CMG helicase and DNA polymerase ε form a functional 15-subunit holoenzyme for eukaryotic leading-strand DNA replication.

Science.gov (United States)

Langston, Lance D; Zhang, Dan; Yurieva, Olga; Georgescu, Roxana E; Finkelstein, Jeff; Yao, Nina Y; Indiani, Chiara; O'Donnell, Mike E

2014-10-28

DNA replication in eukaryotes is asymmetric, with separate DNA polymerases (Pol) dedicated to bulk synthesis of the leading and lagging strands. Pol α/primase initiates primers on both strands that are extended by Pol ε on the leading strand and by Pol δ on the lagging strand. The CMG (Cdc45-MCM-GINS) helicase surrounds the leading strand and is proposed to recruit Pol ε for leading-strand synthesis, but to date a direct interaction between CMG and Pol ε has not been demonstrated. While purifying CMG helicase overexpressed in yeast, we detected a functional complex between CMG and native Pol ε. Using pure CMG and Pol ε, we reconstituted a stable 15-subunit CMG-Pol ε complex and showed that it is a functional polymerase-helicase on a model replication fork in vitro. On its own, the Pol2 catalytic subunit of Pol ε is inefficient in CMG-dependent replication, but addition of the Dpb2 protein subunit of Pol ε, known to bind the Psf1 protein subunit of CMG, allows stable synthesis with CMG. Dpb2 does not affect Pol δ function with CMG, and thus we propose that the connection between Dpb2 and CMG helps to stabilize Pol ε on the leading strand as part of a 15-subunit leading-strand holoenzyme we refer to as CMGE. Direct binding between Pol ε and CMG provides an explanation for specific targeting of Pol ε to the leading strand and provides clear mechanistic evidence for how strand asymmetry is maintained in eukaryotes.

Energy transfer and downconversion near-infrared material of Tb{sup 3+} and Yb{sup 3+} doped Ca{sub 5}(BO{sub 3}){sub 3}F

Energy Technology Data Exchange (ETDEWEB)

Hou, Dejian; Li, Jin-Yan [School of Metallurgy and Chemistry Engineering, Jiangxi University of Science and Technology, Ganzhou 341000, Jiangxi (China); Lin, Huihong, E-mail: linhh@hstc.edu.cn [School of Chemical and Environmental Engineering, Hanshan Normal University, Chaozhou 521041, Guangdong (China); Zhang, Jingxiang [School of Chemical and Environmental Engineering, Hanshan Normal University, Chaozhou 521041, Guangdong (China)

2016-11-01

Yb{sup 3+} and Tb{sup 3+} singly doped and Tb{sup 3+}–Yb{sup 3+} co-doped Ca{sub 5}(BO{sub 3}){sub 3}F phosphors were prepared by a solid state reaction method. The luminescence emission and excitation spectra as well as the luminescence decay curves were investigated. The emission bands of Yb{sup 3+} ion are located around 1000 nm, matching well with the optimal response of Si-based solar cells. Tb{sup 3+} can be a sensitizer for Yb{sup 3+} in the host. The energy transfer from Tb{sup 3+} to Yb{sup 3+} was investigated, the energy transfer mechanism was proposed as cooperative energy transfer. Tb{sup 3+} concentration dependent quantum efficiency was calculated and the maximum efficiency approached 115.5%.

The influence of dose on the kinetic parameters and dosimetric features of the main thermoluminescence glow peak in α-Al{sub 2}O{sub 3}:C,Mg

Energy Technology Data Exchange (ETDEWEB)

Kalita, J.M.; Chithambo, M.L., E-mail: m.chithambo@ru.ac.za

2017-03-01

Highlights: • Influence of dose on thermoluminescence features of α-Al{sub 2}O{sub 3}:C,Mg have been studied. • Kinetic parameters of the main peak are independent of dose (0.1–100 Gy). • Dose response of the main peak: 0.1–30 Gy, superlinear; 30–100 Gy, sublinear. • Fading of the main peak: ∼22% within 2400 s. • Reproducibility: coefficient of variation in the results of 10 re-cycles: >0.071%. - Abstract: The influence of dose (0.1–100 Gy) on the kinetic parameters and the dosimetric features of the main glow peak of α-Al{sub 2}O{sub 3}:C,Mg have been investigated. Thermoluminescence (TL) measured at 1 °C/s shows a very high intensity glow peak at 161 °C and six secondary peaks at 42, 72, 193, 279, 330, 370 °C respectively. Analysis shows that the main peak follows first order kinetics irrespective of the irradiation dose. The activation energy is found to be consistent at 1.37 eV and the frequency factor is of the order of 10{sup 14} s{sup −1} for any dose between 0.1 and 100 Gy. Further, the analysis for thermal quenching of the main peak of 0.1 Gy irradiated sample shows that the activation energy for thermal quenching is (0.94 ± 0.04) eV. Regarding the dosimetric features of α-Al{sub 2}O{sub 3}:C,Mg, the dose response of the main peak is superlinear within 0.1 to 30 Gy of beta dose and then it becomes sublinear up to 100 Gy. Fading analysis shows that the intensity of the main peak drops to ∼22% of its initial value within 2400 s after irradiation and thereafter to ∼14% within 64,800 s. Analysis of the reproducibility shows that the coefficient of variation in the results for 10 identical TL measurements show that reproducibility improves with increase in dose.

Luminescence Properties of Ca19Ce(PO4)14:A (A = Eu3+/Tb3+/Mn2+) Phosphors with Abundant Colors: Abnormal Coexistence of Ce4+/3+-Eu3+ and Energy Transfer of Ce3+ → Tb3+/Mn2+ and Tb3+-Mn2.

Science.gov (United States)

Shang, Mengmeng; Liang, Sisi; Lian, Hongzhou; Lin, Jun

2017-06-05

A series of Eu 3+ /Tb 3+ /Mn 2+ -ion-doped Ca 19 Ce(PO 4 ) 14 (CCPO) phosphors have been prepared via the conventional high-temperature solid-state reaction process. Under UV radiation, the CCPO host presents a broad blue emission band from Ce 3+ ions, which are generated during the preparation process because of the formation of deficiency. The Eu 3+ -doped CCPO phosphors can exhibit magenta to red-orange emission as a result of the abnormal coexistence of Ce 3+ /Ce 4+ /Eu 3+ and the metal-metal charge-transfer (MMCT) effect between Ce 3+ and Eu 3+ . When Tb 3+ /Mn 2+ are doped into the hosts, the samples excited with 300 nm UV light present multicolor emissions due to energy transfer (ET) from the host (Ce 3+ ) to the activators with increasing activator concentrations. The emitting colors of CCPO:Tb 3+ phosphors can be tuned from blue to green, and the CCPO:Mn 2+ phosphors can emit red light. The ET mechanism from the host (Ce 3+ ) to Tb 3+ /Mn 2+ is demonstrated to be a dipole-quadrapole interaction for Ce 3+ → Tb 3+ and an exchange interaction for Ce 3+ → Mn 2+ in CCPO:Tb 3+ /Mn 2+ . Abundant emission colors containing white emission were obtained in the Tb 3+ - and Mn 2+ -codoped CCPO phosphors through control of the levels of doped Tb 3+ and Mn 2+ ions. The white-emitted CCPO:Tb 3+ /Mn 2+ phosphor exhibited excellent thermal stability. The photoluminescence properties have shown that these materials might have potential for UV-pumped white-light-emitting diodes.

Synthesis and crystal structure of terbium(III) meta-oxoborate Tb(BO{sub 2}){sub 3} ({identical_to} TbB{sub 3}O{sub 6}); Synthese und Kristallstruktur von Terbium(III)-meta-Oxoborat Tb(BO{sub 2}){sub 3} ({identical_to} TbB{sub 3}O{sub 6})

Energy Technology Data Exchange (ETDEWEB)

Nikelski, Tanja; Schleid, Thomas [Institut fuer Anorganische Chemie der Universitaet Stuttgart (Germany)

2003-06-01

The terbium meta-oxoborate Tb(BO{sub 2}){sub 3} ({identical_to} TbB{sub 3}O{sub 6}) is obtained as single crystals by the reaction of terbium, Tb{sub 4}O{sub 7} and TbCl{sub 3} with an excess of B{sub 2}O{sub 3} in gastight sealed platinum ampoules at 950 C after three weeks. The compound appears to be air- and water-resistant and crystallizes as long, thin, colourless needles which tend to growth-twinning due to their marked fibrous habit. The crystal structure of Tb(BO{sub 2}){sub 3} (orthorhombic, Pnma; a = 1598.97(9), b = 741.39(4), c = 1229.58(7) pm; Z = 16) contains strongly corrugated oxoborate layers {sub {infinity}}{sup 2}{l_brace}(BO{sub 2}){sup -}{r_brace} built of vertex-linked [BO{sub 4}]{sup 5-} tetrahedra (d(B-O) = 143 - 154 pm, and angsph;(O-B-O) = 102-115 ) which spread out parallel (100). The four crystallographically different Tb{sup 3+} cations all exhibit coordination numbers of eight towards the oxygen atoms (d(Tb-O) = 228-287 pm). The corresponding metal cation polyhedra [TbO{sub 8}]{sup 13+} too convene to layers (composition: {sub {infinity}}{sup 2}{l_brace}(Tb{sub 2}O{sub 11}){sup 16-}{r_brace}) which are likewise oriented parallel to the (100) plane. (Abstract Copyright [2003], Wiley Periodicals, Inc.) [German] Das Terbium-meta-Oxoborat Tb(BO{sub 2}){sub 3} ({identical_to} TbB{sub 3}O{sub 6}) entsteht einkristallin bei der Reaktion von Terbium, Tb{sub 4}O{sub 7} und TbCl{sub 3} mit einem Ueberschuss von B{sub 2}O{sub 3} in gasdicht verschlossenen Platinampullen nach drei Wochen bei 950 C. Die Verbindung ist luft- und wasserstabil und faellt in langen, duennen, farblosen Nadeln an, die aufgrund ihres ausgepraegt faserigen Habitus zur Wachstumsverzwillingung neigen. Die Kristallstruktur von Tb(BO{sub 2}){sub 3} (orthorhombisch, Pnma; a = 1598, 97(9), b = 741, 39(4), c = 1229, 58(7) pm; Z = 16) enthaelt parallel (100) verlaufende, stark gewellte Oxoborat-Schichten {sub {infinity}}{sup 2}{l_brace}(BO{sub 2}){sup -}{r_brace} aus

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

International Nuclear Information System (INIS)

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

2008-01-01

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

Lithium-aluminum-zinc phosphate glasses activated with Tb3+ and Tb3+/Eu3+ for green laser medium, reddish-orange and white phosphor applications

Science.gov (United States)

Francisco-Rodriguez, H. I.; Lira, A.; Soriano-Romero, O.; Meza-Rocha, A. N.; Bordignon, S.; Speghini, A.; Lozada-Morales, R.; Caldiño, U.

2018-05-01

A spectroscopic analysis of Tb3+ and Tb3+/Eu3+ doped lithium-aluminum-zinc phosphate glasses is performed through their absorbance and photoluminescence spectra, and decay time profiles. Laser parameter values (stimulated emission cross section, effective bandwidth, gain bandwidth and optical gain) were obtained for the terbium 5D4 → 7F5 green emission from the Tb3+ singly-doped glass (LAZT) excited at 350 nm to judge the suitability of the glass phosphor for fiber lasers. A quantum yield of (47.68 ± 0.49)% was measured for the 5D4 level luminescence. Upon 350 nm excitation the LAZT glass phosphor emits green light with a color purity of 65.6% and chromaticity coordinates (0.285, 0.585) very close to those (0.29, 0.60) of European Broadcasting Union illuminant green. The Tb3+/Eu3+codoped glass emission color can be tuned from reddish-orange of 1865 K upon 318 nm excitation to warm white of 3599 K and neutral white of 4049 K upon 359 and 340 nm excitations, respectively. Upon Tb3+ excitation at 340 nm Eu3+ is sensitized by Tb3+ through a non-radiative energy transfer with an efficiency of 0.23-0.26. An electric dipole-dipole interaction might be the dominant mechanism in the Tb3+ to Eu3+ energy transfer taking place into Tb3+ - Eu3+ clusters.

Factors that influence length of stay for in-patient gynaecology surgery: is the Case Mix Group (CMG) or type of procedure more important?

Science.gov (United States)

Carey, Mark S; Victory, Rahi; Stitt, Larry; Tsang, Nicole

2006-02-01

To compare the association between the Case Mix Group (CMG) code and length of stay (LOS) with the association between the type of procedure and LOS in patients admitted for gynaecology surgery. We examined the records of women admitted for surgery in CMG 579 (major uterine/adnexal procedure, no malignancy) or 577 (major surgery ovary/adnexa with malignancy) between April 1997 and March 1999. Factors thought to influence LOS included age, weight, American Society of Anesthesiologists (ASA) score, physician, day of the week on which surgery was performed, and procedure type. Procedures were divided into six categories, four for CMG 579 and two for CMG 577. Data were abstracted from the hospital information costing system (T2 system) and by retrospective chart review. Multivariable analysis was performed using linear regression with backwards elimination. There were 606 patients in CMG 579 and 101 patients in CMG 577, and the corresponding median LOS was four days (range 1-19) for CMG 579 and nine days (range 3-30) for CMG 577. Combined analysis of both CMGs 577 and 579 revealed the following factors as highly significant determinants of LOS: procedure, age, physician, and ASA score. Although confounded by procedure type, the CMG did not significantly account for differences in LOS in the model if procedure was considered. Pairwise comparisons of procedure categories were all found to be statistically significant, even when controlled for other important variables. The type of procedure better accounts for differences in LOS by describing six statistically distinct procedure groups rather than the traditional two CMGs. It is reasonable therefore to consider changing the current CMG codes for gynaecology to a classification based on the type of procedure.

Direct two-photon excitation of Sm3+, Eu3+, Tb3+, Tb.DOTA-, and Tb.propargylDO3A in solution

Science.gov (United States)

Sørensen, Thomas Just; Blackburn, Octavia A.; Tropiano, Manuel; Faulkner, Stephen

2012-07-01

We have observed direct two-photon excitation of samarium, europium and terbium ions in solution upon near IR excitation using a tuneable pulsed light source, and have also studied two-photon processes in a pair of related terbium complexes, namely [Tb.DOTA]- and Tb.propargylDO3A. Direct two-photon excitation of lanthanides is observed in simple systems in the absence of sensitizing chromophores. Where even simple chromophores such as a triple bond are present in the complex, then single and two-photon excitation of chromophore excited states competes with direct two-photon excitation of the ions and is the dominant pathway for sensitizing formation of the lanthanide excited state.

Effects of Tb{sup 3+} concentration on the La{sub 2}Sr{sub 3}(BO{sub 3}){sub 4}: X% Tb{sup 3+} polycrystalline nanophosphor

Energy Technology Data Exchange (ETDEWEB)

Mlotswa, D.V. [Physics Department, University of the Free State, Private Bag x13, Phuthaditjhaba 9866 (South Africa); Madihlaba, R.M. [Chemistry Department, University of the Western Cape, Private Bag x17, Bellville 7535 (South Africa); Koao, L.F. [Physics Department, University of the Free State, Private Bag x13, Phuthaditjhaba 9866 (South Africa); Onani, M.O., E-mail: monani@uwc.ac.za [Chemistry Department, University of the Western Cape, Private Bag x17, Bellville 7535 (South Africa); Dejene, F.B. [Physics Department, University of the Free State, Private Bag x13, Phuthaditjhaba 9866 (South Africa)

2016-01-01

A new green phosphor, La{sub 2}Sr{sub 3}(BO{sub 3}){sub 4}): x% Tb{sup 3+} was fabricated by solution-combustion method using urea as a fuel and ammonium nitrate as an oxidizer. The phosphor was characterised using Fourier transform infrared spectroscopy (FTIR), Thermogravimetric analysis (TGA), Differential scanning calorimetry (DSC), Energy dispersive spectroscopy, X-ray diffraction (XRD), scanning electron microscopy (SEM) and photoluminescence spectroscopy (PL. The results exhibit that La{sub 2}Sr{sub 3}(BO{sub 3}){sub 4}): x% Tb{sup 3+} phosphor has the strongest excitation at 209 nm with a full-width at half-maximum (FWHM) of 20 nm, and can emit bright green light at 545 nm under 209 nm excitation. The optimum concentration for Tb{sup 3+} in La{sub 2}Sr{sub 3}(BO{sub 3}){sub 4}): x% Tb{sup 3+} is 0.033 mol%. The prominent green luminescence was due to the {sup 5}D{sub 4}–{sup 7}F{sub 5} transition of Tb{sup 3+} ion. Herein, the green phosphors are promising good candidates employed in tri-color lamps.

