EuO and Gd-doped EuO thin films. Epitaxial growth and properties

Energy Technology Data Exchange (ETDEWEB)

Sutarto, Ronny

2009-07-06

this respect the quality of many of the doped EuO samples used in the past bulk studies. The focus of this thesis is on the preparation and the properties of high-quality single-crystalline EuO and Gd-doped EuO thin films. The so-called Eu-distillation-assisted molecular beam epitaxy (MBE) has been employed to achieve full control of the stoichiometry. The films have been epitaxially grown on yttria-stabilized cubic zirconia (YSZ) (001) substrates. By a systematic variation of the oxygen deposition rates, we have been able to observe sustained oscillations in the intensity of the reflection high-electron energy diffraction (RHEED) pattern during growth. We thus have demonstrated that layer-by-layer growth has been achieved for the first time. We also have confirmed that YSZ indeed supplies oxygen during the initial stages of growth, yet the EuO stoichiometry can still be well maintained. In the case of Gd-doped EuO films, the presence of Gd even helps to stabilize the layer-by-layer growth mode. It is important to achieve this growth mode, since it enables the preparation of films with very smooth and at surfaces. This in turn facilitates the capping of the films with a thin Al overlayer in order to protect the films against degradation under ambient conditions. More important, the smoothness of the lm will enable the preparation of high quality device structures. By using ex-situ soft x-ray absorption spectroscopy (XAS) at the Eu and Gd M{sub 4,5} edges, we have confirmed that the films are completely free from Eu{sup 3+} contaminants, and we were able to determine reliably the actual Gd concentration. This actual Gd concentration could in fact significantly deviate from the nominal Gd/Eu evaporation ratio. From magnetization and susceptibility measurements, we found the Curie temperature to increase smoothly as a function of doping from 69 K up to a maximum of 125 K, all with a saturation moment of 7 {mu}B. A threshold behavior was not observed for Gd concentrations

Isomer decay spectroscopy of 164Sm and 166Gd: midshell collectivity around N=100.

Science.gov (United States)

Patel, Z; Söderström, P-A; Podolyák, Zs; Regan, P H; Walker, P M; Watanabe, H; Ideguchi, E; Simpson, G S; Liu, H L; Nishimura, S; Wu, Q; Xu, F R; Browne, F; Doornenbal, P; Lorusso, G; Rice, S; Sinclair, L; Sumikama, T; Wu, J; Xu, Z Y; Aoi, N; Baba, H; Bello Garrote, F L; Benzoni, G; Daido, R; Fang, Y; Fukuda, N; Gey, G; Go, S; Gottardo, A; Inabe, N; Isobe, T; Kameda, D; Kobayashi, K; Kobayashi, M; Komatsubara, T; Kojouharov, I; Kubo, T; Kurz, N; Kuti, I; Li, Z; Matsushita, M; Michimasa, S; Moon, C-B; Nishibata, H; Nishizuka, I; Odahara, A; Şahin, E; Sakurai, H; Schaffner, H; Suzuki, H; Takeda, H; Tanaka, M; Taprogge, J; Vajta, Zs; Yagi, A; Yokoyama, R

2014-12-31

Excited states in the N=102 isotones 166Gd and 164Sm have been observed following isomeric decay for the first time at RIBF, RIKEN. The half-lives of the isomeric states have been measured to be 950(60) and 600(140) ns for 166Gd and 164Sm, respectively. Based on the decay patterns and potential energy surface calculations, including β6 deformation, a spin and parity of 6- has been assigned to the isomeric states in both nuclei. Collective observables are discussed in light of the systematics of the region, giving insight into nuclear shape evolution. The decrease in the ground-band energies of 166Gd and 164Sm (N=102) compared to 164Gd and 162Sm (N=100), respectively, presents evidence for the predicted deformed shell closure at N=100.

Isomer Decay Spectroscopy of Sm 164 and Gd 166 : Midshell Collectivity Around N =100

Science.gov (United States)

Patel, Z.; Söderström, P.-A.; Podolyák, Zs.; Regan, P. H.; Walker, P. M.; Watanabe, H.; Ideguchi, E.; Simpson, G. S.; Liu, H. L.; Nishimura, S.; Wu, Q.; Xu, F. R.; Browne, F.; Doornenbal, P.; Lorusso, G.; Rice, S.; Sinclair, L.; Sumikama, T.; Wu, J.; Xu, Z. Y.; Aoi, N.; Baba, H.; Bello Garrote, F. L.; Benzoni, G.; Daido, R.; Fang, Y.; Fukuda, N.; Gey, G.; Go, S.; Gottardo, A.; Inabe, N.; Isobe, T.; Kameda, D.; Kobayashi, K.; Kobayashi, M.; Komatsubara, T.; Kojouharov, I.; Kubo, T.; Kurz, N.; Kuti, I.; Li, Z.; Matsushita, M.; Michimasa, S.; Moon, C.-B.; Nishibata, H.; Nishizuka, I.; Odahara, A.; Şahin, E.; Sakurai, H.; Schaffner, H.; Suzuki, H.; Takeda, H.; Tanaka, M.; Taprogge, J.; Vajta, Zs.; Yagi, A.; Yokoyama, R.

2014-12-01

Excited states in the N =102 isotones Gd 166 and Sm 164 have been observed following isomeric decay for the first time at RIBF, RIKEN. The half-lives of the isomeric states have been measured to be 950(60) and 600(140) ns for Gd 166 and Sm 164 , respectively. Based on the decay patterns and potential energy surface calculations, including β6 deformation, a spin and parity of 6- has been assigned to the isomeric states in both nuclei. Collective observables are discussed in light of the systematics of the region, giving insight into nuclear shape evolution. The decrease in the ground-band energies of Gd 166 and Sm 164 (N =102 ) compared to Gd 164 and Sm 162 (N =100 ), respectively, presents evidence for the predicted deformed shell closure at N =100 .

Re-dispersion and film formation of GdVO4 :  Ln3+ (Ln3+ = Dy3+, Eu3+, Sm3+, Tm3+) nanoparticles: particle size and luminescence studies.

Science.gov (United States)

Shanta Singh, N; Ningthoujam, R S; Phaomei, Ganngam; Singh, S Dorendrajit; Vinu, A; Vatsa, R K

2012-04-21

GdVO(4) : Ln(3+) (Ln(3+) = Dy(3+), Eu(3+), Sm(3+), Tm(3+)) nanoparticles are prepared by a simple chemical route at 140 °C. The crystallite size can be tuned by varying the pH of the reaction medium. Interestingly, the crystallite size is found to increase significantly when pH increases from 6 to 12. This is related to slower nucleation of the GdVO(4) formation with increase of VO(4)(3-) present in solution. The luminescence study shows an efficient energy transfer from vanadate absorption of GdVO(4) to Ln(3+) and thereby enhanced emissions are obtained. A possible reaction mechanism at different pH values is suggested in this study. As-prepared samples are well dispersed in ethanol, methanol and water, and can be incorporated into polymer films. Luminescence and its decay lifetime studies confirm the decrease in non-radiative transition probability with the increase of heat treatment temperature. Re-dispersed particles will be useful in potential applications of life science and the film will be useful in display devices.

Orange and reddish-orange light emitting phosphors: Sm{sup 3+} and Sm{sup 3+}/Eu{sup 3+} doped zinc phosphate glasses

Energy Technology Data Exchange (ETDEWEB)

Meza-Rocha, A.N., E-mail: ameza@fis.cinvestav.mx [Departamento de Física, Universidad Autónoma Metropolitana-Iztapalapa, P.O. Box 55-534, 09340 México D.F., México (Mexico); Speghini, A. [Dipartimento di Biotecnologie, Universita di Verona and INSTM, UdR Verona, Strada Le Grazie 15, I-37314 Verona (Italy); IFAC CNR, Nello Carrara Institute of Applied Physics, MDF Lab, I-50019 Sesto Fiorentino, FI (Italy); Bettinelli, M. [Dipartimento di Biotecnologie, Universita di Verona and INSTM, UdR Verona, Strada Le Grazie 15, I-37314 Verona (Italy); Caldiño, U. [Departamento de Física, Universidad Autónoma Metropolitana-Iztapalapa, P.O. Box 55-534, 09340 México D.F., México (Mexico)

2015-11-15

A spectroscopy study of Sm{sup 3+} and Sm{sup 3+}/Eu{sup 3+} doped zinc phosphate glasses is performed through photoluminescence spectra and decay time profile measurements. Under Sm{sup 3+} excitation at 344 nm, the Sm{sup 3+} singly doped glass shows an orange global emission with x=0.579 and y=0.414 CIE1931 chromaticity coordinates, whereas the Sm{sup 3+}/Eu{sup 3+} co-doped sample exhibits orange overall emissions (x=0.581 and y=0.398, and x=0.595 and y=0.387) and reddish-orange overall emission (x=0.634 and y=0.355) upon excitations at 344, 360 and 393 nm, respectively. Such luminescence from the co-doped sample is originated by the simultaneous emission of Sm{sup 3+} and Eu{sup 3+}. Under Sm{sup 3+} excitation at 344 and 360 nm, the Eu{sup 3+} emission is sensitized and enhanced by Sm{sup 3+} through a non-radiative energy transfer process. The non-radiative nature was inferred from the shortening of the Sm{sup 3+} lifetime observed in the Sm{sup 3+}/Eu{sup 3+} co-doped sample. An analysis of the Sm{sup 3+} emission decay time profiles using the Inokuti–Hirayama model suggests that an electric quadrupole–quadrupole interaction into Sm–Eu clusters might dominate the energy transfer process, with an efficiency of 0.17. - Highlights: • Zinc phosphate glasses are optically activated with Sm{sup 3+}/Eu{sup 3+} (ZPOSmEu). • Non-radiative energy transfer Sm{sup 3+}→Eu{sup 3+} takes place in ZPOSmEu. • ZPOSmEu overall emission can be modulated with the excitation wavelength. • ZPOSmEu might be useful as orange/reddish-orange phosphor for UV-white LEDs.

Rare earth elements in the Pacific and Atlantic Oceans. [Pr, Tb, Ho, Tm, Lu, La, Nd, Sm, Eu, Gd, Yb, Ce

Energy Technology Data Exchange (ETDEWEB)

Baar, H J.W. de; Bacon, M P; Brewer, P G; Bruland, K W

1985-09-01

The first profiles of Pr, Tb, Ho, Tm and Lu in the Pacific Ocean, as well as profiles of La, Ce, Nd, Sm, Eu, Gd and Yb are reported. Concentrations of REE (except Ce) in the deep water are two to three times higher than those observed in the deep Atlantic Ocean. Surface water concentrations are typically lower than in the Atlantic Ocean, especially for the heavier elements Ho,Tm,Yb and Lu. Cerium is strongly depleted in the Pacific water column, but less so in the oxygen minimum zone. The distribution of the REE group is consistent with two simultaneous processes: (1) cycling similar to that of opal and calcium carbonate, and (2) adsorptive scavenging by settling particles and possibly by uptake at ocean boundaries. However, the first process can probably not be sustained by the low REE contents of shells, unless additional adsorption on surfaces is invoked. The second process, adsorptive scavenging, largely controls the oceanic distribution and typical seawater pattern of the rare earths. (author).

Synthesis and characterization of La(III), Pr(III), Nd(III), Sm(III), Eu(III), Gd(III), Tb(III) and Dy(III) complexes of 2-acetylfuran-2-thenoylhydrazone

International Nuclear Information System (INIS)

Singh, B.; Singh, Praveen K.

1998-01-01

The reaction of 2-acetylfuran-2-thenoylhydrazone(afth) with Ln(III) trichlorides yields complexes of the type [Ln(afth)Cl 2 (H 2 O)(EtOH)]Cl, [Ln(III) = La, Pr, Nd, Sm, Eu, Gd, Tb and Dy]. The complexes have been characterized by molar conductance, magnetic susceptibility and TGA and DTA measurements, magnetic susceptibility and TGA and DTA measurements, FAB mass, infrared, proton NMR, electronic absorption and emission spectra. The terbium complex is found to be monomer from the FAB mass spectrum. The IR and NMR spectra suggest neutral tridentate behaviour of the Schiff base. A coordination number seven is proposed around the metal ions. Emission spectra suggest C 3v , symmetry around the metal ion with capped octahedron geometry for the europium complex. (author)

Analysis of the magnetic anisotropy in SmCo5 and GdCo5

International Nuclear Information System (INIS)

Zhao, T.; Jin, H.; Groessinger, R.; Kou, X.; Kirchmayr, H.R.

1991-01-01

The temperature dependence of the magnetic anisotropy constant K 1 for SmCo 5 and GdCo 5 is well reproduced by calculations based on a single-ion model taking into account the anisotropies of the R--Co exchange interaction and the Co-sublattice magnetic moment. The anisotropy of the R--Co exchange interaction plays an important role in reproducing the experimental K 1 (T) for SmCo 5 and GdCo 5 . It is found that the absolute value of the second order crystalline electric field parameter A 0 2 in SmCo 5 decreases monotonically with increasing temperature

Ion-irradiation resistance of the orthorhombic Ln_2TiO_5 (Ln = La, Pr, Nd, Sm, Eu, Gd, Tb and Dy) series

International Nuclear Information System (INIS)

Aughterson, Robert D.; Lumpkin, Gregory R.; Ionescu, Mihail; Reyes, Massey de los; Gault, Baptiste; Whittle, Karl R.; Smith, Katherine L.; Cairney, Julie M.

2015-01-01

The response of Ln_2TiO_5 (where Ln is a lanthanide) compounds exposed to high-energy ions was used to test their suitability for nuclear-based applications, under two different but complementary conditions. Eight samples with nominal stoichiometry Ln_2TiO_5 (Ln = La, Pr, Nd, Sm, Eu, Gd, Tb and Dy), of orthorhombic (Pnma) structure were irradiated, at various temperatures, with 1 MeV Kr"2"+ ions in-situ within a transmission electron microscope. In each case, the fluence was increased until a phase transition from crystalline to amorphous was observed, termed critical dose D_c. At certain elevated temperatures, the crystallinity was maintained irrespective of fluence. The critical temperature for maintaining crystallinity, T_c, varied non-uniformly across the series. The T_c was consistently high for La, Pr, Nd and Sm_2TiO_5 before sequential improvement from Eu to Dy_2TiO_5 with T_c's dropping from 974 K to 712 K. In addition, bulk Dy_2TiO_5 was irradiated with 12 MeV Au"+ ions at 300 K, 723 K and 823 K and monitored via grazing-incidence X-ray diffraction (GIXRD). At 300 K, only amorphisation is observed, with no transition to other structures, whilst at higher temperatures, specimens retained their original structure. The improved radiation tolerance of compounds containing smaller lanthanides has previously been attributed to their ability to form radiation-induced phase transitions. No such transitions were observed here. - Highlights: • First ion-irradiation studies on a number of novel compounds including Pr_2TiO_5, Eu_2TiO_5 and Tb_2TiO_5. • Systematic in-situ ion-irradiation study of almost complete Ln_2TiO_5 series (Ln = lanthanides) with orthorhombic crystal structure type. • The first grazing incidence study of bulk irradiated Dy_2TiO_5 looking for irradiation induced phase transition.

Vacuum ultraviolet excited photoluminescence properties of Gd2O2CO3:Eu3+ phosphor

Institute of Scientific and Technical Information of China (English)

WANG Zhilong; WANG Yuhua; ZHANG Jiachi

2008-01-01

The Gd2O2CO3:Eu3+ with type-II structure phosphor was successfully synthesized via flux method at 400℃ and their photoluminescence properties in vacuum ultraviolet (VUV) region were examined. The broad and strong excitation bands in the range of 153-205 nm owing to the CO32- host absorption and charge transfer (CT) of Gd3+-O2- were observed for Gd2O2CO3:Eu3+. Under 172 nm excitation, Gd2O2CO3:Eu3+ exhibited strong red emission with good color purity, indicating Eu3+ ions located at low symmetry sites and the chromaticity coordination of luminescence for Gd2O2CO3:Eu3+ was (x=0.652, y=0.345). The photoluminescence quenching concentration of Eu3+ excited by 172 nm for Gd2O2CO3:Eu3+ was about 5%. Gd2O2CO3:Eu3+ would be a potential VUV-excited red phosphor applied in mercury-free fluorescent lamps.

152Eu decay

International Nuclear Information System (INIS)

Artamonova, K.P.; Vinogradov, V.M.; Grigor'ev, E.P.; Zolotavin, A.V.; Makarov, V.M.; Sergeev, V.O.; Usynko, T.M.

1978-01-01

The purpose of this paper is the measurement of the relative intensities of the most intensive conversion lines of 152 Eu, the determination of as reliable as possible magnitudes of the intensities of γ-quanta using all the available data on γ-radiation of 152 Eu, the measurement of the interval conversion coefficients (ICC) for the most intensive γ-transitions, the determination of the probabilities of the 152 Eu β-decays to the 152 Sm and 152 Gd levels. The conversion lines of the most intensive γ-transitions in the 152 Eu decay are studied and the corresponding ICC are measured on the beta-spectrometers of π√2 and UMB type. The balance for the γ-transitions in the 152 Sm and 152 Gd daughter nuclei are presented. This balance is used to determine the absolute intensities of γ-rays (in terms of the percentage of the 152 Eu decays) and the probabilities of β-transitions to the levels of daughter nuclei. More accurate data on γ-rays and conversion electrons obtained can be used for the calibration of gamma and beta spectrometers

Luminescence and energy transfer of Sm3+ and Eu3+ in Ca2PO4Cl

International Nuclear Information System (INIS)

Wang, Zhijun; Li, Panlai; Yang, Zhiping; Guo, Qinglin

2014-01-01

Sm 3+ , Eu 3+ , and Sm 3+ –Eu 3+ doped Ca 2 PO 4 Cl phosphors are synthesized by a solid-state method. Ca 2 PO 4 Cl:Sm 3+ can produce red emission under the 400 nm radiation excitation, and the emission peak is located at 601 nm, which is assigned to the 4 G 5/2 → 6 H 7/2 transition of Sm 3+ . Ca 2 PO 4 Cl:Eu 3+ can create red emission under the 392 nm radiation excitation, and the strongest peak is located at 620 nm, which is attributed to the 5 D 0 → 7 F 2 transition of Eu 3+ . The energy transfer from Sm 3+ to Eu 3+ in Ca 2 PO 4 Cl has been validated and the critical distance (R c ) of Sm 3+ to Eu 3+ in Ca 2 PO 4 Cl is calculated to be 1.14 nm. With increasing Eu 3+ doping concentration, the energy transfer efficiency (Sm 3+ →Eu 3+ ) gradually increases to 53.7%. The luminescence property of Ca 2 PO 4 Cl:Sm 3+ , Eu 3+ can be tuned by properly tuning the relative ratio of Sm 3+ –Eu 3+ , and the emission intensity of Ca 2 PO 4 Cl:Eu 3+ can be greatly enhanced by codoped Sm 3+ . - Highlights: • Ca 2 PO 4 Cl:Sm 3+ , Eu 3+ can produce red emission under the 400 nm radiation excitation. • The energy transfer from Sm 3+ to Eu 3+ in Ca 2 PO 4 Cl has been validated. • The critical distance of Sm 3+ to Eu 3+ in Ca 2 PO 4 Cl is calculated to be 1.14 nm

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.

ions (RE = La, Pr, Nd, Sm, Gd and Dy)

Indian Academy of Sciences (India)

) zirconia), tendency of phase transformation (tetragonal to monoclinic () zirconia) and lattice strain were studied with mechanical property e.g. tensile strength of sol–gel derived ZrO2–2 mol% RE2O3 (RE = La, Pr, Nd, Sm, Gd and Dy) spun ...

Transition to intermediate valence state and x-ray photoemission in Sm/sub 1-x/Gd/sub x/S

International Nuclear Information System (INIS)

Campagna, M.; Chui, S.T.; Wertheim, G.K.; Tosatti, E.

1976-01-01

We report a systematic x-ray photoemission study of the alloys Sm 1 /sub -//subx/Gd/subx/S for 0 2+ → Sm 3+ photoemission line shape using a model which has some similarities with the Jaccarino-Walker model for magnetic alloys. It assumes the existence of only two different kinds of Sm 2+ ions in Sm 1 /sub -//subx/Gd/subx/S for x approximately-less-than 16%. We discuss possible reasons for the fact that Gd does not show the usual clustering effects known to occur in many substitutional rare-earth alloys. Lattice-constant measurements for various substituents further illustrate the importance of electronic effects in the phase transition

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+

Cross Section Measurements for Some Elements Suited as Thermal Spectrum indicators: Cd, Sm, Gd and Lu

Energy Technology Data Exchange (ETDEWEB)

Sokolowski, E.; Pekarek, H.; Jonsson, E.

1964-05-15

The effective cross sections of Cd, Sm, Gd and Lu have been measured by the oscillator technique in the spectrum of the central channel of the Swedish reactor R1. For Cd, Sm and Gd the 2200 m/s cross sections were deduced on the basis of Westcott's g and s factors. The values obtained were generally in agreement with other recent values obtained by integral methods, although a systematic trend indicated that the value T{sub n} - T{sub m} = 29 {+-} 10 deg C for the neutron spectrum, measured with a fast chopper, was slightly too high. A new value of T{sub n} - T{sub m} = 22.5 {+-} 3.5 deg C was deduced and new 2200 m/s cross sections were obtained by iteration. For natural Lu, the energy dependence of the cross section is not well known. Certain assumptions about the cross section function led to unreasonably high values for the 2200 m/s cross section. Complementary differential measurements of the cross sections of Cd, Sm and Gd were made with the Rl fast chopper. For Cd and Sm the 2200 m/s cross section thus obtained agreed within experimental error with those obtained from the integral measurements. For Gd, the chopper measured value was higher, confirming earlier findings and indicating that the Westcott g factor for Gd is too high. Cd: Integral meas. : {sigma}(2200) = 2,390 {+-} 45 b; Differential meas. : {sigma}(2200) = 2,445 {+-} 25 b; Sm: Integral meas. : {sigma}(2200) = 5,880 {+-} 90 b; Differential meas. : {sigma}(2200) = 5,740 {+-} 150 b; Gd: Integral meas. : {sigma}(2200) = 46,470 {+-} 550 b; Differential meas. : {sigma}(2200) = 47,900 {+-} 700 b.

Cross Section Measurements for Some Elements Suited as Thermal Spectrum indicators: Cd, Sm, Gd and Lu

Energy Technology Data Exchange (ETDEWEB)

Sokolowski, E; Pekarek, H; Jonsson, E

1964-05-15

The effective cross sections of Cd, Sm, Gd and Lu have been measured by the oscillator technique in the spectrum of the central channel of the Swedish reactor R1. For Cd, Sm and Gd the 2200 m/s cross sections were deduced on the basis of Westcott's g and s factors. The values obtained were generally in agreement with other recent values obtained by integral methods, although a systematic trend indicated that the value T{sub n} - T{sub m} = 29 {+-} 10 deg C for the neutron spectrum, measured with a fast chopper, was slightly too high. A new value of T{sub n} - T{sub m} = 22.5 {+-} 3.5 deg C was deduced and new 2200 m/s cross sections were obtained by iteration. For natural Lu, the energy dependence of the cross section is not well known. Certain assumptions about the cross section function led to unreasonably high values for the 2200 m/s cross section. Complementary differential measurements of the cross sections of Cd, Sm and Gd were made with the Rl fast chopper. For Cd and Sm the 2200 m/s cross section thus obtained agreed within experimental error with those obtained from the integral measurements. For Gd, the chopper measured value was higher, confirming earlier findings and indicating that the Westcott g factor for Gd is too high. Cd: Integral meas. : {sigma}(2200) = 2,390 {+-} 45 b; Differential meas. : {sigma}(2200) = 2,445 {+-} 25 b; Sm: Integral meas. : {sigma}(2200) = 5,880 {+-} 90 b; Differential meas. : {sigma}(2200) = 5,740 {+-} 150 b; Gd: Integral meas. : {sigma}(2200) = 46,470 {+-} 550 b; Differential meas. : {sigma}(2200) = 47,900 {+-} 700 b.

Enhanced photoluminescence of Sm{sup 3+}/Bi{sup 3+} co-doped Gd{sub 2}O{sub 3} phosphors by combustion synthesis

Energy Technology Data Exchange (ETDEWEB)

Liu Guangsheng; Zhang Ying [Institute of Micro-system Physics, School of Physics and Electronics, Henan University, Kaifeng 475001 (China); Yin Jiang [Department of Physics, Nanjing University, Nanjing 210093 (China); Zhang, W.F. [Institute of Micro-system Physics, School of Physics and Electronics, Henan University, Kaifeng 475001 (China)], E-mail: wfzhang@henu.edu.cn

2008-12-15

Gd{sub 2}O{sub 3}:Sm{sup 3+} and Gd{sub 2}O{sub 3}:Sm{sup 3+},Bi{sup 3+} powders were prepared by a combustion method. Their structures were determined using X-ray diffraction. UV-visible absorption and photoluminescence spectra were investigated for Gd{sub 2}O{sub 3}:Sm{sup 3+} and Gd{sub 2}O{sub 3}:Sm{sup 3+},Bi{sup 3+} at different annealing temperatures and different doping concentrations. The emission spectra of all samples presented the characteristic emission narrow lines arising from the {sup 4}G{sub 5/2}{yields}{sup 6}H{sub J} transitions (J=5/2, 7/2, and 9/2) of Sm{sup 3+} ions upon excitation with UV irradiation. The emission intensity of Sm{sup 3+} ions was largely enhanced with introducing Bi{sup 3+} ions into Gd{sub 2}O{sub 3}:Sm{sup 3+} and the maximum occurred at a Bi{sup 3+} concentration of 0.5 mol%. The relevant mechanisms were discussed with the sensitization theory by Dexter and the aggregation behavior of Bi{sup 3+} ions.

Hyperfine fields at some 4d, 5d and 4f impurities in ferromagnetic GdZn and GdCd

International Nuclear Information System (INIS)

Kasamatsu, Y.; Kojima, K.; Hihara, T.

1995-01-01

Hyperfine (hf) fields at 4d (Y, Nb, Rh, Pd), 5d (Lu, Ta, Ir) and 4f (La, Nd, Sm, Eu) impurities in ferromagnetic GdZn and GdCd have been measured by NMR at 4.2 K. The local moment contributions to the hf field suggest that the impurity moments at the beginning and end of the d series are parallel and antiparallel to Gd moments, respectively. The hf results for 4f impurities are also discussed. ((orig.))

Luminescence study of Eu3+ doped GdVO4 nanoparticles: Concentration, particle size, and core/shell effects

Science.gov (United States)

Singh, N. Shanta; Ningthoujam, R. S.; Devi, L. Romila; Yaiphaba, N.; Sudarsan, V.; Singh, S. Dorendrajit; Vatsa, R. K.; Tewari, R.

2008-11-01

Nanoparticles of GdVO4 doped with Eu3+ and core/shell of GdVO4:Eu3+/GdVO4 are prepared by urea hydrolysis method using ethylene glycol as capping agent as well as reaction medium at 130 °C. Unit cell volume increases when GdVO4 is doped with Eu3+ indicating the substitution of Gd3+ lattice sites by Eu3+. From luminescence study, it is confirmed that there is no particle size effect on emission positions of Eu3+. Optimum luminescence intensity is found to be in 5-10 at. % Eu3+. Above these concentrations, luminescence intensity decreases due to concentration quenching effect. There is an enhancement in luminescence intensity of core/shell nanoparticles. This has been attributed to the reduction in surface inhomogenities of Eu3+ surroundings by bonding to GdVO4 shell. The lifetime for D50 level increases with annealing and core/shell formation.

Distribution behavior of uranium, neptunium, rare-earth elements (Y, La, Ce, Nd, Sm, Eu, Gd) and alkaline-earth metals (Sr,Ba) between molten LiCl-KCl eutectic salt and liquid cadmium or bismuth

International Nuclear Information System (INIS)

Kurata, M.; Sakamura, Y.; Hijikata, T.; Kinoshita, K.

1995-01-01

Distribution coefficients of uranium neptunium, eight rare-earth elements (Y, La, Ce, Pr, Nd, Sm, Eu and Gd) and two alkaline-earth metals (Sr and Ba) between molten LiCl-KCl eutectic salt and either liquid cadmium or bismuth were measured at 773 K. Separation factors of trivalent rare-earth elements to uranium or neptunium in the LiCl-KCl/Bi system were by one or two orders of magnitude larger than those in the LiCl-KCl/Cd system. On the contrary, the separation factors of alkaline-earth metals and divalent rare-earth elements to trivalent rare-earth elements were by one or two orders of magnitude smaller in the LiCl-KCl/Bi system. (orig.)

Isomer Decay Spectroscopy of Sm-164 and Gd-166: Midshell Collectivity Around N=100

OpenAIRE

Patel, Z; Soederstroem, P-A; Podolyak, Z; Regan, PH; Walker, PM; Watanabe, H; Ideguchi, E; Simpson, GS; Liu, HL; Nishimura, S; Wu, Q; Xu, FR; Browne, F; Doornenbal, P; Lorusso, G

2014-01-01

© 2014 American Physical Society. Excited states in the N=102 isotones Gd166 and Sm164 have been observed following isomeric decay for the first time at RIBF, RIKEN. The half-lives of the isomeric states have been measured to be 950(60) and 600(140) ns for Gd166 and Sm164, respectively. Based on the decay patterns and potential energy surface calculations, including β6 deformation, a spin and parity of 6- has been assigned to the isomeric states in both nuclei. Collective observables are disc...

Deposition of GdVO4:Eu3+ nanoparticles on silica nanospheres by a simple sol gel method

Science.gov (United States)

Liu, Guixia; Hong, Guangyan; Wang, Jinxian; Dong, Xiangting

2006-07-01

The deposition and coating of GdVO4:Eu3+ nanoparticles on spherical silica was carried out using a simple sol-gel method at low temperature. The GdVO4:Eu3+-coated silica composites obtained were characterized by differential thermal analysis (DTA), thermogravimetric (TG) analysis, x-ray diffraction (XRD), Fourier-transform IR spectroscopy (FT-IR), transmission electron microscopy (TEM), x-ray photoelectron spectroscopy (XPS), photoluminescence spectra, and kinetic decay. It is found that the ~5 nm GdVO4:Eu3+ nanoparticles coating the silica spheres are crystal in the as-prepared samples and the crystallinity increases with increasing annealing temperature. The composites obtained are spherical in shape with an average size of 100 nm. The GdVO4:Eu3+ nanoparticles are linked with silica cores by a chemical bond. The photoluminescence spectra of the obtained GdVO4:Eu3+-coated silica composites are similar to those of the bulk GdVO4:Eu3+ phosphors. The strongest peak is near 617 nm, which indicates that Eu3+ is located in the low symmetry site with non-inversion centre.

Energy transfer phenomena and Judd-Ofelt analysis on Sm{sup 3+} ions in K{sub 2}GdF{sub 5} crystal

Energy Technology Data Exchange (ETDEWEB)

Do, Phan Van [Thuyloi University, 175 Tay Son, Dong da Dist, Hanoi (Viet Nam); Tuyen, Vu Phi, E-mail: vptuyen@gust-edu.vast.vn [Graduate University of Science and Technology - VAST, 18 Hoang quoc Viet, Hanoi (Viet Nam); DuyTan University, K7/25 QuangTrung, Danang (Viet Nam); Quang, Vu Xuan [DuyTan University, K7/25 QuangTrung, Danang (Viet Nam); Khaidukov, Nicholas M. [Kurnakov Institute of General and Inorganic Chemistry, Moscow (Russian Federation); TrongThanh, Nguyen [Institute of Materials Science - VAST, 18 Hoang quoc Viet, Hanoi (Viet Nam); Sengthong, Bounyavong [DuyTan University, K7/25 QuangTrung, Danang (Viet Nam); Huy, Bui The, E-mail: buithehuy.nt@gmail.com [Department of Chemistry, Changwon National University, Changwon 641-773 (Korea, Republic of)

2016-11-15

The Raman, absorption, luminescence spectra and lifetimes curves of Sm{sup 3+}-doped K{sub 2}GdF{sub 5}were measured. Based on the Judd-Ofelt analysis, the values of radiative transition probabilities, branching ratios, integrated emission cross-sections and radiative lifetimes of excited states of Sm{sup 3+} in K{sub 2}GdF{sub 5} crystal were calculated. The migration of excitation energy between the Gd{sup 3+} ions and the trapping processes of Gd{sup 3+} excitation energy by Sm{sup 3+} and Tb{sup 3+}ions in K{sub 2}GdF{sub 5} crystal are reported. The role of the overlapping between the broad, allowed absorption bands of the RE{sup 3+} ions and the narrow absorption lines {sup 6}I{sub J} and {sup 6}P{sub J} of Gd{sup 3+} ions on the trapping rates of the RE{sup 3+} was discussed. The energy transfer between the Sm{sup 3+} ions was studied by the decay measurement, which has been fitted by Inokuti-Hirayama energy transfer model and revealed that electric dipole–quadrupole interaction is responsible for the energy transfer process in Sm{sup 3+} ions doped K{sub 2}GdF{sub 5} crystal.

Vacuum ultraviolet excited luminescence properties of sol–gel derived GdP5O14:Eu3+ powders

International Nuclear Information System (INIS)

Mbarek, Aïcha; Chadeyron, Geneviève; Boyer, Damien; Avignant, Daniel; Fourati, Mohieddine; Zambon, Daniel

2014-01-01

Sol–gel route has successfully been used to synthesize pure and Eu 3+ doped polycrystalline samples of the GdP 5 O 14 pentaphosphates. The as-prepared samples have structurally been characterized using X-ray diffraction. Optical properties in the vacuum ultraviolet (VUV) of Eu 3+ activated GdP 5 O 14 samples prepared either by sol–gel process or solid-state reaction were investigated at room temperature for comparison. In this GdP 5 O 14 host matrix the P 5 O 14 ultraphosphate groups were proved to exhibit an efficient absorption in the VUV range. The excitation spectra recorded in the VUV-UV spectral region from 120 nm to 350 nm have revealed the presence of Gd 3+ 4f–5d interconfiguration transitions, Gd 3+ –O 2− and Eu 3+ –O 2− charge transfer states(CTS)in addition to intraconfiguration transitions of Gd 3+ ions.Furthermore the Gd 3+ →Eu 3+ energy transfer process was investigated and discussed in the framework of the multiphonon relaxation process. Besides, the GdP 5 O 14 :Eu 3+ phosphor led to a strong red emission under 147/172 nm excitation, so that it can be considered as a promising red phosphor for mercury-free lamps and plasma display panels applications. -- Highlights: • Lanthanide pentaphosphates were synthesized by the sol–gel process. • A broad absorption was evidenced in the VUV range for GdP 5 O 14 :Eu 3+ . • An efficient energy transfer was proved from pentaphosphate lattice to Eu 3+ ions

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"+.

Muon spin depolarization in Gd- and EuBa2Cu3Ox

International Nuclear Information System (INIS)

Cooke, D.W.; Hutson, R.L.; Kwok, R.S.; Maez, M.; Rempp, H.; Schillaci, M.E.; Smith, J.L.; Willis, J.O.; Lichti, R.L.; Chan, K.C.; Boekema, C.; Weathersby, S.; Oostens, J.

1989-01-01

Positive muon spin rotation (μSR) measurements on Gd- and EuBa 2 Cu 3 O x (x ∼ 7) have been conducted in the temperature interval 4 - 300 K. For each sample, muons stop both at grain boundaries and within the superconducting grains. Measured magnetic field penetration depths are 1550 and 1900 Angstrom for two specimens of GdBa 2 Cu 3 O x , and 1350 Angstrom for EuBa 2 Cu 3 O x

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+}.

Molecular electrophosphorescence in (Sm, Gd)-β-diketonate complex blend for OLED applications

International Nuclear Information System (INIS)

Reyes, R.; Cremona, M.; Teotonio, E.E.S.; Brito, H.F.; Malta, O.L.

2013-01-01

In this work the preparation and characterization of the triple-layer organic light-emitting diode (OLED) using a mixture of the samarium and gadolinium β-diketonate complexes [Sm 0.5 Gd 0.5 (TTA) 3 (TPPO) 2 ] as emitting layer is reported. The OLED's devices contain 1-(3-methylphenyl)-1,2,3,4-tetrahydroquinoline-6-carboxyaldehyde-1, 1'-diphenylhydrazone (MTCD) as hole-transporting layer and tris(8-hydroxyquinoline aluminum) (Alq 3 ) as electron transporting layer. The electroluminescence spectrum present emission narrow bands from the 4 G 5/2 → 6 H J transitions (where J=5/2, 7/2 and 9/2) characteristic of the Sm 3+ ion. These sharp lines are overlapped with a broad band attributed to the electrophosphorescence from the T 1 →S 0 transition in the ligand TTA. The intramolecular energy transfer is discussed and applied on the change of the emission color of the organic LEDs at different bias voltages. - Highlights: ► Samarium and gadolinium complexes. ► OLED with complex blend (Sm,Gd). ► Electrophosphorescence emission detection. ► Application in OLED changing the color emission.

The Preparation and Optical Properties of Novel LiLa(MoO42:Sm3+,Eu3+ Red Phosphor

Directory of Open Access Journals (Sweden)

Jiaxi Wang

2018-02-01

Full Text Available Novel LiLa1−x−y(MoO42: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(MoO42: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.

Crystal structure of RCoIn5 (R - Ce, Pr, Nd, Sm, Gd, Tb, Dy, Ho, Y) and R2CoIn8 (R - Ce, Pr, Nd, Sm, Gd, Dy, Ho, Er, Tm, Y) compounds

International Nuclear Information System (INIS)

Kalychak, Ya.M.; Zaremba, V.I.; Baranyak, V.M.; Bruskov, V.A.; Zavalij, P.Yu.

1989-01-01

Usng X-ray diffraction method of monocrystal, crystal structure of HoCoIn 5 compound belonging to the HoCoGa 5 structural type is determined. Using the method of powder belonging of CeCoIn 5 structure to the HoCoGa 5 structural type is confirmed. Isostructural compounds with Y, Pr, Nd, Sm, Gd, Tb, Dy are detected. Their lattice periods are determined. Using the method of powder belonging of Ce 2 CoIn 8 compound structure to Ho 2 CoGa 8 structural type is determined. Isostructural compounds with Y, Pr, Nd, Sm, Gd, Dy, Ho, Er, Tm are detected and their lattice periods are determined

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

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

New neutron-rich isotope production in 154Sm+160Gd

Directory of Open Access Journals (Sweden)

Ning Wang

2016-09-01

Full Text Available Deep inelastic scattering in 154Sm+160Gd at energies above the Bass barrier is for the first time investigated with two different microscopic dynamics approaches: improved quantum molecular dynamics (ImQMD model and time dependent Hartree–Fock (TDHF theory. No fusion is observed from both models. The capture pocket disappears for this reaction due to strong Coulomb repulsion and the contact time of the di-nuclear system formed in head-on collisions is about 700 fm/c at an incident energy of 440 MeV. The isotope distribution of fragments in the deep inelastic scattering process is predicted with the simulations of the latest ImQMD-v2.2 model together with a statistical code (GEMINI for describing the secondary decay of fragments. More than 40 extremely neutron-rich unmeasured nuclei with 58≤Z≤76 are observed and the production cross sections are at the order of μb to mb. The multi-nucleon transfer reaction of Sm+Gd could be an alternative way to synthesize new neutron-rich lanthanides which are difficult to be produced with traditional fusion reactions or fission of actinides.

Weak ferromagnetism in Re0.67Ca0.33FeO3 (Re=La, Sm, Gd) nanoparticles

International Nuclear Information System (INIS)

Li Jiangong; Kou Xinli; Qin Yong; He Haiying

2003-01-01

Perovskite-type complex ferrite Re 0.67 Ca 0.33 FeO 3 (Re=La, Sm, Gd) nanoparticles of nearly the same particle size were prepared using sol-gel method. The influence of rare-earth ions on weak ferromagnetism in the Re 0.67 Ca 0.33 FeO 3 nanoparticles has been studied. The spontaneous magnetization M s of the Sm 0.67 Ca 0.33 FeO 3 nanoparticles is greater than that of Gd 0.67 Ca 0.33 FeO 3 nanoparticles; and M s of Gd 0.67 Ca 0.33 FeO 3 nanoparticles is greater than that of La 0.67 Ca 0.33 FeO 3 nanoparticles. The ferromagnetic component arising from the Fe sublattice increases with the decreasing rare-earth ionic radii. The magnetization of the rare-earth ions in the Sm 0.67 Ca 0.33 FeO 3 nanoparticles is smaller than that in the Gd 0.67 Ca 0.33 FeO 3 nanoparticles. The influences of the geometric and intrinsic magnetic characters of rare-earth ions as well as the particle size of the nanoparticles on weak ferromagnetism are discussed

Luminescent properties and energy transfer of Gd{sup 3+}/Eu{sup 3+} co-doped cubic CaCO{sub 3}

Energy Technology Data Exchange (ETDEWEB)

Sun, Yidi; Zou, Haifeng; Zhang, Bowen; Zhou, Xiuqing; Song, Yanhua; Zheng, Keyan [College of Chemistry, Jilin University, Changchun 130012 (China); Shi, Zhan [State Key Laboratory of Inorganic Synthesis and Preparative Chemistry, College of Chemistry, Jilin University, Changchun 130012 (China); Sheng, Ye, E-mail: shengye@jlu.edu.cn [College of Chemistry, Jilin University, Changchun 130012 (China)

2016-10-15

Gd{sup 3+} and Eu{sup 3+} ions co-doped CaCO{sub 3} nanoparticles have been successfully synthesized via carbonization method. The emission spectra of co-doped CaCO{sub 3} phosphors in the range of VUV–vis spectral were studied. The results reveal that the co-doped CaCO{sub 3} phosphors show intense red emission in the VUV range because of the Gd{sup 3+} ions as sensitizers. The energy transfer process from Gd{sup 3+} to Eu{sup 3+} in CaCO{sub 3}:Gd{sup 3+}/Eu{sup 3+} phosphors was investigated and discussed in terms of the luminescence spectra and the decay curves, which demonstrated that the energy transfer of Gd{sup 3+}→Eu{sup 3+} is efficient. The mechanism of energy transfer from Gd{sup 3+} to Eu{sup 3+} is a resonant transfer, in which electric dipole–dipole interaction plays a leading role. Furthermore, the effect of doping concentration of Eu{sup 3+} ions on the energy transfer efficiency was also investigated. From the photoluminescence (PL) spectra, it was also found that the incorporation of Na{sup +} ions into CaCO{sub 3}:Gd{sup 3+}/Eu{sup 3+} could lead to a remarkable increase of luminescent intensity due to the charge compensation.

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.

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)

Luminescent GdVO_4:Sm"3"+ quantum dots enhance power conversion efficiency of bulk heterojunction polymer solar cells by Förster resonance energy transfer

International Nuclear Information System (INIS)

Bishnoi, Swati; Gupta, Vinay; Sharma, Gauri D.; Chand, Suresh; Sharma, Chhavi; Kumar, Mahesh; Haranath, D.; Naqvi, Sheerin

2016-01-01

In this work, we report enhanced power conversion efficiency (PCE) of bulk heterojunction polymer solar cells by Förster resonance energy transfer (FRET) from samarium-doped luminescent gadolinium orthovanadate (GdVO_4:Sm"3"+) quantum dots (QDs) to polythieno[3,4-b]-thiophene-co-benzodithiophene (PTB7) polymer. The photoluminescence emission spectrum of GdVO_4:Sm"3"+ QDs overlaps with the absorption spectrum of PTB7, leading to FRET from GdVO_4:Sm"3"+ to PTB7, and significant enhancements in the charge-carrier density of excited and polaronic states of PTB7 are observed. This was confirmed by means of femtosecond transient absorption spectroscopy. The FRET from GdVO_4:Sm"3"+ QDs to PTB7 led to a remarkable increase in the power conversion efficiency (PCE) of PTB7:GdVO_4:Sm"3"+:PC_7_1BM ([6,6]-phenyl-C_7_1-butyric acid methyl ester) polymer solar cells. The PCE in optimized ternary blend PTB7:GdVO_4:Sm"3"+:PC_7_1BM (1:0.1:1.5) is increased to 8.8% from 7.2% in PTB7:PC_7_1BM. This work demonstrates the potential of rare-earth based luminescent QDs in enhancing the PCE of polymer solar cells.

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.

Voltage color tunable OLED with (Sm,Eu)-β-diketonate complex blend

Science.gov (United States)

Reyes, R.; Cremona, M.; Teotonio, E. E. S.; Brito, H. F.; Malta, O. L.

2004-09-01

Light emission from organic electroluminescent diodes (OLEDs) in which mixed samarium and europium β-diketonate complexes, [Sm 0.7Eu 0.3(TTA) 3(TPPO) 2], was used as the emitting layer is described. The electroluminescence spectra exhibit narrow peaks arising from 4f-intraconfigurational transitions of the Sm 3+ and Eu 3+ ions and a broad emission band attributed to the electrophosphorescence of the TTA ligand. The intensity ratio of the peaks determined by the bias voltage applied to the OLED, together with the ligand electrophosphorescence, allows to obtain a voltage-tunable color light source.

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

Molecular electrophosphorescence in (Sm, Gd)-{beta}-diketonate complex blend for OLED applications

Energy Technology Data Exchange (ETDEWEB)

Reyes, R., E-mail: fisicaplic@hotmail.com [Facultad de Ingenieria Quimica y Textil, Universidad Nacional de Ingenieria, UNI, Av. Tupac Amaru 210, Lima 31, Peru (Peru); Cremona, M. [DIMAT - Divisao de Metrologia de Materiais, Instituto Nacional de Metrologia, Normalizacao e Qualidade Industrial, INMETRO, Duque de Caxias, RJ (Brazil); Departamento de Fisica, Pontificia Universidade Catolica do Rio de Janeiro, PUC-Rio, C.P. 38071, Rio de Janeiro, RJ, CEP 22453-970 (Brazil); Teotonio, E.E.S. [Departamento de Quimica, CCEN, Universidade Federal da Paraiba, UFPB, C.P. 5093, Joao Pessoa, PB, CEP 5805-970 (Brazil); Brito, H.F. [Instituto de Quimica, Universidade de Sao Paulo, USP, C.P. 26077, Sao Paulo, SP, CEP 05599-970 (Brazil); Malta, O.L. [Departamento de Quimica Fundamental, CCEN, Universidade Federal de Pernambuco, Cidade Universitaria, Recife, PE, CEP 50670-901 (Brazil)

2013-02-15

In this work the preparation and characterization of the triple-layer organic light-emitting diode (OLED) using a mixture of the samarium and gadolinium {beta}-diketonate complexes [Sm{sub 0.5}Gd{sub 0.5}(TTA){sub 3}(TPPO){sub 2}] as emitting layer is reported. The OLED's devices contain 1-(3-methylphenyl)-1,2,3,4-tetrahydroquinoline-6-carboxyaldehyde-1, 1'-diphenylhydrazone (MTCD) as hole-transporting layer and tris(8-hydroxyquinoline aluminum) (Alq{sub 3}) as electron transporting layer. The electroluminescence spectrum present emission narrow bands from the {sup 4}G{sub 5/2}{yields}{sup 6}H{sub J} transitions (where J=5/2, 7/2 and 9/2) characteristic of the Sm{sup 3+} ion. These sharp lines are overlapped with a broad band attributed to the electrophosphorescence from the T{sub 1}{yields}S{sub 0} transition in the ligand TTA. The intramolecular energy transfer is discussed and applied on the change of the emission color of the organic LEDs at different bias voltages. - Highlights: Black-Right-Pointing-Pointer Samarium and gadolinium complexes. Black-Right-Pointing-Pointer OLED with complex blend (Sm,Gd). Black-Right-Pointing-Pointer Electrophosphorescence emission detection. Black-Right-Pointing-Pointer Application in OLED changing the color emission.

Synthesis RMn{sub 2}O{sub 5} (R = Gd and Sm) nano- and microstructures by a simple hydrothermal method

Energy Technology Data Exchange (ETDEWEB)

Zhu Gangqiang, E-mail: zgq2006@snnu.edu.cn [School of Physics and Information Technology, Shaanxi Normal University, Xi' an 710062 (China); Liu Peng [School of Physics and Information Technology, Shaanxi Normal University, Xi' an 710062 (China); Hojamberdiev, Mirabbos [Shaanxi Key Laboratory of Nano-materials and Technology, Xi' an University of Architecture and Technology, Xi' an 710055 (China); Ge Bao [School of Physics and Information Technology, Shaanxi Normal University, Xi' an 710062 (China); Liu Yun; Miao Hongyan; Tan Guoqiang [College of Materials Science and Engineering, Shaanxi University of Science and Technology, Xi' an 710021 (China)

2009-12-15

Single-phase RMn{sub 2}O{sub 5} (R = Gd and Sm) nano- and microstructures have been successfully synthesized via a simple hydrothermal process at 250 deg. C for 24 h using NaOH as mineralizer. X-ray diffraction (XRD), scanning electron microscopy (SEM), X-ray energy dispersive spectroscopy (EDS), transmission electron microscopy (TEM), high-resolution transmission electron microscopy (HRTEM) and selective area electron diffraction patterns (SAED) were used to characterize the as-synthesized GdMn{sub 2}O{sub 5} and SmMn{sub 2}O{sub 5} samples. The effect of NaOH concentration and the molar ratio of Mn{sup 2+}/Mn{sup 7+} on the morphology and size of the final products was studied, and a possible formation mechanism of RMn{sub 2}O{sub 5} (R = Gd and Sm) nanoplates and nanorods under hydrothermal conditions was proposed.

Ferro-paramagnetic coupled resonant modes in GdEuCuO4

International Nuclear Information System (INIS)

Fainstein, A.; Tovar, M.

1990-01-01

Two paramagnetic resonances were observed in compound GdEuCuO 4 : one was originated in trivalent gadolinium paramagnetism, while the other is associated to a weak ferromagnetic mode in Cu-O planes. In this work, experimental results are presented that show an anisotropy and a strongly anomalous temperature dependence of Gd 3+ . A theoretical model was introduced which explains the data in terms of coupled ferro-paramagnetic resonant modes originated in spin exchange coupling of Cu and Gd. (Author). 9 refs., 4 figs

Energy transfer and tunable multicolor emission and paramagnetic properties of GdF3:Dy(3+),Tb(3+),Eu(3+) phosphors.

Science.gov (United States)

Guan, Hongxia; Sheng, Ye; Xu, Chengyi; Dai, Yunzhi; Xie, Xiaoming; Zou, Haifeng

2016-07-20

A series of Dy(3+), Tb(3+), Eu(3+) singly or doubly or triply doped GdF3 phosphors were synthesized by a glutamic acid assisted one-step hydrothermal method. The samples were characterized by X-ray diffraction (XRD), field-emission scanning electron microscopy (FE-SEM) and photoluminescence (PL) spectroscopy. The results show that the synthesized samples are all pure GdF3. The obtained samples have a peanut-like morphology with a diameter of about 270 nm and a length of about 600 nm. Under UV excitation, GdF3:Dy(3+), GdF3:Tb(3+) and GdF3:Eu(3+) samples exhibit strong blue, green and red emissions, respectively. By adjusting their relative doping concentrations in the GdF3 host, the different color hues of green and red light are obtained by co-doped Dy(3+), Tb(3+) and Tb(3+), Eu(3+) ions in the GdF3 host, respectively. Besides, there exist two energy transfer pairs in the GdF3 host: (1) Dy(3+) → Tb(3+) and (2) Tb(3+) → Eu(3+). More significantly, in the Dy(3+), Tb(3+), and Eu(3+) tri-doped GdF3 phosphors, white light can also be achieved upon excitation of UV light by adjusting the doping concentration of Eu(3+). In addition, the obtained samples also exhibit paramagnetic properties at room temperature (300 K) and low temperature (2 K). It is obvious that multifunctional Dy(3+), Tb(3+), Eu(3+) tri-doped GdF3 materials including tunable multicolors and intrinsic paramagnetic properties may have potential applications in the field of full-color displays.

An electrochemical approach for removal of radionuclidic contaminants of Eu from 153Sm for effective use in metastatic bone pain palliation.

Science.gov (United States)

Chakravarty, Rubel; Chakraborty, Sudipta; Khan, Mohammed Sahiralam; Ram, Ramu; Sarma, Haladhar Dev; Dash, Ashutosh

2018-03-01

Thermal neutron activation of 152 Sm [ 152 Sm(n,γ) 153 Sm] using natural or isotopically enriched (by 152 Sm) samarium target is the established route for production of 153 Sm used for preparation of 153 Sm-EDTMP for pain palliation in cancer patients with disseminated bone metastases. However, some long-lived radionuclidic contaminants of Eu, such as, 154 Eu (t ½ =8.6y) are also produced during the target activation process. This leads to detectable amount of Eu radionuclidic contaminants in patients' skeleton even years after administration with therapeutic doses of 153 Sm-EDTMP. Further, the presence of such contaminants in 153 Sm raises concerns related to radioactive waste management. The aim of the present study was to develop and demonstrate a viable method for large-scale purification of 153 Sm from radionuclidic contaminants of Eu. A radiochemical separation procedure adopting electroamalgamation approach has been critically evaluated. The influence of different experimental parameters for the quantitative removal radionuclidic contaminants of Eu from 153 Sm was investigated and optimized. The effectiveness of the method was demonstrated by purification of ~37 GBq of 153 Sm in several batches. As a proof of concept, 153 Sm-EDTMP was administered in normal Wistar rats and ex vivo γ-spectrometry of bone samples were carried out. After carrying out the electrolysis under the optimized conditions, the radionuclidic contaminants of Eu could not be detected in purified 153 Sm solution by γ-spectrometry. The overall yield of 153 Sm obtained after the purification process was >85%. The reliability of this approach was amply demonstrated in several batches, wherein the performance remained consistent. Ex vivo γ-spectrometry of bone samples of Wistar rats administered with 153 Sm-EDTMP (prepared using electrochemically purified 153 Sm) did not show photo peaks corresponding to radionuclidic contaminants of Eu. A viable electrochemical strategy for the large

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

Science.gov (United States)

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

2017-07-01

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

Magnetism of cyano-bridged hetero-one-dimensional Ln3+-M3+ complexes (Ln3+ = Sm, Gd, Yb; M3+ = FeLS, Co).

Science.gov (United States)

Figuerola, Albert; Diaz, Carmen; Ribas, Joan; Tangoulis, Vassilis; Sangregorio, Claudio; Gatteschi, Dante; Maestro, Miguel; Mahía, José

2003-08-25

The reaction of Ln(NO(3))(3).aq with K(3)[Fe(CN)(6)] or K(3)[Co(CN)(6)] and 2,2'-bipyridine in water led to five one-dimensional complexes: trans-[M(CN)(4)(mu-CN)(2)Ln(H(2)O)(4) (bpy)](n)().XnH(2)O.1.5nbpy (M = Fe(3+) or Co(3+); Ln = Sm(3+), Gd(3+), or Yb(3+); X = 4 or 5). The structures for [Fe(3)(+)-Sm(3+)] (1), [Fe(3)(+)-Gd(3+)] (2), [Fe(3)(+)-Yb(3+)] (3), [Co(3)(+)-Gd(3+)] (4), and [Co(3)(+)-Yb(3+)] (5) have been solved; they crystallize in the triclinic space P1 and are isomorphous. The [Fe(3+)-Sm(3+)] complex is a ferrimagnet, its magnetic studies suggesting the onset of weak ferromagnetic 3-D ordering at 3.5 K. The [Fe(3+)-Gd(3+)] interaction is weakly antiferromagnetic. The isotropic nature of Gd(3+) allowed us to evaluate the exchange interaction (J = 0.77 cm(-)(1)).

Electronic and magnetic properties of SmCrSb3 and GdCrSb3: A first principles study

International Nuclear Information System (INIS)

Sandeep; Ghimire, M.P.; Thapa, R.K.

2011-01-01

The density of states (DOS) and the magnetic moments of SmCrSb 3 and GdCrSb 3 have been studied by first principles full-potential linearized augmented plane wave (FP-LAPW) method based on density functional theory (DFT). For the exchange-correlation potential, the local-spin density approximations with correlation energy (LSDA+U) method have been used. Total and partial DOS have been computed using the WIEN2k code. DOS result shows the exchange-splittings of Cr-3d and rare-earth (R) 4f states electrons, which are responsible for the ground state ferromagnetic (FM) behavior of the systems. The FM behavior of these systems is strongly influenced by the average number of Cr-3d and Sm (Gd) 4f-electrons. The effective moment of SmCrSb 3 is found to be 7.07 μ B while for GdCrSb 3 it is 8.27 μ B . The Cr atom plays a significant role on the magnetic properties due to the hybridization between Cr-3d and Sb-5p states. - Highlights: → DOS and the magnetic moments of SmCrSb 3 and GdCrSb 3 are studied by full-FP-LAPW method. → Exchange splitting of eg and t2g of Cr-3d states and the rare-earth 4f state electrons are responsible for ground state ferromagnetism. → Rare-earth magnetic moments are greater than Cr moment indicating presence of 4f states.

Synthesis and luminescence behavior of SrGd1.76Eu0.24O4 host for display and dosimetric applications

Science.gov (United States)

Singh, Jyoti; Manam, J.; Singh, Fouran

2018-05-01

Novel SrGd1.76Eu0.24O4 materials were synthesized by conventional high-temperature solid-state reaction method in air ambiance. The structural and luminescence properties of as-prepared phosphors were explored by XRD, FESEM, TEM, PL and TL techniques. The confirmation of orthorhombic phase formation was obtained by XRD studies. The agglomerated ginger-like morphology of as-synthesized SrGd1.76Eu0.24O4 samples was unfolded by FESEM and TEM studies. Upon 276 and 395 nm UV excitation, SrGd1.76Eu0.24O4 phosphors showed intense red emission. The TL glow curve of SrGd1.76Eu0.24O4 irradiated with γ-rays exhibits two well-resolved peaks at 393 K and 598 K having a shoulder at 537 K. Linearity in a wide dose range 500 Gy-3 kGy are observed in the as-formed SrGd1.76Eu0.24O4 samples. Intense red emission, linear dose response and high reproducibility of SrGd1.76Eu0.24O4 samples broadly indicated its suitability for display and TL dosimetry applications.

Photoluminescence properties of Eu(3+)/ Sm(3+) activated CaZr4(PO4)6 phosphors.

Science.gov (United States)

Nair, Govind B; Dhoble, S J

2016-09-01

Solid state reaction method was employed for the synthesis of a series of CaZr4(PO4)6: Eu(3+)/Sm(3+) phosphors. The red-emitting CaZr4(PO4)6:Eu(3+) phosphors can be efficiently excited at 396 nm and thereby, exhibit a strong red luminescence predominantly corresponding to the electric dipole transition at 615 nm. Under 405 nm excitation, CaZr4(PO4)6:Sm(3+) phosphors display orange emission with color temperatures approximately around 2200 K. The acquired results reveal that CaZr4(PO4)6: RE(3+) (RE = Eu, Sm) phosphors could be potential candidates for red and orange emitting phosphor, respectively, for UV/blue-pump LEDs.

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 one-step hydrothermal synthesis and luminescence properties of Eu{sup 3+}-doped NaGd(WO{sub 4}){sub 2} nanophosphors

Energy Technology Data Exchange (ETDEWEB)

Jiang, Zehan; Cai, Peiqing; Chen, Cuili; Pu, Xipeng; Kim, Sun Il, E-mail: sikim@pknu.ac.kr; Jin Seo, Hyo, E-mail: hjseo@pknu.ac.kr

2017-06-01

Eu{sup 3+}-doped NaGd(WO{sub 4}){sub 2} nanophosphors were synthesized via a facile one-step hydrothermal method without any surfactants or a further heat treatment. X-ray powder diffraction (XRD), scanning electron microscope (SEM), fourier transform infrared spectroscopy (FT-IR), the photoluminescence (PL) excitation and emission spectra, and decay curves were used to characterize NaGd(WO{sub 4}){sub 2}:Eu{sup 3+} phosphors. The results show that the Eu{sup 3+}-concentration has little influence on the structure and morphology of the as-synthesized samples. However, pH value plays a vital role on the structure and morphology of NaGd(WO{sub 4}){sub 2}. The well-crystallized sheet-like NaGd(WO{sub 4}){sub 2} phosphors can be obtained only at pH = 5–7. On the basis of the time-dependent synthesis, a possible growth mechanism of sheet-like architectures is proposed. The luminescence properties of NaGd{sub 1-x}Eu{sub x}(WO{sub 4}){sub 2} (0 ≤ x ≤ 1) are investigated. It is found that the charge transfer band of Eu{sup 3+} shifts to lower energy and broadens with increasing the Eu{sup 3+}-concentration. - Highlights: • NaGd(WO{sub 4}){sub 2}:Eu{sup 3+} nanosheets were synthesized by facile one-step hydrothermal method. • Luminescence properties of NaGd(WO{sub 4}){sub 2}:Eu{sup 3+} phosphor were firstly reported. • The CT band of Eu{sup 3+} depends strongly on Eu{sup 3+}-concentrations.

Synthesis and photoluminescence properties of GdBO3:Ln3+ (Ln = Eu, Tb) nanofibers by electrospinning

International Nuclear Information System (INIS)

Shen, Hongzhi; Feng, Shuo; Wang, Ying; Gu, Yipeng; Zhou, Jing; Yang, Hang; Feng, Guanlin; Li, Liang; Wang, Wenquan; Liu, Xiaoyang; Xu, Dapeng

2013-01-01

Highlights: ► GdBO 3 :Ln 3+ nanofibers were synthesized successfully by electrospinning. ► The samples have the average diameter of 150 nm and the flexible morphology. ► The GdBO 3 : Eu 3+ nanofibers have the stronger orange emission. ► The luminescence properties are different from the reported bulk material. ► We describe the energy transform process of GdBO 3 :Ln 3+ system. - Abstract: GdBO 3 :Ln 3+ (Ln = Eu, Tb) nanofibers were synthesized using electrospinning combined with heat treatment. The synthesized nanofibers were characterized by X-ray diffraction, Raman spectroscopy, field emission-scanning electron microscopy, thermogravimetric and differential thermal analyses, and photoluminescence. The experimental results show that the flexible synthesized nanofibers have an average diameter of approximately 150 nm. The nanofibers consist of crystalline grains with diameters of about 40 nm and have a vaterite-type structure of GdBO 3 . The GdBO 3 :Eu 3+ nanofibers exhibit strong orange and weak red emissions with a low ratio of red to orange emission intensities, which is different from those of the reported bulk materials and nanoparticles. The luminescence properties of the synthesized GdBO 3 :Tb 3+ nanofibers are essentially consistent with those of the synthesized GdBO 3 :Tb 3+ powders by solid-state reaction.

Surprising luminescent properties of the polyphosphates Ln(PO3)3:Eu (Ln = Y, Gd, Lu).

Science.gov (United States)

Höppe, Henning A; Kazmierczak, Karolina; Kacprzak, Sylwia; Schellenberg, Inga; Pöttgen, Rainer

2011-10-21

The optical emission properties of the lanthanoid catena-polyphosphates Ln(PO(3))(3) (Ln = Y, Gd, Lu) doped with europium were investigated. Incommensurately modulated β-Y(PO(3))(3):Eu (super space group Cc (0|0.364|0)0) and Gd(PO(3))(3):Eu (space group I2/a) show the usual emission characteristics of Eu(3+), while in Lu(PO(3))(3):Eu (space group Cc) the europium is unprecedentedly partially reduced to the divalent state, as proven by both a broad emission band at 406 nm excited at 279 nm and an EPR spectroscopic investigation. (151)Eu-Mössbauer spectroscopy showed that only a very small part of the europium is reduced in Lu(PO(3))(3):Eu. An explanation for this unusual behaviour is given. This journal is © The Royal Society of Chemistry 2011

Muon spin depolarization in Gd- and EuBa1Cu3O/sub x/

International Nuclear Information System (INIS)

Cooke, D.W.; Hutson, R.L.; Kwok, R.S.

