Tunable multicolor and white-light upconversion luminescence in Yb3+/Tm3+/Ho3+ tri-doped NaYF4 micro-crystals.

Science.gov (United States)

Lin, Hao; Xu, Dekang; Teng, Dongdong; Yang, Shenghong; Zhang, Yueli

2015-09-01

NaYF4 micro-crystals with various concentrations of Yb(3+) /Tm(3+) /Ho(3+) were prepared successfully via a simple and reproducible hydrothermal route using EDTA as the chelating agent. Their phase structure and surface morphology were studied using powder X-ray diffraction (XRD) and scanning electron microscopy (SEM). The XRD patterns revealed that all the samples were pure hexagonal phase NaYF4. SEM images showed that Yb(3+)/Tm(3+)/Ho(3+) tri-doped NaYF4 were hexagonal micro-prisms. Upconversion photoluminescence spectra of Yb(3+)/Tm(3+)/Ho(3+) tri-doped NaYF4 micro-crystals with various dopant concentrations under 980 nm excitation with a 665 mW pump power were studied. Tunable multicolor (purple, purplish blue, yellowish green, green) and white light were achieved by simply adjusting the Ho(3+) concentration in 20%Yb(3+)/1%Tm(3+)/xHo(3+) tri-doped NaYF4 micro-crystals. Furthermore, white-light emissions could be obtained using different pump powers in 20%Yb(3+)/1%Tm(3+)/1%Ho(3+) tri-doped NaYF4 micro-crystals at 980 nm excitation. The pump power-dependent intensity relationship was studied and relevant energy transfer processes were discussed in detail. The results suggest that Yb(3+)/Tm(3+) Ho(3+) tri-doped NaYF4 micro-crystals have potential applications in optoelectronic devices such as photovoltaic, plasma display panel and white-light-emitting diodes. Copyright © 2014 John Wiley & Sons, Ltd.

Fabrication and evaluation of chitosan/NaYF4:Yb3+/Tm3+ upconversion nanoparticles composite beads based on the gelling of Pickering emulsion droplets.

Science.gov (United States)

Yan, Huiqiong; Chen, Xiuqiong; Shi, Jia; Shi, Zaifeng; Sun, Wei; Lin, Qiang; Wang, Xianghui; Dai, Zihao

2017-02-01

The rare earth ion doped upconversion nanoparticles (UCNPs) synthesized by hydrophobic organic ligands possess poor solubility and low fluorescence quantum yield in aqueous media. To conquer this issue, NaYF 4 :Yb 3+ /Tm 3+ UCNPs, synthesized by a hydrothermal method, were coated with F127 and then assembled with chitosan to fabricate the chitosan/NaYF 4 :Yb 3+ /Tm 3+ composite beads (CS/NaYF 4 :Yb 3+ /Tm 3+ CBs) by Pickering emulsion system. The characterization results revealed that the as-synthesized NaYF 4 :Yb 3+ /Tm 3+ UCNPs with an average size of 20nm exhibited spherical morphology, high crystallinity and characteristic emission upconversion fluorescence with an overall blue color output. The NaYF 4 :Yb 3+ /Tm 3+ UCNPs were successfully conjugated on the surface of chitosan beads by the gelling of emulsion droplets. The resultant CS/NaYF 4 :Yb 3+ /Tm 3+ CBs showed good upconversion luminescent property, drug-loading capacity, release performance and excellent biocompatibility, exhibiting great potentials in targeted drug delivery and tissue engineering with potential tracking capability and lasting release performance. Copyright © 2016 Elsevier B.V. All rights reserved.

1.8 μm luminescent properties and energy transfer of Yb{sup 3+}/Tm{sup 3+} co-doped α-NaYF{sub 4} single crystals

Energy Technology Data Exchange (ETDEWEB)

Feng, Zhigang [Key Laboratory of Photo-electronic Materials, Ningbo University, Ningbo, Zhejiang, 315211 (China); Xia, Haiping, E-mail: hpxcm@nbu.edu.cn [Key Laboratory of Photo-electronic Materials, Ningbo University, Ningbo, Zhejiang, 315211 (China); Wang, Cheng; Zhang, Zhixiong; Jiang, Dongsheng; Zhang, Jian; He, Shinan; Tang, Qingyang; Sheng, Qiguo; Gu, Xuemei; Zhang, Yuepin [Key Laboratory of Photo-electronic Materials, Ningbo University, Ningbo, Zhejiang, 315211 (China); Chen, Baojiu [Department of Physics, Dalian Maritime University, Dalian, Liaoning Province, 116026 (China); Jiang, Haochuan, E-mail: jianghaochuan@nimte.ac.cn [Ningbo Institute of Materials Technology and Engineering, The Chinese Academy of Sciences, Ningbo, Zhejiang, 315211 (China)

2016-09-25

This paper reports on successful preparation of α-NaYF{sub 4} single crystals co-doped with ∼1.9 mol% Tm{sup 3+} and various concentrations (3.85 mol%, 7.69 mol%, 11.54 mol%, 15.38 mol%) of Yb{sup 3+} by using a flux-Bridgman method. The fluorescence decay curve was measured to investigate the luminescent properties of the Yb{sup 3+}/Tm{sup 3+} co-doped α-NaYF{sub 4}, and the energy transfer process from Yb{sup 3+} to Tm{sup 3+}; the J-O intensity parameters of Tm{sup 3+} were further calculated and analyzed according to the absorption spectra. Results show that, an intense 1.8 μm emission was achieved with Yb{sup 3+} as sensitizer for Tm{sup 3+} in the α-NaYF{sub 4} single crystal under the excitation of 980 nm LD (Laser Diode) because of the strong energy transfer from Yb{sup 3+} to Tm{sup 3+}. The maximum emission intensity at 1.8 μm is obtained at about 15.38 mol% doping concentration of Yb{sup 3+} when the concentration of Tm{sup 3+} ions is fixed at ∼1.90 mol% in the current research. Moreover, the calculated maximum value of emission cross section at 1.8 μm is 1.63 × 10{sup −20} cm{sup 2} for 3.85 mol% Yb{sup 3+}/1.9 mol% Tm{sup 3+} sample, and the obtained energy transfer rate (W{sub ET}) and energy transfer efficiency (η) are 1543 s{sup −1} and 83.8%, respectively. Our analysis of the fluorescence dynamics indicates that electric dipole-dipole interaction is dominant for the energy transfer from Yb{sup 3+} ions to Tm{sup 3+} ions by using Inokuti-Hirayama’s model. - Highlights: • The Tm{sup 3+}/Yb{sup 3+} co-doped α-NaYF{sub 4} single crystals were grown by Bridgman method. • The 1.8 μm emission intensity is obtained at 15.38 mol% Yb{sup 3+}/1.90 mol% Tm{sup 3+} sample. • The maximum value of emission cross section at 1.8 μm is 1.63 × 10{sup −20} cm{sup 2}. • The energy transfer rate is 1543 s{sup −1} and energy transfer efficiency is 83.8%. • The physical mechanism for energy transfer from Yb{sup 3+} to Tm{sup 3+} ions

Spectroscopic investigations of OH- influence on near-infrared fluorescence quenching of Yb3+/Tm3+ co-doped sodium-metaphosphate glasses

International Nuclear Information System (INIS)

Terra, I.A.A.; Camargo, A.S.S. de; Terrile, M.C.; Nunes, L.A.O.

2008-01-01

Energy transfer processes were studied in two sets of Yb 3+ and Tm 3+ co-doped sodium-metaphosphate glasses, prepared in air and nitrogen atmospheres. Using Foerster, Dexter, and Miyakawa theoretical models, the energy transfer parameters were calculated. The main ion-ion energy transfer processes analyzed were energy migration among Yb 3+ ions, cross-relaxations between Yb 3+ and Tm 3+ ions, and interactions with OH - radicals. The results indicated that Yb→Tm energy transfer favors 1.8 μm emissions, and there is no evidence of concentration quenching up to 2% Tm 2 O 3 doping. As expected, samples prepared in nitrogen atmosphere present higher fluorescence quantum efficiency than those prepared in air, and this feature is specially noted in the near-infrared region, where the interaction with the OH - radicals is more pronounced

Tm3+/Yb3+ co-doped tellurite glass with silver nanoparticles for 1.85 μm band laser material

Science.gov (United States)

Huang, Bo; Zhou, Yaxun; Cheng, Pan; Zhou, Zizhong; Li, Jun; Jin, Wei

2016-10-01

Tm3+/Yb3+ co-doped tellurite glasses with different silver nanoparticles (Ag NPs) concentrations were prepared using the conventional melt-quenching technique and characterized by the UV/Vis/NIR absorption spectra, 1.85 μm band fluorescence emission spectra, transmission electron microscopy (TEM) images, differential scanning calorimeter (DSC) curves and X-ray diffraction (XRD) patterns to investigate the effects of Ag NPs on the 1.85 μm band spectroscopic properties of Tm3+ ions, thermal stability and structural nature of glass hosts. Under the excitation of 980 nm laser diode (LD), the 1.85 μm band fluorescence emission of Tm3+ ions enhances significantly in the presence of Ag NPs with average diameter of ∼8 nm and local surface Plasmon resonance (LSPR) band of ∼590 nm, which is mainly attributed to the increased local electric field induced by Ag NPs at the proximity of doped rare-earth ions on the basis of energy transfer from Yb3+ to Tm3+ ions. An improvement by about 110% of fluorescence intensity is observed in the Tm3+/Yb3+ co-doped tellurite glass containing 0.5 mol% amount of AgNO3 while the prepared glass samples possess good thermal stability and amorphous structural nature. Meanwhile, the Judd-Ofelt intensity parameters Ωt (t = 2,4,6), spontaneous radiative transition probabilities, fluorescence branching ratios and radiative lifetimes of relevant excited levels of Tm3+ ions were determined based on the Judd-Ofelt theory to reveal the enhanced effects of Ag NPs on the 1.85 μm band spectroscopic properties, and the energy transfer micro-parameters and phonon contribution ratios were calculated based on the non-resonant energy transfer theory to elucidate the energy transfer mechanism between Yb3+ and Tm3+ ions. The present results indicate that the prepared Tm3+/Yb3+ co-doped tellurite glass with an appropriate amount of Ag NPs is a promising lasing media applied for 1.85 μm band solid-state lasers and amplifiers.

Blue and red emission in wide band gap BaZrO{sub 3}:Yb{sup 3+},Tm{sup 3+}

Energy Technology Data Exchange (ETDEWEB)

Borja-Urby, R. [Centro de Investigaciones en Optica, A. C., C. P. 37150 Leon, Gto. (Mexico); Diaz-Torres, L.A., E-mail: ditlacio@cio.mx [Centro de Investigaciones en Optica, A. C., C. P. 37150 Leon, Gto. (Mexico); Salas, P. [Centro de Fisica Aplicada y Tecnologia Avanzada, Universidad Nacional Autonoma de Mexico, A. P. 1-1010, Queretaro 76000 (Mexico); Vega-Gonzalez, M. [Centro de Geociencias-Universidad Nacional Autonoma de Mexico, A. P. 1-1010, Queretaro 76000 (Mexico); Angeles-Chavez, C. [Instituto Mexicano del Petroleo, Programa de Ingenieria Molecular, Cd. Mexico D.F. 07730 (Mexico)

2010-10-25

Under NIR excitation at 967 intense blue and red photoluminescence (PL) emissions are observed at room temperature in codoped Tm{sup 3+}-Yb{sup 3+} barium zirconate (BaZrO{sub 3}:Yb,Tm) powders. Powders were prepared by a simple hydrothermal method, and present a wide band gap that depends on the total rare earth content due to the degree of disorder induced in the BaZrO{sub 3} lattice by the substitution of the rare earth ions. Rietveld refinements of the XRD patterns indicated the presence of primary nanocrystallites with sizes between 50 and 70 nm depending on the Tm{sup 3+} content. Scanning transmission electron microscopy (STEM) shows that these primary particles self-aggregated in larger secondary particles which present a regular morphology with sizes around 1 {mu}m. The intense blue and red PL emissions in BaZrO{sub 3} powders under 967 nm excitation are governed by energy transfer processes from Yb{sup 3+} ions to Tm{sup 3+} ions and crossrelaxation among Tm{sup 3+} ions.

Intrinsic Bistability and Critical Slowing in Tm3+/Yb3+ Codoped Laser Crystal with the Photon Avalanche Mechanism

International Nuclear Information System (INIS)

Li, Li; Li-Xue, Chen; Xin-Lu, Zhang

2009-01-01

We present theoretically a novel intrinsic optical bistability (IOB) in the Tm 3+ /Yb 3+ codoped system with a photon avalanche mechanism. Numerical simulations based on the rate equation model demonstrate distinct IOB hysteresis and critical slowing dynamics around the avalanche thresholds. Such an IOB characteristic in Tm 3+ /Yb 3+ codoped crystal has potential applications in solid-state bistable optical displays and luminescence switchers in visible-infrared spectra. (fundamental areas of phenomenology (including applications))

Synthesis and characterization of KY3F10 and KY3F10:Yb:Nd:Tm crystals for optical applications

International Nuclear Information System (INIS)

Linhares, Horacio Marconi da Silva Dantas

2009-01-01

In this work, crystals of KY 3 F 10 pure and doped with Yb, Nd and Tm were grown aiming at the attainment of blue emission via Tm 3+ ions up conversion. It was established the best conditions to synthesis and purification of KY 3 F 10 . Crystals doped with 1.3 mol% Nd, 0.5 mol% Tm and some concentrations of Yb (5, 10, 20, 30 and 40 mol%) were obtained by slow cooling of the charge from the melt, using an usual conventional synthesis system and in a reactive HF atmosphere. It was taken into account parameters as cooling rate and different configurations of boats to conditioning the materials. The limit of Yb concentration to obtain a unique cubic phase was determined as 30mol%, for the cooling rates used in this work. The physical and chemical characterizations of the samples were performed by X-ray diffraction, differential thermal analysis, inductively coupled plasma-optical emission spectroscopy (ICP-OES), scanning electron microscopy, optical absorption and emission. An initial spectroscopic study was performed to verify the effect of the Yb 3+ concentration regarding the blue emission efficiency in the KY 3 F 10 :Yb:Nd:Tm. When the Nd 3+ is pumped at 797 nm, it was determined that the suitable Yb concentrations are between 10 and 20 mol% to obtain blue emission at 480 nm, and between 20 and 30 mol% to obtain emission at 450 nm. It was observed that two emissions bands in the UV (350 and 360nm) enhanced proportionally with the Yb 3+ concentration. (author)

Effect of silica surface coating on the luminescence lifetime and upconversion temperature sensing properties of semiconductor zinc oxide doped with gallium(III) and sensitized with rare earth ions Yb(III) and Tm(III).

Science.gov (United States)

Li, Yuemei; Li, Yongmei; Wang, Rui; Zheng, Wei

2018-02-26

Optical sensing of temperature by measurement of the ratio of the intensities of the 700 nm emission and the 800 nm emission of Ga(III)-doped ZnO (GZO) nanoparticles (NPs) and of GZO NPs coated with a silica shell are demonstrated at 980 nm excitation. It is found that the relative sensitivity of SiO 2 @Yb/Tm/GZO is 6.2% K -1 at a temperature of 693 K. This is ~3.4 times higher than that of Yb/Tm/GZO NPs. Obviously, the SiO 2 shell structure decreases the rate of the nonradiative decay. The decay time of the 800 nm emission of the Yb/Tm/GZO NPs (15 mol% Ga; 7 mol% Yb; 0.5 mol% Tm) displays a biexponential decay with a dominant decay time of 148 μs and a second decay time of ~412 μs. The lifetime of the Yb/Tm/GZO NPs at 293 K, and of the SiO 2 @Yb/Tm/GZO NPs are ~412 μs. Both the Yb/Tm/GZO and SiO 2 @Yb/Tm/GZO can be used up to 693 K. These results indicate that the SiO 2 shell on the Yb/Tm/GZO is beneficial in terms of sensitivity and resolution. Graphical abstract The enhancement the decay time and thermal sensitivity in the SiO 2 @Yb/Tm/GZO shell@core structure have been studied compared to the Ga(III)-doped Yb/Tm-doped ZnO (Yb/Tm/GZO). The SiO 2 @Yb/Tm/GZO have good thermal accuracy up to 693 °C.

Enhancing photovoltaic performance of dye-sensitized solar cell by rare-earth doped oxide of Lu2O3:(Tm3+, Yb3+)

International Nuclear Information System (INIS)

Li Qingbei; Lin Jianming; Wu Jihuai; Lan Zhang; Wang Yue; Peng Fuguo; Huang Miaoliang

2011-01-01

Highlights: → Tm 3+ /Yb 3+ codoped oxide is introduced into the TiO 2 film in dye-sensitized solar cell. → The RE improves light harvest via conversion luminescence and increases photocurrent. → The RE elevates the oxide film energy level and increases the cell photovoltage. → The cell efficiency is increased by 11.1% compared to the cell lacking of RE doping. - Abstract: In order to increase of the photocurrent, photovoltage and energy conversion efficiency of dye-sensitized solar cell (DSSC), rare-earth doped oxide of Lu 2 O 3 :(Tm 3+ , Yb 3+ ) is prepared and introduced into the TiO 2 film in the DSSC. As a luminescence medium, Lu 2 O 3 :(Tm 3+ , Yb 3+ ) improves incident light harvest via a conversion luminescence process and increases photocurrent; as a p-type dopant, the rare-earth ions elevate the energy level of the oxide film and increase the photovoltage. Under a simulated solar light irradiation of 100 mW cm -2 , the light-to-electric energy conversion efficiency of the DSSC with Lu 2 O 3 :(Tm 3+ , Yb 3+ ) doping reaches 6.63%, which is increased by 11.1% compared to the DSSC without Lu 2 O 3 :(Tm 3+ , Yb 3+ ) doping.

Spectroscopic investigations of OH{sup -} influence on near-infrared fluorescence quenching of Yb{sup 3+}/Tm{sup 3+} co-doped sodium-metaphosphate glasses

Energy Technology Data Exchange (ETDEWEB)

Terra, I.A.A. [Instituto de Fisica de Sao Carlos, Universidade de Sao Paulo, Av. Trabalhador Saocarlense 400, CEP 13566-590, USP-Sao Carlos, SP (Brazil)], E-mail: idelma@ifsc.usp.br; Camargo, A.S.S. de; Terrile, M.C.; Nunes, L.A.O. [Instituto de Fisica de Sao Carlos, Universidade de Sao Paulo, Av. Trabalhador Saocarlense 400, CEP 13566-590, USP-Sao Carlos, SP (Brazil)

2008-05-15

Energy transfer processes were studied in two sets of Yb{sup 3+} and Tm{sup 3+} co-doped sodium-metaphosphate glasses, prepared in air and nitrogen atmospheres. Using Foerster, Dexter, and Miyakawa theoretical models, the energy transfer parameters were calculated. The main ion-ion energy transfer processes analyzed were energy migration among Yb{sup 3+} ions, cross-relaxations between Yb{sup 3+} and Tm{sup 3+} ions, and interactions with OH{sup -} radicals. The results indicated that Yb{yields}Tm energy transfer favors 1.8 {mu}m emissions, and there is no evidence of concentration quenching up to 2% Tm{sub 2}O{sub 3} doping. As expected, samples prepared in nitrogen atmosphere present higher fluorescence quantum efficiency than those prepared in air, and this feature is specially noted in the near-infrared region, where the interaction with the OH{sup -} radicals is more pronounced.

A comprehensive phononics of phonon assisted energy transfer in the Yb{sup 3+} aided upconversion luminescence of Tm{sup 3+} and Ho{sup 3+} in solids

Energy Technology Data Exchange (ETDEWEB)

Debnath, Radhaballabh, E-mail: drdebnathr@gmail.com; Bose, Saptasree

2015-05-15

The theory of phonon assisted energy transfer is being widely used to explain the Yb{sup 3+} ion aided normal and upconversion emission of various rare earth ions in different Yb{sup 3+} co-doped solids. The reported phonon dynamics in many of these studies are either incomplete or erroneous. Here we report Yb{sup 3+} aided upconversion luminescence properties of Tm{sup 3+} and Ho{sup 3+} in (Yb{sup 3+}/Tm{sup 3+}) and (Yb{sup 3+}/Ho{sup 3+}) co-doped two BaO–tellurite glasses and explain their phononics in the light of Dexter's theory by proposing a comprehensive scheme. The approach is valid for other systems of different phonon structures. - Highlights: • Yb{sup 3+} aided upconversion luminescence properties of Tm{sup 3+} and Ho{sup 3+} in (Yb{sup 3+}/Tm{sup 3+}) and (Yb{sup 3+}/Ho{sup 3+}) co-doped two BaO–tellurite glasses, are reported. • Phonon assisted energy transfer in these systems are explained in the light of Dexter's theory by proposing a comprehensive scheme of phononics. • The approach is valid for other systems of different phonon structures.

Fabrication and evaluation of chitosan/NaYF{sub 4}:Yb{sup 3+}/Tm{sup 3+} upconversion nanoparticles composite beads based on the gelling of Pickering emulsion droplets

Energy Technology Data Exchange (ETDEWEB)

Yan, Huiqiong; Chen, Xiuqiong; Shi, Jia; Shi, Zaifeng; Sun, Wei; Lin, Qiang, E-mail: linqianggroup@163.com; Wang, Xianghui; Dai, Zihao

2017-02-01

The rare earth ion doped upconversion nanoparticles (UCNPs) synthesized by hydrophobic organic ligands possess poor solubility and low fluorescence quantum yield in aqueous media. To conquer this issue, NaYF{sub 4}:Yb{sup 3+}/Tm{sup 3+} UCNPs, synthesized by a hydrothermal method, were coated with F127 and then assembled with chitosan to fabricate the chitosan/NaYF{sub 4}:Yb{sup 3+}/Tm{sup 3+} composite beads (CS/NaYF{sub 4}:Yb{sup 3+}/Tm{sup 3+} CBs) by Pickering emulsion system. The characterization results revealed that the as-synthesized NaYF{sub 4}:Yb{sup 3+}/Tm{sup 3+} UCNPs with an average size of 20 nm exhibited spherical morphology, high crystallinity and characteristic emission upconversion fluorescence with an overall blue color output. The NaYF{sub 4}:Yb{sup 3+}/Tm{sup 3+} UCNPs were successfully conjugated on the surface of chitosan beads by the gelling of emulsion droplets. The resultant CS/NaYF{sub 4}:Yb{sup 3+}/Tm{sup 3+} CBs showed good upconversion luminescent property, drug-loading capacity, release performance and excellent biocompatibility, exhibiting great potentials in targeted drug delivery and tissue engineering with potential tracking capability and lasting release performance. - Highlights: • NaYF{sub 4}:Yb{sup 3+}/Tm{sup 3+} UCNPs were coated by F127 to improve aqueous dispersibility. • NaYF{sub 4}:Yb{sup 3+}/Tm{sup 3+} UCNPs were assembled with chitosan to fabricate the composite beads (CMs). • Pickering emulsions stabilized by UCNPs exhibited uniform and satisfactory emulsion droplets. • The CMs prepared by the gelling of emulsion droplet preserved upconversion luminescent property. • The resultant CMs showed good drug-loading capacity, release performance and biocompatibility.

Structural, Electronic and Elastic Properties of Heavy Fermion YbTM2 (TM= Ir and Pt) Laves Phase Compounds

Science.gov (United States)

Pawar, H.; Shugani, M.; Aynyas, M.; Sanyal, S. P.

2018-02-01

The structural, electronic and elastic properties of YbTM2 (TM = Ir and Pt) Laves phase intermetallic compounds which crystallize in cubic (MgCu2-type) structure, have been investigated using ab-initio full potential linearized augmented plane wave (FP-LAPW) method with LDA and LDA+U approximation. The calculated ground state properties such as lattice parameter (a0), bulk modulus (B) and its pressure derivative (B‧) are in good agreement with available experimental and theoretical data. The electronic properties are analyzed from band structures and density of states. Elastic constants are predicted first time for these compounds which obey the stability criteria for cubic system.

Yb3+,Er3+,Eu3+-codoped YVO4 material for bioimaging with dual mode excitation

International Nuclear Information System (INIS)

Thao, Chu Thi Bich; Huy, Bui The; Sharipov, Mirkomil; Kim, Jin-Ik.; Dao, Van-Duong; Moon, Ja-Young; Lee, Yong-Ill

2017-01-01

We propose an efficient bioimaging strategy using Yb 3+ ,Er 3+ ,Eu 3+ -triplet doped YVO 4 nanoparticles which were synthesized with polymer as a template. The obtained particles possess nanoscale, uniform, and flexible excitation. The effect of Eu 3+ ions on the luminescence properties of YVO 4 :Yb 3+ ,Er 3+ ,Eu 3+ was investigated. The upconversion mechanism of the prepared material was also discussed. The structure and optical properties of the prepared material were characterized by using X-ray diffraction (XRD), Fourier-transform IR spectroscopy (FTIR), scanning electron microscopy (SEM), Transmission electron microscopy (TEM) upconversion and photoluminescence spectra. The Commission International de I′Eclairage (CIE) chromaticity coordinates was investigated to confirm the performance of color luminescent emission. The prepared YVO 4 :Yb 3+ ,Er 3+ ,Eu 3+ nanoparticles could be easily dispersed in water by surface modification with cysteine (Cys) and glutathione (GSH). The aqueous dispersion of the modified YVO 4 :Yb 3+ ,Er 3+ ,Eu 3+ exhibits bright upconversion and downconversion luminescence and has been applied for bioimaging of HeLa cells. Our developed material with dual excitation offers a promising advance in bioimaging. - Highlights: • Prepared particles possess nanoscale size, uniform, and larger scale. • The material exhibits strong emission under dual mode excitations. • The surface material has been applied for bioimaging of HeLa cell. • Low cytotoxicity, no auto-fluorescence

White phosphor using Yb3+-sensitized Er3+-and Tm3+-doped sol-gel derived lead-fluorosilicate transparent glass ceramic excited at 980 nm

Science.gov (United States)

Tavares, M. C. P.; da Costa, E. B.; Bueno, L. A.; Gouveia-Neto, A. S.

2018-01-01

Generation of primary colors and white light through frequency upconversion using sol-gel derived 80SiO2:20PbF2 vitroceramic phosphors doped with Er3+, Er3+/Yb3+, Tm3+/Yb3+, and Er3+/Tm3+/Yb3+ excited at 980 nm is demonstrated. For Er3+ and Er3+/Yb3+ doped samples emissions were obtained in the blue (410 nm), green (530, and 550 nm) and red (670 nm) regions, corresponding to the 2H9/2 → 4I15/2,2H11/2 → 4I15/2, 4S3/2 → 4I152 and 4F9/2 → 4I15/2 transitions of Er3+, respectively. The codoping with Yb3+ ions altered the spectral profile of most of the emissions compared to the single doped samples, resulting in changes in the emitted color, in addition to a significant increase in the emission intensity. In Tm3+/Yb3+ co-doped samples visible emissions in the blue (480 nm), and red (650 nm), corresponding to transitions 1G4 → 3H6 and 1G4 → 3F4 of Tm3+, respectively, were obtained. The emission intensity around 480 nm overcome the red emission, and luminescence showed a predominantly blue tone. White light with CIE-1931 coordinates (0.36; 0.34) was produced by homogeneously mixing up powders of heat treated at 400 °C co-doped samples 5.0Er3+/5.0Yb3+ and 0.5Tm3+/2.5Yb3+ in the mass ratio of 13%, and 87%, respectively. The measured emission spectrum for a sample resulting from the mixture showed a profile with very good agreement with the spectrum found from the superimposition of the spectra of the co-doped samples.

Quantum sized Ag nanocluster assisted fluorescence enhancement in Tm3+-Yb3+ doped optical fiber beyond plasmonics

International Nuclear Information System (INIS)

Chattopadhyay, Rik; Haldar, Arindam; Paul, Mukul C.; Das, Shyamal; Bhadra, Shyamal K.

2015-01-01

We report a process for enhancing fluorescence emission from conventional rare earth ions in optical fiber by metal nanocluster (MNC) in nonresonant indirect pumping. The process is completely different from formal metal enhanced fluorescence phenomenon as the MNCs are too small in size to support localized surface plasmon and the excitation wavelength is far from plasmon resonance frequency. We used an established theory of two coupled oscillators to explain the simultaneous enhancement of Ytterbium (Yb 3+ ) and Thulium (Tm 3+ ) emission by silver (Ag) NCs under nonresonant pumping in optical fiber. The fiber is pumped with a 980 nm fiber pigtailed laser diode with input power of 20–100 mW to excite the Yb 3+ . Four times enhancement of Yb 3+ emission of 900–1100 nm and Tm 3+ upconversion emission around 474 nm, 650 nm, and 790 nm is observed in the fiber with Ag NCs

Influence of gold nanoparticles on the 805 nm gain in Tm3+/Yb3+ codoped PbO-GeO2 pedestal waveguides

Science.gov (United States)

de Assumpção, T. A. A.; Camilo, M. E.; Alayo, M. I.; da Silva, D. M.; Kassab, L. R. P.

2017-10-01

The production and characterization of pedestal waveguides based on PbO-GeO2 amorphous thin films codoped with Tm3+/Yb3+, with and without gold nanoparticles (NPs), are reported. Pedestal structure was obtained by conventional photolithography and plasma etching. Tm3+/Yb3+ codoped PGO amorphous thin film was obtained by RF Magnetron Sputtering deposition and used as core layer in the pedestal optical waveguide. The minimum propagation losses in the waveguide were 3.6 dB/cm at 1068 nm. The internal gain at 805 nm was enhanced and increased to 8.67 dB due to the presence of gold NPs. These results demonstrate for the first time that Tm3+/Yb3+ codoped PbO-GeO2 waveguides are promising for first telecom window and integrated photonics, especially for applications on fiber network at short distances.

Formation enthalpies of LaLn'O{sub 3} (Ln'=Ho, Er, Tm and Yb) interlanthanide perovskites

Energy Technology Data Exchange (ETDEWEB)

Qi, Jianqi [Peter A. Rock Thermochemistry Laboratory and NEAT ORU, University of California, Davis, CA 95616 (United States); College of Physical Science and Technology, Sichuan University, Chengdu 610064 (China); Key Laboratory of Radiation Physics and Technology of Ministry of Education, Sichuan University, Chengdu 610064 (China); Key Laboratory of High Energy Density Physics of Ministry of Education, Sichuan University, Chengdu 610064 (China); Guo, Xiaofeng [Peter A. Rock Thermochemistry Laboratory and NEAT ORU, University of California, Davis, CA 95616 (United States); Mielewczyk-Gryn, Aleksandra [Peter A. Rock Thermochemistry Laboratory and NEAT ORU, University of California, Davis, CA 95616 (United States); Faculty of Applied Physics and Mathematics, Department of Solid State Physics, Gdansk University of Technology, Narutowicza 11/12, 80-233 Gdansk (Poland); Navrotsky, Alexandra, E-mail: anavrotsky@ucdavis.edu [Peter A. Rock Thermochemistry Laboratory and NEAT ORU, University of California, Davis, CA 95616 (United States)

2015-07-15

High-temperature oxide melt solution calorimetry using 3Na{sub 2}O·MoO{sub 3} at 802 °C was performed for interlanthanide perovskites LaLn'O{sub 3} (Ln'=Ho, Er, Tm and Yb) and lanthanide oxides (La{sub 2}O{sub 3}, Ho{sub 2}O{sub 3}, Er{sub 2}O{sub 3}, Tm{sub 2}O{sub 3} and Yb{sub 2}O{sub 3}). The enthalpies of formation of these interlanthanide perovskites from binary lanthanide oxides at room temperature (25 °C) were determined to be −8.3±3.4 kJ/mol for LaHoO{sub 3}, −9.9±3.0 kJ/mol for LaErO{sub 3}, −10.8±2.7 kJ/mol for LaTmO{sub 3} and −12.3±2.9 kJ/mol for LaYbO{sub 3}. There is a roughly linear relationships between these enthalpy values and the tolerance factor for these and for other LaM{sup 3+}O{sub 3} (M=In, Sc, Ga, Al, Fe and Cr) perovskites, confirming that the distortion of the perovskites as results from ionic radius difference of A-site and B-site cations, is the main factor determining the stability of these compounds. - Graphical abstract: A linear relationship between the enthalpy of formation and the tolerance factor for interlanthanide LaLn'O{sub 3} (Ln'=Ho, Er, Tm, and Yb) and other LaM{sup 3+}O{sub 3} (M=In, Sc, Ga, Al, Fe and Cr) perovskites. - Highlights: • Interlanthanide perovskites were synthesized by solid state reactions. • Their enthalpies of formation were measured by oxide melt solution calorimetry. • ΔH{sub f,ox} shows a linear relationship with tolerance factor.

Development of separation process of Dy, Y, Tm and Yb from heavier rare earth residue by solvent impregnated resin

International Nuclear Information System (INIS)

Shibata, J.; Matsumoto, S.

1998-01-01

Full text: Heavier rare earth which is contained in a small amount in ores such as bastnesite and monazite has been accumulated as heavier rare earth residue without doing separation and purification due to lack of suitable methods. The heavier rare earth residue includes seven rare earth elements such as Tb, Dy, Ho, Y, Er, Tm and Yb. Separation and recovery process of Dy, Y, Tm and Yb from leached solution of the heavier rare earth residue was investigated by using a column method with a solvent impregnated resin. The solvent impregnated resin was prepared by impregnation of organophosphorous extractant whose trade name is PC-88A into a macro porous resin, Amberlite XAD-7. It was almost impossible to separate them in simple adsorption and elution steps. However, we attained to individually separate Dy, Y, Tm and Yb from the leached solution first by changing eluent concentration gradually from pH 2 to 2mol/ l HCl in the elution step, and secondly by using a development column and changing eluent concentration in the elution step. The separation process flow was proposed for heavier rare earth residue by using the solvent impregnated resin method

Sequential coating upconversion NaYF{sub 4}:Yb,Tm nanocrystals with SiO{sub 2} and ZnO layers for NIR-driven photocatalytic and antibacterial applications

Energy Technology Data Exchange (ETDEWEB)

Tou, Meijie; Luo, Zhenguo; Bai, Song; Liu, Fangying; Chai, Qunxia; Li, Sheng; Li, Zhengquan, E-mail: zqli@zjnu.edu.cn

2017-01-01

ZnO is one of the most promising materials for both photocatalytic and antibacterial applications, but its wide bandgap requires the excitation of UV light which limits their applications under visible and NIR bands. Herein, we demonstrate a facile approach to synthesize core-shell-shell hybrid nanoparticles consisting of hexagonal NaYF{sub 4}:Yb,Tm, amorphous SiO{sub 2} and wurtzite ZnO. The upconversion nanocrystals are used as the core seeds and sequentially coated with an insulting shell and a semiconductor layer. Such hybrid nanoparticles can efficiently utilize the NIR light through the upconverting process, and display notable photocatalytic performance and antibacterial activity under NIR irradiation. The developed NaYF{sub 4}:Yb,Tm@SiO{sub 2}@ZnO nanoparticles are characterized with TEM, XRD, EDS, XPS and PL spectra, and their working mechanism is also elucidated. - Highlights: • Core-shell NaYF{sub 4}:Yb,Tm@SiO{sub 2}@TiO{sub 2} NPs were synthesized via a sequential coating method. • Hybrid NaYF{sub 4}:Yb,Tm@SiO{sub 2}@TiO{sub 2} NPs show NIR-light enhanced photocatalytic activity. • NIR-driven antibacterial performance has been realized with NaYF{sub 4}:Yb,Tm@SiO{sub 2}@TiO{sub 2} NPs. • Working mechanism of the hybrid photocatalysts as antibacterial agents was proposed.

Emission properties of hydrothermal Yb{sup 3+}, Er{sup 3+} and Yb{sup 3+}, Tm{sup 3+}-codoped Lu{sub 2}O{sub 3} nanorods: upconversion, cathodoluminescence and assessment of waveguide behavior

Energy Technology Data Exchange (ETDEWEB)

Barrera, Elixir William; Pujol, MarIa Cinta; DIaz, Francesc [Fisica i Cristal.lografia de Materials, Universitat Rovira i Virgili, Campus Sescelades c/ Marcel.lI Domingo s/n, E-43007 Tarragona (Spain); Choi, Soo Bong; Rotermund, Fabian [Division of Energy Systems Research, Ajou University, 443-749 Suwon (Korea, Republic of); Park, Kyung Ho [Korea Advanced Nano Fab Center, 443-270 Suwon (Korea, Republic of); Jeong, Mun Seok [Advanced Photonics Research Institute, Gwangju Institute of Science and Technology, 500-712 Gwangju (Korea, Republic of); Cascales, Concepcion, E-mail: ccascales@icmm.csic.es [Instituto de Ciencia de Materiales de Madrid, Consejo Superior de Investigaciones CientIficas, c/Sor Juana Ines de la Cruz, 3 Cantoblanco, E-28049 Madrid (Spain)

2011-02-18

Yb{sup 3+} and Ln{sup 3+} (Ln{sup 3+} = Er{sup 3+} or Tm{sup 3+}) codoped Lu{sub 2}O{sub 3} nanorods with cubic Ia3-bar symmetry have been prepared by low temperature hydrothermal procedures, and their luminescence properties and waveguide behavior analyzed by means of scanning near-field optical microscopy (SNOM). Room temperature upconversion (UC) under excitation at 980 nm and cathodoluminescence (CL) spectra were studied as a function of the Yb{sup +} concentration in the prepared nanorods. UC spectra revealed the strong development of Er{sup 3+4}F{sub 9/2} {yields} 4I{sub 15/2} (red) and Tm{sup 3+1}G{sub 4} {yields} {sup 3}H{sub 6} (blue) bands, which became the pre-eminent and even unique emissions for corresponding nanorods with the higher Yb{sup 3+} concentration. Favored by the presence of large phonons in current nanorods, UC mechanisms that privilege the population of {sup 4}F{sub 9/2} and {sup 1}G{sub 4} emitting levels through phonon-assisted energy transfer and non-radiative relaxations account for these observed UC luminescence features. CL spectra show much more moderate development of the intensity ratio between the Er{sup 3+4}F{sub 9/2} {yields}{sup 4}I{sub 15/2} (red) and {sup 2}H{sub 11/2}, {sup 4}S{sub 3/2} {yields} {sup 4}I{sub 15/2} (green) emissions with the increase in the Yb{sup 3+} content, while for Yb{sup 3+}, Tm{sup 3+}-codoped Lu{sub 2}O{sub 3} nanorods the dominant CL emission is Tm{sup 3+1}D{sub 2} {yields} {sup 3}F{sub 4} (deep-blue). Uniform light emission along Yb{sup 3+}, Er{sup 3+}-codoped Lu{sub 2}O{sub 3} rods has been observed by using SNOM photoluminescence images; however, the rods seem to be too thin for propagation of light.

Role of the stimulated radiation of Yb3+ ions in the formation of luminescence of the Y0.8Yb0.2F3:Tm3+ solid solution

Science.gov (United States)

Mikheev, A. V.; Kazakov, B. N.

2015-09-01

A new mechanism has been proposed for the transfer of the energy of exciting laser radiation through the donor subsystem (Yb3+) to acceptors (Tm3+), which induces multiphoton transitions in the acceptor subsystem. The coherence of the induced radiation of donors is of key importance in this mechanism. An analytical dependence of the intensity of the up-conversion luminescence of Tm3+ (1G4 → 3H6) ions in the Y0.8Yb0.2F3:Tm3+ system on the pump power at the steady-state excitation by 934-nm infrared radiation of a laser diode has been obtained using the mathematical technique of the theory of Poisson processes. In contrast to known mechanisms, this dependence approximates the experimental dependence well in a wide power range (200-1200 mW). The proposed model is applicable for any system where the energy of pump radiation is transferred to acceptors through the subsystem of donor ions.

Downshifting by energy transfer in Eu{sup 3+}/Yb{sup 3+} codoped Ba{sub 4}La{sub 6}(SiO{sub 4}){sub 6}O glass ceramics

Energy Technology Data Exchange (ETDEWEB)

Zhang, W.J., E-mail: wjzhang03@163.com [School of Material Science and Engineering and Shandong Provincial Key Lab of Preparation and Measurement of Building Materials, University of Jinan, Jinan 250022 (China); State Key Lab of Luminescent Materials and Devices and Institute of Optical Communication Materials, South China University of Technology, Guangzhou 510641 (China); Li, X.B.; Wu, L.J.; Yu, Y.Y.; Wang, X.Z.; Liu, S.Q.; Wang, Z. [School of Material Science and Engineering and Shandong Provincial Key Lab of Preparation and Measurement of Building Materials, University of Jinan, Jinan 250022 (China); Wang, W.C.; Liu, Y. [State Key Lab of Luminescent Materials and Devices and Institute of Optical Communication Materials, South China University of Technology, Guangzhou 510641 (China)

2017-03-01

We report on an efficient near-infrared downshifting in Eu{sup 3+}/Yb{sup 3+} codoped glass ceramics containing Ba{sub 4}La{sub 6}(SiO{sub 4}){sub 6}O crystals. The structural and luminescence properties were characterized by X-ray diffraction (XRD), scanning electron microscopy (SEM), static and dynamic photoemission and excitation spectroscopy. After crystallization, the doping ions are found to be selectively incorporated into the precipitated oxyapatite crystals on La{sup 3+} sites, contributing to the remarkably enhanced visible emission of Eu{sup 3+} under 394 nm excitation. The Eu{sup 3+}/Yb{sup 3+} codoped glass ceramics additionally exhibits efficient near-infrared luminescence of Yb{sup 3+} around 1000 nm upon photon excitation of Eu{sup 3+} within the 300–550 nm range. The reduced visible emission and decay time of {sup 5}D{sub 0} state with Yb{sup 3+} codoping further confirm the energy transfer from Eu{sup 3+} to Yb{sup 3+}, which is promoted due to the shortened distance between Eu{sup 3+} and Yb{sup 3+} within crystals. The maximum energy transfer efficiency is evaluated to be 61%. It is revealed that energy transfer process occurs predominantly through the cross relaxation of Eu{sup 3+}({sup 5}D{sub 0}) + Yb{sup 3+}({sup 2}F{sub 7/2}) → Eu{sup 3+}({sup 7}F{sub 6}) + Yb{sup 3+}({sup 7}F{sub 5/2}).

Quantum sized Ag nanocluster assisted fluorescence enhancement in Tm{sup 3+}-Yb{sup 3+} doped optical fiber beyond plasmonics

Energy Technology Data Exchange (ETDEWEB)

Chattopadhyay, Rik; Haldar, Arindam; Paul, Mukul C.; Das, Shyamal; Bhadra, Shyamal K., E-mail: skbhadra@cgcri.res.in [Fiber Optics and Photonics Division, CSIR-Central Glass and Ceramic Research Institute, 196, Raja S. C. Mullick Road, Kolkata 700032 (India)

2015-12-07

We report a process for enhancing fluorescence emission from conventional rare earth ions in optical fiber by metal nanocluster (MNC) in nonresonant indirect pumping. The process is completely different from formal metal enhanced fluorescence phenomenon as the MNCs are too small in size to support localized surface plasmon and the excitation wavelength is far from plasmon resonance frequency. We used an established theory of two coupled oscillators to explain the simultaneous enhancement of Ytterbium (Yb{sup 3+}) and Thulium (Tm{sup 3+}) emission by silver (Ag) NCs under nonresonant pumping in optical fiber. The fiber is pumped with a 980 nm fiber pigtailed laser diode with input power of 20–100 mW to excite the Yb{sup 3+}. Four times enhancement of Yb{sup 3+} emission of 900–1100 nm and Tm{sup 3+} upconversion emission around 474 nm, 650 nm, and 790 nm is observed in the fiber with Ag NCs.

Intense blue upconversion emission and intrinsic optical bistability in Tm3+/Yb3+/Zn2+ tridoped YVO4 phosphors

Science.gov (United States)

Yadav, Manglesh; Mondal, Manisha; Mukhopadhyay, Lakshmi; Rai, Vineet Kumar

2018-04-01

Tm3+/Yb3+/Zn2+:yttrium metavanadate (YVO4) phosphors prepared through chemical coprecipitation and the solid state reaction method have been structurally characterized by an x-ray diffraction (XRD) study. Photoluminescence study of the developed phosphors under ultraviolet (UV) and near infrared (NIR) excitation has been performed. The excitation spectrum of the tetragonal zircon type YVO4 phosphors corresponding to the emission at ˜476 nm exhibits a broad excitation peak in the 250-350 nm region, which is due to charge distribution in the {{{{VO}}}4}3- group. Under 980 nm CW diode laser excitation, enhancements of about ˜3000 times and ˜40 times have been observed for the blue band in the tridoped Tm3+Yb3+Zn2+:YVO4 phosphors compared to those of the Tm3+:YVO4 singly and Tm3+/Yb3+:YVO4 codoped phosphors, respectively. A downconversion (DC) emission study shows an enhancement of about ˜50 times for the blue band in the tridoped phosphors compared to that of the singly doped phosphors. Optical bistability (OB) behavior of the developed phosphors has been also investigated upon 980 nm excitation. The calculated Commission Internationale de l’Éclairage (CIE) color coordinates lie in the blue region with 96.5% color purity under 980 nm excitation, having a color temperature of ˜3400 K. Our observations show that the developed phosphors may be suitably used in dual mode luminescence spectroscopy, display devices, and UV LED chips.

Bright white upconversion luminescence from Er3+/Tm3+/Yb3+-doped titanate-based glasses prepared by aerodynamic levitation method

Science.gov (United States)

Zhang, Minghui; Yu, Jianding; Jiang, Wan; Liu, Yan; Ai, Fei; Wen, Haiqin; Jiang, Meng; Yu, Huimei; Pan, Xiuhong; Tang, Meibo; Gai, Lijun

2017-10-01

Aerodynamic levitation method was employed to prepare Er3+/Tm3+/Yb3+-doped titanate-based glasses. DTA results show that the glass performs high thermal stability with the glass transition temperature of 799 °C. The interaction among rare earth ions has been discussed by adjusting the relative concentration. Er3+ ions can quench the upconversion luminescence of Tm3+ ions. Tm3+ ions play a strong role in quenching the emissions of Er3+ and Tm3+ when the content of Tm3+ ions is greater than or equal 0.05. From the view of the ratio of red emission to green emission, Tm3+ ions can improve the red emission of Er3+ ions to some extent in contrast with the green emissions of Er3+ ions. 980 nm incident laser can be efficiently absorbed by Yb3+ ions. The relative intensity of red, green, and blue upconversion luminescence has been tuned to obtain white light. The composition with white upconversion luminescence of the color coordinate (0.291, 0.3292) has been found. Moreover, white upconversion luminescence mechanism is a two-photon process of ET, ESA, and cooperative sensitization. Rare earth ions doped titanate-based glasses with bright upconversion luminescence perform potential applications in color display, back light, et al.

Spectroscopic characterization and temporal dynamics of energy transfer process between Tm3+ -Ho3+ and Yb3+ -Tm3+ ions in LiYF4 and LiLuF4 crystals

International Nuclear Information System (INIS)

Tarelho, Luiz Vicente Gomes

2001-01-01

In this work, we perform spectroscopic studies to characterize the energy transfer processes occurring in rare-earth doped lithium fluoride systems, aiming the optimization of the population inversion of these media. Yb 3+ ion was used in order to probe the electron-phonon coupling in LiYF 4 , LiGdF 4 and LiLuF 4 matrices. In these systems it was obtained the average phononenergy, the vibronic transition probability and Huang-Rhys coupling constant. These parameters are dependent on the crystal host and the LiLuF 4 system presents excluded correlation effects, an electronic repulsion that weakens the vibronic coupling. The Tm:Ho:LiYF 4 system was studied under diode laser pumping at 796 nm, aiming the 2 μm emission optimization. The ideal conditions of concentration and laser power were determined favouring the latter emission. Upconversion processes of two photons were identified besides the energy transfer among ions. The dynamic processes of luminescence of donors and acceptors allowed one to classify the energy transfer process as an energy transfer process assisted by fast diffusion among donors. The spectroscopic study of the Yb:Tm:LiYF 4 allowed the determination of efficient non resonant transfer mechanisms between ( 2 F 5/2 ) Ytterbium level and ( 3 H 5 ) Thulium level, assisted by two phonon with hopping migration among donors ( Foerster-Burshtein model). The repopulation process of the Yb donor level is due to a cooperative sensitization between Yb-Tm pairs followed by an energy transfer process. (author)

Enhancement of blue upconversion luminescence in hexagonal NaYF{sub 4}:Yb,Tm by using K and Sc ions

Energy Technology Data Exchange (ETDEWEB)

Kale, Vishal, E-mail: vishal.kale@utu.fi; Soukka, Tero [University of Turku, Department of Biochemistry and Food Chemistry/Biotechnology (Finland); Hoelsae, Jorma; Lastusaari, Mika [University of Turku, Department of Chemistry (Finland)

2013-08-15

Hexagonal ({beta})-NaYF{sub 4} is recognized as one of the most efficient hosts for NIR to blue and green upconversion (UC). A new method to tune the blue UC emission in {beta}-NaYF{sub 4}:Yb,Tm nanocrystals through the possible substitution of the host material with different concentrations of K{sup +} and Sc{sup 3+} ions was investigated in detail. In this work, Na{sub 1-x}K{sub x}YF{sub 4}:Yb,Tm and NaY{sub 1-x}Sc{sub x}F{sub 4}:Yb,Tm nanocrystals were synthesized with varying Na:K and Y:Sc ratios. X-ray diffraction, transmission electron microscopy, and UC luminescence spectroscopy showed that size, morphology, and UC luminescence intensity were affected by the addition of K{sup +} and Sc{sup 3+} ions. Substituted ions disturbed the local symmetry and also resulted in changes in the crystal field. The distance between Yb{sup 3+} and Tm{sup 3+} was affected by different concentration of K{sup +} and Sc{sup 3+} ions, and those differences in the distance are responsible for tuning UC luminescence. This study revealed that when the concentration of K{sup +} and Sc{sup 3+} ions were nominally increased from 20 to 100 mol% during synthesis, hexagonal NaYF{sub 4} changed to structurally different KYF{sub 4} and Na{sub 3}ScF{sub 6} so that the solid solubility became difficult. We also demonstrate that the added K{sup +} does not enter into the NaYF{sub 4} lattice, but it still plays an important role by controlling the Na/R ratio. K{sup +} and Sc{sup 3+} ion concentration of 20 mol% during the synthesis was found to result in materials with size 30-35 nm, and shows ca. four times brighter UC emission than the previously reported lanthanide based nanocrystals. The enhancement in UC luminescence intensity makes upconversion nanophosphors versatile imaging tools for diagnosis.Graphical Abstract.

Red, green, blue and white light upconversion emission in Yb3+/Tm3+/Ho3+ co-doped tellurite glasses

International Nuclear Information System (INIS)

Desirena, H; De la Rosa, E; Meza, O; Salas, P

2011-01-01

Several Yb 3+ /Tm 3+ /Ho 3+ co-doped transparent TeO 2 -ZnO-Na 2 O-Yb 2 O 3 -Ho 2 O 3 -Tm 2 O 3 glasses were prepared and luminescence properties were characterized. Simultaneous red, green and blue (RGB) emission were obtained after excitation at 970 nm. Colour emission was tuned from multicolour to white light with colour coordinate (0.32, 0.33) matching very well with the white reference (0.33, 0.33). Changes in colour emission were obtained by varying the intensity ratios between RGB bands that are strongly concentration dependent because of the interaction of co-dopants. The colour tunability, high quality of white light and high intensity of the emitted signal make these transparent glasses excellent candidates for applications in solid-state lighting.

Optical transitions of Tm3+ in oxyfluoride glasses and compositional and thermal effect on upconversion luminescence of Tm3+/Yb3+-codoped oxyfluoride glasses.

Science.gov (United States)

Feng, Li; Wu, Yinsu; Liu, Zhuo; Guo, Tao

2014-01-24

Optical properties of Tm(3+)-doped SiO2-BaF2-ZnF2 glasses have been investigated on the basis of the Judd-Ofelt theory. Judd-Ofelt intensity parameters, radiative transition probabilities, fluorescence branching ratios and radiative lifetimes have been calculated for different glass compositions. Upconversion emissions were observed in Tm(3+)/Yb(3+)-codoped SiO2-BaF2-ZnF2 glasses under 980 nm excitation. The effects of composition, concentration of the doping ions, temperature, and excitation pump power on the upconversion emissions were also systematically studied. Copyright © 2013 Elsevier B.V. All rights reserved.

White upconversion luminescence in Tm3+/Ho3+/Yb3+ triply doped K+-Na+ ion-exchanged aluminum germanate glass channel waveguide

Science.gov (United States)

Liu, Xiao; Chen, Baojie; Pun, Edwin Yue Bun; Lin, Hai

2013-01-01

Rare-earth ions doped K+-Na+ ion-exchanged aluminum germanate (NMAG) glass channel waveguides have been designed and fabricated. Under 980 nm laser pumping, an intense upconversion white light transmission trace was observed in Tm3+/Ho3+/Yb3+ triply doped NMAG glass channel waveguide and a high-brightness light spot was achieved from the output end of the fiber connected to the waveguide channel. The fluorescent colors were diverse and located within or near the white region in CIE chromaticity diagram under various pumping powers. These admirable results indicate that Tm3+/Ho3+/Yb3+ triply doped NMAG channel waveguide is a promising light source for medical and high-precision processing illumination.

Yb{sup 3+},Er{sup 3+},Eu{sup 3+}-codoped YVO{sub 4} material for bioimaging with dual mode excitation

Energy Technology Data Exchange (ETDEWEB)

Thao, Chu Thi Bich [Department of Chemistry, Changwon National University, Changwon 641-773 (Korea, Republic of); Huy, Bui The [Department of Chemistry, Changwon National University, Changwon 641-773 (Korea, Republic of); Institute of Research and Development, Duy Tan University, K7/25 Quang Trung, Da Nang (Viet Nam); Sharipov, Mirkomil [Department of Chemistry, Changwon National University, Changwon 641-773 (Korea, Republic of); Kim, Jin-Ik. [Department of Biochemistry and Health Science, Changwon National University, Changwon 641-773 (Korea, Republic of); Dao, Van-Duong [Department of Chemical Engineering & Applied Chemistry, Chungnam National University, Daejeon 305-764 (Korea, Republic of); Moon, Ja-Young [Department of Biochemistry and Health Science, Changwon National University, Changwon 641-773 (Korea, Republic of); Lee, Yong-Ill, E-mail: yilee@changwon.ac.kr [Department of Chemistry, Changwon National University, Changwon 641-773 (Korea, Republic of)

2017-06-01

We propose an efficient bioimaging strategy using Yb{sup 3+},Er{sup 3+},Eu{sup 3+}-triplet doped YVO{sub 4} nanoparticles which were synthesized with polymer as a template. The obtained particles possess nanoscale, uniform, and flexible excitation. The effect of Eu{sup 3+} ions on the luminescence properties of YVO{sub 4}:Yb{sup 3+},Er{sup 3+},Eu{sup 3+} was investigated. The upconversion mechanism of the prepared material was also discussed. The structure and optical properties of the prepared material were characterized by using X-ray diffraction (XRD), Fourier-transform IR spectroscopy (FTIR), scanning electron microscopy (SEM), Transmission electron microscopy (TEM) upconversion and photoluminescence spectra. The Commission International de I′Eclairage (CIE) chromaticity coordinates was investigated to confirm the performance of color luminescent emission. The prepared YVO{sub 4}:Yb{sup 3+},Er{sup 3+},Eu{sup 3+} nanoparticles could be easily dispersed in water by surface modification with cysteine (Cys) and glutathione (GSH). The aqueous dispersion of the modified YVO{sub 4}:Yb{sup 3+},Er{sup 3+},Eu{sup 3+} exhibits bright upconversion and downconversion luminescence and has been applied for bioimaging of HeLa cells. Our developed material with dual excitation offers a promising advance in bioimaging. - Highlights: • Prepared particles possess nanoscale size, uniform, and larger scale. • The material exhibits strong emission under dual mode excitations. • The surface material has been applied for bioimaging of HeLa cell. • Low cytotoxicity, no auto-fluorescence.

Syntheses, and crystal and electronic structures of the new Zintl phases Na2ACdSb2 and K2ACdSb2 (A=Ca, Sr, Ba, Eu, Yb): Structural relationship with Yb2CdSb2 and the solid solutions Sr2-xAxCdSb2, Ba2-xAxCdSb2 and Eu2-xYbxCdSb2

International Nuclear Information System (INIS)

Saparov, Bayrammurad; Saito, Maia; Bobev, Svilen

2011-01-01

Presented are the details of the syntheses, crystal and electronic structures of a new family of Zintl phases Na 2 ACdSb 2 and K 2 ACdSb 2 (A=Ca, Sr, Ba, Eu, Yb), as well as the solid solutions Sr 2-x A x CdSb 2 , Ba 2-x A x CdSb 2 and Eu 2-x Yb x CdSb 2 . The structures of Na 2 ACdSb 2 and K 2 ACdSb 2 (A=Ca, Sr, Ba, Eu, Yb) were determined to be of a new type with the non-centrosymmetric space group Pmc2 1 (no. 26), Pearson symbol oP12, with lattice parameters a=4.684(1)-4.788(1) A; b=9.099(3)-9.117(2) A; c=7.837(1)-8.057(2) A for the Na 2 ACdSb 2 series, and a=4.6637(9)-5.0368(8) A; b=9.100(2)-9.8183(15) A; and c=7.7954(15)-8.4924(13) A for K 2 ACdSb 2 , respectively. The solid solutions Sr 2-x A x CdSb 2 , Ba 2-x A x CdSb 2 and Eu 2-x Yb x CdSb 2 (x∼1) are isostructural and isoelectronic to the recently reported Yb 2 CdSb 2 (space group Cmc2 1 (no. 36), Pearson symbol cP20). All discussed structures are based upon CdSb 2 4- polyanionic layers, similar to the ones observed in Yb 2 CdSb 2 , with various alkali- and/or alkaline-earth cations coordinated to them. Magnetic susceptibility and Seebeck coefficient measurements on selected Eu 2-x Yb x CdSb 2 samples, taken at low temperatures up to 300 K, are also reported. -- Graphical abstract: The quaternary Zintl phases Na 2 ACdSb 2 and K 2 ACdSb 2 (A=Ca, Sr, Ba, Eu, Yb) with novel layered structures have been synthesized for the first time and structurally characterized by single-crystal X-ray diffraction. Reported as well are the results from crystallographic and property studies of the closely related solid solutions Sr 2-x A x CdSb 2 , Ba 2-x A x CdSb 2 (x∼1), and Eu 2-x Yb x CdSb 2 (1 2 ACdSb 2 and K 2 ACdSb 2 (A=Ca, Sr, Ba, Eu, Yb) are new quaternary Zintl phases. → Sr 2-x A x CdSb 2 , Ba 2-x A x CdSb 2 (x∼1), and Eu 2-x Yb x CdSb 2 (1 4 tetrahedra. → Eu 2-x Yb x CdSb 2 (1< x<2) exhibit high Seebeck coefficient (217 μV/K at RT).

The investigation of the decay of the deformed 167Yb, 164Tm, 225Ac, 221Fr nuclei. Beta-spectrograph with positional-sensitive detector

International Nuclear Information System (INIS)

Butabaev, Yu.S.

1994-01-01

The decay of the deformed 167 Yb, 164 Tm, 225 Ac, 221 Fr nuclei is investigated in this work. For 167 Yb and 164 Tm decays the specters of the conversion electrons were measured. 32 γ-transitions were found for 167 Yb decay, 6 of which were found for the first time. The multipolarities for 9 γ-transitions were found. For 164 Tm decay 23 new γ-transitions were found. The theoretical investigations of the collective states in the nucleus were carried out. Octupole-rotatory line with k=1 - was found in the measurement of conversion electrons specters of the short-life nuclei. Device' nonlinearity was 0,04%. Resolution was Δβρ/βρ 0,11%. Effective light yield was 1-2 %. The decay of 225 Ac and 221 Fr nuclei were investigated. The investigations of α-γ -coincidence, α-γ - rays were carried out. 24 new γ -transitions for 225 Ac and 13 ones for 221 Fr were found. The new levels and their intensities were defined more precisely. Intensity balance calculations were carried out and the full populations of the nuclear levels were calculated. (author). 3 tabs.; 10 figs

Synthesis of g-C{sub 3}N{sub 4}-based NaYF{sub 4}:Yb,Tm@TiO{sub 2} ternary composite with enhanced Vis/NIR-driven photocatalytic activities

Energy Technology Data Exchange (ETDEWEB)

Cheng, Erjian, E-mail: ejcheng6@gmail.com [Department of Materials Physics, Zhejiang Normal University, Jinhua, Zhejiang 321004 (China); Zhou, Shiqi; Li, Mohua [Institute of Physical Chemistry, Zhejiang Normal University, Jinhua, Zhejiang 321004 (China); Li, Zhengquan, E-mail: zqli@zjnu.edu.cn [Department of Materials Physics, Zhejiang Normal University, Jinhua, Zhejiang 321004 (China); Institute of Physical Chemistry, Zhejiang Normal University, Jinhua, Zhejiang 321004 (China)

2017-07-15

Highlights: • The g-C{sub 3}N{sub 4}-based NaYF{sub 4}:Yb,Tm@TiO{sub 2} nanocomposite was fabricated by a facile approach. • The as-prepared composites exhibit enhanced activities under Vis and/or NIR lights. • Upconversion and semiconductor heterojunction lie behind the improved photocatalysis. • Photocatalytic working mechanism of this ternary nanocomposite was proposed. - Abstract: Upconversion (UC) NaYF{sub 4}:Yb,Tm nanocrystals (NCs) are capable of converting low-energy near-infrared (NIR) photons to high-energy ultraviolet (UV) and visible (Vis) photons. Integration of NaYF{sub 4}:Yb,Tm with graphitic carbon nitride (g-C{sub 3}N{sub 4}) can extend the spectral response of g-C{sub 3}N{sub 4} to the NIR range. However, photocatalytic activity of NaYF{sub 4}:Yb,Tm/g-C{sub 3}N{sub 4} is still severely limited by the high recombination rate of photo-generated (PG) electrons and holes (e{sup –}/h{sup +}) in the g-C{sub 3}N{sub 4}. Herein, we report a facile approach to fabricate a ternary nanocomposite consisting of NaYF{sub 4}:Yb,Tm, TiO{sub 2} and g-C{sub 3}N{sub 4}. When NaYF{sub 4}:Yb,Tm NCs were coated with a TiO{sub 2} shell and sequentially assembled with g-C{sub 3}N{sub 4} nanosheets (NSs), a semiconductor heterojunction can be fabricated on the UC particles. The as-prepared nanocomposites possess an enhanced photocatalytic activity under Vis and/or NIR lights due to the formation of heterojunction and UC effect. The ternary nanocomposites have been characterized in detail and their photocatalytic mechanism is proposed. Such kind of ternary nanocomposites may provide a new scenario for the design and synthesis of composite photocatalysts for efficiently utilizing the Vis/NIR lights in environmental remedy.

Aptamer biosensor for Salmonella typhimurium detection based on luminescence energy transfer from Mn2 +-doped NaYF4:Yb, Tm upconverting nanoparticles to gold nanorods

Science.gov (United States)

Cheng, Keyi; Zhang, Jianguo; Zhang, Liping; Wang, Lun; Chen, Hongqi

2017-01-01

A highly sensitive luminescent bioassay for the detection of Salmonella typhimurium was fabricated using Mn2 +-doped NaYF4:Yb,Tm upconversion nanoparticles (UCNPs) as the donor and gold nanorods (Au NRs) as the acceptor and utilizing an energy transfer (LET) system. Mn2 +-doped NaYF4:Yb,Tm UCNPs with a strong emission peak at 807 nm were obtained by changing the doped ion ratio. Carboxyl-terminated Mn2 +-doped NaYF4:Yb,Tm UCNPs were coupled with S. typhimurium aptamers, which were employed to capture and concentrate S. typhimurium. The electrostatic interactions shorten the distance between the negatively charged donor and the positively charged acceptor, which results in luminescence quenching. The added S. typhimurium leads to the restoration of luminescence due to the formation of UCNPs-aptamers-S. typhimurium, which repels the UCNPs-aptamers from the Au NRs. The LET system does not occur because of the nonexistence of the luminescence emission band of Mn2 +-doped NaYF4:Yb,Tm UCNPs, which had large spectral overlap with the absorption band of Au NRs. Under optimal conditions, the linear range of detecting S. typhimurium was 12 to 5 × 105 cfu/mL (R = 0.99). The limit of detection for S. typhimurium was as low as 11 cfu/mL in an aqueous buffer. The measurement of S. typhimurium in milk samples was satisfied in accordance with the plate-counting method, suggesting that the proposed method was of practical value in the application of food security.

Yb3+ can be much better than Dy3+: SMM properties and controllable self-assembly of novel lanthanide 3,5-dinitrobenzoate-acetylacetonate complexes.

Science.gov (United States)

Gavrikov, Andrey V; Efimov, Nikolay N; Ilyukhin, Andrey B; Dobrokhotova, Zhanna V; Novotortsev, Vladimir M

2018-05-01

The first representatives of the binuclear lanthanide 3,5-dinitrobenzoate-acetylacetonate complexes, namely isostructural compounds [Ln(dnbz)(acac)2(H2O)(EtOH)]2 (Ln = Eu (1), Gd (2), Tb (3), Dy (4), Ho (5), Er (6), Tm (7), and Yb (8); dnbz - 3,5-dinitrobenzoate anion; acac - acetylacetonate (pentane-2,4-dionate) anion) were prepared and characterized. The SMM behavior of the Yb compound 8 was shown to be surprisingly less sensitive to the composition of the Yb3+ coordination environment in comparison with that of the Dy derivative. For Yb compound 8, the anisotropy barrier is Δeff/kB = 26 K under the dc field of 2000 Oe. This value is the highest one currently known for binuclear Yb complexes.

Controllable synthesis and crystal structure determined upconversion luminescence properties of Tm{sup 3+} (Er{sup 3+}) ions doped YbF{sub 3} and NaYbF{sub 4} crystals

Energy Technology Data Exchange (ETDEWEB)

Jiang, Tao [Institute of Photonics, Faculty of Science, Ningbo University, Ningbo 315211 (China); Qin, Weiping, E-mail: wpqin@jlu.edu.cn [State Key Laboratory on Integrated Optoelectronics, College of Electronic Science and Engineering, Jilin University, Changchun 130012 (China); Zhou, Jun [Institute of Photonics, Faculty of Science, Ningbo University, Ningbo 315211 (China)

2014-04-01

Graphical abstract: - Highlights: • The synthesis of YbF{sub 3} and NaYbF{sub 4} crystals was successfully fulfilled by hydrothermal method. • The phase and morphology of products were adjusted by changing the hydrothermal conditions. • Relatively enhanced ultraviolet upconversion emissions were observed in YbF{sub 3} nanocrystals. • The crystalline phase impact on the upconversion luminescence was systematically studied. - Abstract: The synthesis of YbF{sub 3} and NaYbF{sub 4} crystals was successfully fulfilled by a facial hydrothermal method. The phase and morphology of the products were adjusted by changing the surfactant additive and fluorine source and tuning the pH value of the initial solution. The products with various morphologies range from octahedral nanoparticles, corn-like nanobundles, nanospheres, microrods, and hollow microprisms were prepared at different conditions. The growth mechanism of these products has been systematically studied. Impressively, relatively enhanced high order ultraviolet (UV) upconversion (UC) luminescence was observed in Tm{sup 3+} (Er{sup 3+}) ions doped YbF{sub 3} nanocrystals (NCs) compared with NaYbF{sub 4} microcrystals under the excitation of 980 nm infrared laser. The investigation results reveal that the crystal symmetry of matrix has significant effect on the spectra and lifetimes of the doping lanthanide ions. The simply synthesized water soluble YbF{sub 3} NCs with efficient UV UC luminescence may find potential application in biochemistry.