Antigen-Specific Interferon-Gamma Responses and Innate Cytokine Balance in TB-IRIS

NARCIS (Netherlands)

Goovaerts, Odin; Jennes, Wim; Massinga-Loembé, Marguerite; Ceulemans, Ann; Worodria, William; Mayanja-Kizza, Harriet; Colebunders, Robert; Kestens, Luc; Loembé, Marguerite Massinga; Mayanja, Harriet; Mascart, Francoise; van den Bergh, Rafael; Locht, Camille; Reiss, Peter; Cobelens, Frank; Ondoa, Pascale; Pakker, Nadine; Mugerwa, Roy

2014-01-01

Background: Tuberculosis-associated immune reconstitution inflammatory syndrome (TB-IRIS) remains a poorly understood complication in HIV-TB patients receiving antiretroviral therapy (ART). TB-IRIS could be associated with an exaggerated immune response to TB-antigens. We compared the recovery of

Tb3O2Cl[SeO3]2 and Tb5O4Cl3[SeO3]2: Oxide Chloride Oxoselenates(IV) of Trivalent Terbium with ''Lone-Pair'' Channel or Layer Structures

International Nuclear Information System (INIS)

Wontcheu, Joseph; Schleid, Thomas

2005-01-01

Orthorhombic Tb 3 O 2 Cl[SeO 3 ] 2 (Pnma; a = 535.16(4), b = 1530.51(9), c = 1081.72(7) pm; Z = 4) is formed by reacting a stoichiometric mixture of Tb 4 O 7 , Tb, TbCl 3 , and SeO 2 in a suitable molar ratio (12: 8: 7: 42) within seven days in an evacuated sealed silica tube at 850 C. The needle-shaped, colourless single crystals (light, water and air stable) exhibit one-dimensional strands [(Tb1) 3/3 (Tb2) 2/1 O 4/2 ] 5+ [O 2 Tb 3 ] 5+ along [100] formed by two parallel chains [OTb 4/2 ] 4+ of trans-edge connected [OTb 4 ] 10+ tetrahedra (d(O-Tb) = 220 - 231 pm) which share an extra edge per chain link. The crystal structure contains two crystallographically different Tb 3+ cations: Tb1 is coordinated as bicapped trigonal prism, while Tb2 resides in square antiprismatic coordination. The Se 4+ coordination is best described as Ψ 1 tetrahedral ([SeO 3 E] 2- ; E: non-binding electron pair). The non-binding ''lone-pair'' electrons of four [SeO 3 ] 2- groups and two Cl - anions form pseudo-hexagonal empty channels along [100] between four cationic double chains. Tb 5 O 4 Cl 3 [SeO 3 ] 2 was prepared likewise as plate-like, colourless single crystals by solid-state reaction of an admixture of Tb 4 O 7 , Tb, TbOCl, TbCl 3 , and SeO 2 (molar ratio: 9: 6: 21: 7: 28) in an evacuated sealed silica tube during seven days at 850 C. This compound crystallizes in the monoclinic system (C2/m; a = 1229.13(9), b = 546.17(4), c = 978.79(7) pm, β = 90.485(6) ; Z = 2) and contains three crystallographically different Tb 3+ cations in seven- and eightfold coordination of O 2- and Cl - anions, respectively. The crystal structure of Tb 5 O 4 Cl 3 [SeO 3 ] 2 is layered and built up of corrugated terbium-oxygen sheets [O 4 Tb 5 ] 7+ formed by edge- and vertex-shared [OTb 4 ] 10+ tetrahedra (d(O-Tb) = 226-232 pm) spreading parallel (001). The structure is strongly related to the ''lone-pair'' channel structures of Tb 2 O[SeO 3 ] 2 and Tb 3 O 2 Cl[SeO 3 ] 2 , where single ([OTb 2 ] 4

Luminescence properties and energy transfer investigations of Sr_3Lu(PO_4)_3:Ce"3"+, Tb"3"+ phosphors

International Nuclear Information System (INIS)

Yang, Zaifa; Xu, Denghui; Sun, Jiayue; Du, Jiangnan; Gao, Xuedong

2016-01-01

Highlights: • A phosphor Sr_3Lu(PO_4)_3:Ce"3"+, Tb"3"+ for UV-based white LEDs was firstly synthesized successfully. • The phase structure and photoluminescence properties of samples were studied in detail. • The energy transfer process from Ce"3"+ to Tb"3"+ ions was illustrated in detail. • Sr_3Lu(PO_4)_3:Ce"3"+, Tb"3"+ phosphor has potential applications as an UV-convertible phosphor for white light emitting diodes. - Abstract: A series of Ce"3"+ or Tb"3"+ doped and Ce"3"+/Tb"3"+ co-doped Sr_3Lu(PO_4)_3 phosphors were prepared via the conventional high temperature solid-state reaction. The phase structure, photoluminescence and energy transfer properties of samples were studied in detail. The optimal proportion of Ce"3"+ single doping is 4 mol% with maximal fluorescence intensity. The Sr_3Lu(PO_4)_3:Ce"3"+, Tb"3"+ phosphor shows both a blue emission (428 nm) from Ce"3"+ and a yellowish-green emission (545 nm) from Tb"3"+ with considerable intensity under ultraviolet (UV) excitation (268 nm). The energy transfer from Ce"3"+ to Tb"3"+ ions takes place in the Sr_3Lu(PO_4)_3:Ce"3"+, Tb"3"+ phosphor on the basis of the analysis of the luminescence spectra. The energy transfer mechanism from Ce"3"+ to Tb"3"+ ions was proved to be dipole–dipole interaction. The energy transfer behaviors in Sr_3Lu(PO_4)_3:Ce"3"+, Tb"3"+ phosphor is also investigated by the lifetime measurement. The results show that this phosphor has potential applications for UV white-light LEDs.

Crystal structure of CsTb(PO3)4 compound

International Nuclear Information System (INIS)

Palkina, K.K.; Maksimova, S.I.; Kuznetsov, V.G.; Chibiskova, N.T.

1978-01-01

The X-ray structural study of compounds of the CsLn(PO 3 ) 4 series has been made. Found is the presence of two structural types for CsPr(PO 3 ) 4 (cubic and monoclinic modifications), one type for CsNd(PO 3 ) 4 (cubic modification) and for CsTb(PO 3 ) 4 (monoclinic modification). For the CsTb(PO 3 ) 4 monocrystal the lattice parameters are determined: a=7.032 +- 0.001; b=8.705 +- 0.001; c=9.051 +- 0.001 A; α=90 deg, β=90 deg, γ=100 deg, Z=2, V=545.68 A 3 , dsub(exp)=3.70 g/cm 3 . The structure character is presented as infinite chains of (PO 4 ) tetrahedrons, stretched along the ''C'' period. Tb and Cs atoms are rounded by 8 atoms of oxygen. Tb polyhedron are irregular octaapexes or strongly deformed tetragonal antiprisms. Tb-Tb shortest distance is 6.59 A

Magnetic ordering of Hf{sub 3}Ni{sub 2}Si{sub 3}-type {Sm, Tb, Er}{sub 3}Co{sub 2}Ge{sub 3} and {Tb, Ho}{sub 3}Ni{sub 2}Ge{sub 3} compounds

Energy Technology Data Exchange (ETDEWEB)

Morozkin, A.V., E-mail: morozkin@tech.chem.msu.ru [Department of Chemistry, Moscow State University, Leninskie Gory, House 1, Building 3, Moscow, GSP-1, 119991 (Russian Federation); Yapaskurt, V.O. [Department of Petrology, Geological Faculty Moscow State University, Leninskie Gory, Moscow 119991 (Russian Federation); Nirmala, R. [Indian Institute of Technology Madras, Chennai 600036 (India); Quezado, S.; Malik, S.K. [Departamento de Física Teórica e Experimental, Universidade Federal do Rio Grande do Norte, Natal 59082-970 (Brazil); Mozharivskyj, Y. [Department of Chemistry and Chemical Biology, McMaster University, 1280 Main Street West, Hamilton, Ontario, Canada L8S 4M1 (Canada); Isnard, O. [CNRS, Institut. Néel, 25 rue des Martyrs BP166 x, F-38042 Grenoble (France); Université Grenoble Alpes, Inst. Néel, F-38042 Grenoble (France)

2017-02-15

The magnetic ordering of Hf{sub 3}Ni{sub 2}Si{sub 3}-type {Sm, Tb, Er}{sub 3}Co{sub 2}Ge{sub 3} and {Tb, Ho}{sub 3}Ni{sub 2}Ge{sub 3} compounds (space group Cmcm, oC32) was investigated via magnetization measurements and neutron diffraction study in a zero-applied field. {Sm, Tb, Er}{sub 3}Co{sub 2}Ge{sub 3} and Ho{sub 3}Ni{sub 2}Ge{sub 3} exhibit field sensitive complex antiferromagnetic orderings with T{sub N}=51 K, T{sub m}=10 K for Sm{sub 3}Co{sub 2}Ge{sub 3}, T{sub N}=34 K, T{sub m}=13 K for Tb{sub 3}Co{sub 2}Ge{sub 3}, T{sub N}=7 K for Er{sub 3}Co{sub 2}Ge{sub 3} and T{sub N}=11 K for Ho{sub 3}Ni{sub 2}Ge{sub 3}. At 2 K and above the critical field of ~5 kOe, 20 kOe, 4 kOe and 7 kOe for Sm{sub 3}Co{sub 2}Ge{sub 3}, Tb{sub 3}Co{sub 2}Ge{sub 3}, Er{sub 3}Co{sub 2}Ge{sub 3} and Ho{sub 3}Ni{sub 2}Ge{sub 3}, respectively, saturation magnetizations per rare-earth atom are 6.5 μ{sub B} for Tb{sub 3}Co{sub 2}Ge{sub 3}, 7.0 μ{sub B} for Er{sub 3}Co{sub 2}Ge{sub 3} and 8.0 μ{sub B} for Ho{sub 3}Ni{sub 2}Ge{sub 3} in the field of 140 kOe, whereas magnetization of Sm{sub 3}Co{sub 2}Ge{sub 3} has an antiferromagnetic behaviour. The isothermal magnetic entropy change, ΔS{sub m}, indicates a field-induced ferromagnetic ordering in Sm{sub 3}Co{sub 2}Ge{sub 3}, Tb{sub 3}Co{sub 2}Ge3, Er{sub 3}Co{sub 2}Ge{sub 3} and Ho{sub 3}Ni{sub 2}Ge{sub 3} with a maximal ΔS{sub m} value of −10.9 J/kg K for Ho{sub 3}Ni{sub 2}Ge{sub 3} at 11 K for a field change of 50 kOe. In a zero-applied magnetic field, below T{sub N}=33 K and down to T{sub m}{sup ND}=15 K Tb{sub 3}Ni{sub 2}Ge{sub 3} shows an ac-antiferromagnetic ordering with the C2′/c magnetic space group, a K{sub 0}=[0, 0, 0] propagation vector and a a{sub Tb3Ni2Ge3}×b{sub Tb3Ni2Ge3}×c{sub Tb3Ni2Ge3} magnetic unit cell. Below T{sub m}{sup ND}=15 K, its magnetic structure is a sum of the ac-antiferromagnetic component with the C2′/c magnetic space group of the K{sub 0} vector and a sine-modulated a

Down-shifting by energy transfer in Tb{sup 3+}/Dy{sup 3+} co-doped zinc phosphate glasses

Energy Technology Data Exchange (ETDEWEB)

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

2015-05-15

An optical spectroscopy investigation of zinc phosphate glasses activated with Tb{sup 3+}/Dy{sup 3+} ions is carried out through photoluminescence spectra and decay time measurements. The emission color can be adjusted from yellow–green light, with CIE1931 chromaticity coordinates (0.36,0.44), toward the white light region (0.35,0.39) by decreasing the Tb{sup 3+} content from 1.0 to 0.1 mol% of Tb(PO{sub 3}){sub 3} upon Dy{sup 3+} excitation at 423 nm. Such visible region luminescence is generated by {sup 5}D{sub 4}→{sup 7}F{sub 5} and {sup 5}D{sub 4}→{sup 7}F{sub 3} emissions of Tb{sup 3+} in addition to {sup 4}I{sub 15/2}→{sup 6}H{sub 15/2}, {sup 4}F{sub 9/2}→{sup 6}H{sub 15/2}, {sup 4}F{sub 9/2}→{sup 6}H{sub 13/2} and {sup 4}F{sub 9/2}→{sup 6}H{sub 11/2} emissions of Dy{sup 3+}, so that Tb{sup 3+} emission is sensitized by Dy{sup 3+} through a non-radiative resonant energy transfer. A dominant {sup 5}D{sub 4}→{sup 7}F{sub 5} green emission is observed in detriment of the {sup 5}D{sub 3}→{sup 7}F{sub J} blue emissions upon 282 nm excitation, as well as an extended excitation range (280–500 nm), due to multiple Dy{sup 3+} and Tb{sup 3+} transitions, which might contribute to enhance the spectral response of solar photovoltaic cells by down-shifting of the incident solar spectrum. - Highlights: • Zn(PO{sub 3}){sub 2} glasses are optically activated with Tb{sup 3+}/Dy{sup 3+} (ZPTbDy). • Non-radiative resonant energy transfer takes place between Tb{sup 3+} and Dy{sup 3+}. • Luminescence can be adjusted from yellow–green light toward the white light region. • ZPTbDy phosphor exhibits spectroscopic properties for photovoltaic applications.

Pulmonary Immune-Compartment-Specific Interferon Gamma Responses in HIV-Infected Individuals with Active Tuberculosis (TB in an Area of High TB Prevalence

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S. Buldeo

2012-01-01

Full Text Available There is a paucity of data on the pulmonary immune-compartment interferon gamma (IFNγ response to M. tuberculosis, particularly in settings of high tuberculosis (TB prevalence and in HIV-coinfected individuals. This data is necessary to understand the diagnostic potential of commercially available interferon gamma release assays (IGRAs in both the pulmonary immune-compartment and peripheral blood. We used intracellular cytokine staining by flow cytometry to assess the IFNγ response to purified protein derivative (PPD and early secretory antigen 6 (ESAT6 in induced sputa (ISp and blood samples from HIV-infected, smear-negative, TB suspects. We found that individuals with active TB disease produced significantly less IFNγ in response to PPD in their induced sputa samples than individuals with non-active TB (control group. This difference was not reflected in the peripheral blood, even within the CD27− CD4+ memory T lymphocyte population. These findings suggest that progression to active TB disease may be associated with the loss of IFNγ secretion at the site of primary infection. Our findings highlight the importance of studying pulmonary immune-compartment M. tuberculosis specific responses to elucidate IFNγ secretion across the spectrum of TB disease.

The candidate TB vaccine, MVA85A, induces highly durable Th1 responses.

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Michele Tameris

Full Text Available Vaccination against tuberculosis (TB should provide long-term protective immunity against Mycobacterium tuberculosis (M.tb. The current TB vaccine, Bacille Calmette-Guerin (BCG, protects against disseminated childhood TB, but protection against lung TB in adolescents and adults is variable and mostly poor. One potential reason for the limited durability of protection may be waning of immunity through gradual attrition of BCG-induced T cells. We determined if a MVA85A viral-vector boost could enhance the durability of mycobacteria-specific T cell responses above those induced by BCG alone.We describe a long-term follow-up study of persons previously vaccinated with MVA85A. We performed a medical history and clinical examination, a tuberculin skin test and measured vaccine-specific T cell responses in persons previously enrolled as adults, adolescents, children or infants into three different Phase II trials, between 2005 and 2011.Of 252 potential participants, 183 (72.6% consented and completed the study visit. Vaccine-induced Ag85A-specific CD4+ T cell responses were remarkably persistent in healthy, HIV-uninfected adults, adolescents, children and infants, up to 6 years after MVA85A vaccination. Specific CD4+ T cells expressed surface markers consistent with either CD45RA-CCR7+ central memory or CD45RA-CCR7- effector memory T cells. Similarly durable Ag85A-specific CD4+ T cell responses were detected in HIV-infected persons who were on successful antiretroviral therapy when MVA85A was administered. By contrast, Ag85A-specific CD4+ T cell frequencies in untreated MVA85A-vaccinated HIV-infected persons were mostly undetectable 3-5 years after vaccination.MVA85A induces remarkably durable T cell responses in immunocompetent persons. However, results from a recent phase IIb trial of MVA85A, conducted in infants from the same geographic area and study population, showed no vaccine efficacy, suggesting that these durable T cell responses do not

Lu{sub 2}O{sub 3}:Tb,Hf storage phosphor

Energy Technology Data Exchange (ETDEWEB)

Kulesza, Dagmara; Trojan-Piegza, Joanna [Faculty of Chemistry, University of Wroclaw, 14 F. Joliot-Curie Street, 50-383 Wroclaw (Poland); Zych, Eugeniusz, E-mail: zych@wchuwr.p [Faculty of Chemistry, University of Wroclaw, 14 F. Joliot-Curie Street, 50-383 Wroclaw (Poland)

2010-03-15

Lu{sub 2}O{sub 3}:Tb,Hf ceramics containing 0.1% of Tb and 0-1.5% of Hf were prepared in reducing atmosphere at 1700 {sup o}C and their thermoluminescence properties were systematically studied. For comparison Tb,Ca co-doped specimen was also fabricated and investigated. The Tb,Hf ceramics shows basically a single TL band located around 180 {sup o}C as found with heating rate of 15 {sup o}C/min. Ceramics singly doped with Tb show complex TL glow curves indicating the presence of traps of very different depths. On the other hand Tb,Ca co-doping is beneficial for the development of shallow traps with the main TL band around 70 {sup o}C. Hence, the aliovalent impurities, Ca{sup 2+} and Hf{sup 4+}, strongly influenced the traps structure in Lu{sub 2}O{sub 3}:Tb ceramics, each of them in its own specific way. Isothermal decay of Lu{sub 2}O{sub 3}:Tb,Hf at 185 {sup o}C was recorded and its shape suggest that multiple hole trapping occurs in the Lu{sub 2}O{sub 3}:Tb,Hf ceramics. Due to the different traps depths the Lu{sub 2}O{sub 3}:Tb,Hf ceramics possess properties typical for storage phosphors, while Lu{sub 2}O{sub 3}:Tb,Ca is a persistent luminescent material rather.

