Strategies to tailor the UV absorption band of Eu3+:La2O3 downshifting nanocrystals

Science.gov (United States)

Méndez, M.; Cesteros, Y.; Marsal, L. F.; Salagre, P.; Formentín, P.; Pallarès, J.; Aguiló, M.; Díaz, F.; Carvajal, J. J.

2012-06-01

The charge transfer state (CTS) band of the Eu3+:La2O3 nanocrystals were studied in detail in order to understand the shift of the maximum of this band. Eu3+:La2O3 nanoparticles present a broad CTS band. However, the maximum is peaking below 300 nm, far below the limit of the solar spectrum arriving to the surface of the Earth and it makes difficult the application of this material as down-shifting in solar cells. In order to shift the CTS band towards blue wavelengths, different synthesis methods such as hydrothermal and sol-gel modified Pechini methods were used to prepare these nanoparticles, and adding additional CTS bands with co-doping ions such as Bi3+ was explored as well. The crystalline structure of Eu3+:La(OH)3, Eu3+:La2O3, Bi3+:Eu3+:La(OH)3 and Bi3+:Eu3+:La2O3 and the cell parameters of Eu3+:La2O3 and Bi3+:Eu3+:La2O3 were analyzed by X-ray powder diffraction technique and their morphology was observed by transmission electron microscopy. Once we obtained the cell parameters refining the XRD patterns by Full-prof software, we were able to calculate the Eu3+-O distance by ATOMS software through the structure previously represented following the Pauling model. The results found suggest that we need to take into account another parameter apart from the Eu3+-O distance to explain the CTS band small shift.

Synthesis and Downconversion Emission Property of Yb2O3:Eu3+ Nanosheets and Nanotubes

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Chao Qian

2013-01-01

Full Text Available Ytterbium oxide (Yb2O3 nanocrystals with different Eu3+ (1%, 2%, 5%, and 10% doped concentrations were synthesized by a facile hydrothermal method, subsequently by calcination at 700°C. The crystal phase, size, and morphology of prepared samples were characterized by X-ray diffraction (XRD and transmission electron microscopy (TEM. The results show that the as-prepared Yb2O3 nanocrystals with sheet- and tube-like shape have cubic phase structure. The Eu3+ doped Yb2O3 nanocrystals were revealed to have good down conversion (DC property and intensity of the DC luminescence can be modified by Eu3+ contents. In our experiment the 1% Eu3+ doped Yb2O3 nanocrystals showed the strongest DC luminescence among the obtained Yb2O3 nanocrystals.

Photoluminescence of rare-earth ion (Eu3+, Tm3+, and Er3+)-doped and co-doped ZnNb2O6 for solar cells

Science.gov (United States)

Gao, Sen-Pei; Qian, Yan-Nan; Wang, Biao

2015-08-01

Visible converted emissions produced at an excitation of 286 nm in ZnNb2O6 ceramics doped with rare-earth ions (RE = Eu3+, Tm3+, Er3+ or a combination of these ions) were investigated with the aim of increasing the photovoltaic efficiency of solar cells. The structure of RE:ZnNb2O6 ceramics was confirmed by x-ray diffraction patterns. The undoped ZnNb2O6 could emit a blue emission under 286-nm excitation, which is attributed to the self-trapped excitons’ recombination of the efficient luminescence centers of edge-shared NbO6 groups. Upon 286-nm excitation, Eu:ZnNb2O6, Tm:ZnNb2O6, and Er:ZnNb2O6 ceramics showed blue, green, and red emissions, which correspond to the transitions of 5D0 → 7FJ (J = 1-4) (Eu3+), 1G4 → 3H6 (Tm3+), and 2H11/2/4S3/2 → 4I15/2 (Er3+), respectively. The calculated CIE chromaticity coordinates of Eu:ZnNb2O6, Tm:ZnNb2O6, and Er:ZnNb2O6 are (0.50, 0.31), (0.14, 0.19), and (0.29, 0.56), respectively. RE ion-co-doped ZnNb2O6 showed a combination of characteristic emissions. The chromaticity coordinates of Eu/Tm:ZnNb2O6, Eu/Er:ZnNb2O6, and Tm/Er:ZnNb2O6 were calculated to be (0.29, 0.24), (0.45, 0.37), and (0.17, 0.25). Project supported by the National Natural Science Foundation of China (Grant Nos. 10572155 and 10732100) and the Research Fund for the Doctoral Program of Ministry of Education, China (Grant No. 20130171130003).

Crossrelaxations and non-radiative energy transfer from (4G5/2) Sm3+ → (5D0) Eu3+: B2O3–ZnO glasses

International Nuclear Information System (INIS)

Naresh, V.; Rudramadevi, B.H.; Buddhudu, S.

2015-01-01

Graphical abstract: The energy transfer process occurring from Sm 3+ to Eu 3+ in B 2 O 3 –ZnO (BZn) glasses is analyzed. Based on the Foster–Dexter theory, the possibility of energy transfer between Sm 3+ and Eu 3+ has been demonstrated from the spectral overlap of Eu 3+ absorption and Sm 3+ emission, photoluminescence spectra, energy level diagram and lifetime measurements. The energy transfer mechanism in (Sm 3+ + Eu 3+ ) co-doped glass is governed by dipole–dipole interaction. - Highlights: • Spectroscopic properties of individually doped Sm 3+ , Eu 3+ & co-doped (Sm 3+ + Eu 3+ ) in BZn glasses were studied separately. • The effect of Eu 3+ concentration on luminescence properties is explained from cross-relaxations. • Energy transfer from Sm 3+ ( 4 G 5/2 ) to Eu 3+ ( 5 D 0 ) has been explained from Foster–Dexter theory. • Dipole–dipole mechanism governs the energy transfer from Sm 3+ to Eu 3+ . - Abstract: The present paper reports on the results concerning to photoluminescence features of Eu 3+ , Sm 3+ ions and energy transfer process occurring from Sm 3+ to Eu 3+ doped in 45 B 2 O 3 –55 ZnO (BZn) glasses prepared by melt quenching technique. Luminescence quenching as a function of Eu 3+ concentration in BZn glasses has been discussed. Among the studied concentrations, 0.5 mol% of Eu 3+ is optimized because it has exhibited red emission transition 5 D 0 → 7 F 2 . With regard to Sm 3+ glasses, orange emission at 602 nm ( 4 G 5/2 → 6 H 7/2 ) has been noticed on exciting with λ exci = 403 nm. Based on the Foster–Dexter theory, the possibility of energy transfer between Sm 3+ and Eu 3+ has been explained from the spectral overlap of Eu 3+ absorption and Sm 3+ emission. The optimized concentration 0.5 mol% of Eu 3+ is co-doped with Sm 3+ in various concentrations ranging from 0.1 to 1.5 mol% inorder to study the sensitization effect of Sm 3+ on Eu 3+ luminescence. The results have revealed that with the addition of Sm 3+ to Eu 3+ : BZn

Influence of annealing temperature on structural and optical properties of Lu2O3:Eu3+, Tb3+ transparent films

International Nuclear Information System (INIS)

Morales-Ramírez, Ángel de Jesús; García-Murillo, Antonieta; Carrillo-Romo, Felipe de Jesús; Garrido-Hernández, Aristeo; García-Hernández, Margarita

2015-01-01

Highlights: • Lu 2 O 3 :Eu 3+ , Tb 3+ films were synthesized by sol–gel and by dip-coating technique. • Effects of annealing treatment on structural and optical properties were studied. • Optogeometrical characteristics of synthesized films were analyzed. • X-ray diffraction results showed that Lu 2 O 3 :Eu 3+ , Tb 3+ crystallizes at 700 °C. • High reddish emission on transparent films with at least 1 μm thick was observed. - Abstract: High-optical quality Lu 2 O 3 :Eu 3+ 5 mol%, X Tb 3+ (X = 0–0.04 mol%) thin films were prepared by the sol–gel process and dip-coating technique. The procedure was as follows: lutetium, europium and terbium nitrates were used as precursors, and ethanol as a solvent. Etylenglycol (EG) was added as a sol stabilizer, and the pH was adjusted by acetic acid. After 10 dipping-cycles, followed by an annealing process (600–900 °C) for 1 h, transparent, smooth and crack-free films (ra = 8–9 nm) were formed. The X-ray diffraction (XRD) results showed crystallized films into the cubic structure at 800 °C. The ellipsometry results showed that the thickness of the films varied from 1 to 1.4 μm at 1000 and 600 °C, respectively. Finally, the films presented a typical Eu 3+ red emission at 611 nm ( 5 D 0 → 7 F 2 ); furthermore, the effect of the Tb 3+ content showed that the highest emission intensity corresponded to the lower Tb 3+ content

The photoluminescent properties of Y2O3:Bi3+, Eu3+, Dy3+ phosphors for white-light-emitting diodes.

Science.gov (United States)

Han, Xiumei; Feng, Xu; Qi, Xiwei; Wang, Xiaoqiang; Li, Mingya

2014-05-01

Bi3+, Eu3+, Dy3+ activated Y2O3 phosphors were prepared through the sol-gel process. X-ray diffraction (XRD), Fourier transform infrared (FT-IR) spectra, and photoluminescence (PL) spectra were used to characterize the resulting phosphors. The XRD patterns show the refined crystal structure of Y2O3. The energy transfer processes of Bi(3+)-Eu3+ occurred in the host lattices. The thermal stability of Y2O3:Bi3+, Eu3+, Dy3+ phosphors was studied. Under short wavelength UV excitation, the phosphors show excellent characteristic red, blue, and yellow emission with medium intensity.

Self-reduction process and enhanced blue emission in SrAl{sub 2}Si{sub 2}O{sub 8}: Eu, Tb via electron transfer from Tb{sup 3+} to Eu{sup 3+}

Energy Technology Data Exchange (ETDEWEB)

Xu, Hongwei; Wang, Lili; Li, Minhong; Ran, Weiguang; Deng, Zhihan; Houzong, Ruizhi; Shi, Jinsheng [Department of Chemistry and Pharmaceutical Science, Qingdao Agricultural University, Qingdao 266109, Shandong, (China)

2017-06-15

Eu, Tb co-doped SrAl{sub 2}Si{sub 2}O{sub 8} luminescent materials were synthesized via a high-temperature solid-state reaction. Excitation spectra of SrAl{sub 2}Si{sub 2}O{sub 8}: Eu{sup 2+} gives two broad excitation bands maximizing at 270 and 330 nm, resulting from splitting Eu{sup 2+} energy levels in octahedral crystal field. Eu single doped SrAl{sub 2}Si{sub 2}O{sub 8} luminescent material exhibits two emission bands at about 406 and 616 nm. Intensity of the blue emission from Eu{sup 2+} is always strong, compared with that of the red emission band of Eu{sup 3+}. Reduction from Eu{sup 3+} to Eu{sup 2+} can be explained with the model of charge compensation. Blue emission in SrAl{sub 2}Si{sub 2}O{sub 8}: xEu was strengthened after incorporation of Tb, which can be explained by electron transfer from Tb{sup 3+} to Eu{sup 3+} (Tb{sup 3+} + Eu{sup 3+} → Tb{sup 4+} + Eu{sup 2+}). Under 230 nm excitation, intensity of Tb{sup 3+} emission was nearly unchanged and that of Eu{sup 2+} was increased, obviously due to the delivery of more electrons to Eu{sup 3+}. The strongest emission of Eu{sup 2+} in 0.09Eu/0.06Tb co-doped SrAl{sub 2}Si{sub 2}O{sub 8} and excited at 270 and 330 nm was remarkably enhanced by about four times compared to that of 0.15Eu Single doped SrAl{sub 2}Si{sub 2}O{sub 8}. All of the results indicate that SrAl{sub 2}Si{sub 2}O{sub 8}:xEu, yTb are potential blue emitting luminescent materials for UV-LEDs. More importantly, this research may provide a new perspective in designing broad band blue luminescent materials. (copyright 2017 WILEY-VCH Verlag GmbH and Co. KGaA, Weinheim)

Synthesis, characterization and photocatalysis enhancement of Eu2O3-ZnO mixed oxide nanoparticles

Science.gov (United States)

Mohamed, W. S.; Abu-Dief, Ahmed M.

2018-05-01

Pure ZnO nanoparticles (NPs) and mixed Eu2O3 and ZnO NPs with different Eu2O3 ratios (5%, 10%, and 15%) were synthesized by a precipitation method under optimum conditions. The synthesized samples were characterized by means of X-ray diffraction, scanning electron microscopy (SEM), energy-dispersive X-ray spectroscopy, transmission electron microscopy (TEM), Fourier transform infrared (FTIR) spectroscopy, Raman spectroscopy, and UV-vis diffuse reflectance spectroscopy. The as-synthesized ZnO NPs exhibit high phase purity and a highly crystalline wurtzite ZnO structure. The mixed Eu2O3 and ZnO NPs exhibit a Eu2O3 zinc blend phase in addition to the wurtzite phase of pure ZnO, confirming the high purity and good crystallinity of the as-synthesized samples. The high-purity formation of ZnO and Eu2O3 phases was confirmed by FTIR and Raman spectra. Microstructural analysis by SEM and TEM confirmed the sphere-like morphology with different particle sizes (29-40 nm) of the as-synthesized samples. The photocatalytic activities of pure ZnO NPs and mixed Eu2O3 and ZnO NPs for the degradation of methylene blue were evaluated under ultraviolet (UV) irradiation. The results show that Eu2O3 plays an important role in the enhancement of the photocatalytic properties of ZnO NPs. We found that mixed 5% Eu2O3 and ZnO NPs exhibit the highest photocatalytic activity (degradation efficiency of 96.5% after 180 min of UV irradiation) as compared with pure ZnO NPs (degradation efficiency of 80.3% after 180 min of UV irradiation). The increased photocatalytic activity of the optimum mixed Eu2O3 and ZnO NPs is due to the high crystallinity, high surface area with small particle size, and narrow energy gap.

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

Energy transfer and colorimetric properties of Eu3+/Dy3+ co-doped Gd2(MoO4)3 phosphors

International Nuclear Information System (INIS)

Wan Jing; Cheng Lihong; Sun Jiashi; Zhong Haiyang; Li Xiangping; Lu Weili; Tian Yue; Lin Hai; Chen Baojiu

2010-01-01

Dy 3+ single-doped and Eu 3+ /Dy 3+ co-doped gadolinium molybdate (Gd 2 (MoO 4 ) 3 ) phosphors were synthesized by a traditional solid-state reaction method. The XRD was used to confirm the crystal structure of the phosphors. The energy transfer between Eu 3+ and Dy 3+ was observed and studied. The Eu 3+ concentration can hardly affect the blue and yellow emission intensities of Dy 3+ , and the Eu 3+ emission intensity increases with the increase of Eu 3+ concentration. Co-doping with Eu 3+ compensated the red emission component of the Dy 3+ doped Gd 2 (MoO 4 ) 3 phosphor. Introducing proper amount of Eu 3+ can improve the colorimetric performance of the phosphors.

Photoluminescence properties of Gd_2O_3:Eu"3"+ for solid state lighting

International Nuclear Information System (INIS)

Ukare, R.S.; Zade, G.D.; Dhoble, S.J.

2016-01-01

We synthesized Gd_2O_3 doped europium (III) (1 m%) nanophosphors using the precipitation method and combustion method. The synthesized nanophosphors were characterized by X-ray diffraction (XRD) and SEM techniques. The optical properties of the synthesized nanophosphors were investigated by photoluminescence spectroscopy. The XRD patterns of Gd_2O_3 revealed formation of desired cubic phase by both methods. The XRD of nanophosphors synthesized by both methods were highly consistent with standard JCPDS file of Gd_2O_3 indicating no structural change with incorporation of the Eu"3"+ ions in the Gd_2O_3 matrix. Both XRD and SEM result confirms the particle size of prepared sample in nanometer range. The phosphor could be effectively excited by near UV at 395 nm. The Eu"3"+ doping of Gd_2O_3 produced red luminescence around 613 nm. The stimulated CIE chromaticity coordinates were also calculated. (author)

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

Luminescent properties of green- or red-emitting Eu2+-doped Sr3Al2O6 for LED

International Nuclear Information System (INIS)

Zhang Jilin; Zhang Xinguo; Shi Jianxin; Gong Menglian

2011-01-01

Eu 2+ -doped Sr 3 Al 2 O 6 (Sr 3-x Eu x Al 2 O 6 ) was synthesized by a solid-state reaction under either H 2 and N 2 atmosphere or CO atmosphere. When H 2 was used as the reducing agent, the phosphor exhibited green emission under near UV excitation, while CO was used as the reducing agent, the phosphor mainly showed red emission under blue light excitation. Both emissions belong to the d-f transition of Eu 2+ ion. The relationship between the emission wavelengths and the occupation of Eu 2+ at different crystallographic sites was studied. The preferential substitution of Eu 2+ into different Sr 2+ cites at different reaction periods and the substitution rates under different atmospheres were discussed. Finally, green-emitting and red-emitting LEDs were fabricated by coating the phosphor onto near UV- or blue-emitting InGaN chips. - Highlights: →Sr 3 Al 2 O 6 :Eu 2+ is synthesized by a solid-state reaction under different atmospheres. →Phosphor obtained under H 2 +N 2 atmosphere emits green light under NUV excitation. →Phosphor obtained under CO atmosphere emits red light under blue light excitation. →Different emission wavelengths are due to Eu 2+ in different Sr 2+ sites. →The preferential substitution and the substitution rates of Eu 2+ are discussed.

Tunable Yellow-Red Photoluminescence and Persistent Afterglow in Phosphors Ca4LaO(BO3)3:Eu3+ and Ca4EuO(BO3)3.

Science.gov (United States)

Chen, Zhen; Pan, Yuexiao; Xi, Luqing; Pang, Ran; Huang, Shaoming; Liu, Guokui

2016-11-07

In most Eu 3+ activated phosphors, only red luminescence from the 5 D 0 is obtainable, and efficiency is limited by concentration quenching. Herein we report a new phosphor of Ca 4 LaO(BO 3 ) 3 :Eu 3+ (CLBO:Eu) with advanced photoluminescence properties. The yellow luminescence emitted from the 5 D 1,2 states is not thermally quenched at room temperature. The relative intensities of the yellow and red emission bands depend strongly on the Eu 3+ doping concentration. More importantly, concentration quenching of Eu 3+ photoluminescence is absent in this phosphor, and the stoichiometric compound of Ca 4 EuO(BO 3 ) 3 emits stronger luminescence than the Eu 3+ doped compounds of CLBO:Eu; it is three times stronger than that of a commercial red phosphor of Y 2 O 3 :Eu 3+ . Another beneficial phenomenon is that ligand-to-metal charge transfer (CT) transitions occur in the long UV region with the lowest charge transfer band (CTB) stretched down to about 3.67 eV (∼330 nm). The CT transitions significantly enhance Eu 3+ excitation, and thus result in stronger photoluminescence and promote trapping of excitons for persistent afterglow emission. Along with structure characterization, optical spectra and luminescence dynamics measured under various conditions as a function of Eu 3+ doping, temperature, and excitation wavelength are analyzed for a fundamental understanding of electronic interactions and for potential applications.

Hydrothermal synthesis of Gd2O3:Eu3+ nanophosphors: Effect of surfactant on structural and luminescence properties

International Nuclear Information System (INIS)

Dhananjaya, N.; Nagabhushana, H.; Sharma, S.C.; Rudraswamy, B.; Shivakumara, C.; Nagabhushana, B.M.

2014-01-01

Highlights: • Gd(OH) 3 :Eu 3+ , GdOOH:Eu 3+ and Gd 2 O 3 :Eu 3+ phases were prepared by hydrothermal method. • Phosphors were well characterized by XRD, SEM, TEM, Raman, UV–Vis, FT-IR. • Cubic Gd 2 O 3 :Eu 3+ show intense red emission, which was highly useful for photonics application. • HDA surfactant plays an important role in conversion of cubic to hexagonal phases. -- Abstract: Various morphologies of Eu 3+ activated gadolinium oxide have been prepared by hydrothermal method using hexadecylamine (HDA) as surfactant at different experimental conditions. The powder X-ray diffraction studies reveal as-formed product is hexagonal Gd(OH) 3 :Eu 3+ phase and subsequent heat treatment at 350 and 600 °C transforms to monoclinic GdOOH:Eu 3+ and cubic Gd 2 O 3 :Eu 3+ phases respectively. SEM pictures of without surfactant show irregular shaped rods along with flakes. However, in the presence of HDA surfactant, the particles are converted into rods of various sizes. The temperature dependent morphological evolution of Gd 2 O 3 :Eu 3+ without and with HDA surfactant is studied. TEM micrographs of Gd(OH) 3 :Eu 3+ sample with HDA confirms smooth nanorods with various diameters in the range 20–100 nm. FTIR studies reveal that HDA surfactant plays an important role in conversion of cubic to hexagonal phases. Among these three phases, cubic phase Gd 2 O 3 :Eu 3+ (λ ex = 254 nm) show red emission at 612 nm corresponding to 5 D 0 → 7 F 2 and is more efficient host than the monoclinic counterpart. The band gap for hexagonal Gd(OH) 3 :Eu 3+ is more when compared to monoclinic GdOOH:Eu 3+ and cubic Gd 2 O 3 :Eu 3+

Synthesis, characterization, photocatalytic activity and ethanol-sensing properties of In{sub 2}O{sub 3} and Eu{sup 3+}:In{sub 2}O{sub 3} nanoparticles

Energy Technology Data Exchange (ETDEWEB)

Anand, Kanica; Thangaraj, R., E-mail: rthangaraj@rediffmail.com [Semiconductors Laboratory, Department of Physics, GND University, Amritsar (India); Kumar, Praveen [Department of Physics, DAV University, Jalandhar (India); Kaur, Jasmeet; Singh, R. C. [Laboratory for sensors and physical education, Department of Physics, GND University, Amritsar (India)

2015-05-15

In the present endeavor, Indium oxide (In{sub 2}O{sub 3}) and Europium doped In{sub 2}O{sub 3} (In{sub 2}O{sub 3}:0.5%Eu{sup 3+} and In{sub 2}O{sub 3}:5%Eu{sup 3+}) nanoparticles were prepared by co-precipitation method. Synthesized nanoparticles were characterized using X-Ray Diffraction (XRD), Scanning Electron Microscopy (SEM) and UV-Visible spectrophotometry (UV-vis). XRD revealed that nanoparticles were of pure bixbyite-type cubic phase and the crystallite size decreased with the Eu{sup 3+} doping. SEM micrographs showed that particles were spherical in shape. Synthesized nanoparticles were used for photo degradation of methylene blue (MB) dye under sunlight and the results clearly showed that In{sub 2}O{sub 3}:5%Eu{sup 3+} nanoparticles exhibited higher activity than pure In{sub 2}O{sub 3} nanoparticles. For gas sensing characteristics, the nanoparticles were applied as thick film onto alumina substrate and tested at different operating temperatures. The results showed that the optimum operating temperature of the gas sensors prepared from synthesized nanoparticles is 300°C. The investigations revealed that the addition of Eu{sup 3+} as a dopant enhanced the sensing response of In{sub 2}O{sub 3} nanoparticles appreciably.

Photoluminescent properties of Sr2CeO4: Eu3+ and Sr2CeO4: Eu2+ phosphors suitable for near ultraviolet excitation

International Nuclear Information System (INIS)

Suresh, K.; Poornachandra Rao, N.V.; Murthy, K.V.R.

2014-01-01

Powder phosphors of 1 mol% Eu 3+ - and Eu 2+ -doped strontium cerium oxide (Sr 2 CeO 4 ) were synthesized by standard solid-state reaction method. Eu 3+ - and Eu 2+ -doped Sr 2 CeO 4 phosphors fired at 1100 ℃ for 2 h were analysed by X-ray diffraction (XRD) and photoluminescence (PL) techniques. The XRD patterns confirm that the obtained phosphors are a single phase of Sr 2 CeO 4 composed of orthorhombic structure. Room temperature PL excitation spectrum of air-heated Sr 2 CeO 4 : Eu phosphor has exhibited bands at 260, 280 and 350 nm. Whereas the excitation spectrum of Sr 2 CeO 4 : Eu phosphor heated under reducing (carbon) atmosphere exhibited single broadband range from 260 to 390 nm. The (PL) emission peaks of both the phosphors at 467 (blue), 537 (green) and 616 nm (red) generate white light under 260, 280 and 350 nm excitation wavelengths. The Commission International de l'Eclairage (CIE) colour coordinates conforms that these phosphors emitting white light. The results reveal that these phosphors are multifunctional phosphors which emit white light under these excitations that they could be used as white components for display and lamp devices and as well as possible good light-conversion phosphor LEDs under near-ultraviolet (nUV) chip. (author)

Phase transformation, morphology evolution and luminescence property variation in Y2O3: Eu hollow microspheres

International Nuclear Information System (INIS)

Wang, Qin; Guo, Jing; Jia, Wenjing; Liu, Baocang; Zhang, Jun

2012-01-01

Highlights: ► We report a general and facile method for the synthesis of Y 2 O 3 : Eu hollow microspheres. ► This method may be of great significance in the synthesis of many other hollow spherical materials. ► Phase, morphology and luminescence property were found to be strongly dependent on temperature and pH. ► The evolution process under various temperatures and pH values were discussed. ► The sample shows a strong red emission under short UV irradiation, and the lifetime is determined to be 7.0 ms. - Abstract: Y 2 O 3 : Eu hollow microspheres with average size of 500–600 nm have been successfully synthesized via a solvothermal method in the presence of sodium citrate as surfactant followed by a subsequent heat treatment process. High polymer F127(EO 106 PO 70 EO 106 ) served as a soft template in the formation of as prepared hollow microspheres. It is found that the pH values and the reaction temperature are two crucial factors in determining the phase, morphology and luminescence properties of the Y 2 O 3 : Eu hollow microspheres. Morphology evolution can be achieved by changing the pH and the reaction temperature. The properties of the Eu 3+ -doped Y 2 O 3 : Eu nanocrystals were characterized by XRD, FE-SEM, HR-TEM and UV–vis spectroscopy.

ESR of Gd3+ in magnetically ordered Eu2CuO4

International Nuclear Information System (INIS)

Rettori, C.; Oseroff, S.B.; Rao, D.; Valdivia, J.A.; Barberis, G.E.; Martins, G.B.; Sarrao, J.; Fisk, Z.; Tovar, M.