Spectroscopic characterization and temporal dynamics of energy transfer process between Tm{sup 3+} -Ho{sup 3+} and Yb{sup 3+} -Tm{sup 3+} ions in LiYF{sub 4} and LiLuF{sub 4} crystals; Caracterizacao espectroscopica e dinamica temporal dos processos de transferencia de energia entre os ions Tm{sup 3+} -Ho{sup 3+} e Yb{sup 3+} -Tm{sup 3+} em cristais de LiYF{sub 4} and LiLuF{sub 4}

Energy Technology Data Exchange (ETDEWEB)

Tarelho, Luiz Vicente Gomes

2001-07-01

In this work, we perform spectroscopic studies to characterize the energy transfer processes occurring in rare-earth doped lithium fluoride systems, aiming the optimization of the population inversion of these media. Yb{sup 3+} ion was used in order to probe the electron-phonon coupling in LiYF{sub 4}, LiGdF{sub 4} and LiLuF{sub 4} matrices. In these systems it was obtained the average phononenergy, the vibronic transition probability and Huang-Rhys coupling constant. These parameters are dependent on the crystal host and the LiLuF{sub 4} system presents excluded correlation effects, an electronic repulsion that weakens the vibronic coupling. The Tm:Ho:LiYF{sub 4} system was studied under diode laser pumping at 796 nm, aiming the 2 {mu}m emission optimization. The ideal conditions of concentration and laser power were determined favouring the latter emission. Upconversion processes of two photons were identified besides the energy transfer among ions. The dynamic processes of luminescence of donors and acceptors allowed one to classify the energy transfer process as an energy transfer process assisted by fast diffusion among donors. The spectroscopic study of the Yb:Tm:LiYF{sub 4} allowed the determination of efficient non resonant transfer mechanisms between ({sup 2}F{sub 5/2}) Ytterbium level and ({sup 3}H{sub 5}) Thulium level, assisted by two phonon with hopping migration among donors ( Foerster-Burshtein model). The repopulation process of the Yb donor level is due to a cooperative sensitization between Yb-Tm pairs followed by an energy transfer process. (author)

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.

Investigation of Upconversion, downshifting and quantum –cutting behavior of Eu3+, Yb3+, Bi3+ co-doped LaNbO4 phosphor as a spectral conversion material

Science.gov (United States)

Dwivedi, A.; Mishra, K.; Rai, S. B.

2018-06-01

This work presents the spectral conversion characteristics [upconversion (UC), downshifting (DS) and quantum–cutting (QC) optical processes] of Eu3+, Yb3+ and Bi3+ co-doped LaNbO4 (LBO) phosphor samples synthesized by solid state reaction technique. The crystal structure and the pure phase formation have been confirmed by x-ray diffraction (XRD) measurements. The surface morphology and particle size are studied by scanning electron microscopy (SEM). The rarely observed intense red UC emission from Eu3+ ion has been successfully obtained in Eu3+/Yb3+ co-doped LaNbO4 phosphor (on excitation with 980 nm) by optimizing the concentrations of Eu3+ and Yb3+ ions. The downshifting (DS) behavior has been studied by photoluminescence (PL) measurements on excitation with 265 nm wavelength from a Xe lamp source. A broad blue emission in the region 300–550 nm with its maximum ∼415 nm due to charge transfer band (CTB) of the host and large number of sharp peaks due to f-f transitions of Eu3+ ion have been observed. The energy transfer has been observed from (NbO4)3‑ to Eu3+ ion and the fluorescence emission has been optimized by varying the concentration of Eu3+ ion. An intense red emission has also been observed corresponding to 5D0 → 7F2 transition of Eu3+ ion at 611 nm in LBO: 0.09Eu3+ phosphor on excitation with 394 nm. The luminescence properties of Eu3+ ion are enhanced further through the sensitization effect of Bi3+ ion. The near infra-red (NIR) quantum cutting (QC) behavior due to Yb3+ ion has been monitored on excitation with 265 as well as 394 nm. The NIR QC is observed due to 2F5/2 → 2F7/2 transition of Yb3+ ion via co-operative energy transfer (CET) process from (NbO4)3‑ as well as Eu3+ ions to Yb3+ ion. This multimodal behavior (UC, DS and QC) makes this a promising phosphor material for multi-purpose spectral converter.

Synthesis, crystal structure, and magnetism of A{sub 2}Co{sub 12}As{sub 7} (A=Ca, Y, Ce–Yb)

Energy Technology Data Exchange (ETDEWEB)

Tan, Xiaoyan [Department of Chemistry and Biochemistry, Florida State University, Tallahassee, FL 32306 (United States); Ovidiu Garlea, V. [Quantum Condensed Matter Division, Oak Ridge National Laboratory, Oak Ridge, TN 37831 (United States); Chai, Ping [Department of Chemistry and Biochemistry, Florida State University, Tallahassee, FL 32306 (United States); Geondzhian, Andrey Y. [National Research Nuclear University “Moscow Engineering Physics Institute”, 115409 Moscow (Russian Federation); Yaroslavtsev, Alexander A. [National Research Nuclear University “Moscow Engineering Physics Institute”, 115409 Moscow (Russian Federation); European XFEL GmbH, 22761 Hamburg (Germany); Xin, Yan [National High Magnetic Field Laboratory, Tallahassee, FL 32310 (United States); Menushenkov, Alexey P. [National Research Nuclear University “Moscow Engineering Physics Institute”, 115409 Moscow (Russian Federation); Chernikov, Roman V. [DESY Photon Science, 22603 Hamburg (Germany); Shatruk, Michael, E-mail: shatruk@chem.fsu.edu [Department of Chemistry and Biochemistry, Florida State University, Tallahassee, FL 32306 (United States)

2016-04-15

Ternary intermetallics, A{sub 2}Co{sub 12}As{sub 7} (A=Ca, Y, Ce–Yb), have been synthesized by annealing mixtures of elements in molten Bi at 1223 K. The materials obtained crystallize in the P6{sub 3}/m variant of the Zr{sub 2}Fe{sub 12}P{sub 7} structure type. The unit cell volume shows a monotonic decrease with the increasing atomic number of the rare-earth metal, with the exception of Ce-, Eu-, and Yb-containing compounds. An examination of these outliers with X-ray absorption near edge structures (XANES) spectroscopy revealed mixed valence of Ce, Eu, and Yb, with the average oxidation states of +3.20(1), +2.47(5), and +2.91(1), respectively, at room temperature. Magnetic behavior of A{sub 2}Co{sub 12}As{sub 7} is generally characterized by ferromagnetic ordering of Co 3d moments at 100–140 K, followed by low-temperature ordering of rare-earth 4f moments. The 3d-4f magnetic coupling changes from antiferromagnetic for A=Pr–Sm to ferromagnetic for A=Ce and Eu–Yb. Polarized neutron scattering experiments were performed to support the postulated ferro- and ferrimagnetic ground states for Ce{sub 2}Co{sub 12}As{sub 7} and Nd{sub 2}Co{sub 12}As{sub 7}, respectively. - Graphical abstract: Title arsenides were synthesized by Bi‐flux method. They exhibit mixed valence for A = Ce, Eu, Yb, ferrimagnetism for A = Ca, Y, Pr–Sm, and ferromagnetism for A = Eu–Tm. - Highlights: • A2Co12As7 (A=Ca, Y, Ce–Yb) were synthesized in Bi flux. • Ce, Eu, Yb exhibit mixed valence in the corresponding structures. • The character of 3d‐4f magnetic coupling changes at the half‐filled f shell. • Materials behave as ferrimagnets for A=Ca, Y, Pr–Sm and as ferromagnets for A=Eu–Yb.

Fluorescence resonance energy transfer between NaYF4:Yb,Tm upconversion nanoparticles and gold nanorods: Near-infrared responsive biosensor for streptavidin

International Nuclear Information System (INIS)

Zhang, Shuang; Wang, Jing; Xu, Wen; Chen, Boting; Yu, Wei; Xu, Lin; Song, Hongwei

2014-01-01

We represent a fluorescence resonance energy transfer (FRET) system using upconversion nanoparticles (UCNPs) and the gold nanorods (GNRs) as the energy donor–acceptor pair for directly determining streptavidin in near-infrared (NIR) region. NaYF 4 :Yb,Tm UCNPs, which had a strong emission at 800 nm under 980-nm excitation, were adopted as the energy donor. The GNRs, which demonstrated strong surface plasmon absorption around 800 nm, were chosen as acceptor to quench the 800 nm emissions of the UCNPs. There had the spectral overlap between the emission of the donor nanoparticles (UCNPs) and the absorption of the acceptor nanoparticles (GNRs). This UCNP-based FRET system was then used to determine the amount of streptavidin. In this system, NaYF 4 :Yb,Tm UCNPs conjugated with biotin, while GNRs conjugated with streptavidin. When added GNRs into UCNPs, the streptavidin were preferred to bind with biotin and decreased spacing between the donor and acceptor NPs. Consequently, FRET occurred and a linear relationship between the luminescence quenching efficiency and the concentration of streptavidin was obtained. Owing to the aforementioned merits of UCNPs as an energy donor and the strong quenching ability of GNRs, satisfactory analytical performances have been acquired. -- Highlights: • NaYF4:Yb,Tm and GNRs are as NIR energy donor and quenching acceptor for FRET. • Linkage between biotin and streptavidin make the distance between the donors and the acceptors short enough for FRET. • The FRET system in this work was applicable for the detection of streptavidin. • The donor and acceptor NPs can be modified by proper molecules for other biological molecules detection

Broadband down-conversion based near infrared quantum cutting in Eu{sup 2+}–Yb{sup 3+} co-doped SrAl{sub 2}O{sub 4} for crystalline silicon solar cells

Energy Technology Data Exchange (ETDEWEB)

Tai, Yuping, E-mail: yupingtai@126.com [Key Laboratory of Synthetic and Natural Functional Molecule Chemistry (Ministry of Education), College of Chemistry & Materials Science, Northwest University, Xi’an 710069 (China); Zheng, Guojun, E-mail: zhengguojun88@126.com [Key Laboratory of Synthetic and Natural Functional Molecule Chemistry (Ministry of Education), College of Chemistry & Materials Science, Northwest University, Xi’an 710069 (China); Wang, Hui, E-mail: huiwang@nwu.edu.cn [Key Laboratory of Synthetic and Natural Functional Molecule Chemistry (Ministry of Education), College of Chemistry & Materials Science, Northwest University, Xi’an 710069 (China); National Key Laboratory of Photoelectric Technology and Functional Materials Culture Base, National Photoelectric Technology and Functional Materials & Application of International Science and Technology Cooperation Base, Institute of Photonics & Photon-Technology, Northwest University, Xi' an 710069 (China); Bai, Jintao, E-mail: baijt@nwu.edu.cn [National Key Laboratory of Photoelectric Technology and Functional Materials Culture Base, National Photoelectric Technology and Functional Materials & Application of International Science and Technology Cooperation Base, Institute of Photonics & Photon-Technology, Northwest University, Xi' an 710069 (China)

2015-03-15

Near infrared (NIR) quantum cutting involving the down conversion of an absorbed visible photon to emission of two NIR photons was achieved in SrAl{sub 2}O{sub 4}:0.01Eu{sup 2+}, xYb{sup 3+} (x=0, 1, 2, 5, 10, 20, 30 mol%) samples. The photoluminescence properties of samples in visible and NIR regions were measured to verify the energy transfer (ET) from Eu{sup 2+} to Yb{sup 3+}. The results demonstrated that Eu{sup 2+} was an efficient sensitizer for Yb{sup 3+} in the SrAl{sub 2}O{sub 4} host lattice. According to Gaussian fitting analysis and temperature-dependent luminescence experiments, the conclusion was drawn that the cooperative energy transfer (CET) process dominated the ET process and the influence of charge transfer state (CTS) of Yb{sup 3+} could be negligible. As a result, the high energy transfer efficiency (ETE) and quantum yield (QY) have been acquired, the maximum value approached 73.68% and 147.36%, respectively. Therefore, this down-conversion material has potential application in crystalline silicon solar cells to improve conversion efficiency. - Graphical abstract: Near infrared quantum cutting was achieved in Eu{sup 2+}–Yb{sup 3+} co-doped SrAl{sub 2}O{sub 4} samples. The cooperative energy transfer process dominated energy transfer process and high energy transfer efficiency was acquired. - Highlights: • The absorption spectrum of Eu{sup 2+} ion is strong in intensity and broad in bandwidth. • The spectra of Eu{sup 2+} in SrAl{sub 2}O{sub 4} lies in the strongest region of solar spectrum. • The cooperative energy transfer (CET) dominated the energy transfer process. • The domination of CET is confirmed by experimental analysis. • SrAl{sub 2}O{sub 4}:Eu{sup 2+},Yb{sup 3+} show high energy transfer efficiency and long lifetime.

Fluorescence resonance energy transfer between NaYF{sub 4}:Yb,Tm upconversion nanoparticles and gold nanorods: Near-infrared responsive biosensor for streptavidin

Energy Technology Data Exchange (ETDEWEB)

Zhang, Shuang; Wang, Jing; Xu, Wen; Chen, Boting; Yu, Wei; Xu, Lin; Song, Hongwei, E-mail: songhw@jlu.edu.cn

2014-03-15

We represent a fluorescence resonance energy transfer (FRET) system using upconversion nanoparticles (UCNPs) and the gold nanorods (GNRs) as the energy donor–acceptor pair for directly determining streptavidin in near-infrared (NIR) region. NaYF{sub 4}:Yb,Tm UCNPs, which had a strong emission at 800 nm under 980-nm excitation, were adopted as the energy donor. The GNRs, which demonstrated strong surface plasmon absorption around 800 nm, were chosen as acceptor to quench the 800 nm emissions of the UCNPs. There had the spectral overlap between the emission of the donor nanoparticles (UCNPs) and the absorption of the acceptor nanoparticles (GNRs). This UCNP-based FRET system was then used to determine the amount of streptavidin. In this system, NaYF{sub 4}:Yb,Tm UCNPs conjugated with biotin, while GNRs conjugated with streptavidin. When added GNRs into UCNPs, the streptavidin were preferred to bind with biotin and decreased spacing between the donor and acceptor NPs. Consequently, FRET occurred and a linear relationship between the luminescence quenching efficiency and the concentration of streptavidin was obtained. Owing to the aforementioned merits of UCNPs as an energy donor and the strong quenching ability of GNRs, satisfactory analytical performances have been acquired. -- Highlights: • NaYF4:Yb,Tm and GNRs are as NIR energy donor and quenching acceptor for FRET. • Linkage between biotin and streptavidin make the distance between the donors and the acceptors short enough for FRET. • The FRET system in this work was applicable for the detection of streptavidin. • The donor and acceptor NPs can be modified by proper molecules for other biological molecules detection.

The effect of intentional potassium co-doping on the luminescent properties of Yb3+ and Tm3+ doped α-NaYF4 core and core–shell nanoparticles

International Nuclear Information System (INIS)

Misiak, Małgorzata; Stręk, Wiesław; Arabasz, Sebastian; Bednarkiewicz, Artur

2016-01-01

Simple and effective ways to circumvent limited luminescence efficiency of up-converting nanoparticles (UCNPs) are sought. One of the methods relays on distorting the crystallographic structure of host material by co-doping the nanocrystals with optically inactive co-dopants. Here we study the influence of K + doping and surface passivation on the up-converting properties of the α-NaYF 4 nanocrystals co-doped with 20% Yb 3+ and 0.1 or 2% Tm 3+ . The intentionally chosen concentrations of K + ions, which were meant to replaced sodium ions were fixed to 0, 5, 10, 20 to 30%. Potassium ions modified the spectroscopic properties of both core and core–shell NPs, but the differences were noticed between samples doped with 0.1% Tm 3+ and 2% Tm 3+ ions. Replacement of sodium by potassium ions decreased up-conversion luminescence intensity as well as shortened thulium excited states lifetimes in the samples doped with 0.1% Tm 3+ , while the opposite behavior was found in the samples co-doped with higher 2% thulium concentration. - Highlights: • We studied the influence of K + doping on luminescent properties of α-NaYF 4 :YbTm. • The 0.1 and 2% Tm doped core and core–shell samples were investigated. • K + -doping influence on UC properties was different in low and highly Tm doped NPs. • The explanations of the observed variations were proposed.

Alloying of Yb-Cu and Yb-Ag utilizing liquid ammonia metal solutions of ytterbium

International Nuclear Information System (INIS)

Imamura, H.; Yoshimura, T.; Sakata, Y.

2003-01-01

In the course of the studies on preparation of novel compounds using the dissolution of Eu or Yb metals in liquid ammonia, the formation of Yb-Cu and Yb-Ag intermetallic films has been found. When Cu or Ag metal powders were placed in a reactor containing a solution of Yb metal in liquid ammonia, the dissolved Yb readily react with the Cu or Ag metal particles to form surface alloy compounds. X-ray diffraction of Yb-Cu showed that upon thermal treatment above 673 K, the Yb metal deposited on the Cu particles reacted together to be transformed into the YbCu 6.5 intermetallic compound. A characteristic endothermic peak at 749 K, due to alloying of Yb-Cu, was observed by the differential scanning calorimeter measurements. By use of the high reactivity of liquid ammonia metal solutions of ytterbium, it was found that the ytterbium intermetallic films were readily formed under mild conditions. Yb-Cu and Yb-Ag exhibited enhanced catalytic activity for the hydrogenation of ethene as a result of alloying

Activation of SO2 with [(η(5) -C5 Me5 )2 Ln(THF)2 ] (Ln=Eu, Yb) leading to dithionite and sulfinate complexes.

Science.gov (United States)

Klementyeva, Svetlana V; Gamer, Michael T; Schmidt, Anna-Corina; Meyer, Karsten; Konchenko, Sergey N; Roesky, Peter W

2014-10-13

The reaction of decamethylytterbocene [(η(5) -C5 Me5 )2 Yb(THF)2 ] with SO2 at low temperature gave two new compounds, namely, the Yb(III) dithionite/sulfinate complex [{(η(5) -C5 Me5 )2 Yb(μ3 ,1κ(2) O(1,3) ,2κ(3) O(2,2',4) -S2 O4 )}2 {(η(5) -C5 Me5 )Yb(μ,1κO,2κO'-C5 Me5 SO2 )}2 ] (1) and the Yb(III) dithionite complex [{(η(5) -C5 Me5 )2 Yb}2 (μ,1κ(2) O(1,3) ,2κ(2) O(2,4) -S2 O4 )] (2). After extraction of 1, the mixture was heated to give the dinuclear tetrasulfinate complex [{(η(5) -C5 Me5 )Yb}2 (μ,κO,κO'-C5 Me5 SO2 )4 ] (3 a). In contrast, from the reaction of [(η(5) -C5 Me5 )2 Eu(THF)2 ] with SO2 only the tetrasulfinate complex [{(η(5) -C5 Me5 )Eu}2 (μ,κO,κO'-C5 Me5 SO2 )4 ] (3 b) was isolated. Two major reaction pathways were observed: 1) reductive coupling of two SO2 molecules to form the dithionite anion S2 O4 (2-) ; and 2) nucleophilic attack of one metallocene C5 Me5 ligand on the sulfur atom of SO2 . The compounds presented are the first dithionite and sulfinate complexes of the f-elements. © 2014 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

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

Science.gov (United States)

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

2015-08-01

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

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.

Transparent glass–ceramics with (Eu{sup 3+},Yb{sup 3+}):YNbO{sub 4} nanocrystals: Crystallization, structure, optical spectroscopy and cooperative upconversion

Energy Technology Data Exchange (ETDEWEB)

Loiko, P.A. [Center for Optical Materials and Technologies (COMT), Belarusian National Technical University, 65/17 Nezavisimosti Ave., Minsk 220013 (Belarus); Dymshits, O.S., E-mail: vodym@goi.ru [NITIOM Vavilov State Optical Institute, 36/1 Babushkin St, Saint-Petersburg 192171 (Russian Federation); Alekseeva, I.P.; Zhilin, A.A.; Tsenter, M.Ya. [NITIOM Vavilov State Optical Institute, 36/1 Babushkin St, Saint-Petersburg 192171 (Russian Federation); Vilejshikova, E.V. [Center for Optical Materials and Technologies (COMT), Belarusian National Technical University, 65/17 Nezavisimosti Ave., Minsk 220013 (Belarus); Bogdanov, K.V. [National Research University of Information Technologies, Mechanics and Optics, Kronverkskiy pr., 49, 197101 Saint-Petersburg (Russian Federation); Mateos, X. [Física i Cristallografia de Materials i Nanomaterials (FiCMA-FiCNA), Universitat Rovira i Virgili (URV), Campus Sescelades, C/Marcellí Domingo, s/n, Tarragona E-43007 (Spain); Yumashev, K.V. [Center for Optical Materials and Technologies (COMT), Belarusian National Technical University, 65/17 Nezavisimosti Ave., Minsk 220013 (Belarus)

2016-11-15

In the present work, we report on a comprehensive study of crystallization, structure and optical spectroscopy of transparent glass–ceramics with (Eu{sup 3+},Yb{sup 3+}):YNbO{sub 4} nanocrystals synthesized by secondary heat-treatments of glass of the Li{sub 2}O–Al{sub 2}O{sub 3}–SiO{sub 2} system, for the first time, to the best of our knowledge. Heat treatments result in volume crystallization of RENbO{sub 4} with the sizes of 4–15 nm. Crystals of rare-earth niobates with disordered fluorite structure (T′) appear during heat-treatment at 720–740 °C for 6 h, crystals with tetragonal structure (T) appear at higher temperatures or longer durations of heat-treatment, and in samples heat-treated at 1000 °C, the monoclinic form (M) is detected additionally. Rare-earth niobates act as nucleating agents for bulk crystallization of β-quartz solid solutions, the main crystalline phase of the glass–ceramics, which ensures their good thermo-mechanical properties. Optical spectroscopy confirms entering of both Eu{sup 3+} and Yb{sup 3+} ions into the RENbO{sub 4} nanophase and their specroscopic properties variation according to the T′→T→M phase transformations. Under UV excitation, glass–ceramics heat-treated at 900 °C provide intense red emission with the color coordinates x=0.665, y=0.335 (CIE 1931). In the sample, heat-treated at 1000 °C, a partial reduction of Eu{sup 3+} to Eu{sup 2+} is observed which allows for tuning the color properties of emission. When excited in the near-IR by an InGaAs diode, the initial glass and glass–ceramics show red cooperative upconversion due to the 2Yb{sup 3+}→Eu{sup 3+} energy transfer. The efficiency of the latter is ~10%. The developed materials due to the good emission and thermo-mechanical properties are promising for the development of color-tunable red phosphors.

Single-crystal structure refinement of YbF{sub 2} with a remark about YbH{sub 2}

Energy Technology Data Exchange (ETDEWEB)

Reckeweg, Olaf; DiSalvo, Francis J. [Cornell Univ., Ithaca, NY (United States). Dept. of Chemistry and Chemical Biology

2017-07-01

Transparent-yellow single crystals of YbF{sub 2} were obtained as only crystalline product from the solid-state reaction of Yb and teflon designed to yield 'Yb{sub 3}C{sub 3}F{sub 2}' in addition to some amorphous black material. The first single-crystal structure determination of YbF{sub 2} (cubic space group Fm anti 3m, CaF{sub 2}-type structure, a = 559.46(16) pm; R1 = 1.2%, wR2 = 3.2%) was the starting point to compare isostructural binary fluorides MF{sub 2} and hydrides MH{sub 2} (M = Ca, Yb, Eu, Sr and Ba) exhibiting an as-yet unexplained small volume per formula unit for YbH{sub 2}.

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.)

Potentiometric investigation into complexing of Pr,Eu,Yb with new β-diketones containing oxygen atom in fluorinated radical

International Nuclear Information System (INIS)

Gritsenko, T.V.; Lozinskij, M.O.; Panyushkin, V.T.; Fialkov, Yu.A.; Berenblit, V.V.; AN Ukrainskoj SSR, Kiev. Inst. Organicheskoj Khimii)

1983-01-01

Potentiometric method in the aqueous-methanol media at 25 deg and ionic torce of 0.15 (NaCl) has been used to determine the constants of acidic dissociation of the next β-diketones; Rsub(F)-CO-CHsub(2)-CO-R, where R=-C 6 H 5 , Rsub(F) C 3 F 7 OCF(CF 3 ) - (1), CF 3 O(CF 2 ) 3 OCF(CF 3 ) - (2), CF 3 O(CF 2 O) 4 CF 2 - (3), CF 3 O(CF 2 ) 2 - (4) and R=-C 4 H 3 S, Rsub(F) CF 3 O(CF 2 ) 3 OCF(CF 3 ) - (5), CF 3 O(CF 2 O) 4 CF 2 - (6). Synthesis of the 1-3, 5, 6 is described. Stability constants of Pr 3+ , Eu 3+ , Yb 3+ with 1-6 are calculated. Stability of the complexes for the each β-diketone increases in Pr-Eu-Yb series. Correlation between stability of the chelates and acidic properties of the β-diketonates is traced for the complexes of one metal with different ligands. Thus, the acidic properties of the β-diketones increase in the 1, 6-4 series; stability of their complexes with rare earths decreases in such order

Template-free synthesis and luminescent properties of hollow Ln:YOF (Ln = Eu or Er + Yb) microspheres

Energy Technology Data Exchange (ETDEWEB)

Martinez-Castro, E. [Instituto de Ciencia de Materiales de Sevilla (CSIC-US), Americo Vespucio 49, Isla de La Cartuja, 41092 Sevilla (Spain); García-Sevillano, J.; Cussó, F. [Dpto. Física de Materiales, C-04, Universidad Autónoma de Madrid, Avda. Francisco Tomás y Valiente, 7, 28049 Madrid (Spain); Ocaña, M., E-mail: mjurado@icmse.csic.es [Instituto de Ciencia de Materiales de Sevilla (CSIC-US), Americo Vespucio 49, Isla de La Cartuja, 41092 Sevilla (Spain)

2015-01-15

Highlights: • Hollow lanthanide doped YOF spheres have been synthesised through a template-free procedure. • Strong red emissions are observed for Eu-doped spheres under UV illumination. • Concentration quenching of luminescence takes place in the spheres at very high Eu doping levels. • Bright red emission is observed for Er, Yb codoped spheres, making this matrix advantageous for biomedical imaging. - Abstract: A method for the synthesis of hollow lanthanide doped yttrium oxyfluoride (YOF) spheres in the micrometer size range with cubic structure based on the pyrolysis at 600 °C of liquid aerosols generated from aqueous solutions containing the corresponding rare earth chlorides and trifluoroacetic acid has been developed. This procedure, which has been used for the first time for the synthesis of YFO based materials, is simpler and advantageous when compared with other methods usually employed for the production of hollow spheres since it does not require the use of sacrificial templates. In addition, it is continuous, which is desirable because of practical reasons. The procedure is also suitable for doping the YOF spheres with europium cations resulting in down converting red phosphors when activated with UV light, or for co-doping with both Er{sup 3+} and Yb{sup 3+} giving rise to up-converting phosphors, which emit intense red light under near infrared (NIR) irradiation. Because of their optical properties and hollow architecture, the developed materials may find applications in optoelectronic devices and biotechnology.

High-efficiency 2 μm Tm-doped fiber laser

International Nuclear Information System (INIS)

Dvornikov, D.

2013-01-01

Full text: Tm doped fiber laser operating in so called 'eye safe' wavelength region and designed in a MOPA configuration has been demonstrated. Large-mode-area fiber design and availability of high-brightness, high-power pump diodes at 795 nm made possible maximum output power of 25 W achieved at incident pump power of 72 W resulting in optical conversion efficiency about 35%. An important factor that led to an interest in 2 μm Tm-doped lasers is significantly broader spectral tunability of Tm-doped fibers compared to Yb-doped fibers, spanning wavelengths from below 1850 nm to beyond 2100 nm, corresponding to more than 200 nm of available bandwidth. This wavelength region covers the water absorption peaks around 1940 nm, making these lasers a valuable tool for precise medical procedures including noninvasive surgery, as well as several atmospheric transmission windows that are useful for remote sensing, laser radar and range-finding. This work was carried out as part of the EU funded Joint Operational Programme 'Black Sea Basin 2007-2013' and project 2.2.1.74459.339, MIS-ETC 1443 'Research networking for the environmental monitoring and mitigation of adverse ecological effects in the Black Sea Basin (BSB Net-Eco)'.

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 ...

Catalytic properties of lanthanide amide, imide and nitride formed by thermal degradation of liquid ammonia solutions of Eu and Yb metal

International Nuclear Information System (INIS)

Imamura, H.; Mizuno, K.; Ohishi, K.; Suda, E.; Kanda, K.; Sakata, Y.; Tsuchiya, S.

1998-01-01

The catalytic properties of lanthanide amide, imide and nitride prepared by the use of liquid ammonia solutions of lanthanide metals (Ln=Eu and Yb) were studied for catalytic hydrogenation. The reaction of Eu or Yb metal solutions in liquid ammonia with silica yielded SiO 2 -grafted lanthanide amide in the divalent state. The divalent amide showed catalytic activity for the selective hydrogenation of dienes and benzene. It was found that partial hydrogenation of benzene occurred with a very high selectivity for cyclohexene. Amides of calcium, strontium and barium were examined similarly in connection with catalytic studies on divalent amides. Imide and nitride, into which the lanthanide (Ln/AC) deposited by impregnation of active carbon (AC) with liquid ammonia solutions of lanthanide metals were converted thermally, were studied catalytically. It was concluded that imide or imide-like species generated during the thermal degradation of lanthanide amide to nitride were very active in the hydrogenation of ethene. Lanthanide nitride was virtually inactive, but the nitride highly dispersed on active carbon was activated when subjected to evacuation treatment above about 1000 K. (orig.)

Thermodynamic modeling of the Eu–Te and Te–Yb systems

Energy Technology Data Exchange (ETDEWEB)

Ghamri, H., E-mail: ghamri.houda@hotmail.fr; Djaballah, Y.; Belgacem-Bouzida, A.

2015-09-15

Highlights: • The Eu–Te and Te–Yb binary systems were not previously thermodynamically assessed. • The Eu–Te and Te–Yb systems were assessed by using the CALPHAD technique. • A coherent set of thermodynamic parameters was obtained for both systems. • An agreement between the calculated results and experimental data was obtained for both systems. - Abstract: In this work, thermodynamic assessments of the Eu–Te and Te–Yb binary systems were carried out by using the CALculation of PHase Diagrams (CALPHAD) method based on the available experimental data including thermodynamic properties and phase equilibria. Reasonable models were constructed for all the phases of the two systems. The liquid phases were described by the substitutional solution model with the Redlich–Kister polynomial. The three intermetallic compounds, Eu{sub 4}Te{sub 7}, Eu{sub 3}Te{sub 7} and TeYb in the two systems, were treated as stoichiometric phases, while the non-stoichiometric phase (EuTe), which has an homogeneity range, was treated by a two-sublattice model following the schema: (Eu,Te){sub 0.5}(Te){sub 0.5}. A consistent set of thermodynamic parameters leading to reasonable agreement between the calculated results and experimental data was obtained.

Design, synthesis and luminescence properties of Ba2 YB2 O6 Cl- and Ba2 YB2 O6 F-based phosphors.

Science.gov (United States)

Chen, Wanping; Yang, Xin; Liu, Yan; Dai, Xiaoyan

2015-05-01

Using a high-temperature solid-state reaction, the chlorine in Ba2 YB2 O6 Cl is gradually replaced by F, and a new compound with the nominal chemical formula Ba2 YB2 O6 F and two phosphors doped with Ce(3+) and Eu(3+) , respectively, are obtained. X-Ray diffraction and photoluminescence spectroscopy are used to characterize the as-synthesized samples. The as-synthesized Ba2 YB2 O6 Cl exhibits bright blue emission in the spectral range ~ 330-410 nm with a maximum around 363 nm under X-ray or UV excitation. Ba2 YB2 O6 F:0.01Ce(3+) exhibits blue emission in the range ~ 340-570 nm with a maximum around 383 nm. Ba2 YB2 O6 F:0.01Eu(3+) exhibits a predominantly (5) D0 -(7)  F2 emission (~610 nm) and the relative intensities of the (5) D0 -(7)  F0,1,2 emissions are tunable under different wavelength UV excitation. The luminescence behaviors of the two phosphors are explained simply in terms of the host composition and site occupancy probability of Ce(3+) and Eu(3+) , respectively. The results indicate that these phosphors have potential application as a blue phosphor or as a red phosphor. Copyright © 2014 John Wiley & Sons, Ltd.

Energy transfer and colour tunability in UV light induced Tm3+/Tb3+/Eu3+: ZnB glasses generating white light emission.

Science.gov (United States)

Naresh, V; Gupta, Kiran; Parthasaradhi Reddy, C; Ham, Byoung S

2017-03-15

A promising energy transfer (Tm 3+ →Tb 3+ →Eu 3+ ) approach is brought forward to generate white light emission under ultraviolet (UV) light excitation for solid state lightening. Tm 3+ /Tb 3+ /Eu 3+ ions are combinedly doped in zinc borate glass system in view of understanding energy transfer process resulting in white light emission. Zinc borate (host) glass displayed optical and luminescence properties due to formation of Zn(II) x -[O(-II)] y centres in the ZnB glass matrix. At 360nm (UV) excitation, triply doped Tm 3+ /Tb 3+ /Eu 3+ : ZnB glasses simultaneously shown their characteristic emission bands in blue (454nm: 1 D 2 → 3 F 4 ), green (547nm: 5 D 4 → 7 F 5 ) and red (616nm: 5 D 0 → 7 F 2 ) regions. In triple ions doped glasses, energy transfer dynamics is discussed in terms of Forster-Dexter theory, excitation & emission profiles, lifetime curves and from partial energy level diagram of three ions. The role of Tb 3+ in ET from Tm 3+ →Eu 3+ was discussed using branch model. From emission decay analysis, energy transfer probability (P) and efficiency (η) were evaluated. Colour tunability from blue to white on varying (Tb 3+ , Eu 3+ ) content is demonstrated from Commission Internationale de L'Eclairage (CIE) chromaticity coordinates. Based on chromaticity coordinates, other colour related parameters like correlated colour temperature (CCT) and colour purity are also computed for the studied glass samples. An appropriate blending of such combination of rare earth ions could show better suitability as potential candidates in achieving multi-colour and warm/cold white light emission for white LEDs application in the field of solid state lightening. Copyright © 2016 Elsevier B.V. All rights reserved.

Fiber-optic thermometer application of thermal radiation from rare-earth end-doped SiO2 fiber

International Nuclear Information System (INIS)

Katsumata, Toru; Morita, Kentaro; Komuro, Shuji; Aizawa, Hiroaki

2014-01-01

Visible light thermal radiation from SiO 2 glass doped with Y, La, Ce, Pr, Nd, Eu, Tb, Dy, Ho, Er, Tm, Yb, and Lu were studied for the fiber-optic thermometer application based on the temperature dependence of thermal radiation. Thermal radiations according to Planck's law of radiation are observed from the SiO 2 fibers doped with Y, La, Ce, Pr, Eu, Tb, and Lu at the temperature above 1100 K. Thermal radiations due to f-f transitions of rare-earth ions are observed from the SiO 2 fibers doped with Nd, Dy, Ho, Er, Tm, and Yb at the temperature above 900 K. Peak intensities of thermal radiations from rare-earth doped SiO 2 fibers increase sensitively with temperature. Thermal activation energies of thermal radiations by f-f transitions seen in Nd, Dy, Ho, Er, Tm, and Yb doped SiO 2 fibers are smaller than those from SiO 2 fibers doped with Y, La, Ce, Pr, Eu, Tb, and Lu. Thermal radiation due to highly efficient f-f transitions in Nd, Dy, Ho, Er, Tm, and Yb ions emits more easily than usual thermal radiation process. Thermal radiations from rare-earth doped SiO 2 are potentially applicable for the fiber-optic thermometry above 900 K

Potentiometric investigation into complexing of Pr,Eu,Yb with new. beta. -diketones containing oxygen atom in fluorinated radical

Energy Technology Data Exchange (ETDEWEB)

Gritsenko, T.V.; Lozinskij, M.O.; Panyushkin, V.T.; Fialkov, Yu.A.; Berenblit, V.V. (Kubanskij Gosudarstvennyj Univ., Krasnodar (USSR); AN Ukrainskoj SSR, Kiev. Inst. Organicheskoj Khimii)

1983-01-01

Potentiometric method in the aqueous-methanol media at 25 deg and ionic torce of 0.15 (NaCl) has been used to determine the constants of acidic dissociation of the next ..beta..-diketones; Rsub(F)-CO-CHsub(2)-CO-R, where R=-C/sub 6/H/sub 5/, Rsub(F) C/sub 3/F/sub 7/OCF(CF/sub 3/) - (1), CF/sub 3/O(CF/sub 2/)/sub 3/OCF(CF/sub 3/) - (2), CF/sub 3/O(CF/sub 2/O)/sub 4/CF/sub 2/ - (3), CF/sub 3/O(CF/sub 2/)/sub 2/ - (4) and R=-C/sub 4/H/sub 3/S, Rsub(F) CF/sub 3/O(CF/sub 2/)/sub 3/OCF(CF/sub 3/) - (5), CF/sub 3/O(CF/sub 2/O)/sub 4/CF/sub 2/ - (6). Synthesis of the 1-3, 5, 6 is described. Stability constants of Pr/sup 3 +/, Eu/sup 3 +/, Yb/sup 3 +/ with 1-6 are calculated. Stability of the complexes for the each ..beta..-diketone increases in Pr-Eu-Yb series. Correlation between stability of the chelates and acidic properties of the ..beta..-diketonates is traced for the complexes of one metal with different ligands. Thus, the acidic properties of the ..beta..-diketones increase in the 1, 6-4 series; stability of their complexes with rare earths decreases in such order.

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

Energy Technology Data Exchange (ETDEWEB)

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

2010-11-24

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

Hydrothermal synthesis of NaLuF4:153Sm,Yb,Tm nanoparticles and their application in dual-modality upconversion luminescence and SPECT bioimaging.

Science.gov (United States)

Yang, Yang; Sun, Yun; Cao, Tianye; Peng, Juanjuan; Liu, Ying; Wu, Yongquan; Feng, Wei; Zhang, Yingjian; Li, Fuyou

2013-01-01

Upconversion luminescence (UCL) properties and radioactivity have been integrated into NaLuF(4):(153)Sm,Yb,Tm nanoparticles by a facile one-step hydrothermal method, making these nanoparticles potential candidates for UCL and single-photon emission computed tomography (SPECT) dual-modal bioimaging in vivo. The introduction of small amount of radioactive (153)Sm(3+) can hardly vary the upconversion luminescence properties of the nanoparticles. The as-designed nanoparticles showed very low cytotoxicity, no obvious tissue damage in 7 days, and excellent in vitro and in vivo performances in dual-modal bioimaging. By means of a combination of UCL and SPECT imaging in vivo, the distribution of the nanoparticles in living animals has been studied, and the results indicated that these particles were mainly accumulated in the liver and spleen. Therefore, the concept of (153)Sm(3+)/Yb(3+)/Tm(3+) co-doped NaLuF(4) nanoparticles for UCL and SPECT dual-modality imaging in vivo of whole-body animals may serve as a platform for next-generation probes for ultra-sensitive molecular imaging from the cellular scale to whole-body evaluation. It also introduces an easy methodology to quantify in vivo biodistribution of nanomaterials which still needs further understanding as a community. Copyright © 2012 Elsevier Ltd. All rights reserved.

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.

Thermal evolution of the spin ordering at the concomitant spin–orbital rearrangement temperature in RVO{sub 3} (R=Lu, Yb and Tm)

Energy Technology Data Exchange (ETDEWEB)

Sarkar, Tapati, E-mail: tapati.sarkar@angstrom.uu.se [Department of Engineering Sciences, Uppsala University, Box 534, SE-75121 Uppsala (Sweden); Ivanov, Sergey A. [Department of Engineering Sciences, Uppsala University, Box 534, SE-75121 Uppsala (Sweden); Center of Materials Science, Karpov Institute of Physical Chemistry, 105064 Moscow K-64 (Russian Federation); Bazuev, G.V. [Institute of Solid State Chemistry, Ural Branch of the Russian Academy of Science, 620999 Ekaterinburg GSP-145 (Russian Federation); Nordblad, Per; Mathieu, Roland [Department of Engineering Sciences, Uppsala University, Box 534, SE-75121 Uppsala (Sweden)

2016-07-01

Synthesis, crystal structure and magnetization measurements of phase pure polycrystalline RVO{sub 3} (R=Lu, Yb and Tm) are reported. The compounds were stabilized in the orthorhombic structure by thermal treatment of the respective precursors (RVO{sub 4}) in a reducing atmosphere. Special pressure treatment was carried out during the synthesis to ensure phase pure samples without secondary phases. Magnetization measurements reveal the presence of two spin ordering temperatures in the samples. Interestingly, at the lower spin ordering temperature, T{sub SO2}, the uncompensated excess moment of the antiferromagnetic spin structure has different field dependences above and below T{sub SO2}, causing a jump in the thermal evolution of the magnetization that changes sign with increasing field strength. This jump is associated with the reported magnetic and orbital rearrangement in the samples, and the different spin configurations in the C- and G-type antiferromagnetic structures. - Highlights: • Magnetization measurements of polycrystalline RVO{sub 3} (R=Lu, Yb, Tm) are reported. • The samples have two spin ordering temperatures, T{sub SO1} and T{sub SO2} (T{sub SO1}>T{sub SO2}). • A magnetic field dependent jump of the excess magnetization, ΔM is observed at T{sub SO2.} • The jump in ΔM is associated with magnetic and orbital rearrangement in the samples. • ΔM is probably affected by possible phase coexistence in the samples.

Ag2O dependent up-conversion luminescence properties in Tm3+/Er3+/Yb3+ co-doped oxyfluorogermanate glasses

International Nuclear Information System (INIS)

Hu, Yuebo; Qiu, Jianbei; Song, Zhiguo; Zhou, Dacheng

2014-01-01

Up-conversion (UC) luminescence properties of Ag/Tm 3+ /Er 3+ /Yb 3+ co-doped oxyfluorogermanate glasses have been studied to assess the effective role of silver nanoparticles as a sensitizer for Tm 3+ and Er 3+ ions. The X-ray diffraction patterns obtained in this work do not reveal any crystalline phase in the glass. However, the absorption spectra reveal that surface plasmons resonance band of Ag undergoes a distinct split with two maxima and a very broad absorption peak with a background that extends toward the near infrared (NIR) with the increasing of Ag 2 O added concentration. Transmission electron microscope images confirm that silver nanoparticles have been precipitated from matrix glasses and show their distribution, size, and shapes. In addition, changes in UC luminescence intensity of four emission bands 476, 524, 546, and 658 nm corresponding to 1 G 4 → 3 H 6 (Tm 3+ ), ( 2 H 11/2 , 4 S 3/2 ) → 4 I 15/2 (Er 3+ ), and 4 F 9/2 → 4 I 15/2 (Er 3+ ) transitions, respectively, as a function of silver addition to the base composition have been measured under 980 nm excitation. It is confirmed that Ag 2 O added concentration plays an important role in increasing the UC luminescence intensity; however, further increase in Ag 2 O added concentration reduces the intensity

Spectrum fluctuations from regular and damped rotational structures in {sup 16}`8Yb and {sup 163}Tm nuclei

Energy Technology Data Exchange (ETDEWEB)

Herskind, B; Dossing, T; Ninel, N; Atac, A; Jensen, H J; Hagemann, G B; Lieder, R M; Maj, A; Nyberg, J; Piiparinen, M; Sugawara, M; Virtanen, A [Niels Bohr Inst., Copenhagen (Denmark); Leoni, S; Vigezzi, E; Bosetti, P; Bracco, A; Broglia, R A; Million, B [Milan Univ. (Italy); Matsuo, M [Kyoto Univ., Uji (Japan). Uji Research Center of Yukawa Inst. for Theoretical Physics; Bergstrom, M; Brockstedt, A; Carlsson, H; Ekstrom, P; Nordlund, A; Ryde, H [Lund Univ. (Sweden). Dept. of Physics; Jongman, J [Rijksuniversiteit Groningen (Netherlands). Kernfysisch Versneller Inst.; Ingebretsen, F; Tjom, P O [Oslo Univ. (Norway); Lonnroth, T [Aabo Akademi, Turku (Finland). Dept. of Physics

1992-08-01

A new method has been developed for analyzing fluctuations of count in two-dimensional gamma ray energy coincidence spectra of deformed nuclei formed in heavy ion fusion reactions. Most of the gamma decay cascades flow through regions of high level density, and the method is based upon assumptions about average properties of the excited states. Transition energies along discrete rotational bands are viewed as randomly selected from a continuous distribution of rotational frequencies and moments of inertia. For damped rotational motion, implying a mixing of the rotational bands, a random matrix model is assumed, leading to smooth energy spectra, and strong fluctuations of the transition strengths. The method is illustrated for {sup 168}Yb and {sup 163}Tm. 4 refs., 4 figs.

Synthesis and up-conversion emissions of Yb3+/Er3+, Yb3+/Tm3+

Indian Academy of Sciences (India)

42

which has received considerable attention for material studies [25-28]. ... Though the energy gap between the ground state 8S7/2 and the first excited state 6P7/2 of ... XRD pattern (Figure 1a) of the 20 mol% Yb3+, 2 mol% Er3+ co-doped ...

Intense upconversion luminescence and effect of local environment for Tm3+/Yb3+ co-doped novel TeO2-BiCl3 glass system.

Science.gov (United States)

Wang, Guonian; Dai, Shixun; Zhang, Junjie; Wen, Lei; Yang, Jianhu; Jiang, Zhonghong

2006-05-15

We present the results of a study that uses theoretical and experimental methods to investigate the characteristics of the upconversion luminescence of Tm3+/Yb3+ codoped TeO2-BiCl3 glass system as a function of the BiCl3 fraction. These glasses are potentially important in the design of upconversion fiber lasers. Effect of local environment around Tm3+ on upconversion fluorescence intensity was analyzed by theoretical calculations. The structure and spectroscopic properties were investigated in the experiments by measuring the Raman spectra, IR transmission spectra, and absorption and fluorescence intensities at room temperature. The results indicate that blue luminescence quantum efficiency increases with increasing BiCl3 content from 10 to 60 mol%, which were interpreted by the increase of asymmetry of glass structure, decrease of phonon energy and removing of OH- groups.

Study of quantitative analysis of rare earth elements (Sc, Y, La, Ce, Pr, Nd, Sm, Eu, Gd, Tb, Dy, Ho, Er, Tm, Yb, Lu) in soil samples by inductively couple plasma mass spectrometry

International Nuclear Information System (INIS)

Truong Duc Toan; Nguyen Giang; Vo Tran Quang Thai; Do Tam Nhan; Nguyen Le Anh; Nguyen Viet Duc; Luong Thi Tham; Truong Thi Phuong Mai

2015-01-01

Method for the determination of 16 rare earth elements (REEs) in soil samples without separating by inductively coupled plasma mass spectrometry (ICP-MS) has been studied at Dalat Nuclear Research Institute. The optimal conditions for ICP-MS NexION 300X with three modes: Standard, Collision (KED), and Reaction (DRC) have been studied on the Montana II soil reference material. The result analysis shows that: DRC mode only gives good analysis result for Sc, Y, La, Ce, Pr, Nd, Tm, Yb, and Lu; Standard mode exhibits good analysis results for all elements with error from 1.2 - 29.0% and KED mode is the best one with error less than 15%. The concentrations of elements in the soil samples of Cau Dat, Bao Loc, and Da Lat were determined, which concentrations of REEs in soil samples of Cau Dat are higher than that of the other areas in Lam Dong Province. (author)

Influence of the diluents on the extraction behaviour of Eu(III), and tm (III) by thenoytrifluoro acetone and/or 18-crown-6 or 15-crown-5 from nitrate aqueous medium. Vol. 3

Energy Technology Data Exchange (ETDEWEB)

Shehata, F A; El-Hefny, N; Aly, H F [Hot Laboratories Center, Atomic Energy Authority, Cairo (Egypt)

1996-03-01

The effects of different diluents on the synergistic extraction of Eu(III), and Tm (III) by thenoyltrifluoroacetone (HTTA) and/or 18-crown-5 was investigated from nitrate aqueous medium. For these systems, it is found that the diluent affects the extracted species in the organic phase. The composition of the extracted species have been proposed on the basis of slope analysis method. With HTTA alone, the stoichiometry of the extracted species was found to be M(TTA){sub 3} or M(NO{sub 3}) (TTA){sub 2} (HTTA) where M=Eu(III) or Tm(III). With HTA-Crown mixture the extracted species were M(TTA){sub 3}. CE or M(NO{sub 3}) (TTA){sub 2}. CE. The respective extraction and formation constants were evaluated. Different thermodynamic parameters of Eu (III), and Tm (III) extraction were determined from the experimental results. The variations obtained in the distribution was explained in terms of the interaction between the solute and the diluents. Correlations between the extraction and formation constants of the extracted species of Eu and Tm and the physicochemical parameter of the diluents used are given and discussed. 3 figs.,1 tab.

Electrical resistivity of YbRh2Si2 and EuT2Ge2 (T=Co,Cu) at extreme conditions of pressure and temperature

International Nuclear Information System (INIS)

Dionicio, G.A.

2006-01-01

This investigation addresses the effect that pressure, p, and temperature, T, have on 4f states of the rare-earth elements in the isostructural YbRh 2 Si 2 , EuCo 2 Ge 2 , and EuCu 2 Ge 2 compounds. Upon applying pressure the volume of the unit cell reduces, enforcing either the enhancement of the hybridization of the 4f localized electrons with the ligand or a change in the valence state of the rare-earth ions. Here, we probe the effect of a pressure-induced lattice contraction on these system by means of electrical-resistivity measurements, ρ(T), from room temperature down to 100 mK. (orig.)

Specific features of magnetoresistance during the antiferromagnet—paramagnet transition in Tm1−xYbxB12

International Nuclear Information System (INIS)

Sluchanko, N. E.; Azarevich, A. N.; Bogach, A. V.; Glushkov, V. V.; Demishev, S. V.; Levchenko, A. V.; Filippov, V. B.; Shitsevalova, N. Yu.

2013-01-01

The transverse magnetoresistance Δρ/ρ(H, T) of Tm 1−x Yb x B 12 single crystals is studied in the ytterbium concentration range corresponding to the antiferromagnet-paramagnet transition in a magnetic field up to 80 kOe at low temperatures. A magnetic H-T phase diagram is constructed for the antiferromagnetic state of substitutional Tm 1−x Yb x B 12 solid solutions with x ≤ 0.1. The contributions to the magnetoresistance in the antiferromagnetic and paramagnetic phases of the dodecaborides under study are separated. Along with negative quadratic magnetoresistance -Δρ/ρ ∝ H 2 , the magnetically ordered phase of these compounds is found to have component Δρ/ρ ∝ H that linearly changes in a magnetic field. The negative contribution to the magnetoresistance of Tm 1−x Yb x B 12 is analyzed in terms of the Yosida model for a local magnetic susceptibility.

A broadening temperature sensitivity range with a core-shell YbEr@YbNd double ratiometric optical nanothermometer

Science.gov (United States)

Marciniak, L.; Prorok, K.; Francés-Soriano, L.; Pérez-Prieto, J.; Bednarkiewicz, A.

2016-02-01

The chemical architecture of lanthanide doped core-shell up-converting nanoparticles can be engineered to purposely design the properties of luminescent nanomaterials, which are typically inaccessible to their homogeneous counterparts. Such an approach allowed to shift the up-conversion excitation wavelength from ~980 to the more relevant ~808 nm or enable Tb or Eu up-conversion emission, which was previously impossible to obtain or inefficient. Here, we address the issue of limited temperature sensitivity range of optical lanthanide based nano-thermometers. By covering Yb-Er co-doped core nanoparticles with the Yb-Nd co-doped shell, we have intentionally combined temperature dependent Er up-conversion together with temperature dependent Nd --> Yb energy transfer, and thus have expanded the temperature response range ΔT of a single nanoparticle based optical nano-thermometer under single ~808 nm wavelength photo-excitation from around ΔT = 150 K to over ΔT = 300 K (150-450 K). Such engineered nanocrystals are suitable for remote optical temperature measurements in technology and biotechnology at the sub-micron scale.The chemical architecture of lanthanide doped core-shell up-converting nanoparticles can be engineered to purposely design the properties of luminescent nanomaterials, which are typically inaccessible to their homogeneous counterparts. Such an approach allowed to shift the up-conversion excitation wavelength from ~980 to the more relevant ~808 nm or enable Tb or Eu up-conversion emission, which was previously impossible to obtain or inefficient. Here, we address the issue of limited temperature sensitivity range of optical lanthanide based nano-thermometers. By covering Yb-Er co-doped core nanoparticles with the Yb-Nd co-doped shell, we have intentionally combined temperature dependent Er up-conversion together with temperature dependent Nd --> Yb energy transfer, and thus have expanded the temperature response range ΔT of a single nanoparticle

Lanthanide-doped Sr2YF7 nanoparticles: controlled synthesis, optical spectroscopy and biodetection

Science.gov (United States)

Yang, Yuhan; Tu, Datao; Zheng, Wei; Liu, Yongsheng; Huang, Ping; Ma, En; Li, Renfu; Chen, Xueyuan

2014-09-01

Sr2YF7, as an important matrix for trivalent lanthanide (Ln3+) ions to fabricate upconversion (UC) or downshifting (DS) phosphors, has been rarely reported. Herein, monodisperse and size-controllable tetragonal-phase Ln3+-doped Sr2YF7 nanoparticles (NPs) were synthesized via a facile thermal decomposition method. Upon excitation at 980 nm, UC luminescence properties of Sr2YF7:Ln3+/Yb3+ (Ln = Tm, Er) NPs were systematically surveyed. Particularly, after coating an inert Sr2YF7 shell, the UC luminescence intensities of Sr2YF7:Tm3+/Yb3+ and Sr2YF7:Er3+/Yb3+ NPs were enhanced by ~22 and 4 times, respectively. Furthermore, intense multicolor DS luminescence was also achieved in Ce3+/Tb3+ or Eu3+ doped Sr2YF7 NPs, with absolute quantum yields of 55.1% (Tb3+) and 11.2% (Eu3+). The luminescence lifetimes of 5D4 (Tb3+) and 5D0 (Eu3+) were determined to be 3.7 and 8.1 ms, respectively. By utilizing the long-lived luminescence of Ln3+ in these Sr2YF7 NPs, we demonstrated their application as sensitive heterogeneous time-resolved photoluminescence bioprobes to detect the protein of avidin and the tumor marker of the carcinoembryonic antigen (CEA) with their limits of detection down to 40.6 and 94.9 pM, and thus reveal the great potential of these Sr2YF7:Ln3+ nanoprobes in cancer diagnosis.Sr2YF7, as an important matrix for trivalent lanthanide (Ln3+) ions to fabricate upconversion (UC) or downshifting (DS) phosphors, has been rarely reported. Herein, monodisperse and size-controllable tetragonal-phase Ln3+-doped Sr2YF7 nanoparticles (NPs) were synthesized via a facile thermal decomposition method. Upon excitation at 980 nm, UC luminescence properties of Sr2YF7:Ln3+/Yb3+ (Ln = Tm, Er) NPs were systematically surveyed. Particularly, after coating an inert Sr2YF7 shell, the UC luminescence intensities of Sr2YF7:Tm3+/Yb3+ and Sr2YF7:Er3+/Yb3+ NPs were enhanced by ~22 and 4 times, respectively. Furthermore, intense multicolor DS luminescence was also achieved in Ce3+/Tb3+ or Eu3

Spectral properties and anti-Stokes luminescence of TeO2-BaF2:Ho3+, Ho3+/Yb3+ ceramics and glass excited by 1.9-μm radiation of a Tm:LiYF4 laser

Science.gov (United States)

Savikin, A. P.; Egorov, A. S.; Budruev, A. V.; Perunin, I. Yu.; Krasheninnikova, O. V.; Grishin, I. A.

2017-07-01

We demonstrate the up-conversion of Tm:LiYF4 infrared (IR) laser radiation with 1908-nm wavelength into visible light with a spectral maximum at 650 nm by ceramics with a composition of (100 - x)TeO2- xBaF2 - 1 wt % HoF3- yYbF3, where x = 20, 30, or 40 mol % and y = 0 or 0.5 wt %. The samples of 60TeO2-40BaF2 - 1 wt % HoF3 - 0.5 wt % YbF3 exhibited anti-Stokes luminescence at a threshold radiation power density of 1.0-1.5 W cm-2.

BaYb2F8, a new radiation hard Cherenkov radiator for electromagnetic calorimeters

International Nuclear Information System (INIS)

Aseev, A.A.; Devitsin, E.G.; Komar, A.A.; Kozlov, V.A.; Hovsepyan, Yu.I.; Potashov, S.Yu.; Sokolovsky, K.A.; Uvarova, T.V.; Vasilchenko, V.G.

1992-01-01

Radiation hardness and optical properties of a new Cherenkov radiator, heavy fluoride BaYb 2 F 8 doped with various elements, have been studied. The above mentioned crystal has the density of 7 g/cm 3 , the radiation length is 1.28 cm and the Moliere radius 2.44 cm. High radiation hardness has been demonstrated for BaYb 2 F 8 doped with Tm, Pr, Tb. (orig.)

Specific heat of the chiral-soliton-lattice phase in Yb(Ni0.94Cu0.06)3Al9

Science.gov (United States)

Ninomiya, Hiroki; Sato, Takaaki; Inoue, Katsuya; Ohara, Shigeo

2018-05-01

We have studied the monoaxial-chiral helimagnet YbNi3Al9 and its-substituted analogue Yb(Ni0.94Cu0.06)3Al9. These compounds belong to a chiral space group R32. In Yb(Ni0.94Cu0.06)3Al9 with the magnetic ordering temperature TM = 6.4 K , only when the magnetic field is applied perpendicular to the helical axis, the chiral soliton lattice is observed below Hc = 10 kOe . YbNi3Al9 with TM = 3.4 K exhibits a metamagnetic transition at Hc = 1 kOe in 2 K. To study the formation of chiral helimagnetic state and chiral soliton lattice, we have measured the specific heat in magnetic fields applied parallel and perpendicular to the helical axis. In zero field, with decreasing temperature, specific heat shows λ-type phase transition from paramagnetic state to chiral helimagnetic one. At the temperature where the chiral soliton lattice emerges, we have found that the specific heat shows a sharp peak. In addition, at around the crossover between paramagnetic state and forced-ferromagnetic one, a broad maximum has been observed. We have determined the magnetic phase diagrams of YbNi3Al9 and Yb(Ni0.94Cu0.06)3Al9.

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).

Spectroscopic properties and energy levels of Yb{sup 3+} ion in huntite structure

Energy Technology Data Exchange (ETDEWEB)

Malakhovskii, A.V. [L.V. Kirensky Institute of Physics, Siberian Branch Russian Academy of Sciences, 660036 Krasnoyarsk (Russian Federation)], E-mail: malakha@iph.krasn.ru; Sukhachev, A.L. [L.V. Kirensky Institute of Physics, Siberian Branch Russian Academy of Sciences, 660036 Krasnoyarsk (Russian Federation); Gnatchenko, S.L.; Kachur, I.S.; Piryatinskaya, V.G. [B. Verkin Institute for Low Temperature Physics and Engineering, National Academy of Sciences of Ukraine, 61103 Kharkov (Ukraine); Temerov, V.L.; Krylov, A.S.; Edelman, I.S. [L.V. Kirensky Institute of Physics, Siberian Branch Russian Academy of Sciences, 660036 Krasnoyarsk (Russian Federation)

2009-05-12

Temperature dependence of Yb{sup 3+} optical absorption spectrum has been studied in crystals Yb{sub x}Tm{sub 1-x}Al{sub 3}(BO{sub 3}){sub 4} (x = 0.1, 0.2 and 1) in the temperature range 1.7-293 K. The spectra of the crystals appeared to be practically identical for the studied ytterbium concentrations. Raman scattering spectrum of YbAl{sub 3}(BO{sub 3}){sub 4} crystal has been measured. Group theory analysis of the optical absorption spectra is made, and new energy structure of the ground and excited states of Yb{sup 3+} ion, based on the experimental data obtained, is presented. Transformation of the local environment of Yb{sup 3+} ion depending on temperature has been found out. Spectrum of luminescence has been calculated from the absorption spectrum by reciprocity method with the use of the proposed energy structure.

K-shell absorption jump factors and jump ratios in elements between Tm ( Z = 69) and Os ( Z = 76) derived from new mass attenuation coefficient measurements

Science.gov (United States)

Kaya, Necati; Tıraşoğlu, Engin; Apaydın, Gökhan; Aylıkcı, Volkan; Cengiz, Erhan

2007-08-01

The K-shell absorption jump factors and jump ratios were derived from new mass attenuation coefficients measured using an energy dispersive X-ray fluorescence (EDXRF) spectrometer for Tm, Yb elements being Tm 2O 3, Yb 2O 3 compounds and pure Lu, Hf, Ta, W, Re and Os. The measurements, in the region 56-77 keV, were done in a transmission geometry utilizing the K α1 , K α2 , K β1 and K β2 X- rays from different secondary source targets (Yb, Ta, Os, W, Re and Ir, etc.) excited by the 123.6 keV γ-photons from an 57Co annular source and detected by an Ultra-LEGe solid state detector with a resolution of 150 eV at 5.9 keV. Experimental results have been compared with theoretically calculated values. The measured values of Tm, Yb, Lu, Hf, Ta, W, Re and Os are reported here for the first time.

K-shell absorption jump factors and jump ratios in elements between Tm (Z = 69) and Os (Z = 76) derived from new mass attenuation coefficient measurements

International Nuclear Information System (INIS)

Kaya, Necati; Tirasoglu, Engin; Apaydin, Goekhan; Aylikci, Volkan; Cengiz, Erhan

2007-01-01

The K-shell absorption jump factors and jump ratios were derived from new mass attenuation coefficients measured using an energy dispersive X-ray fluorescence (EDXRF) spectrometer for Tm, Yb elements being Tm 2 O 3 , Yb 2 O 3 compounds and pure Lu, Hf, Ta, W, Re and Os. The measurements, in the region 56-77 keV, were done in a transmission geometry utilizing the K α1 , K α2 , K β1 and K β2 X- rays from different secondary source targets (Yb, Ta, Os, W, Re and Ir, etc.) excited by the 123.6 keV γ-photons from an 57 Co annular source and detected by an Ultra-LEGe solid state detector with a resolution of 150 eV at 5.9 keV. Experimental results have been compared with theoretically calculated values. The measured values of Tm, Yb, Lu, Hf, Ta, W, Re and Os are reported here for the first time

Observation of superconductivity at 30∼46K in AxFe2Se2 (A = Li, Na, Ba, Sr, Ca, Yb, and Eu)

OpenAIRE

Ying, T. P.; Chen, X. L.; Wang, G.; Jin, S. F.; Zhou, T. T.; Lai, X. F.; Zhang, H.; Wang, W. Y.

2012-01-01

New iron selenide superconductors by intercalating smaller-sized alkali metals (Li, Na) and alkaline earths using high-temperature routes have been pursued ever since the discovery of superconductivity at about 30 K in KFe2Se2, but all have failed so far. Here we demonstrate that a series of superconductors with enhanced Tc=30~46 K can be obtained by intercalating metals, Li, Na, Ba, Sr, Ca, Yb, and Eu in between FeSe layers by the ammonothermal method at room temperature. Analysis on their p...

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)

Magnetism of cyano-bridged Ln3+-M3+ complexes. Part II: one-dimensional complexes (Ln3+ = Eu, Tb, Dy, Ho, Er, Tm; M3+ = Fe or Co) with bpy as blocking ligand.

Science.gov (United States)

Figuerola, Albert; Ribas, Joan; Casanova, David; Maestro, Miguel; Alvarez, Santiago; Diaz, Carmen

2005-10-03

The reaction of Ln(NO3)3(aq) with K3[Fe(CN)6] or K3[Co(CN)6] and 2,2'-bipyridine in water/ethanol led to 13 one-dimensional complexes: trans-[M(CN)4(mu-CN)2Ln(H2O)4(bpy)]n.4nH2O.1.5nbpy (Ln = Eu3+, Tb3+, Dy3+, Ho3+, Er3+, Tm3+, Lu3+; M = Fe3+, Co3+). The structures for [EuFe]n (1), [TbFe]n (2), [DyFe]n (3), [HoFe]n (4), [ErFe]n (5), [TmFe]n (6), [LuFe]n (7), [EuCo]n (8), [TbCo]n (9), [DyCo]n (10), [HoCo]n (11), [ErCo]n (12), and [TmCo]n (13) have been solved: they crystallize in the triclinic space group P and are isomorphous. They exhibit a supramolecular architecture created by the interplay of coordinative, hydrogen bonding, and pi-pi interactions. A stereochemical study of the eight-vertex polyhedra of the lanthanide ions, based on continuous shape measures, is presented. The Ln3+-Fe3+ interaction is antiferromagnetic in [DyFe]n and [TbFe]n. For [EuFe]n, [HoFe]n, [ErFe]n, and [TmFe]n, there is no sign of any significant interaction. The magnetic behavior of [DyFe]n suggests the onset of weak long-range ferromagnetic ordering at 2.5 K.

Upconversion luminescence and blackbody radiation in tetragonal YSZ co-doped with Tm(3+) and Yb(3+).

