-coated LNMO electrode can reach 114 mAh g −1 . • Al-doped ZnO (AZO) modification improved cyclic performance of LNMO at high temperatures. - Abstract: Al-doped ZnO (AZO)-coated LiNi 0.5 Mn 1.5 O 4 (LNMO) was prepared by sol–gel method. Transmission electron microscopy (TEM) analysis indicates that AZO layer grown on the surface of LNMO is high ordered. The results of electrochemical performance measurements reveal that the AZO-coated LNMO electrode displays the best rate capability compared with the bare LNMO and ZnO-coated LNMO, even at a high rate of 10 C. The discharge capacity of the AZO-coated LNMO electrode can still reach 114.3 mAh g −1 , about 89% of its discharge capacity at 0.1 C. Moreover, AZO-coated LNMO electrode shows a remarkable improvement in the cyclic performance at a high rate at elevated temperature due to the protective effect of AZO coating layer. The electrode delivers a capacity of 120.3 mAh g −1 with the capacity retention of 95% at 5 C in 50 cycles at 50 °C. The analysis of electrochemical impedance spectra (EIS) indicates that AZO-coated LNMO possesses the lowest charge transfer resistance compared to the bare LNMO and ZnO-coated LNMO, which may be responsible for improved rate capability

  7. Ce-doped nanoparticles of TiO2: Rutile-to-brookite phase transition and evolution of Ce local-structure studied with XRD and XANES

    International Nuclear Information System (INIS)

    Kityakarn, Sutasinee; Worayingyong, Attera; Suramitr, Anwaraporn; Smith, M.F.

    2013-01-01

    The crystal and electronic structural changes undergone by TiO 2 nanoparticles when Ce is introduced were studied using X-ray diffraction (XRD) and X-ray absorption near-edge spectroscopy (XANES). A small amount of Ce (less than 1% molar concentration) resulted in i/a significant reduction of the average size of the TiO 2 nanoparticles and ii/a phase transition in which brookite replaced rutile as the minority phase component (anatase was the majority phase component at all Ce concentrations studied up to 10% molar concentration). The Ce L3 edge XANES revealed changes in the local environment of Ce impurities. As Ce concentration was increased the fraction of Ce that have formal valence of +3 decreased and, for the remaining Ce with valence +4, the 4f orbitals became less-strongly hybridized with the p-orbitals of oxygen neighbors. The results have implications for photocatalytic and gas sensing properties of Ce-doped TiO 2 . - Highlights: ► Ce-doping: TiO 2 nanoparticles shrink and minority phase changes rutile-> brookite. ► XANES reveals phase change for arbitrarily small particles (while XRD fails). ► As Ce added: fraction of Ce +3 dopants falls, hybridization of Ce +4 with O weakens

  8. Hydrazinium lanthanide oxalates: synthesis, structure and thermal reactivity of N_2H_5[Ln_2(C_2O_4)_4(N_2H_5)].4H_2O, Ln = Ce, Nd

    International Nuclear Information System (INIS)

    De Almeida, Lucie; Grandjean, Stephane; Abraham, Francis; Rivenet, Murielle; Patisson, Fabrice

    2014-01-01

    New hydrazinium lanthanide oxalates N_2H_5[Ln_2(C_2O_4)_4(N_2H_5)].4H_2O, Ln = Ce (Ce-H_yO_x) and Nd (Nd- H_yO_x), were synthesized by hydrothermal reaction at 150 C between lanthanide nitrate, oxalic acid and hydrazine solutions. The structure of the Nd compound was determined from single-crystal X-ray diffraction data, space group P2_1/c with a = 16.315(4), b = 12.127(3), c = 11.430(2) Angstroms, β = 116.638(4) degrees, V = 2021.4(7) Angstroems"3, Z = 4, and R1 = 0.0313 for 4231 independent reflections. Two distinct neodymium polyhedra are formed, NdO_9 and NdO_8N, an oxygen of one monodentate oxalate in the former being replaced by a nitrogen atom of a coordinated hydrazinium ion in the latter. The infrared absorption band at 1005 cm"-"1 confirms the coordination of N_2H_5"+ to the metal. These polyhedra are connected through μ"2 and μ"3 oxalate ions to form an anionic three-dimensional neodymium-oxalate arrangement. A non-coordinated charge-compensating hydrazinium ion occupies, with water molecules, the resulting tunnels. The N-N stretching frequencies of the infrared spectra demonstrate the existence of the two types of hydrazine ions. Thermal reactivity of these hydrazinium oxalates and of the mixed isotypic Ce/Nd (CeNd-H_yO_x) oxalate were studied by using thermogravimetric and differential thermal analyses coupled with gas analyzers, and high temperature X-ray diffraction. Under air, fine particles of CeO_2 and Ce_0_._5Nd_0_._5O_1_._7_5 are formed at low temperature from Ce-H_yO_x and CeNd-H_yO_x, respectively, thanks to a decomposition/oxidation process. Under argon flow, dioxy-mono-cyanamides Ln_2O_2CN_2 are formed. (authors)

  9. Effect of alkali-earth ions on local structure of the LaAlO3-La0.67A0.33MnO3 (A = Ca, Sr, Ba) diluted solid solutions: 27Al NMR studies

    International Nuclear Information System (INIS)

    Charnaya, E.V.; Cheng Tien; Lee, M.K.; Sun, S.Y.; Chejina, N.V.

    2007-01-01

    27 Al Magic Angle Spinning (MAS) NMR studies are carried out for diluted alkali-earth metal doped lanthanum manganite solid solutions in the lanthanum aluminate (1-y)LaAlO 3 -yLa 0.67 A 0.33 MnO 3 (A = Ca, Sr, Ba) with y = 0, 2, 3, and 5 mol %. The spectra depend on the dopant species and show higher substitutional ordering for the Ba containing mixed crystals. Magnetically shifted lines are observed in all solid solutions and attributed to Al in the octahedral oxygen environment near manganese trivalent ions. Nonlinear dependences of their intensity are referred to the manganese-rich cluster formation. An additional MAS NMR line corresponding to aluminium at sites different from the octahedral site in pure LaAlO 3 is observed only in solutions doped with Ba. 3Q MAS NMR revealed that the broadening of this line is governed mainly by quadrupole coupling and allowed calculating the isotropic chemical shift [ru

  10. Ce-doped LuAG single-crystal fibers grown from the melt for high-energy physics

    CERN Document Server

    Xu, X; Moretti, F; Pauwels, K; Lecoq, P; Auffray, E; Dujardin, C

    2014-01-01

    Under a stationary stable regime undoped and Ce-doped LuAG (Lu3Al5O12) single-crystal fibers were grown by a micro-pulling-down technique. The meniscus length corresponding to the equilibrium state was <200 mu m. Fluctuations in the fiber composition and pulling rate were found to have a significant effect on the properties of the fibers grown. A great improvement in the performance was found in samples containing low Ce concentrations (<= 0.1 at.\\%) and produced using pulling rates <0.5 mm min(-1). Under such conditions a good lateral surface fiber quality was obtained and light propagation was significantly improved. Conversely, a high Ce concentration and a high pulling rate resulted in a strong degradation of the fiber surface quality causing defects to appear and a decrease in light output. (C) 2014 Acta Materialia Inc. Published by Elsevier Ltd. All rights reserved.

  11. Luminescence properties of Y2O3:Bi3+, Yb3+ co-doped phosphor for application in solar cells

    Science.gov (United States)

    Lee, E.; Kroon, R. E.; Terblans, J. J.; Swart, H. C.

    2018-04-01

    Bismuth (Bi3+) and ytterbium (Yb3+) co-doped yttrium oxide (Y2O3) phosphor powder was successfully synthesised using the co-precipitation technique. The X-ray diffraction (XRD) patterns confirmed that a single phase cubic structure with a Ia-3 space group was formed. The visible emission confirmed the two symmetry sites, C2 and S6, found in the Y2O3 host material and revealed that Bi3+ ions preferred the S6 site as seen the stronger emission intensity. The near-infrared (NIR) emission of Yb3+ increased significantly by the presence of the Bi3+ ions when compared to the singly doped Y2O3:Yb3+ phosphor with the same Yb3+ concentration. An increase in the NIR emission intensity was also observed by simply increasing the Yb3+ concentration in the Y2O3:Bi3+, Yb3+ phosphor material where the intensity increased up to x = 5.0 mol% of Yb3+ before decreasing due to concentration quenching.

  12. Comparative study of phase structure and dielectric properties for K0.5Bi0.5TiO3-BiAlO3 and LaAlO3-BiAlO3

    International Nuclear Information System (INIS)

    Hou, Yudong; Zheng, Mupeng; Si, Meiju; Cui, Lei; Zhu, Mankang; Yan, Hui

    2013-01-01

    In this work, two perovskite-type compounds, K 0.5 Bi 0.5 TiO 3 and LaAlO 3 , have been selected as host material to incorporate with BiAlO 3 using a solid-state reaction route. The phase evolution and dielectric properties for both systems have been investigated in detail. For the K 0.5 Bi 0.5 TiO 3 -BiAlO 3 system, it is interesting to find that when using Bi 2 O 3 , Al 2 O 3 , K 2 CO 3 , and TiO 2 as starting materials, the formed compounds are K 0.5 Bi 0.5 TiO 3 -K 0.5 Bi 4.5 Ti 4 O 15 and Al 2 O 3 only plays a dopant role. There are two distinct dielectric peaks appearing in the patterns of temperature dependence of dielectric constant, corresponding to the phase-transition points of perovskite-type K 0.5 Bi 0.5 TiO 3 and Aurivillius-type K 0.5 Bi 4.5 Ti 4 O 15 , independently. In comparison, using Bi 2 O 3 , Al 2 O 3 , and La 2 O 3 as starting materials, the pure perovskite phase LaAlO 3 -BiAlO 3 can be obtained. Compared to the inherent paraelectric behavior in LaAlO 3 , the diffuse phase-transition phenomena can be observed in the LaAlO 3 -BiAlO 3 binary system, which corresponds well to the Vogel-Fulcher (VF) relationship. Moreover, compared to pure LaAlO 3 , the synthesized LaAlO 3 -BiAlO 3 compound shows enhanced dielectric properties, which are promising in application as gate dielectric materials. (copyright 2013 WILEY-VCH Verlag GmbH and Co. KGaA, Weinheim)

  13. Tunable white light generation from Ce{sup 3+}-Tb{sup 3+}-Mn{sup 2+} doped metaphosphate glass for LED and solar cell applications

    Energy Technology Data Exchange (ETDEWEB)

    Ghosh, Debarati; Biswas, K.; Balaji, S. [CSIR-Network of Institute for Solar Energy (NISE) (India); Glass Division, Glass Science and Technology Section, CSIR-Central Glass and Ceramic Research Institute, 196, Raja S.C. Mullick Road, Kolkata 700032 (India); Annapurna, K., E-mail: annapurnak@cgcri.res.in [CSIR-Network of Institute for Solar Energy (NISE) (India); Glass Division, Glass Science and Technology Section, CSIR-Central Glass and Ceramic Research Institute, 196, Raja S.C. Mullick Road, Kolkata 700032 (India)

    2017-03-15

    Alkali free Ba-Al metaphosphate glasses doped with Ce, Tb and Mn are prepared and their concentration is tuned to achieve white light emission for production of LEDs and luminescent concentrator for Si-PV applications. The occurrence of a redox reaction among dopant ions (Ce{sup 4+}, Tb{sup 3+}→Ce{sup 3+}, Tb{sup 4+}) is observed from the absorption spectra while there is no change in oxidation state of Mn{sup 2+} ions. This is confirmed from ESR studies. Emission spectra indicated effective downshifting of radiation from near visible to green and red region of the spectrum. On tuning the concentration of Tb{sup 3+} and Mn{sup 2+}, bright white light emission (CIE coordinates: x=3.32, y=3.33) corresponding to CCT of 5900 K is obtained. This white light produced has been further tuned to different hues by varying the excitation wavelength of this triply doped glass.

  14. Solution-combustion synthesis of Tb3+-doped Y3Al5O12 nanoparticles

    International Nuclear Information System (INIS)

    Fadlalla, H.M.H.; Tang, C.C.; Elsanousi, A.; Ding, X.X.; Qi, S.R.

    2009-01-01

    Nano-sized YAG:Tb powder phosphors were prepared by a solution-combustion method, using the general inorganic salts as starting materials. The X-ray diffraction (XRD) measurements showed that the precursor can be well-crystallized at 900 deg. C. As-prepared particles have sizes mostly in the range between 30 and 100 nm as obtained by scanning electron microscope (SEM) and transition electron microscope (TEM). Selected area electron diffraction (SAED) patterns proved that the larger particles are monocrystalline. The effects of annealing temperature and Tb-doping concentration on the luminescence intensity were studied

  15. Structural/surface characterization and catalytic evaluation of rare-earth (Y, Sm and La) doped ceria composite oxides for CH{sub 3}SH catalytic decomposition

    Energy Technology Data Exchange (ETDEWEB)

    He, Dedong; Chen, Dingkai; Hao, Husheng; Yu, Jie; Liu, Jiangping; Lu, Jichang; Liu, Feng [Faculty of Environmental Science and Engineering, Kunming University of Science and Technology, Kunming, 650500 (China); Wan, Gengping [Faculty of Environmental Science and Engineering, Kunming University of Science and Technology, Kunming, 650500 (China); Research Center for Analysis and Measurement, Hainan University, Haikou, 570228 (China); He, Sufang [Research Center for Analysis and Measurement, Kunming University of Science and Technology, Kunming, 650093 (China); Luo, Yongming, E-mail: environcatalysis222@yahoo.com [Faculty of Environmental Science and Engineering, Kunming University of Science and Technology, Kunming, 650500 (China)

    2016-12-30

    Highlights: • Ce{sub 0.75}RE{sub 0.25}O{sub 2-δ} (RE = Y, Sm and La) were synthesized by citrate complexation method. • Ce{sub 0.75}Y{sub 0.25}O{sub 2-δ} exhibited the best stability for the decomposition of CH{sub 3}SH. • Cation radius played a key role in determining structure and surface characteristics. • Catalytic behavior depended on synergistic role of oxygen vacancies and basic sites. • Ce{sub 2}S{sub 3} accumulation on the surface was responsible for the deactivation of catalyst. - Abstract: A series of rare earth (Y, Sm and La) doped ceria composite oxides and pure CeO{sub 2} were synthesized and evaluated by conducting CH{sub 3}SH catalytic decomposition test. Several characterization studies, including XRD, BET, Raman, H{sub 2}-TPR, XPS, FT-IR, CO{sub 2}-TPD and CH{sub 3}SH-TPD, were undertaken to correlate structural and surface properties of the obtained ceria-based catalysts with their catalytic performance for CH{sub 3}SH decomposition. More oxygen vacancies and increased basic sites exhibited in the rare earth doped ceria catalysts. Y doped ceria sample (Ce{sub 0.75}Y{sub 0.25}O{sub 2-δ}), with a moderate increase in basic sites, contained more oxygen vacancies. More structural defects and active sites could be provided, and a relatively small amount of sulfur would accumulate, which resulted in better catalytic performance. The developed catalyst presented good catalytic behavior with stability very similar to that of typical zeolite-based catalysts reported previously. However, La doped ceria catalyst (Ce{sub 0.75}La{sub 0.25}O{sub 2-δ}) with the highest alkalinity was not the most active one. More sulfur species would be adsorbed and a large amount of cerium sulfide species (Ce{sub 2}S{sub 3}) would accumulate, which caused deactivation of the catalysts. The combined effect of increased oxygen vacancies and alkalinity led to the catalytic stability of Ce{sub 0.75}Sm{sub 0.25}O{sub 2-δ} sample was comparable to that of pure CeO

  16. Synthesis, structural and luminescence properties of Bi3+ co-doped Y2Sn2O7:Tb nanoparticles

    International Nuclear Information System (INIS)

    Nigam, S.; Sudarsan, V.; Vatsa, R.K.

    2010-01-01

    Full text: In recent years, advanced materials derived from Pyrochlore-type oxides (A 2 B 2 O 7 ) have been of extensive scientific and technological interest. Chemical substitution of A or B sites of pyrochlore oxide by rare earth ions is a widely used approach to prepare thermally stable, lanthanide ion doped luminescent materials. Due to the higher symmetry around the A and B sites in the lattice lanthanide ions like Eu 3+ and Tb 3+ when incorporated at the A or B sites give very poor luminescence. This problem can be avoided by incorporating other ions like Bi 3+ in the lattice so that the lattice gets distorted and luminescent intensity from the lanthanide ions increases. The present study deals with the synthesis and characterization of Bi 3+ co-doped Y 2 Sn 2 O 7 :Tb nanoparticles. For the preparation of Tb 3+ and Bi 3+ doped Y 2 Sn 2 O 7 nano-materials, Sn metal, Bi(NO 3 ) 3 , Tb 4 O 7 , Y 2 CO 3 , were used as starting materials. The solution containing Y 3+ , Sn 4+ ,and Bi 3+ -Tb 3+ in ethylene glycol medium was slowly heated up to 120 deg C and then subjected to urea hydrolysis. The obtained precipitate after washing was heated to 700 deg C. As prepared samples are amorphous in nature and 700 deg C heated sample showed well crystalline pyrochlore structure as revealed by the XRD studies. Average particles size is calculated from the width of the X-ray diffraction peaks and found to be ∼ 5 nm. TEM images of the nanoparticles obtained at 700 deg C shows very fine spherical particles having a diameter in the range of 2-5 nm. Luminescence measurements were carried out for as prepared and 700 deg C heated samples of 2.5%Tb doped Y 2 Sn 2 O 7 nanoparticles. Green emission characteristic 5 D 4 7 F 5 transition of Tb 3+ has been observed from as prepared sample but on heating to 700 deg C the emission characteristic of Tb 3+ ions got completely removed . However, there is a significant improvement in Tb 3+ emission from 2.5% Bi 3+ co-doped Y 2 Sn 2 O 7 :Tb 3

  17. White-emission in single-phase Ba2Gd2Si4O13:Ce3 +,Eu2 +,Sm3 + phosphor for white-LEDs

    Science.gov (United States)

    Jiang, Xiumin; Zhang, Yuqian; Zhang, Jia

    2018-03-01

    To develop new white-light-emitting phosphor, a series of Ce3 +-Eu2 +-Sm3 + doped Ba2Gd2Si4O13 (BGS) phosphors were prepared by the solid-state reaction method, and their photoluminescence properties were studied. The Ce3 + and Eu2 + single-doped BGS show broad emission bands around in the region of 350-550 and 420-650 nm, respectively. By co-doping Ce3 +-Eu2 + into BGS, the energy transfer (ET) from Ce3 + to Eu2 + is inefficient, which could be due to the competitive absorption between the two activator ions. The Sm3 +-activated BGS exhibits an orangey-red emission in the region of 550-750 nm. To achieve white emission, the BGS:0.06Ce3 +,0.04Eu2 +,ySm3 + (0 ≤ y ≤ 0.18) phosphors were designed, in which the ET from Ce3 +/Eu2 + to Sm3 + was observed. The emission color can be tuned by controlling the Sm3 + concentration, and white emission was obtained in the BGS:0.06Ce3 +,0.04Eu2 +,0.06Sm3 + sample. The investigation of thermal luminescence stability for the typical BGS:0.06Ce3 +,0.04Eu2 +,0.06Sm3 + sample reveals that the emission intensities of both Eu2 + and Sm3 + demonstrate continuous decrease but the Ce3 + emission is enhanced gradually with increasing temperature. The corresponding reason has been discussed.

  18. Raman scattering study of the anharmonic effects in CeO2-y nanocrystals

    Science.gov (United States)

    Popović, Z. V.; Dohčević-Mitrović, Z.; Cros, A.; Cantarero, A.

    2007-12-01

    We have studied the temperature dependence of the F2g Raman mode phonon frequency and broadening in CeO2-y nanocrystals. The phonon softening and phonon linewidth are calculated using a model which takes into account the three-and four-phonon anharmonic processes. A detailed comparison of the experimental data with theoretical calculations revealed the predominance of four-phonon anharmonic processes in the temperature dependence of the phonon energy and broadening of the nanocrystals. On the other hand, three-phonon processes dominate the temperature behavior of phonons in polycrystalline samples. The anti-Stokes/Stokes peak intensity ratio was also investigated and found to be smaller for nanosized CeO2 powders than in the bulk counterpart.

  19. Raman scattering study of the anharmonic effects in CeO2-y nanocrystals

    International Nuclear Information System (INIS)

    Popovic, Z V; Dohcevic-Mitrovic, Z; Cros, A; Cantarero, A

    2007-01-01

    We have studied the temperature dependence of the F 2g Raman mode phonon frequency and broadening in CeO 2-y nanocrystals. The phonon softening and phonon linewidth are calculated using a model which takes into account the three-and four-phonon anharmonic processes. A detailed comparison of the experimental data with theoretical calculations revealed the predominance of four-phonon anharmonic processes in the temperature dependence of the phonon energy and broadening of the nanocrystals. On the other hand, three-phonon processes dominate the temperature behavior of phonons in polycrystalline samples. The anti-Stokes/Stokes peak intensity ratio was also investigated and found to be smaller for nanosized CeO 2 powders than in the bulk counterpart

  20. 1887 nm lasing in Tm3+-doped TeO2-BaF2-Y2O3 glass microstructured fibers

    Science.gov (United States)

    Wang, Shunbin; Yao, Chuanfei; Jia, Zhixu; Qin, Guanshi; Qin, Weiping

    2017-04-01

    In this paper, we demonstrate ∼2 μm lasing in Tm3+-doped fluorotellurite microstructured fibers. The Tm3+-doped fibers are based on TeO2-BaF2-Y2O3 glasses and fabricated by using a rod-in-tube method. Under the pump of a 1570 nm Er3+-doped fiber laser, lasing at 1887 nm is obtained in a ∼42.5 cm long Tm3+-doped fiber with a threshold pump power of 94 mW. As the pump power increases to 780 mW, the obtained maximum unsaturated power reaches up to ∼408 mW with a slop efficiency of ∼58.1%. This result indicates that the Tm3+-doped fluorotellurite fibers are promising gain media for ∼2 μm fiber lasers.