1996-01-01

Electron spin resonance (ESR) experiments of Gd 3+ in the antiferromagnetic (AF) ordered phase (T N ) of Eu 2 CuO 4 can be interpreted in terms of four magnetically nonequivalent rare-earth sites with local internal fields H i =±310(30) Oe along the [100] and [010] directions. The internal field is well described by a dipolar magnetic field of a noncollinear AF array of 0.35(4) μ B per Cu moment aligned along the [100] and [010] directions. This is consistent with recent results of magnetic-field-dependent neutron-diffraction experiments. From the ESR and magnetic susceptibility data, the crystal field parameters for Gd 3+ and Eu 3+ in Eu 2 CuO 4 are determined. The exchange parameters between the rare earths are also estimated. copyright 1996 The American Physical Society

Facile synthesis of luminescent and amorphous La2O3-ZrO2:Eu3+ nanofibrous membranes with robust softness

Science.gov (United States)

Han, Weidong; Ding, Bin; Park, Mira; Cui, Fuhai; Ghouri, Zafar Khan; Saud, Prem Singh; Kim, Hak-Yong

2015-08-01

Novel luminescent and amorphous La2O3-ZrO2:Eu3+ (LZE) nanofibrous membranes with robust softness are fabricated for the first time via a facile electrospinning technique. By incorporating zirconium oxide, the as-prepared lanthanum oxide nanofibrous membranes can be dramatically changed from extreme fragility to robust softness. Meanwhile, the softness and luminescent performance of LZE nanofibrous membranes can be finely controlled by regulating the doping concentration of zirconium oxide and europium in lanthanum oxide nanofibers. Additionally, the crystal structure analysis using X-ray diffractometer and high resolution transmission electron microscopy measurements have confirmed the correlation between the amorphous structure and softness. Furthermore, LZE membranes show the characteristic emission of Eu3+ corresponding to 5D0, 1, 2-7F0, 1, 2, 3, 4 transitions due to an efficient energy transfer from O2- to Eu3+. The LZE nanofibrous membranes with the optimum doping Eu3+ concentration of 3 mol% exhibit excellent softness and luminescent properties, which make the materials to have potential applications in fluorescent lamps and field emission displays.Novel luminescent and amorphous La2O3-ZrO2:Eu3+ (LZE) nanofibrous membranes with robust softness are fabricated for the first time via a facile electrospinning technique. By incorporating zirconium oxide, the as-prepared lanthanum oxide nanofibrous membranes can be dramatically changed from extreme fragility to robust softness. Meanwhile, the softness and luminescent performance of LZE nanofibrous membranes can be finely controlled by regulating the doping concentration of zirconium oxide and europium in lanthanum oxide nanofibers. Additionally, the crystal structure analysis using X-ray diffractometer and high resolution transmission electron microscopy measurements have confirmed the correlation between the amorphous structure and softness. Furthermore, LZE membranes show the characteristic emission of Eu3

Effect of structural evolution of ZnO/HfO2 nanocrystals on Eu2+/Eu3+ emission in glass-ceramic waveguides for photonic applications.

Science.gov (United States)

Ghosh, Subhabrata; Bhaktha B N, Shivakiran

2018-06-01

Eu-doped 70SiO 2 -23HfO 2 -7ZnO (mol%) glass-ceramic waveguides have been fabricated by sol-gel method as a function of heat-treatment temperatures for on-chip blue-light emitting source applications. Structural evolution of spherical ZnO and spherical as well as rod-like HfO 2 nanocrystalline structures have been observed with heat-treatments at different temperatures. Initially, in the as-prepared samples at 900 ◦ C, both, Eu 2+ as well as Eu 3+ ions are found to be present in the ternary matrix. With controlled heat-treatments of up to 1000 ◦ C for 2 h, local environment of Eu-ions become more crystalline in nature and the reduction of Eu 3+ to Eu 2+ takes place in such ZnO/HfO 2 crystalline environments. In these ternary glass-ceramic waveguides, heat-treated at higher temperatures, the blue-light emission characteristic, which is the signature of 4f 6 5d [Formula: see text] 4f 7 energy level transition of Eu 2+ ions is found to be greatly enhanced. The as-prepared glass-ceramic waveguides exhibit a propagation loss of 0.4 ± 0.2 dB cm -1 at 632.8 nm. Though the propagation losses increase with the growth of nanocrystals, the added functionalities achieved in the optimally heat-treated Eu-doped 70SiO 2 -23HfO 2 -7ZnO (mol%) waveguides, make them a viable functional optical material for the fabrication of on-chip blue-light emitting sources for integrated optic applications.

Effect of structural evolution of ZnO/HfO2 nanocrystals on Eu2+/Eu3+ emission in glass-ceramic waveguides for photonic applications

Science.gov (United States)

Ghosh, Subhabrata; N, Shivakiran Bhaktha B.

2018-06-01

Eu-doped 70SiO2–23HfO2–7ZnO (mol%) glass-ceramic waveguides have been fabricated by sol-gel method as a function of heat-treatment temperatures for on-chip blue-light emitting source applications. Structural evolution of spherical ZnO and spherical as well as rod-like HfO2 nanocrystalline structures have been observed with heat-treatments at different temperatures. Initially, in the as-prepared samples at 900 ◦C, both, Eu2+ as well as Eu3+ ions are found to be present in the ternary matrix. With controlled heat-treatments of up to 1000 ◦C for 2 h, local environment of Eu-ions become more crystalline in nature and the reduction of Eu3+ to Eu2+ takes place in such ZnO/HfO2 crystalline environments. In these ternary glass-ceramic waveguides, heat-treated at higher temperatures, the blue-light emission characteristic, which is the signature of 4f 65d \\to 4f 7 energy level transition of Eu2+ ions is found to be greatly enhanced. The as-prepared glass-ceramic waveguides exhibit a propagation loss of 0.4 ± 0.2 dB cm‑1 at 632.8 nm. Though the propagation losses increase with the growth of nanocrystals, the added functionalities achieved in the optimally heat-treated Eu-doped 70SiO2–23HfO2–7ZnO (mol%) waveguides, make them a viable functional optical material for the fabrication of on-chip blue-light emitting sources for integrated optic applications.

Observation of red electroluminescence from an Eu2O3/ p +-Si device and improved performance by introducing a Tb2O3 layer

International Nuclear Information System (INIS)

Yin, Xue; Wang, Shenwei; Mu, Guangyao; Wan, Guangmiao; Huang, Miaoling; Yi, Lixin

2017-01-01

We report red electroluminescence (EL) from an Eu 2 O 3 / p + -Si device with Eu 2 O 3 film annealed in oxygen ambient at 700 °C. The red EL is ascribed to the characteristic emissions of Eu 3+ ions in Eu 2 O 3 film and the luminescence mechanism is discussed in detail. In order to optimize the device performance, Eu 2 O 3 /Tb 2 O 3 multiple films were deposited on Si wafer, and the result showed EL intensity of the device was obviously enhanced and the turn-on voltage was reduced to about 10 V. Moreover, intensity ratio I ( 5 D 0 – 7 F 2 )/ I ( 5 D 0 – 7 F 1 ) was also significantly increased with the hypersensitive transition 5 D 0 – 7 F 2 as the most prominent group at about 611 nm. The improved performance was attributed to the added Tb 2 O 3 film that it can be served as the hole-injection layer to afford extra holes injected into the Eu 2 O 3 layer. (paper)

Investigation on photoluminescence, electrical and positron lifetime of Eu"3"+ activated Gd_2O_3 phosphors

International Nuclear Information System (INIS)

Selvalakshmi, Thangaraj; Sellaiyan, Selvakumar; Uedono, Akira; Chandra Bose, Arumugam

2015-01-01

In the present study, red emitting Gd_2O_3:Eu"3"+ phosphors are prepared by citrate-based sol–gel process and the as-prepared samples are annealed at various annealing temperatures. The photoluminescence properties of Gd_2O_3:Eu"3"+ is explained from the excitation and emission spectra. The excitation spectra include peaks corresponding to charge transfer and 4f–4f transitions of Eu"3"+ and Gd"3"+. The phosphors exhibit a weak energy transfer process from Gd"3"+ to Eu"3"+. Under the excitation of 254 nm, a sharp red emission peak is observed at 611 nm and the emission intensity increases with the annealing temperature. The presence of defects in the phosphor is investigated by positron annihilation lifetime and Doppler broadening spectroscopy. The relation between visible emission and lattice defects of the phosphors is presented. The electrical and dielectric properties of the phosphor are also discussed in detail. Such red emitting phosphors pave the way towards the fabrication of light emitting diodes (LEDs). - Highlights: • Positron annihilation lifetime spectroscopy of Gd_2O_3:Eu"3"+. • Relation between positron lifetime and photoluminescence. • Conductivity and dielectric properties of Gd_2O_3:Eu"3"+.

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)

Photo- and radio-excited luminescence properties of Eu-doped La2O3–Al2O3 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

Luminescence and energy transfer properties of Eu3+ and Gd3+ in ZrO2

International Nuclear Information System (INIS)

Villabona-Leal, E.G.; Diaz-Torres, L.A.; Desirena, H.; Rodríguez-López, J.L.; Pérez, Elías; Meza, Octavio

2014-01-01

Red luminescence emission in ZrO2:Gd 3+ –Eu 3+ nanocrystal under 250 nm radiation excitation is achieved. These materials exhibit a tetragonal phase that is retained by the presence of lanthanide ions. Thus, a study of the optical properties as a function of the dopant concentration was been carried out without the deleterious effects of having segregation of other crystalline phases. We analyze the emission and lifetime curves as a function of dopant concentration through a rate equation simulation, finding an excellent fitting. As results, the nonradiative and radiative relaxation constants, as well as a quantitative estimation of the energy transfer processes among Eu 3+ , Gd 3+ and O 2− ions are reported for the first time. The proposed model can be extended (or applicable) to explain the fluorescence dynamics in other nanomaterials doped with Eu 3+ and Gd 3+ under UV excitation. -- Highlights: • ZrO 2 nanocrystal exhibits a tetragonal phase in the presence of Eu and Gd dopants. • Emission and lifetimes as a function of dopant concentration were analyzed by rate equation model. • Quantitative estimation of the energy transfer processes among Eu 3+ , Gd 3+ and O 2− ions are reported

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.

Synthesis and luminescent properties of CaCO3:Eu3+@SiO2 phosphors with core-shell structure

Science.gov (United States)

Liu, Min; Kang, Ming; Chen, Kexu; Mou, Yongren; Sun, Rong

2018-03-01

Integrating the processes of preparation of CaCO3:Eu3+ and its surface-coating, core-shell structured CaCO3:Eu3+@SiO2 phosphors with red emission were synthesized by the carbonation method and surface precipitation procedure using sodium silicate as silica source. The phase structure, thermal stability, morphology and luminescent property of the as-synthesized samples were characterized by X-ray diffraction, Fourier transform infrared spectrum, thermal analysis, field-emission scanning electron microscopy, transmission electron microscope and photoluminescence spectra. The experimental results show that Eu3+ ions as the luminescence center are divided into two types: one is at the surface of the CaCO3 and the other inhabits the site of Ca2+. For CaCO3:Eu3+@SiO2 phosphors, the SiO2 layers are continuously coated on the surface of CaCO3:Eu3+ and show a typical core-shell structure. After coated with SiO2 layer, the luminous intensity and the compatibility with the rubber matrix increase greatly. Additionally, the luminous intensity increases with the increasing of Eu3+ ions concentration in CaCO3 core and concentration quenching occurs when Eu3+ ions concentration exceeds 7.0 mol%, while it is 5.0 mol% for CaCO3:Eu3+ phosphors. Therefore, preparation of CaCO3:Eu3+@SiO2 phosphors can not only simplify the experimental process through integrating the preparation of CaCO3:Eu3+ and SiO2 layer, but also effectively increase the luminous intensities of CaCO3:Eu3+ phosphors. The as-obtained phosphors may have potential applications in the fields of optical materials and functional polymer composite materials, such as plastics and rubbers.

PROPERTIES OF Eu3+ LUMINESCENCE IN THE MONOCLINIC Ba2MgSi2O7

Directory of Open Access Journals (Sweden)

Shansh an Yao

2011-09-01

Full Text Available Red-emitting phosphors Ba2-xMgSi2O7: Eux3+ was prepared by combustion-assisted synthesis method and an efficient red emission under near-ultraviolet (UV was observed. The luminescence and crystallinity were investigated using luminescence spectrometry and X-ray diffractometer. The emission spectrum shows that the most intense peak is located at 614 nm, which corresponds to the 5D0 → 7F2 transitions of Eu3+. The phosphor has two main excitation peaks located at 394 and 465 nm, which match the emission of UV and blue light-emitting diodes, respectively. The effect of Eu3+ concentration on the emission spectrum of Ba2MgSi2O7:Eu3+ phosphor was studied. The results showed that the emission intensity increased with increasing Eu3+ concentration, and then decreased because of concentration quenching. The critical quenching concentration of Eu3+ in Ba2MgSi2O7: Eu3+ phosphor is about 0.05 mol. The mechanism of concentration quenching of Ba2MgSi2O7: Eu3+ luminescence is energy transfer between Eu3+ ions casued by the dipole-dipole interaction.

Eu/Tb ions co-doped white light luminescence Y2O3 phosphors

International Nuclear Information System (INIS)

Tu Dong; Liang Yujun; Liu Rong; Li Daoyi

2011-01-01

Y 2 O 3 :Eu 3+ , Tb 3+ phosphors with white emission are prepared with different doping concentration of Eu 3+ and Tb 3+ ions and synthesizing temperatures from 750 to 950 deg. C by the co-precipitation method. The resulted phosphors were characterized by X-ray diffraction (XRD) and photoluminescence (PL) spectroscopy. The results of XRD indicate that the crystallinity of the synthesized samples increases with enhancing the firing temperature. The photoluminescence spectra indicate the Eu 3+ and Tb 3+ co-doped Y 2 O 3 phosphors show five main emission peaks: three at 590, 611 and 629 nm originate from Eu 3+ and two at 481 and 541 nm originate from Tb 3+ , under excitation of 250-320 nm irradition. The white light luminescence color could be changed by varying the excitation wavelength. Different concentrations of Eu 3+ and Tb 3+ ions were induced into the Y 2 O 3 lattice and the energy transfer from Tb 3+ →Eu 3+ ions in these phosphors was found. The Commission International de l'Eclairage (CIE) chromaticity shows that the Y 2 O 3 :Eu 3+ , Tb 3+ phosphors can obtain an intense white emission. - Highlights: → Novel phosphors Y 2 O 3 :Eu 3+ , Tb 3+ have been synthesized by co-precipitation method. → Samples emit white light with excellent color coordinates under UV excitation. → Luminescence color could be changed by varying the excitation wavelength. → Energy transfer from Tb 3+ →Eu 3+ ions in these phosphors was found.

Eu3+-doped β-Ga2O3 nanophosphors: annealing effect, electronic structure and optical spectroscopy.

Science.gov (United States)

Zhu, Haomiao; Li, Renfu; Luo, Wenqin; Chen, Xueyuan

2011-03-14

A comprehensive survey of electronic structure and optical properties of rare-earth ions-doped semiconductor is of vital importance for their potential applications. In this work, Eu(3+)-doped β-Ga(2)O(3) nanocrystals were synthesized via a combustion method. The evolution of the optical properties of nanophosphors with increasing the annealing temperature was investigated in detail by means of excitation and emission spectra at room temperature and 10 K. Eu(3+) ions were proved to be incorporated into the crystal lattice of the β-Ga(2)O(3) phase after annealing the as-prepared nanoparticles at 1100 °C. It was observed that the substitution of Eu(3+) for Ga(3+) occurred at merely single site, in spite of two crystallographically nonequivalent sites of Ga(3+) in β-Ga(2)O(3). Spectroscopic evidence corroborated and clarified the local symmetry of C(s) for Eu(3+) at this single site. From the high-resolution excitation and emission spectra, 71 crystal-field levels of Eu(3+) in β-Ga(2)O(3) were identified and analyzed in terms of 19 freely varied free-ions and crystal-field parameters based on C(s) symmetry. The standard deviation of the final fitting is as low as 12.9 cm(-1), indicating an excellent agreement between experimental and calculated energy levels. The temperature-dependent luminescence dynamics of the (5)D(0) multiplet for Eu(3+) in β-Ga(2)O(3) phosphors has also been revealed for the first time from 10 to 300 K.

Hydrothermal synthesis, characterization, and luminescence of Ca_2B_2O_5:RE (RE = Eu"3"+, Tb"3"+, Dy"3"+) nanofibers

International Nuclear Information System (INIS)

Yang, Li; Wan, Yingpeng; Li, Yuze; Pu, Yinfu; Huang, Yanlin; Chen, Cuili; Seo, Hyo Jin

2016-01-01

Ca_2B_2O_5:RE (RE = Eu"3"+, Tb"3"+, Dy"3"+) nanofibers were synthesized by the hydrothermal reaction method. The structural refinement was conducted on the base of the X-ray powder diffraction (XRD) measurements. The surface properties of the Ca_2B_2O_5:RE (RE = Eu"3"+, Tb"3"+, Dy"3"+) nanofibers were investigated by the measurements such as the scanning electron microscope (SEM), transmission electron microscope (TEM), and the energy dispersive spectrum (EDS). The nanofiber has a diameter of about 100 nm and a length of several micrometers. The luminescence properties such as photoluminescence excitation (PLE) and emission spectra (PL), decay lifetime, color coordinates, and the absolute internal quantum efficiency (QE) were reported. Ca_2B_2O_5:Eu"3"+ nanofibers show the red luminescence with CIE coordinates of (x = 0.41, y = 0.51) and the luminescence lifetime of 0.63 ms. The luminescence of Ca_2B_2O_5:Tb"3"+ nanofibers is green color (x = 0.29, y = 0.53) with the lifetime of 2.13 ms. However, Dy"3"+-doped Ca_2B_2O_5 nanofibers present a single-phase white-color phosphor with the fluorescence decay of 3.05 ms. Upon near-UV excitation, the absolute quantum efficiency is measured to be 65, 35, and 37 % for Eu"3"+-, Tb"3"+-, Dy"3"+-doped Ca_2B_2O_5 nanofibers, respectively. It is suggested that Ca_2B_2O_5:RE (RE = Eu"3"+, Tb"3"+, Dy"3"+) nanofibers could be an efficient phosphor for lighting and display.

Microstructural characterization of Al{sub 2}O{sub 3}: Eu with dosimetric purposes; Cracterizacion microestructural de Al{sub 2}O{sub 3}: Eu con fines dosimetricos

Energy Technology Data Exchange (ETDEWEB)

Mendoza A, D.; Espinosa P, M.E.; Gonzalez M, P.R. [ININ, 52045 Ocoyoacac, Estado de Mexico (Mexico); Rubio, E. [BUAP, Facultad de Ingenieria Quimica, 72570 Puebla (Mexico)

2004-07-01

In this work a microstructural analysis is presented, through Sem, EDS and XRD, of the alumina with Europium (Al{sub 2}O{sub 3}: Eu) synthesized by the sol gel method. According to those obtained results, a previous thermal treatment to 1000 C to the samples, induces the formation of the {gamma}-alumina phase for the samples that does not contain Eu; however when there is presence of this element, the {theta} alumina phase is obtained. Likewise, it was observed that the particle size is increased with the presence of Eu. When analyzing the thermoluminescent response (TL) induced by the gamma radiation, it was observed that the pure Al{sub 2}O{sub 3} presents an intense TL sign; while the Al{sub 2}O{sub 3}: Eu, the sign suffers a marked decrement. (Author)

The influence of Pr3+ co-doping on the photoluminescence and cathodoluminescence properties of SiO2:Eu3+/Tb3+

CSIR Research Space (South Africa)

Mhlongo, GH

2011-07-01

Full Text Available Tb3+-Pr3+, and Eu3+-Pr3+ ion pairs co-doped in a SiO2 matrix were prepared by a sol-gel method. Co-doping of Eu3+ and Tb3+ ions with Pr3+ in SiO2 resulted in the quenching of Eu3+ and Tb3+ emissions with increasing Pr3+ concentrations. The quenching...

Modelling Eu(III) speciation in a Eu(III)/PAHA/α-Al2O3 ternary system

International Nuclear Information System (INIS)

Janot, Noemie; Reiller, Pascal E.; Benedetti, Marc F.

2013-01-01

In this work, modelling of Eu(III) speciation in a ternary system, i.e., in presence of purified Aldrich humic acid (PAHA) and α-Al 2 O 3 , is presented. First, the mineral surface charge is measured by potentiometric titrations and then described using the CD-MUSIC model. This model is also used to describe Eu(III) binding to the α-Al 2 O 3 surface at different pH values, ionic strength and mineral concentrations. Time resolved luminescence spectroscopy (TRLS) is then used to study the binding of Eu(III) to PAHA at pH 4 with different humic acid concentrations. The spectra are used to calculate a spectroscopic 'titration curve', used to determine Eu(III)/PAHA binding parameters in the NICA-Donnan model. Following a previous study (Janot et al., Water Res. 46, 731-740), modelling of the ternary system is based upon the definition of two PAHA pools where one fraction remains in solution and the other is adsorbed onto the mineral surface, with each possessing different proton and metal binding parameters. The modification of protonation behaviour for both fractions is examined using spectrophotometric titrations of the non adsorbed PAHA fraction at different organic/mineral ratios. These data are then used to describe Eu(III) interactions in the ternary system: Eu(III) re-partitioning in the ternary system is calculated for different pH, ionic strength and PAHA concentrations, and results are compared to experimental observations. The model is in good agreement with experimental data, except at high PAHA fractionation rates. Results show that organic complexation dominates over a large pH range, with the predominant species existing as the surface-bound fraction. Above pH 8, Eu(III) seems to be mostly complexed to the mineral surface, which is in agreement with previous spectroscopic observations (Janot et al., Environ. Sci. Technol. 45, 3224-3230). (authors)

Photoluminescence properties of a novel red phosphor Sr{sub 3}Ga{sub 2}O{sub 5}Cl{sub 2}:Eu{sup 3+}

Energy Technology Data Exchange (ETDEWEB)

Wang, Zhonghua; Hu, Yihua; Zhang, Shaoan; Lin, Jun [Guangdong University of Technology, School of Physics and Optoelectronic Engineering, Guangzhou (China)

2016-02-15

Eu{sup 3+}-doped Sr{sub 3}Ga{sub 2}O{sub 5}Cl{sub 2} phosphors were synthesized successfully via a two-step solid-state reaction method. Phase purity and morphology of the phosphor were confirmed by XRD and SEM techniques. In the excitation spectra of Sr{sub 3}Ga{sub 2}O{sub 5}Cl{sub 2}:Eu{sup 3+} phosphor, the broad excitation band centering at 310 nm is due to the combination of charge transfer from Eu{sup 3+}→O{sup 2-} and host absorption. And it matches well the emission wavelength from UV LEDs. Sr{sub 3}Ga{sub 2}O{sub 5}Cl{sub 2}:Eu{sup 3+} phosphors show a bright orange-red luminescence under excitation with 301 nm. However, concentration quenching of Eu{sup 3+} in Sr{sub 3}Ga{sub 2}O{sub 5}Cl{sub 2}:Eu{sup 3+} occurs at a low content of 0.07 in this work. The quenching mechanism of Sr{sub 3}Ga{sub 2}O{sub 5}Cl{sub 2}:Eu{sup 3+} was discussed in detail on the basis of the experimental results. (orig.)

Completing the series. New coordination networks of composition {sup 3}{sub ∞}[RE{sub 2}(ADC){sub 3}(H{sub 2}O){sub 6}].2H{sub 2}O with RE = Pr, Nd, Sm, Eu, Tb, Dy, Ho, Er, Y and ADC{sup 2-} = acetylenedicarboxylate ({sup -}O{sub 2}C-C≡C-CO{sub 2}{sup -})

Energy Technology Data Exchange (ETDEWEB)

Gramm, Verena K.; Schuy, Andrea; Ruschewitz, Uwe [Institut fuer Anorganische Chemie, Koeln Univ. (Germany); Suta, Markus; Wickleder, Claudia [Anorganische Chemie, Universitaet Siegen (Germany); Sternemann, Christian [Fakultaet Physik / DELTA, Technische Universitaet Dortmund (Germany)

2018-02-01

The crystal structures of {sup 3}{sub ∞}[RE{sub 2}(ADC){sub 3}(H{sub 2}O){sub 6}].2H{sub 2}O (RE = Pr, Nd, Sm, Eu, Tb, Dy) were solved and refined from X-ray single crystal data. They crystallize in a structure type already known for RE = La, Ce and Gd (P1, no. 2, Z = 2), which is characterized by REO{sub 9} polyhedra forming dimeric units being the nodes of a 3D framework structure linked by ADC{sup 2-} anions ({sup -}O{sub 2}C-C≡C-CO{sub 2}{sup -} = acetylenedicarboxylate). From synchrotron powder diffraction data it was shown that isostructural coordination networks are formed for RE = Ho, Er, Y, whereas for RE = Tm, Yb, Lu a new structure type crystallizing in a highly complex crystal structure with a large orthorhombic unit cell is found. All compounds are obtained by slow evaporation of an aqueous solution containing RE(OAc){sub 3}.xH{sub 2}O and acetylenedicarboxylic acid (H{sub 2}ADC). The coordination networks of composition {sup 3}{sub ∞}[RE{sub 2}(ADC){sub 3}(H{sub 2}O){sub 6}].2H{sub 2}O were thoroughly investigated by thermal analysis and for RE = Eu, Tb, a strong red and green photoluminescence was observed and investigated by means of UV/Vis spectroscopy. (copyright 2018 WILEY-VCH Verlag GmbH and Co. KGaA, Weinheim)

Efficiencies of Eu{sup 3+} ions and hydrogen atoms as donors in ZnO thin films

Energy Technology Data Exchange (ETDEWEB)

Akazawa, Housei, E-mail: akazawa.housei@lab.ntt.co.jp [NTT Device Innovation Center, NTT Corporation, 3-1 Morinosato Wakamiya, Atsugi, Kanagawa 243-0198 (Japan)

2016-09-15

The donor efficiencies of Eu{sup 3+} ions and hydrogen atoms in ZnO crystalline films were investigated with reference to that of Ga{sup 3+} ions. It was found that Eu{sup 3+} ions acted as extrinsic donors in ZnO:Eu films, yielding a resistivity of 1.8 × 10{sup −3} Ω cm at a doping level of 1 at. %. This value is comparable to one for intrinsic donors in undoped ZnO films. The conductivity was maintained as the deposition temperature was increased to 200 °C, and this is evidence for the contribution of extrinsic donors. Deposition of Ga-doped and Eu-doped ZnO films in an H{sub 2}O gas flow produced oxyhydrogenated ZnO:(Ga, H) and ZnO:(Eu, H) films in which the Ga{sup 3+} and Eu{sup 3+} donors were deactivated by oxidization. Nevertheless, hydrogen donors contributed to electrical conduction yielding a resistivity of 1 × 10{sup −2} Ω cm. Postannealing in an H{sub 2} gas ambient alleviated the excessive oxidization of the films and thereby reactivated the donor action of Ga{sup 3+} and Eu{sup 3+} ions, causing the resistivity to recover to 10{sup −3} Ω cm for ZnO:(Ga, H) and 10{sup −2} Ω cm for ZnO:(Eu, H). In contrast, vacuum annealing of ZnO:(Ga, H) and ZnO:(Eu, H) films increased resistivity through removal of hydrogen donors while not affecting the oxidized condition of the samples.

A highly triflated rare-earth ion in [Eu(O_3SCF_3)_8]"5"-

International Nuclear Information System (INIS)

Bruns, Joern; Kluener, Thorsten; Kraeuter, Jessica; Wickleder, Mathias S.; Krueger, Sascha; Adlung, Matthias; Wickleder, Claudia; Niehaus, Oliver; Poettgen, Rainer

2015-01-01

The reaction of Eu_2O_3 with fuming nitric acid, trifluormethanesulfonic acid, and its anhydride in torch-sealed glass ampoules at 120 C gave the europium compound (NO)_5[Eu(O_3SCF_3)_8] (orthorhombic, Fddd, Z=16, a=1932.69(4), b=2878.44(7), c=2955.12(7) pm, V=16439.7(7) Aa"3). The compound exhibits the [Eu(O_3SCF_3)_8]"5"- anion showing for the first time a lanthanide ion that is exclusively coordinated by eight triflate anions. The anion has been further investigated by DFT calculations, which also allowed clear assignment of the vibrational spectra. Moreover, magnetochemical and luminescence measurements gave additional insight into the properties of this complex. The luminescence spectra revealed that the Eu"3"+ ions are in a pseudo D_4_d symmetric environment. (copyright 2015 WILEY-VCH Verlag GmbH and Co. KGaA, Weinheim)

Structural and optical characterization of Eu3+ doped beta-Ga2O3 nanoparticles using a liquid-phase precursor method.