Science.gov (United States)

Soares, M R N; Ferro, M; Costa, F M; Monteiro, T

2015-12-21

Lanthanide doped inorganic nanoparticles with upconversion luminescence are of utmost importance for biomedical applications, solid state lighting and photovoltaics. In this work we studied the downshifted luminescence, upconversion luminescence (UCL) and blackbody radiation of tetragonal yttrium stabilized zirconia co-doped with Tm(3+) and Yb(3+) single crystals and nanoparticles produced by laser floating zone and laser ablation in liquids, respectively. The photoluminescence (PL) and PL excitation (PLE) were investigated at room temperature (RT). PL spectra exhibit the characteristic lines in UV, blue/green, red and NIR regions of the Tm(3+) (4f(12)) under resonant excitation into the high energy (2S+1)LJ multiplets. Under NIR excitation (980 nm), the samples placed in air display an intense NIR at ∼800 nm due to the (1)G4→(3)H5/(3)H4→(3)H6 transitions. Additionally, red, blue/green and ultraviolet UCL is observed arising from higher excited (1)G4 and (1)D2 multiplets. The power excitation dependence of the UCL intensity indicated that 2-3 low energy absorbed photons are involved in the UCL for low power levels, while for high powers, the identified saturation is dependent on the material size with a enhanced effect on the NPs. The temperature dependence of the UCL was investigated for single crystals and targets used in the ablation. An overall increase of the integrated intensity was found to occur between 12 K and the RT. The thermally activated process is described by activation energies of 10 meV and 30 meV for single crystals and targets, respectively. For the NPs, the UCL was found to be strongly sensitive to pressure conditions. Under vacuum conditions, instead of the narrow lines of the Tm(3+), a wide blackbody radiation was detected, responsible for the change in the emission colour from blue to orange. This phenomenon is totally reversible when the NPs are placed at ambient pressure. The UCL/blackbody radiation in the nanosized material exhibits

Electrical resistivity of YbRh{sub 2}Si{sub 2} and EuT{sub 2}Ge{sub 2} (T=Co,Cu) at extreme conditions of pressure and temperature

Energy Technology Data Exchange (ETDEWEB)

Dionicio, G.A.

2006-07-01

This investigation addresses the effect that pressure, p, and temperature, T, have on 4f states of the rare-earth elements in the isostructural YbRh{sub 2}Si{sub 2}, EuCo{sub 2}Ge{sub 2}, and EuCu{sub 2}Ge{sub 2} compounds. Upon applying pressure the volume of the unit cell reduces, enforcing either the enhancement of the hybridization of the 4f localized electrons with the ligand or a change in the valence state of the rare-earth ions. Here, we probe the effect of a pressure-induced lattice contraction on these system by means of electrical-resistivity measurements, {rho}(T), from room temperature down to 100 mK. (orig.)

Strong broad green UV-excited photoluminescence in rare earth (RE = Ce, Eu, Dy, Er, Yb) doped barium zirconate

Energy Technology Data Exchange (ETDEWEB)

Borja-Urby, R. [Grupo de Espectroscopia de Materiales Avanzados y Nanoestructurados (EMANA), Centro de Investigaciones en Optica A. C., Leon, Gto. 37150 (Mexico); Diaz-Torres, L.A., E-mail: ditlacio@cio.mx [Grupo de Espectroscopia de Materiales Avanzados y Nanoestructurados (EMANA), Centro de Investigaciones en Optica A. C., Leon, Gto. 37150 (Mexico); Salas, P. [Centro de Fisica Aplicada y Tecnologia Avanzada, Universidad Nacional Autonoma de Mexico, A.P. 1-1010, Queretaro, Qro. 76000 (Mexico); Angeles-Chavez, C. [Instituto Mexicano del Petroleo, Ciudad de Mexico, D. F. 07730 (Mexico); Meza, O. [Grupo de Espectroscopia de Materiales Avanzados y Nanoestructurados (EMANA), Centro de Investigaciones en Optica A. C., Leon, Gto. 37150 (Mexico)

2011-10-25

Highlights: > Trivalent rare earth (RE) substitution on Zr{sup 4+} sites in BaZrO{sub 3} lead to band gap narrowing. > RE substitution lead to enhanced blue-green intrinsic emission of nanocrystalline BaZrO{sub 3} > Blue-green hue of BaZrO3:RE depends on RE dopant and excitation UV wavelength > BaZrO3: Dy{sup 3+} PL chromatic coordinates correspond to pure white color coordinates of CIE 1931 model - Abstract: The wet synthesis hydrothermal method at 100 deg. C was used to elaborate barium zirconate (BaZrO{sub 3}) unpurified with 0.5 mol% of different rare earth ions (RE = Yb, Er, Dy, Eu, Ce). Morphological, structural and UV-photoluminescence properties depend on the substituted rare earth ionic radii. While the crystalline structure of RE doped BaZrO{sub 3} remains as a cubic perovskite for all substituted RE ions, its band gap changes between 4.65 and 4.93 eV. Under 267 nm excitation the intrinsic green photoluminescence of the as synthesized BaZrO{sub 3}: RE samples is considerably improved by the substitution on RE ions. For 1000 deg. C annealed samples, under 267 nm, the photoluminescence is dominated by the intrinsic BZO emission. It is interesting to notice that Dy{sup 3+}, Er{sup 3+} and Yb{sup 3+} doped samples present whitish emissions that might be useful for white light generation under 267 nm excitation. CIE color coordinates are reported for all samples.

Contribution for study on positron annihilation in tris (dipivaloilmethanates) lanthanides (III)

International Nuclear Information System (INIS)

Ribeiro e Silva, M.E.S.

1988-01-01

Some data on life time of positron and annihilation by Doppler effect in tris (dipivaloilmethanates) lanthanides (III), Ln (dpm) 3 , and Ln = Eu, Gd, Dy, Ho, Er, Tm and Yb are shown. Some results from positronium (Ps) in complexes except Eu (dpm) 3 , chemical aspects and properties of positron and positronium are evaluated. (M.J.C.) [pt

Mixed phosphates of the Na3PO4 - LnPO4 systems

International Nuclear Information System (INIS)

Slivko, T.A.; Smirnova, I.N.; Zimina, G.V.; Spiridonov, F.M.; Chudinova, N.N.

2002-01-01

The phase relationships in the systems Na 3 PO 4 - LnPO 4 (subsolidus 950 Deg C cross-sections), where Ln=Sm, Eu, Tb, Dy, Ho, Tm, Yb, Lu, were studied by X-ray analysis. Reactions of the components were deduced, formed phases were separated and identified. The Na 6 Ln 3 (PO 4 ) 5 (Ln=Dy, Ho, Tm), Na 3 Ln 2 (PO 4 ) 3 (Ln=Tm, Yb, Lu) compounds and phases of the unstable composition Na 6+x Ln 3-x/3 (PO 4 ) 5 (Ln=Yb, Lu, 0 ≤ x ≤ 1.5) were detected for the first time. In all systems the existence of the Na 3-x Ln x/3 PO 4 unstable composition phase on the basis of the high temperature modification of sodium phosphate (sp. gr. Fm3m) is established, suggesting that stabilization of this modification by rare earth ions is possible [ru

Multifunctional Optical Sensors for Nanomanometry and Nanothermometry: High-Pressure and High-Temperature Upconversion Luminescence of Lanthanide-Doped Phosphates-LaPO4/YPO4:Yb3+-Tm3.

Science.gov (United States)

Runowski, Marcin; Shyichuk, Andrii; Tymiński, Artur; Grzyb, Tomasz; Lavín, Víctor; Lis, Stefan

2018-05-23

Upconversion luminescence of nano-sized Yb 3+ and Tm 3+ codoped rare earth phosphates, that is, LaPO 4 and YPO 4 , has been investigated under high-pressure (HP, up to ∼25 GPa) and high-temperature (293-773 K) conditions. The pressure-dependent luminescence properties of the nanocrystals, that is, energy red shift of the band centroids, changes of the band ratios, shortening of upconversion lifetimes, and so forth, make the studied nanomaterials suitable for optical pressure sensing in nanomanometry. Furthermore, thanks to the large energy difference (∼1800 cm -1 ), the thermalized states of Tm 3+ ions are spectrally well-separated, providing high-temperature resolution, required in optical nanothermometry. The temperature of the system containing such active nanomaterials can be determined on the basis of the thermally induced changes of the Tm 3+ band ratio ( 3 F 2,3 → 3 H 6 / 3 H 4 → 3 H 6 ), observed in the emission spectra. The advantage of such upconverting optical sensors is the use of near-infrared light, which is highly penetrable for many materials. The investigated nanomanometers/nanothermometers have been successfully applied, as a proof-of-concept of a novel bimodal optical gauge, for the determination of the temperature of the heated system (473 K), which was simultaneously compressed under HP (1.5 and 5 GPa).

Laser-diode-excited blue upconversion in Tm3+/Yb3+ -codoped TeO2-Ga2O3-R2O (R=Li, Na, K) glasses.

Science.gov (United States)

Zhao, Chun; Zhang, Qinyuan; Yang, Gangfeng; Jiang, Zhonghong

2008-01-01

This paper reports on intense blue upconversion in Tm(3+)/Yb(3+) codoped TeO(2)-Ga(2)O(3)-R(2)O(R=Li, Na, K) glasses upon excitation with commercial available laser diode (LD). Effects of alkali ions on the Raman spectra, thermal stability and spectroscopic properties of the tellurite-gallium glasses have also been investigated. Energy transfer and the involved upconversion mechanisms have been discussed. Intense blue upconversion emission centered at 476 nm along with a weak red emission at 650 nm has been observed upon excitation of 977 nm LD, assigned to the transitions of 1G4-->3H6, and 1G4-->3H4 and/or 3F(2,3)-->3H6 of Tm(3+), respectively. The blue upconversion intensity has a cubelike dependence on incident pump laser power, indicating a three-photon process. However, a quadratic dependence of the 476 nm upconversion intensity on the incident pump laser power has been observed when samples under excitation of 808 nm LD due to a two-photon absorption process. Enhanced upconversion luminescence have been observed with replacing K(+) for Na(+) and Li(+).

Structure, photo- and triboluminescence of the lanthanoid dibenzoylmethanates: HNEt3[Ln(dbm)4

International Nuclear Information System (INIS)

Akerboom, Sebastiaan; Meijer, Michael S.; Siegler, Maxime A.; Fu, Wen Tian; Bouwman, Elisabeth

2014-01-01

A series of lanthanoid coordination compounds with the general formula HNEt 3 [Ln(dbm) 4 ] (Ln=La, Nd, Sm, Eu, Tb, Dy, Ho, Er, Tm, and Yb; dbm=dibenzoylmethanate) has been prepared and characterized. In addition, single crystals with Ln=La, Nd and Sm were obtained. Single crystal X-ray diffraction studies reveal that the compounds with Ln=La and Nd crystallize in the P2 1 /c space group, while the Sm-compound crystallizes in the Pc space group. Based on powder XRD data, the compounds with Ln=Eu–Yb can be described with a monoclinic cell. Photoluminescence studies indicate that compounds with Ln=Sm and Eu exhibit bright photoluminescence characteristic of the lanthanoid ion upon excitation in the near UV range. Furthermore, HNEt 3 [Sm(dbm) 4 ] has been identified as a novel triboluminescent compound. -- Highlights: • The compounds HNEt 3 [Ln(dbm) 4 ], Ln=La, Nd, Sm, Eu, Tb, Dy, Ho Er, Tm, and Yb, have been prepared and their photophysical properties have been studied. • Crystal structures of HNEt 3 [La(dbm) 4 ], HNEt 3 [Nd(dbm) 4 ] and HNEt 3 [Sm(dbm) 4 ] are reported for the first time. • A novel, brightly triboluminescent Sm compound is reported

Raman and Fluorescence Spectroscopy of CeO2, Er2O3, Nd2O3, Tm2O3, Yb2O3, La2O3, and Tb4O7

Directory of Open Access Journals (Sweden)

Jianlan Cui

2015-01-01

Full Text Available To better understand and ascertain the mechanisms of flotation reagent interaction with rare earth (RE minerals, it is necessary to determine the physical and chemical properties of the constituent components. Seven rare earth oxides (CeO2, Er2O3, Nd2O3, Tm2O3, Yb2O3, La2O3, and Tb4O7 that cover the rare earth elements (REEs from light to heavy REEs have been investigated using Raman spectroscopy. Multiple laser sources (wavelengths of 325 nm, 442 nm, 514 nm, and 632.8 nm for the Raman shift ranges from 100 cm−1 to 5000 cm−1 of these excitations were used for each individual rare earth oxide. Raman shifts and fluorescence emission have been identified. Theoretical energy levels for Er, Nd, and Yb were used for the interpretation of fluorescence emission. The experimental results showed good agreement with the theoretical calculation for Er2O3 and Nd2O3. Additional fluorescence emission was observed with Yb2O3 that did not fit the reported energy level diagram. Tb4O7 was observed undergoing laser induced changes during examination.

Lifetimes Measurements in 160Yb,162Yb,164Yb,166Yb,168Yb

International Nuclear Information System (INIS)

Araddad, S. Y.; El-barouni, A. M.; Rateb, G. M.; Mosbah, D. S.; Elahrash, M. S.; Sergiwa, S. M.

2004-01-01

From our measurements of the lifetimes of high spin states in 168 Yb along with the published lifetime data for the nearby even even ytterbium isotopes, 160-168 Yb using the Recoil Distance Method (RDM) and the Doppler Shift Attenuation Method (DSAM) present a great opportunity to probe systematically the relationship between the nuclear shape changes and the reduction in collectivity. (authors)

Color tunability in green, red and infra-red upconversion emission in Tm{sup 3+}/Yb{sup 3+}/Ho{sup 3+} co-doped CeO{sub 2} with potential application for improvement of efficiency in solar cells

Energy Technology Data Exchange (ETDEWEB)

Carvalho, Luiz G.A.; Rocha, Leonardo A.; Buarque, Juliana M.M. [Laboratório de Materiais Inorgânicos Fotoluminescentes e Polímeros Biodegradáveis (LAFOP), Grupo de Pesquisa em Química de Materiais – (GPQM), Departamento de Ciências Naturais, Universidade Federal de São João Del Rei, Campus Dom Bosco, Praça Dom Helvécio, 74, 36301-160 São João Del Rei, MG (Brazil); Gonçalves, Rogéria Rocha [Departamento de Química, Faculdade de Filosofia, Ciências e Letras de Ribeirão Preto, USP, Av. Bandeirantes, 3900, 14040-901 Ribeirão Preto, SP (Brazil); Nascimento Jr, Clébio S. [Laboratório de Química Teórica e Computacional – (LQTC), Departamento de Ciências Naturais, Universidade Federal de São João del-Rei, Campus Dom Bosco, Praça Dom Helvécio, 74, 36301-160 São João del-Rei, MG (Brazil); and others

2015-03-15

The preparation of Tm{sup 3+}/Yb{sup 3+}/Ho{sup 3+} co-doped CeO{sub 2} prepared by the precipitation method using ammonium hydroxide as a precursor is presented. By X-ray diffraction the materials show the phase-type of fluorite structure and the crystallite sizes were calculated by the Scherrer's equation. No other phase was observed evincing that the rare earth ions were inserted into the fluorite phase as substitutional or interstitial dopants. The microstrain calculated by the Williamson–Hall method do not show significant changes in their values, indicating that the inclusion of rare earths does not causes structural changes in the CeO{sub 2} used as a host matrix. All material showed intense upconversion emission at red and green region under excitation with diode laser at 980 nm. The color of emission changes from green to red with increasing excitation power pump. The materials showed suitable photoluminescent properties for applications as a laser source, solar cells, and great emitter at 800 nm. - Highlights: • Tm{sup 3+}/Yb{sup 3+}/Ho{sup 3+} co-doped CeO{sub 2} prepared by the simple way. • Intense upconversion emission regions and the tunability of emission color by the laser power pump. • The materials showed suitable photoluminescent properties for different applications.

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).

Near infrared emission of TbAG:Ce{sup 3+},Yb{sup 3+} phosphor for solar cell applications

Energy Technology Data Exchange (ETDEWEB)

Meshram, N. D., E-mail: meshramnileshsd@gmail.com [Shri. Mathuradas Mohota College of Science, Sakkardara Square, Nagpur-440009 (India); Yadav, P. J., E-mail: yadav.pooja75@yahoo.in [Department of Electronics, Nagpur University campus, Nagpur-440010 (India); Pathak, A. A., E-mail: aapathak@yahoo.com [National power Training Institute, South ambazari road, Nagpur-440022 (India); Joshi, C. P., E-mail: charusheela-4253@yahoo.co.in [Ramdeobaba College of Engineering and Management, Katol road, Gittikhadan Nagpur-440012 (India); Moharil, S. V., E-mail: svmoharil@yahoo.com [Department of Physics, Nagpur University campus, Nagpur-440010 (India)

2016-05-06

Luminescent materials doped with rare earth ions are used for many devices such as optical amplifiers in telecommunication, phosphors for white light emitting diodes (LEDs), displays, and so on. Recently, they also have attracted a great interest for photovoltaic applications to improve solar cell efficiency by modifying solar spectrum. Crystal silicon (c-Si) solar cells most effectively convert photons of energy close to the semiconductor band gap. The mis-match between the incident solar spectrum and the spectral response of solar cells is one of the main reasons to limit the cell efficiency. The efficiency limit of the c-Si has been estimated to be 29% by Shockley and Queisser. However, this limit is estimated to be improved up to 38.4% by modifying the solar spectrum by a quantum cutting (down converting) phosphor which converts one photon of high energy into two photons of lower energy. The phenomenon such as the quantum cutting or the down conversion of rare earth ions have been investigated since Dexter reported the possibility of a luminescent quantum yield greater than unity in 1957. In the past, the quantum cutting from a vacuum ultraviolet photon to visible photons for Pr{sup 3+}, Gd{sup 3+},Gd{sup 3+}–Eu{sup 3+}, and Er{sup 3+}–Tb{sup 3+} had been studied. Recently, a new quantum cutting phenomenon from visible photon shorter than 500 nm to two infrared photons for Tb{sup 3+}–Yb{sup 3+}, Pr{sup 3+}–Yb{sup 3+}, and Tm{sup 3+}–Yb{sup 3+} has been reported. The Yb{sup 3+} ion is suitable as an acceptor and emitter because luminescent quantum efficiency of Yb{sup 3+} is close to 100% and the energy of the only excited level of Yb{sup 3+} (1.2 eV) is roughly in accordance with the band gap of Si (1.1 eV). In addition, the Ce{sup 3+}-doped Tb{sub 3}Al{sub 5}O{sub 12} (TbAG), used as a phosphor for white LED, has broad absorption bands in the range of 300–500 nm due to strong ligand field and high luminescent quantum efficiency. Therefore, the

Effect of mixing RE elements (Nd, Sm, Gd, Eu, Y, Yb) on the RE2BaCuO5/Nd4-2xBa2+2xCu2-xO10-2x phases in RE cuprate high-Tc superconductors

International Nuclear Information System (INIS)

Langhorn, J.B.; Black, M.A.; McGinn, P.J.

1999-01-01

The phases RE 2 BaCuO 5 /RE 4 Ba 2 Cu 2 O 10 phases (where RE is a mixture of Nd, Sm, Gd, Eu, Y and Yb) have been synthesized in an oxygen atmosphere and subsequently characterized. The mixing of RE elements which inherently form the RE 2 BaCuO 5 phase through the peritectic decomposition of REBa 2 Cu 3 O 7-x (RE123) (i.e. Sm, Gd, Eu, Y, Yb), was observed to give homogeneous mixing of the elements in the 211 phase. In contrast it was found that on mixing Nd with other RE elements a mixture of the Nd 4-2x Ba 2+2x Cu 2-x O 10-2x (Nd422) and RE 2 BaCuO 5 (RE211) phases resulted. It was also observed that on mixing Nd with other REs a finite amount of the RE is substituted into the Nd422 phase and Nd into the RE211. (author)

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.

Structural and Magnetothermal Properties of Compounds: Yb₅Si_xGe_4-x,Sm₅Si_xGe_4-x, EuO, and Eu₃O₄

Energy Technology Data Exchange (ETDEWEB)

Ahn, Kyunghan [Iowa State Univ., Ames, IA (United States)

2007-01-01

The family of R₅Si_xGe_4-x alloys demonstrates a variety of unique physical phenomena related to magneto-structural transitions associated with reversible breaking and reforming of specific bonds that can be controlled by numerous external parameters such as chemical composition, magnetic field, temperature, and pressure. Therefore, R₅Si_xGe_4-x systems have been extensively studied to uncover the mechanism of the extraordinary magneto-responsive properties including the giant magnetoresistance (GMR) and colossal magnetostriction, as well as giant magnetocaloric effect (GMCE). Until now, more than a half of possible R₅Si_xGe_4-x pseudobinary systems have been completely or partially investigated with respect to their crystallography and phase relationships (R = La, Pr, Nd, Gd, Tb, Dy, Er, Lu, Y). Still, there are other R₅Si_xGe_4-x systems (R = Ce, Sm, Ho, Tm, and Yb) that are not studied yet. Here, we report on phase relationships and structural, magnetic, and thermodynamic properties in the Yb₅Si_xGe_4-xand Sm₅Si_xGe_4-x pseudobinary systems, which may exhibit mixed valence states. The crystallography, phase relationships, and physical properties of Yb₅Si_xGe_4-x alloys with 0 ≤ x ≤ 4 have been examined by using single crystal and powder x-ray diffraction at room temperature, and dc magnetization and heat capacity measurements between 1.8 K and 400 K in magnetic fields ranging from 0 to 7 T. Unlike the majority of R₅Si_xGe_4-x systems studied to date, where R is the rare earth metal, all Yb-based germanide-silicides with the 5:4 stoichiometry crystallize in the same Gd₅Si₄-type structure. The magnetic properties of Yb₅Si_xGe_4-x materials are nearly composition

Spectroscopy and energy level location of the trivalent lanthanides in LiYP4O12

International Nuclear Information System (INIS)

Dorenbos, P.; Shalapska, T.; Stryganyuk, G.; Gektin, A.; Voloshinovskii, A.

2011-01-01

The excitation and emission properties of the lanthanides Ce 3+ , Pr 3+ , Nd 3+ , Sm 3+ , Eu 3+ , Tb 3+ , Er 3+ , Tm 3+ , and Yb 3+ in LiYP 4 O 12 were studied by vacuum ultra-violet spectroscopy at 10 K. It provides information on the energies of 4f-5d excitation and emission bands. In the case of Er 3+ spin forbidden emission was observed. Charge transfer excitation bands were identified for Eu 3+ , Sm 3+ , Tm 3+ , and Yb 3+ , and in the case of Yb 3+ charge transfer luminescence is observed. All data appear to be consistent with each other and have been used to construct a level scheme showing the location of the energy levels of all trivalent and divalent lanthanides in LiYP 4 O 12 . - Research Highlights: → The spectroscopy of most of the trivalent lanthanides in LiYP 4 O 12 is presented for the first time. → Charge transfer luminescence of Yb3+ is reported. → We demonstrate that the energy of the first 4f-5d transition and the charge transfer band agree with predictive models. → For the first time a scheme with the location of all lanthanide states (divalent and trivalent ) w.r.t. de-valence and conduction band of LIP 4 O 12 is presented.

Luminescence properties of Tm3+ ions single-doped YF3 materials in an unconventional excitation region.

Science.gov (United States)

Chen, Yuan; Liu, Qing; Lin, Han; Yan, Xiaohong

2018-05-01

According to the spectral distribution of solar radiation at the earth's surface, under the excitation region of 1150 to 1350 nm, the up-conversion luminescence of Tm 3+ ions was investigated. The emission bands were matched well with the spectral response region of silicon solar cells, achieved by Tm 3+ ions single-doped yttrium fluoride (YF 3 ) phosphor, which was different from the conventional Tm 3+ /Yb 3+ ion couple co-doped materials. Additionally, the similar emission bands of Tm 3+ ions were achieved under excitation in the ultraviolet region. It is expected that via up-conversion and down-conversion routes, Tm 3+ -sensitized materials could convert photons to the desired wavelengths in order to reduce the energy loss of silicon solar cells, thereby enhancing the photovoltaic efficiency. Copyright © 2018 John Wiley & Sons, Ltd.

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

Evaluating the performance of the ORTECR DetectiveTM for emergency urine bioassay

International Nuclear Information System (INIS)

Li, C.; Ko, R.; Moodie, G.; Kramer, G. H.

2011-01-01

The performance of the ORTEC R Detective TM as a field deployable tool for emergency urine bioassay of 137 Cs, 60 Co, 192 Ir, 169 Yb and 75 Se was evaluated against ANSI N13.30. The tested activity levels represent 10 % RL (reference level) and 1 % RL defined by [Li C., Vlahovich S., Dai X., Richardson R. B., Daka J. N. and Kramer G. H. Requirements for radiation emergency urine bioassay techniques for the public and first responders. Health Phys (in press, 99(5), 702-707 (2010)]. The tests were conducted for both single radionuclide and mixed radionuclides at two geometries, one conventional geometry (CG) and one improved geometry (IG) which improved the MDAs (minimum detectable amounts) by a factor of 1.6-2.7. The most challenging radionuclide was 169 Yb. The measurement of the mixture radionuclides for 169 Yb at the CG did not satisfy the ANSI N13.30 requirements even at 10 % RL. At 1 % RL, 169 Yb and 192 Ir were not detectable at either geometry, while the measurement of 60 Co in the mixed radionuclides satisfied the ANSI N13.30 requirements only at the IG. (authors)

Cooperative emission in ion implanted Yb:YAG waveguides

Energy Technology Data Exchange (ETDEWEB)

Vazquez, G V; Desirena, H; De la Rosa, E [Centro de Investigaciones en Optica, Loma del Bosque 115, Lomas del Campestre, 37150 Leon, Guanajuato (Mexico); Flores-Romero, E; Rickards, J; Trejo-Luna, R [Instituto de Fisica, UNAM, Apartado Postal 20364, 01000 Mexico, D. F. (Mexico); Marquez, H, E-mail: gvvazquez@cio.mx [Departamento de Optica, CICESE, Km 107 Carr. Tijuana-Ensenada, 22860 Ensenada, B. C. (Mexico)

2011-01-01

In this work, we report the analysis of spectroscopic properties of waveguides fabricated by ion implantation in YAG doped with Yb{sup 3+} ions. Three emission bands were detected in the blue, green and red regions under 970-nm excitation. The strong blue-green emission can be explained by a cooperative process between ytterbium ion pairs, leading to emission centered at 514 nm. The additional blue bands as well as green and red emission bands are attributed to the presence of Tm{sup 3+} and Er{sup 3+} traces. The results include absorption and emission curves as well as decay time rates.

Cooperative emission in ion implanted Yb:YAG waveguides

International Nuclear Information System (INIS)

Vazquez, G V; Desirena, H; De la Rosa, E; Flores-Romero, E; Rickards, J; Trejo-Luna, R; Marquez, H

2011-01-01

In this work, we report the analysis of spectroscopic properties of waveguides fabricated by ion implantation in YAG doped with Yb 3+ ions. Three emission bands were detected in the blue, green and red regions under 970-nm excitation. The strong blue-green emission can be explained by a cooperative process between ytterbium ion pairs, leading to emission centered at 514 nm. The additional blue bands as well as green and red emission bands are attributed to the presence of Tm 3+ and Er 3+ traces. The results include absorption and emission curves as well as decay time rates.

Hydrothermal synthesis, characterization and up/down-conversion luminescence of barium rare earth fluoride nanocrystals

International Nuclear Information System (INIS)

Jia, Li-Ping; Zhang, Qiang; Yan, Bing

2014-01-01

Graphical abstract: Lanthanide ions doped bare earth rare earth fluoride nanocrystals are synthesized by hydrothermal technology and characterized. The down/up-conversion luminescence of them are discussed. - Highlights: • Mixed hydrothermal system H 2 O–OA (EDA)–O-A(LO-A) is used for synthesis. • Barium rare earth fluoride nanocrystals are synthesized comprehensively. • Luminescence for down-conversion and up-conversion are obtained for these systems. - Abstract: Mixed hydrothermal system H 2 O–OA (EDA)–O-A(LO-A) is developed to synthesize barium rare earth fluorides nanocrystals (OA = oleylamine, EDA = ethylenediamine, O-A = oleic acid and LO-A = linoleic acid). They are presented as BaREF 5 (RE = Ce, Pr, Nd, Eu, Gd, Tb, Dy, Y, Tm, Lu) and Ba 2 REF 7 (RE = La, Sm, Ho, Er, Yb). The influence of reaction parameters (rare earth species, hydrothermal system and temperature) is checked on the phase and shape evolution of the fluoride nanocrystals. It is found that reaction time and temperature of these nanocrystals using EDA (180 °C, 6 h) is lower than those of them using OA (220 °C, 10 h). The photoluminescence properties of these fluorides activated by some rare earth ions (Nd 3+ , Eu 3+ , Tb 3+ ) are studied, and especially up-conversion luminescence of the four fluoride nanocrystal systems (Ba 2 LaF 7 :Yb, Tm(Er), Ba 2 REF 7 :Yb, Tm(Er) (RE = Gd, Y, Lu)) is observed

Absorption Spectra Of Rbcl:Yb Rbbr:Yb And Rbi:Yb Crystals ...

African Journals Online (AJOL)

Single crystals of rubidium chloride, bromide and iodide were doped with substitutional divalent ytterbium, Yb ions, by heating them in ytterbium atmosphere. The absorption spectra of the Yb doped crystals were measured at room and liquid nitrogen temperatures. The spectra were found to consist of intense broad ...

TmDOTA-tetraglycinate encapsulated liposomes as pH-sensitive LipoCEST agents.

Directory of Open Access Journals (Sweden)

Ana Christina L Opina

Full Text Available Lanthanide DOTA-tetraglycinate (LnDOTA-(gly₄⁻ complexes contain four magnetically equivalent amide protons that exchange with protons of bulk water. The rate of this base catalyzed exchange process has been measured using chemical exchange saturation transfer (CEST NMR techniques as a function of solution pH for various paramagnetic LnDOTA-(gly₄⁻ complexes to evaluate the effects of lanthanide ion size on this process. Complexes with Tb(III, Dy(III, Tm(III and Yb(III were chosen because these ions induce large hyperfine shifts in all ligand protons, including the exchanging amide protons. The magnitude of the amide proton CEST exchange signal differed for the four paramagnetic complexes in order, Yb>Tm>Tb>Dy. Although the Dy(III complex showed the largest hyperfine shift as expected, the combination of favorable chemical shift and amide proton CEST linewidth in the Tm(III complex was deemed most favorable for future in vivo applications where tissue magnetization effects can interfere. TmDOTA-(gly₄⁻ at various concentrations was encapsulated in the core interior of liposomes to yield lipoCEST particles for molecular imaging. The resulting nanoparticles showed less than 1% leakage of the agent from the interior over a range of temperatures and pH. The pH versus amide proton CEST curves differed for the free versus encapsulated agents over the acidic pH regions, consistent with a lower proton permeability across the liposomal bilayer for the encapsulated agent. Nevertheless, the resulting lipoCEST nanoparticles amplify the CEST sensitivity by a factor of ∼10⁴ compared to the free, un-encapsulated agent. Such pH sensitive nano-probes could prove useful for pH mapping of liposomes targeted to tumors.

A near-infrared luminescent Mn2+-doped NaYF4:Yb,Tm/Fe3+ upconversion nanoparticles redox reaction system for the detection of GSH/Cys/AA.

Science.gov (United States)

Zhang, Liping; Ling, Bo; Wang, Lun; Chen, Hongqi

2017-09-01

An upconversion luminescence method was developed for the determination of glutathione (GSH), L-cysteine (Cys) or L-ascorbic acid (AA) based on redox reaction. We synthesized poly(acrylic acid) (PAA)-modified Mn 2+ -doped NaYF 4 :Yb,Tm upconversion nanoparticles (UCNPs), and the luminescence of these UCNPs was effectively quenched due to their carboxyl groups coordinating with Fe 3+ to form a UCNPs/Fe 3+ system. GSH, Cys or AA reduced Fe 3+ to Fe 2+ , which induced the luminescence recovery of the UCNPs. Under the optimized conditions, wide linear concentration ranges from 0.25-300μM for GSH, 0.5-875μM for Cys and 0.5-350μM for AA were found, and the detection limits (3S/K) were 0.2μM, 0.5μM and 0.2μM, respectively. Thus, the UCNPs/Fe 3+ system was successfully applied for sensing GSH, Cys or AA. Copyright © 2017 Elsevier B.V. All rights reserved.

Yb valence state in Yb{sub 5}Rh{sub 4}Ge{sub 10}

Energy Technology Data Exchange (ETDEWEB)

Sato, Hitoshi; Arita, Masashi; Shimada, Kenya; Namatame, Hirofumi; Taniguchi, Masaki [Hiroshima Synchrotron Radiation Center, Hiroshima University, Higashi-Hiroshima (Japan); Utsumi, Yuki [Synchrotron SOLEIL, L' Orme des Merisiers, Gif-sur-Yvette (France); Katoh, Kenichi [Department of Applied Physics, National Defense Academy, Yokosuka (Japan); Mimura, Kojiro [Graduate School of Engineering, Osaka Prefecture University, Sakai (Japan); Ueda, Shigenori [Synchrotron X-ray Station at SPring-8, National Institute for Materials Science, Hyogo (Japan); Quantum Beam Unit, National Institute for Materials Science, Tsukuba (Japan); Yamaoka, Hitoshi [RIKEN SPring-8 Center, Hyogo (Japan); Rousuli, Awabaikeli [Graduate School of Science, Hiroshima University, Higashi-Hiroshima (Japan); Umeo, Kazunori [NBARD, Hiroshima University, Higashi-Hiroshima (Japan)

2017-06-15

Temperature- and pressure-dependent Yb valence state in Yb{sub 5}Rh{sub 4}Ge{sub 10} has been investigated by means of Yb 3d hard X-ray photoemission spectroscopy (HAXPES) and Yb L{sub 3} absorption spectroscopy (XAS). The mean Yb valence derived from the Yb 3d HAXPES is estimated to be ∝2.78 at 300 K and decreases to ∝2.74 at 20 K. On the other hand, the Yb valence deduced from the Yb L{sub 3} XAS at 300 K is almost constant with ∝2.81 in the pressure range between 9.2 and 34.7 GPa. (copyright 2017 WILEY-VCH Verlag GmbH and Co. KGaA, Weinheim)

Stability field diagrams for Ln–O–Cl systems

Indian Academy of Sciences (India)

at 1000 K. All the lanthanide elements form stable LnCl3 and LnOCl. Dichlorides of Nd, Sm, Eu, Dy, Tm and Yb ... tion of lanthanide elements from oxide ores involves carbo- chlorination [4], although other chlorinating ... versa. The purpose of this communication is to gather data on. LnOCl compounds, estimate missing ...

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

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%

Spectral shapes and a beta-gamma directional correlation in the beta decay of 172Tm (Jpi = 2-)

DEFF Research Database (Denmark)

Gregers Hansen, P.; Loft Nielsen, H.; Wilsky, K.

1966-01-01

The isotope 172Tm populates the 0+, 2+ and 4+ states of the 172Yb ground-state rotational band directly in beta decay. The shapes and intensities of the three beta groups have been measured by means of a six-gap magnetic spectrometer operated in coincidence with a Nal(Tl) crystal. The experimenta...

Nuclear Data Sheets for A=164

Science.gov (United States)

Singh, Balraj; Chen, Jun

2018-01-01

Experimental nuclear structure data for the known A=164 isobaric nuclides (Sm, Eu, Gd, Tb, Dy, Ho, Er, Tm, Yb, Lu, Hf, Ta, W, Re, Os, Ir) have been evaluated, and presented together with Adopted properties of level energies, and associated γ rays. The decay data for these nuclides have also been evaluated, providing Adopted values of γ and β radiations, and log ft values. No excited states are known in 164Eu, 164Tb, and 164Ir. Information for 164Gd, 164Re and 164Os is limited due to insufficient experimental data. For radioactive nuclides, decay schemes of 164Sm, 164Gd and 164Re are not known, and those of 164W, 164Tb, 164Lu, 164Hf, 164Ta and 164W are incomplete. The decay schemes of 164Ho and the two activities of 164Tm seem fairly complete. The decay scheme of 164Yb presents a major problem that the Q(ε) value of 887 keV 29 recommended in 2017Wa10 is in disagreement with the population of levels at 928, 952 and 1060 keV in the daughter nucleus. This decay scheme, which so far has been mainly reported in a secondary reference (1982AdZZ) needs further investigation. Also the masses of 164Yb and 164Tm need either new measurements or a re-evaluation to resolve discrepancy of about 220 keV in the Q value of 164Yb decay to 164Tm. The reactions and decays for which no new experimental information has become available since the 2001 update have undergone revisions to incorporate conversion coefficients from BrIcc code, and evaluated Q values from 2017Wa10, but the essential content of such datasets may have remained the same as in previous evaluations. In this respect the present work greatly benefited from all the previous NDS evaluations (2001Si27,1992Sh07, 1986Sh03,1974Bu30), but at the same time data presented herein supersede all the previous published evaluations.

Synthesis of Halide- and Solvent free metal borohydrides

DEFF Research Database (Denmark)

Grinderslev, Jakob; Møller, Kasper Trans; Jensen, Torben René

chloride or LiBH4 is present in the sample. The synthesis pathway has been shown to work for most of the already known metal borohydrides, M = Na, Ca, Sr, Ba, Y, La, Eu, Gd, Tb, Dy, Ho, Er, Tm, and Yb, but also new borohydrides are formed, M = Pr, Nd and Lu. Besides new compounds, new polymorphs...

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.

Double NIR laser stimulation and enhancing the thermal sensitivity of Er3+/Tm3+/Nd3+ doped multilayer core-shell nanoparticles.

Science.gov (United States)

Ba, Zhaojing; Hu, Min; Zhao, Yiming; Wang, Yiqing; Wang, Jing; Zhang, Zhenxi

2018-06-04

Non-contact thermal sensors are important devices to study cellular processes and monitor temperature in vivo. Herein, a novel highly sensitive nanothermometer based on NaYF4:Yb,Er@ NaYF4@NaYF4:Yb,Tm@ NaYF4:Nd (denoted as Er@Y@Tm@Nd) was prepared by a facile solvothermal method. When excited by the NIR light of 808 and 980 nm, the as-prepared Er@Y@Tm@Nd nanoparticles could emit both blue and green light respectively, since the lanthanide cations responsible for these emissions are gathered inside this nanostructure. The green and blue light intensity ratio exhibits obvious temperature dependence in the range of the physiological temperature. Additionally, the fluorescence intensity of Er3+ and Tm3+ are also greatly enhanced due to the multilayer structure that implies avoiding the Er3+ and Tm3+ energy cross-relaxation by introduction of a NaYF4 wall between them. The as-prepared core-shell-shell-shell structure with Er3+ and Tm3+ in different layers improves dozens of times of the thermal sensitivity based on the non-thermal coupling levels of the probe: the maximum values for the sensitivity are 2.95% K-1 (IEr-521/ITm-450) and 6.30% K-1 (ITm-474/IEr-541) when excited by 980 and 808 nm laser sources respectively. These values are well above those previously reported (< 0.7% K-1), indicating that the prepared nanostructures are temperature sensors with excellent thermal sensitivity and sensitive to NIR wavelength excitation that makes them highly preferred for thermal detection. © 2018 IOP Publishing Ltd.

Physical properties of superbulky lanthanide metallocenes: synthesis and extraordinary luminescence of [Eu(II)(Cp(BIG))2] (Cp(BIG) = (4-nBu-C6H4)5-cyclopentadienyl).

Science.gov (United States)

Harder, Sjoerd; Naglav, Dominik; Ruspic, Christian; Wickleder, Claudia; Adlung, Matthias; Hermes, Wilfried; Eul, Matthias; Pöttgen, Rainer; Rego, Daniel B; Poineau, Frederic; Czerwinski, Kenneth R; Herber, Rolfe H; Nowik, Israel

2013-09-09

The superbulky deca-aryleuropocene [Eu(Cp(BIG))2], Cp(BIG) = (4-nBu-C6H4)5-cyclopentadienyl, was prepared by reaction of [Eu(dmat)2(thf)2], DMAT = 2-Me2N-α-Me3Si-benzyl, with two equivalents of Cp(BIG)H. Recrystallizyation from cold hexane gave the product with a surprisingly bright and efficient orange emission (45% quantum yield). The crystal structure is isomorphic to those of [M(Cp(BIG))2] (M = Sm, Yb, Ca, Ba) and shows the typical distortions that arise from Cp(BIG)⋅⋅⋅Cp(BIG) attraction as well as excessively large displacement parameter for the heavy Eu atom (U(eq) = 0.075). In order to gain information on the true oxidation state of the central metal in superbulky metallocenes [M(Cp(BIG))2] (M = Sm, Eu, Yb), several physical analyses have been applied. Temperature-dependent magnetic susceptibility data of [Yb(Cp(BIG))2] show diamagnetism, indicating stable divalent ytterbium. Temperature-dependent (151)Eu Mössbauer effect spectroscopic examination of [Eu(Cp(BIG))2] was examined over the temperature range 93-215 K and the hyperfine and dynamical properties of the Eu(II) species are discussed in detail. The mean square amplitude of vibration of the Eu atom as a function of temperature was determined and compared to the value extracted from the single-crystal X-ray data at 203 K. The large difference in these two values was ascribed to the presence of static disorder and/or the presence of low-frequency torsional and librational modes in [Eu(Cp(BIG))2]. X-ray absorbance near edge spectroscopy (XANES) showed that all three [Ln(Cp(BIG))2] (Ln = Sm, Eu, Yb) compounds are divalent. The XANES white-line spectra are at 8.3, 7.3, and 7.8 eV, for Sm, Eu, and Yb, respectively, lower than the Ln2O3 standards. No XANES temperature dependence was found from room temperature to 100 K. XANES also showed that the [Ln(Cp(BIG))2] complexes had less trivalent impurity than a [EuI2(thf)x] standard. The complex [Eu(Cp(BIG))2] shows already at room temperature

Preparation and spectroscopic properties of Yb-doped and Yb-Al-codoped high silica glasses

International Nuclear Information System (INIS)

Qiao Yanbo; Wen Lei; Wu Botao; Ren Jinjun; Chen Danping; Qiu Jianrong

2008-01-01

Yb-doped and Yb-Al-codoped high silica glasses have been prepared by sintering nanoporous glasses. The absorption, fluorescent spectra and fluorescent lifetimes have been measured and the emission cross-section and minimum pump intensities were calculated. Codoping aluminum ions enhanced the fluorescence intensity of Yb-doped high silica glass obviously. The emission cross-sections of Yb-doped and Yb-Al-codoped high silica glasses were 0.65 and 0.82 pm 2 , respectively. The results show that Yb-Al-codoped high silica glass has better spectroscopic properties for a laser material. The study of high silica glass doped with ytterbium is helpful for its application in Yb laser systems, especially for high-power and high-repetition lasers

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

tmRDB (tmRNA database)

DEFF Research Database (Denmark)

Zwieb, Christian; Gorodkin, Jan; Knudsen, Bjarne

2003-01-01

Maintained at the University of Texas Health Science Center at Tyler, Texas, the tmRNA database (tmRDB) is accessible at the URL http://psyche.uthct.edu/dbs/tmRDB/tmRDB.html with mirror sites located at Auburn University, Auburn, Alabama (http://www.ag.auburn.edu/mirror/tmRDB/) and the Bioinforma......Maintained at the University of Texas Health Science Center at Tyler, Texas, the tmRNA database (tmRDB) is accessible at the URL http://psyche.uthct.edu/dbs/tmRDB/tmRDB.html with mirror sites located at Auburn University, Auburn, Alabama (http......://www.ag.auburn.edu/mirror/tmRDB/) and the Bioinformatics Research Center, Aarhus, Denmark (http://www.bioinf.au.dk/tmRDB/). The tmRDB collects and distributes information relevant to the study of tmRNA. In trans-translation, this molecule combines properties of tRNA and mRNA and binds several proteins to form the tmRNP. Related RNPs are likely...

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 ...

Energy levels, oscillator strengths, line strengths, and transition probabilities in Si-like ions of La XLIII, Er LIV, Tm LV, and Yb LVI

Energy Technology Data Exchange (ETDEWEB)

Chen, Zhan-Bin, E-mail: chenzb008@qq.com [College of Science, National University of Defense Technology, Changsha, Hunan 410073 (China); Ma, Kun [School of Information Engineering, Huangshan University, Huangshan 245041 (China); Wang, Hong-Jian [Chongqing Key Laboratory for Design and Control of Manufacturing Equipment, Chongqing Technology and Business University, Chongqing 40067 (China); Wang, Kai, E-mail: wangkai@hbu.edu.cn [Hebei Key Lab of Optic-electronic Information and Materials, The College of Physics Science and Technology, Hebei University, Baoding 071002 (China); Liu, Xiao-Bin [Department of Physics, Tianshui Normal University, Tianshui 741001 (China); Zeng, Jiao-Long [College of Science, National University of Defense Technology, Changsha, Hunan 410073 (China)

2017-01-15

Detailed calculations using the multi-configuration Dirac–Fock (MCDF) method are carried out for the lowest 64 fine-structure levels of the 3s{sup 2}3p{sup 2}, 3s{sup 2}3p3d, 3s3p{sup 3}, 3s3p{sup 2}3d, 3s{sup 2}3d{sup 2}, and 3p{sup 4} configurations in Si-like ions of La XLIII, Er LIV, Tm LV, and Yb LVI. Energies, oscillator strengths, wavelengths, line strengths, and radiative electric dipole transition rates are given for all ions. A parallel calculation using the many-body perturbation theory (MBPT) method is also carried out to assess the present energy levels accuracy. Comparisons are performed between these two sets of energy levels, as well as with other available results, showing that they are in good agreement with each other within 0.5%. These high accuracy results can be used to the modeling and the interpretation of astrophysical objects and fusion plasmas. - Highlights: • Energy levels and E1 transition rates of Si-like ions are presented. • Breit interaction and Quantum Electrodynamics effects are discussed. • Present results should be useful in the astrophysical application and plasma modeling.

Electronic Spectra of Cs2NaYb(NO2)6: Is There Quantum Cutting?

Science.gov (United States)

Luo, Yuxia; Liu, Zhenyu; Hau, Sam Chun-Kit; Yeung, Yau Yuen; Wong, Ka-Leung; Shiu, Kwok Keung; Chen, Xueyuan; Zhu, Haomiao; Bao, Guochen; Tanner, Peter A

2018-05-03

The crystal structure and electronic spectra of the T h symmetry hexanitritoytterbate(III) anion have been studied in Cs 2 NaY 0.96 Yb 0.04 (NO 2 ) 6 , which crystallizes in the cubic space group Fm3̅. The emission from Yb 3+ can be excited via the NO 2 - antenna. The latter electronic transition is situated at more than twice the energy of the former, but at room temperature, one photon absorbed at 470 nm in the triplet state produces no more than one photon emitted. Some degree of quantum cutting is observed at 298 K under 420 nm excitation into the singlet state and at 25 K using excitation into either state. The quantum efficiency is ∼10% at 25 K. The energy level scheme of Yb 3+ has been deduced from excitation and emission spectra and calculated by crystal field theory. New improved energy level calculations are also reported for the Cs 2 NaLn(NO 2 ) 6 (Ln = Pr, Eu, Tb) series using the f- Spectra package. The neat crystal Cs 2 NaYb(NO 2 ) 6 has also been studied, but results were unsatisfactory due to sample decomposition, and this chemical instability makes it unsuitable for applications.

Upward Trend in Catalytic Efficiency of Rare-Earth Triflate Catalysts in Friedel-Crafts Aromatic Sulfonylation Reactions

DEFF Research Database (Denmark)

Duus, Fritz; Le, Thach Ngoc; Nguyen, Vo Thu An

2014-01-01

A series of 14 lanthanide (Ln) triflates were investigated as sustainable catalysts for aromatic sulfonylation reactions under microwave irradiation. The catalytic efficiency of the early triflates La(OTf)3–Eu(OTf)3 is good for long irradiation times. For the later lanthanides, yields reaching over...... 90 % were achieved for short irradiation periods. This was the case especially for Tm(OTf)3, Yb(OTf)3, and Lu(OTf)3, of which Yb(OTf)3 was the most efficient. The upward trend in catalytic efficiency therefore correlates with the lanthanide sequence in the periodic table. The results can be explained...

Color-tunable up-conversion emission of luminescent-plasmonic, core/shell nanomaterials – KY{sub 3}F{sub 10}:Yb{sup 3+},Tm{sup 3+}/SiO{sub 2}-NH{sub 2}/Au

Energy Technology Data Exchange (ETDEWEB)

Runowski, Marcin, E-mail: runowski@amu.edu.pl

2017-06-15

Multifunctional luminescent-plasmonic KY{sub 3}F{sub 10}:Yb{sup 3+},Tm{sup 3+}/SiO{sub 2}-NH{sub 2}/Au nanomaterials were successfully obtained. The lanthanide-doped fluoride nanoparticles (NPs), synthesized under hydrothermal conditions exhibited bright blue up-conversion luminescence (λ{sub ex}=980 nm). Such lanthanide nanocrystals (20–40 nm) were coated with amine modified silica shell, forming core/shell nanostructures. Their surface was further uniformly covered with ultra-small gold NPs (4–7 nm). The as-prepared luminescent-plasmonic core/shell nanomaterials exhibited tunable up-conversion emission, due to the interactions between plasmonic and luminescent phases. The emission of Tm{sup 3+} ion was affected by the surface Au NPs, which exhibited strong plasmonic absorption in the visible range (450–650 nm). The increasing amount of the surface Au NPs, led to the significant alterations in a ratio of the Tm{sup 3+} emission bands. The NIR band ({sup 3}H{sub 4}→{sup 3}H{sub 6}) was unchanged, whereas the ratio and relative intensity of the bands in a visible range ({sup 1}G{sub 4}→{sup 3}H{sub 6} and {sup 1}G{sub 4}→{sup 3}F{sub 4}) was altered. This led to the significant change of the emission spectra shape and influenced color of emission, tuning it from bright blue to blue-violet. The products obtained were characterized by transmission electron microscopy (TEM), energy dispersive X-ray analysis (EDX), powder X-ray diffraction (XRD), UV–vis absorption spectroscopy and luminescence spectroscopy (excitation/emission spectra and luminescence decay curves).

Improvement of routes and production of CaSO{sub 4}-based dosimeters with unusual doping; Aprimoramento de rotas e producao de dosimetros a base de CaSO{sub 4} com dopagens nao usuais

Energy Technology Data Exchange (ETDEWEB)

Junot, Danilo Oliveira

2017-07-01

The widespread use of ionizing radiation in medicine and industry, associated with the known risks that this type of radiation can cause, has motivated the search for new radiation detectors, seeking improvements in the dosimetric characteristics and in the cost of production in comparison with commercial dosimeters disseminated. The motivation of this work is, therefore, to produce new thermoluminescent detectors through improved routes. Unusual elements in CaSO{sub 4} matrix doping, such as terbium (Tb) and ytterbium (Yb), were used as dopants in this matrix, as well as the europium (Eu), the thulium (Tm) and the silver (Ag), resulting in samples of CaSO{sub 4}:Eu,Tb, CaSO{sub 4}:Tb,Yb, CaSO{sub 4}:Tm,Ag and CaSO{sub 4}:Eu,Ag that were prepared by means of an adaptation of the method developed by Yamashita (1971). The route of synthesis is based on the mixture of calcium carbonate (CaCO{sub 3}) and dopant oxide (except for silver, incorporated in the form of metallic nanoparticles) in a solution of sulfuric acid. The mixture is heated until all the acid evaporates and only the powder of the material remains. In this route, the sulfuric acid is collected and can be reused. The phosphors produced were characterized by X-ray diffraction and radioluminescence techniques. The silver particles, produced by the polyol method, were characterized by scanning electron microscopy. Composites were obtained from the addition of Teflon to the phosphors. The thermoluminescence (TL) and the optically stimulated luminescence (OSL) of the new materials produced were investigated. Thermoluminescent characteristics such as sensitivity, linearity, reproducibility, minimum detectable dose, kinetic order and fading were evaluated and discussed. The CaSO{sub 4}:Tb,Eu composites showed TL glow curves with peaks at temperatures of 170 °C, 270 °C and 340 °C. The CaSO{sub 4}:Tb,Yb composites presented TL glow curves with peaks at temperatures of 90 °C, 160 °C, 240 °C and 340 °C. Ca

Improvement of routes and production of CaSO4-based dosimeters with unusual doping

International Nuclear Information System (INIS)

Junot, Danilo Oliveira

2017-01-01

The widespread use of ionizing radiation in medicine and industry, associated with the known risks that this type of radiation can cause, has motivated the search for new radiation detectors, seeking improvements in the dosimetric characteristics and in the cost of production in comparison with commercial dosimeters disseminated. The motivation of this work is, therefore, to produce new thermoluminescent detectors through improved routes. Unusual elements in CaSO 4 matrix doping, such as terbium (Tb) and ytterbium (Yb), were used as dopants in this matrix, as well as the europium (Eu), the thulium (Tm) and the silver (Ag), resulting in samples of CaSO 4 :Eu,Tb, CaSO 4 :Tb,Yb, CaSO 4 :Tm,Ag and CaSO 4 :Eu,Ag that were prepared by means of an adaptation of the method developed by Yamashita (1971). The route of synthesis is based on the mixture of calcium carbonate (CaCO 3 ) and dopant oxide (except for silver, incorporated in the form of metallic nanoparticles) in a solution of sulfuric acid. The mixture is heated until all the acid evaporates and only the powder of the material remains. In this route, the sulfuric acid is collected and can be reused. The phosphors produced were characterized by X-ray diffraction and radioluminescence techniques. The silver particles, produced by the polyol method, were characterized by scanning electron microscopy. Composites were obtained from the addition of Teflon to the phosphors. The thermoluminescence (TL) and the optically stimulated luminescence (OSL) of the new materials produced were investigated. Thermoluminescent characteristics such as sensitivity, linearity, reproducibility, minimum detectable dose, kinetic order and fading were evaluated and discussed. The CaSO 4 :Tb,Eu composites showed TL glow curves with peaks at temperatures of 170 °C, 270 °C and 340 °C. The CaSO 4 :Tb,Yb composites presented TL glow curves with peaks at temperatures of 90 °C, 160 °C, 240 °C and 340 °C. CaSO 4 :Tm showed peaks at

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...

Luminescence properties of LiSr2Y1-xLnxO4 (Ln=Eu,Tb,Tm) (0≤x≤1)

International Nuclear Information System (INIS)

Kubota, S.; Suzuyama, Y.; Yamane, H.; Shimada, M.

1998-01-01

Investigations of the luminescence properties of LiSr 2 Y 1-x Eu x O 4 , LiSr 2 Y 1-x Tb x O 4 and LiSr 2 Y 1-x Tm x O 4 (0≤x≤1) at room temperature are reported. These samples were synthesized by a solid state reaction. The excitation spectra of Tb 3+ emission in LiSr 2 Y 1-x Tb x O 4 (0≤x≤1) consist of broad bands corresponding to a transition between the 4f 8 and 4f 7 5d 1 states of Tb 3+ . The maximum intensity is situated at about 318 nm. This is at a much longer wavelength than those of other Tb 3+ doped phosphors. This is explained by a large offset of the adiabatic potential curve of the 4f 7 5d 1 state. (orig.)

Thermodynamic properties of thulium and ytterbium in fused NaCl-KCl-CsCl eutectic

Energy Technology Data Exchange (ETDEWEB)

Novoselova, A., E-mail: A.Novoselova@ihte.uran.ru [Institute of High-Temperature Electrochemistry, Ural Division, Russian Academy of Science, S. Kovalevskaya Str., 22, Ekaterinburg 620990 (Russian Federation); Smolenski, V. [Institute of High-Temperature Electrochemistry, Ural Division, Russian Academy of Science, S. Kovalevskaya Str., 22, Ekaterinburg 620990 (Russian Federation)

2011-07-15

Research highlights: > Tm and Yb chloride compounds as fission products. > The investigation of electrochemical properties of lanthanides. > Determination of the apparent standard redox potentials of the couple Ln(III)/Ln(II) in fused NaCl-KCl-CsCl eutectic at (823 to 973) K. > The calculation of the basic thermodynamic properties of redox reaction in molten salt. - Abstract: This work presents the results of a study of the Tm{sup 3+}/Tm{sup 2+} and Yb{sup 3+}/Yb{sup 2+} couple redox potentials vs. Cl{sup -}/Cl{sub 2} reference electrode at the temperature range (823 to 973) K in fused NaCl-KCl-CsCl eutectic by direct potentiometric method. Initial concentrations of TmCl{sub 3} and YbCl{sub 3} in solvents did not exceed 5.0 mol%. Basic thermodynamic properties of the reactions TmCl{sub 2(l)} + 1/2 Cl{sub 2(g)} {r_reversible} TmCl{sub 3(l)} and YbCl{sub 2(l)} + 1/2 Cl{sub 2(g)} {r_reversible} YbCl{sub 3(l)} were calculated using the temperature dependencies of apparent standard potentials of the couples E{sub Tm{sup 3+}/Tm{sup 2+*}} and E{sub Yb{sup 3+}/Yb{sup 2+*}}.

Sequential growth of sandwiched NaYF{sub 4}:Yb/Er@NaYF{sub 4}:Yb@NaNdF{sub 4}:Yb core–shell–shell nanoparticles for photodynamic therapy

Energy Technology Data Exchange (ETDEWEB)

Peng, Huang-Yong; Ding, Bin-Bin; Ma, Yin-Chu [Department of Medical Materials and Rehabilitation Engineering, School of Medical Engineering, Hefei University of Technology, Hefei 230009 (China); Sun, Shi-Qi [State Key Laboratory of Veterinary Etiological Biology and Key Laboratory of Animal Virology of Ministry of Agriculture, Lanzhou Veterinary Research Institute, Chinese Academy of Agricultural Sciences, Xujiaping 1, Lanzhou, Gansu 730046 (China); Tao, Wei [Department of Medical Materials and Rehabilitation Engineering, School of Medical Engineering, Hefei University of Technology, Hefei 230009 (China); Guo, Yan-Chuan [Technical Institute of Physics and Chemistry, Chinese Academy of Sciences, Beijing 100190 (China); Guo, Hui-Chen, E-mail: ghch-2004@hotmail.com [State Key Laboratory of Veterinary Etiological Biology and Key Laboratory of Animal Virology of Ministry of Agriculture, Lanzhou Veterinary Research Institute, Chinese Academy of Agricultural Sciences, Xujiaping 1, Lanzhou, Gansu 730046 (China); Yang, Xian-Zhu, E-mail: yangxz@hftu.edu.cn [Department of Medical Materials and Rehabilitation Engineering, School of Medical Engineering, Hefei University of Technology, Hefei 230009 (China); Qian, Hai-Sheng, E-mail: shqian@hfut.edu.cn [Department of Medical Materials and Rehabilitation Engineering, School of Medical Engineering, Hefei University of Technology, Hefei 230009 (China)

2015-12-01

Graphical abstract: The monodisperse elliptical NaYF{sub 4}:Yb/Er@NaYF{sub 4}:Yb@NaNdF{sub 4}:Yb core–shell–shell nanoparticles have been synthesized successfully by a facile sequential growth process, which can be used as transducer for photodynamic therapy of cancer cells. - Highlights: • The NaYF{sub 4}:Yb/Er@NaYF{sub 4}:Yb@NaNdF{sub 4}:Yb nanoparticles have been fabricated successfully. • The as-prepared nanoparticles show strong fluorescence excited at 980 or 808 nm. • The nanoparticles were transferred into the aqueous phase via a facile process. • Photosensitizers were loaded into the composites for photodynamic therapy. - Abstract: Upconversion (UC) nanostructures have attracted much interest for their extensive biological applications. In this work, we describe a sequential synthetic route to prepare sandwiched NaYF{sub 4}:Yb/Er@NaYF{sub 4}:Yb@NaNdF{sub 4}:Yb core–shell upconversion nanoparticles. The as-prepared products were investigated by X-ray diffraction (XRD) and transmission electron microscopy (TEM, JEM 2100F), respectively. The as-prepared core–shell nanoparticles of NaYF{sub 4}:Yb/Er@NaYF{sub 4}:Yb@NaNdF{sub 4}:Yb are composed of elliptical nanoparticles with a length of 80 nm and width of 42 nm, which show efficient upconversion fluorescence excited at 808 nm indicating the formation of core–shell–shell sandwiched nanostructures. In addition, the as-prepared sandwiched NaYF{sub 4}:Yb/Er@NaYF{sub 4}:Yb@NaNdF{sub 4}:Yb core–shell upconversion nanoparticles also show strong upconversion fluorescence excited at 980 nm. Amphiphilic mPEG{sub 2k}-b-PEBEP{sub 6K} copolymers (denoted as PPE) were chosen to transfer these hydrophobic UCNPs into the aqueous phase for biological application. In vitro photodynamic therapy of cancer cells show that the viability of cells incubated with the nanoparticles loaded with MC 540 was significantly lower as compared to the nanoparticles without photosensitizers exposed to NIR laser.

Transportin-1-dependent YB-1 nuclear import

International Nuclear Information System (INIS)

Mordovkina, Daria A.; Kim, Ekaterina R.; Buldakov, Ilya A.; Sorokin, Alexey V.; Eliseeva, Irina A.; Lyabin, Dmitry N.; Ovchinnikov, Lev P.

2016-01-01

The DNA/RNA-binding protein YB-1 (Y-box binding protein 1) performs multiple functions both in the cytoplasm and the nucleus of the cell. Generally localized to the cytoplasm, under certain conditions YB-1 is translocated to the nucleus. Here we report for the first time a transport factor that mediates YB-1 nuclear import – transportin-1. The YB-1/transportin-1 complex can be isolated from HeLa cell extract. Nuclear import of YB-1 and its truncated form YB-1 (1-219) in in vitro transport assay was diminished in the presence of a competitor substrate and ceased in the presence of transportin-1 inhibitor M9M. Inhibitors of importin β1 had no effect on YB-1 transport. Furthermore, transport of YB-1 (P201A/Y202A) and YB-1 (1–219) (P201A/Y202A) bearing inactivating mutations in the transportin-1-dependent nuclear localization signal was practically abolished. Together, these results indicate that transportin-1 mediates YB-1 nuclear translocation. - Highlights: • Transportin-1 mediates YB-1 nuclear import. • YB-1 nuclear translocation is diminished in the presence of transportin-1 inhibitors. • Mutations in the PY motif of YB-1 NLS prevent its translocation to the nucleus.

Synthesis and characterisation of some lanthanon-tris (chlorosulphate) complexes with nitrogen and oxygen donors

International Nuclear Information System (INIS)

Zaidi, S.A.A.; Zaidi, S.R.A.; Zahoor, M.A.; Khan, T.A.

1992-01-01

Some eight-coordinated complexes of Eu II , Tm II and Yb II chlorosulphates with pyridine, pyridine-N-oxide, acridine and bipyridine have been prepared and characterised by elemental analyses, conductance magnetic and infrared spectral data. Spectroscopic investigation has shown that SO 3 Cl - groups and bipyridyl ligand are all coordinated to the metal ions in a bidentate manner whereas the other ligand groups are coordinated monodentately. (author). 5 refs., 1 tab

Rare earths refining by vacuum sublimation method

International Nuclear Information System (INIS)

Rytus, N.N.

1983-01-01

The process of rare earths refining by the sUblimation; method in high and superhigh oil-free vacuum, is investigated. The method is effective for rare earths obtaining and permits to prepare metal samples with a high value of electric resistance ratio γ=RsUb(298 K)/Rsub(4.2 K). The estimation of general purity is performed for Sm, Eu, Yb, Tm, Dy, Ho, Er and Se

Kondo effect and heavy fermions in Yb compounds

International Nuclear Information System (INIS)

Bonville, P.

1987-01-01

The Kondo properties of Yb dilute alloys and intermetallics have been investigated using Moessbauer spectroscopy on 170 Yb. In the dilute alloys AuYb and LaBe 13 Yb, the Kondo logarithmic anomaly of the impurity relaxation rate has been detected, and in the concentrated Yb compounds YbBe 13 , YbP and YbAs, and YbCuAl, the manifestations of the interplay between the Kondo effect and the magnetic ordering due to the RKKY interaction have been characterized

Gamma ray induced decomposition of lanthanide nitrates

International Nuclear Information System (INIS)

Joshi, N.G.; Garg, A.N.

1992-01-01

Gamma ray induced decomposition of the lanthanide nitrates, Ln(NO 3 ) 3 .xH 2 O where Ln=La, Ce, Pr, Nd, Sm, Eu, Gd, Tb, Dy, Ho, Tm and Yb has been studied at different absorbed doses up to 600 kGy. G(NO 2 - ) values depend on the absorbed dose and the nature of the outer cation. It has been observed that those lanthanides which exhibit variable valency (Ce and Eu) show lower G-values. An attempt has been made to correlate thermal and radiolytic decomposition processes. (author). 20 refs., 3 figs., 1 tab

Luminescent properties of LuAG:Yb and YAG:Yb single crystalline films grown by Liquid Phase Epitaxy method

International Nuclear Information System (INIS)

Zorenko, Yu; Zorenko, T.; Gorbenko, V.; Voznyak, T.; Popielarski, P.; Batentschuk, M.; Osvet, A.; Brabec, Ch; Kolobanov, V.; Spasky, D.; Fedorov, A.

2016-01-01

In this work, investigation of the spectroscopic parameters of the luminescence of Yb"3"+ ions in single crystalline films of Lu_3Al_5O_1_2 and Y_3Al_5O_1_2 garnets was performed using the synchrotron radiation excitation with the energy in the range of Yb"3"+ charge transitions (CT), exciton range and the onset of interband transitions of these garnets. The basic spectroscopic parameters of the Yb"3"+ CT luminescence in LuAG and YAG hosts were determined and summarized with taking into account the differences in the band gap structure of these garnets. - Highlights: • Single crystalline films of Yb doped LuAG and YAG garnets were grown by LPE method. • Yb"3"+ luminescence of LuAG:Yb and YAG:Yb film were studied using synchrotron radiation. • Basic parameters of Yb"3"+ charge transfer luminescence in LuAG and YAG were determined.

The effect of core and lanthanide ion dopants in sodium fluoride-based nanocrystals on phagocytic activity of human blood leukocytes

Science.gov (United States)

Sojka, Bartlomiej; Liskova, Aurelia; Kuricova, Miroslava; Banski, Mateusz; Misiewicz, Jan; Dusinska, Maria; Horvathova, Mira; Ilavska, Silvia; Szabova, Michaela; Rollerova, Eva; Podhorodecki, Artur; Tulinska, Jana

2017-02-01

Sodium fluoride-based β-NaLnF4 nanoparticles (NPs) doped with lanthanide ions are promising materials for application as luminescent markers in bio-imaging. In this work, the effect of NPs doped with yttrium (Y), gadolinium (Gd), europium (Eu), thulium (Tm), ytterbium (Yb) and terbium (Tb) ions on phagocytic activity of monocytes and granulocytes and the respiratory burst was examined. The surface functionalization of toxic with respect to conducted test; however, some cause toxic effects (they have statistically significant deviations compared to reference) in some selected doses tested. Both core types of NPs (Y-core and Gd-core) impaired the phagocytic activity of monocytes the strongest, having minimal or none whatsoever influence on granulocytes and respiratory burst of phagocytic cells. The lowest toxicity was observed in Gd-core, Yb, Tm dopants and near-infrared nanoparticles. Clear dose-dependent effect of NPs on phagocytic activity of leukocytes and respiratory burst of cells was observed for limited number of samples.