1988-01-01

Positive muon spin rotation (μSR) measurements on Gd- and EuBa 2 Cu 3 O/sub x/ (x ∼ 7) have been conducted in the temperature interval 4-300K. For each sample, muons stop both at grain boundaries and within the superconducting grains. Measured magnetic field penetration depths are 1550 and 1900/angstrom/ for two specimens of GdBa 2 Cu 3 O/sub x/, and 1350/angstrom/ for EuBa 2 Cu 3 O/sub x/. 2 refs., 5 figs

Calculations of the Low-Lying Structures in the Even-Even Nd/Sm/Gd/Dy Isotopes

Science.gov (United States)

Lee, Su Youn; Lee, J. H.; Lee, Young Jun

2018-05-01

The nuclear structure of deformed nuclei has been studied using the interacting boson model (IBM). In this study, energy levels and E2 transition probabilities were determined for even nuclei in the Nd/Sm/Gd/Dy chains which have a transition characteristic between the rotational, SU(3) and vibrational, U(5) limits. The structure of the nuclei exhibits a slight breaking of the SU(3) symmetry in the direction of U(5), and therefore, we add the d-boson number operator n d , which is the main term of the U(5) symmetric Hamiltonian, to the SU(3) Hamiltonian of the IBM. The calculated results for low-lying energy levels and E2 transition rates in Nd/Sm/Gd/Dy isotopes are in reasonably good agreement with known experimental results.

Luminescent GdVO{sub 4}:Sm{sup 3+} quantum dots enhance power conversion efficiency of bulk heterojunction polymer solar cells by Förster resonance energy transfer

Energy Technology Data Exchange (ETDEWEB)

Bishnoi, Swati [CSIR-Network of Institutes for Solar Energy, New Delhi 110001 (India); Luminescent Materials and Devices Group, CSIR-National Physical Laboratory, New Delhi 110012 (India); Academy of Scientific and Innovative Research (AcSIR), CSIR-National Physical Laboratory, Dr. K. S. Krishnan Marg, New Delhi 110012 (India); Gupta, Vinay, E-mail: drvinaygupta@netscape.net; Sharma, Gauri D.; Chand, Suresh [CSIR-Network of Institutes for Solar Energy, New Delhi 110001 (India); Organic and Hybrid Solar Cells Group, Physics of Energy Harvesting Division, CSIR-National Physical Laboratory, New Delhi 110012 (India); Sharma, Chhavi; Kumar, Mahesh [Ultrafast Optoelectronics and Terahertz Photonics Lab, Physics of Energy Harvesting Division, CSIR-National Physical Laboratory, New Delhi 110012 (India); Haranath, D. [CSIR-Network of Institutes for Solar Energy, New Delhi 110001 (India); Luminescent Materials and Devices Group, CSIR-National Physical Laboratory, New Delhi 110012 (India); Naqvi, Sheerin [Luminescent Materials and Devices Group, CSIR-National Physical Laboratory, New Delhi 110012 (India)

2016-07-11

In this work, we report enhanced power conversion efficiency (PCE) of bulk heterojunction polymer solar cells by Förster resonance energy transfer (FRET) from samarium-doped luminescent gadolinium orthovanadate (GdVO{sub 4}:Sm{sup 3+}) quantum dots (QDs) to polythieno[3,4-b]-thiophene-co-benzodithiophene (PTB7) polymer. The photoluminescence emission spectrum of GdVO{sub 4}:Sm{sup 3+} QDs overlaps with the absorption spectrum of PTB7, leading to FRET from GdVO{sub 4}:Sm{sup 3+} to PTB7, and significant enhancements in the charge-carrier density of excited and polaronic states of PTB7 are observed. This was confirmed by means of femtosecond transient absorption spectroscopy. The FRET from GdVO{sub 4}:Sm{sup 3+} QDs to PTB7 led to a remarkable increase in the power conversion efficiency (PCE) of PTB7:GdVO{sub 4}:Sm{sup 3+}:PC{sub 71}BM ([6,6]-phenyl-C{sub 71}-butyric acid methyl ester) polymer solar cells. The PCE in optimized ternary blend PTB7:GdVO{sub 4}:Sm{sup 3+}:PC{sub 71}BM (1:0.1:1.5) is increased to 8.8% from 7.2% in PTB7:PC{sub 71}BM. This work demonstrates the potential of rare-earth based luminescent QDs in enhancing the PCE of polymer solar cells.

Co-precipitation synthesis and photoluminescence properties of K2GdZr (PO4)3:Eu3+—a deep red luminomagnetic nanophosphor

International Nuclear Information System (INIS)

Chawla, Santa; Ravishanker,; Rajkumar,; Khan, A.F.; Kotnala, R.K.

2013-01-01

Nanoparticles of Eu 3+ activated K 2 GdZr(PO 4 ) 3 has been successfully synthesized by controlled inclusive co-precipitation method in high alkaline environment to enable complex crystalline phase formation. Much enhanced deep red luminescence, broadened emission bands with unusually prominent 5 D 0 – 7 F 4 transition at 699 nm are defining characteristics of the nanoparticles compared to bulk counterpart synthesized by solid state reaction route. Among various excitation pathways such as charge transfer from O 2− –Eu 3+ , Gd 3+ –Eu 3+ , the direct excitation of Eu 3+ at 394 nm is the most effective as revealed by photoluminescence and time resolved studies. Occurrence and variation of superparamagnetism in undoped and Eu 3+ doped nanoparticles indicate the role of unpaired 4f electron spin of Gd 3+ in making the nanoparticles superparamagnetic. A room temperature cost effective synthesis process of Eu 3+ doped multimetallic complex phosphate supermagnetic nanophosphor can pave way for applications requiring such functionality. -- Highlights: ► Eu 3+ doped K 2 GdZr(PO 4 ) 3 nanocrystals have been synthesized successfully by coprecipitation. ► K 2 GdZr(PO 4 ) 3 :Eu 3+ emit intense deep red fluorescence. ► Red emitting K 2 GdZr(PO 4 ) 3 :Eu 3+ nanocrystals show superparamagnetism due to Gd 3+ . ► Luminomagnetic KGP:Eu 3+ have application potential in biology, lighting and display

Site selective spectroscopy in BaYF{sub 5}:RE{sup 3+} (RE = Eu, Sm) nano-glass–ceramics

Energy Technology Data Exchange (ETDEWEB)

Castillo, J. del, E-mail: fjvargas@ull.edu.es [Dpto. Física, Universidad de La Laguna, 38206 La Laguna, Tenerife (Spain); Yanes, A.C. [Dpto. Física, Universidad de La Laguna, 38206 La Laguna, Tenerife (Spain); Abe, S.; Smet, P.F. [LumiLab, Department of Solid State Sciences, Ghent University, Krijgslaan 281-S1, 9000 Gent (Belgium); Center for Nano- and Biophotonics (NB Photonics), Ghent University (Belgium)

2015-06-25

Highlights: • We obtained sol–gel transparent nGCs with Eu{sup 3+}, Sm{sup 3+}-doped cubic BaYF{sub 5} nanocrystals. • Eu{sup 3+}-doped BaYF{sub 5} NCs were prepared by solvothermal method. • Their luminescent properties were studied and compared with the Eu{sup 3+}-doped nGCs. • Eu{sup 3+}/Sm{sup 3+} were used as probe ions in the nGCs to distinguish different environments. • The incorporation of a large fraction of RE ions into the BaYF{sub 5} NCs was confirmed. - Abstract: Trivalent rare-earth (RE = Eu, Sm) doped transparent nano-glass–ceramics comprising BaYF{sub 5} nanocrystals were successfully obtained by appropriate heat-treatment of the corresponding precursor sol–gel glasses. Their structural and spectroscopic properties were investigated and compared with those for Eu{sup 3+}-doped-BaYF{sub 5} nanocrystals prepared by a solvothermal method. X-ray Diffraction, Transmission Electron Microscopy and Energy Dispersive X-ray Spectroscopy measurements confirmed the distribution of BaYF{sub 5} nanocrystals in the glass matrix, presenting a cubic phase structure with space group Fm-3m. In order to achieve a further structural characterization, the luminescence properties of the Eu{sup 3+} and Sm{sup 3+} dopants were also used as sensitive probes. The reduction in the emission intensities of hypersensitive transitions {sup 5}D{sub 0} → {sup 7}F{sub 2} and {sup 4}G{sub 5/2} → {sup 6}H{sub 9/2} for Eu{sup 3+} and Sm{sup 3+} ions respectively, along with time-resolved measurements, confirm the distribution of a significant fraction of RE ions into the fluoride nanocrystal environment. These results suggest that BaYF{sub 5} nano-glass–ceramics doped with Eu{sup 3+} or Sm{sup 3+} can be considered as potential red-emitting phosphors for the development of white LEDs under near UV excitation.

Tunable photoluminescence and magnetic properties of Dy(3+) and Eu(3+) doped GdVO4 multifunctional phosphors.

Science.gov (United States)

Liu, Yanxia; Liu, Guixia; Dong, Xiangting; Wang, Jinxian; Yu, Wensheng

2015-10-28

A series of Dy(3+) or/and Eu(3+) doped GdVO4 phosphors were successfully prepared by a simple hydrothermal method and characterized by X-ray diffraction (XRD), field emission scanning electron microscopy (FE-SEM), energy-dispersive X-ray spectrometry (EDS), photoluminescence (PL) spectroscopy and vibrating sample magnetometry (VSM). The results indicate that the as-prepared samples are pure tetragonal phase GdVO4, taking on nanoparticles with an average size of 45 nm. Under ultraviolet (UV) light excitation, the individual Dy(3+) or Eu(3+) ion activated GdVO4 phosphors exhibit excellent emission properties in their respective regions. The mechanism of energy transfer from the VO4(3-) group and the charge transfer band (CTB) to Dy(3+) and Eu(3+) ions is proposed. Color-tunable emissions in GdVO4:Dy(3+),Eu(3+) phosphors are realized through adopting different excitation wavelengths or adjusting the appropriate concentration of Dy(3+) and Eu(3+) when excited by a single excitation wavelength. In addition, the as-prepared samples show paramagnetic properties at room temperature. This kind of multifunctional color-tunable phosphor has great potential applications in the fields of photoelectronic devices and biomedical sciences.

Luminescent properties of (Y,Gd)BO3:Bi3+,RE3+ (RE=Eu, Tb) phosphor under VUV/UV excitation

International Nuclear Information System (INIS)

Zeng Xiaoqing; Im, Seoung-Jae; Jang, Sang-Hun; Kim, Young-Mo; Park, Hyoung-Bin; Son, Seung-Hyun; Hatanaka, Hidekazu; Kim, Gi-Young; Kim, Seul-Gi

2006-01-01

Bi 3+ - and RE 3+ -co-doped (Y,Gd)BO 3 phosphors were prepared and their luminescent properties under vacuum ultraviolet (VUV)/UV excitation were investigated. Strong red emission for (Y,Gd)BO 3 :Bi 3+ ,Eu 3+ and strong green emission for (Y,Gd)BO 3 :Bi 3+ ,Tb 3+ are observed under VUV excitation from 147 to 200 nm with a much broader excitation region than that of single Eu 3+ -doped or Tb 3+ -doped (Y,Gd)BO 3 phosphor. Strong emissions are also observed under UV excitation around 265 nm where as nearly no luminescence is observed for single Eu 3+ -doped or Tb 3+ -doped (Y,Gd)BO 3 . The luminescence enhancement of Bi 3+ - and RE 3+ -co-doped (Y,Gd)BO 3 phosphors is due to energy transfer from Bi 3+ ion to Eu 3+ or Tb 3+ ion not only in the VUV region but also in the UV region. Besides, host sensitization competition between Bi 3+ and Eu 3+ or Tb 3+ is also observed. The investigated phosphors may be preferable for devices with a VUV light 147-200 nm as an excitation source such as PDP or mercury-free fluorescent lamp

Luminescence properties of NaY(WO{sub 4}){sub 2}:Sm{sup 3+}, Eu{sup 3+} phosphors prepared by molten salt method

Energy Technology Data Exchange (ETDEWEB)

Liu, Ting; Meng, Qingyu, E-mail: qingyumeng163@163.com; Sun, Wenjun

2016-02-15

Sm{sup 3+} singly doped NaY(WO{sub 4}){sub 2} and Sm{sup 3+}, Eu{sup 3+} co-doped NaY(WO{sub 4}){sub 2} phosphors have been synthesized by molten salt method. The crystal structure and morphology were characterized by means of X-ray powder diffraction (XRD) and field emission scanning electron microscopy (FE-SEM). In Sm{sup 3+} singly doped NaY(WO{sub 4}){sub 2} phosphors, the suitable doping concentration was proved. In Sm{sup 3+}, Eu{sup 3+} co-doped NaY(WO{sub 4}){sub 2} phosphors, the energy transfer from Sm{sup 3+} to Eu{sup 3+} is confirmed by the luminescent spectra. A strong absorption line at 405 nm can be generated from {sup 6}H{sub 5/2}-{sup 4}K{sub 11/2} ({sup 4}F{sub 7/2}) transition of Sm{sup 3+} in Sm{sup 3+}, Eu{sup 3+} co-doped NaY(WO{sub 4}){sub 2} phosphors, which is suitable for the emission of the near-ultraviolet light-emitting diodes. The energy transfer efficiency, energy transfer rate and average distance between Sm{sup 3+} and Eu{sup 3+} in the NaY(WO{sub 4}){sub 2}:Sm{sup 3+}, Eu{sup 3+} phosphors have been calculated based on the fluorescent dynamic analysis. Finally, the energy transfer mechanism between Sm{sup 3+} and Eu{sup 3+} is confirmed, the energy transfer occurs between {sup 4}G{sub 5/2} state of Sm{sup 3+} ions and {sup 5}D{sub 0} state rather than {sup 5}D{sub 1} state of Eu{sup 3+} ions.

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.

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.

Synthesis, electronic structure and luminescent properties of a new red-emitting phosphor GdBiW2O9:Eu3+

Science.gov (United States)

Xie, Zhi; Zhou, Weiwei; Zhao, Wang; Zhang, Hao; Hu, Qichang; Xu, Xuee

2017-10-01

Red phosphor of GdBiW2O9:Eu3+ was prepared by solid-state reaction method. The phase purity and structure of the samples were characterized by XRD. The electronic structures of GdBiW2O9 host were estimated by DFT calculation. The PLE and PL spectra were also investigated. The optimal luminescent properties of GdBiW2O9:Eu3+ phosphors were obtained at 900 °C with 40 mol% of Eu3+ concentration. The phosphors can be excited efficiently by 396 nm NUV light and emit intense red light peaking at 618 nm. The results indicate GdBiW2O9:Eu3+ can act as a potential red-emitting phosphor for LEDs application.

Hydrothermal synthesis of controllable size, morphology and optical properties of β-NaGdF{sub 4}: Eu{sup 3+} microcrystals

Energy Technology Data Exchange (ETDEWEB)

Zhou, Ting; Jiang, Xiaojiao [College of Chemistry and Materials Science, Sichuan Normal University, No. 5 Jing' an Road, Jinjiang District, Chengdu 610068 (China); Zhong, Cheng [Department of Basic Education, Dazhou Vocational and Technical College, No. 448 Xu' jiaba Road, Tongchuan District, Dazhou 635001 (China); Tang, Xiaoxue; Ren, Shanshan; Zhao, Yan; Liu, Mengjiao; Lai, Xin; Bi, Jian [College of Chemistry and Materials Science, Sichuan Normal University, No. 5 Jing' an Road, Jinjiang District, Chengdu 610068 (China); Gao, Daojiang, E-mail: daojianggao@126.com [College of Chemistry and Materials Science, Sichuan Normal University, No. 5 Jing' an Road, Jinjiang District, Chengdu 610068 (China)

2016-07-15

Eu{sup 3+}-doped β-NaGdF{sub 4} (hexagonal NaGdF{sub 4}) microcrystals with various sizes and morphologies have been prepared via a facile hydrothermal route with and without trisodium citrate (Na{sub 3}Cit) under different Ln{sup 3+}/NaF (Ln=Gd, Eu) molar ratios and pH values. The microstructures and luminescence properties of the as-synthesized microcrystals were characterized through X-ray diffraction (XRD), scanning electron microscopy (SEM), Fourier transform infrared spectroscopy (FT-IR) and photoluminescence (PL) spectroscopy. Moreover, the photoluminescent properties of Eu{sup 3+}-doped β-NaGdF{sub 4} samples synthesized at different pH values were systematically discussed. As a result, monodisperse and uniform spherical and rod-like crystals were successfully synthesized by varying Ln{sup 3+}/NaF molar ratio, Ln{sup 3+}/Na{sub 3}Cit molar ratio and pH value, and the obtained feasible range of pH value is 8–11, the optimal molar ratios of Ln{sup 3+}/NaF and Ln{sup 3+}/Na{sub 3}Cit are 1:6 and 1:3, respectively. Our results show that there is an energy transfer process between the host and activator ions, emissions from high energy configurations to ground state are gradually quenched in the β-NaGdF{sub 4}: Eu{sup 3+} phosphors obtained in the strong alkaline solution. In addition, pure orange-red photoluminescent color can be obtained from β-NaGdF{sub 4}: 2 mol% Eu{sup 3+} phosphors synthesized under the obtained processing conditions. - Highlights: • A facile hydrothermal technique is used to prepare β-NaGdF{sub 4}: Eu{sup 3+} microcrystals. • Phosphors with higher performance can be obtained in proper hydrothermal conditions. • The as-synthesized β-NaGdF{sub 4}: Eu{sup 3+} microcrystals can exhibit orange-red emissions.

Observation of magnetization reversal behavior in Sm0.9Gd0.1Cr0.85Mn0.15O3 orthochromites

Science.gov (United States)

Panwar, Neeraj; Joby, Jostin P.; Kumar, Surendra; Coondoo, Indrani; Vasundhara, M.; Kumar, Nitu; Palai, Ratnakar; Singhal, Rahul; Katiyar, Ram S.

2018-05-01

Impact of co-doping (Gd and Mn) on the magnetic properties has been systematically investigated in SmCrO3 compound. For the synthesized compound Sm0.9Gd0.1Cr0.85Mn0.15O3 (SGCMO), below the Neel transition temperature and under low applied magnetic field, temperature induced magnetization reversal at 105 K (crossover temperature) was noticed in the field cooled magnetization curve. Magnetization reversal attained maximum value of -1.03 emu/g at 17 K where spin reorientation occurred. The magnetization reversal disappeared under higher applied field. From the M-H plots an enhancement in the magnetization was observed due to Gd doping. Magnetocaloric effect at low temperatures measured through the magnetic entropy change was found sixteen times higher for this compound as compared to pristine SmCrO3 and twice to that of SmCr0.85Mn0.15O3 compound. The study reveals the importance of co-doping in tailoring the magnetic properties of rare-earth chromites.

Orange-red emitting Gd2Zr2O7:Sm3+: Structure-property correlation, optical properties and defect spectroscopy

Science.gov (United States)

Gupta, Santosh K.; Reghukumar, C.; Sudarshan, K.; Ghosh, P. S.; Pathak, Nimai; Kadam, R. M.

2018-05-01

Local structure analysis of dopant ion, understanding host to dopant energy transfer dynamics and defects characterization in a doped material which plays an important role in the designing a highly efficient opto-electronic material. In this connection a new Sm3+ doped Gd2Zr2O7 pyrochlore material was synthesized using gel-combustion technique and was characterized systematically using X-ray diffraction (XRD), time resolved photoluminescence spectroscopy (TRPLS), positron annihilation lifetime spectroscopy (PALS) and density functional theory (DFT) based ab-initio calculation. Based on DFT site selective energetics calculation and luminescence decay measurement, it was observed that the Sm3+ was distributed at both Gd3+ and Zr4+ site with higher Sm3+ fraction at the Gd3+ site. PALS was used to probe the presence of defects in the phosphor. In this work intense orange-red emission is realized through manipulating the energy transfer from host defect emission (oxygen vacancies) to Sm3+ which allows color emission from green in undoped to orange-red in doped samples. Effect of dopant concentration and annealing temperature was probed using TRPLS and PALS. These all information is highly important for researcher looking to achieve pyrochlore based phosphor materials with high quantum yield.

1,3-thiazole as suitable antenna ligand for lanthanide photoluminescence in [LnCl{sub 3}(thz){sub 4}].0.5thz, Ln = Sm, Eu, Gd, Tb, Dy

Energy Technology Data Exchange (ETDEWEB)

Dannenbauer, Nicole; Mueller-Buschbaum, Klaus [Wuerzburg Univ. (Germany). Inst. for Inorganic Chemistry; Kuzmanoski, Ana; Feldmann, Claus [Karlsruhe Institute of Technology (KIT), Karlsruhe (Germany). Inst. for Inorganic Chemistry

2014-02-15

The series of luminescent monomeric lanthanide thiazole complexes [LnCl{sub 3}(thz){sub 4}].0.5thz (Ln = Sm, Eu, Gd, Tb, Dy; thz = 1,3-thiazole) has been synthesised and characterised by powder and single-crystal X-ray diffraction, IR and photoluminescence spectroscopy, DTA/TG as well as elemental analysis. The colourless compounds exhibit photoluminescence in the visible region with varying quantum efficiencies up to QY = 48 % for [LnCl{sub 3}(thz){sub 4}].0.5thz. Both, the lanthanide ions as well as the thiazole ligand contribute to the luminescence. Excitation can be achieved via intra-4f transitions and by exciting the ligand, emission is observed mainly from the lanthanide ions again by 4f transitions. Thiazole can transfer energy to the lanthanide ions, which further feeds the lanthanide emission by an efficient antenna effect even at room temperature. The lanthanide ions show pentagonal-bipyramidal coordination by three chloride anions and four N atoms of 1,3-thiazole, which leads to a strong {sup 5}D{sub 0} → {sup 7}F{sub 4} transition for europium. Significant differences arise as compared to thiophene complexes because no sulphur atom is involved in the metal coordination, as the thiazole ligand is solely coordinated via its nitrogen function. (orig.)

The spectral characteristics of Gd sub 2 SiO sub 5 :Eu sup 3 sup + in VUV-UV range

CERN Document Server

Chen Yong; Wei Ya Guang; Tao Ye

2002-01-01

Synchrotron radiation source was used to investigated the spectral characteristics of Gd sub 2 SiO sub 5 :Eu sup 3 sup + in VUV-UV range. The various energy transfers at room temperature and 10 K, including from host or Gd sup 3 sup + ions to Eu sup 3 sup + ions and transfer between Eu sup 3 sup + ions at two different lattice sites, were discussed. In addition the emission spectra under 186 nm and 276 nm excitation were compared from the view of quantum cutting. The results indicate that Gd sub 2 SiO sub 5 :Eu sup 3 sup + is a kind of material with potential high efficiency quantum cutting

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 .

Mechanism of luminescent enhancement in Ba{sub 2}GdNbO{sub 6}:Eu{sup 3+} perovskite by Li{sup +} co-doping

Energy Technology Data Exchange (ETDEWEB)

Rezende, Marcos Vinicius dos Santos [Departamento de Física, Universidade Federal de Sergipe, 49500-000, Itabaiana, SE (Brazil); Valério, Mario Ernesto Giroldo [Departamento de Física, Universidade Federal de Sergipe, 49100-000 São Cristóvão, SE (Brazil); Mouta, Rodolpho; Diniz, Eduardo Moraes [Departamento de Física, CCET, Universidade Federal do Maranhão, 65085-580 São Luís, MA (Brazil); Paschoal, Carlos William de Araujo, E-mail: paschoal@ufma.br [Departamento de Física, CCET, Universidade Federal do Maranhão, 65085-580 São Luís, MA (Brazil); Department of Materials Science and Engineering, University of California Berkeley, 94720-1760 Berkeley, CA (United States); Department of Physics, University of California Berkeley, 94720-7300 Berkeley, CA (United States)

2015-02-15

We investigated the Li{sup +} ion incorporation in Ba{sub 2}GdNbO{sub 6}:Eu{sup 3+} perovskite by atomistic simulations based on energy minimization. We predicted the most probable sites occupied by Eu{sup 3+} and Li{sup +} ions and the related charge-compensation mechanisms involved into these substitutions. The results show that the Eu{sup 3+} and Li{sup +} ions are incorporated mainly at the Gd{sup 3+} site. In the Li{sup +} ion case, there is a charge compensation by Nb{sub Gd}{sup •} {sup •} antisite. The crystal field parameters and the transition levels for the Eu{sup 3+} ion in the BGN:Eu{sup 3+} were calculated with basis on the simulated local symmetry of the Eu{sup 3+} site. The results show that the mechanism of luminescent properties enhancement is the symmetry distortion induced by the Li{sup +} co-doping. - Highlights: • We performed a full defect calculations in Ba{sub 2}GdNbO{sub 6} double perovskite. • We modeled with excellent agreement the optical transition of Ba{sub 2}GdNbO{sub 6}:Eu{sup 3+} crystal. • We explained the mechanism of luminescent enhancement in Ba{sub 2}GdNbO{sub 6}:Eu{sup 3+} perovskite by Li{sup +} co-doping.

Magnetic properties of Eu doped BiGdO{sub 3}

Energy Technology Data Exchange (ETDEWEB)

Nithya, R., E-mail: nithya@igcar.gov.in; Yadagiri, K. [Materials Science Group, Indira Gandhi Centre for Atomic Research, Kalpakkam, 603 102, TN (India); Shukla, Neeraj [UGC-DAE-CSR Kalpakkam Node, Kokilamedu-603 104, TN (India)

2016-05-23

Bulk Bismuth Gadolinium Oxide, BiGdO{sub 3} and Eu doped BiGdO{sub 3} compounds were synthesized by the conventional solid state reaction in air. Phase formation of these compounds was tracked using powder X-ray characterization technique since single phase formation was found to be sensitive to thermal treatment parameters such as cooling and heating rates. Analysis of X-ray diffraction patterns revealed cubic structure with Pm-3m symmetry. An antiferromagnetic transition around 3.8 K was observed in the pristine compound whereas doped samples showed paramagnetic nature in the whole measured temperature range.

Luminescent GdVO4:Eu3+ functionalized mesoporous silica nanoparticles for magnetic resonance imaging and drug delivery.

Science.gov (United States)

Huang, Shanshan; Cheng, Ziyong; Ma, Ping'an; Kang, Xiaojiao; Dai, Yunlu; Lin, Jun

2013-05-14

Luminescent GdVO4:Eu(3+) nanophosphor functionalized mesoporous silica nanoparticles (MSN) were prepared (denoted as GdVO4:Eu(3+)@MSN). The in vitro cytotoxicity tests show that the sample has good biocompatibility, which indicates that the nanocomposite could be a promising candidate for drug delivery. Flow cytometry and confocal laser scanning microscopy (CLSM) confirm that the sample can be effectively taken up by SKOV3 ovarian cancer cells and A549 lung adenocarcinoma cells. It was also shown that the GdVO4:Eu(3+)@MSN brightened the T1-weighted images and enhanced the r1 relaxivity of water protons, which suggested that they could act as T1 contrast agents for magnetic resonance (MR) imaging. It was found that the carriers present a pH-dependent drug release behavior for doxorubicin (DOX). The composites show a red emission under UV irradiation due to the GdVO4:Eu(3+) nanophosphors. Furthermore, the PL intensity of the composite shows correlation with the cumulative release of DOX. These results suggest that the composite can potentially act as a multifunctional drug carrier system with luminescent tagging, MR imaging and pH-controlled release property for DOX.

Crystal structure and magnetic properties of RCu5-xPdx (R=Pr, Nd, Sm and Eu) alloys

International Nuclear Information System (INIS)

Shah, K.V.; Bonville, P.; Manfrinetti, P.; Provino, A.; Dhar, S.K.

2009-01-01

We report the effect of replacing Cu by Pd in RCu 5 (R=Pr, Nd, Sm and Eu). The parent RCu 5 compounds crystallize in the hexagonal CaCu 5 -type structure. The hexagonal symmetry is retained in PrCu 4 Pd and EuCu 5-x Pd x (x=1 and 2) but the crystal structure changes to cubic AuBe 5 -type in PrCu 3 Pd 2 , NdCu 5-x Pd x (x=1 and 2) and SmCu 4 Pd. Substitution with Pd leads to lattice expansion and modifies the magnetic behavior. While PrCu 5 is known to be a van-Vleck paramagnet with a singlet ground state, PrCu 4 Pd and PrCu 3 Pd 2 show ferromagnetic-like behavior at low temperatures. SmCu 4 Pd orders ferromagnetically near 28 K in contrast to the antiferromagnetic nature of the parent SmCu 5 . The divalent nature of the Eu ions in EuCu 5 is retained in the ternary alloys, but the Curie temperature is reduced from 57 to 24.5 and 14.5 K in EuCu 4 Pd and EuCu 3 Pd 2 , respectively, inferred from the location of peak in the heat capacity of these two compounds. The magnetic hyperfine field at the Eu nucleus measured with 151 Eu Moessbauer spectroscopy in the ternary Eu-alloys is comparable to that in EuCu 5 . The magnetic behavior of NdCu 4 Pd is similar to that reported in NdCu 5 . The zero-field-cooled, low-field magnetization of NdCu 3 Pd 2 shows a region of diamagnetic behavior roughly between 21 and 4 K, but the field-cooled response is positive.

Shape tunable synthesis of Eu- and Sm-doped ZnO microstructures ...

Indian Academy of Sciences (India)

Shape tunable synthesis of Eu- and Sm-doped ZnO microstructures: a morphological ... different microstructures material at relatively low temper- ..... Chem. C 114. 2776. 5. Gao P X and Wang Z L 2003 J. Am. Chem. Soc. 125 11299. 6.

High-Precision Measurement of Eu/Eu* in Geological Glasses via LA-ICP-MS Analysis

Science.gov (United States)

Tang, Ming; McDonough, William F.; Arevalo, Ricardo, Jr.

2014-01-01

Elemental fractionation during laser ablation inductively coupled plasma mass spectrometry (LA-ICP-MS) analysis has been historically documented between refractory and volatile elements. In this work, however, we observed fractionation between light rare earth elements (LREEs) and heavy rare earth elements (HREEs) when using ablation strategies involving large spot sizes (greater than 100 millimeters) and line scanning mode. In addition: (1) ion yields decrease when using spot sizes above 100 millimeters; (2) (Eu/Eu*)(sub raw) (i.e. Europium anomaly) positively correlates with carrier gas (He) flow rate, which provides control over the particle size distribution of the aerosol reaching the ICP; (3) (Eu/Eu*)(sub raw) shows a positive correlation with spot size, and (4) the changes in REE signal intensity, induced by the He flow rate change, roughly correlate with REE condensation temperatures. The REE fractionation is likely driven by the slight but significant difference in their condensation temperatures. Large particles may not be completely dissociated in the ICP and result in preferential evaporation of the less refractory LREEs and thus non-stoichiometric particle-ion conversion. This mechanism may also be responsible for Sm-Eu-Gd fractionation as Eu is less refractory than Sm and Gd. The extent of fractionation depends upon the particle size distribution of the aerosol, which in turn is influenced by the laser parameters and matrix. Ablation pits and lines defined by low aspect ratios produce a higher proportion of large particles than high aspect ratio ablation, as confirmed by measurements of particle size distribution in the laser induced aerosol. Therefore, low aspect ratio ablation introduces particles that cannot be decomposed and/or atomized by the ICP and thus results in exacerbated elemental fractionation. Accurate quantification of REE concentrations and Eu/Eu* requires reduction of large particle production during laser ablation. For the reference

Eu{sup 3+}/Tb{sup 3+} doped cubic BaGdF{sub 5} multifunctional nanophosphors: Multicolor tunable luminescence, energy transfer and magnetic properties

Energy Technology Data Exchange (ETDEWEB)

Li, Honglan; Liu, Guixia, E-mail: liuguixia22@163.com; Wang, Jinxian; Dong, Xiangting; Yu, Wensheng

2017-06-15

A series of BaGdF{sub 5}:Eu{sup 3+}/Tb{sup 3+} orange-green-yellow-white emitting nanophosphors (NPs) were successfully synthesized via hydrothermal method without assistance of any surfactant, catalyst, or template. The nanocrystals are in sphere-like morphology with an average size of approximately 46 nm. The quenching concentrations of Eu{sup 3+} and Tb{sup 3+} single doped BaGdF{sub 5} phosphors are 5.5% and 15%, respectively. The tunable color tone can be obtained in Eu{sup 3+} and Tb{sup 3+} co-doped BaGdF{sub 5} phosphors, the strong orange-white and green-yellow emissions can be seen in BaGdF{sub 5}:5.5%Eu{sup 3+}, y%Tb{sup 3+} and BaGdF{sub 5}:3.5%Tb{sup 3+}, x%Eu{sup 3+} phosphors, especially. More significantly, we realize the more standard white emission with a CIE chromaticity diagram point at (0.317, 0.321) and a lower correlated color temperature of 6979 K in the BaGdF{sub 5}: 5.5%Eu{sup 3+}, 4.5%Tb{sup 3+} sample. In addition, the energy transfer phenomenon from Tb{sup 3+} to Eu{sup 3+} ions is clearly observed in Tb{sup 3+}, Eu{sup 3+} co-doped BaGdF{sub 5} phosphors and the energy transfer efficiency can reach a maximum of 75%. Moreover, the as-prepared samples exhibit paramagnetic properties at room temperature. This type of multifunctional multicolor emitting nanophosphor has promising applications in the fields of full-color displays, biomedical science, MRI, and so on. - Graphical abstract: The cubic phase BaGdF{sub 5}:Eu{sup 3+}/Tb{sup 3+} sphere-like nanophosphors were prepared. Energy transfer mechanism, color-tunable emissions and magnetic properties of BaGdF{sub 5}:Eu{sup 3+}/Tb{sup 3+} have been studied, which could have promising applications in the fields of full-color displays, MRI and biomedical science, and so on.

Fabrication and photoluminescence properties of color-tunable light emitting lanthanide doped GdVO4 hierarchitectures

International Nuclear Information System (INIS)

Amurisana, Bao; Bao, Lihong; Bao, Liang; Tegus, O.

2017-01-01

The flower-like GdVO 4 :Ln 3+ ( Ln 3+ =Eu 3+ , Dy 3+ , Sm 3+ , Tm 3+ ) hierarchitectures have been successfully synthesized on a glass slide substrate through a one-pot hydrothermal route assisted by disodium ethylenediaminetetraacetic acid (Na 2 H 2 L, where L 4- =(CH 2 COO) 2 N(CH 2 ) 2 N(CH 2 COO) 2 4- ). A high density and ordered flower-like GdVO 4 :Ln 3+ hierarchitectures grew epitaxially on glass substrate. The as-prepared flower-like architectures with the size about 6 μm are constructed by the numerous radially oriented single-crystalline nanorods with the width from 20 nm to 200 nm and the length from 500 nm to 3 μm. The morphologies, the thickness, and the density of as-grown flower clusters can be readily tuned by tailoring the growth time and Na 2 H 2 L/Gd 3+ molar ratio. The possible formation mechanism of flower-like GdVO 4 :Ln 3+ hierarchitectures is discussed on the basis of the results from the controlled experiments under hydrothermal conditions. Because of an energy transfer from vanadate groups to dopants, the flower-like GdVO 4 :Ln 3+ ( Ln 3+ =Eu 3+ , Dy 3+ , Sm 3+ and Tm 3+ ) superstructures showed strong characteristic dominant emissions of the Eu 3+ , Dy 3+ , Sm 3+ and Tm 3+ ions at 617 nm ( 5 D 0 → 7 F 2 , strong red), 575 nm ( 4 F 9/2 → 6 H 13/2 , yellow), 604 nm ( 4 G 5/2 → 6 H 7/2 , orange-red) and 476 nm ( 1 G 4 – 3 H 6 , blue) under ultraviolet excitation, respectively.Further, the emission color of the product can also be tuned by selecting the dopant Ln 3+ with characteristic emissions and varying the concentration ratio of co-doping activators. This approach could be extended to the fabrication of hierarchical structures for other oxide micro/nanomaterials, and may provide a general way to achieve multicolor-tunable emission for many applications.

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

Effective lattice stabilization of gadolinium aluminate garnet (GdAG via Lu3+ doping and development of highly efficient (Gd,LuAG:Eu3+ red phosphors

Directory of Open Access Journals (Sweden)

Jinkai Li, Ji-Guang Li, Zhongjie Zhang, Xiaoli Wu, Shaohong Liu, Xiaodong Li, Xudong Sun and Yoshio Sakka

2012-01-01

Full Text Available The metastable garnet lattice of Gd3Al5O12 is stabilized by doping with smaller Lu3+, which then allows an effective incorporation of larger Eu3+ activators. The [(Gd1−xLux1−yEuy]3Al5O12 (x = 0.1–0.5, y = 0.01–0.09 garnet solid solutions, calcined from their precursors synthesized via carbonate coprecipitation, exhibit strong luminescence at 591 nm (the 5D0 → 7F1 magnetic dipole transition of Eu3+ upon UV excitation into the charge transfer band (CTB at ~239 nm, with CIE chromaticity coordinates of x = 0.620 and y = 0.380 (orange-red. The quenching concentration of Eu3+ was estimated at ~5 at.% (y = 0.05, and the quenching was attributed to exchange interactions. Partial replacement of Gd3+ with Lu3+ up to 50 at.% (x = 0.5 while keeping Eu3+ at the optimal content of 5 at.% does not significantly alter the peak positions of the CTB and 5D0 → 7F1 emission bands but slightly weakens both bands owing to the higher electronegativity of Lu3+. The effects of processing temperature (1000–1500 °C and Lu/Eu contents on the intensity, quantum efficiency, lifetime and asymmetry factor of luminescence were thoroughly investigated. The [(Gd0.7Lu0.30.95Eu0.05]3Al5O12 phosphor processed at 1500 °C exhibits a high internal quantum efficiency of ~83.2% under 239 nm excitation, which, in combination with the high theoretical density, favors its use as a new type of photoluminescent and scintillation material.

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.

Photoluminescent properties of LiSrxBa1-xPO4:RE3+ (RE = Sm3+, Eu3+) f-f transition phosphors

International Nuclear Information System (INIS)

Tu Dong; Liang Yujun; Liu Rong; Cheng Zheng; Yang Fan; Yang Wenlong

2011-01-01

Highlights: → Novel phosphors LiSr x Ba 1-x PO 4 : Sm 3+ and LiSr x Ba 1-x PO 4 : Eu 3+ have been synthesized by solid-state reaction method. → The LiSr x Ba 1-x PO 4 : Sm 3+ and LiSr x Ba 1-x PO 4 : Eu 3+ phosphors may be potential f-f transition phosphors used in LED. → The emission intensity of the LiSr x Ba 1-x PO 4 : Sm 3+ and LiSr x Ba 1-x PO 4 : Eu 3+ phosphors can be enhanced by increasing the value of x. - Abstract: Rare-earth ions (Sm 3+ or Eu 3+ ) doped LiSr x Ba 1-x PO 4 (x = 0, 0.2, 0.4, 0.6, 0.8, 1.0) f-f transition phosphor powders were prepared by a high temperature solid-state reaction. The resulted phosphors were characterized by X-ray diffraction (XRD) and photoluminescence (PL) spectroscopy. The results of XRD indicate that the phase structure of the sample changes from LiBaPO 4 to LiSrPO 4 when x changes from 0 to 1.0. The excitation spectra indicate that only direct excitation of rare earth ions (Sm 3+ or Eu 3+ ) can be observed. The doped rare earth ions show their characteristic emission in LiSr x Ba 1-x PO 4 , i.e., Eu 3+5 D 0 - 7 F J (J = 0, 1, 2, 3, 4), Sm 3+4 G 5/2 → 6 H J (J = 5/2, 7/2, 9/2, 11/2), respectively. The dependence of the emission intensities of the LiSr x Ba 1-x PO 4 :Sm 3+ and LiSr x Ba 1-x PO 4 :Eu 3+ phosphors on the x value and Ln 3+ (Ln 3+ = Sm 3+ , Eu 3+ ) concentration is also investigated.

Combustion synthesis and characterization of MV0.5P0.5O4: Sm3+, Tm3+ (M = Gd, La, Y)

Science.gov (United States)

Motloung, Selepe J.; Lephoto, Mantwa A.; Tshabalala, Kamohelo G.; Ntwaeaborwa, Odireleng M.

2018-04-01

In this paper, GdV0.5P0.5O4: Sm3+, Tm3+, LaV0.5P0.5O4: Sm3+, Tm3+ and YV0.5P0.5O4: Sm3+, Tm3+ phosphor powders were prepared by solution combustion method using urea as a fuel. The phase purity, surface morphology, optical and photoluminescence properties were investigated by X-ray diffraction (XRD), scanning electron microscopy (SEM), UV-vis spectroscopy and photoluminescence spectroscopy. The XRD results indicated that the prepared powders are of a single phase and crystallized in tetragonal structure for Gd and Y systems while monoclinic phase was observed for La system. SEM showed that the samples consisted of mixed structures. The estimated band gaps were 2.2, 2.4 and 2.3 eV for Y, Gd and La systems respectively. The photoluminescence results showed four emission peaks. One peak is assigned to 1G4 - 3H6 transition of Tm3+, and three other emission peaks are attributed to 6G5/2 - 6H5/2, 6G5/2 - 6H7/2 and 6G5/2 - 6H9/2 transitions of Sm3+. The photoluminescent intensity was the highest in the gadolinium system.

A template-free solvothermal synthesis and photoluminescence properties of multicolor Gd2O2S:xTb3+, yEu3+ hollow spheres

Science.gov (United States)

Sang, Xiaotong; Xu, Guangxi; Lian, Jingbao; Wu, Nianchu; Zhang, Xue; He, Jiao

2018-06-01

The multicolor Gd2O2S:xTb3+, yEu3+ hollow spheres were successfully synthesized via a template-free solvothermal route without the use of surfactant from commercially available Ln (NO3)3·6H2O (Ln = Gd, Tb and Eu), absolute ethanol, ethanediamine and sublimed sulfur as the starting materials. The phase, structure, particle morphology and photoluminescence (PL) properties of the as-obtained products were investigated by X-ray diffraction (XRD), fourier transform infrared spectroscopy (FT-IR), field emission scanning electron microscopy (FE-SEM) and photoluminescence spectra. The influence of synthetic time on phase, structure and morphology was systematically investigated and discussed. The possible formation mechanism depending on synthetic time t for the Gd2O2S phase has been presented. These results demonstrate that the Gd2O2S hollow spheres could be obtained under optimal condition, namely solvothermal temperature T = 220 °C and synthetic time t = 16 h. The as-obtained Gd2O2S sample possesses hollow sphere structure, which has a typical size of about 2.5 μm in diameter and about 0.5 μm in shell thickness. PL spectroscopy reveals that the strongest emission peak for the Gd2O2S:xTb3+ and the Gd2O2S:yEu3+ samples is located at 545 nm and 628 nm, corresponding to 5D4→7F5 transitions of Tb3+ ions and 5D0→7F2 transitions of Eu3+ ions, respectively. The quenching concentration of Tb3+ ions and Eu3+ ions is 7%. In the case of Tb3+ and Eu3+ co-doped samples, when the concentration of Tb3+ or Eu3+ ions is 7%, the optimum concentration of Eu3+ or Tb3+ ions is determined to be 1%. Under 254 nm ultraviolet (UV) light excitation, the Gd2O2S:7%Tb3+, the Gd2O2S:7%Tb3+,1%Eu3+ and the Gd2O2S:7%Eu3+ samples give green, yellow and red light emissions, respectively. And the corresponding CIE coordinates vary from (0.3513, 0.5615), (0.4120, 0.4588) to (0.5868, 0.3023), which is also well consistent with their luminous photographs.

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.

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.

Internal fields on Gd3+ ions diluted in Eu2CuO4

International Nuclear Information System (INIS)

Zysler, R.D.

1990-01-01

The EPR spectrum of dilute Gd 3+ ions substituting for Eu 3+ in Eu 2 CuO 4 at 9 GHz and 35 GHz in the temperature range of room temperature down 1.5K have been measured. Each one of the resonance lines shows a splitting into two or more weaker lines below T N ∼ 215K. The simultaneous appearance of a low field microwave absorption signal is attributed to the onset of long range antiferromagnetic ordering with a weak ferromagnetic component. The splitting of the EPR spectrum is associated with different Gd sites in the magnetically ordered structure. A reduction of the local symmetry of the rare earth sites below T N is described in terms of an internal magnetic field lying in the ab-plane. Dipolar and exchange contributions to the internal field are discussed. A strong dependence of the GdEPR spectrum and the microwave absorption on the magnetic history of the samples has been observed, suggesting the formation of magnetic domains or a glassy state. (Author) [es

Luminescent properties of Eu2+-doped BaGdF5 glass ceramics a potential blue phosphor for ultra-violet light-emitting diode

International Nuclear Information System (INIS)

Zhang, Weihuan; Zhang, Yuepin; Ouyang, Shaoye; Zhang, Zhixiong; Wang, Qian; Xia, Haiping

2015-01-01

Eu 2+ doped transparent oxyfluoride glass ceramics containing BaGdF 5 nanocrystals were successfully fabricated by melt-quenching technique under a reductive atmosphere. The structure of the glass and glass ceramics were investigated by differential scanning calorimetry, X-ray diffraction (XRD), and transmission electron microscopy (TEM). The luminescent properties were investigated by transmission, excitation, and emission spectra. The decay time of the Gd 3+ ions at 312 nm excited with 275 nm were also investigated. The results of XRD and TEM indicated the existence of BaGdF5 nanocrystals in the transparent glass ceramics. The excitation spectra of Eu 2+ doped glass ceramics showed an excellent overlap with the main emission region of an ultraviolet light-emitting diode (UV-LED). Compared with the as-made glass, the emission of glass ceramics is much stronger by a factor of increasing energy transfer efficiency from Gd 3+ to Eu 2+ ions, the energy transfer efficiency from Gd 3+ to Eu 2+ ions was discussed. In addition, the chromaticity coordinates of glass and glass ceramics specimens were also discussed, which indicated that the Eu 2+ doped BaGdF 5 glass ceramics may be used as a potential blue-emitting phosphor for UV-LED

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.)

Bi3+ sensitized Y2WO6:Ln3+ (Ln=Dy, Eu, and Sm) phosphors for solar spectral conversion.

Science.gov (United States)

Huang, M N; Ma, Y Y; Xiao, F; Zhang, Q Y

2014-01-01

The phosphors of Y2WO6:Bi3+, Ln3+ (Ln=Dy, Eu and Sm) were synthesized by solid-state reaction in this study. The crystal structure, photoluminescence properties and energy transfer mechanism were investigated. By introducing Bi3+ ions, the excitation band of the phosphors was broadened to be 250-380 nm, which could be absorbed by the dye-sensitized solar cells (DSSCs). The overlap between excitation of W-O groups/Bi3+ and the emission of Ln3+ (Dy, Eu, and Sm) indicated that the probability of energy transfer from W-O groups and Bi3+ to Ln3+. The energy transfer efficiency from Bi3+ to Ln3+ (Ln=Dy, Eu and Sm) are calculated to be 16%, 20% and 58%. This work suggested that Y2WO6:Bi3+, Ln3+ (Ln=Dy, Eu and Sm) might be a promising ultraviolet-absorbing luminescent converter to enhance the photoelectrical conversion efficiency of dye-sensitized solar cells (DSSCs). Copyright © 2013 Elsevier B.V. All rights reserved.

Luminescence enhancement in Eu3+, Sm3+ co-doped liy(MoO4)2 nano-phosphors by sol-gel process.

Science.gov (United States)

Zhou, Xianju; Wang, Guangchuan; Zhou, Tonghui; Zhou, Kaining; Li, Qingxu; Wang, Zhongqing

2014-05-01

A series of LiY(0.95-x)Eu(0.05)Sm(x)(MoO4)2 red light emitting phosphors were synthesized by sol-gel technique. The phase impurity and spectroscopic properties were characterized by X-ray Diffraction (XRD), Photo-Luminescence (PL) and Photo-Luminescence Excitation (PLE) spectra, respectively. It is found that the PLE spectra of the Eu3+, Sm3+ co-doped nanoparticles are enhanced and broadened as compared with the solely doped samples, which will make the co-doped phosphors match better with blue and/or UV GaN based LED chips. The red emission intensity of Eu3+ is largely enhanced by the energy transfer from Sm3+. The mechanism of the enhancement is clearly proven to be the increase in the quantum efficiency of 5D0 state of Eu3+ rather than the increase in the absorption of Eu3+. Meanwhile, the characteristic f-f transitions of Sm3+ are greatly reduced, resulting in little influence in the color purity of the co-doped phosphors. The present material is an amendatory promising red light emitting phosphor for white LEDs.

Systems Ln-Fe-O ( Ln=Eu, Gd): thermodynamic properties of ternary oxides using solid-state electrochemical cells

Science.gov (United States)

Parida, S. C.; Rakshit, S. K.; Dash, S.; Singh, Ziley; Prasad, R.; Venugopal, V.

2003-05-01

The standard molar Gibbs energies of formation of LnFeO 3(s) and Ln3Fe 5O 12(s) where Ln=Eu and Gd have been determined using solid-state electrochemical technique employing different solid electrolytes. The reversible e.m.f.s of the following solid-state electrochemical cells have been measured in the temperature range from 1050 to 1255 K. Cell (I): (-)Pt / { LnFeO 3(s)+ Ln2O 3(s)+Fe(s)} // YDT/CSZ // {Fe(s)+Fe 0.95O(s)} / Pt(+); Cell (II): (-)Pt/{Fe(s)+Fe 0.95O(s)}//CSZ//{ LnFeO 3(s)+ Ln3Fe 5O 12(s)+Fe 3O 4(s)}/Pt(+); Cell (III): (-)Pt/{ LnFeO 3(s)+ Ln3Fe 5O 12(s)+Fe 3O 4(s)}//YSZ//{Ni(s)+NiO(s)}/Pt(+); and Cell(IV):(-)Pt/{Fe(s)+Fe 0.95O(s)}//YDT/CSZ//{ LnFeO 3(s)+ Ln3Fe 5O 12(s)+Fe 3O 4(s)}/Pt(+). The oxygen chemical potentials corresponding to the three-phase equilibria involving the ternary oxides have been computed from the e.m.f. data. The standard Gibbs energies of formation of solid EuFeO 3, Eu 3Fe 5O 12, GdFeO 3 and Gd 3Fe 5O 12 calculated by the least-squares regression analysis of the data obtained in the present study are given by Δ fG°m(EuFeO 3, s) /kJ mol -1 (± 3.2)=-1265.5+0.2687( T/K) (1050 ⩽ T/K ⩽ 1570), Δ fG°m(Eu 3Fe 5O 12, s)/kJ mol -1 (± 3.5)=-4626.2+1.0474( T/K) (1050 ⩽ T/K ⩽ 1255), Δ fG°m(GdFeO 3, s) /kJ mol -1 (± 3.2)=-1342.5+0.2539( T/K) (1050 ⩽ T/K ⩽ 1570), and Δ fG°m(Gd 3Fe 5O 12, s)/kJ·mol -1 (± 3.5)=-4856.0+1.0021( T/K) (1050 ⩽ T/K ⩽ 1255). The uncertainty estimates for Δ fG°m include the standard deviation in the e.m.f. and uncertainty in the data taken from the literature. Based on the thermodynamic information, oxygen potential diagrams for the systems Eu-Fe-O and Gd-Fe-O and chemical potential diagrams for the system Gd-Fe-O were computed at 1250 K.

The RELixSn2 (RE=La–Nd, Sm, and Gd; 0≤x<1) series revisited. Synthesis, crystal chemistry, and magnetic susceptibilities

International Nuclear Information System (INIS)

Makongo, Julien P.A.; Suen, Nian-Tzu; Guo, Shengping; Saha, Shanta; Greene, Richard; Paglione, Johnpierre; Bobev, Svilen

2014-01-01

This study is concerned with the ternary compounds RELi x Sn 2 (RE=La–Nd, Sm, and Gd; 0≤x 2 phases. These materials crystallize with the base-centered orthorhombic space group Cmcm (No. 63), and can be formally assigned with the CeNiSi 2 structure type (Pearson symbol oC16). Our systematic single-crystal X-ray diffraction studies revealed substantial Li-deficiencies in all cases, with SmSn 2 (space group Cmmm, ZrGa 2 structure type, Pearson symbol oC12) and GdSn 2 (space group Cmcm, ZrSi 2 structure type, Pearson symbol oC12) being completely lithium-free. The structure refinements also uncovered positional disorder on the Sn site neighboring the vacancies. The Sn-disorder and the Li-deficiency correlate, and vary monotonically with the decreased size of the rare-earth atoms in the order RE=La–Nd. The SmSn 2 and GdSn 2 structures are devoid of any disorder. Temperature-dependent studies of the magnetic response of the title compounds are also presented and discussed. -- Graphical abstract: RELi x Sn 2 (RE=La–Nd, 0≤x 2 structure type (a). The Sn-disorder and the Li-deficiency correlate, and vary monotonically with the decreased size of the rare-earth atoms in the order RE=La–Nd. The SmSn 2 (b) and GdSn 2 (c) structures are devoid of any disorder. Highlights: • The crystal structures of the RELi x Sn 2 (RE=La–Nd, 0≤x 2 structure type or defect variant of the CeNiSi 2 structure type. • SmSn 2 is isotypic with the ZrGa 2 structure, while RESn 2 (RE=Gd–Lu) are isotypic with the ZrSi 2 structure

Absorption Spectra of BaF2 Sm2O3, Sm, Gd, and Ho Plasmas

Science.gov (United States)

Martin, Michael; Bastiani-Ceccotti, Serena

2009-11-01

Knowledge of the opacities of high Z element plasmas is important in indirect drive ICF and the study of stellar evolution. There are few experimental measurements of this quantity, and its theoretical determination is difficult due to the number of possible bound electron configurations. This study aims to better the theoretical understanding of this parameter by looking at the 3d-4f transitions of BaF2, Sm2O3, Sm, Gd, and Ho plasmas at the LULI2000 facility. The plasmas are produced by radiative heating and are cold, 15 -- 40 eV, and relatively dense, ˜ .01gm/cm^3 A plasma is produced by a .5 ns laser pulse irradiating a gold hohlraum and then probed by an x-ray source created by a gold foil irradiated by a 10 ps laser pulse. The transmission is found with simultaneous source and absorption measurements by an x-ray spectrometer in the 8 - 20 å range We will compare the results with statistical atomic structure codes. From this experiment we will gain further insight into the spectral broadening of neighboring Z elements due to changing plasma temperature and into mixture thermodynamics. This is a first step towards an experimental study of astrophysical domains.

Mixing of the odd-parity excitations in Nd, Sm and Gd nuclei with 86 and 87 neutrons

International Nuclear Information System (INIS)

Hammaren, Esko.

1978-08-01

The low- and medium-spin structure of the four nuclei 148 Sm 86 , 147 Nd 87 , 149 Sm 87 and 151 Gd 87 has been investigated experimentally and theoretically. The low-spin states of 151 Gd were obtained in the EC and β + decay of 151 Tb. The proposed level scheme, based on gamma-gamma coincidence and conversion-electron measurements, contains several new energy levels, among them a 5/2 - state at 427 keV. Nanosecond lifetimes of the states in 147 Nd were studied using the reaction 146 Nd(d,pγ) 147 Nd with 10 MeV deuterons. The reactions sup(148,150)Nd( 3 He,xn) at Esup(3sub(He)) = 19 - 27 MeV were used to study excited states in the nuclei 148 Sm and 149 Sm. Gamma-ray excitation fuctions, angular and time distributions, gamma-gamma coincidences and conversion electrons were measured. The presence of the Z = 64 closed proton core is proposed to be important for the structure of the even and odd isotones considered. Calculations performed for 148 Sm using the interacting-boson-approximation model and related to the N = 82, Z = 64 and N = 82, Z = 50 cores are discussed. The properties of the negative-parity low-spin states of the N = 87 isotones are explained with an axial particle-plus-rotor model. The calculated B(M1) and B(E2) probabilities are compared with a compilation of experimental values. Most of the spectroscopic factors of 149 Sm are reproduced well in the calculation. The consequences of nonaxiality are discussed for the fsub(7/2)- and hsub(9/2)-based excitations. The standard Meyer-ter-Vehn model calculation indicates different asymmetries for the fsub(7/2) and hsub(9/2) shells. (author)

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.

Preparation and luminescence properties of Ca3(VO4)2: Eu3+, Sm3+ phosphor for light-emitting diodes

International Nuclear Information System (INIS)

Huang Jiaping; Li Qiuxia; Chen Donghua

2010-01-01

Rare-earth ions co-activated red phosphors Ca 3 (VO 4 ) 2 : Eu 3+ , Sm 3+ were synthesized by modified solid-state reactions. The samples were characterized by X-ray powder diffractometer (XRD), energy-dispersive X-ray spectrometer (EDS), transmission electron microscopy (TEM) and luminescence spectrometer (LS). The results showed that the Eu-Sm system exhibits higher emission intensity than those of the Eu single-doped system and Sm separate-doped system under blue light. Samarium (III) ions are effective in broadening and strengthening absorptions around 467 nm. Furthermore, they exhibit enhanced luminescence emission. Luminescent measurements showed that the phosphors can be efficiently excited by ultraviolet (UV) to visible region, emitting a red light with a peak wavelength of 616 nm. The material has potential application as a phosphor for light-emitting diodes (LEDs).

Preparation, structural characterization, and enhanced electrical conductivity of pyrochlore-type (Sm{sub 1-x}Eu{sub x}){sub 2}Zr{sub 2}O{sub 7} ceramics

Energy Technology Data Exchange (ETDEWEB)

Xia, X.L. [Institute for Advanced Ceramics, School of Materials Science and Engineering, Harbin Institute of Technology, Harbin (China); Institute of Oceanography Instruments, Shandong Academy of Science, Chinese National Engineering Research Center for Marine Monitoring Equipment, Qingdao (China); Liu, Z.G.; Ouyang, J.H. [Institute for Advanced Ceramics, School of Materials Science and Engineering, Harbin Institute of Technology, Harbin (China); Zheng, Y. [Institute of Oceanography Instruments, Shandong Academy of Science, Chinese National Engineering Research Center for Marine Monitoring Equipment, Qingdao (China)

2012-08-15

(Sm{sub 1-x}Eu{sub x}){sub 2}Zr{sub 2}O{sub 7} (0 {<=} x {<=} 1.0) samples are prepared by solid state reaction method using Sm{sub 2}O{sub 3}, Eu{sub 2}O{sub 3}, and ZrO{sub 2} as starting materials. The phase composition and microstructure of (Sm{sub 1-x}Eu{sub x}){sub 2}Zr{sub 2}O{sub 7} ceramics are investigated by X-ray diffraction (XRD), scanning electron microscopy, high-resolution transmission electron microscopy (HRTEM) coupled with selected area electron diffraction and Raman spectroscopy. XRD and TEM show that all the samples exhibit a single pyrochlore-type structure. HRTEM observation indicates that the whole grain interior of Sm{sub 2}Zr{sub 2}O{sub 7} ceramic is a perfect crystal free of any dislocation. Raman spectroscopy reveals that the degree of structural disorder of (Sm{sub 1-x}Eu{sub x}){sub 2}Zr{sub 2}O{sub 7} ceramics increases gradually with increasing Eu content. The electrical conductivity of (Sm{sub 1-x}Eu{sub x}){sub 2}Zr{sub 2}O{sub 7} ceramics is investigated by impedance spectroscopy in the air and hydrogen atmospheres, respectively. The electrical conductivity of (Sm{sub 1-x}Eu{sub x}){sub 2}Zr{sub 2}O{sub 7} ceramics increases with increasing Eu content at identical temperature levels. Both the activation energy E{sub g} and the pre-exponential factor {sigma}{sub 0g} for the grain conductivity gradually increase with increasing Eu content. As the ionic conductivity shows no obvious change in both air and hydrogen atmospheres, the conduction of (Sm{sub 1-x}Eu{sub x}){sub 2}Zr{sub 2}O{sub 7} is purely ionic with negligible electronic conduction. (Copyright copyright 2012 WILEY-VCH Verlag GmbH and Co. KGaA, Weinheim)

Thermoelectric power of RFeAsO (R = Ce, Pr, Nd, Sm and Gd)

International Nuclear Information System (INIS)

Poddar, Asok; Mukherjee, Sanjoy; Samanta, Tanmay; Saha, Rajat S.; Mukherjee, Rajarshi; Dasgupta, Papri; Mazumdar, Chandan; Ranganathan, R.

2009-01-01

Thermoelectric powers of a series of compounds RFeAsO (R = Ce, Pr, Nd, Sm and Gd) have been reported for temperatures ranging from 77 K up to room temperature. The behavior of S(T) in this temperature range can be divided into three regions. Every region has been fitted with mathematical functions of T. The physical significance of separate terms in the mathematical functions has been discussed. Some kind of universality has been observed between different members of the series.

Thermoelectric power of RFeAsO (R = Ce, Pr, Nd, Sm and Gd)

Energy Technology Data Exchange (ETDEWEB)

Poddar, Asok, E-mail: asok.poddar@saha.ac.i [Saha Institute of Nuclear Physics, 1/AF Bidhannagar, Kolkata 700 064, West Bengal (India); Mukherjee, Sanjoy [Department of Physics, The University of Burdwan, Golapbag, Burdwan 713 104, West Bengal (India); Samanta, Tanmay [Rishra High School, 15 Tilakram Dan Ghat Lane, Rishra, Hooghly, West Bengal (India); Saha, Rajat S.; Mukherjee, Rajarshi [Department of Physics, University of Burdwan, Golapbag, Burdwan 713 104, West Bengal (India); Dasgupta, Papri; Mazumdar, Chandan; Ranganathan, R. [Saha Institute of Nuclear Physics, 1/AF Bidhannagar, Kolkata 700 064, West Bengal (India)

2009-07-15

Thermoelectric powers of a series of compounds RFeAsO (R = Ce, Pr, Nd, Sm and Gd) have been reported for temperatures ranging from 77 K up to room temperature. The behavior of S(T) in this temperature range can be divided into three regions. Every region has been fitted with mathematical functions of T. The physical significance of separate terms in the mathematical functions has been discussed. Some kind of universality has been observed between different members of the series.

The study of structural and optical properties of (Eu, La, Sm) codoped ZnO nanoparticles via a chemical route

Energy Technology Data Exchange (ETDEWEB)

Lang, Jihui; Zhang, Qi; Han, Qiang; Fang, Yue; Wang, Jiaying; Li, Xiuyan; Liu, Yanqing [Key Laboratory of Functional Materials Physics and Chemistry of the Ministry of Education, Jilin Normal University, Siping, 136000 (China); Wang, Dandan [Changchun Institute of Optics, Fine Mechanics and Physics, Chinese Academy of Sciences, Changchun, 130033 (China); Yang, Jinghai, E-mail: jhyang1@jlnu.edu.cn [Key Laboratory of Functional Materials Physics and Chemistry of the Ministry of Education, Jilin Normal University, Siping, 136000 (China); Changchun Institute of Optics, Fine Mechanics and Physics, Chinese Academy of Sciences, Changchun, 130033 (China)

2017-06-15

The (Eu, La, Sm) ions were doped into ZnO nanoparticles by a chemical route, and the substitution of (Eu, La, Sm) for Zn{sup 2+} ions was proved by analytic techniques of X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS), Raman, transmission electron microscope (TEM), photoluminescence (PL) and UV–vis absorption spectroscopy. The results revealed that the codoping did not change the wurtzite structure of ZnO nanoparticles, but the diameter of the nanoparticles decreased with increasing the rare earth (RE) doping concentrations. The optical bandgaps calculated through UV–visible absorption spectroscopy were found to decrease from 3.26 to 3.14 eV with increasing the RE doping concentrations, which also proved by the slight shift of UV positions in PL spectra. The sharp red emissions located at 578.2, 590.1 and 615.7 nm were originated from the 4f-4f transitions in Eu{sup 3+} ions under excitation of 325 nm. And these red emissions of Eu{sup 3+} ions showed a strong correlation with the energy storage centers of oxygen vacancies in the samples which was introduced by the other RE ions of La{sup 3+} and Sm{sup 3+} codoping. - Highlights: • Doping of (Eu, La, Sm) ions into ZnO nanoparticles is realized by a chemical route. • Eu{sup 3+}-related red emissions from intra-4f follow a similar trend as broad defect emission. • Red emissions of Eu{sup 3+} enhance with RE codoping due to oxygen vacancies as energy storage centers. • The bandgap can be tuned by RE codoping, which shows a prospect for the visible utilization.