  1. Fabrication of cerium-doped β-Ga2O3 epitaxial thin films and deep ultraviolet photodetectors.

    Science.gov (United States)

    Li, Wenhao; Zhao, Xiaolong; Zhi, Yusong; Zhang, Xuhui; Chen, Zhengwei; Chu, Xulong; Yang, Hujiang; Wu, Zhenping; Tang, Weihua

    2018-01-20

    High-quality cerium-doped β-Ga 2 O 3 (Ga 2 O 3 :Ce) thin films could be achieved on (0001)α-Al 2 O 3 substrates using a pulsed-laser deposition method. The impact of dopant contents concentration on crystal structure, optical absorption, photoluminescence, and photoelectric properties has been intensively studied. X-ray diffraction analysis results have shown that Ga 2 O 3 :Ce films are highly (2¯01) oriented, and the lattice spacing of the (4¯02) planes is sensitive to the Ce doping level. The prepared Ga 2 O 3 :Ce films show a sharp absorption edge at about 250 nm, meaning a high transparency to deep ultraviolet (DUV) light. The photoluminescence results revealed that the emissions were in the violet-blue-green region, which are associated with the donor-acceptor transitions with the Ce 3+ and oxygen vacancies related defects. A simple DUV photodetector device with a metal-semiconductor-metal structure has also been fabricated based on Ga 2 O 3 :Ce thin film. A distinct DUV photoresponse was obtained, suggesting a potential application in DUV photodetector devices.

  2. Microstructure and enhanced dielectric properties of yttrium and zirconium co-doped CaCu{sub 3}Ti{sub 4}O{sub 12} ceramics

    Energy Technology Data Exchange (ETDEWEB)

    Xu, Zunping, E-mail: xzp16213@163.com [Faculty of Materials and Energy, Southwest University, Chongqing 400715 (China); Qiang, Hua [College of Electromechanical Engineering, Chongqing College of Humanities, Science and Technology, Chongqing 401524 (China); Chen, Yi; Chen, Zhiqian [Faculty of Materials and Energy, Southwest University, Chongqing 400715 (China)

    2017-04-15

    CaCu{sub 3}Ti{sub 4}O{sub 12} (CCTO) ceramics doped with Y{sub 2}O{sub 3}, ZrO{sub 2}, and (Y{sub 2}O{sub 3}+ZrO{sub 2}) were prepared by the citrate-nitrate combustion derived powders in order to investigate the effect of dopants on the microstructure and electrical properties. The results showed that giant dielectric response was enhanced by co-doping of Y{sup 3+} and Zr{sup 4+} ions at the Ti site. Y{sub 2}O{sub 3} and ZrO{sub 2} additive can inhibit the grain growth. Compared with other samples, (Y{sub 2}O{sub 3}+ZrO{sub 2}) co-doped ceramics exhibit a dense and homogenous fine-grained microstructure. A much better temperature and frequency stability of dielectric properties were realized in these ceramics. The dielectric loss (tan δ) < 0.05 in the frequency range of 200 Hz–60 kHz at room temperature, and in the temperature range of 15–72 °C at 10 kHz was successfully accomplished in (Y{sub 2}O{sub 3}+ZrO{sub 2}) co-doped CCTO ceramics. Low tan δ ∼0.039 and high dielectric constant (ε{sub r} ∼10196) were observed at room temperature and 10 kHz for the above ceramic samples, and the characteristic frequency shifts to higher frequency with increasing measuring temperature. The present results indicate that (Y{sub 2}O{sub 3}+ZrO{sub 2}) co-doping may improve the dielectric properties and increase the grain boundary resistance of CCTO. - Highlights: • Y and Zr co-doped CCTO exhibits a dense and homogenous fine-grained microstructure. • Y and Zr co-doped CCTO performs a lower dielectric loss in wide-range of frequency. • Temperature and frequency stability of dielectric properties were greatly enhanced.

  3. Formation and nitrile hydrogenation performance of Ru nanoparticles on a K-doped Al2O3 surface.

    Science.gov (United States)

    Muratsugu, Satoshi; Kityakarn, Sutasinee; Wang, Fei; Ishiguro, Nozomu; Kamachi, Takashi; Yoshizawa, Kazunari; Sekizawa, Oki; Uruga, Tomoya; Tada, Mizuki

    2015-10-14

    Decarbonylation-promoted Ru nanoparticle formation from Ru3(CO)12 on a basic K-doped Al2O3 surface was investigated by in situ FT-IR and in situ XAFS. Supported Ru3(CO)12 clusters on K-doped Al2O3 were converted stepwise to Ru nanoparticles, which catalyzed the selective hydrogenation of nitriles to the corresponding primary amines via initial decarbonylation, the nucleation of the Ru cluster core, and the growth of metallic Ru nanoparticles on the surface. As a result, small Ru nanoparticles, with an average diameter of less than 2 nm, were formed on the support and acted as efficient catalysts for nitrile hydrogenation at 343 K under hydrogen at atmospheric pressure. The structure and catalytic performance of Ru catalysts depended strongly on the type of oxide support, and the K-doped Al2O3 support acted as a good oxide for the selective nitrile hydrogenation without basic additives like ammonia. The activation of nitriles on the modelled Ru catalyst was also investigated by DFT calculations, and the adsorption structure of a nitrene-like intermediate, which was favourable for high primary amine selectivity, was the most stable structure on Ru compared with other intermediate structures.

  4. Growth and luminescence properties of Pr3+-doped single crystalline films of garnets and perovskites

    International Nuclear Information System (INIS)

    Gorbenko, V.; Zorenko, Yu.; Savchyn, V.; Zorenko, T.; Pedan, A.; Shkliarskyi, V.

    2010-01-01

    Peculiarities of growth of single crystalline films (SCF) of Pr 3+ doped Y 3 Al 5 O 12 and Lu 3 Al 5 O 12 garnets and YAlO 3 and LuAlO 3 perovskites by the liquid phase epitaxy method from melt-solutions based on PbO-B 2 O 3 flux as well as luminescent and scintillation properties of these SCFs were studied in this work. Dependence the intensity of the Pr 3+ d-f and f-f-luminescence on the activator concentration and influence of Pb 2+ flux dopant on the light yield of SCFs of the mentioned garnets and perovskites were analyzed.

  5. Redetermination of Ce[B5O8(OH(H2O]NO3·2H2O

    Directory of Open Access Journals (Sweden)

    Ya-Xi Huang

    2012-05-01

    Full Text Available The crystal structure of Ce[B5O8(OH(H2O]NO3·2H2O, cerium(III aquahydroxidooctaoxidopentaborate nitrate dihydrate, has been redetermined from single-crystal X-ray diffraction data. In contrast to the previous determination [Li et al. (2003. Chem. Mater. 15, 2253–2260], the present study reveals the location of all H atoms, slightly different fundamental building blocks (FBBs of the polyborate anions, more reasonable displacement ellipsoids for all non-H atoms, as well as a model without disorder of the nitrate anion. The crystal structure is built from corrugated polyborate layers parallel to (010. These layers, consisting of [B5O8(OH(H2O]2− anions as FBBs, stack along [010] and are linked by Ce3+ ions, which exhibit a distorted CeO10 coordination sphere. The layers are additionally stabilized via O—H...O hydrogen bonds between water molecules and nitrate anions, located at the interlayer space. The [BO3(H2O]-group shows a [3 + 1] coordination and is considerably distorted from a tetrahedral configuration. Bond-valence-sum calculation shows that the valence sum of boron is only 2.63 valence units (v.u. when the contribution of the water molecule (0.49 v.u. is neglected.

  6. ZnO and Al doped ZnO thin films deposited by Spray Plasma: Effect of the growth time and Al doping on microstructural, optical and electrical properties

    International Nuclear Information System (INIS)

    Baba, Kamal; Lazzaroni, Claudia; Nikravech, Mehrdad

    2015-01-01

    Nanostructured zinc oxide (ZnO) and Al doped ZnO (ZnO:Al) thin films are deposited on glass substrate by the Spray Plasma technique. Zinc nitrate and aluminium nitrate are used as Zn and Al precursors, respectively. The effect of the growth time on structural and optical properties of undoped films is studied by X-ray diffraction, atomic force microscopy, and UV–Vis spectroscopy. The effect of Al doping on microstructural, optical and electrical characteristics of ZnO:Al films is also investigated. The results show that the grain size and the film thickness both increase with the growth time. The band gap of the layers varies from 3.17 to 3.24 eV depending on the thickness. The increase of the Al doping results in the enlargement of the peak (002) and the shift of its position to higher 2θ values. Average optical transmittance decreases from 90 to 65% with the growth time because of the thickness increase while there is no significant influence of the aluminium doping on the transmittance which is above 80% in most of the visible and near-IR range for all ZnO:Al films. The electrical properties characterized by Hall measurements show that all the deposited films exhibit high resistivity, between 4 and 10 4 Ω cm. The carrier concentration decreases from 2.10 19 to 2.10 13 cm −3 when the concentration of Al increases from 1.5 to 5 atm%. - Highlights: • The original Spray Plasma technique is used for ZnO and ZnO:Al thin film deposition. • Investigation of the effect of growth time and Al doping on the structural and optical properties • Increase of grain size and film thickness with the growth time • Optical transmittance decreases from 90 to 65% with the growth time and is above 80% for ZnO:Al films in UV–Vis-NIR range. • The peak position of the (002) plane is shifted to high 2θ values with Al doping.

  7. Surface passivation of n-type doped black silicon by atomic-layer-deposited SiO2/Al2O3 stacks

    Science.gov (United States)

    van de Loo, B. W. H.; Ingenito, A.; Verheijen, M. A.; Isabella, O.; Zeman, M.; Kessels, W. M. M.

    2017-06-01

    Black silicon (b-Si) nanotextures can significantly enhance the light absorption of crystalline silicon solar cells. Nevertheless, for a successful application of b-Si textures in industrially relevant solar cell architectures, it is imperative that charge-carrier recombination at particularly highly n-type doped black Si surfaces is further suppressed. In this work, this issue is addressed through systematically studying lowly and highly doped b-Si surfaces, which are passivated by atomic-layer-deposited Al2O3 films or SiO2/Al2O3 stacks. In lowly doped b-Si textures, a very low surface recombination prefactor of 16 fA/cm2 was found after surface passivation by Al2O3. The excellent passivation was achieved after a dedicated wet-chemical treatment prior to surface passivation, which removed structural defects which resided below the b-Si surface. On highly n-type doped b-Si, the SiO2/Al2O3 stacks result in a considerable improvement in surface passivation compared to the Al2O3 single layers. The atomic-layer-deposited SiO2/Al2O3 stacks therefore provide a low-temperature, industrially viable passivation method, enabling the application of highly n- type doped b-Si nanotextures in industrial silicon solar cells.

  8. Neutron irradiation damage in Al2O3 and Y2O3

    International Nuclear Information System (INIS)

    Clinard, F.W. Jr.; Bunch, J.M.; Ranken, W.A.

    1975-01-01

    Two ceramics under consideration for use in fusion reactors, Al 2 O 3 and Y 2 O 3 , were irradiated in the EBR-II fission reactor at 650, 875, and 1025 0 K to fluences between 2 and 6 x 10 21 n/cm 2 (E greater than 0.1 MeV). Samples evaluated include sapphire, Lucalox, alumina, Y 2 O 3 , and Y 2 O 3 -10 percent ZrO 2 (Yttralox). All Al 2 O 3 specimens swelled significantly (1 to 3 percent), with most of the growth observed in sapphire along the c-axis at the higher temperatures. Al 2 O 3 samples irradiated at 875 to 1025 0 K contained a high density of small aligned ''pores''. Irradiated Y 2 O 3 -based ceramics exhibited dimensional stability and a defect content consisting primarily of unresolved damage and/or dislocation loops. The behavior of these ceramics under irradiation is discussed, and the relevance of fission neutron damage studies to fusion reactor applications is considered. (auth)

  9. Inverted opal luminescent Ce-doped silica glasses

    Directory of Open Access Journals (Sweden)

    R. Scotti

    2006-01-01

    Full Text Available Inverted opal Ce-doped silica glasses (Ce : Si molar ratio 1 ⋅ 10−3 were prepared by a sol-gel method using opals of latex microspheres as templates. The rare earth is homogeneously dispersed in silica host matrix, as evidenced by the absence of segregated CeO2, instead present in monolithic Ce-doped SG with the same cerium content. This suggests that the nanometric dimensions of bridges and junctions of the host matrix in the inverted opal structures favor the RE distribution avoiding the possible segregation of CeO2.

  10. Optical Properties and Photoactivity of The Pigmentary TiO2 Doped with P2O5, K2O, Al2O3 and Sb2O3

    International Nuclear Information System (INIS)

    Glen, M; Grzmil, B

    2011-01-01

    The influence of the increasing content of antimony calculated to Sb 2 O 3 (0.08-0.57 mol%) with the constant amount of the other additives (calculated to P 2 O 5 , K 2 O, Al 2 O 3 ) on the optical properties and photostability of doped rutile has been investigated. The properties of the obtained TiO 2 -PKAlSb samples were compared to the commercial TiO 2 -PKAl composition. The starting material was the concentrated suspension of technical-grade hydrated titanium dioxide (HTD). The dopant agents' solutions were introduced to HTD. Prepared samples were calcined with gradually increasing process temperature. The XRD analysis was used to determine the rutile content in the TiO 2 samples. Optical properties of modified titanium dioxide have been determined spectrophotometrically by measuring the colour in the white (brightness, white tone) and grey system (relative lightening power, grey tone). Photostability was characterized by the white lead-glycerin test with UV-Vis light. It was observed that with the increasing content of antimony in rutile TiO 2 , doped with phosphates, potassium and aluminium, the brightness and grey tone were increasing but white tone decreased. The changes of the relative lightening power values were insignificant. Comparing the samples of TiO 2 -PKAlSb with the TiO 2 -PKAl composition it was observed that titanium dioxide doped with antimony had better white and grey tone. The increasing Sb 2 O 3 content in the TiO 2 caused the improvement of the photostability.

  11. Local microstructure and photoluminescence of Er-doped 12CaO·7Al2O3 powder

    Institute of Scientific and Technical Information of China (English)

    WANG Dan; LIU Yuxue; XU Changshan; LIU Yichun; WANG Guorui; LI Xinghua

    2008-01-01

    Er-doped 12CaO·7Al2O3 (C12A7:Er) powders were prepared using the sol-gel method followed by annealing inorganic precursors. X-ray diffraction (XRD), Raman and absorption spectra revealed that Er ions existed and substituted Ca2+ lattice site in C12A7. The photoluminescence of C12A7:Er at room temperature was observed in the visible and infrared region using 488 nm (2.54 eV) Ar+ line as excitation source, respectively. The sharp and intense green emission bands with multi-peaks around 520 nm and 550 nm correspond to the transitions from the excited states 2H11/2 and 4S3/2 to the ground state 4I15/2, respectively. Furthermore, red emission band around 650 nm was also observed. It was attributed to the electronic transition from excited states 4F9/2 to the ground state 4I15/2 inside 4f-shell of Er3+ ions. The intensive infrared emission at 1.54μm was attributed to the transition from the first excited states of 4I13/2 to the ground state (4I15/2). The temperature dependent photoluminescence of infrared emission showed that the integrated intensity reached a maximum value at near room temperature. The forbidden transitions of intra-4f shell electrons in free Er3+ ions were allowed in C12A7 owing to lack of the inversion symmetry in the Er3+ position in C12A7 crystal field. Our results suggested that C12A7:Er was a candidate for applications in Er-doped laser materials, and full color display.

  12. Crystallization in Y-Si-Al-O-N glasses

    Energy Technology Data Exchange (ETDEWEB)

    Leng-Ward, G; Lewis, M H

    1985-05-01

    The development of crystallization in oxynitride glasses has been characterized using transmission electron microscopy and scanning electron microscopy, X-ray (energy-dispersive) microanalysis, and powder X-ray diffraction techniques. A series of glasses was prepared while maintaining the ratio of yttrium-to-silicon-to-aluminium, but replacing oxygen with nitrogen up to the nitrogen solubility limit. On annealing at 1250 C, the oxide glass fully crystallized into yttrium disilicate (Y2Si2O7). Al2O3 and mullite (Al6Si2O13) while, with increasing nitrogen content, the disilicate phase was progressively replaced by yttrium aluminium garnet (Y3Al5O12) and nitrogen was mainly incorporated into Si2N2O. Annealing of the nitrogen glasses at 1100 C produced partial crystallization involving an intermediate phase related to nitrogen-wollastonite. Phase separation in an as-quenched SiO2-rich Y-Si-Al-O composition glass is illustrated. 9 references.

  13. Er{sup 3+}-doped Y{sub 2}O{sub 3} obtained by polymeric precursor: Synthesis, structure and upconversion emission properties

    Energy Technology Data Exchange (ETDEWEB)

    Perrella, Rafael V.; Santos, Daniela P. dos [Grupo de Pesquisa em Química de Materiais – (GPQM), Departamento de Ciências Naturais, Universidade Federal de São João del-Rei, Campus Dom Bosco, Praça Dom Helvécio, 74, 36301-160 São João del-Rei, MG (Brazil); Poirier, Gael Y. [Instituto de Ciência e Tecnologia, Universidade Federal de Alfenas, Cidade Universitária, 37715400 Poços de Caldas, MG (Brazil); Góes, Márcio S. [Universidade Federal da Integração Latino-Americana (UNILA), Av. Tancredo Neves, 6731 – Bloco 4, Cx P. 2044, CEP: 85867-970 Foz do Iguaçu, PR (Brazil); Ribeiro, Sidney José L. [Instituto de Química, UNESP, P.O. Box 355, 14800-970 Araraquara, SP (Brazil); Schiavon, Marco A. [Grupo de Pesquisa em Química de Materiais – (GPQM), Departamento de Ciências Naturais, Universidade Federal de São João del-Rei, Campus Dom Bosco, Praça Dom Helvécio, 74, 36301-160 São João del-Rei, MG (Brazil); and others

    2014-05-01

    The relentless pursuit for materials containing rare earth ions with photoluminescent properties has led to several studies with applications in the development of new technologies. The main focus of this work is the preparation of Er{sup 3+}-doped polycrystalline Y{sub 2}O{sub 3} with photoluminescent properties using PEG as an organic precursor and heat-treated at different temperatures. The methodology used in this synthesis is highly attractive due to its high feasibility for improved technology and low cost for preparing materials. The behavior of the viscous resin has been evaluated and the final compounds exhibited the formation of a cubic polycrystalline phase, which is able to support variations in Er{sup 3+} doping concentrations up to 10 mol%, without significant changes in the polycrystalline parameters. The values of the nanocrystallite size calculated by Scherrer's equation showed direct dependence on the heat-treatment temperature as well as the Er{sup 3+} concentration. Intense emission in the visible region under excitation at 980 nm was attributed to an upconversion phenomenon assigned to the intraconfigurational f–f transitions of Er{sup 3+} ions. The upconversion mechanism was investigated and it was demonstrated that the higher intense emission in the red region in comparison to the emission in the green region is related to the crystallite size. The studies about the intensity showed the dependence of upconversion emission of power source, indicating that two-photon are responsible for the green and red photoluminescence. These polycrystalline materials exhibit properties that make them promising for use in solar energy systems, C-telecom band or solid-state laser devices. - Highlights: • Intense red upconversion emission. • Very easy way to prepare the material. • Potential application in solar cells. • Application for C-telecom band.

  14. Structural and photoluminescence studies of pure and Eu3+ doped Y2O3 oxide nanoparticles

    International Nuclear Information System (INIS)

    Packiyaraj, P.; Thangadurai, P.

    2013-01-01

    Pure and Eu 3+ doped Y 2 O 3 nanoparticles were synthesized by a hydrolysis assisted co-precipitation method. Structural characterization was carried out by X-ray diffraction. The as-prepared Eu:Y 2 O 3 was amorphous yttrium hydroxides in nature and become crystalline Y 2 O 3 once annealed at 600℃ and 900℃. The particle size (13-23 nm) was dependent on annealing temperatures and Eu 3+ ion concentration. Photoluminescence studies showed weak emission bands at 581, 587, 593, and 599 nm, corresponding to the 5 D 0 → 7 F 1 transitions, and sharp peaks with a maximum intensity occurring at 611 nm, due to the 5 D 0 → 7 F 2 transitions of Eu 3+ . (author)

  15. Effect of Ce Doping on RGO-TiO2 Nanocomposite for High Photoelectrocatalytic Behavior

    Directory of Open Access Journals (Sweden)

    Md. Rakibul Hasan

    2014-01-01

    Full Text Available Ce doped RGO-TiO2 composite films on ITO substrates were prepared by sol-gel process using tetrabutyl titanate and reduced graphene oxide (RGO as the starting materials. The sample was designed for the photoelectrocatalytic applications. The obtained samples were characterized by X-ray diffraction, UV-vis absorption spectroscopy, scanning electron microscopy, and Fourier transformed infrared spectroscopy. The results showed that doping of Ce on RGO-TiO2 composite film inhibited the TiO2 anatase-rutile phase transformation. In this case, Ce atoms could serve as dispersion oxide and suppress the recombination of photoinduced electron-hole pairs. Besides, the change in absorbance from UV to visible region was observed in Ce doped RGO-TiO2 nanocomposite films. The Ce doped RGO-TiO2 composite film showed higher photoelectrochemical performance than that of RGO-TiO2 composite and pure TiO2 under solar simulator irradiation. The main reason might be attributed to the optimum content of Ce that could act as electrons acceptor to hinder the recombination loss and facilitate the better transportation for photoinduced charge carriers.