X-ray absorption experiments on rare earth and uranium compounds under high pressure

International Nuclear Information System (INIS)

Schmiester, G.

1987-01-01

After an introduction into the phenomenon of the mixed valency and the method of measuring the microstructures by X-ray absorption spectroscopy in the area of the L edges under pressure, the results of investigations at selected substitutes of the chalcogenides and puictides of the rare earths and the uranium were given. Thus, pressure-induced valency transitions in YbS and YbTe, instabilities in valency and structural phase transitions in EUS and SmTe as well as the change in the electron structure in USb under pressure were investigated in order to answer questions of solid state physics (e.g. semiconductor-metal transitions, correlation between valency and structural phase transitions). Hybridization effects in L III spectra of formally tetravalent Ca are analyzed at CeF 4 and CeO 2 (insulators) and the role of final state effects in the L III spectra are analyzed at EuP 2 P 2 and TmSe-TmTe (semiconductor systems). (RB) [de

General synthesis and structural evolution of a layered family of Ln8(OH)20Cl4 x nH2O (Ln = Nd, Sm, Eu, Gd, Tb, Dy, Ho, Er, Tm, and Y).

Science.gov (United States)

Geng, Fengxia; Matsushita, Yoshitaka; Ma, Renzhi; Xin, Hao; Tanaka, Masahiko; Izumi, Fujio; Iyi, Nobuo; Sasaki, Takayoshi

2008-12-03

The synthesis process and crystal structure evolution for a family of stoichiometric layered rare-earth hydroxides with general formula Ln(8)(OH)(20)Cl(4) x nH(2)O (Ln = Nd, Sm, Eu, Gd, Tb, Dy, Ho, Er, Tm, and Y; n approximately 6-7) are described. Synthesis was accomplished through homogeneous precipitation of LnCl(3) x xH(2)O with hexamethylenetetramine to yield a single-phase product for Sm-Er and Y. Some minor coexisting phases were observed for Nd(3+) and Tm(3+), indicating a size limit for this layered series. Light lanthanides (Nd, Sm, Eu) crystallized into rectangular platelets, whereas platelets of heavy lanthanides from Gd tended to be of quasi-hexagonal morphology. Rietveld profile analysis revealed that all phases were isostructural in an orthorhombic layered structure featuring a positively charged layer, [Ln(8)(OH)(20)(H(2)O)(n)](4+), and interlayer charge-balancing Cl(-) ions. In-plane lattice parameters a and b decreased nearly linearly with a decrease in the rare-earth cation size. The interlamellar distance, c, was almost constant (approximately 8.70 A) for rare-earth elements Nd(3+), Sm(3+), and Eu(3+), but it suddenly decreased to approximately 8.45 A for Tb(3+), Dy(3+), Ho(3+), and Er(3+), which can be ascribed to two different degrees of hydration. Nd(3+) typically adopted a phase with high hydration, whereas a low-hydration phase was preferred for Tb(3+), Dy(3+), Ho(3+), Er(3+), and Tm(3+). Sm(3+), Eu(3+), and Gd(3+) samples were sensitive to humidity conditions because high- and low-hydration phases were interconvertible at a critical humidity of 10%, 20%, and 50%, respectively, as supported by both X-ray diffraction and gravimetry as a function of the relative humidity. In the phase conversion process, interlayer expansion or contraction of approximately 0.2 A also occurred as a possible consequence of absorption/desorption of H(2)O molecules. The hydration difference was also evidenced by refinement results. The number of coordinated water

Cross sections for fast-neutron interaction with ytterbium isotopes

International Nuclear Information System (INIS)

Luo, Junhua; Liu, Rong; Jiang, Li; Ge, Suhong; Liu, Zhenlai; Sun, Guihua

2013-01-01

Highlights: ► The cross sections for the (n,x) reactions on ytterbium isotopes have been measured. ► Mono-energetic neutron beams using the D + T reaction; Energies: 13.5 and 14.8 MeV. ► Neutron cross-section measurements by means of the activation technique. ► Reference reactions 93 Nb(n,2n) 92m Nb and 27 (n,α) 24 Na. ► Data for 172 Yb(n,p) 172 Tm and 176 Yb(n,d * ) 175 Tm are reported for the first time. - Abstract: Measurements of (n,2n), (n,p), and (n,d * ) (The expression (n,d * ) cross section used in this work includes a sum of (n,d), (n,np) and (n,pn) cross sections.) reaction cross-sections on ytterbium isotopes have been carried out in the range of 13.5–14.8 MeV using the activation technique. The monoenergetic neutron beams were produced via the 3 H(d,n) 3 He reaction. The neutron energies of different directions were determined using the Nb/Zr method. Samples were activated along with along with Nb and Al monitor foils to determine the incident neutron flux. Data are reported for the following reactions: 168 Yb(n,2n) 167 Yb, 170 Yb(n,2n) 169m+g Yb, 176 Yb(n,2n) 175m+g Yb, 172 Yb(n,p) 172 Tm, 173 Yb(n,p) 173 Tm, 176 Yb(n,d * ) 175 Tm, 174 Yb(n,p) 174 Tm, and 176 Yb(n,p) 176 Tm. The experimentally deduced cross-sections are compared with the existing experimental data. Furthermore, theoretical statistical model, based on the Hauser–Feshbach formalism, have been carried out using the HFTT

Application of Sm/Eu/, Rb/Sr, Ce/Yb and F-Rb ratios to discriminate between Tin mineralized and non-mineralized S-type granites

International Nuclear Information System (INIS)

Karimpour, M.H.

1998-01-01

Mash had granites and Gran diorites are divided into three groups bas sed on their ages and composition: (1) Deh Now-Vakilabad-Kuhsangi Granodiorites and Quartz monzodiorites, (2) Sang bast Granite and (3) Khalaj- Gheshlagh Biotite-muscovite Granite. All these intrusive s belong to S-type granite, The oldest are in the range of intermediate and the youngest are acidic in composition. Intrusive rocks in the area of Deh now to Kuhsangi show trend of differentiation. Major, trace and rare earth elements within the source rocks of porphyry Sn, Mo, and Cu deposits were compared and very distinct differences were noticed. Differentiation index, Rb/Sr, Ce/Yb, and (Sr 87 /Sr 86 ) ratios can be used to identify the source rocks for porphyry Sn, Mo, or Cu. Major, as well as trace and rare earth elements of Mash had Granites and Granodiorites were compared with tin mineralized granites of the world. As a result, four diagrams were presented to be utilized in order to discriminate between Sn mineralized and non-mineralized granites. Such as Rb to the ratio of Sm/Eu, F to Rb and the three angle of F, Rb, Sr + Ba

Chemical composition of Kiscellian silty sediment (sivica from the Trobni Dol area, Eastern Slovenia

Directory of Open Access Journals (Sweden)

Miha Mišič

2003-06-01

Full Text Available Kiscellian marine silt termed »sivica« is widely developed in Tertiary basins of Eastern Slovenia. Chemical composition is rather uniform and reflects the dominance of filosilicates (mainly illite/muscovite, chlorite and montmorillonite and carbonates. PAAS normalised REE and Y abundances are slightly depleted for La, Ce, Pr and Nd, very close to PAAS for Sm, Eu, Gd and Tb, and depleted for Y, Ho, Er, Tm, Yb and Lu.

White photoluminescence emission from ZrO_2 co-doped with Eu"3"+, Tb"3"+ and Tm"3"+

International Nuclear Information System (INIS)

Lovisa, L.X.; Araújo, V.D.; Tranquilin, R.L.; Longo, E.; Li, M.S.; Paskocimas, C.A.; Bomio, M.R.D.; Motta, F.V.

2016-01-01

The search for high efficiency, reliable, low power consumption and environmental friendly materials for white light-emitting diodes has become a proficient field. Single-phase doped materials have been made to solve some of these challenges. Particles with color-tunable emission can be obtained by a combination of some lanthanide ions in the host material. The luminescence properties and crystalline structure of ZrO_2 particles co-doped with rare earth ions (RE"3"+ = Tb"3"+, Eu"3"+ and Tm"3"+) calcined at different temperatures were studied. We aimed to investigate the emission spectrum of the particles in the red, green, and blue regions under UV excitation. The x and y coordination chromaticity - (x = 0.34, y = 0.34) and (x = 0.31, y = 0.34) - presented values close to those of the white color (x = y = 0.33). In conclusion, the ZrO_2:RE"3"+ powers were successfully obtained by the complex polymerization method and are promising candidates for white light-emitting applications. - Highlights: The ZrO_2:RE materials presented here are promising photoluminescent materials. The CIE coordinates calculated are disposed in the blank region in the CIE diagram. The results for the Raman confirm the response obtained by XRD: stabilization of cubic phase.

Strategy for thermometry via Tm³⁺-doped NaYF₄ core-shell nanoparticles.

Science.gov (United States)

Zhou, Shaoshuai; Jiang, Guicheng; Li, Xinyue; Jiang, Sha; Wei, Xiantao; Chen, Yonghu; Yin, Min; Duan, Changkui

2014-12-01

Optical thermometers usually make use of the fluorescence intensity ratio of two thermally coupled energy levels, with the relative sensitivity constrained by the limited energy gap. Here we develop a strategy by using the upconversion (UC) emissions originating from two multiplets with opposite temperature dependences to achieve higher relative temperature sensitivity. We show that the intensity ratio of the two UC emissions, ³F(2,3) and ¹G₄, of Tm³⁺ in β-NaYF₄:20%Yb³⁺, 0.5%Tm³⁺/NaYF₄:1%Pr³⁺ core-shell nanoparticles under 980 nm laser excitation exhibits high relative temperature sensitivity between 350 and 510 K, with a maximum of 1.53%  K⁻¹ at 417 K. This demonstrates the validity of the strategy, and that the studied material has the potential for high-performance optical thermometry.

Monodisperse and hollow structured Y{sub 2}O{sub 3}:Ln{sup 3+} (Ln = Eu, Dy, Er, Tm) nanospheres: A facile synthesis and multicolor-tunable luminescence properties

Energy Technology Data Exchange (ETDEWEB)

Li, Ruiqing; Zi, Wenwen; Li, Linlin; Liu, Lu; Zhang, Junjun [College of Chemistry, Jilin University, Changchun 130026 (China); Zou, Lianchun, E-mail: zoulianchun@126.com [Teaching Center of Basic Courses, Jilin University, Changchun 130062 (China); Gan, Shucai, E-mail: gansc@jlu.edu.cn [College of Chemistry, Jilin University, Changchun 130026 (China)

2014-12-25

Highlights: • We reported a simple route to synthesize the Y{sub 2}O{sub 3} HNSs. • A possible formation mechanism of the Y{sub 2}O{sub 3} HNSs was proposed. • The Ln-doped Y{sub 2}O{sub 3} HNSs exhibit characteristic emission with different colors. • White-light-emitting phosphor Y{sub 2}O{sub 3}:Tm{sup 3+}, Dy{sup 3+} was also successfully synthesized. - Abstract: A novel, fast and simple method was developed to synthesize the undoped and lanthanide-doped yttrium oxide hollow nanospheres (Y{sub 2}O{sub 3}⋅HNSs) with multicolored downconversion emission under mild conditions by employing poly (acrylic acid sodium salt) microspheres (PAAS MSs) as active templates followed by a subsequent calcination process. The structure, morphology, formation process, and fluorescent properties are well investigated using various techniques. The results show that the samples can be well indexed to the pure cubic phase of Y{sub 2}O{sub 3}. The possible formation mechanism of the PAAS MSs, PAA-Y precursor, and Y{sub 2}O{sub 3} HNSs are proposed and discussed in detail. Upon ultraviolet excitation, the obtained Y{sub 2}O{sub 3}:Ln{sup 3+} (Ln = Eu, Dy, Er, Tm) HNSs exhibit strong red, yellow–green, blue, yellow emission, respectively. Moreover, a novel single-phased and near-UV-pumped white-light-emitting phosphor Y{sub 2}O{sub 3}:Tm{sup 3+}, Dy{sup 3+} was also successfully fabricated through optimizing the molar ratio among Tm{sup 3+} and Dy{sup 3+} in the Y{sub 2}O{sub 3} host. This material may find potential applications in field-emission display devices and white ultraviolet light-emitting diodes (UV LEDs). Furthermore, this synthesis route may be of great significance in the preparation of other hollow spherical materials.

Functional conservation of rice OsNF-YB/YC and Arabidopsis AtNF-YB/YC proteins in the regulation of flowering time

KAUST Repository

Hwang, Yoon-Hyung; Kim, SoonKap; Lee, Keh Chien; Chung, Young Soo; Lee, Jeong Hwan; Kim, Jeong-Kook

2016-01-01

Plant NUCLEAR FACTOR Y (NF-Y) transcription factors play important roles in plant development and abiotic stress. In Arabidopsis thaliana, two NF-YB (AtNF-YB2 and AtNF-YB3) and five NF-YC (AtNF-YC1, AtNF-YC2, AtNF-YC3, AtNF-YC4, and AtNF-YC9) genes regulate photoperiodic flowering by interacting with other AtNF-Y subunit proteins. Three rice NF-YB (OsNF-YB8, OsNF-YB10, and OsNF-YB11) and five rice OsNF-YC (OsNF-YC1, OsNF-YC2, OsNF-YC4, OsNF-YC6, and OsNF-YC7) genes are clustered with two AtNF-YB and five AtNF-YC genes, respectively. To investigate the functional conservation of these NF-YB and NF-YC genes in rice and Arabidopsis, we analyzed the flowering phenotypes of transgenic plants overexpressing the respective OsNF-YB and OsNF-YC genes in Arabidopsis mutants. Overexpression of OsNF-YB8/10/11 and OsNF-YC2 complemented the late flowering phenotype of Arabidopsis nf-yb2 nf-yb3 and nf-yc3 nf-yc4 nf-yc9 mutants, respectively. The rescued phenotype of 35S::OsNF-YC2 nf-yc3 nf-yc4 nf-yc9 plants was attributed to the upregulation of FLOWERING LOCUS T (FT) and SUPPRESSOR OF OVEREXPRESSION OF CONSTANS 1 (SOC1). In vitro and in planta protein–protein analyses revealed that OsNF-YB8/10/11 and OsNF-YC1/2/4/6/7 interact with AtNF-YC3/4/9 and AtNF-YB2/3, respectively. Our data indicate that some OsNF-YB and OsNF-YC genes are functional equivalents of AtNF-YB2/3 and AtNF-YC3/4/9 genes, respectively, and suggest functional conservation of Arabidopsis and rice NF-Y genes in the control of flowering time.

Functional conservation of rice OsNF-YB/YC and Arabidopsis AtNF-YB/YC proteins in the regulation of flowering time

KAUST Repository

Hwang, Yoon-Hyung

2016-01-11

Plant NUCLEAR FACTOR Y (NF-Y) transcription factors play important roles in plant development and abiotic stress. In Arabidopsis thaliana, two NF-YB (AtNF-YB2 and AtNF-YB3) and five NF-YC (AtNF-YC1, AtNF-YC2, AtNF-YC3, AtNF-YC4, and AtNF-YC9) genes regulate photoperiodic flowering by interacting with other AtNF-Y subunit proteins. Three rice NF-YB (OsNF-YB8, OsNF-YB10, and OsNF-YB11) and five rice OsNF-YC (OsNF-YC1, OsNF-YC2, OsNF-YC4, OsNF-YC6, and OsNF-YC7) genes are clustered with two AtNF-YB and five AtNF-YC genes, respectively. To investigate the functional conservation of these NF-YB and NF-YC genes in rice and Arabidopsis, we analyzed the flowering phenotypes of transgenic plants overexpressing the respective OsNF-YB and OsNF-YC genes in Arabidopsis mutants. Overexpression of OsNF-YB8/10/11 and OsNF-YC2 complemented the late flowering phenotype of Arabidopsis nf-yb2 nf-yb3 and nf-yc3 nf-yc4 nf-yc9 mutants, respectively. The rescued phenotype of 35S::OsNF-YC2 nf-yc3 nf-yc4 nf-yc9 plants was attributed to the upregulation of FLOWERING LOCUS T (FT) and SUPPRESSOR OF OVEREXPRESSION OF CONSTANS 1 (SOC1). In vitro and in planta protein–protein analyses revealed that OsNF-YB8/10/11 and OsNF-YC1/2/4/6/7 interact with AtNF-YC3/4/9 and AtNF-YB2/3, respectively. Our data indicate that some OsNF-YB and OsNF-YC genes are functional equivalents of AtNF-YB2/3 and AtNF-YC3/4/9 genes, respectively, and suggest functional conservation of Arabidopsis and rice NF-Y genes in the control of flowering time.

n-aminobenzoates of rare earths

International Nuclear Information System (INIS)

Efremova, G.I.; Buchkova, R.T.; Lapitskaya, A.V.; Pirkes, S.B.

1977-01-01

N-aminobenzoates of r.e.e. have been synthesized. Their composition corresponds to the general formula Me(C 6 H 4 NH 2 COO) 3 xnH 2 O, where Me stands for La, Ce, Pr, Nd, Sm, Eu, Gd, Tb, Dy, Ho, Er, Tm, Yb, Lu; n=1.2. The compounds obtained are identified by chemical analysis and roentgenographically. Their solubility products, which are values of the order of 10 -9 -10 -10 , are determined

A novel high color purity blue-emitting phosphor: CaBi{sub 2}B{sub 2}O{sub 7}:Tm{sup 3+}

Energy Technology Data Exchange (ETDEWEB)

Li, Jiangong, E-mail: lijiangong01@gmail.com [Department of Electronic Science and Engineering, Huanghuai University, Zhumadian 463000 (China); Yan, Huifang [Department of Foreign Languages and Literature, Huanghuai University, Zhumadian 463000 (China); Yan, Fengmei [Department of Chemistry and Chemical Engineering, Huanghuai University, Zhumadian 463000 (China)

2016-07-15

Graphical abstract: - Highlights: • A series of Tm{sup 3+}-doped CaBi{sub 2}B{sub 2}O{sub 7} blue-emitting phosphors were prepared. • The optimum doping content of Tm{sup 3+} ions was found. • The critical distance and concentration quenching mechanism was discussed. • The color purity of as prepared sample was analyzed and compared. - Abstract: A series of Tm{sup 3+}-doped CaBi{sub 2−x}B{sub 2}O{sub 7}:xTm{sup 3+} (0.02 ≤ x ≤ 0.12) blue-emitting phosphors with high color purity were prepared by solid-state reaction method. The crystal structure and luminescence properties of the as-prepared phosphors were studied. This phosphor shows a satisfactory blue performance (peak at 453 nm) due to the {sup 1}D{sub 2} → {sup 3}F{sub 4} transition of Tm{sup 3+} excited by 357 nm light. Investigation of Tm{sup 3+} content dependent emission spectra indicates that x = 0.04 is the optimum doping content of Tm{sup 3+} ions in the CaBi{sub 2}B{sub 2}O{sub 7} host. The critical distance and the concentration quenching mechanism were also investigated. In particular, the color purity of as prepared sample was analyzed and the result shows that the color purity of CaBi{sub 2}B{sub 2}O{sub 7}:Tm{sup 3+} is higher than the commercial blue phosphor BaMgAl{sub 10}O{sub 17}:Eu{sup 2+} (BAM:Eu{sup 2+}) and the latest reported Tm{sup 3+} doped blue phosphors. The present work suggests that the CaBi{sub 2}B{sub 2}O{sub 7}:Tm{sup 3+} phosphor is a potential blue-emitting candidate for the application in the near-UV WLEDs.

Thulium oxide fuel characterization study: Part 2, Environmental behavior and mechanical, thermal and chemical stability enhancement

International Nuclear Information System (INIS)

Nelson, C.A.

1970-12-01

A study was performed of the correlation between fuel form stability and exposure environment of (temperature and atmosphere). 100% Tm 2 O 3 , 80% Tm 2 O 3 /20% Yb 2 O 3 and 100% Yb 2 O 3 wafers were subjected to air, dynamic vacuum and static vacuum at temperatures to 2000 0 C for times to 100 hours. Results showed the Tm 2 O 3 /Yb 2 O 3 cubic structure to be unaffected by elemental levels of iron, aluminum, magnesium and silicon and unaffected by the environmental conditions imposed on the wafers. A second task emphasized the optimization of the thermal, mechanical and chemical stability of Tm 2 O 3 fuel forms. Enhancement was sought through process variable optimization and the addition of metal oxides to Tm 2 O 3 . CaO, TiO 2 and Al 2 O 3 were added to form a grain boundary precipitate to control fines generation. The presence of 1% additive was inadequate to depress the melting point of Tm 2 O 3 or to change the cubic crystalline structure of Tm 2 O 3 /Yb 2 O 3 . Tm 2 O 3 /Yb 2 O 3 wafers containing CaO developed a grain boundary phase that improved the resistance to fines generation. The presence of Yb 2 O 3 did not appear to measurably influence behavior

Structure analysis of complex metallic alloys in the Eu-Ag-In system by X-ray diffraction

International Nuclear Information System (INIS)

Gomez, Cesar Pay; Morita, Yoshiki; Tsai, An Pang; Yamamoto, Akiji

2009-01-01

In this work we investigate the complex atomic structures of two CMAs in the Eu-Ag-In system, these are quasicrystal approximants and their structures are similar to those of the 1/1 and 2/1 approximants found in the Yb-Cd system. The similarities between the Yb-Cd and Eu-Ag-In systems indicate that the RE-Ag-In systems in several ways can be treated as pseudo-binary. The investigated phases however also show some interesting differences; when Cd is replaced by the elements Ag and In partial chemical disorder is introduced into the system. As a response, the positional disorder which is usually observed in certain atomic positions for these types of approximants tends to disappear. The complete structures refined from single crystal data are described in detail and the differences with other related phases are highlighted. The 2/1 approximant in the Eu-Ag-In system is the first to exhibit such a degree of structural perfection in terms of positional order, a feature which makes this phase very suitable for further studies of chemical order and also can give insight into the local structures of related disordered phases. Electron diffraction studies on the 1/1 approximant phase have previously shown the presence of weak superlattice reflections, indicating a superstructure similar to that of the related phase Eu 4 Cd 25 . However, no superlattice reflections could be observed by single crystal diffraction and it is thus concluded that the phase has a disordered average structure with possible short to medium range superlattice ordering.

Genome-wide analysis of the human Alu Yb-lineage

Directory of Open Access Journals (Sweden)

Carter Anthony B

2004-03-01

Full Text Available Abstract The Alu Yb-lineage is a 'young' primarily human-specific group of short interspersed element (SINE subfamilies that have integrated throughout the human genome. In this study, we have computationally screened the draft sequence of the human genome for Alu Yb-lineage subfamily members present on autosomal chromosomes. A total of 1,733 Yb Alu subfamily members have integrated into human autosomes. The average ages of Yb-lineage subfamilies, Yb7, Yb8 and Yb9, are estimated as 4.81, 2.39 and 2.32 million years, respectively. In order to determine the contribution of the Alu Yb-lineage to human genomic diversity, 1,202 loci were analysed using polymerase chain reaction (PCR-based assays, which amplify the genomic regions containing individual Yb-lineage subfamily members. Approximately 20 per cent of the Yb-lineage Alu elements are polymorphic for insertion presence/absence in the human genome. Fewer than 0.5 per cent of the Yb loci also demonstrate insertions at orthologous positions in non-human primate genomes. Genomic sequencing of these unusual loci demonstrates that each of the orthologous loci from non-human primate genomes contains older Y, Sg and Sx Alu family members that have been altered, through various mechanisms, into Yb8 sequences. These data suggest that Alu Yb-lineage subfamily members are largely restricted to the human genome. The high copy number, level of insertion polymorphism and estimated age indicate that members of the Alu Yb elements will be useful in a wide range of genetic analyses.

Are there non-statistical effects in /sup 173/Yb(n,gamma)/sup 174/Yb?

International Nuclear Information System (INIS)

Pospisil, S.; Becvar, F.; Chrien, R.E.; Kopecky, J.

1987-01-01

The resonance-averaged capture of neutrons in 173 Yb has been studied at energy of 2 keV. With a statistical significance of 99.5% an enhancement of E1-transition to the neutron 2QP levels in 174 Yb is observed. 8 refs

Growth and laser action of Yb: YVO4 crystals with low Yb doping concentration

Science.gov (United States)

Zhong, Degao; Teng, Bing; Li, Jianhong; Zhang, Shiming; Zhang, Bingtao; Wang, Chao; Tian, Xueping; Liu, Junhai

2012-11-01

Yb: YVO4 single crystals with low doping concentrations of Yb3+ less than 0.3 at% were grown using the Czochralski method. The polarized absorption spectra were measured at room temperature. Strong anisotropy exists in the absorption spectra, resulting in almost entirely different features for π-polarization and σ-polarization. The laser emission spectrum and relationship curve between the output power and absorbed pump power (Pabs) were measured. The continuous-wave laser action of Yb: YVO4 single crystal in a range of 1020.4-1026.3 nm was realized by using a high-power diode laser as the pump source.

Synthesis and investigation of rare earth tris-acetylacetonates addUcts with acetylaceoneimine

International Nuclear Information System (INIS)

Trembovetskij, G.V.; Smirnov, E.V.; Murav'eva, I.A.; Martynenko, L.I.

1983-01-01

Adducts of tris-acetylacetonates of pare earths With acetylacetonimine of the composition MA 3 x2L (M=La, Pr, Nd, Eu, Gd, Tb) and MA 3 XL (M=Dy, Ho, Er, Tm, Yb, LU) have been synthesized. The compounds prepared are studied using the methods of elemental analysis, IR spectroscopy, PMR spectroscopy, X-ray phase analysis. Volatile tris-acetylacetonates of the yttrium subgroUp rare earths have been prepared by thermal decomposition of MA 3 xL in vacuum

Rare earth elements in the Pacific and Atlantic Oceans

International Nuclear Information System (INIS)

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

1985-01-01

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)

Cryogenic Yb: YAG Thin-Disk Laser

Science.gov (United States)

2016-09-09

as a 4- level laser. Its absorption and emission cross-sections increase, and its thermal conductivity improves. Yb:YAG thin disk laser performance...Air Force Base, NM USA 87117 4RINI Technologies, 582 South Econ Circle, Oviedo, FL USA 32765 Keywords: Laser materials; Lasers, ytterbium...temperatures, Yb:YAG behaves as a 4- level laser. Its absorption and emission cross-sections increase, and its thermal conductivity improves. Yb:YAG

Dielectric relaxation in Yb-doped SrZrO3

International Nuclear Information System (INIS)

Kamishima, O; Abe, Y; Ishii, T; Kawamura, J; Hattori, T

2004-01-01

The dielectric constant of the proton conductor SrZr 1-x Yb x O 3 (x 0-0.1) was measured as a function of temperature and frequency. Two well-defined relaxation peaks were observed in SrZrO 3 doped with more than 1 mol% of Yb. The assignment of the two dielectric relaxations is discussed in terms of IR spectra and by free energy calculation for a miscibility of dopant Yb ions. The Yb concentration dependence of the relaxation strength of the two dielectric relaxations is in agreement with the results calculated from the free energy. The two relaxations can be assigned to a reorientation of a single Yb-OH dipole and of Yb-OH dipoles associated with Yb-clusters. The attractive energy for Yb-clustering in SrZrO 3 is evaluated at about -85 meV

Luminescent Afterglow Behavior in the M2Si5N8: Eu Family (M = Ca, Sr, Ba

Directory of Open Access Journals (Sweden)

Koen Van den Eeckhout

2011-05-01

Full Text Available Persistent luminescent materials are able to emit light for hours after being excited. The majority of persistent phosphors emit in the blue or green region of the visible spectrum. Orange- or red-emitting phosphors, strongly desired for emergency signage and medical imaging, are scarce. We prepared the nitrido-silicates Ca2Si5N8:Eu (orange, Sr2Si5N8:Eu (reddish, Ba2Si5N8:Eu (yellowish orange, and their rare-earth codoped variants (R = Nd, Dy, Sm, Tm through a solid state reaction, and investigated their luminescence and afterglow properties. In this paper, we describe how the persistent luminescence is affected by the type of codopant and the choice and ratio of the starting products. All the materials exhibit some form of persistent luminescence, but for Sr2Si5N8:Eu,R this is very weak. In Ba2Si5N8:Eu the afterglow remains visible for about 400 s, and Ca2Si5N8:Eu,Tm shows the brightest and longest afterglow, lasting about 2,500 s. For optimal persistent luminescence, the dopant and codopant should be added in their fluoride form, in concentrations below 1 mol%. A Ca3N2 deficiency of about 5% triples the afterglow intensity. Our results show that Ba2Si5N8:Eu(,R and Ca2Si5N8:Eu(,R are promising persistent phosphors for applications requiring orange or red light.

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)

Gibbs free energy of formation of liquid lanthanide-bismuth alloys

International Nuclear Information System (INIS)

Sheng Jiawei; Yamana, Hajimu; Moriyama, Hirotake

2001-01-01

The linear free energy relationship developed by Sverjensky and Molling provides a way to predict Gibbs free energies of liquid Ln-Bi alloys formation from the known thermodynamic properties of aqueous trivalent lanthanides (Ln 3(5(6+ ). The Ln-Bi alloys are divided into two isostructural families named as the LnBi 2 (Ln=La, Ce, Pr, Nd and Pm) and LnBi (Ln=Sm, Eu, Gd, Tb, Dy, Ho, Er, Tm and Yb). The calculated Gibbs free energy values are well agreed with experimental data

Level Densities and Radiative Strength Functions in 170,171Yb

International Nuclear Information System (INIS)

Agvaanluvsan, U.; Schiller, A.; Becker, J.A.; Berstein, L.A.; Guttormsen, M.; Mitchell, G.E.; Rekstad, J.; Siem, S.; Voinov, A.

2003-01-01

Level densities and radiative strength functions in 171 Yb and 170 Yb nuclei have been measured with the 171 Yb( 3 He, 3 He(prime) γ) 171 Yb and 171 Yb( 3 He, αγ) 170 Yb reactions. A simultaneous determination of the nuclear level density and the radiative strength function was made. The present data adds to and is consistent with previous results for several other rare earth nuclei. The method will be briefly reviewed and the result from the analysis will be presented. The radiative strength function for 171 Yb is compared to previously published work.

Measurement of cross sections producing short-lived nuclei by 14 MeV neutron. Br, Te, Dy, Ho, Yb

Energy Technology Data Exchange (ETDEWEB)

Sakane, H.; Matsumoto, T.; Yamamoto, H.; Kawade, K. [Nagoya Univ. (Japan); Iida, T.; Takahashi, A.

1997-03-01

Nine neutron activation cross sections producing the nuclei with half-lives between 2 min and 57 min have been measured at energy range between 13.4 and 14.9 MeV for Br, Te, Dy, Ho, Yb. The cross sections of {sup 81}Br(n,p){sup 81m}Se, {sup 128}Te(n,p){sup 128m}Sb, {sup 128}Te(n,{alpha}){sup 125m}Sn, {sup 164}Dy(n,p){sup 164}Tb, {sup 165}Ho(n,{alpha}){sup 162}Tb, {sup 176}Yb(n,p){sup 176}Tm were newly obtained at the six energy points between 13.4-14.9 MeV, although the previous results have been obtained at one energy point. {sup 79}Br(n,2n){sup 78}Br, {sup 164}Dy(n,p){sup 164}Tb are compared with evaluated data of JENDL-3.2. The evaluations for these reactions agree reasonably well with experimental results. The cross sections of (n,p) reaction are compared with systematics by Kasugai et. al. The systematics agrees with experimental results. (author)

Spectral properties of hydrothermally-grown Nd:LuAG, Yb:LuAG, and Yb:Lu{sub 2}O{sub 3} laser materials

Energy Technology Data Exchange (ETDEWEB)

Brown, David C., E-mail: DBrown@snakecreeklasers.com [Snake Creek Lasers LLC, Friendsville, PA 18818 (United States); McMillen, Colin D.; Moore, Cheryl; Kolis, Joseph W. [Department of Chemistry and Center for Optical Materials Science and Engineering Technologies, Clemson University, Clemson, SC 29634-0973 (United States); Envid, Victoria [Snake Creek Lasers LLC, Friendsville, PA 18818 (United States)

2014-04-15

We have investigated the hydrothermal growth of, and spectrally characterized, the lutetium based laser materials Nd:LuAG, Yb:LuAG, and Yb:Lu{sub 2}O{sub 3}. Absorption cross-section data are presented for Nd:LuAG at 83, 175, and 295 K. Absorption cross-section data was also obtained for Yb:LuAG at 83, 175, and 295 K; the 295 K data was used to generate emission cross-sections using the method of reciprocity. For Yb:Lu{sub 2}O{sub 3}, we present absorption cross-sections at 295 K as well as emission cross-sections derived using reciprocity. -- Highlights: • We present spectral properties for hydrothermally-grown laser crystals. • Absorption cross-section data are presented for Nd:LuAG and Yb:LuAG at 83, 175, and 295 K. • Emission cross-sections are presented for Yb:LuAG at 295 K derived by reciprocity. • We present absorption cross-sections at 295 K as well as emission cross-sections derived using reciprocity for the laser material Yb:Lu{sub 2}O{sub 3}.

Study of the production of 177Lu through 176Yb (n, γ) 177Yb → 177Lu nuclear reaction

International Nuclear Information System (INIS)

Silva, Giovana Pasqualini da; Osso Junior, Joao Alberto

2007-01-01

The beta minus emitter 177 Lu is a promising therapeutic radioisotope for the curative treatment of cancer using labelled proteins. It has a half - life of T 1/2 = 6.71 day and maximum and average β - energies of 421 and 133 keV, resulting in a short range of radiation in tissue. The decay is accompanied by the emission of low energy γ-radiation with 208.3 keV (11%) and 113 keV (6.4%) suitable for simultaneous imaging, 177 Lu can be produced by two different routes, namely, by irradiation of natural Lu 2 O 3 target ( 176 Lu, 2.6%) or enriched (in 176 Lu) Lu 2 O 3 target, as also by irradiation of Yb target (Yb 2 O 3 ) followed by radiochemical separation of 177 Lu from Yb isotopes. The objective of this work is to study the production of 177 Lu through the indirect 176 Yb(n,γ) 177 Yb → 177 Lu nuclear reaction. The results of the production yield of 177 Lu will be shown and compared with the direct reaction. The method of choice for the chemical separation between Lu and Yb was the ion exchange, using an cation exchange resin in Cl - form and α-HIBA as eluent. Preliminary results showed a good separation of 177 Lu from Yb 2 O 3 indirect targets. (author)

Vaporization thermodynamics of Pd-rich intermediate phases in the Pd–Yb system

Energy Technology Data Exchange (ETDEWEB)

Ciccioli, A., E-mail: andrea.ciccioli@uniroma1.it [Dipartimento di Chimica, Sapienza Università di Roma, p.le Aldo Moro 5, 00185 Roma (Italy); Balducci, G.; Gigli, G. [Dipartimento di Chimica, Sapienza Università di Roma, p.le Aldo Moro 5, 00185 Roma (Italy); Provino, A. [Dipartimento di Chimica e Chimica Industriale, Università degli Studi di Genova, via Dodecaneso 31, 16146 Genova (Italy); Istituto SPIN-CNR, Corso Perrone 24, 16152 Genova (Italy); Palenzona, A. [Dipartimento di Chimica e Chimica Industriale, Università degli Studi di Genova, via Dodecaneso 31, 16146 Genova (Italy); Manfrinetti, P. [Dipartimento di Chimica e Chimica Industriale, Università degli Studi di Genova, via Dodecaneso 31, 16146 Genova (Italy); Istituto SPIN-CNR, Corso Perrone 24, 16152 Genova (Italy)

2016-02-20

Highlights: • Vaporization equilibria of Pd–Yb intermediate phases investigated by effusion techniques. • Heats of formation of Pd–Yb compounds determined from decomposition/atomization enthalpies. • Phase diagram of the Pd–Yb system re-drawn. • Influence of the Yb valence state on the thermodynamic properties observed. - Abstract: The vaporization thermodynamics of several intermediate phases in the Pd–Yb system was investigated by means of vaporization experiments performed under Knudsen conditions (KEML, Knudsen Effusion Mass Loss). The following thermal decomposition processes were studied in the overall temperature range 819–1240 K and their enthalpy changes determined: 4 PdYb(s) = Pd{sub 4}Yb{sub 3}(s) + Yb(g); 5/3 Pd{sub 4}Yb{sub 3}(s) = 4/3 Pd{sub 5}Yb{sub 3}(s) + Yb(g); 21/13 Pd{sub 5}Yb{sub 3}(s) = 5/13 Pd{sub 21}Yb{sub 10}(s) + Yb(g); 1/3 Pd{sub 21}Yb{sub 10}(s) = 21/9 Pd{sub 3}Yb(s) + Yb(g). Additional measurements were performed by KEMS (Knudsen Effusion Mass Spectrometry) on a Pd-rich two-phase sample, which allowed to detect both Yb(g) and Pd(g) in the vapor phase and to determine the atomization enthalpy of the Pd{sub 3}Yb phase (Pd-rich composition boundary, Pd{sub 3.08}Yb{sub 0.92}): Pd{sub 3.08}Yb{sub 0.92}(s) = 0.92 Yb(g) + 3.08 Pd(g). The enthalpy of formation of this compound was thereafter determined as −68 ± 2 kJ/mol at. and, by combining this value with the decomposition enthalpies derived by KEML, the enthalpies of formation of the studied Pd–Yb intermediate phases were evaluated (kJ/mol at.): −75 ± 4 (Pd{sub 21}Yb{sub 10}), −75 ± 3 (Pd{sub 5}Yb{sub 3}), −73 ± 3 (Pd{sub 4}Yb{sub 3}), and −66 ± 3 (PdYb). A modified version of the Pd–Yb phase diagram is also reported, re-drawn on the basis of literature data and of new experimental information recently become available.

Optical waveguide formed in Yb:GdCOB and Yb:YCOB crystals by 3.0MeV O{sup +} implantation

Energy Technology Data Exchange (ETDEWEB)

Jiao, Yang, E-mail: sdujy@163.com [College of Physics and Electronics, Shandong Normal University, Jinan 250014 (China)

2013-07-15

Planar optical waveguides were formed in Yb:GdCOB and Yb:YCOB crystals by 3.0 MeV O{sup +} ion implantation at fluence of 2 × 10{sup 15} ions/cm{sup 2} at room temperature, respectively. The prism coupling method was performed to characterize the dark-mode property of the waveguides. The refractive index profiles in the waveguides were reconstructed by reflectivity calculation method (RCM). The results show that after the implantation, a 1.5 μm-wide region with enhanced refractive-index was formed beneath the sample surfaces to act as waveguide structures for both Yb:GdCOB and Yb:YCOB.

The effect of core and lanthanide ion dopants in sodium fluoride-based nanocrystals on phagocytic activity of human blood leukocytes

Energy Technology Data Exchange (ETDEWEB)

Sojka, Bartlomiej [Wroclaw University of Science and Technology, Department of Experimental Physics (Poland); Liskova, Aurelia; Kuricova, Miroslava [Slovak Medical University, Medical Faculty, Department of Immunology and Immunotoxicology (Slovakia); Banski, Mateusz; Misiewicz, Jan [Wroclaw University of Science and Technology, Department of Experimental Physics (Poland); Dusinska, Maria [Norwegian Institute for Air Research, Health Effects Laboratory, Department of Environmental Chemistry (Norway); Horvathova, Mira; Ilavska, Silvia; Szabova, Michaela [Slovak Medical University, Medical Faculty, Department of Immunology and Immunotoxicology (Slovakia); Rollerova, Eva [Slovak Medical University, Faculty of Public Health, Department of Toxicology (Slovakia); Podhorodecki, Artur, E-mail: artur.p.podhorodecki@pwr.edu.pl [Wroclaw University of Science and Technology, Department of Experimental Physics (Poland); Tulinska, Jana, E-mail: jana.tulinska@szu.sk [Slovak Medical University, Medical Faculty, Department of Immunology and Immunotoxicology (Slovakia)

2017-02-15

Sodium fluoride-based β-NaLnF4 nanoparticles (NPs) doped with lanthanide ions are promising materials for application as luminescent markers in bio-imaging. In this work, the effect of NPs doped with yttrium (Y), gadolinium (Gd), europium (Eu), thulium (Tm), ytterbium (Yb) and terbium (Tb) ions on phagocytic activity of monocytes and granulocytes and the respiratory burst was examined. The surface functionalization of <10-nm NPs was performed according to our variation of patent pending ligand exchange method that resulted in meso-2,3-dimercaptosuccinic acid (DMSA) molecules on their surface. Y-core-based NCs were doped with Eu ions, which enabled them to be excited with UV light wavelengths. Cultures of human peripheral blood (n = 8) were in vitro treated with five different concentrations of eight NPs for 24 h. In summary, neither type of nanoparticles is found toxic with respect to conducted test; however, some cause toxic effects (they have statistically significant deviations compared to reference) in some selected doses tested. Both core types of NPs (Y-core and Gd-core) impaired the phagocytic activity of monocytes the strongest, having minimal or none whatsoever influence on granulocytes and respiratory burst of phagocytic cells. The lowest toxicity was observed in Gd-core, Yb, Tm dopants and near-infrared nanoparticles. Clear dose-dependent effect of NPs on phagocytic activity of leukocytes and respiratory burst of cells was observed for limited number of samples.

The effect of core and lanthanide ion dopants in sodium fluoride-based nanocrystals on phagocytic activity of human blood leukocytes

International Nuclear Information System (INIS)

Sojka, Bartlomiej; Liskova, Aurelia; Kuricova, Miroslava; Banski, Mateusz; Misiewicz, Jan; Dusinska, Maria; Horvathova, Mira; Ilavska, Silvia; Szabova, Michaela; Rollerova, Eva; Podhorodecki, Artur; Tulinska, Jana

2017-01-01

Sodium fluoride-based β-NaLnF4 nanoparticles (NPs) doped with lanthanide ions are promising materials for application as luminescent markers in bio-imaging. In this work, the effect of NPs doped with yttrium (Y), gadolinium (Gd), europium (Eu), thulium (Tm), ytterbium (Yb) and terbium (Tb) ions on phagocytic activity of monocytes and granulocytes and the respiratory burst was examined. The surface functionalization of <10-nm NPs was performed according to our variation of patent pending ligand exchange method that resulted in meso-2,3-dimercaptosuccinic acid (DMSA) molecules on their surface. Y-core-based NCs were doped with Eu ions, which enabled them to be excited with UV light wavelengths. Cultures of human peripheral blood (n = 8) were in vitro treated with five different concentrations of eight NPs for 24 h. In summary, neither type of nanoparticles is found toxic with respect to conducted test; however, some cause toxic effects (they have statistically significant deviations compared to reference) in some selected doses tested. Both core types of NPs (Y-core and Gd-core) impaired the phagocytic activity of monocytes the strongest, having minimal or none whatsoever influence on granulocytes and respiratory burst of phagocytic cells. The lowest toxicity was observed in Gd-core, Yb, Tm dopants and near-infrared nanoparticles. Clear dose-dependent effect of NPs on phagocytic activity of leukocytes and respiratory burst of cells was observed for limited number of samples.

Lanthanide phosphonates: Synthesis, thermal stability and magnetic characterization

Energy Technology Data Exchange (ETDEWEB)

Amghouz, Z., E-mail: amghouz.uo@uniovi.es [Departamentos de Quimica Fisica y Analitica y Quimica Organica e Inorganica, Universidad de Oviedo - CINN, 33006 Oviedo (Spain); Garcia, J.R.; Garcia-Granda, S. [Departamentos de Quimica Fisica y Analitica y Quimica Organica e Inorganica, Universidad de Oviedo - CINN, 33006 Oviedo (Spain); Clearfield, A. [Department of Chemistry, Texas A and M University, College Station, TX 77842-3012 (United States); Rodriguez Fernandez, J.; Pedro, I. de [CITIMAC, Facultad de Ciencias, Universidad de Cantabria, 39005 Santander (Spain); Blanco, J.A. [Departamento de Fisica, Universidad de Oviedo, 33007 Oviedo (Spain)

2012-09-25

Highlights: Black-Right-Pointing-Pointer Report of the complete series of lanthanide 1,4-phenylbis(phosphonate). Black-Right-Pointing-Pointer Synthesis under conventional hydrothermal synthesis or microwave-assisted hydrothermal synthesis. Black-Right-Pointing-Pointer Cation size is the key factor for the structural and particles size variations. Black-Right-Pointing-Pointer Thermal behaviour is characterized by unusual very high thermal stability. - Abstract: Series of novel organic-inorganic hybrids materials based on trivalent lanthanides (Ln = Y, La, Ce, Pr, Nd, Sm, Eu, Gd, Tb, Dy, Ho, Er, Tm, Yb, Lu) and 1,4-phenylbis(phosphonate) obtained under hydrothermal conditions either by oven heat or microwave irradiation. The anhydrous compounds containing La, Ce, Pr, Nd, Sm, Eu, Gd, Tb, Dy, and Ho, are isostructural. However, the compounds based on Y, Er, Tm, Yb, and Lu are hydrated and their structures have not yet been solved. The series of compounds are characterized by PXRD, TEM, SEM-EDX and thermal analyses (TG-MS and DSC). TEM study show a variable particles size with a minimum mean-particle size of ca. 30 nm. These compounds exhibit unusual very high thermal stability. The size of particles and the thermal stability are depending on lanthanide(III) cation features. All the investigated materials show paramagnetic behaviour. The magnetic susceptibility data follow a Curie-Weiss laws with paramagnetic effective moments in good agreement with those expected for Ln{sup 3+} free ions.

Transport, Thermal, and Magnetic Properties of YbNi3X9 (X = Al, Ga): A Newly Synthesized Yb-Based Kondo Lattice System

Science.gov (United States)

Yamashita, Tetsuro; Miyazaki, Ryoichi; Aoki, Yuji; Ohara, Shigeo

2012-03-01

We have succeeded in synthesizing a new Yb-based Kondo lattice system, YbNi3X9 (X = Al, Ga). Our study reveals that YbNi3Al9 shows typical features of a heavy-fermion antiferromagnet with a Néel temperature of TN = 3.4 K. All of the properties reflect a competition between the Kondo effect and the crystalline electric field (CEF) effect. The moderate heavy-fermion state leads to an enhanced Sommerfeld coefficient of 100 mJ/(mol\\cdotK2), even if ordered antiferromagnetically. On the other hand, the isostructural gallide YbNi3Ga9 is an intermediate-valence system with a Kondo temperature of TK = 570 K. A large hybridization scale can overcome the CEF splitting energy, and a moderately heavy Fermi-liquid ground state with high local moment degeneracy should form at low temperatures. Note that the quality of single-crystalline YbNi3X9 is extremely high compared with those of other Yb-based Kondo lattice compounds. We conclude that YbNi3X9 is a suitable system for investigating the electronic structure of Yb-based Kondo lattice systems from a heavy-fermion system with an antiferromagnetically ordered ground state to an intermediate-valence system.

Yb-based heavy fermion compounds and field tuned quantum chemistry

Energy Technology Data Exchange (ETDEWEB)

Mun, Eundeok [Iowa State Univ., Ames, IA (United States)

2010-01-01

The motivation of this dissertation was to advance the study of Yb-based heavy fermion (HF) compounds especially ones related to quantum phase transitions. One of the topics of this work was the investigation of the interaction between the Kondo and crystalline electric field (CEF) energy scales in Yb-based HF systems by means of thermoelectric power (TEP) measurements. In these systems, the Kondo interaction and CEF excitations generally give rise to large anomalies such as maxima in ρ(T) and as minima in S(T). The TEP data were use to determine the evolution of Kondo and CEF energy scales upon varying transition metals for YbT₂Zn₂₀ (T = Fe, Ru, Os, Ir, Rh, and Co) compounds and applying magnetic fields for YbAgGe and YbPtBi. For YbT₂Zn₂₀ and YbPtBi, the Kondo and CEF energy scales could not be well separated in S(T), presumably because of small CEF level splittings. A similar effect was observed for the magnetic contribution to the resistivity. For YbAgGe, S(T) has been successfully applied to determine the Kondo and CEF energy scales due to the clear separation between the ground state and thermally excited CEF states. The Kondo temperature, T_K, inferred from the local maximum in S(T), remains finite as magnetic field increases up to 140 kOe. In this dissertation we have examined the heavy quasi-particle behavior, found near the field tuned AFM quantum critical point (QCP), with YbAgGe and YbPtBi. Although the observed nFL behaviors in the vicinity of the QCP are different between YbAgGe and YbPtBi, the constructed H-T phase diagram including the two crossovers are similar. For both YbAgGe and YbPtBi, the details of the quantum criticality turn out to be complicated. We expect that YbPtBi will provide an additional example of field tuned quantum criticality, but clearly there are further experimental investigations left and more ideas needed to understand the basic physics of field-induced quantum

Magnetic structure of the YbMn2SbBi compound

International Nuclear Information System (INIS)

Morozkin, A.V.; Manfrinetti, P.

2011-01-01

Graphical abstract: Display Omitted Research highlights: → A neutron diffraction investigation in zero applied field of La 2 O 2 S-type YbMn 2 SbBi shows antiferromagnetic ordering below 138(3) K and ferrimagnetic ordering below 112(3) K. → Between 138 and 112 K, the magnetic structure of YbMn 2 SbBi consists of antiferromagnetically coupled ab-plane magnetic moments of the manganese atoms (D 1d magnetic point group). → Below 112(3) K, the magnetic structure of YbMn 2 SbBi becames the sum antiferromagnetic component with D 1d magnetic point group and ferromagnetic one with C 2 magnetic point group. → The magnitude of Yb and Mn magnetic moments in YbMn 2 SbBi at 2 K (M Yb = 3.6(2) μ B , M Mn = 3.5(2) μ B ) correspond to the trivalent state of the Yb ions and tetravalent state of the Mn ions. - Abstract: A neutron diffraction investigation has been carried out on the trigonal La 2 O 2 S-type (hP5, space group P3-bar ml, No. 164; also CaAl 2 Si 2 -type) YbMn 2 SbBi intermetallic compound. The YbMn 2 SbBi presents antiferromagnetic ordering below 138(3) K and ferrimagnetic ordering below 112(3) K. Between 138 and 112 K, the magnetic structure of YbMn 2 SbBi consists of antiferromagnetically coupled ab-plane magnetic moments of the manganese atoms (D 1d magnetic point group). Below 112(3) K, the ferromagnetic components of Yb and Mn begin to develop, and the magnetic structure of YbMn 2 SbBi becames the sum antiferromagnetic component with D 1d magnetic point group and ferromagnetic one with C 2 magnetic point group. The magnitude of Yb and Mn magnetic moments in YbMn 2 SbBi at 2 K (M Yb = 3.6(2) μ B , M Mn = 3.5(2) μ B ) correspond to the trivalent state of the Yb ions and tetravalent state of the Mn ions.

A mass spectrometric study of the neutral and ionic vapor components of ytterbium chlorides; formation enthalpies of YbCl2 and YbCl3 molecules, and YbCl3- and YbCl4- ions in the gas phase

International Nuclear Information System (INIS)

Kuznetsov, F.Yh.; Kudin, L.S.; Pogrebnoj, A.M.; Butman, M.F.; Burdukovskaya, G.G.

1997-01-01

Ionic and neutral components of saturated vapour over the ytterbium di-and trichloride is studied through the Knudsen effusive method with mass-spectromic registration of evaporated products within the temperature range of 1000-1300 K. It is found that ytterbium trichloride is subjected to thermal decomposition with formation of ytterbium dichloride and molecular chloride. Sublimation enthalpy and enthalpy of YbCl 2 and YbCl 3 molecules formation in a gaseous phase at 298 K, comprising 356±6, 293±8, -425±6 and -667±6 kJ/mole correspondingly, are determined with application of 2 and 3 thermodynamical laws. Enthalpies of YbCl 3 - and YbCl 4 - negative ions formation in a gaseous phase at 298 K equal to -895 and -1211±30 kJ/mole correspondingly are calculated by measured equilibrium constants ion-molecular reaction. 30 refs., 3 figs., 3 tabs

YB0 SERVICES INSTALLATION COMPLETED

CERN Document Server

The beauty of the completed YB0 was briefly visible at P5 as preparations continue for Tracker installation. A tremendous effort, lasting 7 months and involving more than 100 workers on the busiest days, resulted in 5700 electrical cables, 780 optical cables with 65k fibre channels, and 550 pipes laid on YB0 for HB, EB and Tracker.

Utilization of visible to NIR light energy by Yb"+"3, Er"+"3 and Tm"+"3 doped BiVO_4 for the photocatalytic degradation of methylene blue

International Nuclear Information System (INIS)

Regmi, Chhabilal; Kshetri, Yuwaraj K.; Ray, Schindra Kumar; Pandey, Ramesh Prasad; Lee, Soo Wohn

2017-01-01

Highlights: • Lanthanide doped BiVO_4 as highly efficient upconversion and photocatalytic material. • Well defined beads like morphology for better photocatalytic activity. • Effective utilization of NIR and visible light for efficient photocatalytic degradation of methylene blue. • Nontoxic to human cells, potential for application in biological fields. - Abstract: Lanthanide-doped BiVO_4 semiconductors with efficient photocatalytic activities over a broad range of the solar light spectrum have been synthesized by the microwave hydrothermal method using ethylenediaminetetraacetic acid (EDTA). The structural, morphological, and optical properties of the as-synthesized samples were evaluated by Scanning Electron Microscopy (SEM), Transmission Electron Microscopy (TEM), X-ray powder diffraction (XRD), Raman spectroscopy, FT-IR spectroscopy, UV–vis diffuse reflectance spectroscopy (DRS), and photoluminescence spectroscopy (PL). The chemical compositions were analyzed by X-ray photoelectron spectroscopy (XPS). The toxicity of the samples was measured using Mus musculus skin melanoma cells (B16-F10 (ATCC"® CRL-6475™)) and were found to be nontoxic for human cells. The photocatalytic efficiency of the prepared samples was evaluated by methylene blue (MB) degradation. The best photocatalytic activity was shown by BiVO_4 with 6:3:3 mol percentage of Yb"+"3:Er"+"3:Tm"+"3 in all solar light spectrum. The synthesized samples possess low band gap energy and a hollow structure suitable for the better photocatalytic activity. The observed NIR photoactivity supports that the upconversion mechanism is involved in the overall photocatalytic process. Therefore, this approach provides a better alternative upconversion material for integral solar light absorption.

Buffer layers and articles for electronic devices

Science.gov (United States)

Paranthaman, Mariappan P.; Aytug, Tolga; Christen, David K.; Feenstra, Roeland; Goyal, Amit

2004-07-20

Materials for depositing buffer layers on biaxially textured and untextured metallic and metal oxide substrates for use in the manufacture of superconducting and other electronic articles comprise RMnO.sub.3, R.sub.1-x A.sub.x MnO.sub.3, and combinations thereof; wherein R includes an element selected from the group consisting of La, Ce, Pr, Nd, Pm, Sm, Eu, Gd, Tb, Dy, Ho, Er, Tm, Yb, Lu, and Y, and A includes an element selected from the group consisting of Be, Mg, Ca, Sr, Ba, and Ra.

Neutron activation analysis of ultrabasis rock by Ge(Li) γ-ray spectrometry and group separation

International Nuclear Information System (INIS)

Chen Baoguan; Yuan Ling; Fang Chanmeng

1986-01-01

The analytical procedure for determination of 21 elements in two ultrabasis rock samples with Ge(Li) gamma-ray spectrometry and group separation was described. 8 elements including Cr, Fe, Co, Sc, Mn, Na, Cl and Br have been directly determined by INAA. 13 elements including La, Ce, Nd, Sm, Gd, Eu, Tb, Ho, Tm, Yb, Lu, Zn and Cs have been determined by radiochemical separation. The samples of international standard AGV-1 (Andesite) have also been analyzed. The agreement of the results with the values proposed by F.J.Flanagan is satisfactory

Identification and characterization of NF-YB family genes in tung tree.

Science.gov (United States)

Yang, Susu; Wang, Yangdong; Yin, Hengfu; Guo, Haobo; Gao, Ming; Zhu, Huiping; Chen, Yicun

2015-12-01

The NF-YB transcription factor gene family encodes a subunit of the CCAAT box-binding factor (CBF), a highly conserved trimeric activator that strongly binds to the CCAAT box promoter element. Studies on model plants have shown that NF-YB proteins participate in important developmental and physiological processes, but little is known about NF-YB proteins in trees. Here, we identified seven NF-YB transcription factor-encoding genes in Vernicia fordii, an important oilseed tree in China. A phylogenetic analysis separated the genes into two groups; non-LEC1 type (VfNF-YB1, 5, 7, 9, 11, 13) and LEC1-type (VfNF-YB 14). A gene structure analysis showed that VfNF-YB 5 has three introns and the other genes have no introns. The seven VfNF-YB sequences contain highly conserved domains, a disordered region at the N terminus, and two long helix structures at the C terminus. Phylogenetic analyses showed that VfNF-YB family genes are highly homologous to GmNF-YB genes, and many of them are closely related to functionally characterized NF-YBs. In expression analyses of various tissues (root, stem, leaf, and kernel) and the root during pathogen infection, VfNF-YB1, 5, and 11 were dominantly expressed in kernels, and VfNF-YB7 and 9 were expressed only in the root. Different VfNF-YB family genes showed different responses to pathogen infection, suggesting that they play different roles in the pathogen response. Together, these findings represent the first extensive evaluation of the NF-YB family in tung tree and provide a foundation for dissecting the functions of VfNF-YB genes in seed development, stress adaption, fatty acid synthesis, and pathogen response.

Kinetics of electrophilic exchange of lanthanide(3) and copper(2) ions in aqueous solutions of ethylenediaminetetraacetates. [Rare earths: La,Pr,Nd,Eu,Gd,Tb,Er,Yb

Energy Technology Data Exchange (ETDEWEB)

Nikitenko, S.I.; Martynenko, L.I.; Pechurova, N.I.; Spitsyn, V.I. (Moskovskij Gosudarstvennyj Univ. (USSR))

1984-05-01

Electrophilic exchange in the MA/sup -/ - Cu/sup 2 +/ (M/sup 3 +/=La/sup 3 +/, PUPSILON/sup 3 +/, Nd/sup 3 +/, Eu/sup 3 +/, Gd/sup 3 +/, Tb/sup 3 +/, Er/sup 3 +/, Yb/sup 3 +/, A/sup 4 -/=ethylenediaminetetraacetate) systems is studied. Copper is chosen as a constituent cation, because the stability of the CuA/sup 2 +/- complex is higher than that of the MA/sup -/ complex, besides the CuA/sup 2 -/, is characterized by a high extinction coefficient E/sub 280/=3200. Electrophilic exchange in the systems is shown to be realized through the acid dissociation mechanism and through the association mechanism. Consideration of the acid dissociation mechanism assumes that the exchange is limited by a break in the metal-oxygen bond in the intermediate protonated complex. In case of the association mechanism it is limited by a break in the metal-nitrogen bond in the intermediate binuclear complex. Rate constants of the limiting stage are calculated. Dependences of the rate constants of exchange on the stability of the complexes, the order number of the element, acidity of medium, Cu/sup 2 +/ concentration are given. Differences are shown to exist between the exchange mechanisms in the studied: systems for the REE of cerium and yttrium subgroups.

Properties of the divalent-Yb compound YbAu{sub 2}Si{sub 2} under extreme conditions

Energy Technology Data Exchange (ETDEWEB)

Kaštil, J.; Míšek, M.; Kamarád, J.; Arnold, Z. [Institute of Physics AS CR, v.v.i., Na Slovance 1999/2, 182 21 Prague 8 (Czech Republic); Vlášková, K. [Charles University, Faculty of Mathematics and Physics, Department of Condensed Matter Physics, Ke Karlovu 5, 12116 Prague 2 (Czech Republic); Prchal, J., E-mail: prchal@karlov.mff.cuni.cz [Charles University, Faculty of Mathematics and Physics, Department of Condensed Matter Physics, Ke Karlovu 5, 12116 Prague 2 (Czech Republic); Diviš, M.; Doležal, P.; Prokleška, J.; Valenta, J.; Fikáček, J.; Rudajevová, A.; Kriegner, D. [Charles University, Faculty of Mathematics and Physics, Department of Condensed Matter Physics, Ke Karlovu 5, 12116 Prague 2 (Czech Republic)

2017-01-15

Polycrystalline YbAu{sub 2}Si{sub 2} has been prepared by arc melting and a non-standard anisotropic thermal expansion is observed at low temperatures. A non-magnetic Yb{sup 2+} valence state is derived from magnetization, magnetic-susceptibility, heat-capacity and electrical-conductivity measurements in the temperature range from 0.3 to 300 K and at external pressures up to 3.2 GPa. By both experimental and theoretical investigations, YbAu{sub 2}Si{sub 2} is confirmed to be a system with a weak electron-electron correlations and a small electron-phonon interaction. Application of hydrostatic pressure does not reveal any change of state in the range of applied pressures.

Novel Sr{sub 2}LuF{sub 7}–SiO{sub 2} nano-glass-ceramics: Structure and up-conversion luminescence

Energy Technology Data Exchange (ETDEWEB)

Yanes, A.C.; Castillo, J. del, E-mail: fjvargas@ull.edu.es; Luis, D.; Puentes, J.

2016-02-15

Novel transparent nano-glass-ceramics comprising RE-doped Sr{sub 2}LuF{sub 7} nanocrystals have been obtained by thermal treatment of precursor sol–gel glasses. The precipitated Sr{sub 2}LuF{sub 7} nanocrystals with sizes from 4.5 to 11.5 nm, confirmed by X-Ray Diffraction and Transmission Electron Microscopy images, show a cubic phase structure. The luminescent features of Eu{sup 3+} ions, used as structural probes, evidence the distribution of RE ions into the fluoride nanocrystals. Under 980 nm laser excitation, intense UV, vis and NIR up-conversion emissions were observed and studied in Yb{sup 3+}–Tm{sup 3+}, Yb{sup 3+}–Er{sup 3+} and Yb{sup 3+}–Ho{sup 3+} co-doped nano-glass-ceramics. These results suggest considering these nano-glass-ceramics for potential optical applications as high efficient UV up-conversion materials in UV solid state lasers, infrared tuneable phosphors and photonic integrated devices. - Highlights: • Novel sol-gel glass-ceramics with RE{sup 3+}-Sr{sub 2}LuF{sub 7} doped nanocrystals were obtained. • Eu{sup 3+} probe ion was used to distinguish between amorphous and crystalline environments. • The incorporation of an important fraction of RE ions into nanocrystals was confirmed. • Under 980 nm excitation, intense UV-vis-NIR up-conversion emissions were observed.

Development of Yb-169 radiation source for new nondestructive inspection

International Nuclear Information System (INIS)

Yamabayashi, Hisamichi

1994-01-01

As the nondestructive inspection method for large structures, there has been radiography, and X-ray and γ-ray have been used as the radiation. The transmissivity of radiation through materials changes by the energy of the radiation and the density and thickness of the materials. At present about 880 γ-ray radiography apparatuses are used in Japanese private enterprises, and about 70% of them use 192 Ir γ-ray sources, and about 30% use 60 Co or 137 Cs sources. Recently the defect inspection for the worlded parts of thin wall small tubes and so on have become to be regarded as important, and the 169 Yb source that emits lower energy γ-ray is suitable to the purpose. There are many reports that 169 Yb radiography was applied successfully. As the 169 Yb radiation source, pellets and balls are on the market. 169 Yb is made by the neutron irradiation of 168 Yb in nuclear reactors. The characteristics of 169 Yb, the manufacture of 169 Yb radiation sources and the applicability of 169 Yb radiation sources to nondestructive inspection are reported. Also in Japan, many basic experiments on 169 Yb radiation sources have been carried out, and the irradiation apparatuses are small and light, and the control area can be set small. (K.I.)

Laser-diode pumped 40-W Yb:YAG ceramic laser.

Science.gov (United States)

Hao, Qiang; Li, Wenxue; Pan, Haifeng; Zhang, Xiaoyi; Jiang, Benxue; Pan, Yubai; Zeng, Heping

2009-09-28

We demonstrated a high-power continuous-wave (CW) polycrystalline Yb:YAG ceramic laser pumped by fiber-pigtailed laser diode at 968 nm with 400 mum fiber core. The Yb:YAG ceramic laser performance was compared for different Yb(3+) ion concentrations in the ceramics by using a conventional end-pump laser cavity consisting of two flat mirrors with output couplers of different transmissions. A CW laser output of 40 W average power with M(2) factor of 5.8 was obtained with 5 mol% Yb concentration under 120 W incident pump power. This is to the best of our knowledge the highest output power in end-pumped bulk Yb:YAG ceramic laser.

Parameters of thermoelectric power and electronic structure of Yb-based compounds of YbM2X2(M=Fe,Co,Ni,Cu; X=Si,Ge) type

International Nuclear Information System (INIS)

Levin, E.M.; Kuzhel', B.S.

1990-01-01

Thermoelectric power of Yb-based intermetallic alloys YbM 2 Si 2 (M-Co,Ni,Cu) and YbM 2 Ge 2 (M=Fe,Co,Ni) have been investigated and found to have anomalous low-temperature peaks conditioned by intermediate Yb valency. Calculation of electronic structure parameters performed in frames of the localized Fermi-liquid model using experimental data on the thermoelectric power is in good agreement with results of YbCu 2 Si 2 band structure calculation based on the experimental value of the electronic heat capacity with regard for the (2J+1) - fold Yb 2+ degeneration

The contribution of valence unstable ytterbium states into kinetic properties of YbNi2-xGe2+x and YbCu2-xSi2+x

International Nuclear Information System (INIS)

Kuzhel, B.C.; Shcherba, I.D.; Kravchenko, I.I.