Science.gov (United States)

Kim, Moung-O; Kang, Bongkyun; Yoon, Daeho

2013-08-01

Eu3+ doped beta-Ga2O3 and non-doped beta-Ga2O3 nanoparticles were synthesized at 800 degrees C using a liquid-phase precursor (LPP) method, with different annealing times and Eu3+ ion concentrations. Eu3+ doped beta-Ga2O3 nanoparticles showed broad XRD peaks, revealing a second phase compared with the non-doped beta-Ga2O3 nanoparticles. The cathode luminescence (CL) spectra of beta-Ga2O3 and Eu3+ doped beta-Ga2O3 nanoparticles showed a broad band emission (300-500 nm) of imperfection and two component emissions. The luminescence quenching properties of Eu3+ dopant ion concentration appeared gradually beyond 5 mol% in our investigation.

Effect of structure, particle size and relative concentration of Eu3+ and Tb3+ ions on the luminescence properties of Eu3+ co-doped Y2O3:Tb nanoparticles

International Nuclear Information System (INIS)

Mukherjee, S; Sudarsan, V; Vatsa, R K; Tyagi, A K; Godbole, S V; Kadam, R M; Bhatta, U M

2008-01-01

Eu 3+ co-doped Y 2 O 3 :Tb nanoparticles were prepared by the combustion method and characterized for their structural and luminescence properties as a function of annealing temperatures and relative concentration of Eu 3+ and Tb 3+ ions. For Y 2 O 3 :Eu,Tb nanoparticles annealed at 600 and 1200 deg. C, variation in the relative intensity of excitation transitions between the 7 F 6 ground state and low spin and high spin 4f 7 5d 1 excited states of Tb 3+ is explained due to the combined effect of distortion around Y 3+ /Tb 3+ in YO 6 /TbO 6 polyhedra and the size of the nanoparticles. Increase in relative intensity of the 285 nm peak (spin-allowed transition denoted as peak B) with respect to the 310 nm peak (spin-forbidden transition denoted as peak A) with decrease of Tb 3+ concentration in the Y 2 O 3 :Eu,Tb nanoparticles heated at 1200 deg. C is explained based on two competing effects, namely energy transfer from Tb 3+ to Eu 3+ ions and quenching among the Tb 3+ ions. Back energy transfer from Tb 3+ to Eu 3+ in these nanoparticles is found to be very poor

Nd(BrO3)3-Yb(BrO3)3-H2O and Nd2(SeO4)3-Yb2(SeO4)3-H2O systems at 25 deg C

International Nuclear Information System (INIS)

Serebrennikov, V.V.; Batyreva, V.A.; Tsybukova, T.N.

1981-01-01

Using the methods of isothermal solubility the Nd(BrO 3 ) 3 - Yb(BrO 3 ) 3 -H 2 O and Nd 2 (SeO 4 ) 3 -Yb 2 (SeO 4 ) 3 -H 2 O systems are studied at 25 deg C. The compositions of the solid phases are determined by the method of ''residues''. The formation of two series of solid solutions in both systems is established. Besides, there is a crystallization region of Nd 2 (SeO 4 ) 3 in the system of selenates. The solubility diagrams of the systems are presented [ru

Solubility limit and luminescence properties of Eu{sup 3+} ions in Al{sub 2}O{sub 3} powder

Energy Technology Data Exchange (ETDEWEB)

Onishi, Yuya; Nakamura, Toshihiro, E-mail: tnakamura@gunma-u.ac.jp; Adachi, Sadao, E-mail: adachi@gunma-u.ac.jp

2016-08-15

Al–Eu–O compounds are synthesized from Al{sub 2}O{sub 3}:Eu{sub 2}O{sub 3}=(1–x):x mixtures (x=0–0.15) by the metal organic decomposition method and subsequently calcined at various temperatures from T{sub c}=750 to 1200 °C in dry O{sub 2} atmosphere. The structural and luminescence properties of these compounds are investigated using X-ray diffraction analysis, photoluminescence (PL) analysis, PL excitation spectroscopy, and luminescence lifetime measurements. The present study focuses on the effects of the Eu{sub 2}O{sub 3} addition (x) on the material and phosphor properties of Al{sub 2}O{sub 3}:Eu{sup 3+}. The stable phase of α-Al{sub 2}O{sub 3} is synthesized at T{sub c}>1100 °C and cubic γ-Al{sub 2}O{sub 3} phase at T{sub c}≤1100 °C. The calcination temperature dependence of the PL intensity yields an activation of E{sub a}~0.8 eV for Eu{sup 3+} ions in the Al{sub 2}O{sub 3} host. The luminescence decay time is determined to be ~0.8 ms, independent of x. Temperature dependence of the PL intensity at T=20–450 K exhibits thermal quenching behavior with energies of 17 meV and 0.28 eV at low (<200 K) and high temperatures (>200 K), respectively. The solubility limit of Eu{sup 3+} ions in α-Al{sub 2}O{sub 3} is determined to be ~1%. The schematic energy-level diagram of Eu{sup 3+} in α-Al{sub 2}O{sub 3} is also proposed for the sake of a better understanding of the luminescence process of this phosphor system.

Heat Treatment Effect on Eu3+ Doped TeO2-BaO-Bi2O3 Glass Systems with Ag Nanoparticles

Directory of Open Access Journals (Sweden)

Tomasz Lewandowski

2017-01-01

Full Text Available Glass systems of 73TeO2-4BaO-3Bi2O3-2Eu2O3-xAg (in molar ratio where x = 0, 1, 2, and 3 compositions have been successfully synthesized. Silver nanoparticles were obtained with the employment of heat treatment (HT procedure executed at 350°C. Glass transition temperatures of different compositions have been determined through DSC measurements. XRD results presented characteristic amorphous halo indicating lack of long range order in the samples. FTIR structural studies revealed that glass matrix is mainly composed of TeO3 and TeO4 species and is stable after different applied heat treatment times. X-ray photoelectron spectroscopy (XPS measurements confirmed that in selected samples part of Ag ions changed oxidation state to form Ag0 species. TEM measurements revealed nanoparticles of size in the range of 20–40 nm. UV-vis absorption results demonstrated characteristic transitions of Eu3+ ions. Additionally, UV-vis spectra of samples heat-treated for 6, 12, 24, and 48 hours presented bands related to silver nanoparticles. Photoluminescence (PL studies have been performed with excitation wavelength of λexc=395 nm. Obtained spectra exhibited peaks due to 5D0-7FJ (where J=2,3,4 and 5D1-7FJ (where J=1,2,3 transitions of Eu3+. Moreover, luminescence measurement indicated enhancement of rare earth ions emissions in several of the annealed samples. Increase of emission intensity of about 35% has been observed.

Structure of LaH(PO3H)2.3H2O

International Nuclear Information System (INIS)

Loukili, M.; Durand, J.; Larbot, A.; Cot, L.; Rafiq, M.

1991-01-01

Lanthanum hydrogen bis(hydrogenphosphite) trihydrate, LaH(Po 3 H) 2 .3H 2 O, M r =353.8, monoclinic, P2 1 /c, a=9.687 (3), b=7.138 (2), c=13.518 A, β=104.48 (3) deg, V=905.0 (5) A 3 , Z=4, D m =2.56 (2), D x =2.598 Mg m -3 , λ(MoKα)=0.71073 A, μ(MoKα)=5.103 mm -1 , F(000)=672, T=300 K, R=0.032 for 1018 independent observed reflections. The structure contains two phosphite anions connected by a hydrogen bond. The La 3+ cation is eight coordinated by seven O atoms from phosphite anions and one O atom of a water molecule. (orig.)

Synthesis and tunable luminescent properties of Eu-doped Ca2NaSiO4F – Coexistence of the Eu2+ and Eu3+ centers

Directory of Open Access Journals (Sweden)

Mubiao Xie

Full Text Available Novel phosphors Ca2NaSiO4F:Eu were synthesized successfully by the conventional solid-state method in CO atmosphere, and their spectroscopic properties in UV−vis region were investigated. The photoluminescence properties show that Eu3+ ions were partially reduced to Eu2+ in Ca2NaSiO4F. As a result of radiation and re-absorption energy transfer from Eu2+ to Eu3+, both Eu2+ bluish-green emission at around 520 nm and Eu3+ red emission are observed in the emission spectra under the n-UV light excitation. Furthermore, the ratio between Eu2+ and Eu3+ emissions varies with increasing content of overall Eu. Because relative intensity of the red component from Eu3+ became systematically stronger, white light emission can be realized by combining the emission of Eu2+ and Eu3+ in a single host lattice under n-UV light excitation. These results indicate that the Ca2NaSiO4F:Eu phosphors have potential applications as a n-UV convertible phosphor for light-emitting diodes. Keywords: Phosphors, Luminescence, White LED, Optical materials

Investigation of structural and optical properties of CaTiO3 powders doped with Mg2+ and Eu3+ ions

International Nuclear Information System (INIS)

Oliveira, Larissa H.; Savioli, Julia; Moura, Ana P. de; Nogueira, Içamira C.; Li, Maximo S.; Longo, Elson; Varela, José A.; Rosa, Ieda L.V.

2015-01-01

In this work, CaTiO 3 powders doped with Mg 2+ ions and CaTiO 3 powders co-doped with Mg 2+ and Eu 3+ ions were prepared by the polymeric precursor method (PPM). These powders were characterized by different characterization techniques to study the influence of Mg 2+ doping as well as Mg 2+ and Eu 3+ co-doping in structural and optical properties of CaTiO 3 perovskite-type structure. The Rietveld refinement and Micro-Raman analyses suggested the substitution Mg 2+ and Eu 3+ ions in the A-site of CaTiO 3 perovskite. The influence of Mg 2+ doping can be detected by the displacement of calcium and oxygen atomic positions when compared to the non-doped CaTiO 3 powder. When Eu 3+ ions are added to the A-site of this perovskite the excess of positive charge can be compensated by the formation of calcium vacancies. Luminescence data showed that Ca 1-x Mg x TiO 3 and Ca 1x Mg x/2 Eu 2y/3 TiO 3 powders are potential materials for fabrication of lighting devices based on near-UV and blue LED using an excitation wavelength of 397 and/or 450 nm. - Highlights: • CaTiO 3 co-doped with Mg 2+ and Eu 3+ were obtained by the Polymeric Precursor Method. • Incorporation of Mg 2+ and Eu 3+ ions in the CaTiO 3 lattice. • Enhancement of the Eu 3+ photoluminescence

Synthesis and optical properties of red/blue-emitting Sr2MgSi2O7:Eu3+/Eu2+ phosphors for white LED

Directory of Open Access Journals (Sweden)

Tong Thi Hao Tam

2016-06-01

Full Text Available Phosphor-converted white light emitting diodes (white LEDs have received great attention in recent years since they have several excellent features such as high lumen output, low power consumption, long lifetime and environmentally friendly. In this work, we report the co-precipitation synthesis of red/blue Sr2MgSi2O7:Eu3+/Eu2+ phosphors with various Eu doping concentration. The results show that the obtained Sr2MgSi2O7:Eu3+/Eu2+ phosphors have good crystallinity and emit strong red (Sr2MgSi2O7:Eu3+ and blue (Sr2MgSi2O7:Eu2+ emissions under near UV light excitation. The sharp emission peaks at 577, 590, 612, 653, and 701 nm corresponded to the typical 5D0 → 7Fj (j = 0,1,2,3,4 transitions of Eu3+, and the blue emission peaking at 460 nm is attributed to the typical 4f65d1-4f7 transition of Eu2+ in the same Sr2MgSi2O7 host lattice. Both phosphors can be well excited in the wavelength range of 260–400 nm where the near UV-LED is well matched. The above results suggest that the Sr2MgSi2O7:Eu3+/Eu2+ phosphors are promising red/blue-emitting phosphors for the application in near UV pumped phosphor-converted white LEDs.

Experimental and theoretical study of pure and doped crystals: Gd2O2S, Gd2O2S:Eu3+ and Gd2O2S:Tb3+

Science.gov (United States)

Wang, Fei; Chen, Xiumin; Liu, Dachun; Yang, Bin; Dai, Yongnian

2012-08-01

Quantum chemistry and experimental method were used to study on pure and doped Gd2O2S crystals in this paper. The band structure and DOS diagrams of pure and doped Gd2O2S crystals which calculated by using DFT (Density Functional Theory) method were illustrated to explain the luminescent properties of impurities in crystals. The calculations of the crystal structure were finished by using the program of CASTEP (Cambridge Sequential Total Energy Package). The samples showed the characteristic emissions of Tb3+ ions with 5D4-7FJ transitions and Eu3+ ions with 5D0-7FJ transitions which emit pure green luminescence and red luminescence respectively. The experimental excitation spectra of Tb3+ and Eu3+ doped Gd2O2S are in agreement of the DOS diagrams over the explored energy range, which has allowed a better understanding of different luminescence mechanisms of Tb3+ and Eu3+ in Gd2O2S crystals.

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.

Preparation and properties of multifunctional Fe-C-Y2O3:Eu3+ nanocomposites

International Nuclear Information System (INIS)

Yang Jingxing; Yang Xuwei; Yang Hua

2012-01-01

Highlights: ► Multifunctional Fe/Fe 3 O 4 -Y 2 O 3 : Eu nanocomposites were prepared by a solvothermal method. ► Their structure, magnetic and luminescent properties were characterized by XRD, SEM, TEM, excitation and emission spectra and vibration sample magnetometry (VSM). ► It is shown that the nanocomposites exhibit high saturation magnetization and strong red emission under UV-light. - Abstract: Multifunctional Fe-C-Y 2 O 3 :Eu 3+ nanocomposites were prepared by the solvo thermal method, and their structure, magnetic and luminescent properties were characterized by X-ray diffraction (XRD), vibrating sample magnetometer (VSM) and scanning electron microscope (SEM). Results show that the nanocomposites are spherical with a mean diameter of 700 nm and there are high special saturation magnetization (47.4 emu/g) and strong red emission under UV-light. Even dispersed in water solution, the nanocomposites also exhibit a strong red emission under ultraviolet light radiation, and it could be manipulated using an external magnet. Thus it looks promising for application in biomedicine field, especially in drug targeting and fluorescence label. And we also discussed the effect of the electron transfer process between the Fe magnetic core and Y 2 O 3 :Eu 3+ shell.

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.

Influence of annealing temperature on structural and optical properties of Lu{sub 2}O{sub 3}:Eu{sup 3+}, Tb{sup 3+} transparent films

Energy Technology Data Exchange (ETDEWEB)

Morales-Ramírez, Ángel de Jesús [Instituto Politécnico Nacional, CIITEC IPN, Cerrada de Cecati S/N, 02250 México D.F. (Mexico); García-Murillo, Antonieta, E-mail: angarciam@ipn.mx [Instituto Politécnico Nacional, CIITEC IPN, Cerrada de Cecati S/N, 02250 México D.F. (Mexico); Carrillo-Romo, Felipe de Jesús [Instituto Politécnico Nacional, CIITEC IPN, Cerrada de Cecati S/N, 02250 México D.F. (Mexico); Garrido-Hernández, Aristeo [Instituto Politécnico Nacional, CIITEC IPN, Cerrada de Cecati S/N, 02250 México D.F. (Mexico); Universidad Tecnológica de Tecámac, División de Nanotecnología, Carretera Federal México- Pachuca Km 37.5, Sierra Hermosa, 55740, Edo. De México (Mexico); García-Hernández, Margarita [Universidad Autónoma Metropolitana, Departamento de Ciencias Naturales, Unidad Cuajimalpa, Pedro Antonio de los Santos 84, 11850 México D.F. (Mexico)

2015-10-15

Highlights: • Lu{sub 2}O{sub 3}:Eu{sup 3+}, Tb{sup 3+} films were synthesized by sol–gel and by dip-coating technique. • Effects of annealing treatment on structural and optical properties were studied. • Optogeometrical characteristics of synthesized films were analyzed. • X-ray diffraction results showed that Lu{sub 2}O{sub 3}:Eu{sup 3+}, Tb{sup 3+} crystallizes at 700 °C. • High reddish emission on transparent films with at least 1 μm thick was observed. - Abstract: High-optical quality Lu{sub 2}O{sub 3}:Eu{sup 3+} 5 mol%, X Tb{sup 3+} (X = 0–0.04 mol%) thin films were prepared by the sol–gel process and dip-coating technique. The procedure was as follows: lutetium, europium and terbium nitrates were used as precursors, and ethanol as a solvent. Etylenglycol (EG) was added as a sol stabilizer, and the pH was adjusted by acetic acid. After 10 dipping-cycles, followed by an annealing process (600–900 °C) for 1 h, transparent, smooth and crack-free films (ra = 8–9 nm) were formed. The X-ray diffraction (XRD) results showed crystallized films into the cubic structure at 800 °C. The ellipsometry results showed that the thickness of the films varied from 1 to 1.4 μm at 1000 and 600 °C, respectively. Finally, the films presented a typical Eu{sup 3+} red emission at 611 nm ({sup 5}D{sub 0} → {sup 7}F{sub 2}); furthermore, the effect of the Tb{sup 3+} content showed that the highest emission intensity corresponded to the lower Tb{sup 3+} content.

Technology and optical characterization of luminophore coordination compounds Eu(o-MBA)3Phen and NC PEPC/Eu(o-MBA)3Phen

Science.gov (United States)

Bordian, Olga; Verlan, Victor; Culeac, Ion; Iovu, Mihail; Zubareva, Vera

2016-12-01

Were obtained a new nanocomposite (NC) based on poly N-epoxy prolyl carbazol (PEPC) and the coordination compound luminophore Eu(o-MBA)3Phen, where o-MBA is o- methylbenzoic acid and Phen - phenanthroline. Nanocrystals of Eu(o-MBA)3Phen with the dimensions 50 nm were uniformly incorporated into the PEPC polymer matrix with various concentrations. The absorption spectra of coordination compounds and thin layers of NC PEPC/Eu(o-MBA)3Phen revealed 1 intensive absorption bands at 2.02 eV. Photoluminescence (PL) spectra showed an intense red luminescence at 578 - 699 nm, which is assigned to the transitions 4D0->7Fi (i= 0,1,2 3 4) in the 4f-shell of the Eu3+ ion.

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.

Li{sub 3}Gd{sub 3}Te{sub 2}O{sub 12}:Eu{sup 3+}- an intense red phosphor for solid state lighting applications

Energy Technology Data Exchange (ETDEWEB)

Tiwari, Hansnath [Department of Chemistry, Indian Institute of Technology Madras, Chennai 600036 (India); Asiri Naidu, S. [Department of Chemistry, Rajiv Gandhi University of Knowledge Technologies, Nuzvid, Andhra Pradesh 521202 (India); Varadaraju, U.V., E-mail: varada@iitm.ac.in [Department of Chemistry, Indian Institute of Technology Madras, Chennai 600036 (India)

2017-02-15

Li{sub 3}Gd{sub 3−3x}Eu{sub 3x}Te{sub 2}O{sub 12} (x=0.05−1.0) phases with garnet structure were synthesized by high temperature solid state reaction and the photoluminescence properties were investigated. The appearance of bands due to intra 4 f transitions of Gd{sup 3+} in the excitation spectra recorded by monitoring the 612 nm emission line of the activator indicates Gd{sup 3+}→Eu{sup 3+} energy transfer in this host lattice. Under 395 nm excitation, the electric dipole transition is predominant in the emission spectrum of Eu{sup 3+} and is in agreement with the C{sub 2} point group (noncentrosymmetric) of the EuO{sub 8} polyhedron. The critical concentration of the Eu{sup 3+} activator in this series was found to be 0.6 (x=0.2) above which, concentration quenching occurs. The emission intensity of the phosphor composition, Li{sub 3}Gd{sub 2.4}Eu{sub 0.6}Te{sub 2}O{sub 12} is ~4 times that of the commercial sample of Y{sub 2}O{sub 3}:Eu{sup 3+} phosphor. - Highlights: • New Eu{sup 3+} doped garnet. • Intense electric dipole emission. • Gd{sup 3+}→Eu{sup 3+} energy transfer.

Enhanced photoluminescence and thermal stability of divalent ions (Zn2+, Mg2+) assisted CaTiO3:Eu3+ perovskite phosphors for lighting applications

Science.gov (United States)

Singh, Dhananjay Kumar; Manam, J.

2018-03-01

Current study proposes the improved red emission of Zn2+ and Mg2+ ions incorporated CaTiO3:Eu3+ phosphors synthesized via the well-known solid-state reaction method. Under the 397 nm UV excitation, the Zn2+- and Mg2+-incorporated CaTiO3:0.15Eu3+ phosphor having orthorhombic structure with space group Pbnm exhibited an intense red emission at 619 nm. This can be credited to the hypersensitive 5D0 → 7F2 transition of Eu3+ ions, which is also indicative of the fact that the Eu3+ ions populated the non-inversion symmetry sites in the CaTiO3 lattices. The optimized composition CaTiO3:0.15Eu3+, 0.20Zn2+ and CaTiO3:0.15Eu3+, 0.10Mg2+ phosphors, pronounces in a magnificent enhancement of PL intensity by 5.5 and 2.5 times, respectively, as compared to CaTiO3:0.15 Eu3+ phosphor. From the temperature-dependent emission spectra, ΔEa were enunciated to be 0.101 and 0.086 eV for CaTiO3:0.15Eu3+, 0.20Zn2+ and CaTiO3:0.15Eu3+, 0.10Mg2+ phosphors, respectively, for thermal quenching. In addition, it can be better understood as related to the adequate thermal stability of 60% even at 450 and 420 K, respectively. Furthermore, the Judd-Ofelt theory was used to study the radiative intensity parameters of Eu3+ ions in the CaTiO3 lattices. The experimental results incited the bright prospects of synthesized ceramics as a promising candidate for lighting applications.

Structural, photoluminescent and photocatalytic properties of TiO{sub 2}:Eu{sup 3+} coatings formed by plasma electrolytic oxidation

Energy Technology Data Exchange (ETDEWEB)

Stojadinović, Stevan, E-mail: sstevan@ff.bg.ac.rs [University of Belgrade, Faculty of Physics, Studentski trg 12–16, Belgrade 11000 (Serbia); Radić, Nenad; Grbić, Boško [University of Belgrade, Institute of Chemistry, Technology and Metallurgy, Department of Catalysis and Chemical Engineering, Njegoševa 12, Belgrade 11000 (Serbia); Maletić, Slavica [University of Belgrade, Faculty of Physics, Studentski trg 12–16, Belgrade 11000 (Serbia); Stefanov, Plamen [Institute of General and Inorganic Chemistry, Bulgarian Academy of Sciences, Acad. G. Bonchev Str., Block 11, Sofia 1113 (Bulgaria); Pačevski, Aleksandar [University of Belgrade, Faculty of Mining and Geology, Đušina 7, 11000 Belgrade (Serbia); Vasilić, Rastko [University of Belgrade, Faculty of Physics, Studentski trg 12–16, Belgrade 11000 (Serbia)

2016-05-01

Graphical abstract: - Highlights: • TiO{sub 2}:Eu{sup 3+} coatings are formed by plasma electrolytic oxidation (PEO). • Photoluminescence is related to transitions of Eu{sup 3+} from level {sup 5}D{sub 0} to levels {sup 7}F{sub J}. • Eu{sup 3+} ions occupy non-inversion symmetry sites in the coatings. • PEO time is an important factor affecting photocatalytic activity. - Abstract: In this paper, we used plasma electrolytic oxidation (PEO) of titanium in water solution containing 10 g/L Na{sub 3}PO{sub 4}·12H{sub 2}O + 2 g/L Eu{sub 2}O{sub 3} powder for preparation of TiO{sub 2}:Eu{sup 3+} coatings. The surfaces of obtained coatings exhibit a typical PEO porous structure. The energy dispersive X-ray spectroscopy analysis showed that the coatings are mainly composed of Ti, O, P, and Eu; it is observed that Eu content in the coatings increases with PEO time. The X-ray diffraction analysis indicated that the coatings are crystallized and composed of anatase and rutile TiO{sub 2} phases, with anatase being the dominant one. X-ray photoelectron spectroscopy revealed that Ti 2p spin-orbit components of TiO{sub 2}:Eu{sup 3+} coatings are shifted towards higher binding energy, with respect to pure TiO{sub 2} coatings, suggesting that Eu{sup 3+} ions are incorporated into TiO{sub 2} lattice. Diffuse reflectance spectroscopy showed that TiO{sub 2}:Eu{sup 3+} coatings exhibit evident red shift with respect to the pure TiO{sub 2} coatings. Photoluminescence (PL) emission spectra of TiO{sub 2}:Eu{sup 3+} coatings are characterized by sharp emission bands in orange–red region ascribed to f–f transitions of Eu{sup 3+} ions from excited level {sup 5}D{sub 0} to lower levels {sup 7}F{sub J} (J = 0, 1, 2, 3, and 4). The excitation PL spectra of TiO{sub 2}:Eu{sup 3+} coatings can be divided into two regions: the broad band region from 250 nm to 350 nm associated with charge transfer state of Eu{sup 3+} and the series of sharp peaks in the range from 350 nm to 550 nm

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.

Synthesis and thermoluminescence behavior of ZrO2:Eu3+ with variable concentration of Eu3+ doped phosphor

Directory of Open Access Journals (Sweden)

Raunak Kumar Tamrakar

2014-10-01

Full Text Available Cubical ZrO2 phosphor doped with the europium synthesized by conventional solid state synthesis method. The prepared phosphor was characterized by X-ray diffraction (XRD technique, field emission gun scanning electron microscopy (FEGSEM and transmission electron microscopy (TEM. In this paper, we focused on the thermoluminescence glow curves and kinetic parameters, activation energy, order of kinetics, and the frequency factor of ZrO2:Eu3+ phosphor under different doses of UV irradiations at a heating rate of 6.7 °C/s. The kinetic parameters activation energy E, the order of kinetics b, and the frequency factor s of synthesized phosphor of ZrO2:Eu3+ have been calculated by using a peak shape method.

Phase stabilization in transparent Lu2O3:Eu ceramics by lattice expansion

Science.gov (United States)

Seeley, Z. M.; Dai, Z. R.; Kuntz, J. D.; Cherepy, N. J.; Payne, S. A.

2012-11-01

Gadolinium lutetium oxide transparent ceramics doped with europium (Gd,Lu)2O3:Eu were fabricated via vacuum sintering and hot isostatic pressing (HIP). Nano-scale starting powder with the composition GdxLu1.9-xEu0.1O3 (x = 0, 0.3, 0.6, 0.9, 1.0, and 1.1) were uniaxially pressed and sintered under high vacuum at 1625 °C to obtain ˜97% dense structures with closed porosity. Sintered compacts were then subjected to 200 MPa argon gas at temperatures between 1750 and 1900 °C to reach full density. It was observed that a small portion of the Eu3+ ions were exsolved from the Lu2O3 cubic crystal lattice and concentrated at the grain boundaries, where they precipitated into a secondary monoclinic phase creating optical scattering defects. Addition of Gd3+ ions into the Lu2O3 cubic lattice formed the solid solution (Gd,Lu)2O3:Eu and stretched the lattice parameter allowing the larger Eu3+ ions to stay in solid solution, reducing the secondary phase and improving the transparency of the ceramics. Excess gadolinium, however, resulted in a complete phase transformation to monoclinic at pressures and temperatures sufficient for densification. Light yield performance was measured and all samples show equal amounts of the characteristic Eu3+ luminescence, indicating gadolinium addition had no adverse effect. This material has potential to improve the performance of high energy radiography devices.