  16. Effects of (Al,Ge) double doping on the thermoelectric properties of higher manganese silicides

    Energy Technology Data Exchange (ETDEWEB)

    Chen, Xi; Salta, Daniel; Zhang, Libin [Materials Science and Engineering Program, Texas Materials Institute, The University of Texas at Austin, Austin, Texas 78712 (United States); Weathers, Annie [Department of Mechanical Engineering, The University of Texas at Austin, Austin, Texas 78712 (United States); Zhou, Jianshi; Goodenough, John B.; Shi, Li [Materials Science and Engineering Program, Texas Materials Institute, The University of Texas at Austin, Austin, Texas 78712 (United States); Department of Mechanical Engineering, The University of Texas at Austin, Austin, Texas 78712 (United States)

    2013-11-07

    Experiments and analysis have been carried out to investigate the effects of Al and (Al,Ge) doping on the microstructure and thermoelectric properties of polycrystalline higher manganese silicide (HMS) samples, which were prepared by solid-state reaction, ball milling, and followed by spark plasma sintering. It has been found that Al doping effectively increases the hole concentration, which leads to an increase in the electrical conductivity and power factor. By introducing the second dopant Ge into Al-doped HMS, the electrical conductivity is increased, and the Seebeck coefficient is decreased as a result of further increased hole concentration. The peak power factor is found to occur at a hole concentration between 1.8 × 10{sup 21} and 2.2 × 10{sup 21} cm{sup −3} measured at room temperature. The (Al,Ge)-doped HMS samples show lower power factors owing to their higher hole concentrations. The mobility of Mn(Al{sub 0.0035}Ge{sub y}Si{sub 0.9965-y}){sub 1.8} with y = 0.035 varies approximately as T{sup −3/2} above 200 K, suggesting acoustic phonon scattering is the dominant scattering mechanism. The thermal conductivity of HMS does not change appreciably by Al or (Al,Ge) doping. The maximum ZT of (Al,Ge)-doped HMS is 0.57 at 823 K, which is similar to the highest value found in the Al-doped HMS samples. The ZT values were reduced in the Mn(Al{sub 0.0035}Ge{sub y}Si{sub 0.9965-y}){sub 1.8} samples with high Ge concentration of y = 0.025 and 0.035, because of reduced power factor. In addition, a two-band model was employed to show that the hole contribution to the thermal conductivity dominates the bipolar and electron contributions for all samples from 300 to 823 K and accounts for about 12% of the total thermal conductivity at about 800 K.

  17. Effects of (Al,Ge) double doping on the thermoelectric properties of higher manganese silicides

    International Nuclear Information System (INIS)

    Chen, Xi; Salta, Daniel; Zhang, Libin; Weathers, Annie; Zhou, Jianshi; Goodenough, John B.; Shi, Li

    2013-01-01

    Experiments and analysis have been carried out to investigate the effects of Al and (Al,Ge) doping on the microstructure and thermoelectric properties of polycrystalline higher manganese silicide (HMS) samples, which were prepared by solid-state reaction, ball milling, and followed by spark plasma sintering. It has been found that Al doping effectively increases the hole concentration, which leads to an increase in the electrical conductivity and power factor. By introducing the second dopant Ge into Al-doped HMS, the electrical conductivity is increased, and the Seebeck coefficient is decreased as a result of further increased hole concentration. The peak power factor is found to occur at a hole concentration between 1.8 × 10 21 and 2.2 × 10 21  cm −3 measured at room temperature. The (Al,Ge)-doped HMS samples show lower power factors owing to their higher hole concentrations. The mobility of Mn(Al 0.0035 Ge y Si 0.9965-y ) 1.8 with y = 0.035 varies approximately as T −3/2 above 200 K, suggesting acoustic phonon scattering is the dominant scattering mechanism. The thermal conductivity of HMS does not change appreciably by Al or (Al,Ge) doping. The maximum ZT of (Al,Ge)-doped HMS is 0.57 at 823 K, which is similar to the highest value found in the Al-doped HMS samples. The ZT values were reduced in the Mn(Al 0.0035 Ge y Si 0.9965-y ) 1.8 samples with high Ge concentration of y = 0.025 and 0.035, because of reduced power factor. In addition, a two-band model was employed to show that the hole contribution to the thermal conductivity dominates the bipolar and electron contributions for all samples from 300 to 823 K and accounts for about 12% of the total thermal conductivity at about 800 K

  18. Photoluminescence study of Dy3+ doped SrCeVO5 phosphor

    International Nuclear Information System (INIS)

    Suresh, K.; Dai, Ch. Vijay Anil; Murthy, K.V.R.

    2016-01-01

    Dy 3+ doped SrCeVO 5 phosphor was synthesized by the solid-state reaction method. Photoluminescence (PL) technique was performed to characterize the sample. The excitation spectra monitored under 520 nm and 610 nm wavelength was characterized by a broad band ranging from 220-400 nm. From the excitation spectra two main bands at 265 nm and 325 nm were observed. The PLE intensity of 520 nm monitored shows high intensity than 610 nm spectrum. The emission spectra of SrCeVO 5 phosphor under excitations at 265 nm and 325 nm exhibited main peak at 515 nm (cyan) which is a strong, intense well resolved peak with FWHM (full width at half maximum) of 130 nm is observed. This emission is mainly may be due to Ce ion but not Dy ion. The same emission under 640 and 670 nm excitations (up conversion) with good intensity was also observed. Commission international de l'eclairage (CIE) co-ordinates under these excitations revealed that this phosphor emit cyan colour and could be used for the generation of white light in display and lamp devices. (author)

  19. Probing the doping mechanisms and electrical properties of Al, Ga and In doped ZnO prepared by spray pyrolysis

    KAUST Repository

    Maller, Robert

    2016-05-24

    The measured structural, optical and electrical properties of Al, Ga and In doped ZnO films deposited using spray pyrolysis are reported over the doping range 0.1 - 3 atomic percent (at. %). Over the entire doping series highly transparent, polycrystalline thin films are prepared. Using the AC Hall effect we probe the electronic properties of our doped films separating the impact of doping on the measured charge carrier concentrations and Hall mobility, with an emphasis on the low doping, < 1 at. %, range. In this doping range highly resistive films are formed and we highlight AC Hall as a reliable and highly reproducible technique for analysing the doping mechanism. The implementation of a simple, post-deposition heat treatment of our AZO films creates typical films with charge carrier concentrations exceeding > 1019 cm-3 and electron mobilities over 10 cm2/Vs. We describe in detail the nature of the defect chemistry and the role of intrinsic defects, particularly traps, and show that despite significant variations in dopant species and grain boundary concentrations that the defect chemistry dominates the electrical characteristics.

  20. Probing the doping mechanisms and electrical properties of Al, Ga and In doped ZnO prepared by spray pyrolysis

    KAUST Repository

    Maller, Robert; Porte, Yoann; Alshareef, Husam N.; McLachlan, Martyn

    2016-01-01

    The measured structural, optical and electrical properties of Al, Ga and In doped ZnO films deposited using spray pyrolysis are reported over the doping range 0.1 - 3 atomic percent (at. %). Over the entire doping series highly transparent, polycrystalline thin films are prepared. Using the AC Hall effect we probe the electronic properties of our doped films separating the impact of doping on the measured charge carrier concentrations and Hall mobility, with an emphasis on the low doping, < 1 at. %, range. In this doping range highly resistive films are formed and we highlight AC Hall as a reliable and highly reproducible technique for analysing the doping mechanism. The implementation of a simple, post-deposition heat treatment of our AZO films creates typical films with charge carrier concentrations exceeding > 1019 cm-3 and electron mobilities over 10 cm2/Vs. We describe in detail the nature of the defect chemistry and the role of intrinsic defects, particularly traps, and show that despite significant variations in dopant species and grain boundary concentrations that the defect chemistry dominates the electrical characteristics.

  1. Effect of Y2O3-Al2O3 ratio on inter-granular phases and films in tape-casting α-SiC with high toughness

    International Nuclear Information System (INIS)

    Huang Rong; Gu Hui; Zhang Jingxian; Jiang Dongliang

    2005-01-01

    Silicon carbide (SiC) ceramics prepared from liquid phase sintering after aqueous-tape-casting can yield high toughness when appropriate amount of Y 2 O 3 -Al 2 O 3 are added, even though no elongated grains are present. Grain boundaries (GB), second-phases and hetero-phase boundaries (HB) in 2 samples with additive mole ratios of 3:5 and 3:7 are investigated using high-resolution and analytical electron microscopy (HREM and AEM). The meta-stable YAlO 3 (YAP) was nucleated from SiC surfaces in the sample with Y/Al = 3:5 as revealed by crystallographic relations across the HB, whilst relatively thick amorphous films were found at GB. In contrary, the higher level of Al 2 O 3 additives decreases the GB film thickness in the sample with Y/Al = 3:7, and the homogeneous nucleation of Y 3 Al 5 O 12 (YAG) occurs at triple pockets accompanying with thick HB films. The strong variation of GB widths is a result of GB wetting in the sample with Y/Al = 3:5 and HB wetting in the sample of Y/Al = 3:7, both by liquid Al 2 O 3 . The energy of GB in the former sample is higher than the energy of HB as exhibited by the preferential nucleation of meta-stable YAP on SiC surfaces, which results in wetting of GB by the liquid; the situation is opposite in the latter sample as the wetting of HB occurs, leading to de-wetting of GB. The thermal mismatch between SiC and YAP or YAG as well as the presence of amorphous films facilitate the creation of micro-crack to promote inter-granular fracture and result in high toughness in both SiC ceramics

  2. Electrical and microstructural properties of Yb-doped CeO2

    Directory of Open Access Journals (Sweden)

    B. Matović

    2014-06-01

    Full Text Available Nanopowdered Ce1−xYbxO2−δ solid solutions (0 ≤ x ≤ 0.2 were synthesized by a self-propagating room temperature synthesis. XRD and SEM were used to study the properties of these materials as well as the Yb solubility in CeO2 lattice. Results showed that all the obtained powders were solid solutions with a fluorite-type crystal structure and with nanometric particle size. The average size of Ce1−xYbxO2−δ particles was approximately 3 nm. Electrochemical impedance spectroscopy for the sintered pellets depicted that it was possible to separate Rbulk and Rgb in the temperature interval of 550–800 °C. The activation energy for the bulk conduction was 1.03 eV and for grain boundary conduction was 1.14 eV. Grain boundary resistivity dominates over the other resistivities. These measurements confirmed that Yb3+-doped CeO2 material had a potential as electrolyte for intermediate-temperature solid oxide fuel cell applications.

  3. Luminescence study on Eu3+ doped Y2O3 nanoparticles: particle size, concentration and core-shell formation effects

    International Nuclear Information System (INIS)

    Singh, L Robindro; Ningthoujam, R S; Sudarsan, V; Srivastava, Iti; Singh, S Dorendrajit; Dey, G K; Kulshreshtha, S K

    2008-01-01

    Nanoparticles of Eu 3+ doped Y 2 O 3 (core) and Eu 3+ doped Y 2 O 3 covered with Y 2 O 3 shell (core-shell) are prepared by urea hydrolysis for 3 h in ethylene glycol medium at a relatively low temperature of 140 deg. C, followed by heating at 500 and 900 deg. C. Particle sizes determined from x-ray diffraction and transmission electron microscopic studies are 11 and 18 nm for 500 and 900 deg. C heated samples respectively. Based on the luminescence studies of 500 and 900 deg. C heated samples, it is confirmed that there is no particle size effect on the peak positions of Eu 3+ emission, and optimum luminescence intensity is observed from the nanoparticles with a Eu 3+ concentration of 4-5 at.%. A luminescence study establishes that the Eu 3+ environment in amorphous Y (OH) 3 is different from that in crystalline Y 2 O 3 . For a fixed concentration of Eu 3+ doping, there is a reduction in Eu 3+ emission intensity for core-shell nanoparticles compared to that of core nanoparticles, and this has been attributed to the concentration dilution effect. Energy transfer from the host to Eu 3+ increases with increase of crystallinity

  4. Characterization of 12CaO x 7Al2O3 doped indium tin oxide films for transparent cathode in top-emission organic light-emitting diodes.

    Science.gov (United States)

    Jung, Chul Ho; Hwang, In Rok; Park, Bae Ho; Yoon, Dae Ho

    2013-11-01

    12CaO x 7Al2O3, insulator (C12A7) doped indium tin oxide (ITO) (ITO:C12A7) films were fabricated using a radio frequency magnetron co-sputtering system with ITO and C12A7 targets. The qualitative and quantitative properties of ITO:C12A7 films, as a function of C12A7 concentration, were examined via X-ray photoemission spectroscopy and synchrotron X-ray scattering as well as by conducting atomic force microscopy. The work function of ITO:C12A7 (1.3%) films of approximately 2.8 eV obtained by high resolution photoemission spectroscopy measurements make them a reasonable cathode for top-emission organic light-emitting diodes.

  5. Investigation of spectroscopic properties and energy transfer between Ce and Dy in (Lu0.2Gd0.8−x−yCexDyy)2SiO5 single crystals

    International Nuclear Information System (INIS)

    Strzęp, A.; Martin, I.R.; Głowacki, M.; Ryba-Romanowski, W.; Berkowski, M.; Pérez-Rodríguez, C.

    2015-01-01

    In this paper we present results of spectroscopic investigations of single crystals with general formula (Lu 0.2 Gd 0.8−x−y ) 2 SiO 5 codoped with x% of Ce 3+ and y% of Dy 3+ ions. Investigated materials exhibit strong optical anisotropy what can be easily observed in polarized absorption and emission spectra. Based on room temperature polarized absorption spectra calculations in framework of phenomenological Judd–Ofelt model was carried out. Intensity parameters Ω t were evaluated to be Ω 2 =7.08 (±0.39), Ω 4 =2.76 (±0.44), and Ω 6 =3.36 (±0.21) [10 −20 cm 2 ] for sample doped with 1% of cerium and Ω 2 =10.72 (±0.33), Ω 4 =1.98 (±0.37), and Ω 6 =2.11 (±0.18) [10 −20 cm 2 ] for sample doped with 3% of cerium. Influence of cerium admixture on Judd Ofelt intensity parameters is discussed. Value of experimental lifetime of 4 F 9/2 multiplet of Dy 3+ ion in sample doped with 1 at% Ce is 0.5 ms (τ rad =0.45 ms), while for sample doped with 3 at% of Ce, experimental lifetime is 0.45 ms (τ rad =0.43 ms). Absorption bands located between 440 and 460 nm, can be utilized for optical pumping of material by GaN laser diodes. Intense and broad emission bands at 465–495 and 560–590 nm, with experimental branching ratio strongly depending on polarization, give high chance for obtaining white luminophore, due to appropiate mixing of blue and yellow luminescence. By means of a pump and probe experiment optical amplification was demonstrated in the codoped sample with 1 at% of Ce and 1 at% Dy at 575 nm corresponding to the emission of Dy 3+ with a high net gain coefficient of 34 cm −1 . Such high amplification was obtained under 359 nm excitation (at the maximum of intense absorption band of Ce 3+ ions). - Highlights: • Influence of anisotropy on properties of LGSO: Ce, Dy crystals was investigated. • ET between Ce 3+ and Dy 3+ ions enhanced luminous properties of material investigated. • High optical amplification net gain in yellow

  6. Microstructures and luminescent properties of Ce-doped transparent mica glass-ceramics

    International Nuclear Information System (INIS)

    Taruta, Seiichi; Iwasaki, Yoshitomo; Nishikiori, Hiromasa; Yamakami, Tomohiko; Yamaguchi, Tomohiro; Kitajima, Kunio; Okada, Kiyoshi

    2012-01-01

    Highlights: ► Ce-doped transparent glass-ceramics and their parent glasses. ► TEM and STEM images for the microstructures. ► Each mica crystal did not contain Ce uniformly. ► Emission due to Ce 3+ ions in the glass phase and/or Ce 3+ ions in the mica crystals. - Abstract: Transparent mica glass-ceramics were prepared by heating parent glasses that had been doped with 0.5–15 mol% CeO 2 . During the melting and heat treatment, Ce 4+ ions in the specimens were reduced to Ce 3+ ions, and one or both of these ion species were then replaced with Li + ions in the interlayers of the separated mica crystals. However, scanning transmission electron microscope (STEM) and Z-contrast imaging revealed that the mica crystals did not contain the same amount of Ce. On excitation at 254 nm, the parent glasses and glass-ceramics emitted blue light, which originated from the 5d to 4f transition of the Ce 3+ ions. The emission of the glass-ceramic containing a smaller amount of Ce was attributed to the Ce 3+ ions in both the glass phase and the mica crystals, whereas that of the glass-ceramics containing a larger amount of Ce was caused mainly by Ce 3+ ions in the mica crystals. The dependence of the emission band of the parent glasses on the amount of Ce was a unique feature of the Ce-doped transparent mica glass-ceramics and was not observed in previous studies of Eu-doped parent glasses and mica glass-ceramics.

  7. Preparation and characterization of Au/CeO{sub 2}-Al{sub 2}O{sub 3} monoliths

    Energy Technology Data Exchange (ETDEWEB)

    Gawel, Bartlomiej; Lambrechts, Kalle [Ugelstad Laboratory, Department of Chemical Engineering, Norwegian University of Science and Technology (NTNU), N-7491 Trondheim (Norway); Oye, Gisle, E-mail: gisle.oye@chemeng.ntnu.no [Ugelstad Laboratory, Department of Chemical Engineering, Norwegian University of Science and Technology (NTNU), N-7491 Trondheim (Norway)

    2012-05-15

    Highlights: Black-Right-Pointing-Pointer A facile method for preparing Au/CeO{sub 2}-Al{sub 2}O{sub 3} monoliths with hierarchical porosity. Black-Right-Pointing-Pointer Continuous-flow testing of the monoliths in liquid-phase oxidation of glucose. Black-Right-Pointing-Pointer Increased catalytic activity in the presence of cerium oxide (stirred-batch tests). - Abstract: Porous CeO{sub 2}-Al{sub 2}O{sub 3} monoliths with hierarchical pore structure were prepared by mixing boehmite particles with solutions containing different amounts of cerium chloride and aluminum nitrate. The monoliths were functionalized with gold nanoparticles using the incipient wetness method. The resulting materials were characterized by X-ray diffraction, nitrogen sorption, mercury porosimetry, UV-vis spectroscopy and transmission electron microscopy. The catalysts were tested in liquid phase glucose oxidation, comparing continuously stirred batch reactor and continuous-flow fix-bed reactor setups.

  8. Study of cerium doped magnetite (Fe{sub 3}O{sub 4}:Ce)/PMMA nanocomposites

    Energy Technology Data Exchange (ETDEWEB)

    Padalia, Diwakar, E-mail: Padalia.diwakar@gmail.com [Department of Physics, G.B. Pant University of Agriculture and Technology, Pantnagar, Uttrakhand (India); Johri, U.C. [Department of Physics, G.B. Pant University of Agriculture and Technology, Pantnagar, Uttrakhand (India); Zaidi, M.G.H. [Supercritical Fluid Processing Laboratory, Department of Chemistry, G.B. Pant University of Agriculture and Technology, Pantnagar, Uttrakhand (India)

    2012-03-01

    The paper presents the synthesis and properties of polymer nanocomposite material based on cerium doped magnetite (Fe{sub 3}O{sub 4}) as filler material and poly methyl methacrylate (PMMA) as host matrix. The magnetite (Fe{sub 3}O{sub 4}) particles were synthesized by co-precipitation route using stable ferrous and ferric salts with ammonium hydroxide as precipitating agent. Further, they doped by cerium oxide (CeO{sub 2}) non-stoichiometrically. The composite material was fabricated by solvent evaporation method. Here 2.4 GHz microwaves were used to study the effect of microwaves heating on polymerization. The phase and crystal structure is determined by X-ray diffraction (XRD). The average crystallite size of the composites varies from 28 to 35 nm. The chemical structure is confirmed by Fourier transform infrared (FTIR) spectroscopy. The magnetic and thermal properties are investigated by vibrating sample magnetometer (VSM) and differential scanning calorimetry (DSC). The thermal study shows that the microwave heated samples possess higher glass transition temperature (T{sub g}). The magnetic results suggest that coercivity (H{sub C}) and squareness (M{sub r}/M{sub s}) of the loop increases with increasing doping percent of cerium.

  9. Effect of Phosphine Doping and the Surface Metal State of Ni on the Catalytic Performance of Ni/Al2O3 Catalyst

    Directory of Open Access Journals (Sweden)

    Xiaoru Li

    2015-04-01

    Full Text Available Ni-based catalysts as replacement for noble metal catalysts are of particular interest in the catalytic conversion of biomass due to their cheap and satisfactory catalytic activity. The Ni/SiO2 catalyst has been studied for the hydrogenolysis of glycerol, and doping with phosphorus (P found to improve the catalytic performance significantly because of the formation of Ni2P alloys. However, in the present work we disclose a different catalytic phenomenon for the P-doped Ni/Al2O3 catalyst. We found that doping with P has a significant effect on the state of the active Ni species, and thus improves the selectivity to 1,2-propanediol (1,2-PDO significantly in the hydrogenolysis of glycerol, although Ni-P alloys were not observed in our catalytic system. The structure and selectivity correlations were determined from the experimental data, combining the results of X-ray diffraction (XRD, X-ray photoelectron spectroscopy (XPS, hydrogen temperature-programmed reduction (H2-TPR and ammonia temperature-programmed desorption (NH3-TPD. The presence of NiO species, formed from P-doped Ni/Al2O3 catalyst, was shown to benefit the formation of 1,2-PDO. This was supported by the results of the Ni/Al2O3 catalyst containing NiO species with incomplete reduction. Furthermore, the role the NiO species played in the reaction and the potential reaction mechanism over the P-doped Ni/Al2O3 catalyst is discussed. The new findings in the present work open a new vision for Ni catalysis and will benefit researchers in designing Ni-based catalysts.

  10. Magnetorresistência colossal em La5/8-yPr yCa3/8MnO3 Magnetoresistance in La5/8-yPr yCa3/8MnO3

    Directory of Open Access Journals (Sweden)

    S. H. Masunaga

    2007-09-01

    Full Text Available Amostras policristalinas de La5/8-yPr yCa3/8MnO3, 0 0,35 também mostram uma transição para o estado de ordenamento de carga/orbital T OC. Uma análise das medidas de ro(T, H sugere a coexistência de pelo menos duas fases distintas nesses materiais: uma ferromagnética-metálica FMM e uma segunda, com ordenamento de carga/orbital e comportamento isolante OCI. Os resultados também permitem concluir que as frações volumétricas dessas fases podem ser manipuladas, alterando-se parâmetros termodinâmicos como T e H. A magnetorresistência MR(T, determinada através das medidas de ro(T, H, foi observada ocorrer em uma larga faixa de temperatura e em todas as amostras pertencentes à série. Amostras ricas em Pr (y > 0,35 revelam um efeito de magnetorresistência colossal amplificado devido à coexistência e competição das FMM e OCI cujas frações volumétricas podem ser alteradas via mudança da temperatura e aplicação de um campo magnético externo.Polycrystalline samples of La5/8-yPr yCa3/8MnO3; 0 0.35 a transition to a charge and orbital-ordered state was also observed. The rho(T, H data analyses suggest the coexistence of at least two ordered phases in these samples: a ferromagnetic metallic phase FMM and a charge and orbital-ordered insulating COI phase.The data also indicate that the volume fraction of these phases can be changed by the variation of thermodynamic parameters like temperature T and magnetic field H. The magnetoresistance MR(T determined from rho(T, H data were observed in a large temperature range for all samples. In addition, samples with y > 0.35 were found to display a pronounced colossal magnetoresistance effect due to a severe competition between FMM and COI coexisting phases.