2006-01-01

The intermetalic YbNi 2-x Ge 2+x (-0.25>=x>=0.25) and YbCu 2-x Si 2+x (-0.20>=x>=0.20) alloy systems (CeGa 2 Al 2 -type crystal structure) were studied by measuring X-ray absorption and diffraction at room temperatures as well as electrical resistivity and thermopower in the 4.2-300K temperature range. The temperature dependence of the contribution of valence unstable Yb ions to the total electrical resistance has been analyzed. The qualitative estimation of this contribution has been performed by utilizing the following equation:Δρ Yb (T)=ρ exp (T)-ρ YbCu 2 Ge 2 (T)-Δρ 4.2K ,where Δρ YbCu 2 Ge 2 (T) is the temperature dependence of YbCu 2 Ge 2 electrical resistance, Δρ 4.2 =ρ 4.2 (exp)-ρ 4.2 (YbCu 2 Ge 2 )

White photoluminescence emission from ZrO{sub 2} co-doped with Eu{sup 3+}, Tb{sup 3+} and Tm{sup 3+}

Energy Technology Data Exchange (ETDEWEB)

Lovisa, L.X., E-mail: lovisaengmat@ig.com.br [Departamento de Engenharia de Materiais, Universidade Federal do Rio Grande do Norte, 59072-970, Natal, RN (Brazil); Araújo, V.D. [UACSA, Universidade Federal Rural de Pernambuco, 54510-000, Cabo de Santo Agostinho, PE (Brazil); Tranquilin, R.L.; Longo, E. [LIEC, Universidade Federal de São Carlos, 13565-905, São Carlos, SP (Brazil); Li, M.S. [Instituto de Física de São Carlos, Universidade de São Paulo, 13566-590, São Carlos, SP (Brazil); Paskocimas, C.A.; Bomio, M.R.D.; Motta, F.V. [Departamento de Engenharia de Materiais, Universidade Federal do Rio Grande do Norte, 59072-970, Natal, RN (Brazil)

2016-07-25

The search for high efficiency, reliable, low power consumption and environmental friendly materials for white light-emitting diodes has become a proficient field. Single-phase doped materials have been made to solve some of these challenges. Particles with color-tunable emission can be obtained by a combination of some lanthanide ions in the host material. The luminescence properties and crystalline structure of ZrO{sub 2} particles co-doped with rare earth ions (RE{sup 3+} = Tb{sup 3+}, Eu{sup 3+} and Tm{sup 3+}) calcined at different temperatures were studied. We aimed to investigate the emission spectrum of the particles in the red, green, and blue regions under UV excitation. The x and y coordination chromaticity - (x = 0.34, y = 0.34) and (x = 0.31, y = 0.34) - presented values close to those of the white color (x = y = 0.33). In conclusion, the ZrO{sub 2}:RE{sup 3+} powers were successfully obtained by the complex polymerization method and are promising candidates for white light-emitting applications. - Highlights: The ZrO{sub 2}:RE materials presented here are promising photoluminescent materials. The CIE coordinates calculated are disposed in the blank region in the CIE diagram. The results for the Raman confirm the response obtained by XRD: stabilization of cubic phase.

A [Cyclentetrakis(methylene)]tetrakis[2-hydroxybenzamide]Ligand That Complexes and Sensitizes Lanthanide(III) Ions

Energy Technology Data Exchange (ETDEWEB)

D' Aleo, Anthony; Xu, Jide; Do, King; Muller, Gilles; Raymond, Kenneth N.

2009-04-30

The synthesis of a cyclen derivative containing four isophthalamide groups (L{sup 1}) is described. The spectroscopic properties of the Ln(III) complexes of L{sup 1} (Ln = Gd, Tb, Yb, Eu) reveal changes of the UV/visible absorption, circular dichroism absorption, luminescence and circularly polarized luminescence properties. It is shown that at least two metal complex species are present in solution, whose relative amounts are pH dependent. When at pH > 8.0, an intense long lived emission is observed (for [L{sup 1}Tb] and [L{sup 1}Yb]) while at pH < 8.0, a weaker, shorter-lived species predominates. Unconventional Ln(III) emitters (Pr, Nd, Sm, Dy and Tm) were sensitized in basic solution, both in the visible and in the near infra-red, to measure the emission of these ions.

Magnetocaloric effect in In doped YbMnO{sub 3}

Energy Technology Data Exchange (ETDEWEB)

Sattibabu, Bhumireddi, E-mail: bsb.satti@gmail.com [School of Engineering Sciences and Technology, University of Hyderabad, Hyderabad 500046 (India); Department of Electronics and Physics, Institute of Science, GITAM University, Visakhapatnam 530045 (India); Bhatnagar, A.K., E-mail: anilb42@gmail.com [School of Physics, University of Hyderabad, Hyderabad 500046 (India); Vinod, K.; Mani, Awadhesh [Condensed Matter Physics Division, Materials Science Group, Indira Gandhi Centre for Atomic Research, Kalpakkam 603102 (India)

2017-06-01

Magnetic and magnetocaloric (MCE) properties of Yb{sub 0.9}In{sub 0.1}MnO{sub 3} and Yb{sub 0.8}In{sub 0.2}MnO{sub 3} polycrystalline samples are presented in this paper. Isothermal magnetization measurements reveal a field induced magnetic transition. Magnetic entropy change of 2.34±0.35 J/mole-K for Yb{sub 0.9}In{sub 0.1}MnO{sub 3} and 2.64±0.38 J/mole-K for Yb{sub 0.8}In{sub 0.2}MnO{sub 3} field change ΔH =10 KOe is observed around the ferromagnetic ordering temperature of Yb{sup 3+}. Values of relative cooling power for the same field change are found to be 38.03±9 J /mol, and 40.90±10 J/mol for Yb{sub 0.9}In{sub 0.1}MnO{sub 3} and Yb{sub 0.8}In{sub 0.2}MnO{sub 3}, respectively. These values suggest In doped YbMnO{sub 3} may be a potential candidate for magnetic refrigerant at low temperatures.

Laser-cooling effects in few-ion clouds of Yb+

International Nuclear Information System (INIS)

Edwards, C.S.; Gill, P.; Klein, H.A.; Levick, A.P.; Rowley, W.R.C.

1994-01-01

We report some laser-cooling effects in a few 172 Yb + ions held in a Paul trap. Pronounced cloud-to-crystal phase transitions have been observed as discontinuities in the Yb + fluorescence spectrum of the 369 nm cooling transition. The first reported two-dimensional images of Yb + clouds with evidence of crystal structure have been recorded using a photon-counting position-sensitive detector. An ion temperature of 100 mK has been estimated from the size of a single ion image. Stepwise cooling of a re-heated, few-ion Yb + cloud was also observed. (orig.)

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.

Magnetic linear dichroism in x-ray emission spectroscopy: Yb in Yb3 Fe5 O12

NARCIS (Netherlands)

Groot, F.M.F. de; Krisch, M.H.; Sette, F.; Vogel, J.

2000-01-01

A magnetic linear dichroism MLD effect of up to 5% has been observed in the 2p 1/2 4d x-ray emission spectrum of Yb in Yb 3 Fe 5 O 12 . The spectral shape is well reproduced with an atomic multiplet calculation of the 4d to 2p decay. It is shown that the details of the spectral shapes are

Electron spin resonance in Yb-based Kondo-lattice systems; Elektronenspinresonanz in Yb-basierten Kondogitter-Systemen

Energy Technology Data Exchange (ETDEWEB)

Wykhoff, Jan

2010-07-07

The systems Yb{sub 1-w}A{sub 1-w}(Rh{sub 1-x}Co{sub x})(Si{sub 1-y}Ge{sub y}){sub 2} with A=La respectively Lu, as well as YbIr{sub 2}Si{sub 2} are studied. The measurements are presented sortedly for systems, dopings, and external parameters. Beside these external parameters furthermore the orientation of the sample related to the quasistatic magnetic field and the microwave magnetic field was varied.

Post-adsorption process of Yb phosphate nano-particle formation by Saccharomyces cerevisiae

Science.gov (United States)

Jiang, MingYu; Ohnuki, Toshihiko; Tanaka, Kazuya; Kozai, Naofumi; Kamiishi, Eigo; Utsunomiya, Satoshi

2012-09-01

In this study, we have investigated the post-adsorption process of ytterbium (Yb) phosphate nano-particle formation by Saccharomyces cerevisiae (yeast). The yeast grown in P-rich medium were exposed to 1.44 × 10-4 mol/L Yb(III) solution for 2-120 h, and 2 months at 25 ± 1 °C at an initial pH of 3, 4, or 5, respectively. Ytterbium concentrations in solutions decreased as a function of exposure time. Field-emission scanning electron microscopy equipped with energy-dispersive X-ray spectroscopy (FESEM), transmission electron microscopy (TEM), and synchrotron-based extended X-ray absorption fine structure (EXAFS) analyses revealed that nano-sized blocky Yb phosphate with an amorphous phase formed on the yeast cells surfaces in the solutions with Yb. These nano-sized precipitates that formed on the cell surfaces remained stable even after 2 months of exposure at 25 ± 1 °C around neutral pHs. The EXAFS data revealed that the chemical state of the accumulated Yb on the cell surfaces changed from the adsorption on both phosphate and carboxyl sites at 30 min to Yb phosphate precipitates at 5 days, indicating the Yb-phosphate precipitation as a major post-adsorption process. In addition, the precipitation of Yb phosphate occurred on cell surfaces during 7 days of exposure in Yb-free solution after 2 h of exposure (short-term Yb adsorption) in Yb solution. These results suggest that the released P from the inside of yeast cells reacted with adsorbed Yb on cell surfaces, resulting in the formation of Yb precipitates, even though no P was added to the exposure solution. In an abiotic system, the EXAFS data showed that the speciation of sorbed Yb on the reference materials, carboxymethyl cellulose and Ln resin, did not change even when the Yb was exposed to P solution, without forming Yb phosphate precipitates. This result strongly suggests that the cell surface of the yeast plays an important role in the Yb-phosphate precipitation process, not only as a carrier of the

Labelling of ethylenediaminetetramethylene phosphonic acid (EDTMP) with 175Yb

International Nuclear Information System (INIS)

Azmairit Aziz

2009-01-01

Ytterbium-175 ( 175 Yb) is one of radioisotopes that can be used for therapy due to its β-particle emission (T 1/2 = 4.2 d, E β(max) = 480 keV). Beside that, this radioisotope also emits γ-rays of 113 keV (1.9%), 282 keV (3.1%) and 396 keV (6.5%) which are suitable energy for imaging as long as therapeutic applications. EDTMP could be labeled with radionuclide of 175 Yb as an alternative radiopharmaceutical for bone pain palliation due to bone metastases. Labeling of ethylenediaminetetramethylenephosphonic acid with 175 Yb has been studied. Various influential parameters in labeling conditions i.e. the amount of EDTMP ligand, the pH of labeling, incubation time and the amount of 175 Yb solution were studied in order to obtain high labeling efficiency of 175 Yb-EDTMP. The labeling efficiency was obtained by radiochemical purity that was determined by paper chromatography and paper electrophoresis techniques. The optimum labeling condition was obtained at pH 7, 4 mg of EDTMP ligand, 100 µL (105 µg; 0.6 µmol) of 175 Yb solution and 30 minutes incubation time at room temperature. The complex formed was gave maximum labeling efficiency of 98.81 ± 0.15%. Owing to the results, EDTMP ligand can be labeled with 175 Yb radionuclide with labeling efficiency more than 95%. (author)

Lifetimes of high-spin states in {sup 162}Yb

Energy Technology Data Exchange (ETDEWEB)

Carpenter, M.P.; Janssens, R.V.F.; Henry, R.G. [and others

1995-08-01

A measurement on lifetimes of high-spin states in the yrast and near-yrast rotational bands in {sup 162}Yb was carried out at ATLAS in order to determine the evolution of collectivity as a function of angular momentum using the {sup 126}Te({sup 40}Ar,4n){sup 162}Yb reaction at 170 MeV. Previous lifetime measurements in the {sup 164,166,168}Yb isotopes showed a dramatic decrease in the transition quadrupole moment Q{sub t} with increasing spin. It was suggested that this decrease in Q{sub t} is brought about by the rotationally-induced deoccupation of high-j configurations, mainly i{sub 13/2} neutrons. If this interpretation is correct, the heavier isotopes should have a larger decrease in Q{sub t} than the lighter mass nuclides due to the position of the Fermi surface in the i{sub 13/2} subshell. Indeed, {sup 160}Yb does not show a clear decrease in Q{sub t} at high spin. No high spin lifetime information exists for {sup 162}Yb, thus this experiment fills the gap of measured Q{sub t}`s in the light Yb series. The data is currently being analyzed.

Near-yrast spectroscopy of 164Yb and neighbouring nuclei

International Nuclear Information System (INIS)

Jonsson, S.; Roy, H. and others.

1983-03-01

High-spin states in 164 Yb have been populated in the 152 Sm( 16 0,4n) and 150 Sm( 18 0,4n) reactions. From studies of γ-γ coincidences, γ-ray angular distributions and conversion electron measurements the level scheme has been constructed. The g-band and the S-band have been established to spin and parity 22(sup)+ and 26(sup)+, respectively, and the rotational sequences (π,α)=(-,1) 1 , (-,0) 1 and (-,0) 2 to 23(sup)-, 24(sup)- and 18(sup)-, respectively. The sidebands in 162 , 164 Er and 164 , 166 Yb are discussed. Constructed two-quasineutron configurations and cranked shell model (CSM) calculations are compared with the experimental results in 164 Yb. Residual interactions between quasiparticles in 164 Yb are calculated. Crossing frequencies and the gain in alignment are summarized for the Yb isotopes and the main features are discussed. (author)

Yb5Ni4Sn10 and Yb7Ni4Sn13: New polar intermetallics with 3D framework structures

International Nuclear Information System (INIS)

Lei Xiaowu; Sun Zhongming; Li Longhua; Zhong Guohua; Hu Chunli; Mao Jianggao

2010-01-01

The title compounds have been obtained by solid state reactions of the corresponding pure elements at high temperature, and structurally characterized by single-crystal X-ray diffraction studies. Yb 5 Ni 4 Sn 10 adopts the Sc 5 Co 4 Si 10 structure type and crystallizes in the tetragonal space group P4/mbm (No. 127) with cell parameters of a=13.785(4) A, c=4.492 (2) A, V=853.7(5) A 3 , and Z=2. Yb 7 Ni 4 Sn 13 is isostructural with Yb 7 Co 4 InGe 12 and crystallizes in the tetragonal space group P4/m (No. 83) with cell parameters of a=11.1429(6) A, c=4.5318(4) A, V=562.69(7) A 3 , and Z=1. Both structures feature three-dimensional (3D) frameworks based on three different types of one-dimensional (1D) channels, which are occupied by the Yb atoms. Electronic structure calculations based on density functional theory (DFT) indicate that both compounds are metallic. These results are in agreement with those from temperature-dependent resistivity and magnetic susceptibility measurements. - Graphical abstract: Two new ytterbium nickel stannides, namely, Yb 5 Ni 4 Sn 10 and Yb 7 Ni 4 Sn 13 , have been synthesized and structurally characterized by single-crystal X-ray diffraction studies. Both their structures feature three-dimensional (3D) frameworks based on three different types of one-dimensional (1D) channels, which are situated by all the Yb atoms. Electronic structure calculations based on density functional theory (DFT) indicate that both compounds are metallic, which are in accordance with the results from temperature-dependent resistivity and magnetic susceptibility measurements.

Cold shock protein YB-1 is involved in hypoxia-dependent gene transcription

International Nuclear Information System (INIS)

Rauen, Thomas; Frye, Bjoern C.; Wang, Jialin; Raffetseder, Ute; Alidousty, Christina; En-Nia, Abdelaziz; Floege, Jürgen; Mertens, Peter R.

2016-01-01

Hypoxia-dependent gene regulation is largely orchestrated by hypoxia-inducible factors (HIFs), which associate with defined nucleotide sequences of hypoxia-responsive elements (HREs). Comparison of the regulatory HRE within the 3′ enhancer of the human erythropoietin (EPO) gene with known binding motifs for cold shock protein Y-box (YB) protein-1 yielded strong similarities within the Y-box element and 3′ adjacent sequences. DNA binding assays confirmed YB-1 binding to both, single- and double-stranded HRE templates. Under hypoxia, we observed nuclear shuttling of YB-1 and co-immunoprecipitation assays demonstrated that YB-1 and HIF-1α physically interact with each other. Cellular YB-1 depletion using siRNA significantly induced hypoxia-dependent EPO production at both, promoter and mRNA level. Vice versa, overexpressed YB-1 significantly reduced EPO-HRE-dependent gene transcription, whereas this effect was minor under normoxia. HIF-1α overexpression induced hypoxia-dependent gene transcription through the same element and accordingly, co-expression with YB-1 reduced HIF-1α-mediated EPO induction under hypoxic conditions. Taken together, we identified YB-1 as a novel binding factor for HREs that participates in fine-tuning of the hypoxia transcriptome. - Highlights: • Hypoxia drives nuclear translocation of cold shock protein YB-1. • YB-1 physically interacts with hypoxia-inducible factor (HIF)-1α. • YB-1 binds to the hypoxia-responsive element (HRE) within the erythropoietin (EPO) 3′ enhancer. • YB-1 trans-regulates transcription of hypoxia-dependent genes such as EPO and VEGF.

Trace diffusion of different nuclear reactions products in polycrystalline tantalum

International Nuclear Information System (INIS)

Beyer, G.J.; Fromm, W.D.; Novgorodov, A.F.

1976-07-01

Measurements of the lattice diffusion coefficients for carrier free isotopes of Hf, Lu, Yb, Tm, Tb, Gd, Eu, Ba, Cs, Y, Sr, Rb and As in polycrystalline tantalum were made over the temperature range 1700 Fsub(As)>Fsub(lanthanides)>Fsub(Sr)>Fsub(Ba)>Fsub(Hf)>Fsub(Rb)>Fsub(Cs). The data indicate, that the Arrhenius relation was obeyed over the entire temperature range. Within the lanthanide-group no differences in the diffusion velocities could be detected, this fact points to a diffusion mechanism of Me 3+ -ions of lanthanides, Me 2+ -ions of earth alkaline elements and Me + -ions of alkaline elements. (author)

Ultraviolet and near-infrared luminescence of LaBO3:Ce3+,Yb3+

Science.gov (United States)

Wei, Heng-Wei; Shao, Li-Ming; Jiao, Huan; Jing, Xi-Ping

2018-01-01

Ce3+ or Yb3+ singly doped LaBO3 and Ce3+-Yb3+ co-doped LaBO3 were prepared by conventional solid state reactions at 1100 °C and their photoluminescence (PL) properties were investigated. The emission spectrum of LaBO3:Ce3+,Yb3+ contains both the Ce3+ ultraviolet (UV) emissions (355 nm and 380 nm) and the Yb3+ near infrared (NIR) emission (975 nm) when excited by the UV light at 270 nm. By using the data of the Ce3+ decay curves and the PL intensities of both Ce3+ and Yb3+, the energy transfer efficiency (η) from Ce3+ to Yb3+, the actual energy transfer efficiency (AE) and the quantum efficiency (Q) of the Yb3+ emission were calculated. In the Ce3+-Yb3+ co-doped LaBO3, Ce3+ can transfer its absorbed energy to Yb3+ efficiently (η can be over 60%), and Yb3+ shows the Q value over 50% when it accepts the energy from Ce3+, which results in the low AE value ∼30%. The energy transfer process from Ce3+ to Yb3+ may be understood by the charge transfer mechanism: Ce3+ + Yb3+ ↔ Ce4+ + Yb2+. Particularly the Ce3+-Yb3+ co-doped LaBO3 phosphor gives the emissions mainly in the UV range and the NIR range with a portion of visible emissions in eye-insensitive range. This unique property may be suitable for applications in anti-counterfeiting techniques and public security affairs.

Nuclear spectroscopic studies in 162Yb

International Nuclear Information System (INIS)

Behrens, H.

1980-01-01

The decay of the highly excited 162 Yb nuclei formed in the reaction 150 Sm( 16 O,4n) 162 Yb to the ground state was studied using different gamma detectors and an electron spectrometer, a so called mini-orange. The isotope 162 Yb was moreover produced and spectroscoped by the beta-decay of 162 Lu. For the identification of decay cascades, which were passed after the fusion, and for the determination of the multipolarity of the contributing energy transitions a series of experiments took place: The excitation functions and the angular distributions of the emitted gamma radiation was measured, the conversion coefficients of important transitions were determined, and coincidence events between two detectors occasionally were registrated and analyzed. In the beta decay measurement an assignment of gamma transitions to 162 Yb followed due to the lifetime, under which they occured. The found states of 162 Yb upto spins of 22 h/2π and excitation energies above 5 MeV belong to five rotational bands. The yrast band shows a weak backbending. Corresponding to their spins and parities the bands can be reduced to intrinsic excitation of two quasineutrons. The analysis of the beta-decay of 162 Lu, which takes place from three states in 162 Lu, leads to the lowest levels of the gamma-vibrational band and the band head of the beta band. The microscopic interpretation of the rotational bands and the description of the backbending behaviour are as the interpretation of the states involved at the beta decay in agreement with experimental and theoretical results for neighbouring ytterbium isotopes. (orig.) [de

Assessment of effect of Yb3+ ion pairs on a highly Yb-doped double-clad fibre laser

Science.gov (United States)

Vallés, J. A.; Martín, J. C.; Berdejo, V.; Cases, R.; Álvarez, J. M.; Rebolledo, M. Á.

2018-03-01

Using a previously validated characterization method based on the careful measurement of the characteristic parameters and fluorescence emission spectra of a highly Yb-doped double-clad fibre, we evaluate the contribution of ion pair induced processes to the output power of a double-clad Yb-doped fibre ring laser. This contribution is proved to be insignificant, contrary to analysis by other authors, who overestimate the role of ion pairs.

Synthesis and characterisation of YbPdSb

Energy Technology Data Exchange (ETDEWEB)

Haines, Charles R.S.; Brown, Philip A.C.; Grosche, Friedrich M. [Department of Physics, Cavendish Laboratory, University of Cambridge (United Kingdom)

2016-07-01

The intermetallic compound YbPdSb can form in two structures: the low temperature (LT) half-Heusler phase, in which the Yb atoms form a frustrated fcc structure, and the high temperature (HT) Pnma modification. We have prepared phase pure samples of both structures and report resistivity, magnetisation and heat capacity measurements on both. The LT phase is a Kondo lattice system showing large-moment Curie-Weiss paramagnet behaviour without any phase transition anomalies down to the lowest temperatures measured. The resistivity is rather insensitive to temperature from room temperature down to ∝50 K where it decreases steeply with further cooling. By contrast, in the HT phase the magnetic susceptibility displays weak temperature dependence and the resistivity falls with decreasing temperature in the way expected of a weakly correlated metal. These findings suggest that in contrast to the electronic state in the LT structure, the 4f-shell of Yb is completely filled in the HT structure of YbPdSb, presenting an interesting opportunity to study the interplay between lattice and electronic structure within the same compound.

Effect of rare-earth ion size on local electron structure in RBa2Cu3O7-δ (R = Tm, Dy, Gd, Eu, Nd and Y) superconductors: A positron study

International Nuclear Information System (INIS)

Chen Zhenping; Zhang Jincang; Su Yuling; Xue Yuncai; Cao Shixun

2006-01-01

The effects of rare-earth ionic size on the local electron structure, lattice parameters and superconductivity have been investigated by positron annihilation technique (PAT) and related experiments for RBa 2 Cu 3 O 7-δ (R = Tm, Dy, Gd, Eu, Nd and Y) superconductors. The local electron density n e is evaluated as a function of the rare-earth radius. The results show that both the bulk-lifetime τ B and the defect lifetime τ 2 increase with increasing rare-earth ionic radius, while the local electron density n e decrease with increasing rare-earth ionic radius. These results prove that the changes of n e , the degree of orthorhombic distortion and the coupling between the Cu-O chains and the CuO 2 planes all have an effect on the superconductivity of RBa 2 Cu 3 O 7-δ systems

A family of acetato-diphenoxo triply bridged dimetallic Zn(II)Ln(III) complexes: SMM behavior and luminescent properties.

Science.gov (United States)

Oyarzabal, Itziar; Artetxe, Beñat; Rodríguez-Diéguez, Antonio; García, JoséÁngel; Seco, José Manuel; Colacio, Enrique

2016-06-21

Eleven dimetallic Zn(II)-Ln(III) complexes of the general formula [Zn(µ-L)(µ-OAc)Ln(NO3)2]·CH3CN (Ln(III) = Pr (1), Nd (2), Sm (3), Eu (4), Gd (5), Tb (6), Dy (7), Ho (8), Er (9), Tm (10), Yb (11)) have been prepared in a one-pot reaction from the compartmental ligand N,N'-dimethyl-N,N'-bis(2-hydroxy-3-formyl-5-bromo-benzyl)ethylenediamine (H2L). In all these complexes, the Zn(II) ions occupy the internal N2O2 site whereas the Ln(III) ions show preference for the O4 external site. Both metallic ions are bridged by an acetate bridge, giving rise to triple mixed diphenoxido/acetate bridged Zn(II)Ln(III) compounds. The Nd, Dy, Er and Yb complexes exhibit field induced single-ion magnet (SIM) behaviour, with Ueff values ranging from 14.12 to 41.55 K. The Er complex shows two relaxation processes, but only the second relaxation process with an energy barrier of 21.0 K has been characterized. The chromophoric L(2-) ligand is able to act as an "antenna" group, sensitizing the near-infrared (NIR) Nd(III) and Yb(III)-based luminescence in complexes 2 and 11 and therefore, both compounds can be considered as magneto-luminescent materials. In addition, the Sm(III), Eu(III) and Tb(III) derivatives exhibit characteristic emissions in the visible region.

Laser-cooling effects in few-ion clouds of Yb[sup +

Energy Technology Data Exchange (ETDEWEB)

Edwards, C.S. (National Physical Lab., Teddington (United Kingdom)); Gill, P. (National Physical Lab., Teddington (United Kingdom)); Klein, H.A. (National Physical Lab., Teddington (United Kingdom)); Levick, A.P. (National Physical Lab., Teddington (United Kingdom)); Rowley, W.R.C. (National Physical Lab., Teddington (United Kingdom))

1994-08-01

We report some laser-cooling effects in a few [sup 172]Yb[sup +] ions held in a Paul trap. Pronounced cloud-to-crystal phase transitions have been observed as discontinuities in the Yb[sup +] fluorescence spectrum of the 369 nm cooling transition. The first reported two-dimensional images of Yb[sup +] clouds with evidence of crystal structure have been recorded using a photon-counting position-sensitive detector. An ion temperature of 100 mK has been estimated from the size of a single ion image. Stepwise cooling of a re-heated, few-ion Yb[sup +] cloud was also observed. (orig.)

Study of the production of {sup 177}Lu through {sup 176}Yb (n, {gamma}) {sup 177}Yb {yields} {sup 177}Lu nuclear reaction

Energy Technology Data Exchange (ETDEWEB)

Silva, Giovana Pasqualini da; Osso Junior, Joao Alberto [Instituto de Pesquisas Energeticas e Nucleares (IPEN/CNEN-SP), Sao Paulo, SP (Brazil)]. E-mail: gpsilva@ipen.br; jaosso@ipen.br

2007-07-01

The beta minus emitter {sup 177}Lu is a promising therapeutic radioisotope for the curative treatment of cancer using labelled proteins. It has a half - life of T{sub 1/2} = 6.71 day and maximum and average {beta}{sup -} energies of 421 and 133 keV, resulting in a short range of radiation in tissue. The decay is accompanied by the emission of low energy {gamma}-radiation with 208.3 keV (11%) and 113 keV (6.4%) suitable for simultaneous imaging, {sup 177}Lu can be produced by two different routes, namely, by irradiation of natural Lu{sub 2}O{sub 3} target ({sup 176}Lu, 2.6%) or enriched (in {sup 176}Lu) Lu{sub 2}O{sub 3} target, as also by irradiation of Yb target (Yb{sub 2}O{sub 3}) followed by radiochemical separation of {sup 177}Lu from Yb isotopes. The objective of this work is to study the production of {sup 177}Lu through the indirect {sup 176}Yb(n,{gamma}){sup 177}Yb {yields} {sup 177}Lu nuclear reaction. The results of the production yield of {sup 177}Lu will be shown and compared with the direct reaction. The method of choice for the chemical separation between Lu and Yb was the ion exchange, using an cation exchange resin in Cl{sup -} form and {alpha}-HIBA as eluent. Preliminary results showed a good separation of {sup 177}Lu from Yb{sub 2}O{sub 3} indirect targets. (author)

YB-1 promotes microtubule assembly in vitro through interaction with tubulin and microtubules

Directory of Open Access Journals (Sweden)

Baconnais Sonia

2008-09-01

Full Text Available Abstract Background YB-1 is a major regulator of gene expression in eukaryotic cells. In addition to its role in transcription, YB-1 plays a key role in translation and stabilization of mRNAs. Results We show here that YB-1 interacts with tubulin and microtubules and stimulates microtubule assembly in vitro. High resolution imaging via electron and atomic force microscopy revealed that microtubules assembled in the presence of YB-1 exhibited a normal single wall ultrastructure and indicated that YB-1 most probably coats the outer microtubule wall. Furthermore, we found that YB-1 also promotes the assembly of MAPs-tubulin and subtilisin-treated tubulin. Finally, we demonstrated that tubulin interferes with RNA:YB-1 complexes. Conclusion These results suggest that YB-1 may regulate microtubule assembly in vivo and that its interaction with tubulin may contribute to the control of mRNA translation.

Luminescence studies on Dy3+ and Dy3+:Eu3+ co-doped boro-phosphate glasses for WLED applications

Science.gov (United States)

Vijayakumar, M.; Uma, V.; Arunkumar, S.; Marimuthu, K.

2015-06-01

Dy3+ and Dy3+:Eu3+ co-doped boro-phosphate glasses have been prepared and optically characterized using absorption, luminescence and decay measurements. The Nephelauxetic ratios (β), Bonding parameters (δ) and Judd-Ofelt (JO) intensity parameters Ωλ (λ = 2, 4 and 6) were calculated to study the nature of the environment around the RE3+ ions in the prepared glasses. The yellow to blue (Y/B) intensity ratio and the chromaticity color coordinates were calculated from the luminescence measurements. The lifetimes of the 4F9/2 excited level were measured using decay curves and is found to decrease in the Dy3+:Eu3+ co-doped glass due to the occurrence of resonant energy transfer between Dy3+-Eu3+ ions and the non-exponential decay rates have been fitted with Inokuti-Hirayama (IH) model. The decay curves are well fitted for S= 6 suggesting that the interaction between active ions for the energy transfer is of dipole-dipole nature.

Electronic structure and X-ray spectroscopic properties of YbNi_2P_2

International Nuclear Information System (INIS)

Shcherba, I.D.; Bekenov, L.V.; Antonov, V.N.; Noga, H.; Uskokovic, D.; Zhak, O.; Kovalska, M.V.

2016-01-01

Highlights: • We present new experimental and theoretical data for YbNi_2P_2. • The presence of divalent and trivalent Yb ion found in YbNi_2P_2. • The calculation show good agreement with the experimental measurements. - Abstract: X-ray absorption spectrum at the Yb L_3 edge and X-ray emission spectra of Ni and P at the K and L_2_,_3 edges have been studied experimentally and theoretically in the mixed valent compound YbNi_2P_2 with ThCr_2Si_2 type crystal structure. The electronic structure of YbNi_2P_2 is investigated using the fully relativistic Dirac linear muffin-tin orbital (LMTO) band-structure method. The effect of the spin–orbit (SO) interaction and Coulomb repulsion U on the electronic structure of YbNi_2P_2 is examined in the frame of the LSDA + SO + U method. The core-hole effect in the final states as well as the effect of the electric quadrupole E_2 transitions have been investigated. A good agreement between the theory and the experiment was found. Both the trivalent and the divalent Yb ions in YbNi_2P_2 are reflected in the experimentally measured Yb L_3 X-ray absorption spectrum simultaneously. We found that the best agreement between the experimental spectrum and sum of the theoretically calculated Yb"2"+ and Yb"3"+ spectra is achieved with 73% ytterbium ions in 2+ state and 27% ions in 3+ state.

Thermodynamic and transport properties of YbNi 4Cd

Science.gov (United States)

Lee, J.; Park, H.; Lee-Hone, N. R.; Broun, D. M.; Mun, E.

2018-05-01

The single crystal growth and the physical properties of the intermetallic compounds R Ni4Cd (R =Y and Yb) which crystallize in the face-centered cubic (fcc) MgCu4Sn -type structure (space group F 4 ¯3 m ) are discussed. Thermodynamic and transport properties of YbNi4Cd are studied by measuring the magnetization, electrical resistivity, and specific heat. The magnetic susceptibility measurement shows that the 4 f electrons of Yb3 + ions are well localized. The electrical resistivity and specific heat exhibits an antiferromagnetic ordering below TN=0.97 K. Applying the field along the [111] direction results in the suppression of TN below 0.4 K at the critical field Hc˜4.5 kOe. No non-Fermi liquid behavior has been observed in the vicinity of Hc. Above Hc, the magnetoresistivity shows an unconventional temperature dependence ρ (T ) =ρ0+A Tn with n >2 , suggesting that an additional scattering mechanism in the resistivity needs to be considered. Based on the analysis of experimental results, we conclude that the Yb3 + moments and conduction electrons are weakly coupled. Despite the antiferromagnetic ordering below TN, YbNi4Cd exhibits a large frustration parameter | θp/TN|˜16 , where the magnetic Yb3 + ions occupy the tetrahedra on the fcc lattice.

Synthesis, properties, and crystal structure of complex Cp2Yb(DAD)

International Nuclear Information System (INIS)

Trifonov, A.A.; Kirillov, E.N.; Bochkarev, M.N.; Shumani, G.; Myule, S.

1999-01-01

Diazadiene complex of trivalent ytterbium Cp 2 Yb(DAD) (1) (DAD = Bu 1 -N CH-CH = N-Bu 1 ) was obtained by three routes: the oxidation of Cp 2 Yb(THF) 2 by diazadiene in tetrahydrofuran (THF), the reaction of Cp 2 YbCl with DAD 2- Na 2 + (2:1), and the reaction of Cp 2 YbCl(THF) with DAD - K + in the 1:1 ratio. Complex 1 was characterized by microanalysis, IR spectroscopy, magnetochemistry, and X-ray structural analysis [ru

Growth and continuous-wave laser operation of disordered crystals of Yb3+:NaLa(WO4)2 and Yb3+:NaLa(MoO4)2

Science.gov (United States)

Liu, J.; Cano-Torres, J. M.; Cascales, C.; Esteban-Betegón, F.; Serrano, M. D.; Volkov, V.; Zaldo, C.; Rico, M.; Griebner, U.; Petrov, V.

2005-03-01

Single crystals of disordered NaLa(WO4)2 and NaLa(MoO4)2 doped with Yb3+ are grown by the Czochralski method from the melt. Continuous-wave laser operation with Ti:sapphire laser pumping is demonstrated at room temperature without special cooling. Tunability from 1017 to 1057 nm and from 1015 to 1053 nm is achieved for Yb:NaLa(WO4)2 and Yb:NaLa(MoO4)2, respectively. A maximum output power of 205 mW is obtained with Yb:NaLa(WO4)2.

YB-1 overexpression promotes a TGF-β1-induced epithelial–mesenchymal transition via Akt activation

International Nuclear Information System (INIS)

Ha, Bin; Lee, Eun Byul; Cui, Jun; Kim, Yosup; Jang, Ho Hee

2015-01-01

The Y-box binding protein-1 (YB-1) is a transcription/translation regulatory protein, and the expression thereof is associated with cancer aggressiveness. In the present study, we explored the regulatory effects of YB-1 during the transforming growth factor-β1 (TGF-β1)-induced epithelial-to-mesenchymal transition (EMT) in lung adenocarcinoma cells. Downregulation of YB-1 increased E-cadherin promoter activity, and upregulation of YB-1 decreased promoter activity, suggesting that the YB-1 level may be correlated with the EMT. TGF-β1 induced YB-1 expression, and TGF-β1 translocated cytosolic YB-1 into the nucleus. YB-1 overexpression promoted TGF-β1-induced downregulation of epithelial markers, upregulation of mesenchymal markers, and cell migration. Moreover, YB-1 overexpression enhanced the expression of E-cadherin transcriptional repressors via TGF-β1-induced Akt activation. Our findings afford new insights into the role played by YB-1 in the TGF-β1 signaling pathway. - Highlights: • YB-1 regulates E-cadherin expression in A549 cells. • TGF-β1 induces upregulating and nuclear localization of YB-1. • YB-1 overexpression accelerates TGF-β1-induced EMT and cell migration. • YB-1 regulates Snail and Slug expression via Akt activation

Sol-Gel Derived Active Material for Yb Thin-Disk Lasers.

Science.gov (United States)

Almeida, Rui M; Ribeiro, Tiago; Santos, Luís F

2017-09-02

A ytterbium doped active material for thin-disk laser was developed based on aluminosilicate and phosphosilicate glass matrices containing up to 30 mol% YbO 1.5 . Thick films and bulk samples were prepared by sol-gel processing. The structural nature of the base material was assessed by X-ray diffraction and Raman spectroscopy and the film morphology was evidenced by scanning electron microscopy. The photoluminescence (PL) properties of different compositions, including emission spectra and lifetimes, were also studied. Er 3+ was used as an internal reference to compare the intensities of the Yb 3+ PL peaks at ~ 1020 nm. The Yb 3+ PL lifetimes were found to vary between 1.0 and 0.5 ms when the Yb concentration increased from 3 to 30 mol%. Based on a figure of merit, the best active material selected was the aluminosilicate glass composition 71 SiO₂-14 AlO 1.5 -15 YbO 1.5 (in mol%). An active disk, ~ 36 μm thick, consisting of a Bragg mirror, an aluminosilicate layer doped with 15 mol% Yb and an anti-reflective coating, was fabricated.

Downconversion in Pr3+–Yb3+ co-doped ZBLA fluoride glasses

International Nuclear Information System (INIS)

Maalej, O.; Boulard, B.; Dieudonné, B.; Ferrari, M.; Dammak, M.; Dammak, M.

2015-01-01

Fluorozirconate ZBLA glasses with molar composition 57ZrF 4 –34BaF 2 –5LaF 3 –4AlF 3 –0.5PrF 3 –xYbF 3 (from x=0 to 10) were synthesized to evaluate the rate of the conversion of visible photons into infrared photons. The emission spectra in the near infrared (NIR) at 950–1100 nm and the luminescence decays in the visible and NIR indicate an energy transfer from Pr 3+ to Yb 3+ upon blue excitation of Pr 3+ at 440 nm. The energy transfer efficiency increases with Yb 3+ concentration to reach 86% with 0.5Pr 3+ –10Yb 3+ co-doping (in mol%). However, the quenching of the Yb 3+ emission strongly reduces the efficiency of the downconversion process: the decay time values decrease from 600 µs (x=0.5 mol%) to 85 µs (x=10 mol%). - Highlights: • We synthesized 0.5Pr 3+ –xYb 3+ co-doped ZBLA glasses (from x=0 to 10 mol %). • Photoluminescence of Yb 3+ was observed at 980 nm under blue excitation. • Time resolved measurements have been performed in the visible and near infrared. • Energy transfer efficiency from Pr 3+ to Yb 3+ reaches 86% in 0.5 Pr 3+ –10Yb 3+ glass

Mass fabrication of homogeneously Yb-doped silica nanoparticles and their spectroscopic properties

International Nuclear Information System (INIS)

Xiong Liangming; Sekiya, Edson H; Saito, Kazuya

2009-01-01

A large number of homogeneously Yb-doped silica nanoparticles were continually fabricated in a vapor synthesis route, in which the Yb doping level can be well controlled by varying either the heating temperature or the carrier gas flow rate of the Yb precursor. The sizes, shapes, and morphologies of the nanoparticles were examined, and no crystallites and no Yb 2 O 3 clusters were observed in the nanoparticles. These nanoparticles exhibit a clear Yb 3+ -derived absorption at around 973-975 nm and a dependence of the emission intensity and decay time on the doping level, much different from that of sintered pellets.

The contribution of valence unstable ytterbium states into kinetic properties of YbNi{sub 2-x}Ge{sub 2+x} and YbCu{sub 2-x}Si{sub 2+x}

Energy Technology Data Exchange (ETDEWEB)

Kuzhel, B.C. [Department of Physics, Ivan Franko National University of Lviv, 50 Dragomanow Str., 79005, Lviv (Ukraine)]. E-mail: kuzhelb@org.lviv.net; Shcherba, I.D. [Department of Physics, Ivan Franko National University of Lviv, 50 Dragomanow Str., 79005, Lviv (Ukraine); Institute of Techniques, Academy of Pedagogy, Podchorozych 2, 30-084, Krakow (Poland); Kravchenko, I.I. [Department of Physics, University of Florida, P.O. Box 118440, Gainesville, FL 32611 (United States)]. E-mail: kravch@phys.ufl.edu

2006-11-30

The intermetalic YbNi{sub 2-x}Ge{sub 2+x} (-0.25>=x>=0.25) and YbCu{sub 2-x}Si{sub 2+x} (-0.20>=x>=0.20) alloy systems (CeGa{sub 2}Al{sub 2} -type crystal structure) were studied by measuring X-ray absorption and diffraction at room temperatures as well as electrical resistivity and thermopower in the 4.2-300K temperature range. The temperature dependence of the contribution of valence unstable Yb ions to the total electrical resistance has been analyzed. The qualitative estimation of this contribution has been performed by utilizing the following equation:{delta}{rho}{sub Yb}(T)={rho}{sub exp}(T)-{rho}{sub YbCu{sub 2}Ge{sub 2}}(T)-{delta}{rho}{sub 4.2K},where {delta}{rho}{sub YbCu{sub 2}Ge{sub 2}}(T) is the temperature dependence of YbCu{sub 2}Ge{sub 2} electrical resistance, {delta}{rho}{sub 4.2}={rho}{sub 4.2}(exp)-{rho}{sub 4.2}(YbCu{sub 2}Ge{sub 2})

Melt processing of Yb-123 tapes

International Nuclear Information System (INIS)

Athur, S. P.; Balachandran, U.; Salama, K.

2000-01-01

The innovation of a simple, scalable process for manufacturing long-length conductors of HTS is essential to potential commercial applications such as power cables, magnets, and transformers. In this paper the authors demonstrate that melt processing of Yb-123 tapes made by the PIT route is an alternative to the coated conductor and Bi-2223 PIT tape fabrication techniques. Ag-clad Yb-123 tapes were fabricated by groove rolling and subsequently, melt processed in different oxygen partial pressures in a zone-melting furnace with a gradient of 140 C/cm. The transition temperatures measured were found to be around 81 K undermost processing conditions. EPMA of the tapes processed under different conditions show the 123 phase to be Ba deficient and Cu and Yb rich. Critical current was measured at various temperatures from 77 K to 4.2 K. The J c increased with decrease in pO 2 . The highest I c obtained was 52 A at 4.2 K

Comparing Zeeman qubits to hyperfine qubits in the context of the surface code: +174Yb and +171Yb

Science.gov (United States)

Brown, Natalie C.; Brown, Kenneth R.

2018-05-01

Many systems used for quantum computing possess additional states beyond those defining the qubit. Leakage out of the qubit subspace must be considered when designing quantum error correction codes. Here we consider trapped ion qubits manipulated by Raman transitions. Zeeman qubits do not suffer from leakage errors but are sensitive to magnetic fields to first order. Hyperfine qubits can be encoded in clock states that are insensitive to magnetic fields to first order, but spontaneous scattering during the Raman transition can lead to leakage. Here we compare a Zeeman qubit (+174Yb) to a hyperfine qubit (+171Yb) in the context of the surface code. We find that the number of physical qubits required to reach a specific logical qubit error can be reduced by using +174Yb if the magnetic field can be stabilized with fluctuations smaller than 10 μ G .

The physical and chemical characteristics of 175Yb-EDTMP labelled compound

International Nuclear Information System (INIS)

Azmairit Aziz; Marlina; Muhammad Basit Febrian

2010-01-01

Bone pain is a common complication for patient with bone metastases from breasts, prostate and lung cancers. The derivative of phosphonate groups, i.e. diphosphonate as well as poly phosphonate ligands e.g. EDTMP have high affinity in bone matrix. The labeled compound of 175 Yb-EDTMP can be used as an alternative radiopharmaceutical for bone pain palliation. The compound of 175 Yb-EDTMP can be produced by labeling of ethylenediamine tetramethylene phosphonic acid (EDTMP) with itterbium-175 ( 175 YbCl 3 ). Before 175 Yb-EDTMP is used for bone pain palliation in nuclear medicine, the compound have to be characterized to full fill the criteria of the good radiopharmaceutical. The physical and chemical characteristics of 175 Yb-EDTMP had been studied. It consists of: pH, solution clearity, the radiochemical purity that was determined by paper chromatography and paper electrophoresis techniques, electricity charge was determined by paper electrophoresis, stability, lipophilicity of 175 Yb-EDTMP was obtained by determination of octanol-water partition and the plasma binding protein was in-vitro investigated with precipitation method using 5% of trichloroacetic acid solution, and the binding to hydroxyapatite. From the experiment, it was obtained that the 175 Yb-EDTMP solution has the pH of 7, clear, the radiochemical purity of 98.66 ± 0.53%, and the negative electric charge. The compound of 175 Yb-EDTMP has lipophilicity (P) of 0.0135 ± 0.003%, the human plasma binding protein of 8.94 ± 0.66%, and the hydroxyapatite binding of 94.78 ± 2.16%. Stability evaluation indicated that 175 Yb-EDTMP solution was still stable for nine days at room temperature with the radiochemical purity more than 95% (98.62 ± 0.83%). This study expects that 175 Yb-EDTMP compound can fulfill the requirement as radiopharmaceutical for use in palliative treatment of painful bone metastases and supports the development of nuclear medicine in Indonesia. (author)

Utilization of visible to NIR light energy by Yb{sup +3}, Er{sup +3} and Tm{sup +3} doped BiVO{sub 4} for the photocatalytic degradation of methylene blue

Energy Technology Data Exchange (ETDEWEB)

Regmi, Chhabilal [Research Center for Eco-Multifunctional Nanomaterials, Sun Moon University, Chungnam 31460 (Korea, Republic of); Kshetri, Yuwaraj K. [Department of Advanced Materials Engineering, Sun Moon University, Chungnam 31460 (Korea, Republic of); Ray, Schindra Kumar [Research Center for Eco-Multifunctional Nanomaterials, Sun Moon University, Chungnam 31460 (Korea, Republic of); Pandey, Ramesh Prasad [Institute of Biomolecule Reconstruction, Department of BT-Convergent Pharmaceutical Engineering, Sun Moon University, Chungnam 31460 (Korea, Republic of); Lee, Soo Wohn, E-mail: swlee@sunmoon.ac.kr [Research Center for Eco-Multifunctional Nanomaterials, Sun Moon University, Chungnam 31460 (Korea, Republic of)

2017-01-15

Highlights: • Lanthanide doped BiVO{sub 4} as highly efficient upconversion and photocatalytic material. • Well defined beads like morphology for better photocatalytic activity. • Effective utilization of NIR and visible light for efficient photocatalytic degradation of methylene blue. • Nontoxic to human cells, potential for application in biological fields. - Abstract: Lanthanide-doped BiVO{sub 4} semiconductors with efficient photocatalytic activities over a broad range of the solar light spectrum have been synthesized by the microwave hydrothermal method using ethylenediaminetetraacetic acid (EDTA). The structural, morphological, and optical properties of the as-synthesized samples were evaluated by Scanning Electron Microscopy (SEM), Transmission Electron Microscopy (TEM), X-ray powder diffraction (XRD), Raman spectroscopy, FT-IR spectroscopy, UV–vis diffuse reflectance spectroscopy (DRS), and photoluminescence spectroscopy (PL). The chemical compositions were analyzed by X-ray photoelectron spectroscopy (XPS). The toxicity of the samples was measured using Mus musculus skin melanoma cells (B16-F10 (ATCC{sup ®} CRL-6475™)) and were found to be nontoxic for human cells. The photocatalytic efficiency of the prepared samples was evaluated by methylene blue (MB) degradation. The best photocatalytic activity was shown by BiVO{sub 4} with 6:3:3 mol percentage of Yb{sup +3}:Er{sup +3}:Tm{sup +3} in all solar light spectrum. The synthesized samples possess low band gap energy and a hollow structure suitable for the better photocatalytic activity. The observed NIR photoactivity supports that the upconversion mechanism is involved in the overall photocatalytic process. Therefore, this approach provides a better alternative upconversion material for integral solar light absorption.

Yb-doped aluminophosphosilicate ternary fiber with high efficiency and excellent laser stability

Science.gov (United States)

Li, Yuwei; Peng, Kun; Zhan, Huan; Liu, Shuang; Ni, Li; Wang, Yuying; Yu, Juan; Wang, Xiaolong; Wang, Jianjun; Jing, Feng; Lin, Aoxiang

2018-03-01

By using chelate precursor doping technique and traditional modified chemical vapor deposition system, we fabricated Yb-doped aluminophosphosilicate (Al2O3-P2O5-SiO2, ternary Yb-APS) large-mode-area fiber and reported on its laser performance. The fiber preform was doped with Al, P and Yb with concentration of ∼8000 ppm, ∼1700 ppm and ∼400 ppm in molar percent, respectively. Tested with master oscillator power amplifier system, the home-made Yb-APS fiber was found to present 1.02 kW at 1061.1 nm with a high slope efficiency of 81.2% and excellent laser stability with power fluctuation less than ±1.1% for over 10 h. Compared with Yb-doped aluminosilicate (Al2O3-SiO2, binary Yb-AS) fiber, the introduction of P2O5 effectively suppressed photodarkening effect even the P/Al ratio is much less than 1, indicating that Yb-APS fiber is a better candidate for high power fiber lasers.

Coexistence of metallic and insulating channels in compressed YbB6

Science.gov (United States)

Ying, Jianjun; Tang, Lingyun; Chen, Fei; Chen, Xianhui; Struzhkin, Viktor V.

2018-03-01

It remains controversial whether compressed YbB6 material is a topological insulator or a Kondo topological insulator. We performed high-pressure transport, x-ray diffraction (XRD), x-ray absorption spectroscopy, and Raman-scattering measurements on YbB6 samples in search for its topological Kondo phase. Both high-pressure powder XRD and Raman measurements show no trace of structural phase transitions in YbB6 up to 50 GPa. The nonmagnetic Yb2 + gradually change to magnetic Yb3 + above 18 GPa concomitantly with the increase in resistivity. However, the transition to the insulating state occurs only around 30 GPa, accompanied by the increase in the shear stress, and anomalies in the pressure dependence of the Raman T2 g mode and in the B atomic position. The resistivity at high pressures can be described by a model taking into account coexisting insulating and metallic channels with the activation energy for the insulating channel about 30 meV. We argue that YbB6 may become a topological Kondo insulator at high pressures above 35 GPa.

Selective separation of yttrium by CA-100 in the presence of a complexing agent

International Nuclear Information System (INIS)

Sun Xiaobo; Wang Yige; Li Deqian

2006-01-01

The selective separation of Y from yttrium solution containing small heavy rare earth (HRE) impurities (Ho, Er, Tm, Yb, Lu) by liquid-liquid extraction using CA-100 in the presence of a water-soluble complexing agent of ethylenediaminetetraacetic acid (EDTA) was experimentally studied at 298 K. Experiments were carried out in two feeds, Feed-I: [RE] f = 4.94 x 10 -3 M, Y = 98.5%, HRE (Ho, Er, Tm, Yb, Lu) = 1.5%; Feed-II: [RE] f = 4.94 x 10 -3 M, Y = 99.9%, HRE (Ho, Er, Tm, Yb, Lu) = 0.1%, as a function of equilibrium pH (pH eq ), the concentration ratio of [EDTA]:[HRE impurities]. It was shown that the extraction of HRE in the presence of EDTA was suppressed when compared to that of Y because of the masking effect, while the selective extraction of Y was enhanced and the separation factors increased to maximum at appropriate condition for Feed-I: Y/Ho = 1.53, Y/Er 3.09, Y/Tm = 5.61, Y/Yb = 12.04, Y/Lu = 27.51 at pH 4.37 and [EDTA]:[HRE impurities] = 4:1, for Feed-II: Y/Ho = 1.32, Y/Er = 1.91, Y/Tm = 2.00, Y/Yb 3.05, Y/Lu = 3.33 at pH 4.42 and [EDTA]:[HRE impurities] = 8:1. The separation and purification of Y by this method was discussed

Phase precipitation of Yb 2+ ions in RbCl monocrystals monitored ...

African Journals Online (AJOL)

Optical absorption spectra of RbCl:Yb2+ crystals have been measured at several elevated temperatures up to 300C. Results showed that in hot RbCl:Yb2+ crystals, the Yb2+ ions occupied lattice sites with effective octahedral, O, point symmetry. Values of an energy parameter , which is an approximate measure of the ...

Electrodynamically trapped Yb+ ions for quantum information processing

International Nuclear Information System (INIS)

Balzer, Chr.; Braun, A.; Hannemann, T.; Wunderlich, Chr.; Paape, Chr.; Ettler, M.; Neuhauser, W.

2006-01-01

Highly efficient, nearly deterministic, and isotope selective generation of Yb + ions by one- and two-color photoionization is demonstrated. State preparation and state selective detection of hyperfine states in 171 Yb + is investigated in order to optimize the purity of the prepared state and to time-optimize the detection process. Linear laser-cooled Yb + ion crystals confined in a Paul trap are demonstrated. Advantageous features of different previous ion trap experiments are combined, while at the same time the number of possible error sources is reduced by using a comparatively simple experimental apparatus. This opens a new path toward quantum state manipulation of individual trapped ions, and in particular, to scalable quantum computing

Investigation of optical properties and the photocatalytic activity of synthesized YbYO4 nanoparticles and YbVO4/NiWO4 nanocomposites by polymeric capping agents

Science.gov (United States)

Pourmasoud, Saeid; Sobhani-Nasab, Ali; Behpour, Mohsen; Rahimi-Nasrabadi, Mehdi; Ahmadi, Farhad

2018-04-01

YbVO4 nanoparticles YbVO4/NiWO4 nanocomposites were synthesized by simple and new method. The effect of various polymeric capping agents such as Tween 80, Tween 20 and PEG on the shape and size of YbVO4/NiWO4 nanocomposites were investigated. YbVO4/NiWO4 nanocomposites were analyzed through some techniques including, X-ray diffraction (XRD), Fourier-transform infrared (FT-IR) spectroscopy, vibrating sample magnetometer (VSM), thermogravimetry differential thermal analysis (TG-DTA), transmission electron microscopy (TEM), field emission electron microscopy (FESEM), ultraviolet-visible spectroscopy (UV-Vis), and energy-dispersive X-ray spectroscopy (EDX). This attempt is the first study on the photocatalytic performance of the YbVO4/NiWO4 nanocomposites in various conditions such as size of particles and kind of dyes (rhodamine B (Rh B), methylene blue (MB), methyl orange (MO), and phenol red (Ph R)), under visible light.

Down-conversion luminescence from (Ce, Yb) co-doped oxygen-rich silicon oxides

International Nuclear Information System (INIS)

Heng, C. L.; Wang, T.; Su, W. Y.; Wu, H. C.; Yin, P. G.; Finstad, T. G.

2016-01-01

We have studied down-conversion photoluminescence (PL) from (Ce, Yb) co-doped “oxygen rich” silicon oxide films prepared by sputtering and annealing. The Ce"3"+ ∼510 nm PL is sensitive to the Ce concentration of the films and is much stronger for 3 at. % Ce than for 2 at. % Ce after annealing at 1200 °C. The PL emission and excitation spectroscopy results indicate that the excitation of Yb"3"+ is mainly through an energy transfer from Ce"3"+ to Yb"3"+, oxide defects also play a role in the excitation of Yb"3"+ after lower temperature (∼800 °C) annealing. The Ce"3"+ 510 nm photon excites mostly only one Yb"3"+ 980 nm photon. Temperature-dependent PL measurements suggest that the energy transfer from Ce"3"+ to Yb"3"+ is partly thermally activated.

Growth and continuous-wave laser operation of disordered crystals of Yb3+:NaLa(WO4)2 and Yb3+:NaLa(MoO4)2

International Nuclear Information System (INIS)

Liu, J.; Rico, M.; Griebner, U.; Petrov, V.; Cano-Torres, J.M.; Cascales, C.; Esteban-Betegon, F.; Serrano, M.D.; Volkov, V.; Zaldo, C.

2005-01-01

Single crystals of disordered NaLa(WO 4 ) 2 and NaLa(MoO 4 ) 2 doped with Yb 3+ are grown by the Czochralski method from the melt. Continuous-wave laser operation with Ti:sapphire laser pumping is demonstrated at room temperature without special cooling. Tunability from 1017 to 1057 nm and from 1015 to 1053 nm is achieved for Yb:NaLa(WO 4 ) 2 and Yb:NaLa(MoO 4 ) 2 , respectively. A maximum output power of 205 mW is obtained with Yb:NaLa(WO 4 ) 2 . (copyright 2005 WILEY-VCH Verlag GmbH and Co. KGaA, Weinheim) (orig.)

Nuclear Data Sheets for A=158

Energy Technology Data Exchange (ETDEWEB)

Nica, N. [Cyclotron Institute, Texas A& M University, College Station, TX 77843-3366 (United States); On leave from the National Institute for Physics and Nuclear Engineering “Horia Hulubei”, Bucharest (Romania); Under Subcontract No. 100586 with National Nuclear Data Center, Brookhaven National Laboratory, Upton, NY 11973 (United States)

2017-03-15

The experimental results published before February 2017 from the various reaction and decay studies leading to nuclides {sup 158}Nd, {sup 158}Pm, {sup 158}Sm, {sup 158}Eu, {sup 158}Gd, {sup 158}Tb, {sup 158}Dy, {sup 158}Ho, {sup 158}Er, {sup 158}Tm, {sup 158}Yb, {sup 158}Lu, {sup 158}Hf, {sup 158}Ta, {sup 158}W in the A=158 mass chain have been reviewed. These data are summarized and presented, together with adopted level schemes and properties. Large sections of the mass chain are almost identical to the ones in the previous 2004He05 NDS publication by R.G. Helmer.

Luminescence of YbP3O9 upon excitation in the UV-VUV range

International Nuclear Information System (INIS)

Stryganyuk, G; Trots, D; Berezovskaya, I; Shalapska, T; Voloshinovskii, A; Dotsenko, V; Zimmerer, G

2007-01-01

X-ray powder diffraction and luminescence spectral-kinetic studies have been performed for ytterbium metaphosphate (YbP 3 O 9 ) in the 12-290 K temperature range. The diffraction investigation has shown YbP 3 O 9 to be of monoclinic P 2 1 /c structure at T = 12-290 K. Charge transfer luminescence originating from Yb 3+ ion has been revealed. The carrier confinement within the Yb 3+ charge transfer state is pronounced at T = 12 K. A tendency has been revealed for charge carriers in YbP 3 O 9 to be localized in a trapped exciton state at room temperature. The quenching mechanisms for Yb 3+ charge transfer luminescence and processes competing with the formation of the Yb 3+ charge transfer state are discussed

Level structures in Yb nuclei far from stable nuclei

International Nuclear Information System (INIS)

Hashizume, Akira

1982-01-01

Applying n-γ, γ-γ coincidence techniques, the excited levels in 158 Yb and in 157 Yb nuclei were studied. Stress is placed ona neutron detection technique to assign (HI,xn) reactions which produce the nuclei far from β stability line. (author)

Concentration effect of Tm3+ on cathodoluminescence properties of SiO2: Tm3+ and SiO2:Ho3+, Tm3+ systems

CSIR Research Space (South Africa)

Dhlamini, MS

2012-05-01

Full Text Available .physb.2011.09.091 Concentration effect of Tm3+ on cathodoluminescence properties of SiO2: Tm 3+ and SiO2:Ho 3+, Tm3+ systems M.S. Dhlamini, G.H. Mhlongo, H.C. Swart, O.M. Ntwaeaborwa, K.T. Hillie ABSTRACT: Cathodoluminescence (CL) properties of Si...O2 powders activated with thulium (Tm3+) and holmium (Ho3+) ions prepared by a sol–gel process were investigated. Different molar concentrations of Tm3+ co-doped with Ho3+ were studied. The 460 nm peak was monitored and the influence of the beam...

Crystal growth, optical properties, and laser operation of Yb3+-doped NYW single crystal

Science.gov (United States)

Cheng, Y.; Xu, X. D.; Yang, X. B.; Xin, Z.; Cao, D. H.; Xu, J.

2009-11-01

Laser crystal Yb3+-doped NaY(WO4)2 (Yb:NYW) with excellent quality has been grown by Czochralski technique. The rocking curves from (400) plane of as-grown Yb:NYW crystal was measured and the full-width value at half-maximum was 19.92″. The effective segregation coefficients were measured by the X-ray fluorescence method. The polarized absorption spectra and the fluorescence spectra of Yb:NYW crystal were measured at room temperature. The fluorescence decay lifetime of Yb3+ ion in NYW crystal has been investigated. The spectroscopic parameters of Yb:NYW crystal are calculated and compared with those of Yb:YAG crystal. A continuous wave output power of 3.06 W at 1031 nm was obtained with a slope efficiency of 42% by use of diode pumping.

YB0 HAS LANDED

CERN Multimedia

  On Feb 28th after a majestic descent of 90m taking 11 hours, the 2000t YB0 central wheel of CMS, containing the superconducting solenoid, gently touched down on the floor of the experimental cavern UXC55.

Synthesis and molecular structure of YbI(bipy)(DME)2 complex

International Nuclear Information System (INIS)

Petrovskaya, T.V.; Fedyushkin, I.L.; Nevodchikov, V.I.; Bochkarev, M.N.; Borodina, N.V.; Eremenko, I.L.; Nefedov, S.E.

1998-01-01

The reaction of the ytterbium naphthaline complex [Yb(DME) 2 ] 2 (μ-C 10 H 8 ) with 2,2 ' -bipyridine in DME is found to lead to the formation of the complex with the Yb 2+ atom, YbI(bipy)(DME) 2 (1) containing 2,2 ' -bipyridine radical anion. Complex 1 is characterized by IR and UV spectroscopy, magnetic methods and X-ray analysis [ru

Preparation, Biological Evaluation and Dosimetry Studies of 175Yb-Bis-Phosphonates for Palliative Treatment of Bone Pain

Directory of Open Access Journals (Sweden)

Ashraf Fakhari

2015-10-01

Full Text Available Objective: Optimized production and quality control of ytterbium-175 (Yb-175 labeled pamidronate and alendronate complexes as efficient agents for bone pain palliation has been presented. Methods: Yb-175 labeled pamidronate and alendronate (175Yb-PMD and 175Yb-ALN complexes were prepared successfully at optimized conditions with acceptable radiochemical purity, stability and significant hydroxyapatite absorption. The biodistribution of complexes were evaluated up to 48 h, which demonstrated significant bone uptake ratios for 175Yb-PAM at all-time intervals. It was also detected that 175Yb-PAM mostly washed out and excreted through the kidneys. Results: The performance of 175Yb-PAM in an animal model was better or comparable to other 175Yb-bone seeking complexes previously reported. Conclusion: Based on calculations, the total body dose for 175Yb-ALN is 40% higher as compared to 175Yb-PAM (especially kidneys indicating that 175Yb-PAM is probably a safer agent than 175Yb-ALN.

Synthesis and up-conversion emissions of Yb , Yb and Yb co-doped ...

Indian Academy of Sciences (India)

2017-09-23

Sep 23, 2017 ... Green/red UC emissions of Er3+, UV/blue/IR UC emissions of Tm3+, and UV UC emissions of Gd3+ ... In the last few decades, rare earth (RE) materials have been ... age, colour displays, IR sensors, environmental monitoring,.

Powernext Day-AheadTM. Powernext futuresTM. Activity report - 2004

International Nuclear Information System (INIS)

2004-01-01

The introduction of a power exchange in France is a direct response to the opening up of the European electricity markets. Powernext SA is a Multilateral Trading Facility in charge of managing the French power exchange through an optional and anonymous organised exchange offering: - Day-ahead contracts for the management of volume risk on Powernext Day-Ahead TM since 21 November 2001, - Medium term contracts for the management of price risk on Powernext Futures TM since 18 June 2004. This document is the 2004 activity report of Powernext SA, it presents the key figures of the power market and of Powernext in 2004: - Increasing volumes: Powernext Day-Ahead TM 's traded volumes increased by 89%, from 7.48 to 14.18 TWh. Powernext Futures TM kicks off to a promising debut with 12.86 TWh traded in less than 7 months. - Less volatile prices: During 2004, the base price averaged 28.13 euro/MWh, and the peak prices averaged 33.71 euro/MWh. Compared to 2003, these prices decreased by an average of 3.7% on base-load and 10.9% on peak-load. In comparison to the two previous years, the daily volatility has noticeably settled down with 27% on base-load and 37% on peak-load. - Increasing liquidity: 10 new members joined Powernext Day-Ahead TM in 2004. The activity level of the members remains very high as 89% of them trade on an actual daily basis during 2004. The market resiliency stays strong. In December, an additional market 50 MW order on each hour resulted in a balance price variation of only 0.16 euro/MWh, or 0.53% of this balance price. For a 100 MW order, the resiliency is 0.32 euro/MWh, or 1.07% of the balance price. Thus, in 2004, Powernext Day-Ahead TM consolidates its role as a short term reference price. Moreover, in 2004, Powernext launched a futures market, Powernext Futures TM . This new market segment proposes contracts tradable up to 2 years ahead of delivery

Characterization of the electronic properties of YB{sub 4} and YB{sub 6} using {sup 11}B NMR and first-principles calculations

Energy Technology Data Exchange (ETDEWEB)

Jaeger, B.; Paluch, S.; Wolf, W.; Herzig, P.; Zogal, O.J.; Shitsevalova, N.; Paderno, Y

2004-11-30

Two compounds, tetragonal YB{sub 4} and cubic YB{sub 6}, have been investigated by electric-field gradient (EFG) and Knight shift measurements at the boron sites using the {sup 11}B nuclear magnetic resonance (NMR) technique and by performing first-principles calculations. In YB{sub 6} {sup 11}B (I=3/2) NMR spectra reveal patterns typical for an axially symmetric field gradient with a quadrupole coupling frequency of {nu}{sub Q}=600{+-}15 kHz. In the second boride (YB{sub 4}) three different EFGs were observed corresponding to the three inequivalent crystallographic sites for the boron atoms (4h, 4e, and 8j). They correspond to: {nu}{sub Q}(4h)=700{+-}30 kHz with an asymmetry parameter {eta}=0.02{+-}0.02, {nu}{sub Q}(4e)=515{+-}30 kHz, {eta}=0.00+0.02/-0.00, and {nu}{sub Q}(8j)=515{+-}40 kHz, {eta}=0.46{+-}0.08. The Knight shifts measured by magic-angle spinning (MAS) NMR at room temperature are very small being 0.6{+-}8 and -1{+-}8 ppm for YB{sub 4} and YB{sub 6}, respectively. For the theoretical calculations structure optimizations were performed as a first step. For the obtained structural parameters the EFGs were computed within the local-density approximation. Very satisfactory agreement between experimental and theoretical results is obtained both for the structural parameters and the B EFGs, thus confirming the underlying structural models. In addition to the EFGs, band structures, densities of states, and valence-electron densities are presented and the bonding situation in the two yttrium borides is discussed. The band-structure results are compatible with the very low values for the Knight shifts mentioned above.

Luminescence properties and energy transfer processes in YAG:Yb,Er single crystalline films

International Nuclear Information System (INIS)

Zorenko, Yu.; Gorbenko, V.; Savchyn, V.; Batentschuk, M.; Osvet, A.; Brabec, C.