Host-Sensitized and Tunable Luminescence of GdNbO4:Ln3+ (Ln3+ = Eu3+/Tb3+/Tm3+) Nanocrystalline Phosphors with Abundant Color.

Science.gov (United States)

Liu, Xiaoming; Chen, Chen; Li, Shuailong; Dai, Yuhua; Guo, Huiqin; Tang, Xinghua; Xie, Yu; Yan, Liushui

2016-10-17

Up to now, GdNbO 4 has always been regarded as an essentially inert material in the visible region with excitation of UV light and electron beams. Nevertheless, here we demonstrate a new recreating blue emission of GdNbO 4 nanocrystalline phosphors with a quantum efficiency of 41.6% and host sensitized luminescence in GdNbO 4 :Ln 3+ (Ln 3+ = Eu 3+ /Tb 3+ /Tm 3+ ) nanocrystalline phosphors with abundant color in response to UV light and electron beams. The GdNbO 4 and GdNbO 4 :Ln 3+ (Ln 3+ = Eu 3+ /Tb 3+ /Tm 3+ ) nanocrystalline phosphors were synthesized by a Pechini-type sol-gel process. With excitation of UV light and low-voltage electron beams, the obtained GdNbO 4 nanocrystalline phosphor presents a strong blue luminescence from 280 to 650 nm centered around 440 nm, and the GdNbO 4 :Ln 3+ nanocrystalline phosphors show both host emission and respective emission lines derived from the characterize f-f transitions of the doping Eu 3+ , Tb 3+ , and Tm 3+ ions. The luminescence color of GdNbO 4 :Ln 3+ nanocrystalline phosphors can be tuned from blue to green, red, blue-green, orange, pinkish, white, etc. by varying the doping species, concentration, and relative ratio of the codoping rare earth ions in GdNbO 4 host lattice. A single-phase white-light-emission has been realized in Eu 3+ /Tb 3+ /Tm 3+ triply doped GdNbO 4 nanocrystalline phosphors. The luminescence properties and mechanisms of GdNbO 4 and GdNbO 4 :Ln 3+ (Ln 3+ = Eu 3+ /Tb 3+ /Tm 3+ ) are updated.

Is there lattice contraction in multicomponent metal oxides? Case study for GdVO4:Eu3+ nanoparticles

Science.gov (United States)

Yang, Liusai; Li, Liping; Zhao, Minglei; Fu, Chaochao; Li, Guangshe

2013-08-01

Metal oxide nanomaterials have been found to have great potential for diverse applications due to their unique relationships between structure and properties. Lattice expansion as particle size reduces was previously considered to be general for metal oxide nanomaterials. It is now a great challenge to see if lattice contraction could be induced by the size effect for metal oxide nanomaterials. ABO4 metal oxides (e.g., CaWO4, GdVO4, and CdWO4) are some of the most important functional materials with many applications, while such oxides at the nanoscale are never reported to show a lattice contraction. This work presents a first report on the variation from lattice expansion to lattice contraction by tuning the microstructures of GdVO4:Eu3+ nanocrystals. A hydrothermal method was adopted to synthesize GdVO4:Eu3+ nanocrystals, and then these nanoparticles were calcined at 600 ° C in air. It is found that particle size reduction led to a lattice contraction for the calcined samples, which is in contrast to the lattice expansion observed for the hydrothermally synthesized counterparts or many other metal oxide nanomaterials. In addition, the lattice symmetry of the calcined samples remained almost a constant. The results indicate that the negative surface stress was eliminated by calcination treatment, leading to a homogeneous compression process in the lattice structure of the calcined GdVO4:Eu3+ nanocrystals. Furthermore, Eu3+ was taken as a structural probe and a luminescence center to study the local environments pertinent to these structural changes and to optimize the photoluminescence performance.

Influence of Y, Gd and Sm on the glass forming ability and thermal crystallization of aluminum based alloy

International Nuclear Information System (INIS)

Aliaga, L.C.R.; Bolfarini, C.; Kiminami, C.S.; Botta Filho, W.J.; Danez, G.P.

2010-01-01

Al-based amorphous alloys represent an important family of metals and a great scientific activity has been devoted to determine the main features of both glass forming ability (GFA) and crystallization behavior in order to have a comprehensive framework aimed at potential technological applications. Nowadays, it is well known that the best Al-based amorphous alloys are formed in ternary systems such as Al- RE-TM, where RE is a rare earth and TM a transition metal. This paper presents results of research in Al 85 Ni 10 RE 5 alloys (RE = Y, Gd and Sm). Amorphous ribbons were processed by melt-spinning under the same conditions and subsequently characterized by x-ray diffraction (XRD) and differential scanning calorimetry (DSC). Results show appreciable micro structural differences as function of the rare earth, thus crystal is obtained for Y, nano-glassy for Gd and, fully amorphous structure for Sm. (author)

Possibilities for standardization of {sup 152}Eu by liquid scintillation and gamma spectrometry; Possibilidades para padronização do {sup 152}Eu por cintilação líquida e por espectrometria gama

Energy Technology Data Exchange (ETDEWEB)

Ferreira Filho, A.L.; Cruz, P.A.L. da; Silva, R.L. da; Delgado, J.U., E-mail: alfredo@ird.gov.br [Instituto de Radioproteção e Dosimetria (LNMRI/IRD/CNEN-RJ), Rio de Janeiro, RJ (Brazil). Lab. Nacional de Metrologia das Radiações Ionizantes; Lopes, R.T. [Coordenacao de Pos-Graduacao e Pesquisa de Engenharia (LIN/PEN/COPPE/UFRJ), Rio de Janeiro, RJ (Brazil). Lab. de Instrumentação Nuclear

2017-07-01

The {sup 152}Eu has a half-life of 13.5 years and a very complex decay scheme with two branches of decay. It disintegrates in {sup 152}Sm by electronic capture (72.1%) or by emission of positrons (0.027%) and in {sup 152}Gd by beta emission minus (27.9%). The child nucleus, {sup 152}Sm, has 19 excited levels, while {sup 152}Gd has 15. The direct decay of the parent nucleus to the fundamental state of the child nucleus does not exist. The decay of a {sup 152}Eu source results in emissions of 4 KX photons and 132 gamma rays, which is the reason for a lot of true coincidence-sum. The particular interest in this radionuclide is explained by its wide use in the calibration in energy and efficiency of gamma spectrometers with semiconductor detectors, since the range of energy of the emitted photons, varying from 40 to 1769 keV. But, because of such a complex decay scheme, the determination of {sup 152}Eu activity presents many difficulties. The CIEMAT / NIST liquid scintillation counting method and the peak-sum coincidence method, an absolute measurement technique using coincidence counts and photon spectrometry, have been tested in the LNMRI-IRD to standardize {sup 152}Eu solutions.

A first-principles study of B2 NiAl alloyed with rare earth elements Pr, Pm, Sm, and Eu

Institute of Scientific and Technical Information of China (English)

He Jun-Qi; Wang You; Yan Mu-Fu; Pan Zhao-Yi; Guo Li-Xin

2013-01-01

The structural,elastic,and electronic properties of NiAl alloyed with rare earth elements Pr,Pm,Sm,and Eu are investigated by using density functional theory (DFT).The study suggests that Pr,Pm,Sm,and Eu all tend to be substituted for an Al site.Ni8Al7Pm possesses the largest ductility.Only the hardness and ductility of Ni8Al7Eu are enhanced simultaneously.The covalency strength of the Ni-Al bond in Ni8Al7Pm is higher than that in Ni8Al7Eu.The covalency strength of an Al-Al bond and that of a Ni-Ni bond in Ni8Al7Eu are higher than that in Ni8Al7Pm.The Ni-Pm bond and the Ni-Eu bond are covalent,and the covalency strength of the Ni-Pm bond is greater.The Al-Pm bond and the Al-Eu bond show great covalency strength and ionicity,respectively.

Charge Carrier Trapping Processes in RE2O2S (RE = La, Gd, Y, and Lu)

NARCIS (Netherlands)

Luo, H.; Bos, A.J.J.; Dorenbos, P.

2017-01-01

Two different charge carrier trapping processes have been investigated in RE2O2S:Ln3+ (RE = La, Gd, Y, and Lu; Ln = Ce, Pr, and Tb) and RE2O2S:M (M = Ti4+ and Eu3+). Cerium, praseodymium and terbium act as recombination centers and hole trapping centers while host intrinsic defects provide the

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

Study of the influence of the codopant over the photoluminescent properties of PAA doped with Eu3+, Gd3+, and Tb3+

International Nuclear Information System (INIS)

Flores, M.; Arroyo, R.

2003-01-01

The results are presented obtained about the synthesis of acrylic poly acid characterization (PAA) doped with Eu 3+ , Gd 3+ and Tb 3+ . They got ready materials with even of these ions and it was studied the influence of the co dopant in the processes of emission of Eu 3+ (λ em = 618 nm), Gd 3+ (λ em = 624 nm) and Tb 3+ (λ em = 546 nm), as well as their effect in the phosphorescence (λ em = 450 nm) of the polymeric matrix. It was found that the intensity of the emission of Eu 3+ diminishes substantially due to the presence of the ions Gd 3+ , contrary to what happens when the co dopant is Tb 3+ , which causes an increase. In the one case of the emission of Tb 3+ , this it increases with the presence of Gd 3+ but it diminishes when Eu 3+ is present. These results are consequence of the homogeneous distribution of those dopants and of the phenomena of energy transfer that happen in the materials synthesized. (Author)

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.)

Study of the influence of the codopant over the photoluminescent properties of PAA doped with Eu{sup 3+}, Gd{sup 3+}, and Tb{sup 3+}; Estudio de la influencia del codopante sobre las propiedades fotoluminiscentes de PAA dopado con Eu{sup 3+}, Gd{sup 3+} y Tb{sup 3+}

Energy Technology Data Exchange (ETDEWEB)

Flores, M.; Arroyo, R. [Departamento de Fisica, UAM-I, A.P. 55-534, 09820 Mexico D.F. (Mexico)

2003-07-01

The results are presented obtained about the synthesis of acrylic poly acid characterization (PAA) doped with Eu{sup 3+}, Gd{sup 3+} and Tb{sup 3+}. They got ready materials with even of these ions and it was studied the influence of the co dopant in the processes of emission of Eu{sup 3+} ({lambda}{sub em} = 618 nm), Gd{sup 3+} ({lambda}{sub em} = 624 nm) and Tb{sup 3+} ({lambda}{sub em} = 546 nm), as well as their effect in the phosphorescence ({lambda}{sub em} = 450 nm) of the polymeric matrix. It was found that the intensity of the emission of Eu{sup 3+} diminishes substantially due to the presence of the ions Gd{sup 3+}, contrary to what happens when the co dopant is Tb{sup 3+} , which causes an increase. In the one case of the emission of Tb{sup 3+}, this it increases with the presence of Gd{sup 3+} but it diminishes when Eu{sup 3+} is present. These results are consequence of the homogeneous distribution of those dopants and of the phenomena of energy transfer that happen in the materials synthesized. (Author)

Controlled synthesis of different multilayer architectures of GdBO{sub 3}:Eu{sup 3+} phosphors and shape-dependent luminescence properties

Energy Technology Data Exchange (ETDEWEB)

Leng, Zhihua; Zhang, Nannan; Liu, Yali; Li, Linlin; Gan, Shucai, E-mail: gansc@jlu.edu.cn

2015-03-01

Graphical abstract: - Highlights: • Pancake-like/flower-like/leaf-like GdBO{sub 3} were obtained via a hydrothermal method. • Gd(OH){sub 3} nanorods and borates were used as the precursors for the first time. • A dissolution and recrystallization process was happened induced by the excess borax. • Three products have the similar stacked arrangements to reduce the surface energy. • The luminescence properties of GdBO{sub 3}:Eu{sup 3+} are related to shape and crystallinity. - Abstract: Monodisperse pancake-like/flower-like/leaf-like GdBO{sub 3} samples have been successfully synthesized via a designed hydrothermal conversion method using H{sub 3}BO{sub 3}, Na{sub 2}B{sub 4}O{sub 7}·10H{sub 2}O, or NaBO{sub 2}·4H{sub 2}O as boron sources, respectively. It was found that different boron sources have crucial influences on the formation and morphology of the products. The Gd(OH){sub 3} nanorods precursors were prepared through a simple hydrothermal process, which then served as sacrificial templates for the fabrication of GdBO{sub 3} micropancakes/microflowers/microleaves via a hydrothermal conversion process. FT-IR spectra confirm that vaterite-type GdBO{sub 3} can be synthesized by this method. The possible formation mechanisms for different microstructures were put forward on the basis of a series of time-dependent control experiments. The products have similar stacked arrangements driven by the minimization of the interfacial and surface energy of the hydrothermal system. An investigation on the photoluminescence (PL) properties of GdBO{sub 3}:Eu{sup 3+} samples with different morphologies indicates that the PL properties of as-obtained GdBO{sub 3}:Eu{sup 3+} phosphors are strongly dependent on their morphology and crystallinity. The flower-like structure exhibits the strongest red emission.

Influence of Y, Gd and Sm on the glass forming ability and thermal crystallization of aluminum based alloy; Efeito das terras raras Y, Gd e Sm na tendencia a formacao de amorfo e na cristalizacao termica em ligas a base de aluminio

Energy Technology Data Exchange (ETDEWEB)

Aliaga, L.C.R.; Bolfarini, C.; Kiminami, C.S.; Botta Filho, W.J., E-mail: aliaga@ufscar.b [Universidade Federal de Sao Carlos (DEMa/UFSCar), SP (Brazil). Dept. de Engenharia de Materiais; Danez, G.P. [Universidade Federal de Sao Carlos (PPG-CEMUFSCar), SP (Brazil). Programa de Pos-Graduacao em Ciencia e Engenharia de Materiais

2010-07-01

Al-based amorphous alloys represent an important family of metals and a great scientific activity has been devoted to determine the main features of both glass forming ability (GFA) and crystallization behavior in order to have a comprehensive framework aimed at potential technological applications. Nowadays, it is well known that the best Al-based amorphous alloys are formed in ternary systems such as Al- RE-TM, where RE is a rare earth and TM a transition metal. This paper presents results of research in Al{sub 85}Ni{sub 10}RE{sub 5} alloys (RE = Y, Gd and Sm). Amorphous ribbons were processed by melt-spinning under the same conditions and subsequently characterized by x-ray diffraction (XRD) and differential scanning calorimetry (DSC). Results show appreciable micro structural differences as function of the rare earth, thus crystal is obtained for Y, nano-glassy for Gd and, fully amorphous structure for Sm. (author)

Luminescence thermometry with Eu{sup 3+} doped GdAlO{sub 3}

Energy Technology Data Exchange (ETDEWEB)

Lojpur, Vesna, E-mail: vesna.lojpur@yahoo.com; Ćulubrk, Sanja; Medić, Mina; Dramicanin, Miroslav

2016-02-15

Eu{sup 3+} doped GdAlO{sub 3} powder synthesized by solid state reaction was investigated for application in luminescence thermometry. Phase composition of material was confirmed by X-ray powder diffraction analysis. The photoluminescence emission spectra were collected under excitation of 399 nm, while elevating the temperature of the sample from the room temperature to 793 K. Emissions from {sup 5}D{sub 1}→{sup 7}F{sub 1} and {sup 5}D{sub 0}→{sup 7}F{sub 2} characteristic transitions of Eu{sup 3+} ions are selected for the temperature-dependence study using the fluorescence intensity ratio method. Emission decay curves measured at the strongest emission peak centered at 614 nm were recorded in a same temperature range. Data analysis showed that thermometry by fluorescence intensity ratio method can be used over the temperature region 293–793 K with the maximal relative sensitivity of 2.96% K{sup −1} (at 293 K). Temporal dependence of emission (lifetime) provides temperature sensing from 620 to 793 K with the maximal relative sensitivity of 2.28% K{sup −1}. - Highlights: • GdAlO{sub 3}: 4 at% of Eu{sup 3+} can be used for luminescence thermometry in the 293–793 K range. • Combined FIR and lifetime thermometry provide >0.5% K{sup −1} relative sensitivity. • Temperature dependence of lifetime is well described energy gap law model.

Synthesis of three-dimensional flower-like BiOCl:RE{sup 3+} (RE{sup 3+} = Eu{sup 3+}, Sm{sup 3+}) globular microarchitectures and their luminescence properties

Energy Technology Data Exchange (ETDEWEB)

Guo, Yang-Yang; Zhang, Zhi-Jun [Department of Physics, Dongguk University, Seoul, 100715 (Korea, Republic of); Zhu, Gang-Qiang [Department of Physics, Shanxi Normal University, Xi’an, 710062 (China); Yang, Woochul, E-mail: wyang@dongguk.edu [Department of Physics, Dongguk University, Seoul, 100715 (Korea, Republic of)

2016-12-01

Graphical abstract: - Highlights: • Three-dimensional flower-like Eu{sup 3+} and Sm{sup 3+}-activated BiOCl globular microarchitectures have been synthesized. • Ostwald ripening and recrystallization are responsible for the growth mechanism of BiOCl microarchitectures. • Efficient red-emission from Eu{sup 3+}:BiOCl is observed due to the well-crystallized structures of the microarchitectures. - Abstract: Three-dimensional flower-like Eu{sup 3+} and Sm{sup 3+}-activated BiOCl globular microarchitectures were synthesized by the solvothermal method employing urea as a dispersing agent for the first time. The crystal structure, morphologies and luminescence properties of Eu{sup 3+} and Sm{sup 3+} doped BiOCl have been systematically investigated by powder X-ray diffraction (XRD) and scanning electron microscopy (SEM) and spectroscopy, respectively. The unit cell volumes show a nearly linear decrease by about 0.18 and 0.15% with increasing Eu{sup 3+} and Sm{sup 3+} concentration up to 9 mol%, respectively. All of the prepared samples show flower-like globular microarchitectures with an average diameter about 3–5 μm with different Eu{sup 3+} and Sm{sup 3+} concentrations. Possible formation mechanism for the flower-like microarchitectures is proposed on the basis of time-dependent experiment. Both BiOCl:Eu{sup 3+} and BiOCl:Sm{sup 3+} samples show a strong red emission corresponding to the {sup 5}D{sub 0} → {sup 7}F{sub 4} transition (700 nm) of Eu{sup 3+} and {sup 4}G{sub 5/2} → {sup 6}H{sub 7/2} transition (600 nm) of Sm{sup 3+}, respectively. This work sheds some light on the design and preparation of red-emitting phosphors with novel microstructures.

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.

Predictions of thermomagnetic properties of Laves phase compounds: TbAl2, GdAl2 and SmAl2 performed with ATOMIC MATTERS MFA computation system

Science.gov (United States)

Michalski, Rafał; Zygadło, Jakub

2018-04-01

Recent calculations of properties of TbAl2 GdAl2 and SmAl2 single crystals, performed with our new computation system called ATOMIC MATTERS MFA are presented. We applied localized electron approach to describe the thermal evolution of Fine Electronic Structure of Tb3+, Gd3+ and Sm3+ ions over a wide temperature range and estimate Magnetocaloric Effect (MCE). Thermomagnetic properties of TbAl2, GdAl2 and SmAl2 were calculated based on the fine electronic structure of the 4f8, 4f7 and 4f5 electronic configuration of the Tb3+ and Gd3+ and Sm3+ ions, respectively. Our calculations yielded: magnetic moment value and direction; single-crystalline magnetization curves in zero field and in external magnetic field applied in various directions m(T,Bext); the 4f-electronic components of specific heat c4f(T,Bext); and temperature dependence of the magnetic entropy and isothermal entropy change with external magnetic field - ΔS(T,Bext). The cubic universal CEF parameters values used for all CEF calculations was taken from literature and recalculated for universal cubic parameters set for the RAl2 series: A4 = +7.164 Ka04 and A6 = -1.038 Ka06. Magnetic properties were found to be anisotropic due to cubic Laves phase C15 crystal structure symmetry. These studies reveal the importance of multipolar charge interactions when describing thermomagnetic properties of real 4f electronic systems and the effectiveness of an applied self-consistent molecular field in calculations for magnetic phase transition simulation.

Preparation of SmBCO layer for the surface optimization of GdYBCO film by MOCVD process based on a simple self-heating technology

Science.gov (United States)

Zhao, Ruipeng; Zhang, Fei; Liu, Qing; Xia, Yudong; Lu, Yuming; Cai, Chuanbing; Tao, Bowan; Li, Yanrong

2018-07-01

The MOCVD process was adopted to grow the REBa2Cu3O7-δ ((REBCO), RE = rare earth elements) films on the LaMnO3 (LMO) templates. Meanwhile, the LMO-template tapes are heated by the joule effect after applying a heating current through the Hastelloy metal substrates. The surface of GdYBCO films prepared by MOCVD method is prone to form outgrowths. So the surface morphology of GdYBCO film is optimized by depositing the SmBCO layer, which is an important process method for the preparation of high-quality multilayer REBCO films. At last, the GdYBCO/SmBCO/GdYBCO multilayer films were successfully prepared on the LMO templates based on the simple self-heating method. It is demonstrated that the GdYBCO surface was well improved by the characterization analysis of scanning electron microscope. And the Δω of REBCO (005) and Δφ of REBCO (103), which were performed by an X-ray diffraction system, are respectively 1.3° and 3.3° What's more, the critical current density (Jc) has been more than 3 MA/cm2 (77 K, 0 T) and the critical current (Ic) basically shows a trend of good linear increase with the increase of the number of REBCO layers.

Fabrication and photoluminescence properties of color-tunable light emitting lanthanide doped GdVO{sub 4} hierarchitectures

Energy Technology Data Exchange (ETDEWEB)

Amurisana, Bao, E-mail: amurisana@163.com [Institute of Chemical Biology, Hohhot Vocational College, Hohhot 010051 (China); Inner Mongolia Key Laboratory for Physics and Chemistry of Functional Materials, Inner Mongolia Normal University, Hohhot 010022 (China); Bao, Lihong [Inner Mongolia Key Laboratory for Physics and Chemistry of Functional Materials, Inner Mongolia Normal University, Hohhot 010022 (China); Bao, Liang [Institute of Chemical Biology, Hohhot Vocational College, Hohhot 010051 (China); Tegus, O., E-mail: tegusph@imnu.edu.cn [Inner Mongolia Key Laboratory for Physics and Chemistry of Functional Materials, Inner Mongolia Normal University, Hohhot 010022 (China)

2017-04-15

The flower-like GdVO{sub 4}:Ln{sup 3+}( Ln{sup 3+}=Eu{sup 3+}, Dy{sup 3+}, Sm{sup 3+}, Tm{sup 3+}) hierarchitectures have been successfully synthesized on a glass slide substrate through a one-pot hydrothermal route assisted by disodium ethylenediaminetetraacetic acid (Na{sub 2}H{sub 2}L, where L{sup 4-}=(CH{sub 2}COO){sub 2}N(CH{sub 2}){sub 2}N(CH{sub 2}COO){sub 2}{sup 4-}). A high density and ordered flower-like GdVO{sub 4}:Ln{sup 3+} hierarchitectures grew epitaxially on glass substrate. The as-prepared flower-like architectures with the size about 6 μm are constructed by the numerous radially oriented single-crystalline nanorods with the width from 20 nm to 200 nm and the length from 500 nm to 3 μm. The morphologies, the thickness, and the density of as-grown flower clusters can be readily tuned by tailoring the growth time and Na{sub 2}H{sub 2}L/Gd{sup 3+} molar ratio. The possible formation mechanism of flower-like GdVO{sub 4}:Ln{sup 3+} hierarchitectures is discussed on the basis of the results from the controlled experiments under hydrothermal conditions. Because of an energy transfer from vanadate groups to dopants, the flower-like GdVO{sub 4}:Ln{sup 3+}( Ln{sup 3+}=Eu{sup 3+}, Dy{sup 3+}, Sm{sup 3+} and Tm{sup 3+}) superstructures showed strong characteristic dominant emissions of the Eu{sup 3+}, Dy{sup 3+}, Sm{sup 3+} and Tm{sup 3+} ions at 617 nm ({sup 5}D{sub 0}→{sup 7}F{sub 2}, strong red), 575 nm ({sup 4}F{sub 9/2}→{sup 6}H{sub 13/2}, yellow), 604 nm ({sup 4}G{sub 5/2}→{sup 6}H{sub 7/2}, orange-red) and 476 nm ({sup 1}G{sub 4}–{sup 3}H{sub 6}, blue) under ultraviolet excitation, respectively.Further, the emission color of the product can also be tuned by selecting the dopant Ln{sup 3+} with characteristic emissions and varying the concentration ratio of co-doping activators. This approach could be extended to the fabrication of hierarchical structures for other oxide micro/nanomaterials, and may provide a general way to achieve multicolor

Influence of the Gd.sub.2./sub.BaCuO.sub.5./sub. fine particles on thermoelectric power of melt-textured (Nd-Sm-Gd) Ba.sub.2./sub.Cu.sub.3./sub.O.sub.7 -.delta../sub.

Czech Academy of Sciences Publication Activity Database

Okram, G. A.; Muralidhar, M.; Jirsa, Miloš; Murakami, M.

2004-01-01

Roč. 402, - (2004), s. 94-97 ISSN 0921-4534 Institutional research plan: CEZ:AV0Z1010914 Keywords : melt-textured materials * thermoelectric power * (Nd,Sm,Gd)Ba 2 Cu 3 O y * Gd 2 BaCuO 5 Subject RIV: BM - Solid Matter Physics ; Magnetism Impact factor: 1.072, year: 2004

In pursuit of the rhabdophane crystal structure: from the hydrated monoclinic LnPO{sub 4}.0.667H{sub 2}O to the hexagonal LnPO{sub 4} (Ln = Nd, Sm, Gd, Eu and Dy)

Energy Technology Data Exchange (ETDEWEB)

Mesbah, Adel, E-mail: adel.mesbah@cea.fr [ICSM, UMR 5257 CNRS – CEA – ENSCM – Université de Montpellier, Site de Marcoule - Bât 426, BP 17171, 30207 Bagnols/Cèze (France); Clavier, Nicolas [ICSM, UMR 5257 CNRS – CEA – ENSCM – Université de Montpellier, Site de Marcoule - Bât 426, BP 17171, 30207 Bagnols/Cèze (France); Elkaim, Erik [Synchrotron SOLEIL, L' Orme des Merisiers, Saint-Aubin, BP 48, 91192 Gif-sur-Yvette Cedex (France); Szenknect, Stéphanie; Dacheux, Nicolas [ICSM, UMR 5257 CNRS – CEA – ENSCM – Université de Montpellier, Site de Marcoule - Bât 426, BP 17171, 30207 Bagnols/Cèze (France)

2017-05-15

The dehydration process of the hydrated rhabdophane LnPO{sub 4}.0.667H{sub 2}O (Ln = La to Dy) was thoroughly studied over the combination of in situ high resolution synchrotron powder diffraction and TGA experiments. In the case of SmPO{sub 4}.0.667H{sub 2}O (monoclinic, C2), a first dehydration step was identified around 80 °C leading to the formation of SmPO{sub 4}.0.5H{sub 2}O (Monoclinic, C2) with Z =12 and a =17.6264(1) Å, b =6.9704(1) Å, c =12.1141(1) Å, β=133.74(1) °, V =1075.33(1) Å{sup 3}. In agreement with the TGA and dilatometry experiments, all the water molecules were evacuated above 220 °C yielding to the anhydrous form, which crystallizes in the hexagonal P3{sub 1}21 space group with a =7.0389(1) Å, c =6.3702(1) Å and V =273.34(1) Å{sup 3}. This study was extended to selected LnPO{sub 4}.0.667H{sub 2}O samples (Ln= Nd, Gd, Eu, Dy) and the obtained results confirmed the existence of two dehydration steps before the stabilization of the anhydrous form, with the transitory formation of LnPO{sub 4}.0.5H{sub 2}O. - Graphical abstract: The dehydration process of the rhabdophane SmPO{sub 4}.0.667H{sub 2}O was studied over combination of in situ high resolution synchrotron powder diffraction and TGA techniques, a first dehydration was identified around 80 °C leading to the formation of SmPO{sub 4}.0.5H{sub 2}O (Monoclinic, C2). Then above 220 °C, the anhydrous form of the rhabdophane SmPO{sub 4} was stabilized and crystallizes in the hexagonal P3{sub 1}21 space group. - Highlights: • In situ synchrotron powder diffraction was carried out during the dehydration of the rhabdopahe LnPO{sub 4}.0.667H{sub 2}O. • The heat of the rhabdophane LnPO{sub 4}.0.667H{sub 2}O leads to LnPO{sub 4}.0.5H{sub 2}O then to anhydrous rhabdophane LnPO{sub 4}. • LnPO{sub 4}.0.5H{sub 2}O (monoclinic, C2) and LnPO{sub 4} (Hexagonal, P3{sub 1}21) were solved over the use of direct methods.

Implantation sites of Ce and Gd in diamond

CERN Document Server

Bharuth-Ram, K; Hofsäss, H C; Ronning, C; Dietrich, M

2002-01-01

The implantation sites of rare earth (RE) probes /sup 141/Ce (t/sub 1 /2/=32 d) and /sup 149/Gd (t/sub 1/2/=9.28 d) in diamond have been investigated using the emission channeling (EC) technique. Parent isotopes /sup 141/Cs and /sup 149/Dy were implanted into type IIa, diamond samples at an energy of 60 keV at the online isotope separator ISOLDE at CERN. /sup 141/Cs decays through the chain /sup 141/Cs-/sup 141/Ba-/sup 141/La-/sup 141/Ce-/sup 141/ Pr. EC measurements were made on the 102 keV conversion electrons emitted in the decay of /sup 141/Pr to its ground state. The decay of /sup 149 /Dy follows the chain /sup 149/Dy-/sup 149/Tb-/sup 149/Gd-/sup 149 /Eu-/sup 149/Sm. EC measurements were made on the 101 keV electrons emitted in the decay of /sup 149/Eu. Two-dimensional channeling patterns of the conversion electrons were obtained along and axial directions by raster scans with a Si surface barrier detector. Comparison of the observed patterns with simulated spectra show that in diamond 45-50% of the RE...

The new carbodiimide Li_2Gd_2Sr(CN_2)_5 having a crystal structure related to that of Gd_2(CN_2)_3

International Nuclear Information System (INIS)

Unverfehrt, Leonid; Stroebele, Markus; Meyer, H. Juergen

2013-01-01

The new carbodiimide compounds Li_2RE_2Sr(CN_2)_5 (RE = Sm, Gd, Eu, Tb) were prepared by a straight forward solid state metathesis reaction of REF_3, SrF_2, and Li_2(CN_2) at around 600 C. The crystal structure of Li_2Gd_2Sr(CN_2)_5 was solved based on X-ray single-crystal diffraction data. Corresponding Li_2RE_2Sr(CN_2)_5 compounds were analyzed by isotypic indexing of their powder patterns. The crystal structure of Li_2Gd_2Sr(CN_2)_5 can be well related to that of Gd_2(CN_2)_3, because both structures are based on layered structures composed of close packed layers of [N=C=N]"2"- sticks, alternating with layers of metal ions. The crystal structure of Li_2Gd_2Sr(CN_2)_5 can be considered to contain an ABC layer sequence of [N = C=N]"2"- layers with the interlayer voids being occupied by (three) distinct types of cations. (Copyright copyright 2013 WILEY-VCH Verlag GmbH and Co. KGaA, Weinheim)

Photoluminescence varied by selective excitation in BiGdWO6:Eu3+ phosphor

Science.gov (United States)

Pavani, K.; Graça, M. P. F.; Kumar, J. Suresh; Neves, A. J.

2017-12-01

Eu3+ doped bismuth gadolinium tungstate (BGW), a simplest member of Aurivillius family of layered perovskites, was synthesized by solid-state reaction method. Structural characterisation has been performed by X-Ray diffraction (XRD), Raman spectroscopy, Fourier Transform Infrared spectroscopy (FTIR) and scanning electron microscopy (SEM). Band gap of the host matrix has been calculated using reflectance and absorption spectra. Three different mechanisms were found to explain the excitation of Eu3+ ions and are described in detail. Photoluminescence (PL) spectra of the BGW phosphor doped with Eu3+ ions consist of major emission lines associated with 5D0 → 7FJ (J = 0, 1, 2, 3 and 4) of Eu3+ ion. Site selective PL excitation and emission indicates that Eu3+ ions doped in BiGdWO6 are sensitive to the excitation wavelength without change in the structure. Change in emission spectra were observed when the excitation wavelength was changed. Judd-Ofelt (J-O) parameters were determined from the indirect method to interpret the interactions between the host and dopant ions along with detailed analysis of lifetime measurements.

Integral-capture measurements and cross-section adjustments for Nd, Sm, and Eu

International Nuclear Information System (INIS)

Anderl, R.A.; Schmittroth, F.; Harker, Y.D.

1981-07-01

Integral-capture reaction rates are reported for 143 Nd, 144 Nd, 145 Nd, 147 Sm, 151 Eu, 152 Eu, 153 Eu, and 154 Eu irradiated in different neutron spectra in EBR-II. These reaction rates are based primarily on mass-spectrometric measurements of the isotopic atom ratios of the capture product to the target nuclide. The neutron spectra are characterized using passive neutron dosimetry and spectrum-unfolding with the FERRET least-squares data analysis code. Reaction rates for the neutron spectrum monitors were determined by the radiometric technique using Ge(Li) spectrometers. These rates are also reported here. The integral data for the rare-earth samples and for the spectrum monitors were used in multigroup flux/cross-section adtustment analyses with FERRET to generate adjustments to 47 group representations of the ENDF/B-IV capture cross sections for the rare-earth isotopes. These adjusted cross sections are in good agreement with recent differential data and with adjusted cross sections based on STEK integral data. Examples are given of the use of the adjusted cross sections and covariance matrices for cross-section evaluation

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

Tune color of single-phase LiGd(MoO4)2-X(WO4)X: Sm3+, Tb3+ via adjusting the proportion of matrix and energy transfer to create white-light phosphor

Science.gov (United States)

Wu, Hongyue; Yang, Junfeng; Wang, Xiaoxue; Gan, Shucai; Li, Linlin

2018-03-01

A series of LiGd(MO4)2: Sm3+, Tb3+ (M = Mo, W) phosphors was prepared by a conventional solid state reaction method. Powder X-Ray diffraction (XRD) analysis reveals that the compounds are of the same structure type. Their luminescent properties have been studied. The optimal doping concentrations are 8% for Sm3+ and 18% for Tb3+ in the LiGd(MoO4)2 host. Sm3+ and Tb3+ have different sensitivity to the Mo/W ratio. For LiGd(MoO4)2-X(WO4)X: Sm3+ (X = 0, 0.4, 0.8, 1.2, 1.6, 2.0), the strongest emission intensity is 1.766 times than that of the weakest, while 171 times for LiGd(MoO4)2-X(WO4)X: Tb3+. The experimental results show that Mo/W ratio strong influences on the properties of LiGd(MoO4)2-X(WO4)X: Tb3+. With the increasing of WO42- groups concentration, the shape of characteristic excitation peaks of Tb3+ is almost the same and the excitation intensity gradually increase. Moreover, the energy transfer from Tb3+ to Sm3+ has been realized in the co-doped phosphors. The experimental analysis and theoretical calculations reveal that the quadrupole-quadrupole interaction is the dominant mechanism for the Tb3+→Sm3+ energy transfer. Therefore, luminous intensity can be adjusted by different sensitivities to matrix composition and energy transfer from Tb3+→Sm3+. By this tuning color method, white-light-emitting phosphor has been prepared. The excitation wavelength is 378 nm, and this indicates that the white-light-emitting phosphor could be pumped by near-UV light.

Luminescence and thermal stability tuning in (Ba,Mn)3(Gd,Y)Na(PO4)5F:Eu2+ phosphors via cation-substitution

Science.gov (United States)

Mei, Juan; Lv, Lemin; Gao, Junsong; Wei, Yi; Feng, Yuxin; Yan, Chunjie; Li, Guogang

2018-04-01

In this work, [Y3+-Gd3+] and [Mn2+-Ba2+] substitutions were designed in Ba3GdNa(PO4)5F:Eu2+ system, which were marked as BG1-xYxNPF:Eu2+ and B1-yMyGNPF:Eu2+, respectively. It is found that their luminescence properties and thermal stability could be obviously tuned. For BG1-xYxNPF:Eu2+ series, under 365 nm UV light, the emission spectra exhibited a continuous red-shift from 458 nm (x = 0) to 485 nm (x = 1) with the corresponding luminescence varying from blue light to cyan light. For B1-yMyGNPF:Eu2+ series, it was observed the coexistence of blue-green and enhanced red emission of Eu2+ and the appearance of Eu3+ emission when Mn2+ partly substituted Ba2+, resulting in a final white emission. In addition, the thermal stabilities of B1-yMyGNPF:Eu2+ were obviously improved with Mn2+ doping. The corresponding luminescence and thermal stability tuning mechanisms were investigated.

Phase relations and linear thermal expansion of cubic solid solutions in the Th1-xMxO2-x/2 (M=Eu, Gd, Dy) systems

International Nuclear Information System (INIS)

Mathews, M.D.; Ambekar, B.R.; Tyagi, A.K.

2005-01-01

Cell parameters and linear thermal expansion studies of the Th-M oxide systems with general compositions Th 1-x M x O 2-x/2 (M=Eu 3+ , Gd 3+ and Dy 3+ , 0.0= 1.5 in the ThO 2 lattice. The upper solid solubility limits of EuO 1.5 , GdO 1.5 and DyO 1.5 in the ThO 2 lattice under conditions of slow cooling from 1673K are represented as Th 0.50 Eu 0.50 O 1.75 , Th 0.60 Gd 0.40 O 1.80 and Th 0.85 Dy 0.15 O 1.925 , respectively. The linear thermal expansion (293-1123K) of MO 1.5 and their single-phase solid solutions with thoria were investigated by dilatometery. The average linear thermal expansion coefficients (α-bar ) of the compounds decrease on going from EuO 1.5 to DyO 1.5 . The values of α-bar for EuO 1.5 , GdO 1.5 and DyO 1.5 containing solid solutions showed a downward trend as a function of the dopant concentration. The linear thermal expansion (293-1473K) of the solid solutions investigated by high-temperature XRD also showed a similar trend

Noticeable red emission and Raman active modes in nanoscale gadolinium oxyfluoride (Gd4O3F6) systems with Eu3+ inclusion

International Nuclear Information System (INIS)

Hazarika, Samiran; Mohanta, Dambarudhar

2017-01-01

Eu 3+ doped gadolinium oxyfluoride (Gd 4 O 3 F 6 , GOF) nanoscale systems have been synthesized following a modified Pechini method. While exhibiting a tetragonal crystal structure, the GOF nanosystem gave an average crystallite size (d) of ∝21-26 nm. The Lotgering factor (L F ), which is a measure of orientation of crystallites along the preferred direction was found to vary between 0.22 and 0.48. In the photoluminescence spectra, ∝595 and ∝613 nm peaks were identified as magnetically driven ( 5 D 0 → 7 F 1 ) and electrically driven ( 5 D 0 → 7 F 2 ) transitions with latter (red emission) being strongly manifested with Eu 3+ doping concentration and intrinsic defects. Moreover, several Raman active modes have been probed in the Raman spectra with low frequency peaks (<300 cm -1 ) and moderate frequency peaks (∝481 and 567 cm -1 ) assigned to observable vibration of heavy atom Gd-Gd pairs and Gd-O groups, respectively. Apart from manifestation of phononic features, inclusion of Eu 3+ in the host lattice would bring new insight on improving the red emission response prior to concentration quenching. (orig.)

An investigation on photoluminescence and energy transfer of Eu{sup 3+}/Sm{sup 3+} single-doped and co-doped Ca{sub 4}YO(BO{sub 3}){sub 3} phosphors

Energy Technology Data Exchange (ETDEWEB)

Bandi, Vengala Rao; Grandhe, Bhaskar Kumar [Department of Physics, Changwon National University, Changwon 641-773 (Korea, Republic of); Jang, Kiwan, E-mail: kwjang@changwon.ac.kr [Department of Physics, Changwon National University, Changwon 641-773 (Korea, Republic of); Shin, Dong-Soo [Department of Chemistry, Changwon National University, Changwon (Korea, Republic of); Yi, Soung-Soo [Department of Photonics, Silla University, Busan (Korea, Republic of); Jeong, Jung-Hyun [Department of Physics, Pukyong National University, Busan (Korea, Republic of)

2013-07-15

The present investigation aims to demonstrate the potentiality of Eu{sup 3+}/Sm{sup 3+} single-doped and co-doped Ca{sub 4}YO(BO{sub 3}){sub 3} phosphors, which were prepared by a sol–gel method. The X-ray diffraction (XRD) profiles showed that all the observed peaks could be attributed to the monoclinic phase of Ca{sub 4}YO(BO{sub 3}){sub 3}. From the measured emission profiles, we have noticed that both the single-doped Eu{sup 3+}/Sm{sup 3+} phosphors shows four emission transitions of {sup 5}D{sub 0} → {sup 7}F{sub 0,1,2,3} and {sup 4}G{sub 5/2} → {sup 6}H{sub 5/2,7/2,9/2,11/2} respectively. Among them, the {sup 5}D{sub 0} → {sup 7}F{sub 2} of Eu{sup 3+} and {sup 4}G{sub 5/2} → {sup 6}H{sub 7/2} of Sm{sup 3+} are intense emission transitions, leading to an intense red color emission from the prepared phosphors. The excitation spectra showed that Eu{sup 3+}/Sm{sup 3+} doped samples can be excited efficiently by 394 nm and 402 nm respectively, incidentally which matches well with the characteristic emission from UVLED. The co-doping of Sm{sup 3+} ions can broaden and strengthen the absorption of near UV region and to be efficient to sensitize the emission of the Ca{sub 4}YO(BO{sub 3}){sub 3}:Eu{sup 3+} phosphor. The mechanism involved in the energy transfer between Eu{sup 3+} and Sm{sup 3+} has been explained and elucidated by an energy level diagram. - Highlights: • Eu{sup 3+} or/and Sm{sup 3+}:Ca{sub 4}YO(BO{sub 3}){sub 3} phosphors were prepared by sol–gel method. • The co-doping of Sm{sup 3+} to Ca{sub 4}YO(BO{sub 3}){sub 3}:Eu{sup 3+} extends its absorption of NUV region. • It has intense absorption in NUV region, which is suitable for NUV LED. • The energy transfer process between Eu{sup 3+} and Sm{sup 3+} ions were discussed.

Magnetic properties of the germanides RE3Pt4Ge6 (RE=Y, Pr, Nd, Sm, Gd-Dy)

International Nuclear Information System (INIS)

Eustermann, Fabian; Eilers-Rethwisch, Matthias; Renner, Konstantin; Hoffmann, Rolf-Dieter; Poettgen, Rainer; Janka, Oliver; Oldenburg Univ.

2017-01-01

The germanides RE 3 Pt 4 Ge 6 (RE=Y, Pr, Nd, Sm, Gd-Dy) have been synthesized by arc-melting of the elements followed by inductive annealing to improve the crystallinity and allow for structural order. The compounds have been studied by powder X-ray diffraction; additionally the structure of Y 3 Pt 4 Ge 6 has been refined from single-crystal X-ray diffractometer data. It exhibits a (3+1)D modulated structure, indicating isotypism with Ce 3 Pt 4 Ge 6 . The crystal structure can be described as an intergrowth between YIrGe 2 - and CaBe 2 Ge 2 -type slabs along [100]. Temperature-dependent magnetic susceptibility measurements showed Pauli paramagnetism for Y 3 Pt 4 Ge 6 and Curie-Weiss paramagnetism for Pr 3 Pt 4 Ge 6 and Nd 3 Pt 4 Ge 6 . Sm 3 Pt 4 Ge 6 exhibits van Vleck paramagnetism, while antiferromagnetic ordering at T N =8.1(1) K and T N =11.0(1) K is observed for Gd 3 Pt 4 Ge 6 and Tb 3 Pt 4 Ge 6 , respectively.

Symmetry-Breaking Transitions in RECuAs_2-xP_x (RE=Sm, Gd, Ho, and Er)

Energy Technology Data Exchange (ETDEWEB)

Mozharivskyj, Yurij [Iowa State Univ., Ames, IA (United States)

2002-01-01

Structural changes resulting in lower symmetries can be understood in terms of electronic instabilities and Coulomb interactions. The interplay of these two interrelated factors is complicated and difficult to analyze. The RECuAs_2-xP _x phases, because of the variation in the chemical content (As/P substitution), allow, with the aid of band structures, Madelung energies and Landau theory, a partial unraveling of the forces important in the symmetry-breaking transitions in RECuAs_2-xP _x (RE = Sm, Gd, Ho and Er). Distortions of the P layers in SmCu_1.15P₂, GdCuP_2.20 and ErCuP₂ are usefully thought of as generalized Peierls distortions, i.e., they lower the electronic (and total) energy and lead to more stable structures. On the other hand, the P4/nmm → Pmmn transitions, which are observed in all studied arsenophosphide series and occur upon substitution of P for As, originate from the B1g vibrational mode and are structural adaptations to smaller P atoms. These transitions provide tighter atomic packing and better Coulomb interactions. Configurational contribution to the entropy becomes important in stabilizing the mixed occupancy in the RECuAs _2-xP _x arsenophosphides. While geometric and electronic factors favor separation of the As and P atoms over two different crystallographic sites, configurational entropy stabilizes the As/P mixing on these two sites.;Progress in the research on RECuAs_2-xP _x was dependent upon the ability of Landau theory to predict, explain and dismiss structural models and transitions. The space group Pmmn (arising from the B 1g vibrational mode) in all mixed arsenophosphides and the existence of these mixed arsenophosphides followed from the analysis of GdCuAs ₂ and GdCuP₂, using Landau theory. The impossibility of obtaining the high-symmetry structure (P4/nmm) and the low symmetry structure

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.

Mass of the 158Sm

International Nuclear Information System (INIS)

Zhao Kui; Guo Jiyu; Lu Xiuqin; Cheng Yehao; Huang Xiaolin; Ma Yong; Li Shuyuan; Ruan Ming; Li Zhichang; Jiang Chenglie

1997-01-01

A preliminary result was reported for the experiment to determine the mass of the heavier neutron-rich nucleus 158 Sm using the 160 Gd( 18 O, 20 Ne) two proton transfer reaction in last progress report. The average Q-value of (4.046 +- 0.102) MeV for the 160 Gd( 18 O, 20 Ne) 158 Sm reaction is given. A mass excess for 158 Sm of (-65.738 +- 0.102) MeV was derived. This is the first experimentally measured value of the mass of 158 Sm which is about 450 keV higher than the evaluation value from systematic trends listed in the 1993 atomic mass table. The new prediction shows better agreement with the measured values and a significant improvement over the earlier FRDM (finite-range droplet model) value

Synthesis and photoluminescence properties of Eu{sup 3+}, Sm{sup 3+} and Pr{sup 3+} doped Ca{sub 2}ZnWO{sub 6} phosphors for phosphor converted LED

Energy Technology Data Exchange (ETDEWEB)

Dabre, K.V. [Department of Physics, Arts, Commerce and Science College, Koradi, Nagpur-441111, Maharashtra (India); Dhoble, S.J., E-mail: sjdhoble@rediffmail.com [Department of Physics, R.T.M. Nagpur University, Nagpur-440033, Maharashtra (India)

2014-06-01

In this work, we report on the synthesis and photoluminescence (PL) properties of rare earth (Eu{sup 3+}, Sm{sup 3+} and Pr{sup 3+}) doped double perovskite tungstate Ca{sub 2}ZnWO{sub 6} phosphor. The phosphors were synthesized by two step modified solid state method. Phase purity and formation of phosphor were confirmed by XRD technique. PL spectra of Eu{sup 3+}, Sm{sup 3+} and Pr{sup 3+} doped phosphor show intense emission peaks in red region at 615, 604 and 650 nm respectively, upon the visible excitation of 466 nm (Eu{sup 3+}), 410 nm (Sm{sup 3+}) and 491 nm (Pr{sup 3+}). The CIE coordinates of the phosphors are in the yellow (Sm{sup 3+} doped sample) and orange (Eu{sup 3+} and Pr{sup 3+} doped sample) regions near the edge of color space which confirms their applicability in LEDs. -- Highlights: •Eu{sup 3+}, Sm{sup 3+} and Pr{sup 3+} doped and undoped samples of Ca{sub 2}ZnWO{sub 6} phosphor synthesized by Solid state method. •The phosphors have intense excitation in violet and blue region of visible spectrum. •Phosphors show intense emission peaks in red region. •CIE coordinates of phosphors are lie in yellow (Sm{sup 3+} doped phosphor) and orange (Eu{sup 3+} and Pr{sup 3+} doped phosphor) region near to edge of color space.

Oriented monolayer film of Gd2O3:0.05 Eu crystallites: quasi-topotactic transformation of the hydroxide film and drastic enhancement of photoluminescence properties.

Science.gov (United States)

Hu, Linfeng; Ma, Renzhi; Ozawa, Tadashi C; Sasaki, Takayoshi

2009-01-01

Caught on film: A semitransparent and intensely luminescent monolayer film of oriented Gd(2)O(3):0.05 Eu platelet crystallites is fabricated by annealing the precursor hydroxide film (see scheme). The photoluminescence properties of the as-transformed film are greatly improved over those of the hydroxide film, and are much more pronounced than those of the corresponding Gd(2)O(3):0.05 Eu powder.

Online Determination of Sm, Eu and Yb in Environmental Samples by Inductively Coupled Plasma – Optical Emission Spectrometry

Directory of Open Access Journals (Sweden)

J. Dilip Kumar

2007-01-01

Full Text Available A procedure was developed for the determination of Sm, Eu and Yb in water samples by inductively coupled plasma-optical emission spectrometry (ICP-OES after preconcentration on synthesized 5-(4-pyridyl azo-8-quinolinol supported by Borassus flabellifer inflorescence (BFI. The sorbed element was subsequently eluted with 0.4 M HNO3 and the acid eluates were analyzed by ICP-OES. Under the optimal conditions, Sm, Eu and Yb in aqueous samples were concentrated 100-fold. Recoveries were obtained by the proposed method in the range of 98.6 -99.8%. This method was also applied for the analysis of spiked and natural water samples. The results provide strong evidence to support the hypothesis of an adsorption mechanism.

Czochralski growth and optical properties of Li 6Gd 1-xEu x(BO 3) 3 ( x=0-1) single crystals

Science.gov (United States)

Yavetskiy, R. P.; Dolzhenkova, E. F.; Dubovik, M. F.; Korshikova, T. I.; Tolmachev, A. V.

2005-04-01

It was shown that a continuous series of Li 6Gd 1-xEu x(BO 3) 3 solid solutions exist within the whole concentration range ( x=0-1). Li 6Gd 1-xEu x(BO 3) 3 ( x=0-0.03; 1) single crystals up to 25 mm in length and up to 20 mm in diameter have been grown by the Czochralski method. The structural perfection of the crystals has been estimated from etch patterns and XPA analysis results. The optical absorption and thermally stimulated luminescence of the grown crystals has been studied.

Preparation of MAl O : Eu2+, Sm3+ (M = Ca, Sr, Ba) Phosphors by ...

African Journals Online (AJOL)

NJD

2007-10-15

Oct 15, 2007 ... clearly show that most peaks are assigned to those of the MAl2O4 structure. Moreover, their structures change with change of M. Samples A and B exhibit monoclinic crystal systems and sample. C a hexagonal structure. The doping Eu2+ and co-doping Sm3+ have very little influence on the structure of the ...

Preparation of MAl 2 O 4 : Eu 2+ , Sm 3+ (M = Ca, Sr, Ba) Phosphors ...

African Journals Online (AJOL)

A series of MAl2O4: Eu2+, Sm3+ (M = Ca, Sr, Ba) phosphors was prepared by the combustion method, and the influence of these alkaline earth metals on the structure and luminescent performances for these phosphors was investigated. A relationship was established between their composition, crystallization capacity and ...

Efficient and thermally stable red luminescence from nano-sized phosphor of Gd6MoO12:Eu3+

International Nuclear Information System (INIS)

Qin, Lin; Wei, Donglei; Huang, Yanlin; Kim, Sun Il; Yu, Young Moon; Seo, Hyo Jin

2013-01-01

A novel red-emitting nano-phosphor of Eu 3+ -doped Gd 6 MoO 12 was successfully synthesized by the Pechini method. The crystalline phase was confirmed by X-ray powder diffraction analysis. The morphology of the nano-phosphor was analyzed by scanning electron microscopy, indicating a good crystallization with particles smaller than 500 nm. The luminescence properties such as photoluminescence spectra and decay curves were investigated. The phosphors can be efficiently excited by near-ultraviolet (near-UV) light and exhibit a bright red luminescence around 613 nm ascribed to the forced electric dipole transition 5 D 0 → 7 F 2 of Eu 3+ ions. The thermal stabilities were investigated from the temperature-dependent luminescence decay curves (lifetimes) and spectra intensities. The luminescence properties in relation to applications in white light-emitting diodes (W-LEDs) such as the absolute luminescence quantum efficiency, excitation wavelength, and color coordinates were discussed. The Gd 6 MoO 12 :Eu 3+ nano-phosphor is a promising red-emitting candidate for the fabrication of W-LEDs with near-UV chips

Ortho-vanadates K3RE(VO4)2 (RE = La, Pr, Eu, Gd, Dy, Y) for near UV-converted phosphors

International Nuclear Information System (INIS)

Qin, Lin; Wei, Dong-Lei; Huang, Yanlin; Qin, Chuanxiang; Cai, Peiqing; Kim, Sun-Il; Seo, Hyo-Jin

2014-01-01

The orthovanadate poly-crystals K 3 RE(VO 4 ) 2 (RE = La, Pr, Eu, Gd, Dy, Y) were synthesized via the solid-state reaction route. The crystal phase formation was verified through X-ray diffraction (XRD) studies and was performed by structural refinements. The optical properties were also investigated in detail. K 3 RE(VO 4 ) 2 (RE = Eu, Dy, Gd, Pr, La, Y) phosphors present different luminescence behaviors: the profiles of excitation and emission spectra, the spectra shift, the luminescence decay lifetimes, the absolute quantum efficiency (QE), and the CIE color coordinates are very different. The luminescence of K 3 RE(VO 4 ) 2 (RE = La, Gd, Y, Pr) presents yellow or yellowish green color, while, K 3 Dy(VO 4 ) 2 and K 3 Eu(VO 4 ) 2 show white and red luminescence, respectively. This was discussed on the base of the different micro-structure, activator centers, and the charge transfer transitions from [VO 4 ] 3− groups in the lattices. K 3 Y(VO 4 ) 2 and K 3 Eu(VO 4 ) 2 show higher QE values of 47.0% and 45.0% at room temperature, respectively. All the phosphors have efficient absorption in the region of near-UV wavelengths or blue wavelength region. This can well match with the light from UV-LED (360–400 nm) or blue LED chips (450–480 nm) based on GaN semiconductor. K 3 RE(VO 4 ) 2 could be suggested to be a potential candidate to give further investigations for the application on near-UV excited white LEDs. - Graphical abstract: A series of orthovanadates K 3 RE(VO 4 ) 2 (RE = Eu, Dy, Gd, Pr, La, Y) have been developed to be new phosphors with rich luminescence colors; there are efficiency excitation in the near UV wavelength region. Compared with the reported vanadate phosphors K 3 R(VO 4 ) 2 has rich luminescence color, rich color, no concentration quenching, and comparable luminescence QE. - Highlights: • A new phosphor of non-doped of K 3 R(VO 4 ) 2 (R = Eu, Dy, Gd, Pr, La, Y) were developed by solid-state reaction route. • The phosphor

The temperature-sensitive luminescence of (Y,Gd)VO4:Bi3+,Eu3+ and its application for stealth anti-counterfeiting

International Nuclear Information System (INIS)

Chen, Lei; Zhang, Yao; Luo, Anqi; Liu, Fayong; Jiang, Yang; Hu, Qingzhuo; Chen, Shifu; Liu, Ru-Shi

2012-01-01

Anti-counterfeiting technologies are desired to protect products far away from the violation of dummy, fake and shoddy goods. The phosphor of (Y,Gd)VO 4 :Bi 3+ ,Eu 3+ was synthesized for the application of this purpose. Its photoluminescence was investigated by exciting with different wavelengths at variant temperatures. Wide emission color ranged from green through yellow to orange was tuned up by tailor-ing Bi 3+ and Eu 3+ concentrations. The temperature dependent luminescence and wavelength selective excitation of (Y,Gd)VO 4 :Bi 3+ ,Eu 3+ were observed, which provide different encryptions in anti-counterfeiting. To verify the feasibility in application, two anti-counterfeiting patterns were fabricated practically and excellent performance was obtained. Moreover, the physical mechanisms for the different phenomena of luminescence were elucidated from excitation spectra combining with the configuration coordinate model. (copyright 2012 WILEY-VCH Verlag GmbH and Co. KGaA, Weinheim) (orig.)

Valence and magnetic state of transition-metal and rare-earth ions in single-crystal multiferroics RMn{sub 2}O{sub 5} (R = Y, Bi, Eu, Gd) from X-ray photoelectron spectroscopy data

Energy Technology Data Exchange (ETDEWEB)

Kozakov, A.T. [Scientific-Research Institute of Physics at Southern Federal University, 194 Stachki, Rostov-na-Donu 344194 (Russian Federation); Kochur, A.G., E-mail: agk@rgups.ru [Rostov State University of Transport Communication, 2 Narodnogo Opolcheniya, Rostov-na-Donu 344038 (Russian Federation); Nikolsky, A.V.; Googlev, K.A.; Smotrakov, V.G.; Eremkin, V.V. [Scientific-Research Institute of Physics at Southern Federal University, 194 Stachki, Rostov-na-Donu 344194 (Russian Federation)

2011-11-15

Highlights: {yields} Single crystals RMn{sub 2}O{sub 5} (R = Y, Bi, Eu, Gd) and YMnO{sub 3} are grown. {yields} Core level XPS are measured and calculated with inclusion of temperature effect. {yields} Mn2p, Mn3s, R4s, and R4d (R = Eu, Gd) XPS are sensitive to valence and spin state. {yields} Paramagnetic moments per structural cell are estimated. - Abstract: Single crystals of orthorhombic multiferroics RMn{sub 2}O{sub 5} (R = Y, Bi, Eu, Gd), and of hexagonal manganite YMnO{sub 3} are grown. X-ray photoelectron spectra of the core levels of the Mn, Y, Bi, Eu, Gd, and O atoms in multiferroics are obtained at room temperature with the ESCALAB 250 microprobe system with monochromatization of the exciting X-ray radiation. X-ray photoelectron spectra of Mn2p, Mn3s, R4s, and R4d (R = Eu, Gd) levels are assigned based on one-configuration isolated-ion approximation calculations with taking the temperature effect into account. It is shown using the photoelectron spectroscopy methods that both Mn{sup 3+} and Mn{sup 4+} ions are present in orthorhombic multiferroics, while Eu and Gd are in trivalent state. Paramagnetic moments per structural unit are calculated and compared with those determined from our spectroscopic data and with the data from other authors.

Synthesis and characterization of novel red emitting nanocrystal Gd6WO12:Eu3+ phosphors

International Nuclear Information System (INIS)

Tian Yue; Chen Baojiu; Hua Ruinian; Zhong Haiyang; Cheng Lihong; Sun Jiashi; Lu Weili; Wan Jing

2009-01-01

Novel nanosized Gd 6 WO 12 :Eu 3+ phosphors were synthesized via a co-precipitation reaction. The crystal structure and morphology of the phosphors were characterized by using X-ray diffraction (XRD) and field emission scanning electron microscopy (FE-SEM). It was found that the resultant powders show a regular and sphere-like shape with average particle size of 60 nm. Intrinsic red emission originating from Eu 3+ was observed while excited at the W 6+ →O 2- and Eu 3+ →O 2- charge transfer bands or f-f absorption bands. The color coordinates of the phosphors were calculated to be x=0.625, y=0.375. The concentration dependence of the luminescence was studied, and optimum doping concentration for obtaining maximum emitting intensity was confirmed to be around 12 mol%. It was also found that the electric dipole-dipole interaction plays an important role for quenching luminescence of Eu 3+ .

Multifunctional Eu3+- and Er3+/Yb3+-doped GdVO4 nanoparticles synthesized by reverse micelle method.

Science.gov (United States)

Gavrilović, Tamara V; Jovanović, Dragana J; Lojpur, Vesna; Dramićanin, Miroslav D

2014-02-27

Synthesis of Eu(3+)- and Er(3+)/Yb(3+)-doped GdVO4 nanoparticles in reverse micelles and their multifunctional luminescence properties are presented. Using cyclohexane, Triton X-100, and n-pentanol as the oil, surfactant, and co-surfactant, respectively, crystalline nanoparticles with ~4 nm diameter are prepared at low temperatures. The particle size assessed using transmission electron microscopy is similar to the crystallite size obtained from X-ray diffraction measurements, suggesting that each particle comprises a single crystallite. Eu(3+)-doped GdVO4 nanoparticles emit red light through downconversion upon UV excitation. Er(3+)/Yb(3+)-doped GdVO4 nanoparticles exhibit several functions; apart from the downconversion of UV radiation into visible green light, they act as upconvertors, transforming near-infrared excitation (980 nm) into visible green light. The ratio of green emissions from (2)H11/2 → (2)I15/2 and (4)S3/2 → (4)I15/2 transitions is temperature dependent and can be used for nanoscale temperature sensing with near-infrared excitation. The relative sensor sensitivity is 1.11%K(-1), which is among the highest sensitivities recorded for upconversion-luminescence-based thermometers.

Multifunctional Eu3+- and Er3+/Yb3+-doped GdVO4 nanoparticles synthesized by reverse micelle method

Science.gov (United States)

Gavrilović, Tamara V.; Jovanović, Dragana J.; Lojpur, Vesna; Dramićanin, Miroslav D.

2014-02-01

Synthesis of Eu3+- and Er3+/Yb3+-doped GdVO4 nanoparticles in reverse micelles and their multifunctional luminescence properties are presented. Using cyclohexane, Triton X-100, and n-pentanol as the oil, surfactant, and co-surfactant, respectively, crystalline nanoparticles with ~4 nm diameter are prepared at low temperatures. The particle size assessed using transmission electron microscopy is similar to the crystallite size obtained from X-ray diffraction measurements, suggesting that each particle comprises a single crystallite. Eu3+-doped GdVO4 nanoparticles emit red light through downconversion upon UV excitation. Er3+/Yb3+-doped GdVO4 nanoparticles exhibit several functions; apart from the downconversion of UV radiation into visible green light, they act as upconvertors, transforming near-infrared excitation (980 nm) into visible green light. The ratio of green emissions from 2H11/2 --> 2I15/2 and 4S3/2 --> 4I15/2 transitions is temperature dependent and can be used for nanoscale temperature sensing with near-infrared excitation. The relative sensor sensitivity is 1.11%K-1, which is among the highest sensitivities recorded for upconversion-luminescence-based thermometers.