  11. Nanofrictional behavior of amorphous, polycrystalline and textured Y-Cr-O films

    International Nuclear Information System (INIS)

    Gervacio-Arciniega, J.J.; Flores-Ruiz, F.J.; Diliegros-Godines, C.J.; Broitman, E.; Enriquez-Flores, C.I.; Espinoza-Beltrán, F.J.; Siqueiros, J.; Cruz, M.P.

    2016-01-01

    Highlights: • Friction coefficient (μ) of ferroelectric textured and polycrystalline YCrO_3 films. • A simple method to evaluate μ from a single AFM image is presented. • The AFM-cantilever spring constant was determined from its dynamic response. • Polycrystalline and amorphous films have a lower μ than textured samples. - Abstract: Differences in friction coefficients (μ) of ferroelectric YCrO_3, textured and polycrystalline films, and non-ferroelectric Y-Cr-O films are analyzed. The friction coefficient was evaluated by atomic force microscopy using a simple quantitative procedure where the dependence of friction force with the applied load is obtained in only one topographical image. A simple code was developed with the MATLAB"® software to analyze the experimental data. The code includes a correction of the hysteresis in the forward and backward scanning directions. The quantification of load exerted on the sample surface was obtained by finite element analysis of the AFM cantilever starting from its experimental dynamic information. The results show that the ferroelectric YCrO_3 film deposited on a Pt(150 nm)/TiO_2(30 nm)/SiO_2/Si (100) substrate is polycrystalline and has a lower friction coefficient than the deposited on SrTiO_3 (110), which is highly textured. From a viewpoint of industrial application in ferroelectric memories, where the writing process is electrical or mechanically achieved by sliding AFM tips on the sample, polycrystalline YCrO_3 films seem to be the best candidates due to their lower μ.

  12. Nanofrictional behavior of amorphous, polycrystalline and textured Y-Cr-O films

    Energy Technology Data Exchange (ETDEWEB)

    Gervacio-Arciniega, J.J. [Centro de Nanociencias y Nanotecnología (CNyN), Universidad Nacional Autónoma de México (UNAM), km. 107, Carretera Tijuana-Ensenada, 22860 Ensenada, B.C. (Mexico); Flores-Ruiz, F.J., E-mail: fcojfloresr@gmail.com [Centro de Nanociencias y Nanotecnología (CNyN), Universidad Nacional Autónoma de México (UNAM), km. 107, Carretera Tijuana-Ensenada, 22860 Ensenada, B.C. (Mexico); Diliegros-Godines, C.J. [Centro de Nanociencias y Nanotecnología (CNyN), Universidad Nacional Autónoma de México (UNAM), km. 107, Carretera Tijuana-Ensenada, 22860 Ensenada, B.C. (Mexico); Broitman, E. [Thin Film Physics Division, IFM, Linköping University, SE-58183 Linköping (Sweden); Enriquez-Flores, C.I.; Espinoza-Beltrán, F.J. [CINVESTAV Unidad Querétaro, Lib. Norponiente 2000, Real de Juriquilla, 76230 Querétaro, Qro. (Mexico); Siqueiros, J.; Cruz, M.P. [Centro de Nanociencias y Nanotecnología (CNyN), Universidad Nacional Autónoma de México (UNAM), km. 107, Carretera Tijuana-Ensenada, 22860 Ensenada, B.C. (Mexico)

    2016-08-15

    Highlights: • Friction coefficient (μ) of ferroelectric textured and polycrystalline YCrO{sub 3} films. • A simple method to evaluate μ from a single AFM image is presented. • The AFM-cantilever spring constant was determined from its dynamic response. • Polycrystalline and amorphous films have a lower μ than textured samples. - Abstract: Differences in friction coefficients (μ) of ferroelectric YCrO{sub 3}, textured and polycrystalline films, and non-ferroelectric Y-Cr-O films are analyzed. The friction coefficient was evaluated by atomic force microscopy using a simple quantitative procedure where the dependence of friction force with the applied load is obtained in only one topographical image. A simple code was developed with the MATLAB{sup ®} software to analyze the experimental data. The code includes a correction of the hysteresis in the forward and backward scanning directions. The quantification of load exerted on the sample surface was obtained by finite element analysis of the AFM cantilever starting from its experimental dynamic information. The results show that the ferroelectric YCrO{sub 3} film deposited on a Pt(150 nm)/TiO{sub 2}(30 nm)/SiO{sub 2}/Si (100) substrate is polycrystalline and has a lower friction coefficient than the deposited on SrTiO{sub 3} (110), which is highly textured. From a viewpoint of industrial application in ferroelectric memories, where the writing process is electrical or mechanically achieved by sliding AFM tips on the sample, polycrystalline YCrO{sub 3} films seem to be the best candidates due to their lower μ.

  13. Doping of low-T{sub g} phosphate glass with Al{sub 2}O{sub 3}, B{sub 2}O{sub 3} and SiO{sub 2}: Part I- effect on glass property and stability

    Energy Technology Data Exchange (ETDEWEB)

    Rajbhandari, P., E-mail: p.rajbhandari@sheffield.ac.uk [UCCS UMR-CNRS 8181, Universite de Lille1, Villeneuve d' Ascq (France); Montagne, L. [UCCS UMR-CNRS 8181, Universite de Lille1, Villeneuve d' Ascq (France); Tricot, G. [UCCS UMR-CNRS 8181, Universite de Lille1, Villeneuve d' Ascq (France); LASIR UMR-CNRS 8516, Universite de Lille1, Villeneuve d' Ascq (France)

    2016-11-01

    A zinc alkali pyrophosphate system 46.6ZnO-20Na{sub 2}O-33.5P{sub 2}O{sub 5} presenting low-T{sub g} (339 °C) and good thermal stability has been doped with (1–4) mol% of Al{sub 2}O{sub 3}, B{sub 2}O{sub 3} and SiO{sub 2} to improve the stability of the glass with a minimal increase in glass transition temperature (T{sub g}). XRD and 1D {sup 31}P solid state NMR were used to monitor the isothermal crystallization process occurring at 130 °C above T{sub g}. If the Al{sub 2}O{sub 3} and B{sub 2}O{sub 3} doping significantly improved thermal stability, this property was marginally affected by SiO{sub 2} doping. Viscosity measurements were performed to observe the crystallization effects induced by the doping. It is noteworthy that the T{sub g} values of all the doped compositions with improved stability presented in this work are below 400 °C. Raman spectroscopy, 1D {sup 31}P, {sup 27}Al, {sup 11}B and {sup 29}Si solid state NMR were carried out to determine the structural modifications and coordination states of the doping elements all along the composition line. - Highlights: • Low-Tg phosphate glasses doped with Al{sub 2}O{sub 3}, B{sub 2}O{sub 3} and SiO{sub 2} have been formulated. • Thermal stability of the glass has been improved significantly. • The structural modification induced by doping elements has been studied by employing solid state NMR technique.

  14. Magnetism mediated by a majority of [Fe³⁺ + VO²⁻] complexes in Fe-doped CeO₂ nanoparticles.

    Science.gov (United States)

    Paidi, V K; Ferreira, N S; Goltz, D; van Lierop, J

    2015-08-26

    We examine the role of Fe(3+) and vacancies (V(O)) on the magnetism of Fe-doped CeO2 nanoparticles. Magnetic nanoparticles of Ce(100-x)Fe(x)O2 (x  =  0, 0.26, 1.82, 2.64, 5.26, 6.91, and 7.22) were prepared by a co-precipitation method, and their structural, compositional and magnetic properties were investigated. The CeO2 nanoparticles had a mixed valance of Ce(4+) and Ce(3+) ions, and doping introduced Fe(3+) ions. The decrease in Ce(3+) and increase in Fe(3+) concentrations indicated the presence of more [Fe(3+) + V(O)(2-)] complexes with Fe loading in the particles. Charge neutralization, Fe(3+) + V(O)(2-) + 2Ce(4+) ↔ 2Ce(3+) + Fe(3+), identified the impact of V(O) on the magnetism, where our results suggest that the Fe-doped CeO2 nanoparticle magnetism is mediated by a majority of [Fe(3+) + V(O)(2-)]-Ce(3+) -[Fe(3+) + V(O)(2-)] complexes.

  15. Luminescence properties of Ce{sup 3+} and Tb{sup 3+} co-activated ZnAl{sub 2}O{sub 4} phosphor

    Energy Technology Data Exchange (ETDEWEB)

    Tshabalala, K.G. [Department of Physics, University of the Free State, Bloemfontein, ZA 9300 (South Africa); Cho, S.-H.; Park, J.-K. [Nano-Materials Center, Korea Institute of Science and Technology, Cheongryang, Seoul 130-650 (Korea, Republic of); Pitale, Shreyas S.; Nagpure, I.M.; Kroon, R.E.; Swart, H.C. [Department of Physics, University of the Free State, Bloemfontein, ZA 9300 (South Africa); Ntwaeaborwa, O.M., E-mail: ntwaeab@ufs.ac.za [Department of Physics, University of the Free State, Bloemfontein, ZA 9300 (South Africa)

    2012-05-15

    In this study, a solution combustion method was used to prepare green emitting Ce{sup 3+}-Tb{sup 3+} co-activated ZnAl{sub 2}O{sub 4} phosphor. The samples were annealed at 700 Degree-Sign C in air or hydrogen atmosphere to improve their crystallinity and optical properties. X-ray diffraction study confirmed that both as-prepared and post-preparation annealed samples crystallized in the well known cubic spinel structure of ZnAl{sub 2}O{sub 4}. An agglomeration of irregular platelet-like particles whose surfaces were encrusted with smaller spheroidal particles was confirmed by scanning electron microscopy (SEM). The fluorescence data collected from the annealed samples with different concentrations of Ce{sup 3+} and Tb{sup 3+} show the enhanced green emission at 543 nm associated with {sup 5}D{sub 4}{yields}{sup 7}F{sub 5} transitions of Tb{sup 3+}. The enhancement was attributed to energy transfer from Ce{sup 3+} to Tb{sup 3+}. Possible mechanism of energy transfer via a down conversion process is discussed. Furthermore, cathodoluminescence (CL) intensity degradation of this phosphor was also investigated and the degradation data suggest that the material was chemically stable and the CL intensity was also stable after 10 h of irradiation by a beam of high energy electrons.

  16. Dehydrogenation of Surface-Oxidized Mixtures of 2LiBH4 + Al/Additives (TiF3 or CeO2

    Directory of Open Access Journals (Sweden)

    Juan Luis Carrillo-Bucio

    2017-11-01

    Full Text Available Research for suitable hydrogen storage materials is an important ongoing subject. LiBH4–Al mixtures could be attractive; however, several issues must be solved. Here, the dehydrogenation reactions of surface-oxidized 2LiBH4 + Al mixtures plus an additive (TiF3 or CeO2 at two different pressures are presented. The mixtures were produced by mechanical milling and handled under welding-grade argon. The dehydrogenation reactions were studied by means of temperature programmed desorption (TPD at 400 °C and at 3 or 5 bar initial hydrogen pressure. The milled and dehydrogenated materials were characterized by scanning electron microscopy (SEM, X-ray diffraction (XRD, and Fourier transformed infrared spectroscopy (FT-IR The additives and the surface oxidation, promoted by the impurities in the welding-grade argon, induced a reduction in the dehydrogenation temperature and an increase in the reaction kinetics, as compared to pure (reported LiBH4. The dehydrogenation reactions were observed to take place in two main steps, with onsets at 100 °C and 200–300 °C. The maximum released hydrogen was 9.3 wt % in the 2LiBH4 + Al/TiF3 material, and 7.9 wt % in the 2LiBH4 + Al/CeO2 material. Formation of CeB6 after dehydrogenation of 2LiBH4 + Al/CeO2 was confirmed.

  17. Processes of the excitation energy migration and transfer in Ce3+-doped alkali gadolinium phosphates studied with time-resolved photoluminescence spectroscopy technique

    International Nuclear Information System (INIS)

    Stryganyuk, G.; Shalapska, T.; Voloshinovskii, A.; Gektin, A.; Krasnikov, A.; Zazubovich, S.

    2011-01-01

    Spectral-kinetic characteristics of Gd 3+ and Ce 3+ luminescence from a series of Ce 3+ -doped alkali gadolinium phosphates of MGdP 4 O 12 type (M=Li, Na, Cs) have been studied within 4.2-300 K temperature range using time-resolved luminescence spectroscopy techniques. The processes of energy migration along the Gd 3+ sub-lattice and energy transfer between the Gd 3+ and Ce 3+ ions have been investigated. Peculiarities of these processes have been compared for MGdP 4 O 12 phosphate hosts with different alkali metal ions. A contribution of different levels from the 6 P j multiplet of the lowest Gd 3+ excited state into the energy migration and transfer processes has been clarified. The phonon-assisted occupation of high-energy 6 P 5/2,3/2 levels by Gd 3+ in the excited 6 P j state has been revealed as a shift of Gd 3+6 P j → 8 S 7/2 emission into the short-wavelength spectral range upon the temperature increase. The relaxation of excited Gd 3+ via phonon-assisted population of Gd 3+6 P 5/2 level (next higher one to the lowest excited 6 P 7/2 ) is supposed to be responsible for the rise in probability of energy migration within the Gd 3+ sub-lattice initiating the Gd 3+ →Ce 3+ energy transfer at T 3+ →Ce 3+ energy transfer at T>150 K is explained by the increase in probability of Gd 3+ relaxation into the highest 6 P 3/2 level of the 6 P j multiplet. An efficient reversed Ce 3+ →Gd 3+ energy transfer has been revealed for the studied phosphates at 4.2 K. - Highlights: →We investigate the Gd 3+ -Ce 3+ energy transfer in alkali gadolinium phosphates. → Thermal population of Gd 3+6 P 5/2 level improves migration along the Gd sub-lattice. → Increasing overlap of Gd 3+ and Ce 3+ states enhances the Gd 3+ -Ce 3+ energy transfer. → In LiGdP 4 O 12 :Ce and NaGdP 4 O 12 :Ce an efficient Ce 3+ -Gd 3+ transfer occurs at 4-300 K. → An effective reverse Gd 3+ -Ce 3+ energy transfer becomes possible at T>150 K.

  18. Effect of Al and Fe doping in ZnO on magnetic and magneto-transport properties

    International Nuclear Information System (INIS)

    Kumar, Santosh; Deepika; Tripathi, Malvika; Vaibhav, Pratyush; Kumar, Aman; Kumar, Ritesh; Choudhary, R.J.; Phase, D.M.

    2016-01-01

    The structural, magnetic and magneto-transport of undoped ZnO, Zn_0_._9_7Al_0_._0_3O, Zn_0_._9_5Fe_0_._0_5O and Zn_0_._9_2Al_0_._0_3Fe_0_._0_5O thin films grown on Si(100) substrate using pulsed laser deposition were investigated. The single phase nature of the films is confirmed by X-ray diffraction and Raman spectroscopy measurements. The possibility of Fe metal cluster in Fe doped/co-doped films is ruled out by Fe 2p core level photoelectron spectra. From O 1s core level spectra it is observed that oxygen vacancy is present in all the films. The undoped ZnO film shows magnetic ordering below ∼175 K, whereas Fe doped/codoped samples show magnetic ordering even at 300 K. The Al doped sample reveals paramagnetic behavior. The magneto-transport measurements suggest that the mobile carriers undergo exchange interaction with local magnetic moments. - Highlights: • Al, Fe, Al–Fe co-doped and undoped films of ZnO are deposited on Si by PLD. • Single phase (002) oriented Wurtzite ZnO phase is formed for all films. • Fe doped and Fe–Al co-doped ZnO films reveal magnetic hysteresis at 300 K. • Negative magnetoresistance is observed in undoped and Fe–Al co-doped ZnO film. • It is apparent that charge carriers are coupled with the local magnetic moment.

  19. Magnetic and magnetocaloric properties of amorphous Y{sub 3}Fe{sub 5}O{sub 12} compound

    Energy Technology Data Exchange (ETDEWEB)

    Nóbrega, E.P., E-mail: pilad@cbpf.br; Costa, S.S.; Alvarenga, T.S.T.; Alho, B.P.; Caldas, A.; Ribeiro, P.O.; Sousa, V.S.R de; Oliveira, N.A. de; Ranke, P.J. von

    2017-01-15

    We report a theoretical model formed by two coupled magnetic sublattices of localized spins in the presence of an applied magnetic field to investigate the magnetic characteristics and magnetocaloric properties of amorphous yttrium iron garnet. The magnetic state equation is based on Handrich–Kobe´s theory, where the amorphization is taken into account by introducing fluctuations in the exchange parameters. Experimental results report that Y{sub 3}Fe{sub 5}O{sub 12} presents a structural phase transition from crystalline to amorphous caused by a variation of external pressure. This phase transition on Y{sub 3}Fe{sub 5}O{sub 12} leads to interesting results in the magnetic properties and magnetocaloric quantities. - Highlights: • Study of magnetic and magnetocaloric properties of amorphous Y{sub 3}Fe{sub 5}O{sub 12} compound. • Theoretical model formed by two coupled magnetic sublattices of localized spins in the presence of an applied magnetic field. • The influence of crystalline/amorphous transition on the magnetocaloric effect.

  20. Highly Efficient Green-Emitting Phosphors Ba2Y5B5O17 with Low Thermal Quenching Due to Fast Energy Transfer from Ce3+ to Tb3.

    Science.gov (United States)

    Xiao, Yu; Hao, Zhendong; Zhang, Liangliang; Xiao, Wenge; Wu, Dan; Zhang, Xia; Pan, Guo-Hui; Luo, Yongshi; Zhang, Jiahua

    2017-04-17

    This paper demonstrates a highly thermally stable and efficient green-emitting Ba 2 Y 5 B 5 O 17 :Ce 3+ , Tb 3+ phosphor prepared by high-temperature solid-state reaction. The phosphor exhibits a blue emission band of Ce 3+ and green emission lines of Tb 3+ upon Ce 3+ excitation in the near-UV spectral region. The effect of Ce 3+ to Tb 3+ energy transfer on blue to green emission color tuning and on luminescence thermal stability is studied in the samples codoped with 1% Ce 3+ and various concentrations (0-40%) of Tb 3+ . The green emission of Tb 3+ upon Ce 3+ excitation at 150 °C can keep, on average, 92% of its intensity at room temperature, with the best one showing no intensity decreasing up to 210 °C for 30% Tb 3+ . Meanwhile, Ce 3+ emission intensity only keeps 42% on average at 150 °C. The high thermal stability of the green emission is attributed to suppression of Ce 3+ thermal de-excitation through fast energy transfer to Tb 3+ , which in the green-emitting excited states is highly thermally stable such that no lifetime shortening is observed with raising temperature to 210 °C. The predominant green emission is observed for Tb 3+ concentration of at least 10% due to efficient energy transfer with the transfer efficiency approaching 100% for 40% Tb 3+ . The internal and external quantum yield of the sample with Tb 3+ concentration of 20% can be as high as 76% and 55%, respectively. The green phosphor, thus, shows attractive performance for near-UV-based white-light-emitting diodes applications.

  1. Epitaxial patterning of nanometer-thick Y3Fe5O12 films with low magnetic damping.

    Science.gov (United States)

    Li, Shaozhen; Zhang, Wei; Ding, Junjia; Pearson, John E; Novosad, Valentine; Hoffmann, Axel

    2016-01-07

    Magnetic insulators such as yttrium iron garnet, Y3Fe5O12, with extremely low magnetic damping have opened the door for low power spin-orbitronics due to their low energy dissipation and efficient spin current generation and transmission. We demonstrate here reliable and efficient epitaxial growth and nanopatterning of Y3Fe5O12 thin-film based nanostructures on insulating Gd3Ga5O12 substrates. In particular, our fabrication process is compatible with conventional sputtering and lift-off, and does not require aggressive ion milling which may be detrimental to the oxide thin films. Their structural and magnetic properties indicate good qualities, in particular low magnetic damping of both films and patterned structures. The dynamic magnetic properties of the nanostructures are systematically investigated as a function of the lateral dimension. By comparing with ferromagnetic nanowire structures, a distinct edge mode in addition to the main mode is identified by both experiments and simulations, which also exhibit cross-over with the main mode upon varying the width of the wires. The non-linear evolution of dynamic modes over nanostructural dimensions highlights the important role of size confinement to their material properties in magnetic devices where Y3Fe5O12 nanostructures serve as the key functional component.

  2. Red, yellow, blue and green emission from Eu3+, Dy3+ and Bi3+ doped Y2O3 nanophosphors

    International Nuclear Information System (INIS)

    Loitongbam, Romeo Singh; Rameshwor Singh, W.

    2014-01-01

    Rare earth elements (RE = Eu 3+ and Dy 3+ ) and Bi 3+ doped Y 2 O 3 nanoparticles were synthesized by urea hydrolysis method in ethylene glycol, which acts as reaction medium as well as capping agent, at a low temperature (140℃), followed by calcination of the obtained product. Scanning electron microscopy (SEM) images reveal that a highly uniform ovoid shaped Y 2 O 3 nanoparticles of around 100 nm size range were obtained in this method. The respective RE and Bi 3+ doped Y 2 O 3 precursor nanoparticles when heated at 600 and 750℃, retains the same shape as that of the as-synthesized Y 2 O 3 precursor samples. XRD pattern reveals the crystalline nature of the heated nanoparticles and indicate the absence of any impurity phase other than cubic Y 2 O 3

  3. Interface phenomena in the Y2O3/(Al-Cu) system

    International Nuclear Information System (INIS)

    Barzilai, S.; Aizenshtein, M.; Froumin, N.; Frage, N.