Light emission efficiency and imaging performance of Lu{sub 2}O{sub 3}:Eu nanophosphor under X-ray radiography conditions: Comparison with Gd{sub 2}O{sub 2}S:Eu

Energy Technology Data Exchange (ETDEWEB)

Seferis, I. [Faculty of Chemistry, Wroclaw University, 14F Joliot-Curie Street, 50-383 Wroclaw (Poland); Department of Medical Physics, Medical School, University of Patras, 265 00 Patras (Greece); Michail, C.; Valais, I. [Department of Biomedical Engineering, Technological Educational Institute of Athens, 122 10 Athens (Greece); Zeler, J. [Faculty of Chemistry, Wroclaw University, 14F Joliot-Curie Street, 50-383 Wroclaw (Poland); Liaparinos, P.; Fountos, G.; Kalyvas, N.; David, S. [Department of Biomedical Engineering, Technological Educational Institute of Athens, 122 10 Athens (Greece); Stromatia, F. [Department of Radiology and Nuclear Medicine, “IASO” General Hospital, Mesogion 264, 15562 Holargos (Greece); Zych, E. [Faculty of Chemistry, Wroclaw University, 14F Joliot-Curie Street, 50-383 Wroclaw (Poland); Kandarakis, I., E-mail: kandarakis@teiath.gr [Department of Biomedical Engineering, Technological Educational Institute of Athens, 122 10 Athens (Greece); Panayiotakis, G. [Department of Medical Physics, Medical School, University of Patras, 265 00 Patras (Greece)

2014-07-01

Nanocrystallic europium-activated lutetium oxide (Lu{sub 2}O{sub 3}:Eu) is a strong candidate for use in digital medical imaging applications, due to its spectroscopic and structural properties. The aim of the present study was to investigate the imaging and efficiency properties of a 33.3 mg/cm{sup 2} Lu{sub 2}O{sub 3}:Eu scintillating screen coupled to a high resolution RadEye HR CMOS photodetector under radiographic imaging conditions. Since Lu{sub 2}O{sub 3}:Eu emits light in the red wavelength range, the light emission efficiency and the imaging performance were compared with results for a Gd{sub 2}O{sub 2}S:Eu phosphor screen. Parameters such as the Absolute Efficiency (AE), the X-ray Luminescence Efficiency (XLE), and the Detector Quantum Gain (DQG), were investigated. The imaging characteristics of Lu{sub 2}O{sub 3}:Eu nanophosphor screen were investigated in terms of the Modulation Transfer Function (MTF), the Normalized Noise Power Spectrum (NNPS) and the Detective Quantum Efficiency (DQE). It was found that Lu{sub 2}O{sub 3}:Eu nanophosphor has higher AE and XLE by a factor of 1.32 and 1.37 on average, respectively, in the whole radiographic energy range in comparison with the Gd{sub 2}O{sub 2}S:Eu screen. DQG was also found higher in the energy range from 50 kVp to 100 kVp and comparable thereafter. The imaging quality of Lu{sub 2}O{sub 3}:Eu nanophosphor coupled to the CMOS sensor was found to outmatch in any aspect in comparison with the Gd{sub 2}O{sub 2}S:Eu screen. These results indicate that Lu{sub 2}O{sub 3}:Eu nanophosphor could be considered for further research in order to be used in medical imaging applications. - Highlights: • AE and XLE of Lu{sub 2}O{sub 3}:Eu nanophosphor were higher by a factor of 1.32 and 1.37 than Gd{sub 2}O{sub 2}S:Eu. • DQG was higher from 50 to 100 kVp and comparable thereafter. • Imaging performance of Lu{sub 2}O{sub 3}:Eu/CMOS was better than that of Gd{sub 2}O{sub 2}S:Eu/CMOS.

Structural and luminescent study of TeO2-BaO-Bi2O3-Ag glass system doped with Eu3+ and Dy3+ for possible color-tunable phosphor application

Science.gov (United States)

Lewandowski, Tomasz; Seweryński, Cezary; Walas, Michalina; Łapiński, Marcin; Synak, Anna; Sadowski, Wojciech; Kościelska, Barbara

2018-05-01

Tellurite glass systems of 73TeO2-4BaO-3Bi2O3-1Ag:xEu2O3-(2-x)Dy2O3 (where x = 0.5, 1, 1.5, 2 in molar ratio) composition have been successfully synthesized. In order to acquire Ag nanoparticles, materials have been heat treated at 350 °C in the air atmosphere. Structural properties of obtained samples were evaluated with various techniques. X-Ray Diffraction (XRD) measurements indicated that obtained materials are amorphous in nature. UV-vis results presented transitions characteristic to Dy3+ and Eu3+ ions. Additionally, X-Ray Photoelectron Spectroscopy (XPS) analysis indicated the presence of silver in metallic form. Photoluminescence measurements shown influence of Ag nanoparticles on emission characteristics. Simultaneous emission of Dy3+ and Eu3+ has been observed when samples were excited with λexc = 390 nm. Change of the emission color induced by heat treatment has been observed and described in case of x = 1 glass series. According to CIE results emission color changes as Eu/Dy ratio and heat treatment time are changed. Emission shifts from reddish-orange to yellowish white color. Obtained photoluminescence results confirm that synthesized materials are good candidates for color tunable phosphors.

Host-sensitized luminescence properties in CaNb2O6:Ln(3+) (Ln(3+) = Eu(3+)/Tb(3+)/Dy(3+)/Sm(3+)) phosphors with abundant colors.

Science.gov (United States)

Li, Kai; Liu, Xiaoming; Zhang, Yang; Li, Xuejiao; Lian, Hongzhou; Lin, Jun

2015-01-05

A series of Ln(3+) (Ln(3+) = Eu(3+)/Tb(3+)/Dy(3+)/Sm(3+)) ion doped CaNb2O6 (CNO) phosphors have been prepared via the conventional high-temperature solid-state reaction route. The X-ray diffraction (XRD) and structure refinement, diffuse reflection, photoluminescence (PL), and fluorescent decay curves were used to characterize the as-prepared samples. Under UV radiation, the CNO host present a broad emission band from about 355 to 605 nm centered around 460 nm originating from the NbO6 octahedral groups, which has spectral overlaps with the excitation of f-f transitions of Eu(3+)/Tb(3+)/Dy(3+)/Sm(3+) in CNO:Eu(3+)/Tb(3+)/Dy(3+)/Sm(3+) samples. They show both host emission and respective emission lines derived from the characteristic f-f transitions of activators, which present different emission colors owing to the energy transfer from the NbO6 group in the host to Eu(3+)/Tb(3+)/Dy(3+)/Sm(3+) with increasing activator concentrations. The decreases of decay lifetimes of host emissions in CNO:Eu(3+)/Tb(3+)/Dy(3+)/Sm(3+) demonstrate the energy transfer from the hosts to Eu(3+)/Tb(3+)/Dy(3+)/Sm(3+). The energy transfer mechanisms in CNO:Eu(3+)/Tb(3+)/Dy(3+) phosphors have been determined to be a resonant type via dipole-dipole mechanisms. For CNO:Sm(3+), the metal-metal charge transfer transition (MMCT) might contribute to the different variations of decay lifetimes and emission intensity from CNO:Eu(3+)/Tb(3+)/Dy(3+) samples. The best quantum efficiency is 71.2% for CNO:0.01/0.02Dy(3+). The PL properties of as-prepared materials indicate the promising application in UV-pumped white-emitting lighting diodes field.

Hydrothermal synthesis of Gd{sub 2}O{sub 3}:Eu{sup 3+} nanophosphors: Effect of surfactant on structural and luminescence properties

Energy Technology Data Exchange (ETDEWEB)

Dhananjaya, N., E-mail: dhanu.siri@yahoo.co.in [B.S. Narayan Centre of Excellence for Advanced Materials, B.M.S. Institute of Technology, Bangalore 560 064 (India); Department of Physics, B.M.S. Institute of Technology, Bangalore 560 064 (India); Nagabhushana, H., E-mail: bhushanvlc@gmail.com [Prof. C.N.R. Rao Centre for Advanced Materials, Tumkur University, Tumkur 572 103 (India); Sharma, S.C. [B.S. Narayan Centre of Excellence for Advanced Materials, B.M.S. Institute of Technology, Bangalore 560 064 (India); Department of Mechanical Engineering, B.M.S. Institute of Technology, Bangalore 560 064 (India); Rudraswamy, B. [Department of Physics, J.B. Campus, Bangalore University, Bangalore 560 056 (India); Shivakumara, C. [Solid State and Structural Chemistry Unit, Indian Institute of Science, Bangalore 560 012 (India); Nagabhushana, B.M. [Department of Chemistry, M.S. Ramaiah Institute of Technology, Bangalore 560 054 (India)

2014-02-25

Highlights: • Gd(OH){sub 3}:Eu{sup 3+}, GdOOH:Eu{sup 3+} and Gd{sub 2}O{sub 3}:Eu{sup 3+} phases were prepared by hydrothermal method. • Phosphors were well characterized by XRD, SEM, TEM, Raman, UV–Vis, FT-IR. • Cubic Gd{sub 2}O{sub 3}:Eu{sup 3+} show intense red emission, which was highly useful for photonics application. • HDA surfactant plays an important role in conversion of cubic to hexagonal phases. -- Abstract: Various morphologies of Eu{sup 3+} activated gadolinium oxide have been prepared by hydrothermal method using hexadecylamine (HDA) as surfactant at different experimental conditions. The powder X-ray diffraction studies reveal as-formed product is hexagonal Gd(OH){sub 3}:Eu{sup 3+} phase and subsequent heat treatment at 350 and 600 °C transforms to monoclinic GdOOH:Eu{sup 3+} and cubic Gd{sub 2}O{sub 3}:Eu{sup 3+} phases respectively. SEM pictures of without surfactant show irregular shaped rods along with flakes. However, in the presence of HDA surfactant, the particles are converted into rods of various sizes. The temperature dependent morphological evolution of Gd{sub 2}O{sub 3}:Eu{sup 3+} without and with HDA surfactant is studied. TEM micrographs of Gd(OH){sub 3}:Eu{sup 3+} sample with HDA confirms smooth nanorods with various diameters in the range 20–100 nm. FTIR studies reveal that HDA surfactant plays an important role in conversion of cubic to hexagonal phases. Among these three phases, cubic phase Gd{sub 2}O{sub 3}:Eu{sup 3+} (λ{sub ex} = 254 nm) show red emission at 612 nm corresponding to {sup 5}D{sub 0} → {sup 7}F{sub 2} and is more efficient host than the monoclinic counterpart. The band gap for hexagonal Gd(OH){sub 3}:Eu{sup 3+} is more when compared to monoclinic GdOOH:Eu{sup 3+} and cubic Gd{sub 2}O{sub 3}:Eu{sup 3+}.

Effect of annealing on luminescence of Eu{sup 3+}- and Sm{sup 3+}-doped Mg{sub 2}TiO{sub 4} nanoparticles

Energy Technology Data Exchange (ETDEWEB)

Medić, Mina; Antić, Željka; Đorđević, Vesna [University of Belgrade, Vinča Institute of Nuclear Sciences, P.O. Box 522, 11001 Belgrade (Serbia); Ahrenkiel, Phillip S. [South Dakota School of Mines & Technology, Rapid City, SD (United States); Marinović-Cincović, Milena [University of Belgrade, Vinča Institute of Nuclear Sciences, P.O. Box 522, 11001 Belgrade (Serbia); Dramićanin, Miroslav D., E-mail: dramican@vinca.rs [University of Belgrade, Vinča Institute of Nuclear Sciences, P.O. Box 522, 11001 Belgrade (Serbia)

2016-02-15

This work explores the influence of annealing temperature on the structure and luminescence of 2 at% Eu{sup 3+} and 1 at% Sm{sup 3+}-doped Mg{sub 2}TiO{sub 4} nanopowders produced via Pechini-type polymerized complex route. Mg{sub 2}TiO{sub 4} samples were annealed at 7 different temperatures (400 °C, 450 °C, 500 °C, 550 °C, 600 °C, 650 °C and 700 °C) to determine the temperature range in which cubic inverse spinel structure is stable and to follow the changes of material luminescence properties. X-ray diffraction revealed that crystallization of both Eu{sup 3+} and Sm{sup 3+}-doped Mg{sub 2}TiO{sub 4} nanopowders starts at 400 °C, and that Sm{sup 3+} doped Mg{sub 2}TiO{sub 4} starts to decompose at 650 °C, while Eu{sup 3+} doped Mg{sub 2}TiO{sub 4} starts to decompose at 700 °C. Samples annealed at higher temperatures show higher crystallinity and larger crystallite size. Mg{sub 2}TiO{sub 4} powder annealed at 600 °C is composed of ~5 nm size nanoparticles agglomerated in micron-size and dense chunks. The emission spectra of nanoparticles are composed of emissions from defects in Mg{sub 2}TiO{sub 4} host and characteristic emissions of Eu{sup 3+} ({sup 5}D{sub 0}→{sup 7}F{sub J}) and Sm{sup 3+} ({sup 4}G{sub 5/2}→{sup 6}H{sub J}) ions. The stronger emission and longer emission decays are observed with samples annealed at high temperatures. In the case of the Eu{sup 3+} ions emission intensity increased one order of magnitude between samples annealed at 400 °C and 650 °C. - Highlights: • Mg{sub 2}TiO{sub 4} nanoparticles of 5–10 nm in size are prepared by polymerized complex route. • Emission spectra and decays of Eu{sup 3+} and Sm{sup 3+} doped Mg{sub 2}TiO{sub 4} nanoparticles are shown. • Eu{sup 3+}(Sm{sup 3+}) doped Mg{sub 2}TiO{sub 4} can be annealed at temperatures <700 °C (650 °C). • Emission intensity of nanoparticles increases with increase of annealing temperature.

Electrochemical behaviours of Eu(III/E(II and Ce(IV/Ce(III in H3PO4-H2O media : solvation and complexation reactions

Directory of Open Access Journals (Sweden)

Belqat B.

2018-01-01

Full Text Available Many kinds of rare earth elements (REE such as europium and cerium have been make them essential elements in many high-tech components. The electrochemical studies can be presented as an interesting indication for europium and cerium extraction from phosphoric solutions, including solvation and complexation reactions. The normal redox potentials of Eu3+/Eu2+ and Ce4+/Ce3+ systems have been determined in H3PO4-H2O media with various phosphoric acid concentration. The solvation of these elements in phosphoric media is characterized by their transfer activity coefficients "f" calculated from the corresponding normal redox potentials. The corresponding solvation increases with increasing the H3PO4 concentration. For each REE, the electrochemical properties depend on its number of charges and on its basic properties. Results suggest that solvation and complexation of REE phosphates are important in controlling REE concentration.

Influence of hydroxybenzoic acids on the adsorption of Eu(III) onto α,γ-Al_2O_3 particles in mildly acidic conditions: A macroscopic and spectroscopic study

International Nuclear Information System (INIS)

Moreau, Pauline; Colette-Maatouk, Sonia; Gareil, Pierre; Reiller, Pascal E.

2016-01-01

The influence of hydroxybenzoic acids (HAH_n), namely p-hydroxybenzoic acid (4-hydroxybenzoic acid, HPhbH) and protocatechuic acid (3,4-dihydroxybenzoic acid, HProtoH_2), on the adsorption of europium(III) onto α,γ-Al_2O_3 particles is studied as a function of acid concentration. After measuring the adsorption edge of the Eu(III)/α,γ-Al_2O_3 binary system, and using the previously studied binary component system Eu(III)/HAH_n—Moreau et al. (2015) Inorg. Chim. Acta432, 81—, and HAH_n/α,γ-Al_2O_3—Moreau et al. (2013) Colloids Surf. A435, 97—, it is evidenced that HPhbH does not enhance Eu(III) adsorption onto α,γ-Al_2O_3 in the Eu(III)/HPhbH/α,γ-Al_2O_3 ternary system. Conversely, HProtoH_2 enhances Eu(III) adsorption onto α,γ-Al_2O_3 in the Eu(III)/HProtoH_2/α,γ-Al_2O_3 ternary system. Adsorption of the acids are also found higher in the Eu(III)/acid/α,γ-Al_2O_3 ternary systems as compared with the corresponding binary systems assessing synergetic effects. For high HPhbH concentrations, a ternary surface species involving ≡AlOH surface sites, Eu(III), and PhbH"– is evidenced by time-resolved luminescence spectroscopy (TRLS). However, in the Eu(III)/HProtoH_2/α,γ-Al_2O_3 ternary system, chemical environment of Eu(III) is found to be very close to that in the Eu(III)/HProtoH_2 binary system. Ternary surface species could not be evidenced in the Eu(III)/HProtoH_2/α,γ-Al_2O_3 ternary system with TRLS because of the very short decay time of Eu(III) in the presence of protocatechuic acid. - Highlights: • Adsorption in the Eu(III) – hydroxybenzoic acid – alumina system is studied. • Adsorption is quantified and luminescence parameters are obtained independently. • Synergistic effect of organic acids adsorption are evidenced in the ternary systems. • A ternary species is clearly shown for the p-hydrobenzoic acid.

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

Phase transformation, morphology evolution and luminescence property variation in Y{sub 2}O{sub 3}: Eu hollow microspheres

Energy Technology Data Exchange (ETDEWEB)

Wang, Qin; Guo, Jing; Jia, Wenjing; Liu, Baocang [College of Chemistry and Chemical Engineering, Inner Mongolia University, Hohhot (China); Zhang, Jun, E-mail: cejzhang@sina.com [College of Chemistry and Chemical Engineering, Inner Mongolia University, Hohhot (China)

2012-11-25

Highlights: Black-Right-Pointing-Pointer We report a general and facile method for the synthesis of Y{sub 2}O{sub 3}: Eu hollow microspheres. Black-Right-Pointing-Pointer This method may be of great significance in the synthesis of many other hollow spherical materials. Black-Right-Pointing-Pointer Phase, morphology and luminescence property were found to be strongly dependent on temperature and pH. Black-Right-Pointing-Pointer The evolution process under various temperatures and pH values were discussed. Black-Right-Pointing-Pointer The sample shows a strong red emission under short UV irradiation, and the lifetime is determined to be 7.0 ms. - Abstract: Y{sub 2}O{sub 3}: Eu hollow microspheres with average size of 500-600 nm have been successfully synthesized via a solvothermal method in the presence of sodium citrate as surfactant followed by a subsequent heat treatment process. High polymer F127(EO{sub 106}PO{sub 70}EO{sub 106}) served as a soft template in the formation of as prepared hollow microspheres. It is found that the pH values and the reaction temperature are two crucial factors in determining the phase, morphology and luminescence properties of the Y{sub 2}O{sub 3}: Eu hollow microspheres. Morphology evolution can be achieved by changing the pH and the reaction temperature. The properties of the Eu{sup 3+}-doped Y{sub 2}O{sub 3}: Eu nanocrystals were characterized by XRD, FE-SEM, HR-TEM and UV-vis spectroscopy.

Photoluminescence and thermoluminescence properties of Eu2+ doped and Eu2+ ,Dy3+ co-doped Ba2 MgSi2 O7 phosphors.

Science.gov (United States)

Sao, Sanjay Kumar; Brahme, Nameeta; Bisen, D P; Tiwari, Geetanjali

2016-11-01

In this work, we report the preparation, characterization, comparison and luminescence mechanisms of Eu 2 + -doped and Eu 2 + ,Dy 3 + -co-doped Ba 2 MgSi 2 O 7 (BMSO) phosphors. Prepared phosphors were synthesized via a high temperature solid-state reaction method. All prepared phosphors appeared white. The phase structure, particle size, and elemental analysis were analyzed using X-ray diffraction (XRD), transmission electron microscopy (TEM) and energy-dispersive X-ray (EDX) analysis. The luminescence properties of the phosphors were investigated by thermoluminescence (TL) and photoluminescence (PL). The PL excitation and emission spectra of Ba 2 MgSi 2 O 7 :Eu 2 + showed the peak to be around 381 nm and 490 nm respectively. The PL excitation spectrum of Ba 2 MgSi 2 O 7 :Eu 2 + Dy 3 + showed the peak to be around 341 nm and 388 nm, and the emission spectrum had a broad band around 488 nm. These emissions originated from the 4f 6 5d 1 to 4f 7 transition of Eu 2 + . TL analysis revealed that the maximum TL intensity was found at 5 mol% of Eu 2 + doping in Ba 2 MgSi 2 O 7 phosphors after 15 min of ultraviolet (UV) light exposure. TL intensity was increased when Dy 3 + ions were co-doped in Ba 2 MgSi 2 O 7 :Eu 2 + and maximum TL intensity was observed for 2 mol% of Dy 3 + . TL emission spectra of Ba 1.95 MgSi 2 O 7 :0.05Eu 2 + and Ba 1.93 MgSi 2 O 7 :0.05Eu 2 + ,0.02Dy 3 + phosphors were found at 500 nm. TL intensity increased with UV exposure time up to 15 min, then decreased for the higher UV radiation dose for both Eu doping and Eu,Dy co-doping. The trap depths were calculated to be 0.54 eV for Ba 1.95 MgSi 2 O 7 :0.05Eu 2 + and 0.54 eV and 0.75 eV for Ba 1.93 MgSi 2 O 7 :0.05Eu 2 + ,0.02Dy 3 + phosphors. It was observed that co-doping with small amounts of Dy 3 + enhanced the thermoluminescence properties of Ba 2 MgSi 2 O 7 phosphor. Copyright © 2016 John Wiley & Sons, Ltd. [Correction added on 5 April 2016, after first online publication: The

Luminescent and magnetic properties of Fe{sub 3}O{sub 4}@SiO{sub 2}:phen:Eu{sup 3+}

Energy Technology Data Exchange (ETDEWEB)

Silva, Raphael Lucas de Sousa; Figueiredo, Alberthmeiry Teixeira de; Barrado, Cristiano Morita, E-mail: alberth@ufg.br [Universidade Federal de Goiás (UFG), Catalão, GO (Brazil). Departamento de Química; Sousa, Marcelo Henrique [Universidade de Brasília (UnB), DF (Brazil). Faculdade de Ceilândia

2017-10-15

Magnetite was doped with rare earth ions (europium) to produce core-shell materials with both magnetic and luminescent properties, i.e., a magnetic Fe{sub 3}O{sub 4} oxide core and a SiO{sub 2} :phen:Eu{sup 3+} shell. The resulting material was analyzed by X-ray powder diffraction and transmission electron microscopy, and subjected to magnetic and luminescence emission measurements. All the synthesized materials exhibited superparamagnetic behavior and luminescence emission. The magnetic behavior of Fe{sub 3}O{sub 4} and luminescence emission of SiO{sub 2} :phen:Eu{sup 3+} of the materials were compared to precursors. (author)

Optimized photoluminescence of SrB 2O 4:Eu 3+ red-emitting phosphor by charge compensation

Science.gov (United States)

Zhao, Lai-Shi; Liu, Jie; Wu, Zhan-Chao; Kuang, Shao-Ping

2012-02-01

A novel red-emitting phosphor, SrB 2O 4:Eu 3+, was synthesized by high temperature solid-state reaction and its photoluminescence properties were studied. The emission spectrum consists of four major emission bands. The emission peaks are located at 593, 612, 650 and 703 nm, corresponding to the 5D0 → 7F1, 5D0 → 7F2, 5D0 → 7F3 and 5D0 → 7F4 typical transitions of Eu 3+, respectively. The effects of Eu 3+ doping content and charge compensators (Li +, Na +, K +) on photoluminescence of SrB 2O 4:Eu 3+ phosphor were studied. The results show that the emission intensity can be affected by above factors and Na + is the optimal charge compensator for SrB 2O 4:Eu 3+. The photoluminescence of NaSrB 2O 4:Eu 3+ was compared with that of Y 2O 2S:Eu 3+. It implies that SrB 2O 4:Eu 3+ is a good candidate as a red-emitting phosphor pumped by near-ultraviolet (NUV) InGaN chip for fabricating white light-emitting diodes (WLEDs).

Core shell structured nanoparticles of Eu3+ doped SnO2 with SiO2 shell: luminescence studies

International Nuclear Information System (INIS)

Ningthoujam, R.S.; Sudarsan, V.; Kulshreshtha, S.K.

2005-01-01

Re dispersible SnO 2 nanoparticles with and without Eu 3+ doping nanoparticles were prepared at 185 deg C by the urea hydrolysis of Sn 4+ in ethylene glycol medium. X-ray diffraction and 119 Sn MAS NMR studies of these particles revealed that these nanoparticles are crystalline with Cassiterite structure having an average crystallite size of 7 nm. Undoped SnO 2 gave a emission peak centered around 470 nm characteristic of the traps present in the nanoparticles. For Eu 3+ doped samples, emission around 590 and 615 nm was observed on both direct excitation as well as indirect excitation through traps, indicating that there is an energy transfer between the traps present in the nanoparticles and Eu 3+ ions. The asymmetric ratio of luminescence (relative intensity ratio of 590 to 615 nm transitions) has been found to be 1.2. For SnO 2 :Eu(5%)-SiO 2 nanoparticles, the asymmetric ratio of luminescence change significantly indicating the formation of nanoparticles with SnO 2 :Eu(5%) core covered with SiO 2 shell. (author)

Preparation and Scintillating Properties of Sol-Gel Eu3+, Tb3+ Co-Doped Lu2O3 Nanopowders

Directory of Open Access Journals (Sweden)

Joel Moreno Palmerin

2011-09-01

Full Text Available Nanocrystalline Eu3+, Tb3+ co-doped Lu2O3 powders with a maximum size of 25.5 nm were prepared by the sol-gel process, using lutetium, europium and terbium nitrates as precursors, and ethanol as a solvent. Differential thermal analysis (DTA and infrared spectroscopy (IR were used to study the chemical changes during the xerogel annealing. After the sol evaporation at 100 °C, the formed gel was annealed from 300 to 900 °C for 30 min under a rich O2 atmosphere, and the yielded product was analyzed by X-ray diffraction (XRD to characterize the microstructural behavior and confirm the crystalline structure. The results showed that Lu2O3 nanopowders start to crystallize at 400 °C and that the crystallite size increases along with the annealing temperature. A transmission electron microscopy (TEM study of samples annealed at 700 and 900 °C was carried out in order to analyze the microstructure, as well as the size, of crystallites. Finally, in regard to scintillating properties, Eu3+ dopant (5 mol%, Tb3+ codoped Lu2O3 exhibited a typical red emission at 611 nm (Do→7F2, furthermore, the effect of Tb3+ molar content (0.01, 0.015 and 0.02% mol on the Eu3+ radioluminiscence was analyzed and it was found that the higher emission intensity corresponds to the lower Tb3+ content.