Red emitting phosphors of Eu{sup 3+} doped Na{sub 2}Ln{sub 2}Ti{sub 3}O{sub 10} (Ln = Gd, Y) for white light emitting diodes

Energy Technology Data Exchange (ETDEWEB)

Zhang, Niumiao [National Key Laboratory of Photoelectric Technology and Functional Materials Culture Base in Shaanxi Province, National Photoelectric Technology and Functional Materials & Application of Science and Technology International Cooperation Base, Institute of Photonics & Photon-Technology, Northwest University, Xi’an 710069 (China); Guo, Chongfeng, E-mail: guocf@nwu.edu.cn [National Key Laboratory of Photoelectric Technology and Functional Materials Culture Base in Shaanxi Province, National Photoelectric Technology and Functional Materials & Application of Science and Technology International Cooperation Base, Institute of Photonics & Photon-Technology, Northwest University, Xi’an 710069 (China); Yin, Luqiao; Zhang, Jianhua [Key Laboratory of Advanced Display and System Applications (Shanghai University), Ministry of Education, Shanghai 200072 (China); Wu, Mingmei, E-mail: ceswmm@mail.sysu.edu.cn [School of Chemistry and Chemical Engineering, Sun Yat-Sen University, No. 135, Xingang Xi Road, Guangzhou 510275 (China)

2015-06-25

Highlights: • Layered red phosphors Na{sub 2}Ln{sub 2}Ti{sub 3}O{sub 10} (Ln = Gd, Y):Eu{sup 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{sup 3+} doped Na{sub 2}Ln{sub 2}Ti{sub 3}O{sub 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{sub 2}Ln{sub 2}Ti{sub 3}O{sub 10}:Eu{sup 3+} (Ln = Gd, Y) red emitting phosphors were fabricated with a near-ultraviolet (n-UV) chip. In comparison with Na{sub 2}Y{sub 1.4}Eu{sub 0.6}Ti{sub 3}O{sub 10}, the Na{sub 2}Gd{sub 0.6}Eu{sub 1.4}Ti{sub 3}O{sub 10} phosphor offers higher brightness, quantum efficiency, and excellent thermal stability. W-LEDs comprising Na{sub 2}Gd{sub 0.6}Eu{sub 1.4}Ti{sub 3}O{sub 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{sub 2}Gd{sub 0.6}Eu{sub 1.4}Ti{sub 3}O{sub 10} is more suitable candidate for application in LEDs.

Characterization and luminescent properties of Eu3+ doped Gd2Zr2O7 nanopowders

International Nuclear Information System (INIS)

Rabasovic, M.S.; Sevic, D.; Krizan, J.; Terzic, M.; Mozina, J.; Marinkovic, B.P.; Savic-Sevic, S.; Mitric, M.; Rabasovic, M.D.; Romcevic, N.

2015-01-01

Highlights: • Nanopowders Gd 2 Zr 2 O 7 doped by europium ions (Eu 3+ ) have been synthesized. • Their luminescence properties have been measured at room temperature. • The temporal evolution of laser induced phenomena are presented using time-resolved technique. • Lifetime analysis for luminescence bands in emission spectra has been done. - Abstract: Nanopowders based on gadolinium zirconium oxide (Gd 2 Zr 2 O 7 ) doped by europium ions (Eu 3+ ) were successfully prepared using a flame combustion method. This material is suitable for various optical devices. The structure of prepared materials has been confirmed and characterized using X-ray powder diffraction (XRD), scanning electron microscope (SEM) and photoluminescence (PL) techniques. The luminescence properties of synthesized nanopowders were characterized by emission spectra and luminescence lifetimes by using the streak camera system. PL spectra were obtained at three different excitation wavelengths (Optical Parametric Oscilator (OPO) at 360 nm, laser diode at 365 nm and Ar laser line at 514.5 nm). The strong emission lines at 611 nm and 630 nm corresponding to the 5 D 0 → 7 F 2 long lived transition could be used as a new red light source in optical devices

Synthesis and luminescent properties of Sr{sub 2}Gd{sub 6.8}Eu{sub 1.2}Si{sub 6(1−x)}P{sub 6x}O{sub 26} oxyapatites

Energy Technology Data Exchange (ETDEWEB)

Ishchenko, A.V., E-mail: a-v-i@mail.ru [Ural Federal University, 620002 Ekaterinburg (Russian Federation); Zuev, M.G. [Ural Federal University, 620002 Ekaterinburg (Russian Federation); Institute of Solid State Chemistry, Ural Branch of the Russian Academy of Sciences, 620990 Ekaterinburg (Russian Federation); Vasin, A.A. [Institute of Solid State Chemistry, Ural Branch of the Russian Academy of Sciences, 620990 Ekaterinburg (Russian Federation); Yagodin, V.V.; Viktorov, L.V.; Shulgin, B.V. [Ural Federal University, 620002 Ekaterinburg (Russian Federation)

2016-01-15

The solid solutions Sr{sub 2}Gd{sub 6.8}Eu{sub 1.2}Si{sub 6(1−x)}P{sub 6x}O{sub 26−δ} (where x=0–0.15 and δ is oxygen nonstoichiometry) were synthesized. The structural properties of the crystal lattice of the solid solutions and the peculiarities of Eu{sup 3+} and P{sup 5+} dopants substitution for matrix ions have been considered. The photo-, X-ray and pulsed cathode luminescence properties have been studied. It has been found that substitution of (SiO{sub 4}){sup 4−} by (PO{sub 4}){sup 3−} tetrahedron in Eu{sup 3+}-doped oxyapatites does not bring significant changes to bands structure Eu{sup 3+} in luminescence spectra under different excitation (UV, X-ray, pulse cathode beam). However, the increase of P{sup 5+} concentration in Sr{sub 2}Gd{sub 6.8}Eu{sub 1.2}Si{sub 6(1−x)}P{sub 6x}O{sub 26–δ} compounds leads to a decrease of integral intensity of Eu{sup 3+} luminescence bands due to local environment symmetry modifications and covalency degree changes. Two nonequivalent optical Eu{sup 3+} centers have been found. These compounds are of interest for efficient X-ray phosphors, display devices and LED engineering material creation. - Highlights: • The luminescence properties were studied upon UV, X-ray and pulse cathode beam. • P{sup 5+} doping of Sr{sub 2}Gd{sub 6.8}Eu{sub 1.2}Si{sub 6}O{sub 26} leads to luminescence intensity reduction. • At least two types of optical centers formed by Eu{sup 3+} ions were found. • The structural features of Sr{sub 2}Gd{sub 6.8}Eu{sub 1.2}Si{sub 6(1−x)}P{sub 6x}O{sub 26} were reported. • Partial replacement of Si by P does not change the Sr{sub 2}Gd{sub 6.8}Eu{sub 1.2}Si{sub 6}O{sub 26} structure.

Study of a new magnetic dipole mode in the heavy deformed nuclei 154Sm, 156Gd, 158Gd, 164Dy, 168Er, and 174Yb by high-resolution electron spectroscopy

International Nuclear Information System (INIS)

Bohle, D.

1985-01-01

By inelastic electron scattering with high energy resolution a new magnetic dipole mode in heavy, deformed nuclei could be detected. For this the nuclei 154 Sm, 156 Gd, 158 Gd, 164 Dy, 168 Er, and 174 Yb were studied at the Darmstadt electron linear accelerator (DALINAC) at small momentum transfer q ≤ 0.6 fm -1 and low excitation energies. A collective magnetic dipole excitation could be discovered in all nuclei at an excitation energy of E x ≅ 66 δA -1/3 MeV whereby δ means the mass deformation. The transition strength extends in the mean to B(M1)↑ ≅ 1.3 μ N 2 . A systematic study of the nucleus 156 Gd yielded hints to a strong fragmentation of the magnetic dipole strength. A comparison of electron scattering, proton scattering, and nuclear resonance fluorescence experiments shows that the new mode is a pure orbital mode. (orig./HSI) [de

L-shell X-ray production cross sections of Ce, Nd, Sm, Eu, Gd, and Dy by impact of {sup 14}N{sup 2+} ions with energies between 7.0 MeV and 10.5 MeV

Energy Technology Data Exchange (ETDEWEB)

Murillo, G.; Méndez, B.; López-Monroy, J. [Departamento de Aceleradores, Instituto Nacional de Investigaciones Nucleares, Carr. México-Toluca S/N, Ocoyoacac, Edo. Méx. 52750 (Mexico); Miranda, J., E-mail: miranda@fisica.unam.mx [Instituto de Física, Universidad Nacional Autónoma de México, A.P. 20-364, México, Cd. Mx. 01000 (Mexico); Villaseñor, P. [Departamento de Aceleradores, Instituto Nacional de Investigaciones Nucleares, Carr. México-Toluca S/N, Ocoyoacac, Edo. Méx. 52750 (Mexico)

2016-09-15

Highlights: • A new data set of L X-ray production cross sections by nitrogen ion impact is given. • The target elements have atomic numbers in the range 58–66 (lanthanoids). • A universal scaling as function of a reduced velocity variable is applied. • The eCPSSR model with EC and MI corrections gives very good results. - Abstract: L-shell X-ray production cross sections from the lanthanoid elements Ce, Nd, Sm, Eu, Gd, and Dy, induced by the impact of {sup 14}N{sup 2+} ions with energies in the interval 7.0 MeV to 10.5 MeV (0.50 MeV/μ to 0.75 MeV/μ), were measured and then compared with theoretical calculations obtained with the ECPSSR model with exact limits of integration (eCPSSR) and related corrections. These include the electron capture by the incoming ion and multiple ionizations of higher shells. Data from this work were contrasted with previously published L X-ray production cross sections for {sup 14}N{sup 2+} ion impact. As with other ions, a universal behavior is found when L{sub α} and L{sub γ} X-ray production cross sections are plotted as a function of reduced velocity parameters. The agreement with theoretical predictions was very good when the corrections were applied to the eCPSSR model.

Formation constants of Sm(III), Dy(III), Gd(III), Pr(III) and Nd(III) complexes of tridentate schiff base, 2-[(1H-benzimidazol-2-yl-methylene) amino] phenol

International Nuclear Information System (INIS)

Omprakash, K.L.; Chandra Pal, A.V.; Reddy, M.L.N.

1982-01-01

A new tridentate schiff base, 2- (1H-benzimidazol-2-yl-methylene)amino phenol derived from benzimididazole-2-carbo-xaldehyde and 2-aminophenol has been synthesised and characterised by spectral and analytical data. Proton-ligand formation constants of the schiff base and metal-ligand formation constants of its complexes with Sm(III), Dy(III), Gd(III), Nd(III) and Pr(III) have been determined potentiometrically in 50% (v/v) aqueous dioxane at an ionic strength of 0.1M (NaClO 4 ) and at 25deg C using the Irving-Rossotti titration technique. The order of stability constants (logβ 2 ) is found to be Sm(III)>Dy(III)>Gd(III)>Pr(III)>Nd(III). (author)

Formation constants of Sm(III), Dy(III), Gd(III), Pr(III) and Nd(III) complexes of tridentate schiff base, 2-((1H-benzimidazol-2-yl-methylene) amino) phenol

Energy Technology Data Exchange (ETDEWEB)

Omprakash, K L; Chandra Pal, A V; Reddy, M L.N. [Osmania Univ., Hyderabad (India). Dept. of Chemistry

1982-03-01

A new tridentate schiff base, 2- (1H-benzimidazol-2-yl-methylene)amino phenol derived from benzimididazole-2-carbo-xaldehyde and 2-aminophenol has been synthesised and characterised by spectral and analytical data. Proton-ligand formation constants of the schiff base and metal-ligand formation constants of its complexes with Sm(III), Dy(III), Gd(III), Nd(III) and Pr(III) have been determined potentiometrically in 50% (v/v) aqueous dioxane at an ionic strength of 0.1M (NaClO/sub 4/) and at 25deg C using the Irving-Rossotti titration technique. The order of stability constants (log..beta../sub 2/) is found to be Sm(III)>Dy(III)>Gd(III)>Pr(III)>Nd(III).

Engineering of Highly Susceptible Paramagnetic Nanostructures of Gd2S3:Eu3+: Potentially an Efficient Material for Room Temperature Gas Sensing Applications

Directory of Open Access Journals (Sweden)

Muhammed M. Radhi

2010-11-01

Full Text Available This research papers throws light into the compositional, morphological and structural properties of novel nanoparticles of Gd2S3:Eu3+ synthesized by a simple co-precipitation technique. Furthermore, we also prognosticate that this material could be useful for gas sensing applications at room temperature. Nanostructures formulation by this method resulted in the formation of orthorhombic crystal structure with primitive lattice having space group Pnma. The material characterizations are performed using X-ray diffraction (XRD, energy dispersive X-ray analysis (EDX, thermo-gravimetric analysis/differential thermal analysis (TGA/DTA and transmission electron microscope (TEM. The calculated crystallite sizes are ~ 2-5 nm and are in well accordance with the HRTEM results. EDX result confirms the presence and homogeneous distribution of Gd and Eu throughout the nanoparticle. The prepared nanoparticles exhibit strong paramagnetic nature with paramagnetic term, susceptibility c = 8.2 ´ 10-5 emg/g Gauss. TGA/DTA analysis shows 27 % weight loss with rise in temperature. The gas sensing capability of the prepared Gd2S3:Eu3+ magnetic nanoparticles are investigated using the amperometric method. These nanoparticles show good I-V characteristics with ideal semiconducting nature at room temperature with and without ammonia dose. The observed room temperature sensitivity with increasing dose of ammonia indicates applicability of Gd2S3 nanoparticles as room temperature ammonia sensors.

An analysis on structural and magnetic properties of La{sub 1-x}RE{sub x}FeO{sub 3} (x = 0.0 and 0.5, RE = Nd, Sm and Gd) nanoparticles

Energy Technology Data Exchange (ETDEWEB)

Blessington Selvadurai, A. Paul; Pazhanivelu, V.; Jagadeeshwaran, C.; Murugaraj, R. [Anna University, Department of Physics, Chennai (India); Gazzali, P.M. Mohammed; Chandrasekaran, G. [Pondicherry University, Department of Physics, Pudhucherry (India)

2017-01-15

La{sub 1-x}RE{sub x}FeO{sub 3} (x = 0.0 and 0.5, RE = Nd, Sm and Gd) is synthesised by sol-gel citrate combustion method. X-ray diffraction (XRD) and Raman spectra show orthorhombic phase with Pbnm symmetry, confirmed by profile fitting and Raman modes analysis for La{sub 1-x}R{sub x}FeO{sub 3} samples. The estimated crystallite size and the orthorhombic strain of La{sub 1-x}RE{sub x}FeO{sub 3} (x = 0.0 and 0.5, RE = Nd, Sm and Gd) from XRD data illustrate the role of ionic size substitution. The temperature- and field-dependent magnetisation M(T) and M(H) were measured using vibrating sample magnetometer. The M(H) curve parameters of La{sub 1-x}RE{sub x}FeO{sub 3}(x = 0.5, RE = Nd and Gd) exhibit a relation of M{sub r} ∝ (1)/(H{sub c}) and H{sub ex} ∝ H{sub C} at 20, 150 and 300 K. The M (T) curve of La{sub 0.5}Nd{sub 0.5}FeO{sub 3} and La{sub 0.5}Gd{sub 0.5}FeO{sub 3} indicates the paramagnetic-like behaviour, whereas the M (H) curve reveals the antiferromagnetic signature in them. The M (H) curve of La{sub 0.5}Sm{sub 0.5}FeO{sub 3} shows a strong AFM pinned ferromagnetism and ferromagnetism (FM) at 150 and 20 K, respectively. Further, field-cooled (FC) and zero-field-cooled (ZFC) measurement of La{sub 0.5}Sm{sub 0.5}FeO{sub 3} indicates a competitive interaction of AFM-FM, which is emphasised by a broad blocking temperature at ∝117 K in ZFC curve. The FM-like ordering of Sm{sup 3+} ions are observed below at ∝150 K in FC curve of La{sub 0.5}Sm{sub 0.5}FeO{sub 3}. In addition, the electron paramagnetic resonance spectra at room temperature show a high g value and a strong non-homogenous broadening for La{sub 0.5}Sm{sub 0.5}FeO{sub 3}. (orig.)

Properties of the (Sm sub 0 sub . sub 3 sub 3 Eu sub 0 sub . sub 3 sub 3 Gd sub 0 sub . sub 3 sub 3)Ba sub 2 Cu sub 3 O sub y superconductor prepared by different processes in air

CERN Document Server

Giovannelli, F; Monot-Laffez, I

2003-01-01

Bars and pellets of the (Sm sub 0 sub . sub 3 sub 3 Eu sub 0 sub . sub 3 sub 3 Gd sub 0 sub . sub 3 sub 3)Ba sub 2 Cu sub 3 O sub x superconductor were processed in air, using the floating zone method and the top-seeded melt-textured growth method, respectively. The samples were prepared using different experimental conditions, i.e. maximal processing temperature, translation rate or cooling rate. Their physical properties and their microstructure were studied. All the samples exhibit a satisfying superconducting transition whereas the critical current density greatly depends on the processing parameters. The sample prepared by the floating zone method at 1070 deg C with a translation rate of 2 mm h sup - sup 1 exhibits a very high J sub c value of 70000 A cm sup - sup 2 in the self-field and more than 30000 A cm sup - sup 2 at 1.7 T. The pellet processed at 1080 deg C with a cooling rate of 2 deg C h sup - sup 1 has a high J sub c reaching about 56000 A cm sup - sup 2 in the self-field and more than 32000 A ...

Effect of Gd doping and O deficiency on the Curie temperature of EuO

KAUST Repository

Jutong, Nuttachai; Eckern, Ulrich; Mairoser, Thomas; Schwingenschlö gl, Udo

2015-01-01

The effect of Gd doping and O deficiency on the electronic structure, exchange interaction, and Curie temperature of EuO in the cubic and tetragonal phases is studied by means of density functional theory. For both defects, the Curie temperature is found to exhibit a distinct maximum as a function of the defect concentration. The existence of optimal defect concentrations is explained by the interplay of the on-site, RKKY, and superexchange contributions to the magnetism.

Effect of Gd doping and O deficiency on the Curie temperature of EuO

KAUST Repository

Jutong, Nuttachai

2015-01-27

The effect of Gd doping and O deficiency on the electronic structure, exchange interaction, and Curie temperature of EuO in the cubic and tetragonal phases is studied by means of density functional theory. For both defects, the Curie temperature is found to exhibit a distinct maximum as a function of the defect concentration. The existence of optimal defect concentrations is explained by the interplay of the on-site, RKKY, and superexchange contributions to the magnetism.

Synthesis and photoluminescence properties of microcrystalline Sr{sub 2}ZnWO{sub 6}:RE{sup 3+} (RE = Eu, Dy, Sm and Pr) phosphors

Energy Technology Data Exchange (ETDEWEB)

Dabre, K.V. [Department of Physics, Arts, Commerce and Science College, Koradi, Nagpur 441111 (India); Park, K. [Faculty of Nanotechnology and Advanced Materials Engineering, Sejong University, Seoul 143-747 (Korea, Republic of); Dhoble, S.J., E-mail: sjdhoble@rediffmail.com [Department of Physics, R.T.M. Nagpur University, Nagpur 440033 (India)

2014-12-25

Graphical abstract: CIE chromaticity coordinate diagram (1931) indicating different colors of Sr{sub 2}ZnWO{sub 6}:RE{sup 3+} (RE = Eu (a), Dy (b and c), Sm (d–f) and Pr (g and h)) phosphor under different excitation 466 nm (a), 312 nm (b), 454 nm (c), 313 nm (d), 408 nm (e), 482 nm (f), 315 nm (g) and 450 nm (h). - Highlights: • Microcrystalline Sr{sub 2}ZnWO{sub 6}:RE{sup 3+} (RE = Eu, Dy, Sm and Pr) phosphors were synthesized by solid state method. • Photoluminescence properties of phosphor were investigated. • Color of the phosphor for different excitation has been verified by chromaticity diagram. • The host absorption and energy transfer were investigated. - Abstract: The novel microcrystalline Sr{sub 2}ZnWO{sub 6}:RE{sup 3+} (RE = Eu, Dy, Sm and Pr) phosphors were synthesized by solid-state reaction method at 1250 °C and their photoluminescence properties were investigated. The Eu{sup 3+} and Dy{sup 3+} activated phosphors show intense red (616 nm) and yellow (574 nm) emission respectively; which indicate that the rare earth ions are substituted at non-centrosymmetric site in the host lattice. Near white (Dy{sup 3+}) and reddish-orange (Sm{sup 3+}) emissions of rare earth ions in the host lattice show strong host absorption and energy transfer from the host to activator ion. Pr{sup 3+} activated phosphor shows a series of emission peaks in the visible region with the most intense peak in the blue region at 491 and 499 nm.

Synthesis and photoluminescence characteristics of (Y,Gd)BO3:RE (RE = Eu(3+), Ce(3+), Dy(3+) and Tb(3+)) phosphors for blue chip and near-UV white LEDs.

Science.gov (United States)

Rangari, V V; Singh, V; Dhoble, S J

2016-03-01

A series of Eu(3+)-, Ce(3+)-, Dy(3+)- and Tb(3+)-doped (Y,Gd)BO3 phosphors was synthesized by a solid-state diffusion method. X-Ray diffraction confirmed their hexagonal structure and the scanning electron microscopy results showed crystalline particles. The excitation spectra revealed that (Y,Gd)BO3 phosphors doped with Eu(3+), Ce(3+), Dy(3+) and Tb(3+) are effectively excited with near UV-light of 395 nm/blue light, 364, 351 and 314 nm, respectively. Photoluminescence spectra of Eu(3+)-, Ce(3+)- and Tb(3+)/Dy(3+)-doped phosphor showed intense emission of reddish orange, blue and white light, respectively. The phosphor Y0.60Gd0.38BO3:Ce0.02 showed CIE 1931 color coordinates of (0.158, 0.031) and better color purity compared with commercially available blue BAM:Eu(2+) phosphor. The phosphor (Y,Gd)BO3 doped with Eu(3+), Dy(3+) and Tb(3+) showed CIE 1931 color coordinates of (0.667, 0.332), (0.251, 0.299) and (0.333, 0.391) respectively. Significant photoluminescence characteristics of the prepared phosphors indicate that they might serve as potential candidates for blue chip and near-UV white light-emitting diode applications. Copyright © 2015 John Wiley & Sons, Ltd.

Prism inside. Spectroscopic and magnetic properties of the lanthanide(III) chloride oxidotungstates(VI) Ln{sub 3}Cl{sub 3}[WO{sub 6}] (Ln = La - Nd, Sm - Tb)

Energy Technology Data Exchange (ETDEWEB)

Dorn, Katharina V.; Blaschkowski, Bjoern; Hartenbach, Ingo [Institute for Inorganic Chemistry, University of Stuttgart (Germany); Foerg, Katharina; Netzsch, Philip; Hoeppe, Henning A. [Institute for Physics, University of Augsburg (Germany)

2017-11-17

The lanthanide(III) chloride oxidotungstates(VI) with the formula Ln{sub 3}Cl{sub 3}[WO{sub 6}] for Ln = La - Nd, Sm - Tb were synthesized by solid-state reactions utilizing the respective lanthanide trichloride, lanthanide sesquioxide (where available), and tungsten trioxide together with lithium chloride as flux. The title compounds crystallize hexagonally in space group P6{sub 3}/m (no. 176, a = 941-909, c = 543-525 pm, Z = 2). The structures comprise crystallographically unique Ln{sup 3+} cations surrounded by six O{sup 2-} and four Cl{sup -} anions (C.N. = 10) forming distorted tetracapped trigonal prisms as well as rather uncommon trigonal prismatic [WO{sub 6}]{sup 6-} units, whose edges are coordinated by nine Ln{sup 3+} cations. Thus, a {sup 3}{sub ∞}{([WO_6]Ln"e_9_/_3)"3"+} framework (e = edge-sharing) is created, which contains tube-shaped channels along [001] lined with chloride anions. To elucidate the spectroscopic and magnetic properties of the obtained pure phase samples, single-crystal Raman (for Ln = La - Nd, Sm-Tb), diffuse reflectance (for Ln = La, Pr, Nd, Gd), and luminescence spectroscopy (for bulk Ln{sub 3}Cl{sub 3}[WO{sub 6}] (Ln = La, Eu, Gd, Tb) and Eu{sup 3+}- or Tb{sup 3+}-doped derivatives of La{sub 3}Cl{sub 3}[WO{sub 6}] and Gd{sub 3}Cl{sub 3}[WO{sub 6}], respectively) were performed and their temperature-dependent magnetic moments (for Ln = Pr, Nd, Gd) were determined. (copyright 2017 WILEY-VCH Verlag GmbH and Co. KGaA, Weinheim)

Phase transformation and spectroscopic adjustment of Gd{sub 2}O{sub 3}:Eu{sup 3+} synthesized by hydrothermal method

Energy Technology Data Exchange (ETDEWEB)

Wang, Zijun; Wang, Pei; Zhong, Jiuping, E-mail: zhongjp@mail.sysu.edu.cn; Liang, Hongbin; Wang, Jing

2014-08-01

The microcrystalline Gd{sub 2}O{sub 3}:Eu{sup 3+} phosphors were synthesized by the hydrothermal method with post annealing treatment. The powder X-ray diffraction (XRD) indicated the phase transformation from cubic to monoclinic occurred at about 1673 K. The morphologies and sizes were characterized by scanning electron microscopy (SEM). It was found that the morphology of Gd{sub 2}O{sub 3}:Eu{sup 3+} was altered from nanorod to microparticle as the phase changed from cubic to monoclinic. In order to evaluate the effects of sites and phases on luminescence behaviors, the photoluminescence (PL) properties of both phases were investigated. Dominant red emission was observed due to an efficient energy transfer among the sites as well as the strong excitation of O{sup 2−}–Eu{sup 3+} charge transfer band. It was calculated that the monoclinic structure has a higher degree of distortion. More importantly, the phase transformation resulted in the red shift of the strongest emission peak of Eu{sup 3+} from 610.5 to 622.5 nm, closer to the optical transmission window for bioimaging. - Highlights: • Raising annealing temperature induces phase transformation from cubic to monoclinic. • Different phases and sites lead to distinct photoluminescence properties. • Monoclinic structure has higher degree of distortion and it is calculated. • Monoclinic phase emitting at longer wavelength is proposed for bioimaging.

Pinning performance of (Nd,Eu,Gd)-123 superconductors: Comparison of melt-textured pellet and single crystal

Czech Academy of Sciences Publication Activity Database

Jirsa, Miloš; Rameš, Michal; Jurek, Karel; Muralidhar, M.; Das, P.; Koblischka, M.R.; Wolf, T.

2008-01-01

Roč. 151, č. 1 (2008), s. 25-30 ISSN 0921-5107 R&D Projects: GA ČR GA202/05/0173; GA MŠk 1P05ME728 Institutional research plan: CEZ:AV0Z10100520 Keywords : high-temperature superconductors * cuprous oxides * superconductivity perovskites, * (Nd,Eu,Gd)BaCuO * ternary compounds * melt-textured materials Subject RIV: BM - Solid Matter Physics ; Magnetism

Tunable luminescence and energy transfer properties in Na{sub 3}Bi(PO4){sub 2}:Eu{sup 3+}, Tb{sup 3+}, Dy{sup 3+}, Sm{sup 3+} phosphors with high thermal stability

Energy Technology Data Exchange (ETDEWEB)

Zhu, Zizhong; Fu, Guangsheng; Yang, Yong; Yang, Zhiping, E-mail: yangzp2005@sohu.com; Li, Panlai, E-mail: li_panlai@126.com

2017-04-15

Na{sub 3}Bi(PO{sub 4}){sub 2}:Eu{sup 3+}/Tb{sup 3+}/Dy{sup 3+}/Sm{sup 3+} phosphors were synthesized via a high-temperature solid-state reaction method. The X-ray diffraction (XRD), field emission scanning electron microscopy (FE-SEM), diffuse reflection, photoluminescence (PL) and fluorescent decay curves were utilized to characterize the obtained phosphors. Under n-UV excitation, Na{sub 3}Bi(PO{sub 4}){sub 2}:Eu{sup 3+}/Tb{sup 3+}/Dy{sup 3+}/Sm{sup 3+} samples show the characteristic f-f emissions and present red, green, yellow and orange emission, respectively. When Tb{sup 3+}, Dy{sup 3+} and Sm{sup 3+} were co-doped into the Na{sub 3}Bi(PO{sub 4}){sub 2}:Eu{sup 3+} phosphors, tunable emission colors can be obtained and can be efficiently adjusted by varying the doping ions and the doping concentration. The energy transfer mechanisms were investigated in detail and demonstrated that there is an efficient energy transfer from Tb{sup 3+}, Dy{sup 3+} and Sm{sup 3+} to Eu{sup 3+} via a dipole-dipole interaction mechanism. Additional, as the temperature increases from RT to 150 °C, the PL intensity of Tb{sup 3+}-Eu{sup 3+}, Dy{sup 3+}-Eu{sup 3+} and Sm{sup 3+}-Eu{sup 3+} co-doped phosphors decreased to 86%, 85% and 88%, respectively, which prove good thermal stability. All the CIE coordinates of as-prepared phosphors are displayed and show abundant colors, making these materials have potential applications for n-UV-excited white-LEDs.

A study of luminescence from Eu"3"+, Ce"3"+, Tb"3"+ and Ce"3"+/Tb"3"+ in new potassium gadolinium phosphate K_3Gd_5(PO_4)_6

International Nuclear Information System (INIS)

Meng, Fangui; Zhang, Hongzhi; Chen, Cuili; Kim, Sun Il; Seo, Hyo Jin; Zhang, Xinmin

2016-01-01

New potassium gadolinium phosphate [K_3Gd_5(PO_4)_6] doped with Eu"3"+, Ce"3"+, Tb"3"+ and co-doped with Ce"3"+ and Tb"3"+ phosphors were prepared by high temperature solid state synthesis. Phase purity of the powders was checked by X-ray powder diffraction. Luminescence and excitation spectra of samples were reported. In particular, the interaction mechanism between Eu"3"+ ions was investigated in terms of the Inokuti–Hirayama model; it was found that the interactions between Eu"3"+ can be assigned to dipole–dipole interaction. K_3Gd_5(PO_4)_6:Eu"3"+ could act as a candidate for solid state lighting due to its strong absorption band in the near-UV region (350–400 nm). The energy transfer from Ce"3"+ to Tb"3"+ was confirmed and the mechanism was studied using Dexter's theory; it is concluded that electric dipole–dipole interaction predominates in the energy transfer process from Ce"3"+ to Tb"3"+ in the K_3Gd_5(PO_4)_6 host. The energy transfer efficiency and critical distance were also investigated. - Highlights: • Optical properties of K_3Gd_5(PO_4)_6:RE"3"+ are investigated for the first time. • The interaction mechanism between Eu"3"+ ions is attributed to dipole–dipole type. • K_3Eu_5(PO_4)_6 is a candidate phosphor for application to solid state lighting. • There exists an efficient energy transfer from Ce"3"+ to Tb"3"+ (η is up to 95%). • The mechanism of energy transfer process is electric dipole–dipole interaction.

Noticeable red emission and Raman active modes in nanoscale gadolinium oxyfluoride (Gd{sub 4}O{sub 3}F{sub 6}) systems with Eu{sup 3+} inclusion

Energy Technology Data Exchange (ETDEWEB)

Hazarika, Samiran; Mohanta, Dambarudhar [Tezpur University, Nanoscience and Soft Matter Laboratory, Department of Physics, Tezpur, Assam (India)

2017-05-15

Eu{sup 3+} doped gadolinium oxyfluoride (Gd{sub 4}O{sub 3}F{sub 6}, GOF) nanoscale systems have been synthesized following a modified Pechini method. While exhibiting a tetragonal crystal structure, the GOF nanosystem gave an average crystallite size (d) of ∝21-26 nm. The Lotgering factor (L{sub F}), which is a measure of orientation of crystallites along the preferred direction was found to vary between 0.22 and 0.48. In the photoluminescence spectra, ∝595 and ∝613 nm peaks were identified as magnetically driven ({sup 5}D{sub 0} → {sup 7}F{sub 1}) and electrically driven ({sup 5}D{sub 0} → {sup 7}F{sub 2}) transitions with latter (red emission) being strongly manifested with Eu{sup 3+} doping concentration and intrinsic defects. Moreover, several Raman active modes have been probed in the Raman spectra with low frequency peaks (<300 cm{sup -1}) and moderate frequency peaks (∝481 and 567 cm{sup -1}) assigned to observable vibration of heavy atom Gd-Gd pairs and Gd-O groups, respectively. Apart from manifestation of phononic features, inclusion of Eu{sup 3+} in the host lattice would bring new insight on improving the red emission response prior to concentration quenching. (orig.)

Thermoelectric properties, crystal and electronic structure of semiconducting RECuSe2 (RE = Pr, Sm, Gd, Dy and Er)

International Nuclear Information System (INIS)

Esmaeili, Mehdi; Tseng, Yu-Chih; Mozharivskyj, Yurij

2014-01-01

Highlights: • Crystal and electronic structure of monoclinic and trigonal RECuSe 2 phases. • Thermoelectric properties of the RECuSe 2 phases. • Temperature stability of the RECuSe 2 phases. - Abstract: The ternary RECuSe 2 phases have been prepared and structurally characterized. They adopt either a monoclinic structure (P2 1 /c, z = 4) for lighter rare earths (RE = Pr, Sm and Gd) or Cu-disordered trigonal structure for heavier rare-earths (P3 ¯ m1, z = 1, RE = Dy and Er). The resistivity and Seebeck coefficient measurements on GdCuSe 2 , DyCuSe 2 and ErCuSe 2 indicate that the studied phases are p-type semiconductors with relatively small activation energies (0.045–0.11 eV). However, their electrical resistivities are too high (0.45–220 Ω cm at room temperature) to make them competitive thermoelectric materials. Electronic structure calculations indicate presence of a band gap in the RECuSe 2 phases

Synthesis, structure and luminescence properties of binary and ternary complexes of lanthanide (Eu{sup 3+}, Sm{sup 3+} and Tb{sup 3+}) with salicylic acid and 1,10-phenanthroline

Energy Technology Data Exchange (ETDEWEB)

Shen, Chen-Qi; Yan, Tian-Lu; Wang, Yi-Ting; Ye, Zi-Jun; Xu, Cun-Jin, E-mail: cjxu@hznu.edu.cn; Zhou, Wen-Jun

2017-04-15

A series of binary and ternary complexes of lanthanide (Eu{sup 3+}, Sm{sup 3+} and Tb{sup 3+}) with salicylic acid (Hsal) and 1,10-phenanthroline (phen) were synthesized, and characterized by element analysis, coordination titration analysis, IR, UV and TG-DTA. Their compositions were (NH{sub 4})[Ln(sal){sub 4}(H{sub 2}O){sub 2}] (Ln=Eu (1), Sm (2), Tb (3)) and (NH{sub 4})[Ln(sal){sub 4}(phen){sub 2}] (Ln=Eu (4), Sm (5), Tb (6)), respectively. In particular, the ternary complex of Eu{sup 3+}, 4, was characterized by X-ray diffraction, and luminescence intensities of binary and ternary complexes were compared. In case of Eu{sup 3+} and Sm{sup 3+} complexes, ternary complexes emitted stronger luminescence than corresponding binary complexes of salicylic acid and Ln{sup 3+}. On the other hand, the ternary Tb{sup 3+} complex had weaker luminescence than the binary complex because of back energy transfer from Tb{sup 3+} to phen. The CIE coordinates of 1–6 were calculated as (0.65, 0.35), (0.52, 0.48), (0.33, 0.59), (0.67, 0.33), (0.62, 0.38) and (0.36, 0.58), respectively, which enable these complexes to be promising candidates for red, green, or yellow component in OLEDs.

Colloidal GdVO4:Eu3+@SiO2 nanocrystals for highly selective and sensitive detection of Cu2+ ions

Science.gov (United States)

Liang, Yanjie; Noh, Hyeon Mi; Park, Sung Heum; Choi, Byung Chun; Jeong, Jung Hyun

2018-03-01

Nowadays, in view of health and safety demands, the controlled design of selective and sensitive sensors for Cu2+ detection is of considerable importance. Therefore, we construct herein core-shell colloidal GdVO4:Eu3+@SiO2 nanocrystals (NCs) as optical sensor for the detection of Cu2+, which were synthesized by a facile hydrothermal reaction and encapsulated with a uniform layer of ultrathin silica through a sol-gel strategy. The NCs present strong red emission due to energy transfer from VO43- groups to Eu3+ when exciting with ultraviolet (UV) light. This intense red emission from Eu3+ could be selectively quenched in the presence of Cu2+ in comparison to other metal ions and the limit of detection is as low as 80 nM in aqueous solution. It is revealed that the spectral overlap between the emission band of NCs and the absorption of Cu2+ accounts for this intriguing luminescence behavior. The detection ability is highly reversible by the addition of ethylenediaminetetraacetic acid (EDTA) with the recovery of almost 100% of the original luminescence. The luminescence quenching and recovery processes can be performed repeatedly with good sensing ability. These remarkable performances allow the colloidal GdVO4:Eu3+@SiO2 NCs a promising fluorescence chemosensor for detecting Cu2+ ions in aqueous solution.

The temperature-sensitive luminescence of (Y,Gd)VO{sub 4}:Bi{sup 3+},Eu{sup 3+} and its application for stealth anti-counterfeiting

Energy Technology Data Exchange (ETDEWEB)

Chen, Lei; Zhang, Yao; Luo, Anqi; Liu, Fayong; Jiang, Yang; Hu, Qingzhuo [School of Materials Science and Engineering, Hefei University of Technology (China); Chen, Shifu [Department of Chemistry, Huaibei Normal University (China); Liu, Ru-Shi [Department of Chemistry, National Taiwan University, Taipei (China)

2012-07-15

Anti-counterfeiting technologies are desired to protect products far away from the violation of dummy, fake and shoddy goods. The phosphor of (Y,Gd)VO{sub 4}:Bi{sup 3+},Eu{sup 3+} was synthesized for the application of this purpose. Its photoluminescence was investigated by exciting with different wavelengths at variant temperatures. Wide emission color ranged from green through yellow to orange was tuned up by tailor-ing Bi{sup 3+} and Eu{sup 3+} concentrations. The temperature dependent luminescence and wavelength selective excitation of (Y,Gd)VO{sub 4}:Bi{sup 3+},Eu{sup 3+} were observed, which provide different encryptions in anti-counterfeiting. To verify the feasibility in application, two anti-counterfeiting patterns were fabricated practically and excellent performance was obtained. Moreover, the physical mechanisms for the different phenomena of luminescence were elucidated from excitation spectra combining with the configuration coordinate model. (copyright 2012 WILEY-VCH Verlag GmbH and Co. KGaA, Weinheim) (orig.)

Nitrato-complexes of Y(III), La(III), Ce(III), Pr(III), Nd(III), Sm(III), Gd(III), Tb(III), Dy(III) and Ho(III) with 2-(2'-pyridyl) benzimidazole

Energy Technology Data Exchange (ETDEWEB)

Mishra, A; Singh, M P; Singh, V K

1982-05-01

The nitrato-complexes, (Y(PyBzH)/sub 2/(NO/sub 3/)/sub 2/)NO/sub 3/.H/sub 2/O and Nd, Sm, Gd, Tb, Dy, Ho ; n=1-3, m=0-0.5 ; PyBzh=2-(2 -pyridyl)benzimidazole) are formed on interaction of the ligand with metal nitrates in ethanol. The electrical conductance values (116-129 ohm/sup -1/cm/sup 2/mol/sup -1/) suggest 1:1 electrolyte-nature of the complexes. Magnetic moment values of Ce(2.53 B.M.), Pr(3.62 B.M.), Nd(3.52 B.M.), Sm(1.70 B.M.), Gd(8.06 B.M.), Tb(9.44 B.M.), Dy(10.56 B.M.) and Ho(10.51 B.M.) in the complexes confirm the positive state of the metals. Infrared evidences are obtained for the existance of both coordinated (C/sub 2/v) and uncoordinated (D/sub 3/h) nitrate groups. Electronic absorption spectra of Pr(III)-, Nd(III)-, Sm(III)-, Tb(III)-, Dy(III)- and Ho(III)-complexes have been analysed in the light of LSJ terms.

Nitrato-complexes of Y(III), La(III), Ce(III), Pr(III), Nd(III), Sm(III), Gd(III), Tb(III), Dy(III) and Ho(III) with 2-(2'-pyridyl) benzimidazole

International Nuclear Information System (INIS)

Mishra, A.; Singh, M.P.; Singh, V.K.

1982-01-01

The nitrato-complexes, [Y(PyBzH) 2 (NO 3 ) 2 ]NO 3 .H 2 O and Nd, Sm, Gd, Tb, Dy, Ho ; n=1-3, m=0-0.5 ; PyBzh=2-(2 -pyridyl)benzimidazole] are formed on interaction of the ligand with metal nitrates in ethanol. The electrical conductance values (116-129 ohm -1 cm 2 mol -1 ) suggest 1:1 electrolyte-nature of the complexes. Magnetic moment values of Ce(2.53 B.M.), Pr(3.62 B.M.), Nd(3.52 B.M.), Sm(1.70 B.M.), Gd(8.06 B.M.), Tb(9.44 B.M.), Dy(10.56 B.M.) and Ho(10.51 B.M.) in the complexes confirm the terpositive state of the metals. Infrared evidences are obtained for the existance of both coordinated (C 2 v) and uncoordinated (D 3 h) nitrate groups. Electronic absorption spectra of Pr(III)-, Nd(III)-, Sm(III)-, Tb(III)-, Dy(III)- and Ho(III)-complexes have been analysed in the light of LSJ terms. (author)

Dependence of morphology and photoluminescent properties of GdPO4:Eu3+ nanostructures on synthesis condition

International Nuclear Information System (INIS)

Yu Lixin; Li Dianchao; Yue Mingxin; Yao Jie; Lu Shaozhe

2006-01-01

GdPO 4 :Eu 3+ nanoparticles, nanowires and nanorods phosphors were successfully synthesized by a hydrothermal method. Their photoluminescent properties were investigated and compared. The results indicated that the one-dimensional nanowires and nanorods were formed as the pH value of precursor solution was 1, 5 and 9, while zero-dimensional nanoparticles were formed for the pH value of 9. The crystallization state of nanoparticles was relative lower and the crystal structure belongs to monoclinic phase for other samples. The charge transfer band (CTB) of Eu 3+ ions in nanorods (for pH value of 13) clearly blue-shifted in contrast with other samples. The integrate intensity ratio of 5 D 0 - 7 F 2 to 5 D 0 - 7 F 1 in nanoparticles increased due to high disorder. The lifetime of 5 D 0 level of Eu 3+ in nanoparticles decreased in comparison with other samples and radiative transition rate of 5 D 0 -bar J 7 F J increased

Synthesis and luminescence properties of ZnAl{sub 2}O{sub 4}:RE{sup 3+} (RE = Eu, Sm) phosphors

Energy Technology Data Exchange (ETDEWEB)

Lee, Seung Jin; Cho, Shin Ho [Silla University, Busan (Korea, Republic of)

2014-01-15

ZnAl{sub 2}O{sub 4}:RE{sup 3+} (RE = Eu or Sm) phosphor powders were synthesized with different concentrations of activator ions by using the conventional solid-state reaction method. The effects of the concentration of activator ions on the structural, morphological, and luminescent properties of zinc aluminate phosphors were investigated. The X-ray diffraction patterns revealed that the phosphors synthesized with different concentrations of activator ions showed mixed phases of ZnAl{sub 2}O{sub 4}, ZnO, and Al{sub 2}O{sub 3}. The crystallite size was estimated using the Scherrer formula, and the maximum size was obtained for 0.20 mol of Eu{sup 3+} ions. The emission spectra of of Eu{sup 3+}-doped ZnAl{sub 2}O{sub 4} phosphors under excitation at 303 nm exhibited one intense green band at approximately 520 nm and three weak bands centered at 590, 621, and 701 nm, respectively. The intensity of all the emission bands reached a maximum for 0.05 mol of Eu{sup 3+} ions. For the Sm{sup 3+}-doped ZnAl{sub 2}O{sub 4} phosphors, a broad emission band peak at 526 nm and several weak lines in the range 470 - 700 nm were observed. The results suggest that the luminescent intensity of the phosphors can be enhanced by controlling the amount of activator ions incorporated into the host lattice.

Study of LnBaCo{sub 2}O{sub 6-d}elta (Ln = Pr, Nd, Sm and Gd) double perovskites as new cathode material for IT-SOFC

Energy Technology Data Exchange (ETDEWEB)

Chavez, E; Mueller, M; Mogni, L; Caneiro, A, E-mail: mogni@cab.cnea.gov.a [Centro Atomico Bariloche-CNEA, Instituto Balseiro. Av. Bustillo 9500, S. C. de Bariloche 8400 (Argentina)

2009-05-01

Oxides with double perovskites structures of general composition LnBaCo{sub 2}O{sub 6-d}elta (Ln = Pr, Nd, Sm and Gd) were synthesized by solid state reaction with the purpose to evaluate new materials to be used as cathodes in intermediate temperature solid oxide fuel cell (IT-SOFC). A preliminary study about electrochemical properties was performed by impedance spectroscopy between 500 and 800 deg. C under atmosphere of pure O{sub 2}. Symmetrical cells were obtained by spray deposition of LnBaCo{sub 2}O{sub 6-d}elta (Ln = Pr, Nd, Sm and Gd) at both sides of a dense ceramic electrolyte. The impedance spectroscopy measurements as a function of temperatures show a hysteresis loop which could be associated to a tetragonal/orthorhombic phase transition. The existence of this transition was corroborated by high temperature X-Ray diffraction and Differential Scanning Calorimetry measurements.

Efficient and thermally stable red luminescence from nano-sized phosphor of Gd{sub 6}MoO{sub 12}:Eu{sup 3+}

Energy Technology Data Exchange (ETDEWEB)

Qin, Lin [Soochow University, College of Chemistry, Chemical Engineering and Materials Science (China); Wei, Donglei [Pukyong National University, Department of Physics and Interdisciplinary Program of Biomedical Engineering (Korea, Republic of); Huang, Yanlin [Soochow University, College of Chemistry, Chemical Engineering and Materials Science (China); Kim, Sun Il [Pukyong National University, Department of Physics and Interdisciplinary Program of Biomedical Engineering (Korea, Republic of); Yu, Young Moon [Pukyong National University, LED-Marin Convergence Technology R and BD Center (Korea, Republic of); Seo, Hyo Jin, E-mail: hjseo@pknu.ac.kr [Pukyong National University, Department of Physics and Interdisciplinary Program of Biomedical Engineering (Korea, Republic of)

2013-09-15

A novel red-emitting nano-phosphor of Eu{sup 3+}-doped Gd{sub 6}MoO{sub 12} was successfully synthesized by the Pechini method. The crystalline phase was confirmed by X-ray powder diffraction analysis. The morphology of the nano-phosphor was analyzed by scanning electron microscopy, indicating a good crystallization with particles smaller than 500 nm. The luminescence properties such as photoluminescence spectra and decay curves were investigated. The phosphors can be efficiently excited by near-ultraviolet (near-UV) light and exhibit a bright red luminescence around 613 nm ascribed to the forced electric dipole transition {sup 5}D{sub 0}{yields}{sup 7}F{sub 2} of Eu{sup 3+} ions. The thermal stabilities were investigated from the temperature-dependent luminescence decay curves (lifetimes) and spectra intensities. The luminescence properties in relation to applications in white light-emitting diodes (W-LEDs) such as the absolute luminescence quantum efficiency, excitation wavelength, and color coordinates were discussed. The Gd{sub 6}MoO{sub 12}:Eu{sup 3+} nano-phosphor is a promising red-emitting candidate for the fabrication of W-LEDs with near-UV chips.

Bifunctional ferromagnetic Eu-Gd-Bi-codoped hybrid organo-silica red emitting phosphors synthesized by a modified Pechini sol-gel method

Energy Technology Data Exchange (ETDEWEB)

Abo-Naf, S.M., E-mail: sm.abo-naf@nrc.sci.eg [Glass Research Department, National Research Centre (NRC), El-Buhouth Str., Dokki, 12622 Cairo (Egypt); Abdel-Hameed, S.A.M.; Marzouk, M.A. [Glass Research Department, National Research Centre (NRC), El-Buhouth Str., Dokki, 12622 Cairo (Egypt); Hamdy, Y.M. [Spectroscopy Department, National Research Centre (NRC), El-Buhouth Str., Dokki, 12622 Cairo (Egypt)

2017-06-15

Red phosphor, composed of Eu-Gd-Bi-codoped hybrid organo-silica glass, has been synthesized via a modified Pechini sol-gel process. The synthesized hybrid glass was analyzed with powder X-ray diffraction (XRD), differential thermal analysis coupled with thermogravimetry (DTA-TG) and Fourier transform infrared (FTIR) spectroscopy. XRD and DTA-TG confirmed its amorphous structure up to 1000 °C. Magnetic behavior of the produced phosphor was investigated using vibrating specimen magnetometer (VSM) and the obtained results revealed its unsaturated ferromagnetic behavior. Photoluminescence (PL) properties of the obtained phosphor have been investigated under near-UV excitation at 395 nm. The influence of calcination temperature on the PL intensity and its decay behavior as well as on the ferromagnetic characteristics has been studied to determine the optimal reaction temperature of the phosphor. The PL emission spectra show the characteristic emission bands of Eu{sup 3+} ions in the wavelength range from 580 to 700 nm. These emission spectra have been dominated by the electric dipole {sup 5}D{sub 0}→{sup 7}F{sub 2} transition of the Eu{sup 3+} peaked at 610–620 nm producing the red light emission of the phosphors. It was found that the phosphor performance, expressed by its PL intensity and life time, could be significantly improved by increasing of the heat treatment temperature up to 900 °C. Also, calcination at 900 °C for 6 h greatly increased both of the magnetization and retentivity, while decreased the coercivity value. The organic phenomenon of metal citrate-ethylene glycol chelation and its degradation by calcination were well followed by FTIR spectroscopy. The obtained results are promising and could afford a basis for designing of efficient red phosphors for displays, lighting and bifunctional biosensors for biomedical applications. - Highlights: • Eu-Gd-Bi-codoped hybrid organo-silica phosphor was synthesized by sol-gel method. • Inorganic Eu-Gd

Effect of annealing on the structural, optical and emissive properties of SrWO4:Ln3+ (Dy3+, Eu3+ and Sm3+) nanoparticles

Science.gov (United States)

Maheshwary; Singh, B. P.; Singh, R. A.

2016-01-01

Lanthanide ions, Ln3+ (Dy3+, Eu3+ and Sm3+) doped SrWO4 nanoparticles were synthesized using ethylene glycol (EG) as a capping agent as well as reaction medium. The X-ray diffraction (XRD) study reveals that all the Ln3+ (Dy3+, Eu3+ and Sm3+) doped samples are well crystalline in nature with a tetragonal scheelite structure of SrWO4 phase. TG study reveals that the nanophosphors are thermally stable. Fourier transform infrared spectroscopy (FTIR) and Raman spectroscopy techniques were used to obtain the information about internal and external vibrational modes present in the SrWO4 structure. Optical properties were investigated using UV-vis and photoluminescence (PL) spectroscopy. The average crystallite size was calculated using Debye-Scherrer's for as-prepared and 800 °C annealed samples and is found to be in the range of ∼35-70 nm. The luminescence intensity of Eu3+ doped SrWO4 nanoparticles under 364 nm excitation wavelength reveals that 5D0 → 7F2 transition at ∼613 nm (red) is more prominent than that of 5D0 → 7F1 transition at ∼590 nm (orange). Also upon excitation by UV radiation, the SrWO4:Dy3+ phosphor shows the yellow and blue transition lines appearing at ∼572 and 484 nm which are the characteristic electronic transitions of 4F9/2-6H13/2 and 4F9/2-6H15/2 emission line of Dy3+, respectively. Also Sm3+ doped SrWO4 nanophosphor shows its characteristic emission lines in the range of 550-720 nm, corresponding to 4G5/2 → 6HJ (J = 5/2, 7/2, 9/2 and 11/2) transitions of Sm3+ ions. The predominant orange red color can be attributed to 4G5/2 → 6H9/2 located at ∼642 nm. This is related to the polarizing effect due to the energy transfer from WO42- to the Eu3+, Dy3+ and Sm3+ sites, respectively. Effect of annealing on the photoluminescence properties of samples has been studied and it was found that luminescence intensity increases up to ∼3 times on heating the samples at 800 °C. This may be due to reduction in non-radiative decay channels

Color-tunable and white luminescence properties via energy transfer in single-phase KNaCa2(PO4)2:A (A = Ce3+, Eu2+, Tb3+, Mn2+, Sm3+) phosphors.

Science.gov (United States)

Geng, Dongling; Shang, Mengmeng; Zhang, Yang; Lian, Hongzhou; Lin, Jun

2013-12-02

A series of single-phase phosphors based on KNaCa2(PO4)2 (KNCP):A (A = Ce(3+), Eu(2+), Tb(3+), Mn(2+), Sm(3+)) have been prepared via the Pechini-type sol-gel method. Photoluminescence (PL) and cathodoluminescence (CL) properties of Ce(3+)-, Eu(2+)-, Tb(3+)-, Mn(2+)-, and Sm(3+)-activated KNCP phosphors were investigated. For the A singly doped KNCP samples, they exhibit the characteristic emissions of the A activator. Na(+) ions exhibit the best charge compensation result among Li(+), Na(+), and K(+) ions for Ce(3+)-, Tb(3+)-, and Sm(3+)-doped KNCP samples. The energy transfers from Ce(3+) to Tb(3+) and Mn(2+) ions as well as Eu(2+) to Tb(3+) and Mn(2+) have been validated. The emission colors of KNCP:Ce(3+)/Eu(2+), Tb(3+)/Mn(2+), Na(+) samples can be adjusted by energy transfer process and changing the Tb(3+)/Mn(2+) concentration. More importantly, white light emission in KNCP:Eu(2+), Mn(2+) system has been obtained. The KNCP:Tb(3+), Na(+) sample shows tunable luminescence from blue to cyan and then to green with the change of Tb(3+) concentration due to the cross-relaxation from (5)D3 to (5)D4. A white emission can also be realized in the single-phase KNCP host by reasonably adjusting the doping concentrations of Tb(3+) and Sm(3+) (reddish-orange emission) under low-voltage electron beam excitation. Additionally, the temperature-dependent PL properties of as-prepared phosphors reveal that the KNCP host has good thermal stability. Therefore, the KNCP:A (A = Ce(3+), Eu(2+), Tb(3+), Mn(2+), Sm(3+)) phosphors could be regarded as good candidates for UV W-LEDs and FEDs.

Study of the R-(Zr,W)-(O,N) (R = Y, Nd, Sm, Gd, Yb) oxynitride system

Energy Technology Data Exchange (ETDEWEB)

Tessier, Franck, E-mail: Franck.Tessier@univ-rennes1.fr [UMR CNRS 6226 ' Sciences Chimiques de Rennes' , equipe ' Verres et Ceramiques' , Universite de Rennes 1, 35042 Rennes cedex (France); Maillard, Pascal [UMR CNRS 6226 ' Sciences Chimiques de Rennes' , equipe ' Verres et Ceramiques' , Universite de Rennes 1, 35042 Rennes cedex (France); Orhan, Emmanuelle [Laboratoire Science des Procedes Ceramiques et Traitements de Surface, UMR CNRS 6638, Universite de Limoges, 123 Avenue Albert Thomas, 87060 Limoges cedex (France); Chevire, Francois [UMR CNRS 6226 ' Sciences Chimiques de Rennes' , equipe ' Verres et Ceramiques' , Universite de Rennes 1, 35042 Rennes cedex (France)

2010-02-15

The replacement of tantalum by the couple Zr/W within the RTa-O-N systems (R = Y, Nd, Sm, Gd, Yb), enables the preparation of novel oxide and oxynitride phases in the R-Zr-W-O-N system. R{sub 2}Zr{sub 2-x}W{sub x}O{sub 7+x} oxides exhibit the fluorite-type (x < 0.9) and scheelite (x {approx} 1) structures. Corresponding oxynitride compositions are of the fluorite-type and show different colors, for example in the case of ytterbium: pale yellow (x = 0.2 or 0.25), green (x = 0.5-0.8) and brown for the tungsten-rich samples (x = 0.9, 1). Photocatalytic activity measurements have been performed to investigate the overall water splitting behavior of these colored phases.

Magnetic properties of the germanides RE{sub 3}Pt{sub 4}Ge{sub 6} (RE=Y, Pr, Nd, Sm, Gd-Dy)

Energy Technology Data Exchange (ETDEWEB)

Eustermann, Fabian; Eilers-Rethwisch, Matthias; Renner, Konstantin; Hoffmann, Rolf-Dieter; Poettgen, Rainer [Muenster Univ. (Germany). Inst. fuer Anorganische und Analytische Chemie; Janka, Oliver [Muenster Univ. (Germany). Inst. fuer Anorganische und Analytische Chemie; Oldenburg Univ. (Germany). Inst. fuer Chemie

2017-07-01

The germanides RE{sub 3}Pt{sub 4}Ge{sub 6} (RE=Y, Pr, Nd, Sm, Gd-Dy) have been synthesized by arc-melting of the elements followed by inductive annealing to improve the crystallinity and allow for structural order. The compounds have been studied by powder X-ray diffraction; additionally the structure of Y{sub 3}Pt{sub 4}Ge{sub 6} has been refined from single-crystal X-ray diffractometer data. It exhibits a (3+1)D modulated structure, indicating isotypism with Ce{sub 3}Pt{sub 4}Ge{sub 6}. The crystal structure can be described as an intergrowth between YIrGe{sub 2}- and CaBe{sub 2}Ge{sub 2}-type slabs along [100]. Temperature-dependent magnetic susceptibility measurements showed Pauli paramagnetism for Y{sub 3}Pt{sub 4}Ge{sub 6} and Curie-Weiss paramagnetism for Pr{sub 3}Pt{sub 4}Ge{sub 6} and Nd{sub 3}Pt{sub 4}Ge{sub 6}. Sm{sub 3}Pt{sub 4}Ge{sub 6} exhibits van Vleck paramagnetism, while antiferromagnetic ordering at T{sub N}=8.1(1) K and T{sub N}=11.0(1) K is observed for Gd{sub 3}Pt{sub 4}Ge{sub 6} and Tb{sub 3}Pt{sub 4}Ge{sub 6}, respectively.

Determination of diffusion coefficients for sulfide ions in solid electrolytes on the basis of BaSm2S4 and CaGd2S4

International Nuclear Information System (INIS)

Yurlov, I.S.; Ushakova, Yu.N.; Medvedeva, O.V.; Kalinina, L.A.; Shirokova, G.I.; Ananchenko, B.A.

2007-01-01

Coefficients of self-diffusion and coefficients of diffusion of the sulfur ion in solid electrolytes BaSm 2 S 4 and CaGd 2 S 4 are determined with recourse to methods of conductometry and potentiostatic chronoamperometry. A vacancy mechanism for the defect formation in solid solutions on the basis of barium thiosamarate and calcium thiogadolynate is proposed [ru

Structural relative stabilities and pressure-induced phase transitions for lanthanide trihydrides REH{sub 3} (RE=Sm, Gd, Tb, Dy, Ho, Er, Tm, and Lu)

Energy Technology Data Exchange (ETDEWEB)

Kong Bo, E-mail: kong79@yeah.net [National Key Laboratory for Shock Wave and Detonation Physics Research, Institute of Fluid Physics, Chinese Academy of Engineering Physics, Mianyang 621900 (China); College of Physical Science and Technology, Sichuan University, Chengdu 610064 (China); Zhang Lin, E-mail: zhanglinbox@263.net [National Key Laboratory for Shock Wave and Detonation Physics Research, Institute of Fluid Physics, Chinese Academy of Engineering Physics, Mianyang 621900 (China); Chen Xiangrong [College of Physical Science and Technology, Sichuan University, Chengdu 610064 (China); Zeng Tixian [College of Physics and Electronic Information, China West Normal University, Nanchong 637002 (China); Cai Lingcang [National Key Laboratory for Shock Wave and Detonation Physics Research, Institute of Fluid Physics, Chinese Academy of Engineering Physics, Mianyang 621900 (China)

2012-06-15

The structures, structural relative stabilities, pressure-induced phase transitions, and equations of state for lanthanide trihydrides REH{sub 3} (RE=Sm, Gd, Tb, Dy, Ho, Er, Tm, and Lu) are systematically studied using ab initio calculations under a core state model (CSM). The obtained ground-state parameters, such as lattice constants and bulk modulus, agree well with the available data. Among the P6{sub 3}/mm, P3-bar c1, and P6{sub 3}cm structures, the P6{sub 3}cm structure is found to be the most stable structure for lanthanide trihydride via the comparison of the calculated total energies. With the help of Birch-Murnaghan equation of state, the structural transitions from hexagonal to cubic for REH{sub 3} (RE=Sm, Gd, Ho, Er, and Lu) under pressure are affirmed; especially, the similar behavior of REH{sub 3} (RE= Tb, Dy, and Tm) is reasonably predicted for the first time by this means. For the transitions, the repulsive interactions of H-H atoms may play an important role in terms of the analysis of the structures in the vicinity of the theoretical phase transition.

Ordered perovskites with cationic vacancies. 9. Compounds of the type Sr/sub 2/Srsub(1/4)Bsub(1/2)sup(III)vacantsub(1/4)WO/sub 6/ equivalent to Sr/sub 8/SrB/sub 2/sup(III)vacantW/sub 4/O/sub 24/ (Bsup(III) = La, Pr, Nd, Sm - Tm, Y)

Energy Technology Data Exchange (ETDEWEB)

Kemmler-Sack, S; Ehmann, A [Tuebingen Univ. (Germany, F.R.). Lehrstuhl fuer Anorganische Chemie 2

1981-08-01

The compounds Sr/sub 2/Srsub(1/4)Bsub(1/2)sup(III)vacantsub(1/4)WO/sub 6/ equivalent to Sr/sub 8/SrB/sub 2/sup(III)vacantW/sub 4/O/sub 24/ belong to the group of perovskites with octahedral cationic vacancies (cation/vacancy ratio (CN 6) = 7:1). For the larger Bsup(III) ions (La, Pr, Nd, Sm-Dy) different ordering effects are observed. The perovskites with Bsup(III) = Sm, Eu, Gd are polymorphic too (HT modification: higher ordered cubic perovskite (Bsup(III) = Gd: a = 2 x 8.23/sub 4/ A); LT modification: hexagonal perovskite stacking polytype (Bsup(III) = Gd: a = 9.95/sub 4/ A; c = 19.0/sub 4/ A)). With the smaller Bsup(III) ions (Ho, Er, Tm and Y) a cubic, 1:1 ordered perovskite type is observed.

Radiochemical separations of target-like reaction products from Au-, Pt-, and Th-targets after irradiation with GeV protons

International Nuclear Information System (INIS)

Szweryn, B.; Bruechle, W.; Schausten, B.; Schaedel, M.

1988-08-01

Chemical separation procedures for separations of reaction products after spallation reactions with 2.6 GeV protons and heavy element targets are presented. To determine independent cross sections of individual isotopes the elements Au, Pt, Ir, Os, Re, W, Ta, Hf, (Lu, Yb, Tm, Er), (Gd, Eu, Sm), were separated from gold targets, Pt, Ir, Os, W, Ta, Hf, (Lu, Yb, Tm, Er), (Gd, Eu, Sm) from a platinum target and Au, Tl from a thorium target. (orig.)