2013-01-01

The paper is dedicated to the study of the optical properties of YAG:Yb,Er single-crystalline films (SCF) grown by liquid phase epitaxy. The absorption, cathodoluminescence and time-resolved photoluminescence spectra and photoluminescence decay curves were measured for the SCFs with different doping levels of Er 3+ (from 0.6 to 4.2 at.%) and Yb 3+ (from 0.1 to 0.6 at.%). The spectra, excited by synchrotron radiation in the fundamental absorption range of the YAG and in the intraionic absorption bands of both dopants, reveal energy transfer from the YAG host to the Er 3+ and Yb 3+ ions and between these ions. -- Highlights: •Growth of YAG:Yb,Er single crystalline films by LPE method. •Peculiarities of luminescence of YAG:Yb,Er films with different Er–Yb content. •Yb–Er energy transfer processes in YAG hosts

Effect of silver nanoparticles on the 1.53 μm fluorescence in Er3+/Yb3+ codoped tellurite glasses

Science.gov (United States)

Wu, Libo; Zhou, Yaxun; Zhou, Zizhong; Cheng, Pan; Huang, Bo; Yang, Fengjing; Li, Jun

2016-07-01

Improving the spectroscopic properties of rare earth (RE) doped glass materials is a challenging task. In the present work the metallic silver nanoparticles (Ag NPs) were embedded into Er3+/Yb3+ codoped tellurite glasses with composition TeO2-Bi2O3-TiO2, prepared using melt-quenching and subsequent heat-treated techniques, and the improved effect of Ag NPs on the 1.53 μm band fluorescence of Er3+ ions was investigated. About 24 h heat-treatment of Er3+/Yb3+ codoped tellurite glass containing 1 mol % amount of AgNO3 at the temperature 370 °C yielded the well-dispersed and near-spherical Ag NPs with ∼11.4 nm average diameter as evidenced by transmission electron microscopy (TEM) image. The intense 1.53 μm band fluorescence was observed in the prepared Er3+/Yb3+ codoped tellurite glasses under the excitation of 980 nm and was further improved with the presence of Ag NPs in the glass matrix, which is attributed to the enhanced local electric field around doped RE ions induced by Ag NPs and the possible energy transfer from Ag NPs to Er3+ ions. The enhanced local electric field was well demonstrated by comparing the variation of emission spectra of hypersensitive probe Eu3+ ions in tellurite glasses with and without Ag NPs. From the Judd-Ofelt analysis, it was also found that the value of Ω6 intensity parameter increased slightly with the increase of Ag NPs concentration in a certain range, also confirming the possibility of realizing strong fluorescence emission. In addition, the amorphous structural nature was demonstrated by the measured X-ray diffraction (XRD) patterns with no sharp diffraction peak. The enhanced 1.53 μm band fluorescence indicates that the Er3+/Yb3+ codoped tellurite glass with an appropriate amount of Ag NPs is a promising candidate for the development of Er3+-doped fiber amplifiers (EDFAs) applied in the WDM systems.

The tmRDB and SRPDB resources

DEFF Research Database (Denmark)

Andersen, Ebbe Sloth; Rosenblad, Magnus Alm; Larsen, Niels

2006-01-01

Maintained at the University of Texas Health Science Center at Tyler, Texas, the tmRNA database (tmRDB) is accessible at the URL http://psyche.uthct.edu/dbs/tmRDB/tmRDB.html with mirror sites located at Auburn University, Auburn, Alabama (http://www.ag.auburn.edu/mirror/tmRDB/) and the Royal...

Effects of Yb on the mechanical properties and microstructures of an Al-Mg alloy

International Nuclear Information System (INIS)

Song Min; Wu Zhenggang; He Yuehui

2008-01-01

This paper reported a first study of the effects of Yb on the microstructures and mechanical properties of an extruded Al-Mg alloy. It has been shown that the addition of 0.3 wt.% Yb decreases the mechanical properties of the alloy since Mg- and Yb-containing constituents decrease the concentration of Mg solute atoms in Al matrix, and thus the solution strengthening effect. However, the addition of 1 wt.% Yb substantially improves the mechanical behavior of the alloy because the concentration of Yb solute atoms in Al matrix is high enough to generate solution strengthening effect. The improvement in the mechanical properties is due to the large work-hardening and high dislocation density caused by the interaction between dislocations and Yb and Mg solute atoms. The Yb and Mg atoms inhibit the dynamic recovery and recrystallization of the alloy, thus provide a uniformly distributed dislocation structure with high density

Magnetic ordering in TmGa

DEFF Research Database (Denmark)

Cadogan, J.M.; Stewart, G.A.; Muños Pérez, S.

2014-01-01

We have determined the magnetic structure of the intermetallic compound TmGa by high-resolution neutron powder diffraction and 169Tm Mössbauer spectroscopy. This compound crystallizes in the orthorhombic (Cmcm) CrB-type structure and its magnetic structure is characterized by magnetic order...... of the Tm sublattice along the a-axis. The initial magnetic ordering occurs at 15(1) K and yields an incommensurate antiferromagnetic structure described by the propagation vector k1 = [0 0.275(2) 0]. At 12 K the dominant ferromagnetic ordering of the Tm sublattice along the a-axis develops in what appears...... to be a first-order transition. At 3 K the magnetic structure of TmGa is predominantly ferromagnetic but a weakened incommensurate component remains. The ferromagnetic Tm moment reaches 6.7(2) μB at 3 K and the amplitude of the remaining incommensurate component is 2.7(4) μB. The 169Tm hyperfine magnetic field...

Excited negative parity bands in 160Yb

Science.gov (United States)

Saha, A.; Bhattacharjee, T.; Curien, D.; Dedes, I.; Mazurek, K.; Banerjee, S. R.; Rajbanshi, S.; Bisoi, A.; de Angelis, G.; Bhattacharya, Soumik; Bhattacharyya, S.; Biswas, S.; Chakraborty, A.; Das Gupta, S.; Dey, B.; Goswami, A.; Mondal, D.; Pandit, D.; Palit, R.; Roy, T.; Singh, R. P.; Saha Sarkar, M.; Saha, S.; Sethi, J.

2018-03-01

Negative parity rotational bands in {} 70160Yb{}90 nucleus have been studied. They were populated in the 148Sm(16O, 4n)160Yb reaction at 90 MeV. The gamma-coincidence data have been collected using Indian National Gamma Array composed of twenty Compton suppressed clover germanium (Ge) detectors. Double gating on triple gamma coincidence data were selectively used to develop the decay scheme for these negative parity bands by identifying and taking care of the multiplet transitions. The even- and odd-spin negative parity bands in 160Yb have been studied by comparing the reduced transition probability ratios with the similar bands in neighbouring even-even rare earth nuclei. It is concluded that the concerned odd-spin and even-spin bands are not signature partners and that their structures are compatible with those of the ‘pear-shape’ and ‘pyramid-shape’ oscillations, respectively, the octupole shapes superposed with the quadrupole shape of the ground-state.

Lifetime-broadening-suppressed X-ray absorption spectrum of β-YbAlB4 deduced from Yb 3d → 2p resonant X-ray emission spectroscopy

International Nuclear Information System (INIS)

Kawamura, Naomi; Mizumaki, Masaichiro; Kanai, Noriko; Hayashi, Hisashi; Matsuda, Yasuhiro H.; Kuga, Kentaro; Nakatsuji, Satoru; Watanabe, Shinji

2017-01-01

In this work, the Yb 3d → 2p (Yb Lα 1,2 ) resonant X-ray emission spectrum of β-YbAlB 4 was acquired using excitation energies around the Yb L 3 -edge, at 2 K. Subsequently, the lifetime-broadening-suppressed (LBS) X-ray absorption structure (XAS) spectrum was obtained using the SIM-RIXS program. This spectrum was found to exhibit clearly resolved pre-edge and shoulder structures. Resonant Lα 1 emission spectra were well reproduced from LBS-XAS profiles over wide ranges of excitation and emission energies. In contrast, noticeable discrepancies appeared between the experimental and simulated Lα 2 emission spectra, suggesting an effect resulting from M 4 M 5 O 1 Coster-Kronig transitions. LBS-XAS, in conjunction with partial fluorescence yield (PFY) XAS and transmission XAS, determined a value for the Yb valence (v) in β-YbAlB 4 of 2.76 ± 0.08 at 2 K. Despite this relatively large uncertainty in v, each method provided a consistent variation in valence (δv) as the temperature was raised from 2 to 280 K: 0.060 ± 0.004 (LBS-XAS), 0.061 ± 0.005 (PFY-XAS) and 0.058 ± 0.007 (transmission XAS). The smaller δv associated with LBS-XAS demonstrates the greater precision of this method. (author)

Ab-initio calculation of EuO doped with 5% of (Ti, V, Cr and Fe): GGA and SIC approximation

Science.gov (United States)

Rouchdi, M.; Salmani, E.; Bekkioui, N.; Ez-Zahraouy, H.; Hassanain, N.; Benyoussef, A.; Mzerd, A.

2017-12-01

In this research, a simple theoretical method is proposed to investigate the electronic, magnetic and optical properties of Europium oxide (EuO) doped with 5% of (Ti, V, Cr and Fe). For a basic understanding of these properties, we employed Density-Functional Theory (DFT) based calculations with the Korringa-Kohn-Rostoker code (KKR) combined with the Coherent Potential Approximation (CPA). Also we investigated the half-metallic ferromagnetic behavior of EuO doped with 5% of (Ti, V, Cr and Fe) within the self-interaction-corrected Generalized Gradient Approximation (GGA-SIC). Our calculated results revealed that the Eu0.95TM0.05O is ferromagnetic with a high transition temperature. Moreover, the optical absorption spectra revealed that the half metallicity has been also predicted.

Is YbAs a heavy Fermion system?

International Nuclear Information System (INIS)

Monnier, R.; Degiorgi, L.; Delley, B.; Koelling, D.D.

1989-08-01

Using parameters extracted from a tight binding fit to an ab initio band structure, the specific heat anomaly observed in YbAs around 5 K is computed within the infinite U limit of the degenerate Anderson impurity model. Applying the renormalization procedure derived in variational treatments of the periodic Anderson model, a quasiparticle Fermi surface with strong nesting features and small mass enhancements is obtained. The results suggest that YbAs is not a ''classical'' heavy Fermion system. 28 refs., 3 figs., 1 tab

Translation-Memory (TM) Research

DEFF Research Database (Denmark)

Schjoldager, Anne Gram; Christensen, Tina Paulsen

2010-01-01

to be representative of the research field as a whole. Our analysis suggests that, while considerable knowledge is available about the technical side of TMs, more research is needed to understand how translators interact with TM technology and how TMs influence translators' cognitive translation processes.......  It is no exaggeration to say that the advent of translation-memory (TM) systems in the translation profession has led to drastic changes in translators' processes and workflow, and yet, though many professional translators nowadays depend on some form of TM system, this has not been the object...... of much research. Our paper attempts to find out what we know about the nature, applications and influences of TM technology, including translators' interaction with TMs, and also how we know it. An essential part of the analysis is based on a selection of empirical TM studies, which we assume...

Cooperative up-conversion processes in SrAl{sub 4}O{sub 7}:Yb and SrAl{sub 4}O{sub 7}:Yb,Tb and their dependence on charge compensation by Na

Energy Technology Data Exchange (ETDEWEB)

Puchalska, M., E-mail: malgorzata.puchalska@chem.uni.wroc.pl [Faculty of Chemistry, University of Wroclaw, 14, F. Joliot-Curie Street, 50-383 Wroclaw (Poland); Zych, E. [Faculty of Chemistry, University of Wroclaw, 14, F. Joliot-Curie Street, 50-383 Wroclaw (Poland); Watras, A. [Institute of Low Temperature and Structure Research, Polish Academy of Sciences, 2 Okólna Street, 50-422 Wrocław (Poland)

2017-03-15

A detailed analysis of the luminescence behaviour of Yb{sup 3+}-doped and Yb{sup 3+}-Tb{sup 3+} co-doped strontium aluminates powders: Sr{sub 1-x}Yb{sub x}Al{sub 4}O{sub 7} (x=0.002–0.07) and Sr{sub 1-x-y}Yb{sub x}Tb{sub y}Al{sub 4}O{sub 7} (x=0.03; y=0.002–0.02) were performed. The studies of singly doped samples show that direct excitation of Yb{sup 3+} by means of {sup 2}F{sub 7/2}-{sup 2}F{sub 5/2} absorption at 900–980 nm leads to Stokes Yb{sup 3+} emission in the range of 970–1130 nm as well as bluish-green Yb{sup 3+} cooperative luminescence (CL) whose energy doubles that of the NIR one. The effect of activator concentration and charge compensation through Na{sup +} co-doping on both Yb{sup 3+} emissions were also studied. It was found that Na{sup +} addition enhanced Stokes Yb{sup 3+} photoluminescence brightness, while the cooperative emission intensity appeared to be lower. In doubly Yb{sup 3+}-Tb{sup 3+} doped materials excitation at 980 nm led to cooperative sensitization of the Tb{sup 3+} {sup 5}D{sub 4} level giving rise to its green {sup 5}D{sub 4}→{sup 7}F{sub J} (J={sup 7}F{sub 6}-{sup 7}F{sub 3}) up-conversion luminescence with the dominant component around 542 nm. The cooperative energy transfer (CET) mechanism was proposed basing on the results obtained from emission and absorption spectra, decay kinetics as well as the dependence of UC luminescence intensity on NIR excitation power.

Spin reorientation behavior in Yb doped YMnO3

International Nuclear Information System (INIS)

Sharma, Neetika; Das, A.

2014-01-01

RMnO 3 with smaller rare-earths ions (R = Ho to Lu and Y) crystallize in the non-centrosymmetric hexagonal space group P6 3 cm. The magnetic structure of RMnO 3 compounds with (R=Er,Yb.Lu) are described by irreducible representations (IR) Γ 2,4 and Γ 1,3 for those with higher ionic radii (R=Ho,Y,Y-Er). Of recent the magnetic structure of YMnO 3 has been found to be better described by Γ 3 + Γ 4 IR. YbMnO 3 is another hexagonal manganite, with almost similar transition temperature, and basically shares all the physical properties of YMnO 3 , except for the magnetic structure. The magnetic structure of YbMnO 3 can be explained by Γ 2 or Γ 4 . The non collinear nature of magnetic ordering in these compounds arises due to the frustration inherent in these compounds. In this study we have probed the effect of a magnetic ion (Yb) on the magnetic structure of these frustrated isostructural compounds

Cross-Section Measurement of the 169Tm(n,3n)167Tm Reaction and Constraining the Branching Ratio of 167Tm

Science.gov (United States)

Champine, Brian; Gooden, Matthew; Thomas, Keenan; Krishichayan, F.; Norman, Eric; Scielzo, Nick; Tonchev, Anton; Tornow, Werner

2015-10-01

The cross section of the 169Tm(n,3n)167Tm reaction has been measured from 17.5 to 21.5 MeV using activation technique. This energy region was chosen to resolve the two different trends of the previous (n,3n) cross section measurements on 169Tm. In addition, the branching ratio of the 207.8 keV γ-ray line stemming from electron capture of 167Tm was measured to be 0.419(16). The result of these measurements provide more accurate diagnostic estimation of the so called reaction-in-flight neutrons produced via the internal confinement fusion plasma in deuterium-tritium capsules at the National Ignition Facility.

Thermodynamic properties of multiferroic Mg doped YbMnO{sub 3}

Energy Technology Data Exchange (ETDEWEB)

Sattibabu, Bhumireddi, E-mail: bsb.satti@gmail.com [School of Engineering Sciences and Technology, University of Hyderabad, Hyderabad 500046 (India); Bhatnagar, A.K., E-mail: anilb42@gmail.com [School of Engineering Sciences and Technology, University of Hyderabad, Hyderabad 500046 (India); School of Physics, University of Hyderabad, Hyderabad 500046 (India); Samatham, S. Shanmukharao; Singh, D. [Low Temperature Laboratory, UGC-DAE Consortium for Scientific Research, University Campus, Khandwa Road, Indore 452001, M.P. (India); Rayaprol, S. [UGC-DAE Consortium for Scientific Research, Mumbai Centre, BARC Campus, Mumbai 400085 (India); Das, D. [School of Engineering Sciences and Technology, University of Hyderabad, Hyderabad 500046 (India); Siruguri, V. [UGC-DAE Consortium for Scientific Research, Mumbai Centre, BARC Campus, Mumbai 400085 (India); Ganesan, V. [Low Temperature Laboratory, UGC-DAE Consortium for Scientific Research, University Campus, Khandwa Road, Indore 452001, M.P. (India)

2015-09-25

Highlights: • Specific heat data shows that T{sub N} increases for Mg doped YbMnO{sub 3} from 83 K to 86 K. • Yb{sub 1−x}Mg{sub x}MnO{sub 3} (x = 0.0 and 0.05) shows multiple magnetic transitions. • RCP are found to be 26.1 J/mol and 27.2 J/mol for YbMnO{sub 3} and Yb{sub 0.95}Mg{sub 0.05}MnO{sub 3}. - Abstract: Calorimetric studies of polycrystalline samples Yb{sub 1−x}Mg{sub x}MnO{sub 3} with x = 0.0 and 0.05 are reported. It is revealed that the Mg doping raises the antiferromagnetic ordering temperature, T{sub N,} from 83 K for x = 0.0 to 86 K for x = 0.05. A ferromagnetic ordering is also observed around 3 K. The broad feature in the specific heat data just above ferromagnetic ordering, is attributed to the Schottky anomaly. The estimated effective molecular fields from the Schottky analysis are H{sub mf} = 3.0 and 3.5 T for YbMnO{sub 3} and Yb{sub 0.95}Mg{sub 0.05}MnO{sub 3}, respectively. High temperature shift of Schottky anomaly with Mg doping indicates increase in effective molecular field of Mn at the Yb 4b site. The data supports that the idea that although molecular field is mainly responsible for the Schottky anomaly in Yb{sub 1−x}Mg{sub x}MnO{sub 3} and Mn{sup 3+} spin ordering also affects it. Magnetic part of the specific heat is obtained by subtracting the lattice contribution estimated using two Debye temperatures. The magnetic entropy change (ΔS{sub mag}) for pure and doped samples are 2.0 J mol{sup −1} K{sup −1} and 2.1 J mol{sup −1} K{sup −1} respectively, while the relative cooling power (RCP) calculate 26.1 J/mol, 27.2 J/mol for a field change of 10 T.

Electronic structure and X-ray spectroscopic properties of YbNi{sub 2}P{sub 2}

Energy Technology Data Exchange (ETDEWEB)

Shcherba, I.D., E-mail: ishcherba@gmail.com [Institute of Technology, University of Pedagogy, Podchorazych 2, 30-084 Krakow (Poland); Lviv National University by Ivan Franko, Lviv (Ukraine); Bekenov, L.V.; Antonov, V.N. [Institute for Metal Physics, 36 Vernadsky Street, 03142 Kiev (Ukraine); Noga, H. [Institute of Technology, University of Pedagogy, Podchorazych 2, 30-084 Krakow (Poland); Uskokovic, D. [Institute of Technical Sciences, SASA, Belgrade (Serbia); Zhak, O.; Kovalska, M.V. [Lviv National University by Ivan Franko, Lviv (Ukraine)

2016-10-15

Highlights: • We present new experimental and theoretical data for YbNi{sub 2}P{sub 2}. • The presence of divalent and trivalent Yb ion found in YbNi{sub 2}P{sub 2}. • The calculation show good agreement with the experimental measurements. - Abstract: X-ray absorption spectrum at the Yb L{sub 3} edge and X-ray emission spectra of Ni and P at the K and L{sub 2,3} edges have been studied experimentally and theoretically in the mixed valent compound YbNi{sub 2}P{sub 2} with ThCr{sub 2}Si{sub 2} type crystal structure. The electronic structure of YbNi{sub 2}P{sub 2} is investigated using the fully relativistic Dirac linear muffin-tin orbital (LMTO) band-structure method. The effect of the spin–orbit (SO) interaction and Coulomb repulsion U on the electronic structure of YbNi{sub 2}P{sub 2} is examined in the frame of the LSDA + SO + U method. The core-hole effect in the final states as well as the effect of the electric quadrupole E{sub 2} transitions have been investigated. A good agreement between the theory and the experiment was found. Both the trivalent and the divalent Yb ions in YbNi{sub 2}P{sub 2} are reflected in the experimentally measured Yb L{sub 3} X-ray absorption spectrum simultaneously. We found that the best agreement between the experimental spectrum and sum of the theoretically calculated Yb{sup 2+} and Yb{sup 3+} spectra is achieved with 73% ytterbium ions in 2+ state and 27% ions in 3+ state.

Continuous-wave diode-pumped Yb 3+:LYSO tunable laser

Science.gov (United States)

Du, Juan; Liang, Xiaoyan; Xu, Yi; Li, Ruxin; Yan, Chengfeng; Zhao, Guangjun; Su, Liangbi; Xu, Jun; Xu, Zhizhan

2007-01-01

A new alloyed crystal, Yb:LYSO, has been grown by the Czochralski method in our institute for the first time, and its effective diode-pumped cw tunable laser action was demonstrated. The alloyed crystal retains excellent laser properties of LSO with reduced growth cost, as well as the favorable growth properties of YSO. With a 5-at.% Yb:LYSO sample, we achieved 2.84 W output power at 1085 nm and a slope efficiency of 63.5%. And its laser wavelength could be tuned over a range broader than 80nm, from 1030nm to 1111 nm. This is the broadest tunable range achieved for Yb:LYSO laser, as far as we know.

Valence mixing in YbCuAl: a case study

International Nuclear Information System (INIS)

Mattens, W.

1980-01-01

Results are presented of a study of the valence state of Yb in the intermetallic compound YbCuAl. Both macroscopic physical properties (magnetic susceptibility, heat capacity, thermal expansion, electric resistivity) and microscopic physical properties (neutron inelastic scattering, nuclear magnetic resonance) are determined. The results are compared with a local Fermi liquid theory. (G.T.H.)

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.

Yb:YAG Lasers for Space Based Remote Sensing

Science.gov (United States)

Ewing, J.J.; Fan, T. Y.

1998-01-01

Diode pumped solid state lasers will play a prominent role in future remote sensing missions because of their intrinsic high efficiency and low mass. Applications including altimetry, cloud and aerosol measurement, wind velocity measurement by both coherent and incoherent methods, and species measurements, with appropriate frequency converters, all will benefit from a diode pumped primary laser. To date the "gold standard" diode pumped Nd laser has been the laser of choice for most of these concepts. This paper discusses an alternate 1 micron laser, the YB:YAG laser, and its potential relevance for lidar applications. Conceptual design analysis and, to the extent possible at the time of the conference, preliminary experimental data on the performance of a bread board YB:YAG oscillator will be presented. The paper centers on application of YB:YAG for altimetry, but extension to other applications will be discussed.

Diode-pumped Yb:Sr5(PO4)3F laser performance

International Nuclear Information System (INIS)

Marshall, C.D.; Payne, S.A.; Smith, L.K.

1995-01-01

The performance of the first diode-pumped Yb 3+ -doped Sr 5 (PO 4 ) 3 F (Yb:S-FAP) laser is discussed. We found the pumping dynamics and extraction cross-sections of Yb:S-FAP crystals to be similar to those previously inferred by purely spectroscopic techniques. The saturation fluence for pumping was measured to be 2.2 J/cm 2 using three different methods based on either the spatial, temporal, or energy transmission properties of a Yb:S-FAP rod. The small signal gain implies an emission cross section of 6.0 x 10 -20 cm 2 that falls within error bars of the previously reported value of 7.3 x 10 -20 cm 2 , obtained from spectroscopic techniques. Up to 1.7 J/cm 3 of stored energy density was achieved in a 6 x 6 x 44 mm Yb:S-FAP amplifier rod. An InGaAs diode array has been fabricated that has suitable specifications for pumping a 3 x 3 x 30 mm Yb:S-FAP rod. In a free running configuration diode-pumped slope efficiencies up to 43% were observed with output energies up to ∼0.5 J per 1 ms pulse. When the rod was mounted in a copper block for cooling, 13 W of average power was produced with power supply limited operation at 70 Hz and 500 μs pulses

The recombination channels of luminescence excitation in YAG:Yb single crystalline films

International Nuclear Information System (INIS)

Zakharko, Ya.M.; Luchechko, A.P.; Ubizskii, S.B.; Syvorotka, I.I.; Martynyuk, N.V.; Syvorotka, I.M.

2007-01-01

Absorption and emission spectra, luminescence decay kinetics and thermostimulated luminescence of X-ray irradiated YAG:Yb single crystalline films were studied. Two emission bands peaked at 420 and 488 nm have been detected in the investigated films. The strong thermal quenching of luminescence band at 488 nm was observed above 160 K. The influence of growth conditions and annealing in air on the lifetime of Yb 3+ ion excited state in the IR spectral region have been revealed. The recombination mechanisms of the f-f transition at Yb 3+ ion excitation, as well as the mechanism of lifetime shortening for the excited Yb 3+ luminescence have been discussed

Influence of dopant concentration on spectroscopic properties of Sr2CeO4:Yb nanocrystals

Science.gov (United States)

Stefanski, M.; Kędziorski, A.; Hreniak, D.; Strek, W.

2017-12-01

Optical properties of Sr2CeO4:Yb nanocrystals synthesized via Pechini's method are reported. The samples were characterized by X-ray diffraction data measurements. The unit cell parameters were determined using Rietveld refinement. It was found that they decreased with increasing amount of Yb ions. The absorption, excitation, emission spectra and luminescence decay profiles of the Sr2CeO4:Yb nanocrystals were investigated. It was observed that optical properties were strongly dependent on Yb concentration. It was found that Yb3+-O2- charge transfer transitions have great influence on the absorption spectra. It can be seen in the emission spectra that in addition to standard bands/lines corresponding to Ce-O metal-to-ligand charge transfer of Sr2CeO4 and f-f transitions of Yb3+, there is emission band centered at 744 nm. Its intensity depends on the concentration of the dopant. Recorded decay times become shorter with increasing dopant concentration due to the Yb3+ concentration quenching. Excitation spectra indicate the energy transfer from Ce-O charge transfer states to Yb3+2F5/2 state. The issue of appearance of down-conversion process in Sr2CeO4:Yb nanocrystals is considered.

Affinity of 169Yb, 67Ga and 111In for malignant tumor, (1)

International Nuclear Information System (INIS)

Ando, Itsuko

1975-01-01

The tumor affinity of 169 Yb-citrate, 67 Ga-citrate and 111 In-citrate was examined by using Yoshida sarcoma-bearing rats, and the affinity of these compounds for inflammation was also tested using rats with inflammation induced by croton oil injection. In this investigation there was no great difference in uptake by the tumor tissue of these compounds, but a great difference was observed in the retention value of the blood and uptake rate in the bone. 169 Yb-citrate was cleared rapidly from the blood and was taken mostly into the bone. So the retention values in the soft tissues became very small. On the other hand, 111 In-citrate was slowly and only slightly taken into the bone from the blood, so the retention values in the soft tissue remained relatively high. 67 Ga-citrate showed the intermediate value between the bone uptake rate of 169 Yb-citrate and that of 111 In-citrate. In the following experiments, 169 Yb-citrate and 67 Ga-citrate were compared in four strains: Yoshida sarcoma, Walker carcinosarcoma 256, Sarcoma 180, and Ehrlich tumor. The uptake rate of 169 Yb in tumor tissue was much larger than that of 67 Ga in Ehrlich tumor-bearing mice, but the value of 169 Yb was slightly smaller than those of 67 Ga in Yoshida sarcoma-bearing rats, Walker carcinosarcoma 256-bearing rats and Sarcoma 180-bearing mice. Tumor to organ ratios of 169 Yb, which were most important for tumor scanning, were much larger than those of 67 Ga in all four strains except tumor to bone ratios of 169 Yb. From the above-described facts, it was shown that 169 Yb-citrate had a stronger tumor affinity than 67 Ga-citrate and that the tumor affinity of 169 Yb-citrate was similar in these four strains of tumor bearing animals. These three compounds had a relatively strong affinity with the inflammatory tissue. (auth.)

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

International Nuclear Information System (INIS)

Sugiyama, Makoto; Yanagida, Takayuki; Fujimoto, Yutaka

2014-01-01

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

Investigation of thermal expansion and compressibility of rare-earth orthovanadates using a dielectric chemical bond method.

Science.gov (United States)

Zhang, Siyuan; Zhou, Shihong; Li, Huaiyong; Li, Ling

2008-09-01

The chemical bond properties, lattice energies, linear expansion coefficients, and mechanical properties of ReVO 4 (Re = La, Ce, Pr, Nd, Sm, Eu, Gd, Tb, Dy, Ho, Er, Tm, Yb, Lu, Sc, Y) are investigated systematically by the dielectric chemical bond theory. The calculated results show that the covalencies of Re-O bonds are increasing slightly from La to Lu and that the covalencies of V-O bonds in crystals are decreasing slightly from La to Lu. The linear expansion coefficients decrease progressively from LaVO 4 to LuVO 4; on the contrary, the bulk moduli increase progressively. Our calculated results are in good agreement with some experimental values for linear expansion coefficients and bulk moduli.

Synthesis and upconversion luminescence properties of YF{sub 3}:Yb{sup 3+}/Er{sup 3+} hollow nanofibers derived from Y{sub 2}O{sub 3}:Yb{sup 3+}/Er{sup 3+} hollow nanofibers

Energy Technology Data Exchange (ETDEWEB)

Li Dan; Dong Xiangting, E-mail: dongxiangting888@163.com; Yu Wensheng; Wang Jinxian; Liu Guixia [Changchun University of Science and Technology, Key Laboratory of Applied Chemistry and Nanotechnology at Universities of Jilin Province (China)

2013-06-15

YF{sub 3}:Yb{sup 3+}/Er{sup 3+} hollow nanofibers were successfully fabricated via fluorination of the relevant Y{sub 2}O{sub 3}:Yb{sup 3+}/Er{sup 3+} hollow nanofibers which were obtained by calcining the electrospun PVP/[Y(NO{sub 3}){sub 3} + Yb(NO{sub 3}){sub 3} + Er(NO{sub 3}){sub 3}] composite nanofibers. The morphology and properties of the products were investigated in detail by X-ray diffraction, scanning electron microscope, transmission electron microscope, and fluorescence spectrometer. YF{sub 3}:Yb{sup 3+}/Er{sup 3+} hollow nanofibers were pure orthorhombic phase with space group Pnma and were hollow-centered structure with mean diameter of 174 {+-} 22 nm, and YF{sub 3}:Yb{sup 3+}/Er{sup 3+} hollow nanofibers are composed of nanoparticles with size in the range of 30-60 nm. Upconversion emission spectrum analysis manifested that YF{sub 3}:Yb{sup 3+}/Er{sup 3+} hollow nanofibers emitted strong green and weak red upconversion emissions centering at 523, 545, and 654 nm, respectively. The green and red emissions were, respectively, originated from {sup 2}H{sub 11/2}/{sup 4}S{sub 3/2} {yields} {sup 4}I{sub 15/2} and {sup 4}F{sub 9/2} {yields} {sup 4}I{sub l5/2} energy levels transitions of the Er{sup 3+} ions. Moreover, the emitting colors of YF{sub 3}:Yb{sup 3+}/Er{sup 3+} hollow nanofibers were located in the green region in CIE chromaticity coordinates diagram. This preparation technique could be applied to prepare other rare earth fluoride upconversion luminescence hollow nanofibers.Graphical AbstractYF{sub 3}:Yb{sup 3+}/Er{sup 3+} hollow nanofibers with orthorhombic structure were synthesized by fluorination of the electrospun Y{sub 2}O{sub 3}:Yb{sup 3+}/Er{sup 3+} hollow nanofibers via a double-crucible method using NH{sub 4}HF{sub 2} as fluorinating agent. The mean diameter of YF{sub 3}:Yb{sup 3+}/Er{sup 3+} hollow nanofibers was 174 {+-} 22 nm. The fluorination method we proposed here has been proved to be an important method, as it can not only

Investigation of some lanthanide boron, carbon, nitrogen, chalcogen and halogen systems at elevated temperatures. Progress report, February 1, 1959--March 31, 1976

International Nuclear Information System (INIS)

Eick, H.A.

1976-01-01

Research is summarized on thermodynamic properties of borides, ThC 2 , EuC 2 , oxide-carbide phases, YbOC, Eu bromides, vaporization, fluorides, Y chlorides, etc. Preliminary results are given for the preparation of Gd(III) Cl-I phases and the vaporization of YbBr 2

'Obligate' anaerobic Salmonella strain YB1 suppresses liver tumor growth and metastasis in nude mice.

Science.gov (United States)

Li, Chang-Xian; Yu, Bin; Shi, Lei; Geng, Wei; Lin, Qiu-Bin; Ling, Chang-Chun; Yang, Mei; Ng, Kevin T P; Huang, Jian-Dong; Man, Kwan

2017-01-01

The antitumor properties of bacteria have been demonstrated over the past decades. However, the efficacy is limited and unclear. Furthermore, systemic infection remains a serious concern in bacteria treatment. In this study, the effect of YB1, a rationally designed 'obligate' anaerobic Salmonella typhimurium strain, on liver tumor growth and metastasis in a nude mouse orthotopic liver tumor model was investigated. The orthotopic liver tumor model was established in nude mice using the hepatocellular carcinoma cell line MHCC-97L. Two weeks after orthotopic liver tumor implantation, YB1, SL7207 and saline were respectively administered through the tail vein of the mice. Longitudinal monitoring of tumor growth and metastasis was performed using Xenogen IVIS, and direct measurements of tumor volume were taken 3 weeks after treatment. In vitro , MHCC-97L and PLC cells were incubated with YB1 or SL7207 under anaerobic conditions. YB1 was observed to invade tumor cells and induce tumor cell apoptosis and death. The results revealed that all mice in the YB1 group were alive 3 weeks after YB1 injection while all mice in the SL7207 group died within 11 days of the SL7207 injection. The body weight decreased by ~9% on day 1 after YB1 injection and but subsequently recovered. Liver tumor growth and metastases were significantly inhibited following YB1 treatment. By contrast to the control group, a large number of Gr1-positive cells were detected on days 1 to 21 following YB1 treatment. Furthermore, YB1 also effectively invaded tumor cells and induced tumor cell apoptosis and death. In conclusion, YB1 suppressed liver tumor growth and metastasis in a nude mice liver tumor model. The potential mechanism may be through enhancing innate immune response and inducing tumor cell apoptosis and cell death.

Crystal field excitations of YbMn{sub 2}Si{sub 2}

Energy Technology Data Exchange (ETDEWEB)

Mole, R.A. [Australian Nuclear Science and Technology Organisation, Lucas Heights, NSW 2234 (Australia); School of Physical, Environmental and Mathematical Sciences, The University of New South Wales at the Australian Defence Force Academy, Canberra, ACT 2600 (Australia); Hofmann, M. [School of Physical, Environmental and Mathematical Sciences, The University of New South Wales at the Australian Defence Force Academy, Canberra, ACT 2600 (Australia); Forschungsneutronenquelle Heinz Maier-Leibnitz (FRM II), Technische Universität München, 85747 Garching (Germany); Adroja, D.T. [ISIS Facility, Science and Technology Facilities Council, Rutherford Appleton Laboratory, Didcot, OX11 OQX (United Kingdom); Moze, O. [Dipartimento di Fisica, Università degli Studi di Modena e Reggio Emilia, Modena (Italy); Campbell, S.J., E-mail: stewart.campbell@adfa.edu.au [School of Physical, Environmental and Mathematical Sciences, The University of New South Wales at the Australian Defence Force Academy, Canberra, ACT 2600 (Australia)

2013-12-15

The crystal field excitations of the rare earth intermetallic compound YbMn{sub 2}Si{sub 2} have been measured by inelastic neutron scattering over the temperature range 2.5–50 K. The YbMn{sub 2}Si{sub 2} spectra exhibit three low energy excitations (∼3–7 meV) in the antiferromagnetic AFil region above the magnetic phase transition at T{sub N2} = 30(5) K. The crystal field parameters have been determined for YbMn{sub 2}Si{sub 2} in the antiferromagnetic AFil region. A further two inelastic excitations (∼9 meV, 17 meV) are observed below T{sub N2}=30(5) K, the temperature at which the high temperature antiferromagnetic structure is reported to exhibit doubling of the magnetic cell. Energy level diagrams have been determined for Yb{sup 3+} ions in the different sites above (single site) and below the magnetic transition temperature (two sites). The excitation energies for both sites are shown to be temperature independent with the temperature dependences of the transition intensities for the two sites described well by a simple Boltzmann model. The spectra below T{sub N2} cannot be described fully in terms of molecular field models based on either a single Yb{sup 3+} site or two Yb{sup 3+} sites. This indicates that the magnetic behaviour of YbMn{sub 2}Si{sub 2} is more complicated than previously considered. The inability to account fully for excitations below the magnetic phase transition may be due to an, as yet, unresolved structural transition associated with the magnetic transition. - Highlights: • The inelastic neutron scattering from YbMn{sub 2}Si{sub 2} has been investigated over the temperature range 2.5–50 K. • The crystal field splitting has been monitored through the magnetic transition at 30(5) K. • We have determined the crystal field parameters for the antiferromagnetic AFil region. • The transition intensities are described well by Boltzmann occupancy models. • The spectra below the magnetic transition have been analysed by

Facile synthesis of NaYF4:Yb, Ln/NaYF4:Yb core/shell upconversion nanoparticles via successive ion layer adsorption and one-pot reaction technique

NARCIS (Netherlands)

Zeng, Q.; Xue, B.; Zhang, Y.; Wang, D.; Liu, X.; Tu, L.; Zhao, H.; Kong, X.; Zhang, H.

2013-01-01

The facile one-pot synthesis of NaYF4:Yb, Ln/NaYF4:Yb core/shell (CS) upconversion nanoparticles (UCNPs) was firstly developed through the successive ion layer adsorption and reaction (SILAR) technique, which represents an attractive alternative to conventional synthesis utilizing the chloride of Ln

Thermodynamic description of the Al-Cu-Yb ternary system supported by first-principles calculations

Directory of Open Access Journals (Sweden)

Huang G.

2016-01-01

Full Text Available Phase relationships of the ternary Al-Cu-Yb system have been assessed using a combination of CALPHAD method and first principles calculations. A self-consistent thermodynamic parameter was established based on the experimental and theoretical information. Most of the binary intermetallic phases, except Al3Yb, Al2Yb, Cu2Yb and Cu5Yb, were assumed to be zero solubility in the ternary system. Based on the experimental data, eight ternary intermetallic compounds were taken into consideration in this system. Among them, three were treated as line compounds with large homogeneity ranges for Al and Cu. The others were treated as stoichiometric compounds. The calculated phase diagrams were in agreement with available experimental and theoretical data.

The complexity of the CaF2:Yb system: evidence that CaF2:Yb2+ is not an impurity trapped exciton system

Science.gov (United States)

Mackeen, Cameron; Bridges, Frank; Kozina, Michael; Mehta, Apurva; Reid, M. F.; Wells, J.-P. R.; BarandiaráN, Zoila

Fluorite crystal structures doped with rare-earth elements exhibit an anomalous redshifted luminescence upon UV excitation, generally attributed to the relaxation of impurity trapped excitons (ITE). We find that the intensity of this luminescence decreases as the total concentration of Yb 2+ increases in unexposed samples, which is in conflict with the currently accepted ITE model. Further, using x-ray absorption spectroscopy and UV-vis studies of CaF2:Yb, we find a large (but reversible) Yb valence reduction upon x-ray exposure at 200 K - from mostly 3+ to 2+. This valence reduction is stable for long time periods at low T ITE model; the data appear more consistent with an intervalence charge transfer (IVCT) model. It is likely that many similar ITE systems have also been misidentified.

Local structure investigation of Ga and Yb dopants in Co4Sb12 skutterudites

Science.gov (United States)

Hu, Yanyun; Chen, Ning; Clancy, J. P.; Salvador, James R.; Kim, Chang-Yong; Shi, Xiaoya; Li, Qiang; Kim, Young-June

2017-12-01

We report comprehensive x-ray absorption spectroscopy studies at both the Ga K edge and Yb L2 edge to elucidate the local structure of Ga and Yb dopants in YbxGayCo4Sb12 . Our extended x-ray absorption fine structure (EXAFS) data confirm that Ga atoms occupy two crystallographic sites: one is the 24 g site replacing Sb, and the other is the 2 a site in the off-center void position. We find that the occupancy ratio of these two sites varies significantly as a function of the filling fraction of additional Yb, which exclusively occupies the 2 a on-center site. At low concentrations of Yb, Ga24 g and Ga2 a dopants coexist and they form a charge-compensated compound defect proposed by Qiu et al. [Adv. Funct. Mater. 23, 3194 (2013), 10.1002/adfm.201202571]. The Ga24 g occupancy increases gradually with increasing Yb concentration, and almost all Ga occupies the 24 g site for the highest Yb concentration studied (x =0.4 ). In addition to the local structural evidence provided by our EXAFS data, we also present x-ray absorption near-edge structure (XANES) spectra, which show a small Ga K -edge energy shift as a function of Yb concentration consistent with the change from predominantly Ga2 a to Ga24 g states. Our result suggests that the increased solubility of Yb in Yb-Ga co-doped Co4Sb12 skutterudites is due to the increased Ga24 g electron acceptor, and thus provides an important strategy to optimize the carrier concentration in partially filled skutterudites.

Microscopic analysis of shape transition in neutron-deficient Yb isotopes

Science.gov (United States)

Fu, Y.; Tong, H.; Wang, X. F.; Wang, H.; Wang, D. Q.; Wang, X. Y.; Yao, J. M.

2018-01-01

The development of nuclear collectivity in even-even Yb-170152 is studied with three types of mean-field calculations: the nonrelativistic Hartree-Fock plus BCS calculation using the Skyrme SLy4 force plus a density-dependent δ pairing force and the relativistic mean-field calculation using a point-coupling energy functional supplemented with either a density-independent δ pairing force or a separable pairing force. The low-lying states are obtained by solving a five-dimensional collective Hamiltonian with parameters determined from the three mean-field solutions. The energy surfaces, excitation energies, electric multiple transition strengths, and differential isotope shifts are presented in comparison with available data. Our results show that different treatments of pairing correlations have a significant influence on the speed of developing collectivity as the increase of neutron number. All the calculations demonstrate the important role of dynamic shape-mixing effects in resolving the puzzle in the dramatic increase of charge radius from 152Yb to 154Yb and the role of triaxiality in Yb 160 ,162 ,164 .

Electron spin resonance in Yb-based Kondo-lattice systems

International Nuclear Information System (INIS)

Wykhoff, Jan

2010-01-01

The systems Yb 1-w A 1-w (Rh 1-x Co x )(Si 1-y Ge y ) 2 with A=La respectively Lu, as well as YbIr 2 Si 2 are studied. The measurements are presented sortedly for systems, dopings, and external parameters. Beside these external parameters furthermore the orientation of the sample related to the quasistatic magnetic field and the microwave magnetic field was varied.

Study on the fabrication and photoluminescence characteristics of LiBO2 glass scintillators with the lanthanides activators

International Nuclear Information System (INIS)

Sin, S. W.; Hwang, J. H.; Choi, S. H.; Sumarokov, S. Yu.

2002-01-01

LiBO 2 glass scintillators were fabricated, and lanthanides(except Pm) oxides or chlorides were used as an activator. For the fabrication of LiBO 2 glasses, optimum heating conditions were obtained, and the photoluminescence of the glasses was measured by the monochromator. For the best transparency of the glass samples, optimum heating temperature and time are 1000 .deg. C and 40 min, respectively. The result of photoluminescence analysis shows that Pr, Nd, Gd, Ho, Er, Tm, Yb, and Lu are not good as activator. Because emission spectrum of samples with them was equal to that of sample without activator. In the case of samples with Europium, the peak of emission spectrum of Eu(III) is 810 nm. And Samples with Ce(III) are 760 nm, and Tb(III) are about 535 nm. Samples with Ce(III) and Tb(III) have the best PL intensity with added sugar in Ar reduction atmosphere, and sample with Eu(III) has the best intensity without a reducing process

Up-conversion and near infrared luminescence in Er3+/Yb3+ co-doped glass-ceramic containing MgGa2O4 nano-crystals

International Nuclear Information System (INIS)

Sun, Jiaju; Yu, Lixin; Li, Fuhai; Wei, Shuilin; Li, Songchu

2016-01-01

The MgO–Ga 2 O 3 –SiO 2 (MG-S) glasses and nanocrystalline glass-ceramics (GCs) containing MgGa 2 O 4 nanocrystals codoped with Er 3+ and Yb 3+ were prepared by a simple sol–gel method. The formation of MgGa 2 O 4 nanocrystals in the GCs was confirmed by the X-ray diffraction (XRD). Their morphology was investigated applying high-resolution transmission electron microscopy (HRTEM). Stark splitting of near infrared (NIR) and up-conversion (UC) emission implies that the Er 3+ is incorporated into MgGa 2 O 4 nanocrystals. The effect of the MgO, Ga 2 O 3 content and sintering temperature on the structure of the prepared samples was systematically studied. Under 980 nm excitation, intense UC and NIR emission (1530 nm) were observed in the MG-S GCs by efficient energy transfer from Yb 3+ to Er 3+ . The two-photon process was confirmed to be responsible for both the green and red UC emissions. - Highlights: • It is interesting that the CIE chromaticity coordinates of the several prepared CaMO 4 :Eu samples by a hydrothermal method are very close to the standard of white light.

Investigation of Anderson lattice behavior in Yb1-xLuxAl3

International Nuclear Information System (INIS)

Bauer, E.D.; Booth, C.H.; Lawrence, J.M.; Hundley, M.F.; Sarrao, J.L.; Thompson, J.D.; Riseborough, P.S.; Ebihara, T.

2003-01-01

Measurements of magnetic susceptibility χ(T), specific heat C(T), Hall coefficient R H (T), and Yb valence ν = 2 + n f [f-occupation number n f (T) determined from Yb L 3 x-ray absorption measurements] were carried out on single crystals of Yb 1-x Lu x Al 3 . The low temperature anomalies observed in χ(T) and C(T) corresponding to an energy scale T coh ∼ 40 K in the intermediate valence, Kondo lattice compound YbAl 3 are suppressed by Lu concentrations as small as 5% suggesting these low-T anomalies are extremely sensitive to disorder and, therefore, are a true coherence effect. By comparing the temperature dependence of various physical quantities to the predictions of the Anderson Impurity Model, the slow crossover behavior observed in YbAl 3 , in which the data evolve from a low-temperature coherent, Fermi-liquid regime to a high temperature local moment regime more gradually than predicted by the Anderson Impurity Model, appears to evolve to fast crossover behavior at x ∼ 0.7 where the evolution is more rapid than predicted. These two phenomena found in Yb 1-x Lu x Al 3 , i.e., the low-T anomalies and the slow/fast crossover behavior are discussed in relation to recent theories of the Anderson lattice

Effect of rare-earth ion size on local electron structure in RBa{sub 2}Cu{sub 3}O{sub 7-{delta}} (R = Tm, Dy, Gd, Eu, Nd and Y) superconductors: A positron study

Energy Technology Data Exchange (ETDEWEB)

Chen Zhenping [Department of Technology and Physics, Zhengzhou University of Light Industry, 5 Dongfeng Road, Zhengzhou, Henan 450002 (China)]. E-mail: czhping@zzuli.edu.cn; Zhang Jincang [Department of Physics, Shanghai University, Shanghai 200436 (China); Su Yuling [Department of Technology and Physics, Zhengzhou University of Light Industry, 5 Dongfeng Road, Zhengzhou, Henan 450002 (China); Xue Yuncai [Department of Technology and Physics, Zhengzhou University of Light Industry, 5 Dongfeng Road, Zhengzhou, Henan 450002 (China); Cao Shixun [Department of Physics, Shanghai University, Shanghai 200436 (China)

2006-02-15

The effects of rare-earth ionic size on the local electron structure, lattice parameters and superconductivity have been investigated by positron annihilation technique (PAT) and related experiments for RBa{sub 2}Cu{sub 3}O{sub 7-{delta}} (R = Tm, Dy, Gd, Eu, Nd and Y) superconductors. The local electron density n {sub e} is evaluated as a function of the rare-earth radius. The results show that both the bulk-lifetime {tau} {sub B} and the defect lifetime {tau} {sub 2} increase with increasing rare-earth ionic radius, while the local electron density n {sub e} decrease with increasing rare-earth ionic radius. These results prove that the changes of n {sub e}, the degree of orthorhombic distortion and the coupling between the Cu-O chains and the CuO{sub 2} planes all have an effect on the superconductivity of RBa{sub 2}Cu{sub 3}O{sub 7-{delta}} systems.

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)

Whole-body retention studies of /sup 169/Yb-citrate. Estimation of radiation dose to humans from /sup 169/Yb-citrate

Energy Technology Data Exchange (ETDEWEB)

Ando, A; Hiraki, T [Kanazawa Univ. (Japan). School of Paramedicine; Mori, H; Ando, I; Hisada, K

1977-09-01

For purpose of the estimation of the radiation dose to humans from /sup 169/Yb-citrate, the whole-body retention studies using five rats were carried out. Following intravenous administration of /sup 169/Yb-citrate, the whole-body activity was monitored for 40 days by the animal counter. The whole-body retention curve consisted of three components: the first with a 3.6 hours effective half-time, the second with an 154 hours effective half-time and the third with a 29.9 days effective half-time. Therefore it was assumed that 32% of the administered /sup 169/Yb-citrate clears from the kidney with a short biologic half-time (3.6 hours), 18% remains in the liver and other soft tissues with a relatively long biologic half-time (194 hours) and 50% remains in the bone with a long biologic half-time (850 days). Based on these biological data and the MIRD Committee method, the average dose to the bone and whole-body were 20.8 rads/mCi and 4.5 rads/mCi respectively.

Photoluminescence characterization of porous YAG: Yb{sup 3+}–Er{sup 3+} nanoparticles

Energy Technology Data Exchange (ETDEWEB)

Desirena, H., E-mail: hagdes@cio.mx [Centro de Investigaciones en Óptica, A. P. 1-948, León 37150, Guanajuato (Mexico); Diaz-Torres, L.A. [Centro de Investigaciones en Óptica, A. P. 1-948, León 37150, Guanajuato (Mexico); Rodríguez, R.A. [Centro Universitario de Los Lagos, Universidad de Guadalajara, Lagos de Moreno, Jalisco (Mexico); Meza, O. [Instituto de Física, Benemérita Universidad Autónoma de Puebla, Apartado Postal J-48, Centro Historico 72570, Puebla (Mexico); Salas, P. [Centro de Física Aplicada y Tecnología Avanzada, Universidad Nacional Autónoma de México, Apartado Postal 1-1010, Querétaro 76000, Querétaro México (Mexico); Angeles-Chávez, C. [Instituto Mexicano del Petróleo, Ciudad México, D.F. 07730, México (Mexico); Tobar, E.H.; Castañeda-Contreras, J. [Centro Universitario de Los Lagos, Universidad de Guadalajara, Lagos de Moreno, Jalisco (Mexico); De la Rosa, E., E-mail: elder@cio.mx [Centro de Investigaciones en Óptica, A. P. 1-948, León 37150, Guanajuato (Mexico)

2014-09-15

Yb{sup 3+}/Er{sup 3+} codoped yttrium aluminium garnet (YAG) porous nanocrystals were prepared by glycolate method assisted with poly-vinyl alcohol (PVA) and urea. The typical cubic structure for YAG was confirmed from XRD with crystallite average size of ∼40 nm, calculated from Scherrer formula and corroborated by TEM. Strong green and red upconversion emissions are observed readily with the naked eyes, and the color coordinates were obtained from emission spectra. A theoretical model to calculate CIE coordinate as a function of donor (Yb{sup 3+}) and acceptors (Er{sup 3+}) concentration is proposed. The eye-safe near infrared emitted signal and fluorescence lifetime were also measured and results show lifetime as large as 8.5 ms. The maximum energy transfer efficiency from Yb{sup 3+} to Er{sup 3+} was 72% for 20 mol% of Yb{sub 2}O{sub 3}. The proposed mechanisms for signal emitted are explained in terms of direct and energy back transfer processes, and cross relaxation. - Highlights: • Strong upconversion emission were observed in YAG:Er{sup 3+}–Yb{sup 3+} samples. • Color emission can be tuned from green to red by choosing properly the Yb{sup 3+} concentration. • The experimental colour coordinates match very well with the proposed theoretical model. • Cross relaxation and energy back transfer are mainly responsible for the red emission. • Fluorescence lifetime of {sup 4}I{sub 13/2} level increase with the Yb{sup 3+} concentration.

Structural specifics of the condensate prepared by thermal evaporation of alloys of As2S3-Yb systems

International Nuclear Information System (INIS)

Ehfendiev, Eh.G.; Mamedov, A.I.; Il'yasov, T.M.; Rustamov, P.G.

1987-01-01

The problem aimed at preparation of the films of As 2 S 3 -Yb system, at studying their substructure depending on condensation conditions and defining noncrystallinity region of this system in the film state, is formulated. It is shown that in representative samples of As 2 S 3 -Yb system the vitrification region is extended up to 7 at.% Yb, in the films noncrystallinity region is extended up to 30 at.% Yb. With up to 30 at.% increase of ytterbium amount in initial alloys a tendency to crystallization in amorphous condensate structure is noticed. In evaporation of As 2 S 3 + 40 at.% Yb and As 2 S 3 + 50 at.% Yb, unknown in the film state YbAs 2 S 4 , Yb 3 As 4 S 9 and YbAs 4 S 7 phases are prepared, and the latter is formed in case of As 2 S 3 + 50 at.% Yb alloy at small evaporation rates (∼10 A/s). Substructure of As 2 S 3 + 50 at.% Yb alloy prepared condensate is more dependent on evaporation rate than in evaporation of As 2 S 3 + 40 at.% Yb alloy. In this case, evaporation rates being ∼ 100 A/s, the condensate has a polycrystal structure, and at small rates of ∼ 10 A/c, condensate structure is primarily blocked

Growth and luminescent properties of Yb3+--doped oxide single crystals for scintillator application

International Nuclear Information System (INIS)

Yoshikawa, A.; Ogino, H.; Shim, J.B.; Nikl, M.; Solovieva, N.; Fukuda, T.

2004-01-01

Rod-shaped (Lu 1-x Yb x ) 3 Al 5 O 12 with x=0.05, 0.15, 0.30 and (Y 1-x Yb x )AlO 3 with x=0.05, 0.10, 0.30 single crystals were grown by the micro-pulling-down method. Edge-defined film-fed growth method was used to prepare (Y 0.9 Yb 0.1 )VO 4 crystal, while Ca 8 (La 1.98 Yb 0.02 )(PO 4 ) 6 O 2 crystal was grown by the Czochralski method. Luminescence of these crystals was studied with main attention paid to the charge transfer emission of Yb 3+ . Temperature tuned decay times in the time scale of units--tens of nanosecond was measured as a feature possibly interesting for an application in scintillation detectors in positron emission tomography

Synthesis and characterization of Yb and Er based monosilicate powders and durability of plasma sprayed Yb2SiO5 coatings on C/C–SiC composites

International Nuclear Information System (INIS)

Khan, Zuhair S.; Zou Binglin; Huang Wenzhi; Fan Xizhi; Gu Lijian; Chen Xiaolong; Zeng Shuibing; Wang Chunjie; Cao Xueqiang

2012-01-01

Highlights: ► Ultra-pure rare-earth monosilicate powders based on Er and Yb have been fabricated by solid-state reaction. ► Spray-drying treatment results in powders with free flowing characteristics and rounded surface morphologies. ► CTEs are found to be 7.1 ppm/°C for Yb 2 SiO 5 and 7.5 ppm/°C for Er 2 SiO 5 . ► Plasma spraying has been used to deposit Yb 2 SiO 5 coatings on C/C–SiC substrate. ► Coatings remain strongly intact with the substrate on thermal cycling between ∼400 °C and 1500 °C in gas burner rig experiment. - Abstract: Rare-earth silicates such as Yb 2 SiO 5 and Er 2 SiO 5 are promising environmental barrier coating materials for ceramic matrix composites. In this work, Yb 2 SiO 5 and Er 2 SiO 5 ceramic powders have been synthesized by solid-state reaction using Yb 2 O 3 , Er 2 O 3 and SiO 2 as starting materials. The fabricated powders were subjected to spray drying treatment for subsequent synthesis of coatings by plasma spraying. The spray drying resulted in well-dispersed and spherical powder particles with good flowability. Analytical techniques such as X-ray diffraction (XRD), scanning electron microscopy (SEM), thermogravimetry and differential scanning calorimetry (TGA/DSC) and dilatometry were applied to study the microstructural and thermal characteristics of the powders. Ultra-high purity monosilicate powders formed as a result of heating treatments at 1400 °C in a box furnace for 20 h. TG/DSC revealed the genesis temperatures of the silicate formation (low temperature polymorphs) and also showed that the solid-state reactions to form Yb and Er based monosilicates proceeded without any weight-loss in the tested temperature range. The values of coefficients of thermal expansion (CTE) of the fabricated compounds are found to be 7.1 ppm/°C for Yb 2 SiO 5 and 7.5 ppm/°C for Er 2 SiO 5 by dilatometric measurements. Besides these studies, coating formation by plasma spraying of spray-dried Yb 2 SiO 5 powders on the ceramic

Up-conversion luminescence of Er3+/Yb3+/Nd3+-codoped tellurite glasses

International Nuclear Information System (INIS)

Lu Longjun; Nie Qiuhua; Xu Tiefeng; Dai Shixun; Shen Xiang; Zhang Xianghua

2007-01-01

Up-conversion luminescence and energy transfer (ET) processes in Nd 3+ -Yb 3+ -Er 3+ triply doped TeO 2 -ZnO-Na 2 O glasses have been studied under 800 nm excitation. Intense green up-conversion emissions around 549 nm, which can be attributed to the Er 3+ : 4 S 3/2 →4 I 15/2 transition, are observed in triply doped samples. In contrast, the green emissions are hardly observed in Er 3+ singly doped and Er 3+ -Yb 3+ codoped samples under the same condition. Up-conversion luminescence intensity exhibits dependence of Yb 2 O 3 -concentration and Nd 2 O 3 -concentration. Up-conversion mechanism in the triply doped glasses under 800 nm pump is discussed by analyzing the ET among Nd 3+ , Yb 3+ and Er 3+ . And a possible up-conversion mechanism based on sequential ET from Nd 3+ to Er 3+ through Yb 3+ is proposed for green and red up-conversion emission processes

Characterization and Computation of Yb/TiO2 and Its Photocatalytic Degradation with Benzohydroxamic Acid

Directory of Open Access Journals (Sweden)

Xianping Luo

2017-11-01

Full Text Available Yb-doped TiO2 (Yb/TiO2 compositions were synthesized by sol-gel method, and the prepared materials were characterized by X-ray Diffraction (XRD, X-ray photoelectron spectroscopy (XPS, UV-visible diffuse-reflectance spectrum (UV-Vis DRS, transmission electron microscope (TEM and high resolution transmission electron microscope (HRTEM, energy dispersive spectrometer (EDS, and N2 adsorption. A beneficiation reagent of benzohydroxamic acid (BHA was used to test the photocatalytic activity of Yb/TiO2. The characterizations indicate that the doping of Yb could inhibit the crystal growth of TiO2, enhance the specific surface area, increase the binding energy of Ti2p, and also slightly expand the adsorption ranges to visible light. Furthermore, the computation of band structure also indicates that Yb-doped TiO2 could make the forbidden band narrower than pure anatase TiO2, which presents a red shift in the absorption spectrum. As a result of the photodegradation experiment on BHA, Yb/TiO2 (0.50% in mass sintered at 450 °C displayed the highest catalytic activity for BHA when compared with pure TiO2 or other doped Yb/TiO2 compositions, and more than 89.2% of the total organic carbon was removed after 120 min. Almost all anions, including Cl−, HCO3−, NO3−, and SO42−, inhibited the degradation of BHA by Yb/TiO2, and their inhibition effects followed the order of HCO3− > NO3− > SO42− > Cl−. Cations of Na+, K+, Ca2+, and Mg2+ displayed a slight suppressing effect due to the impact of Cl− coexisting in the solution. In addition, Yb/TiO2 maintained a high photocatalytic ability with respect to BHA after four runs. It is hypothesized that ·OH is one of the main species involved in the photodegradation of BHA, and the mutual transformation of Yb3+ and Yb2+ could promote the separation of electron-hole pairs.

CW Yb:YAG LASER FOR PORTABLE MEASURING SYSTEMS

Directory of Open Access Journals (Sweden)

A. M. Ivashko

2014-01-01

Full Text Available The theoretical and experimental results of longitudinally continuous-wave diode-pumped Yb:Y3Al5O12 (YAG laser performance for compact field-condition measuring systems were demonstrated. Optimization of laser setup in terms of operation condition in the range of -40 ˚С – +65 ˚С without active thermal stabilization was carried out. Using Yb (10 ат.%:YAG crystal with the length of 3 mm the maximal output power more than 2 W was obtained in the whole of temperature range.

Electronic structure of YbNiX{sub 3} (X =Si, Ge) studied by hard X-ray photoemission spectroscopy

Energy Technology Data Exchange (ETDEWEB)

Sato, Hitoshi; Shimada, Kenya; Namatame, Hirofumi [Hiroshima Synchrotron Radiation Center, Hiroshima University, Kagamiyama 2-313, Higashi-Hiroshima 739-0046 (Japan); Utsumi, Yuki [Max-Planck Institute for Chemical Physics of Solids, 01187 Dresden (Germany); Kodama, Junichi; Nagata, Heisuke [Graduate School of Science, Hiroshima University, Kagamiyama 1-3-1, Higashi-Hiroshima 739-8526 (Japan); Avila, Marcos A.; Ribeiro, Raquel A. [Centro de Ciencias Naturais e Humanas, Universidade Federal do ABC, Santo Andre - SP, 09210-580 (Brazil); Umeo, Kazunori [Cryogenics and Instrumental Analysis Division, N-BARD, Hiroshima University, Higashi-Hiroshima 739-8526 (Japan); Takabatake, Toshiro [Department of Quantum Matter, AdSM, Hiroshima University, Higashi-Hiroshima 739-8530 (Japan); Institute for Advanced Materials Research, Hiroshima University, Higashi-Hiroshima 739-8530 (Japan); Mimura, Kojiro; Motonami, Satoru; Anzai, Hiroaki [Graduate School of Engineering, Osaka Prefecture University, Sakai 599-8531 (Japan); Ueda, Shigenori [Synchrotron X-ray Station at SPring-8, National Institute for Materials Science, Hyogo 679-5148 (Japan); Taniguchi, Masaki [Hiroshima Synchrotron Radiation Center, Hiroshima University, Kagamiyama 2-313, Higashi-Hiroshima 739-0046 (Japan); Graduate School of Science, Hiroshima University, Kagamiyama 1-3-1, Higashi-Hiroshima 739-8526 (Japan)

2015-06-15

lectronic structure of the Kondo lattices YbNiX{sub 3} (X =Si, Ge) has been investigated by means of hard x-ray photoemission spectroscopy (HAXPES) with hν = 5.95 keV. From the Yb 3d HAXPES spectra, the Yb valence in YbNiSi{sub 3} is estimated to be ∝ 2.92, which is almost temperature-independent. On the other hand, the valence in YbNiGe{sub 3} is estimated to be 2.48 at 300 K, showing significant valence fluctuation, and gradually decreases to 2.41 at 20 K on cooling. The Ni 2p{sub 3/2} and Yb{sup 3+} 4f peaks exhibit opposite energy shifts amounting to ∝ 0.6 eV between YbNiSi{sub 3} and YbNiGe{sub 3}. We propose a simple model for the electronic structure of YbNiX{sub 3} based on the HAXPES results. (copyright 2015 WILEY-VCH Verlag GmbH and Co. KGaA, Weinheim)

Unusual antiferromagnetic structure of YbCo{sub 2}Si{sub 2}

Energy Technology Data Exchange (ETDEWEB)

Mufti, N. [Max-Planck-Institut fuer Chemische Physik fester Stoffe, Dresden (Germany); Department of Physics, State University of Malang, Malang (Indonesia); Kaneko, K. [Max-Planck-Institut fuer Chemische Physik fester Stoffe, Dresden (Germany); Quantum Beam Science Center, Japan Atomic Energy Agency, Tokai (Japan); Hoser, A. [Helmholtz-Zentrum Berlin fuer Materialien und Energie, Berlin (Germany); Gutmann, M. [ISIS Neutron and Muon Source, Rutherford Appleton Laboratory, Didcot (United Kingdom); Geibel, C.; Stockert, O. [Max-Planck-Institut fuer Chemische Physik fester Stoffe, Dresden (Germany); Krellner, C. [Max-Planck-Institut fuer Chemische Physik fester Stoffe, Dresden (Germany); Physikalisches Institut, Goethe-Universitaet Frankfurt, Frankfurt (Germany)

2016-07-01

We report on extensive powder and single crystal neutron diffraction experiments to study the magnetic structure in YbCo{sub 2}Si{sub 2} below the Neel temperature T{sub N} = 1.7 K in detail. Representation analysis has been used to find the possible magnetic structure models compatible with the experiments. Two different magnetically ordered phases can clearly be distinguished. At lowest temperatures a commensurate magnetic structure with a propagation vector k{sub 1} = (0.25 0.25 1) and equal moments or about 1.4 μ{sub B}/Yb is found, while the intermediate phase (T > 0.9 K) is characterized by an incommensurate amplitude-modulated magnetic structure with k{sub 2} = (0.25 0.086 1). The magnetic structure in YbCo{sub 2}Si{sub 2} is in stark contrast to all other compounds of the RCo{sub 2}Si{sub 2} family (R = rare earth element) likely due to some itineracy of the Yb 4f states being responsible for the magnetism.

Treatment of Neuroblastoma with an Engineered "Obligate" Anaerobic Salmonella typhimurium Strain YB1.

Science.gov (United States)

Ning, Bo-Tao; Yu, Bin; Chan, Shing; Chan, Jian-Liang; Huang, Jian-Dong; Chan, Godfrey Chi-Fung

2017-01-01

Purpose Neuroblastoma is an embryonic solid tumor derived from the progenitors of the sympathetic nervous system. More than half of the patients developed metastatic disease at the time of initial diagnosis and had poor outcome with current therapeutic approaches. In recent years, some obligate and facultative anaerobic bacteria were reported to target the hypoxic and necrotic region of solid tumor models and caused tumor regression. We recently successfully constructed an "obligate" anaerobic Salmonella strain YB1 that was applied in breast cancer nude mice model by us. Here, we report the application of YB1 in neuroblastoma treatment. Methods The anti-cancer effect and side-effects of YB1 was examined in both in vitro and in vivo experiment. Previous established orthotopic neuroblastoma SCID/beige murine model using SK-NLP/luciferase cell line was adopted. Results In vitro , YB1 induced apoptosis for up to 31.4% of the neuroblastoma cells under anaerobic condition, three times more than that under aerobic condition (10.9%). The expression of both Toll like Receptor 4 and 5 (TLR4 and TLR5) in cancer cells were significantly up-regulated ( p anaerobic condition. In mouse model, YB1 preferentially accumulated inside the core of the tumors, rather than in normal tissues as our previous reported. This is suggestive of the hypoxic nature of tumor core. Tumor growth was significantly retarded in YB1 treatment group ( n=6, P<0.01 ). Furthermore, there was no long-term organ damage noted in all the organs examined including heart, lung, liver, spleen and brain in the YB1 treated mice. Conclusion The genetic modified Salmonella strain YB1 is a promising anti-tumor strategy against the tumor bulk for neuroblastoma. Future study can be extended to other common cancer types to verify the relative efficacy on different neoplastic cells.