Luminescent properties of red-emitting LiSr4B3O(9−3x/2)Nx:Eu2+ phosphor for white-LEDs

International Nuclear Information System (INIS)

Yu Hua; Deng Degang; Xu Shiqing; Yu Cuiping; Yin Haoyong; Nie Qiulin

2012-01-01

An Eu 2+ -activated oxynitride LiSr (4−y) B 3 O (9−3x/2) N x :yEu 2+ red-emitting phosphor was synthesized by solid-state reactions. The synthesized phosphor crystallized in a cubic system with space group Ia–3d. The LiSr 4 B 3 O (9−3x/2) N x :Eu 2+ phosphors exhibited a broad red emission band with a peak at 610 nm and a full width at half maximum of 106 nm under 410 nm excitation, which is ascribed to the 4f 6 5d 1 →4f 7 transition of Eu 2+ . The optimal doped nitrogen concentration was observed to be x=0.75. The average decay times of two different emission centers were estimated to be 568 and 489 ns in the LiSr 3.99 B 3 O 8.25 N 0.5 :0.01Eu 2+ phosphors, respectively. Concentration quenching of Eu 2+ ions occurred at y=0.07, and the critical distance was determined as 17.86 Å. The non-radiative transitions via dipole–dipole interactions resulted in the concentration quenching of Eu 2+ -site emission centers in the LiSr 4 B 3 O 9 host. These results indicate LiSr 4 B 3 O (9−3x/2) N x :Eu 2+ phosphor is promising for application in white near-UV LEDs. - Highlights: ► An oxynitride LiSr 4 B 3 O 9 N:Eu 2+ red-emitting phosphor was prepared at low synthesis temperature. ► The introduced nitrogen improved the excitation and emission intensity of the phosphor. ► The wide excitation band matches well with near-UV LED chips. ► The emission spectrum of the phosphor showed a broad full width at half maximum of about 106 nm.

Formation, cationic site exchange and surface structure of mechanosynthesized EuCrO{sub 3} nanocrystalline particles

Energy Technology Data Exchange (ETDEWEB)

Widatallah, H M; Al-Harthi, S H; Gismelseed, A M; Al-Rawas, A D [Department of Physics, Sultan Qaboos University, PO Box 36, 123, Muscat (Oman); Johnson, C; Moore, E A [School of Chemistry and Analytical Sciences, The Open University, Milton Keynes, MK7 6AA (United Kingdom); Klencsar, Z [Chemical Research Center, Hungarian Academy of Sciences, 1025 Budapest (Hungary); Wynter, C I [Nassau Community College, Garden City, NY 11530-6793 (United States); Brown, D E, E-mail: hishammw@squ.edu.om, E-mail: hisham@ictp.it [Department of Physics, Northern Illinois University, De Kalb, IL 60115 (United States)

2011-07-06

Nanocrystalline EuCrO{sub 3} particles ({approx}25 nm) have been prepared by pre-milling a 1 : 1 molar mixture of Eu{sub 2}O{sub 3} and Cr{sub 2}O{sub 3} for 60 h followed by sintering at 700 {sup 0}C (12 h). This temperature is {approx}500-600 {sup 0}C lower than those at which the material, in bulk form, is conventionally prepared. Rietveld analysis of the x-ray powder diffraction pattern of the EuCrO{sub 3} nanoparticles favours a structural model involving a slight degree of cationic exchange where {approx}11% of the Eu{sup 3+} and Cr{sup 3+} ions exchange their normal dodecahedral A- and octahedral B-sites, respectively, in the perovskite-related structure. This cationic site exchange, which is unusual in a perovskite structure, has been well supported by the corresponding room-temperature {sup 151}Eu Moessbauer spectrum of the nanoparticles that in addition to displaying a distribution in the principal component of the EFG tensor (V{sub zz}) at the usual A-sites of the {sup 151}Eu nuclei, also revealed the presence of a subcomponent with {approx}11% area fraction and a considerably increased |V{sub zz}| value that was associated with Eu{sup 3+} ions at octahedral B-sites. X-ray photoelectron and Auger electron spectroscopic techniques reveal a complex surface structure where extremely thin layers of un-reacted Eu{sub 2}O{sub 3} and Cr{sub 2}O{sub 3} cover most of the EuCrO{sub 3} nanoparticles' surfaces together with some traces of elemental Cr. The binding energies associated with Eu{sup 3+} 3d{sub 5/2}, Eu{sup 3+} 4d{sub 3/2}, Cr{sup 3+} 2p{sub 3/2} and O{sup 2-} 1s core-level electrons in EuCrO{sub 3} are estimated from the x-ray photoelectron data for the first time.

Luminescence and energy transfer properties of Eu{sup 3+} and Gd{sup 3+} in ZrO{sub 2}

Energy Technology Data Exchange (ETDEWEB)

Villabona-Leal, E.G. [Posgrado en Ciencias Aplicadas, Facultad de Ciencias, Universidad Autónoma de San Luis Potosí. Av. Salvador Nava, 078290 San Luis Potosí (Mexico); Diaz-Torres, L.A.; Desirena, H. [Grupo de Espectroscopia de Materiales Avanzados y Nanoestrcuturados (EMANA), Centro de Investigaciones en Óptica, A. P.1-948, Gto. 37150 León (Mexico); Rodríguez-López, J.L. [División de Materiales Avanzados, Instituto Potosino de Investigación Científica y Tecnológica, A.C., Camino Presa San José, Lomas 4a Secc, 78216 San Luis Potosí (Mexico); Pérez, Elías [Instituto de Física, Universidad Autónoma de San Luis Potosí, Alvaro Obregón 64, 78000 San Luis Potosí (Mexico); Meza, Octavio, E-mail: omeza@ifuap.buap.mx [Instituto de Física, Benemérita Universidad Autónoma de Puebla, Apartado Postal J-48, Puebla 72570 (Mexico)

2014-02-15

Red luminescence emission in ZrO2:Gd{sup 3+}–Eu{sup 3+} nanocrystal under 250 nm radiation excitation is achieved. These materials exhibit a tetragonal phase that is retained by the presence of lanthanide ions. Thus, a study of the optical properties as a function of the dopant concentration was been carried out without the deleterious effects of having segregation of other crystalline phases. We analyze the emission and lifetime curves as a function of dopant concentration through a rate equation simulation, finding an excellent fitting. As results, the nonradiative and radiative relaxation constants, as well as a quantitative estimation of the energy transfer processes among Eu{sup 3+}, Gd{sup 3+} and O{sup 2−} ions are reported for the first time. The proposed model can be extended (or applicable) to explain the fluorescence dynamics in other nanomaterials doped with Eu{sup 3+} and Gd{sup 3+} under UV excitation. -- Highlights: • ZrO{sub 2} nanocrystal exhibits a tetragonal phase in the presence of Eu and Gd dopants. • Emission and lifetimes as a function of dopant concentration were analyzed by rate equation model. • Quantitative estimation of the energy transfer processes among Eu{sup 3+}, Gd{sup 3+} and O{sup 2−} ions are reported.

Synthesis and characterization of (3-Aminopropyl)trimethoxy-silane (APTMS) functionalized Gd2O3:Eu(3+) red phosphor with enhanced quantum yield.

Science.gov (United States)

Jain, Akhil; Hirata, G A; Farías, M H; Castillón, F F

2016-02-12

We report the surface modification of nanocrystalline Gd2O3:Eu(3+) phosphor by (3-Aminopropyl)trimethoxysilane (APTMS). The nanoparticles were first coated with silica using the Stöber process, and then annealed at 650 °C for 2 h. Afterwards, APTMS was functionalized onto the silica layer to obtain Gd2O3:Eu(3+) nanoparticles bearing amine groups on the surface. The effect of silica coating, and the subsequent annealing process on the crystallization of the nanophosphor were analyzed by x-ray diffraction (XRD). High-resolution transmission electron microscopy (HR-TEM) confirmed the presence of a silica layer of ∼45 nm thickness. X-ray photoelectron (XPS) and Fourier transform infrared (FTIR) spectroscopy confirmed the presence of silica and the amine groups. Photoluminescence (PL) analysis demonstrated an increased emission after functionalization of nanoparticles. Absolute quantum yield (QY) measurements revealed an 18% enhancement in QY in functionalized nanoparticles compared with unmodified nanoparticles, which is of great importance for their biomedical applications.

Synthesis and characterization of (3-Aminopropyl)trimethoxy-silane (APTMS) functionalized Gd2O3:Eu3+ red phosphor with enhanced quantum yield

Science.gov (United States)

Jain, Akhil; Hirata, G. A.; Farías, M. H.; Castillón, F. F.

2016-02-01

We report the surface modification of nanocrystalline Gd2O3:Eu3+ phosphor by (3-Aminopropyl)trimethoxysilane (APTMS). The nanoparticles were first coated with silica using the Stöber process, and then annealed at 650 °C for 2 h. Afterwards, APTMS was functionalized onto the silica layer to obtain Gd2O3:Eu3+ nanoparticles bearing amine groups on the surface. The effect of silica coating, and the subsequent annealing process on the crystallization of the nanophosphor were analyzed by x-ray diffraction (XRD). High-resolution transmission electron microscopy (HR-TEM) confirmed the presence of a silica layer of ∼45 nm thickness. X-ray photoelectron (XPS) and Fourier transform infrared (FTIR) spectroscopy confirmed the presence of silica and the amine groups. Photoluminescence (PL) analysis demonstrated an increased emission after functionalization of nanoparticles. Absolute quantum yield (QY) measurements revealed an 18% enhancement in QY in functionalized nanoparticles compared with unmodified nanoparticles, which is of great importance for their biomedical applications.

Synthesis and characterization of (3-Aminopropyl)trimethoxy-silane (APTMS) functionalized Gd2O3:Eu3+ red phosphor with enhanced quantum yield

International Nuclear Information System (INIS)

Jain, Akhil; Hirata, G A; Farías, M H; Castillón, F F

2016-01-01

We report the surface modification of nanocrystalline Gd 2 O 3 :Eu 3+ phosphor by (3-Aminopropyl)trimethoxysilane (APTMS). The nanoparticles were first coated with silica using the Stöber process, and then annealed at 650 °C for 2 h. Afterwards, APTMS was functionalized onto the silica layer to obtain Gd 2 O 3 :Eu 3+ nanoparticles bearing amine groups on the surface. The effect of silica coating, and the subsequent annealing process on the crystallization of the nanophosphor were analyzed by x-ray diffraction (XRD). High-resolution transmission electron microscopy (HR-TEM) confirmed the presence of a silica layer of ∼45 nm thickness. X-ray photoelectron (XPS) and Fourier transform infrared (FTIR) spectroscopy confirmed the presence of silica and the amine groups. Photoluminescence (PL) analysis demonstrated an increased emission after functionalization of nanoparticles. Absolute quantum yield (QY) measurements revealed an 18% enhancement in QY in functionalized nanoparticles compared with unmodified nanoparticles, which is of great importance for their biomedical applications. (paper)

IR and Raman spectra of LaH(SeO3)2 and FeH(SeO3)2

International Nuclear Information System (INIS)

Ratheesh, R.; Suresh, G.; Nayar, V.U.; Morris, R.E.

1995-01-01

The infrared and Raman spectra of LaH(SeO 3 ) 2 and FeH(SeO 3 ) 2 crystals are recorded and analysed. Bands confirm the coexistence of HSeO 3 - and SeO 3 2- ions in both LaH(SeO 3 ) 2 and FeH(SeO 3 ) 2 crystals. The Se-OH stretching vibrations are observed to be at lower wavenumbers in LaH(SeO 3 ) 2 than that in the iron compound in agreement with the short O-O distance in the former. Observed bands indicate that the SeO 3 2- ions are more angularly distorted in FeH(SeO 3 ) 2 crystal. ABC bands, characteristic of strong hydrogen bonded systems are observed in the infrared spectra of both the crystals. (author). 15 refs., 2 figs., 1 tab

Fabrication and properties of highly luminescent materials from Tb(OH)3-SiO2 and Tb(OH)3-SiO2:Eu3+ nanotubes

International Nuclear Information System (INIS)

Tran Thu Huong; Tran Kim Anh; Le Quoc Minh

2009-01-01

Luminescent nanomaterials with one-dimensional (1D) structures have attracted much attention due to their unique properties and potential applications in nanophotonics and nanobiophotonics. In this paper, we report a synthesis of terbium - hydroxide - at - silica Tb(OH) 3 -SiO 2 and Tb(OH) 3 -SiO 2 :Eu 3+ nanotubes. Terbium - hydroxide tubes were synthesized by soft template method. The size of the tubes can be controlled precisely and have outer diameters ranging from 80 to 120 nm, wall thickness of about 30 nm, and lengths ranging from 300 to 800 nm. To fabricate core/shell materials, the seed growth method is used. FESEM, X-ray diffraction, Raman spectra of Tb(OH) 3 and Tb(OH) 3 -SiO 2 nanotubes were investigated. The photoluminescence (PL) spectrum of Tb(OH) 3 under 325 nm excitation consists of four main peaks at 488, 542, 582, and 618 nm. Furthermore, a preliminary suggestion for the mechanism of growth of the Tb(OH) 3 nanotubes using the soft - template synthesis technique has been proposed. The PL intensity from Tb(OH) 3 -SiO 2 or Tb(OH) 3 -SiO 2 :Eu 3+ nanotubes is much stronger than that of Tb(OH) 3 .

Electric-field gradients at 181Ta impurity sites in Ho2O3 and Eu2O3 bixbyites

International Nuclear Information System (INIS)

Errico, Leonardo A.; Renteria, Mario; Bibiloni, Anibal G.; Freitag, Kristian

2007-01-01

The time-differential γ-γ perturbed-angular-correlation (PAC) technique with ion-implanted 181 Hf tracers has been applied to study the hyperfine interactions of 181 Ta impurities in the cubic bixbyite structure of Ho 2 O 3 and Eu 2 O 3 . The PAC experiments were performed in air in the temperature range 300-1373 K (in the case of Ho 2 O 3 ) and 77-1273 K (in the case of Eu 2 O 3 ). For both oxides, two electric-quadrupole interactions were found and attributed to the electric-field gradients (EFGs) acting on 181 Ta probes substitutionally located at the two free-of-defects nonequivalent cation sites of the bixbyite structure. In the case of Ho 2 O 3 , two additional interactions were found in the temperature range 300-573 K. These results, as well as previous characterizations of the EFG at 181 Ta sites in bixbyites, were compared to those obtained in experiments using 111 Cd as probe, and to point-charge model calculations. Very recent ab initio predictions for the EFG tensor at impurities sites in binary oxides are also discussed. All these results enable us to discuss the validity of the widely used ionic model to describe the EFG in these highly ionic compounds

Long lasting behavior of Gd2O2S:Eu3+ phosphor synthesized by hydrothermal routine

International Nuclear Information System (INIS)

Hang Tao; Liu Qun; Mao Dali; Chang Chengkang

2008-01-01

This paper reports the detailed preparation process and afterglow properties of Eu 3+ activated long lasting Gd 2 O 2 S phosphor by hydrothermal routine. Rod-like Gd(OH) 3 were firstly synthesized by hydrothermal method to serve as the precursor. Long lasting Gd 2 O 2 S:Eu 3+ ,Ti 4+ ,Mg 2+ phosphor was obtained by calcinating the precursor with co-activators and S powder. It was found from the results that the hydrothermally prepared Gd(OH) 3 revealed a rod-like morphology, while the calcinated Gd 2 O 2 S:Eu 3+ ,Ti 4+ ,Mg 2+ phosphor showed a round granular shape. The morphological change can be explained by the etching effect of the melt that was formed by the carbonate and S powder during the high temperature calcination. The obtained Gd 2 O 2 S:Eu 3+ ,Ti 4+ ,Mg 2+ phosphor produced a red emission upon 243 nm UV excitation, which is a typical emission of Eu 3+ from 5 D j to 7 F j states. Long lasting behavior was observed after the UV source was switched off, due to the formation of electron traps with suitable trap depth within the matrix by the codoped Ti 4+ and Mg 2+ ions

Luminescent properties and quenching effects of Pr3+ co-doping in SiO2:Tb3+/Eu3+ nanophosphors

CSIR Research Space (South Africa)

Mhlongo, GH

2014-02-01

Full Text Available Luminescence properties of Pr(sup3+) single doped SiO2 and Pr(sup3+) co-doped SiO(sub2):Tb(sup3+)/Eu(sup3+) nanophosphors synthesized using sol–gel method were investigated. X-ray diffraction (XRD), and scanning electron microscope (SEM) were used...

Crossrelaxations and non-radiative energy transfer from ({sup 4}G{sub 5/2}) Sm{sup 3+} → ({sup 5}D{sub 0}) Eu{sup 3+}: B{sub 2}O{sub 3}–ZnO glasses

Energy Technology Data Exchange (ETDEWEB)

Naresh, V., E-mail: varna.naresh@gmail.com; Rudramadevi, B.H.; Buddhudu, S., E-mail: profsb_svuniv@hotmail.com

2015-05-25

Graphical abstract: The energy transfer process occurring from Sm{sup 3+} to Eu{sup 3+} in B{sub 2}O{sub 3}–ZnO (BZn) glasses is analyzed. Based on the Foster–Dexter theory, the possibility of energy transfer between Sm{sup 3+} and Eu{sup 3+} has been demonstrated from the spectral overlap of Eu{sup 3+} absorption and Sm{sup 3+} emission, photoluminescence spectra, energy level diagram and lifetime measurements. The energy transfer mechanism in (Sm{sup 3+} + Eu{sup 3+}) co-doped glass is governed by dipole–dipole interaction. - Highlights: • Spectroscopic properties of individually doped Sm{sup 3+}, Eu{sup 3+} & co-doped (Sm{sup 3+} + Eu{sup 3+}) in BZn glasses were studied separately. • The effect of Eu{sup 3+} concentration on luminescence properties is explained from cross-relaxations. • Energy transfer from Sm{sup 3+} ({sup 4}G{sub 5/2}) to Eu{sup 3+} ({sup 5}D{sub 0}) has been explained from Foster–Dexter theory. • Dipole–dipole mechanism governs the energy transfer from Sm{sup 3+} to Eu{sup 3+}. - Abstract: The present paper reports on the results concerning to photoluminescence features of Eu{sup 3+}, Sm{sup 3+} ions and energy transfer process occurring from Sm{sup 3+} to Eu{sup 3+} doped in 45 B{sub 2}O{sub 3}–55 ZnO (BZn) glasses prepared by melt quenching technique. Luminescence quenching as a function of Eu{sup 3+} concentration in BZn glasses has been discussed. Among the studied concentrations, 0.5 mol% of Eu{sup 3+} is optimized because it has exhibited red emission transition {sup 5}D{sub 0} → {sup 7}F{sub 2}. With regard to Sm{sup 3+} glasses, orange emission at 602 nm ({sup 4}G{sub 5/2} → {sup 6}H{sub 7/2}) has been noticed on exciting with λ{sub exci} = 403 nm. Based on the Foster–Dexter theory, the possibility of energy transfer between Sm{sup 3+} and Eu{sup 3+} has been explained from the spectral overlap of Eu{sup 3+} absorption and Sm{sup 3+} emission. The optimized concentration 0.5 mol% of Eu{sup 3+} is co

Fracto- mechanoluminescence and thermoluminescence properties of orange-red emitting Eu3+ doped Ca2Al2SiO7 phosphors

International Nuclear Information System (INIS)

Tiwari, Geetanjali; Brahme, Nameeta; Sharma, Ravi; Bisen, D.P.; Sao, Sanjay K.; Khare, Ayush

2017-01-01

The suitability of nano-structured Ca 2 Al 2 SiO 7 :Eu 3+ phosphors for thermoluminescence and mechanoluminescence dosimeter were investigated. Europium doped di-calcium di-aluminum silicate phosphor was synthesised by the combustion assisted method and annealed at 1100 °C for 4 h in reducing and oxidizing environments. The prepared Ca 2 Al 2 SiO 7 :Eu 3+ phosphor was characterized by X-ray diffractometer (XRD), transmission electron microscopy (TEM), scanning electron microscopy (SEM) with energy dispersive x-ray spectroscopy (EDX), photoluminescence (PL) and decay characteristics. The phase structure of sintered phosphor has akermanite type which belongs to the tetragonal crystallography; this structure is a member of the melilite group and forms a layered compound. The chemical composition of the sintered Ca 2 Al 2 SiO 7 :Eu 3+ phosphor was confirmed by EDX spectra. Mechanoluminescence (ML) and thermoluminescence (TL) studies revealed that the ML and TL intensity increases with activator concentration. Optimum ML was observed for the sample having 2 mol% of Eu ions. The TL intensity of Ca 2 Al 2 SiO 7 :Eu 3+ was recorded for different exposure times of γ -irradiation and it was observed that TL intensity is maximum for γ dose of 1770 Gy. The PL spectra indicated that Ca 2 Al 2 SiO 7 :Eu 3+ could be excited effectively by near ultraviolet (NUV) light and exhibited bright orange-red emission with excellent colour stability. CIE colour coordinates of the prepared Ca 2 Al 2 SiO 7 :Eu 3+ phosphor was found suitable as orange-red light emitting phosphor with a CIE value of (x=0.6142, y=0.3849) and correlated colour temperature (CCT) is 1250 K. Therefore, it is considered to be a new promising orange-red emitting phosphor for white light emitting diode (LED) application.

Hydrothermal synthesis and white light emission of cubic ZrO2:Eu3+ nanocrystals

International Nuclear Information System (INIS)

Meetei, Sanoujam Dhiren; Singh, Shougaijam Dorendrajit

2014-01-01

Highlights: • White light emitting cubic ZrO 2 :Eu 3+ nanocrystal is synthesized by hydrothermal technique. • Eu 3+ is used to stabilize crystalline phase and to get red counterpart of the white light. • Defect emission and Eu 3+ emission combined to give white light. • The white light emitted from this nanocrystal resembles vertical daylight of the Sun. • Lifetime corresponding to red counterpart of the sample is far longer than conventional white light emitters. -- Abstract: Production of white light has been a promising area of luminescence studies. In this work, white light emitting nanocrystals of cubic zirconia doped with Eu 3+ are synthesized by hydrothermal technique. The dopant Eu 3+ is used to stabilize crystalline phase to cubic and at the same time to get red counterpart of the white light. The synthesis procedure is simple and precursor required no further annealing for crystallization. X-ray diffraction patterns show the crystalline phase of ZrO 2 :Eu 3+ to be cubic and it is confirmed by Fourier Transform Infrared spectroscopy. From transmission electron microscopy images, size of the crystals is found to be ∼5 nm. Photoluminescence emission spectrum of the sample, on monitoring excitation at O 2− –Eu 3+ charge transfer state shows broad peak due to O 2− of the zirconia and that of Eu 3+ emission. Commission Internationale de l’éclairage co-ordinate of this nanocrystal (0.32, 0.34) is closed to that of the ideal white light (0.33, 0.33). Correlated color temperature of the white light (5894 K) is within the range of vertical daylight. Lifetime (1.32 ms) corresponding to 5 D 0 energy level of the Eu 3+ is found to be far longer than conventional red counterparts of white light emitters. It suggests that the ZrO 2 :Eu 3+ nanocrystals synthesized by hydrothermal technique may find applications in simulating the vertical daylight of the Sun

Two ternary mixed-anion chlorides with divalent europium: Eu{sub 2}H{sub 3}Cl and Eu{sub 7}F{sub 12}Cl{sub 2}

Energy Technology Data Exchange (ETDEWEB)

Reckeweg, Olaf [Baker Laboratory, Department of Chemistry and Chemical Biology, Cornell University, Ithaca, NY 14853-1301 (United States); Institut fuer Anorganische Chemie, Universitaet Stuttgart, Pfaffenwaldring 55, 70569 Stuttgart (Germany); DiSalvo, Francis J. [Baker Laboratory, Department of Chemistry and Chemical Biology, Cornell University, Ithaca, NY 14853-1301 (United States); Wolf, Sarah; Schleid, Thomas [Institut fuer Anorganische Chemie, Universitaet Stuttgart, Pfaffenwaldring 55, 70569 Stuttgart (Germany)

2014-06-15

Dark ruby-red, transparent, triangular plate-shaped single crystals of Eu{sub 2}H{sub 3}Cl and colorless, transparent, needle-shaped single crystals of Eu{sub 7}F{sub 12}Cl{sub 2} were obtained by solid-state reactions of Eu, NaH, NaCl, and Na (2:4:1:2 molar ratio) or Eu, EuCl{sub 3}, and LiF (1:1:4 molar ratio), respectively, in silica-jacketed tantalum ampoules at 900 C for 13 h. Eu{sub 2}H{sub 3}Cl crystallizes isotypically to Ba{sub 2}H{sub 3}X (X = Cl, Br, I) in the trigonal space group P anti 3m1 (no. 164) with lattice parameters a = 409.67(4) and c = 696.18(7) pm, whereas Eu{sub 7}F{sub 12}Cl{sub 2} crystallizes isotypically to Ba{sub 7}F{sub 12}Cl{sub 2} or Sr{sub 7}H{sub 12}Cl{sub 2} in the hexagonal space group P anti 6 (no. 174) with lattice parameters a = 1002.31(5) and c = 392.54(2) pm. Both compounds contain Eu{sup 2+} cations with coordination numbers as high as nine (Eu{sub 7}F{sub 12}Cl{sub 2}) and ten (Eu{sub 2}H{sub 3}Cl) with respect to the halide anions (F{sup -} or H{sup -} and Cl{sup -}). The structural results are corroborated by EUTAX and MAPLE calculations on both ternary mixed-anion europium(II) chlorides in comparison to these for related binary and ternary compounds with divalent europium. (Copyright copyright 2014 WILEY-VCH Verlag GmbH and Co. KGaA, Weinheim)

Preparation and optical properties of Eu3+-doped tin oxide nanoparticles

International Nuclear Information System (INIS)

Wang, Guofeng; Yang, Yiping; Mu, Qiuying; Wang, Yude

2010-01-01

Eu 3+ -doped SnO 2 nanoparticles with high surface area were generated within the template of the cationic surfactant (cetyltrimethylammonium bromide, CTAB) micelle assembly by surfactant-mediated method from the hydrous tin chloride (SnCl 4 .5H 2 O) and europium chloride (EuCl 3 .6H 2 O). The as-synthesized product was amorphous and transformed into crystalline calcined at 500 o C for 2 h. DSC-TGA, X-ray powder diffraction (XRD), transmission electron microscopy (TEM), and X-ray photoelectron spectroscopy (XPS) were used to examine the morphology and microstructure of the final products. The results showed that the Eu 3+ -doped SnO 2 nanoparticles with diameter of 3-7 nm were obtained. The influences of the molar ratios of Eu 3+ and CTAB on the room temperature photoluminescence (RTPL) properties of Eu 3+ -doped SnO 2 nanoparticles were investigated. The results showed that the contents of Eu 3+ and CTAB had a great influence on the crystallite sizes and RTPL properties of Eu 3+ :SnO 2 nanoparticles. The maximum of the RTPL intensity can be observed at the molar ratio 5.0% Eu 3+ and 10.0% CTAB.

Gd2O3:Eu3+/PPO/POPOP/PS composites for digital imaging radiation detectors

International Nuclear Information System (INIS)

Oliveira, J.; Correia, V.; Martins, P.M.; Martins, P.; Lanceros-Mendez, S.; Rocha, J.G.