    2006-01-01

    Wetting behavior and the interface reaction in the Y 2 O 3 /(Cu-Al) system were investigated at 1423 K. A contact angle of about 130 o was measured in the Y 2 O 3 /Cu system. Aluminum addition to copper improves wetting and the transition from non-wetting to wetting (θ ≤ 90 o ) was observed for the alloy with 50 at.% Al. The microstructure examination of the interface indicates that Al reacts with yttria, yttrium dissolves in the melt and a crater of AlYO 3 is formed at the substrate. The interface interaction in the Y 2 O 3 /(Cu-Al) system is in a good agreement with the results of a thermodynamic analysis in the Y-Al-Cu-O system. The crater depth and the macroscopic final contact angles are correlated with the Y and Al activities in the melt

  4. The Poisoning Effect of Na Doping over Mn-Ce/TiO2 Catalyst for Low-Temperature Selective Catalytic Reduction of NO by NH3

    Directory of Open Access Journals (Sweden)

    Liu Yang

    2014-01-01

    Full Text Available Sodium carbonate (Na2CO3, sodium nitrate (NaNO3, and sodium chloride (NaCl were chosen as the precursors to prepare the Na salts deposited Mn-Ce/TiO2 catalysts through an impregnation method. The influence of Na on the performance of the Mn-Ce/TiO2 catalyst for low-temperature selective catalytic reduction of NOx by NH3 was investigated. Experimental results showed that Na salts had negative effects on the activity of Mn-Ce/TiO2 and the precursors of Na salts also affected the catalytic activity. The precursor Na2CO3 had a greater impact on the catalytic activity, while NaNO3 had minimal effect. The characterization results indicated that the significant changes in physical and chemical properties of Mn-Ce/TiO2 were observed after Na was doped on the catalysts. The significant decreases in surface areas and NH3 adsorption amounts were observed after Na was doped on the catalysts, which could be considered as the main reasons for the deactivation of Na deposited Mn-Ce/TiO2.

  5. Evaluation of mechanical hardness and fracture toughness of Co and Al co-doped ZnO

    International Nuclear Information System (INIS)

    Siddheswaran, R.; Mangalaraja, R.V.; Avila, Ricardo E.; Manikandan, D.; Esther Jeyanthi, C.; Ananthakumar, S.

    2012-01-01

    Combustion synthesized nanocrystalline Co and Al co-doped ZnO powders [(Zn 1−x−y Co x Al y O; x=0.04, 0.03, 0.02; y=0.01, 0.02, 0.03)] were fabricated into cylindrical discs by uni-axial pressing and sintered intentionally at 1000 °C for 2 h to assess the mechanical performance. The crystallinity of the pure and doped ZnO was confirmed by X-ray diffraction analysis. The microstructures of the sintered samples were investigated by scanning electron microscopy (SEM) to examine the density, porosity, grain size and its distribution. Grains of 0.53 μm were observed for the samples sintered at 1000 °C. The mechanical properties such as micro-hardness, fracture toughness and strain hardening co-efficient were investigated by the Vickers indentation method. It was found that the crack mode observed during the indentation on the samples belongs to median cracks under a load of 19.6 N. Also, the hardness was enhanced with increasing mol% of Co, while the trend was reversed with the increase of Al content. In addition, the strain hardening coefficient and fracture toughness were calculated using the indentation data.

  6. Influence of P2O5 and Al2O3 content on the structure of erbium-doped borosilicate glasses and on their physical, thermal, optical and luminescence properties

    International Nuclear Information System (INIS)

    Bourhis, Kevin; Massera, Jonathan; Petit, Laeticia; Ihalainen, Heikki; Fargues, Alexandre; Cardinal, Thierry; Hupa, Leena; Hupa, Mikko; Dussauze, Marc; Rodriguez, Vincent; Boussard-Plédel, Catherine; Bureau, Bruno; Roiland, Claire; Ferraris, Monica

    2015-01-01

    Highlights: • Reorganization of the glass structure induced by the addition of P 2 O 5 or Al 2 O 3 . • Emission properties related to the presence of P or Al in the Er 3+ coordination shell. • Declustering observed upon addition of P 2 O 5 . • No declustering upon addition of Al 2 O 3 . - Abstract: The effect of P 2 O 5 and/or Al 2 O 3 addition in Er-doped borosilicate glasses on the physical, thermal, optical, and luminescence properties is investigated. The changes in these glass properties are related to the glass structure modifications induced by the addition of P 2 O 5 and/or Al 2 O 3 , which were probed by FTIR, 11 B MAS NMR and X-ray photoelectron spectroscopies. Variations of the polymerization degree of the silicate tetrahedra and modifications in the [3] B/ [4] B ratio are explained by a charge compensation mechanism due to the formation of AlO 4 , PO 4 groups and the formation of Al-O-P linkages in the glass network. From the absorption and luminescence properties of the Er 3+ ions at 980 nm and 1530 nm, declustering is suspected for the highest P 2 O 5 concentrations while for the highest Al 2 O 3 concentrations no declustering is observed

  7. Room temperature magnetic and dielectric properties of cobalt doped CaCu3Ti4O12 ceramics

    Science.gov (United States)

    Mu, Chunhong; Song, Yuanqiang; Wang, Haibin; Wang, Xiaoning

    2015-05-01

    CaCu3Ti4-xCoxO12 (x = 0, 0.2, 0.4) ceramics were prepared by a conventional solid state reaction, and the effects of cobalt doping on the room temperature magnetic and dielectric properties were investigated. Both X-ray diffraction and energy dispersive X-ray spectroscopy confirmed the presence of Cu and Co rich phase at grain boundaries of Co-doped ceramics. Scanning electron microscopy micrographs of Co-doped samples showed a striking change from regular polyhedral particle type in pure CaCu3Ti4O12 (CCTO) to sheet-like grains with certain growth orientation. Undoped CaCu3Ti4O12 is well known for its colossal dielectric constant in a broad temperature and frequency range. The dielectric constant value was slightly changed by 5 at. % and 10 at. % Co doping, whereas the second relaxation process was clearly separated in low frequency region at room temperature. A multirelaxation mechanism was proposed to be the origin of the colossal dielectric constant. In addition, the permeability spectra measurements indicated Co-doped CCTO with good magnetic properties, showing the initial permeability (μ') as high as 5.5 and low magnetic loss (μ″ < 0.2) below 3 MHz. And the interesting ferromagnetic superexchange coupling in Co-doped CaCu3Ti4O12 was discussed.

  8. Optical characterization of hydrogen-free CeO2 doped DLC films deposited by unbalanced magnetron sputtering

    International Nuclear Information System (INIS)

    Zhang Zhenyu; Zhou Hongxiu; Guo Dongming; Gao Hang; Kang Renke

    2008-01-01

    A novel kind of hydrogen-free CeO 2 doped diamond-like carbon (DLC) films with thickness of 180-200 nm were deposited on silicon by unbalanced magnetron sputtering. Reduced reflectance and increased lifetime are expected with respect to pure DLC films, making these coatings good candidates as optical protective coatings for IR windows and solar cells. X-ray photoelectron spectroscopy confirms that CeO 2 is formed within the DLC films. Auger electron spectroscopy exhibits that the C, O, and Ce elements distribute uniformly across the film thickness, and C element diffuses into the Si substrate at the interface between the substrate and film. AFM shows that nanoparticles with diameter of around 50 nm are formed on the surface of deposited films, whose surface roughness is in the range of 1.3-2.3 nm. Raman spectra show the CeO 2 doped DLC films are amorphous DLC films, and both the G frequency and relative intensity ratio I D /I G are higher than those of pure DLC films. The photoluminescence of CeO 2 doped DLC films is obviously more intense than that of a pure DLC film, which indicates a promising potential as optical protective films for solar cells and IR window

  9. Erbium-doped borosilicate glasses containing various amounts of P2O5 and Al2O3: Influence of the silica content on the structure and thermal, physical, optical and luminescence properties

    International Nuclear Information System (INIS)

    Bourhis, Kevin; Massera, Jonathan; Petit, Laeticia; Koponen, Joona; Fargues, Alexandre; Cardinal, Thierry; Hupa, Leena; Hupa, Mikko; Dussauze, Marc; Rodriguez, Vincent; Ferraris, Monica

    2015-01-01

    Highlights: • Er 3+ doped borosilicate glasses were processed with different compositions and characterizations. • An increase in the SiO 2 content leads to a silicate-rich environment around the Er 3+ site. • An increase in the SiO 2 content decreases the Er 3+ absorption cross-section at 980 nm. • Glasses with 60 mol% of SiO 2 exhibit a stronger emission intensity at 1530 nm than glasses with x = 50. • Highest 1.5 μm emission intensity was achieved for the Al and P containing glass with 60 mol% of SiO 2 . - Abstract: The influence of the silica content on several properties of Er-doped borosilicate glasses in the presence of various amounts of P 2 O 5 and Al 2 O 3 has been investigated. The introduction of P 2 O 5 and/or Al 2 O 3 are responsible for structural modifications in the glass network through a charge-compensation mechanism related to the formation of negatively-charged PO 4 and AlO 4 groups or through the formation of AlPO 4 -like structural units. In this paper, we show that an increase in the SiO 2 content leads to a silicate-rich environment around the Er 3+ site, resulting in an increased dependence of the Er 3+ ions optical and luminescence properties on the P 2 O 5 and/or Al 2 O 3 concentration. The highest emission intensity at 1.5 μm was achieved for the glass with an equal proportion of P and Al in the glass system with 60 mol% of SiO 2

  10. Microstructure and crystallography of Al2O3-Y3Al5O12-ZrO2 ternary eutectic oxide grown by the micropulling down technique

    Science.gov (United States)

    Benamara, Omar; Cherif, Maya; Duffar, Thierry; Lebbou, Kheirreddine

    2015-11-01

    The directional solidification of Al2O3-YAG-ZrO2 eutectic ceramic by a micro-pulling down (μ-PD) technique is investigated. The effect of the pulling rate (0.1-1 mm min-1) on the crystallography and the microstructure is discussed. This ternary eutectic system has a Chinese script microstructure and the eutectic spacing λ depends on the pulling rate υ following the law: λ = 6.5υ-1/2 where λ is in μm and υ in μm/s as derived from the Jackson-Hunt model. With the lower pulling rates, all phases are oriented with the direction parallel to the growth direction; however other orientations appear at the higher pulling rates. The Cr3+ ions R-lines emission in the sapphire phase in the ternary eutectic composite is measured to estimate the stress in the alumina phase which is also shown to depend on the pulling rate.

  11. Structural, optical, and magnetic properties of polycrystalline Co-doped TiO2 synthesized by solid-state method

    International Nuclear Information System (INIS)

    Bouaine, Abdelhamid; Schmerber, G.; Ihiawakrim, D.; Derory, A.

    2012-01-01

    Highlights: ► Influence of Co doping on the TiO 2 tetragonal structure. ► Decrease of the energy band gap after doping with Co atoms. ► Appearance of ferromagnetism in Co-doped TiO 2 diluted magnetic semiconductors. - Abstract: We have used a solid-state method to synthesize polycrystalline Co-doped TiO 2 diluted magnetic semiconductors (DMSs) with Co concentrations of 0, and 0.5 at.%. X-ray diffraction patterns reveal that Co doped TiO 2 crystallizes in the rutile tetragonal structure with no additional peaks. Transmission electron microscopy (TEM) did not indicate the presence of magnetic parasitic phases and confirmed that Co ions are uniformly distributed inside the samples. Optical absorbance measurements showed an energy band gap which decreases after doping with the Co atoms into the TiO 2 matrix. Magnetization measurements revealed a paramagnetic behavior for the as-prepared Co-doped TiO 2 and a ferromagnetic behavior for the same samples after annealed under a mixture of H 2 /N 2 atmosphere.

  12. Photoluminescent and Thermoluminescent Studies of Dy3+ and Eu3+ Doped Y2O3 Phosphors.

    Science.gov (United States)

    Verma, Tarkeshwari; Agrawal, Sadhana

    2018-01-01

    Eu 3+ doped and Dy 3+ codoped yttrium oxide (Y 2 O 3 ) phosphors have been prepared using solid-state reaction technique (SSR). The prepared phosphors were characterized by X-ray diffractometer (XRD), energy dispersive X-ray (EDX) spectroscopy, scanning electron microscopy (SEM) and Fourier transforms infrared spectroscopy (FTIR) techniques. Photoluminescence (PL) and Thermoluminescence (TL) properties were studied in detail. PL emission spectra were recorded for prepared phosphors under excitation wavelength 254 nm, which show a high intense peak at 613 nm for Y 2 O 3 :Dy 3+ , Eu 3+ (1:1.5 mol %) phosphor. The correlated color temperature (CCT) and CIE analysis have been performed for the synthesized phosphors. TL glow curves were recorded for Eu 3+ doped and Dy 3+ codoped phosphors to study the heating rate effect and dose response. The kinetic parameters were calculated using peak shape method for UV and γ exposures through computerized glow curve deconvolution (CGCD) technique. The phosphors show second order kinetics and activation energies varying from 5.823 × 10 - 1 to 18.608 × 10 - 1  eV.

  13. Structural, magnetic and electronic structural properties of Mn doped CeO2 nanoparticles

    Science.gov (United States)

    Kumari, Kavita; Vij, Ankush; Hashim, Mohd.; Chae, K. H.; Kumar, Shalendra

    2018-05-01

    Nanoparticles of Ce1-xMnxO2, (x=0.0, 0.01, and 0.05) have been synthesized by using co-precipitation method, and then characterized by x-ray diffraction (XRD), transmission electron microscopy (TEM), near edge x-ray absorption fine structure (NEXAFS) spectroscopy and dc magnetization measurements. XRD results clearly showed that the all the samples have single phase nature and exclude the presence of any secondary phase. The average particle size calculated using XRD TEM measurements found to decrease with increase in Mn doping in the range of 4.0 - 9.0 nm. The structural parameters such as strain, interplaner distance and lattice parameter is observed to decrease with increase in doping. The morphology of Ce1-xMnxO2 nanoparticles measured using TEM micrographs indicate that nanoparticle have spherical shape morphology. Magnetic hysteresis curve for Ce1-xMnxO2, (x = 0.0, 0.01, and 0.05) confirms the ferromagnetic ordering room temperature. The value of saturation magnetization is observed to decrease with increase in temperature from 10 K to 300 K. The NEXAFS spectra measured at Ce M4,5 edge reveals that Ce-ions are in +4 valance state.

  14. Creation of Y2Ti2O7 nanoprecipitates to strengthen the Fe-14Cr-3Al-2W steels by adding Ti hydride and Y2O3 nanoparticles

    International Nuclear Information System (INIS)

    Wang, Linbo; Bai, Zhonglian; Shen, Hailong; Wang, Chenxi; Liu, Tong

    2017-01-01

    In order to prohibit the formation of large Y-Al-O precipitates, Ti hydride nanoparticles (NPs) were prepared and used to replace Ti as raw particles to fabricate the oxide dispersion strengthened (ODS) Fe-14Cr-3Al-2W-0.35Y 2 O 3 steels by mechanical alloying (MA) and hot isostatic pressing (HIP). As the content of Ti hydride increases from 0.1 to 0.5 and 1.0 wt%, the oxide nanoprecipitates in the ODS steels changes from Y 3 Al 5 O 12 phase to Y 2 Ti 2 O 7 phase (semicoherent with the matrix), and the particle size is successfully reduced. The tensile strength of the ODS steel increases remarkably with increasing Ti hydride content. The sample with 1.0 wt% Ti hydride exhibits a high strength of 1049 MPa at 25 °C and 278 MPa at 700 °C. The creation of Y 2 Ti 2 O 7 nanoprecipitates by adding Ti hydride NPs opens a new way to control the structure and size of the oxide precipitates in the ODS steels. - Graphical abstract: The creation of Y 2 Ti 2 O 7 nanoprecipitates by adding Ti hydride nanoparticles remarkably increases the mechanical properties of the Al-containing ODS steels. - Highlights: •TiH 1.971 reacts with Y 2 O 3 to form Y 2 Ti 2 O 7 in the Al-containing ODS steel. •Addition of TiH 1.971 nanoparticles can prevent the formation of Y-Al-O phases. •Y 2 Ti 2 O 7 nanoparticles share semicoherent interface with the ferrite matrix. •The mean size of oxide dispersion is reduced to 11.2 ± 7.1 nm with 1.0 wt% TiH 1.971 . •The tensile strength of the ODS steel enlarges with increasing TiH 1.971 content.

  15. Nb and Ta layer doping effects on the interfacial energetics and electronic properties of LaAlO3/SrTiO3 heterostructure: first-principles analysis.

    Science.gov (United States)

    Nazir, Safdar; Behtash, Maziar; Cheng, Jianli; Luo, Jian; Yang, Kesong

    2016-01-28

    The two-dimensional electron gas (2DEG) formed at the n-type (LaO)(+1)/(TiO2)(0) interface in the polar/nonpolar LaAlO3/SrTiO3 (LAO/STO) heterostructure (HS) has emerged as a prominent research area because of its great potential for nanoelectronic applications. Due to its practical implementation in devices, desired physical properties such as high charge carrier density and mobility are vital. In this respect, 4d and 5d transition metal doping near the interfacial region is expected to tailor electronic properties of the LAO/STO HS system effectively. Herein, we studied Nb and Ta-doping effects on the energetics, electronic structure, interfacial charge carrier density, magnetic moment, and the charge confinements of the 2DEG at the n-type (LaO)(+1)/(TiO2)(0) interface of LAO/STO HS using first-principles density functional theory calculations. We found that the substitutional doping of Nb(Ta) at Ti [Nb(Ta)@Ti] and Al [Nb(Ta)@Al] sites is energetically more favorable than that at La [Nb(Ta)@La] and Sr [Nb(Ta)@Sr] sites, and under appropriate thermodynamic conditions, the changes in the interfacial energy of HS systems upon Nb(Ta)@Ti and Nb(Ta)@Al doping are negative, implying that the formation of these structures is energetically favored. Our calculations also showed that Nb(Ta)@Ti and Nb(Ta)@Al doping significantly improve the interfacial charge carrier density with respect to that of the undoped system, which is because the Nb(Ta) dopant introduces excess free electrons into the system, and these free electrons reside mainly on the Nb(Ta) ions and interfacial Ti ions. Hence, along with the Ti 3d orbitals, the Nb 4d and Ta 5d orbitals also contribute to the interfacial metallic states; accordingly, the magnetic moments on the interfacial Ti ions increase significantly. As expected, the Nb@Al and Ta@Al doped LAO/STO HS systems show higher interfacial charge carrier density than the undoped and other doped systems. In contrast, Nb@Ti and Ta@Ti doped systems may

  16. Nanopores creation in boron and nitrogen doped polycrystalline graphene: A molecular dynamics study

    Science.gov (United States)

    Izadifar, Mohammadreza; Abadi, Rouzbeh; Nezhad Shirazi, Ali Hossein; Alajlan, Naif; Rabczuk, Timon

    2018-05-01

    In the present paper, molecular dynamic simulations have been conducted to investigate the nanopores creation on 10% of boron and nitrogen doped polycrystalline graphene by silicon and diamond nanoclusters. Two types of nanoclusters based on silicon and diamond are used to investigate their effect for the fabrication of nanopores. Therefore, three different diameter sizes of the clusters with five kinetic energies of 10, 50, 100, 300 and 500 eV/atom at four different locations in boron or nitrogen doped polycrystalline graphene nanosheets have been perused. We also study the effect of 3% and 6% of boron doped polycrystalline graphene with the best outcome from 10% of doping. Our results reveal that the diamond cluster with diameter of 2 and 2.5 nm fabricates the largest nanopore areas on boron and nitrogen doped polycrystalline graphene, respectively. Furthermore, the kinetic energies of 10 and 50 eV/atom can not fabricate nanopores in some cases for silicon and diamond clusters on boron doped polycrystalline graphene nanosheets. On the other hand, silicon and diamond clusters fabricate nanopores for all locations and all tested energies on nitrogen doped polycrystalline graphene. The area sizes of nanopores fabricated by silicon and diamond clusters with diameter of 2 and 2.5 nm are close to the actual area size of the related clusters for the kinetic energy of 300 eV/atom in all locations on boron doped polycrystalline graphene. The maximum area and the average maximum area of nanopores are fabricated by the kinetic energy of 500 eV/atom inside the grain boundary at the center of the nanosheet and in the corner of nanosheet with diameters of 2 and 3 nm for silicon and diamond clusters on boron and nitrogen doped polycrystalline graphene.

  17. Significant improvement in performances of LiNi{sub 0.5}Mn{sub 1.5}O{sub 4} through surface modification with high ordered Al-doped ZnO electro-conductive layer

    Energy Technology Data Exchange (ETDEWEB)

    Sun, Hongdan; Xia, Bingbo [College of Physics, Optoelectronics and Energy & Collaborative Innovation Center of Suzhou Nano Science and Technology, Soochow University, Suzhou 215006 (China); Key Laboratory of Lithium Ion Battery Materials of Jiangsu Province, Institute of Chemical Power Sources, Soochow University, Suzhou 215006 (China); Liu, Weiwei [Changzhou Institute of Energy Storage Materials & Devices, Changzhou 213000 (China); Fang, Guoqing; Wu, Jingjing; Wang, Haibo; Zhang, Ruixue [College of Physics, Optoelectronics and Energy & Collaborative Innovation Center of Suzhou Nano Science and Technology, Soochow University, Suzhou 215006 (China); Key Laboratory of Lithium Ion Battery Materials of Jiangsu Province, Institute of Chemical Power Sources, Soochow University, Suzhou 215006 (China); Kaneko, Shingo [Key Laboratory of Lithium Ion Battery Materials of Jiangsu Province, Institute of Chemical Power Sources, Soochow University, Suzhou 215006 (China); Zheng, Junwei [College of Physics, Optoelectronics and Energy & Collaborative Innovation Center of Suzhou Nano Science and Technology, Soochow University, Suzhou 215006 (China); Key Laboratory of Lithium Ion Battery Materials of Jiangsu Province, Institute of Chemical Power Sources, Soochow University, Suzhou 215006 (China); Wang, Hongyu [Changzhou Institute of Energy Storage Materials & Devices, Changzhou 213000 (China); Li, Decheng, E-mail: lidecheng@suda.edu.cn [College of Physics, Optoelectronics and Energy & Collaborative Innovation Center of Suzhou Nano Science and Technology, Soochow University, Suzhou 215006 (China); Key Laboratory of Lithium Ion Battery Materials of Jiangsu Province, Institute of Chemical Power Sources, Soochow University, Suzhou 215006 (China)

    2015-03-15

    Graphical abstract: Al-doped ZnO (AZO)-coated LiNi{sub 0.5}Mn{sub 1.5}O{sub 4} (LNMO) was prepared by sol–gel method. AZO-coated LNMO electrode shows excellent rate capability and a remarkable improvement in the cyclic performance at a high rate at elevated temperature. - Highlights: • Al-doped ZnO (AZO)-coated LiNi{sub 0.5}Mn{sub 1.5}O{sub 4} (LNMO) was prepared by a traditional sol–gel method. • Al-doped ZnO (AZO) layer grown on the surface of LNMO is high ordered. • At a high rate of 10 C, the discharge capacity of the AZO-coated LNMO electrode can reach 114 mAh g{sup −1}. • Al-doped ZnO (AZO) modification improved cyclic performance of LNMO at high temperatures. - Abstract: Al-doped ZnO (AZO)-coated LiNi{sub 0.5}Mn{sub 1.5}O{sub 4} (LNMO) was prepared by sol–gel method. Transmission electron microscopy (TEM) analysis indicates that AZO layer grown on the surface of LNMO is high ordered. The results of electrochemical performance measurements reveal that the AZO-coated LNMO electrode displays the best rate capability compared with the bare LNMO and ZnO-coated LNMO, even at a high rate of 10 C. The discharge capacity of the AZO-coated LNMO electrode can still reach 114.3 mAh g{sup −1}, about 89% of its discharge capacity at 0.1 C. Moreover, AZO-coated LNMO electrode shows a remarkable improvement in the cyclic performance at a high rate at elevated temperature due to the protective effect of AZO coating layer. The electrode delivers a capacity of 120.3 mAh g{sup −1} with the capacity retention of 95% at 5 C in 50 cycles at 50 °C. The analysis of electrochemical impedance spectra (EIS) indicates that AZO-coated LNMO possesses the lowest charge transfer resistance compared to the bare LNMO and ZnO-coated LNMO, which may be responsible for improved rate capability.