Spin-glass-like behaviour in IrSr2RECu2O8 (RE=Sm and Eu)

International Nuclear Information System (INIS)

Santos-Garcia, A.J. dos; Duijn, J. van; Alario-Franco, M.A.

2008-01-01

We report the results of magnetic and specific heat measurements on the 1212-type compounds IrSr 2 RECu 2 O 8 with RE=Sm and Eu, prepared by high-pressure and high-temperature synthesis. The magnetic susceptibility of these compounds shows a large difference in the temperature dependence of the magnetization measured under zero-field-cooled and field-cooled conditions below 87 and 71 K, respectively, and upon further cooling below ∼10 K substantial maxima are observed too. Further AC susceptibility measurements support a glassy behaviour in lower magnetic transitions whereas the specific heat measurements do not show the typical long-range ordering commonly displayed in ferro, ferri or antiferromagnetic transitions. Hysteresis loops suggest the presence of magnetic clusters in the otherwise paramagnetic zone, indicating that these compounds probably display a reentrant spin-glass transition. Results are presented and discussed. - Graphical abstract: IrSr 2 RECu 2 O 8 with RE=Sm and Eu were prepared by high-pressure and high-temperature synthesis. Both samples adopt a M-1212-type perovskite structure and a microdomain texturing of the long c-axis is observed by TEM. A very interesting magnetic behaviour is observed in these materials. A 'cluster by cluster freezing' model is proposed, instead of the classical individual spin freezing one to explain the spin-glass-like behaviour that seems to coexist with weak ferromagnetism in both compounds

Investigation of Sm(3) and Eu(3) coordination compounds with pyrazolones by IR spectroscopy method

International Nuclear Information System (INIS)

Panyushkin, V.T.; Grishenko, T.V.; Afanas'ev, Yu.A.; Garnovskij, A.D.; Osipov, O.A.

1978-01-01

The synthesis is described of the coordination nitrate compounds of Sm(3) and Eu(3) with pyrazolones: 4-aminoantipyrine (A), 1-ethylpyridyl- 3-phenyl-pyrazolone-5(B); 1-(3'-ethylpyridyl)-3(phenylamine-n)-pyrazolone-5(C). It has been determined by the infrared spectroscopy method that exocyclic oxygen atom is the place of coordination bond localization in the pentioned compounds. The infrared spectra analysis of complexes in the 1700-1800 cm -1 region makes it possible to mention bidentate character of NO 3 -groups in the studied complex compounds

Synthesis and luminescent properties of Eu{sup 3+}-activated Na{sub 0.5}Gd{sub 0.5}MoO{sub 4}: A strong red-emitting phosphor for LED and FED applications

Energy Technology Data Exchange (ETDEWEB)

Du, Peng; Yu, Jae Su, E-mail: jsyu@khu.ac.kr

2016-11-15

A series of Eu{sup 3+}-activated Na{sub 0.5}Gd{sub 0.5}MoO{sub 4} phosphors were prepared by a typical sol–gel method. The as-prepared samples possessed a single tetragonal phase and consisted of closely-packed particles. Under the excitation of 395 nm, all the phosphors exhibited the characteristic emissions of Eu{sup 3+} ions corresponding to the {sup 5}D{sub 0}→ {sup 7}F{sub J} transitions. The photoluminescence (PL) emission intensities were enhanced with the increment of Eu{sup 3+} ion concentration and the optimum doping concentration was 0.25 mol. The energy transfer mechanism between the Eu{sup 3+} ions was dominated by dipole–dipole interaction and the critical distance was found to be 8.45 Å. Furthermore, the temperature-dependent PL emission spectra suggested that the obtained phosphors had good thermal stability (60.4% of the initial intensity at 150 °C). In addition, the color purity, chromatic and cathodoluminescence (CL) properties of the Na{sub 0.5}Gd{sub 0.5}MoO{sub 4}:0.25Eu{sup 3+} phosphor were also investigated. The results indicated that the Eu{sup 3+}-activated Na{sub 0.5}Gd{sub 0.5}MoO{sub 4} phosphors with excellent PL and CL properties may have potential applications in white light-emitting diodes and field-emission displays.

Magnetism and superconductivity in Ru{sub 1-x}Sr{sub 2}RECu{sub 2+x}O{sub 8-d} (RE=Gd, Eu) and RuSr{sub 2}Gd{sub 1-y}Ce{sub y}Cu{sub 2}O{sub 8} compounds

Energy Technology Data Exchange (ETDEWEB)

Klamut, P.W. [Dept. of Physics, Northern Illinois Univ., DeKalb, IL (United States)]|[Inst. of Low Temperature and Structure Research of Polish Academy of Sciences, Wroclaw (Poland); Dabrowski, B.; Mini, S.M.; Kolesnik, S.; Maxwell, M.; Mais, J. [Dept. of Physics, Northern Illinois Univ., DeKalb, IL (United States); Shengelaya, A.; Keller, H. [Physik-Inst., Univ. Zuerich, Zuerich (Switzerland); Khazanov, R. [Physik-Inst., Univ. Zuerich, Zuerich (Switzerland)]|[Lab. for Muon-Spin Spectroscopy, Paul Scherrer Inst., Villigen PSI (Switzerland); Savic, I. [Physik-Inst., Univ. Zuerich, Zuerich (Switzerland)]|[Faculty of Physics, Univ. of Belgrade, Belgrade (Yugoslavia); Sulkowski, C.; Wlosewicz, D.; Matusiak, M. [Inst. of Low Temperature and Structure Research of Polish Academy of Sciences, Wroclaw (Poland); Wisniewski, A.; Puzniak, R.; Fita, I. [Inst. of Physics of Polish Academy of Sciences, Warszawa (Poland)

2002-07-01

We discuss the properties of new superconducting compositions of ruthenocuprates Ru{sub 1-x}Sr{sub 2}RECu{sub 2+x}O{sub 8-d} (RE=Gd, Eu) that were synthesized at 600 atm. of oxygen at 1080 C. By changing ratio between the Ru and Cu, the temperature of superconducting transition (T{sub C}) raises up to T{sub C}{sup max} = 72 K for x=0.3, 0.4. The hole doping achieved along the series increases with Cu{yields}Ru substitution. For x {ne} 0, T{sub C} can be subsequently tuned between T{sub C}{sup max} and 0 K by changing oxygen content in the compounds. The magnetic characteristics of the RE=Gd and Eu based compounds are interpreted as indicative of constrained dimensionality of the superconducting phase. Muon spin rotation experiments reveal the presence of the magnetic transitions at low temperatures (T{sub m}=14-2 K for x=0.1-0.4) that can originate in the response of Ru/Cu sublattice. RuSr{sub 2}Gd{sub 1-y}Ce{sub 1-y}Cu{sub 2}O{sub 8} (0 {<=} y {<=} 0.1) compounds show the simultaneous increase of T{sub N} and decrease of T{sub C} with y. The effect should be explained by the electron doping that occurs with Ce{yields}Gd substitution. Properties of these two series allow us to propose phase diagram for 1212-type ruthenocuprates that links their properties to the hole doping achieved in the systems. Non-superconducting single-phase RuSr{sub 2}GdCu{sub 2}O{sub 8} and RuSr{sub 2}EuCu{sub 2}O{sub 8} are reported and discussed in the context of the properties of substituted compounds. (orig.)

Electric and magnetic properties of Al{sub 86}Ni{sub 8}R{sub 6} (R=Sm, Gd, Ho) alloys in liquid and amorphous states

Energy Technology Data Exchange (ETDEWEB)

Sidorov, V. [Ural State Pedagogical University, Ekaterinburg (Russian Federation); Ural Federal University, Ekaterinburg (Russian Federation); Svec, P.; Svec, P.; Janickovic, D. [Institute of Physics SAS, Bratislava (Slovakia); Mikhailov, V. [Ural State Pedagogical University, Ekaterinburg (Russian Federation); Sidorova, E. [Plekhanov Russian University of Economics, Moscow (Russian Federation); Son, L. [Ural State Pedagogical University, Ekaterinburg (Russian Federation); Ural Federal University, Ekaterinburg (Russian Federation)

2016-06-15

Electrical resistivity and magnetic susceptibility of Al{sub 86}Ni{sub 8}Sm{sub 6}, Al{sub 86}Ni{sub 8}Gd{sub 6} and Al{sub 86}Ni{sub 8}Ho{sub 6} alloys are studied in a wide temperature range including amorphous, crystalline and liquid states. The negative value of resistivity temperature coefficient in amorphous ribbons is explained by the structural separation starting much before the beginning of their crystallization. The effective magnetic moments per Gd and Ho atoms are found to be essentially lower than for R{sup 3+} ions. The results are discussed in supposition of directed bonds between rare earth and aluminum atoms. - Highlights: • Electric and magnetic properties of Al{sub 86}Ni{sub 8}R{sub 6} alloys are studied experimentally. • The negative value of rtc in amorphous ribbons is explained. • The effective magnetic moments per Gd and Ho are found to be lower than for R{sup 3+} ions.

Evaluation of luminescent properties and detection of Eu{sup 2}+ in nano structured particles of Gd{sub 2}-x Eu{sub x}O{sub 3} system (x= 0.05, 0.10 and 0.30); Evaluacion de las propiedades luminiscentes y deteccion de Eu{sup 2}+ en particulas nanoestructuradas del sistema Gd{sub 2}-xEu{sub x} O{sub 3} (x= 0.05, 0.10 y 0.30)

Energy Technology Data Exchange (ETDEWEB)

Barroso, J.; Mena, I.; Gomez, L. S.; Milosevic, O.; Rabanal, M. E.

2012-11-01

Spray Pyrolysis (SP) is performed at 700 degree centigrade in dry air atmosphere using common nitrate aqueous solutions (0,1M) as precursor in order to obtain nano structured particles with the composition Gd{sub 2}-xEu{sub x}O{sub 3} (x= 0.05, 0.10 and 0.30). In this work, three samples with different atomic europium concentration (1, 2 and 6%) were studied. After, the obtained particles were subjected to different thermal treatments with varying temperatures between 800 and 1000 degree centigrade/12 h in dry air atmosphere. The obtained particles were characterized by XRD, SEM techniques, laser dispersion and steady state fluorescence spectroscopy. The existence of two cubic phases with different symmetry cubic phases (Ia-3, Fm-3m) was identified within the as-prepared samples. Moreover, the presence of Gd{sub 2}O{sub 3} monoclinic phase (C{sub 2}/m) which disappears during the thermal treatments was proved. In all thermally treated samples, it was observed the stabilization of an only Ia-3 phase. Fluorescence emission measurements in all studied samples the presence of Eu{sup 2}+ ({lambda}= 430nm), whose intensity increases as long as the content of the monoclinic phase decreases of the Eu{sup 3}+ percentage. (Author) 35 refs.

Thermoelectric properties, crystal and electronic structure of semiconducting RECuSe{sub 2} (RE = Pr, Sm, Gd, Dy and Er)

Energy Technology Data Exchange (ETDEWEB)

Esmaeili, Mehdi [Department of Chemistry and Chemical Biology, McMaster University, 1280 Main Street West, Hamilton, Ontario L8S 4M1 (Canada); Tseng, Yu-Chih [CANMET Materials, Natural Resources Canada, 183 Longwood Road South, Hamilton, Ontario L8P 0A5 (Canada); Mozharivskyj, Yurij, E-mail: mozhar@mcmaster.ca [Department of Chemistry and Chemical Biology, McMaster University, 1280 Main Street West, Hamilton, Ontario L8S 4M1 (Canada)

2014-10-15

Highlights: • Crystal and electronic structure of monoclinic and trigonal RECuSe{sub 2} phases. • Thermoelectric properties of the RECuSe{sub 2} phases. • Temperature stability of the RECuSe{sub 2} phases. - Abstract: The ternary RECuSe{sub 2} phases have been prepared and structurally characterized. They adopt either a monoclinic structure (P2{sub 1}/c, z = 4) for lighter rare earths (RE = Pr, Sm and Gd) or Cu-disordered trigonal structure for heavier rare-earths (P3{sup ¯}m1, z = 1, RE = Dy and Er). The resistivity and Seebeck coefficient measurements on GdCuSe{sub 2}, DyCuSe{sub 2} and ErCuSe{sub 2} indicate that the studied phases are p-type semiconductors with relatively small activation energies (0.045–0.11 eV). However, their electrical resistivities are too high (0.45–220 Ω cm at room temperature) to make them competitive thermoelectric materials. Electronic structure calculations indicate presence of a band gap in the RECuSe{sub 2} phases.

Study of the high pressure effect on nanoparticles GdVO4: Eu3+ optical properties

Science.gov (United States)

Jovanić, B. R.; Bettinelli, M.; Piccinelli, F.; Radenković, B.; Despotović-Zrakić, M.; Bogdanović, Z.

2015-07-01

This study considers the effects of hydrostatic pressure on the line position and fluorescence lifetime τ for 5D0 → 7F2 transitions in GdVO4: Eu3+ nanocrystals. The results indicate that the pressure induced the red shift toward longer wavelengths for all the considered lines with different rate. The fluorescence lifetime τ nonlinearly decreases with pressure in the considered pressure range. High pressure induced the fluorescence lifetime τ that can be explained with a simple theoretical model. The measured line position and τ are in a satisfactory agreement with the theoretical calculations.

Platinum triangles in the Pt/Al framework of the intermetallic REPt6Al3 (RE = Ce-Nd, Sm, Gd, Tb) series

International Nuclear Information System (INIS)

Eustermann, Fabian; Stegemann, Frank; Renner, Konstantin; Janka, Oliver

2017-01-01

The compounds of the REPt 6 Al 3 series (RE = Ce-Nd, Sm, Gd, Tb) were obtained by reaction of the elements via arc-melting. They were characterized by powder and single-crystal X-ray diffraction (NdPt 6 Al 3 : wR = 0.0432, 759 F 2 values, 33 variables) as well as by magnetic susceptibility measurements. The isostructural compounds crystallize with a new structure type in the trigonal crystal system with space group R anti 3c, twelve formula units in the unit cell, and lattice parameters of a = 752-755 and c = 3882-3945 pm. The crystal structure can be described by different slabs stacked along [001]. One layer features Pt 3 triangles, centering the cavities of a flat honeycomb RE layer that are arranged in a..ABCA ' B ' C ' .. sequence. The other layer consists of condensed hexagonal [Pt 6 Al 6 ] prisms, centered by Pt atoms, separating the before mentioned slabs. Magnetic measurements revealed that all rare-earth atoms are in the trivalent oxidation state, however, due to the low lanthanoide content magnetic ordering phenomena were observed only at low temperatures [SmPt 6 Al 3 : T C = 5.0(1) K; GdPt 6 Al 3 : T C = 7.3(1) K; TbPt 6 Al 3 : T N = 3.6(1) K]. (copyright 2017 WILEY-VCH Verlag GmbH and Co. KGaA, Weinheim)

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)

Use of dispersive liquid-liquid microextraction for simultaneous preconcentration of samarium, europium, gadolinium and dysprosium

International Nuclear Information System (INIS)

Mallah, M.H.; Atomic Energy Organization of Iran, Tehran; Shemirani, F.; Ghannadi Maragheh, M.

2008-01-01

A new preconcentration method of dispersive liquid-liquid microextraction (DLLME) was developed for simultaneous preconcentration of samarium, europium, gadolinium and dysprosium. DLLME technique was successfully used as a sample preparation method. In this preconcentration method, an appropriate mixture of extraction solvent, disperser solvent was injected rapidly into an aqueous solution containing Sm, Eu, Gd and Dy after complex formation using chelating reagent of the 1-(2-pyridylazo)-2-naphthol (PAN). After phase separation, 0.5 mL of the settled phase containing enriched analytes was determined by inductively coupled plasma optical emission spectrometry (ICP-OES). The main factors affected the preconcentration of Sm, Eu, Gd and Dy were extraction and dispersive solvent type and their volume, extraction time, volume of chelating agent (PAN), centrifuge speed and drying temperature of the samples. Under the best operating condition simultaneous preconcentration factors of 80, 100, 103 and 78 were obtained for Sm, Eu, Gd and Dy, respectively. (author)

First-principles calculation of structural and energetic properties for A2Ti2O7 (A = Lu, Er, Y, Gd, Sm, Nd, La)

International Nuclear Information System (INIS)

Zhang, Z.L.; Xiao, H.Y.; Zu, Xiaotao T.; Gao, Fei; Weber, William J.

2009-01-01

A first-principles method has been employed to investigate the structural and energetic properties for A2Ti2O7 (A = Lu, Er, Y, Gd, Sm, Nd, La), including the formation energies of the cation antisite-pair, the anion Frenkel pair that defines anion-disorder, and the coupled cation antisite-pair/anion-Frenkel. It is proposed that the interaction may have more significant influence on the radiation resistance behavior of titanate pyrochlores, although the interactions are relatively much stronger than the interactions. It is found that the defect formation energies are not simple functions of the A-site cation radii. The formation energy of the cation antisite-pair increases continuously as the A-site cation varies from Lu to Gd, and then decreases continuously with the variation of the A-site cation from Gd to La, in excellent agreement with the radiation-resistance trend of the titanate pyrochlores. The band gaps in these pyrochlores were also measured, and the band gap widths changed continuously with cation radius.

Multifunctional Eu3+- and Er3+/Yb3+-doped GdVO4 nanoparticles synthesized by reverse micelle method

OpenAIRE

Gavrilović, Tamara V.; Jovanović, Dragana J.; Lojpur, Vesna; Dramićanin, Miroslav D.

2014-01-01

Synthesis of Eu3+- and Er3+/Yb3+-doped GdVO4 nanoparticles in reverse micelles and their multifunctional luminescence properties are presented. Using cyclohexane, Triton X-100, and n-pentanol as the oil, surfactant, and co-surfactant, respectively, crystalline nanoparticles with ~4 nm diameter are prepared at low temperatures. The particle size assessed using transmission electron microscopy is similar to the crystallite size obtained from X-ray diffraction measurements, suggesting that each ...

MBO3: Eu3+ at the rate SiO2 (M = Y, Gd and Al) nano down conversion phosphors with superior asymmetric ratio and colour purity as spectral converters for c-Si solar cells

International Nuclear Information System (INIS)

Rambabu, U.; Munirathnam, N.R.; Prakash, T.L.

2013-01-01

Y 1-x BO 3 :Eu x 3+ (0.07 ≤ x ≤ 0.5 mol) and Y 0.72x (Gd x , Al x )BO 3 : Eu 3+ 0.3 (0.05 ± x ± 0.3 mol) powder phosphors have been synthesized by a novel co-precipitation technique followed by heat treatment. Luminescence optimization was done: by optimizing the dopant Eu 3+ -concentration, substitution of Y 3+ with Gd 3+ /Al 3+ and finally with SiO 2 shell coating. Due to nanosize particle distribution, the optimum activator (Eu 3+ ) concentration (30 mol %) was found to be extremely at higher level, compared to the bulk phosphors. The asymmetric ratio (Red/Orange) and color purity of the optimized phosphors, Y 0.7 BO 3 :Eu 0.3 3+ (with crystallite size, D = 32 nm) and Y 0.3 Gd 0.2 Al 0.2 BO 3 :Eu 3+ (D = 17 nm) were further enhanced with SiO 2 shell coating. Based on the systematic study, the nanophosphor Y 0.7 BO 3 :Eu 0.3 3+ at the rate SiO 2 with R/O ratio as 6.710 and color coordinates (x = 0.6612, y = 0.3357) was optimized as a remarkable phosphor having superior features for its application in thin transparent form as DC layer to improve the energy conversion efficiency of c-Si solar cells

ALnS2:RE (A=K, Rb; Ln=La, Gd, Lu, Y): New optical materials family

International Nuclear Information System (INIS)

Jarý, V.; Havlák, L.; Bárta, J.; Mihóková, E.; Buryi, M.; Nikl, M.

2016-01-01

In the presented review paper, new potentially interesting material family, RE-doped ternary sulfides ALnS 2 (RE=Ce, Pr, Sm, Eu, Tb, Tm; A=Rb, K; Ln=La, Gd, Lu, Y) is discussed. Their synthesis is described and the structural and optical properties, characterized by methods of X-ray diffraction, time-resolved luminescence spectroscopy and electron paramagnetic resonance, are summarized and reviewed especially with respect to the influence of their composition. All samples discussed were synthesized in the form of transparent crystalline hexagonal platelets by chemical reaction under the flow of hydrogen sulfide. Their luminescence characteristics, including absorption, radioluminescence, photoluminescence excitation and emission spectra and decay kinetics, were measured and evaluated in a broad temperature (8–800 K) and concentration (0.002–20% of dopants) range. The application potential of mentioned compounds in the field of white LED solid state lightings or X-ray phosphors is thoroughly discussed. - Highlights: • RE-doped ALnS 2 (A=K, Rb; Ln=La, Gd, Lu, Y) were synthesized. • Their optical characteristics are summarized. • Concentration and temperature dependences of luminescence features investigated. • EPR technique is employed to explain Eu 2+ incorporation into KLuS 2 host. • The application potential in white LED and X-ray phosphors is discussed.

Charge disproportionation in (X0.6Sr0.4)0.99Fe0.8Co0.2O3-δ perovskites (X = La, Pr, Sm, Gd)

DEFF Research Database (Denmark)

Pedersen, Thomas; Saadi, Souheil; Nielsen, K.H.

2005-01-01

The change in crystal structure and the oxidation state in iron of iron-cobalt-based perovskites with different A-site cations is investigated by the use of powder XRD and Mossbauer spectroscopy. The perovskites investigated are (X0.6Sr0.4)(0.99)Fe0.8Co0.2O3-delta, where X is La, Pr, Sm or Gd...

A new series of rhenium VII compounds: sodium-rare earth perrhenates

International Nuclear Information System (INIS)

Slimane, Z.A.A.; Silvestre, J.-P.; Freundlich, William

1978-01-01

Synthesis by solid state reaction or in aqueous solution and radiocrystallographical study of the hexagonal sodium-rare earth perrhenates NaLn(ReO 4 ) 4 (Ln=La, Nd, Sm, Eu, Gd, Er) and of the tetragonal tetrahydrates NaLn(ReO 4 ) 4 , 4H 2 O (Ln=Eu, Gd, Er, Lu) [fr

Linear optical properties of Ca4EuO(BO3)3 and Eu3+ : Ca4GdO(BO3)3 crystals

International Nuclear Information System (INIS)

Antic-Fidancev, E.; Lemaitre-Blaise, M.; Porcher, P.; Caramanian, A.; Aka, G.

1998-01-01

Full text: The title compounds are now intensively studied due to their quadratic nonlinear properties in view of applications, e.g. high power laser frequency conversion. Rare earth calcium oxoborates, Ca 4 REO(BO 3 ) 3 , constitute an isostructural family along the rare earth series with RE = La - Lu, Y included. These compounds crystallize in the monoclinic biaxial crystal system with Cm (N 8) space group. They are isostructural to the calcium fluoroborate Ca 5 (BO 3 ) 3 F which is related to the fluoroapatite structure Ca 5 (PO 4 ) 3 F. The rare earth ions are located in the distorted octahedron with C s point site symmetry in the mirror plane. Two types of distorted octahedral sites exist for calcium ions. The existence of some disorder between calcium and rare earth atoms is suspected from the structural analysis. Good optical quality crystals of europium (or gadolinium) oxoborate, EuCOB (GdCOB) have been grown from the stoichiometric melt by the Czochralski pulling method. From the luminescence of the Eu 3+ doped gadolinium or in the europium stoichiometric compound very complex emission spectra have been obtained. It principally depends on the preparation method of studied samples: i) for a monocrystalline sample, a single phase with a single site is observed; ii) for a polycrystalline sample complex feature occurs. It is probably due to an expanded disorder between calcium and rare earth atoms. Practically, there is one principal site corresponding to the low symmetry site of the rare earth as expected from the structural investigation. Other minor sites are attributed to the local distortion created around the active rare earth ion. The intensity of the emission lines of Eu 3+ used as a local structural probe related to these minor sites increases when the gadolinium in Ca 4 GdO(BO 0 ) 3 is substituted by lanthanum or yttrium ions. It seems therefore evident that the synthesis of these rare earth calcium oxoborates must be realised carefully. The crystal

Synthesis, structures, and luminescent properties of sodium rare-earth metal(III) chloride oxotellurates(IV), Na{sub 2}Ln{sub 3}Cl{sub 3}[TeO{sub 3}]{sub 4} (Ln = Sm, Eu, Gd, Tb, Dy, and Ho)

Energy Technology Data Exchange (ETDEWEB)

Charkin, Dmitri O.; Dorofeev, Sergey G.; Berdonosov, Peter S.; Dolgikh, Valery A. [Department of Chemistry, Lomonosov Moscow State University (Russian Federation); Zitzer, Sabine; Greiner, Stefan; Schleid, Thomas [Institut fuer Anorganische Chemie, Universitaet Stuttgart (Germany); Olenev, Andrei V. [Department of Chemistry, Lomonosov Moscow State University (Russian Federation); Sine Theta Ltd., Moscow (Russian Federation)

2017-11-17

Six sodium rare-earth metal(III) chloride oxotellurates(IV), Na{sub 2}Ln{sub 3}Cl{sub 3}[TeO{sub 3}]{sub 4}, isostructural to Na{sub 2}Y{sub 3}Cl{sub 3}[TeO{sub 3}]{sub 4}, were synthesized by flux techniques and characterized by single-crystal XRD. The compounds crystallize in the monoclinic space group C2/c with lattice constants a = 23.967(1), b = 5.6342(3), c = 16.952(1) Aa, β = 134.456(5) for Ln = Sm, a = 23.932(2), b = 5.6044(5), c = 17.134(1) Aa, β = 135.151(6) for Ln = Eu, a = 23.928(1), b = 5.5928(1), c = 17.1133(8) Aa, β = 135.366(3) for Ln = Gd, a = 23.907(1), b = 5.569(3), c = 16.745(1) Aa, β = 134.205(3) for Ln = Tb, a = 23.870(1), b = 5.547(3), c = 16.665(1) Aa, β = 134.102(3) for Ln = Dy, and a = 23.814(1), b = 5.526(3), c = 16.626(1) Aa, β = 134.016(3) for Ln = Ho and Z = 4. Their crystal structure can be considered as a framework built of intergrowing Ln-O and Na-(O,Cl) slabs with channel walls decorated by tellurium atoms of [TeO{sub 3}]{sup 2-} groups. The luminescent properties of the new compounds due to the Ln{sup 3+} cations are described and discussed. We also discuss the crystal chemistry of various alkali-metal rare-earth metal(III) halide oxochalcogenates(IV). (copyright 2017 WILEY-VCH Verlag GmbH and Co. KGaA, Weinheim)

Characterization and luminescent properties of Eu{sup 3+} doped Gd{sub 2}Zr{sub 2}O{sub 7} nanopowders

Energy Technology Data Exchange (ETDEWEB)

Rabasovic, M.S., E-mail: majap@ipb.ac.rs [Institute of Physics, University of Belgrade (Serbia); Sevic, D. [Institute of Physics, University of Belgrade (Serbia); Krizan, J. [Faculty for Mechanical Engineering, University of Ljubljana (Slovenia); Terzic, M. [Faculty of Science, University of Novi Sad (Serbia); Mozina, J. [Faculty for Mechanical Engineering, University of Ljubljana (Slovenia); Marinkovic, B.P.; Savic-Sevic, S. [Institute of Physics, University of Belgrade (Serbia); Mitric, M. [Vinča Institute of Nuclear Science, University of Belgrade, P.O. Box 522, 11001 Belgrade (Serbia); Rabasovic, M.D.; Romcevic, N. [Institute of Physics, University of Belgrade (Serbia)

2015-02-15

Highlights: • Nanopowders Gd{sub 2}Zr{sub 2}O{sub 7} doped by europium ions (Eu{sup 3+}) have been synthesized. • Their luminescence properties have been measured at room temperature. • The temporal evolution of laser induced phenomena are presented using time-resolved technique. • Lifetime analysis for luminescence bands in emission spectra has been done. - Abstract: Nanopowders based on gadolinium zirconium oxide (Gd{sub 2}Zr{sub 2}O{sub 7}) doped by europium ions (Eu{sup 3+}) were successfully prepared using a flame combustion method. This material is suitable for various optical devices. The structure of prepared materials has been confirmed and characterized using X-ray powder diffraction (XRD), scanning electron microscope (SEM) and photoluminescence (PL) techniques. The luminescence properties of synthesized nanopowders were characterized by emission spectra and luminescence lifetimes by using the streak camera system. PL spectra were obtained at three different excitation wavelengths (Optical Parametric Oscilator (OPO) at 360 nm, laser diode at 365 nm and Ar laser line at 514.5 nm). The strong emission lines at 611 nm and 630 nm corresponding to the {sup 5}D{sub 0} → {sup 7}F{sub 2} long lived transition could be used as a new red light source in optical devices.

Deposition of silica protected luminescent layers of Eu:GdVO_4 nanoparticles assisted by atmospheric pressure plasma jet

International Nuclear Information System (INIS)

Moretti, Elisa; Pizzol, Giorgia; Fantin, Marina; Enrichi, Francesco; Scopece, Paolo; Nuñez, Nuria O.; Ocaña, Manuel; Benedetti, Alvise; Polizzi, Stefano

2016-01-01

Eu:GdVO_4 nanophosphors with an average size of 60 nm, synthesized by a facile solvothermal method, were deposited on monocrystalline silicon wafers by a spray-coating technique with artworks anti-counterfeiting applications in mind. Atmospheric pressure plasma jet (APPJ) was used to deposit a silica-based layer on top of the nanometric luminescent layer, in order to improve its adhesion to the substrate and to protect it from the environment. The nanophosphors were characterized by X-ray diffraction (XRD) and transmission electron microscopy (TEM). Coating composition was investigated by Fourier transform infrared spectroscopy (FT-IR) and its morphology was characterized by scanning electron microscopy (FEG-SEM). The film thickness was evaluated by means of ellipsometry and adhesion was estimated by a peeling test. Luminescent properties of the nanophosphors deposited and fixed on silicon wafers were also measured. The whole layer resulted well-adhered to the silicon substrate, transparent and undetectable in the presence of visible light, but easily activated by UV light source. - Highlights: • Luminescent films were obtained by spray deposition of Eu:GdVO_4 nanophosphors. • Plasma jet deposition of SiO_2 fixed the nanophosphors on the substrate. • Optical properties of nanophosphors were preserved after deposition-fixing process. • Films well-adhered to the substrate, even after a scotch tape peeling test and a scratch test.

Ln28Ti2O7 (Ln = La, Nd, Sm, Gd): a novel series of defective Ruddlesden–Popper phases formed by topotactic dehydration of HLnTiO4

OpenAIRE

Thangadurai, V; Subbanna, GN; Gopalakrishnan, J

1998-01-01

Topotactic dehydration of HLnTiO4 (Ln = La, Nd, Sm or Gd) around 480–500 °C yields a new series of metastable layered perovskite oxides, Ln28Ti2O7, that possess a defective Sr3Ti2O7 structure, where the cubooctahedral sites within the double-perovskite layers are most likely vacant.

Synthesis, structural characterization, luminescent properties and theoretical study of three novel lanthanide metal-organic frameworks of Ho(III), Gd(III) and Eu(III) with 2,5-thiophenedicarboxylate anion

Energy Technology Data Exchange (ETDEWEB)

Marques, Lippy F. [Instituto de Química, Universidade do Estado do Rio de Janeiro, Rio de Janeiro 20550-013 (Brazil); Correa, Charlane C. [Departamento de Química-ICE, Universidade Federal de Juiz de Fora, Juiz de Fora-MG, 36036-330 (Brazil); Ribeiro, Sidney J.L.; Santos, Molíria V. dos [Institute of Chemistry, São Paulo State University − UNESP, CP 355 Araraquara-SP 14801-970 Brazil (Brazil); Dutra, José Diogo L.; Freire, Ricardo O. [Pople Computational Chemistry Laboratory, Departamento de Química, Universidade Federal de Sergipe, São Cristóvão-SE 49100-000 (Brazil); Machado, Flávia C., E-mail: flavia.machado@ufjf.edu.br [Departamento de Química-ICE, Universidade Federal de Juiz de Fora, Juiz de Fora-MG, 36036-330 (Brazil)

2015-07-15

In this paper, the synthesis of three new metal-organic frameworks of lanthanides (LnMOFs) ([Ln{sub 2}(2,5-tdc){sub 3}(dmso){sub 2}]·H{sub 2}O){sub n} (Ln=Ho (1); Gd (2); Eu (3); 2,5-tdc=2,5-thiophenedicarboxylate anion; dmso=dimethylsulfoxide), and their complete characterization, including single crystal X-ray diffraction, FTIR spectroscopy and thermogravimetric analysis are reported. In especial, photophysical properties of Eu(III) complex have been studied in detail via both theoretical and experimental approaches. Crystal structure of (1) reveals that each lanthanide ion is seven-coordinated by oxygen atoms in an overall distorted capped trigonal – prismatic geometry. The 2,5-tdc{sup 2−} ligands connect four Ln(III) centers, adopting (κ{sup 1}–κ{sup 1})–(κ{sup 1}–κ{sup 1})–μ{sub 4} coordination mode, generating an 8-connected uninodal 3D network. In addition, theoretical studies for Eu(III) complex were performed using the Sparkle model for lanthanide complexes. - Graphical abstract: Three new metal-organic frameworks of lanthanides (LnMOFs) ([Ln{sub 2}(2,5-tdc){sub 3}(dmso){sub 2}]·H{sub 2}O){sub n} (Ln=Ho (1); Gd (2); Eu (3); 2,5-tdc=2,5-thiophenedicarboxylate anion; dmso=dimethylsulfoxide), were synthesized and their complete characterization, including single crystal X-ray diffraction, FTIR spectroscopy and thermogravimetric analysis are reported. In especial, photophysical properties of Eu(III) complex have been studied in detail via both theoretical and experimental approaches. - Highlights: • Three new LnMOFs were synthesized and fully characterized. • Ho{sup 3+}, Gd{sup 3+} and Eu{sup 3+} complexes photoluminescence properties were investigated. • Theoretical approaches for Eu{sup 3+} complex luminescence has been performed. • An energy level diagram is used to establish the ligand-to-metal energy transfer. • These metal−organic frameworks can act as light conversion molecular devices.

Phase transition of the orthorhombic fluorite-related compounds Ln{sub 3}IrO{sub 7} (Ln = Pr, Nd, Sm, Eu)

Energy Technology Data Exchange (ETDEWEB)

Hinatsu, Yukio, E-mail: hinatsu@sci.hokudai.ac.j [Division of Chemistry, Graduate School of Science, Hokkaido University, Sapporo 060-0810 (Japan); Doi, Yoshihiro; Nishimine, Hiroaki; Wakeshima, Makoto [Division of Chemistry, Graduate School of Science, Hokkaido University, Sapporo 060-0810 (Japan); Sato, Mineo [Department of Chemistry and Chemical Engineering, Faculty of Engineering, Niigata University, 8050 Ikarashi 2-nocho, Niigata 950-2181 (Japan)

2009-12-04

Rare earth iridium oxides Ln{sub 3}IrO{sub 7} (Ln = Pr, Nd, Sm, and Eu) were prepared and their structures were determined by X-ray diffraction measurements. At room temperature, Pr{sub 3}IrO{sub 7} crystallized in an orthorhombic superstructure of cubic fluorite with space group Cmcm. The differential thermal analysis (DTA) and specific heat measurements for Ln{sub 3}IrO{sub 7} (Ln = Pr, Nd, Sm, and Eu) showed a phase transition at 262, 342, 420, and 485 K, respectively. At low temperatures, Ln{sub 3}IrO{sub 7} crystallized in a monoclinic structure with the space group P2{sub 1}/n. The transition temperatures increased with decreasing the ionic radius of rare earths, which indicates that the transition is stress-induced and occurs with the lattice contraction on cooling. These results for Ln{sub 3}IrO{sub 7} were compared with the phase transitions observed for Ln{sub 3}MoO{sub 7}, Ln{sub 3}RuO{sub 7}, Ln{sub 3}ReO{sub 7}, and Ln{sub 3}OsO{sub 7}.

Nanostructured LnBaCo2O6− (Ln = Sm, Gd with layered structure for intermediate temperature solid oxide fuel cell cathodes

Directory of Open Access Journals (Sweden)

Augusto E. Mejía Gómez

2017-04-01

Full Text Available In this work, we present the combination of two characteristics that are beneficial for solid oxide fuel cell (SOFC cathodic performance in one material. We developed and evaluated for the first time nanostructured layered perovskites of formulae LnBaCo2O6-d with Ln = Sm and Gd (SBCO and GBCO, respectively as SOFC cathodes, finding promising electrochemical properties in the intermediate temperature range. We obtained those nanostructures by using porous templates to confine the chemical reagents in regions of 200-800 nm. The performance of nanostructured SBCO and GBCO cathodes was analyzed by electrochemical impedance spectroscopy technique under different operating conditions using Gd2O3-doped CeO2 as electrolyte. We found that SBCO cathodes displayed lower area-specific resistance than GBCO ones, because bulk diffusion of oxide ions is enhanced in the former. We also found that cathodes synthesized using smaller template pores exhibited better performance.

Zero-field splitting in the isoelectronic aqueous Gd(III) and Eu(II) complexes from a first principles analysis

Science.gov (United States)

Khan, S.; Peters, V.; Kowalewski, J.; Odelius, M.

2018-03-01

The zero-field splitting (ZFS) of the ground state octet in aqueous Eu(II) and Gd(III) solutions was investigated through multi- configurational quantum chemical calculations and ab initio molecular dynamics (AIMD) simulations. Investigation of the ZFS of the lanthanide ions is essential to understand the electron spin dynamics and nuclear spin relaxation around paramagnetic ions and consequently the mechanisms underlying applications like magnetic resonance imaging. We found by comparing clusters at identical geometries but different metallic centres that there is not a simple relationship for their ZFS, in spite of the complexes being isoelectronic - each containing 7 unpaired f electrons. Through sampling it was established that inclusion of the first hydration shell has a dominant (over 90 %) influence on the ZFS. Extended sampling of aqueous Gd(III) showed that the 2 nd order spin Hamiltonian formalism is valid and that the rhombic ZFS component is decisive.

Photoluminescence and cathodoluminescence properties of Sr{sub 2}Gd{sub 8}Si{sub 6}O{sub 26}:RE{sup 3+}(RE{sup 3+}=Tb{sup 3+}or Sm{sup 3+}) phosphors

Energy Technology Data Exchange (ETDEWEB)

Hussain, Sk. Khaja [Department of Electronics and Radio Engineering, Kyung Hee University, 1 Seocheon-dong, Giheung-gu, Yongin-si, Gyeonggi-do 446-701 (Korea, Republic of); Rao, Gattupalli Manikya [Department of Physics, College of Science and Technology, Andhra University, Visakhapatanam, Andhra Pradesh 53003 (India); Raju, G. Seeta Rama; Krishna Bharat, L. [Department of Electronics and Radio Engineering, Kyung Hee University, 1 Seocheon-dong, Giheung-gu, Yongin-si, Gyeonggi-do 446-701 (Korea, Republic of); Subba Rao, P.S.V., E-mail: raopsvs@rediffmail.com [Department of Physics, College of Science and Technology, Andhra University, Visakhapatanam, Andhra Pradesh 53003 (India); Yu, Jae Su, E-mail: jsyu@khu.ac.kr [Department of Electronics and Radio Engineering, Kyung Hee University, 1 Seocheon-dong, Giheung-gu, Yongin-si, Gyeonggi-do 446-701 (Korea, Republic of)

2016-10-15

Trivalent terbium (Tb{sup 3+}) or samarium (Sm{sup 3+}) ions individually activated green and orange emitting Sr{sub 2}Gd{sub 8}Si{sub 6}O{sub 26} (SGSO) phosphors were synthesized by a citrate sol–gel method. The X-ray diffraction patterns of SGSO:Tb{sup 3+} and SGSO:Sm{sup 3+} phosphors exhibited the characteristic diffraction peaks of oxyapatite in a hexagonal lattice structure. The photoluminescence (PL) properties at ultraviolet (UV) or near-UV excitation wavelengths were measured for Tb{sup 3+} or Sm{sup 3+} ions doped SGSO phosphors as a function of its respective concentration. The PL spectra of SGSO:Tb{sup 3+} phosphors revealed the characteristic emission peaks of both Gd{sup 3+} and Tb{sup 3+} ions which are associated with 4f–4f transitions under 274 nm of excitation wavelength. When the concentration of Tb{sup 3+} ions increased over 0.05 mol (5 mol%), the emission intensities of {sup 5}D{sub 3} transitions decreased due to the well-known cross-relaxation process. However, based on the intensities of {sup 5}D{sub 4} transitions, the optimum concentration of Tb{sup 3+} ions was found to be 0.05 mol. Under 404 nm of excitation wavelength, the SGSO:Sm{sup 3+} phosphors exhibited the characteristic orange emission at 600 nm due to the {sup 4}G{sub 5/2}→{sup 6}H{sub 7/2} electronic transition. The optimum concentration of SGSO:Sm{sup 3+} phosphors was found to be 0.02 mol. The decay curves of the optimized SGSO:Tb{sup 3+} and SGSO:Sm{sup 3+} phosphors were well fitted to single exponential functions and their lifetimes were calculated. Furthermore, the optimized phosphor samples showed good thermal stability. Likewise, cathodoluminescence properties were also studied for the optimized samples as a function of filament current and accelerating voltage. The Commission International de I-Eclairage chromaticity coordinates were calculated for the SGSO:Tb{sup 3+} and SGSO:Sm{sup 3+} phosphors.

Preparation and photophysical properties of luminescent nanoparticles based on lanthanide doped fluorides (LaF3:Ce3+, Gd3+, Eu3+), obtained in the presence of different surfactants

International Nuclear Information System (INIS)

Runowski, Marcin; Lis, Stefan

2014-01-01

Highlights: • Synthesis of nanocrystalline lanthanide fluorides doped with Eu 3+ ions. • Inorganic nanomaterials exhibiting bright red luminescence. • Luminescence enhancement by energy transfer (ET) from Ce 3+ → Gd 3+ to Eu 3+ ions. • Decreased agglomeration and morphology control using organic modifiers/surfactants. • Absolute and relative quantum yield (QY) comparison. - Abstract: A series of nanomaterials composed of LaF 3 :Ce 3+ 10%, Gd 3+ 30%, Eu 3+ 1% was synthesized via a facile co-precipitation approach. The reaction between appropriate lanthanide (Ln 3+ ) and fluoride ions resulted in the formation of crystalline, Ln 3+ doped fluorides and was performed in the presence of a series of organic modifiers, acting as surfactants and anti-agglomeration agents. Modifiers such as polyacrylic acid (PAA), ethylenediaminetetraacetic acid (EDTA), citric acid and oleylamine most significantly influenced the morphology and spectroscopic properties of the products. The product obtained in the presence of PAA was composed of the smallest nanoparticles (ca. 5–6 nm), with narrow size/shape distribution. All fluorides synthesized exhibited intensive, bright red luminescence under UV irradiation (λ ex ≈ 250 nm), because of the presence of Eu 3+ ions in their structure. The efficient intensity of luminescence was a result of indirect excitation, via energy transfer (ET) phenomena occurring in the system (Ce 3+ → Gd 3+ → Eu 3+ ). The structure and morphology of the obtained nanomaterials were established by powder X-ray Diffraction (XRD) and Transmission Electron Microscopy (TEM) measurements. Optical properties of the obtained compounds were studied and discussed on the basis of excitation emission spectra and luminescence decay curves. On the basis of the performed measurements, luminescence quantum yield (absolute and relative) and radiative lifetimes were calculated and analyzed. FT-IR spectroscopy was applied to examine the presence of molecules of

Field and sample history dependence of the compensation temperature in Sm0.97Gd0.03Al2

International Nuclear Information System (INIS)

Vaidya, U.V.; Rakhecha, V.C.; Sumithra, S.; Ramakrishnan, S.; Grover, A.K.

2007-01-01

We present magnetization data on three polycrystalline specimens of Sm 0.97 Gd 0.03 Al 2 : (1) as-cast (grainy texture), (2) powder, and (3) re-melted fast-quenched (plate). The data are presented for nominally zero- (ZFC) and high-field-cooling (HFC) histories. A zero cross-over in magnetization curve at some temperature T=T 0 was seen in ZFC data on grainy and powder samples, but not in the plate sample. At fields surpassing magnetocrystalline anisotropy, a 4f magnetic moment flip was still evidenced by HFC data in all samples at a compensation temperature T comp , which must necessarily be treated as distinct from T 0 (T 0 may not even exist). Proper understanding of T comp should take account of thermomagnetic history effects

Deposition of silica protected luminescent layers of Eu:GdVO{sub 4} nanoparticles assisted by atmospheric pressure plasma jet

Energy Technology Data Exchange (ETDEWEB)

Moretti, Elisa, E-mail: elisa.moretti@unive.it [Dipartimento di Scienze Molecolari e Nanosistemi, Università Ca' Foscari Venezia, INSTM Venice Research Unit, Via Torino 155/B, 30172 Mestre, Venezia (Italy); Pizzol, Giorgia [Dipartimento di Scienze Molecolari e Nanosistemi, Università Ca' Foscari Venezia, INSTM Venice Research Unit, Via Torino 155/B, 30172 Mestre, Venezia (Italy); Fantin, Marina; Enrichi, Francesco; Scopece, Paolo [Nanofab-Veneto Nanotech, Via delle Industrie 5, 30175 Marghera, Venezia (Italy); Nuñez, Nuria O.; Ocaña, Manuel [Instituto de Ciencia de Materiales de Sevilla, CSIC-US, Americo Vespucio 49, 41092, Isla de la Cartuja, Sevilla (Spain); Benedetti, Alvise [Dipartimento di Scienze Molecolari e Nanosistemi, Università Ca' Foscari Venezia, INSTM Venice Research Unit, Via Torino 155/B, 30172 Mestre, Venezia (Italy); Polizzi, Stefano [Dipartimento di Scienze Molecolari e Nanosistemi, Università Ca' Foscari Venezia, INSTM Venice Research Unit, Via Torino 155/B, 30172 Mestre, Venezia (Italy); Centro di Microscopia Elettronica “Giovanni Stevanato”, Università Ca' Foscari Venezia, Via Torino 155/B, 30172 Mestre, Venezia (Italy)

2016-01-01

Eu:GdVO{sub 4} nanophosphors with an average size of 60 nm, synthesized by a facile solvothermal method, were deposited on monocrystalline silicon wafers by a spray-coating technique with artworks anti-counterfeiting applications in mind. Atmospheric pressure plasma jet (APPJ) was used to deposit a silica-based layer on top of the nanometric luminescent layer, in order to improve its adhesion to the substrate and to protect it from the environment. The nanophosphors were characterized by X-ray diffraction (XRD) and transmission electron microscopy (TEM). Coating composition was investigated by Fourier transform infrared spectroscopy (FT-IR) and its morphology was characterized by scanning electron microscopy (FEG-SEM). The film thickness was evaluated by means of ellipsometry and adhesion was estimated by a peeling test. Luminescent properties of the nanophosphors deposited and fixed on silicon wafers were also measured. The whole layer resulted well-adhered to the silicon substrate, transparent and undetectable in the presence of visible light, but easily activated by UV light source. - Highlights: • Luminescent films were obtained by spray deposition of Eu:GdVO{sub 4} nanophosphors. • Plasma jet deposition of SiO{sub 2} fixed the nanophosphors on the substrate. • Optical properties of nanophosphors were preserved after deposition-fixing process. • Films well-adhered to the substrate, even after a scotch tape peeling test and a scratch test.

Magnetic and luminescent hybrid nanomaterial based on Fe{sub 3}O{sub 4} nanocrystals and GdPO{sub 4}:Eu{sup 3+} nanoneedles

Energy Technology Data Exchange (ETDEWEB)

Runowski, Marcin; Grzyb, Tomasz; Lis, Stefan, E-mail: blis@amu.edu.pl [Adam Mickiewicz University, Department of Rare Earths, Faculty of Chemistry (Poland)

2012-10-15

A bifunctional hybrid nanomaterial, which can show magnetic and luminescent properties, was obtained. A magnetic phase was synthesized as a core/shell type composite. Nanocrystalline magnetite, Fe{sub 3}O{sub 4} was used as the core and was encapsulated in a silica shell. The luminescent phase was GdPO{sub 4} doped with Eu{sup 3+} ions, as the emitter. The investigated materials were synthesized using a coprecipitation method. Encapsulated Fe{sub 3}O{sub 4} was 'trapped' in a nano-scaffold composed of GdPO{sub 4} crystalline nanoneedles. When an external magnetic field was applied, this hybrid composite was attracted in one direction. Also, the luminescent phase can move simultaneously with magnetite due to a 'trapping' effect. The structure and morphology of the obtained nanocomposites were examined with the use of transmission electron microscopy and X-ray powder diffraction. Spectroscopic properties of the Eu{sup 3+}-doped nanomaterials were studied by measuring their excitation and emission spectra as well as their luminescence decay times.Graphical Abstract.

X-ray spectroscopic and magnetic studies of RBaCo_2O_5_._5, R = Pr, Nd, Sm, Gd and Y

International Nuclear Information System (INIS)

Ganorkar, S.; Priolkar, K. R.; Sarode, P. R.; Emura, S.

2016-01-01

The structural and magnetic properties of layered perovskites of the type RBaCo_2O_5_+_δ with δ ≤0.5 (R=Pr, Nd, Sm, Gd and Y) have been investigated. The samples were prepared by the sol-gel method and characterized by X-ray diffraction, magnetization and X-ray absorption near edge structure (XANES) spectroscopy. It is found that the magnetic properties depend on the size of the rare-earth ion. The critical size of the rare-earth ion introduces structural distortion which affects the Co-O hybridization in these layered perovskites. The detailed analysis of experimental and calculated XANES spectra throws some light on spin states of Co ions in these perovskites.

Complexes of o-Vanillin oxime with La(III), Ce(III), Nd(III), Sm(III), Gd(III), Tb(III), Dy(III), Ho(III) and Yb(III)

International Nuclear Information System (INIS)

Dhar, M.L.; Gupta, V.K.; Singh, Onkar

1988-01-01

Ten complexes of lanthanides with o-vanillin oxime have been swynthesised and characterised. The composition of the complexes as determined by elemental and thermal analyses, infrared electronic spectral and magnetic moment studies is [Ln(C 8 H 8 NO 3 ) 3 .XH 2 O], where X=2 when Ln=La, Ce, Pr, Nd, Sm and X=3 when Ln=Gd, Dy, Tb, Ho, Yb; C 8 H 8 NO 3 - represents the anion of the ligand. (author). 16 refs., 2 figs., 2 tables

A novel fluorescent probe (dtpa-bis(cytosine)) for detection of Eu(III) in rare earth metal ions

Science.gov (United States)

Yang, Fan; Ren, Peipei; Liu, Guanhong; Song, Youtao; Bu, Naishun; Wang, Jun

2018-03-01

In this paper, a novel fluorescent probe, dtpa-bis(cytosine), was designed and synthesized for detecting europium (Eu3 +) ion. Upon addition of Eu3 + ions into the dtpa-bis(cytosine) solution, the fluorescence intensity can strongly be enhanced. Conversely, adding other rare earth metal ions, such as Y3 +, Ce3 +, Pr3 +, Nd3 +, Sm3 +, Gd3 +, Tb3 +, Dy3 +, Ho3 +, Er3 +, Yb3 + and Lu3 +, into dtpa-bis(cytosine) solution, the fluorescence intensity is decreased slightly. Some parameters affecting the fluorescence intensity of dtpa-bis(cytosine) solution in the presence of Eu3 + ions were investigated, including solution pH value, Eu3 + ion concentration and interfering substances. The detection mechanism of Eu3 + ion using dtpa-bis(cytosine) as fluorescent probe was proposed. Under optimum conditions, the fluorescence emission intensities of EuIII-dtpa-bis(cytosine) at 375 nm in the concentration range of 0.50 × 10- 5 mol • L- 1-5.00 × 10- 5 mol • L- 1 of Eu3 + ion display a better linear relationship. The limit of detection (LOD) was determined as 8.65 × 10- 7 mol • L- 1 and the corresponding correlation coefficient (R2) of the linear equation is 0.9807. It is wished that the proposed method could be applied for sensitively and selectively detecting Eu3 + ion.

Luminescent properties of complexly substituted oxides Ме2Ln8 (XO46O2 (Me=Sr, Ca; Ln=La, Gd, Eu; X= Si, P

Directory of Open Access Journals (Sweden)

A. A. Vasin

2014-11-01

Full Text Available In the current work it is established that the maximum intensity of a luminescence of crystalline phosphors with structure silicate-apatite of general formulae: Ca2Eu8Si6(1-xP6xO26, Sr2Gd7.2Eu0.8Si6(1-xP6xO26 and Ca2La8(1-xEu8xSi6O26 is reached at concentration of europium equal 0,15. The maximum intensity of a luminescence of these substances, at replacement in an anion sublattice of tetrahedrons [SiO4]4- on tetrahedrons [PO4]3- takes place at concentration of phosphorus 0,05.

Platinum triangles in the Pt/Al framework of the intermetallic REPt{sub 6}Al{sub 3} (RE = Ce-Nd, Sm, Gd, Tb) series

Energy Technology Data Exchange (ETDEWEB)

Eustermann, Fabian; Stegemann, Frank; Renner, Konstantin [Institut fuer Anorganische und Analytische Chemie, Westfaelische Wilhelms-Universitaet Muenster (Germany); Janka, Oliver [Institut fuer Anorganische und Analytische Chemie, Westfaelische Wilhelms-Universitaet Muenster (Germany); Institut fuer Chemie, Carl von Ossietzky Universitaet Oldenburg (Germany)

2017-12-13

The compounds of the REPt{sub 6}Al{sub 3} series (RE = Ce-Nd, Sm, Gd, Tb) were obtained by reaction of the elements via arc-melting. They were characterized by powder and single-crystal X-ray diffraction (NdPt{sub 6}Al{sub 3}: wR = 0.0432, 759 F{sup 2} values, 33 variables) as well as by magnetic susceptibility measurements. The isostructural compounds crystallize with a new structure type in the trigonal crystal system with space group R anti 3c, twelve formula units in the unit cell, and lattice parameters of a = 752-755 and c = 3882-3945 pm. The crystal structure can be described by different slabs stacked along [001]. One layer features Pt{sub 3} triangles, centering the cavities of a flat honeycomb RE layer that are arranged in a..ABCA{sup '}B{sup '}C{sup '}.. sequence. The other layer consists of condensed hexagonal [Pt{sub 6}Al{sub 6}] prisms, centered by Pt atoms, separating the before mentioned slabs. Magnetic measurements revealed that all rare-earth atoms are in the trivalent oxidation state, however, due to the low lanthanoide content magnetic ordering phenomena were observed only at low temperatures [SmPt{sub 6}Al{sub 3}: T{sub C} = 5.0(1) K; GdPt{sub 6}Al{sub 3}: T{sub C} = 7.3(1) K; TbPt{sub 6}Al{sub 3}: T{sub N} = 3.6(1) K]. (copyright 2017 WILEY-VCH Verlag GmbH and Co. KGaA, Weinheim)

Description and exploitation of benchmarks involving 149Sm, a fission product taking part of the burn up credit in spent fuels

International Nuclear Information System (INIS)

Anno, J.; Poullot, G.

1995-01-01

Up to now, there was no benchmark to validate the Fission Products (FPs) cross sections in criticality safety calculations. The protection and nuclear safety institute (IPSN) has begun an experimental program on 6 FPs ( 103 Rh, 133 Cs, 143 Nd, 149 Sm, 152 Sm, and 155 Gd daughter of 155 Eu) giving alone a decrease of reactivity equal to half the whole FPs in spent fuels (except Xe and I). Here are presented the experiments with the 149 Sm and the results obtained with the APOLLO I-MORET III calculations codes. 11 experiments are carried out in a zircaloy tank of 3.5 1 containing slightly nitric acid solutions of Samarium (96,9% in weight of 149S m) at 0.1048 -0.2148 - 0.6262 g/l concentrations. It was placed in the middle of arrays of UO 2 rods (4.742 % U5 weight %) at square pitch of 13 mm. The underwater height of the rods is the critical parameter. In addition, 7 experiments were performed with the same apparatus with water and boron proving a good experimental representativeness and a good accuracy of the calculations. As the reactivity worth of the Sm tank is between 2000 and 6000 10 -5 , the benchmarks are well representative and the cumulative absorption ratios show that 149 Sm is well qualified under 1 eV. (authors). 8 refs., 7 figs., 6 tabs

A study of luminescence from Eu{sup 3+}, Ce{sup 3+}, Tb{sup 3+} and Ce{sup 3+}/Tb{sup 3+} in new potassium gadolinium phosphate K{sub 3}Gd{sub 5}(PO{sub 4}){sub 6}

Energy Technology Data Exchange (ETDEWEB)

Meng, Fangui; Zhang, Hongzhi [School of Materials Science and Engineering, Central South University of Forestry and Technology, Changsha 410004 (China); Chen, Cuili; Kim, Sun Il [Department of Physics and Interdisciplinary Program of Biomedical, Mechanical & Electrical Engineering, Pukyong National University, Busan 608-737 (Korea, Republic of); Seo, Hyo Jin, E-mail: hjseo@pknu.ac.kr [Department of Physics and Interdisciplinary Program of Biomedical, Mechanical & Electrical Engineering, Pukyong National University, Busan 608-737 (Korea, Republic of); Zhang, Xinmin, E-mail: xmzhuga@163.com [School of Materials Science and Engineering, Central South University of Forestry and Technology, Changsha 410004 (China)

2016-06-25

New potassium gadolinium phosphate [K{sub 3}Gd{sub 5}(PO{sub 4}){sub 6}] doped with Eu{sup 3+}, Ce{sup 3+}, Tb{sup 3+} and co-doped with Ce{sup 3+} and Tb{sup 3+} phosphors were prepared by high temperature solid state synthesis. Phase purity of the powders was checked by X-ray powder diffraction. Luminescence and excitation spectra of samples were reported. In particular, the interaction mechanism between Eu{sup 3+} ions was investigated in terms of the Inokuti–Hirayama model; it was found that the interactions between Eu{sup 3+} can be assigned to dipole–dipole interaction. K{sub 3}Gd{sub 5}(PO{sub 4}){sub 6}:Eu{sup 3+} could act as a candidate for solid state lighting due to its strong absorption band in the near-UV region (350–400 nm). The energy transfer from Ce{sup 3+} to Tb{sup 3+} was confirmed and the mechanism was studied using Dexter's theory; it is concluded that electric dipole–dipole interaction predominates in the energy transfer process from Ce{sup 3+} to Tb{sup 3+} in the K{sub 3}Gd{sub 5}(PO{sub 4}){sub 6} host. The energy transfer efficiency and critical distance were also investigated. - Highlights: • Optical properties of K{sub 3}Gd{sub 5}(PO{sub 4}){sub 6}:RE{sup 3+} are investigated for the first time. • The interaction mechanism between Eu{sup 3+} ions is attributed to dipole–dipole type. • K{sub 3}Eu{sub 5}(PO{sub 4}){sub 6} is a candidate phosphor for application to solid state lighting. • There exists an efficient energy transfer from Ce{sup 3+} to Tb{sup 3+} (η is up to 95%). • The mechanism of energy transfer process is electric dipole–dipole interaction.

First measurement of 153Sm in the SIR

International Nuclear Information System (INIS)

Michotte, C.; Ratel, G.; Lucas, L.

1999-01-01

In June 1998, the NIST sent to the International Reference System (SIR) a solution of 153 Sm standardized in a 4π ionization chamber. As this radionuclide had not previously been measured in the SIR, the resulting equivalent activity A e,NIST is compared with the value calculated from the efficiency curve of the SIR. However, problems occurred owing to the presence of 154 Eu and 156 Eu impurities in the solution. The manner in which the final equivalent activity value for this solution of 153 Sm has been deduced is described in this report. (authors)

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

Science.gov (United States)

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

2018-02-01

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

Preparation of red phosphor (Y, Gd)BO3:Eu by soft chemistry methods

International Nuclear Information System (INIS)

Cui Xiangzhong; Zhuang Weidong; Yu Zhijian; Xia Tian; Huang Xiaowei; Li Hongwei

2008-01-01

The three soft chemistry methods were employed to prepare the red phosphor (Y, Gd)BO 3 :Eu, such as coprecipitation-combustion method, salt assisted combustion method and emulsion method. The main factors affecting particle size, particle distribution and luminescent properties of the product were investigated in detail, and as a result, the preparation processes were optimized. The phosphors were characterized by X-ray diffraction (XRD), scanning electronic microscope (SEM), transmission electronic microscope (TEM) and vacuum ultraviolet (VUV) spectra. Results reveal that phosphors with different morphology, small particle size and high luminescence intensity could be obtained by soft chemistry methods. The difference between the luminescence properties of phosphors in this work and commercial rare earth borate phosphor is discussed. The phosphor with grain shape and high luminescence intensity could be prepared by coprecipitation-combustion method, nanophosphor could be prepared by salt assisted combustion method, and spherical phosphor with a narrow size distribution could be obtained by using emulsion method

K isomerism and collectivity in neutron-rich rare-earth isotopes

Science.gov (United States)

Patel, Zena

Neutron-rich rare-earth isotopes were produced by in-flight fission of 238U ions at the Radioactive Isotope Beam Factory (RIBF), RIKEN, Japan. In-flight fission of a heavy, high-intensity beam of 238U ions on a light target provides the cleanest secondary beams of neutron-rich nuclei in the rare-earth region of isotopes. In-flight fission is advantageous over other methods of nuclear production, as it allows for a secondary beam to be extracted, from which the beam species can be separated and identified. The excited states of nuclei are studied by delayed isomeric or beta-delayed gamma-ray spectroscopy. New K isomers were found in Sm (Z=62), Eu (Z=63), and Gd (Z=64) isotopes. The key results are discussed here. Excited states in the N=102 isotones 166Gd and 164Sm have been observed following isomeric decay for the first time. The K-isomeric states in 166Gd and 164Sm are due to 2-quasiparticle configurations. Based on the decay patterns and potential energy surface calculations, including beta6 deformation, both isomers are assigned a (6-) spin-parity. The half-lives of the isomeric states have been measured to be 950(60)ns and 600(140)ns for 166Gd and 164Sm respectively. Collective observables are discussed in light of the systematics of the region, giving insight into nuclear shape evolution. The decrease in the ground state band energies of 166Gd and 164Sm (N=102) compared to 164Gd and 162Sm (N=100) respectively, presents evidence for the predicted deformed shell closure at N=100. A 4-quasiparticle isomeric state has been discovered in 160Sm: the lightest deformed nucleus with a 4-quasiparticle isomer to date. The isomeric state is assigned an (11+) spin-parity with a measured half-life of 1.8(4)us. The (11+) isomeric state decays into a rotational band structure, based on a (6-) v5/2-[523] ⊗ v7/2+[633] bandhead, determined from the extracted gK-gR values. Potential energy surface and blocked BCS calculations were performed in the deformed midshell region

The temperature dependence studies of rare-earth (Dy.sup.3+./sup., Sm.sup.3+./sup., Eu.sup.3+./sup. and Tb.sup.3+./sup.) activated Gd.sub.3./sub.Ga.sub.3./sub.Al.sub.2./sub.O.sub.12./sub. garnet single crystals

Czech Academy of Sciences Publication Activity Database

Bartosiewicz, Karol; Babin, Vladimir; Beitlerová, Alena; Boháček, Pavel; Jurek, Karel; Nikl, Martin

2017-01-01

Roč. 189, Sep (2017), s. 126-139 ISSN 0022-2313 R&D Projects: GA ČR GA16-15569S EU Projects: European Commission(XE) 316906 - LUMINET Institutional support: RVO:68378271 Keywords : Gd3Ga3Al2O12 * rare earth dopants * energy transfer * thermal quenching * single crystal Sub ject RIV: BH - Optics, Masers, Lasers OBOR OECD: Optics (including laser optics and quantum optics) Impact factor: 2.686, year: 2016

Synthesis, characterization and properties of lanthanide trifluoroacetate complexes with N-(1-adamantyl) acetamide

International Nuclear Information System (INIS)

Miranda Junior, P.; Isolani, P.C.; Vicentini, G.; Zinner, L.B.