2015-01-01

Polymer-based scintillator composites have been produced by combining polystyrene (PS) and Gd 2 O 3 :Eu 3+ scintillator nanoparticles. Polystyrene has been used since it is a flexible and stable binder matrix, resistant to thermal and light deterioration and with suitable optical properties. Gd 2 O 3 :Eu 3+ has been selected as scintillator material due to its wide band gap, high density and visible light yield. The optical, thermal and electrical characteristics of the composites were studied as a function of filler content, together with their performance as scintillator material. Additionally 1 wt.% of 2,5-diphenyloxazole (PPO) and 0.01 wt.% of 1,4 di[2-(5phenyloxazolyl)]benzene (POPOP) were introduced in the polymer matrix in order to strongly improve light yield, i.e., the measured intensity of the output visible radiation, under X-ray irradiation. Increasing scintillator filler concentration (from 0.25 to 7.5 wt.%) increases scintillator light yield and decreases the optical transparency of the composite. The addition of PPO and POPOP strongly increased the overall transduction performance of the composite due to specific absorption and re-emission processes. It is thus shown that Gd 2 O 3 :Eu 3+ /PPO/POPOP/PS composites with 0.25 wt.% of scintillator content with fluorescence molecules are suitable for the development of innovative large-area X-ray radiation detectors with huge demand from the industries. (orig.)

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.

Red emitting phosphors of Eu3+ doped Na2Ln2Ti3O10 (Ln = Gd, Y) for white light emitting diodes

International Nuclear Information System (INIS)

Zhang, Niumiao; Guo, Chongfeng; Yin, Luqiao; Zhang, Jianhua; Wu, Mingmei

2015-01-01

Highlights: • Layered red phosphors Na 2 Ln 2 Ti 3 O 10 (Ln = Gd, Y):Eu 3+ were prepared. • The synthesis parameters of phosphors were optimized. • PL and thermal stability of the samples were investigated. • LED devices were also fabricated including the present red phosphor. - Abstract: A series of Eu 3+ doped Na 2 Ln 2 Ti 3 O 10 (Ln = Gd, Y) red-emitting phosphors for application in ultraviolet based light emitting diodes (LEDs) were successfully synthesized by a modified sol–gel method. Their structure and luminescent properties were characterized by powder X-ray diffraction (XRD), photoluminescence excitation (PLE) and emission (PL) spectra and absorption spectra, according to these results the optimal compositions and synthesis parameters were determined. In addition, the thermal stabilities of the phosphors were investigated according to the temperature-dependent PL spectra. The red and white-LEDs (W-LEDs) comprising the Na 2 Ln 2 Ti 3 O 10 :Eu 3+ (Ln = Gd, Y) red emitting phosphors were fabricated with a near-ultraviolet (n-UV) chip. In comparison with Na 2 Y 1.4 Eu 0.6 Ti 3 O 10 , the Na 2 Gd 0.6 Eu 1.4 Ti 3 O 10 phosphor offers higher brightness, quantum efficiency, and excellent thermal stability. W-LEDs comprising Na 2 Gd 0.6 Eu 1.4 Ti 3 O 10 showed bright white emission with a color rendering index (Ra) of 82, a color temperature of 2151 K, and Commission Internationale de I’Eclairage (CIE) color coordinates of (0.34, 0.37). The phosphor Na 2 Gd 0.6 Eu 1.4 Ti 3 O 10 is more suitable candidate for application in LEDs

Spectra and energy levels of Eu{sup 3+} in cubic phase Gd{sub 2}O{sub 3}

Energy Technology Data Exchange (ETDEWEB)

Smith, Eric R. [Kratos Defense and Security Solutions, Inc., 5030 Bradford Dr., Huntsville, AL 35805 (United States); Gruber, John B. [Department of Physics and Astronomy, University of Texas at San Antonio, San Antonio, TX 78249-0697 (United States); Wellenius, Patrick; Muth, John F. [Department of Electrical and Computer Engineering, NC State University, Raleigh, NC 27606 (United States); Everitt, Henry O. [Department of Physics, Duke University, Durham, NC 27708 (United States); Army Aviation and Missile RD and E Center, Redstone Arsenal, AL 35898 (United States)

2010-07-15

In pulsed laser deposition of the sesquioxide semiconductor Gd{sub 2}O{sub 3}, adjusting the chamber oxygen pressure controls the crystalline structure of the host. This technique was used to deposit thin films of nominally 1.6% by weight europium-doped, cubic phase Gd{sub 2}O{sub 3} using 50 mTorr of oxygen. Structural measurements using high-resolution transmission electron microscopy and selected area electron diffraction confirm the films were polycrystalline, cubic phase Eu:Gd{sub 2}O{sub 3}. The spectroscopic assignment of emission lines to specific radiative transitions within the trivalent Eu ion is confirmed by theoretical analysis of the appropriate crystal field Hamiltonian. Detailed crystal-field splittings are presented for the {sup 5}D{sub J=0-2} and {sup 7}F{sub J=0-5} multiplet manifolds of Eu{sup 3+} in this host material. (Abstract Copyright [2010], Wiley Periodicals, Inc.)

Brilliant blue, green and orange-red emission band on Tm{sup 3+}-, Tb{sup 3+}- and Eu{sup 3+}-doped ZrO{sub 2} nanocrystals

Energy Technology Data Exchange (ETDEWEB)

Romero, V H; De la Rosa, E; Lopez-Luke, T [Centro de Investigaciones en Optica, A.P. 1-948, Leon Gto., 37160 (Mexico); Salas, P [Centro de Fisica Aplicada y TecnologIa Avanzada, Universidad Nacional Autonoma de Mexico, A.P. 1-1010, Queretaro, Qro. 76000 (Mexico); Angeles-Chavez, C, E-mail: elder@cio.m [Instituto Mexicano del Petroleo, Programa de IngenierIa Molecular, A.P. 11-848, Mexico, D.F. 07730 (Mexico)

2010-11-24

Tm{sup 3+}-, Tb{sup 3+}- and Eu{sup 3+}-doped ZrO{sub 2} nanocrystals were prepared by a facile precipitation method with a hydrothermal process. Structural characterization showed a crystallite size ranging from 30 to 40 nm, and monoclinic and tetragonal zirconia phases were observed depending on the dopant concentration. The monoclinic phase was dominant for 0.5 mol% of Tb{sup 3+} and Eu{sup 3+}, and the tetragonal phase was 100% stabilized for 2 mol% of Tm{sup 3+} and Tb{sup 3+}. The structure of emission bands associated with Eu{sup 3+} confirms the substitution of Zr{sup 4+} located at C{sub 1} and D{sub 2h} symmetry sites for the monoclinic and tetragonal phases. The emission of three primary colours, red, green and blue, was obtained from Eu{sup 3+}, Tb{sup 3+} and Tm{sup 3+}, respectively, which makes this nanophosphor an excellent candidate for use in photonics applications. The emitted signal was analysed as a function of ion concentration and the optimum concentration was determined.

Citrate mediated synthesis and tuning of luminescence in Eu3+ incorporated Gd2O3 nanophosphors

Science.gov (United States)

Abhilash Kumar, R. G.; Gopchandran, K. G.

2015-02-01

Gd1.9Eu0.1O3 nanophosphors were prepared successfully by a large-scale facile solution based citrate-metal complex controlled combustion method and was systematically studied by varying the citric acid to metal cation ratio. X-ray diffraction (XRD), scanning electron microscopy (SEM), transmission electron microscopy (TEM), photoluminescence (PL) measurements and radiative properties were done to evaluate the crystal structure, phase formation, phase composition, surface morphology, radiative and luminescent properties of the prepared nanophosphors. Photoluminescent emission intensity of the samples can be correlated with the amount of citric acid, improved crystallinity, uniform morphology, particle size, reduced defects, and proper diffusion of Eu3+ in to the crystal structure of Gd2O3. Higher asymmetricity results in intense red emission (612 nm) due to 5D0-7F2 forced electric dipole transition and found that photoluminescence intensity is highest for the sample prepared with citric acid to metal cation ratio of 2:1. The existence of strong red emission from Gd1.9Eu0.1O3 nanophosphor corresponding to 5D0-7F2 transition (612 nm) of Eu3+ under UV light excitation make it a promising candidate for applications in bio assays, magnetic resonance imaging, deep uv LED's, solid state lighting, fluorescent lamps and flat panel displays.

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.

Influence of Eu{sup 3+} doping content on antioxidant properties of Lu{sub 2}O{sub 3} sol-gel derived nanoparticles

Energy Technology Data Exchange (ETDEWEB)

Olvera Salazar, Arturo [Universidad Del Valle de México Campus Lomas Verde, Paseo de las Aves No.1 Col. San Mateo Nopala. Naucalpan de Juárez, Edo. Méx. C.P. 53220 (Mexico); García Hernández, Margarita, E-mail: margarita.garcia@itcm.edu.mx [Tecnológico Nacional de México-Instituto Tecnológico de Ciudad Madero. Av. 1o. de Mayo esq. Sor Juana Inés de la Cruz s/n Col. Los Mangos Cd. Madero Tamaulipas C.P.89440 (Mexico); López Camacho, Perla Yolanda [Universidad Autónoma Metropolitana, Unidad Cuajimalpa. Av. Vasco de Quiroga 4871, Col. Santa Fé Cuajimalpa, Cuajimalpa D.F. C.P. 05348 (Mexico); López Marure, Arturo [Instituto Politécnico Nacional, CICATA Altamira. Carretera Tampico-Puerto Industrial Altamira, Altamira, Tamaulipas C.P. 89600 (Mexico); Reyes de la Torre, Adriana Isabel [Tecnológico Nacional de México-Instituto Tecnológico de Ciudad Madero. Av. 1o. de Mayo esq. Sor Juana Inés de la Cruz s/n Col. Los Mangos Cd. Madero Tamaulipas C.P.89440 (Mexico); Morales Ramírez, Ángel de Jesús [Instituto Politécnico Nacional, CIITEC Azcapotzalco. Cerrada de Cecati S/N, Col. Santa Catarina, Azcapotzalco, D.F. C.P. 02250 (Mexico); and others

2016-12-01

This paper presents the synthesis of pure and europium-doped lutetium oxide (Lu{sub 2}O{sub 3}) powders prepared by sol-gel method. The influence of europium ion concentration into Lu{sub 2}O{sub 3} nanocrystallites was investigated for first time in an in vitro system using a modified ABTS radical cation decolorization assay to determine the antioxidant activity. The crystalline structure of Lu{sub 2}O{sub 3} and Eu:Lu{sub 2}O{sub 3} powders was elucidated by XRD obtaining cubic phase in all system without secondary products in accordance with FT-IR results. By TEM and Scherrer equation, it was determined that Lu{sub 2}O{sub 3} and Eu:Lu{sub 2}O{sub 3} powders presented nearly spherical particle morphology with crystallites sizes in the range of 8 to 13 nm. The antioxidant assays results revealed that europium ion enhance Lu{sub 2}O{sub 3} powders antioxidant properties, showing that 12.5 mol% of europium is sufficient to reach its maximum capacity. - Highlights: • For first time the effect of the Eu content vs antioxidant properties was studied. • Sol-gel particles of Lu{sub 2}O{sub 3}:Eu{sup 3+} nanopowders showed relevant antioxidant properties. • The antioxidant behavior remains stable at higher Eu levels.

Magnetic and luminescent properties of Fe/Fe{sub 3}O{sub 4}-Y{sub 2}O{sub 3}:Eu nanocomposites

Energy Technology Data Exchange (ETDEWEB)

Wang Qin [College of Chemistry, Jilin University, Changchun 130012 (China); College of Chemistry and Chemical Engineering, Inner Mongolia University, Hohhot (China); Yang Xuwei; Yu Lianxiang [College of Chemistry, Jilin University, Changchun 130012 (China); Yang Hua, E-mail: huayang86@sina.com [College of Chemistry, Jilin University, Changchun 130012 (China)

2011-09-15

Highlights: > We synthesize multifunctional Fe/Fe{sub 3}O{sub 4}-Y{sub 2}O{sub 3}:Eu nanocomposites. > The luminescent and magnetic properties of the nanocomposites are researched. > The nanocomposites showed both ferrimagnetic behavior and unique europium fluorescence properties with high emission intensity. > The spectra changes induced by the UV light irradiation and the magnetic field have been systematically studied and compared in detail. > And the hysteresis curve changes induced by the UV light irradiation have been discussed. - Abstract: Multifunctional nanocomposites with Fe/Fe{sub 3}O{sub 4} nanoparticles as the core and europium-doped yttrium oxide (Y{sub 2}O{sub 3}:Eu) as the shell (Fe/Fe{sub 3}O{sub 4}-Y{sub 2}O{sub 3}:Eu) have been obtained successfully employing a solvothermal method. The nanocomposites showed both ferrimagnetic behavior and unique europium fluorescence properties with high emission intensity. The spectra changes induced by the UV light irradiation and the magnetic field have been systematically studied and compared in detail. The relationship between fluorescence and magnetic properties of the multifunctional nanocomposites has been investigated in our manuscript. These multifunctional nanocomposites could be used in a number of biomedical applications, such as drug targeting, cell separation and bioimaging.

Luminescent properties of codoping Y{sub 2}O{sub 3}: Eu, Me (Me = Mg, Ca) nanorods

Energy Technology Data Exchange (ETDEWEB)

Liu Zhilong; Wang Qin; Yang Yuming; Tao Chunyan; Yang Hua, E-mail: huayang86@sina.co [Jilin University, College of Chemistry (China)

2010-08-15

Phosphors of nanorods Y{sub 2}O{sub 3}: Eu (Mg, Ca) have been prepared by the hydrothermal method. The effect of Mg, Ca co-dopants on the Y{sub 2}O{sub 3}: Eu phosphor photoluminescence (PL) property was investigated. Upon excitation with ultraviolet (UV) irradiation, it is shown that there is a strong emission at around 610 nm corresponding to the forced electric dipole {sup 5}D{sub 0}-{sup 7}F{sub 2} transition of Eu{sup 3+}. At a certain concentration, Mg, Ca ions' doping effectively enhanced the luminescent properties of Y{sub 2}O{sub 3}: Eu{sup 3+} nanorods and did not change the cubic phase of the host. The structure of Y{sub 2}O{sub 3}: Eu{sup 3+} (Mg, Ca) phosphors was characterized by X-Ray diffraction (XRD). From XRD patterns, it is indicated that the phosphor Y{sub 2}O{sub 3}:(Eu, Ca) forms without impurity phase. From SEM, TEM images, it is shown that the crystal size of the nanorods phosphors is about 1-2 {mu}m in length and 30-50 nm in diameter.

Synthesis of Y2O2S:Eu3+, Mg2+, Ti4+ hollow microspheres via homogeneous precipitation route

Directory of Open Access Journals (Sweden)

Peng-Fei Ai, Ying-Liang Liu, Li-Yuan Xiao, Hou-Jin Wang and Jian-Xin Meng

2010-01-01

Full Text Available A phosphorescent material in the form of Y2O2S:Eu3+, Mg2+, Ti4+ hollow microspheres was prepared by homogeneous precipitation using monodispersed carbon spheres as hard templates. Y2O3:Eu3+ hollow microspheres were first synthesized to serve as the precursor. Y2O2S:Eu3+, Mg2+, Ti4+ powders were obtained by calcinating the precursor in a CS2 atmosphere. The crystal structure, morphology and optical properties of the composites were characterized. X-ray diffraction measurements confirmed the purity of the Y2O2S phase. Electron microscopy observations revealed that the Y2O2S:Eu3+, Mg2+, Ti4+ particles inherited the hollow spherical shape from the precursor after being calcined in a CS2 atmosphere and that they had a diameter of 350–450 nm and a wall thickness of about 50–80 nm. After ultraviolet radiation at 265 or 325 nm for 5 min, the particles emitted strong red long-lifetime phosphorescence originating from Eu3+ ions. This phosphorescence is associated with the trapping of charge carriers by Ti4+ and Mg2+ ions.

Combined use of O3/H2O2 and O3/Mn2+ in flotation of dairy wastewater

Directory of Open Access Journals (Sweden)

Marta Cristina Silva Carvalho

2018-05-01

Full Text Available This work investigated the degradation of organic matter present in synthetic dairy wastewater by the combination of ozonation (ozone (O3/hydrogen peroxide (H2O2 and catalytic ozonation (ozone (O3/manganese (Mn2+ associated with dispersed air flotation process. The effect of independent factors such as O3 concentration, pH and H2O2 and Mn2+ concentration was evaluated. For the flotation/O3/H2O2 treatment, the significant variables (p ≤ 0.05 were: O3 concentration (linear and quadratic effect, H2O2 concentration linear and quadratic effect, pH values (linear and quadratic effect and interaction O3 concentration versus pH. For catalytic ozonation, it was observed that the significant variable was the linear effect of O3 concentration. According to the desirability function, it was concluded that the optimal condition for the treatment of flotation/O3/H2O2 can be obtained in acidic solution using O3 concentrations greater than 42.9 mg L-1 combined with higher concentrations of H2O2 to 1071.5 mg L-1. On other hand, at pH values higher than 9.0, the addition of O3 may be neglected when using higher concentrations than 1071.5 mg L-1 of H2O2. For flotation/ozonation catalyzed by Mn2+, it was observed that metal addition did not affect treatment, resulting in an optimum condition: 53.8 mg L-1 of O3 and pH 3.6.

Structural and luminescence studies of Eu3+: TeO2sbnd B2O3sbnd AOsbnd AF2 (A = Pb, Ba, Zn, Cd, Sr) glasses

Science.gov (United States)

Selvi, S.; Marimuthu, K.; Muralidharan, G.

2017-09-01

Eu3+ doped oxyfluoro boro-tellurite (TBXFE) with molar composition 29 TeO2sbnd 30B2O3sbnd 20AOsbnd 20AF2sbnd 1Eu2O3 (where A = Pb, Ba, Zn, Cd, Sr) glasses were prepared and investigated by XRD, FTIR, UV-Vis-NIR, luminescence and decay measurements. XRD patterns confirm the glassy nature of the prepared glasses. The influence of metal ions on the structure of boro-tellurite glasses were investigated through FTIR spectra. The intra band (4f-4f) transitions of Eu3+ ions are discussed through UV-Vis-NIR absorption spectra. The covalent nature around the Eu3+ ions with ligands are discussed using the bonding parameter (δ) and nephelauxetic ratio (β). The fundamental absorption edge, direct, indirect band gap, Urbach energy and band tailing parameters are reported. A bright red emission at 616 nm corresponding to the 5D0 → 7F2 transition of Eu3+ ions could be observed in the title glasses. Judd-Ofelt parameters were estimated from the emission spectra of Eu3+ ions. The dependence of these parameters on the composition of the glass is discussed. Judd-Ofelt parameters were used to derive the radiative parameters such as transition probabilities (A, s-1), branching ratios (βR), radiative lifetime (τrad) and stimulated emission cross-section (σPE) for the 5D0 → 7FJ (J = 0, 1, 2, 3 and 4) transitions. The luminescence intensity ratio (LIR) of 5D0 → 7F2/5D0 → 7F1 transitions was estimated to analyze the local site symmetry around the Eu3+ ions in the present glasses. The chromaticity coordinates and colour purity were calculated from the emission spectra and analyzed with Commission International de I'Eclairage (CIE) 1931 diagram. The experimental lifetime of 5D0 level could be fitted to a single exponential indicating the absence of energy transfer between the Eu3+ ions in the present glasses.

Structure, luminescence, and dynamics of Eu2O3 nanoparticles in MCM-41

International Nuclear Information System (INIS)

Chen, Wei; Joly, Alan G.; Kowalchuk, George A.; Malm, Jan-Olle; Huang, Yining; Bovin, Jan-Olov

2001-01-01

The structure, luminescence spectroscopy, and lifetime decay dynamics of Eu2O3 nanoparticles formed in MCM-41 have been investigated. Both X-ray diffraction and high resolution transmission electron microscope observations indicate that Eu2O3 nanoparticles of monoclinic structure are formed inside channels of MCM-41 by heating at 140 C. However, heat treatment at 600 and 700 C causes migration of Eu2O3 from the MCM-41 channels forming nanoparticles of cubic structure outside of the MCM-41 channels. The feature of the hypersensitive 5D0? 7F2 emission profile of Eu3+ is used to follow the structural changes. Photoluminescence lifetimes show the existence of short (< 1 microsecond) and long (microsecond to millisecond) components for each sample. The fast decay is attributed to quenching by surface states of the nanoparticles or energy transfer to the MCM-41 while the longer time decays show the effects of concentration quenching. The monoclinic sample prepared at 140 C shows a higher luminescence intensity than the cubic samples or the bulk powder

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

A highly triflated rare-earth ion in [Eu(O{sub 3}SCF{sub 3}){sub 8}]{sup 5-}

Energy Technology Data Exchange (ETDEWEB)

Bruns, Joern; Kluener, Thorsten; Kraeuter, Jessica; Wickleder, Mathias S. [Carl von Ossietzky Universitaet Oldenburg, Institut fuer Chemie (Germany); Krueger, Sascha; Adlung, Matthias; Wickleder, Claudia [Universitaet Siegen, Institut fuer Anorganische Chemie (Germany); Niehaus, Oliver; Poettgen, Rainer [Westfaelische Wilhelms Universitaet Muenster, Institut fuer Anorganische und Analytische Chemie (Germany)

2015-08-24

The reaction of Eu{sub 2}O{sub 3} with fuming nitric acid, trifluormethanesulfonic acid, and its anhydride in torch-sealed glass ampoules at 120 C gave the europium compound (NO){sub 5}[Eu(O{sub 3}SCF{sub 3}){sub 8}] (orthorhombic, Fddd, Z=16, a=1932.69(4), b=2878.44(7), c=2955.12(7) pm, V=16439.7(7) Aa{sup 3}). The compound exhibits the [Eu(O{sub 3}SCF{sub 3}){sub 8}]{sup 5-} anion showing for the first time a lanthanide ion that is exclusively coordinated by eight triflate anions. The anion has been further investigated by DFT calculations, which also allowed clear assignment of the vibrational spectra. Moreover, magnetochemical and luminescence measurements gave additional insight into the properties of this complex. The luminescence spectra revealed that the Eu{sup 3+} ions are in a pseudo D{sub 4d} symmetric environment. (copyright 2015 WILEY-VCH Verlag GmbH and Co. KGaA, Weinheim)

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.

Role of Eu"2"+ on the blue‐green photoluminescence of In_2O_3:Eu"2"+ nanocrystals

International Nuclear Information System (INIS)

Devi, Konsam Reenabati; Meetei, Sanoujam Dhiren; Singh, Shougaijam Dorendrajit

2016-01-01

Blue‐green light emitting undoped and europium doped indium oxide nanocrystal were synthesized by simple precipitation method. X-ray diffraction (XRD) pattern confirmed the cubic phase of undoped and europium doped samples. Further, transmission electron microscopy (TEM), scanning electron microscopy (SEM) , energy dispersive analysis of X-rays (EDAX), Fourier transform infra-red (FT-IR), photoluminescence (PL), electron paramagnetic resonance (EPR) studies were performed to characterise the samples. PL analysis of the samples is the core of the present research. It includes excitation, emission and CIE (Commission Internationale de l’e´ clairage) studies of the samples. On doping europium to In_2O_3 lattice, ln"3"+ site is substituted by Eu"2"+ thereby increasing the concentration of singly ionized oxygen vacancy and hence blue–green emission from the host is found to increase. Further, this increase in blue–green emission after doping may also be attributed to 4f → 5d transitions of Eu"2"+. However, the blue–green PL emission is found to decrease after an optimum dopant concentration (Eu"2"+ = 4%) due to luminescence and size quenching. CIE co-ordinates of the samples are calculated to know colour of light emitted from the samples. It suggests that this blue–green light emitting In_2O_3: Eu"2"+ nanocrystals may find application in lighting such as in generation of white light. - Highlight: • XRD and TEM study confirms the synthesis of cubic doped and europium doped nanocrystals. • EPR study reveals the doped europium is in + 2 oxidation state. • Enhance PL emission intensity of host material due to increase in singly ionized oxygen vacancy and 4f–5d transitions of Eu"2"+ • CIE co-ordinates suggest the blue–green colour of the samples.

Red luminescence from Eu3+-doped TeO2-WO3-GeO2 glasses for solid state lasers

Science.gov (United States)

Subrahmanyam, Tallam; Gopal, Kotalo Rama; Suvarna, Reniguntla Padma; Jamalaiah, Bungala Chinna

2018-05-01

Eu3+-doped oxyfluoro tellurite (TWGEu) glasses were prepared by conventional melt quenching method. The optical band gap energy and covalence between Eu3+ and O2-/F- ions were determined from optical absorption spectra. Using the 5D0 → 7F1,2,4 emission transitions, the Ω2 and Ω4 intensity parameters were determined. These intensity parameters were used to evaluate the radiative parameters such as emission probability rate (AR), luminescence branching ratio (βR) and radiative life time (τR) of 5D0 → 7FJ transitions. The laser characteristic parameters such as stimulated emission cross-section, gain bandwidth and quantum efficiency were determined. The luminescence decay profiles of 5D0 emission level were well fitted to single exponential function for all the concentrations. The experimental results show that the 0.5 mol% of Eu3+-doped TWGEu glass could be the best choice to design red laser sources.

Kinetic removal of haloacetonitrile precursors by photo-based advanced oxidation processes (UV/H2O2, UV/O3, and UV/H2O2/O3).

Science.gov (United States)

Srithep, Sirinthip; Phattarapattamawong, Songkeart

2017-06-01

The objective of the study is to evaluate the performance of conventional treatment process (i.e., coagulation, flocculation, sedimentation and sand filtration) on the removals of haloacetonitrile (HAN) precursors. In addition, the removals of HAN precursors by photo-based advanced oxidation processes (Photo-AOPs) (i.e., UV/H 2 O 2 , UV/O 3 , and UV/H 2 O 2 /O 3 ) are investigated. The conventional treatment process was ineffective to remove HAN precursors. Among Photo-AOPs, the UV/H 2 O 2 /O 3 was the most effective process for removing HAN precursors, followed by UV/H 2 O 2 , and UV/O 3 , respectively. For 20min contact time, the UV/H 2 O 2 /O 3 , UV/H 2 O 2 , and UV/O 3 suppressed the HAN formations by 54, 42, and 27% reduction. Increasing ozone doses from 1 to 5 mgL -1 in UV/O 3 systems slightly improved the removals of HAN precursors. Changes in pH (6-8) were unaffected most of processes (i.e., UV, UV/H 2 O 2 , and UV/H 2 O 2 /O 3 ), except for the UV/O 3 system that its efficiency was low in the weak acid condition. The pseudo first-order kinetic constant for removals of dichloroacetonitrile precursors (k' DCANFP ) by the UV/H 2 O 2 /O 3 , UV/H 2 O 2 and standalone UV systems were 1.4-2.8 orders magnitude higher than the UV/O 3 process. The kinetic degradation of dissolved organic nitrogen (DON) tended to be higher than the k' DCANFP value. This study firstly differentiates the kinetic degradation between DON and HAN precursors. Copyright © 2017 Elsevier Ltd. All rights reserved.