  18. Al2O3 doping of TiO2 electrodes and applications in dye-sensitized solar cells

    International Nuclear Information System (INIS)

    Eom, Tae Sung; Kim, Kyung Hwan; Bark, Chung Wung; Choi, Hyung Wook

    2014-01-01

    Dye-sensitized solar cells (DSSCs) have been intensively studied since their discovery in 1991. DSSCs have been extensively researched over the past decades as cheaper alternatives to silicon solar cells due to their high energy-conversion efficiency and their low production cost. However, some problems need to be solved in order to enhance the efficiency of DSSCs. In particular, the electron recombination that occurs due to the contact between the transparent conductive oxide (TCO) and a redox electrolyte is one of the main limiting factors of efficiency. In this work, we report for the first time the improvement of the photovoltaic characteristics of DSSCs by doping TiO 2 with Al 2 O 3 . DSSCs were constructed using composite particles of Al 2 O 3 -doped TiO 2 and TiO 2 nanoparticles. The DSSCs using Al 2 O 3 showed the maximum conversion efficiency of 6.29% due to effective electron transport. DSSCs based on Al 2 O 3 -doped TiO 2 films showed better photovoltaic performance than cells fabricated with only TiO 2 nanoparticles. This result is attributed to the prevention of electron recombination between electrons in the TiO 2 conduction band with holes in the dye or the electrolyte. There mechanism is suggested based on impedance results, which indicated improved electron transport at the TiO 2 /dye/electrolyte interface.

  19. In situ screen-printed BaZr{sub 0.1}Ce{sub 0.7}Y{sub 0.2}O{sub 3-{delta}} electrolyte-based protonic ceramic membrane fuel cells with layered SmBaCo{sub 2}O{sub 5+x} cathode

    Energy Technology Data Exchange (ETDEWEB)

    Lin, Bin; Dong, Yingchao; Zhang, Shangquan; Hu, Mingjun; Zhou, Yang; Meng, Guangyao [Department of Materials Science and Engineering, University of Science and Technology of China (USTC), Hefei, Anhui 230026 (China); Yan, Ruiqiang [Department of Materials Engineering, Taizhou University, Linhai, Zhejiang 317000 (China)

    2009-01-15

    In order to develop a simple and cost-effective route to fabricate protonic ceramic membrane fuel cells (PCMFCs) with layered SmBaCo{sub 2}O{sub 5+x} (SBCO) cathode, a dense BaZr{sub 0.1}Ce{sub 0.7}Y{sub 0.2}O{sub 3-{delta}} (BZCY) electrolyte was fabricated on a porous anode by in situ screen printing. The porous NiO-BaZr{sub 0.1}Ce{sub 0.7}Y{sub 0.2}O{sub 3-{delta}} (NiO-BZCY) anode was directly prepared from metal oxide (NiO, BaCO{sub 3}, ZrO{sub 2}, CeO{sub 2} and Y{sub 2}O{sub 3}) by a simple gel-casting process. An ink of metal oxide (BaCO{sub 3}, ZrO{sub 2}, CeO{sub 2} and Y{sub 2}O{sub 3}) powders was then employed to deposit BaZr{sub 0.1}Ce{sub 0.7}Y{sub 0.2}O{sub 3-{delta}} (BZCY) thin layer by an in situ reaction-sintering screen printing process on NiO-BZCY anode. The bi-layer with 25 {mu}m dense BZCY electrolyte was obtained by co-sintering at 1400 C for 5 h. With layered SBCO cathode synthesized by gel-casting on the bi-layer, single cells were assembled and tested with H{sub 2} as fuel and the static air as oxidant. A high open-circuit potential of 1.01 V, a maximum power density of 382 mW cm{sup -2}, and a low polarization resistance of the electrodes of 0.15 {omega} cm{sup 2} was achieved at 700 C. (author)

  20. Synthesis of High Crystalline Al-Doped ZnO Nanopowders from Al2O3 and ZnO by Radio-Frequency Thermal Plasma

    Directory of Open Access Journals (Sweden)

    Min-Kyeong Song

    2015-01-01

    Full Text Available High crystalline Al-doped ZnO (AZO nanopowders were prepared by in-flight treatment of ZnO and Al2O3 in Radio-Frequency (RF thermal plasma. Micron-sized (~1 μm ZnO and Al2O3 powders were mixed at Al/Zn ratios of 3.3 and 6.7 at.% and then injected into the RF thermal plasma torch along the centerline at a feeding rate of 6.6 g/min. The RF thermal plasma torch system was operated at the plate power level of ~140 kVA to evaporate the mixture oxides and the resultant vapor species were condensed into solid particles by the high flow rate of quenching gas (~7000 slpm. The FE-SEM images of the as-treated powders showed that the multipod shaped and the whisker type nanoparticles were mainly synthesized. In addition, these nanocrystalline structures were confirmed as the single phase AZO nanopowders with the hexagonal wurtzite ZnO structure by the XRD patterns and FE-TEM results with the SAED image. However, the composition changes of 0.3 and 1.0 at.% were checked for the as-synthesized AZO nanopowders at Al/Zn ratios of 3.3 and 6.7 at.%, respectively, by the XRF data, which can require the adjustment of Al/Zn in the mixture precursors for the applications of high Al doping concentrations.

  1. Hydrogenation of carbon monoxide on Co/MgAl2O4 and Ce-Co/MgAl2O4 catalysts

    International Nuclear Information System (INIS)

    Kondoh, S.; Muraki, H.; Fujitani

    1986-01-01

    It is well known that various hydrocarbons are obtained by hydrogenation of CO on Fischer-Tropsch catalysts, the products depending on the catalyst components such as Co, Ni, Fe and Ru: and the reaction conditions, particularly, temperature, pressure, space velocity and H 2 /CO ratio. Further, both reactivity and selectivity of catalysts may be improved by suitable selection of support and an additive. The main program of the present work is to develop a catalyst for producing C 5 + liquid hydrocarbons, as an automobile fuel, by the Fischer-Tropsch synthesis. The authors have studied unique CO catalyst systems consisting of various supports - such as Al 2 O 3 (γ, β, α), MgAl 2 O 4 (alumina magnesia spinel), MgO and additives selected from the lanthanoid elements (LE). The composition of spinel-based supports was altered in a range from 28 mol % excess Al 2 O 3 to 28 mol % excess MgO. Particularly, they found that a MgAl 2 O 4 support with 15-18 mol % excess Al 2 O 3 is the most preferable for our purpose and CeO 2 as the additive for Co/spinel catalyst remarkably improves C 5 + yield. Further, it was confirmed that the catalytic activity of Co-base catalysts agree with the oxidation state of Co-oxides on Co and Co-Ce/spinel catalysts. The performance of Co-based catalysts for the production of higher hydrocarbons from syn-gas were described elsewhere. The items described in this report include (a) selection of supports, (b) selection of optimum reaction conditions for Co-Ce/spinel catalyst, (c) redox characteristics of Co-oxides on a spinel surface, and (d) experimental observation of TPD profiles, adsorption capacities and IR spectra relating to adsorbed CO

  2. Effect of air annealing on the color center in Yb:Y3Al5O12 transparent ceramics with MgO as sintering additive

    Science.gov (United States)

    Lu, Zhongwen; Lu, Tiecheng; Wei, Nian; Zhang, Wei; Ma, Benyuan; Qi, Jianqi; Guan, Yongbing; Chen, Xingtao; Wu, Huajun; Zhao, Yu

    2015-09-01

    High quality Yb:Y3Al5O12 (YAG) transparent ceramics were fabricated by vacuum sintering with MgO as sintering aids. The Yb:YAG samples were annealed at 1250-1450 °C for 20 h in air. The experimental results showed that the transparency of Yb:YAG samples declined markedly with the annealing temperatures of 1250-1450 °C. The samples became increasingly orange-yellow in color with the increase of annealing temperature. The potential reasons of discoloration were discussed for the first time. It was attributed to the complex color center [Mg2+F+] formed during the annealing, which was evidenced by optical absorption in the range of 300-500 nm wavelength and the presence of an electron spin resonance (ESR) line at g = 1.9806. The formation mechanism of the complex color center was explained in detail. The complex color center can be eliminated after post-HIP (hot isostatic pressing). And by air annealing and post-HIP, the transmittance of the samples increased from 80.3% to 83.4%.

  3. Study on fast luminescence component induced by gamma-rays in Ce doped LiCaAlF6 scintillators

    International Nuclear Information System (INIS)

    Watanabe, Kenichi; Kondo, Yoshiyuki; Yamazaki, Atsushi; Uritani, Akira; Iguchi, Tetsuo; Kawaguchi, Noriaki; Fukuda, Kentaro; Ishizu, Sumito; Yanagida, Takayuki; Fujimoto, Yutaka; Yoshikawa, Akira

    2014-01-01

    We discuss the origin of the fast luminescence component induced by fast electrons generated in gamma-ray interactions in Ce doped LiCaAlF 6 scintillators. Although the slow luminescence component induced by Ce 3+ emissions depends on the Ce concentration in the LiCaAlF 6 scintillator, the fast component is independent. The fast component is suggested to be generated in the host matrix of the LiCaAlF 6 crystal. From quantitative considerations based on Frank–Tamm equation, which shows the light yield of the Cherenkov radiation, the Cherenkov radiation was determined as the origin of the fast component. We, additionally, found that the slow rise time of main Ce 3+ emissions in the Ce:LiCaAlF 6 scintillator plays an important role to perform the pulse shape discrimination. - Highlights: • The fast luminescence in Ce:LiCaAlF 6 scintillator is generated in the host matrix. • The origin of the fast luminescence is determined as the Cherenkov radiation. • The slow rise time also plays an important role to perform PSD

  4. Synthesis and photoluminescence characteristics of (Y,Gd)BO3:RE (RE = Eu(3+), Ce(3+), Dy(3+) and Tb(3+)) phosphors for blue chip and near-UV white LEDs.

    Science.gov (United States)

    Rangari, V V; Singh, V; Dhoble, S J

    2016-03-01

    A series of Eu(3+)-, Ce(3+)-, Dy(3+)- and Tb(3+)-doped (Y,Gd)BO3 phosphors was synthesized by a solid-state diffusion method. X-Ray diffraction confirmed their hexagonal structure and the scanning electron microscopy results showed crystalline particles. The excitation spectra revealed that (Y,Gd)BO3 phosphors doped with Eu(3+), Ce(3+), Dy(3+) and Tb(3+) are effectively excited with near UV-light of 395 nm/blue light, 364, 351 and 314 nm, respectively. Photoluminescence spectra of Eu(3+)-, Ce(3+)- and Tb(3+)/Dy(3+)-doped phosphor showed intense emission of reddish orange, blue and white light, respectively. The phosphor Y0.60Gd0.38BO3:Ce0.02 showed CIE 1931 color coordinates of (0.158, 0.031) and better color purity compared with commercially available blue BAM:Eu(2+) phosphor. The phosphor (Y,Gd)BO3 doped with Eu(3+), Dy(3+) and Tb(3+) showed CIE 1931 color coordinates of (0.667, 0.332), (0.251, 0.299) and (0.333, 0.391) respectively. Significant photoluminescence characteristics of the prepared phosphors indicate that they might serve as potential candidates for blue chip and near-UV white light-emitting diode applications. Copyright © 2015 John Wiley & Sons, Ltd.

  5. Optimization of Electrochemically Deposited Highly Doped ZnO Bilayers on Ga-Rich Chalcopyrite Selenide for Cost-Effective Photovoltaic Device Technology

    Directory of Open Access Journals (Sweden)

    Dimitra N. Papadimitriou

    2016-11-01

    Full Text Available High quality polycrystalline bilayers of aluminium doped ZnO (Al:ZnO were successively electrodeposited in the form of columnar structures preferentially oriented along the ( 10 1 ¯ 1 crystallographic direction from aqueous solution of zinc nitrate (Zn(NO32 at negative electrochemical potential of EC = (−0.8–(−1.2 V and moderate temperature of 80 °C on gallium rich (30% Ga chalcopyrite selenide Cu(In,GaSe2 (CIGS with chemically deposited ZnSe buffer (ZnSe/Cu(In,GaSe2/Mo/glass. The aluminium doped ZnO layer properties have initially been probed by deposition of Al:ZnO/i-ZnO bilayers directly on Mo/glass substrates. The band-gap energy of the Al:ZnO/i-ZnO reference layers was found to vary from 3.2 to 3.7 eV by varying the AlCl3 solute dopant concentration from 1 to 20 mM. The electrical resistivity of indium-pellet contacted highly doped Al:ZnO sheet of In/Al:ZnO/i-ZnO/Mo/glass reference samples was of the order ρ ~10−5 Ω·cm; the respective carrier concentration of the order 1022 cm−3 is commensurate with that of sputtered Al:ZnO layers. For crystal quality optimization of the bilayers by maintenance of the volatile selenium content of the chalcopyrite, they were subjected to 2-step annealing under successive temperature raise and N2 flux regulation. The hydrostatic compressive strain due to Al3+ incorporation in the ZnO lattice of bilayers processed successively with 5 and 12 mM AlCl3 dopant was εh = −0.046 and the respective stress σh = −20 GPa. The surface reflectivity of maximum 5% over the scanned region of 180–900 nm and the (optical band gap of Eg = 3.67 eV were indicative of the high optical quality of the electrochemically deposited (ECD Al:ZnO bilayers.

  6. Free carrier absorption in self-activated PbWO_4 and Ce-doped Y_3(Al_0.25Ga_0.75)_3O_12 and Gd_3Al_2Ga_3O_12 garnet scintillators

    OpenAIRE

    Auffray, E.; Korjik, M.; M.T. Lucchini; S. Nargelas; O. Sidletskiy; G. Tamulaitis; Y. Tratsiak; A. Vaitkevičius

    2016-01-01

    Nonequilibrium carrier dynamics in the scintillators prospective for fast timing in high energy physics and medical imaging applications was studied. The time-resolved free carrier absorption investigation was carried out to study the dynamics of nonequilibrium carriers in wide-band-gap scintillation materials: self-activated led tungstate (PbWO_4, PWO) ant two garnet crystals, GAGG:Ce and YAGG:Ce. It was shown that free electrons appear in the conduction band of PWO and YAGG:Ce crystals w...

  7. The electrorheological properties of nano-sized SiO2 particle materials doped with rare earths

    International Nuclear Information System (INIS)

    Liu Yang; Liao Fuhui; Li Junran; Zhang Shaohua; Chen Shumei; Wei Chenguan; Gao Song

    2006-01-01

    Electrorheological (ER) materials of pure SiO 2 and SiO 2 doped with rare earths (RE = Ce, Gd, Y) (non-metallic glasses (silicates)) were prepared using Na 2 SiO 3 and RECl 3 as starting materials. The electrorheological properties are not enhanced by all rare earth additions. The material doped with Ce exhibits the best ER performance

  8. Synthesis, Characterization and Properties of CeO2-doped TiO2 Composite Nanocrystals

    Directory of Open Access Journals (Sweden)

    Oman ZUAS

    2013-12-01

    Full Text Available Pure TiO2 and CeO2-doped TiO2 (3 % CeO2-97 %TiO2 composite nanocrystals were synthesized via co-precipitation method and characterized using TGA, XRD, FTIR, DR-UV-vis and TEM. The XRD data revealed that the phase structure of the synthesized samples was mainly in pure anatase having crystallite size in the range of 7 nm – 11 nm. Spherical shapes with moderate aggregation of the crystal particles were observed under the TEM observation. The presence of the CeO2 at TiO2 site has not only affected morphologically but also induced the electronic property of the TiO2 by lowering the band gap energy from 3.29 eV (Eg-Ti to 3.15 eV (Eg-CeTi. Performance evaluation of the synthesized samples showed that both samples have a strong adsorption capacity toward Congo red (CR dye in aqueous solution at room temperature experiment, where  the capacity of the CeTi was higher than the Ti sample. Based on DR-UV data, the synthesized samples obtained in this study may also become promising catalysts for photo-assisted removal of synthetic dye in aqueous solution. DOI: http://dx.doi.org/10.5755/j01.ms.19.4.2732

  9. Basic study of single crystal fibers of Pr:Lu3Al5O12 scintillator for gamma-ray imaging applications

    International Nuclear Information System (INIS)

    Yanagida, Takayuki; Kamada, Kei; Kawaguchi, Noriaki; Fujimoto, Yutaka; Fukuda, Kentaro; Yokota, Yuui; Chani, Valery; Yoshikawa, Akira

    2011-01-01

    Single-crystalline fibers were grown from 0.25, 0.70, and 1.50 mol% Pr-doped Lu 3 Al 5 O 12 (LuAG) melts by the micro-pulling down (μ-PD) method with a diameter of 0.3-0.5 mm and a length of about 200 mm. They were cut to 10 mm long specimens, and their scintillation properties, including light yield and decay time profile, were examined. These results were compared with corresponding properties of the specimens (0.8x0.8x10 mm 3 ) cut from the bulk crystals produced by conventional Czochralski (CZ) growth. The μ-PD-grown fibers demonstrated relatively low light yield and had the same decay time constant when compared with those of the samples cut from the CZ-grown crystals. The fiber crystals were used to assemble scintillating arrays with dimensions of O 0.5x10 mm 2 x20 pixels and O 0.3x10 mm 2 x30 pixels coated by a BaSO 4 reflector. After optical coupling with a position sensitive photomultiplier tube, the fiber-based arrays demonstrated acceptable imaging capability with a spatial resolution of about 0.5 mm.

  10. Elastic Properties of Synthetic Pyrope (Mg3Al2Si3O12) to 9 GPa and 1000°C

    Science.gov (United States)

    Gwanmesia, G. D.; Zhang, J.; Li, B.; Darling, K.; Kung, J.; Neuville, D.; Raterron, P.; Sullivan, S.; Liebermann, R. C.

    2003-04-01

    We have measured the elastic wave velocities of polycrystalline pyrope (Mg_3Al_2Si_3O12) to 9 GPa and 1000^oC by ultrasonic interferometry, combined with in-situ synchrotron x-ray diffraction and imaging techniques. Fine-grained polycrystalline specimens (99.5% of theoretical density) were hot-pressed from a homogeneous glass starting material in the USSA-2000 apparatus at Stony Brook; the physical properties of the recovered specimens were characterized with density measurements, x-ray diffraction and transmission electron microscopy. Bench-top elastic wave velocities were in excellent agreement with the isotropic averages calculated from single-crystal elastic moduli of Leitner et al. (1980) by the Hashin-Shtrikman method. Travel times of acoustic compressional (P) and shear (S) waves, specimen lengths and PVT equations of state for the specimen and a NaCl standard were measured to 9 GPa and 1000^oC in a DIA-type high pressure apparatus (SAM-85), installed on the superconducting wiggler beamline (X17B) at the National Synchrotron Light Source of the Brookhaven National Laboratory. These data enabled us to determine the pressure and temperature derivatives of the elastic wave velocities and moduli for isotropic pyrope. We compare our new values with those of previous investigators and discuss the implications of these data for interpreting the seismic velocity gradients in the transition zone of the Earth's mantle.

  11. Sequential evolution of different phases in metastable Gd(2-x)Ce(x)Zr(2-x)Al(x)O7 (0.0 ≤ x ≤ 2.0) system: crucial role of reaction conditions.

    Science.gov (United States)

    Shukla, Rakesh; Sayed, Farheen N; Phapale, Suhas; Mishra, Ratikant; Tyagi, Avesh K

    2013-07-15

    The Gd(2-x)Ce(x)Zr(2-x)Al(x)O7 (0.0 ≤ x ≤ 2.0) series was synthesized by the gel combustion method. This system exhibited the presence of a fluorite-type phase, along with a narrow biphasic region, depending upon the Ce/Gd content in the sample. Thermal stability of these new compounds under oxidizing and reducing conditions has been investigated. The products obtained on decomposition of Gd(2-x)Ce(x)Zr(2-x)Al(x)O7 in oxidizing and reducing conditions were found to be entirely different. It was observed that in air the fluorite-type solid solutions of Gd(2-x)Ce(x)Zr(2-x)Al(x)O7 composition undergo phase separation into perovskite GdAlO3 and fluorite-type solid solutions of Gd-Ce-Zr-O or Ce-Zr-Al-O depending upon the extent of Ce and Al substitution. On the other hand, Gd(2-x)Ce(x)Zr(2-x)Al(x)O7 samples on heating under reducing conditions show a phase separation to CeAlO3 perovskite and a defect-fluorite of Gd2Zr2O7. The extent of metastability for a typical composition of Gd(1.2)Ce(0.8)Zr(1.2)Al(0.8)O7 (nano), Gd(1.2)Ce(0.8)Zr(1.2)Al(0.8)O(6.6) (heated under reduced conditions), Gd(1.2)Ce(0.8)Zr(1.2)Al(0.8)O7 (heated in air at 1200 °C) has been experimentally determined employing a high temperature Calvet calorimeter. On the basis of thermodynamic stability data, it could be inferred that the formation of a more stable compound in the presence of two competing cations (i.e., Gd(3+) and Ce(3+)) is guided by the crystallographic stability.