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

International Nuclear Information System (INIS)

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

2016-01-01

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

Construction of Tb3+ PVC-MembraneElectrode Based on N,N’-Bis(pyrrolylmethylene-2-aminobenzylamine

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Hassan Ali Zamani

2011-01-01

Full Text Available In this work, we report as new Tb3+-PVC membrane sensor based on N,N’-bis(pyrrolylmethylene- 2-aminobenzylamine (PMA as a suitable ion carrier. Poly vinylchloride (PVC-based membrane composed of PMA with oleic acid (OA as anionic additives and acetophenone (AP as plasticizing solvent mediators. The Tb3+ sensor exhibits a Nernstian slope of 19.7±0.4 mV per decade over the concentration range of 1.0×10-5 to 1.0×10-2 M and a detection limit of 4.6×10-6 M of Tb3+ ions. The potentiometric response of the sensor is independent of the solution pH in the range of 2.9–8.1. It has a very short response time, in the whole concentration range (∼5 s. The recommended sensor revealed comparatively good selectivity with respect to most alkali, alkaline earth, some transition and heavy metal ions. It was successfully employed as an indicator electrode in the potentiometric titration of Tb(III ions with EDTA. The electrode was also employed for the determination of the fluoride ion in two mouth wash preparations and the determination of Tb3+ ions concentration in mixtures of three different ions.

Tb3+ and Eu3+ luminescence in imidazolium ionic liquids

International Nuclear Information System (INIS)

Hopkins, Todd; Goldey, Matt

2009-01-01

The luminescence properties of Tb 3+ and Eu 3+ dissolved in ionic liquids are studied. Solutes in this study include simple lanthanide compounds (e.g., EuBr 3 , TbCl 3 ) and lanthanide complexes (e.g., Eu(dpa) 3 3- where dpa = 2,6 pyridine dicarboxylate dianion) dissolved in a 1-butyl-3-methylimidazolium bromide(BMIBr)/water mixture. Emission, excitation, and time-resolved emission measurements are utilized to characterize the spectroscopic properties. It is well established in the literature that the solubility and spectroscopic properties of lanthanides in ionic liquids are highly dependent upon environmental factors including purity, and water content [K. Binnemans, Chemical Reviews (2007); I. Billard, S. Mekki, C. Gaillard, P. Hesemann, C. Mariet, G. Moutiers, A. Labet, J.-C.G. Buenzli, European Journal of Inorganic Chemistry 6 (2004) 1190-1197; S. Samikkanu, K. Mellem, M. Berry, P.S. May, Inorganic Chemistry 46 (2007) 7121-7128]. The water in this ionic liquid system acts as a co-solvent to facilitate solubility of Tb 3+ and Eu 3+ compounds. The observed spectroscopic properties of Eu 3+ and Tb 3+ salts are expectedly impacted by the high water content, but unexpectedly impacted by the BMIBr ionic liquid. However, the spectroscopy of Eu(dpa) 3 3- is unaffected by the presence of BMIBr.

Photoluminescence and Energy Transfer Properties with Y+SiO4 Substituting Ba+PO4 in Ba3Y(PO4)3:Ce(3+)/Tb(3+), Tb(3+)/Eu(3+) Phosphors for w-LEDs.

Science.gov (United States)

Li, Kai; Liang, Sisi; Shang, Mengmeng; Lian, Hongzhou; Lin, Jun

2016-08-01

A series of Ce(3+), Tb(3+), Eu(3+) doped Ba2Y2(PO4)2(SiO4) (BYSPO) phosphors were synthesized via the high-temperature solid-state reaction route. X-ray diffraction, high-resolution transmission electron microscopy, Fourier transform infrared, solid-state NMR, photoluminescence (PL) including temperature-dependent PL, and fluorescent decay measurements were conducted to characterize and analyze as-prepared samples. BYSPO was obtained by the substitution of Y+SiO4 for Ba+PO4 in Ba3Y(PO4)3 (BYPO). The red shift of PL emission from 375 to 401 nm occurs by comparing BYSPO:0.14Ce(3+) with BYPO:0.14Ce(3+) under 323 nm UV excitation. More importantly, the excitation edge can be extended from 350 to 400 nm, which makes it be excited by UV/n-UV chips (330-410 nm). Tunable emission color from blue to green can be observed under 365 nm UV excitation based on the energy transfer from Ce(3+) to Tb(3+) ions after codoping Tb(3+) into BYSPO:0.14Ce(3+). Moreover, energy transfer from Tb(3+) to Eu(3+) ions also can be found in BYSPO:Tb(3+),Eu(3+) phosphors, resulting in the tunable color from green to orange red upon 377 nm UV excitation. Energy transfer properties were demonstrated by overlap of excitation spectra, variations of emission spectra, and decay times. In addition, energy transfer mechanisms from Ce(3+) to Tb(3+) and Tb(3+) to Eu(3+) in BYSPO were also discussed in detail. Quantum yields and CIE chromatic coordinates were also presented. Generally, the results suggest their potential applications in UV/n-UV pumped LEDs.

Ufd1-Npl4 Recruit Cdc48 for Disassembly of Ubiquitylated CMG Helicase at the End of Chromosome Replication

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Marija Maric

2017-03-01

Full Text Available Disassembly of the Cdc45-MCM-GINS (CMG DNA helicase is the key regulated step during DNA replication termination in eukaryotes, involving ubiquitylation of the Mcm7 helicase subunit, leading to a disassembly process that requires the Cdc48 “segregase”. Here, we employ a screen to identify partners of budding yeast Cdc48 that are important for disassembly of ubiquitylated CMG helicase at the end of chromosome replication. We demonstrate that the ubiquitin-binding Ufd1-Npl4 complex recruits Cdc48 to ubiquitylated CMG. Ubiquitylation of CMG in yeast cell extracts is dependent upon lysine 29 of Mcm7, which is the only detectable site of ubiquitylation both in vitro and in vivo (though in vivo other sites can be modified when K29 is mutated. Mutation of K29 abrogates in vitro recruitment of Ufd1-Npl4-Cdc48 to the CMG helicase, supporting a model whereby Ufd1-Npl4 recruits Cdc48 to ubiquitylated CMG at the end of chromosome replication, thereby driving the disassembly reaction.

Structural, spectroscopic and cytotoxicity studies of TbF3@CeF3 and TbF3@CeF3@SiO2 nanocrystals

International Nuclear Information System (INIS)

Grzyb, Tomasz; Runowski, Marcin; Dąbrowska, Krystyna; Giersig, Michael; Lis, Stefan

2013-01-01

Terbium fluoride nanocrystals, covered by a shell, composed of cerium fluoride were synthesized by a co-precipitation method. Their complex structure was formed spontaneously during the synthesis. The surface of these core/shell nanocrystals was additionally modified by silica. The properties of TbF 3 @CeF 3 and TbF 3 @CeF 3 @SiO 2 nanocrystals, formed in this way, were investigated. Spectroscopic studies showed that the differences between these two groups of products resulted from the presence of the SiO 2 shell. X-ray diffraction patterns confirmed the trigonal crystal structure of TbF 3 @CeF 3 nanocrystals. High resolution transmission electron microscopy in connection with energy-dispersive X-ray spectroscopy showed a complex structure of the formed nanocrystals. Crystallized as small discs, ‘the products’, with an average diameter around 10 nm, showed an increase in the concentration of Tb 3+ ions from surface to the core of nanocrystals. In addition to photo-physical analyses, cytotoxicity studies were performed on HSkMEC (Human Skin Microvascular Endothelial Cells) and B16F0 mouse melanoma cancer cells. The cytotoxicity of the nanomaterials was neutral for the investigated cells with no toxic or antiproliferative effect in the cell cultures, either for normal or for cancer cells. This fact makes the obtained nanocrystals good candidates for biological applications and further modifications of the SiO 2 shell.Graphical Abstract

TB Terms

Science.gov (United States)

... sputum can also be used to do a culture. TB blood test – a test that uses a blood sample to find out if you are infected with TB bacteria. The test measures the response to TB proteins when they are mixed with a small amount of blood. Examples of these TB blood tests include QuantiFERON ® -TB ...

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

Energy Technology Data Exchange (ETDEWEB)

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

2017-01-15

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

Synthesis, characterisation, luminescence and defect centres in solution combustion synthesised CaZrO3:Tb3+ phosphor

International Nuclear Information System (INIS)

Singh, Vijay; Watanabe, S.; Gundu Rao, T.K.; Al-Shamery, Katharina; Haase, Markus; Jho, Young-Dahl

2012-01-01

Tb 3+ doped CaZrO 3 has been prepared by an easy solution combustion synthesis method. The combustion derived powder was investigated by X-ray diffraction, Fourier-transform infrared spectrometry and scanning electron microscopy techniques. A room temperature photoluminescence study showed that the phosphors can be efficiently excited by 251 nm light with a weak emission in the blue and orange region and a strong emission in green light region. CaZrO 3 :Tb 3+ exhibits three thermoluminescence (TL) glow peaks at 126 °C, 200 °C and 480 °C. Electron Spin Resonance (ESR) studies were carried out to study the defect centres induced in the phosphor by gamma irradiation and also to identify the centres responsible for the TL peaks. The room temperature ESR spectrum of irradiated phosphor appears to be a superposition of two distinct centres. One of the centres (centre I) with principal g-value 2.0233 is identified as an O − ion. Centre II with an axial symmetric g-tensor with principal values g ⊥ =1.9986 and g ⊥ =2.0023 is assigned to an F + centre (singly ionised oxygen vacancy). An additional defect centre is observed during thermal annealing experiments and this centre (assigned to F + centre) seems to originate from an F centre (oxygen vacancy with two electrons). The F centre and also the F + centre appear to correlate with the observed high temperature TL peak in CaZrO 3 :Tb 3+ phosphor. - Highlights: ► Powder phosphor of CaZrO 3 :Tb 3+ was prepared by an easy solution combustion synthesis method. ► The phosphor exhibits a bright green emission at 545 nm ( 5 D 4 → 7 F 5 ) of the Tb 3+ ion. ► Electron Spin Resonance studies have been carried out to identify the defect centres responsible for the observed thermoluminescence peaks.

On the role of the ground state Tb(3)/acetylacetone complex in sensitized emission of Tb(3) in ethanol solution

International Nuclear Information System (INIS)

Lis, S.; Elbanowski, M.; Marciniak, B.

1989-01-01

The Tb(3)-acetylacetone system in ethanol solution has been studied by spectroscopic methods. The formation of a Tb(3)/acetylacetone (1:1) complex in the ground state has been proved and its stability constant determined, K = (0,97 ± 0,06).10 4 dm 3 mol -1 . The role of this complex in the spectrofluorimetric determination of Ln(3) ions in the presence of acetylacetone has been discussed. (Authors)

Temperature and concentration quenching of Tb3+ emissions in Y4Al2O9 crystals

International Nuclear Information System (INIS)

Boruc, Z.; Fetlinski, B.; Kaczkan, M.; Turczynski, S.; Pawlak, D.; Malinowski, M.

2012-01-01

Highlights: ► Spectroscopic properties of Tb 3+ :Y 4 Al 2 O 9 crystals are studied. ► Concentration and temperature dependencies of fluorescence are investigated. ► The cross-relaxation transfer rates are experimentally determined. ► Strong influence of cross relaxation process on 5 D 3 emission quenching is observed. ► Decays are modelled using Inokuti–Hirayama approach. - Abstract: Spectroscopic properties of trivalent terbium (Tb 3+ ) activated Y 4 Al 2 O 9 (abbreviated YAM) crystals were studied. Concentration and temperature dependent emission spectra and fluorescence dynamics profiles have been investigated in YAM:Tb 3+ in order to understand better processes responsible for quenching of the terbium 5 D 3 and 5 D 4 emissions. Decays were modelled using Inokuti–Hirayama approach to obtain information on the energy transfer mechanism. The cross-relaxation transfer rates were experimentally determined as a function of temperature and Tb 3+ concentration. The investigation revealed strong influence of cross-relaxation process on 5 D 3 emission quenching. The two different processes responsible for the increase of fluorescence quenching with growing temperature were observed, both related to thermal activation energy. For temperatures above 700 K, the temperature dependence of the emission intensity ratio ( 5 D 3 / 5 D 4 ) becomes linear and the decay times are rapidly decreasing monotonously with increasing temperature, what is confirming the potential of Y 4 Al 2 O 9 :Tb 3+ material in high temperature luminescence thermometry.

Luminescence, Energy Transfer and Tunable Color of Ce3+- and Tb3+-Activated Na3Gd(BO3)2 Phosphors

Science.gov (United States)

Zhang, Xinguo; Pan, Jialiang; Mo, Fuwang

2017-07-01

A series of blue Na3Gd(BO3)2:Ce3+ and blue-to-green color-tunable Na3Gd (BO3)2:Ce3+,Tb3+ phosphors were synthesized by the solid-state method. The luminescence, concentration quenching and energy transfer (ET) process of Na3Gd(BO3)2:Ce3+,Tb3+ were investigated. Both Ce3+ and Tb3+ occupy the Gd3+ site in the Na3Gd(BO3)2 host. Na3Gd(BO3)2:Ce3+ exhibits strong ultraviolet absorption and broadband blue emission. The Ce3+ sensitization effect on Tb3+ has been verified by the variation of PL/PLE spectra, the Ce3+ decay lifetimes and the energy transfer efficiency of Na3Gd(BO3)2:Ce3+,Tb3+ phosphors. The maximum Ce3+-Tb3+ ET efficiency has been calculated to be 95%. The emitting color of the obtained phosphors can be modulated from blue (0.179, 0.204) through bluish-green (0.271, 0.391) to green (0.349, 0.551) by properly changing the ratio of Ce3+/Tb3+.

Luminescent properties and energy transfer studies of color-tunable LuBO{sub 3}: Ce{sup 3+}/Tb{sup 3+}/Eu{sup 3+} phosphors

Energy Technology Data Exchange (ETDEWEB)

Zhang, Xinguo, E-mail: sysuzxg@gmail.com [School of Pharmaceutical Sciences, Southern Medical University, Guangzhou 510515 (China); School of Chemistry and Chemical Engineering, Guangxi University, Nanning 530004 (China); Fu, Xionghui [Department of Chemistry, Jinan University, Guangzhou 510632 (China); Song, Jiahui [Shenzhou High School, Hengshui 053800 (China); Gong, Menglian [School of Chemistry and Chemical Engineering, Sun Yat-Sen University, Guangzhou 510275 (China)

2016-08-15

Highlights: • A series of color-tunable LuBO{sub 3}: Ce{sup 3+}/Tb{sup 3+}/Eu{sup 3+} phosphors were synthesized. • Phosphors exhibit strong blue/green/red emission under UV excitation. • The reason of high Tb{sup 3+} content required for Ce{sup 3+} → Tb{sup 3+} → Eu{sup 3+} energy transfer is unveiled. • Green and red LED prototypes were fabricated and characterized. - Abstract: A series of LuBO{sub 3}: Ce{sup 3+}/Tb{sup 3+}/Eu{sup 3+} phosphors were synthesized via solid state reaction. The Ce{sup 3+}/Tb{sup 3+} co-doped and Ce{sup 3+}/Tb{sup 3+}/Eu{sup 3+} tri-doped phosphors absorb near UV light through 4f-5d transitions of Ce{sup 3+}, followed by sensitized Tb{sup 3+} green and Eu{sup 3+} red emission. Decay curves investigations for samples with various Tb{sup 3+} and Eu{sup 3+} contents reveal the occurrence of Ce{sup 3+} → Tb{sup 3+} → Eu{sup 3+} energy transfer. It is found that due to relative low Tb{sup 3+} → Eu{sup 3+} energy transfer rate, a high Tb{sup 3+} content (>40%) is required for efficient Ce{sup 3+} → Tb{sup 3+} → Eu{sup 3+} energy transfer. Emission color of LuBO{sub 3}: Ce{sup 3+}, Tb{sup 3+}, Eu{sup 3+} varies from blue through green to red with Ce{sup 3+}/Tb{sup 3+}/Eu{sup 3+} ratio. The quantum efficiency of LuBO{sub 3}: Ce{sup 3+}, Tb{sup 3+} green phosphor and LuBO{sub 3}: Ce{sup 3+}, Tb{sup 3+}, Eu{sup 3+} red phosphor is 50% and 30%, respectively. Green and red LED prototypes were fabricated. The results show that the obtained phosphors are potential candidates as down-converted phosphors for NUV LEDs.

A Comparative Study of Er3+, Er3+-Eu3+, Er3+-Tb3+, and Er3+-Eu3+-Tb3+ Codoped Y2O3 Nanoparticles as Optical Heaters

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G. A. Sobral

2015-01-01

Full Text Available Fluorescence intensity ratio (FIR technique, based on the thermal coupling of H11/22 and S3/24 energy levels of erbium ions, was used to study the optical heating behavior of rare earth doped yttrium oxide nanophosphors (Y2O3:Er3+, Y2O3:Er3+-Eu3+, Y2O3:Er3+-Tb3+, and Y2O3:Er3+-Eu3+-Tb3+ synthesized via PVA-assisted sol-gel route. The samples were optically heated by an 800 nm CW diode laser, while the upconverted green emissions were used to measure their temperatures in real time. The experimental results indicate that the studied nanoparticles are promising candidates to applications such as photothermal treatments and hyperthermia.

Energy transfer and color tunable emission in Tb3+,Eu3+ co-doped Sr3LaNa(PO4)3F phosphors.