Rapid formation of red long afterglow phosphor Sr3Al2O6:Eu2+, Dy3+ by microwave irradiation

International Nuclear Information System (INIS)

Zhang Ping; Xu Mingxia; Zheng Zhentai; Sun Bo; Zhang Yanhui

2007-01-01

A new red long afterglow phosphor Sr 3 Al 2 O 6 :Eu 2+ , Dy 3+ nanocrystalline particles were prepared using a microwave oven operated at a frequency of 2.45 GHz and a power of 680 W in a weak reductive atmosphere. The phosphor nanocrystalline particles were characterized by the X-ray diffraction (XRD), scanning electron microscopy (SEM) and fluorescence spectrophotometer. The results reveal that the samples are composed of single Sr 3 Al 2 O 6 phase. The obtained nanocrystalline particles show small size (80-100 nm) and spherical shape. The excitation and emission spectra indicate that excitation broadband chiefly lies in visible range and the nanocrystalline particles emit strong light at 612 nm under around 473 nm excitation. The effect of Eu 2+ doping concentrations of the samples on the emission intensity is studied systematically. Furthermore, comparing with conventional heating method, the microwave method has the advantages such as short heating time and low energy consumption. However, the decay speed of the afterglow for Sr 3 Al 2 O 6 :Eu 2+ , Dy 3+ nanocrystalline particles is faster than that obtained by the conventional heating method

Broadband sensitized white light emission of g-C_3N_4/Y_2MoO_6:Eu"3"+ composite phosphor under near ultraviolet excitation

International Nuclear Information System (INIS)

Han, Bing; Xue, Yongfei; Li, Pengju; Zhang, Jingtao; Zhang, Jie; Shi, Hengzhen

2015-01-01

The g-C_3N_4/Y_2MoO_6:Eu"3"+ composite phosphors were synthesized and characterized by X-ray diffraction, Fourier transform-infrared spectroscopy, ultraviolet visible diffuse reflection spectra, photoluminescence spectra and luminescence decay curves. Under the excitation of 360 nm near ultraviolet light, these composite phosphors show tunable emission from blue to red region, in which white light emission can be obtained in term of appropriate quality proportion of Y_2MoO_6:Eu"3"+ relative to g-C_3N_4/Y_2MoO_6:Eu"3"+. In addition, the emission color can be also dependent on the excitation wavelength in g-C_3N_4/Y_2MoO_6:Eu"3"+ composite phosphor. - Graphical abstract: Under the excitation of 360 nm near ultraviolet light, the g-C_3N_4/Y_2MoO_6:Eu"3"+ composite phosphors show tunable emission from blue to red region, in which white light emission can be obtained. - Highlights: • The g-C3N4/Y2MoO6:Eu"3"+ composite phosphors were synthesized and characterized. • White light emission was realized in the g-C3N4/Y2MoO6:Eu"3"+ composites under UV excitation. • A novel idea to realize the broadband sensitized white light emission in phosphors was provided.

A novel red phosphor Mg2GeO4 doped with Eu3+ for PDP applications

International Nuclear Information System (INIS)

Yang Hongmei; Shi Jianxin; Liang Hongbin; Gong Menglian

2006-01-01

A novel red emitting phosphor, Eu 3+ -doped Mg 2 GeO 4 , was prepared by the solid-state reaction. X-ray powder diffraction (XRD) analysis confirmed the formation of Mg 2 GeO 4 :Eu 3+ . Field-emission-scanning electron microscopy (FE-SEM) observation indicated a narrow size-distribution of about 0.5-2 μm nm for the particles with spindle-like shape. Photoluminescence (PL) and vacuum ultraviolet (VUV) excitation characteristics of the phosphor Mg 2 GeO 4 :Eu 3+ were studied. We have also studied the effect of preparation conditions such as temperature, heating time on the PL data. Photoluminescence measurements indicated that the phosphor exhibits bright red emission at about 609 nm under UV excitation. And the vacuum ultraviolet spectra present that the novel red phosphor Mg 2 GeO 4 :Eu 3+ shows strong absorption in the VUV region, which ensures the efficient absorption of the Xe plasma emission lines. The phosphor Mg 2 GeO 4 :Eu 3+ shows the strongest emission at 613 nm corresponding to the electric dipole 5 D - 7 F 2 transition of Eu 3+ excited at 147 nm. The optical properties study suggests that it is a potential candidate for plasma display panels (PDPs) application

Sol–gel synthesis of long-lasting phosphors CdSiO3: Mn2+, RE3+ (RE = Tb, Eu, Nd) and luminescence mechanism research

International Nuclear Information System (INIS)

Qu, Xiaofei; Cao, Lixin; Liu, Wei; Su, Ge; Wang, Pingping; Schultz, Isabel

2012-01-01

Highlights: ► New long-lasting CdSiO 3 : Mn 2+ , RE 3+ (RE = Tb, Eu, Nd) phosphors were synthesized by a sol–gel method. ► The afterglow performance of the CdSiO 3 : Mn 2+ , Eu 3+ phosphor was the best. ► The role of RE 3+ co-doped into the CdSiO 3 : Mn 2+ matrix was discussed in this paper. -- Abstract: Mn 2+ and RE 3+ (RE = Tb, Eu, Nd) co-doped CdSiO 3 orange phosphors were prepared at 1050 °C by a sol–gel method. The phase and crystallinity of the synthesized materials were investigated by X-ray powder diffraction (XRD) and scanning electron microscopy (SEM). The luminescence characteristics were analyzed using photoluminescence (PL) spectra, afterglow decay curves, long-lasting phosphorescence spectra, and thermoluminescence (TL) spectra. Due to the difference in co-doped rare earth ionic radii, it varied greatly in trap density and trap depth caused by the different defects deriving from RE 3+ ions co-doping into the CdSiO 3 : Mn 2+ host. The afterglow intensity and time for these samples increased as follows: CdSiO 3 : Mn 2+ 0.2%, Nd 3+ 0.8% 3 : Mn 2+ 0.4%, Tb 3+ 0.8% 3 : Mn 2+ 0.4%, Eu 3+ 0.3%. CdSiO 3 : Mn 2+ 0.4%, Eu 3+ 0.3% had the best afterglow properties, which could be due to the proper traps formed by Eu 3+ ions co-doping into the host. The role of RE 3+ co-doped into the CdSiO 3 : Mn 2+ matrix and the possible long-lasting phosphorescence process was also discussed in this paper.

Hydrothermal synthesis, characterization, and luminescence of Ca{sub 2}B{sub 2}O{sub 5}:RE (RE = Eu{sup 3+}, Tb{sup 3+}, Dy{sup 3+}) nanofibers

Energy Technology Data Exchange (ETDEWEB)

Yang, Li; Wan, Yingpeng; Li, Yuze; Pu, Yinfu; Huang, Yanlin, E-mail: huang@suda.edu.cn [Soochow University, State and Local Joint Engineering Laboratory for Novel Functional Polymeric Materials, College of Chemistry, Chemical Engineering and Materials Science (China); Chen, Cuili; Seo, Hyo Jin, E-mail: hjseo@pknu.ac.kr [Pukyong National University, Department of Physics and Interdisciplinary Program of Biomedical Engineering (Korea, Republic of)

2016-04-15

Ca{sub 2}B{sub 2}O{sub 5}:RE (RE = Eu{sup 3+}, Tb{sup 3+}, Dy{sup 3+}) nanofibers were synthesized by the hydrothermal reaction method. The structural refinement was conducted on the base of the X-ray powder diffraction (XRD) measurements. The surface properties of the Ca{sub 2}B{sub 2}O{sub 5}:RE (RE = Eu{sup 3+}, Tb{sup 3+}, Dy{sup 3+}) nanofibers were investigated by the measurements such as the scanning electron microscope (SEM), transmission electron microscope (TEM), and the energy dispersive spectrum (EDS). The nanofiber has a diameter of about 100 nm and a length of several micrometers. The luminescence properties such as photoluminescence excitation (PLE) and emission spectra (PL), decay lifetime, color coordinates, and the absolute internal quantum efficiency (QE) were reported. Ca{sub 2}B{sub 2}O{sub 5}:Eu{sup 3+} nanofibers show the red luminescence with CIE coordinates of (x = 0.41, y = 0.51) and the luminescence lifetime of 0.63 ms. The luminescence of Ca{sub 2}B{sub 2}O{sub 5}:Tb{sup 3+} nanofibers is green color (x = 0.29, y = 0.53) with the lifetime of 2.13 ms. However, Dy{sup 3+}-doped Ca{sub 2}B{sub 2}O{sub 5} nanofibers present a single-phase white-color phosphor with the fluorescence decay of 3.05 ms. Upon near-UV excitation, the absolute quantum efficiency is measured to be 65, 35, and 37 % for Eu{sup 3+}-, Tb{sup 3+}-, Dy{sup 3+}-doped Ca{sub 2}B{sub 2}O{sub 5} nanofibers, respectively. It is suggested that Ca{sub 2}B{sub 2}O{sub 5}:RE (RE = Eu{sup 3+}, Tb{sup 3+}, Dy{sup 3+}) nanofibers could be an efficient phosphor for lighting and display.

Synthesis of Y{sub 2}O{sub 3}:(Li,Eu) films using phosphor powders coated with SiO{sub 2} nano particles

Energy Technology Data Exchange (ETDEWEB)

Kim, In-Gyu; Park, Sangmoon [Center for Green Fusion Technology and Department of Engineering in Energy and Applied Chemistry, Silla University, Busan 617-736 (Korea, Republic of); Kang, Seong-Gu [Department of Chemical Engineering, Hoseo University, Chungnam 336-795 (Korea, Republic of); Park, Jung-Chul, E-mail: parkjc@silla.ac.k [Center for Green Fusion Technology and Department of Engineering in Energy and Applied Chemistry, Silla University, Busan 617-736 (Korea, Republic of)

2010-08-15

Y{sub 1.9-x}Li{sub 0.1}Eu{sub x}O{sub 3} (x=0.02, 0.05, 0.08, and 0.12) films were fabricated by spin-coating method. A colloidal silica suspension with Y{sub 1.9-x}Li{sub 0.1}Eu{sub x}O{sub 3} phosphor powder was exploited to obtain the highly stable and effective luminescent films onto the glass substrate. After heating as-prepared Y{sub 1.9-x}Li{sub 0.1}Eu{sub x}O{sub 3} films at 700 {sup o}C for 1 h, the phosphor films exhibit a high luminescent brightness as well as a strong adhesiveness on the glass substrate. The emission spectra of spin-coated and pulse-laser deposited Y{sub 1.82}Li{sub 0.1}Eu{sub 0.08}O{sub 3} films were compared. The cathodoluminescence of the phosphor films was carried out at the anode voltage 1 kV.

Synthesis and crystal structure of new uranyl selenite(IV)-selenate(VI) [C5H14N][(UO2)3(SeO4)4(HSeO3)(H2O)](H2SeO3)(HSeO4)

International Nuclear Information System (INIS)

Krivovichev, S.V.; Tananaev, I.G.; Myasoedov, B.F.; Kalenberg, V.

2006-01-01

Crystals of new uranyl selenite(IV)-selenate(VI) [C 5 H 14 N][(UO 2 ) 3 (SeO 4 ) 4 (HSeO 3 )(H 2 O)](H 2 SeO 3 )(HSeO 4 ) are obtained by the method of evaporation from aqueous solutions. Compound has triclinic lattice, space group P1-bar, a=11.7068(9), b=14.8165(12), c=16.9766(15), α=73.899(6), β=76.221(7), γ=89.361(6) Deg, V=2743.0(4) A 3 , Z=2. Laminated complexes (UO 2 ) 3 (SeO 4 ) 4 (HSeO 3 )(H 2 O)] 3- are the basis of the structure. [HSe(VI)O 4 ] - , [H 2 Se(IV)O 3 ] complexes and protonated methylbutylamine cations are disposed between layers [ru

Spectroscopy Study on the Location and Distribution of Eu3+ Ions in TiO2 Nanoparticles

Science.gov (United States)

Tsuboi, Taiju; Setiawati, Elly; Kawano, Katsuyasu

2008-09-01

Eu3+- and non-doped TiO2 nanoparticles were synthesized by the sol-gel method at sintering temperatures of 500 or 900 °C. The photoluminescence spectra of these nanoparticles have been investigated at various temperatures between 290 and 12 K. Two kinds of Eu3+ photoluminescence spectra were observed. One spectrum consists of sharp lines; the other consists of broad bands. The former was obtained by indirect excitation into Eu3+ with light of wavelengths shorter than 330 nm, while the latter was obtained by direct excitation into Eu3+ with light of wavelengths longer than 380 nm which correspond to the Eu3+ absorption bands. In the latter case, different spectra were obtained depending on the excitation wavelength even in the same absorption band. It is suggested that the sharp line spectrum is caused by Eu3+ ions substituted for Ti4+ but with some distortion around the Eu3+ ions in the matrix of TiO2 due to the large difference in ionic radius between the Ti4+ and Eu3+ ions, which are mainly present in the interior region of the nanoparticle. The broad band spectrum is caused by the disordered Eu3+ ions with Eu-O-Ti bonds which are predominantly present in the near surface region.

Eu3+ doped yttrium oxide nano-luminophores from laser synthesis

International Nuclear Information System (INIS)

Ivanov, M.G.; Kynast, U.; Leznina, M.

2016-01-01

Nano-sized Y 2 O 3 :Eu phosphors were obtained from laser synthesis at a production rate of 25 g/h, the initial product consisting of purely monoclinic material, of primary particle sizes of 20–30 nm as could be shown by powder X-ray diffraction, TEM and BET. Despite a large amount of surface adsorbed water and O–H groups, and peculiarly, nitrous oxide species, as shown by mass spectrometer coupled thermoanalysis/thermogravimetry and FTIR, the luminescence efficiency still amounted to approximately 19% relative to bulk Y 2 O 3 :Eu. On thermal conversion at 900 °C, the transformation to cubic Y 2 O 3 :Eu, now yielding particles of approximately 60 nm appeared to be complete and had an efficiency of about 68%, however, an efficiency of 93%, approaching that of bulk Y 2 O 3 :Eu, was obtained on annealing at 1200 °C. Significantly, a rapid re-formation of carbonates takes place on the calcined samples also. - Highlights: • Nano-sized Y 2 O 3 :Eu phosphors were obtained from laser synthesis. • Luminescence efficiency of monoclinic phase 20 nm nanoparticles was about 19% relative to bulk Y 2 O 3 :Eu. • Purely cubic phase 92 nm particles demonstrated efficiency of 93% of bulk Y 2 O 3 :Eu.

Hydrothermal synthesis and crystal structures of Na{sub 2}Be{sub 3}(SeO{sub 3}){sub 4}.H{sub 2}O and Cs{sub 2}[Mg(H{sub 2}O){sub 6}]{sub 3}(SeO{sub 3}){sub 4}

Energy Technology Data Exchange (ETDEWEB)

Shen, Chen; Mei, Dajiang; Sun, Chuanling; Liu, Yunsheng; Wu, Yuandong [College of Chemistry and Chemical Engineering, Shanghai University of Engineering Science (China)

2017-09-04

The selenites, Na{sub 2}Be{sub 3}(SeO{sub 3}){sub 4}.H{sub 2}O and Cs{sub 2}[Mg(H{sub 2}O){sub 6}]{sub 3}(SeO{sub 3}){sub 4}, were synthesized under hydrothermal conditions. The crystal structures of Na{sub 2}Be{sub 3}(SeO{sub 3}){sub 4}.H{sub 2}O and Cs{sub 2}[Mg(H{sub 2}O){sub 6}]{sub 3}(SeO{sub 3}){sub 4} were determined by single-crystal X-ray diffractions. Na{sub 2}Be{sub 3}(SeO{sub 3}){sub 4}.H{sub 2}O crystallizes in the triclinic space group P1 (no. 2) with unit cell parameters a = 4.8493(9), b = 12.013(2), c = 12.077(2) Aa, and Z = 2, whereas Cs{sub 2}[Mg(H{sub 2}O){sub 6}]{sub 3}(SeO{sub 3}){sub 4} crystallizes in the monoclinic space group C2/m (no. 12) with lattice cell parameters a = 12.596(6), b = 7.297(4), c = 16.914(8) Aa, and Z = 2. Na{sub 2}Be{sub 3}(SeO{sub 3}){sub 4}.H{sub 2}O features a three-dimensional open framework structure formed by BeO{sub 4} tetrahedra and SeO{sub 3} trigonal pyramids. Na cations and H{sub 2}O molecules are located in different tunnels. Cs{sub 2}[Mg(H{sub 2}O){sub 6}]{sub 3}(SeO{sub 3}){sub 4} has a structure composed of isolated [Mg(H{sub 2}O){sub 6}] octahedra and SeO{sub 3} trigonal pyramids interacted by hydrogen bonds, and Cs cations are resided in-between. Both compounds were characterized by thermogravimetric analysis and FT-IR spectroscopy. (copyright 2017 WILEY-VCH Verlag GmbH and Co. KGaA, Weinheim)

Synthesis and physicochemical investigation of vanadium tripolyphosphate, H2VP3O10·3H2O (3)

International Nuclear Information System (INIS)

Lyutsko, V.A.; Romanij, T.V.

1987-01-01

The new compound - vanadium dihydrotripolyphosphate, H 2 VP 3 O 10 x3H 2 O of the modification III has been prepared by interaction of the metalic vanadium and orthophosphoric acid at 483 K. It has been investigated by chemical analysis, thin layer chromatography, X-ray phase analysis, infrared spectroscopy and thermal analysis

Optical spectroscopy of Eu3+ doped Th(MoO4)2

International Nuclear Information System (INIS)

Keskar, Meera; Phatak, Rohan; Gupta, Santhosh; Natarajan, V.

2014-01-01

Eu 3+ is often used as a structural probe, because of the relative simplicity of its energy-level structure and dependence on its site symmetry in the host material. The phonon energy of the host for rare-earth ions is a crucial factor to be considered for developing luminescent materials.Thorium molybdate can satisfy both low phonon energy environment for rare-earth ions and good chemical and mechanical stabilities for practical use. Thus Eu 3+ doped Th(MoO 4 ) 2 are expected to be a good promising optical materials. To the best of our knowledge, there is no report on optical spectroscopy of Eu 3+ doped thorium molybdate and thus work has been carried out and discussed in this paper

Ratiometric luminescence thermometry with different combinations of emissions from Eu3+ doped Gd2Ti2O7 nanoparticles

International Nuclear Information System (INIS)

Lojpur, Vesna; Ćulubrk, Sanja; Dramićanin, Miroslav D.

2016-01-01

Herein, Eu 3+ doped Gd 2 Ti 2 O 7 nanoparticles were tested for application in ratiometric luminescence thermometry. It is shown that two combinations of emissions: one that uses two emissions of Eu 3+ ions and one that uses one emission of Eu 3+ ions and trap emission of Gd 2 Ti 2 O 7 provide thermometry over the 303–423 K temperature range with relative sensitivities between 0.14% K −1 and 0.95% K −1 . Thermometry based on two Eu 3+ emissions from 5 D 0 to 5 D 1 levels has a higher relative sensitivity, but lower absolute sensitivity than thermometry based on one Eu 3+ emission and trap emission of Gd 2 Ti 2 O 7 . The tested material is prepared by Pechini-type polymerized complex route and is composed of agglomerated nanoparticles of ~30–50 nm in size with pure-phase cubic structure (space group Fd-3m) as evidenced from electron microscopy and X-ray diffraction measurements. - Highlights: • Eu 3+ doped Gd 2 Ti 2 O 7 nanoparticles can serve as probes for luminescence thermometry. • Gd 2 Ti 2 O 7 trap emission is an excellent internal standard for luminescence thermometry. • Temperature is measured over 303–423 K range with sensitivity ranging 0.14–0.95% K −1 .

The Preparation and Optical Properties of Novel LiLa(MoO4)2:Sm3+,Eu3+ Red Phosphor

Science.gov (United States)

Luo, Li; Huang, Baoyu; He, Jingqi; Zhang, Wei; Zhao, Weiren; Wang, Jianqing

2018-01-01

Novel LiLa1−x−y(MoO4)2:xSm3+,yEu3+ (in short: LL1−x−yM:xSm3+,yEu3+) double molybdate red phosphors were synthesized by a solid-state reaction at as low temperature as 610 °C. The optimal doping concentration of Sm3+ in LiLa1−x(MoO4)2:xSm3+ (LL1−xM:xSm3+) phosphor is x = 0.05 and higher concentrations lead to emission quenching by the electric dipole—electric dipole mechanism. In the samples co-doped with Eu3+ ions, the absorption spectrum in the near ultraviolet and blue regions became broader and stronger than these of the Sm3+ single-doped samples. The efficient energy transfer from Sm3+ to Eu3+ was found and the energy transfer efficiency was calculated. Under the excitation at 403 nm, the chromaticity coordinates of LL0.95−yM:0.05Sm3+,yEu3+ approach to the NTSC standard values (0.670, 0.330) continuously with increasing Eu3+ doping concentration. The phosphor exhibits high luminous efficiency under near UV or blue light excitation and remarkable thermal stability. At 150 °C, the integrated emission intensity of the Eu3+ remained 85% of the initial intensity at room temperature and the activation energy is calculated to be 0.254 eV. The addition of the LL0.83M:0.05Sm3+,0.12Eu3+ red phosphors can improve the color purity and reduce the correlated color temperature of WLED lamps. Hence, LL1−x−yM:xSm3+,yEu3+ is a promising WLED red phosphor. PMID:29443910

Synthesis and fabrication of Y{sub 2}O{sub 3}:Tb{sup 3+} and Y{sub 2}O{sub 3}:Eu{sup 3+} thin films for electroluminescent applications: Optical and structural characteristics

Energy Technology Data Exchange (ETDEWEB)

Alarcón-Flores, G., E-mail: alar_fbeto@yahoo.com [Centro de Investigación en Ciencia Aplicada y Tecnología Avanzada, IPN, Legaría 694, Irrigación, C.P. 11500, México D.F. (Mexico); García-Hipólito, M. [Instituto de Investigaciones en Materiales, UNAM, Apdo. Postal 70-360, Delegación Coyoacán, C.P. 04150, México D.F. (Mexico); Aguilar-Frutis, M. [Centro de Investigación en Ciencia Aplicada y Tecnología Avanzada, IPN, Legaría 694, Irrigación, C.P. 11500, México D.F. (Mexico); Carmona-Téllez, S. [Instituto de Física, UNAM, Coyoacán, C.P. 04150, México D.F. (Mexico); Martinez-Martinez, R. [Universidad Tecnológica de la Mixteca, Carretera Acatlima Km 2.5, Huajuapan de León Oaxaca, C.P. 69000, México (Mexico); Campos-Arias, M.P. [Centro de Investigación en Ciencia Aplicada y Tecnología Avanzada, IPN, Legaría 694, Irrigación, C.P. 11500, México D.F. (Mexico); Zaleta-Alejandre, E. [Universidad Autónoma del Estado de Hidalgo-Escuela Superior de Apan, Carretera Apan-Calpulalpan Km. 8, C.P. 43920, Apan, Hidalgo (Mexico); and others

2015-01-15

Terbium, europium and yttrium β diketonates have been synthesized from acetylacetone and inorganic metal salts and used as precursors for the deposition of Tb{sup 3+} or Eu{sup 3+} doped Y{sub 2}O{sub 3} polycrystalline films by the ultrasonic spray pyrolysis technique. The films were deposited on c-Si substrates at temperatures in the 400–550 °C range. The optical and structural characterization of these films as a function of substrate temperature and Tb{sup 3+} and Eu{sup 3+} concentration was carried out by means of photoluminescence (PL), cathodoluminescence (CL), infrared (IR), ellipsometry, and UV–visible spectroscopy and atomic force microscopy (AFM), energy dispersive spectroscopy (EDS) and X ray diffraction (XRD) measurements respectively. The PL intensity from these films was found to depend on deposition temperature. Films deposited above 450 °C exhibited the characteristic PL peaks associated with either Tb{sup 3+} or Eu{sup 3+} intra electronic energy levels transitions. The most intense PL emission was found for dopant concentration of 10 at% for Tb{sup 3+} and at 8 at% for Eu{sup 3+} ions into precursor solution. In both cases concentration quenching of the PL emission was observed for concentrations above these values. The films had a refractive index (1.81), low average surface roughness (∼62 Å) and a UV–Vis. transmission of the order of 90 %T. - Highlights: • Terbium, europium and yttrium β diketonates have been synthesized. • Luminescent thin films of Y{sub 2}O{sub 3}:Tb{sup 3+} and Y{sub 2}O{sub 3}:Eu{sup 3+} were obtained. • Optical and structural characteristics of these thin films are presented. • The films had a refractive index (1.81) and low average surface roughness (∼62 Å)

Enhanced luminescence in Mg{sup 2+} codoped CaTiO{sub 3}:Eu{sup 3+} phosphor prepared by solid state reaction

Energy Technology Data Exchange (ETDEWEB)

Vandana, C. Sai; Rudramadevi, B. Hemalatha [Department of Physics, Sri Venkateswara University, Tirupati-517 502 (India)

2016-05-23

CaTiO{sub 3} phosphors doped with Eu{sup 3+} and codoped with Mg{sup 2+} were prepared by Solid State Reaction method. The powders were characterized by X-ray diffraction, SEM with EDS, Raman scattering, and photoluminescence spectroscopy. The Crystalline phase and vibrational modes of the phosphors were studied using XRD pattern and Raman Spectrum respectively. The morphological studies of the phosphor samples were carried out using SEM analysis. From PL spectra we have observed two prominent red emission peaks around at 595 nm ({sup 5}D{sub 0}→{sup 7}F{sub 1}), 619 nm ({sup 5}D{sub 0}→{sup 7}F{sub 2}) with the excitation of 399 nm for Eu{sup 3+} doped CaTiO{sub 3} powders. The PL intensity of CaTiO{sub 3}:Eu{sup 3+} phosphor is enhanced significantly on codoping with Mg{sup 2+}. The observed enhanced emissions are due to energy transfer from Mg{sup 2+} to Eu{sup 3+}, which is due to radiative recombination. Eu{sup 3+} doped phosphors are well known to be promising materials for electroluminescent devices, optical amplifiers, and lasers.

Luminescence and energy transfer mechanism in Eu{sup 3+}/Tb{sup 3+}-co-doped ZrO{sub 2} nanocrystal rods

Energy Technology Data Exchange (ETDEWEB)

Ahemen, I., E-mail: ahemior@gmail.com; Dejene, F. B. [University of the Free State-QwaQwa Campus, Department of Physics (South Africa)

2017-01-15

Nanocrystal rods of Eu{sup 3+}/Tb{sup 3+}-co-doped ZrO{sub 2} were synthesized using a simple chemical precipitation technique. Both ions were successfully doped into the Zr{sup 4+} ion site in a mixed structure containing both monoclinic and tetragonal phases. The Eu{sup 3+} or Tb{sup 3+} singly doped zirconia produced red and green luminescence which are characteristics of Eu{sup 3+} and Tb{sup 3+} ions, respectively. The co-doped zirconia samples produced blue emission from defect states transitions in the host ZrO{sub 2}, red and green luminescence from dopant ions giving cool to warm white light emissions. The phosphors were efficiently excited by ultraviolet and near-ultraviolet/blue radiations giving white and red light, respectively. The decay lifetime was found to increase with increasing donor ion concentration contrary to conventional observations reported by previous researchers. Weak quadrupole–quatdrupole multipolar process was responsible for energy transfer from Tb{sup 3+} (donor) ion to Eu{sup 3+} ion. No energy back-transfer from Eu{sup 3+} to Tb{sup 3+} ion was observed from the excitation spectra. Temperature-dependent photoluminescence shows the presence of defects at low temperature, but these defects vanished at room temperature and beyond. The Eu{sup 3+}/Tb{sup 3+}-co-doped ZrO{sub 2} nanocrystal rod is a potential phosphor for white light application using UV as an excitation source. Thermoluminescence measurements show that the inclusion of Tb{sup 3+} ion increases trap depths in the host zirconia.

Luminescent properties of Eu2+ and Ce3+ ions in strontium litho-silicate Li2SrSiO4

International Nuclear Information System (INIS)

Dotsenko, V.P.; Levshov, S.M.; Berezovskaya, I.V.; Stryganyuk, G.B.; Voloshinovskii, A.S.; Efryushina, N.P.