Tm3+ activated lanthanum phosphate: a blue PDP phosphor

International Nuclear Information System (INIS)

Rao, R.P.

2005-01-01

Plasma display panels (PDPs) are gaining attention due to their high performance and scalability as a medium for large format TVs. The performance and life of a PDP strongly depends upon the nature of phosphors. Currently, Eu 2+ activated barium magnesium aluminate (BAM) is being used as a blue component. Because of its low life, efforts are being made to explore new blue emitting phosphors. One of the alternatives to BAM is Tm 3+ activated lanthanum phosphate (LPTM) phosphor. LPTM phosphor samples are prepared by a solid-state as well as sol-gel process in presence of flux. The phosphor of the present investigation, having uniform and spherical shape particles in the range of 0.1-2 μm, is appropriate for thin phosphor screens required for PDP applications. It exhibits a narrow band emission in the blue region, peaking at 452 nm and also a number of narrow bands in the UV region when excited by 147 and 173 nm radiation from a xenon gas mixture. Various possible transitions responsible for UV and visible emission from Tm 3+ ion are presented. These phosphors also exhibit good color saturation and better stability when excited with VUV radiation. To achieve higher brightness, they are blended with other UV excited blue emitting phosphors such as BAM. Results related to morphology, excitation, after glow decay, emission and degradation of these phosphors in the powder form as well as in plasma display panels are presented and discussed

Magnetic susceptibility of YbN

International Nuclear Information System (INIS)

Zhou, Y.; Bowen, S.P.; Koelling, D.D.; Monnier, R.

1991-01-01

Applying the Zwicknagl, Zevin, and Fulde (ZZF) approximation for the spectral densities of the occupied and empty f states resulting from a degenerate-Anderson-impurity model, which incorporates crystal fields, we compute the low-temperature magnetic susceptibility of YbN. The model, in which each crystal-field level couples to the band states with its own hybridization function, has previously been successfully applied without the ZZF approximation to explain the specific-heat structure at low temperatures. The ZZF approximation removes the spurious zero-temperature behavior of the parent noncrossing approximation for the susceptibility. Surprisingly, even at the low crystal-field degeneracy (N=2) of YbN, the Shiba relation is very nearly satisfied. The appropriate experimental impurity susceptibility for comparison is extracted from the measurement by removing an empirical exchange interaction. The resultant Kondo temperature (T 0 =8.49 K) is consistent with previous specific-heat estimates (10--11 K), and the agreement with experiment is good

Study of chromites YbMIICr2O5,5 (MII - Mg, Ca, Sr, Ba by X-ray diffraction

Directory of Open Access Journals (Sweden)

B. Kasenov

2012-03-01

Full Text Available Compounds of composition YbMeMnFeO5,5 (Me – Mg, Ca, Sr, Ba are synthesized from Yb2O3, , Cr2O3 and MgCO3, CaCO3, SrCO3, BaCO3 by solid phase method. X-ray powder diffraction showed that the compound YbMgCr2O5,5, YbCaCr2O5,5, YbSrCr2O5,5, YbBaCr2O5,5 crystallizes in the tetragonal crystal system.

Direct Comparison of Yb.sup.3+./sup.:CaF.sub.2./sub. and heavily doped Yb.sup.3+./sup.:YLF as laser media at room temperature

Czech Academy of Sciences Publication Activity Database

Pirri, A.; Alderighi, D.; Toci, G.; Vannini, M.; Nikl, Martin; Sato, H.

2009-01-01

Roč. 17, č. 20 (2009), s. 18312-18319 ISSN 1094-4087 Grant - others:AV ČR(CZ) M100100910 Institutional research plan: CEZ:AV0Z10100521 Keywords : Yb 3+ :YLF * Yb 3+ :CaF 2 * solid state laser * diode pumped Subject RIV: BM - Solid Matter Physics ; Magnetism Impact factor: 3.278, year: 2009

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

Microscopic evidence for significant ionic disorder in the Yb sup 3 sup + -chain in Yb sub 4 (As sub 1 sub - sub x P sub x) sub 3 : sup 3 sup 1 P NMR studies

CERN Document Server

Tanida, H; Aoki, H; Ochiai, A

2003-01-01

We report unambiguous microscopic evidence from sup 3 sup 1 P NMR under H sub e sub x sub t approx = 7.3 T for significant ionic disorder in the Yb sup 3 sup + chain in Yb sub 4 (As sub 1 sub - sub x P sub x) sub 3 (x=0.05 and 0.40), which have similar characteristic chi(T) and C sub p (T, H sub e sub x sub t) behavior to the antiferromagnetic quantum spin chain (AFQSC) system Yb sub 4 As sub 3. Our conclusion is based on the observations only below the charge-ordering transition at T sub 0 approx = 292 K of clear structures in the spectrum, which can be fitted well by the superpositions of almost equally spaced five Gaussian components. Since perfect ordering of Yb sup 3 sup + in the chain sites would lead to a single-line spectrum also below T sub 0 , the structures should be ascribed to significant ionic disorder in the Yb sup 3 sup + chain and resulting distribution of local configurations of Yb sup 3 sup + in the eight nearest-neighboring Yb sites around sup 3 sup 1 P. Quantitative comparisons with a sim...

Y-box-binding protein-1 (YB-1) promotes cell proliferation, adhesion and drug resistance in diffuse large B-cell lymphoma

Energy Technology Data Exchange (ETDEWEB)

Miao, Xiaobing; Wu, Yaxun [Department of Pathology, Affiliated Cancer Hospital of Nantong University, Nantong 226361, Jiangsu (China); Wang, Yuchan [Department of Pathogen, Medical College, Nantong University, Nantong 226001, Jiangsu (China); Jiangsu Province Key Laboratory for Inflammation and Molecular Drug Target, Nantong University, Nantong 226001, Jiangsu (China); Zhu, Xinghua; Yin, Haibing [Department of Pathology, Affiliated Cancer Hospital of Nantong University, Nantong 226361, Jiangsu (China); He, Yunhua [Jiangsu Province Key Laboratory for Inflammation and Molecular Drug Target, Nantong University, Nantong 226001, Jiangsu (China); Li, Chunsun; Liu, Yushan; Lu, Xiaoyun; Chen, Yali; Shen, Rong [Department of Pathology, Affiliated Cancer Hospital of Nantong University, Nantong 226361, Jiangsu (China); Xu, Xiaohong, E-mail: xuxiaohongnantong@126.com [Department of Oncology, Affiliated Cancer Hospital of Nantong University, Nantong 226361, Jiangsu (China); He, Song, E-mail: hesongnt@126.com [Department of Pathology, Affiliated Cancer Hospital of Nantong University, Nantong 226361, Jiangsu (China)

2016-08-15

YB-1 is a multifunctional protein, which has been shown to correlate with resistance to treatment of various tumor types. This study investigated the expression and biologic function of YB-1 in diffuse large B-cell lymphoma (DLBCL). Immunohistochemical analysis showed that the expression statuses of YB-1 and pYB-1{sup S102} were reversely correlated with the clinical outcomes of DLBCL patients. In addition, we found that YB-1 could promote the proliferation of DLBCL cells by accelerating the G1/S transition. Ectopic expression of YB-1 could markedly increase the expression of cell cycle regulators cyclin D1 and cyclin E. Furthermore, we found that adhesion of DLBCL cells to fibronectin (FN) could increase YB-1 phosphorylation at Ser102 and pYB-1{sup S102} nuclear translocation. In addition, overexpression of YB-1 could increase the adhesion of DLBCL cells to FN. Intriguingly, we found that YB-1 overexpression could confer drug resistance through cell-adhesion dependent and independent mechanisms in DLBCL. Silencing of YB-1 could sensitize DLBCL cells to mitoxantrone and overcome cell adhesion-mediated drug resistance (CAM-DR) phenotype in an AKT-dependent manner. - Highlights: • The expression statuses of YB-1 and pYB-1{sup S102} are reversely correlated with outcomes of DLBCL patients. • YB-1 promotes cell proliferation by accelerating G1/S transition in DLBCL. • YB-1 confers drug resistance to mitoxantrone in DLBCL.

Synthesis and thermoelectric properties of rare earth Yb-doped Ba8−xYbxSi30Ga16 clathrates

International Nuclear Information System (INIS)

Liu, Lihua; Li, Feng; Wei, Yuping; Chen, Ning; Bi, Shanli; Qiu, Hongmei; Cao, Guohui; Li, Yang

2014-01-01

Highlights: • Samples with the chemical formula Ba8− x Yb x Si 30 Ga 16 (x = 0, 0.5, 0.7, 1 and 1.5) were prepared. • Some Yb atoms enter the clathrate lattice to replace Ba, while other Yb atoms are oxidized as Yb 2 O 3 . • The thermal conductivity decreases with Yb-doping. • Thermoelectric figure of merit ZT significantly increased. -- Abstract: The potential thermoelectric and magnetic application of clathrate materials with rare-earth doping is the focus of much of the recent research activity in the synthetic material physics and chemistry. A series of clathrate samples with the chemical formula Ba 8−x Yb x Si 30 Ga 16 (x = 0, 0.5, 0.7, 1 and 1.5) were prepared by combining arc melting, ball milling and spark plasma sintering (SPS) techniques. X-ray diffraction and scanning electronic microscopy combined with energy-dispersive X-ray spectroscopy (EDS) analysis showed the dominant phase to be the type-I clathrate. Whereas, X-ray structural refinement and EDS analysis indicated that some Yb atoms enter the clathrate lattice to replace Ba at 2a sites, while other Yb atoms are oxidized as Yb 2 O 3 precipitated around grain boundaries. The solid solubility of Yb into clathrate lattice yielded x ∼ 0.3. Comparative analysis between Yb-doped and Yb-free clathrates showed that the thermal conductivity decreases with Yb-doping. Consequently, thermoelectric figure of merit ZT significantly increased

Dependence of upconversion emission intensity on Yb3+ concentration in Er3+/Yb3+ co-doped flake shaped Y2(MoO4)3 phosphors

International Nuclear Information System (INIS)

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

2010-01-01

Yttrium molybdate phosphors with fixed Er 3+ and various Yb 3+ concentrations were synthesized via a co-precipitation method. The crystal structure and the morphology of the phosphor were characterized by means of x-ray diffraction and field-emission scanning electron microscopy. Under 980 nm excitation, red and green upconversion emissions centred at 660, 553 and 530 nm were observed. Quantitative analyses on the dependence of upconversion emission intensity on the working current of a laser diode (LD) indicated that two-photon processes are responsible for both red and green upconversion emissions in both cases of low and high Yb 3+ concentrations. The relationship between the emission intensity ratio of 2 H 11/2 → 4 I 15/2 to 4 S 3/2 → 4 I 15/2 and the working current of the LD was studied for the samples doped with low and high Yb 3+ concentrations. Finally, a set of rate equations was established based on the possible upconversion mechanism, and an empirical formula was proposed to describe the Yb 3+ concentration dependence of upconversion emission intensity; the empirical formula fits well with the experimental data.

Synthesis and characterization of Nd3+: Yb3+ co-doped near infrared sensitive fluorapatite nanoparticles as a bioimaging probe

Science.gov (United States)

Karthi, S.; Kumar, G. A.; Sardar, D. K.; Santhosh, C.; Girija, E. K.

2018-03-01

Trivalent Nd and Yb co-doped rod shaped hexagonal phase fluorapatite (FAP) nanoparticles of length and width about 32 and 13 nm, respectively were prepared by hydrothermal method and investigated the ability for 980 nm emission via Nd3+ → Yb3+ energy transfer with the objective of utilizing them in biomedical imaging. Nd3+ → Yb3+ energy transfer in FAP was studied as a function of both Nd3+ and Yb3+ concentrations and found that when Yb3+ concentration was 10 mol% the FAP phase has partially turned in to YbPO4 phase. The Yb3+ emission intensity at 980 nm significantly increased up to 5 mol% Yb3+ doping and then reduced drastically for further increase in its concentration. Nd3+ →Yb3+ energy transfer rates were evaluated from the decay curves and found that a transfer rate of 71% for 2 mol% Nd3+ co-doped with 5 mol% Yb3+. The cytocompatibility test with fibroblast like cells using MTT assay revealed that the nanoparticles are compatible with the cells.

Upconversion dynamics in Yb3+-Ho3+-doped fluoroindate glasses

International Nuclear Information System (INIS)

Martin, I.R.; Rodriguez, V.D.; Lavin, V.; Rodriguez-Mendoza, U.R.

1998-01-01

The mechanisms and dynamics of the upconversion emissions in Yb 3+ -Ho 3+ -doped fluoroindate glasses by exciting at 975 nm have been analysed. The upconversion efficiencies have been measured as a function of temperature in the range from 12 to 295 K. The temporal evolution of the 545- and 650-nm upconversion emissions obtained under flash excitation at 975 nm in codoped samples with 2.25 mol.% of Yb 3+ and 0.75 mol.% of Ho 3+ cannot be described using the energy migration model. This indicates that at this concentration of Yb 3+ the rapid migration regimen between these ions has not been reached. A model is proposed in order to explain the temporal evolution of these emissions taking into account energy migration between donors and backtransfer processes. (orig.)

Laser induced broad band anti-Stokes white emission from LiYbF4 nanocrystals

Institute of Scientific and Technical Information of China (English)

L. Marciniak; R. Tomala; M. Stefanski; D. Hreniak; W. Strek

2016-01-01

Spectroscopic properties of tetragonal LiYbF4 nanocrystals under high dense NIR excitation at vacuum condition were in-vestigated. White, broad band emission covering whole visible part of the spectrum from LiYbF4 nanocrystals was observed. Its in-tensity strongly depended on the excitation power, excitation wavelength and ambient pressure. Temperature of the nanocrystals un-der 975 nm excitation was determined as a function of excitation power. Strong photo-induced current was observed from LiYbF4 pallet. The emission kinetic was analyzed. The mechanism of the anti-Stokes white emission was discussed in terms of the la-ser-induced charge transfer emission from Yb2+ states.

Phase formation and stability of quasicrystal/α-Mg interfaces in the Mg–Cd–Yb system

International Nuclear Information System (INIS)

Ohhashi, S.; Suzuki, K.; Kato, A.; Tsai, A.P.

2014-01-01

Phase formation involving icosahedral quasicrystals (iQc) in the Mg–Cd–Yb system was investigated. The phase diagrams obtained revealed that the iQc is in equilibrium with either (Mg, Cd) 2 Yb or an α-Mg phase over a wide composition range at 673 K. A eutectic reaction, where the melt decomposed to a rod-like lamella structure consisting of iQc and α-Mg phases was observed for Mg 68 Cd 24 Yb 8 at 735 K. High-angle annular dark-field scanning transmission microscopy observation of the iQc in Mg 96 Cd 3 Yb 1 verified the atomic positions of the Yb icosahedra and confirmed that the i-MgCdYb is isostructural to the i-CdYb. The formation of the eutectic structure is responsible for the high stability of the iQc/α-Mg interfaces because of good lattice matching; which is coincident interplanar spacing over several planes for the two phases. This coincidence in interplanar spacing was further confirmed in the real atomic structure, for which the twofold planes of the iQc, and the [0 0 0 2] and [2 −1 −1 0] planes of α-Mg are dominant factors in determining the stability of the interfaces

Near-infrared quantum cutting in Yb3+ ion doped strontium vanadate

Science.gov (United States)

Sawala, N. S.; Bajaj, N. S.; Omanwar, S. K.

2016-05-01

The materials Sr3-x(VO4)2:xYb were successfully synthesized by co-precipitation method varying the concentration of Yb3+ ions from 0 to 0.06 mol. It was characterize by powder X-ray powder diffraction (XRD) and surface morphology was studied by scanning electronic microscope (SEM). The photoluminescence (PL) properties were studied by spectrophotometers in near infra red (NIR) and ultra violet visible (UV-VIS) region. The Yb3+ ion doped tristrontium vanadate (Sr3(VO4)2) phosphors that can convert a photon of UV region (349 nm) into photons of NIR region (978, 996 and 1026 nm). Hence this phosphor could be used as a quantum cutting (QC) luminescent convertor in front of crystalline silicon solar cell (c-Si) panels to reduce thermalization loss due to spectral mismatch of the solar cells. The theoretical value of quantum efficiency (QE) was calculated from steady time decay measurement and the maximum efficiency approached up to 144.43%. The Sr(3-x) (VO4)2:xYb can be potentiality used for betterment of photovoltaic (PV) technology.

Up-conversion mechanisms in Er{sup 3+} doped YbAG crystals

Energy Technology Data Exchange (ETDEWEB)

Kaczkan, Marcin; Borowska, Maja [Institute of Microelectronics and Optoelectronics PW, Warsaw (Poland); Malinowski, Michal [Institute of Microelectronics and Optoelectronics PW, Warsaw (Poland); Institute of Electronic Materials Technology, Warsaw (Poland); Lukasiewicz, Tadeusz; Kolodziejak, Katarzyna [Institute of Electronic Materials Technology, Warsaw (Poland)

2009-07-15

Up-conversion phenomena leading to the red, green and violet emissions in erbium doped ytterbium-aluminum garnet (YbAG) are investigated. Absorption and emission spectra and luminescence dynamics from various excited states of YbAG:Er{sup 3+} were registered. The low temperature absorption spectra were used to determine Stark levels energies of Er{sup 3+} ion in the investigated host. Emissions from the high lying excited states {sup 2}G{sub 9/2}, {sup 4}S{sub 3/2} and {sup 4}F{sub 9/2} of Er{sup 3+} were characterized under pulsed multi-photon IR excitation in the region of wavelength corresponding to the strong {sup 2}F{sub 7/2} {yields} {sup 2}F{sub 5/2} absorption transition of Yb{sup 3+} ions. Using the rate equations formalism the dynamics of the observed emissions were modeled. From the comparison of the measured and calculated decays the energy transfer rates between Yb{sup 3+} and Er{sup 3+} ions were evaluated. (copyright 2009 WILEY-VCH Verlag GmbH and Co. KGaA, Weinheim) (orig.)

Determination of lanthanides in fossil samples using laser induced breakdown spectroscopy

International Nuclear Information System (INIS)

Anzano, J.M.; Lasheras, R.J.; Canudo, I.; Laguna, M.

2017-01-01

As being a fast, simple and relatively non-destructive analytical technique Laser-induced breakdown spectroscopy (LIBS) has a large variety of applications including the analysis of paleontological samples. In this work LIBS is employed for the quantitative determination of lanthanides (Ce, Dy, Er, Eu, Gd, Ho, La, Lu, Nd, Sm, Tb, Tm and Yb) in vertebrate fossil samples comprising teeth, disarticulated complete or fragmented bones, eggshell fragments, and coprolites of dinosaurs, mammals and crocodiles. For emission line data, standard AnalaR grade salts of lanthanides were used. The major components: iron, calcium, magnesium, silicon and aluminum in the samples were also determined. The analytical information may be helpful in studying the samples for their age, formation environment and other paleontological properties. (author)

Isopiestic determination of the activity coefficients of some aqueous rare earth electrolyte solutions at 250C. I. The rare earth chlorides

International Nuclear Information System (INIS)

Spedding, F.H.; Weber, H.O.; Saeger, V.W.; Petheram, H.H.; Rard, J.A.; Habenschuss, A.

1976-01-01

The osmotic coefficients of the aqueous trichlorides of La, Pr, Nd, Sm, Eu, Gd, Tb, Dy, Ho, Er, Tm, Yb, Lu, and Y were determined from 0.1 M to saturation at 25 0 C. Semiempirical least-squares equations were obtained for the osmotic coefficients as a function of molality and these equations were used to calculate water activities and mean molal activity coefficients. The water activities of the light rare earth chlorides at constant molalities are higher than for the heavy rare earths, while the mean molal activity coefficients are larger for the heavy rare earths than for the light ones. The above effects are discussed in terms of changes in the cationic radii and hydration of the rare earth ions

Indium-modified Yb:KLu(WO{sub 4}){sub 2} crystal: Growth, spectroscopy and laser operation

Energy Technology Data Exchange (ETDEWEB)

Serres, J.M. [Física i Cristallografia de Materials i Nanomaterials (FiCMA-FiCNA), Universitat Rovira i Virgili (URV), Campus Sescelades, c/ Marcellí Domingo, s/n., Tarragona E-43007 (Spain); Mateos, X., E-mail: xavier.mateos@urv.cat [Física i Cristallografia de Materials i Nanomaterials (FiCMA-FiCNA), Universitat Rovira i Virgili (URV), Campus Sescelades, c/ Marcellí Domingo, s/n., Tarragona E-43007 (Spain); Max Born Institute for Nonlinear Optics and Short Pulse Spectroscopy, 2A Max-Born-Str., Berlin D-12489 (Germany); Loiko, P. [ITMO University, 49 Kronverkskiy pr., St. Petersburg 197101 (Russian Federation); Griebner, U.; Petrov, V. [Max Born Institute for Nonlinear Optics and Short Pulse Spectroscopy, 2A Max-Born-Str., Berlin D-12489 (Germany); Yumashev, K. [Center for Optical Materials and Technologies (COMT), Belarusian National Technical University, 65/17 Nezavisimosti Ave., Minsk 220013 (Belarus); Aguiló, M.; Díaz, F. [Física i Cristallografia de Materials i Nanomaterials (FiCMA-FiCNA), Universitat Rovira i Virgili (URV), Campus Sescelades, c/ Marcellí Domingo, s/n., Tarragona E-43007 (Spain)

2017-03-15

We report on the growth, spectroscopic and laser characterization of a novel monoclinic laser crystal, Yb,In:KLu(WO{sub 4}){sub 2} (Yb,In:KLuW). The absorption, stimulated-emission and gain cross-section spectra of 3.5 at% Yb, 5.5 at% In-doped KLuW are determined at room temperature with polarized light and compared with those for Yb,In:KYW, as well as singly Yb-doped KLuW and KYW crystals. It is found that the introduction of In results in a decrease of the transition cross-sections and in a spectral broadening of the absorption and emission bands. Such a broadening is more pronounced for light polarization E ||N{sub p}. For Yb,In:KLuW, the maximum σ{sub abs} is 9.9×10{sup –20} cm{sup 2} at 980.9 nm for E ||N{sub m} and the corresponding bandwidth of the absorption peak is 3.7 nm. The radiative lifetime for Yb{sup 3+} ions is 237±5 µs. The stimulated-emission cross-sections are σ{sub SE}(m)=2.4×10{sup –20} cm{sup 2} at 1022.4 nm and σ{sub SE}(p)=1.3×10{sup –20} cm{sup 2} at 1039.1 nm corresponding to an emission bandwidth of >30 nm and >35 nm, respectively. The diode-pumped N{sub g}-cut Yb,In:KLuW microchip laser generated 4.11 W at 1042–1048 nm with a slope efficiency of 78%. The Yb,In:KLuW crystal is very promising for the generation of sub-100 fs pulses in mode-locked lasers due to its broadband emission characteristics.

Study for optimizing the design of optical temperature sensor

Science.gov (United States)

Li, Panpan; Sun, Zhen; Shi, Ruixin; Liu, Guofeng; Fu, Zuoling; Wei, Yanling

2017-12-01

The correlations between temperature sensitivity (relative sensitivity Sr and absolute sensitivity Sa) and thermally coupled level gaps (ΔE) are vital but less-studied for potential applications in scientific research, industrial production, clinical medicine, and so on. We take YbPO4:Ln3+ (Ln = Tm3+, Ho3+, and Er3+) up-conversion phosphors as a case to study the relationships between temperature sensitivity (Sr, Sa) and ΔE. The results of various discussions, including the experimental data of temperature sensitivity based on YbPO4:Ln3+ (Ln = Tm3+, Ho3+, and Er3+) and theoretical derivation from original formulas, show that Sr and ΔE are linearly positive correlation, which is invalid for Sa. Noticeably, YbPO4:Tm3+ nanoparticles display intense near infrared red emission within the biological window, leading to great potential application in biological sensing and biological imaging. All the research studies would benefit the design of optical temperature sensing.

Bismuth silicate glass: A new choice for 2 μm fiber lasers

Science.gov (United States)

Ding, Jia; Zhao, Guoying; Tian, Ying; Chen, Wei; Hu, Lili

2012-11-01

We report on a new Yb3+/Tm3+/Ho3+ co-doped bismuth silicate glass: SiO2-Bi2O3-R2O (R = Li, Na, K) for 2 μm fiber lasers. Bi2O3 was introduced into alkali silicate glass to optimize 2 μm emission properties. Physical, chemical and spectroscopic properties of Yb3+/Tm3+/Ho3+ co-doped SiO2-Bi2O3-R2O (SBR) glass were presented. The Yb3+/Tm3+/Ho3+ co-doped SBR glass shows excellent thermal stability (ΔT = 162 °C), an intense 2.0 μm emission pumped by 980 nm LD with a lifetime of 1.33 ms and width of 168 nm, large maximum emission cross section of Ho3+ (5.3 × 10-21 cm2), thus large σemτ product (7.049 × 10-24 cm2 s), which suggest its application in 2 μm fiber lasers.

Solar-Pumping Upconversion of Interfacial Coordination Nanoparticles.

Science.gov (United States)

Ishii, Ayumi; Hasegawa, Miki

2017-01-30

An interfacial coordination nanoparticle successfully exhibited an upconversion blue emission excited by very low-power light irradiation, such as sunlight. The interfacial complex was composed of Yb ions and indigo dye, which formed a nano-ordered thin shell layer on a Tm 2 O 3 nanoparticle. At the surface of the Tm 2 O 3 particle, the indigo dye can be excited by non-laser excitation at 640 nm, following the intramolecular energy transfer from the indigo dye to the Yb ions. Additionally, the excitation energy of the Yb ion was upconverted to the blue emission of the Tm ion at 475 nm. This upconversion blue emission was achieved by excitation with a CW Xe lamp at an excitation power of 0.14 mW/cm 2 , which is significantly lower than the solar irradiation power of 1.4 mW/cm 2 at 640 ± 5 nm.

Charge transfer luminescence of Yb3+ ions in LiY1-xYbxP4O12 phosphates

International Nuclear Information System (INIS)

Stryganyuk, G; Zazubovich, S; Voloshinovskii, A; Pidzyrailo, M; Zimmerer, G; Peters, R; Petermann, K

2007-01-01

Spectral-kinetic studies have been performed for LiY 1-x Yb x P 4 O 12 (x = 0; 0.1; 0.9) phosphates at T = 8-320 K using synchrotron radiation for excitation within the 5-17 eV energy range. Mechanisms for the excitation of Yb 3+ charge transfer and f-f luminescence are discussed. The quasimolecular character of Yb 3+ charge transfer luminescence (CTL) is pointed out. The central Yb 2+ ion and hole delocalized over the surrounding ligands are proposed for consideration as a 'charge transfer cluster' (Yb 2+ CT cluster). Possible mechanisms of Yb 3+ CTL quenching are presumed

On the valence state of Yb and Ce in transition metal intermetallic compounds

International Nuclear Information System (INIS)

Boer, F.R. de; Dijkman, W.H.; Mattens, W.C.M.

1979-01-01

In the pure state Yb is a divalent metal, similar to Ca; in alloys it can become trivalent like the majority of the rare earth metals. Using a value of 38 kJ (mol Yb) -1 for the energy difference between divalent and trivalent Yb metal and using model calculations for the heat of formation of intermetallic compounds, the authors are able to account for the existing information on the valence state of Yb in transition metal compounds. A similar analysis of compounds of Ce with transition metals shows that a model in which the 4f electron is treated as a core electron, i.e. being absent in the tetravalent modification of Ce and present as a fully localized electron in trivalent Ce, does not apply. (Auth.)

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.

Treatment of Neuroblastoma with an Engineered “Obligate” Anaerobic Salmonella typhimurium Strain YB1

Science.gov (United States)

Ning, Bo-Tao; Yu, Bin; Chan, Shing; Chan, Jian-liang; Huang, Jian-Dong; Chan, Godfrey Chi-Fung

2017-01-01

Purpose Neuroblastoma is an embryonic solid tumor derived from the progenitors of the sympathetic nervous system. More than half of the patients developed metastatic disease at the time of initial diagnosis and had poor outcome with current therapeutic approaches. In recent years, some obligate and facultative anaerobic bacteria were reported to target the hypoxic and necrotic region of solid tumor models and caused tumor regression. We recently successfully constructed an “obligate” anaerobic Salmonella strain YB1 that was applied in breast cancer nude mice model by us. Here, we report the application of YB1 in neuroblastoma treatment. Methods The anti-cancer effect and side-effects of YB1 was examined in both in vitro and in vivo experiment. Previous established orthotopic neuroblastoma SCID/beige murine model using SK-NLP/luciferase cell line was adopted. Results In vitro, YB1 induced apoptosis for up to 31.4% of the neuroblastoma cells under anaerobic condition, three times more than that under aerobic condition (10.9%). The expression of both Toll like Receptor 4 and 5 (TLR4 and TLR5) in cancer cells were significantly up-regulated (panaerobic condition. In mouse model, YB1 preferentially accumulated inside the core of the tumors, rather than in normal tissues as our previous reported. This is suggestive of the hypoxic nature of tumor core. Tumor growth was significantly retarded in YB1 treatment group (n=6, P<0.01). Furthermore, there was no long-term organ damage noted in all the organs examined including heart, lung, liver, spleen and brain in the YB1 treated mice. Conclusion The genetic modified Salmonella strain YB1 is a promising anti-tumor strategy against the tumor bulk for neuroblastoma. Future study can be extended to other common cancer types to verify the relative efficacy on different neoplastic cells. PMID:28775780

Luminescence properties of different Eu sites in LiMgPO4:Eu2+, Eu3+

International Nuclear Information System (INIS)

Baran, A; Mahlik, S; Grinberg, M; Cai, P; Kim, S I; Seo, H J

2014-01-01

The effect of temperature on the luminescence properties of LiMgPO 4 doped with Eu 3+ and Eu 2+ are presented. Depending on the excitation wavelength, luminescence spectra consist of two distinct broad emission bands peaking at 380 nm and 490 nm related to 4f 6 5d 1  → 4f 7 ( 8 S 7/2 ) luminescence of Eu 2+ and to europium-trapped exciton, respectively, and/or several sharp lines between the 580 nm and 710 nm region, ascribed to the 5 D 0  →  7 F J (J = 0, 1, 2, 3 and 4) transitions in Eu 3+ . To explain all the features of the Eu 2+ and Eu 3+ luminescence we discussed the existence of two different Eu sites substituting for Li + , with short and long distance compensation. The evident effect of increasing the intensity of the Eu 2+ luminescence with increasing temperature was observed. It was considered that the charge compensation mechanism for Eu 3+ and Li + as well as Eu 2+ replacing Li + in the LiMgPO 4 is a long distance compensation that allows for the existence of some of the europium ions either as Eu 3+ at low temperature or as Eu 2+ at high temperature. We concluded that Eu 2+ in the Li + site with long distance compensation yields only 4f 6 5d 1  → 4f 7 luminescence, whereas Eu 2+ in the Li + site with short distance compensation yields 4f 6 5d 1  → 4f 7 luminescence and europium-trapped exciton emission. (paper)

Luminescence dosemeter of the Al{sub 2}O{sub 3}:Er,Yb

Energy Technology Data Exchange (ETDEWEB)

Goncalves, Katia A.; Ventieri, Alexandre; Bitencourt, Jose F.S. [Universidade de Sao Paulo (EP/USP), SP (Brazil). Escola Politecnica. Dept. de Engenharia Eletrica; Mittani, Juan C.R.; Tatumi, Sonia H. [Faculdade de Tecnologia de Sao Paulo (CEETEPS), SP (Brazil)

2011-07-01

The present work deals with the thermoluminescence (TL) and Optically Stimulated Luminescence (OSL) properties of {alpha}-Al{sub 2}O{sub 3}: Er,Yb obtained by sol gel process. Nanocrystals formations composed by Er{sub 2}O{sub 3}, Yb{sub 2}O{sub 3} and Yb{sub 3}Al{sub 5}O{sub 12} were observed by TEM images, EDS, electron beam diffraction and RXD, located at the surface of the alumina grains. The sample codoped with 1mol% of Er and 2 mol% of Yb supplied the best results for TL and OSL responses. The growth of the intensity of dosimetric TL peak at 205 deg C was linear with gamma radiation doses and the same behavior was observed in OSL growth curve. The luminescence fading of the sample after a dose of 5 Gy was found initially for a period of 30 days and minimum detectable dose measured for TL was 60.78 mGy and for OSL was 13.09 mGy. (author)

Investigating the evolution of local structure around Er and Yb in ZnO:Er and ZnO:Er, Yb on annealing using X-ray absorption spectroscopy

Science.gov (United States)

Anjana, R.; Jayaraj, M. K.; Yadav, A. K.; Jha, S. N.; Bhattacharyya, D.

2018-04-01

The local structure around Er and Yb centre in ZnO favouring upconversion luminescence was studied using EXAFS (Extended X-ray absorption fine structure spectroscopy). Due to the ionic radii difference between Zn and Er, Yb ions, the dopants cannot replace Zn in the ZnO lattice properly. Er2O3 and Yb2O3 impurity phases are formed at the grain boundaries of ZnO. It is found that the local structure around the Er centre in ZnO is modified on annealing in air. The symmetry around both erbium and ytterbium reduces with increase in annealing temperature. Symmetry reduction will favour the intra-4f transition and the energy transitions causing upconversion luminescence. By fitting the EXAFS data with theoretically simulated data, it is found that the Er centre forms a local structure similar to C4ν symmetry which is a distorted octahedron. On annealing the sample to 1200 °C, all the erbium centres are transformed to C4ν symmetry causing enhanced upconversion emission. Yb centre has also been modified on annealing. The decrease in co-ordination number with annealing temperature will decrease the symmetry and increase the near infrared absorption cross section. The decrease in symmetry around both the erbium and ytterbium centre and formation of C4ν symmetry around Er centre is the reason behind the activation of upconversion luminescence with high temperature annealing in both Er doped and Er, Yb co-doped ZnO samples. The study will be useful for the synthesis of high efficiency upconversion materials.

Measurement of formation cross sections of short-lived nuclei by 14 MeV neutron. Nd, Sm, Dy, Er, Yb

Energy Technology Data Exchange (ETDEWEB)

Sakane, H.; Yamamoto, H.; Kawade, K. [Nagoya Univ. (Japan). School of Engineering; Iida, T.; Takahashi, A.

1997-03-01

Eight neutron activation cross sections producing the nuclei with half-lives between 3 min and 24 min were obtained at the energy range between 13.4 and 14.9 MeV by activation method. The cross sections were {sup 146}Nd(n,p){sup 146}Pr, {sup 154}Sm(n,{alpha}){sup 151}Nd, {sup 162}Dy(n,p){sup 162}Tb, {sup 163}Dy(n,np){sup 162}Tb, {sup 163}Dy(n,p){sup 163}Tb, {sup 164}Dy(n,p){sup 164}Tb, {sup 170}Er(n,{alpha}){sup 167}Dy, {sup 174}Yb(n,p){sup 170}Tm. {sup 163}Dy(n,np){sup 162}Tb (T{sub 1/2}=7.7 min) was obtained for the first time. Present results are compared with previous results and the evaluated data of JENDL-3 and ENDF/B-VI. There are some discrepancies between present results and the JENDL-3 and ENDF/B-VI. (author)

Time reversal symmetry violation in the YbF molecule

Energy Technology Data Exchange (ETDEWEB)

Sauer, B. E., E-mail: ben.sauer@imperial.ac.uk; Devlin, J. A.; Hudson, J. J.; Kara, D. M.; Smallman, I. J.; Tarbutt, M. R.; Hinds, E. A. [Blackett Laboratory Imperial College London, Centre for Cold Matter (United Kingdom)

2013-03-15

We present a summary of the techniques used to test time reversal symmetry by measuring the permanent electric dipole moment of the YbF molecule. The results of a recent measurement (Hudson et al., Nature 473:493, 2011) are reported. We review some systematic effects which might mimic time reversal violation and describe how they are overcome. We then discuss improvements to the sensitivity of the apparatus, including both short term technical enhancements as well as a longer term goal to use laser cooled YbF in the experiment.

Formation and characterization of ZnO : Tm+ optical waveguides fabricated by Tm+ and O+ ion implantation

International Nuclear Information System (INIS)

Ming Xianbing; Lu Fei; Liu Hanping; Chen Ming; Wang Lei

2009-01-01

Planar optical waveguides were formed in ZnO crystal by Tm + and O + ion implantation. The distributions of Tm + in as-implanted and annealed ZnO samples were investigated by the RBS technique. A shift of the Tm + peak towards the sample surface and out diffusion were observed after thermal treatment and subsequent O + ion implantation. Waveguide formation was determined after O + implantation in Tm + -implanted ZnO crystal. By using the prism-coupling method two guided modes were detected. The refractive index profile in the implanted waveguide was reconstructed according to the SRIM and RCM simulation. The RBS/channelling measurements show that the lattice structure of ZnO did not suffer detectable damage after O + implantation.

Optical properties of silica-coated Y2O3:Er,Yb nanoparticles in the presence of polyvinylpyrrolidone

International Nuclear Information System (INIS)

Fujii, Kunio; Kitamoto, Yoshitaka; Hara, Masahiko; Odawara, Osamu; Wada, Hiroyuki

2014-01-01

The optical properties of polyvinylpyrrolidone (PVP)-adsorbed and silica-coated Y 2 O 3 :Er,Yb nanoparticles produced by using PVP were studied for potential bio-applications of upconversion nanoparticles. We utilized PVP to better disperse Y 2 O 3 :Er,Yb nanoparticles in solution and to prepare silica-coated Y 2 O 3 :Er,Yb nanoparticles. The fluorescent intensity of PVP-adsorbed Y 2 O 3 :Er,Yb nanoparticles was 1.25 times higher than non-adsorbed Y 2 O 3 :Er,Yb nanoparticles, which was probably due to surface defects in Y 2 O 3 :Er,Yb nanoparticles being covered by the PVP. However, the fluorescent intensity of silica-coated Y 2 O 3 :Er,Yb nanoparticles decreased as silica layer thickness increased. This could be ascribed to the higher vibrational energy of PVP than that of the silica structure. Therefore, the optimum silica layer thickness is important in bio-applications to avoid deterioration of the optical properties of Y 2 O 3 :Er,Yb nanoparticles. - Highlights: • We prepared the silica-coated upconversion nanoparticles by using PVP. • We showed that PVP played an important role in coating nanoparticles. • PL intensity of silica-coated nanoparticles decreased as silica layer thickness increased

Spectroscopic properties of Er3+ and Yb3+ co-doped glass ceramics containing SrF2 nanocrystals

International Nuclear Information System (INIS)

Qiao Xvsheng; Fan Xianping; Wang Minquan; Zhang Xianghua

2009-01-01

The spectroscopic properties of Er 3+ /Yb 3+ co-doped 50SiO 2 -10Al 2 O 3 -20ZnF 2 -20SrF 2 glass and glass ceramic containing SrF 2 nanocrystals were investigated. The formation of SrF 2 nanocrystals in the glass ceramic was confirmed by XRD. The oscillator strengths for several transitions of the Er 3+ ions in the glass ceramic have been obtained and the Judd-Ofelt parameters were then determined. The XRD result and Judd-Ofelt parameters suggested that Er 3+ and Yb 3+ ions had efficiently enriched in the SrF 2 nanocrystals in the glass ceramic. The lifetime of excited states has been used to reveal the surroundings of luminescent Er 3+ and Yb 3+ and energy transfer (ET) mechanism between Er 3+ and Yb 3+ . Much stronger upconversion luminescence and longer lifetime of the Er 3+ /Yb 3+ co-doped glass ceramic were observed in comparison with the Er 3+ /Yb 3+ co-doped glass, which could be ascribed to more efficient ET from Yb 3+ to Er 3+ due to the enrichment of Yb 3+ and Er 3+ and the shortening of the distance between lanthanide ions in the precipitated SrF 2 nanocrystals.

From EuCARD to EuCARD-2

CERN Multimedia

Chaudron, M

2013-01-01

The one word that best describes the spirit of the EuCARD ’13 event (see here) that took place from 10 to 14 June at CERN is "collaboration". The event brought together more than 180 accelerator specialists from all over the world to celebrate the conclusion of the EuCARD project and to kick off its successor, EuCARD-2.   EuCARD-2 brings a global view to particle accelerator research in order to address challenges for future generations of accelerators. The project officially began on 1 May 2013 and will run for four years. With a total budget of €23.4 million, including an €8 million EU contribution, it will build upon the success of EuCARD and push it into an even more innovative regime. EuCARD-2 aims to significantly enhance multidisciplinary R&D for European accelerators and will actively contribute to the development of a European Research Area in accelerator science. This will be accomplished by promoting complementary expertise, cross-d...

Temperature dependence of LRE-HRE-TM thin films

Science.gov (United States)

Li, Zuoyi; Cheng, Xiaomin; Lin, Gengqi; Li, Zhen; Huang, Zhixin; Jin, Fang; Wang, Xianran; Yang, Xiaofei

2003-04-01

Temperature dependence of the properties of RE-TM thin films is very important for MO recording. In this paper, we studied the temperature dependence of the magnetic and magneto-optical properties of the amorphous LRE-HRE-TM single layer thin films and LRE-HRE-TM/HRE-TM couple-bilayered thin films. For LRE-HRE-TM single layer thin films, the temperature dependence of the magnetization was investigated by using the mean field theory. The experimental and theoretical results matched very well. With the LRE substitution in HRE-TM thin film, the compensation temperature Tcomp decreased and the curie temperature Tc remained unchanged. Kerr rotation angle became larger and the saturation magnetization Ms at room temperature increased. For LRE-HRE-TM/HRE-TM couple-bilayered thin films, comparisons of the temperature dependences of the coercivities and Kerr rotation angles were made between isolated sublayers and couple-bilayered thin film.

Measurement of the 169Tm (n ,3 n ) 167Tm cross section and the associated branching ratios in the decay of 167Tm

Science.gov (United States)

Champine, B.; Gooden, M. E.; Krishichayan, Norman, E. B.; Scielzo, N. D.; Stoyer, M. A.; Thomas, K. J.; Tonchev, A. P.; Tornow, W.; Wang, B. S.

2016-01-01

The cross section for the 169Tm(n ,3 n ) 167Tm reaction was measured from 17 to 22 MeV using quasimonoenergetic neutrons produced by the 2H(d ,n ) 3He reaction. This energy range was studied to resolve the discrepancy between previous (n ,3 n ) cross-section measurements. In addition, the absolute γ -ray branching ratios following the electron-capture decay of 167Tm were measured. These results provide more reliable nuclear data for an important diagnostic that is used at the National Ignition Facility to estimate the yield of reaction-in-flight neutrons produced via the inertial-confinement-fusion plasma in deuterium-tritium capsules.

Instability of Yb3+ and Pr3+ low-symmetry luminescence centers in gallium phosphide

International Nuclear Information System (INIS)

Kasatkin, V.A.

1985-01-01

The stability of γb 3+ and Pr 3+ low-symmetry luminescence centers formed in gallium phosphide during quenching were studied in the process of durable storage and annealing. Observation of the Yb 3+ and Pr 3+ centrer states was accomplished by the photoluminescence spectra at 18 K. It has been established that annealing in the dark under normal conditions results in a reduced integral luminescence intensity of all low-symmetry Yb 3+ and Pr 3+ centers. Annealing of quenched GaP and GaP saples at 400 K results in complete disappearance of intracenter luminescence of Pr 3+ and low-symmetry Yb 3+ centers. Decomposition during storage and low anealing temperature point to the instability of low-symmetry centers of Pr 3+ and Yb 3+ luminescence

Enhanced exciton emission from ZnO nano-phosphor induced by Yb3+ ions

CSIR Research Space (South Africa)

Kabongo, GL

2014-01-01

Full Text Available In this work, the sol–gel method was used to prepare Ytterbium (Yb(sup3+)) doped ZnO nano-phosphors with different concentrations of Yb(sup3+) ions. Their structural, morphological, photoluminescence, electronic states and the chemical composition...

Preparation and radiopharmaceutical control of 169Yb EDTA an agent for kidney function and scintigraphy

International Nuclear Information System (INIS)

Gulbaba, G.; Ozker; Tomek, F.

1976-01-01

169 Yb was produced by thermal neutron irradiation of Yb 2 O 3 in 1 MW research reactor at Cekmece Nuclear Research Center. 169 Yb-EDTA complex was then prepared with a sodium salt of EDTA. Radionuclidic and radiochemical purities of the compound were determined by gama spectral analysis and radiochromatography-electrophoresis following preparation. Ionic Yb(III) which accumulates at bone and liver was not observed on the radiochromatographic and electrophoretic analysis of the final compound. There was no separation of the label for two months of examination in order to determine stability of the compound. In conclusion, the labeled compound has been prepared for use in the external scanning of kidney and determining the glomerular filtration rate. The label appears to be firmly bound so that the agent can be stored for a reasonably long period as 31 days half-life of 169 Yb permits. Administration of the compound is safe from the stand point of radiation dose since a 30 micro-Ci 169 Yb-EDTA for a glomerular filtration study delivers no more than 0.4 mrad whole-body and 5 mrad kidney dose. (author)

EU Udbudsretten

DEFF Research Database (Denmark)

Poulsen, Sune Troels; Jakobsen, Peter Stig; Kalsmose-Hjelmborg, Simon Evers

I bogen, som er en 2. udgave, analyseres EU udbudsdirektiv for offentlige myndigheder og EU's forsyningsvirksomhedsdirektiv. I analyserne inddrages EU-domstolens domme, afgørelser fra Kalgenævnet for Udbud, domme fra danske domstole samt litteratur på dansk og engelsk.......I bogen, som er en 2. udgave, analyseres EU udbudsdirektiv for offentlige myndigheder og EU's forsyningsvirksomhedsdirektiv. I analyserne inddrages EU-domstolens domme, afgørelser fra Kalgenævnet for Udbud, domme fra danske domstole samt litteratur på dansk og engelsk....

Origin of quantum criticality in Yb-Al-Au approximant crystal and quasicrystal

International Nuclear Information System (INIS)

Watanabe, Shinji; Miyake, Kazumasa

2016-01-01

To get insight into the mechanism of emergence of unconventional quantum criticality observed in quasicrystal Yb 15 Al 34 Au 51 , the approximant crystal Yb 14 Al 35 Au 51 is analyzed theoretically. By constructing a minimal model for the approximant crystal, the heavy quasiparticle band is shown to emerge near the Fermi level because of strong correlation of 4f electrons at Yb. We find that charge-transfer mode between 4f electron at Yb on the 3rd shell and 3p electron at Al on the 4th shell in Tsai-type cluster is considerably enhanced with almost flat momentum dependence. The mode-coupling theory shows that magnetic as well as valence susceptibility exhibits χ ∼ T -0.5 for zero-field limit and is expressed as a single scaling function of the ratio of temperature to magnetic field T/B over four decades even in the approximant crystal when some condition is satisfied by varying parameters, e.g., by applying pressure. The key origin is clarified to be due to strong locality of the critical Yb-valence fluctuation and small Brillouin zone reflecting the large unit cell, giving rise to the extremely-small characteristic energy scale. This also gives a natural explanation for the quantum criticality in the quasicrystal corresponding to the infinite limit of the unit-cell size. (author)

The Cold Shock Domain of YB-1 Segregates RNA from DNA by Non-Bonded Interactions.

Directory of Open Access Journals (Sweden)

Vladislav Kljashtorny

Full Text Available The human YB-1 protein plays multiple cellular roles, of which many are dictated by its binding to RNA and DNA through its Cold Shock Domain (CSD. Using molecular dynamics simulation approaches validated by experimental assays, the YB1 CSD was found to interact with nucleic acids in a sequence-dependent manner and with a higher affinity for RNA than DNA. The binding properties of the YB1 CSD were close to those observed for the related bacterial Cold Shock Proteins (CSP, albeit some differences in sequence specificity. The results provide insights in the molecular mechanisms whereby YB-1 interacts with nucleic acids.

Constitutive overexpression of the TaNF-YB4 gene in transgenic wheat significantly improves grain yield.

Science.gov (United States)

Yadav, Dinesh; Shavrukov, Yuri; Bazanova, Natalia; Chirkova, Larissa; Borisjuk, Nikolai; Kovalchuk, Nataliya; Ismagul, Ainur; Parent, Boris; Langridge, Peter; Hrmova, Maria; Lopato, Sergiy

2015-11-01

Heterotrimeric nuclear factors Y (NF-Ys) are involved in regulation of various vital functions in all eukaryotic organisms. Although a number of NF-Y subunits have been characterized in model plants, only a few have been functionally evaluated in crops. In this work, a number of genes encoding NF-YB and NF-YC subunits were isolated from drought-tolerant wheat (Triticum aestivum L. cv. RAC875), and the impact of the overexpression of TaNF-YB4 in the Australian wheat cultivar Gladius was investigated. TaNF-YB4 was isolated as a result of two consecutive yeast two-hybrid (Y2H) screens, where ZmNF-YB2a was used as a starting bait. A new NF-YC subunit, designated TaNF-YC15, was isolated in the first Y2H screen and used as bait in a second screen, which identified two wheat NF-YB subunits, TaNF-YB2 and TaNF-YB4. Three-dimensional modelling of a TaNF-YB2/TaNF-YC15 dimer revealed structural determinants that may underlie interaction selectivity. The TaNF-YB4 gene was placed under the control of the strong constitutive polyubiquitin promoter from maize and introduced into wheat by biolistic bombardment. The growth and yield components of several independent transgenic lines with up-regulated levels of TaNF-YB4 were evaluated under well-watered conditions (T1-T3 generations) and under mild drought (T2 generation). Analysis of T2 plants was performed in large deep containers in conditions close to field trials. Under optimal watering conditions, transgenic wheat plants produced significantly more spikes but other yield components did not change. This resulted in a 20-30% increased grain yield compared with untransformed control plants. Under water-limited conditions transgenic lines maintained parity in yield performance. © The Author 2015. Published by Oxford University Press on behalf of the Society for Experimental Biology.

YB-1 expression promotes epithelial-to-mesenchymal transition in prostate cancer that is inhibited by a small molecule fisetin

Science.gov (United States)

Khan, Mohammad Imran; Adhami, Vaqar Mustafa; Lall, Rahul Kumar; Sechi, Mario; Joshi, Dinesh C.; Haidar, Omar M.; Syed, Deeba Nadeem; Siddiqui, Imtiaz Ahmad; Chiu, Shing-Yan; Mukhtar, Hasan

2014-01-01

Epithelial-to-mesenchymal transition (EMT) plays an important role in prostate cancer (PCa) metastasis. The transcription/translation regulatory Y-box binding protein-1 (YB-1) is known to be associated with cancer metastasis. We observed that YB-1 expression increased with tumor grade and showed an inverse relationship with E-cadherin in a human PCa tissue array. Forced YB-1 expression induced a mesenchymal morphology that was associated with down regulation of epithelial markers. Silencing of YB-1 reversed mesenchymal features and decreased cell proliferation, migration and invasion in PCa cells. YB-1 is activated directly via Akt mediated phosphorylation at Ser102 within the cold shock domain (CSD). We next identified fisetin as an inhibitor of YB-1 activation. Computational docking and molecular dynamics suggested that fisetin binds on the residues from β1 - β4 strands of CSD, hindering Akt's interaction with YB-1. Calculated free binding energy ranged from −11.9845 to −9.6273 kcal/mol. Plasmon Surface Resonance studies showed that fisetin binds to YB-1 with an affinity of approximately 35 μM, with both slow association and dissociation. Fisetin also inhibited EGF induced YB-1 phosphorylation and markers of EMT both in vitro and in vivo. Collectively our data suggest that YB-1 induces EMT in PCa and identify fisetin as an inhibitor of its activation. PMID:24770864

Dual functional NaYF4:Yb3+, Er3+@NaYF4:Yb3+, Nd3+ core-shell nanoparticles for cell temperature sensing and imaging

Science.gov (United States)

Shi, Zengliang; Duan, Yue; Zhu, Xingjun; Wang, Qiwei; Li, DongDong; Hu, Ke; Feng, Wei; Li, Fuyou; Xu, Chunxiang

2018-03-01

Lanthanide-doped up-conversion nanoparticles (UCNPs) provide a remote temperature sensing approach to monitoring biological microenvironments. In this research, the UCNPs of NaYF4:Yb3+, Er3+@NaYF4:Yb3+, Nd3+ with hexagonal (β)-phase were synthesized and applied in cell temperature sensing as well as imaging after surface modification with meso-2, 3-dimercaptosuccinic acid. In the core-shell UCNPs, Yb3+ ions were introduced as energy transfer media between sensitizers of Nd3+ and activators of Er3+ to improve Er3+emission and prevent their quenching behavior due to multiple energy levels of Nd3+. Under the excitations of 808 nm and 980 nm lasers, the NaYF4:Yb3+, Er3+@NaYF4:Yb3+, Nd3+ nanoparticles exhibited an efficient green band with two emission peaks at 525 nm and 545 nm, respectively, which originated from the transitions of 2H11/2 → 4I15/2 and 4S3/2 → 4I15/2 for Er3+ ions. We demonstrate that an occurrence of good logarithmic linearity exists between the intensity ratio of these two emission peaks and the reciprocal of the inside or outside temperature of NIH-3T3 cells. A better thermal stability is proved through temperature-dependent spectra with a heating-cooling cycle. The obtained viability of NIH-3T3 cells is greater than 90% after incubations of about 12 and 24 (h), and they possess a lower cytotoxicity of UCNPs. This work provides a method for monitoring the cell temperature and its living state from multiple dimensions including temperature response, cell images and visual up-conversion fluorescent color.

Evolution of magnetic properties and exchange interactions in Ru doped YbCrO3

International Nuclear Information System (INIS)

Dalal, Biswajit; Sarkar, Babusona; De, S K; Dev Ashok, Vishal

2016-01-01

Magnetic properties of YbCr 1−x Ru x O 3 as a function of temperature and magnetic field have been investigated to explore the intriguing magnetic phenomena in rare-earth orthochromites. A quantitative analysis of x-ray photoelectron spectroscopy confirms the mixed valence state (Yb 3+  and Yb 2+ ) of Yb ions for the highest doped sample. Field-cooled magnetization reveals a broad peak around 75 K and then becomes zero at about 20–24 K, due to the antiparallel coupling between Cr 3+ and Yb 3+ moments. An increase of the Ru 4+ ion concentration leads to a slight increase of compensation temperature T comp from 20 to 24 K, but the Néel temperature remains constant. A larger value of the magnetic moment of Yb ions gives rise to negative magnetization at low temperature. An external magnetic field significantly modifies the temperature dependent magnetization. Simulation of temperature dependent magnetization data, below T N , based on the three (two) magnetic sub-lattice model predicts stronger intra-sublattice exchange interaction than that of inter-sublattice. Thermal hysteresis and Arrot plots suggest first order magnetic phase transition. Random substitution of Ru 4+ ion reduces the magnetic relaxation time. Weak ferromagnetic component in canted antiferromagnetic system and negative internal magnetic field cause zero-field-cooled exchange bias effect. Large magnetocrystalline anisotropy associated with Ru creates high coercivity in the Ru doped sample. A maximum value of magnetocaloric effect is found around the antiferromagnetic ordering of Yb 3+ ions. Antiferromagnetic transition at about 120 K and temperature induced magnetization reversal lead to normal and inverse magnetocaloric effects in the same material. (paper)

Influence of Er3+/Yb3+ concentration ratio on the down-conversion and up-conversion luminescence and lifetime in GdVO4:Er3+/Yb3+ microcrystals

Directory of Open Access Journals (Sweden)

Gavrilović T.V.

2015-01-01

Full Text Available In this paper, we studied the effects of Er3+/Yb3+ concentration ratio on structural, morphological and luminescence properties of GdVO4:Er3+/Yb3+ green phosphors prepared by a high-temperature solid state method. The samples with different concentrations (between 0.5 to 2 mol% of dopant Er3+ emitting ions and different concentrations (between 5 to 20 mol% of sensitizer ions (Yb3+ were studied. The phosphors were characterized by the X-ray diffraction (XRD, scanning electron microscopy (SEM and photoluminescence spectroscopy. For all samples, XRD diffraction patterns confirmed a formation of a pure GdVO4 phase, while the SEM showed that the materials are comprised of chunks of deformed particles with an average diameter ranging from approximately 2 μm to 8 μm. Both, down-conversion and up-conversion emission spectra of GdVO4:Er3+/Yb3+ samples, under near UV and IR excitations, exhibit two strong emission bands in the green spectral region at 525 nm and 552 nm wavelengths corresponding to 2H11/2 →4I15/2 and 4S3/2 → 4I15/2 electronic transitions of Er3+ ions. The intensity of the green emission was changed by changing the Er3+/Yb3+ concentration ratio. This dual-mode luminescence makes these materials ideal as green phosphors for a wide variety of applications in the fields of bioanalysis and biomedical. [Projekat Ministarstva nauke Republike Srbije, br. 45020 i br. 172056

Ferromagnetic correlations in Yb based heavy fermions probed by NMR relaxation: YbNi{sub 4}P{sub 2} vs. Yb(Rh,Ir){sub 2}Si{sub 2}

Energy Technology Data Exchange (ETDEWEB)

Baenitz, M.; Sarkar, R.; Khuntia, P.; Krellner, C.; Geibel, C.; Steglich, F. [Max - Planck Institute of Chemical Physics of Solids, 01187 Dresden, Germany (Germany)

2012-07-01

Intersite correlations in Ce-based heavy fermion systems close to the quantum critical point separating the magnetic ordered state from the paramagnetic Kondo lattice are in almost all cases predominantly antiferromagnetic (AFM) in nature. The NMR relaxation of these systems show an evolution from localized fluctuations with 1/T{sub 1} nearly constant above the Kondo temperature T{sub K}, to a linear in T Korringa- like behavior with a constant and enhanced (1/T{sub 1}T)- value below T{sub K}. We report on {sup 31}P-NMR results on the ferromagnetic (FM) quantum critical system YbNi{sub 4}P{sub 2} over a wide range in temperature (2-300 K) and field (0.2 - 9 T). Here, {sup 31}(1/T{sub 1}T)(T) does not show such a signature at T{sub K}, instead a continuous increase of (1/T{sub 1}T) down to lowest T is observed. A similar behavior has been reported for YbRh{sub 2}Si{sub 2}, which also exhibits strong FM correlations evidenced by {sup 29}Si - NMR and an enhanced Wilson ratio. Furthermore, in CeFePO, which is likely unique among Ce-based quantum critical system because of its strong FM correlations, (1/T{sub 1}T) also diverges continuously for T {yields}0. This suggests that the difference in the relaxation between most of the Ce systems and the Yb systems is predominantly related to a change from AFM to FM intersite correlations. NMR-results (shift, line width, T{sub 1}) are analyzed and discussed in different models (Korringa, Moriya).

Hyper-O-GlcNAcylation of YB-1 affects Ser102 phosphorylation and promotes cell proliferation in hepatocellular carcinoma

Energy Technology Data Exchange (ETDEWEB)

Liu, Qingqing [Department of Gastroenterology, Affiliated Hospital of Nantong University, Nantong 226001, Jiangsu Province (China); Jiangsu Province Key Laboratory for Inflammation and Molecular Drug Target, Nantong University, 19 Qi-xiu Road, Nantong 226001, Jiangsu Province (China); Tao, Tao [Jiangsu Province Key Laboratory for Inflammation and Molecular Drug Target, Nantong University, 19 Qi-xiu Road, Nantong 226001, Jiangsu Province (China); Liu, Fang [Key Laboratory of Neuroregeneration, Nantong University, Nantong 226001, Jiangsu Province (China); Ni, Runzhou [Department of Gastroenterology, Affiliated Hospital of Nantong University, Nantong 226001, Jiangsu Province (China); Lu, Cuihua, E-mail: lch1516@yeah.net [Department of Gastroenterology, Affiliated Hospital of Nantong University, Nantong 226001, Jiangsu Province (China); Shen, Aiguo, E-mail: shag@ntu.edu.cn [Jiangsu Province Key Laboratory for Inflammation and Molecular Drug Target, Nantong University, 19 Qi-xiu Road, Nantong 226001, Jiangsu Province (China); Key Laboratory of Neuroregeneration, Nantong University, Nantong 226001, Jiangsu Province (China)

2016-12-10

As an essential post-translational modification, O-GlcNAcylation has been thought to be able to modulate various nuclear and cytoplasmic proteins and is emerging as a key regulator of multiple biological processes, such as transcription, cell growth, signal transduction, and cell motility. Recently, authoritative glycomics analyses have reported extensive crosstalk between O-GlcNAcylation and phosphorylation, which always dynamically interplay with each other and regulate signaling, transcription, and other cellular processes. Also, plentiful studies have shown close correlation between YB-1 phosphorylation and tumorigenesis. Therefore, our study aimed to determine whether YB-1 was O-GlcNAc modified and whether such modification could interact with its phosphorylation during the process of HCC development. Western blot and immunohistochemistry were firstly conducted to reveal obvious up-regulation of YB-1, OGT and O-GlcNAc modification in HCC tissues. What is more, not only YB-1 was identified to be O-GlcNAcylated but hyper-O-GlcNAcylation was demonstrated to facilitate HCC cell proliferation in a YB-1 dependent manner. Moreover, we detected four specific O-GlcNAc sites and confirmed T126A to be the most effective mutant in HCC cell proliferation via close O-GlcNAcylation-phosphorylation interaction. Even more interestingly, we discovered that T126A-induced HCC cell retardation and subdued transcriptional activity of YB-1 could be partially reversed by T126A/S102E mutant. From all above, it is not difficult to find that glycosylated-YB-1 mainly enhanced cell proliferation through congenerous actions with YB-1 phosphorylation and thus played indispensable roles in fine-tuning cell proliferation and procession of HCC. - Highlights: • YB-1 and OGT are associated with HCC prognosis. • YB-1 is O-GlcNAc modified in HCC. • Hyper-O-GlcNAcylation promotes HCC cell proliferation in dependent of YB-1. • The proliferating role of O-GlcNAcylation is based on Ser102

Creep properties and precipitate evolution in Al-Li alloys microalloyed with Sc and Yb

Energy Technology Data Exchange (ETDEWEB)

Krug, Matthew E. [Department of Materials Science and Engineering, Northwestern University, 2220 Campus Drive, Evanston, IL 60208 (United States); Seidman, David N. [Department of Materials Science and Engineering, Northwestern University, 2220 Campus Drive, Evanston, IL 60208 (United States); Northwestern Center for Atom Probe Tomography, Northwestern University, 2220 Campus Drive, Evanston, IL 60208 (United States); Dunand, David C., E-mail: dunand@northwestern.edu [Department of Materials Science and Engineering, Northwestern University, 2220 Campus Drive, Evanston, IL 60208 (United States)

2012-07-30

Highlights: Black-Right-Pointing-Pointer We examine the creep behavior of Al-alloys with Li and rare earth element additions. Black-Right-Pointing-Pointer These alloys exhibit threshold stresses below which no measurable creep occurs. Black-Right-Pointing-Pointer Larger precipitate size and lattice parameter mismatch increase creep resistance. Black-Right-Pointing-Pointer A simple parameter describes the threshold stress behavior in ternary Al-Sc-X alloys. Black-Right-Pointing-Pointer The findings are explained by a recent model of dislocation-precipitate interactions. - Abstract: A dilute Al-Sc alloy (Al-0.12 Sc, at.%, Al-Sc), its counterpart with a Li addition (Al-2.9 Li-0.11 Sc, at.%, Al-Li-Sc), as well as a quaternary alloy (Al-5.53 Li-0.048 Sc-0.009 Yb, at.%, Al-Li-Sc-Yb) were isothermally aged at 325 Degree-Sign C, and in some cases isochronally aged to 450 Degree-Sign C. As the {alpha} Prime -Al{sub 3}(Li,Sc) and Al{sub 3}(Li,Sc,Yb) precipitates, with L1{sub 2} structure, coarsen in the two Li-containing alloys, their Li and Yb concentrations decrease and their Sc concentration increases. A significant interfacial excess of Li also segregates at the {alpha}-Al matrix/{alpha} Prime -Al{sub 3}Sc(Li,Sc,Yb) precipitate interface: 5.99 {+-} 0.05 atoms nm{sup -2} in Al-Li-Sc and 13.2 {+-} 0.4 atoms nm{sup -2} in Al-Li-Sc-Yb after aging isochronally to 450 Degree-Sign C. During compression creep at 300 Degree-Sign C, the aged alloys exhibit threshold stresses between 8 and 22 MPa. A recent threshold stress model based on elastic interactions between dislocations and precipitates predicts correctly that Li additions in the Al-Li-Sc alloy reduce the threshold stress, while Yb in the Al-Li-Sc-Yb alloy increases it. The model is also in agreement with the threshold stresses of all Al-Sc-X alloys published to date.

Reduction of Kondo lattice effects in Yb1-xLuxAl3 observed by soft x-ray photoelectron spectroscopy

International Nuclear Information System (INIS)

Yamaguchi, J; Sekiyama, A; Imada, S; Yamasaki, A; Tsunekawa, M; Muro, T; Ebihara, T; Onuki, Y; Suga, S

2007-01-01

We have carried out the bulk-sensitive and high-resolution soft x-ray photoelectron spectroscopy on Lu substituted intermediate-valence compound Yb 1-x Lu x Al 3 (x = 0.4) at temperatures from 200 to 20 K. The temperature dependences of the bulk Yb 4f photoelectron spectra revealed in our preceding works on high purity YbAl 3 have not been observed in this Lu substituted system. The temperature dependences of the bulk Yb 4f peak positions and the Yb valence in this system can be well reproduced by the single impurity Anderson model (SIAM), whereas the spectral behaviors in YbAl 3 were not at all reproduced by the SIAM. These results confirm the importance of the Kondo lattice effects for YbAl 3 , for which the coherent lattice periodicity plays essential roles

Synthesis and luminescent properties of two different Y{sub 2}WO{sub 6}:Eu{sup 3+} phosphor phases

Energy Technology Data Exchange (ETDEWEB)

Llanos, Jaime, E-mail: jllanos@ucn.cl [Departamento de Química, Universidad Católica del Norte, Avda. Angamos 0610, Antofagasta (Chile); Olivares, Douglas [Departamento de Química, Universidad Católica del Norte, Avda. Angamos 0610, Antofagasta (Chile); Manríquez, Víctor; Espinoza, Darío [Departamento de Química, Universidad de Chile, Las Palmeras 3425, Santiago (Chile); Brito, Ivan [Departamento de Química, Universidad de Antofagasta, Campus Coloso, Antofagasta (Chile)

2015-04-15

Highlights: • Synthesis of two phases Y{sub 2−x}Eu{sub x}WO{sub 6}. One of them crystallizes as Aurivillius phase. • Optical properties of the phosphors Y{sub 2}WO{sub 6}:Eu{sup 3+} (monoclinic and orthorhombic phases). • The orthorhombic phase was prepared via low-temperature combustion synthesis method. - Abstract: In this paper, two different Y{sub 2−x}Eu{sub x}WO{sub 6} phases were synthesized. The monoclinic phase was prepared via a conventional solid-state reaction, whereas the orthorhombic phase was obtained via a facile, low-temperature combustion synthesis method. X-ray diffraction (XRD), scanning electron microscopy (SEM), differential scanning calorimetry (DSC), and photoluminescence (PL) spectroscopy were used to characterize the resulting phosphors. The XRD results indicate the orthorhombic phase crystallized isostructurally with the Aurivillius Bi{sub 2}WO{sub 6} phase, whereas the other polymorph crystallized isostructurally with Yb{sub 2}WO{sub 6} in the monoclinic system. The SEM studies revealed both phases had a strong tendency to form agglomerates averaging nanometers in size. The photoluminescence emission spectra confirmed all of the samples were efficiently excited by near UV light and were dominated by the electric dipole transition {sup 5}D{sub 0} → {sup 7}F{sub 2}. The orthorhombic Y{sub 2−x}Eu{sub x}WO{sub 6} excitation spectrum possessed a broad band across the entire UV region (220–400 nm); therefore, Y{sub 1.86}Eu{sub 0.14}WO{sub 6} could be considered an efficient spectral converter material for use in dye-sensitized solar cells.