Science.gov (United States)

Li, Shuo; Guo, Ning; Liang, Qimeng; Ding, Yu; Zhou, Huitao; Ouyang, Ruizhuo; Lü, Wei

2018-02-05

A group of color tunable Sr 3 LaNa(PO 4 ) 3 F:Tb 3+ ,Eu 3+ phosphors were prepared by conventional high temperature solid state method. The phase structures, luminescence properties, fluorescence lifetimes and energy transfer were investigated in detail. Under 369nm excitation, owing to efficient energy transfer of Tb 3+ →Eu 3+ , the emission spectra both have green emission of Tb 3+ and red emission of Eu 3+ . An efficient energy transfer occur in Tb 3+ , Eu 3+ co-doped Sr 3 LaNa(PO 4 ) 3 F phosphors. The most possible mechanism of energy transfer is dipole-dipole interaction by Dexter's theoretical model. The energy transfer of Tb 3+ and Eu 3+ was confirmed by the variations of emission and excitation spectra and Tb 3+ /Eu 3+ decay lifetimes in Sr 3 LaNa(PO 4 ) 3 F:Tb 3+ ,Eu 3+ . The color tone can tuned from yellowish-green through yellow and eventually to reddish-orange with fixed Tb 3+ content by changing Eu 3+ concentrations. The results show that the prepared Tb 3+ , Eu 3+ co-doped color tunable Sr 3 LaNa(PO 4 ) 3 F phosphor can be used for white LED. Copyright © 2017 Elsevier B.V. All rights reserved.

Energy transfer and color tunable emission in Tb3 +,Eu3 + co-doped Sr3LaNa(PO4)3F phosphors

Science.gov (United States)

Li, Shuo; Guo, Ning; Liang, Qimeng; Ding, Yu; Zhou, Huitao; Ouyang, Ruizhuo; Lü, Wei

2018-02-01

A group of color tunable Sr3LaNa(PO4)3F:Tb3 +,Eu3 + phosphors were prepared by conventional high temperature solid state method. The phase structures, luminescence properties, fluorescence lifetimes and energy transfer were investigated in detail. Under 369 nm excitation, owing to efficient energy transfer of Tb3 + → Eu3 +, the emission spectra both have green emission of Tb3 + and red emission of Eu3 +. An efficient energy transfer occur in Tb3 +, Eu3 + co-doped Sr3LaNa(PO4)3F phosphors. The most possible mechanism of energy transfer is dipole-dipole interaction by Dexter's theoretical model. The energy transfer of Tb3 + and Eu3 + was confirmed by the variations of emission and excitation spectra and Tb3 +/Eu3 + decay lifetimes in Sr3LaNa(PO4)3F:Tb3 +,Eu3 +. The color tone can tuned from yellowish-green through yellow and eventually to reddish-orange with fixed Tb3 + content by changing Eu3 + concentrations. The results show that the prepared Tb3 +, Eu3 + co-doped color tunable Sr3LaNa(PO4)3F phosphor can be used for white LED.

A new promising phosphor, Na3La2(BO3)3:Ln (Ln=Eu, Tb)

International Nuclear Information System (INIS)

Li Zhihua; Zeng Jinghui; Zhang Guochun; Li Yadong

2005-01-01

We present an efficient way to search a host for ultraviolet (UV) phosphor from UV nonlinear optical (NLO) materials. With the guidance, Na 3 La 2 (BO 3 ) 3 (NLBO), as a promising NLO material with a broad transparency range and high damage threshold, was adopted as a host material for the first time. The lanthanide ions (Tb 3+ and Eu 3+ )-doped NLBO phosphors have been synthesized by solid-state reaction. Luminescent properties of the Ln-doped (Ln=Tb 3+ , Eu 3+ ) sodium lanthanum borate were investigated under UV ray excitation. The emission spectrum was employed to probe the local environments of Eu 3+ ions in NLBO crystal. For red phosphor, NLBO:Eu, the measured dominating emission peak was at 613 nm, which is attributed to 5 D - 7 F 2 transition of Eu 3+ . The luminescence indicates that the local symmetry of Eu 3+ in NLBO crystal lattice has no inversion center. Optimum Eu 3+ concentration of NLBO:Eu 3+ under UV excitation with 395 nm wavelength is about 30 mol%. The green phosphor, NLBO:Tb, showed bright green emission at 543 with 252 nm excited light. The measured concentration quenching curve demonstrated that the maximum concentration of Tb 3+ in NLBO was about 20%. The luminescence mechanism of Ln-doped NLBO (Tb 3+ and Eu 3+ ) was analyzed. The relative high quenching concentration was also discussed

Preparation and tunable luminescence of CaCO{sub 3}: Eu{sup 3+}, Tb{sup 3+} phosphors

Energy Technology Data Exchange (ETDEWEB)

Cheng, Qijun; Dong, Yanwei; Kang, Ming, E-mail: dyw510@126.com; Zhang, Ping

2014-12-15

Luminescent tunable phosphors CaCO{sub 3}: Eu{sup 3+}, Tb{sup 3+} were synthesized by a microwave co-precipitation method. The structure and micro-morphology of samples were characterized and analyzed by an X-ray powder diffraction (XRD) and a scanning electronic microscope (SEM), results showed that Tb{sup 3+} and Eu{sup 3+} ions were uniformly introduced into the host lattice of CaCO{sub 3} entering substitutionally in Ca{sup 2+} sites. The photoluminescence (PL) properties were characterized by PL, PL excitation spectroscopy and chromaticity coordinates. Under the excitation at 235 nm and 267 nm, the transitions of {sup 5}D{sub 4}→{sup 7}F{sub J} (J=3–6) for Tb{sup 3+} and {sup 5}D{sub 0}→{sup 7}F{sub J} (J=0–3) for Eu{sup 3+} were observed, and the luminescent intensities and emitting colors of Eu{sup 3+}–Tb{sup 3+} co-doped CaCO{sub 3} phosphors could be gradually changed between red and green by changing the Eu/Tb atomic ratio and the excitation wavelength. - highlights: • A new phosphor CaCO{sub 3}: Eu{sup 3+}, Tb{sup 3+} was prepared by the microwave co-precipitation method. • The phosphors exhibited green and red color under UV excitation. • The emission color could be gradually tuned between green and red. • The phosphors had the potential as materials for anti-counterfeiting technologies.

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.

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

Science.gov (United States)

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

2016-07-20

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

Differential dependence on N-glycosylation of anthrax toxin receptors CMG2 and TEM8.

Directory of Open Access Journals (Sweden)

Sarah Friebe

Full Text Available ANTXR 1 and 2, also known as TEM8 and CMG2, are two type I membrane proteins, which have been extensively studied for their role as anthrax toxin receptors, but with a still elusive physiological function. Here we have analyzed the importance of N-glycosylation on folding, trafficking and ligand binding of these closely related proteins. We find that TEM8 has a stringent dependence on N-glycosylation. The presence of at least one glycan on each of its two extracellular domains, the vWA and Ig-like domains, is indeed necessary for efficient trafficking to the cell surface. In the absence of any N-linked glycans, TEM8 fails to fold correctly and is recognized by the ER quality control machinery. Expression of N-glycosylation mutants reveals that CMG2 is less vulnerable to sugar loss. The absence of N-linked glycans in one of the extracellular domains indeed has little impact on folding, trafficking or receptor function of the wild type protein expressed in tissue culture cells. N-glycans do, however, seem required in primary fibroblasts from human patients. Here, the presence of N-linked sugars increases the tolerance to mutations in cmg2 causing the rare genetic disease Hyaline Fibromatosis Syndrome. It thus appears that CMG2 glycosylation provides a buffer towards genetic variation by promoting folding of the protein in the ER lumen.

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

Science.gov (United States)

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

2017-07-01

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

Photoluminescence and thermoluminescence properties of Tb3+ doped K3Gd(PO4)2 nanophosphor

International Nuclear Information System (INIS)

Gupta, Palvi; Bedyal, A.K.; Kumar, Vinay; Khajuria, Y.; Lochab, S.P.; Pitale, S.S.; Ntwaeaborwa, O.M.; Swart, H.C.

2014-01-01

Energy level diagram of Tb 3+ ion in the K 3 Gd(PO 4 ) 2 host lattice. - Highlights: • First time, a detailed TL and PL study on undoped and Tb 3+ doped K 3 Gd(PO 4 ) 2 nanophosphor. • Combustion method was employed to synthesize the Tb 3+ doped K 3 Gd(PO 4 ) 2 nanophosphor. • Mechanism of excitation and emission in undoped and Tb 3+ doped K 3 Gd(PO 4 ) 2 nanophosphor was given. - Abstract: Tb 3+ doped nanoparticulate K 3 Gd(PO 4 ) 2 phosphor was prepared by combustion method using urea as a fuel. The structure, optical and luminescent properties of the phosphor were studied by X-ray diffraction (XRD), scanning electron microscopy (SEM), diffuse reflectance spectroscopy (DRS), photoluminescence spectroscopy (PL), and thermoluminescence (TL) spectroscopy. In undoped K 3 Gd(PO 4 ) 2 , the excitation and emission peaks at 273 nm and 323 nm belongs to the 8 S 7/2 → 6 I J(J=7/2) and 6 P J(J=7/2) → 8 S 7/2 transitions of Gd 3+ while green emission was observed in the Tb 3+ doped K 3 Gd(PO 4 ) 2 . TL study was carried out after exposing the samples to γ-radiations (0.1–5 kGy) in the K 3 Gd(PO 4 ) 2 :Tb 3+ (1.5 mol%). The calculated kinetic parameters were compared with different methods. The band gap of the phosphor was estimated as 5.80 eV. The green shade of the Tb 3+ ion with the CIE coordinates (x, y) as (0.29, 0.54) was in good agreement with the well known green phosphors

Formation of Infrared Femtosecond Laser Induced Colour Centres in Tb3+-Doped and Tb3+/Ce3+-Codoped Heavy Germanate Glasses

Institute of Scientific and Technical Information of China (English)

CHEN Guo-Rong(陈国荣); YANG Yun-Xia(杨云霞); QIU Jian-Rong(邱建荣); JIANG Xiong-Wei(姜雄伟); K.Hirao

2003-01-01

The formation of infrared femtosecond laser induced colour centres was observed in Tb3+-doped and Tb3+ /Ce3+-codoped heavy germanate glasses.A rectangular scan was made by focusing the laser beam inside the glass samples.A three-dimensional yellowish block was created from the path and it corresponded to the appearance of broad absorption bands in the absorption spectra.The irradiation induced absorption coefficient μ(λ)was used to characterize the distribution of radiation induced colour centres in the samples,whose peak was located at 380nm and extended to the longer wavelength.Ce3+ ions were found not only to inhibit the formation of colour centres,but also to enhance the recovery.

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

International Nuclear Information System (INIS)

Loitongbam, Romeo Singh; Singh, W. Rameshwor

2013-01-01

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

Solution growth of Tb doped Gd_2O_3 film

International Nuclear Information System (INIS)

Ghosh, M.; Pitale, S.; Desai, D.G.; Patra, G.D.; Sen, S.; Gadkari, S.C.

2016-01-01

Nanomaterials of Gd_2O_3 have proven applications in medical imaging and cancer therapy due to the presence of element Gd. Also Gd_2O_3 films have been grown by vapor phase method as well as self assembly in solution and studied as a high-k dielectric and efficient luminescence material. Here, we report a method to obtain Tb doped Gd_2O_3 film by solution growth method followed by suitable heat treatment. Uniform films of Tb doped Gadolinium hydroxycarbonate have been deposited on fused quartz substrates kept inside a solution containing gadolinium nitrate, terbium nitrate and Urea maintained at 90°C. Gadolinium hydroxy-carbonate films are then treated at 800°C for 2 hour to obtain Tb doped cubic Gd_2O_3 as confirmed by X-ray diffraction measurement. The photoluminescence spectra display characteristic Tb emission at 544 nm when excited at 285 nm. The lifetime of Tb emission is found to be of the order of few microseconds. (author)

Synthesis, characterisation, luminescence and defect centres in solution combustion synthesised CaZrO{sub 3}:Tb{sup 3+} phosphor

Energy Technology Data Exchange (ETDEWEB)

Singh, Vijay, E-mail: vijayjiin2006@yahoo.com [School of Information and Communications, Gwangju Institute of Science and Technology, Gwangju 500-712 (Korea, Republic of); Watanabe, S.; Gundu Rao, T.K. [Institute of Physics, University of Sao Paulo, 05508-090 Sao Paulo/SP (Brazil); Al-Shamery, Katharina [Physical Chemistry, Institute for Pure and Applied Chemistry and Center of Interface Science University of Oldenburg, 26129 Oldenburg (Germany); Haase, Markus [Department of Inorganic Chemistry I-Materials Research, Institute of Chemistry, University of Osnabrueck, Barbarastrabe 7, 49069 Osnabrueck (Germany); Jho, Young-Dahl, E-mail: jho@gist.ac.kr [School of Information and Communications, Gwangju Institute of Science and Technology, Gwangju 500-712 (Korea, Republic of)

2012-08-15

Tb{sup 3+} doped CaZrO{sub 3} has been prepared by an easy solution combustion synthesis method. The combustion derived powder was investigated by X-ray diffraction, Fourier-transform infrared spectrometry and scanning electron microscopy techniques. A room temperature photoluminescence study showed that the phosphors can be efficiently excited by 251 nm light with a weak emission in the blue and orange region and a strong emission in green light region. CaZrO{sub 3}:Tb{sup 3+} exhibits three thermoluminescence (TL) glow peaks at 126 Degree-Sign C, 200 Degree-Sign C and 480 Degree-Sign C. Electron Spin Resonance (ESR) studies were carried out to study the defect centres induced in the phosphor by gamma irradiation and also to identify the centres responsible for the TL peaks. The room temperature ESR spectrum of irradiated phosphor appears to be a superposition of two distinct centres. One of the centres (centre I) with principal g-value 2.0233 is identified as an O{sup -} ion. Centre II with an axial symmetric g-tensor with principal values g{sub Up-Tack }=1.9986 and g{sub Up-Tack }=2.0023 is assigned to an F{sup +} centre (singly ionised oxygen vacancy). An additional defect centre is observed during thermal annealing experiments and this centre (assigned to F{sup +} centre) seems to originate from an F centre (oxygen vacancy with two electrons). The F centre and also the F{sup +} centre appear to correlate with the observed high temperature TL peak in CaZrO{sub 3}:Tb{sup 3+} phosphor. - Highlights: Black-Right-Pointing-Pointer Powder phosphor of CaZrO{sub 3}:Tb{sup 3+} was prepared by an easy solution combustion synthesis method. Black-Right-Pointing-Pointer The phosphor exhibits a bright green emission at 545 nm ({sup 5}D{sub 4}{yields}{sup 7}F{sub 5}) of the Tb{sup 3+} ion. Black-Right-Pointing-Pointer Electron Spin Resonance studies have been carried out to identify the defect centres responsible for the observed thermoluminescence peaks.

Tunable luminescence properties and energy transfer in Ba{sub 3}Lu(PO{sub 4}){sub 3}:Ce{sup 3+},Tb{sup 3+} phosphors

Energy Technology Data Exchange (ETDEWEB)

Jin, Cheng [Department of Physics and Electronic Engineering, Baoding University, Baoding 071002 (China); Ma, Hengxin [College of Science, Agricultural University of Hebei, Baoding 071002 (China); Liu, Yufeng, E-mail: liuyufeng4@126.com [State Key Lab of Power Systems, Department of Thermal Engineering, Tsinghua University, Beijing 100084 (China); Liu, Qingbo [Department of Physics and Electronic Engineering, Baoding University, Baoding 071002 (China); Dong, Guoyi [College of Physics Science and Technology, Hebei University, Baoding 071002 (China); Yu, Quanmao [Institute of Functional Materials, Jiangxi University of Finance and Economics, Nanchang 330013 (China)

2014-11-15

Highlights: • Effective energy transfer from Ce{sup 3+} to Tb{sup 3+} in Ba{sub 3}Lu(PO{sub 4}){sub 3} was confirmed. • The reason of energy transfer from Ce{sup 3+} to Tb{sup 3+} was investigated in detail. • Ba{sub 3}Lu(PO{sub 4}){sub 3}:Ce{sup 3+}, Tb{sup 3+} can be a potential green-emitting phosphor for UV LEDs. - Abstract: A series of novel color-tunable phosphors Ba{sub 3}Lu(PO{sub 4}){sub 3}:Ce{sup 3+},Tb{sup 3+} have been synthesized by solid-state reaction. X-ray diffraction, photoluminescence emission and excitation spectra, lifetime, as well as the effect of Tb{sup 3+} concentration were employed to characterize the resulting samples. The emission spectra of Ba{sub 3}Lu(PO{sub 4}){sub 3}:Ce{sup 3+},Tb{sup 3+} phosphor contains both the asymmetric broad-band Ce{sup 3+} ion emission and the line-type Tb{sup 3+} ion emission. Under ultraviolet light excitation, Ba{sub 3}Lu(PO{sub 4}){sub 3}:Ce{sup 3+},Tb{sup 3+} can achieve tunable emission from deep blue to yellowish-green by changing the concentration of Tb{sup 3+}. The results indicated that these phosphors could be considered as double emission phosphors for field emission displays.

Photoluminescence characterization and energy transfer of color-tunable Li{sub 6}Y(BO{sub 3}){sub 3}:Ce{sup 3+},Tb{sup 3+} phosphors

Energy Technology Data Exchange (ETDEWEB)

Guan, Anxiang; Zhou, Liya, E-mail: zhouliyatf@163.com; Wang, Guofang; Gao, Fangfang; Wang, Qiuping; Chen, Xueting; Li, Yinghao

2016-08-01

Ce{sup 3+} and Tb{sup 3+} singly doped and co-doped Li{sub 6}Y(BO{sub 3}){sub 3} (LYB) phosphors were synthesized through a solid-state reaction. The phosphors were effectively excited by 350 nm, which matched the near-UV emitting InGaN chip. Luminescence spectra and decay lifetime curves of LYB:Ce{sup 3+},Tb{sup 3+} were measured to prove energy transfer from Ce{sup 3+} to Tb{sup 3+}. Through energy transfer, the intensity of the typical emission peak of Tb{sup 3+} at 546 nm in LYB:0.05Ce{sup 3+},0.03Tb{sup 3+} was approximately 1.8 times stronger than that in LYB:0.03Tb{sup 3+}. The mechanism of Ce{sup 3+}→Tb{sup 3+} energy transfer was a dipole–dipole interaction, and the energy transfer efficiency gradually increased to 29.27% with increasing Tb{sup 3+} doping concentration. Furthermore, the emission colors of LYB:Ce{sup 3+},Tb{sup 3+} varied from blue to green by adjusting the Ce{sup 3+}/Tb{sup 3+} ratio, indicating that the phosphors could be used as blue-to-green emitting phosphors for application in ultraviolet light-emitting diodes.