  12. Fabrication of cerium-doped yttrium aluminum garnet thin films by a mist CVD method

    Energy Technology Data Exchange (ETDEWEB)

    Murai, Shunsuke, E-mail: murai@dipole7.kuic.kyoto-u.ac.jp; Sato, Takafumi; Yao, Situ; Kamakura, Ryosuke; Fujita, Koji; Tanaka, Katsuhisa

    2016-02-15

    We synthesized thin films, consisting of yttrium aluminum garnet doped with Ce{sup 3+} (YAG:Ce), using the mist chemical vapor deposition (CVD) method, which allows the fabrication of high-quality thin films under atmospheric conditions without the use of vacuum equipment. Under a deposition rate of approximately 1 μm/h, the obtained thin films had a typical thickness of 2 μm. The XRD analysis indicated that the thin films consisted of single-phase YAG:Ce. The Rutherford backscattering confirmed the stoichiometry; the composition of the film was determined to be (Y, Ce){sub 3}Al{sub 5}O{sub 12}, with a Ce content of Ce/(Y+Ce)=2.5%. The YAG:Ce thin films exhibited fluorescence due to the 5d–4f electronic transitions characteristic of the Ce ions occupying the eight-coordinated dodecahedral sites in the YAG lattice. - Highlights: • We have synthesized thin films of yttrium aluminum garnet doped with Ce{sup 3+} (YAG:Ce) by using a mist chemical vapor deposition (CVD) method for the first time. • The thickness of the single-phase and stoichiometric thin film obtained by 2 h deposition and following heat treatments is 2 μm. • The thin film is porous but optically transparent, and shows yellow fluorescence upon irradiation with a blue light. • Mist-CVD is a green and sustainable technique that allows fabrication of high-quality thin films at atmospheric conditions without vacuum equipment.

  13. Significant enhancement of room temperature ferromagnetism in surfactant coated polycrystalline Mn doped ZnO particles

    Energy Technology Data Exchange (ETDEWEB)

    Jayakumar, O.D. [Chemistry Division, Bhabha Atomic Research Centre, Mumbai 400085 (India); Gopalakrishnan, I.K. [Chemistry Division, Bhabha Atomic Research Centre, Mumbai 400085 (India)]. E-mail: ikgopal@barc.gov.in; Sudakar, C. [Department of Physics and Astronomy, Wayne State University, Detroit, MI 48201 (United States); Kadam, R.M. [Radiochemistry Division, Bhabha Atomic Research Centre, Mumbai 400085 (India); Kulshreshtha, S.K. [Chemistry Division, Bhabha Atomic Research Centre, Mumbai 400085 (India)

    2007-07-12

    We report a surfactant assisted synthesis of Mn doped ZnO polycrystalline samples showing robust room temperature ferromagnetism as characterized by X-ray diffraction analysis, transmission electron microscopy, electron paramagnetic resonance and DC magnetization measurements. This surfactant assisted synthesis method, developed by us, is found to be highly reproducible. Further, it can also be extended to the synthesis of other transition metal doped ZnO.

  14. Studies on Y{sub 2}SiO{sub 5}:Ce phosphors prepared by gel combustion using new fuels

    Energy Technology Data Exchange (ETDEWEB)

    Muresan, L.E., E-mail: laura_muresan2003@yahoo.com [“Raluca Ripan” Institute for Research in Chemistry, Babeş Bolyai University, Fântânele 30, 400294 Cluj-Napoca (Romania); Oprea, B.F.; Cadis, A.I.; Perhaita, I. [“Raluca Ripan” Institute for Research in Chemistry, Babeş Bolyai University, Fântânele 30, 400294 Cluj-Napoca (Romania); Ponta, O. [Faculty of Physics, Babeş Bolyai University, 400084 Cluj-Napoca (Romania)

    2014-12-05

    Highlights: • Y{sub 2}SiO{sub 5}:Ce was prepared by combustion using aspartic or glutamic acid as fuels. • Combustion process occurs differently depending on the fuels amount. • Single phase X2-Y{sub 2}SiO{sub 5} phosphors were obtained in fuel rich conditions. • PL measurements indicate that aspartic acid is a better fuel than glutamic. • Optimal preparative conditions were established for synthesis of Y{sub 2}SiO{sub 5}:Ce. - Abstract: Cerium activated yttrium silicate (Y{sub 2}SiO{sub 5}:Ce) phosphors were prepared by combustion, using yttrium–cerium nitrate as oxidizer, aspartic or glutamic acid as fuel and TEOS as source of silicon. In this study, aspartic and glutamic acid are used for the first time for the synthesis of Y{sub 2}SiO{sub 5}:Ce phosphors. The fuels molar amount was varied from 0.5 mol to 1.5 mol in order to reveal the thermal behavior of intermediary products (gels and ashes) same as the structural and luminescent characteristics of final products (phosphors). According to thermal analysis correlated with FTIR and XPS investigations, the combustion process occurs differently depending on the fuel amount; unreacted nitrate compounds have been identified in fuel lean conditions and carbonate based compounds along with organic residue in rich fuel conditions. The conversion to well crystallized silicates was revealed by changes of FTIR vibration bands and confirmed by XRD measurements. Based on luminescent spectra, aspartic acid is a better fuel than glutamic acid. A positive effect on the luminescence have been observed for samples fired in air due to complete remove of organic residue. The best luminescence was obtained for combustions with 0.75 mol aspartic acid and 1.25 mol glutamic respectively, fired at 1400 °C for 4 h in air atmosphere.

  15. Raman scattering study of the anharmonic effects in CeO{sub 2-y} nanocrystals

    Energy Technology Data Exchange (ETDEWEB)

    Popovic, Z V [Center for Solid State Physics and New Materials, Institute of Physics, Pregrevica 118, 11080 Belgrade (Serbia); Dohcevic-Mitrovic, Z [Center for Solid State Physics and New Materials, Institute of Physics, Pregrevica 118, 11080 Belgrade (Serbia); Cros, A [Materials Science Institute, University of Valencia, P O Box 22085, E-46071, Valencia (Spain); Cantarero, A [Materials Science Institute, University of Valencia, P O Box 22085, E-46071, Valencia (Spain)

    2007-12-12

    We have studied the temperature dependence of the F{sub 2g} Raman mode phonon frequency and broadening in CeO{sub 2-y} nanocrystals. The phonon softening and phonon linewidth are calculated using a model which takes into account the three-and four-phonon anharmonic processes. A detailed comparison of the experimental data with theoretical calculations revealed the predominance of four-phonon anharmonic processes in the temperature dependence of the phonon energy and broadening of the nanocrystals. On the other hand, three-phonon processes dominate the temperature behavior of phonons in polycrystalline samples. The anti-Stokes/Stokes peak intensity ratio was also investigated and found to be smaller for nanosized CeO{sub 2} powders than in the bulk counterpart.

  16. Impact of ultra-thin Al2O3-y layers on TiO2-x ReRAM switching characteristics

    Science.gov (United States)

    Trapatseli, Maria; Cortese, Simone; Serb, Alexander; Khiat, Ali; Prodromakis, Themistoklis

    2017-05-01

    Transition metal-oxide resistive random access memory devices have demonstrated excellent performance in switching speed, versatility of switching and low-power operation. However, this technology still faces challenges like poor cycling endurance, degradation due to high electroforming (EF) switching voltages and low yields. Approaches such as engineering of the active layer by doping or addition of thin oxide buffer layers have been often adopted to tackle these problems. Here, we have followed a strategy that combines the two; we have used ultra-thin Al2O3-y buffer layers incorporated between TiO2-x thin films taking into account both 3+/4+ oxidation states of Al/Ti cations. Our devices were tested by DC and pulsed voltage sweeping and in both cases demonstrated improved switching voltages. We believe that the Al2O3-y layers act as reservoirs of oxygen vacancies which are injected during EF, facilitate a filamentary switching mechanism and provide enhanced filament stability, as shown by the cycling endurance measurements.

  17. Combustion synthesis and photoluminescence properties of LaAlO{sub 3} nanophosphors doped with Yb{sup 3+} ions

    Energy Technology Data Exchange (ETDEWEB)

    Dhahri, A. [Laboratoire de Physico-chimie des Matériaux Minéraux et leurs Applications, Centre National des Recherches en Sciences des Matériaux, Technopole de Borj Cedria, B.P. 73, Soliman 8027 (Tunisia); Horchani-Naifer, K., E-mail: karima_horchani@yahoo.com [Laboratoire de Physico-chimie des Matériaux Minéraux et leurs Applications, Centre National des Recherches en Sciences des Matériaux, Technopole de Borj Cedria, B.P. 73, Soliman 8027 (Tunisia); Benedetti, A. [Dipartimento di Scienze Molecolari e Nanosistemi, Università Ca’ Foscari Venezia, Dorsoduro 2137, 30123 Venezia (Italy); Enrichi, F. [CIVEN – Coordinamento Interuniversitario Veneto per le Nanotecnologie, Via Delle Industrie 5, Marghera, Venice 30175 (Italy); Ferid, M. [Laboratoire de Physico-chimie des Matériaux Minéraux et leurs Applications, Centre National des Recherches en Sciences des Matériaux, Technopole de Borj Cedria, B.P. 73, Soliman 8027 (Tunisia)

    2014-09-15

    Ytterbium doped lanthanum aluminate (LaAlO{sub 3}) nanophosphors have been prepared by a combustion process with glycine as a fuel. The structures of the powders were determined by X-ray diffraction (XRD), the morphology of the annealed materials was observed using scanning electron microscopy (SEM), the average crystalline grain sizes have been determined by transmission electron microscopy (TEM) and photoluminescence properties using fluorescence spectroscopy. Pure LaAlO{sub 3} phase was obtained at 800 °C heated for 4 h, with an average crystal size, as determined by TEM, of 60 nm. Emission spectra and decay times of main luminescence transitions were measured at room temperature. A strong emission is reported at 986 nm from the ({sup 2}F{sub 5/2}→{sup 2}F{sub 7/2}) transition, whose intensity depends on Yb concentration. - Highlights: • Ytterbium doped lanthanum aluminate (LaAlO{sub 3}) nanophosphors have been prepared by a combustion process with glycine as a fuel. • Powders were characterized by DRX, FTIR, TEM and fluorescence spectroscopy. • Pure LaAlO{sub 3} phase was obtained at 800 °C heated for 4 h, with an average crystal size of 60 nm. • A strong emission is reported at 986 nm from the ({sup 2}F{sub 5/2}→{sup 2}F{sub 7/2}) transition, whose intensity depends on Yb concentration.

  18. Optical and structural properties of Cu-doped β-Ga2O3 films

    International Nuclear Information System (INIS)

    Zhang Yijun; Yan Jinliang; Li Qingshan; Qu Chong; Zhang Liying; Xie Wanfeng

    2011-01-01

    Graphical abstract: Highlights: → We prepare polycrystalline Cu-doped β-Ga2O3 films. → Cu dopants cause poor crystal quality and shrinkage of the optical band gap. → Cu-doping enhances the UV and blue emission. → A new blue emission peak centre at 475 nm appears by Cu-doping. → Cu dopants decrease the optical transmittance. - Abstract: The intrinsic and Cu-doped β-Ga 2 O 3 films were grown on Si and quartz substrates by RF magnetron sputtering in an argon and oxygen mixture ambient. The effects of the Cu doping and the post thermal annealing on the optical and structural properties of the β-Ga 2 O 3 films were studied. The surface morphology, microstructure, optical transmittance, optical absorption, optical energy gap and photoluminescence of the β-Ga 2 O 3 films were significantly changed after Cu-doping. After post thermal annealing, Polycrystalline β-Ga 2 O 3 films were obtained, the transmittance decreased. After Cu-doping, the grain size decreased, the crystal quality deteriorated and the optical band gap shrunk. The UV, blue and green emission bands were observed and discussed. The UV and blue emission were enhanced and a new blue emission peak centred at 475 nm appeared by Cu-doping.

  19. Lu.sub.2./sub.SiO.sub.5./sub.:Ce and Y.sub.2./sub.SiO.sub.5./sub.:Ce single crystals and single crystalline film scintillators: comparisom of the luminescent and scintillation properties

    Czech Academy of Sciences Publication Activity Database

    Zorenko, Y.; Gorbenko, V.; Savchyn, V.; Zorenko, T.; Grinyov, B.; Sidletskiy, O.; Fedorov, A.; Mareš, Jiří A.; Nikl, Martin; Kučera, M.

    2013-01-01

    Roč. 56, SEP (2013), s. 84-89 ISSN 1350-4487. [International Conference on Luminescent Detectors and Transformers of Ionizing Radiation 2012 /8./, LUMDETR 2012. Halle (Saale), 10.09.2012-14.09.2012] R&D Projects: GA ČR GAP204/12/0805 Institutional support: RVO:68378271 Keywords : Lu 2 SiO 5 :Ce * Y 2 SiO 2 * single crystalline film, * single crystal * luminescence Subject RIV: BM - Solid Matter Physics ; Magnetism Impact factor: 1.140, year: 2013

  20. The effects of Zn doping on magnetic properties of Cu3Bi(SeO3)2O2Cl

    Science.gov (United States)

    Yang, Pei-Ying; Tseng, Wu-Jyun; Wu, Hung-Cheng; Kakarla, D. Chandrasekhar; Yang, Hung-Duen; Department of Physics, Natl Sun Yat Sen Univ Team

    Recently, layered spin-frustrated Cu3Bi(SeO3)2 O2Cl has received considerable research attention due to its unusual magnetic properties. Two inequivalent Cu2 + ions form a pseudo-kagome lattice that invokes spin frustration and anisotropic magnetic properties. In this study, the influence of Zn doping on the complex magnetic properties has been explored. Polycrystalline (Cu1-xZnx) Bi(SeO3)2 O2Cl (0 x 0.5) samples were synthesized using solid-state reaction and characterized by X-ray diffraction and magnetic measurements. The Zn doping strongly modulates the magnetic ground state of the system. The antiferromagnetic transition temperature TN = 24 K and magnetic field-induced hysteresis observed for x = 0 at low field are systematically shifted to lower temperature and reduced with Zn doping. These results can illustrate the insight of the occurrence of field-induced spin-flip type multiferroics in Cu3Bi(SeO3)2 O2Cl.

  1. Synthesis and characterization of charge-substituted garnets YCaLnGa5O12 (Ln = Ce,Pr,Tb)

    International Nuclear Information System (INIS)

    Gramsch, S.A.

    1993-01-01

    A low temperature method is described for the preparation of the new garnet compounds YCaLnGa 5 O l2 (Ln=Ce, Pr, Th). In this set of compounds (Ca 2+ + Ln 4+ ) replaces 2 Y 3+ in the parent gallium based garnet Y 3 Ga 5 O l2 in order to stabilize as effectively as possible the Ln 4+ species in the eight-coordinate ''A'' site of the garnet structure. Characterization of the oxides by x-ray powder diffraction and thermogravimetric analysis is discussed with regard to the structural relationship of the substituted compound to the parent material. The tetravalent ions Pr 4+ and Tb 4+ exhibit increased thermal stability in reducing conditions as compared to the Ln 4+ states in the fluorite (LnO 2 ) and perovskite (BaLnO 3 ) type structures. This result is discussed with reference to the complex crystal chemistry of these systems

  2. Intermediate-to-low temperature protonic ceramic membrane fuel cells with Ba{sub 0.5}Sr{sub 0.5}Co{sub 0.8}Fe{sub 0.2}O{sub 3-{delta}}-BaZr{sub 0.1}Ce{sub 0.7}Y{sub 0.2}O{sub 3-{delta}} composite cathode

    Energy Technology Data Exchange (ETDEWEB)

    Lin, Bin; Ding, Hanping; Dong, Yingchao; Wang, Songlin; Zhang, Xiaozhen; Fang, Daru; Meng, Guangyao [Department of Materials Science and Engineering, University of Science and Technology of China (USTC), Hefei, Anhui 230026 (China)

    2009-01-01

    The perovskite-type Ba{sub 0.5}Sr{sub 0.5}Co{sub 0.8}Fe{sub 0.2}O{sub 3-{delta}}-BaZr{sub 0.1}Ce{sub 0.7}Y{sub 0.2}O{sub 3-{delta}} (BSCF-BZCY) composite oxides were synthesized by a modified Pechini method and examined as a novel composite cathode for intermediate-to-low temperature protonic ceramic membrane fuel cells (ILT-PCMFCs). Thin proton-conducting BaZr{sub 0.1}Ce{sub 0.7}Y{sub 0.2}O{sub 3-{delta}} (BZCY) electrolyte and NiO-BaZr{sub 0.1}Ce{sub 0.7}Y{sub 0.2}O{sub 3-{delta}} (NiO-BZCY) anode functional layer were prepared over porous anode substrates composed of NiO-BaZr{sub 0.1}Ce{sub 0.7}Y{sub 0.2}O{sub 3-{delta}} by a one-step dry-pressing/co-firing process. A laboratory-sized quad-layer cell of NiO-BZCY/NiO-BZCY({proportional_to}50 {mu}m)/BZCY({proportional_to}20 {mu}m)/BSCF-BZCY({proportional_to}50 {mu}m) was operated from 550 to 700 C with humidified hydrogen ({proportional_to}3% H{sub 2}O) as fuel and the static air as oxidant. A high open-circuit potential of 1.009 V, a maximum power density of 418 mW cm{sup -2}, and a low polarization resistance of the electrodes of 0.10 {omega} cm{sup 2} was achieved at 700 C. These investigations have indicated that proton-conducting BZCY electrolyte with BSCF perovskite cathode is a promising material system for the next generation solid oxide fuel cells (SOFCs). (author)

  3. Narrow in-gap states in doped Al2O3

    KAUST Repository

    Casas-Cabanas, Montse; Fré sard, Marion; Lü ders, Ulrike; Fré sard, Raymond; Schuster, Cosima B.; Schwingenschlö gl, Udo

    2011-01-01

    Based on XRD data testifying that the M ions occupy substitutional sites, transmittance measurement are discussed in comparison to electronic structure calculations for M-doped Al2O3 with M = V, Mn, and Cr. The M 3d states are found approximatively 2 eV above the top of the host valence band. The fundamental band gap of Al2O3 is further reduced in the V and Mn cases due to a splitting of the narrow band at the Fermi energy. Nevertheless the measured transmittance in the visible range remains high in all three cases. © 2011 Elsevier B.V. All rights reserved.

  4. Narrow in-gap states in doped Al2O3

    KAUST Repository

    Casas-Cabanas, Montse

    2011-10-01

    Based on XRD data testifying that the M ions occupy substitutional sites, transmittance measurement are discussed in comparison to electronic structure calculations for M-doped Al2O3 with M = V, Mn, and Cr. The M 3d states are found approximatively 2 eV above the top of the host valence band. The fundamental band gap of Al2O3 is further reduced in the V and Mn cases due to a splitting of the narrow band at the Fermi energy. Nevertheless the measured transmittance in the visible range remains high in all three cases. © 2011 Elsevier B.V. All rights reserved.

  5. Effect of doping concentration and annealing temperature on luminescence properties of Y{sub 2}O{sub 3}:Eu{sup 3+} nanophosphor prepared by colloidal precipitation method

    Energy Technology Data Exchange (ETDEWEB)

    Siddaramana Gowd, G.; Kumar Patra, Manoj; Songara, Sandhya; Shukla, Anuj; Mathew, Manoth; Raj Vadera, Sampat [Materials Development Group, Defence Laboratory, Jodhpur (India); Kumar, Narendra, E-mail: nkjainjd@yahoo.com [Materials Development Group, Defence Laboratory, Jodhpur (India)

    2012-08-15

    Eu{sup 3+} doped Y{sub 2}O{sub 3} nanophosphors have been synthesized using the simple colloidal precipitation method. Doping of Eu{sup 3+} ions in host yttria lattice has been achieved through slow re-crystallization process under wet-chemical conditions followed by annealing at high temperatures (300-1400 Degree-Sign C). The nanophosphors were characterized by using powder X-ray diffraction (XRD), thermogravimetric analysis (TGA), atomic force microscopy (AFM) and spectrofluorometer techniques. XRD analysis reveals formation of pure cubic phase of Y{sub 2}O{sub 3} in samples annealed at 700 Degree-Sign C or above. Further, the XRD data was successfully used to retrieve the crystallite size and size distribution from powder samples using the FW((1/5)/(4/5))M method. Crystallite size (11-50 nm) extracted from XRD has been found to be consistent with AFM measurements. The PL emission spectra of nanophosphors show bright red emission at 612 nm due to hypersensitive electric dipole (ED) {sup 5}D{sub 0}-{sup 7}F{sub 2} transition of Eu{sup 3+} ions in Y{sub 2}O{sub 3} lattice. Further, photoluminescence studies indicate that optimum value of the Eu{sup 3+} to get best luminescence properties is 12 at%. Surface conjugations of these nanophosphors with water soluble dextran biomolecules have also been performed. Surface conjugated rare earth nanophosphors have great potential for bio-applications. - Highlights: Black-Right-Pointing-Pointer Surfactant and catalyst free synthesis of Eu{sup 3+} doped Y{sub 2}O{sub 3} nanophosphor showing bright red emission at 612 nm. Black-Right-Pointing-Pointer Optimization of reaction conditions and Eu{sup 3+}dopant concentration to achieve high luminescence efficiency. Black-Right-Pointing-Pointer Estimation of crystallite size and size distribution of nanophosphor from XRD data. Black-Right-Pointing-Pointer Surface conjugation of Eu{sup 3+} doped Y{sub 2}O{sub 3} nanophosphor with dextran biomolecules.