Simulation of 4f-5d transitions of Yb2+ in potassium and sodium halides

International Nuclear Information System (INIS)

Duan Changkui; Tanner, P A

2008-01-01

The free ion energy level parameters of Yb 2+ are obtained by fitting the 4f 13 5d Yb 2+ free ion energy levels. A model is proposed for scaling these parameters so that they are appropriate for Yb 2+ in crystals. Treating the scaling factor, the barycenter energy E exc of the 4f 13 5d configuration, and the crystal-field splitting parameter B 4 (dd) as free parameters and adopting the 4f crystal-field parameters of the 4f 13 configuration Yb 3+ ion in other hosts with the same ligands, the absorption spectra of Yb 2+ in MX (M = K, Na; X = F, Cl, Br, I) hosts are well simulated. A model is proposed for taking the effect of charge compensation into account and this shows that the inclusion of charge compensation effects does not significantly alter the calculated electronic absorption spectra but may considerably change the dynamics of the system

Virally encoded 7TM receptors

DEFF Research Database (Denmark)

Rosenkilde, M M; Waldhoer, M; Lüttichau, H R

2001-01-01

expression of this single gene in certain lymphocyte cell lineages leads to the development of lesions which are remarkably similar to Kaposi's sarcoma, a human herpesvirus 8 associated disease. Thus, this and other virally encoded 7TM receptors appear to be attractive future drug targets.......A number of herpes- and poxviruses encode 7TM G-protein coupled receptors most of which clearly are derived from their host chemokine system as well as induce high expression of certain 7TM receptors in the infected cells. The receptors appear to be exploited by the virus for either immune evasion...

Structural, mechanical and electronic properties of OsTM and TMOs{sub 2} (TM = Ti, Zr and Hf): First-principles calculations

Energy Technology Data Exchange (ETDEWEB)

Liu, Qi-Jun, E-mail: qijunliu@home.swjtu.edu.cn [Bond and Band Engineering Group, Institute of High Temperature and High Pressure Physics, School of Physical Science and Technology, Southwest Jiaotong University, Chengdu, Sichuan 610031 (China); Zhang, Ning-Chao; Liu, Fu-Sheng [Bond and Band Engineering Group, Institute of High Temperature and High Pressure Physics, School of Physical Science and Technology, Southwest Jiaotong University, Chengdu, Sichuan 610031 (China); Liu, Zheng-Tang [State Key Laboratory of Solidification Processing, School of Materials Science and Engineering, Northwestern Polytechnical University, Xi’an, Shaanxi 710072 (China)

2014-03-15

Highlights: • OsTM and TMOs{sub 2} compounds have no superhard character. • These compounds are mechanically stable and behave in ductile manner. • OsTM has a mixture of covalent-ionic and metallic character. -- Abstract: The first-principles calculations have been performed to study the structural, elastic, mechanical and electronic properties of cubic OsTM (TM = Ti, Zr, and Hf) and hexagonal TMOs{sub 2} compounds. The calculated structural parameters are in good agreement with the available experimental data. To the best of our knowledge, the elastic constants of OsTM and TMOs{sub 2} compounds have been obtained for the first time. The calculated elastic and mechanical properties show that these compounds have no superhard character. These compounds are mechanically stable and behave in ductile manner. The electronic band structures and densities of states of OsTM and TMOs{sub 2} compounds have been analysed. OsTM has a mixture of covalent-ionic and metallic character, and TMOs{sub 2} has strong metallic nature.

Up conversion luminescence of Yb3+–Er3+ codoped CeO2 nanocrystals with imaging applications

International Nuclear Information System (INIS)

Cho, Jung-Hyun; Bass, Michael; Babu, Suresh; Dowding, Janet M.; Self, William T.; Seal, Sudipta

2012-01-01

The effects of Yb 3+ doping on up conversion in Yb 3+ –Er 3+ co-doped cerium oxide nanocrystals are reported. Green emission around 545 and 560 nm attributed to the 2 H 11/2 , 4 S 3/2 → 4 I 15/2 transitions and red emission around 660 and 680 nm due to 4 F 9/2 → 4 I 15/2 transitions under 975 nm excitation were studied at room temperature. Both green and red emission intensities increase as the Yb 3+ concentration increases from 0%. Emission strength starts to decrease after the Yb 3+ concentration exceeds a critical amount. The green emission strength peaks around 1% Yb 3+ concentration while the red emission strength peaks around 4%. An explanation of competition between different decay mechanisms is presented to account for the luminescence dependence on Yb 3+ concentration. Also, the application of up converting nanoparticles in biomedical imaging is demonstrated. - Highlights: ► Up conversion in Yb 3+ –Er 3+ co-doped cerium oxide nanocrystals. ► Different decay mechanisms determine luminescence efficiency. ► Up converting nanoparticles in biomedical imaging is demonstrated.

Infrared emission properties and energy transfer in ZnO-SiO2:Yb3+ composites

International Nuclear Information System (INIS)

Xiao, F.; Chen, R.; Shen, Y.Q.; Liu, B.; Gurzadyan, G.G.; Dong, Z.L.; Zhang, Q.Y.; Sun, H.D.

2011-01-01

Graphical abstract: Highlights: → ZnO-SiO 2 :Yb 3+ composites have been prepared via a facile sol-gel method. Intense near-infrared emission at around 1 μm has been obtained upon broadband ultraviolet light excitation. → Efficient energy transfer from ZnO quantum dots to Yb 3+ ions has been clarified by the systematic measurements and analysis of static and time resolved photoluminescence spectra. → Codoping with Li + ions leads to about twice enhancement of the near-infrared luminescence intensity around 1 μm at room temperature. - Abstract: Intense near-infrared emission at 1 μm has been obtained in ZnO-SiO 2 :Yb 3+ composites via a facile sol-gel method upon broadband ultraviolet light excitation. Systematic optical measurements including static and time-resolved photoluminescence have been performed to elucidate the energy transfer from ZnO quantum dots to Yb 3+ ions. The dependence of energy transfer efficiency on Yb 3+ concentration has been investigated in detail. Codoping with Li + ions leads to about twice enhancement of the near-infrared luminescence intensity around 1 μm at room temperature. The enhancement in the luminescence intensity could be mostly attributed to the modification of the local symmetry around Yb 3+ ions by codoping with Li + ions.

Expression of an enzymatically active Yb3 glutathione S-transferase in Escherichia coli and identification of its natural form in rat brain.

Science.gov (United States)

Abramovitz, M; Ishigaki, S; Felix, A M; Listowsky, I

1988-11-25

Glutathione S-transferases containing Yb3 subunits are relatively uncommon forms that are expressed in a tissue-specific manner and have not been identified unequivocally or characterized. A cDNA clone containing the entire coding sequence of Yb3 glutathione S-transferase mRNA was incorporated into a pIN-III expression vector used to transform Escherichia coli. A fusion Yb3-protein containing 14 additional amino acid residues at its N terminus was purified to homogeneity. Recombinant Yb3 was enzymatically active with both 1-chloro-2,4-dinitrobenzene and 1,2-dichloro-4-nitrobenzene as substrates but lacked glutathione peroxidase activity. Substrate specificity patterns of recombinant Yb3 were more limited than those of glutathione S-transferase isoenzymes containing Yb1- or Yb2-type subunits. Peptides corresponding to unique amino acid sequences of Yb3 as well as a peptide from a region of homology with Yb1 and Yb2 subunits were synthesized. These synthetic peptides were used to raise antibodies specific to Yb3 and others that cross-reacted with all Yb forms. Immunoblotting was utilized to identify the natural counterpart of recombinant Yb3 among rat glutathione transferases. Brain and testis glutathione S-transferases were rich in Yb3 subunits, but very little was found in liver or kidney. Physical properties, substrate specificities, and binding patterns of the recombinant protein paralleled properties of the natural isoenzyme isolated from brain.

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

Energy Technology Data Exchange (ETDEWEB)

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

2008-11-15

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

Structural and optical properties of novel surfactant-coated Yb-TiO2 nanoparticles

International Nuclear Information System (INIS)

Calandra, P.; Lombardo, D.; Pistone, A.; Turco Liveri, V.; Trusso, S.

2011-01-01

In this paper a novel hybrid approach to synthesise composite nanoparticles is presented. It is based on the laser ablation of a bulk target (Yb) immersed in a reversed micellar solution which contains nanoparticles of a different host material (TiO 2 nanoparticles) previously synthesised by chemical method. This approach thus exploits the advantages of the chemical synthesis through reversed micellar solution (size control, nanoparticle stabilisation), and of the laser ablation (“clean” synthesis, no side reactions). Central role is played by the microscopic processes controlling the deposition of the ablated Yb atoms onto the surface of TiO 2 nanoparticles which actually behave as nucleation seeds. The structural features of the resulting Yb-TiO 2 composite nanoparticles have been studied by Transmission Electron Microscopy, whereas their peculiar optical properties have been explored by UV–Vis spectroscopy and steady-state fluorescence. Results consistently show the formation of Yb and TiO 2 glued nanodomains to form nearly spherical and non-interacting nanoparticles with enhanced photophysical properties.

Spectroscopic properties and quenching processes of Yb3+ in Fluoride single crystals for laser applications

International Nuclear Information System (INIS)

Bensalah, A.; Ito, M.; Guyot, Y.; Goutaudier, C.; Jouini, A.; Brenier, A.; Sato, H.; Fukuda, T.; Boulon, G.

2007-01-01

Spectroscopic characterization is carried out to identify Stark's levels of Yb 3+ transitions in several fluoride crystals grown either by the Czochralski technique or by the laser-heated pedestal growth method. Yb 3+ concentration dependence of the decay time is analyzed in order to understand involved concentration quenching mechanisms. Laser tests under saphire:Ti pumping are presented for all our materials as well as under diode pumping for Yb:CaF 2

Influence of temperature on Yb:YAG/Cr:YAG microchip laser operation

Science.gov (United States)

Šulc, Jan; Eisenschreiber, Jan; Jelínková, Helena; Nejezchleb, Karel; Å koda, Václav

2017-02-01

The goal of this work was an investigation of the temperature influence (in range from 80 up to 320 K) on the laser properties of Yb:YAG/Cr:YAG Q-switched diode-pumped microchip laser. This laser was based on monolith crystal (diameter 3mm) which combines in one piece an active laser part (Yb:YAG crystal, 10 at.% Yb/Y, 3mm long) and saturable absorber (Cr:YAG crystal, 1.36mm long, initial transmission 90% @ 1031 nm). The laser resonator pump mirror (HT for pump radiation, HR for generated radiation) was directly deposited on the Yb:YAG monolith part. The output coupler with reflection 55% for the generated wavelength was placed on the Cr:YAG part. The microchip laser was placed in the temperature controlled cupreous holder inside vacuum chamber of the liquid nitrogen cryostat. For Yb:YAG part longitudinal pulsed pumping (pumping pulse length 2.5 ms, rep-rate 20 Hz, power amplitude 21W) a fibre coupled (core diameter 400 μm, NA= 0:22) laser diode, operating at wavelength 933 nm, was used. The microchip laser mean output power, pulse duration, repetition rate, emission wavelength, and laser beam profile were measured in dependence on temperature. The generated pulse length was in range from 2.2 ns to 1.1 ns (FWHM) with the minimum at 230 K. The single pulse energy was peaking (0.4 mJ) at 180 K. The highest peak power (325 kW) was obtained at 220 K. The highest pulse repetition rate (38 kHz) and output mean power (370mW) was reached for temperature 80 K.

Wavelengths, classifications, and ionization energies in the isoelectronic sequences from Yb II and Yb III through Bi XV and Bi XVI

International Nuclear Information System (INIS)

Kaufman, V.; Sugar, J.

1976-01-01

Spectral observations are reported for transitions to the ground term and first excited term of the one-electron configurations in the 4f/sup 14/5p 6 nl isoelectronic sequence from Yb II through Bi XV. Resonance lines are reported for the isoelectronic sequence Yb III through Bi XVI in which the ground state is 4f/sup 14/5p 6 1 S 0 and the upper levels are the J = 1 levels of the 4f/sup 13/5p 6 nd, 4f/sup 14/5p 5 nd, and 4f/sup 14/5p 5 ns configurations. The wavelengths fall in the range 70--3700 A. The spectra were produced by means of sliding and triggered spark discharges and photographed with 10.7 m normal and grazing incidence spectrographs. The data in the Yb III sequence demonstrate the crossing of binding energies of the 4f and 5p shells at W VII. Rydberg series terms were found in a sufficient number of cases to provide extrapolation curves through Bi XV and Bi XVI. These data enabled us to calculate ionization energies for each of these ions with an uncertainty of approx.1% or better

Comparison of radiation shielding requirements for HDR brachytherapy using 169Yb and 192Ir sources

International Nuclear Information System (INIS)

Lymperopoulou, G.; Papagiannis, P.; Sakelliou, L.; Georgiou, E.; Hourdakis, C. J.; Baltas, D.

2006-01-01

169 Yb has received a renewed focus lately as an alternative to 192 Ir sources for high dose rate (HDR) brachytherapy. Following the results of a recent work by our group which proved 169 Yb to be a good candidate for HDR prostate brachytherapy, this work seeks to quantify the radiation shielding requirements for 169 Yb HDR brachytherapy applications in comparison to the corresponding requirements for the current 192 Ir HDR brachytherapy standard. Monte Carlo simulation (MC) is used to obtain 169 Yb and 192 Ir broad beam transmission data through lead and concrete. Results are fitted to an analytical equation which can be used to readily calculate the barrier thickness required to achieve a given dose rate reduction. Shielding requirements for a HDR brachytherapy treatment room facility are presented as a function of distance, occupancy, dose limit, and facility workload, using analytical calculations for both 169 Yb and 192 Ir HDR sources. The barrier thickness required for 169 Yb is lower than that for 192 Ir by a factor of 4-5 for lead and 1.5-2 for concrete. Regarding 169 Yb HDR brachytherapy applications, the lead shielding requirements do not exceed 15 mm, even in highly conservative case scenarios. This allows for the construction of a lead door in most cases, thus avoiding the construction of a space consuming, specially designed maze. The effects of source structure, attenuation by the patient, and scatter conditions within an actual treatment room on the above-noted findings are also discussed using corresponding MC simulation results

Comparison of NMR and crystal structures for the proteins TM1112 and TM1367

International Nuclear Information System (INIS)

Mohanty, Biswaranjan; Serrano, Pedro; Pedrini, Bill; Jaudzems, Kristaps; Geralt, Michael; Horst, Reto; Herrmann, Torsten; Elsliger, Marc-André; Wilson, Ian A.; Wüthrich, Kurt

2010-01-01

NMR structures of the proteins TM1112 and TM1367 solved by the JCSG in solution at 298 K could be superimposed with the corresponding crystal structures at 100 K with r.m.s.d. values of <1.0 Å for the backbone heavy atoms. For both proteins the structural differences between multiple molecules in the asymmetric unit of the crystals correlated with structural variations within the bundles of conformers used to represent the NMR solution structures. A recently introduced JCSG NMR structure-determination protocol, which makes use of the software package UNIO for extensive automation, was further evaluated by comparison of the TM1112 structure obtained using these automated methods with another NMR structure that was independently solved in another PSI center, where a largely interactive approach was applied. The NMR structures of the TM1112 and TM1367 proteins from Thermotoga maritima in solution at 298 K were determined following a new protocol which uses the software package UNIO for extensive automation. The results obtained with this novel procedure were evaluated by comparison with the crystal structures solved by the JCSG at 100 K to 1.83 and 1.90 Å resolution, respectively. In addition, the TM1112 solution structure was compared with an NMR structure solved by the NESG using a conventional largely interactive methodology. For both proteins, the newly determined NMR structure could be superimposed with the crystal structure with r.m.s.d. values of <1.0 Å for the backbone heavy atoms, which provided a starting platform to investigate local structure variations, which may arise from either the methods used or from the different chemical environments in solution and in the crystal. Thereby, these comparative studies were further explored with the use of reference NMR and crystal structures, which were computed using the NMR software with input of upper-limit distance constraints derived from the molecular models that represent the results of structure

Influence of O_2 exposure on the interaction between CH_4 and amorphous AlYB_1_4

International Nuclear Information System (INIS)

Hunold, Oliver; Wiesing, Martin; Arcos, Teresa de los; Music, Denis; Grundmeier, Guido; Schneider, Jochen M.

2017-01-01

Highlights: • Influence of O_2 exposure on the surface chemistry of a-AlYB_1_4 on the interaction with CH_4 and PE studied by ab initio and UHV-AFM. • Predicted stronger interaction is consistent with experimentally observed trends. • Upon O_2 exposure surface bonding becomes more semiconducting causing a charge redistribution within the adsorbed CH_4 molecule. • The data serve as proof of concept for exploring polymer − hard coating interactions in varying atmospheres. - Abstract: The influence of surface oxidation on the interaction between CH_4 and amorphous AlYB_1_4 (a-AlYB_1_4) has been studied theoretically by using density functional theory and experimentally by ultra-high vacuum atomic force microscopy (UHV-AFM). CH_4 mimics the –CH_3 termination and aliphatic subunits of a polymer chain. Low-energy ion scattering measurements of magnetron sputtered thin films suggest that the bonding at the surfaces of pristine a-AlYB_1_4 and O_2 exposed a-AlYB_1_4 (O_2//a-AlYB_1_4) is metal-boron and metal-oxygen dominated, respectively. Based on the ab initio calculations the adsorption energies of CH_4 on a-AlYB_1_4 and O_2//a-AlYB_1_4 decreases from −0.07 to −0.30 eV, respectively. This trend is consistent with experimental data obtained by colloidal probe UHV-AFM studies with a polyethylene sphere, where larger adhesion forces for the O_2 exposed surface as compared to the pristine a-AlYB_1_4 surface were measured. No charge transfer takes place between CH_4 and the pristine as well as the O_2 exposed a-AlYB_1_4. Oxygen chemisorption induces changes in surface bonding. States at the Fermi level are depleted upon oxidation, hence the surface bonding becomes more semiconducting causing a charge redistribution within the adsorbed CH_4 molecule. Hence, these data serve as proof of concept for exploring the effect of O_2 exposure on the interaction between aliphatic polymers and a-AlYB_1_4 using a correlative experimental and theoretical research approach.

Transport and magnetic properties of new heavy-fermion antiferromagnet YbNi{sub 3}Al{sub 9}

Energy Technology Data Exchange (ETDEWEB)

Ohara, S; Yamashita, T; Mori, Y; Sakamoto, I, E-mail: ohara.shigeo@nitech.ac.jp [Department of Engineering Physics, Electronics and Mechanics, Graduate School of Engineering, Nagoya Institute of Technology, Nagoya 466-8555 (Japan)

2011-01-01

We have synthesized a new Yb-based Kondo-lattice compound YbNi{sub 3}Al{sub 9}. This compound crystallizes in a trigonal ErNi{sub 3}Al{sub 9}-type structure (space group R32), in which the Yb-ion is arranged in a two-dimensional honey-comb lattice perpendicular to the c-axis. We report the first measurements of electrical resistivity and magnetization for single-crystalline samples of YbNi{sub 3}Al{sub 9}. The electrical resistivity of YbNi{sub 3}Al{sub 9} is characteristic of the typical properties of heavy-fermion antiferromagnets with a Neel temperature of T{sub N} = 3.4 K. The transport and magnetic properties exhibit large anisotropy in the low-temperature region owing to an interplay among the crystalline-electric-field effect, the Ruderman-Kittel-Kasuya-Yoshida interaction, and the Kondo effect. Below T{sub N}, the metamagnetic transition is observed at a very low magnetic field of around 1 kOe with the field applied along the a-axis. The magnetic structure of YbNi{sub 3}Al{sub 9} is highly sensitive to the applied magnetic field.

Yb-doped rod-type photonic crystal fibers for single-mode amplification

DEFF Research Database (Denmark)

Poli, Frederica; Passaro, Davide; Cucinotta, Annamaria

2009-01-01

The competition among the guided modes in rod-type photonic crystal fibers with a low refractive index ring in the Yb-doped core is investigated with an amplifier model to demonstrate the effective higher-order mode suppression.......The competition among the guided modes in rod-type photonic crystal fibers with a low refractive index ring in the Yb-doped core is investigated with an amplifier model to demonstrate the effective higher-order mode suppression....

Topotactic Transformation Route to Monodisperse β-NaYF4:Ln(3+) Microcrystals with Luminescence Properties.

Science.gov (United States)

Shao, Baiqi; Feng, Yang; Song, Yan; Jiao, Mengmeng; Lü, Wei; You, Hongpeng

2016-02-15

A novel nonorganic wet route for direct synthesis of uniform hexagonal β-NaYF4:Ln(3+) (Ln = Eu, Tb, Ce/Tb, Yb/Er, and Yb/Tm) microcrystals with various morphologies has been developed wherein the intermediate routine cubic-hexagonal (α → β) phase transfer process was avoided. The morphology can be effectively tuned into hexagonal disc, prism, and novel hierarchical architectures by systematically fine manipulating the Na2CO3/F(-) feeding ratio. It has been found that the routine α → β phase transfer for NaYF4 was not detected during the growth, while NaY(CO3)F2 emerged in the initial reaction stage and fast transformed into β-NaYF4 via a novel topotactic transformation behavior. Detailed structural analysis showed that β-NaYF4 preferred the [001] epitaxial growth direction of NaY(CO3)F2 due to the structural matching of [001]NaY(CO3)F2//[0001]β-NaYF4. Besides, the potential application of the as-prepared products as phosphors is emphasized by demonstrating multicolor emissions including downconversion, upconversion, and energy transfer (Ce-Tb) process by lanthanides doping.

ThSi_2 type ytterbium disilicide and its analogues YbT_xSi_2_-_x (T = Cr, Fe, Co)

International Nuclear Information System (INIS)

Peter, Sebastian C.; Kanatzidis, Mercouri G.

2012-01-01

YbSi_2 and the derivatives YbT_xSi_2_-_x (T = Cr, Fe, Co) crystallizing in the α-ThSi_2 structure type were obtained as single crystals from reactions run in liquid indium. All silicides were investigated by single-crystal X-ray diffraction, I4_1/amd space group and the lattice constants are: a = 3.9868(6) Aa and c = 13.541(3) Aa for YbSi_2, a = 4.0123(6) Aa and c = 13.542(3) Aa for YbCr_0_._2_7Si_1_._7_3, a = 4.0142(6) Aa and c = 13.830(3) Aa for YbCr_0_._7_1Si_1_._2_9, a = 4.0080(6) Aa and c = 13.751(3) Aa for YbFe_0_._3_4Si_1_._6_6, and a = 4.0036(6) Aa, c = 13.707(3) Aa for YbCo_0_._2_1Si_1_._7_9. YbSi_2 and YbT_xSi_2_-_x compounds are polar intermetallics with three-dimensional Si and M (T+Si) polyanion sub-networks, respectively, filled with ytterbium atoms. The degree of substitution of transition metal at the silicon site is signficant and leads to changes in the average bond lengths and bond angles substantially. (Copyright copyright 2012 WILEY-VCH Verlag GmbH and Co. KGaA, Weinheim)

Mobility of rare earth element in hydrothermal process and weathering product: a review

Science.gov (United States)

Lintjewas, L.; Setiawan, I.

2018-02-01

The Rare Earth Element (REE), consists of La, Ce, Pr, Nd, Pm, Sm, Eu, Gd, Tb, Dy, Lu, Ho, Er, Tm, Yb, are important elements to be used as raw materials of advanced technology such as semiconductors, magnets, and lasers. The research of REE in Indonesia has not been done. Several researches were conducted on granitic rocks and weathering product such as Bangka, Sibolga, West Kalimantan, West Sulawesi and Papua. REE can be formed by hydrothermal processes such as Bayan Obo, South China. The REE study on active hydrothermal system (geothermal) in this case also has the potential to produce mineral deposits. The purpose of this review paper is to know the mobility of REE on hydrothermal process and weathering products. Mobility of REE in the hydrothermal process can change the distribution patterns and REE content such as Ce, Eu, La, Lu, Nd, Sm, and Y. Another process besides the hydrothermal is weathering process. REE mobility is influenced by weathering products, where the REE will experience residual and secondary enrichment processes in heavier minerals.

Valence determination of rare earth elements in lanthanide silicates by L 3-XANES spectroscopy

International Nuclear Information System (INIS)

Kravtsova, Antonina N; Guda, Alexander A; Soldatov, Alexander V; Goettlicher, Joerg; Taroev, Vladimir K; Suvorova, Lyudmila F; Tauson, Vladimir L; Kashaev, Anvar A

2016-01-01

Lanthanide silicates have been hydrothermally synthesized using Cu and Ni containers. Chemical formulae of the synthesized compounds correspond to K 3 Eu[Si 6 O 15 ] 2H 2 O, HK 6 Eu[Si 10 O 25 ], K 7 Sm 3 [Si 12 O 32 ], K 2 Sm[AlSi 4 O 12 ] 0.375H 2 O, K 4 Yb 2 [Si 8 O 21 ], K 4 Ce 2 [Al 2 Si 8 O 24 ]. The oxidation state of lanthanides (Eu, Ce, Tb, Sm, Yb) in these silicates has been determined using XANES spectroscopy at the Eu, Ce, Tb, Sm, Yb, L 3 - edges. The experimental XANES spectra were recorded using the synchrotron radiation source ANKA (Karlsruhe Institute of Technology) and the X-ray laboratory spectrometer Rigaku R- XAS. By comparing the absorption edge energies and white line intensities of the silicates with the ones of reference spectra the oxidation state of lanthanides Eu, Ce, Tb, Sm, Yb has been found to be equal to +3 in all investigated silicates except of the Ce-containing silicate from the run in Cu container where the cerium oxidation state ranges from +3 (Ce in silicate apatite and in a KCe silicate with Si 12 O 32 layers) to +4 (starting CeO 2 or oxidized Ce 2 O 3 ). (paper)

Phase stability of AlYB14 sputtered thin films

International Nuclear Information System (INIS)

Koelpin, Helmut; Music, Denis; Emmerlich, Jens; Schneider, Jochen M; Henkelman, Graeme; Munnik, Frans

2009-01-01

AlYB 14 (Imma) thin films were synthesized by magnetron sputtering. On the basis of x-ray diffraction, no phases other than crystalline AlYB 14 could be identified. According to electron probe microanalysis, energy dispersive x-ray analysis and elastic recoil detection analysis, the Al and Y occupancies vary in the range of 0.73-1.0 and 0.29-0.45, respectively. Density functional theory based calculations were carried out to investigate the effect of occupancy on the stability of Al x Y y B 14 (x,y = 0.25, 0.5, 0.75, 1). The mean effective charge per icosahedron and the bulk moduli were also calculated. It is shown that the most stable configuration is Al 0.5 YB 14 , corresponding to a charge transfer of two electrons from the metal atoms to the boron icosahedra. Furthermore, it is found that the stability of a configuration is increased as the charge is homogeneously distributed within the icosahedra. The bulk moduli for all configurations investigated are in the range between 196 and 220 GPa, rather close to those for known hard phases such as α- Al 2 O 3 .

Properties of melt-grown single crystals of 'YB/sub 68/'

Energy Technology Data Exchange (ETDEWEB)

Slack, G A; Oliver, D W; Brower, G D; Young, J D [General Electric Co., Schenectady, N.Y. (USA). Research and Development Center

1977-01-01

Single crystals of yttrium boride YB/sub n/ with n = 61 +- 3 were grown from the melt. Precision density and lattice parameter measurements indicate a congruent melting point at n = 61.7 and a stoichiometric composition at n = 68. Measurements of elastic constants, acoustic attenuation, electrical resistivity and optical absorption are presented. High resolution transmission electron microscopy reveals a complex crystal structure similar to that found by using X-rays. A comparison of the properties of YB/sub n/ with those of ..beta..-boron show that there are many similarities.

Statistical γ-ray multiplicity distributions in Dy and Yb nuclei

International Nuclear Information System (INIS)

Tveter, T.S.; Bergholt, L.; Guttormsen, M.; Rekstad, J.

1994-03-01

The statistical γ-ray multiplicity distributions following the reactions 163 Dy( 3 He,αxn) 162-x Dy and 173 Yb( 3 He,αxn) 172-x Yb have been studied. The mean value and standard deviation have been extracted as functions of excitation energy. The method is based on the probability distribution of k-fold events, where an α-particle is observed in coincidence with signals in k γ-ray detectors. Techniques for isolating statistical γ-rays and subtracting random background, cross-talk and neutron contributions are discussed. 22 refs., 10 figs., 3 tabs

Ternary oxide nanostructures and methods of making same

Science.gov (United States)

Wong, Stanislaus S [Stony Brook, NY; Park, Tae-Jin [Port Jefferson, NY

2009-09-08

A single crystalline ternary nanostructure having the formula A.sub.xB.sub.yO.sub.z, wherein x ranges from 0.25 to 24, and y ranges from 1.5 to 40, and wherein A and B are independently selected from the group consisting of Ag, Al, As, Au, B, Ba, Br, Ca, Cd, Ce, Cl, Cm, Co, Cr, Cs, Cu, Dy, Er, Eu, F, Fe, Ga, Gd, Ge, Hf, Ho, I, In, Ir, K, La, Li, Lu, Mg, Mn, Mo, Na, Nb, Nd, Ni, Os, P, Pb, Pd, Pr, Pt, Rb, Re, Rh, Ru, S, Sb, Sc, Se, Si, Sm, Sn, Sr, Ta, Tb, Tc, Te, Ti, Tl, Tm, U, V, W, Y, Yb, and Zn, wherein the nanostructure is at least 95% free of defects and/or dislocations.

Studies on elemental analysis of widely consumed traditional herbs in Libya by ko instrumental neutron activation analysis

International Nuclear Information System (INIS)

Abugassa, I. O.; Abunawael, M. E.

2012-12-01

Herbs are accepted as an alternative medicine for specific treatment of illness of among different ethnic groups worldwide. It is vital to know the contents of these herbs used in Libya were analysed by k-0 instrumental neutron activation analysis. A total of 32 trace and major elements (Ag, As, Au, Ba, Br, Ca, Ce, Co, Cr, Cs, Eu, Fe, Hf, Hg, K, La, Mo, Na, Nd, Rb, Sb, Sc, Se, Sm, Sr, Tb, Th, Tm, U, Yb and Zn) were determined. The concentration of elements varied depending on the origin of the herb. The study showed that the toxic elements found in the samples were below the levels prescribed by health regulations. The method was justified by analyzing two SRM. All the results are in good agreement with the certified values. (Author)

Characterization of Loma Venturilla pegmatites using nuclear techniques; Caracterizacion de las pegmatitas de Loma Venturilla mediante el uso de tecnicas nucleares

Energy Technology Data Exchange (ETDEWEB)

Pena Fortes, B; Caopte Rodriguez, G; Toujague La Rosa, R [Centro de Estudios Aplicados al Desarrollo Nuclear (CEADEN), La Habana (Cuba); Sukar Satraputa, K [Instituto de Geofisica y Astronomia, La Habana (Cuba)

1996-10-01

Neutron Activation Analysis (NAA) and gamma spectrometry Analysis (GEA) were used for the determination of 21 trace elements in geological samples of pegmatites of Loma Venturilla area. Both methods permitted, in general, the determination of K, Cr, Co, Sc, Rb, Cs, Ba, Ta, HF, Th, and U and 10 rare earths elements: La, Ce, Nd, Sm, Eu, Tb, Ho, Tm, Yb, and Lu. The results were obtained with good precision and accuracy The knowledge of such concentrations is of great interest in geosciences. The values of the concentrations obtained can be extensively used in petrogenetic studies of those rocks, since they facilitate the evaluation and estimation of the extent of the main process, involved in the generation and differentiation of the melts from which the pegmatites were derivates.

Characterization of Loma Venturilla pegmatites using nuclear techniques

International Nuclear Information System (INIS)

Pena Fortes, B.; Caopte Rodriguez, G.; Toujague La Rosa, R.; Sukar Satraputa, K.

1996-01-01

Neutron Activation Analysis (NAA) and gamma spectrometry Analysis (GEA) were used for the determination of 21 trace elements in geological samples of pegmatites of Loma Venturilla area. Both methods permitted, in general, the determination of K, Cr, Co, Sc, Rb, Cs, Ba, Ta, HF, Th, and U and 10 rare earths elements: La, Ce, Nd, Sm, Eu, Tb, Ho, Tm, Yb, and Lu. The results were obtained with good precision and accuracy The knowledge of such concentrations is of great interest in geosciences. The values of the concentrations obtained can be extensively used in petrogenetic studies of those rocks, since they facilitate the evaluation and estimation of the extent of the main process, involved in the generation and differentiation of the melts from which the pegmatites were derivates

Twist and YB-1 gene expression in cervical cancer and precancerous tissue and their correlation with cell invasion

Directory of Open Access Journals (Sweden)

Qin Tian

2017-04-01

Full Text Available Objective: To study the correlation of Twist and YB-1 gene expression in cervical cancer and precancerous tissue with cell invasion. Methods: Cervical cancer tissue, precancerous tissue and normal cervical tissue surgically removed in our hospital between May 2013 and April 2015 were collected; immunohistochemical staining kits were used to detect the positive protein expression rate of Twist and YB-1 gene; fluorescence quantitative PCR kits were used to detect Twist, YB-1 and invasion gene mRNA expression. Results: Twist and YB-1 mRNA expression and positive protein expression rate as well as USP22, Rab11, Rac1 and ANXA5 mRNA expression in cervical cancer tissue and precancerous tissue were significantly higher than those in normal cervical tissue, Twist and YB-1 mRNA expression and positive protein expression rate as well as USP22, Rab11, Rac1 and ANXA5 mRNA expression in cervical cancer tissue were significantly higher than those in precancerous tissue; USP22, Rab11, Rac1 and ANXA5 mRNA expression in cervical cancer tissue and precancerous tissue with positive Twist and YB-1 expression were significantly higher than those in cervical cancer tissue and precancerous tissue with negative Twist and YB-1 expression. Conclusion: Highly expressed Twist and YB-1 in cervical cancer and precancerous tissue can promote cell invasion.

Multimodal emissions from Tb{sup 3+}/Yb{sup 3+} co-doped lithium borate glass: Upconversion, downshifting and quantum cutting

Energy Technology Data Exchange (ETDEWEB)

Bahadur, A.; Yadav, R.S.; Yadav, R.V.; Rai, S.B., E-mail: sbrai49@yahoo.co.in

2017-02-15

This paper reports the optical properties of Tb{sup 3+}/Yb{sup 3+} co-doped lithium borate (LB) glass prepared by melt quench method. The absorption spectrum of the Yb{sup 3+} doped LB glass contains intense NIR band centered at 976 nm due to {sup 2}F{sub 7/2}→{sup 2}F{sub 5/2} transition. The emission spectra of the prepared glasses have been monitored on excitation with 266, 355 and 976 nm. The Yb{sup 3+} doped glass emits a broad NIR band centered at 976 nm whereas the Tb{sup 3+} doped glass gives off visible bands on excitations with 266 and 355 nm. When the Tb{sup 3+} and Yb{sup 3+} ions are co-doped together, the emission intensity in the visible region decreases whereas it increases in the NIR region significantly. The increase in the emission intensity in the NIR region is due to efficient cooperative energy transfer (CET) from Tb{sup 3+} to Yb{sup 3+} ions. The quantum cutting efficiency for Tb{sup 3+}/Yb{sup 3+} co-doped glass has been calculated and compared for 266 and 355 nm excitations. The quantum cutting efficiency is larger for 355 nm excitation (137%). The Tb{sup 3+}/Yb{sup 3+} co-doped LB glass also emits upconverted visible bands on excitation with 976 nm. The mechanisms involved in the energy transfer have been discussed using schematic energy level diagram. The Tb{sup 3+}/Yb{sup 3+} co-doped LB glass may be used in the optical devices and in solar cell for solar spectral conversion and behaves as a multi-modal photo-luminescent material. - Graphical abstract: The Tb{sup 3+}/Yb{sup 3+} co-doped lithium borate (LB) glass prepared by melt quench method emits upconverted visible emissions through upconversion CET from Yb{sup 3+} to Tb{sup 3+} ions and quantum cutting emissions through downconversion CET from Tb{sup 3+} to Yb{sup 3+} ions. Therefore, the Tb{sup 3+}/Yb{sup 3+} co-doped LB glass may find applications in optical devices and solar cell and behaves as a multi-modal photo-luminescent material. - Highlights: • The Tb{sup 3+}/Yb{sup 3

Intracellular distribution of TM4SF1 and internalization of TM4SF1-antibody complex in vascular endothelial cells

International Nuclear Information System (INIS)

Sciuto, Tracey E.; Merley, Anne; Lin, Chi-Iou; Richardson, Douglas; Liu, Yu; Li, Dan; Dvorak, Ann M.; Dvorak, Harold F.; Jaminet, Shou-Ching S.

2015-01-01

Transmembrane-4 L-six family member-1 (TM4SF1) is a small plasma membrane-associated glycoprotein that is highly and selectively expressed on the plasma membranes of tumor cells, cultured endothelial cells, and, in vivo, on tumor-associated endothelium. Immunofluorescence microscopy also demonstrated TM4SF1 in cytoplasm and, tentatively, within nuclei. With monoclonal antibody 8G4, and the finer resolution afforded by immuno-nanogold transmission electron microscopy, we now demonstrate TM4SF1 in uncoated cytoplasmic vesicles, nuclear pores and nucleoplasm. Because of its prominent surface location on tumor cells and tumor-associated endothelium, TM4SF1 has potential as a dual therapeutic target using an antibody drug conjugate (ADC) approach. For ADC to be successful, antibodies reacting with cell surface antigens must be internalized for delivery of associated toxins to intracellular targets. We now report that 8G4 is efficiently taken up into cultured endothelial cells by uncoated vesicles in a dynamin-dependent, clathrin-independent manner. It is then transported along microtubules through the cytoplasm and passes through nuclear pores into the nucleus. These findings validate TM4SF1 as an attractive candidate for cancer therapy with antibody-bound toxins that have the capacity to react with either cytoplasmic or nuclear targets in tumor cells or tumor-associated vascular endothelium. - Highlights: • Anti-TM4SF1 antibody 8G4 was efficiently taken up by cultured endothelial cells. • TM4SF1–8G4 internalization is dynamin-dependent but clathrin-independent. • TM4SF1–8G4 complexes internalize along microtubules to reach the perinuclear region. • Internalized TM4SF1–8G4 complexes pass through nuclear pores into the nucleus. • TM4SF1 is an attractive candidate for ADC cancer therapy

Intracellular distribution of TM4SF1 and internalization of TM4SF1-antibody complex in vascular endothelial cells

Energy Technology Data Exchange (ETDEWEB)

Sciuto, Tracey E.; Merley, Anne; Lin, Chi-Iou [Center for Vascular Biology Research and Department of Pathology, Beth Israel Deaconess Medical Center and Harvard Medical School (United States); Richardson, Douglas [Department of Molecular and Cellular Biology, Harvard University (United States); Liu, Yu [Department of Pharmacology, Shanxi Medical University, Xinjiannanlu 56, Shanxi Province, Taiyuan 030001 (China); Li, Dan; Dvorak, Ann M. [Center for Vascular Biology Research and Department of Pathology, Beth Israel Deaconess Medical Center and Harvard Medical School (United States); Dvorak, Harold F., E-mail: hdvorak@bidmc.harvard.edu [Center for Vascular Biology Research and Department of Pathology, Beth Israel Deaconess Medical Center and Harvard Medical School (United States); Jaminet, Shou-Ching S., E-mail: sjaminet@bidmc.harvard.edu [Center for Vascular Biology Research and Department of Pathology, Beth Israel Deaconess Medical Center and Harvard Medical School (United States)

2015-09-25

Transmembrane-4 L-six family member-1 (TM4SF1) is a small plasma membrane-associated glycoprotein that is highly and selectively expressed on the plasma membranes of tumor cells, cultured endothelial cells, and, in vivo, on tumor-associated endothelium. Immunofluorescence microscopy also demonstrated TM4SF1 in cytoplasm and, tentatively, within nuclei. With monoclonal antibody 8G4, and the finer resolution afforded by immuno-nanogold transmission electron microscopy, we now demonstrate TM4SF1 in uncoated cytoplasmic vesicles, nuclear pores and nucleoplasm. Because of its prominent surface location on tumor cells and tumor-associated endothelium, TM4SF1 has potential as a dual therapeutic target using an antibody drug conjugate (ADC) approach. For ADC to be successful, antibodies reacting with cell surface antigens must be internalized for delivery of associated toxins to intracellular targets. We now report that 8G4 is efficiently taken up into cultured endothelial cells by uncoated vesicles in a dynamin-dependent, clathrin-independent manner. It is then transported along microtubules through the cytoplasm and passes through nuclear pores into the nucleus. These findings validate TM4SF1 as an attractive candidate for cancer therapy with antibody-bound toxins that have the capacity to react with either cytoplasmic or nuclear targets in tumor cells or tumor-associated vascular endothelium. - Highlights: • Anti-TM4SF1 antibody 8G4 was efficiently taken up by cultured endothelial cells. • TM4SF1–8G4 internalization is dynamin-dependent but clathrin-independent. • TM4SF1–8G4 complexes internalize along microtubules to reach the perinuclear region. • Internalized TM4SF1–8G4 complexes pass through nuclear pores into the nucleus. • TM4SF1 is an attractive candidate for ADC cancer therapy.

Investigation of A = 152 radioactivities with mass-separated sources: Identification of /sup 152/Lu

International Nuclear Information System (INIS)

Toth, K.S.; Sousa, D.C.; Nitschke, J.M.; Wilmarth, P.A.

1987-01-01

Nuclides with A = 152 were produced in /sup 58/Ni bombardments of /sup 96/Ru and their decay properties were investigated following on-line mass separation. The isotope /sup 152/Lu (T/sub 1/2/ = 0.7 +- 0.1 s) was identified by γ rays in its β-decay daughter, /sup 152/Yb. Based on its decay characteristics, the parent state has a probable spin and parity assignment of (4,5,6 - ). Several new transitions were observed to follow the β decays of /sup 152/Yb and the /sup 152/Tm low-spin isomer; they established previously unknown levels in both /sup 152/Tm and /sup 152/Er. The additional γ rays in /sup 152/Yb decay reduce from 100% to 88% the direct feeding to the one excited state in /sup 152/Tm that had been known earlier. Nevertheless, the corresponding logft value is calculated to be 3.5, indicating that this is an allowed β transition which connects the 0 + parent with a 1 + excited state in /sup 152/Tm. By comparing the β-decay rates of /sup 148/Dy and /sup 152/Ho, and the α- and β-decay rates of /sup 152/Er, an α branch of 90 +- 4 % was deduced for /sup 152/Er

The EU agencies’ role in policy diffusion beyond the EU

DEFF Research Database (Denmark)

Chatzopoulou, Sevasti

and health quality within the risk assessment. This paper shows that the EU agencies develop various entrepreneurial methods and that they actively promote policy diffusion beyond the EU through socialisation and learning within international arrangements and collaborations. However, variations......The extensive literature on the EU agencies has mainly focused on their role in the harmonisation and expansion of regulatory standards within the EU. This paper joins this literature and investigates the role of EU agencies in policy diffusion beyond the EU borders. To operationalise this...

Optical and magnetic properties of Yb ion-doped cobalt-based ZnO ...

Indian Academy of Sciences (India)

Administrator

The X-ray photoelectron spectral peaks for Yb 4f ions ... temperature with high coercivity due to the contribution of both 3d and 4f exchange interaction with the host ... Mn,4,5 Co,6–9 Ni2,10 Fe11–13 and Cu,2,14 and reported to .... water separately under stirring. .... different concentrations of Yb added ZnO : Co, nanopar-.

Family C 7TM receptor dimerization and activation

DEFF Research Database (Denmark)

Bonde, Marie Mi; Sheikh, Søren P; Hansen, Jakob Lerche

2006-01-01

The family C seven transmembrane (7TM) receptors constitutes a small and especially well characterized subfamily of the large 7TM receptor superfamily. Approximately 50% of current prescription drugs target 7TM receptors, this biologically important family represents the largest class of drug...... to be fully defined. This review presents the biochemical support for family C 7TM receptor dimerization and discusses its importance for receptor biosynthesis, surface expression, ligand binding and activation, since lessons learnt here may well be applicable to the whole superfamily of 7TM receptors.......-targets today. It is well established that family C 7TM receptors form homo- or hetero-dimers on the cell surface of living cells. The large extra-cellular domains (ECD) have been crystallized as a dimer in the presence and absence of agonist. Upon agonist binding, the dimeric ECD undergoes large conformational...

Ytterbium doped silicon clusters YbSi{sub n} (n = 4–10) and their anions: Structures, thermochemistry, and electron affinities

Energy Technology Data Exchange (ETDEWEB)

Xie, Xiaohong [School of Chemical Engineering, Inner Mongolia University of Technology, Hohhot 010051 (China); Hao, Dongsheng [School of Chemical Engineering, Inner Mongolia University of Technology, Hohhot 010051 (China); School of Mining and Technology, Inner Mongolia University of Technology, Hohhot 010051 (China); Yang, Jucai, E-mail: yangjc@imut.edu.cn [School of Chemical Engineering, Inner Mongolia University of Technology, Hohhot 010051 (China); School of Energy and Power Engineering, Inner Mongolia University of Technology, Hohhot 010051 (China)

2015-11-05

Highlights: • The ground-state structure of YbSi{sub n} and its anion is substitutional structure. • The four DFT AEAs are in excellent agreement with the experimental data. • Theoretical AEA of 2.33 eV of YbSi{sub 9} is more reasonable than the experimental 2.60 eV. • Hardness analysis reveals that doping Yb to Si{sub n} raises photochemical sensitivity. • Relative stabilities of YbSi{sub n} and their anions are examined. - Abstract: The structures, electron affinities, dissociation energies, hardness, and dipole moments of YbSi{sub n} (n = 4–10) and their anions were examined using B3LYP, TPSSh, PBE and wB97X methods. The lowest-energy structures can be regarded as replacing a Si of the ground-state structure of Si{sub n+1} with a Yb atom. The theoretical adiabatic electron affinities (AEAs) of YbSi{sub n} are in excellent agreement with experimental data. The average absolute errors from experiment are by 0.08, 0.07, 0.05 and 0.08 eV at the B3LYP, the TPSSh, the PBE and the wB97X levels, respectively. Theoretical AEAs of 2.33 ± 0.05 eV for YbSi{sub 9} are more reliable than the experimental value of 2.60 ± 0.05 eV. The hardness analysis reveals that doping Yb atom to Si{sub n} (n = 4–10) clusters raises the photochemical sensitivity. The dissociation energies of Yb atom from YbSi{sub n} and their anions were calculated to examine relative stabilities.

Coulomb-nuclear interference measurements of hexadecapole deformations in 168Yb and 178,180Hf

International Nuclear Information System (INIS)

Nettles, W.G.; Mississippi Coll., Clinton; Ramayya, A.V.; Hamilton, J.H.

1988-01-01

Coulomb-nuclear interference studies of 168 Yb and 178,180 Hf have been carried out with alpha particles from the Pittsburgh tandem. From coupled channel fits to the data at 18 MeV for 168 Yb and 19.5 MeV for 178,180 Hf, β 4 c values of -0.030(20), -0.166(18), and -0.180(6) were obtained, respectively. These data agree with the positive M 04 value from sub-Coulomb studies of 168 Yb but with the large negative M 04 values from sub-Coulomb studies of 178,180 Hf. (author)

Spectroscopy of Yb-doped tungsten-tellurite glass and assessment of its lasing properties

Science.gov (United States)

Merzliakov, M. A.; Kouhar, V. V.; Malashkevich, G. E.; Pestryakov, E. V.

2018-01-01

Glasses of the TeO2-WO3-Yb2O3 system are synthesized for wide range of Yb3+ concentrations of up to 6.0 × 1021 ions/cm3. The spectral-luminescent properties of lightly doped samples are investigated at room temperature and at the boiling point of liquid nitrogen. The energies of the Stark levels of the ground and excited states of Yb3+ ions incorporated into tungsten-tellurite glass are determined by analyzing the low-temperature spectra. The absorption, emission, and gain cross section spectra are obtained. The excess of the measured fluorescence decay time over the radiative lifetime ∼0.3 ms derived from the absorption spectra is attributed to the reabsorption effect in bulk samples. Measurements of lightly doped glass powder in the immersion liquid are made to reduce the effect of reabsorption. The fluorescence decay time of the powder is very close to the calculated radiative lifetime. Compared with phosphate, silicate, and other Yb3+-doped glasses, the tungsten-tellurite glass has a promising potential as a gain medium for lasers and amplifiers.

Luminescence properties of Y2O3:Bi3+, Yb3+ co-doped phosphor for application in solar cells

Science.gov (United States)

Lee, E.; Kroon, R. E.; Terblans, J. J.; Swart, H. C.

2018-04-01

Bismuth (Bi3+) and ytterbium (Yb3+) co-doped yttrium oxide (Y2O3) phosphor powder was successfully synthesised using the co-precipitation technique. The X-ray diffraction (XRD) patterns confirmed that a single phase cubic structure with a Ia-3 space group was formed. The visible emission confirmed the two symmetry sites, C2 and S6, found in the Y2O3 host material and revealed that Bi3+ ions preferred the S6 site as seen the stronger emission intensity. The near-infrared (NIR) emission of Yb3+ increased significantly by the presence of the Bi3+ ions when compared to the singly doped Y2O3:Yb3+ phosphor with the same Yb3+ concentration. An increase in the NIR emission intensity was also observed by simply increasing the Yb3+ concentration in the Y2O3:Bi3+, Yb3+ phosphor material where the intensity increased up to x = 5.0 mol% of Yb3+ before decreasing due to concentration quenching.

Rare earth and precious elements in the urban sewage sludge and lake surface sediments under anthropogenic influence in the Republic of Benin.

Science.gov (United States)

Yessoufou, Arouna; Ifon, Binessi Edouard; Suanon, Fidèle; Dimon, Biaou; Sun, Qian; Dedjiho, Comlan Achille; Mama, Daouda; Yu, Chang-Ping

2017-11-09

Nowadays, sewage sludge and water bodies are subjected to heavy pollution due to rapid population growth and urbanization. Heavy metal pollution represents one of the main challenges threatening our environment and the ecosystem. The present work aims to evaluate the contamination state of the sewage sludge and lake sediments in the Republic of Benin. Twenty metallic elements including 15 rare earth elements (Eu, Sb, Cs, Nd, Pr, Gd, La, Ce, Tb, Sm, Dy, Ho, Eu, Yb, and Lu) and five precious elements (Ag, Au, Pd, Pt, and Ru) were investigated using inductive plasma-mass spectrometry. Results showed broad range concentrations of the elements. Ce, La, and Nd were present in both sediments and sewage sludge at concentrations ranging 5.80-41.30 mg/kg dry matter (DM), 3.23-15.60 mg/kg DM, and 2.74-19.26 mg/kg DM, respectively. Pr, Sm, Gd, Tb, Dy, Eu, Er, Yb, Cs, Ho, and Tm concentrations were lower (0.02-5.94 mg/kg DM). Among precious elements, Ag was detected at the highest concentration in all sites (0.43-4.72 mg/kg DM), followed by Pd (0.20-0.57 mg/kg DM) and Au (0.01-0.57 mg/kg DM). Ru and Pt concentrations were sewage sludge. This revealed a growing anthropogenic input which was also implied by principal component analysis. The evaluation of pollution loading index (PLI) indicated a moderate to strong contamination (0.12 ≤ PLI ≤ 0.58; 37 ≤ PLI ≤ 114, respectively, for rare earth elements and precious elements), while the degree of contamination indicated a moderate polymetallic contamination for rare earth elements and significant contamination for precious elements.

Thermal and electron transport studies on the valence fluctuating compound YbNiAl4

Science.gov (United States)

Falkowski, M.; Kowalczyk, A.

2018-05-01

We report the thermoelectric power S and thermal conductivity κ measurements on the valence fluctuating compound YbNiAl4, furthermore taking into account the impact of the applied magnetic field. We discuss our new results with revisiting the magnetic [χ(T)], transport [ρ(T)], and thermodynamic [Cp(T)] properties in order to better understand the phenomenon of thermal and electron transport in this compound. The field dependence of the magnetoresistivity data is also given. The temperature dependence of thermoelectric power S(T) was found to exhibit a similar behaviour as expected for Yb-based compounds with divalent or nearly divalent Yb ions. In addition, the values of total thermal conductivity as a function of temperature κ(T) of YbNiAl4 are fairly low compared to those of pure metals which may be linked to the fact that the conduction band is perturbed by strong hybridization. A deeper analysis of the specific heat revealed the low-T anomaly of the ratio Cp(T)/T3, most likely associated with the localized low-frequency oscillators in this alloy. In addition, the Kadowaki-Woods ratio and the Wilson ratio are discussed with respect to the electronic correlations in YbNiAl4.

Bulk and surface electron transport in topological insulator candidate YbB{sub 6-δ}

Energy Technology Data Exchange (ETDEWEB)

Glushkov, Vladimir V.; Demishev, Sergey V.; Sluchanko, Nikolay E. [Prokhorov General Physics Institute of RAS, Vavilov str. 38, 119991, Moscow (Russian Federation); Moscow Institute of Physics and Technology, Institutskii per. 9, 141700, Dolgoprudny, Moscow Region (Russian Federation); Bozhko, Alexey D.; Bogach, Alexey V.; Semeno, Alexey V.; Voronov, Valeriy V. [Prokhorov General Physics Institute of RAS, Vavilov str. 38, 119991, Moscow (Russian Federation); Dukhnenko, Anatoliy V.; Filipov, Volodimir B.; Shitsevalova, Natalya Yu. [Frantsevich Institute for Problems of Materials Science NAS, Krzhyzhanovsky str. 3, 03680, Kiev (Ukraine); Kondrin, Mikhail V. [Vereshchagin Institute of High Pressure Physics of RAS, 142190, Troitsk, Moscow (Russian Federation); Kuznetsov, Alexey V.; Sannikov, Ilia I. [National Research Nuclear University ' ' MEPhI' ' , Kashirskoe Shosse 31, 115409, Moscow (Russian Federation)

2016-04-15

We report the study of transport and magnetic properties of the YbB{sub 6-δ}single crystals grown by inductive zone melting. A strong disparity in the low temperature resistivity, Seebeck and Hall coefficients is established for the samples with the different level of boron deficiency. The effective parameters of the charge transport in YbB{sub 6-δ} are shown to depend on the concentration of intrinsic defects, which is estimated to range from 0.09% to 0.6%. The pronounced variation of Hall mobility μ{sub H} found for bulk holes is induced by the decrease of transport relaxation time from τ ∼ 7.7 fs for YbB{sub 5.994} to τ ∼ 2.2 fs for YbB{sub 5.96}. An extra contribution to conductivity from electrons with μ{sub H}∼ -1000 cm{sup 2} V{sup -1} s{sup -1} and the very low concentration n /n{sub Yb}∼ 10{sup -6} discovered below 20 K for all the single crystals under investigation is suggested to arise from the surface electron states appeared in the inversion layer due to the band bending. (copyright 2016 WILEY-VCH Verlag GmbH and Co. KGaA, Weinheim)

YB-1 facilitates basal and 5-fluorouracil-inducible expression of the human major vault protein (MVP) gene.

Science.gov (United States)

Stein, Ulrike; Bergmann, Stephan; Scheffer, George L; Scheper, Rik J; Royer, Hans-Dieter; Schlag, Peter M; Walther, Wolfgang

2005-05-19

Vaults have been suggested to play a direct role in multidrug resistance (MDR) to anticancer drugs. The human major vault protein (MVP) also known as lung resistance-related protein (LRP) represents the predominant component of vaults that may be involved in the defense against xenobiotics. Here, we demonstrate that besides MDR-related cytostatics, also the non-MDR-related drug 5-fluorouracil (5-FU) was able to induce MVP mRNA and protein expression. Treatment with 5-FU amplified the binding activity and interaction of the transcription factor Y-box binding protein-1 (YB-1) with the Y-box of the human MVP gene promoter in a time-dependent manner. 5-FU also induced reporter expressions driven by a panel of newly generated MVP promoter deletion mutants. Interestingly, stably YB-1 overexpressing cell clones showed enhanced binding of YB-1 to the Y-box motif, associated with enhanced basal as well as 5-FU-inducible MVP promoter-driven reporter expressions. Moreover, transduction of YB-1 cDNA led to increased expression of endogenous MVP protein. Under physiological conditions, we observed a strong coexpression of MVP and YB-1 in human colon carcinoma specimen. In summary, our data demonstrate a direct involvement of YB-1 in controlling basal and 5-FU-induced MVP promoter activity. Therefore, YB-1 is directly linked to MVP-mediated drug resistance.

Resonance transition array of Yb IV

International Nuclear Information System (INIS)

Kaufman, V.; Sugar, J.

1976-01-01

Nineteen pairs of lines in the wavelength range of 800--1300 A were identified as transitions to the two levels of the ground term of Yb IV, 4f 13 2 F. The 2 F 5 / 2 -- 2 F 7 / 2 interval is 10 214.0 cm -1 with an rms deviation of 0.4 cm -1

Preparation and characteristics of various rare earth nitrides

International Nuclear Information System (INIS)

Imamura, H.; Imahashi, T.; Zaimi, M.; Sakata, Y.

2008-01-01

Active nanocrystalline nitrides of EuN and YbN with high surface areas were successfully prepared by the thermal decomposition of the rare earth amides (Eu(NH 2 ) 2 , Yb(NH 2 ) 2 and Yb(NH 2 ) 3 ). For the preparation of CeN, PrN and NdN, the direct reaction of the rare earth metals with ammonia was extensively studied to determine optimal conditions. In the reaction of rare earth metals with ammonia, hydrides besides the nitrides were competitively formed. The reaction conditions such as temperatures and ratios of ammonia to rare earth metal were crucial in preferential formation of nitride. The nanocrystalline YbN and EuN readily absorbed large amounts of ammonia even at room temperature upon contact with ammonia (13.3 kPa). The absorbed ammonia existed in at least two forms on/in the nitride; the one was surface-adsorbed ammonia and the other ammonia absorbed in the nitride in a decomposed state. The properties of ammonia absorbed by the nitride were further evaluated by temperature-programmed desorption (TPD), FT-IR and XRD techniques

Guided mode gain competition in Yb-doped rod-type photonic crystal fibers

DEFF Research Database (Denmark)

Poli, Federica; Passaro, Davide; Cucinotta, Annamaria

2009-01-01

The gain competition among the guided modes in Yb-doped rod-type photonic crystal fibers with a low refractive index core is investigated with a spatial model to demonstrate the fiber effective single-mode behaviour.......The gain competition among the guided modes in Yb-doped rod-type photonic crystal fibers with a low refractive index core is investigated with a spatial model to demonstrate the fiber effective single-mode behaviour....

Radio metal (169Yb) uptake in normal and tumour cells in vitro. Influence of metabolic cell activity and complex structure

International Nuclear Information System (INIS)

Franke, W.G.; Kampf, G.

1996-01-01

Trivalent radio metal tracers have been used for tumour imaging and metastatic pain palliation. For better understanding their tumour accumulation, basic model studies of uptake of different 169 Yb complexes into cultured normal and tumour cells were performed. Whereas the uptake of 169 Yb citrate is strongly dependent on the metabolic activity and is not tumour-cell pacific, the uptake of 169 Yb complexed with amino carbonic acid (NTA, EDTA, DTPA) does not correlate to the metabolic activities. These complexes are taken up to a greater amount by the tumour cells (by a factor of about 2). Uptake of both complex types leads to a stable association to cellular compounds, 169 Yb is not releasable by the strong complexing agent DTPA. Protein binding of the 169 Yb complexes shows great influence on their cellular uptake. The bound proportion is no more available,for cellular uptake. The results indicate that i 0 uptake of 169 Yb citrate is an active cellular transport process which i not tumor-specific, ii) the 169 Yb amino carbonic acid complexes show a weak favouring by the tumour cells, iii) different from earlier acceptions the Yb complexes studied are not taken up by the cells in protein-bound form. The structure of the Yb complex is decisive for its protein binding and cellular uptake. (author). 13 refs., 6 figs

Photoluminescence study of Sm{sup 3+}–Yb{sup 3+}co-doped tellurite glass embedding silver nanoparticles

Energy Technology Data Exchange (ETDEWEB)

Reza Dousti, M., E-mail: mrdousti@ifsc.usp.br [Laboratório de Espectroscopia de Materiais Funcionais (LEMAF), Instituto de Fisica de São Carlos, Universidade de São Paulo, Av. Trabalhador So-carlense 400, São Carlos, SP 13566-590 (Brazil); Department of Physics, Tehran-North Branch, Islamic Azad University Tehran (Iran, Islamic Republic of); Department of Physics, Faculty of Science, Universiti Teknologi Malaysia, Skudai 81310, Johor (Malaysia); Amjad, R.J. [Department of Physics, Faculty of Science, Universiti Teknologi Malaysia, Skudai 81310, Johor (Malaysia); Department of Physics, COMSATS Institute of Information Technology, Lahore 54000 (Pakistan); Hosseinian S, R.; Salehi, M.; Sahar, M.R. [Department of Physics, Faculty of Science, Universiti Teknologi Malaysia, Skudai 81310, Johor (Malaysia)

2015-03-15

We report on the upconversion emission of Sm{sup 3+} ions doped tellurite glass in the presence of Yb{sup 3+} ions and silver nanoparticles. The enhancement of infrared-to-visible upconversion emissions is achieved under 980 nm excitation wavelength and attributed to the high absorption cross section of Yb{sup 3+} ions and an efficient energy transfer to Sm{sup 3+} ions. Further enhancements are attributed to the plasmonic effect via metallic nanoparticles resulting in the large localized field around rare earth ions. However, under excitation at 406 nm, the addition of Yb{sup 3+} content and heat-treated silver nanoparticles quench the luminescence of Sm{sup 3+} ions likely due to quantum cutting and plasmonic diluent effects, respectively. - Highlights: • Sm{sup 3+} tellurite glasses co-doped with Yb{sup 3+} ions and tri-doped with Yb{sup 3+}:Ag NPs were prepared. • In first step, Yb{sup 3+} ions enhanced the upconversion emissions of Sm{sup 3+} doped samples. • In second step, Ag NPs further enhanced the upconversion emissions in tri-doped glasses. • Finally, the quench in luminescence under 406 nm excitation is observed and discussed.

Spin re-orientation in heavy fermion system α - YbAl1 - x FexB4

Science.gov (United States)

Wu, Shan; Broholm, C.; Kuga, K.; Suzuki, Shintaro; Nakatsuji, S.; Mourigal, M.; Stone, M.; Tian, Wei; Qiu, Y.; Rodriguez-Rivera, Jose

Non centro-symmetric α - YbAlB4 has a heavy Fermi liquid ground state and shares many characteristics with centro-symmetric β - YbAlB4 . Both isomorphs display intermediate valence, associated with a fluctuation scale of T0 = 200 K and a Kondo lattice scale of T* = 8 K. Unlike β - YbAlB4 , α - YbAlB4 is at the boundary of a transition from a Fermi liquid metallic state to an antiferromagnetic (AFM) insulating state, driven by Fe substitution of Al. Magnetization and specific heat measurements reveal two different antiferromagnetic phases with TN = 9 K and TN = 2 K for Fe concentration above and below x =0.07. We report single crystal neutron scattering experiments on Fe doped YbAlB4 with x =0.035 and x =0.125. While the ordering wave vector is identical, k -> = (1 , 0 , 0) , the spin orientation switches from c to a with increasing Fe concentration. This suggests different anisotropic hybridization between 4f and conduction electrons that we confirmed by determining the crystal field levels. Supported by DOE, BES through DE-FG02-08ER46544.

Exploring strategies for the production of ultracold RbYb molecules in conservative traps

Energy Technology Data Exchange (ETDEWEB)

Bruni, Cristian

2015-07-14

Within the scope of this thesis, the production of ultracold molecules at a temperature of a few μK with various isotopes of rubidium (Rb) and ytterbium (Yb) was examined by means of photoassociation spectroscopy and magnetic Feshbach resonances in combined conservative traps. The long-term goal of this experiment is the production of ultracold RbYb molecules in the rovibronic ground state. It was possible to produce electronically excited {sup 87}Rb {sup 176}Yb molecules in a novel hybrid trap (HT) at a combined temperature of 1.7 μK by means of 1-photon photoassociation close to the Rb D1 line at 795 nm. This HT takes advantage of the different magnetic properties of Rb and Yb and allows for independent trapping and manipulation of the atomic species. It combines an Ioffe-Pritchard type magnetic trap for Rb and a near-resonant optical dipole trap for Yb. The excited molecular {sup 2}Π{sub 1/2} state could be characterized further extending previous works in a combined MOT and vibrational levels reaching binding energies up to E{sub b}=-h x 2.2 THz could be assigned by trap-loss spectroscopy. Almost every detected vibrational state consists of two resonances that could be assigned to the molecular analogue of the hyperfine structure of {sup 87}Rb. An important experimental observation is a decrease in hyperfine splitting with increasing binding energy of a vibrational level. For the deepest found vibrational state the hyperfine splitting amounts only 70 % of the atomic value (817 MHz) which emphasizes a gradual passage from weakly to tightly bound molecules. Furthermore, detailed attempts were undertaken to induce magnetic Feshbach resonances in {sup 85}Rb and different Yb isotopes, especially {sup 171}Yb in a crossed optical dipole trap at 1064 nm at temperatures of 10 μK. For this purpose, a homogeneous magnetic field was applied and scanned in small steps over the range of 495 G ∼ 640 G. Unfortunately, our efforts were without success. Additionally, well

Overview of Nintendo WiiTM use and potential applications for the Microsoft KinectTM in residential facilities