Effect of calcinations temperature on the luminescence intensity and fluorescent lifetime of Tb3+-doped hydroxyapatite (Tb-HA nanocrystallines

Directory of Open Access Journals (Sweden)

Hairong Yin

2017-06-01

Full Text Available Hydroxyapatite luminescent nanocrystallines doped with 6 mol.% Tb3+ (Tb-HA were prepared via chemical deposition method and calcined at different temperature, and the effects of calcinations temperature on the luminescence intensity and fluorescent lifetime were studied. TEM image of Tb-HA revealed that the shape of nanocrystallines changed from needle-like to short rod-like and sphere-like with the increase of calcinations temperature; while the particles sizes decreased from 190 nm to 110 nm. The crystallinity degree increased. The typical emission peaks attributed to Tb3+ ions were observed in emission spectra of 6 mol.% Tb-HA under 378 nm excitation. The luminescent intensity of Tb-HA, which showed the fluorescence quenching, firstly enhanced and then decreased at 700 °C; while the fluorescent lifetime increased firstly and then decreased after 600 °C. Furthermore, the ratio of intensity between 545 nm and 490 nm corresponding to electric-dipole and magnetic-dipole transition (IR: IO increases firstly and then decreases, which revealed that the proportion of substitute type and site of Ca2+ ions by Tb3+ ions were helpful to realize the substitute process and functional structure design.

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

NARCIS (Netherlands)

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

2012-01-01

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

Optically stimulated luminescence of Tb{sup 3+}/Sm{sup 3+} doubly doped K{sub 2}YF{sub 5} single crystals

Energy Technology Data Exchange (ETDEWEB)

Camargo, L.; Marcazzo, J.; Santiago, M.; Caselli, E. [Universidad Nacional del Centro de la Provincia de Buenos Aires, Instituto de Fisica Arroyo Seco, Gral. Pinto 399, B7000GHG, Tandil (Argentina); Khaidukov, N. M., E-mail: jmarcass@exa.unicen.edu.ar [Kurnakov Institute of General and Inorganic Chemistry, RAS, Leninskii Prospekt 31, 119991 Moscow (Russian Federation)

2014-08-15

In this work optically stimulated luminescence (OSL) properties of K{sub 2}YF{sub 5} crystals doubly doped with Tb{sup 3+} and Sm{sup 3+} ions have been investigated for the first time. OSL responses for different dopant concentration and for optical stimulation with different wavelengths have been analyzed for each compound. Dosimetric properties of the most efficient composition, namely, K{sub 2}YF{sub 5}:1.0 at.% Tb{sup 3+}; 1.0 at.% Sm{sup 3+}, have been studied. Finally, the possible application of this single crystal as OSL dosimeter has been evaluated. (Author)

Mcm10 regulates DNA replication elongation by stimulating the CMG replicative helicase.

Science.gov (United States)

Lõoke, Marko; Maloney, Michael F; Bell, Stephen P

2017-02-01

Activation of the Mcm2-7 replicative DNA helicase is the committed step in eukaryotic DNA replication initiation. Although Mcm2-7 activation requires binding of the helicase-activating proteins Cdc45 and GINS (forming the CMG complex), an additional protein, Mcm10, drives initial origin DNA unwinding by an unknown mechanism. We show that Mcm10 binds a conserved motif located between the oligonucleotide/oligosaccharide fold (OB-fold) and A subdomain of Mcm2. Although buried in the interface between these domains in Mcm2-7 structures, mutations predicted to separate the domains and expose this motif restore growth to conditional-lethal MCM10 mutant cells. We found that, in addition to stimulating initial DNA unwinding, Mcm10 stabilizes Cdc45 and GINS association with Mcm2-7 and stimulates replication elongation in vivo and in vitro. Furthermore, we identified a lethal allele of MCM10 that stimulates initial DNA unwinding but is defective in replication elongation and CMG binding. Our findings expand the roles of Mcm10 during DNA replication and suggest a new model for Mcm10 function as an activator of the CMG complex throughout DNA replication. © 2017 Lõoke et al.; Published by Cold Spring Harbor Laboratory Press.

New reddish-orange and greenish-yellow light emitting phosphors: Eu3+ and Tb3+/Eu3+ in sodium germanate glass

International Nuclear Information System (INIS)

Álvarez, E.; Zayas, Ma. E.; Alvarado-Rivera, J.; Félix-Domínguez, F.; Duarte-Zamorano, R.P.; Caldiño, U.

2014-01-01

A spectroscopic analysis of sodium germanate glasses activated with Eu 3+ , Tb 3+ and Eu 3+ /Tb 3+ is performed from their photoluminescence spectra and decay times. In the Eu 3+ -singly doped glass reddish-orange light emission, with x=0.64 and y=0.35 CIE1931 chromaticity coordinates, is obtained upon Eu 3+ excitation at 393 nm. Such chromaticity coordinates are close to those (0.67, 0.33) proposed by the National Television Standard Committee for the red phosphor. When the sodium germanate glass is co-doped with Tb 3+ and Eu 3+ greenish-yellow light emission, with (0.41, 0.46) CIE1931 chromaticity coordinates, is obtained upon Tb 3+ excitation at 344 nm. Such greenish-yellow luminescence is due mainly to the terbium 5 D 4 → 7 F 6,5 and europium 5 D 0 → 7 F 1,2 emissions, Eu 3+ being sensitized by Tb 3+ through a non-radiative energy transfer. The non-radiative nature of this energy transfer is inferred from the increase in the decay rate of the Tb 3+ emission when the glass is co-doped with Eu 3+ . From an analysis of the Tb 3+ emission decay time curves it is inferred that such energy transfer might take place between Tb 3+ and Eu 3+ clusters through a short-range interaction mechanism. - Highlights: • Sodium germanate glasses are optically activated with Eu 3+ (GNE) and Tb 3+ /Eu 3+ (GNTE). • Reddish-orange light (0.64, 0.35) is generated by GNE pumped with 393 nm light. • Greenish-yellow light (0.41, 0.46) is generated by GNTE pumped with 344 nm light. • Non-radiative energy transfer Tb 3+ →Eu 3+ takes place in GNTE

High quality TbMnO3 films deposited on YAlO3

International Nuclear Information System (INIS)

Glavic, Artur; Voigt, Joerg; Persson, Joerg; Su, Yixi; Schubert, Juergen; Groot, Joost de; Zande, Willi; Brueckel, Thomas

2011-01-01

Research highlights: → We found a good substrate and suitable deposition parameters to create untwinned, epitaxial thin films of TbMnO 3 . → Laboratory experiments prove the crystalline quality of the films. → We were able to measure the micro magnetic structure in the films by polarized neutron diffraction (to our knowledge the first neutron investigations on TbMnO 3 thin films). - Abstract: High quality thin films of TbMnO 3 were grown by pulsed laser deposition on orthorhombicYAlO 3 (1 0 0). The interface and surface roughness of a 55 nm thick film were probed by X-ray reflectometry and atomic force microscopy, yielding a roughness of 1 nm. X-ray diffraction revealed untwinned films and a small mosaic spread of 0.04 o and 0.2 o for out-of-plane and in-plane reflections, respectively. This high degree of epitaxy was also confirmed by Rutherford backscattering spectrometry. Using polarized neutron diffraction we could identify a magnetic structure with the propagation vector (0 0.27 0), identical to the bulk magnetic structure of TbMnO 3 .

Features of the low-frequency polarization response in the region of the ferroelectric phase transition in multiferroic TbMnO.sub.3./sub.

Czech Academy of Sciences Publication Activity Database

Trepakov, Vladimír; Kvyatkovskii, O.E.; Savinov, Maxim; Dejneka, Alexandr; Wang, X.; Cheong, S.W.

2016-01-01

Roč. 58, č. 10 (2016), s. 2021-2026 ISSN 1063-7834 Institutional support: RVO:68378271 Keywords : low-frequency * polarization response * ferroelectric, phase * transition * multiferroic * TbMnO 3 Subject RIV: BM - Solid Matter Physics ; Magnetism OBOR OECD: Condensed matter physics (including formerly solid state physics, supercond.) Impact factor: 0.860, year: 2016

Enhancement of CdSiO3: Tb3+ green long-lasting phosphors by co-doping with Re3+ (Re3+=Gd3+, Y3+, La3+) ions

International Nuclear Information System (INIS)

Zeng, Wei; Wang, Yuhua; Han, Shaochun; Chen, Wenbo; Li, Gen

2014-01-01

CdSiO 3 : Tb 3+ , Re 3+ long-lasting phosphors were synthesized by the conventional high temperature solid-state method. A green-light phosphorescence phenomenon, which was associated with the 5 D 4 → 7 F J (J=6, 5, 4, 3) transitions of the Tb 3+ ion, was observed. Introduction of Re 3+ (Re 3+ =Gd 3+ , Y 3+ , La 3+ ) ions, which deepens the depth (E t ) or/and increases the density (n 0 ) of traps, greatly improved the afterglow properties of CdSiO 3 : Tb 3+ . Possible mechanism of CdSiO 3 : Tb 3+ , Re 3+ was discussed in this work. - Highlights: • CdSiO 3 : Tb 3+ , Re 3+ samples enrich the color of long-lasting afterglow phosphors in CdSiO 3 host. • Both the afterglow intensity and the lasting time are greatly enhanced for the co-doped samples, especially for Cd 0.96 SiO 3 : Tb 0.03 3+ , La 0.01 3+ . • Introduction of Re 3+ (Re 3+ =Gd 3+ , Y 3+ , La 3+ ) ions, which deepens the depth (E t ) or increase density(n 0 ) of traps, greatly improved the afterglow properties of CdSiO 3 : Tb 3+

Luminescence properties and energy transfer investigations of Sr{sub 3}Lu(PO{sub 4}){sub 3}:Ce{sup 3+}, Tb{sup 3+} phosphors

Energy Technology Data Exchange (ETDEWEB)

Yang, Zaifa; Xu, Denghui, E-mail: xudh@btbu.edu.cn; Sun, Jiayue; Du, Jiangnan; Gao, Xuedong

2016-09-15

Highlights: • A phosphor Sr{sub 3}Lu(PO{sub 4}){sub 3}:Ce{sup 3+}, Tb{sup 3+} for UV-based white LEDs was firstly synthesized successfully. • The phase structure and photoluminescence properties of samples were studied in detail. • The energy transfer process from Ce{sup 3+} to Tb{sup 3+} ions was illustrated in detail. • Sr{sub 3}Lu(PO{sub 4}){sub 3}:Ce{sup 3+}, Tb{sup 3+} phosphor has potential applications as an UV-convertible phosphor for white light emitting diodes. - Abstract: A series of Ce{sup 3+} or Tb{sup 3+} doped and Ce{sup 3+}/Tb{sup 3+} co-doped Sr{sub 3}Lu(PO{sub 4}){sub 3} phosphors were prepared via the conventional high temperature solid-state reaction. The phase structure, photoluminescence and energy transfer properties of samples were studied in detail. The optimal proportion of Ce{sup 3+} single doping is 4 mol% with maximal fluorescence intensity. The Sr{sub 3}Lu(PO{sub 4}){sub 3}:Ce{sup 3+}, Tb{sup 3+} phosphor shows both a blue emission (428 nm) from Ce{sup 3+} and a yellowish-green emission (545 nm) from Tb{sup 3+} with considerable intensity under ultraviolet (UV) excitation (268 nm). The energy transfer from Ce{sup 3+} to Tb{sup 3+} ions takes place in the Sr{sub 3}Lu(PO{sub 4}){sub 3}:Ce{sup 3+}, Tb{sup 3+} phosphor on the basis of the analysis of the luminescence spectra. The energy transfer mechanism from Ce{sup 3+} to Tb{sup 3+} ions was proved to be dipole–dipole interaction. The energy transfer behaviors in Sr{sub 3}Lu(PO{sub 4}){sub 3}:Ce{sup 3+}, Tb{sup 3+} phosphor is also investigated by the lifetime measurement. The results show that this phosphor has potential applications for UV white-light LEDs.

Hierarchy Low CD4+/CD8+ T-Cell Counts and IFN-γ Responses in HIV-1+ Individuals Correlate with Active TB and/or M.tb Co-Infection.

Science.gov (United States)

Shao, Lingyun; Zhang, Xinyun; Gao, Yan; Xu, Yunya; Zhang, Shu; Yu, Shenglei; Weng, Xinhua; Shen, Hongbo; Chen, Zheng W; Jiang, Weimin; Zhang, Wenhong

2016-01-01

Detailed studies of correlation between HIV-M.tb co-infection and hierarchy declines of CD8+/CD4+ T-cell counts and IFN-γ responses have not been done. We conducted case-control studies to address this issue. 164 HIV-1-infected individuals comprised of HIV-1+ATB, HIV-1+LTB and HIV-1+TB- groups were evaluated. Immune phenotyping and complete blood count (CBC) were employed to measure CD4+ and CD8+ T-cell counts; T.SPOT.TB and intracellular cytokine staining (ICS) were utilized to detect ESAT6, CFP10 or PPD-specific IFN-γ responses. There were significant differences in median CD4+ T-cell counts between HIV-1+ATB (164/μL), HIV-1+LTB (447/μL) and HIV-1+TB- (329/μL) groups. Hierarchy low CD4+ T-cell counts (500/μL) were correlated significantly with active TB but not M.tb co-infection. Interestingly, hierarchy low CD8+ T-cell counts were not only associated significantly with active TB but also with M.tb co-infection (PHierarchy low CD8+ T-cell counts and effector function in HIV-1-infected individuals are correlated with both M.tb co-infection and active TB. Hierarchy low CD4+ T-cell counts and Th1 effector function in HIV-1+ individuals are associated with increased frequencies of active TB, but not M.tb co-infection.

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

Science.gov (United States)

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

2015-09-01

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

Long persistent luminescence property of a novel green emitting SrLaGaO{sub 4}: Tb{sup 3+} phosphor

Energy Technology Data Exchange (ETDEWEB)

Fu, Xiaoyan, E-mail: fuxiaoyan@xmut.edu.cn [College of Materials Science and Engineering, Xiamen University of Technology, Xiamen 361024 (China); Jiangsu Collaborative Innovation Center of Atmospheric Environment and Equipment Technology (CICAEET), Nanjing University of Information Science & Technology, Jiangsu Key Laboratory of Atmospheric Environment Monitoring and Pollution Control (AEMPC), Nanjing 210044 (China); Zheng, Shenghui [College of Materials Science and Engineering, Xiamen University of Technology, Xiamen 361024 (China); Institute of Urban Environment, Chinese Academy of Sciences, Xiamen 361021 (China); Shi, Junpeng [Institute of Urban Environment, Chinese Academy of Sciences, Xiamen 361021 (China); Li, Yuechan [College of Materials Science and Engineering, Xiamen University of Technology, Xiamen 361024 (China); Zhang, Hongwu, E-mail: hwzhang@iue.ac.cn [Institute of Urban Environment, Chinese Academy of Sciences, Xiamen 361021 (China)

2017-04-15

A novel long persistent green emitting phosphor SrLaGaO{sub 4}: Tb{sup 3+} was synthesized via a conventional high temperature solid-state method. The obtained results indicated that the green long persistent emitting was similar to the photoluminescence, originating from the f-f transitions of Tb{sup 3+} centers which were supposed to occupy the random distribution Sr{sup 2+} and La{sup 3+} sites. The duration of green afterglow can be observed in the dark by naked eyes even after more than 3.5 h. The thermoluminescence results revealed that SrLaGaO{sub 4}: Tb{sup 3+} possessed three main traps calculated to be 0.62, 0.68 and 0.77 eV, which were responsible for the long persistent green luminescence. The further structure analysis revealed that the Tb{sup 3+} dopants not only acted as emission centers but also significantly influenced the density of traps, and the trapping centers were postulated nonrandom distribution under the assistance of high temperature, which resulted in the efficient persistent luminescence of Tb{sup 3+}. All the results showed that SrLaGaO{sub 4}: Tb{sup 3+} was a potential long persistent luminescent material.

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

International Nuclear Information System (INIS)

Tu Dong; Liang Yujun; Liu Rong; Li Daoyi

2011-01-01

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

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

International Nuclear Information System (INIS)

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

2013-01-01

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

In situ 119Sn Moessbauer spectroscopy used to study lithium insertion in c-Mg2Sn

International Nuclear Information System (INIS)

Aldon, L.; Ionica, C. M.; Lippens, P. E.; Larcher, D.; Tarascon, J.-M.; Olivier-Fourcade, J.; Jumas, J.-C.

2006-01-01

The electrochemical reactions of Li with c-Mg 2 Sn have been investigated by in situ Moessbauer spectroscopy of 119 Sn and X-ray diffraction. The lithiation transforms initially c-Mg 2 Sn part into Li x Mg 2 Sn alloy (x 2 MgSn ternary alloy. In situ Moessbauer spectroscopy provides valuable information on local environment of tin and swelling behavior and cracking of the particles during discharge and charge processes.