2011-01-01

The luminescent properties of Eu 2+ and Ce 3+ ions in Li 2 SrSiO 4 have been studied upon excitation in the 2-20 eV region. Based on the results of luminescent measurements, values of the crystal field splitting and the centroid shift of the Ce 3+ 5d configuration in Li 2 SrSiO 4 were found and compared with those of Ce 3+ ions in some other inorganic compounds. The Eu 2+ ions in Li 2 SrSiO 4 exhibit a broad band emission with a maximum at 576 nm, which is due to the 4f 6 5d→4f 7 transition. It was shown that the long-wavelength position of the Eu 2+ emission in Li 2 SrSiO 4 is caused by the large crystal-field splitting of the Eu 2+ 4f 6 5d configuration and relatively high degree of covalency of the Eu-O bond. The stabilization of Eu 2+ ions in Li 2 SrSiO 4 during the synthesis process requires a strong reducing agent. Two phenomenological approaches to explain the low stability of Eu 2+ in Li 2 SrSiO 4 are also discussed.

Thermoluminescence properties of Eu and Li co-doped Gd2O3, induced by UV light

International Nuclear Information System (INIS)

Hristov, H; Arhangelova, N; Velev, V; Uzunov, N M; Baneva, Y; Nedeva, D; Penev, I; Moschini, G; Rossi, P

2012-01-01

For some specific biomedical applications, connected with in-situ measurements of the absorbed dose of ultraviolet (UV) light, we have developed materials, sensitive to the light emission with a wavelength up to 320nm. Thermoluminescence (TL) yield of Gd 2 O 3 , doped with Eu and Li has been analysed with respect to the quantity of Li co-dopant. Lithium has been added as Li 2 CO 3 to a mixture of Gd 2 O 3 with 10 wt% Eu 2 O 3 . Pellets with the mixture have been sintered at a temperature of 1000°C. The kinetic parameters of the phosphors thus obtained have been studied from the TL glow curves after irradiation with UV light. It has been demonstrated that the addition of 16 wt% of Li 2 CO 3 to the Eu-doped Gd 2 O 3 yields a maximum intensity of the peaks at 87°C and at 145°C. Studies on the kinetic parameters as well as the TL properties of Eu-doped Gd 2 O 3 with the addition of 16% of Li 2 CO 3 have been conducted. It has been measured that two of the TL peaks of this phosphor have relatively long fading. Analysis of the TL properties of the phosphors obtained from Gd 2 O 3 , doped with Eu and Li, shows that they possess good sensitivity to the UV emission and could be used as appropriate phosphors for detection and quantitative measurements of UV light.

Effect of Al{sup 3+} ions on fluorescence properties of Eu{sup 3+} ions in YbO{sub 3} phosphors

Energy Technology Data Exchange (ETDEWEB)

Balakrishnaiah, R.; Kim, Dong Woo; Yi, Soung Soo [Silla Univ., Busan (Korea, Republic of); Balakrishnaiah, R.; Jang, Kiwan; Lee, Ho Sueb [Changwon National Univ., Changwon (Korea, Republic of); Jeong, Jung Hyun [Pukyong National Univ., Busan (Korea, Republic of)

2008-11-15

Over the past few years, much attention has been paid to the synthesis and development of luminescence properties, of various lanthanide (Ln)doped materials that are useful for plasma display panels (PDPs). In order to display full colors in PDPs, red, green and blue phosphors are required. The PDP phosphors emit visible light under VUV excitation. The VUV pump photon is absorbed by the host lattice and the absorbed energy is transferred to the activator. Since the red emission, which comes from the {sup 5D0→7F2t}ransition, is hypersensitive to the lattice symmetry of the host crystal and will be relatively strong if the symmetry of the crystal is low, it is possible to tune the intensity of red emission by modifying the neighboring network design around Eu{sup 3}+{sup i}ons on introducing other atoms such as Ca, Sr, Ba, Zn, Al, Li, Sc, Bi, La, Gd, etc., into the ortho borate host lattice. Incorporation of these metal atoms into the host lattice of YBO{sup 3d}istorts the lattice to modify the energy absorption and transfer behaviors, resulting in an increased emission intensity. In this work, we have prepared Y{sup (}0.95-X)Eu{sup 0}.05{sup B}O{sup 3:}Al{sup 3}+{sup (}X){sup (}x=0, 0.05, 0.10, 0.15 and 0.20)phosphors by solid state reaction method by using the high purity chemicals of Y{sup 2O3,} H{sup 3B}O{sup 3,} Eu{sup 2O3a}nd Al{sup 2O3t}o study the effect of concentration of Al{sup 3}+{sup i}ons on the luminescence properties of Eu{sup 3}+{sup i}ons in YBO{sup 3p}hosphor. The prepared samples are characterized by XRD, SEM, photoluminescence excitation, photoluminescence emission and lifetime measurements. The results are also compared with those of earlier reported works.

High colour purity single-phased full colour emitting white LED phosphor Sr2V2O7:Eu3+

International Nuclear Information System (INIS)

Zhou Zhi; Zhou Nan; He Zhangxing; Liu Suqin; Liu Younian; Tian Ziwei; Wang Nanfang; Mao Zhiyong; Hintzen, H T

2013-01-01

Single-phased white-light-emitting phosphor Sr 2 V 2 O 7 :Eu 3+ was successfully synthesized by the solid-state method. The result of x-ray diffraction analysis indicated that the obtained phosphor has the same crystal structure as that of Sr 2 V 2 O 7 . The synthesized Sr 2 V 2 O 7 :Eu 3+ was combined with near-UV light (365 nm) chips and then assembled into ligtht-emitting diodes (LED) devices, which generated white light with colour coordinates of (0.324, 0.317). The white light was generated from yellow-green and red emissions, which should be attributed to the host Sr 2 V 2 O 7 and dopant Eu ions, respectively. The effects of the concentration of Eu ions and charge compensation on the emission intensity were carefully investigated. The results show that the energy migrates from the host to the dopant and also that Li 2 CO 3 should be the best charge compensator for this single-phased phosphor. In addition, the colour rendering index and luminescence efficiency of the fabricated LED devices with Sr 1.90 V 2 O 7 :0.10Eu 3+ phosphor were 91 and 32 lm W -1 , respectively, suggesting that Sr 1.90 V 2 O 7 :0.10Eu 3+ phosphor is a potential candidate for the phosphor-converted white-light-emitting diodes with near-UV chips.

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.

Effect of Gd substitution on structure and spectroscopic properties of (Lu,Gd)2O3:Eu ceramic scintillator

Science.gov (United States)

Cao, Maoqing; Hu, Zewang; Ivanov, Maxim; Dai, Jiawei; Li, Chaoyu; Kou, Huamin; Shi, Yun; Chen, Haohong; Xu, Jiayue; Pan, Yubai; Li, Jiang

2018-02-01

In this paper, (Lu1-xGdx)2O3:Eu (x = 0, 0.1, 0.3, 0.5, 0.7, 0.9) ceramics were consolidated by the solid-state reaction method combined with vacuum sintering without sintering aids. We investigated the effect of the varying contents of Gd2O3 on the structure and spectroscopic properties of (Lu1-xGdx)2O3:Eu ceramics. X-ray diffraction (XRD) patterns indicate that proper amount of Gd2O3 can incorporate well with Lu2O3 and form Lu2O3-Gd2O3 solid solution. However, excessive Gd3+-doping in Lu2O3 will lead to the cubic phase transforming into monoclinic even hexagonal phase. The Gd3+ substitution no more than 50% of Lu2O3 enhances the radioluminescence, and reduces the fluorescence lifetime. Transmittance, photoluminescence, and radiation damage of the (Lu1-xGdx)2O3:Eu scintillation ceramics were also studied.

Luminescent Polymer Electrolyte Composites Using Silica Coated-Y2O3:Eu as Fillers

Directory of Open Access Journals (Sweden)

Mikrajuddin Abdullah

2003-05-01

Full Text Available Luminescent polymer electrolyte composites composed of silica coated Y2O3:Eu in polyethylene glycol (PEG matrix has been produced by initially synthesizing silica coated Y2O3:Eu and mixing with polyethylene glycol in a lithium salt solution. High luminescence intensity at round 600 nm contributed by electron transitions in Eu3+ (5D0 -> 7F0, 5D0 -> 7F1, and 5D0 -> 7F3 transitions were observed. The measured electrical conductivity was comparable to that reported for polymer electrolyte composites prepared using passive fillers (non luminescent. This approach is therefore promising for production of high intensity luminescent polymer electrolyte composites for use in development of hybrid battery/display.

Synthesis and photocatalytic activity of Eu3+-doped nanoparticulate TiO2 sols and thermal stability of the resulting xerogels

International Nuclear Information System (INIS)

Borlaf, Mario; Moreno, Rodrigo; Ortiz, Angel L.; Colomer, María T.

2014-01-01

The synthesis of nanoparticulate TiO 2 sols without and with Eu 3+ doping (1, 2, or 3 mol%) by the colloidal sol–gel method in aqueous media was investigated, with emphasis on the effect of the Eu 3+ doping on the peptization time and rheological properties of the sols. It was found that the addition of Eu 3+ increasingly retards the peptization process, and also results in sols with greater aggregate sizes which are therefore more viscous, although in all cases the distributions of aggregate sizes are unimodal and the flow behavior is Newtonian. The shifting of the isoelectric point of the sols toward greater pH with increasing Eu 3+ doping indicates that the aforementioned trends are due to the chemical adsorption of europium ionic complexes in the form of solvated species. Furthermore, the effect of Eu 3+ doping on the ultraviolet–visible spectrum and photocatalytic activity of the peptized sols was also explored. It was found that the Eu 3+ doping increasingly shifts slightly the absorption edge from the ultraviolet to the visible range, and that its effect on the photocatalytic activity is certainly complex because this is enhanced only if the Eu 3+ cations have some electronic transition (charge transfer transition or transitions between the ground state and the excited states) at the wavelength of the incident radiation, in which case the photocatalytic activity first increases with increasing Eu 3+ content and then decreases perhaps due to occurrence of Eu–Eu interactions or simply to the greater aggregation state. Finally, the influence of the Eu 3+ doping on the thermal stability of the nanoparticulate xerogels resulting from the drying of the peptized sols was also examined by X-ray thermo-diffractometry together with transmission electron microscopy, selected area electron diffractometry, and X-ray energy-dispersive spectrometry. It was found that although the xerogels crystallize all as anatase phase, this is increasingly more thermally stable

Nanostructured ZnO/Y2O3:Eu for use as fillers in luminescent polymer electrolyte composites

International Nuclear Information System (INIS)

Abdullah, Mikrajuddin; Panatarani, Camellia; Kim, Tae-Oh; Okuyama, Kikuo

2004-01-01

Nanostructured ZnO/Eu and ZnO/Y 2 O 3 :Eu composites have been produced by hydrolizing a mixture of zinc acetate, yttrium acetate and europium acetate in ethanol solution, followed by mixing with lithium hydroxide. By analyzing the ICP data, XRD patterns and luminescence emission spectra we concluded that the europium and yttrium compounds appeared as coating layer on the surface of ZnO nanoparticles. Without heating, these layers were in amorphous state and transformed into crystalline state after annealing at temperatures of above 600 deg. C around 30 min. We observed the presence of lithium hydroxide concentration threshold below which no coating layer was formed on the surface of ZnO nanoparticles. The emission intensity of ZnO/Y 2 O 3 :Eu was found to increase with increasing annealing temperature, while the crystalline size of Y 2 O 3 (close to 20 nm) decreased with increasing the annealing temperature. The powder produced might be used as fillers in luminescent polymer electrolyte composites, which can produce two colors, i.e., red (Eu emission) when excited using a wavelength of around 254 nm and green (emitted by ZnO nanoparticles) when excited using a wavelength of around 365 nm

Sr(1.7)Zn(0.3)CeO4: Eu3+ novel red-emitting phosphors: synthesis and photoluminescence properties.

Science.gov (United States)

Li, Haifeng; Zhao, Ran; Jia, Yonglei; Sun, Wenzhi; Fu, Jipeng; Jiang, Lihong; Zhang, Su; Pang, Ran; Li, Chengyu

2014-03-12

A series of novel red-emitting Sr1.7Zn0.3CeO4:Eu(3+) phosphors were synthesized through conventional solid-state reactions. The powder X-ray diffraction patterns and Rietveld refinement verified the similar phase of Sr1.7Zn0.3CeO4:Eu(3+) to that of Sr2CeO4. The photoluminescence spectrum exhibits that peak located at 614 nm ((5)D0-(7)F2) dominates the emission of Sr1.7Zn0.3CeO4:Eu(3+) phosphors. Because there are two regions in the excitation spectrum originating from the overlap of the Ce(4+)-O(2-) and Eu(3+)-O(2-) charge-transfer state band from 200 to 440 nm, and from the intra-4f transitions at 395 and 467 nm, the Sr1.7Zn0.3CeO4:Eu(3+) phosphors can be well excited by the near-UV light. The investigation of the concentration quenching behavior, luminescence decay curves, and lifetime implies that the dominant mechanism type leading to concentration quenching is the energy transfer among the nearest neighbor or next nearest neighbor activators. The discussion about the dependence of photoluminescence spectra on temperature shows the better thermal quenching properties of Sr1.7Zn0.3CeO4:0.3Eu(3+) than that of Sr2CeO4:Eu(3+). The experimental data indicates that Sr1.7Zn0.3CeO4:Eu(3+) phosphors have the potential as red phosphors for white light-emitting diodes.

Synthesis and Characterization of SiO2@Y2MoO6:Eu3+ Core-Shell Structured Spherical Phosphors by Sol-Gel Process.

Science.gov (United States)

Li, G Z; Liu, F H; Chu, Z S; Wu, D M; Yang, L B; Li, J L; Wang, M N; Wang, Z L

2016-04-01

SiO2@Y2MoO6:Eu3+ core-shell phosphors were prepared by the sol-gel process. X-ray diffraction (XRD), Fourier transform infrared spectroscopy (FT-IR), field emission scanning electron microscopy (FESEM), energy-dispersive X-ray spectra (EDS), transmission electron microscopy (TEM), photoluminescence (PL) spectra as well as kinetic decays were used to characterize the resulting SiO2@Y2MoO6:Eu3+ core-shell phosphors. The XRD results demonstrated that the Y2MoO6:Eu3+ layers on the SiO2 spheres crystallized after being annealed at 700 °C and the crystallinity increased with raising the annealing temperature. The obtained core-shell phosphors have spherical shape with narrow size distribution (average size ca. 640 nm), non-agglomeration, and smooth surface. The thickness of the Y2MoO6:Eu3+ shells on the SiO2 cores could be easily tailored by varying the number of deposition cycles (70 nm for four deposition cycles). The Eul+ shows a strong PL emission (dominated by 5D0-7F2 red emission at 614 nm) under the excitation of 347 nm UV light. The PL intensity of Eu3+ increases with increasing the annealing temperature and the number of coating cycles.

Enhancement of Color Rendering Index for White Light LED Lamps by Red Y2O3:EU3+ Phosphor

Directory of Open Access Journals (Sweden)

Tran Hoang Quang Minh

2016-01-01

Full Text Available We present an application of the red Y2O3:Eu3+ dopant phosphor compound for reaching the color rendering index as high as 86. The Multi-Chip White LED lamps (MCW-LEDs with high Correlated Color Temperatures (CCTs including 7000 K and 8500 K are employed in this study. Besides, the impacts of the Y2O3:Eu3+ phosphor on the attenuation of light through phosphor layers of the various packages is also demonstrated based on the Beer-Lambert law. Simulation results provide important conclusion for selecting and developing the phosphor materials in MCW-LEDs manufacturing.

Synthesis and photoluminescence properties of Ba2CaZn2Si6O17:Eu3+ red phosphors for white LED applications

International Nuclear Information System (INIS)

Annadurai, G.; Kennedy, S. Masilla Moses

2016-01-01

Novel pellyite type Ba 2 CaZn 2 Si 6 O 17 :Eu 3+ red emitting phosphors with different Eu 3+ contents were synthesized by the solid state reaction method. The crystal structure, photoluminescence properties and concentration quenching of Ba 2 CaZn 2 Si 6 O 17 :Eu 3+ phosphors were investigated. Powder X-ray diffraction measurements confirmed the structure of the samples. The photoluminescence emission (PL) and excitation (PLE) spectra were measured. The results showed that the dominant hypersensitive red emission peak of the phosphors Ba 2 CaZn 2 Si 6 O 17 :Eu 3+ was located at 613 nm attributed to the Eu 3+ transition ( 5 D 0 → 7 F 2 ) which could be effectively excited by 395 nm (near-UV). The latter band matched well with the emission from the near-UV LED chips. The intensity ratio of 5 D 0 → 7 F 2 to 5 D 0 → 7 F 1 transition showed slight variation with Eu 3+ concentrations. The Eu 3+ emission intensity was maximum for 9 mol%. The luminescence quantum efficiency was determined and also the decay profiles were obtained and analyzed. In addition, the Commission International del'Eclairage (CIE) chromaticity coordinates of Ba 2 CaZn 2 Si 6 O 17 :0.09Eu 3+ phosphor were calculated to be 0.637 and 0.362. The experimental results demonstrated that the Ba 2 CaZn 2 Si 6 O 17 :Eu 3+ red emitting phosphor is a potential candidate for white light emitting diodes (WLEDs) pumped by near-UV chip. - Highlights: • A novel Ba 2 CaZn 2 Si 6 O 17 :Eu 3+ red phosphor was synthesized. • The samples yielded a dominant PL emission of Eu 3+ at 613 nm. • Eu 3+ concentration was optimized to be 9 mol% in Ba 2 CaZn 2 Si 6 O 17. • CIE chromaticity coordinates were estimated from the emission spectrum.

Correlation of Structure, Tunable Colors, and Lifetimes of (Sr, Ca, Ba)Al2O4:Eu2+, Dy3+ Phosphors

OpenAIRE

Qidi Xie; Bowen Li; Xin He; Mei Zhang; Yan Chen; Qingguang Zeng

2017-01-01

(Sr, Ca, Ba)Al2O4:Eu2+, Dy3+ phosphors were prepared via a high temperature solid-state reaction method. The correlation of phase structure, optical properties and lifetimes of the phosphors are investigated in this work. For the (Sr, Ca)Al2O4:Eu2+, Dy3+ phosphors, the different phase formation from monoclinic SrAl2O4 phase to hexagonal SrAl2O4 phase to monoclinic CaAl2O4 phase was observed when the Ca content increased. The emission color of SrAl2O4:Eu2+, Dy3+ phosphors varied from green to ...

Novel 2D or 3D alkaline-earth metal sulfonate-phosphonates based on [O 3S-C 2H 4-PO 3H] 2- ligand

Science.gov (United States)

Du, Zi-Yi; Wen, He-Rui; Xie, Yong-Rong

2008-11-01

Three novel alkaline-earth metal sulfonate-phosphonates based on [O 3S-C 2H 4-PO 3H] 2- ligand, namely, [Ca(O 3SC 2H 4PO 3H)(H 2O) 2] ( 1), [Sr(O 3SC 2H 4PO 3H)] ( 2) and [Ba 2(O 3SC 2H 4PO 3H) 2] ( 3), have been synthesized by hydrothermal reactions. They represent the first structurally characterized alkaline-earth metal complexes of phosphonic acid attached with a sulfonate group. The structure of compound 1 features a 2D layer based on 1D chains of [Ca 2(PO 3) 2] bridged by -CH 2-CH 2-SO 3- groups. Compounds 2 and 3 show pillar-layer architecture based on two different inorganic layers linked by -CH 2-CH 2- groups. The inorganic layer in compound 2 features a 1D chain of edge-sharing SrO 8 polyhedra whereas that in compound 3 features an edge-sharing Ba 2O 14 di-polyhedral unit which is further corner-shared with four neighboring ones. The [O 3S-C 2H 4-PO 3H] 2- ligand shows diverse coordination modes in the three alkaline-earth metal sulfonate-phosphonates.

Correlation of Structure, Tunable Colors, and Lifetimes of (Sr, Ca, Ba)Al2O4:Eu2+, Dy3+ Phosphors

Science.gov (United States)

Xie, Qidi; Li, Bowen; He, Xin; Zhang, Mei; Chen, Yan; Zeng, Qingguang

2017-01-01

(Sr, Ca, Ba)Al2O4:Eu2+, Dy3+ phosphors were prepared via a high temperature solid-state reaction method. The correlation of phase structure, optical properties and lifetimes of the phosphors are investigated in this work. For the (Sr, Ca)Al2O4:Eu2+, Dy3+ phosphors, the different phase formation from monoclinic SrAl2O4 phase to hexagonal SrAl2O4 phase to monoclinic CaAl2O4 phase was observed when the Ca content increased. The emission color of SrAl2O4:Eu2+, Dy3+ phosphors varied from green to blue. For the (Sr, Ba)Al2O4:Eu2+, Dy3+ phosphors, different phase formation from the monoclinic SrAl2O4 phase to the hexagonal BaAl2O4 phase was observed, along with a shift of emission wavelength from 520 nm to 500 nm. More interestingly, the decay time of SrAl2O4:Eu2+, Dy3+ changed due to the different phase formations. Lifetime can be dramatically shortened by the substitution of Sr2+ with Ba2+ cations, resulting in improving the performance of the alternating current light emitting diode (AC-LED). Finally, intense LEDs are successfully obtained by combining these phosphors with Ga(In)N near UV chips. PMID:29057839

Correlation of Structure, Tunable Colors, and Lifetimes of (Sr, Ca, BaAl2O4:Eu2+, Dy3+ Phosphors

Directory of Open Access Journals (Sweden)

Qidi Xie

2017-10-01

Full Text Available (Sr, Ca, BaAl2O4:Eu2+, Dy3+ phosphors were prepared via a high temperature solid-state reaction method. The correlation of phase structure, optical properties and lifetimes of the phosphors are investigated in this work. For the (Sr, CaAl2O4:Eu2+,Dy3+ phosphors, the different phase formation from monoclinic SrAl2O4 phase to hexagonal SrAl2O4 phase to monoclinic CaAl2O4 phase was observed when the Ca content increased. The emission color of SrAl2O4:Eu2+, Dy3+ phosphors varied from green to blue. For the (Sr, BaAl2O4:Eu2+, Dy3+ phosphors, different phase formation from the monoclinic SrAl2O4 phase to the hexagonal BaAl2O4 phase was observed, along with a shift of emission wavelength from 520 nm to 500 nm. More interestingly, the decay time of SrAl2O4:Eu2+, Dy3+changed due to the different phase formations. Lifetime can be dramatically shortened by the substitution of Sr2+ with Ba2+ cations, resulting in improving the performance of the alternating current light emitting diode (AC-LED. Finally, intense LEDs are successfully obtained by combining these phosphors with Ga(InN near UV chips.

Investigations of gamma irradiation on the properties of luminescent films of polycarbonate(PC) matrix doped with europium complex [Eu(tta)3(H2O)2

International Nuclear Information System (INIS)

Forster, Pedro L.; Lugao, Ademar B.; Martins, Natalia A.; Egute, Nayara S.; Parra, Duclerc F.; Brito, Hermi F.

2009-01-01

Luminescent lanthanide complexes have attracted much recent interest for their application as luminescent materials. The combination of unique spectroscopic properties from rare earth complexes associated to physical and chemical intrinsic properties of polymers became more attractive in the last years. A number of advantages of these substances have been reported or realized over the much studied conjugated polymers and nonlanthanide. Luminescent films composed by diaquatris(thenoyltrifluoroacetonate)europium(III) complex [Eu(tta) 3 (H 2 O) 2 ] doped into a polycarbonate (PC) matrix were prepared and irradiated at gamma radiation with 5, 10, and 20 kGy. The PC polymer was doped with 1% (w/w) of the Eu 3+ complex. The thermal properties was investigated by utilization of differential scanning calorimeter (DSC) changes in thermal stability was observed due to the addition of doping agent into the polycarbonate matrix. Changes in photophysical properties due of gamma radiation was observed by emission, excitation spectra and fourier transformed infrared spectra (FTIR). Based on the emission spectra of PC:1% Eu(tta)3 film were observed the characteristic bands arising from the 5 D 0 7 F J transitions of Eu 3+ ion (J=0-4), indicating the ability to obtain the luminescence films. (author)

Fabrication of Au{sub nanoparticle}@mSiO{sub 2}@Y{sub 2}O{sub 3}:Eu nanocomposites with enhanced fluorescence

Energy Technology Data Exchange (ETDEWEB)

Li, Huiqin [Key Laboratory of Synthetic and Natural Functional Molecule Chemistry (Ministry of Education), Shaanxi Key Laboratory of Physico-Inorganic Chemistry, College of Chemistry & Materials Science, Northwest University, Xi' an, 710069 (China); College of Chemistry & Chemical Engineering, Baoji University of Arts & Sciences, Baoji, 721013 (China); Kang, Jianmiao [Key Laboratory of Synthetic and Natural Functional Molecule Chemistry (Ministry of Education), Shaanxi Key Laboratory of Physico-Inorganic Chemistry, College of Chemistry & Materials Science, Northwest University, Xi' an, 710069 (China); Yang, Jianhui, E-mail: jianhui@nwu.edu.cn [Key Laboratory of Synthetic and Natural Functional Molecule Chemistry (Ministry of Education), Shaanxi Key Laboratory of Physico-Inorganic Chemistry, College of Chemistry & Materials Science, Northwest University, Xi' an, 710069 (China); Wu, Biao, E-mail: wubiao@nwu.edu.cn [Key Laboratory of Synthetic and Natural Functional Molecule Chemistry (Ministry of Education), Shaanxi Key Laboratory of Physico-Inorganic Chemistry, College of Chemistry & Materials Science, Northwest University, Xi' an, 710069 (China)

2016-07-15

Herein, Au{sub nanoparticle}@mSiO{sub 2}@Y{sub 2}O{sub 3}:Eu nanocomposites are synthesized through layer-by-layer assembly technology. Au{sub nanoparticle}@mSiO{sub 2} core–shell nanospheres were prepared at first in the presence of CTAB in aqueous solution system by the modified one-pot method. A chemical precipitation method and a succeeding calcination process were adopted to the growth of Y{sub 2}O{sub 3}:Eu shells on the surfaces of Au{sub nanoparticle}@mSiO{sub 2} core–shell nanospheres. The structure, morphology and composition of the nanocomposites were confirmed by XRD, TEM and UV–vis absorption spectrum. The prepared Au{sub nanoparticle}@mSiO{sub 2}@Y{sub 2}O{sub 3}:Eu nanocomposites have showed the emission intensity enhances to 6.23 times at 30 nm thickness of the silica spacer between the core of Au nanoparticle and the shell of Y{sub 2}O{sub 3}:Eu. According to the observations of fluorescent lifetime and the modeling of local electric field, the metal-enhanced and quenched fluorescence is closely related with the enhancement of excitation and radiative decay rate and the quenching by NRET comes as a result of competition between the distance-dependent mechanisms. This kind of multifunctional inorganic material will be widely used in electronics, biology and medical drug loading, etc. - Highlights: • Fabrication of Au{sub nanoparticle}@mSiO{sub 2}@Y{sub 2}O{sub 3}:Eu nanocomposites with core-spacer-shell structure. • The controllable fluorescence is achieved by adjusting the spacer thickness of silica. • The fluorescence enhancement is 6.23-fold at an optimal spacer thickness about 30 nm. • The metal-enhanced fluorescence mechanism is proposed.