1999-01-01

Complexes of lanthanide trifluoacetates and N-(1-adamantyl) acetamide (ADA) with composition Ln (TFA) 3 .ADA (Ln=Nd, Sm, Eu, Gd, Tb, Dy; TFA trifluoroacetate) were synthesized by titration of lanthanides with EDTA and CHN microanalytical procedures. According to IR spectra the bonding of ADA occurs through the carbonyl oxygen. Compounds of Nd 3+ , Sm 3+ and Eu 3+ present two bands attributed to v aa COO and that of Gd 3+ Tb 3+ only one. In all cases only one band is attributed to v a -s COO. The absorption spectra of the neodymium and the emission spectra of the europium compounds were determined and interpreted. (author)

Description and exploitation of benchmarks involving {sup 149}Sm, a fission product taking part of the burn up credit in spent fuels

Energy Technology Data Exchange (ETDEWEB)

Anno, J.; Poullot, G. [CEA Centre d`Etudes de Fontenay-aux-Roses, 92 (France). Inst. de Protection et de Surete Nucleaire; Fouillaud, P.; Grivot, P. [CEA Centre d`Etudes de Valduc, 21 - Is-sur-Tille (France)

1995-12-31

Up to now, there was no benchmark to validate the Fission Products (FPs) cross sections in criticality safety calculations. The protection and nuclear safety institute (IPSN) has begun an experimental program on 6 FPs ({sup 103}Rh, {sup 133}Cs, {sup 143}Nd, {sup 149}Sm, {sup 152}Sm, and {sup 155}Gd daughter of {sup 155}Eu) giving alone a decrease of reactivity equal to half the whole FPs in spent fuels (except Xe and I). Here are presented the experiments with the {sup 149}Sm and the results obtained with the APOLLO I-MORET III calculations codes. 11 experiments are carried out in a zircaloy tank of 3.5 1 containing slightly nitric acid solutions of Samarium (96,9% in weight of {sup 149S}m) at 0.1048 -0.2148 - 0.6262 g/l concentrations. It was placed in the middle of arrays of UO{sub 2} rods (4.742 % U5 weight %) at square pitch of 13 mm. The underwater height of the rods is the critical parameter. In addition, 7 experiments were performed with the same apparatus with water and boron proving a good experimental representativeness and a good accuracy of the calculations. As the reactivity worth of the Sm tank is between 2000 and 6000 10{sup -5}, the benchmarks are well representative and the cumulative absorption ratios show that {sup 149}Sm is well qualified under 1 eV. (authors). 8 refs., 7 figs., 6 tabs.

Strongly coupled band in 140Gd

International Nuclear Information System (INIS)

Falla-Sotelo, F.; Oliveira, J.R.B.; Rao, M.N.

2005-01-01

Several high-K states are known to exist in the mass 130-140 region. For the N=74 even-even isotopes, Kπ = 8 - isomers, with lifetimes ranging from ns to ms, are known in 128 Xe, 130 Ba, 132 Ce, 134 Nd, 136 Sm, and 138 Gd[. In 140 Gd, we have observed for the first time a band also based on an Iπ = 8 - state. This could be the first case of a Kπ = 8 - state observed in an N=76 even-even isotope. The systematics of the Kπ = 8 - isomeric states in N=74 isotopes has been studied by A.M. Bruce et al. These states decay towards the K = 0 ground state band, and the transitions are K-forbidden. The 140 Gd case presents strong similarities but also some significant differences with relation to the N=74 isotopes. We propose the same configuration but with larger deformation in 140 Gd

Multielemental nondestructive neutron activation analysis of Dy, Mn, Eu, Na, Ga, W, La and Sm involving cyclic irradiations with 252Cf

International Nuclear Information System (INIS)

Narkhede, S.S.; Turel, Z.R.

1995-01-01

Dy, Mn, Eu, Na, Ga, W, La and Sm respond very well to INAA technique because of their favourable nuclear properties such as high thermal neutron cross-section or abundance. In the present work a method has been developed for the determination of these elements employing cycle irradiation with 252 Cf thermal neutron source. Radioassaying of the irradiated sample and standard was done employing HPGe detector in conjunction with a PC based MCA units. (author). 2 tabs

Theoretical and experimental spectroscopic studies of the first highly luminescent binuclear hydrocinnamate of Eu(III), Tb(III) and Gd(III) with bidentate 2,2'-bipyridine ligand

Energy Technology Data Exchange (ETDEWEB)

Marques, Lippy F.; Correa, Charlane C.; Garcia, Humberto C. [Departamento de Química-ICE, Universidade Federal de Juiz de Fora, Juiz de Fora-MG 36036-330 (Brazil); Martins Francisco, Thiago [Departamento de Física-ICEx, Universidade Federal de Minas Gerais, Pampulha, Belo Horizonte-MG 30123-970 (Brazil); Ribeiro, Sidney J.L. [Instituto de Química, Universidade Estadual Paulista Júlio de Mesquita Filho-UNESP, CP 355, Araraquara-SP 14801-970 (Brazil); Dutra, José Diogo L.; Freire, Ricardo O. [Pople Computational Chemistry Laboratory, Departamento de Química, Universidade Federal de Sergipe, São Cristóvão-SE 49100-000 (Brazil); Machado, Flávia C., E-mail: flavia.machado@ufjf.edu.br [Departamento de Química-ICE, Universidade Federal de Juiz de Fora, Juiz de Fora-MG 36036-330 (Brazil)

2014-04-15

In this paper, the synthesis of three new binuclear lanthanide (III) complexes [Ln{sub 2}(cin){sub 6}(bpy){sub 2}] (Ln=Eu (1), Tb (2), Gd (3), cin=hydrocinnamate anion; bpy=2,2'-bipyridine), and their complete characterization, including single crystal X-ray diffraction, FTIR spectroscopy and thermal analysis (TGA/DTA) are reported. In especial, photophysical properties of Eu(III) complex have been studied in detail via both theoretical and experimental approaches. Crystal structures of 1–3 reveal that all compounds are isostructural and that each lanthanide ion is nine-coordinated by oxygen and nitrogen atoms in an overall distorted tricapped trigonal-prismatic geometry. Eu(III) complex structure was also calculated using the Sparkle model for lanthanide complexes and the intensity parameters (Ω{sub 2}, Ω{sub 4}, and Ω{sub 6}), calculated from the experimental data and from Sparkle/PM3 model. The theoretical emission quantum efficiencies obtained for Sparkle/PM3 structures are in excellent agreement with the experimental values, clearly attesting to the efficacy of the theoretical models. The theoretical procedure applied here shows that the europium binuclear compound displays a quantum yield about 65% suggesting that the system can be excellent for the development of efficient luminescent devices. Highlights: • First binuclear Ln{sup 3+}-hydrocinnamate have been synthesized and characterized. • Eu{sup 3+}, Tb{sup 3+} and Gd{sup 3+} complexes photoluminescence properties were investigated. • Theoretical approaches for Eu{sup 3+} complex luminescence has been performed. • An energy level diagram is used to establish the ligand-to-metal energy transfer. • 65% Quantum yield suggests an excellent system for luminescent devices.

β-Y(BO{sub 2}){sub 3}. A new member of the β-Ln(BO{sub 2}){sub 3} (Ln = Nd, Sm, Gd-Lu) structure family

Energy Technology Data Exchange (ETDEWEB)

Schmitt, Martin K.; Huppertz, Hubert [Innsbruck Univ. (Austria). Inst. fuer Allgemeine, Anorganische und Theoretische Chemie

2017-07-01

β-Y(BO{sub 2}){sub 3} was synthesized in a Walker-type multianvil module at 5.9 GPa/1000 C. The crystal structure has been elucidated through single-crystal X-ray diffraction. β-Y(BO{sub 2}){sub 3} crystallizes in the orthorhombic space group Pnma (no. 62) with the lattice parameters a = 15.886(2), b = 7.3860(6), and c = 12.2119(9) Aa. Its crystal structure will be discussed in the context of the isotypic lanthanide borates β-Ln(BO{sub 2}){sub 3} (Ln = Nd, Sm, Gd-Lu).

Octupole excitations in 146Sm

International Nuclear Information System (INIS)

Bizzeti, P.G.; Bizzetti-Sona, A.M.

1998-01-01

The mean lives of the lowest 9 - and 12 + states of 146 Sm have been measured by means of the RDM. Their (preliminary) values are r m (9 - )=0.97±0.05 ns and r m (12 + )=15±2 ps, respectively. The strengths of the collective E3 transitions of the 12 + →9 - →6 6 cascade are compared with the corresponding ones in 148 Gd

Complexes of light lanthanides with 2,4-dimethoxybenzoic acid

Directory of Open Access Journals (Sweden)

WIESLAWA FERENC

2000-01-01

Full Text Available The complexes of light lanthanides with 2,4-dimethoxybenzoic acid of the formula: Ln(C9H9O43·nH2O where Ln = La(III, Ce(III, Pr(III, Nd(III, Sm(III, Eu(III, Gd(IIII, and n = 3 for La(III, Gd(III, n = 2 for Sm(III, Eu(III, and n = 0 for Ce(III, Pr(III, Nd(III have been synthesized and characterized by elemental analysis, IR spectroscopy, thermogravimetric studies and X-ray diffraction measurements. The complexes have colours typical for Ln3+ ions (La, Ce, Eu, Gd-white, Sm-cream, Pr-green, Nd-violet. The carboxylate group in these complexes is a symmetrical, bidentate, chelating ligand. They are crystalline compounds characterized by various symmetry. On heating in air to 1273 K the 2,4-dimethoxybenzoates of the light lanthanides decompose in various ways. The hydrated complexes decompose in two or three steps while those of anhydrous ones only in one or two. The trihydrate of lanthanum 2,4-dimethoxybenzoate first dehydrates to form the anhydrous salt, which then decomposes to La2O3via the intermediate formation of La2O2CO3. The hydrates of Sm(III, Eu(III, Gd(III decompose in two stages. First, they dehydrate forming the anhydrous salts, which then decompose directly to the oxides of the respective metals. The anhydrous complexes of Ce(III, Pr(III decompose in one step, while that of Nd(III in two. The solubilities of the 2,4-dimethoxybenzoates of the light lanthanides in water and ethanol at 293 K are in the order of: 10-3 mol dm-3 and 10-4-10-3 mol dm-3, respectively.

Hydrothermal synthesis and photoluminescent properties of hierarchical GdPO4·H2O:Ln3+ (Ln3+ = Eu3+, Ce3+, Tb3+) flower-like clusters

Science.gov (United States)

Amurisana, Bao.; Zhiqiang, Song.; Haschaolu, O.; Yi, Chen; Tegus, O.

2018-02-01

3D hierarchical GdPO4·H2O:Ln3+ (Ln3+ = Eu3+, Ce3+, Tb3+) flower clusters were successfully prepared on glass slide substrate by a simple, economical hydrothermal process with the assistance of disodium ethylenediaminetetraacetic acid (Na2H2L, where L4- = (CH2COO)2N(CH2)2N(CH2COO)24-). In this process, Na2H2L was used as both a chelating agent and a structure-director. The hierarchical flower clusters have an average diameter of 7-12 μm and are composed of well-aligned microrods. The influence of the molar ratio of Na2H2L/Gd3+ and reaction time on the morphology was systematically studied. A possible crystal growth and formation mechanism of hierarchical flower clusters is proposed based on the evolution of morphology as a function of reaction time. The self-assembled GdPO4·H2O:Ln3+ superstructures exhibit strong orange-red (Eu3+, 5D0 → 7F1), green (Tb3+, 5D4 → 7F5) and near ultraviolet emissions (Ce3+, 5d → 7F5/2) under ultraviolet excitation, respectively. This study may provide a new channel for building hierarchically superstructued oxide micro/nanomaterials with optical and new properties.

Determination of lanthanides in rare earths concentrates by emission optical spectrography

International Nuclear Information System (INIS)

Friedmann, R.; Lordello, A.R.; Abrao, A.

1978-01-01

A spectrochemical method has been developed for the determination of Y, Pr, Sm, Eu, Gd and Dy in purified lanthanum oxide; Y, La, Nd, Sm, Gd and Dy in purified cerium oxide and Y, La, Sm, Eu, Gd and Dy in purified neodymium oxide. The technique consists of an almost total consumption of the sample in a 17 ampere direct current arc. The rare earth oxides are mixed with an equal amount by weight of spectrographic graphite and the electrodes are arced in an argon (80%)-oxygen (20%) atmosphere, inside a specially desingned chamber, to suppress cyanogen bands. The concentration ranges are approximatelly 0.002 - 2%, depending on the matrix and the elements to be analysed. The presicion, accuracy and acceptability of the method are calculated for all elements. The total error values are approximately in the range of 18-48%. The method was developed for quality control of the individual fractions held by pulsed and ion exchange columns in the lanthanide separations, in the Chemical Engineering Centre, Atomic Energy Institute, Sao Paulo [pt

Control of rare earths fractioning in a pilot unit, by emission optical spectrography

International Nuclear Information System (INIS)

Friedmann, R.

1978-01-01

A spectrochemical method has been developed for the determination of Y, Pr, Sm, Eu, Gd and Dy in purified lanthanum oxide; Y, La, Nd, Sm, Gd and Dy in purified cerium oxide and Y, La, Sm, Eu, Gd and Dy in neodymium oxide. The technique consists of an almost total consumption of the sample in a 17 amperes direct current arc. The rare erath oxides are mixed with an equal amount by weight of spectrographic graphite powder and the electrodes are arced in an argon(80%)-oxygen (20%) atmosphere, inside a specially designed chamber, to suppress cyanogen bands. The concentration ranges are approximately 0.002-2%, depending on the matrix and the elements to be analysed. The precision, accuracy and acceptability of the method are calculated for all elements. The total error values are approximately in the range of 18-48%. The method was developed for the quality control of the individual fractions held by pulsed and ion exchange columns in the lanthanide separations, in the Centro de Engenharia Quimica, Instituto de Energia Atomica, Sao Paulo [pt

High temperature properties of rare-earth tungstates RE{sub 2}W{sub 2}O{sub 9}

Energy Technology Data Exchange (ETDEWEB)

Marrero-López, D., E-mail: damarre@uma.es [Dpto. de Física Aplicada I, Universidad de Málaga, 29071-Málaga (Spain); Canales-Vázquez, J. [Renewable Energy Research Institute, University of Castilla-La Mancha, 02071-Albacete (Spain); Ruiz-Morales, J.C.; Núñez, P. [Dpto. de Química, U.D. Química Inorgánica, Universidad de la Laguna, 38206-Tenerife (Spain)

2015-02-15

Highlights: • RE{sub 2}W{sub 2}O{sub 9} (RE = Nd, Pr, Sm, Eu and Gd) are prepared by freeze-drying precursor. • The samples crystallize in the monoclinic s.g. P2{sub 1}/c. • A first order phase transition was detected between 330 and 590 °C. • These materials exhibit low ionic conductivity of 10{sup -5} S cm{sup -1} at 800 °C. - Abstract: RE{sub 2}W{sub 2}O{sub 9} (RE = Ce, Nd, Pr, Sm, Eu, Gd and Tb) compounds have been prepared by a freeze-drying precursor method in order to explore their high temperature thermal properties by different techniques. Samples with Nd, Pr, Sm, Eu and Gd crystallize in the same monoclinic structure with space group P2{sub 1}/c. The thermal, X-ray diffraction, and electrical analysis reveal the existence of a reversible first order phase transition, which is accompanied by a sudden decrease of the unit cell volume and conductivity. A large thermal hysteresis of about 250 °C is also observed during the heating and cooling processes. These materials exhibit low electrical conductivity of the order of 10{sup -5} S cm{sup -1} at 800 °C.

Superconductivity and magnetism in Ir-doped GdFeAsO

International Nuclear Information System (INIS)

Cui, Y.J.; Chen, Y.L.; Cheng, C.H.; Yang, Y.; Jiang, J.; Wang, Y.Z.; Zhang, Y.; Zhao, Y.

2010-01-01

The 5d-transition metal, Ir has successfully been doped at Fe site and induced superconductivity in GdFeAsO at T c = 18.9 K and ∼20 atom%. The Ir-doping shortened the c-axis length and stretched the a-axis one, which led to enhance the coupling between the FeAs- and SmO-layer, and to weaken the bonding between Fe and As atom. Paramagnetism was observed in all of the samples, which was resulted from the magnetic Gd ion as in the F-doped GdFeAsO. An upper critical field of GdFe 0.8 Ir 0.2 AsO was extrapolated to around 24 T, much smaller than that of F-doped GdFeAsO owing to a relatively low T c and small value of dH c2 /dT.

Preparation, characterization and luminescence of Sm~(3+) or Eu~(3+) doped Sr_2CeO_4 by a modified sol-gel method

Institute of Scientific and Technical Information of China (English)

张春祥; 史建设; 杨绪杰; 陆路德; 汪信

2010-01-01

Superfine Sr2CeO4:RE3+ (RE=Eu, Sm) phosphors were synthesized at relatively low temperature by a modified sol-gel method using nitrates as raw materials, ethylenediaminetetraacetic acid (EDTA) as complexing agent. Single phase phosphors could be obtained at calcination temperature above 800 °C and pH value higher than 6.4 of initial solution. The as-prepared powders consisted of uniform crotch-like grains. The preparation process was monitored by thermogravimetric and differential thermal analysis (TG-DTA) ...

Evaluation of luminescent properties and detection of Eu2+ in nano structured particles of Gd2-x EuxO3 system (x= 0.05, 0.10 and 0.30)

International Nuclear Information System (INIS)

Barroso, J.; Mena, I.; Gomez, L. S.; Milosevic, O.; Rabanal, M. E.

2012-01-01

Spray Pyrolysis (SP) is performed at 700 degree centigrade in dry air atmosphere using common nitrate aqueous solutions (0,1M) as precursor in order to obtain nano structured particles with the composition Gd 2 -xEu x O 3 (x= 0.05, 0.10 and 0.30). In this work, three samples with different atomic europium concentration (1, 2 and 6%) were studied. After, the obtained particles were subjected to different thermal treatments with varying temperatures between 800 and 1000 degree centigrade/12 h in dry air atmosphere. The obtained particles were characterized by XRD, SEM techniques, laser dispersion and steady state fluorescence spectroscopy. The existence of two cubic phases with different symmetry cubic phases (Ia-3, Fm-3m) was identified within the as-prepared samples. Moreover, the presence of Gd 2 O 3 monoclinic phase (C 2 /m) which disappears during the thermal treatments was proved. In all thermally treated samples, it was observed the stabilization of an only Ia-3 phase. Fluorescence emission measurements in all studied samples the presence of Eu 2 + (λ= 430nm), whose intensity increases as long as the content of the monoclinic phase decreases of the Eu 3 + percentage. (Author) 35 refs.

Spin-phonon and lattice contributions to the ground-state splitting of Gd3+ and Eu2+ in scheelite crystals

Science.gov (United States)

Gorlov, A. D.

2015-07-01

The EPR spectra of Gd3+ in CaWO4 single crystals have been studied at temperatures T = 1.8, 4.2, and 114-300 K, and the temperature dependence of the parameters b {/n m } ( T) of the spin Hamiltonian has been found. The behavior of b {2/0}( T) has been analyzed. The spin-phonon and static lattice contributions b {2/0}( F) and b {2/0}( L) to b {2/0}( T) have been revealed. For this purpose, the variation of b {2/0}( L) has been calculated taking into account the thermal shifts of oxygen ions in CaWO4. Similar analysis has been carried out for CaWO4: Eu2+ based on the EPR data of other authors (Bronstein, Voterra and Harvey, Kiefte). It has been shown that at b {2/0}( F) > 0, the variation of b {2/0}( F) as a function of T for these impurity centers is described well by the Pfister model and a sign change of b {2/0}( T) for Eu2+ is determined by thermal expansion of the lattice.

Superconductivity and magnetism in Ir-doped GdFeAsO

Energy Technology Data Exchange (ETDEWEB)

Cui, Y.J.; Chen, Y.L. [Key Laboratory of Magnetic Levitation and Maglev Trains (Ministry of Education of China), Superconductivity R and D Center (SRDC), Mail Stop 165, Southwest Jiaotong University, Chengdu, Sichuan 610031 (China); Cheng, C.H. [School of Materials Science and Engineering, University of New South Wales, Sydney 2052 NSW (Australia); Yang, Y.; Jiang, J.; Wang, Y.Z.; Zhang, Y. [Key Laboratory of Magnetic Levitation and Maglev Trains (Ministry of Education of China), Superconductivity R and D Center (SRDC), Mail Stop 165, Southwest Jiaotong University, Chengdu, Sichuan 610031 (China); Zhao, Y., E-mail: yzhao@swjtu.edu.c [Key Laboratory of Magnetic Levitation and Maglev Trains (Ministry of Education of China), Superconductivity R and D Center (SRDC), Mail Stop 165, Southwest Jiaotong University, Chengdu, Sichuan 610031 (China); School of Materials Science and Engineering, University of New South Wales, Sydney 2052 NSW (Australia)

2010-11-01

The 5d-transition metal, Ir has successfully been doped at Fe site and induced superconductivity in GdFeAsO at T{sub c} = 18.9 K and {approx}20 atom%. The Ir-doping shortened the c-axis length and stretched the a-axis one, which led to enhance the coupling between the FeAs- and SmO-layer, and to weaken the bonding between Fe and As atom. Paramagnetism was observed in all of the samples, which was resulted from the magnetic Gd ion as in the F-doped GdFeAsO. An upper critical field of GdFe{sub 0.8}Ir{sub 0.2}AsO was extrapolated to around 24 T, much smaller than that of F-doped GdFeAsO owing to a relatively low T{sub c} and small value of dH{sub c2}/dT.

Synthesis, crystal structure and photoluminescent properties of Eu{sup 3+} ion-activated R{sub 4}MoO{sub 9} (R = Y, Gd, and Lu)

Energy Technology Data Exchange (ETDEWEB)

Li, Huaiyong [Department of Materials Science and Engineering, Liaocheng University, Liaocheng 252059 (China); Moon, Byung Kee; Choi, Byung Chun [Department of Physics, Pukyong National University, Busan 608-737 (Korea, Republic of); Jeong, Jung Hyun, E-mail: jhjeong@pknu.ac.kr [Department of Physics, Pukyong National University, Busan 608-737 (Korea, Republic of); Yang, Hyun Kyoung [Jeju Global Research Center, Korea Institute of Energy Research, Jeju 695-971 (Korea, Republic of); Jang, Kiwan; Lee, Ho Sueb [Department of Physics, Changwon National University, Changwon 641-773 (Korea, Republic of); Yi, Soung Soo [Department of Electronic Material Engineering, Silla University, Busan 617-736 (Korea, Republic of)

2013-05-15

Rare earth molybdates R{sub 4}MoO{sub 9} (R = Y, Gd, and Lu) with Eu{sup 3+} ion-doped were synthesized by solid-state reaction. The phase structure, optical absorption and photoluminescence properties of the as-prepared powder samples were studied. The powder X-ray diffraction patterns indicated that all the compounds crystallized in a hexagonal structure, and the lattice parameters reduced in the order of the ionic radii of R. The UV–visible diffuse reflectance spectra revealed that the compounds had a strong absorption of near-UV light due to the excitation of MoO{sub 6} groups in the host lattices. The energy absorbed by the host lattices could then be transferred to doped Eu{sup 3+} ions, resulting in red emission due to the f–f transitions of Eu{sup 3+} ions. The optical absorption and photoluminescence properties of the compounds indicated that they might be candidates as the color-conversion red phosphors for solid-state lighting. - Highlights: ► Structure, optical and photoluminescence properties of Eu{sup 3+} ion-activated R{sub 4}MoO{sub 9} were studied. ► Energy transfer from MoO{sub x} to Eu{sup 3+} can be used to convert near-UV to red light. ► R{sub 4}MoO{sub 9}:Eu might be candidate for color-conversion red phosphors excited by near-UV light.

X-ray induced Sm{sup 3+} to Sm{sup 2+} conversion in fluorophosphate and fluoroaluminate glasses for the monitoring of high-doses in microbeam radiation therapy

Energy Technology Data Exchange (ETDEWEB)

Vahedi, Shahrzad; Okada, Go; Morrell, Brian; Muzar, Edward; Koughia, Cyril; Kasap, Safa [Department of Electrical and Computer Engineering, University of Saskatchewan, Saskatoon, Saskatchewan S7N 5A9 (Canada); Edgar, Andy; Varoy, Chris [School of Chemical and Physical Sciences and MacDiarmid Institute, Victoria University of Wellington, Kelburn Parade (New Zealand); Belev, George; Wysokinski, Tomasz [Canadian Light Source, Inc., University of Saskatchewan, Saskatoon, Saskatchewan S7N 0X4 (Canada); Chapman, Dean [Department of Anatomy and Cell Biology, University of Saskatchewan, Saskatoon, Saskatchewan S7N 5E5 (Canada)

2012-10-01

Fluorophosphate and fluoroaluminate glasses doped with trivalent samarium were evaluated as sensors of x-ray radiation for microbeam radiation therapy at the Canadian Light Source using the conversion of trivalent Sm{sup 3+} to the divalent form Sm{sup 2+}. Both types of glasses show similar conversion rates and may be used as a linear sensor up to {approx}150 Gy and as a nonlinear sensor up to {approx}2400 Gy, where saturation is reached. Experiments with a multi-slit collimator show high spatial resolution of the conversion pattern; the pattern was acquired by a confocal fluorescence microscopy technique. The effects of previous x-ray exposure may be erased by annealing at temperatures exceeding the glass transition temperature T{sub g} while annealing at T{sub A} < T{sub g} enhances the Sm conversion. This enhancement is explained by a thermally stimulated relaxation of host glass ionic matrix surrounding x-ray induced Sm{sup 2+} ions. In addition, some of the Sm{sup 3+}-doped glasses were codoped with Eu{sup 2+}-ions but the results show that there is no marked improvement in the conversion efficiency by the introduction of Eu{sup 2+}.

Magnetization fluctuation analysis and superconducting parameters of La0.5RE0.5BaCaCu3O7-δ(RE=Y, Sm, Gd, Dy, Ho, Yb) superconductor

International Nuclear Information System (INIS)

Parra Vargas, C.A.; Pimentel, J.L.; Pureur, P.; Landinez Tellez, D.A.; Roa-Rojas, J.

2009-01-01

In this work we report the analysis of magnetization experimental data of the La 0.5 RE 0.5 BaCaCu 3 O 7-δ (RE=Y, Sm, Gd, Dy, Ho, Yb) superconducting system. The data are analyzed in terms of thermal fluctuations on the magnetization excess ΔM(T) for different values of temperature in each one of the samples. We describe a procedure for extracting the penetration depth λ ab (∼1571A) and the coherence length ξ ab (∼1.52A) parameters from the magnetization, as a function of the applied magnetic field. This procedure was performed for polycrystalline samples of La 0.5 RE 0.5 BaCaCu 3 O 7-δ by using the theory of Bulaevskii, Ledvij and Kogan, which analyzes the vortex fluctuation in superconducting materials within the Lawrence-Doniach framework. These data allowed to determine the characteristic temperature value T * (73, 58, 48, 57, 56, 71 K, for RE=Y, Sm, Gd, Dy, Ho, Yb, respectively) in the magnetization curves for several magnetic fields. We calculated the data of magnetization excess from the curves of magnetization as a function of logarithm of applied field. We notice that the values for these superconducting parameters are in agreement with the reports for high temperature superconductors. The obtained value of superconducting volumetric fraction is compared with that obtained through the measure of the Meissner effect.

In vivo immunotoxicity of SiO2@(Y0.5Gd0.45Eu0.05)2O3 as dual-modality nanoprobes.

Science.gov (United States)

Tian, Xiumei; Li, Ermao; Yang, Fanwen; Peng, Ye; Zhu, Jixiang; He, Fupo; Chen, Xiaoming

2014-08-07

We have successfully synthesized SiO2@(Y0.5Gd0.45Eu0.05)2O3 nanocomposites as a potential dual-modality nanoprobe for molecular imaging in vitro. However, their immunotoxicity assessment in vivo remains unknown. In this article, the in vitro biocompatibility of our dual-modality nanoprobes was assayed in terms of cell viability and apoptosis. In vivo immunotoxicity was investigated by monitoring the generation of reactive oxygen species (ROS), cluster of differentiation (CD) markers and cytokines in Balb/c mice. The data show that the in vitro biocompatibility was satisfactory. In addition, the immunotoxicity data revealed there are no significant changes in the expression levels of CD11b and CD71 between the nanoprobe group and the Gd in a diethylenetriaminepentaacetic acid (DTPA) chelator (Gd-DTPA) group 24 h after injection in Balb/c mice (p>0.05). Importantly, there are significant differences in the expression levels of CD206 and CD25 as well as the secretion of IL-4 and the generation of ROS 24 h after injection (pimmunotoxicity of these rare earth-based biomaterials at the molecular level before molecular imaging in vivo.

Elemental content in ground and soluble/instant coffee

International Nuclear Information System (INIS)

Vega-Carrillo, H.R.; Manzanares-Acuna, E.; Iskander, F.Y.

2002-01-01

The concentration of thirty-four elements in twelve coffee brands has been measured using instrumental neutron activation analysis. The samples investigated included four brands of commercially available ground coffee and eight brands of soluble/instant coffee. The elements measured were Al, As, Ba, Ca, Ce, Co, Cr, Cs, Dy, Eu, Fe, Gd, Hf, K, La, Lu, Mg, Mn, Na, Rb, Sb, Sc, Se, Sm, Sr, Ta, Tb, Th, Ti, Tm, U, V, Yb and Zn. Twenty four elements were found to be below the detection limit in one or more samples. These elements were Ce, Cr, Fe, V, As, Eu, Ba, Dy, Gd, Hf, La, Lu, Sb, Sc, Se, Sm, Sr, Ta, Tb, Th, Ti, Yb, Tm, and U. (author)

Electronic and magnetic properties of rare earth-Sn3 compounds for 119Sn Moessbauer spectroscopy

International Nuclear Information System (INIS)

Sanchez, J.P.; Friedt, J.M.; Shenoy, G.K.; Percheron, A.; Achard, J.C.

1975-01-01

The electronic and magnetic properties of RESn 3 compounds (RE=La, Ce, Pr, Nd, Sm, Eu, Gd, Yb) have been investigated using the 23.8keV Moessbauer resonance of 119 Sn. The isomer shifts and quadrupole interactions are nearly the same in all compounds. The transferred magnetic fields and their orientation with respect to the principal electric field gradient axis at various Sn sites in the magnetically ordered state of RESn 3 (RE=Pr, Nd, Sm, Eu, Gd) have been utilized to get information about the magnetic structure. An evaluation of the transferred fields in PrSn 3 and NdSn 3 shows that the spin density at the Sn nucleus is nearly the same in both compounds [fr

Strongly coupled band in {sup 140}Gd

Energy Technology Data Exchange (ETDEWEB)

Falla-Sotelo, F.; Oliveira, J.R.B.; Rao, M.N. [Instituto de Fisica, Universidade de Sao Paulo, Sao Paulo (Brazil)] (and others)

2005-07-01

Several high-K states are known to exist in the mass 130-140 region. For the N=74 even-even isotopes, K{pi} = 8{sup -} isomers, with lifetimes ranging from ns to ms, are known in {sup 128}Xe, {sup 130}Ba, {sup 132}Ce, {sup 134}Nd, {sup 136}Sm, and {sup 138}Gd[. In {sup 140}Gd, we have observed for the first time a band also based on an I{pi} = 8{sup -} state. This could be the first case of a K{pi} = 8{sup -} state observed in an N=76 even-even isotope. The systematics of the K{pi} = 8{sup -} isomeric states in N=74 isotopes has been studied by A.M. Bruce et al. These states decay towards the K = 0 ground state band, and the transitions are K-forbidden. The {sup 140}Gd case presents strong similarities but also some significant differences with relation to the N=74 isotopes. We propose the same configuration but with larger deformation in {sup 140}Gd.

Optical and crystal chemistry studies of Na3Ln(PO4)2-K3Ln(PO4)2 (Ln=Eu, Gd)

International Nuclear Information System (INIS)

Mesnaoui, M.; Maazaz, M.

1987-01-01

In these systems, large single phase domains are separated by two phase regions. The structural evolution as a function of composition is analysed both by X-ray diffraction and by using Eu 3+ and Gd 3+ as luminescent local structural probes. Due to layer type structure of the K 3 Ln(PO 4 ) 2 phases an exchange reaction resulting in total substitution of sodium for potassium can be carried out with formation of metastable Na 3 Ln(PO 4 ) 2 phases, the structure of which is close to those of the potassium compounds. 10 refs.; 18 figs [fr

AC susceptibility, XRD and DSC studies of Sm1-xGdxMn2Si2 silicides

International Nuclear Information System (INIS)

Kervan, S.; Kilic, A.; Gencer, A.

2004-01-01

X-ray powder diffraction, AC susceptibility and differential scanning calorimetry (DSC) studies were performed on the polycrystalline Sm 1-x Gd x Mn 2 Si 2 (0≤x≤1) compounds. All compounds investigated crystallize in the body-centered tetragonal ThCr 2 Si 2 -type structure with the space group I4/mmm. Substitution of Gd for Sm leads to a linear decrease of the lattice constants and the unit cell volume. The lattice constants and the unit cell volume obey Vegard's law. At low temperatures, the rare earth sublattice orders and reconfigures the ordering in the Mn sublattice. The samples with x=0.6 and 0.8 exhibit spin reorientation phenomenon. The Neel temperature T N (Mn) determined by DSC technique and the Curie temperature T C (RE) increase linearly with increasing Gd content x. The results are summarized in the x-T magnetic phase diagram

Effects of rare-earth substitution on the stability and electronic structure of REZnOSb (RE = La-Nd, Sm-Gd) investigated via first-principles calculations

International Nuclear Information System (INIS)

Guo Kai; Man Zhenyong; Cao Qigao; Chen Haohong; Guo Xiangxin; Zhao Jingtai

2011-01-01

Graphical abstract: The structure stability of REZnOSb decreases with varying rare-earth from La to Gd because of the increased binding energy. Research highlights: → As increasing the atomic number of the RE, the structural stability of REZnOSb decreases. → Varying the rare-earth elements from La to Gd, the covalent interactions between [ZnSb] and [LaO] layer are enhanced by 4f-electrons. → The electrical transport properties of REZnOSb could be improved using the large atomic number of the RE. - Abstract: The structural stability, chemical bonding, Mulliken populations, and charge-density distribution of REZnOSb (RE = La-Nd, Sm-Gd) were investigated by first-principles calculations. Unit cell parameters calculated by the generalized gradient approximation (GGA) are in better agreement with experimental results than those derived from the local density approximation (LDA). Binding energy comparisons indicate that the structural stability of REZnOSb decreases with the increment of the atomic number of the RE, as confirmed by X-ray diffraction (XRD) results. Semimetal or narrow band-gap semiconductor behaviors are found for selected REZnOSb. Moreover, chemical bonding analysis shows that there exist considerable polar covalent interactions between the participating atoms. It also reveals that the [ZnSb] layers receive some electrons from the [LaO] layers (donor) as an electrons acceptor and holes transport tunnel. The covalent interactions between the [ZnSb] and [LaO] layers, which are enhanced by 4f-electrons of the RE, are supposed to improve the electrical transport properties.

Functionalization of atomic force microscope tips by dielectrophoretic assembly of Gd2O3:Eu3+ nanorods

International Nuclear Information System (INIS)

Macedo, Andreia G; Ananias, Duarte; Andre, Paulo S; Ferreira, Rute A sa; Carlos, Luis D; Kholkin, Andrei L; Rocha, J

2008-01-01

An atomic force microscopy (AFM) tip has been coated with photoluminescent Eu 3+ -doped Gd 2 O 3 nanorods using a dielectrophoresis technique, which preserves the red emission of the nanorods (quantum yield 0.47). The performance of the modified tips has been tested by using them for regular topography imaging in tapping and contact modes. Both a regular AFM standard grid and a patterned surface (of an organic-inorganic methacrylate Zr-based oxo-cluster and poly(oxyethylene)/siloxane hybrid) have been used. Similar depth values have been measured using a conventional silicon tip and the nanorod-modified tip. The tips before and after use exhibit similar SEM images and photoluminescence spectra and, thus, seem to be stable under working conditions. These tips should find applications in scanning near-field optical microscopy and other scanning techniques

Crystal phase transition in LixNa1-xGdF4 solid solution nanocrystals - Tuning of optical properties

KAUST Repository

Bański, Mateusz

2014-01-01

The influence of precursor composition on the crystallization of LixNa1-xGdF4 is investigated and discussed. Nanocrystals are prepared from the thermal decomposition of trifluoroacetates in the presence of trioctylphosphine oxide to provide control over particle size. A crystal phase transition from hexagonal to cubic and to tetragonal is observed by increasing lithium trifluoroacetate (Li-TFA) in the solution. Controlling the composition of LixNa1-xGdF4 nanocrystals results in modified crystal field symmetry and emission properties from doped europium (Eu3+) ions. We report that for lithium (Li+) substitution <15%, the hexagonal crystal field is preferred, while the Eu3+ emission is already tuned, whereas at higher Li+ substitution, a phase change takes place and the number of crystalline matrix defects increases which is reflected in the optical properties of Eu3+. From Eu3+ emission properties, the optimum Li+ content is determined to be ∼6.2% in the prepared LixNa1-xGdF4 nanocrystals.

Dependences on RE of superconducting properties of transition metal co-doped (Ca, RE)FeAs_2 with RE = La–Gd

International Nuclear Information System (INIS)

Yakita, H.; Ogino, H.; Sala, A.; Okada, T.; Yamamoto, A.; Kishio, K.; Iyo, A.; Eisaki, H.; Shimoyama, J.

2015-01-01

Highlights: • We synthesized Co or Ni co-doped (Ca, RE)FeAs_2 with RE = La–Gd. • Co or Ni co-doping improved superconducting properties of all (Ca, RE)FeAs_2 samples. • T_c of (Ca, RE)FeAs_2 decreased with decreasing ionic radii of RE"3"+. • Eu doped samples showed exceptionally low T_c and long interlayer distance. • Long interlayer distance of Eu doped samples suggested co-existence of Eu"2"+ and Eu"3"+. - Abstract: Dependence of superconducting properties of (Ca, RE)(Fe, TM)As_2 [(Ca, RE)112, TM: Co, Ni)] on RE elements (RE = La–Gd) was systematically investigated. Improvement of superconducting properties by Co or Ni co-doping was observed for all (Ca, RE)112, which is similar to Co-co-doped (Ca, La)112 or (Ca, Pr)112. T_c of Co-co-doped samples decreased from 38 K for RE = La to 29 K for RE = Gd with decreasing ionic radii of RE"3"+. However, Co-co-doped (Ca, Eu)112 showed exceptionally low T_c = 21 K probably due to the co-existence of Eu"3"+ and Eu"2"+ suggested by longer interlayer distance d_F_e_–_F_e of (Ca, Eu)112 than other (Ca, RE)112.

Half Life Measurements in 155Gd

International Nuclear Information System (INIS)

Malmskog, S.G.

1966-08-01

In the literature there exists a definite difference for the half life of the 86.5 keV level in Gd depending on whether 155 Eu or 155 Tb sources have been used. Using a good energy resolution electron-electron coincidence spectrometer and a 155 Eu source, a half life of 6.48 ± 0.26 nsec was obtained for the 86.5 keV level. This is in agreement with the values previously measured with 155 Tb sources. The half life of the 105.4 keV level was measured to be 1.12 ± 0.05 nsec

Raman and infrared spectroscopy of pure and doped GdAlO3 with rare earth ions

International Nuclear Information System (INIS)

Bagnato, V.S.

1983-01-01

IR and Raman measurements were carried out in pure and Eu +3 - doped GdAlO 3 with the purpose of understanding their K=O phonom modes and the Eu +3 electronic transitions. Starting from the GdAlO 3 symmetry, (D1 6 sub(2h)), the correlation method allows the classification of the number and symmetries of the modes, as well their assignement as either internal or external. Experimental and theoretical results are in good agreement and show three well defined absorption bands in GdAlO 3 . The internal modes are found to be located around 670 cm -1 (stretching) and 480 cm -1 (bending), while the external modes are around 200 cm -1 . The interaction of Eu +3 electronic states with the GdAlO 3 crystal field were studied by taking into account a small perturbative orthorrombic (C sub(s)) distortion on a crystal field with symmetry O sub(h). This small distortion lifts completely the degeneracy of the 7 F sub(J) (J=0,1,...,6) levels and allows the 7 J sub(o) → 7 F sub(J) transitions. (Author) [pt

Sorption of lanthanoids by polymer-supported diaza-18-crown-6

International Nuclear Information System (INIS)

Bel'tyukova, S.I.; Malinka, E.V.; Kravchenko, T.B.; Roska, A.S.; Zitsmanis, A.Kh.

1990-01-01

Sorption of thenoyltrifluoroacetonates of rare earths on polymeric sorbent (copolymer of styrene-divinylbenzene) containing the functional groups of macrocyclic polyether diazo-18-crown-6 is studied. Sorption capacity of a sorbent and sorption coefficients are calculated. It is shgown that Eu 3+ , Sm 3+ and Gd 3+ are sorbed most of all, and Ce 3+ , Pr 3+ , Yb 3+ , Lu 3+ - worst of all. Luminescence properties of the sorption europium adduct is studied. The Eu detection limit in the sorbent is 0.00005 μg/ml, Sm - 0.01 μg/ml

Crystallographic and 119Sn and 155Gd Moessbauer analyses of Gd5Ge2(Si1-xSnx)2 (x = 0.23 and x = 0.40)

International Nuclear Information System (INIS)

Campoy, J. C. P.; Santos, A. O. dos; Cardoso, L. P.; Paesano, A.; Raposo, M. T.; Fabris, J. D.

2010-01-01

We report the structural characterization of Gd 5 Ge 2 (Si 1-x Sn x ) 2 (x = 0.23 and x = 0.40) compounds by means of 100 and 298 K-X-ray diffractometry (XRD) and 4 K- 155 Gd and 298 K- 119 Sn Moessbauer spectroscopy. These compounds order ferromagnetically at 218.4 and 172.7 K, respectively. At ∼100 K, it was identified the Gd 5 Si 4 -orthorhombic phase (type I) for both samples. At ∼298 K, it was identified a Gd 5 Si 2 Ge 2 -monoclinic phase, for x = 0.23 and a Sm 5 Sn 4 -orthorhombic phase (type II), for x 0.40. The Rietveld analysis of XRD data suggests a first order magneto-structural transition at Curie temperature for both compositions. Moessbauer results are well consistent with the proposed crystallographic models for these systems.

Structures, magnetic, and thermal properties of Ln3MoO7 (Ln=La, Pr, Nd, Sm, and Eu)

International Nuclear Information System (INIS)

Nishimine, Hiroaki; Wakeshima, Makoto; Hinatsu, Yukio

2005-01-01

Ternary lanthanide-molybdenum oxides Ln 3 MoO 7 (Ln=La, Pr, Nd, Sm, Eu) have been prepared. Their structures were determined by X-ray diffraction measurements. They crystallize in a superstructure of cubic fluorite and the space group is P2 1 2 1 2 1 . The Mo ion is octahedrally coordinated by six oxygens and the slightly distorted octahedra share corners forming a zig-zag chain parallel to the b-axis. These compounds have been characterized by magnetic susceptibility and specific heat measurements. The La 3 MoO 7 shows complex magnetic behavior at 150 and 380K. Below these temperatures, there is a large difference in the temperature-dependence of the magnetic susceptibility measured under zero-field-cooled condition and under field-cooled condition. The Nd 3 MoO 7 show a clear antiferromagnetic transition at 2.5K. From the susceptibility measurements, both Pr 3 MoO 7 and Sm 3 MoO 7 show the existence of magnetic anomaly at 8.0 and 2.5K, respectively. The results of the specific heat measurements also show anomalies at the corresponding magnetic transition temperatures. The differential scanning calorimetry measurements indicate that two phase-transitions occur for any Ln 3 MoO 7 compound in the temperature range between 370 and 710K

High-pressure synthesis and magnetic behavior of A-site columnar-ordered double perovskites, LnMn(Ga{sub 0.5}Ti{sub 0.5}){sub 2}O{sub 6} (Ln = Sm, Gd)

Energy Technology Data Exchange (ETDEWEB)

Shimura, Gen; Niwa, Ken; Shirako, Yuichi; Hasegawa, Masashi [Department of Crystalline Materials Science, Nagoya University, 464-8601, Nagoya (Japan)

2017-01-26

A-site columnar-ordered double perovskites, LnMn(Ga{sub 0.5}Ti{sub 0.5}){sub 2}O{sub 6} (Ln = Sm, Gd), were successfully synthesized under high pressure and high temperature (6 GPa, 1375 K). From the synchrotron powder X-ray diffraction patterns, all of the diffraction peaks can be indexed by the P4{sub 2}/nmc space group with lattice parameters a, c ∼ 2a{sub p} (a{sub p}: primitive cubic perovskite lattice) and no ordering of the B-site cations. Rietveld analysis of the synchrotron powder X-ray diffraction patterns and Curie-Weiss fitting of their magnetizations reveal that the ionic formulae of these perovskites are Ln{sup 3+}Mn{sup 2+}(Ga{sup 3+}{sub 0.5}Ti{sup 4+}{sub 0.5}){sub 2}O{sup 2-}{sub 6}. SmMn(Ga{sub 0.5}Ti{sub 0.5}){sub 2}O{sub 6} shows canted-antiferromagnetic behavior, whereas GdMn(Ga{sub 0.5}Ti{sub 0.5}){sub 2}O{sub 6} exhibits two different magnetic states at low temperature depending on the applied magnetic field and shows an unusual magnetization curve. These magnetic behaviors originate by decreasing the antiferromagnetic interaction by substituting Ga{sup 3+}(d{sup 10}) for Ti{sup 4+}(d{sup 0}) and by decreasing the ferromagnetic interaction between columnar-ordered Ln{sup 3+} and Mn{sup 2+}. (copyright 2017 WILEY-VCH Verlag GmbH and Co. KGaA, Weinheim)

Monte-Carlo Modelling and Verification of Photoluminescence of Gd{sub 2}O{sub 3}:Eu Scintillator by Using the GEANT4 Simulation Code

Energy Technology Data Exchange (ETDEWEB)

Cho, Gyu-Seok; Kim, Kum-Bae; Choi, Sang-Hyoun [Korea Institute of Radiological and Medical Science, Seoul (Korea, Republic of); Song, Yong-Keun [Inje University, Gimhae (Korea, Republic of); Lee, Soon-Sung [University of Science and Technology, Daejeon (Korea, Republic of)

2017-01-15

Recently, Monte Carlo methods have been used to optimize the design and modeling of radiation detectors. However, most Monte Carlo codes have a fixed and simple optical physics, and the effect of the signal readout devices is not considered because of the limitations of the geometry function. Therefore, the disadvantages of the codes prevent the modeling of the scintillator detector. The modeling of a comprehensive and extensive detector system has been reported to be feasible when the optical physics model of the GEomerty ANd Tracking 4 (GEANT 4) simulation code is used. In this study, we performed a Gd{sub 2}O{sub 3}:Eu scintillator modelling by using the GEANT4 simulation code and compared the results with the measurement data. To obtain the measurement data for the scintillator, we synthesized the Gd{sub 2}O{sub 3}:Eu scintillator by using solution combustion method and we evaluated the characteristics of the scintillator by using X-ray diffraction and photoluminescence. We imported the measured data into the GEANT4 code because GEANT4 cannot simulate a fluorescence phenomenon. The imported data were used as an energy distribution for optical photon generation based on the energy deposited in the scintillator. As a result of the simulation, a strong emission peak consistent with the measured data was observed at 611 nm, and the overall trends of the spectrum agreed with the measured data. This result is significant because the characteristics of the scintillator are equally implemented in the simulation, indicating a valuable improvement in the modeling of scintillator-based radiation detectors.

Effect of oxygen annealing on magnetic performance of (Nd,Eu,Gd)Ba.sub.2./sub.Cu.sub.3./sub.O.sub.y./sub. with a lamelar pinning nanostructure

Czech Academy of Sciences Publication Activity Database

Jirsa, Miloš; Rameš, Michal; Muralidhar, M.; Diko, P.

2009-01-01

Roč. 153, č. 1 (2009), 012015/1-012015/15 ISSN 1742-6588. [International Conference On Superconductivity and Magnetism (ICSM2008). Side-Antalya, 25.08.2008–29.08.2008] R&D Projects: GA ČR GA202/08/0722 Institutional research plan: CEZ:AV0Z10100520 Keywords : (Nd,Eu,Gd)Ba 2 Cu 3 O y * annealing effect * pinning * critical currents Subject RIV: BM - Solid Matter Physics ; Magnetism

Studies on ion transport of Eu (III) and Gd (III) through supported liquid membranes containing Di-(2-ethylhexyl) phosphate, as a carrier

Energy Technology Data Exchange (ETDEWEB)

Hernandez, L.; Bolarin, A.M.; Sanchez, F.; Patino, F.; Rivera, I.; Salinas, E. [Area de Investigaciones en Materiales y Metalurgia, Universidad Autonoma del Estado de Hidalgo, Carretera Pachuca-Tulancingo Km. 4.5, 42072 Pachuca, Hidalgo (Mexico)]. e-mail: hcruz@uaeh.reduaeh.mx

2007-07-01

In this work, permeation of Eu (III) and Gd (III) between aqueous oxide solutions through supported membrane containing di-(2-ethylhexyl) phosphate as a carrier and kerosene has been studied. Mass transfer of these cations has been determined in terms of permeability coefficients (P) by measurement of metal concentrations in strip solution. The permeability coefficient increases with increase in pH acidity of feed solution ranged from pH 0.5 to 2.5 while that of strip solution was kept constant at 0.1 mol L{sup -1} HNO{sub 3}. Thus, the results obtained show that it is possible to get up to 93% of percentage of extraction. (Author)

Studies on ion transport of Eu (III) and Gd (III) through supported liquid membranes containing Di-(2-ethylhexyl) phosphate, as a carrier

International Nuclear Information System (INIS)

Hernandez, L.; Bolarin, A.M.; Sanchez, F.; Patino, F.; Rivera, I.; Salinas, E.

2007-01-01

In this work, permeation of Eu (III) and Gd (III) between aqueous oxide solutions through supported membrane containing di-(2-ethylhexyl) phosphate as a carrier and kerosene has been studied. Mass transfer of these cations has been determined in terms of permeability coefficients (P) by measurement of metal concentrations in strip solution. The permeability coefficient increases with increase in pH acidity of feed solution ranged from pH 0.5 to 2.5 while that of strip solution was kept constant at 0.1 mol L -1 HNO 3 . Thus, the results obtained show that it is possible to get up to 93% of percentage of extraction. (Author)

Luminescence and magnetic properties of novel nanoparticle-sheathed 3D Micro-Architectures of Fe0.5R0.5(MoO4)1.5:Ln3+ (R = Gd3+, La3+), (Ln = Eu, Tb, Dy) for bifunctional application

Science.gov (United States)

Krishnan, Rajagopalan; Thirumalai, Jagannathan; Kathiravan, Arunkumar

2015-01-01

For the first time, we report the successful synthesis of novel nanoparticle-sheathed bipyramid-like and almond-like Fe0.5R0.5(MoO4)1.5:Ln3+ (R = Gd3+, La3+), (Ln = Eu, Tb, Dy) 3D hierarchical microstructures through a simple disodium ethylenediaminetetraacetic acid (Na2EDTA) facilitated hydrothermal method. Interestingly, time-dependent experiments confirm that the assembly-disassembly process is responsible for the formation of self-aggregated 3D architectures via Ostwald ripening phenomena. The resultant products are characterized by x-ray diffraction (XRD), field emission scanning electron microscopy (FESEM), high resolution transmission electron microscopy (HRTEM), photoluminescence (PL), and magnetic measurements. The growth and formation mechanisms of the self-assembled 3D micro structures are discussed in detail. To confirm the presence of all the elements in the microstructure, the energy loss induced by the K, L shell electron ionization is observed in order to map the Fe, Gd, Mo, O, and Eu components. The photo luminescence properties of Fe0.5R0.5(MoO4)1.5 doped with Eu3+, Tb3+, Dy3+ are investigated. The room temperature and low temperature magnetic properties suggest that the interaction between the local-fields introduced by the magnetic Fe3+ ions and the R3+ (La, Gd) ions in the dodecahedral sites determine the magnetism in Fe0.5R0.5(MoO4)1.5:Eu3+. This work provides a new approach to synthesizing the novel Fe0.5R0.5(MoO4)1.5:Ln3+ for bi-functional magnetic and luminescence applications.

Reactive oxygen species generation in aqueous solutions containing GdVO4:Eu3+ nanoparticles and their complexes with methylene blue

Science.gov (United States)

Hubenko, Kateryna; Yefimova, Svetlana; Tkacheva, Tatyana; Maksimchuk, Pavel; Borovoy, Igor; Klochkov, Vladimir; Kavok, Nataliya; Opolonin, Oleksander; Malyukin, Yuri

2018-04-01

It this letter, we report the study of free radicals and reactive oxygen species (ROS) generation in water solutions containing gadolinium orthovanadate GdVO4:Eu3+ nanoparticles (VNPs) and their complexes with methylene blue (MB) photosensitizer. The catalytic activity was studied under UV-Vis and X-ray irradiation by three methods (conjugated dienes test, OH· radical, and singlet oxygen detection). It has been shown that the VNPs-MB complexes reveal high efficiency of ROS generation under UV-Vis irradiation associated with both high efficiency of OH· radicals generation by VNPs and singlet oxygen generation by MB due to nonradiative excitation energy transfer from VNPs to MB molecules. Contrary to that under X-ray irradiation, the strong OH . radicals scavenging by VNPs has been observed.

Half Life Measurements in {sup 155}Gd

Energy Technology Data Exchange (ETDEWEB)

Malmskog, S G

1966-08-15

In the literature there exists a definite difference for the half life of the 86.5 keV level in Gd depending on whether {sup 155}Eu or {sup 155}Tb sources have been used. Using a good energy resolution electron-electron coincidence spectrometer and a {sup 155}Eu source, a half life of 6.48 {+-} 0.26 nsec was obtained for the 86.5 keV level. This is in agreement with the values previously measured with {sup 155}Tb sources. The half life of the 105.4 keV level was measured to be 1.12 {+-} 0.05 nsec.

Addition compounds between same phosphinoxides and hexafluorophosphates of rare earths (III)

International Nuclear Information System (INIS)

Silva, A.M. da; Melo, S.M.; Souza, E.F. de; Almeida, M.A. de

1984-01-01

Coordination compounds were prepared from salts of lanthanide hexafluorophosphates and three different phosphine oxides: methyldiphenylphosphine oxide (MDPPO), diphenylcyclohexylphosphine oxide (DPcHPO) and phosphoric acid trimethylester (TMxPO). The analytical results indicated the following general formulae : Ln(PF 6 ) 3 .5DPChPO where Ln = La, Eu, Gd, Tb and Dy; Ln(PF 6 ) 3 6MDPPO, where Ln = La, Ce, Nd, Eu, Gd, and Tm; Ln(PF 6 ) 3 .7TMxPO, where Ln = La, Ce, Pr, Nd, Sm, Eu, Gd, Tb, Dy, Ho, Er, Tm and Yb. The vibrational studies in the infrared region showed that all the phosphine oxides coordination are through the oxygen of the phosphoryl group and confirmed the non-coordination character of the PF - 6 ion. Fluorescence spectra in the visible region for the Eu (III) compounds, at the liquid nitrogen temperature indicated the microsymmetry C sub(3v) as the most probable for the Eu (III) in the compounds Eu (PF 6 ) 3 .5DPChPO and Eu (PF 6 ) 3 .7TMxPO. The symmetry site of the Eu (PF 6 ) 3 .6MDPPO compound is octahedral with tetragonal distortion. (Author) [pt

UV and VUV characteristics of (YGd)2O3:Eu phosphor particles prepared by spray pyrolysis from polymeric precursors

International Nuclear Information System (INIS)

Kim, E.J.; Kang, Y.C.; Park, H.D.; Ryu, S.K.

2003-01-01

Red-emitting (YGd) 2 O 3 :Eu phosphor particles, with high luminescence efficiency under vacuum ultraviolet (VUV) and ultraviolet (UV) excitation, were prepared by a large-scale spray pyrolysis process. To control the morphology of phosphor particles under severe preparation conditions, spray solution with polymeric precursors were introduced in spray pyrolysis. The prepared (YGd) 2 O 3 :Eu phosphor particles had spherical shape and filled morphology even after post-treatment irrespective of Gd/Y ratio. In the case of solution with polymeric precursors, long polymeric chains formed by esterification reaction in a hot tubular reactor; the droplets turned into viscous gel, which retarded the precipitation of nitrate salts and promoted the volume precipitation of droplets. The brightness of (YGd) 2 O 3 :Eu phosphor particles increased with increasing gadolinium content, and the Gd 2 O 3 :Eu phosphor had the highest luminescence intensity under UV and VUV excitation. The maximum peak intensity of Gd 2 O 3 :Eu phosphor particles under UV and VUV were 118 and 110% of the commercial Y 2 O 3 :Eu phosphor particles, respectively

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.

Characterization of element and mineral content in Artemisia annua ...

African Journals Online (AJOL)

Dr DIALLO

2013-06-26

Jun 26, 2013 ... The mineral elements are present in different kinds of herbal leaves in various proportions .... rare earth elements (Dy, Eu, Gd, Sm, Tb and Yb) were not detected in ..... behaviour of leached aluminum in tea infusions. The Sci.

Morphology-controllable growth of GdVO4:Eu3+ nano/microstructures for an optimum red luminescence

Science.gov (United States)

Yang, Liusai; Li, Guangshe; Zhao, Minglei; Zheng, Jing; Guan, Xiangfeng; Li, Liping

2012-06-01

Chemically tailoring microstructures for an optimum red luminescence is a subject at the forefront of many disciplines, which still remains a challenge due to a poor knowledge about the roles of defects in structures. In this work, GdVO4 :Eu3+ nano/microstructures of different morphologies, including tomato-like, cookie-circle-like, and ellipsoidal-like nanoparticles, and microspheroids were synthesized via a simple hydrothermal route using trisodium citrate as a capping agent. During the growth processes, the types of vanadyl ions were adjusted by varying pH value to control the morphologies and nano/microstructures with the help of trisodium citrate. The possible mechanisms for the growth processes into diverse morphologies are presented. Further, a systematic study on defect characteristics pertinent to these diverse morphologies has been explored to achieve an optimum red luminescence. The ability is clearly shown to generate different nano/microstructures of diverse morphologies and varied defect concentrations, which provides a great opportunity for morphological control in tailoring the red luminescence property for many technological applications.

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.

Power-law index and penetration depth of (Nd_xSm_xGd_1−2x)Ba2Cu₃O_7−δ films studied by AC susceptibility

DEFF Research Database (Denmark)

Li, Xiaofen; He, Dong; Grivel, Jean-Claude

2012-01-01

Superconducting (NdxSmxGd1−2x)Ba2Cu3O7−δ films with x=0, 0.1, 0.25, 0.33 were grown by PLD on STO single crystal substrates. The power-law index n and penetration depth λ are studied by AC susceptibility. During cooling, n in films with x ≠ 0 increases much slower compared with the films with x =....... The films with x ≠ 0 also tend to have a longer penetration depth. These properties might be related to the higher possibility for disorder in the mixed (Nd,Sm,Gd)BCO films....

Komatiites of the Onverwacht Group, S. Africa: REE geochemistry, Sm/Nd age and mantle evolution

Science.gov (United States)

Jahn, Bor-Ming; Gruau, G.; Glikson, A. Y.

1982-08-01

Komatiites of the Tjakastad Subgroup of the Onverwacht Group (S. Africa) were dated by the Sm/Nd method. A whole-rock isochron yields an age of 3.56±0.24 (2 σ) AE, with initial 143Nd/144Nd ratio of 0.50818±23 (2 σ), corresponding to ɛ Nd( T)= + 1.9±4.5. This age is interpreted as the time of initial Onverwacht volcanism. This result agrees with earlier Sm/Nd data of Hamilton et al. (1979) and is consistent with the Rb-Sr result of Jahn and Shih (1974). Komatiites may be divided into 3 groups based on the typology of heavy REE distributions (Jahn and Gruau 1981). According to this scheme, the Onverwacht komatiites of the present study belong to two groups: the predominant Group II rocks showing (Gd/Yb)N≃1.4, CaO/Al2O3 = 1.33, Al2O3/TiO2≃10.6; and the subordinate Group III rocks with (Gd/Yb)Nconnotation of the chemical parameters, such as CaO/Al2O3, (Gd/Yb)N or Al2O3/TiO2 ratio has not been firmly established. The characteristic “high” CaO/Al2O3 or (Gd/Yb)N ratios in many Onverwacht Group rocks can also be explained as a result of local short-term mantle heterogeneity.

Decay pathway and high-temperature luminescence of Eu{sup 3+} in Ca{sub 2}Gd{sub 8}Si{sub 6}O{sub 26}

Energy Technology Data Exchange (ETDEWEB)

Chambers, M.D. [Engineering Materials Department, College of Engineering, University of California, Santa Barbara, CA 93106-5050 (United States)], E-mail: chambers@engineering.ucsb.edu; Rousseve, P.A.; Clarke, D.R. [Engineering Materials Department, College of Engineering, University of California, Santa Barbara, CA 93106-5050 (United States)

2009-03-15

The temperature-dependent luminescence of Eu:Ca{sub 2}Gd{sub 8}Si{sub 6}O{sub 26} and its decay pathways are investigated in order to assess the utility of the material as a thermometric phosphor. Non-radiative decays are found to compete with radiative processes even at room temperature. A decay pathway involving decay through charge-transfer states is proposed based on the decay profiles of emissions from {sup 5}D{sub 1} and {sup 5}D{sub 0} levels and on the temperature sensitivity of the spectra as observed after excitation by several wavelengths. The implications of this on solid-state lighting are also discussed.

Effect of oxygen pressure on the structure and luminescence of Eu-doped Gd{sub 2}O{sub 3} thin films

Energy Technology Data Exchange (ETDEWEB)

Wellenius, Patrick; Muth, John F. [Department of Electrical and Computer Engineering, NC State University, Raleigh, NC 27606 (United States); Smith, Eric R. [Kratos Defense and Security Solutions, Inc., 5030 Bradford Dr., Huntsville, AL 35805 (United States); Wu, Pae C [Department of Electrical and Computer Engineering, Duke University, Durham, NC 27708 (United States); Everitt, Henry O. [Department of Electrical and Computer Engineering, Duke University, Durham, NC 27708 (United States); Army Aviation and Missile RD and E Center, Redstone Arsenal, AL 35898 (United States)

2010-08-15

Europium-doped gadolinium oxide (Gd{sub 2}O{sub 3}) thin films were deposited on sapphire substrates by pulsed laser deposition (PLD). The effect of oxygen pressure during deposition on the structure of the thin films, investigated by transmission electron microscopy (TEM) and X-ray diffraction (XRD), was correlated to photoluminescence spectra. The polycrystalline films, like the one deposited in 5 mTorr oxygen environment, were primarily monoclinic phase; however the rarer cubic phase was achieved at 50 mTorr pressure. Time-integrated and time-resolved photoluminescence (TIPL and TRPL) spectra of the bright {sup 5}D{sub 0} to {sup 7}F{sub 2} radiative transition revealed how the differing host material phases altered the local environment of the Eu dopants. (Abstract Copyright [2010], Wiley Periodicals, Inc.)