Determination of terbium in phosphate rock by Tb{sup 3+}-selective fluorimetric optode based on dansyl derivative as a neutral fluorogenic ionophore

Energy Technology Data Exchange (ETDEWEB)

Hosseini, Morteza, E-mail: smhosseini@khayam.ut.ac.ir [Department of Chemistry, Islamic Azad University, Savadkooh Branch, Savadkooh (Iran, Islamic Republic of); Ganjali, Mohammad Reza [Center of Excellence in Electrochemistry, Faculty of Chemistry, University of Tehran, Tehran (Iran, Islamic Republic of); Endocrinology and Metabolism Research Center, Tehran University of Medical Sciences, Tehran (Iran, Islamic Republic of); Veismohammadi, Bahareh [Center of Excellence in Electrochemistry, Faculty of Chemistry, University of Tehran, Tehran (Iran, Islamic Republic of); Faridbod, Farnoush [Endocrinology and Metabolism Research Center, Tehran University of Medical Sciences, Tehran (Iran, Islamic Republic of); Abkenar, Shiva Dehghan [Department of Chemistry, Islamic Azad University, Savadkooh Branch, Savadkooh (Iran, Islamic Republic of); Norouzi, Parviz [Endocrinology and Metabolism Research Center, Tehran University of Medical Sciences, Tehran (Iran, Islamic Republic of); Center of Excellence in Electrochemistry, Faculty of Chemistry, University of Tehran, Tehran (Iran, Islamic Republic of)

2010-04-07

For the first time a highly sensitive and selective fluorimetric optode membrane was prepared for determination of trace amounts of Tb(III) ions in phosphate rock samples. The Tb(III) sensing system was constructed by incorporating 5-(dimethylamino)-N'-(2-hydroxy-1-naphthoyl) naphthalene-1-sulfonohydrazine (L) as a neutral Tb(III)-selective fluoroionophore, in the plasticized PVC membrane containing sodium tetraphenyl borate as a liphophilic anionic additive. The response of the optode is based on the strong fluorescence quenching of L by Tb{sup 3+} ions. At a pH value of 5.0, the optode displays a wide concentration range of 1.0 x 10{sup -7} to 1.0 x 10{sup -2} M, with a relatively fast response time of less than 45 s. In addition, to high stability and reproducibility, the sensor shows a unique selectivity towards Tb{sup 3+} ion with respect to common cations. The optode was applied successfully to the trace determination of terbium ion in binary mixture and water samples and the determination of Tb{sup 3+} in phosphate rock samples.

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

Determination of terbium in phosphate rock by Tb3+-selective fluorimetric optode based on dansyl derivative as a neutral fluorogenic ionophore.

Science.gov (United States)

Hosseini, Morteza; Ganjali, Mohammad Reza; Veismohammadi, Bahareh; Faridbod, Farnoush; Abkenar, Shiva Dehghan; Norouzi, Parviz

2010-04-07

For the first time a highly sensitive and selective fluorimetric optode membrane was prepared for determination of trace amounts of Tb(III) ions in phosphate rock samples. The Tb(III) sensing system was constructed by incorporating 5-(dimethylamino)-N'-(2-hydroxy-1-naphthoyl) naphthalene-1-sulfonohydrazine (L) as a neutral Tb(III)-selective fluoroionophore, in the plasticized PVC membrane containing sodium tetraphenyl borate as a liphophilic anionic additive. The response of the optode is based on the strong fluorescence quenching of L by Tb(3+) ions. At a pH value of 5.0, the optode displays a wide concentration range of 1.0 x 10(-7) to 1.0 x 10(-2)M, with a relatively fast response time of less than 45 s. In addition, to high stability and reproducibility, the sensor shows a unique selectivity towards Tb(3+) ion with respect to common cations. The optode was applied successfully to the trace determination of terbium ion in binary mixture and water samples and the determination of Tb(3+) in phosphate rock samples. Crown Copyright 2010. Published by Elsevier B.V. All rights reserved.

Structural, spectroscopic and cytotoxicity studies of TbF{sub 3}@CeF{sub 3} and TbF{sub 3}@CeF{sub 3}@SiO{sub 2} nanocrystals

Energy Technology Data Exchange (ETDEWEB)

Grzyb, Tomasz; Runowski, Marcin [Adam Mickiewicz University, Department of Rare Earths, Faculty of Chemistry (Poland); Dabrowska, Krystyna [Polish Academy of Sciences, Bacteriophage Laboratory, Institute of Immunology and Experimental Therapy (Poland); Giersig, Michael; Lis, Stefan, E-mail: blis@amu.edu.pl [Adam Mickiewicz University, Department of Rare Earths, Faculty of Chemistry (Poland)

2013-10-15

Terbium fluoride nanocrystals, covered by a shell, composed of cerium fluoride were synthesized by a co-precipitation method. Their complex structure was formed spontaneously during the synthesis. The surface of these core/shell nanocrystals was additionally modified by silica. The properties of TbF{sub 3}@CeF{sub 3} and TbF{sub 3}@CeF{sub 3}@SiO{sub 2} nanocrystals, formed in this way, were investigated. Spectroscopic studies showed that the differences between these two groups of products resulted from the presence of the SiO{sub 2} shell. X-ray diffraction patterns confirmed the trigonal crystal structure of TbF{sub 3}@CeF{sub 3} nanocrystals. High resolution transmission electron microscopy in connection with energy-dispersive X-ray spectroscopy showed a complex structure of the formed nanocrystals. Crystallized as small discs, 'the products', with an average diameter around 10 nm, showed an increase in the concentration of Tb{sup 3+} ions from surface to the core of nanocrystals. In addition to photo-physical analyses, cytotoxicity studies were performed on HSkMEC (Human Skin Microvascular Endothelial Cells) and B16F0 mouse melanoma cancer cells. The cytotoxicity of the nanomaterials was neutral for the investigated cells with no toxic or antiproliferative effect in the cell cultures, either for normal or for cancer cells. This fact makes the obtained nanocrystals good candidates for biological applications and further modifications of the SiO{sub 2} shell.Graphical Abstract.

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

Science.gov (United States)

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

2017-11-01

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

CMG-Biotools, a Free Workbench for Basic Comparative Microbial Genomics

DEFF Research Database (Denmark)

Vesth, Tammi Camilla; Lagesen, Karin; Acar, Öncel

2013-01-01

This paper shows the strength and diverse use of the CMG-biotools system. The system can be installed on a vide range of host operating systems and utilizes as much of the host computer as desired. It allows the user to compare multiple genomes, from various sources using standardized data formats...

Evaluation of immune responses in HIV infected patients with pleural tuberculosis by the QuantiFERON® TB-Gold interferon-gamma assay

Directory of Open Access Journals (Sweden)

Lekabe Jacob M

2008-03-01

Full Text Available Abstract Background Diagnosis of tuberculous (TB pleuritis is difficult and better diagnostic tools are needed. New blood based interferon-gamma (IFN-γ tests are promising, but sensitivity could be low in HIV positive patients. The IFN-γ tests have not yet been validated for use in pleural fluid, a compartment with higher level of immune activation than in blood. Methods The QuantiFERON TB®-Gold (QFT-TB test was analysed in blood and pleural fluid from 34 patients presenting with clinically suspected pleural TB. Clinical data, HIV status and CD4 cell counts were recorded. Adenosine deaminase activity (ADA analysis and TB culture were performed on pleural fluid. Results The patients were categorised as 'confirmed TB' (n = 12, 'probable TB' (n = 16 and 'non-TB' pleuritis (n = 6 based on TB culture results and clinical and biochemical criteria. The majority of the TB patients were HIV infected (82%. The QFT-TB in pleural fluid was positive in 27% and 56% of the 'confirmed TB' and 'probable TB' cases, respectively, whereas the corresponding sensitivities in blood were 58% and 83%. Indeterminate results in blood (25% were caused by low phytohemagglutinin (PHA = positive control IFN-γ responses, significantly lower in the TB patients as compared to the 'non-TB' cases (p = 0.02. Blood PHA responses correlated with CD4 cell count (r = 0.600, p = 0.028. In contrast, in pleural fluid indeterminate results (52% were caused by high Nil (negative control IFN-γ responses in both TB groups. Still, the Nil IFN-γ responses were lower than the TB antigen responses (p Conclusion The QFT-TB test in blood could contribute to the diagnosis of TB pleuritis in the HIV positive population. Still, the number of inconclusive results is too high to recommend the commercial QFT-TB test for routine use in pleural fluid in a TB/HIV endemic resource-limited setting.

Dosimetric characterization of KMgF{sub 3}:Tb+PTFE; Caracterizacion dosimetrica de KMgF{sub 3}:Tb+PTFE

Energy Technology Data Exchange (ETDEWEB)

Ramirez R, M. I.; Garcia S, L.; Villicana M, M.; Huirache A, R.; Apolinar C, J. [Universidad Michoacana de San Nicolas de Hidalgo, Facultad de Ingenieria Quimica, Francisco J. Mujica s/n, Ciudad Universitaria, Col. Felicitas del Rio, 58030 Morelia, Michoacan (Mexico); Gonzalez M, P. R., E-mail: itcraf_15@hotmail.com [ININ, Carretera Mexico-Toluca s/n, 52750 Ocoyoacac, Estado de Mexico (Mexico)

2017-10-15

In this work the results obtained from the dosimetric characterization of the new radiation detectors of KMgF{sub 3}:Tb+PTFE are presented. The host salt was obtained by means of the microwave technique, with the polycrystalline powder obtained, dosimeters were made in tablet form, using as Ptfe binder. The thermoluminescent response of these new detectors presented a linear behavior, in the dose range between 1 and 1000 Gy of {sup 60}Co gamma radiation, the reproducibility test in the measurements, during ten cycles of heat treatment, irradiation and reading presented ± 3.7% Ds, in the stability test of thermoluminescent signal, during two months showed that the fading is practically null. Due to the results obtained, this new detector could be very useful for the dosimetry of ionizing radiation in different clinical applications. (Author)

The equilibrium diagram and some properties of alloys Gd5Sb3-Tb5Sb3 system

International Nuclear Information System (INIS)

Azizov, Yu.S.; Abulkhaev, V.D.; Ganiev, I.N.

2001-01-01

The purpose of present work is investigation equilibrium diagram of Gd 5 Sb 3 -Tb 5 Sb 3 system in total range of concentrations. Equilibrium diagram of Gd 5 Sb 3 -Tb 5 Sb 3 system investigated by methods of difference-thermal, roentgen-phase and metallographic analyses. For the first time on the base of difference-thermal, roentgen-phase and metallographic analyses was formed the equilibrium diagram of Gd 5 Sb 3 -Tb 5 Sb 3 system. Was determined the cristal-chemical parameters of solid solutions with general formula Gd x Tb 5 - x Sb 3

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

Science.gov (United States)

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

2015-01-05

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

Optical spectroscopy and optical waveguide fabrication in Eu3+ and Eu3+/Tb3+ doped zinc–sodium–aluminosilicate glasses

International Nuclear Information System (INIS)

Caldiño, U.; Speghini, A.; Berneschi, S.; Bettinelli, M.; Brenci, M.; Pasquini, E.; Pelli, S.; Righini, G.C.

2014-01-01

Optical and spectroscopic properties of 2.0% Eu(PO 3 ) 3 singly doped and 5.0% Tb(PO 3 ) 3 –2.0% Eu(PO 3 ) 3 codoped zinc–sodium–aluminosilicate glasses were investigated. Reddish-orange light emission, with x=0.64 and y=0.36 CIE1931 chromaticity coordinates, is obtained in the europium singly doped glass excited at 393 nm. Such chromaticity coordinates are close to those (0.67,0.33) standard of the National Television System Committee for the red phosphor. When the sodium–zinc–aluminosilicate glass is co-doped with Tb 3+ and Eu 3+ , reddish-orange light emission, with (0.61,0.37) CIE1931 chromaticity coordinates, is obtained upon Tb 3+ excitation at 344 nm. This reddish-orange luminescence is generated mainly by 5 D 0 → 7 F 1 and 5 D 0 → 7 F 2 emissions of Eu 3+ , europium being sensitized by terbium through a non-radiative energy transfer. From an analysis of the Tb 3+ emission decay curves it is inferred that the Tb 3+ →Eu 3+ energy transfer might take place between Tb 3+ and Eu 3+ clusters through a short-range interaction mechanism, so that an electric dipole–quadrupole interaction appears to be the most probable transfer mechanism. The efficiency of this energy transfer is about 62% upon excitation at 344 nm. In the singly doped and codoped glasses multimode optical waveguides were successfully produced by Ag + –Na + ion exchange, and they could be characterized at various wavelengths. -- Highlights: • Reddish-orange light emission can be generated from Tb 3+ and Eu 3+ codoped zinc–sodium–aluminosilicate glasses excited at 344 nm. • The Eu 3+ is sensitized by Tb 3+ through a non-radiative energy transfer. • Highly multimode waveguides can be fabricated by diluted silver–sodium exchange. • This type of AlGaN LEDs pumped glass phosphors might be useful for generation of reddish-orange light

Synthesis, structural and luminescence properties of Bi3+ co-doped Y2Sn2O7:Tb nanoparticles

International Nuclear Information System (INIS)

Nigam, S.; Sudarsan, V.; Vatsa, R.K.

2010-01-01

+ (2.5%) nanoparticles compared to Y 2 Sn 2 O 7 :Tb 3+ (2.5%) nanoparticles. Lattice distortion brought about by Bi 3+ incorporation at the Y 3+ site in the Y 2 Sn 2 O 7 lattice is responsible for the improved Tb 3+ luminescence

Optical and structural properties of nanostructured CeO2:Tb3+ film

International Nuclear Information System (INIS)

Ansari, Anees A.; Singh, S.P.; Malhotra, B.D.

2011-01-01

Nanostructured CeO 2 :Tb 3+ film has been fabricated on glass substrate through sol-gel technique via dip-coating process. (NH 4 ) 2 Ce(NO 3 ) 6 , Tb(NO 3 ) 3 .6H 2 O, ethylene glycol have been used as precursors for sol preparation. X-ray diffraction (XRD), scanning electron microscopy (SEM), UV/VIS and photoluminescence (PL) spectral studies have been employed to analyze the structural and optical properties of the film. XRD pattern has been used to analyze the crystallite nature and calculated particle size by Scherrer equation of nanostructured CeO 2 :Tb 3+ film, found in the range 3-4 nm. SEM image has been observed to analyze the surface topography of the film which is well porous, highly agglomerated and uniformly distributed nanoparticles on the film surface. Optical band gap of nanostructured CeO 2 :Tb 3+ film has been estimated as 3.57 eV. A significant enhancement in band shape of CeO 2 :Tb 3+ spectrum has been observed in PL spectra, showed their promising usages as optical materials in optoelectronic devices.

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

CSIR Research Space (South Africa)

Mhlongo, GH

2011-07-01

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

CMG-biotools, a free workbench for basic comparative microbial genomics.

Science.gov (United States)

Vesth, Tammi; Lagesen, Karin; Acar, Öncel; Ussery, David

2013-01-01

Today, there are more than a hundred times as many sequenced prokaryotic genomes than were present in the year 2000. The economical sequencing of genomic DNA has facilitated a whole new approach to microbial genomics. The real power of genomics is manifested through comparative genomics that can reveal strain specific characteristics, diversity within species and many other aspects. However, comparative genomics is a field not easily entered into by scientists with few computational skills. The CMG-biotools package is designed for microbiologists with limited knowledge of computational analysis and can be used to perform a number of analyses and comparisons of genomic data. The CMG-biotools system presents a stand-alone interface for comparative microbial genomics. The package is a customized operating system, based on Xubuntu 10.10, available through the open source Ubuntu project. The system can be installed on a virtual computer, allowing the user to run the system alongside any other operating system. Source codes for all programs are provided under GNU license, which makes it possible to transfer the programs to other systems if so desired. We here demonstrate the package by comparing and analyzing the diversity within the class Negativicutes, represented by 31 genomes including 10 genera. The analyses include 16S rRNA phylogeny, basic DNA and codon statistics, proteome comparisons using BLAST and graphical analyses of DNA structures. This paper shows the strength and diverse use of the CMG-biotools system. The system can be installed on a vide range of host operating systems and utilizes as much of the host computer as desired. It allows the user to compare multiple genomes, from various sources using standardized data formats and intuitive visualizations of results. The examples presented here clearly shows that users with limited computational experience can perform complicated analysis without much training.

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

Energy Technology Data Exchange (ETDEWEB)

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

2016-06-25

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

Tunable emission and concentration quenching of Tb{sup 3+} in magnesium phosphate lithium

Energy Technology Data Exchange (ETDEWEB)

Shi, Mingming; Zhang, Dongyun, E-mail: dyz@sit.edu.cn; Chang, Chengkang

2015-04-05

Highlights: • It is very likely the first time to realize tunable emission using Tb{sup 3+} as emitting centers. • Tb{sup 3+}:LiMgPO{sub 4} with colorful emissions are obtained by simply adjusting the Tb concentration. • The energy transfer method is implied by calculating the index of electric multipole interaction. • Either the dipole–dipole or exchange interaction method is proposed for each emission. - Abstract: Tunable photoluminescence of Tb{sup 3+}-doped LiMgPO{sub 4} (Tb{sup 3+}:LiMgPO{sub 4}) phosphors with different Tb{sup 3+} concentrations are successfully synthesized by a high temperature solid-state reaction routine. X-ray diffraction (XRD) and photoluminescent spectroscope (PLS) are employed to characterize the phosphors. It is found that a suitable firing temperature is important for the synthesis of the phosphors, and pure phase material can only be obtained around 900 °C. PL spectra reveals typical {sup 5}D{sub 4} to {sup 7}F{sub j} energy transition of Tb{sup 3+} ions, and the emission colors varied from red to green with Tb{sup 3+} concentration increasing, which is caused by the concentration quenching of Tb{sup 3+} emission centers in the LiMgPO{sub 4} matrix. The emissions peaking at 591, 619 and 695 nm are quenched at concentration of 1.5%, while the emissions at 489 nm and 543 nm are quenched at concentration of 8%. Further analysis of the data reveals two different energy transfer mechanisms for the five emission bands. The dipole–dipole model is proposed for the energy transfer of the red bands peaking at 694 nm, 619 nm and 591 nm, while the exchange interaction model is suggested for that of the green bands (543 nm and 489 nm), due to the different ion separations caused by different Tb concentrations.