  6. Fabrication and evaluation of green-light emitting Ta2O5:Er, Ce co-sputtered thin films

    Directory of Open Access Journals (Sweden)

    K. Miura

    2015-01-01

    Full Text Available Erbium and cerium co-doped tantalum-oxide (Ta2O5:Er, Ce thin films were fabricated using radio-frequency co-sputtering of Ta2O5, Er2O3, and CeO2 for the first time. Enhanced green-light emission due to Er3+ that seems to be sensitized by Ce3+ was observed from the film annealed at 900 °C for 20 min. From XRD measurements of the films, the β-Ta2O5 (orthorhombic, δ-Ta2O5 (hexagonal, and (201 Ta2O5 phases seem to be very important for obtaining green PL from them. Such Ta2O5:Er, Ce co-sputtered films can be used as high-refractive-index materials of autocloned photonic crystals that can be applied to novel green-light-emitting devices, and they will also be used as multi-functional coating films that can work both as anti-reflection and down-conversion films for realizing high-efficiency silicon solar cells.

  7. Synthesis and characterization of polycrystalline brownmillerite cobalt doped Ca{sub 2}Fe{sub 2}O{sub 5}

    Energy Technology Data Exchange (ETDEWEB)

    Dhankhar, Suchita; Baskar, K.; Singh, Shubra, E-mail: shubra6@gmail.com [Crystal Growth Centre, Anna University, Chennai-600 025 (India); Bhalerao, Gopal [UGC-DAE CSR Kalpakkam node, Kalpakkam-603104 (India)

    2016-05-23

    Brownmillerite compounds with general formula A{sub 2}BB’O{sub 5} (BB’ = Mn, Al, Fe, Co) have attracted attention in wide range of applications such as in solid oxide fuel cell, oxygen separation membrane and photocatalysis. Brownmillerite compounds have unique structure with alternate layers of BO{sub 6} octahedral layers and BO{sub 4} tetrahedral layers. Presence of dopants like Co in place of Fe increases oxygen vacancies. In the present work we have synthesized polycrystalline Ca{sub 2}Fe{sub 2}O{sub 5} and Ca{sub 2}Fe{sub 1-x}Co{sub x}O{sub 5} (x = 0.01, 0.03) by citrate combustion route. The as prepared samples were characterized by XRD using PANalytical X’Pert System, DRS (Diffuse reflectance spectroscopy) and SEM (Scanning electron microscopy).

  8. Electronic property and structure of double-doping Y1-2xPrxCaxBa2Cu3O7-δ with 0 ≤ x ≤ 0.14

    International Nuclear Information System (INIS)

    Wang Yang; Shi Lei; Chu Songnan

    2010-01-01

    Equal amount Pr and Ca double-doping Y 1-2x Pr x Ca x Ba 2 Cu 3 O 7-δ with 0 ≤ x ≤ 0.14 have been investigated by X-ray diffraction, resistivity, and X-ray photoemission spectroscopy (XPS). The deviation of the linearly decreasing of T c vs. x curve was observed when x 1-2x Pr x Ca x Ba 2 Cu 3 O 7-δ with low Pr content (x 0.10), which suggests a change of Pr valence with the Pr content. XPS measurement shows that the relative amount of Pr 3+ and Pr 4+ is closely related to the total Pr content x. The valence of Pr is close to +3 when x 0.10, which implies a different mechanism for depression of superconductivity of Pr content x 0.10 in Pr doping Y-123.

  9. XAS study of V2O5/Al2O3 catalysts doped with rare earth oxides

    International Nuclear Information System (INIS)

    Centeno, M.A.; Malet, P.; Capitan, M.J.; Benitez, J.J.; Carrizosa, I.; Odriozola, J.A.

    1995-01-01

    This paper reports on XAS studies of well dispersed V 2 O 5 /Al 2 O 3 and V 2 O 5 /Sm 2 O 3 /Al 2 O 3 samples. XAS spectra at V-K and Sm-L III edges show that the rare earth oxide favours the formation of regular tetrahedral units, [VO 4 ], over the surface of the support. Positions of the preedge peak at the V-K edge, and intensities of the white line at the Sm-L III edge also suggest modifications in the electronic density around V and Sm atoms when they are simultaneously supported over Al 2 O 3 . ((orig.))

  10. Ce decay curves in Ce, Tb co-doped LaF3 and the energy transfer mechanism

    International Nuclear Information System (INIS)

    Kroon, R.E.; Swart, H.C.; Ntwaeaborwa, O.M.; Seed Ahmed, H.A.A.

    2014-01-01

    Energy transfer phenomena can play an important role in the development of luminescent materials, and hosts co-doped with Ce 3+ and Tb 3+ ions continue to be actively studied. Several recent reports on Ce, Tb co-doped phosphors suggest different mechanisms for the energy transfer from Ce 3+ to Tb 3+ ions and further study is required to reach consensus on the mechanism or to understand why different mechanisms dominate in different hosts. A more direct method of analysis is proposed to distinguish between the different types of multipole energy transfer mechanisms. When applied to Ce, Tb co-doped LaF 3 , the experimental data shows a poor match to any of these models but is consistent with energy transfer through the exchange mechanism. The decay curves of Ce emission in Ce, Tb co-doped LaF 3 were also studied to obtain further insight on the energy transfer mechanism. Although the decrease in lifetime with increasing Tb concentration shows that energy transfer occurs through a non-radiative mechanism, the form of the decay curves does not correspond to what is expected for energy transfer via multipole interactions.

  11. The crystal structure of galgenbergite-(Ce), CaCe2(CO3)4•H2O

    Science.gov (United States)

    Walter, Franz; Bojar, Hans-Peter; Hollerer, Christine E.; Mereiter, Kurt

    2013-04-01

    Galgenbergite-(Ce) from the type locality, the railroad tunnel Galgenberg between Leoben and St. Michael, Styria, Austria, was investigated. There it occurs in small fissures of an albite-chlorite schist as very thin tabular crystals building rosette-shaped aggregates associated with siderite, ancylite-(Ce), pyrite and calcite. Electron microprobe analyses gave CaO 9.49, Ce2O3 28.95, La2O3 11.70, Nd2O3 11.86, Pr2O3 3.48, CO2 30.00, H2O 3.07, total 98.55 wt.%. CO2 and H2O calculated by stoichiometry. The empirical formula (based on Ca + REE ∑3.0) is C{{a}_{1.00 }}{{( {C{{e}_{1.04 }}L{{a}_{0.42 }}N{{d}_{0.42 }}P{{r}_{0.12 }}} )}_{2.00 }}{{( {C{{O}_3}} )}_4}\\cdot {{H}_2}O , and the simplified formula is CaC{{e}_2}{{( {C{{O}_3}} )}_4}\\cdot {{H}_2}O . According to X-ray single crystal diffraction galgenbergite-(Ce) is triclinic, space group Poverline{1},a=6.3916(5) , b = 6.4005(4), c = 12.3898(9) Å, α = 100.884(4), β = 96.525(4), γ = 100.492(4)°, V = 483.64(6) Å3, Z = 2. The eight strongest lines in the powder X-ray diffraction pattern are [ d calc in Å/( I)/ hkl]: 5.052/(100)/011; 3.011/(70)/0-22; 3.006/(66)/004; 5.899/(59)/-101; 3.900/(51)/1-12; 3.125/(46)/-201; 2.526/(42)/022; 4.694/(38)/-102. The infrared absorption spectrum reveals H2O (OH-stretching mode at 3,489 cm-1, HOH bending mode at 1,607 cm-1) and indicates the presence of distinctly non-equivalent CO3-groups by double and quadruple peaks of their ν1, ν2, ν3 and ν4 modes. The crystal structure of galgenbergite-(Ce) was refined with X-ray single crystal data to R1 = 0.019 for 2,448 unique reflections ( I > 2 σ( I)) and 193 parameters. The three cation sites of the structure Ca(1), Ce(2) and Ce(3) have a modest mixed site occupation by Ca and small amount of REE (Ce, La, Pr, Nd) and vice versa. The structure is based on double layers parallel to (001), which are composed of Ca(1)Ce(2)(CO3)2 single layers with an ordered chessboard like arrangement of Ca and Ce, and with a roof tile

  12. Tailoring the piezoelectric and relaxor properties of (Bi1/2 Na1/2) TiO3- BaTiO3 via zirconium doping

    DEFF Research Database (Denmark)

    Glaum, Julia; Simons, Hugh; Acosta, Matias

    2013-01-01

    This article details the influence of zirconium doping on the piezoelectric properties and relaxor characteristics of 94(Bi1/2Na1/2)TiO3-6Ba(ZrxTi1-x)O3 (BNT-6BZT) bulk ceramics. Neutron diffraction measurements of BNT-6BZT doped with 0%-15% Zr revealed an electric-field-induced transition...

  13. Nano-phases of ZrO2 doped with Y2O3

    International Nuclear Information System (INIS)

    Duteanu, Narcis; Monty, Claude

    2001-01-01

    This work reports the method of obtaining oxygen sensors by using nano-phases of ZrO 2 doped with Y 2 O 3 95% molar in thin layers. In the first phase it is necessary to prepare a substratum based on La 1-x Sr 30 MnO 3 . This substratum is obtained by grinding powders of base, followed by mixing and then by baking of the product. The nano-phases of ZrO 2 doped with Y 2 O 3 95% molar are obtained using solar energy in a solar furnace; in the focus the temperature has value of 3000 deg. C. Such temperatures are enough to realize the process of vapor condensation. The nano-phases obtained will have used in thin layers, representing the active element. This layers are obtained directly through the process of vapor condensation in solar focus or using the spray method. The goal of this work was obtaining oxygen sensors which function at low temperatures (below 300 deg. C), because the sensors which are found on market, operate at a temperature of 800 deg. C. Those sensors are used to obtain a good combustion with engines with internal combustion. (authors)

  14. Effect of cerium addition on the microstructure, electrical and relaxor behavior of Sr{sub 0.5}Ba{sub 0.5}Nb{sub 2}O{sub 6} ceramics

    Energy Technology Data Exchange (ETDEWEB)

    Velayutham, T.S., E-mail: t_selvi@um.edu.my; Salim, N.I.F.; Gan, W.C.; Abd Majid, W.H.

    2016-05-05

    Sr{sub 0.5}Ba{sub 0.5}Nb{sub 2}O{sub 6} (SBN50) ceramic doped with different concentrations of Cerium (Ce) according to the stoichiometry formulation of Sr{sub 0.5-3y/2}Ba{sub 0.5}Ce{sub y}Nb{sub 2}O{sub 6} (Ce-SBN) with y = 0, 0.01, 0.02, 0.03, 0.04 and 0.05 was prepared using the conventional solid state reaction method. The morphology, structure, and electrical properties of the samples were studied using field emission scanning electron microscope (FESEM), X-ray diffraction (XRD), ferroelectric and dielectric spectroscopy, respectively. The FESEM images reveal a strong influence of cerium on the SBN microstructure. The X-ray diffraction patterns show that all compositions of SBN ceramic exhibit tetragonal tungsten bronze structure. As the dopant concentration, y increased, both unit cell volume and axial ratio c/a decreased gradually. In addition, dopant incorporation lowers the phase transition temperature, T{sub m}. As a result, all practical parameters are sufficiently increased, i.e. the dielectric constant and remnant polarization. SBN50 doped with a 3% Ce sample is most attractive for practical applications due to its high remnant polarization, P{sub r} = 58.6 μC/cm{sup 2} and dielectric constant, ε’ ≈ 8000 (10 kHz) at room temperature, respectively. - Highlights: • Sr{sub 0.5-3y/2}Ba{sub 0.5}Ce{sub y}Nb{sub 2}O{sub 6} synthesized using solid-state reaction method. • Cerium dopant improved the overall properties of SBN. • Dopant incorporation lowers the phase transition temperature, T{sub m}. • 3% Ce dopant exhibits best functional properties among the rest of the composition. • The P{sub r} of 3%Ce-doped SBN is 58.6 μC/cm{sup 2} and ε’ ≈ 8000 (10 kHz) at room temperature.

  15. Chemical durability and Structural approach of the glass series (40-y) Na2O-yFe2O3-5Al2O3-55P2O5-by IR, X-ray diffraction and Mössbauer Spectroscopy

    International Nuclear Information System (INIS)

    Aqdim, S; Sayouty, El H; Elouad, B; Greneche, J M

    2012-01-01

    The relationship between the composition and structure for the glasses of general composition (40-y)Na 2 O-yFe 2 O 3 -5Al 2 O 3 -55P 2 O 5 (5≤y≤20), has been studied. The chemical durability and density of these glasses increase with increasing Fe 2 O 3 content. The dissolution rate (D R ), calculated from the weight loss in distilled water at 90°C for up to 20 days was ≈ 3.10 −9 g/cm 2 /mn which is 30 times lower than that of window glass. The structure and valence states of the iron ions in the glasses were investigated using, X-ray diffraction, 57Fe Mössbauer spectrometry, potentiometric analysis, and infrared spectroscopy. Both Mössbauer spectrometry and potentiometric analysis allow to estimate both Fe 2+ and Fe 3+ contents in all these glasses. X-ray diffraction indicates that the local structure of iron phosphate glasses is related to the short range structures of NaFeP 2 O 7 . Infrared spectra indicate the formation of P–O–Fe bonds in the pyrophosphate glasses that replace P–O–Na bonds. The presence of a small content of Al 2 O 3 in the glass seems to play a role as a network modifier. The addition of Fe 2 O 3 to Al 2 O 3 in phosphate glasses favours the enhancement of the formation of pyrophosphate units because iron ions have stronger effect on the depolymerization of metaphosphate chains than the aluminium ions. Finally, the I.R spectra indicate that the presence of P-O-Fe bands of these glasses containing more than 15 mol%Fe 2 O 3 is consistent with their good chemical durability.

  16. Synthesis by sol-gel and characterization of catalysts Ag/Al2O3- CeO2 for the elimination of nitric oxide

    International Nuclear Information System (INIS)

    Zayas R, M.L.

    2005-01-01

    The environmental pollution is one from the big problems to solve at the present time, because the quality of the alive beings life is affected. For such reason, more clean and economic technologies are required, that it conduces to develop new catalytic alternatives to diminish the nitrogen oxides that due to its chemical processes in the environment contribute considerably in the air pollution. The main objective of the present work, is the preparation and characterization of catalytic materials with base of silver supported in simple and mixed aluminium oxides (Al 2 O 3 ) and Cerium oxide (CeO 2 ), and its catalytic evaluation that through of the reduction of nitric oxide (NO) using hydrogen (H 2 ) as reducer agent. It was synthesized alumina (Al 2 O 3 ) and Cerium oxide (CeO 2 ) and mixed oxides (Al 2 O 3 - CeO 2 ), by the sol-gel method and the cerium oxide (CeO 2 ) by precipitation of the cerium nitrate (III) hexa hydrated. The oxides were stabilized thermally at 900 C by 5 hr. The catalysts were prepared by impregnation using silver nitrate (AgNO 3 ), the nominal concentration of Ag was of 5% in weight. The catalysts were reduced at 400 C by 2 hr, in hydrogen flow of 60 cc/min. The characterization of the catalytic materials was carried out through different techniques as: nitrogen adsorption to determine the surface area BET, scanning electron microscopy (SEM) to observe the final morphology of the catalysts, X-ray diffraction (XRD) to identify the crystalline phases of the catalytic materials, Infrared spectroscopy (DRIFT) to know the structural characterization of the catalysts, reduction to programmed temperature (TPR) to evidence the interaction metal-support. The catalytic properties of the catalysts were evaluated in the model reaction NO + H 2 , to determine the activity and selectivity. The results indicate that the preparation technique, the precursors and the thermal treatments that underwent these materials influence in the catalyst and by

  17. Magnesium doping on brownmillerite Ca2FeAlO5

    International Nuclear Information System (INIS)

    Malveiro, J.; Ramos, T.; Ferreira, L.P.; Waerenborgh, J.C.; Nunes, M.R.; Godinho, M.; Carvalho, M.D.

    2007-01-01

    Ca 2 FeAl 1- x Mg x O 5 (x=0, 0.05 and 0.1) compounds adopting the brownmillerite-type structure were prepared by a self-combustion route using two different fuels. Characterisation was performed using X-ray powder diffraction, Moessbauer spectroscopy, magnetisation measurements, chemical analysis, scanning electron microscopy and 4-point dc conductivity measurements. Global results indicate that the solubility limit was reached for x=0.1. An antiferromagnetic behaviour was detected for all studied compositions, with magnetic ordering temperatures of 340 and 290 K for x=0 and 0.05, respectively. Mg doping increases the number of iron cations in tetrahedral sites, which induces magnetisation enhancement at low temperatures through the coupling between octahedral iron cations in different octahedral planes. The compounds exhibit semiconductor behaviour and Mg 2+ doping yields a significant enhancement of the total conductivity, which can be essentially attributed to the presence of Fe 4+ ions. - Graphical abstract: Ca 2 FeAl 1- x Mg x O 5 (x=0, 0.05, 0.1) compounds with the brownmillerite structure were prepared and characterised. The paramagnetic Moessbauer spectra presented were obtained at T=363 K (x=0); T=297 K (x=0.05) and T=353 K (x=0.1)

  18. Bioactivity of Y2O3 and CeO2 doped SiO2-SrO-Na2O glass-ceramics.

    Science.gov (United States)

    Placek, L M; Keenan, T J; Wren, A W

    2016-08-01

    The bioactivity of yttrium and cerium are investigated when substituted for Sodium (Na) in a 0.52SiO2-0.24SrO-0.24-xNa2O-xMO glass-ceramics (where x = 0.08 and MO = Y2O3 or CeO2). Bioactivity is monitored through pH and inductively coupled plasma-optical emission spectrometry where pH of simulated body fluid ranged from 7.5 to 7.6 and increased between 8.2 and 10.0 after 14-day incubation with the glass-ceramic disks. Calcium (Ca) and phosphorus (P) levels in simulated body fluid after incubation with yttrium and cerium containing disks show a continual decline over the 14-day period. In contrast, Con disks (not containing yttrium or cerium) caused the elimination of Ca in solution after 1 day and throughout the incubation period, and initially showed a decline in P levels followed by an increase at 14 days. Scanning electron microscopy and energy dispersive spectroscopy confirmed the presence of Ca and P on the surface of the simulated body fluid-incubated disks and showed precipitates on Con and HCe (8 mol% cerium) samples. Cell viability of MC3T3 osteoblasts was not significantly affected at a 9% extract concentration. Optical microscopy after 24 h cell incubation with disks showed that Con samples do not support osteoblast or Schwann cell growth, while all yttrium and cerium containing disks have direct contact with osteoblasts spread across the wells. Schwann cells attached in all wells, but only showed spreading with the HY-S (8 mol% yttrium, heated to sintering temperature) and YCe (4 mol% yttrium and cerium) disks. Scanning electron microscopy of the compatible disks shows osteoblast and sNF96.2 Schwann cells attachment and spreading directly on the disk surfaces. © The Author(s) 2016.

  19. Synthesis of Mn-doped CeO 2 nanorods and their application as ...

    Indian Academy of Sciences (India)

    Mn-doped CeO2 nanorods have been prepared from CeO2 particles through a facile compositehydroxide-mediated (CHM) approach. The products were characterized by X-ray diffraction (XRD), scanning electron microscopy (SEM) and transmission electron microscopy (TEM). The analysis from the X-ray photoelectron ...

  20. A novel gamma-ray detector with submillimeter resolutions using a monolithic MPPC array with pixelized Ce:LYSO and Ce:GGAG crystals

    Energy Technology Data Exchange (ETDEWEB)

    Kato, T., E-mail: katou.frme.8180@asagi.waseda.jp [Research Institute for Science and Engineering, Waseda University, 3-4-1, Ohkubo, Shinjuku, Tokyo (Japan); Kataoka, J.; Nakamori, T.; Miura, T.; Matsuda, H.; Kishimoto, A. [Research Institute for Science and Engineering, Waseda University, 3-4-1, Ohkubo, Shinjuku, Tokyo (Japan); Sato, K.; Ishikawa, Y.; Yamamura, K.; Nakamura, S.; Kawabata, N. [Solid State Division, Hamamatsu Photonics K. K., 1126-1, Ichino-cho, Hamamatsu, Shizuoka (Japan); Ikeda, H. [ISAS/JAXA, 3-1-1, Yoshinodai, Chuo-ku, Sagamihara-shi, Kanagawa (Japan); Yamamoto, S. [Kobe City College of Technology, 8-3, Gakuenhigashimati, Nishi-ku, Kobe-shi, Hyougo 651-2194 (Japan); Kamada, K. [Materials Research Laboratory, Furukawa Co., Ltd., 1-25-13, Kannondai, Tsukuba, Ibaraki 305-0856 (Japan)

    2013-01-21

    We have developed a large-area monolithic Multi-Pixel Photon Counter (MPPC) array consisting of 4×4 channels with a three-side buttable package. Each channel has a photosensitive area of 3×3 mm{sup 2} and 3600 Geiger mode avalanche photodiodes (APDs). For typical operational gain of 7.5×10{sup 5} at +20 °C, gain fluctuation over the entire MPPC device is only ±5.6%, and dark count rates (as measured at the 1 p.e. level) amount to ≤400kcps per channel. We first fabricated a gamma-ray camera consisting of the MPPC array with one-to-one coupling to a Ce-doped (Lu,Y){sub 2}(SiO{sub 4})O (Ce:LYSO) crystal array (4×4 array of 3×3×10 mm{sup 3} crystals). Energy and time resolutions of 11.5±0.5% (FWHM at 662 keV) and 493±22ps were obtained, respectively. When using the charge division resistor network, which compiles signals into four position-encoded analog outputs, the ultimate positional resolution is estimated as 0.19 mm in both X and Y directions, while energy resolution of 10.2±0.4% (FWHM) was obtained. Finally, we fabricated submillimeter Ce:LYSO and Ce-doped Gd{sub 3}Ga{sub 3}Al{sub 2}O{sub 12} (Ce:GGAG) scintillator matrices each consisting of 1.0×1.0, 0.7×0.7 and 0.5×0.5 mm{sup 2} pixels, to further improve the spatial resolution. In all types of Ce:LYSO and Ce:GGAG matrices, each crystal was clearly resolved in the position histograms when irradiated by a {sup 137}Cs source. The energy resolutions for 662 keV gamma-rays for each Ce:LYSO and Ce:GGAG scintillator matrix were ≤14.3%. These results suggest excellent potential for its use as a high spatial medical imaging device, particularly in positron emission tomography (PET). -- Highlights: ► We developed a newly designed large-area monolithic MPPC array. ► We obtained fine gain uniformity, and good energy and time resolutions when coupled to the LYSO scintillator. ► We fabricated gamma-ray camera consisting of the MPPC array and submillimeter pixelized LYSO and GGAG scintillators. ► In