In Vivo Immunotoxicity of SiO2@(Y0.5Gd0.45Eu0.052O3 as Dual-Modality Nanoprobes

Directory of Open Access Journals (Sweden)

Xiumei Tian

2014-08-01

Full Text Available We have successfully synthesized SiO2@(Y0.5Gd0.45Eu0.052O3 nanocomposites as a potential dual-modality nanoprobe for molecular imaging in vitro. However, their immunotoxicity assessment in vivo remains unknown. In this article, the in vitro biocompatibility of our dual-modality nanoprobes was assayed in terms of cell viability and apoptosis. In vivo immunotoxicity was investigated by monitoring the generation of reactive oxygen species (ROS, cluster of differentiation (CD markers and cytokines in Balb/c mice. The data show that the in vitro biocompatibility was satisfactory. In addition, the immunotoxicity data revealed there are no significant changes in the expression levels of CD11b and CD71 between the nanoprobe group and the Gd in a diethylenetriaminepentaacetic acid (DTPA chelator (Gd-DTPA group 24 h after injection in Balb/c mice (p > 0.05. Importantly, there are significant differences in the expression levels of CD206 and CD25 as well as the secretion of IL-4 and the generation of ROS 24 h after injection (p < 0.05. Transmission electron microscopy (TEM images showed that few nanoprobes were localized in the phagosomes of liver and lung. In conclusion, the toxic effects of our nanoprobes may mainly result from the aggregation of particles in phagosomes. This accumulation may damage the microstructure of the cells and generate oxidative stress reactions that further stimulate the immune response. Therefore, it is important to evaluate the in vivo immunotoxicity of these rare earth-based biomaterials at the molecular level before molecular imaging in vivo.

Titration of thorium and rare earths with ethylenediaminetetraacetic acid using semimethylthymol blue by visual end-point indication

International Nuclear Information System (INIS)

Hafez, M.A.H.; Kenawy, I.M.M.; Ramadan, M.A.M.

1994-01-01

The precision and accuracy attainable in direct complexometric titrations of Thsup(4+) consecutively with either lighter (La 3+ , Nd 3+ , Sm 3+ , Eu 3+ or Gd 3+ ) or heavier lanthanides (Dy 3+ ) in different proportions using Semimethylthymol Blue (SMTB) as a metallochromic indicator and disodium dihydrogen ethylenediaminetetraacetate were studied. Thorium (IV) was titrated at pH 2, the Ph was adjusted to 5.5-6.0 by adding hexamethylenetetramine (hexamine) buffer and acetylacetone-acetone solution and La 3+ (or Nd 3+ , Sm 3+ , Eu 3+ , Gd 3+ or Dy 3+ ) was then titrated. A comparison of the indicators SMTB and Methylthymol Blue (MTB) for successive titrations of Th 4+ and any of the rare earth ions was carried out. The proposed titration method was applied successfully to some naturally occurring ores and minerals containing thorium and some lanthanides and the results were satisfactory. (Author)

Enrichment method for trace amounts of rare earth elements using chemofiltration and XRF determination

International Nuclear Information System (INIS)

De Vito, I.E.; Olsina, R.A.; Masi, A.N.

2000-01-01

A preconcentration method for subsequent determination of rare earth elements (REE) by X-ray fluorescence (XRF) spectrometry was developed. The method is based on using (o-[3,6-disulfo-2-hydroxy-1-naphthylazo]-benzenearsonic acid) (Thorin) as a complexing agent which is retained on a polyamide membrane by a chemofiltration process. The pH dependence of the chemofiltration of these metal ions on the membrane and other variables, such as flow-rate, contact time, kinetic of complex formation, etc. were determined. The membrane containing the chemofiltrate formed a thin film, which eliminated the interelemental effects when measured by XRF. The detection limits were 23, 23 and 49 ng/mL for Sm(III), Eu(III) and Gd(III), respectively. High enrichment factors were obtained. The method was successfully applied to the preconcentration of Sm(III), Eu(III) and Gd(III) from different samples. (orig.)

Solid-state amorphization of SmFe3 by hydrogenation

International Nuclear Information System (INIS)

Mueller, K.H.; Kubis, M.; Handstein, A.; Gutfleisch, O.

2000-01-01

Hydrogen-induced amorphization (HIA) has received much attention as a method for the preparation of amorphous compounds since its discovery by Yeh et al. Meanwhile it has been observed for a large number of intermetallic compounds with C15, C23, B8 2 , DO 19 and L1 2 structures. E.G. the C15 Laves-type compounds (MgCu 2 -type structure) of rare earth (R) - transition metal (T) compounds RT 2 show HIA for R = Y, Ce, Pr, Nd, Sm, Gd, Tb, Dy, Ho and Er. Aoki et al. postulated that new amorphizing compounds can be expected at high hydrogen pressures. In this work, the structural changes of SmFe 3 (PuNi 3 -type structure) during heating in high hydrogen pressures are reported

Magnetocaloric effect and refrigeration cooling power in amorphous Gd7Ru3 alloys

OpenAIRE

Pramod Kumar; Rachana Kumar

2015-01-01

In this paper, we report the magnetic, heat capacity and magneto-caloric effect (MCE) of amorphous Gd7Ru3 compound. Both, temperature dependent magnetization and heat capacity data reveals that two transitions at 58 K and 34 K. MCE has been calculated in terms of isothermal entropy change (ΔSM) and adiabatic temperature change (ΔTad) using the heat capacity data in different fields. The maximum values of ΔSM and ΔTad are 21 Jmol−1K−1 and 5 K respectively, for field change of 50 kOe whereas re...

Chemiluminescent Diagnostics of Free-Radical Processes in an Abiotic System and in Liver Cells in the Presence of Nanoparticles Based on Rare-Earth Elements nReVO4:Eu3+ (Re = Gd, Y, La) and CeO2

Science.gov (United States)

Averchenko, E. A.; Kavok, N. S.; Klochkov, V. K.; Malyukin, Yu. V.

2014-11-01

We have used luminol-dependent chemiluminescence with Fenton's reagent to study the effect of nanoparticles based on rare-earth elements of different sizes and shapes on free-radical processes in abiotic and biotic cell-free systems, and also in isolated cells in vitro. We have estimated the effects of rare-earth orthovanadate nanoparticles of spherical (GdYVO4:Eu3+, 1-2 nm), spindle-shaped (GdVO4:Eu3+, 25 ×8 nm), and rod-shaped (LaVO4:Eu3+, 57 × (6-8) nm) nanoparticles and spherical CeO2 nanoparticles (sizes 1-2 nm and 8-10 nm). We have shown that in contrast to the abiotic system, in which all types of nanoparticles exhibit antiradical activity, in the presence of biological material, extra-small spherical (1-2 nm) nanoparticles of both types exhibit pro-oxidant activity, and also enhance pro-oxidant induced oxidative stress (for the pro-oxidants hydrogen peroxide and tert-butyl hydroperoxide). The effect of rare-earth orthovanadate spindle and rod shaped nanoparticles in this system was neutral; a moderate antioxidant effect was exhibited by 8-10 nm CeO2 nanoparticles.

Synthesis and Structural Investigation of New Bio-Relevant Complexes of Lanthanides with 5-Hydroxyflavone: DNA Binding and Protein Interaction Studies

Directory of Open Access Journals (Sweden)

Alexandra-Cristina Munteanu

2016-12-01

Full Text Available In the present work, we attempted to develop new metal coordination complexes of the natural flavonoid 5-hydroxyflavone with Sm(III, Eu(III, Gd(III, Tb(III. The resultant hydroxo complexes have been characterized by a variety of spectroscopic techniques, including fluorescence, FT-IR, UV-Vis, EPR and mass spectral studies. The general chemical formula of the complexes is [Ln(C15H9O33(OH2(H2Ox]·nH2O, where Ln is the lanthanide cation and x = 0 for Sm(III, x = 1 for Eu(III, Gd(III, Tb(III and n = 0 for Sm(III, Gd(III, Tb(III, n = 1 for Eu(III, respectively. The proposed structures of the complexes were optimized by DFT calculations. Theoretical calculations and experimental determinations sustain the proposed structures of the hydroxo complexes, with two molecules of 5-hydroxyflavone acting as monoanionic bidentate chelate ligands. The interaction of the complexes with calf thymus DNA has been explored by fluorescence titration and UV-Vis absorption binding studies, and revealed that the synthesized complexes interact with DNA with binding constants (Kb ~ 104. Human serum albumin (HSA and transferrin (Tf binding studies have also been performed by fluorescence titration techniques (fluorescence quenching studies, synchronous fluorescence spectra. The apparent association constants (Ka and thermodynamic parameters have been calculated from the fluorescence quenching experiment at 299 K, 308 K, and 318 K. The quenching curves indicate that the complexes bind to HSA with smaller affinity than the ligand, but to Tf with higher binding affinities than the ligand.

Dynamics of the lattice and spins in the phase-separated manganite (Eu{sub 1−x}Gd{sub x}){sub 0.6}Sr{sub 0.4}MnO{sub 3}

Energy Technology Data Exchange (ETDEWEB)

Taniguchi, Haruka, E-mail: tanig@iwate-u.ac.jp [Department of Physical Science and Materials Engineering, Iwate University, Morioka 020-8551 (Japan); Kimura, Daichi; Matsukawa, Michiaki; Inomata, Tasuku; Kobayashi, Satoru [Department of Physical Science and Materials Engineering, Iwate University, Morioka 020-8551 (Japan); Nimori, Shigeki [National Institute for Materials Science, Tsukuba 305-0047 (Japan); Suryanarayanan, Ramanathaan [Laboratoire de Physico-Chimie de l’Etat Solide, CNRS, UMR8182, Université Paris-Sud, 91405 Orsay (France)

2017-06-15

We investigated slow relaxations of the magnetostriction and residual magnetostriction of the phase-separated system (Eu{sub 1−x}Gd{sub x}){sub 0.6}Sr{sub 0.4}MnO{sub 3}, in which the metamagnetic transition from a paramagnetic insulating state to a ferromagnetic metallic state is accompanied by a lattice shrinkage. The relaxations are well fitted by a stretched exponential function, suggesting the strong frustration between the double exchange interaction and Jahn-Teller effect. We have revealed that the Gd substitution suppresses the frozen phase-separated phase at low temperatures and stabilizes the paramagnetic insulating state in the dynamic phase-separated phase at intermediate temperatures. The former origin would be the randomness effect and the latter would be the suppression of the double exchange interaction.

Long-wave UVA radiation excited warm white-light emitting NaGdTiO4: Tm3+/Dy3+/Eu3+ ions tri-doped phosphors: Synthesis, energy transfer and color tunable properties

International Nuclear Information System (INIS)

Bharat, L. Krishna; Du, Peng; Yu, Jae Su

2016-01-01

NaGdTiO 4 (NGT) phosphors doped with different activator ions (Tm 3+ , Dy 3+ , and Eu 3+ ) were synthesized by a conventional solid-state reaction method in an ambient atmosphere. These phosphors were characterized by scanning electron microscope images, transmission electron microscope images, X-ray diffraction patterns, Fourier transform infrared spectra, and photoluminescence spectra. All the samples were crystallized in an orthorhombic phase with a space group of Pbcm (57). In Tm 3+ /Dy 3+ ions co-doped samples, white-light emission was observed under near-ultraviolet (NUV) excitation. In addition, the energy transfer between Tm 3+ and Dy 3+ ions was proved to be a resonant type via an electric dipole–dipole mechanism and the critical distance of energy transfer was calculated to be 19.91 Å. Furthermore, Tm 3+ /Dy 3+ /Eu 3+ ions tri-doped NGT phosphors demonstrated warm white-light emission by appropriately tuning the activator content, based on the principle of energy transfer. These NUV wavelength excitable phosphors exhibit great potential as a single-phase full-color emitting phosphor for white light-emitting diode applications. - Highlights: • The pebble shaped NaGdTiO 4 particles were prepared by solid-state reaction method. • Tm 3+ and Dy 3+ single doping gives respective blue and cool white light emission. • The Tm 3+ /Dy 3+ ions co-doped samples give CIE values near to standard white light. • Addition of Eu 3+ ions shifts the CIE values towards warm white light region. • This single phase white light emitting phosphors have lower CCT values (<5000 K).

Oxygen perovskites with pentavalent ruthenium A/sub 2/sup(II)Bsup(III)Rusup(V)O/sub 6/ with Asup(II) = Ba, Sr

Energy Technology Data Exchange (ETDEWEB)

Bader, H; Kemmler-Sack, S [Tuebingen Univ. (Germany, F.R.). Lehrstuhl fuer Anorganische Chemie 2

1980-07-01

The perovskites Ba/sub 2/Bsup(III)Rusup(V)O/sub 6/ with Bsup(III) = La, Nd, Sm, Eu, Gd, Dy, Y are cubic (Bsup(III) = La: a = 8.54 A; Y: a = 8.33 A) with a partial order for Bsup(III) and Rusup(V). The Sc compound, Ba/sub 2/ScRuO/sub 6/, has a hexagonal 6L structure (a = 5.79 A; c = 14.22 A; sequence (hcc)/sub 2/). The lattice of the Sr perovskites, Sr/sub 2/Bsup(III)Rusup(V)O/sub 6/, with Bsup(III) = Eu, Gd, Dy, Y is rhombic distorted. The IR and FIR spectra are discussed.

RE{sub 3}Ga{sub 9}Ge (RE=Y, Ce, Sm, Gd and Yb): compounds with an open three-dimensional polygallide framework synthesized from liquid gallium

Energy Technology Data Exchange (ETDEWEB)

Zhuravleva, M A; Kanatzidis, M G

2003-07-01

The RE{sub 3}Ga{sub 9}Ge compounds (RE=Y, Ce, Sm, Gd and Yb) were synthesized at 850 deg. C in quantitative yield from reactions containing excess liquid Ga. The orthorhombic crystal structure is characterized by a unique three-dimensional open Ga framework with parallel straight tunnels. In the tunnels, inserted are arrays of the RE atoms together with interpenetrated monoatomic RE-Ga-Ge planes. A complex disordered arrangement of the RE and Ga atoms is observed in the monoatomic plane. Depending on the extent of disorder, the crystal structure could be presented either in a sub-cell (no ordering) or in a super-cell (partial ordering). Single-crystal X-ray data for Ce{sub 3}Ga{sub 9}Ge sub-structure: space group Immm, Z=2, cell parameters a=4.3400(12) A; b=10.836(3) A; and c=11.545(3) A; super-structure: space group Cmma, Z=8, cell parameters a=8.680(3) A; b=23.090(7) A; and c=10.836(3) A. The refinement based on the full-matrix least squares on F{sub o}{sup 2}[I>2{sigma}(I)] converged to final residuals R{sub 1}/wR{sub 2}=0.0226/0.0528 and 0.0729/0.1569 for the sub- and super-structures, respectively. The relationship between the disordered sub-structure and partially ordered super-structure is discussed. Magnetic susceptibility measurements show Curie-Weiss behavior at the temperatures above 30 K with the negative Weiss constants {theta}=-49(1) and-7.7 K for Gd and Ce analogs, respectively. An antiferromagnetic transition is observed in the Gd analog at T{sub N}=26.1 K. The {mu}{sub eff} obtained for both analogs is close to the RE{sup 3+} free-ion value.

Ultraviolet photoluminescence in Gd-doped silica and phosphosilicate fibers

Directory of Open Access Journals (Sweden)

Y. Wang

2017-04-01

Full Text Available Optical fiber lasers operating in the near infrared and visible spectral regions have relied on the spectroscopic properties of rare earth ions such as Yb3+, Er3+, Tm3+, Nd3+, and Sm3+. Here, we investigate Gd3+ doping in phosphosilicate and pure silica fibers using solution doping and sol-gel techniques, respectively, for potential applications in the ultraviolet. Photoluminescence spectra for optical fiber bundles and fiber preforms were recorded and compared. Emissions at 312 nm (phosphosilicate and 314 nm (pure silica were observed when pumping to the Gd3+ 6DJ, 6IJ, and 6PJ = 5/2, 3/2 energy levels. Oxygen deficient center was observed in solution doping sample with a wide absorption band centered at around 248 nm not affecting pumping to 6IJ states.

Investigation of BaMoO4-Ln2(MoO4)3 systems (Ln = Nd, Sm, Yb)

International Nuclear Information System (INIS)

Vakulyuk, V.V.; Evdokimov, A.A.; Khomchenko, G.P.

1982-01-01

Using the methods of X-ray phase and differential-thermal analyses phase ratios in the systems BaMoO 4 -Ln 2 (MoO 4 ) 3 (Ln=Nd, Sm, Yb); BaNd 2 (MoO 4 ) 4 -MaGd 2 (MoO 4 ) are studied. Unit cell parameters and the character of melting of the compounds BaLn 2 (MoO 4 ) 4 are specified. Effect of growth conditions on laminated nature of BaGd 2 (MoO 4 ) 4 monocrystals is studied

Enhancing the performance of photovoltaic cells by using down-converting KCaGd(PO4)2∶Eu3+ phosphors

Institute of Scientific and Technical Information of China (English)

Yen-Chi Chen; Woan-Yu Huang; Teng-Ming Chen

2011-01-01

The goal of this work is aimed to improve the power conversion efficiency of single crystalline silicon-based photovoltaic (PV) cells by using the solar spectral conversion principle,which employed a down-converting phosphor to convert a high-energy ultraviolet photon to the less energetic red-emitting photons to improve the spectral response of Si solar cells.In this study,the surface of silicon solar cells was coated with a red-emitting KCaGd(PO4)2∶Eu3+ phosphor by using the screen-printing technique.In addition to the investigation on the microstructure using scanning electron microscopy (SEM),we measured the short circuit current (Isc),open circuit voltage (Voc),and power conversion efficiency (η) of spectral-conversion cells and compared with those of bare solar cells as a reference.Preliminary experimental results revealed that in an optimized PV cell,an enhancement of (0.64+0.01)％ (from 16.03％ to 16.67％) in △η ofa Si-based PV cell was achieved.

Comparative magnetic studies of (Sm, Nd) trichloroacetates and their heteronuclear CuLn2(CCl3COO)8.6H2O systems: structure and spectroscopy of a new type of Eu trichloroacetate

International Nuclear Information System (INIS)

Wojciechowski, W.; Legendziewicz, J.; Puchalska, M.; Ciunik, Z.

2004-01-01

Two series of compounds: heteronuclear CuLn 2 (CCl 3 COO) 8 .6H 2 O (Ln = Nd and Sm) and their simple analogues Ln(CCl 3 COO) 3 .2H 2 O (Ln = Eu, Nd, Sm) were synthesized. New Eu(III) trichloroacetate; Eu(CCl 3 COO) 3 .3H 2 O.CH 3 OH was obtained, its molecular structure was determined by X-ray diffraction and compared with the data of respective systems reported earlier. Magnetization was measured and the susceptibility was derived in the limit of low field. Magnetic susceptibilities were calculated and discussed for series of homo- and hetero-nuclear chloroacetates.Untypical hysteresis was found (two loops) in samarium trichloroacetate. This phenomenon is most probably the effect of flops of spins in magnetic fields of 30,000Oe and very weak (if any) interaction intermediated by weak hydrogen bonding between the chains. A similar magnetic behavior was observed in neodymium carboxylate where the magnetic ordering was observed as a result of Nd-Nd interaction at low temperature (1.6K). For this system, the magnetic moment depends on magnitude of the magnetic field and ferromagnetic ordering appears at low temperatures. The strongest interactions of coupled ions and antiferromagnetic ordering with T N =6.5K were found in CuSm 2 (CCl 3 COO) 8 .6H 2 O single crystals.Heisenberg model was applied in the calculations for three interacting ions located linearly. The following relation was derived: χ M =Ng 2 μ β 2 kT(12)+(12)exp(J 2 /kT)+5exp(J 2 /kT)-exp(1,5J 1 /kT)2+2exp(J 2 /kT)+4exp(J 2 /kT)-exp(1,5J 1 /kT) and applied in calculations of the exchange integrals. Mechanism of the exchange interaction was discussed on the basis of the obtained results.

Synthesis and characterization of BaAl{sub 2}O{sub 4}:Eu{sup 2+} co-doped with different rare earth ions

Energy Technology Data Exchange (ETDEWEB)

Lephoto, M.A. [Department of Physics, University of the Free State, Private bag X 13, Phuthaditjaba 9866, P.O. Box 339, Bloemfontein, ZA 9300 (South Africa); Ntwaeaborwa, O.M., E-mail: ntwaeab@ufs.ac.za [Department of Physics, University of the Free State, Private bag X 13, Phuthaditjaba 9866, P.O. Box 339, Bloemfontein, ZA 9300 (South Africa); Pitale, Shreyas S.; Swart, H.C. [Department of Physics, University of the Free State, Private bag X 13, Phuthaditjaba 9866, P.O. Box 339, Bloemfontein, ZA 9300 (South Africa); Botha, J.R. [Department of Physics, Nelson Mandela Metropolitan University, Port Elizabeth, ZA 6031 (South Africa); Mothudi, B.M. [Department of Physics, University of South Africa, P.O Box 392, Pretoria, ZA 6031 (South Africa)

2012-05-15

Combustion method was used in this study to prepare BaAl{sub 2}O{sub 4}:Eu{sup 2+} phosphors co-doped with different trivalent rare-earths (Re{sup 3+}=Dy{sup 3+}, Nd{sup 3+}, Gd{sup 3+}, Sm{sup 3+}, Ce{sup 3+}, Er{sup 3+}, Pr{sup 3+} and Tb{sup 3+}) ions at an initiating temperature of 600 Degree-Sign C. The phosphors were annealed at 1000 Degree-Sign C for 3 h. As confirmed from the X-ray diffraction (XRD) data, both as prepared and post annealed samples crystallized in the well known hexagonal structure of BaAl{sub 2}O{sub 4}. All samples exhibited bluish-green emission associated with the 4f{sup 6}5d{sup 1}{yields}4f{sup 7} transitions of Eu{sup 2+} at {approx}500 nm. Although the highest intensity was observed from Er{sup 3+} co-doping, the longest afterglow (due to trapping and detrapping of charge carriers) was observed from Nd{sup 3+} followed by Dy{sup 3+} co-doping. The traps responsible for the long afterglow were studied using thermoluminescence (TL) spectroscopy.

Study on Yen Phu rare earth ore concentrate treatment technology and separation of major heavy rare earth elements by solvent extraction method

International Nuclear Information System (INIS)

Le Ba Thuan; Pham Quang Trung; Vu Lap Lai

2003-01-01

1. Yenphu rare earth ore concentrate treatment by alkali under pressure: On the base of studying mineral and chemical compositions of Yenphu rare earth ore concentrate containing 28% TREO and conditions for digestion of ore concentrate by alkali under pressure such as ore concentrate/ NaOH ratio, alkali concentration, pressure and temperature at bench scale (100 gram and 5 kg per batch), the optimal conditions for decomposition of REE ore concentrate have been determined. The yield of the decomposition stage is about 90%. The studies on alkali washing, REE leaching by HCl, pH for leaching process, and iron and radioactive impurities removing by Na 2 S + Na 2 PO 4 have been carried out. The obtained results show that mixture of Na 2 S 5% + Na2PO 4 1% is effective in iron and radioactive impurities removing. The obtained REE oxides get purity of > 99% and meet the need of solvent extraction (SX) individual separation of rare earth elements. The schema for recovery of REEs from Yenphu REE ore concentrate by alkali decomposition under high pressure has been proposed. 2. Fractionation of Yenphu rare earth mixture into subgroups by solvent extraction with PC88A: On the base of simulation program, the parameters for fractional process of rare earths mixture into subgroups by solvent extraction with PC88A have been proposed and determined by experimental verification on mixer-settler set. According to this process, rare earths mixture fractionated into yttrium and light subgroups. In their turn, the light subgroup was separated into light (La, Ce, Pr, Nd) and middle (Sm, Eu, Gd) subgroups. The average yield of the process reached value > 95%. The composition of light subgroup meets the needs for individual separation of Gd, Eu, and Sm. 3. Separation and purification of yttrium: The process for recovery of yttrium consists of two stages: upgrade to get high quality Y concentrate by PC88A and purification by Aliquat 336 in NH 4 SCN-NH 4 Cl medium. The process parameter for

Bulletin of Materials Science | Indian Academy of Sciences

Indian Academy of Sciences (India)

Permanent link: https://www.ias.ac.in/article/fulltext/boms/039/03/0603-0611. Keywords. Predominance area diagram; Kellogg diagram; lanthanide oxychloride; rare-earth mineral processing; thermodynamic properties. Abstract. Isothermal stability field diagrams for Ln−O−Cl systems (Ln = La, Ce, Pr, Nd, Sm, Eu, Gd, Tb, Dy, ...

Guided ion beam and theoretical studies of the bond energy of SmS+

Science.gov (United States)

Armentrout, P. B.; Demireva, Maria; Peterson, Kirk A.

2017-12-01

Previous work has shown that atomic samarium cations react with carbonyl sulfide to form SmS+ + CO in an exothermic and barrierless process. To characterize this reaction further, the bond energy of SmS+ is determined in the present study using guided ion beam tandem mass spectrometry. Reactions of SmS+ with Xe, CO, and O2 are examined. Results for collision-induced dissociation processes with all three molecules along with the endothermicity of the SmS+ + CO → Sm+ + COS exchange reaction are combined to yield D0(Sm+-S) = 3.37 ± 0.20 eV. The CO and O2 reactions also yield a SmSO+ product, with measured endothermicities that indicate D0(SSm+-O) = 3.73 ± 0.16 eV and D0(OSm+-S) = 1.38 ± 0.27 eV. The SmS+ bond energy is compared with theoretical values characterized at several levels of theory, including CCSD(T) complete basis set extrapolations using all-electron basis sets. Multireference configuration interaction calculations with explicit spin-orbit calculations along with composite thermochemistry using the Feller-Peterson-Dixon method and all-electron basis sets were also explored for SmS+, and for comparison, SmO, SmO+, and EuO.

Triple energy transfer and color tuning in Tb3+ and Eu3+-coactivated apatite-type gadolinium-containing phosphors

Science.gov (United States)

Guo, Ning; Liang, Qimeng; Li, Shuo; Ouyang, Ruizhuo; Lü, Wei

2017-11-01

A family of apatite-type fluorophosphate phosphors with general formula Sr3Gd(1-m-n)Na(PO4)3F:mTb3+,nEu3+ (SGN:mTb3+,nEu3+) have been synthesized via the high-temperature solid-state reaction method. Triple energy transfer processes from Gd3+ in the host to both Tb3+ and Eu3+, as well as from Tb3+ to Eu3+ have been verified by the photoluminescence spectra. Under the excitation of UV light, both green line from the transitions of Tb3+ and red line origin from the transitions of Eu3+ have been simultaneously observed in a single phase phosphor, which makes a promise for tunable color emissions from yellowish-green through yellow and ultimately to reddish-orange by simply adjusting the Eu3+ content (n) in SGN:0.20Tb3+,nEu3+ phosphors. Additionally, the energy transfer from the Tb3+ to the Eu3+ ions has been demonstrated to be a resonant type via a quadrupole-quadrupole mechanism based on the Dexter's theoretical model, and the energy transfer efficiency increases with an increase in Eu3+ concentration.

Angular non-critical phase-matching second-harmonic-generation characteristics of RECOB (RE = Tm, Y, Gd, Sm, Nd and La) crystals.

Science.gov (United States)

Liu, Yanqing; Wang, Zhengping; Yu, Fapeng; Qi, Hongwei; Yang, Xiuqin; Yu, Xiaoqiang; Zhao, Xian; Xu, Xinguang

2017-05-15

For the first time, the angular non-critical phase-matching (A-NCPM) second-harmonic-generation (SHG) characteristics of a family of monoclinic oxoborate crystals, RECa 4 O(BO 3 ) 3 (RECOB, RE = Tm, Y, Gd, Sm, Nd and La), were comprehensively investigated. For all of the realizable A-NCPM SHG styles, the feature parameters including PM wavelength, angular, wavelength and temperature acceptance bandwidths, have been derived from the theory and verified by the experiments. We discovered that the closer the ion radius between RE 3+ and Ca 2+ , the smaller the birefringence, and the better the A-NCPM SHG properties. As a result, for the Type-I SHG on Y-axis which has the largest effective nonlinear optical coefficient (d eff ) among the three realizable A-NCPM styles, NdCOB crystal presents the longest PM wavelength (927 nm), the largest angular acceptance bandwidth (Δθ⋅l 1/2 = 84.3 mrad·cm 1/2 , Δϕ⋅l 1/2 = 58.8 mrad·cm 1/2 ), and the broadest wavelength acceptance bandwidth (8.7 nm). This discovery will contribute to the design of new NCPM materials, at the same time the parameter formula will be helpful for the theoretical prediction of NCPM performance.

Multicolor Tunable Luminescence Based on Tb3+/Eu3+ Doping through a Facile Hydrothermal Route.

Science.gov (United States)

Wang, Chao; Zhou, Ting; Jiang, Jing; Geng, Huiyuan; Ning, Zhanglei; Lai, Xin; Bi, Jian; Gao, Daojiang

2017-08-09

Ln 3+ -doped fluoride is a far efficient material for realizing multicolor emission, which plays an important part in full-color displays, biolabeling, and MRI. However, studies on the multicolor tuning properties of Ln 3+ -doped fluoride are mainly concentrated on a complicated process using three or more dopants, and the principle of energy transfer mechanism is still unclear. Herein, multicolor tunable emission is successfully obtained only by codoping with Tb 3+ and Eu 3+ ions in β-NaGdF 4 submicrocrystals via a facile hydrothermal route. Our work reveals that various emission colors can be obtained and tuned from red, orange-red, pink, and blue-green to green under single excitation energy via codoping Tb 3+ and Eu 3+ with rationally changed Eu 3+ /Tb 3+ molar ratio due to the energy transfer between Tb 3+ and Eu 3+ ions in the β-NaGdF 4 host matrix. Meanwhile, the energy transfer mechanism in β-NaGdF 4 : x Eu 3+ /y Tb 3+ (x + y = 5 mol %) submicrocrystals is investigated. Our results evidence the potential of the dopants' distribution density as an effective way for analyzing energy transfer and multicolor-controlled mechanism in other rare earth fluoride luminescence materials. Discussions on the multicolor luminescence under a certain dopant concentration based on single host and wavelength excitation are essential toward the goal of the practical applications in the field of light display systems and optoelectronic devices.

Structural trends in a series of isostructural lanthanide-copper metallacrown sulfates (Ln(III) = Pr, Nd, Sm, Eu, Gd, Dy and Ho): hexaaquapentakis[μ3-glycinehydroxamato(2-)]sulfatopentacopper(II)lanthanide(III) heptaaquapentakis[μ3-glycinehydroxamato(2-)]sulfatopentacopper(II)lanthanide(III) sulfate hexahydrate.

Science.gov (United States)

Pavlishchuk, Anna V; Kolotilov, Sergey V; Fritsky, Igor O; Zeller, Matthias; Addison, Anthony W; Hunter, Allen D

2011-07-01

The seven isostructural complexes, [Cu(5)Ln(C(2)H(4)N(2)O(2))(5)(SO(4))(H(2)O)(6.5)](2)(SO(4))·6H(2)O, where Ln(III) = Pr, Nd, Sm, Eu, Gd, Dy and Ho, are representatives of the 15-metallacrown-5 family. Each dianion of glycinehydroxamic acid (GlyHA) links two Cu(II) cations forming a cyclic [CuGlyHA](5) frame. The Ln(III) cations are located at the centre of the [CuGlyHA](5) rings and are bound by the five hydroxamate O atoms in the equatorial plane. Five water molecules are coordinated to Cu(II) cations, and one further water molecule, located close to an inversion centre between two adjacent [Cu(5)Ln(GlyHA)(5)](2+) cations, is disordered around this inversion centre and coordinated to a Cu(II) cation of either the first or second metallacrown ether. Another water molecule and one of the two crystallographically independent sulfate anions are coordinated, the latter in a bidentate fashion, to the Ln(III) cation in the axial positions. The second sulfate anion is not coordinated to the cation, but is located in an interstitial position on a crystallographic inversion centre, thus leading to disorder of the O atoms around the centre of inversion. The Ln-O bond distances follow the trend of the lanthanide contraction. The apical Ln-O bond distances are very close to the sums of the ionic radii. However, the Ln-O distances within the metallacrown units are slightly compressed and the Ln(III) cations protrude significantly from the plane of the otherwise flat metallacrown ligand, thus indicating that the cavity is somewhat too small to accommodate the Ln(III) ions comfortably. This effect decreases with the size of the lanthanide cation from complex (I) (Ln(III) = Pr; 0.459) to complex (VII) (Ln(III) = Ho; 0.422), which indicates that the smaller lanthanide cations fit the cavity of the pentacopper metallacrown ring better than the larger ones. The diminished contraction of Ln-O distances within the metallacrown planes leads to an aniostropic contraction of the unit

Solvothermal syntheses, crystal structures, and properties of lanthanide(III) thioarsenates [Ln(dien)2(μ-1κ,2κ2-AsS4)]n (Ln==Sm, Eu, Gd) and [Ln(dien)2(1κ2-AsS4)] (Ln==Tb, Dy, Ho)

International Nuclear Information System (INIS)

Wang, Fang; Tang, Chunying; Chen, Ruihong; Zhang, Yong; Jia, Dingxian

2013-01-01

Solvothermal reactions of Ln 2 O 3 , As and S in diethylenetriamine (dien) at 170 °C for 6 days afforded two structural types of lanthanide thioarsenates with the general formulae [Ln(dien) 2 (μ-1κ,2κ 2 -AsS 4 )] n [Ln=Sm(1), Eu(2), Gd(3)] and [Ln(dien) 2 (1κ 2 -AsS 4 )] [Ln=Tb(4), Dy(5), Ho(6)]. The Ln 2 O 3 oxides were converted to [Ln(dien) 2 ] 3+ complex units in the solvothermal reactions. The As atom binds four S atoms, forming a tetrahedral AsS 4 unit. In 1−3, the AsS 4 units interconnect the [Ln(dien) 2 ] 3+ cations via Ln−S bonds as tridentate μ-1κ,2κ 2 -AsS 4 bridging ligands, resulting in the neutral coordination polymers [Ln(dien) 2 (μ-1κ,2κ 2 -AsS 4 )] n (Ln1). In 4−6, the AsS 4 units coordinate with the Ln 3+ ion of [Ln(dien) 2 ] 3+ as 1κ 2 -AsS 4 chelating ligands to form neutral coordination compounds [Ln(dien) 2 (1κ 2 -AsS 4 )] (Ln2). The Ln 3+ ions are in nine- and eight-coordinated environments in Ln1 and Ln2, respectively. The formation of Ln1 and Ln2 is related with ionic size of the Ln 3+ ions. Optical absorption spectra showed that 1−6 have potential use as semiconductors with the band gaps in the range 2.18−3.21 eV. - Graphical abstract: Two types of Ln-thioarsenates [Ln(dien) 2 (μ-1κ,2κ 2 -AsS 4 )] n and [Ln(dien) 2 (1κ 2 -AsS 4 )] were prepared by solvothermal methods and the soft Lewis basic AsS 4 3– ligand to Ln(III) centers with polyamine co-ligand was obtained. Display Omitted - Highlights: • Lanthanide thioarsenates were prepared by solvothermal methods. • The soft Lewis basic AsS 4 ligand coordinate Ln 3+ ions with coexistence polyamine ligands. • Two structural types of Ln-thioarsenates with structural turnover at Tb were obtained along Ln series. • The Ln-thioarsenates are potential semiconductors with optical band gaps in the range 2.18−3.21 eV

Solid-state amorphization of SmFe{sub 3} by hydrogenation

Energy Technology Data Exchange (ETDEWEB)

Mueller, K.H.; Kubis, M.; Handstein, A.; Gutfleisch, O.

2000-05-10

Hydrogen-induced amorphization (HIA) has received much attention as a method for the preparation of amorphous compounds since its discovery by Yeh et al. Meanwhile it has been observed for a large number of intermetallic compounds with C15, C23, B8{sub 2}, DO{sub 19} and L1{sub 2} structures. E.G. the C15 Laves-type compounds (MgCu{sub 2}-type structure) of rare earth (R) - transition metal (T) compounds RT{sub 2} show HIA for R = Y, Ce, Pr, Nd, Sm, Gd, Tb, Dy, Ho and Er. Aoki et al. postulated that new amorphizing compounds can be expected at high hydrogen pressures. In this work, the structural changes of SmFe{sub 3} (PuNi{sub 3}-type structure) during heating in high hydrogen pressures are reported.

A superdeformed band in {sup 142}Sm

Energy Technology Data Exchange (ETDEWEB)

Hackman, G; Mullins, J M; Kuehner, J A; Prevost, D; Waddington, J C [McMaster Univ., Hamilton, ON (Canada). Dept. of Physics; Galindo-Uribarri, A; Janzen, V P; Radford, D C; Schmeing, N; Ward, D [Atomic Energy of Canada Ltd., Chalk River, ON (Canada). Chalk River Nuclear Labs.

1992-08-01

Observation of {gamma}-{gamma} coincidences from the reaction {sup 124}Sn({sup 24}Mg,6n){sup 142}Sm at 145 MeV indicates the existence of a rotational band with dynamic moment of inertia J{sup (2)} similar to that of the superdeformed band in the isotone {sup 143}Eu. This result is consistent with calculations predicting superdeformed structures in N = 80, Z {approx} 64 nuclei. (author). 8 refs., 4 figs.

Distribution patterns of rare earth elements in various plant species

Energy Technology Data Exchange (ETDEWEB)

Wyttenbach, A.; Tobler, L.; Furrer, V. [Paul Scherrer Inst. (PSI), Villigen (Switzerland)

1997-09-01

The elements La, Ce, Nd, Sm, Eu, Gd, Tb, Yb and Lu have been determined in 6 different plant species by neutron activation analysis. When the concentrations of each species were normalized to Norway spruce, smooth curves were obtained which revealed systematic inter-species differences. (author) 3 figs., 4 refs.

Distribution patterns of rare earth elements in various plant species

International Nuclear Information System (INIS)

Wyttenbach, A.; Tobler, L.; Furrer, V.

1997-01-01

The elements La, Ce, Nd, Sm, Eu, Gd, Tb, Yb and Lu have been determined in 6 different plant species by neutron activation analysis. When the concentrations of each species were normalized to Norway spruce, smooth curves were obtained which revealed systematic inter-species differences. (author) 3 figs., 4 refs

Moessbauer and channeling experiments on TeSi and SmSi

International Nuclear Information System (INIS)

Kemerink, G.J.; Boerma, D.O.; Waard, H. de; Wit, J.C. de; Drentje, S.A.

1980-01-01

Considerable effort is made to obtain an insight in the structural and electronic properties of ion implanted elemental semiconductors. This research is strongly stimulated by the many applications of semi-conductor devices. We report here on Moessbauer studies of 129 TeSi and 153 SmSi, using the 27.8 keV transition in 129 I and the 103.2 keV transition in 153 Eu, respectively, and on channeling experiments on 128 TeSi and 152 SmSi with a 2 MeV α-beam from the Groningen Van de Graaff generator. In the Moessbauer experiments we used Cu 129 I and EuF 3 .1/2H 2 O as absorber materials. Source and absorber were held at 4.2 K. The implantations were generally done at room temperature with an implantation energy of 100-115 keV. For the Moessbauer and channeling measurements we applied similar Si single crystals and the same implantation and annealing conditions. Crystals with low doses could only be investigated with the Moessbauer effect

Extraction of 152Gd from HFIR control plates

International Nuclear Information System (INIS)

Kohring, M.W.

1986-01-01

The primary method of 153 Gd production at the Oak Ridge National Lab. (ORNL) research reactors since 1980 has been the irradiation of a natural europium oxide powder (Eu 2 O 3 ) followed by the chemical extraction of the gadolinium fraction. The specific activity of the resulting source is 45 to 50 Ci/g with a radiochemical purity of > 99.99%. A potential alternative method involves the extraction of gadolinium from the europium-bearing region of highly radioactive, spent control plates used in the High Flux Isotope Reactor (HFIR), followed by neutron irradiation. This alternative to the traditional process is attractive in that chemical separation of the europium and gadolinium occurs before the 153 Gd production irradiation, thus reducing process and decay losses and, most significantly, the gadolinium is highly enriched in the parent isotope, 152 Gd. Investigation into the usefulness of the gadolinium isotopes contained in spent HFIR control plates began in the late 1960s. However, separation of the gadolinium from the europium to the purity levels required for a marketable specific activity could not be attained. Due to the recent increase in 153 Gd demand and separation process improvements, research into this valuable source of parent material was resurrected

Recent experiments at Brookhaven: level structure of N = 86 isotones 156Yb and 150Gd

International Nuclear Information System (INIS)

Sunyar, A.W.

1980-01-01

States of the N = 86 isotones 156 Yb and 150 Gd have been studied by means of the 144 Sm( 16 O,4n) 156 Yb, 113 In( 46 Ti,p2n) 156 Yb, and 124 Sn( 30 Si,4n) 150 Gd reactions. Levels have been established to spin 36 h-bar and over 12.5 MeV in excitation in 150 Gd and to beyond spin 25 h-bar in 156 Yb. The systematics of levels in the N = 86 isotones from 150 Gd to 156 Yb are described, and the near-spherical shell model description for states in this region to near spin 30 h-bar is discussed. A T/sub 1/2/ = 6 ns, 72-keV isomeric transition in 156 Yb has been discovered, and an E1 multipolarity is assigned to this transition. The spin-parity of the isomeric state is established as 11 - . 6 figures

Mid-temperature deep removal of hydrogen sulfide on rare earth (RE = Ce, La, Sm, Gd) doped ZnO supported on KIT-6: Effect of RE dopants and interaction between active phase and support matrix

Science.gov (United States)

Li, Lu; Zhou, Pin; Zhang, Hongbo; Meng, Xianglong; Li, Juexiu; Sun, Tonghua

2017-06-01

Rare earth oxides (RE = Ce, La, Sm and Gd) doped ZnO supported on KIT-6 sorbents (RE-ZnO/KIT-6) were synthesized by sol-gel method and their performance for deep removal of H2S (bellow 0.1 ppmv) from gas stream at medium temperature was tested. The RE dopants (except Ce) significantly enhance the deep desulfurization capacity of ZnO/KIT-6 sorbent and maintained higher sulfur uptake capacities upon multiple cycles of regeneration by a simple thermal oxidation in 10 v% of O2 in N2 atmosphere. The results of SAXS, XRD, N2 physisorption, TEM, FIIR, and XPS implied that the KIT-6 structure of loading metal oxides remained intact. It was found that RE could hinder the ZnO crystal ripening during calcination resulted in smaller ZnO particles, enhance the interaction of ZnO and silica matrix to improve the dispersion of active phase on KIT-6. Furthermore, by increasing the outlayer electron density of Zn atom and oxygen transfer ability, the synergistic effect considered to be favorable for RE-ZnO/KIT-6 sulfidation. Even though the performance of improving ZnO dispersion was weaker than that of Sm and Gd, La-ZnO/KIT-6 performs the best deep desulfurizers by changing the surface chemical atmosphere for ZnO. Steam in the gas stream inhibited the capture of H2S by ZnO in the sorbents, in the case of La-ZnO/KIT-6, the steam content should control as lower as 5 v% to ensure the desulfurization efficiency and precision.

Static magnetic susceptibility, crystal field and exchange interactions in rare earth titanate pyrochlores

NARCIS (Netherlands)

Malkin, B. Z.; Lummen, T. T. A.; van Loosdrecht, P. H. M.; Dhalenne, G.; Zakirov, A. R.

2010-01-01

The experimental temperature dependence (T = 2-300 K) of single crystal bulk and site susceptibilities of rare earth titanate pyrochlores R2Ti2O7 (R = Sm, Eu, Gd, Tb, Dy, Ho, Er, Yb) is analyzed in the framework of crystal field theory and a mean field approximation. Analytical expressions for the

Probing structural homogeneity of La{sub 1-x}Gd{sub x}PO{sub 4} monazite-type solid solutions by combined spectroscopic and computational studies

Energy Technology Data Exchange (ETDEWEB)

Huittinen, N., E-mail: n.huittinen@hzdr.de [Helmholtz-Zentrum Dresden - Rossendorf, Institute of Resource Ecology, Bautzner Landstraße 400, 01328 Dresden (Germany); Arinicheva, Y. [Forschungszentrum Jülich GmbH, Institute of Energy and Climate Research, Nuclear Waste Management and Reactor Safety (IEK-6), 52425 Jülich (Germany); Kowalski, P.M.; Vinograd, V.L. [Forschungszentrum Jülich GmbH, Institute of Energy and Climate Research, Nuclear Waste Management and Reactor Safety (IEK-6), 52425 Jülich (Germany); JARA High-Performance Computing, Schinkelstraße 2, 52062 Aachen (Germany); Neumeier, S. [Forschungszentrum Jülich GmbH, Institute of Energy and Climate Research, Nuclear Waste Management and Reactor Safety (IEK-6), 52425 Jülich (Germany); Bosbach, D. [Forschungszentrum Jülich GmbH, Institute of Energy and Climate Research, Nuclear Waste Management and Reactor Safety (IEK-6), 52425 Jülich (Germany); JARA High-Performance Computing, Schinkelstraße 2, 52062 Aachen (Germany)

2017-04-01

Here we study the homogeneity of Eu{sup 3+}-doped La{sub 1-x}Gd{sub x}PO{sub 4} (x = 0, 0.11, 0.33, 0.55, 0.75, 0.92, 1) monazite-type solid solutions by a combination of Raman and time-resolved laser fluorescence spectroscopies (TRLFS) with complementary quasi-random structure-based atomistic modeling studies. For the intermediate La{sub 0.45}Gd{sub 0.55}PO{sub 4} composition we detected a significant broadening of the Raman bands corresponding to the lattice vibrations of the LnO{sub 9} polyhedron, indicating much stronger distortion of the lanthanide cation site than the PO{sub 4} tetrahedron. A distortion of the crystal lattice around the dopant site was also confirmed in our TRLFS measurements of Eu{sup 3+} doped samples, where both the half width (FWHM) of the excitation peaks and the {sup 7}F{sub 2}/{sup 7}F{sub 1} ratio derived from the emission spectra increase for intermediate solid-solution compositions. The observed variation in FWHM correlates well with the simulated distribution of Eu···O bond distances within the investigated monazites. The combined results imply that homogenous Eu{sup 3+}-doped La{sub 1-x}Gd{sub x}PO{sub 4} monazite-type solid solutions are formed over the entire composition range, which is of importance in the context of using these ceramics for immobilization of radionuclides. - Highlights: •Homogenous Eu{sup 3+}-doped La{sub 1-x}Gd{sub x}PO{sub 4} monazite-type solid solutions have been synthesized. •Solid solution formation is accompanied by slight distortion of the LnO{sub 9} polyhedron. •Raman and laser spectroscopic trends are observed within the monazite series. •Results are explained with atomistic simulations of Eu-O bond distance distribution.

Preparation of high-temperature superconducting ceramics

International Nuclear Information System (INIS)

Causa, M.T.; Dutrus, S.M.; Esparza, Daniel; Fainstein, Carlos; Malachevsky, M.T.; Salva, Horacio; Sanchez, Rodolfo; Steren, L.B.; Tovar, Manuel; Veglio, Nestor

1987-01-01

We have prepared samples of the family ABa2Cu3Ox (A=Y, Gd, Eu, Dy, Sm, Er). The powdered samples were characterized by X-ray diffraction at room temperature. We have also studied the effect of Fe impurities in YBa2Cu3Ox and EuBa2Cu3Ox. Moreover, single crystals of YBa2Cu3Ox and La(1-x)SrxCuO4 were grown using cooper oxide flux. (Author) [es

Anisotropic magnetization and transport properties of RAgSb₂ (R=Y, La-Nd, Sm, Gd-Tm)

Energy Technology Data Exchange (ETDEWEB)

Myers, Kenneth D. [Iowa State Univ., Ames, IA (United States)

1999-11-08

This study of the RAgSb₂ series of compounds arose as part of an investigation of rare earth intermetallic compounds containing antimony with the rare earth in a position with tetragonal point symmetry. Materials with the rare earth in a position with tetragonal point symmetry frequently manifest strong anisotropies and rich complexity in the magnetic properties, and yet are simple enough to analyze. Antimony containing intermetallic compounds commonly possess low carrier densities and have only recently been the subject of study. Large single grain crystals were grown of the RAgSb₂ (R=Y, La-Nd, Sm, Gd-Tm) series of compounds out of a high temperature solution. This method of crystal growth, commonly known as flux growth is a versatile method which takes advantage of the decreasing solubility of the target compound with decreasing temperature. Overall, the results of the crystal growth were impressive with the synthesis of single crystals of LaAgSb₂ approaching one gram. However, the sample yield diminishes as the rare earth elements become smaller and heavier. Consequently, no crystals could be grown with R=Yb or Lu. Furthermore, EuAgSb₂ could not be synthesized, likely due to the divalency of the Eu ion. For most of the RAgSb₂ compounds, strong magnetic anisotropies are created by the crystal electric field splitting of the Hund's rule ground state. This splitting confines the local moments to lie in the basal plane (easy plane) for the majority of the members of the series. Exceptions to this include ErAgSb₂ and TmAgSb₂, which have moments along the c-axis (easy axis) and CeAgSb₂, which at intermediate temperatures has an easy plane, but exchange coupling at low temperatures is anisotropic with an easy axis. Additional anisotropy is also observed within the basal plane of DyAgSb₂, where the moments are restricted to align along one of the <110> axes. Most of

Cu k-edge studies of the charge carries in Th-doped cuprate system R2-xThxCuO4-δ (R = Nd, Sm and Gd)

International Nuclear Information System (INIS)

Liang, G.; Yi, Y.; Jardim, R.F.; Wang, L.V.

1999-01-01

To further study the charge carrier concentration in electron doped cuprate superconductors, a systematic x-ray absorption near edge structure (XANES) measurement has been carried out on Th-doped superconductor system R 2-x Th x CuO 4-δ (R = Nd, Sm, and Gd). The XANES results show that, similar to the Ce-doped compounds, while the intensity of the Cu 1+ 4p π feature increase with the increase of the Th doping level x, the intensities of the Cu 2+ 4p π and 4p σ features decreases. This clearly indicates that the electrons doped by the Th atoms are injected into the local Cu 3d-orbitals. The normalized Cu 1+ 4p π intensity data show that the Cu 1+ concentration in the Th-doped compound series with different R-elements is linearly proportional to the Th doping-level x. The data suggest that both Ce and Th donate the same fraction of electrons into the Cu sites

Determination of Psub(K) values to the 172, 103 and 97 keV levels and the fluorescence yield. omega. sub(K) of Eu after electron capture by /sup 153/Gd

Energy Technology Data Exchange (ETDEWEB)

Singh, K; Grewal, B S; Sahota, H S [Punjabi Univ., Patiala (India). Dept. of Physics

1985-03-01

From an analysis of K x-ray-..gamma..-ray sum peaks observed with an intrinsic Ge detector the K-capture probabilities (Psub(K)) to the 172, 103 and 97 keV levels in the decay of /sup 153/Gd have been determined; these yield an electron-capture energy Qsub(EC)=245 +- 2. The K-capture probability to the 172 keV level differs significantly from that found in the literature. With these results the K-shell fluorescence yield of Eu is ..omega..sub(K)=0.935 +- 0.019.

Lattice dynamical investigation of the Raman and infrared wave numbers and heat capacity properties of the pyrochlores R2Zr2O7 (R = La, Nd, Sm, Eu)

Science.gov (United States)

Nandi, S.; Jana, Y. M.; Gupta, H. C.

2018-04-01

A short-range electrostatic forcefield model has been applied for the first time to investigate the Raman and infrared wave numbers in pyrochlore zirconates R2Zr2O7 (R3+ = La, Nd, Sm, Eu). The calculations of phonons involve five stretching and four bending force constants in the Wilson GF matrix method. The calculated phonon wave numbers are in reasonable agreement with the observed spectra in infrared and Raman excitation zones for all of these isomorphous compounds. The contributions of force constants to each mode show a similar trend of variation for all of these compounds. Furthermore, to validate the established forcefield model, we calculated the standard thermodynamic functions, e.g., molar heat capacity, entropy and enthalpy, and compared the results with the previous experimental data for each compound. Using the derived wave numbers for the acoustic and optical modes, the total phonon contribution to the heat capacity was calculated for all these zirconate compounds. The Schottky heat capacity contributions were also calculated for the magnetic compounds, Nd2Zr2O7, Sm2Zr2O7 and Eu2Zr2O7, taking account of crystal-field level schemes of the lanthanide ions. The derived total heat capacity and the integrated values of molar entropy and molar enthalpy showed satisfactory correlations at low temperatures with the experimental results available in the literature for these compounds. At higher temperatures, the discrepancies may be caused by the anharmonic effects of vibrations, phonon dispersion, distribution of phonon density of states, etc.

Instrumental neutron activation analysis of rocks from Cayajabos petroleum ore

International Nuclear Information System (INIS)

Montero Cabrera, M.E.; Herrera Hernandez, H.; Herrera Peraza, E.; Rodriguez Martinez, N.; Lopez Reyes, M.C.

2000-01-01

The relative INAA method under statistical control was used to measure the concentrations of Sb, La, Eu, Co, Rb, Tb, Cs, Hf, Th, Cr, Lu, Yb, Ce, Sm, Gd, Nd. Rare earth element (REE) Chondrite-normalized patterns are presented. The La cond /Lu cond normalized concentration ratios obtained confirm the carbonaceous character of the rocks

Lanthanide-doped NaGdF4 core-shell nanoparticles for non-contact self-referencing temperature sensors.

Science.gov (United States)

Zheng, Shuhong; Chen, Weibo; Tan, Dezhi; Zhou, Jiajia; Guo, Qiangbing; Jiang, Wei; Xu, Cheng; Liu, Xiaofeng; Qiu, Jianrong

2014-06-07

We report that non-contact self-referencing temperature sensors can be realized with the use of core-shell nanostructures. These lanthanide-based nanothermometers (NaGdF4:Yb(3+)/Tm(3+)@Tb(3+)/Eu(3+)) exhibit higher sensitivity in a wide range from 125 to 300 K based on two emissions of Tb(3+) at 545 nm and Eu(3+) at 615 nm under near-infrared laser excitation.

Structure–function analysis and genetic interactions of the SmG, SmE, and SmF subunits of the yeast Sm protein ring

Science.gov (United States)

Schwer, Beate; Kruchten, Joshua; Shuman, Stewart

2016-01-01

A seven-subunit Sm protein ring forms a core scaffold of the U1, U2, U4, and U5 snRNPs that direct pre-mRNA splicing. Using human snRNP structures to guide mutagenesis in Saccharomyces cerevisiae, we gained new insights into structure–function relationships of the SmG, SmE, and SmF subunits. An alanine scan of 19 conserved amino acids of these three proteins, comprising the Sm RNA binding sites or inter-subunit interfaces, revealed that, with the exception of Arg74 in SmF, none are essential for yeast growth. Yet, for SmG, SmE, and SmF, as for many components of the yeast spliceosome, the effects of perturbing protein–RNA and protein–protein interactions are masked by built-in functional redundancies of the splicing machine. For example, tests for genetic interactions with non-Sm splicing factors showed that many benign mutations of SmG, SmE, and SmF (and of SmB and SmD3) were synthetically lethal with null alleles of U2 snRNP subunits Lea1 and Msl1. Tests of pairwise combinations of SmG, SmE, SmF, SmB, and SmD3 alleles highlighted the inherent redundancies within the Sm ring, whereby simultaneous mutations of the RNA binding sites of any two of the Sm subunits are lethal. Our results suggest that six intact RNA binding sites in the Sm ring suffice for function but five sites may not. PMID:27417296

94 β-Decay Half-Lives of Neutron-Rich _{55}Cs to _{67}Ho: Experimental Feedback and Evaluation of the r-Process Rare-Earth Peak Formation.

Science.gov (United States)

Wu, J; Nishimura, S; Lorusso, G; Möller, P; Ideguchi, E; Regan, P-H; Simpson, G S; Söderström, P-A; Walker, P M; Watanabe, H; Xu, Z Y; Baba, H; Browne, F; Daido, R; Doornenbal, P; Fang, Y F; Gey, G; Isobe, T; Lee, P S; Liu, J J; Li, Z; Korkulu, Z; Patel, Z; Phong, V; Rice, S; Sakurai, H; Sinclair, L; Sumikama, T; Tanaka, M; Yagi, A; Ye, Y L; Yokoyama, R; Zhang, G X; Alharbi, T; Aoi, N; Bello Garrote, F L; Benzoni, G; Bruce, A M; Carroll, R J; Chae, K Y; Dombradi, Z; Estrade, A; Gottardo, A; Griffin, C J; Kanaoka, H; Kojouharov, I; Kondev, F G; Kubono, S; Kurz, N; Kuti, I; Lalkovski, S; Lane, G J; Lee, E J; Lokotko, T; Lotay, G; Moon, C-B; Nishibata, H; Nishizuka, I; Nita, C R; Odahara, A; Podolyák, Zs; Roberts, O J; Schaffner, H; Shand, C; Taprogge, J; Terashima, S; Vajta, Z; Yoshida, S

2017-02-17

The β-decay half-lives of 94 neutron-rich nuclei ^{144-151}Cs, ^{146-154}Ba, ^{148-156}La, ^{150-158}Ce, ^{153-160}Pr, ^{156-162}Nd, ^{159-163}Pm, ^{160-166}Sm, ^{161-168}Eu, ^{165-170}Gd, ^{166-172}Tb, ^{169-173}Dy, ^{172-175}Ho, and two isomeric states ^{174m}Er, ^{172m}Dy were measured at the Radioactive Isotope Beam Factory, providing a new experimental basis to test theoretical models. Strikingly large drops of β-decay half-lives are observed at neutron-number N=97 for _{58}Ce, _{59}Pr, _{60}Nd, and _{62}Sm, and N=105 for _{63}Eu, _{64}Gd, _{65}Tb, and _{66}Dy. Features in the data mirror the interplay between pairing effects and microscopic structure. r-process network calculations performed for a range of mass models and astrophysical conditions show that the 57 half-lives measured for the first time play an important role in shaping the abundance pattern of rare-earth elements in the solar system.

Rare earth analysis in human biological samples by atomic absorption using electrothermal atomization

International Nuclear Information System (INIS)

Citron, I.M.; Holtzman, R.B.; Leiman, J.

1982-01-01

The determination of Sc and seven rare earth elements, Nd, Sm, Dy, Ho, Eu, Tm, and Yb, in biological samplesby atomic absorption spectrophotometric analysis (AAS) using electrothermal atomization in a pyrolytic graphite tube is shown to be rapid, precise and accurate. The technique utilizes the method of standard additions and linear regression analysis to determine results from peak area data. Inter-elemental interferences are negligible. The elements found sensitive enough for this type of analysis are, in order of decreasing sensitivity, Yb, Eu, Tm, Dy, Sc, Ho, Sm and Nd. The determination in these types of materials of Gd and elements less sensitive to AAS detection than Gd does not appear to be feasible. Results are presented on the concentrations of these elements in 41 samples from human subjects, cows and vegetables with normal environmental exposure to the rare earth elements. The composite percent mean deviation in peak-area readings for all samples and all elements examined was 4%. The mean standard error in the results among samples was about 6.5%

Proton configurations and pairing correlations at the N=80 superdeformed shell closure: Study of 145Tb

International Nuclear Information System (INIS)

Mullins, S.M.; Schmeing, N.C.; Flibotte, S.; Hackman, G.; Rodriguez, J.L.; Waddington, J.C.; Yao, L.; Andrews, H.R.; Galindo-Uribarri, A.; Janzen, V.P.; Radford, D.C.; Ward, D.; DeGraaf, J.; Drake, T.E.; Pilotte, S.; Paul, E.S.

1994-01-01

A superdeformed band has been observed in the N=80 nucleus 145 Tb which was produced with the reactions 112 Sn( 37 Cl,2p2n) and 118 Sn( 31 P,4n) at bombarding energies of 187 and 160 MeV, respectively. Since superdeformed bands also exist in the three lighter N=80 isotones 142 Sm, 143 Eu, and 144 Gd, it is now possible to understand the valence-proton configurations of these bands in a systematic way. The T (2) dynamic moment of inertia in 145 Tb shows no evidence for the N = 6 quasiproton crossing that is observed in 144 Gd. Comparison with cranked Woods-Saxon and total Routhian surface calculations suggests that the proton configuration in 145 Tb is 6 1 direct-product[404] 9/2 + 2 in which the quasiproton crossing is blocked. Furthermore, like 143 Eu and 142 Sm, there is no evidence in the T (2) for the N=6 quasineutron crossing predicted by the calculations. This may indicate that static neutron pairing correlations are quenched at the N=80 superdeformed shell closure

NaGd(MoO4)2 nanocrystals with diverse morphologies: controlled synthesis, growth mechanism, photoluminescence and thermometric properties.

Science.gov (United States)

Li, Anming; Xu, Dekang; Lin, Hao; Yang, Shenghong; Shao, Yuanzhi; Zhang, Yueli

2016-08-10

Pure tetragonal phase, uniform and well-crystallized sodium gadolinium molybdate (NaGd(MoO4)2) nanocrystals with diverse morphologies, e.g. nanocylinders, nanocubes and square nanoplates have been selectively synthesized via oleic acid-mediated hydrothermal method. The phase, structure, morphology and composition of the as-synthesized products are studied. Contents of both sodium molybdate and oleic acid of the precursor solutions are found to affect the morphologies of the products significantly, and oleic acid plays a key role in the morphology-controlled synthesis of NaGd(MoO4)2 nanocrystals with diverse morphologies. Growth mechanism of NaGd(MoO4)2 nanocrystals is proposed based on time-dependent morphology evolution and X-ray diffraction analysis. Morphology-dependent down-shifting photoluminescence properties of NaGd(MoO4)2: Eu(3+) nanocrystals, and upconversion photoluminescence properties of NaGd(MoO4)2: Yb(3+)/Er(3+) and Yb(3+)/Tm(3+) nanoplates are investigated in detail. Charge transfer band in the down-shifting excitation spectra shows a slight blue-shift, and the luminescence intensities and lifetimes of Eu(3+) are decreased gradually with the morphology of the nanocrystals varying from nanocubes to thin square nanoplates. Upconversion energy transfer mechanisms of NaGd(MoO4)2: Yb(3+)/Er(3+), Yb(3+)/Tm(3+) nanoplates are proposed based on the energy level scheme and power dependence of upconversion emissions. Thermometric properties of NaGd(MoO4)2: Yb(3+)/Er(3+) nanoplates are investigated, and the maximum sensitivity is determined to be 0.01333 K(-1) at 285 K.

Structure-function analysis and genetic interactions of the SmG, SmE, and SmF subunits of the yeast Sm protein ring.