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

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

International Nuclear Information System (INIS)

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

2006-01-01

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

Ionic liquid-assisted hydrothermal synthesis of dendrite-like NaY(MoO{sub 4}){sub 2}:Tb{sup 3+} phosphor

Energy Technology Data Exchange (ETDEWEB)

Tian Yue [Department of Physics, Dalian Maritime University, Dalian, Liaoning 116026 (China); College of Life Science, Dalian Nationalities University, Dalian, Liaoning 116600 (China); Chen Baojiu, E-mail: chenmbj@sohu.com [Department of Physics, Dalian Maritime University, Dalian, Liaoning 116026 (China); Tian Bining [Department of Physics, Dalian Maritime University, Dalian, Liaoning 116026 (China); College of Life Science, Dalian Nationalities University, Dalian, Liaoning 116600 (China); Sun Jiashi; Li Xiangping; Zhang Jinsu; Cheng Lihong; Zhong Haiyang; Zhong Hua [Department of Physics, Dalian Maritime University, Dalian, Liaoning 116026 (China); Meng Qingyu [School of Physics and Electronic Engineering, Harbin Normal University, Harbin 150025 (China); Hua Ruinian, E-mail: rnhua@dlnu.edu.cn [College of Life Science, Dalian Nationalities University, Dalian, Liaoning 116600 (China)

2012-07-01

Micro-sized NaY(MoO{sub 4}){sub 2}:Tb{sup 3+} phosphors with dendritic morphology was synthesized by a ionic liquid-assisted hydrothermal process. X-ray diffraction (XRD) indicated that the as-prepared product is pure tetragonal phase of NaY(MoO{sub 4}){sub 2}. Field emission scanning electron microscopy (FE-SEM) images showed that the as-prepared NaY(MoO{sub 4}){sub 2}:Tb{sup 3+} phosphors have dendritic morphology. The photoluminescent (PL) spectra displayed that the as-prepared NaY(MoO{sub 4}){sub 2}:Tb{sup 3+} phosphors show a stronger green emission with main emission wavelength 545 nm corresponding to the {sup 5}D{sub 4}{yields}{sup 7}F{sub 5} transition of Tb{sup 3+} ion, and the optimal Tb{sup 3+} doping concentration for obtaining maximum emission intensity was confirmed to be 10 mol%. Based on Van Uitert's and Dexter's models the electric dipole-dipole (D-D) interaction was confirmed to be responsible for the concentration quenching of {sup 5}D{sub 4} fluorescence of Tb{sup 3+} in the NaY(MoO{sub 4}){sub 2}:Tb{sup 3+} phosphors. The intrinsic radiative transition lifetime of {sup 5}D{sub 4} level is found to be 0.703 ms.

Fiscal 2000 project on measures for assisting and diffusing environmentally-friendly coal utilization system introduction. CMG recovery/utilization system joint demonstration project; 2000 nendo kankyo chowagata sekitan riyo system donyu shien nado fukyu taisaku jigyo chosa hokoku. CMG kaishu riyo system kyodo jissho jigyo

Energy Technology Data Exchange (ETDEWEB)

NONE

2001-03-01

A CMG (coal mine gas) recovery/utilization system was designed, constructed, and then demonstrated at a model coal mining district in Liaoning Province for the purpose of contributing to the solution of energy and environment related problems in China. The recovery system demonstration test, aiming to improve on safety and productivity of coal mining and to supply recovered gas with stability, involved gas drainage test boring, mine sealing, sealed gas induction control, centralized gas monitoring, etc., which were carried out at the coal mine working face. A utilization system demonstration test was conducted, and CMG would continue to be supplied to the current users and CMG utilization would be started at the other 6 coal mines. For the supply of CMG to large-scale gas consuming areas, steel materials were manufactured and processed for spherical gas holders and denitrification facilities, gas holders were constructed, pipe lines were installed, and a provisional gas supply was carried out. For the transfer and diffusion of the technology, Chinese engineers were trained in Japan and Japanese engineers were dispatched to China. (NEDO)

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

Science.gov (United States)

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

2017-08-09

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

Prominent blue emission through Tb3+ doped La2O3 nano-phosphors for white LEDs

Science.gov (United States)

Jain, Neha; Singh, Rajan Kr; Srivastava, Amit; Mishra, S. K.; Singh, Jai

2018-06-01

In this article, we report the tunable luminescence emission of Tb3+ doped La2O3 nanophosphors synthesized by a facile and effective Polyol method. The structural and surface morphological studies have been carried out by employing X-ray diffraction (XRD) and scanning electron microscopy (SEM), respectively. The XRD studies elucidate the proper phase formation and the results emanate from Raman spectroscopy of the as synthesized nanophosphor affirms it. The optical properties of the as fabricated nanoparticles have been investigated by Raman and photoluminescence (PL) spectroscopy. The PL spectroscopy shows the occurrence of excitation peaks at 305, 350 and 375 nm for 543 nm emissions, correspond to transition 5D4 →7F5. Emission spectra with 305 nm excitation exhibits characteristic emission peaks of Tb3+ion at 472, 487, 543 and 580 nm. The intensity of emission increases with Tb3+ concentration and is most prominent for 7 at% Tb3+ ion. The characteristic emissions of Tb3+ ion owes to the transition in which intensities of blue and green emission are prominent. The dominant intensity has been found for 472 nm (for blue emission). Commission international d 'Eclairage (CIE) co-ordinates have found in the light blue to green region. The research work provides a new interesting insight dealing with tunable properties with Tb3+ doping in La2O3 nanophosphors, to be useful for display devices, solar cells, LEDs and optoelectronic devices.

The phase transition of the incommensurate phases β-Ln(PO3)3(Ln=Y,Tb...Yb), crystal structures of α-Ln(PO3)3(Ln=Y,Tb...Yb) and Sc(PO3)3

International Nuclear Information System (INIS)

Hoeppe, Hennig A.

2009-01-01

The incommensurately modulated room-temperature phases β-Ln(PO 3 ) 3 (Ln=Y,Tb...Yb) undergo a topotactic phase transition monitored by vibrational spectroscopy below 180 K leading to α-Ln(PO 3 ) 3 (Ln=Y,Dy...Yb), above 200 K the incommensurate phases are reobtained. The low-temperature phases exhibit a new structure type (α-Dy(PO 3 ) 3 ,P2 1 /c,Z=12,a=14.1422(6),b=20.0793(9),c=10.1018(4)A, β=127.532(3) 0 ). α-Tb(PO 3 ) 3 is isotypic with Gd(PO 3 ) 3 (α-Tb(PO 3 ) 3 ,I2/a,Z=16,a=25.875(6),b=13.460(3),c=10.044(2)A, β=119.13(3) 0 ). The symmetry relations between the involved phases of the phase transition are discussed. The crystal structure of Sc(PO 3 ) 3 is isotypic with that of Lu(PO 3 ) 3 and C-type phosphates. The polyphosphates consist of infinite zig-zag chains of corner-sharing PO 4 tetrahedra, the cations are coordinated sixfold in an almost octahedral arrangement. To confirm the quality of the determined crystal structures the deviation of the phosphate tetrahedra from ideal symmetry was determined and discussed. - Abstract: Basic structure from which all crystal structures of the late lanthanoids' polyphosphates at room temperature and below can be derived.

Na3Tb(PO4)2: Synthesis, crystal structure and greenish emitting properties

Science.gov (United States)

Zhao, Dan; Ma, Zhao; Liu, Bao-Zhong; Zhang, Rui-Juan; Wu, Zhi-Qiang; Wang, Jian; Duan, Pei-Gao

2018-03-01

A anhydrous orthoborate Na3Tb(PO4)2 has been prepared and its crystal structure was determined by X-Ray diffraction of a non-merohedral twinned single crystal. The results show that the compound crystallizes in monoclinic space group C2/c and the structure features a 3D framework containing PO4, NaO6, NaO7, NaO8 and TbO8 polyhedra. Under near-UV excitation (370 nm), Na3Tb(PO4)2 shows intense characteristic emission bands of Tb3+ (490 nm, 543 nm, 585 nm and 620 nm) with the CIE coordinate of (0.3062, 0.5901), corresponding to greenish color. The excitation spectrum covers a wide range from 340 nm to 390 nm, which indicates that phosphor Na3Tb(PO4)2 can be efficiently activated by near-UV LED ship.

Microstructural and photoluminescence properties of sol–gel derived Tb3+ doped ZnO nanocrystals

CSIR Research Space (South Africa)

Kabongo, GL

2014-04-01

Full Text Available Un-doped and Tb(Sup3+) doped ZnO nanocrystals with different concentrations of Tb(Sup3+) were synthesized by a sol–gel method and their photoluminescence (PL) properties were investigated. The successful incorporation of Tb(sup3+) ions...

Luminescence and energy transfer studies on Sm3+/Tb3+codoped telluroborate glasses for WLED applications

Science.gov (United States)

Uma, V.; Vijayakumar, M.; Marimuthu, K.; Muralidharan, G.

2018-01-01

A new series of Sm3+/Tb3+ codoped telluroborate glasses have been prepared by conventional melt quenching technique with the chemical composition (40-x-y)B2O3+15TeO2+15Li2O+15LiF+15NaF+xTb2O3+ySm2O3 (where x = 0, 0.5; y = 0, 0.05, 0.1, 0.25, 0.5, 1 and 2 wt%). The structural and optical behaviour of the prepared glasses were investigated through Fourier transform infrared spectroscopy (FTIR), optical absorption, photoluminescence and lifetime measurements. The fundamental vibrational units of the borate and tellurite network have been identified through FTIR spectra. Nephelauxetic ratio (βbar) and bonding parameter (δ) values indicate that the Smsbnd O bonds are ionic in nature. The characteristic emissions of terbium (543 nm, green) and samarium (645 nm, orange-red) were observed while exciting the Tb3+ ions. Higher magnitude of asymmetric intensity ratio (AIR) values confirms the higher asymmetry around the Sm3+ ion site. Decay profiles of Tb3+ ions (5D4 state) and Sm3+ ions (4G9/2 state) exhibit double exponential nature. The nature of interaction between the donor (Tb3+) and acceptor (Sm3+) has been analyzed through Inokuti-Hirayama (IH) model. Energy transfer from Tb3+ to Sm3+ ions is dominated by dipole-dipole type interaction. TBLT0.5S glass possess the better colour coordinates (0.41, 0.45) and colour correlated temperature (CCT) value (3524 K) and the same is suggested for eye safe warm white light emitting applications.

Tunable emission and the systematic study on energy-transfer properties of Ce3+- and Tb3+-co-doped Sr3(PO4)2 phosphors

International Nuclear Information System (INIS)

Liu, Zhijun

2015-01-01

An emitting color tunable phosphor Sr 3 (PO 4 ) 2 :Ce 3+ , Tb 3+ was synthesized by the traditional high-temperature solid-state reaction method. The photoluminescence and energy-transfer (ET) properties of Ce 3+ - and Tb 3+ -doped Sr 3 (PO 4 ) 2 host were studied in detail. The obtained phosphors show both a blue emission from Ce 3+ and a yellowish green emission from Tb 3+ with considerable intensity under ultraviolet (UV) excitation (∝311 nm). When the content of Ce 3+ was fixed at 0.03, the emission chromaticity coordinates could be adjusted from blue to green region by tuning the contents of Tb 3+ ions with the aid of ET process. The critical distance between Ce 3+ and Tb 3+ is 14.69 A. The ET mechanism from Ce 3+ to Tb 3+ ions was identified with dipole-dipole interaction. The obtained phosphor exhibits a strong excitation in UV spectral region and high-efficient ET from Ce 3+ to Tb 3+ ions. It may find applications as a green light-emitting UV-convertible phosphor in white LED devices. (orig.)

Dosimetric characterization of KMgF3:Tb+PTFE

International Nuclear Information System (INIS)

Ramirez R, M. I.; Garcia S, L.; Villicana M, M.; Huirache A, R.; Apolinar C, J.; Gonzalez M, P. R.

2017-10-01

In this work the results obtained from the dosimetric characterization of the new radiation detectors of KMgF 3 :Tb+PTFE are presented. The host salt was obtained by means of the microwave technique, with the polycrystalline powder obtained, dosimeters were made in tablet form, using as Ptfe binder. The thermoluminescent response of these new detectors presented a linear behavior, in the dose range between 1 and 1000 Gy of 60 Co gamma radiation, the reproducibility test in the measurements, during ten cycles of heat treatment, irradiation and reading presented ± 3.7% Ds, in the stability test of thermoluminescent signal, during two months showed that the fading is practically null. Due to the results obtained, this new detector could be very useful for the dosimetry of ionizing radiation in different clinical applications. (Author)

Tb{sup 3+}/Eu{sup 3+}: YF{sub 3} nanophase embedded glass ceramics: Structural characterization, tunable luminescence and temperature sensing behavior

Energy Technology Data Exchange (ETDEWEB)

Chen, Daqin, E-mail: dqchen@hdu.edu.cn [College of Materials & Environmental Engineering, Hangzhou Dianzi University, Hangzhou, 310018 (China); Wang, Zhongyi; Zhou, Yang [College of Materials & Environmental Engineering, Hangzhou Dianzi University, Hangzhou, 310018 (China); Huang, Ping, E-mail: phuang@fjirsm.ac.cn [State Key Laboratory of Structural Chemistry, Fujian Institute of Research on The Structure of Matter, Chinese Academy of Sciences, Fuzhou, Fujian 350002 (China); Ji, Zhenguo, E-mail: jizg@hdu.edu.cn [College of Materials & Environmental Engineering, Hangzhou Dianzi University, Hangzhou, 310018 (China)

2015-10-15

Tb{sup 3+}/Eu{sup 3+} co-doped transparent bulk glass ceramics containing orthorhombic β-YF{sub 3} nanocrystals were successfully synthesized by melt-quenching and subsequent heating. The partition of the active centers into the YF{sub 3} crystalline lattice was confirmed by elemental mapping in the scanning transmission electron microscope, emission spectra and decay curves. As a consequence, Tb{sup 3+} → Eu{sup 3+} energy transfer was demonstrated to be more efficient in the glass ceramic than in the precursor glass, which resulted in color tunable luminescence by simply modifying Eu{sup 3+} content and induced the linearly temperature-dependent fluorescence intensity ratio between the Tb{sup 3+}: {sup 5}D{sub 4} → {sup 7}F{sub 5} transition and the Eu{sup 3+}: {sup 5}D{sub 0} → {sup 7}F{sub 4} one in the Tb{sup 3+}/Eu{sup 3+} co-doped glass ceramic. It is expected that the investigated glass ceramic might be a promising candidate for solid-state lighting as well as optical temperature sensor. - Highlights: • Lanthanide doped glass ceramics containing YF{sub 3} nanocrystals were fabricated. • Tb{sup 3+} and Eu{sup 3+} dopants were confirmed to incorporate into YF{sub 3} lattice. • Tunable luminescence was realized via Tb{sup 3+} → Eu{sup 3+} energy transfer. • Linearly temperature-dependent fluorescence intensity ratio was detected.

Luminescence properties and dynamical processes of energy transfer in BiPO{sub 4}: Tb{sup 3+},Eu{sup 3+} phosphor

Energy Technology Data Exchange (ETDEWEB)

Zhong, Jianming; Zhao, Weiren, E-mail: zwren123@126.com; Song, Enhai; Deng, Yongqiang

2014-10-15

A series of new emission-tunable phosphors Bi{sub 0.95−y}PO{sub 4}:0.05Tb{sup 3+},yEu{sup 3+} were synthesized by a facile hydrothermal method with surfactant-free environment. XRD results indicated that phosphors possess the standard BiPO{sub 4} monoclinic structure. From the luminescence spectra and decay curves, the energy transfer from Tb{sup 3+} to Eu{sup 3+} was confirmed. The efficient Tb{sup 3+} to Eu{sup 3+} energy transfer can be used to tune the emission color from green, yellow to orange by simply changing the concentration of europium, making the materials have potential applications in three-color-based displays and white light illumination. Finally, the energy transfer mechanism between Tb{sup 3+} and Eu{sup 3+} was demonstrated to be the electric quadrupole–quadrupole interaction based on Dexter's energy transfer formula and the Inokuti–Hirayama model. - Highlights: • BiPO{sub 4}: Tb{sup 3+}, Eu{sup 3+} phosphor was synthesized by a facile hydrothermal method. • Energy transfer from Tb{sup 3+} to Eu{sup 3+} in BiPO{sub 4} was firstly studied. • The Q–Q interaction is the main mechanism for energy transfer from Tb{sup 3+} to Eu{sup 3+}. • BiPO{sub 4}: Tb{sup 3+}, Eu{sup 3+} has potential applications in white LEDs and display devices.