Science.gov (United States)

Schwer, Beate; Kruchten, Joshua; Shuman, Stewart

2016-09-01

A seven-subunit Sm protein ring forms a core scaffold of the U1, U2, U4, and U5 snRNPs that direct pre-mRNA splicing. Using human snRNP structures to guide mutagenesis in Saccharomyces cerevisiae, we gained new insights into structure-function relationships of the SmG, SmE, and SmF subunits. An alanine scan of 19 conserved amino acids of these three proteins, comprising the Sm RNA binding sites or inter-subunit interfaces, revealed that, with the exception of Arg74 in SmF, none are essential for yeast growth. Yet, for SmG, SmE, and SmF, as for many components of the yeast spliceosome, the effects of perturbing protein-RNA and protein-protein interactions are masked by built-in functional redundancies of the splicing machine. For example, tests for genetic interactions with non-Sm splicing factors showed that many benign mutations of SmG, SmE, and SmF (and of SmB and SmD3) were synthetically lethal with null alleles of U2 snRNP subunits Lea1 and Msl1. Tests of pairwise combinations of SmG, SmE, SmF, SmB, and SmD3 alleles highlighted the inherent redundancies within the Sm ring, whereby simultaneous mutations of the RNA binding sites of any two of the Sm subunits are lethal. Our results suggest that six intact RNA binding sites in the Sm ring suffice for function but five sites may not. © 2016 Schwer et al.; Published by Cold Spring Harbor Laboratory Press for the RNA Society.

Adsorption study of a macro-RAFT agent onto SiO2-coated Gd2O3:Eu3+ nanorods: Requirements and limitations

Science.gov (United States)

Zou, Hua; Melro, Liliana; de Camargo Chaparro, Thaissa; de Souza Filho, Isnaldi Rodrigues; Ananias, Duarte; Bourgeat-Lami, Elodie; dos Santos, Amilton Martins; Barros-Timmons, Ana

2017-02-01

The use of a macromolecular RAFT (macro-RAFT) agent to encapsulate anisotropic nano-objects via emulsion polymerization is an emerging route to prepare polymer/inorganic colloidal nanocomposites. However, a number of requirements have to be fulfilled. This work aims at highlighting the effects of the preparative procedure and dispersion method on the amount of macro-RAFT agent adsorbed onto SiO2-coated Gd2O3:Eu3+ nanorods. The adsorption of macro-RAFT agent was studied using the depletion method with UV-vis spectrophotometry. Measurements were performed at a fixed concentration of nanorods and varying concentrations of the macro-RAFT agent in aqueous dispersion at room temperature. The adsorption isotherms showed that for the same initial macro-RAFT agent concentration, the highest adsorption capacity of the macro-RAFT agent on nanorods was usually achieved for non-calcined thin SiO2-coated nanorods under mild bath sonication.

DTA AND MOSSBAUER STUDIES IN RARE EARTH ORTHOFERRITES

Energy Technology Data Exchange (ETDEWEB)

Eibschuetz, M.; Gorodetsky, G.; Shtrikman, S.; Treves, D.

1963-11-15

Curie temperatures of 14 different orthoferrites with the chemical formula RFeO/sub 3/ (R = Y, La, Pr, Nd, Sm, Eu, Gd, Tb, Dy, Ho, Er, Tm, Yb, Lu) were measured by differential thermal analysis. Hyperfine interactions of the Fe/ sup 57/ nucleus in the same materials were determined from their Mossbauer spectra. It is found that the quadrupole splitting with the exception of the case of Sm, isomer shift, Curie temperature, and internal field vary regularly with the ionic size of R. (auth)

Quantitative spark-source analysis of UO2-PuO2 for rare earths and tantalum, tungsten

International Nuclear Information System (INIS)

Alkire, G.J.

A quantitative analytical technique good to 20% for the determination of Sm, Eu, Gd, Dy, Ta, and W in Pu-U mixed oxides by spark source mass spectrography has been developed. The technique uses La as an added internal standard and an electronic integrator to measure peak areas of each line photometered on the densitometer. 3 tables

Evaluation of optoelectronic response and Raman active modes in Tb{sup 3+} and Eu{sup 3+}-doped gadolinium oxide (Gd{sub 2}O{sub 3}) nanoparticle systems

Energy Technology Data Exchange (ETDEWEB)

Paul, Nibedita [National Institute of Technology Nagaland, Department of Physics, Dimapur, Nagaland (India); Tezpur University, Department of Physics, Tezpur, Assam (India); Mohanta, D. [Tezpur University, Department of Physics, Tezpur, Assam (India)

2016-09-15

Rare earth oxide (Tb{sup 3+}:Gd{sub 2}O{sub 3} and Eu{sup 3+}:Gd{sub 2}O{sub 3}) nanophosphors are exploited through spectroscopic and microscopic tools with special emphasis on D-F mediated radiative emission and Raman active vibrational modes. Powder X-ray diffraction measurements have revealed cubic crystal structure of the nanosystems and with an average crystallite size varying between ∝3.2 and 4.8 nm. Photoluminescence (PL) spectra of Tb{sup 3+} doped systems signify intense blue-green (∝490 nm) and green (∝544 nm) emissions mediated by {sup 5}D{sub 4} → {sup 7}F{sub 6} and {sup 5}D{sub 4} → {sup 7}F{sub 5} transitional events; respectively. In the PL responses of Eu{sup 3+} doped nanoparticle systems, we also identify magnetically-driven {sup 5}D{sub 0} → {sup 7}F{sub 1} (∝591 nm) and electrically driven {sup 5}D{sub 0} → {sup 7}F{sub 2} (∝619 nm) radiative features which seem to improve with increasing doping level. However, the magnitude of Judd-Ofelt (J-O) intensity parameters (Ω {sub 2,} {sub 4}), is significantly lowered for the high doping cases. Raman spectra of the undoped and RE doped systems exhibited several A{sub g} and F{sub g} modes in the range of Raman shift ∝100-600 cm{sup -1}. In the Raman spectra, the peaks located at ∝355 cm{sup -1} are assigned to the mixed mode of F{sub g} + A{sub g}, the line width of which was found to increase with RE doping. Moreover, owing to the enhanced defect concentration in the doped systems than its undoped counterpart, we anticipate a faster phonon relaxation and consequently, a suppression of phonon lifetime in the former case. (orig.)

Reversible white-purple photochromism in europium doped Sr{sub 3}GdLi(PO{sub 4}){sub 3}F powders

Energy Technology Data Exchange (ETDEWEB)

Lv, Yang; Jin, Yahong, E-mail: yhjin@gdut.edu.cn; Wang, Chuanlong; Ju, Guifang; Xue, Feihong; Hu, Yihua, E-mail: huyh@gdut.edu.cn

2017-06-15

Inorganic photochromic materials have attracted growing attention in recent years. Here, a reversible white-purple photochromic powder material Sr{sub 3}GdLi(PO{sub 4}){sub 3}F:Eu{sup 2+} was synthesized by conventional solid-state method. The surface color shows reversible white-purple changes after irradiated alternatively by UV and visible light (or thermal treat). Diffuse reflectance spectra were used to characterize the photochromic properties including coloring and bleaching. The results indicated that the optimal Eu{sup 2+} doping concentration was found to be about 0.5 mol%. Several cycles measurements including photo- and thermal-induced bleaching indicates that Sr{sub 3}GdLi(PO{sub 4}){sub 3}F:Eu{sup 2+} posses high fatigue resistance in photochromism performance. Based on thermoluminescence curves, the photochromism property related factors that the critical role of traps and the motion of charge carriers between traps were discussed. Finally, a schematic diagram for illustrating the photochromic mechanism was proposed.

Neutron activation analysis of NBS oyster tissue (SRM 1566) and IAEA animal bone (H-5)

International Nuclear Information System (INIS)

Lepel, E.A.; Laul, J.C.

1983-10-01

Data have been presented for 35 elements determined by INAA for NBS oyster tissue (SRM 1566) and for 38 elements determined by INAA and RNAA for IAEA animal bone (H-5). The experimental data showed excellent agreement with published values wherever the comparison exists. Additional trace-element data in the ppb range have been presented for the elements Sc, Sb, Cs, La, Ce, Nd, Sm, Eu, Tb, Dy, Ho, Yb, Lu, Hf, Ta, W and Th in NBS oyster tissue. Also, additional trace-element data for IAEA animal bone (H-5) in the ppb range for the elements Al, Sc, Co, Rb, Cs, La, Ce, Pr, Nd, Sm, Eu, Gd, Tb, Dy, Ho, Tm, Yb, lu, Hf, Ta and Th have been presented

Peculiarities of component interaction in {Gd, Er}-V-Sn Ternary systems at 870 K and crystal structure of RV6Sn6 stannides

International Nuclear Information System (INIS)

Romaka, L.; Stadnyk, Yu.; Romaka, V.V.; Demchenko, P.; Stadnyshyn, M.; Konyk, M.

2011-01-01

Highlights: → {Gd, Er}-V-Sn ternary systems at 870 K are characterized by formation of stannides with general compositions RV 6 Sn 6 . → Isostructural RV 6 Sn 6 compounds were also found with Y, Dy, Ho, Tm, and Lu. → The crystal structure of RV 6 Sn 6 compounds was determined by powder diffraction method. → Structural analysis showed that RV 6 Sn 6 compounds (R = Gd, Dy-Tm, Lu) are disordered; YV 6 Sn 6 is characterized by structure ordering. - Abstract: The phase equilibria in the Gd-V-Sn and Er-V-Sn ternary systems were studied at 870 K by means of X-ray and metallographic analyses in the whole concentration range. Both Gd-V-Sn and Er-V-Sn systems are characterized by formation of one ternary compound at investigated temperature, with stoichiometry RV 6 Sn 6 (SmMn 6 Sn 6 -type, space group P6/mmm, a = 0.55322(3) nm, c = 0.91949(7) nm for Gd, a = 0.55191(2) nm, c = 0.91869(8) nm for Er). Solubility of the third component in the binary compounds was not observed. Compounds with the SmMn 6 Sn 6 -type were also found with Dy, Ho, Tm, and Lu, while YV 6 Sn 6 compound crystallizes in HfFe 6 Ge 6 structure type. All investigated compounds are the first ternary stannides with rare earth elements and vanadium.

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)

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

International Nuclear Information System (INIS)

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

2013-01-01

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

The mercury-richest europium amalgam Eu{sub 10}Hg{sub 55}

Energy Technology Data Exchange (ETDEWEB)

Tambornino, Frank; Hoch, Constantin [Department of Chemistry, Ludwig-Maximilians-Universitaet Muenchen (Germany)

2015-03-15

The mercury-richest europium amalgam Eu{sub 10}Hg{sub 55} was synthesized by isothermal electrocrystallization from a solution of EuI{sub 3}.8DMF in DMF on a reactive mercury cathode. The crystal structure shows remarkable complexity and polar metal-metal bonding. Closely related to the structures of mercury-rich amalgams A{sub 11-x}Hg{sub 55+x} (A = Na, Ca, Sr), it shows underoccupied Hg positions along [00z]. Eu{sub 10}Hg{sub 55} can be described as hettotype structure of the Gd{sub 14}Ag{sub 51} structure type. (Copyright copyright 2015 WILEY-VCH Verlag GmbH and Co. KGaA, Weinheim)

K2Ln2As2Se9 (Ln = Sm, Gd): the first quaternary rare-earth selenoarsenate compounds with a 3D framework containing chairlike As2Se4 units.

Science.gov (United States)

Wu, Yuandong; Bensch, Wolfgang

2009-04-06

The new compounds K(2)Ln(2)As(2)Se(9) (Ln = Sm, Gd) were obtained by applying the reactive flux method. The structure consists of a three-dimensional (3D) [Ln(2)As(2)Se(9)](2-) framework with K(+) ion-filling tunnels running along the b axis. The two unique Ln(3+) cations are coordinated by two Se(2)(2-) dumbbells, two AsSe(3)(3-) pyramids, and one chairlike As(2)Se(4)(2-) unit in a bicapped trigonal-prismatic geometry. The Ln(3+)-centered trigonal prisms share triangular faces with neighboring prisms, forming one-dimensional chains along the b axis. These chains are linked to each other to form layers by sharing Se(2-) anions on the capped sites of the trigonal prisms. The As(2)Se(4) units connect these layers to form the 3D framework.

ZZ MATXSLIBJ33, JENDL-3.3 based, 175 N-42 photon groups (VITAMIN-J) MATXS library for discrete ordinates multi-group

International Nuclear Information System (INIS)

Kosako, K.; Yamano, N.; Fukahori, T.; Shibata, K.; Hasegawa, A.

2006-01-01

1 - Description of program or function: JENDL-3.3 based, 175 neutron-42 photon groups (VITAMIN-J) MATXS library for discrete ordinates multi-group transport codes. Format: MATXS. Number of groups: 175 neutron, 42 gamma-ray. Nuclides: 337 nuclides contained in JENDL-3.3: H-1, H-2, He-3, He-4, Li-6, Li-7, Be-9, B-10, B-11, C-Nat, N-14, N-15, O-16, F-19, Na-23, Mg-24, Mg-25, Mg-26, Al-27, Si-28, Si-29, Si-30, P-31, S-32, S-33, S-34, S-36, Cl-35, Cl-37, Ar-40, K-39, K-40, K-41, Ca-40, Ca-42, Ca-43, Ca-44, Ca-46, Ca-48, Sc-45, Ti-46, Ti-47, Ti-48, Ti-49, Ti-50, V-Nat, Cr-50, Cr-52, Cr-53, Cr-54, Mn-55, Fe-54, Fe-56, Fe-57, Fe-58, Co-59, Ni-58, Ni-60, Ni-61, Ni-62, Ni-64, Cu-63, Cu-65, Ga-69, Ga-71, Ge-70, Ge-72, Ge-73, Ge-74, Ge-76, As-75, Se-74, Se-76, Se-77, Se-78, Se-79, Se-80, Se-82, Br-79, Br-81, Kr-78, Kr-80, Kr-82, Kr-83, Kr-84, Kr-85, Kr-86, Rb-85, Rb-87, Sr-86, Sr-87, Sr-88, Sr-89, Sr-90, Y-89, Y-91, Zr-90, Zr-91, Zr-92, Zr-93, Zr-94, Zr-95, Zr-96, Nb-93, Nb-94, Nb-95, Mo-92, Mo-94, Mo-95, Mo-96, Mo-97, Mo-98, Mo-99, Mo-100, Tc-99, Ru-96, Ru-98, Ru-99, Ru-100, Ru-101, Ru-102, Ru-103, Ru-104, Ru-106, Rh-103, Rh-105, Pd-102, Pd-104, Pd-105, Pd-106, Pd-107, Pd-108, Pd-110, Ag-107, Ag-109, Ag-110m, Cd-106, Cd-108, Cd-110, Cd-111, Cd-112, Cd-113, Cd-114, Cd-116, In-113, In-115, Sn-112, Sn-114, Sn-115, Sn-116, Sn-117, Sn-118, Sn-119, Sn-120, Sn-122, Sn-123, Sn-124, Sn-126, Sb-121, Sb-123, Sb-124, Sb-125, Te-120, Te-122, Te-123, Te-124, Te-125, Te-126, Te-127m, Te-128, Te-129m, Te-130, I-127, I-129, I-131, Xe-124, Xe-126, Xe-128, Xe-129, Xe-130, Xe-131, Xe-132, Xe-133, Xe-134, Xe-135, Xe-136, Cs-133, Cs-134, Cs-135, Cs-136, Cs-137, Ba-130, Ba-132, Ba-134, Ba-135, Ba-136, Ba-137, Ba-138, Ba-140, La-138, La-139, Ce-140, Ce-141, Ce-142, Ce-144, Pr-141, Pr-143, Nd-142, Nd-143, Nd-144, Nd-145, Nd-146, Nd-147, Nd-148, Nd-150, Pm-147, Pm-148, Pm-148m, Pm-149, Sm-144, Sm-147, Sm-148, Sm-149, Sm-150, Sm-151, Sm-152, Sm-153, Sm-154, Eu-151, Eu-152, Eu-153, Eu-154, Eu-155, Eu

Highly luminescent Eu{sup 3+}-doped benzenetricarboxylate based materials

Energy Technology Data Exchange (ETDEWEB)

Silva, Ivan G.N. [Departamento de Química Fundamental, Instituto de Química da Universidade de São Paulo, Av. Prof. Lineu Prestes 748, São Paulo 05508-900, SP (Brazil); Mustafa, Danilo, E-mail: dmustafa@iq.usp.br [Departamento de Química Fundamental, Instituto de Química da Universidade de São Paulo, Av. Prof. Lineu Prestes 748, São Paulo 05508-900, SP (Brazil); Andreoli, Bruno [Departamento de Química Fundamental, Instituto de Química da Universidade de São Paulo, Av. Prof. Lineu Prestes 748, São Paulo 05508-900, SP (Brazil); Felinto, Maria C.F.C. [Centro de Química do Meio Ambiente, Instituto de Pesquisas Energéticas e Nucleares, Av. Prof. Lineu Prestes 2242, São Paulo 05508-000, SP (Brazil); Malta, Oscar L. [Departamento de Química Fundamental, Universidade Federal de Pernambuco, Av. Prof. Moraes Rego, 1235, Recife 50670-90, PE (Brazil); Brito, Hermi F., E-mail: hefbrito@iq.usp.br [Departamento de Química Fundamental, Instituto de Química da Universidade de São Paulo, Av. Prof. Lineu Prestes 748, São Paulo 05508-900, SP (Brazil)

2016-02-15

[RE(TMA)] anhydrous complexes (RE{sup 3+}: Y, Gd and Lu) present high red emission intensity with a quantum efficiency (~45%) for the [Y(TMA):Eu{sup 3+}] complexes, due to the absence of non-radioactive decay pathways mediated by water molecules. The complexes were prepared in mild conditions. All the compounds are crystalline and thermostable up to 460 °C. Phosphorescence data of the complexes with Y, Gd and Lu show that the T{sub 1} state of the TMA{sup 3−} anion has energy higher than the {sup 5}D{sub 0} emitting level of the Eu{sup 3+} ion, indicating that the ligand can act as an intramolecular energy sensitizer. The photoluminescence properties of the doped materials were studied based on the excitation and emission spectra and luminescence decay curves. The experimental intensity parameters (Ω{sub λ}), lifetimes (τ), radiative (A{sub rad}) and non-radiative (A{sub nrad}) decay rates were determined and discussed. - Highlights: • Highly luminescent Europium doped anhydrous complexes. • Efficient monochromatic red light conversion molecular devices (LCMDs). • High emission quantum efficiencies.

Electrochemical properties of composite cathodes using Sm doped layered perovskite for intermediate temperature-operating solid oxide fuel cell

Science.gov (United States)

Baek, Seung-Wook; Azad, Abul K.; Irvine, John T. S.; Choi, Won Seok; Kang, Hyunil; Kim, Jung Hyun

2018-02-01

SmBaCo2O5+d (SBCO) showed the lowest observed Area Specific Resistance (ASR) value in the LnBaCo2O5+d (Ln: Pr, Nd, Sm, and Gd) oxide system for the overall temperature ranges tested. The ASR of a composite cathode (mixture of SBCO and Ce0.9Gd0.1O2-d) on a Ce0.9Gd0.1O2-d (CGO91) electrolyte decreased with respect to the CGO91 content; the percolation limit was also achieved for a 50 wt% SBCO and 50 wt% CGO91 (SBCO50) composite cathode. The ASRs of SBCO50 on the dense CGO91 electrolyte in the overall temperature range of 500-750 °C were relatively lower than those of SBCO50 on the CGO91 coated dense 8 mol% yttria-stabilized zirconia (8YSZ) electrolyte for the same temperature range. From 750 °C and for all higher temperatures tested, however, the ASRs of SBCO50 on the CGO91 coated dense 8YSZ electrolyte were lower than those of the CGO91 electrolyte. The maximum power densities of SBCO50 on the Ni-8YSZ/8YSZ/CGO91 buffer layer were 1.034 W cm-2 and 0.611 W cm-2 at 800 °C and 700 °C.

Stabilization of the ferromagnetic metallic state in rare earth-doped La0.49X0.01Ca0.50MnO3+δ (X=Nd, Sm, Gd and Yb)

International Nuclear Information System (INIS)

Aslam, Affia; Hasanain, S.K.; Akhtar, M.J.; Nadeem, M.

2006-01-01

We report the effects of disorder induced by a small amount of substitution of the smaller cations (Nd, Sm, Gd and Yb) for La in the La 0.50 Ca 0.50 MnO 3+δ system. With decreasing size of the dopant, the ferromagnetic and metallic state is stabilized while the AFM and insulating behaviour is completely eliminating. The magnetic moment below T c increases in general, with decreasing dopant size. The behaviour is interpreted in terms of the destabilization of the charge ordering (CO) due to the disorder induced by the size mismatch of the cations. Our data support the view that close to the COI-FM phase boundary, the effect of disorder is to weaken the CO that is more sensitive to disorder, whereas it leaves the more robust double exchange relatively unaffected, thereby extending the region in phase space where the FM phase is stable

Ternary rhombohedral Laves phases RE_2Rh_3Ga (RE = Y, La-Nd, Sm, Gd-Er)

International Nuclear Information System (INIS)

Seidel, Stefan; Benndorf, Christopher; Heletta, Lukas; Poettgen, Rainer; Eckert, Hellmut; Sao Paulo Univ., Sao Carlos

2017-01-01

The ordered Laves phases RE_2Rh_3Ga (RE=Y, La-Nd, Sm, Gd-Er) were synthesized by arc-melting of the elements and subsequent annealing. The samples were characterized by powder X-ray diffraction (XRD). They crystallize with the rhombohedral Mg_2Ni_3Si type structure, space group R3m. Three structures were refined from single crystal X-ray diffractometer data: a=557.1(1), c=1183.1(2), wR2=0.0591, 159 F"2 values, 10 variables for Y_2Rh_3Ga, a=562.5(2), c=1194.4(2) pm, wR2=0.0519, 206 F"2 values, 11 variables for Ce_2Rh_3Ga and a=556.7(2), c=1184.1(3) pm, wR2=0.0396, 176 F"2 values, 11 variables for Tb_2Rh_3Ga. The Rh_3Ga tetrahedra are condensed via common corners and the large cavities left by the network are filled by the rare earth atoms. The RE_2Rh_3Ga Laves phases crystallize with a translationengleiche subgroup of the cubic RERh_2 Laves phases with MgCu_2 type. Magnetic susceptibility measurements reveal Pauli paramagnetism for Y_2Rh_3Ga and La_2Rh_3Ga. Ce_2Rh_3Ga shows intermediate cerium valence while all other RE_2Rh_3Ga phases are Curie-Weiss paramagnets which order magnetically at low temperatures. The "8"9Y and "7"1Ga solid state nuclear magnetic resonance (NMR) spectra of the diamagnetic representative Y_2Rh_3Ga show well-defined single resonances in agreement with an ordered bulk phase. In comparison to the binary Laves phase YRh_2 a strongly increased "8"9Y resonance frequency is observed owing to a higher s-electron spin density at the "8"9Y nuclei as proven by density of states (DOS) calculations.

Estimation of tau1 for the host Kramers' Ln3+ ions (Ln = Nd, Sm and Yb) from the EPR linewidths of Gd3+ impurity ions in Ln2(SO4)3.8H2O

International Nuclear Information System (INIS)

Malhotra, V.M.; Buckmaster, H.A.

1981-01-01

It is shown that the EPR linewidth data published by Misra and Mikolajczak for Gd 3+ impurity ions in Ln 2 (SO 4 ) 3 .8H 2 O (Ln = Nd, Sm and Yb) single crystals at 77 and 300 K can be used to estimate the effective spin-lattice relaxation time of Kramers' host ions. The various relaxation mechanisms which are operative in the lanthanides are reviewed and discussed. The estimated relaxation times are shown to be a sensitive function of the host ion energy level splittings and the temperature. The estimated effective spin-lattice relaxation times in these hosts are in reasonable agreement with those expected from a resonance Orbach process

Relaxor-ferroelectric BaLnZT (Ln = La, Nd, Sm, Eu, and Sc) ceramics for actuator and energy storage application

Science.gov (United States)

Ghosh, Sarit K.; Mallick, Kaushik; Tiwari, B.; Sinha, E.; Rout, S. K.

2018-01-01

Lead free ceramics Ba1-x Ln2x/3Zr0.3Ti0.7O3 (Ln = La, Nd, Sm, Eu and Sc), x = 0.02-0.10 are investigated for electrostrictive effect and energy storage properties in the proximity of relaxor-paraelectric phase boundary. Relaxor phase evidence from slim hysteresis loop and low remnant polarization are the key parameters responsible for improve the electrostrictive effect and energy storage properties simultaneously. With increase in rare earth content negative strain disappeared and almost hysteresis free strain is achieved. Strain-hysteresis profile in term of S-E, S-E 2 and S-P 2 is used to analyze the electrostrictive behavior of these ceramics. An average strain (S%) ˜ 0.03%, is accomplished at initial concentrations of x = 0.02-0.04 and electrostrictive coefficients (Q 11, and M 11) as well as the energy storage density is improved by a factor of 1.2 and 2.6 respectively when compare with pure (x = 0.0) ceramic. Above x ≥ 0.06, all compositions show a stable behavior which suggested the possibilities of these relaxor ceramics towards high precision actuators and energy storage application.

BaFCl:Eu2+, a new phosphor for X-ray-intensifying screens

International Nuclear Information System (INIS)

Stevels, A.L.N.; Pingault, F.

1975-01-01

A number of phosphors for X-ray-intensifying screens have been evaluated by calculating figures of merit. On use in combination with standard (''blue''-sensitive) X-ray film, BaFCl:Eu 2+ and BaFBr:Eu 2+ give better performance than the traditional CaWO 4 and more recently developed UV or blue-emitting materials (e.g., sulphates and y-oxysulphides). The calculated figures of merit of BaFCl:Eu 2+ or BaFBr:Eu 2+ /standard-film combinations are comparable to those of Gd 2 O 2 S:Tb/green-sensitive X-ray film systems. The preparation of optimal fluorohalide:Eu 2+ phosphors involves proper formation of the host lattice, complete reduction of Eu 3+ ions as well as elimination of afterglow. Measurements on powders and experimental screens indicate that by using BaFCl:Eu 2+ screens in radiography, important dose reductions can be achieved without the necessity of using other than standard (''blue''-sensitive) X-ray films

Journal of Earth System Science | Indian Academy of Sciences

Indian Academy of Sciences (India)

The rare earth elements like La, Ce, Pr, Nd, Sm, Eu, Gd, Tb, Dy, Ho, Er, Tm, Yb, Lu and the heavy metals like Mg, V, Cr, Mn, Fe, Cu, Zn, U, Th were analysed by using standard analytical methods. The Post-Archean Australian Shale composition was used to normalise the rare earth elements. It was found that the sediments ...

Synthesis and luminescent properties of Y(As, Nb, P, V)O4:Eu3+ red phosphors by combinatorial chemistry method

International Nuclear Information System (INIS)

Zeon, Il Woon; Park, Hee Dong; Sohn, Kee Sun; Ryu, Seung Kon

2001-01-01

Eu doped YRO 4 (R=As, Nb, P, V)red phosphors were prepared by the combinatorial chemistry method. The quaternary material library of tetrahedron-type composition array was designed to investigate the luminescence of the host material under UV and VUV excitations (254, 147 nm). The photoluminescent characteristics of the samples were comparable to the commercially available red phosphors such as (Y, Gd)BO 3 :Eu 3+ and Y 2 O 3 :Eu 3+ . In view of the luminescence yield, V rich region was found to be optimum under UV excitation. But the results under VUV excitation were different from those of UV excitation, the samples of the composition containing a large amount of P shows the highest luminescence. Especially, higher luminescence was obtained in Y 0.9 (As 0.06 Nb 0.06 P 0.83 V 0.06 )O 4 :Eu 0.1 phosphors than commercial (Y, Gd)BO 3 red phosphors under 147 nm excitation

Identification of 162Gd and a new type of identical bands

International Nuclear Information System (INIS)

Jones, E. F.; Gore, P. M.; Hamilton, J. H.; Ramayya, A. V.; Dodder, R. S.; Beyer, C. J.; Hwang, J. K.; Zhang, X. Q.; Kormicki, J.; Zhu, S. J.; Lima, A. P. de; Cole, J. D.; Aryaeinejad, R.; Ma, W. C.; Ter-Akopian, G. M.; Daniel, A. V.; Oganessian, Yu. Ts.; Rasmussen, J. O.; Asztalos, S. J.; Lee, I. Y.

1998-01-01

From γ-γ-γ coincidence measurements in spontaneous fission of 252 Cf, level energies were established to spins 14 + to 20 + in many neutron-rich nuclei. New isotope 162 Gd was identified. Yrast bands of 152,154,156 Nd, 156,158,160 Sm, and 160,162 Gd exhibit near-identical transition energies and moments of inertia (MOI) shifted by the same constant amounts for every spin state from 2 + to 12 + or 14 + for nuclei differing by 2n, 4n, 2p, 4p, α, α+2p, and α+2n. These shifted identical bands (SIB) are a new phenomenon. Analysis of all known even-even proton- to neutron-rich nuclei from Ba(Z=56) to Os(Z=76) reveal no SIB for proton-rich nuclei and few cases of SIB for the most neutron-rich pairs around N=98-102 separated by 2n and 2p

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.

Phase transitions of rare earth compounds during immobilization by foamed corundum

International Nuclear Information System (INIS)

Potemkina, T.I.; Zakharov, M.A.; Plotnikova, T.E.

1992-01-01

Expansion of work on the environmentally safe handling of radioactive materials has become very important in recent years. The proposed method for immobilizing radionuclides by injection into a porous matrix and subsequent fixation has a definite advantage over other techniques, because of its simplicity and low cost. This raises a number of problems that require careful study. The authors can distinguish the following: choice of porous matrix materials; thermal decomposition of nitrates directly in the matrix itself, which determines the minimum firing temperature; behavior and properties of oxides produced in nitrate decomposition; conditions for compound formation between injected solutions and matrix material; processes occurring during immobilizer storage. The rare earth nitrate series can be divided into two groups on the basis of behavior during thermal decomposition: the elements preceding and following Gd. The first group includes La, Pr, And Eu, for which decomposition begins simultaneously with conclusion of dehydration; the second includes Dy, Tb, and Yb, for which nitrate group decomposition begins before dehydration is complete. The authors utilized DTA, XPA, and IR analysis to study the physicochemical properties of the immobilizer produced by a single impregnation of the foamed corundum with rare earth (La, Eu, Dy, Tb, and Yb) nitrate solutions and subsequent firing at 900 degrees C for 30 min. The choice of these rare earths was dictated by the fact that the Ln 2 O 3 -AlO 3 system can be divided into three groups on the basis of phase ratios: La-Nd, Sm-Eu, and Gd-Lu. Lanthanide monoaluminates are formed in all these groups, and the difference lies in the other reaction products generated: LnAl 11 O 18 for La-Nd, LnAl 11 O 18 and Ln 4 Al 2 O 9 for Sm-Eu, and Ln 4 Al 2 O 9 and Ln 3 Al 5 O 12 for Gd-Lu

Ion chromatography separation of lanthanides at trace concentrations from Gd Matrix and quantification by ICP-MS

International Nuclear Information System (INIS)

Raut, V.V.; Jeyakumar, S.; Nagar, B.K.; Deb, S.B.; Saxena, M.K.; Tomar, B.S.

2014-01-01

Gadolinium compounds are mainly used as burnable poison. The presence of certain impurities is undesirable in the nuclear grade Gd compounds. Gd 2 O 3 , a most common raw material used for the preparation of nuclear grade Gd compounds. Analysis of rare earth impurities in Gd-matrices is one of the important exercises carried out to ensure the purity of Gd 2 O 3 . Determination of lanthanides at trace concentrations in lanthanide (Gd) matrix is complicated and difficult to realize. This is because the selective separation of REE's in one of the lanthanide elements is a challenging task. The present study was carried out to explore the feasibility of separating trace level lanthanides from Gd matrix by ion interaction chromatography (IIC) and to develop an analytical methodology for the determination of lanthanides by inductively coupled plasma mass spectrometry (ICP-MS). In the present investigation, the reversed phase column was dynamically modified into sulphonic acid functionalized surface by using 0.025 M n-Octane sulphonic acid (OSA). With α-HIBA eluent system, the elution order follows as Lu to La. The separations are employed with gradient elution mode. Since the sample has large excess of Gd, elution profiles with concentration gradient of HIBA were attempted. Separated fractions of Light lanthanides (LLn) and Heavy lanthanides (HLn) were collected and analyzed by ICP-MS. During MS analysis, it was observed that due to high concentration of salt (Na salt of OSA) present in the collected fractions caused difficulty in ICP-MS . Hence the experiments were carried out using another ion interacting reagent viz. 0.03 M camphor-10-sulphonic acid (CSA). Initial concentration of HIBA was kept at 0.025 M up to 15 min for the elution of HLns i.e. from Lu to Tb and it was then increased to 0.05 M to 0.3 M in 30 min. After elution of Tb, outlet of the column was switched to drain for 7 min to separate bulk Gd fraction. From 22 to 35 min effluent fraction containing Eu

X-ray powder diffraction data on miscellaneous lanthanide compounds

International Nuclear Information System (INIS)

Ferguson, I.F.; Hughes, T.E.

1978-08-01

Recent work on neutron absorbing materials has produced various new X-ray diffraction powder patterns of compounds of the lanthanides. Various inconsistencies in previously published data have been noted, and accurate measurements have been made of the lattice parameters of the rare earth oxides Sm 2 0 3 , Eu 2 0 3 , Gd 2 0 3 which have the monoclinic rare earth type B- structure, as well as Eu0. These data are recorded for reference. The optimum conditions for obtaining X-ray powder diffraction data from europium compounds are also noted. (author)

Long-wave UVA radiation excited warm white-light emitting NaGdTiO{sub 4}: Tm{sup 3+}/Dy{sup 3+}/Eu{sup 3+} ions tri-doped phosphors: Synthesis, energy transfer and color tunable properties

Energy Technology Data Exchange (ETDEWEB)

Bharat, L. Krishna; Du, Peng; Yu, Jae Su, E-mail: jsyu@khu.ac.kr

2016-05-05

NaGdTiO{sub 4} (NGT) phosphors doped with different activator ions (Tm{sup 3+}, Dy{sup 3+}, and Eu{sup 3+}) were synthesized by a conventional solid-state reaction method in an ambient atmosphere. These phosphors were characterized by scanning electron microscope images, transmission electron microscope images, X-ray diffraction patterns, Fourier transform infrared spectra, and photoluminescence spectra. All the samples were crystallized in an orthorhombic phase with a space group of Pbcm (57). In Tm{sup 3+}/Dy{sup 3+} ions co-doped samples, white-light emission was observed under near-ultraviolet (NUV) excitation. In addition, the energy transfer between Tm{sup 3+} and Dy{sup 3+} ions was proved to be a resonant type via an electric dipole–dipole mechanism and the critical distance of energy transfer was calculated to be 19.91 Å. Furthermore, Tm{sup 3+}/Dy{sup 3+}/Eu{sup 3+} ions tri-doped NGT phosphors demonstrated warm white-light emission by appropriately tuning the activator content, based on the principle of energy transfer. These NUV wavelength excitable phosphors exhibit great potential as a single-phase full-color emitting phosphor for white light-emitting diode applications. - Highlights: • The pebble shaped NaGdTiO{sub 4} particles were prepared by solid-state reaction method. • Tm{sup 3+} and Dy{sup 3+} single doping gives respective blue and cool white light emission. • The Tm{sup 3+}/Dy{sup 3+} ions co-doped samples give CIE values near to standard white light. • Addition of Eu{sup 3+} ions shifts the CIE values towards warm white light region. • This single phase white light emitting phosphors have lower CCT values (<5000 K).

High-efficient, bicolor-emitting GdVO_4:Dy"3"+ phosphor under near ultraviolet excitation

International Nuclear Information System (INIS)

Lu, Jinjin; Zhou, Jia; Jia, Huayu; Tian, Yue

2015-01-01

Bicolor emitting GdVO_4:Dy"3"+ phosphor with short columniation-shape was prepared via a simple co-precipitation process. The optimal doping concentration for obtaining maximal luminescent intensity was confirmed to be 0.3 mol% and the electric dipole–dipole interaction is responsible for concentration quenching of Dy"3"+ emission in GdVO_4 phosphor. In order to evaluate the luminescent performance of as-prepared phosphor, the luminescent efficiency and color coordinates were studied. The results show that luminescent efficiency of this phosphor is very high under near UV excitation and twice times higher than commercial Y_2O_2S:Eu"3"+ phosphor. In addition, the color coordinates for optimal Dy"3"+ concentration are (0.339, 0.379), which are close to equal energy point. Therefore, the GdVO_4:Dy"3"+ phosphor may have potential application for solid state lighting.

Macrocyclic Gd(3+) complexes with pendant crown ethers designed for binding zwitterionic neurotransmitters.

Science.gov (United States)

Oukhatar, Fatima; Meudal, Hervé; Landon, Céline; Logothetis, Nikos K; Platas-Iglesias, Carlos; Angelovski, Goran; Tóth, Éva

2015-07-27

A series of Gd(3+) complexes exhibiting a relaxometric response to zwitterionic amino acid neurotransmitters was synthesized. The design concept involves ditopic interactions 1) between a positively charged and coordinatively unsaturated Gd(3+) chelate and the carboxylate group of the neurotransmitters and 2) between an azacrown ether appended to the chelate and the amino group of the neurotransmitters. The chelates differ in the nature and length of the linker connecting the cyclen-type macrocycle that binds the Ln(3+) ion and the crown ether. The complexes are monohydrated, but they exhibit high proton relaxivities (up to 7.7 mM(-1)  s(-1) at 60 MHz, 310 K) due to slow molecular tumbling. The formation of ternary complexes with neurotransmitters was monitored by (1) H relaxometric titrations of the Gd(3+) complexes and by luminescence measurements on the Eu(3+) and Tb(3+) analogues at pH 7.4. The remarkable relaxivity decrease (≈80 %) observed on neurotransmitter binding is related to the decrease in the hydration number, as evidenced by luminescence lifetime measurements on the Eu(3+) complexes. These complexes show affinity for amino acid neurotransmitters in the millimolar range, which can be suited to imaging concentrations of synaptically released neurotransmitters. They display good selectivity over non-amino acid neurotransmitters (acetylcholine, serotonin, and noradrenaline) and hydrogenphosphate, but selectivity over hydrogencarbonate was not achieved. © 2015 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

Medium-spin levels and the character of the 20.4 ns 13/2+ isomer in 145Gd

International Nuclear Information System (INIS)

Pakkanen, A.; Muhonen, J.; Piiparinen, M.

1981-06-01

Levels of the N = 81 nucleus 145 Gd have been investigated by in-beam γ-ray and conversion electron spectroscopy with the 144 Sm( 3 He,2n) reaction. Fourteen new low- and medium-spin states between 1.0 and 2.4 MeV excitation, the known yrast levels up to spin (21/2) + , five other high-spin non-yrast states and a new 20.4 ns (13/2) + isomer at 2200.2 keV in 145 Gd have been observed. The isomer decays via a fast 927.3 keV E3 transition with B(E3) = 48 +- 7 W.u. Another weaker decay branch is a mixed, strongly hindered E1+M2+E3 transition to the νhsub(11/2)sup(-1) state. We propose an octupole νfsub(7/2)jsub(0)sup(-2)x3 - main configuration for the isomer, analogous to the 997 keV (13/2) + isomer in 147 Gd. The levels of 145 Gd are discussed on the basis of the spherical shell model. (author)

Optical properties of Eu(III) doped strontium gadolinium niobate oxide

Energy Technology Data Exchange (ETDEWEB)

Vishwnath, Verma, E-mail: mnsmsu@gmail.com, E-mail: vermavicky.1988@gmail.com; Srinivas, M.; Patel, Nimesh; Modi, Dhaval [Luminescent Materials Laboratory, Physics Department, Faculty of Science, The M. S. University of Baroda, Vadodara-390002 (India); Murthy, K. V. R. [Display Materials Laboratory, Applied Physics Department, Faculty of Technology and Engineering, The M. S. University of Baroda, Vadodara-390001, Gujarat (India)

2016-05-23

Sr{sub 2}GdNbO{sub 6} doped with trivalent ion of Eu phosphors having monoclinic phase of space group P2{sub 1}/n have been synthesized via solid state reaction method, and their photoluminescence properties have been examined under UV excitation. The emission peaks exhibited around 580, 596, and 610 nm wavelength. By using xenon lamp as a source of excitation having wavelengths at 254 and 262 nm, it is observed that the maximum light emission yielded in red region. It is inferred that the dopant Eu{sup +3} ions may take the substitutional positions at non-centrosymmetric site.

Syntheses of rare-earth metal oxide nanotubes by the sol-gel method assisted with porous anodic aluminum oxide templates

International Nuclear Information System (INIS)

Kuang Qin; Lin Zhiwei; Lian Wei; Jiang Zhiyuan; Xie Zhaoxiong; Huang Rongbin; Zheng Lansun

2007-01-01

In this paper, we report a versatile synthetic method of ordered rare-earth metal (RE) oxide nanotubes. RE (RE=Y, Ce, Pr, Nd, Sm, Eu, Gd, Tb, Dy, Ho, Er, Yb) oxide nanotubes were successfully prepared from corresponding RE nitrate solution via the sol-gel method assisted with porous anodic aluminum oxide (AAO) templates. Scanning electron microscopy (SEM), transmission electron microscopy (TEM), high-resolution TEM, and X-ray diffraction (XRD) have been employed to characterize the morphology and composition of the as-prepared nanotubes. It is found that as-prepared RE oxides evolve into bamboo-like nanotubes and entirely hollow nanotubes. A new possible formation mechanism of RE oxide nanotubes in the AAO channels is proposed. These high-quantity RE oxide nanotubes are expected to have promising applications in many areas such as luminescent materials, catalysts, magnets, etc. - Graphical abstract: A versatile synthetic method for the preparation of ordered rare-earth (RE) oxide nanotubes is reported, by which RE (RE=Y, Ce, Pr, Nd, Sm, Eu, Gd, Tb, Dy, Ho, Er, Yb) oxide nanotubes were successfully prepared from corresponding RE nitrate solution via the sol-gel method assisted with porous anodic aluminum oxide (AAO) templates

Fixation of carbon dioxide by macrocyclic lanthanide(III) complexes under neutral conditions producing self-assembled trimeric carbonato-bridged compounds with μ3-η2:η2:η2 bonding.

Science.gov (United States)

Bag, Pradip; Dutta, Supriya; Biswas, Papu; Maji, Swarup Kumar; Flörke, Ulrich; Nag, Kamalaksha

2012-03-28

A series of mononuclear lanthanide(III) complexes [Ln(LH(2))(H(2)O)(3)Cl](ClO(4))(2) (Ln = La, Nd, Sm, Eu, Gd, Tb, Lu) of the tetraiminodiphenolate macrocyclic ligand (LH(2)) in 95 : 5 (v/v) methanol-water solution fix atmospheric carbon dioxide to produce the carbonato-bridged trinuclear complexes [{Ln(LH(2))(H(2)O)Cl}(3)(μ(3)-CO(3))](ClO(4))(4)·nH(2)O. Under similar conditions, the mononuclear Y(III) complex forms the dimeric compound [{Y(LH(2))(H(2)O)Cl}(μ(2)-CO(3)){Y(LH(2))(H(2)O)(2)}](ClO(4))(3)·4H(2)O. These complexes have been characterized by their IR and NMR ((1)H, (13)C) spectra. The X-ray crystal structures have been determined for the trinuclear carbonato-bridged compounds of Nd(III), Gd(III) and Tb(III) and the dinuclear compound of Y(III). In all cases, each of the metal centers are 8-coordinate involving two imine nitrogens and two phenolate oxygens of the macrocyclic ligand (LH(2)) whose two other imines are protonated and intramolecularly hydrogen-bonded with the phenolate oxygens. The oxygen atoms of the carbonate anion in the trinuclear complexes are bonded to the metal ions in tris-bidentate μ(3)-η(2):η(2):η(2) fashion, while they are in bis-bidentate μ(2)-η(2):η(2) mode in the Y(III) complex. The magnetic properties of the Gd(III) complex have been studied over the temperature range 2 to 300 K and the magnetic susceptibility data indicate a very weak antiferromagnetic exchange interaction (J = -0.042 cm(-1)) between the Gd(III) centers (S = 7/2) in the metal triangle through the carbonate bridge. The luminescence spectral behaviors of the complexes of Sm(III), Eu(III), and Tb(III) have been studied. The ligand LH(2) acts as a sensitizer for the metal ions in an acetonitrile-toluene glassy matrix (at 77 K) and luminescence intensities of the complexes decrease in the order Eu(3+) > Sm(3+) > Tb(3+).

Frenkel effect in EuLaGa3S7

International Nuclear Information System (INIS)

Tagiev, O.B.; Musaev, N.N.; Musaeva, S.M.

1998-01-01

The Frenkel effect in the EuLaGdGa 3 S monocrystals with specific resistance of 10 9 -10 13 Ohm cm and forbidden zone width of 3.0 eV is studied. The following parameters: di-electrical permittivity (ε 8), the electron free run length (λ = 6x10 -6 cm -3 ) and traps concentration (N t =1.2x10 15 cm -3 ) are determined on the basis of studies on volt-ampere characteristics of the In-EuLaGa 3 S 7 -In structures in the electrical fields up to 10 4 V/cm within the temperature interval of 300-360 K [ru

Molecular imaging of alpha v beta3 integrin expression in atherosclerotic plaques with a mimetic of RGD peptide grafted to Gd-DTPA.

Science.gov (United States)

Burtea, Carmen; Laurent, Sophie; Murariu, Oltea; Rattat, Dirk; Toubeau, Gérard; Verbruggen, Alfons; Vansthertem, David; Vander Elst, Luce; Muller, Robert N

2008-04-01

The integrin alpha v beta3 is highly expressed in atherosclerotic plaques by medial and intimal smooth muscle cells and by endothelial cells of angiogenic microvessels. In this study, we have assessed non-invasive molecular magnetic resonance imaging (MRI) of plaque-associated alpha v beta3 integrin expression on transgenic ApoE-/- mice with a low molecular weight peptidomimetic of Arg-Gly-Asp (mimRGD) grafted to gadolinium diethylenetriaminepentaacetate (Gd-DTPA-g-mimRGD). The analogous compound Eu-DTPA-g-mimRGD was employed for an in vivo competition experiment and to confirm the molecular targeting. The specific interaction of mimRGD conjugated to Gd-DTPA or to 99mTc-DTPA with alpha v beta3 integrin was furthermore confirmed on Jurkat T lymphocytes. The mimRGD was synthesized and conjugated to DTPA. DTPA-g-mimRGD was complexed with GdCl3.6H2O, EuCl3.6H2O, or with [99mTc(CO)3(H2O)3]+. MRI evaluation was performed on a 4.7 T Bruker imaging system. Blood pharmacokinetics of Gd-DTPA-g-mimRGD were assessed in Wistar rats and in c57bl/6j mice. The presence of angiogenic blood vessels and the expression of alpha v beta3 integrin were confirmed in aorta specimens by immunohistochemistry. Gd-DTPA-g-mimRGD produced a strong enhancement of the external structures of the aortic wall and of the more profound layers (possibly tunica media and intima). The aortic lumen seemed to be restrained and distorted. Pre-injection of Eu-DTPA-g-mimRGD diminished the Gd-DTPA-g-mimRGD binding to atherosclerotic plaque and confirmed the specific molecular targeting. A slower blood clearance was observed for Gd-DTPA-g-mimRGD, as indicated by a prolonged elimination half-life and a diminished total clearance. The new compound is potentially useful for the diagnosis of vulnerable atherosclerotic plaques and of other pathologies characterized by alpha v beta3 integrin expression, such as cancer and inflammation. The delayed blood clearance, the significant enhancement of the signal

Structural Characterization and Absolute Luminescence Efficiency Evaluation of Gd2O2S High Packing Density Ceramic Screens Doped with Tb3+ and Eu3+ for further Applications in Radiology

Science.gov (United States)

Dezi, Anna; Monachesi, Elenasophie; D'Ignazio, Michela; Scalise, Lorenzo; Montalto, Luigi; Paone, Nicola; Rinaldi, Daniele; Mengucci, Paolo; Loudos, George; Bakas, Athanasios; Michail, Christos; Valais, Ioannis; Fountzoula, Christine; Fountos, George; David, Stratos

2017-11-01

Rare earth activators are impurities added in the phosphor material to enhance probability of visible photon emission during the luminescence process. The main activators employed are rare earth trivalent ions such as Ce+3, Tb+3, Pr3+ and Eu+3. In this work, four terbium-activated Gd2O2S (GOS) powder screens with different thicknesses (1049 mg/cm2, 425.41 mg/cm2, 313 mg/cm2 and 187.36 mg/cm2) and one europium-activated GOS powder screen (232.18 mg/cm2) were studied to investigate possible applications for general radiology detectors. Results presented relevant differences in crystallinity between the GOS:Tb doped screens and GOS:Eu screens in respect to the dopant agent present. The AE (Absolute efficiency) was found to rise (i) with the increase of the X-ray tube voltage with the highest peaking at 110kVp and (ii) with the decrease of the thickness among the four GOS:Tb. Comparing similar thickness values, the europium-activated powder screen showed lower AE than the corresponding terbium-activated.

Facile combustion synthesis of novel CaZrO3:Eu , Gd red phosphor ...

Indian Academy of Sciences (India)

When the Gd3+ ions were introduced in this compound, the emissions of ... a doped nanostructure may suppress resonant energy trans- ... light.17,18 In this paper, we report a fast and efficient pro- cedure for .... stages of weight loss at temperatures between 258 and 600 ... or particle size as the dopant ions are introduced.

Chiroptical methods in a wide wavelength range for obtaining Ln3+ complexes with circularly polarized luminescence of practical interest.

Science.gov (United States)

Górecki, Marcin; Carpita, Luca; Arrico, Lorenzo; Zinna, Francesco; Di Bari, Lorenzo

2018-05-29

We studied enantiopure chiral trivalent lanthanide (Ln3+ = La3+, Sm3+, Eu3+, Gd3+, Tm3+, and Yb3+) complexes with two fluorinated achiral tris(β-diketonate) ligands (HFA = hexafluoroacetylacetonate and TTA = 2-thenoyltrifluoroacetonate), incorporating a chiral bis(oxazolinyl)pyridine (PyBox) unit as a neutral ancillary ligand, by the combined use of optical and chiroptical methods, ranging from UV to IR both in absorption and circular dichroism (CD), and including circularly polarized luminescence (CPL). Ultimately, all the spectroscopic information is integrated into a total and a chiroptical super-spectrum, which allows one to characterize a multidimensional chemical space, spanned by the different Ln3+ ions, the acidity and steric demand of the diketone and the chirality of the PyBox ligand. In all cases, the Ln3+ ions endow the systems with peculiar chiroptical properties, either allied to f-f transitions or induced by the metal onto the ligand. In more detail, we found that Sm3+ complexes display interesting CPL features, which partly superimpose and partly integrate the more common Eu3+ properties. Especially, in the context of security tags, the pair Sm/Eu may be a winning choice for chiroptical barcoding.

Definition of an intramolecular Eu-to-Eu energy transfer within a discrete [Eu2L] complex in solution.

Science.gov (United States)

Nonat, Aline; Regueiro-Figueroa, Martín; Esteban-Gómez, David; de Blas, Andrés; Rodríguez-Blas, Teresa; Platas-Iglesias, Carlos; Charbonnière, Loïc J

2012-06-25

Ligand L, based on two do3a moieties linked by the methylene groups of 6,6'-dimethyl-2,2'-bipyridine, was synthesized and characterized. The addition of Ln salts to an aqueous solution of L (0.01 M Tris-HCl, pH 7.4) led to the successive formation of [LnL] and [Ln(2)L] complexes, as evidenced by UV/Vis and fluorescence titration experiments. Homodinuclear [Ln(2)L] complexes (Ln = Eu, Gd, Tb, Yb, and Lu) were prepared and characterized. The (1)H and (13)C NMR spectra of the Lu and Yb complexes in D(2)O solution (pD = 7.0) showed C(1) symmetry of these species in solution, pointing to two different chemical environments for the two lanthanide cations. The analysis of the chemical shifts of the Yb complex indicated that the two coordination sites present square antiprismatic (SAP) coordination environments around the metal ions. The spectroscopic properties of the [Tb(2)L] complex upon ligand excitation revealed conventional behavior with τ(H2O) = 2.05(1) ms and ϕ(H2O) = 51%, except for the calculation of the hydration number obtained from the luminescent lifetimes in H(2)O and D(2)O, which pointed to a non-integer value of 0.6 water molecules per Tb(III) ion. In contrast, the Eu complex revealed surprising features such as: 1) the presence of two and up to five components in the (5)D(0)→(7)F(0) and (5)D(0)→(7)F(1) emission bands, respectively; 2) marked differences between the normalized spectra obtained in H(2)O and D(2)O solutions; and 3) unconventional temporal evolution of the luminescence intensity at certain wavelengths, the intensity profile first displaying a rising step before the occurrence of the expected decay. Additional spectroscopic experiments performed on [Gd(2-x)Eu(x)L] complexes (x = 0.1 and 1.9) confirmed the presence of two distinct Eu sites with hydration numbers of 0 (site I) and 2 (site II), and showed that the unconventional temporal evolution of the emission intensity is the result of an unprecedented intramolecular Eu-to-Eu

Highly Luminescent Lanthanide Complexes of 1 Hydroxy-2-pyridinones

Energy Technology Data Exchange (ETDEWEB)

University of California, Berkeley; Lawrence National Laboratory; Raymond, Kenneth; Moore, Evan G.; Xu, Jide; Jocher, Christoph J.; Castro-Rodriguez, Ingrid; Raymond, Kenneth N.

2007-11-01

The synthesis, X-ray structure, stability, and photophysical properties of several trivalent lanthanide complexes formed from two differing bis-bidentate ligands incorporating either alkyl or alkyl ether linkages and featuring the 1-hydroxy-2-pyridinone (1,2-HOPO) chelate group in complex with Eu(III), Sm(III) and Gd(III) are reported. The Eu(III) complexes are among some of the best examples, pairing highly efficient emission ({Phi}{sub tot}{sup Eu} {approx} 21.5%) with high stability (pEu {approx} 18.6) in aqueous solution, and are excellent candidates for use in biological assays. A comparison of the observed behavior of the complexes with differing backbone linkages shows remarkable similarities, both in stability and photophysical properties. Low temperature photophysical measurements for a Gd(III) complex were also used to gain insight into the electronic structure, and were found to agree with corresponding TD-DFT calculations for a model complex. A comparison of the high resolution Eu(III) emission spectra in solution and from single crystals also revealed a more symmetric coordination geometry about the metal ion in solution due to dynamic rotation of the observed solid state structure.

Dependence of the Q10 values on the depth of the soil temperature measuring point

Czech Academy of Sciences Publication Activity Database

Pavelka, Marian; Acosta, Manuel; Marek, Michal V.; Kutsch, W.; Janouš, Dalibor

2007-01-01

Roč. 292, - (2007), s. 171-179 ISSN 0032-079X R&D Projects: GA ČR GD526/03/H036; GA MŽP SM/640/18/03 Grant - others:EU(XE) GOCE-CT-2003-505572 Institutional research plan: CEZ:AV0Z60870520 Keywords : respiration * soil * temperature * Q10 * Norway spruce * grassland Subject RIV: EH - Ecology, Behaviour Impact factor: 1.821, year: 2007

Miljøundersøgelser ved Kvanefjeldet 2001

DEFF Research Database (Denmark)

Asmund, G.

jordarter' (La Ce Pr Nd Sm Eu Gd Tb Dy Ho Er Tm Yb Lu) Af de mange grundstoffer, der er undersøgt er det kun 'Sjældne jordarter', zirkonium, niobium og thorium, der viser forhøjelser i forhold til baggrundsværdier og samtidigt er stærkt forhøjede i det vand, der siver ud fra minen. Imidlertid fandtes denne...

Mid-temperature deep removal of hydrogen sulfide on rare earth (RE = Ce, La, Sm, Gd) doped ZnO supported on KIT-6: Effect of RE dopants and interaction between active phase and support matrix

International Nuclear Information System (INIS)

Li, Lu; Zhou, Pin; Zhang, Hongbo; Meng, Xianglong; Li, Juexiu; Sun, Tonghua

2017-01-01

Highlights: • Various rare earth (RE)-doped ZnO/KIT-6 sorbents were prepared via sol-gel method. • La showed the highest efficiency on promoting ZnO/KIT-6 desulfurization activity. • The morphology of ZnO on KIT-6 played a crucial role for the reactivity. • The most initial factor of improving reactivity by RE was surface chemical property. • Crystallinity, host-guest interaction were also important to ZnO state on support. - Abstract: Rare earth oxides (RE = Ce, La, Sm and Gd) doped ZnO supported on KIT-6 sorbents (RE-ZnO/KIT-6) were synthesized by sol-gel method and their performance for deep removal of H 2 S (bellow 0.1 ppmv) from gas stream at medium temperature was tested. The RE dopants (except Ce) significantly enhance the deep desulfurization capacity of ZnO/KIT-6 sorbent and maintained higher sulfur uptake capacities upon multiple cycles of regeneration by a simple thermal oxidation in 10 v% of O 2 in N 2 atmosphere. The results of SAXS, XRD, N 2 physisorption, TEM, FIIR, and XPS implied that the KIT-6 structure of loading metal oxides remained intact. It was found that RE could hinder the ZnO crystal ripening during calcination resulted in smaller ZnO particles, enhance the interaction of ZnO and silica matrix to improve the dispersion of active phase on KIT-6. Furthermore, by increasing the outlayer electron density of Zn atom and oxygen transfer ability, the synergistic effect considered to be favorable for RE-ZnO/KIT-6 sulfidation. Even though the performance of improving ZnO dispersion was weaker than that of Sm and Gd, La-ZnO/KIT-6 performs the best deep desulfurizers by changing the surface chemical atmosphere for ZnO. Steam in the gas stream inhibited the capture of H 2 S by ZnO in the sorbents, in the case of La-ZnO/KIT-6, the steam content should control as lower as 5 v% to ensure the desulfurization efficiency and precision.

Synthesis and photoluminescence study of rare earth activated phosphor Na2La2B2O7

International Nuclear Information System (INIS)

Nagpure, P.A.; Omanwar, S.K.

2012-01-01

The photoluminescence properties in UV and N-UV excitable range for the phosphors of Na 2 La 2 B 2 O 7 : RE (RE=Eu, Tb, Ce, Sm, Gd) are investigated. The solution combustion synthesis technique was employed for the synthesis of the phosphors Na 2 La 2 B 2 O 7 : RE. The photoluminescence measurements of the phosphors were carried out on a HITACHI F7000 Fluorescence Spectrophotometer. The PL and PL excitation (PLE) spectra indicate that the main emission wavelength of Na 2 La 2 B 2 O 7 : Eu are 591 and 615 nm, Na 2 La 2 B 2 O 7 : Ce shows dominating emission peak at 387 nm and Na 2 La 2 B 2 O 7 : Tb displays green emission at 493, 544, 593 and 620 nm at 254 nm excitation, while Na 2 La 2 B 2 O 7 : Sm shows the main emission peak wavelengths 566 and 604 nm at 405 nm excitation and Na 2 La 2 B 2 O 7 : Gd shows dominating emission peak at 312 nm at 274 nm excitation. These phosphors may provide a new kind of luminescent materials under ultraviolet and near ultraviolet excitation for various applications. - Highlights: ► We use the combustion technique for synthesis of Na 2 La 2 B 2 O 7 : RE phosphor. ► Phosphor Na 2 La 2 B 2 O 7 : Eu 3+ shows intense red emission under UV excitation. ► Phosphor Na 2 La 2 B 2 O 7 : Tb 3+ shows intense green emission under UV excitation. ► Phosphor Na 2 La 2 B 2 O 7 : Sm 3+ shows orange red emission under near UV excitation. ► Phosphors Na 2 La 2 B 2 O 7 : Ce 3+ and Na 2 La 2 B 2 O 7 : Gd 3+ show near UV and UVB emissions under UV excitation.

Uranium dioxide in Fe(III)-containing ionic liquids with DMSO: Dissolution, separation, and structural characterization

Energy Technology Data Exchange (ETDEWEB)

Yao, Aining; Chu, Taiwei, E-mail: twchu@pku.edu.cn

2016-11-15

UO{sub 2} can be successfully dissolved in imidazolium-based Fe(III)-containing ionic liquids (ILs) with the help of DMSO. Spectroscopic studies and X-ray diffraction show that UO{sub 2}Cl{sub 4}{sup 2−} is the principal product. The dissolved uranyl species can be easily separated from the ILs via a combination of crystallization and solvent extraction. Moreover, even if 15.2 wt% of the rare-earth elements of Sm, Eu, and Gd, compared with the total amount of uranium and the rare-earth elements, exist in the IL, only uranium-containing crystals would be selectively formed and separated from the system. The solvents of acetone and acetonitrile could be used to separate the rare-earth elements from uranium in the IL with the help of imidazolium chloride. Considering the complete process from the dissolution of UO{sub 2} and some rare-earth oxides to the separation of uranium and rare-earth elements in the IL, the facile approach is promising for the spent nuclear fuel reprocessing. - Graphical abstract: UO{sub 2} can be successfully dissolved in Fe-containing ILs with the help of DMSO to form UO{sub 2}Cl{sub 4}{sup 2−}. The rare earth elements of Sm, Eu, and Gd can be separated from uranium in the IL, and meanwhile, the recovery of dissolved uranyl species and Fe-containing IL can also be achieved. - Highlights: • Dissolution of UO{sub 2} can be successfully achieved in imidazolium-based Fe-containing ILs with the help of DMSO without additional oxidants. • Compared with the total amount of uranium and the rare-earth elements, even if 15.2 wt% of the rare-earth elements of Sm, Eu, and Gd exist in the IL, only uranium-containing crystals would be selectively formed and separated from the system. • The separation of the rare-earth elements from uranium has also been achieved via a combination of crystallization and solvent extraction.

Uranium dioxide in Fe(III)-containing ionic liquids with DMSO: Dissolution, separation, and structural characterization

International Nuclear Information System (INIS)

Yao, Aining; Chu, Taiwei

2016-01-01

UO_2 can be successfully dissolved in imidazolium-based Fe(III)-containing ionic liquids (ILs) with the help of DMSO. Spectroscopic studies and X-ray diffraction show that UO_2Cl_4"2"− is the principal product. The dissolved uranyl species can be easily separated from the ILs via a combination of crystallization and solvent extraction. Moreover, even if 15.2 wt% of the rare-earth elements of Sm, Eu, and Gd, compared with the total amount of uranium and the rare-earth elements, exist in the IL, only uranium-containing crystals would be selectively formed and separated from the system. The solvents of acetone and acetonitrile could be used to separate the rare-earth elements from uranium in the IL with the help of imidazolium chloride. Considering the complete process from the dissolution of UO_2 and some rare-earth oxides to the separation of uranium and rare-earth elements in the IL, the facile approach is promising for the spent nuclear fuel reprocessing. - Graphical abstract: UO_2 can be successfully dissolved in Fe-containing ILs with the help of DMSO to form UO_2Cl_4"2"−. The rare earth elements of Sm, Eu, and Gd can be separated from uranium in the IL, and meanwhile, the recovery of dissolved uranyl species and Fe-containing IL can also be achieved. - Highlights: • Dissolution of UO_2 can be successfully achieved in imidazolium-based Fe-containing ILs with the help of DMSO without additional oxidants. • Compared with the total amount of uranium and the rare-earth elements, even if 15.2 wt% of the rare-earth elements of Sm, Eu, and Gd exist in the IL, only uranium-containing crystals would be selectively formed and separated from the system. • The separation of the rare-earth elements from uranium has also been achieved via a combination of crystallization and solvent extraction.

NEUTRON CROSS SECTION EVALUATIONS OF FISSION PRODUCTS BELOW THE FAST ENERGY REGION

International Nuclear Information System (INIS)

OH, S.Y.; CHANG, J.; MUGHABGHAB, S.