Fabrication and luminescence properties of Al{sub 2}O{sub 3}:Tb{sup 3+} microspheres via a microwave solvothermal route

Energy Technology Data Exchange (ETDEWEB)

Zhu Zhenfeng, E-mail: zhuzf@sust.edu.cn [School of Materials Science and Engineering, Shaanxi University of Science and Technology, Xi' an 710021 (China); Liu Dianguang; Liu Hui; Li Guangjun; Du Juan; He Zuoli [School of Materials Science and Engineering, Shaanxi University of Science and Technology, Xi' an 710021 (China)

2012-02-15

Al{sub 2}O{sub 3}:Tb{sup 3+} green phosphors were synthesized via a microwave solvothermal and thermal decomposition route, and characterized by X-ray diffraction (XRD), scanning electron microscope (SEM), photoluminescence (PL) spectra, and decay curves. XRD results indicate that Tb{sup 3+} doped samples are {gamma}-Al{sub 2}O{sub 3} after being calcined at 773 K. SEM results show that the particles of Al{sub 2}O{sub 3}:Tb{sup 3+} are hierarchically nanostructured microspheres assembled from nanosheets. The PL spectra indicate that the {sup 5}D{sub 4}{yields}{sup 7}F{sub 5} (545 nm) electric dipole transition is the most intensive when excited at 235 nm. It is shown that 0.7 mol% of doping concentration of Tb{sup 3+} ions in {gamma}-Al{sub 2}O{sub 3}:Tb{sup 3+} is optimum. According to Dexter's theory, the critical distance between Tb{sup 3+} ions for energy transfer was determined to be 18.4 A. It is found that the curve followed the single-exponential decay. The excellent chromaticity coordinates of Al{sub 2}O{sub 3}:Tb{sup 3+} phosphors, as defined by the International Commission on Illumination (CIE), indicate that it is a good candidate for use in light display systems and optoelectronic devices. - Highlights: Black-Right-Pointing-Pointer Al{sub 2}O{sub 3}:Tb{sup 3+} phosphors prepared via a microwave solvothermal route. Black-Right-Pointing-Pointer The particles were hierarchically nanostructured microspheres packaged by nanosheets. Black-Right-Pointing-Pointer {sup 5}D{sub 4}{yields}{sup 7}F{sub 5} electric dipole transition is the most intensive when excited at 235 nm. Black-Right-Pointing-Pointer 0.7 mol% of doping concentration of Tb{sup 3+} ions in {gamma}-Al{sub 2}O{sub 3}:Tb{sup 3+} is optimum. Black-Right-Pointing-Pointer Critical distance between Tb{sup 3+} ions for energy transfer is 18.4 A.

Expanded polyfunctional T cell response to mycobacterial antigens in TB disease and contraction post-treatment.

Directory of Open Access Journals (Sweden)

James M Young

2010-06-01

Full Text Available T cells producing multiple factors have been shown to be required for protection from disease progression in HIV but we have recently shown this not to be the case in TB. Subjects with active disease had a greater proportion of polyfunctional cells responding to ESAT-6/CFP-10 stimulation than their infected but non-diseased household contacts (HHC. We therefore wanted to assess this profile in subjects who had successfully completed standard TB chemotherapy.We performed a cross-sectional study using PBMC from TB cases (pre- and post-treatment and HHC. Samples were stimulated overnight with TB antigens (ESAT-6/CFP-10 and PPD and their CD4+ and CD8+ T cells were assessed for production of CD107a, IFN-gamma, IL-2 and TNF-alpha and the complexity of the responses was determined using SPICE and PESTLE software.We found that an increase in complexity (i.e., production of more than 1 factor simultaneously of the T cell profile was associated with TB disease and that this was significantly reduced following TB treatment. This implies that T cells are able to respond adequately to TB antigens with active disease (at least initially but the ability of this response to protect the host from disease progression is hampered, presumably due to immune evasion strategies by the bacteria. These findings have implications for the development of new diagnostics and vaccine strategies.

New reddish-orange and greenish-yellow light emitting phosphors: Eu{sup 3+} and Tb{sup 3+}/Eu{sup 3+} in sodium germanate glass

Energy Technology Data Exchange (ETDEWEB)

Álvarez, E. [Departamento de Física, Universidad de Sonora (UNISON), Boulevard Luis Encinas y Rosales s/n, Hermosillo 83000, Sonora (Mexico); Zayas, Ma. E. [Departamento de Investigación en Física, Universidad de Sonora (UNISON), Boulevard Luis Encinas y Rosales s/n, Hermosillo 83000, Sonora (Mexico); Alvarado-Rivera, J. [Departamento de Física, Universidad de Sonora (UNISON), Boulevard Luis Encinas y Rosales s/n, Hermosillo 83000, Sonora (Mexico); Félix-Domínguez, F. [Departamento de Física, Universidad de Sonora (UNISON), Boulevard Luis Encinas y Rosales s/n, Hermosillo 83000, Sonora (Mexico); Centro de investigación en Materiales Avanzados, S.C. Miguel de Cervantes 120, Complejo industrial Chihuahua, Chihuahua 31109, Chihuahua (Mexico); Duarte-Zamorano, R.P. [Departamento de Física, Universidad de Sonora (UNISON), Boulevard Luis Encinas y Rosales s/n, Hermosillo 83000, Sonora (Mexico); Caldiño, U., E-mail: cald@xanum.uam.mx [Departamento de Física, Universidad Autónoma Metropolitana-Iztapalapa, PO Box 55-534, México City 09340, Distrito Federal (Mexico)

2014-09-15

A spectroscopic analysis of sodium germanate glasses activated with Eu{sup 3+}, Tb{sup 3+} and Eu{sup 3+}/Tb{sup 3+} is performed from their photoluminescence spectra and decay times. In the Eu{sup 3+}-singly doped glass reddish-orange light emission, with x=0.64 and y=0.35 CIE1931 chromaticity coordinates, is obtained upon Eu{sup 3+} excitation at 393 nm. Such chromaticity coordinates are close to those (0.67, 0.33) proposed by the National Television Standard Committee for the red phosphor. When the sodium germanate glass is co-doped with Tb{sup 3+} and Eu{sup 3+} greenish-yellow light emission, with (0.41, 0.46) CIE1931 chromaticity coordinates, is obtained upon Tb{sup 3+} excitation at 344 nm. Such greenish-yellow luminescence is due mainly to the terbium {sup 5}D{sub 4}→{sup 7}F{sub 6,5} and europium {sup 5}D{sub 0}→{sup 7}F{sub 1,2} emissions, Eu{sup 3+} being sensitized by Tb{sup 3+} through a non-radiative energy transfer. The non-radiative nature of this energy transfer is inferred from the increase in the decay rate of the Tb{sup 3+} emission when the glass is co-doped with Eu{sup 3+}. From an analysis of the Tb{sup 3+} emission decay time curves it is inferred that such energy transfer might take place between Tb{sup 3+} and Eu{sup 3+} clusters through a short-range interaction mechanism. - Highlights: • Sodium germanate glasses are optically activated with Eu{sup 3+} (GNE) and Tb{sup 3+}/Eu{sup 3+} (GNTE). • Reddish-orange light (0.64, 0.35) is generated by GNE pumped with 393 nm light. • Greenish-yellow light (0.41, 0.46) is generated by GNTE pumped with 344 nm light. • Non-radiative energy transfer Tb{sup 3+}→Eu{sup 3+} takes place in GNTE.

Temperature and concentration quenching of Tb{sup 3+} emissions in Y{sub 4}Al{sub 2}O{sub 9} crystals

Energy Technology Data Exchange (ETDEWEB)

Boruc, Z., E-mail: z.boruc@stud.elka.pw.edu.pl [Institute of Microelectronics and Optoelectronics, Warsaw University of Technology, ul. Koszykowa 75, 00-662 Warsaw (Poland); Fetlinski, B.; Kaczkan, M. [Institute of Microelectronics and Optoelectronics, Warsaw University of Technology, ul. Koszykowa 75, 00-662 Warsaw (Poland); Turczynski, S.; Pawlak, D. [Institute of Electronic Materials Technology, ul. Wolczynska 133, 01-919 Warsaw (Poland); Malinowski, M. [Institute of Microelectronics and Optoelectronics, Warsaw University of Technology, ul. Koszykowa 75, 00-662 Warsaw (Poland)

2012-08-15

Highlights: Black-Right-Pointing-Pointer Spectroscopic properties of Tb{sup 3+}:Y{sub 4}Al{sub 2}O{sub 9} crystals are studied. Black-Right-Pointing-Pointer Concentration and temperature dependencies of fluorescence are investigated. Black-Right-Pointing-Pointer The cross-relaxation transfer rates are experimentally determined. Black-Right-Pointing-Pointer Strong influence of cross relaxation process on {sup 5}D{sub 3} emission quenching is observed. Black-Right-Pointing-Pointer Decays are modelled using Inokuti-Hirayama approach. - Abstract: Spectroscopic properties of trivalent terbium (Tb{sup 3+}) activated Y{sub 4}Al{sub 2}O{sub 9} (abbreviated YAM) crystals were studied. Concentration and temperature dependent emission spectra and fluorescence dynamics profiles have been investigated in YAM:Tb{sup 3+} in order to understand better processes responsible for quenching of the terbium {sup 5}D{sub 3} and {sup 5}D{sub 4} emissions. Decays were modelled using Inokuti-Hirayama approach to obtain information on the energy transfer mechanism. The cross-relaxation transfer rates were experimentally determined as a function of temperature and Tb{sup 3+} concentration. The investigation revealed strong influence of cross-relaxation process on {sup 5}D{sub 3} emission quenching. The two different processes responsible for the increase of fluorescence quenching with growing temperature were observed, both related to thermal activation energy. For temperatures above 700 K, the temperature dependence of the emission intensity ratio ({sup 5}D{sub 3}/{sup 5}D{sub 4}) becomes linear and the decay times are rapidly decreasing monotonously with increasing temperature, what is confirming the potential of Y{sub 4}Al{sub 2}O{sub 9}:Tb{sup 3+} material in high temperature luminescence thermometry.

Polycrystalline (TbXY1-X)2O3 Faraday rotator.

Science.gov (United States)

Ikesue, Akio; Aung, Yan Lin; Makikawa, Shinji; Yahagi, Akira

2017-11-01

We have succeeded for the first time in synthesizing an optical grade (Tb X Y 1-X ) 2 O 3 (X=0.5-1.0) ceramic Faraday rotator, which greatly exceeds the basic characteristics of the commercial terbium gallium garnet (TGG) (Tb 3 Ga 5 O 12 ) crystal. The Faraday rotation angle increased as the Tb concentration increased, and the Verdet constant increased from 2.1 (82  rad T -1  m -1 at X=0.5) to 3.8 times (154  rad T -1  m -1 at X=1.0) than the TGG single crystal, which is regarded as highest class. Therefore, it is possible to minimize the Faraday rotator length and the magnet in building an optical isolator. It was also confirmed that its optical quality was very comparable to the commercial TGG crystal.

Anisotropy of the Mechanical Properties of TbF3 Crystals

Science.gov (United States)

Karimov, D. N.; Lisovenko, D. S.; Sizova, N. L.; Sobolev, B. P.

2018-01-01

TbF3 (sp. gr. Pnma) crystals up to 40 mm in diameter have been grown from melt by a Bridgman technique. The anisotropy of their mechanical properties is studied for the first time. the technical elasticity constants are calculated, and room-temperature values of Vickers microhardness for the (010) and (100) planes are measured. The shape of indentation impressions is found to correlate with Young's modulus anisotropy for TbF3 crystals.

Synthesis, structural, thermal and optical studies of rare earth coordinated complex: Tb(Sal){sub 3}Phen

Energy Technology Data Exchange (ETDEWEB)

Kaur, Gagandeep; Dwivedi, Y. [Laser and Spectroscopy Laboratory, Department of Physics, Banaras Hindu University, Varanasi 221005 (India); Rai, S.B., E-mail: sbrai49@yahoo.co.in [Laser and Spectroscopy Laboratory, Department of Physics, Banaras Hindu University, Varanasi 221005 (India)

2011-11-01

Highlights: {yields} RE coordinated complex of Tb(Sal){sub 3}Phen in crystalline phases were synthesized. {yields} Enhancement in luminescence of Tb{sup 3+} was observed in complex on 355 nm excitation. {yields} Fluorescence enhancement is due to the efficient energy transfer from Sal to Tb{sup 3+}. {yields} An observed increase in lifetime of Tb{sup 3+} is due to encapsulation in Sal/Phen network. {yields} The present system is a deserving candidate for LSC when coupled with solar cells. - Abstract: Complexes of salicylic acid (Sal) and 1,10-phenanthroline (Phen) were synthesized coordinated with terbium ion (Tb{sup 3+}) in crystalline phases. The structural characterizations of the lanthanide complex were made using FT-IR, NMR ({sup 1}H and {sup 13}C) and XRD techniques. These measurements confirm the formation of Tb(Sal){sub 3}Phen complex structure. The thermal aspects of the complex were examined using DTA and TGA techniques. An enhancement in luminescence intensity of Tb{sup 3+} ion bands were observed in Tb(Sal){sub 3}Phen complex as compared to TbCl{sub 3} crystals on 355 nm laser excitation. Enhancement is reported due to the efficient energy transfer process from Sal to Tb{sup 3+} ions. This is also confirmed by the time resolved photoluminescence spectroscopy with increase in lifetime of Tb{sup 3+} ions due to encapsulation in Sal/Phen network. Our system in itself can be a deserving candidate for luminescent solar collector material when coupled with solar cells.

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

Science.gov (United States)

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

2017-12-05

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

Thermoluminescence properties of Al2O3:Tb nanoparticles irradiated by gamma rays and 85 MeV C6+ ion beam

International Nuclear Information System (INIS)

Salah, Numan; Alharbi, Najlaa D.; Habib, Sami S.; Lochab, S.P.

2015-01-01

Carbon ions beam is recently recognized as an ideal cancer treatment modality, because of its excellent local tumor control. These ions have a high relative biological effectiveness resulting from high linear energy transfer (LET) and their sharp Bragg peak. However, the dose of those energetic ions needs to be measured with great precision using a proper dosimeter. Aluminum Oxide (Al 2 O 3 ) is a highly luminescent phosphor widely used for radiation dosimetry using thermoluminesence (TL) technique. In this work nanoparticles of this material activated by different elements like Eu, Tb, Dy, Cu and Ag were evaluated for their TL response to gamma rays irradiation. Tb doped sample is found to be the most sensitive sample, which could be selected for exposure to 85 MeV C 6+ ion beam in the fluence range 10 9 –10 13 ions/cm 2 . The obtained result shows that C ion beam irradiated sample has a simple glow curve structure with a prominent glow peak at around 230 °C. This glow curve has a dosimetric peak better than those induced by gamma rays. This glow peak exhibits a linear response in the range 10 9 –10 11 ions/cm 2 , corresponding to the equivalent absorbed doses 0.285–28.5 kGy. The absorbed doses, penetration depths and main energy loss were calculated using TRIM code based on the Monte Carlo simulation. The wide linear response of Al 2 O 3 :Tb nanoparticles along with the low fading makes this low cost nanomaterial a good candidate for C ion beam dosimetry. - Highlights: • Nanoparticles of Al 2 O 3 doped with Eu, Tb, Dy, Cu and Ag were synthesised. • They were evaluated for their TL response to gamma rays and C ion beam irradiation. • Tb doped sample is the most sensitive sample to gamma rays. • Al 2 O 3 :Tb was exposed to 85 MeV C 6+ ion beam in the fluence range 10 9 -10 13 ions/cm 2 . • The glow peak induced by C ions has a linear response in the range 10 9 -10 11 ions/cm 2

The TbBr3–LiBr binary system: Experimental thermodynamic investigation and assessment of phase diagram

International Nuclear Information System (INIS)

Rycerz, L.; Gong, W.; Gaune-Escard, M.

2013-01-01

Highlights: ► DSC measurements for the (LiBr + TbBr 3 ) system. ► congruently Li3TbBr 6 and incongruently melting Li5TbBr 8 compounds. ► Thermodynamic description of the liquid phase in the (LiBr + TbBr 3 ) system. ► Assessment with a two-sublattice ionic solution model. - Abstract: DSC was used to study the phase equilibrium in the TbBr 3 –LiBr binary system. The results obtained provided a basis for constructing the phase diagram of this system. It exhibits two compounds: Li 5 TbBr 8 , which decomposes in the solid state at 611 K, and Li 3 TbBr 6 , which melts congruently at 785 K with the related enthalpy 59.1 kJ·mol −1 . The binary LiBr–TbBr 3 system was then optimized using the available experimental information on phase diagram and thermodynamic properties. A two-sub-lattice ionic solution model (Li + ) P :(Br − , TbBr 6 −3 , TbBr 3 ) Q was adopted to describe the liquid phase. The present assessment of the binary LiBr–TbBr 3 system was in good agreement with the corresponding experimental data and confirmed their consistency.

Color-tunable and highly thermal stable Sr_2MgAl_2_2O_3_6:Tb"3"+ phosphors

International Nuclear Information System (INIS)

Zhang, Haiming; Zhang, Haoran; Liu, Yingliang; Lei, Bingfu; Deng, Jiankun; Liu, Wei-Ren; Zeng, Yuan; Zheng, Lingling; Zhao, Minyi

2017-01-01

Tb"3"+ activated Sr_2MgAl_2_2O_3_6 phosphor was prepared by a high-temperature solid-state reaction route. The X-ray diffraction, scanning electron microscopy, and photoluminescence spectroscopy were used to characterize the as-prepared samples. The Sr_2MgAl_2_2O_3_6:Tb"3"+ phosphors show intense green light emission under UV excitation. The phosphor exhibit two groups of emission lines from about 370 to 700 nm, which originating from the characteristic "5D_3-"7F_J and "5D_4-"7F_J transitions of the Tb"3"+ ion, respectively. The cross-relaxation mechanism between the "5D_3 and "5D_4 emission was investigated and discussed. The emission colors of these phosphors can be tuned from bluish-green to green by adjusting the Tb"3"+ doping concentration. Furthermore, the thermal quenching temperature (T_1_/_2) is higher than 500 K. The excellent thermal stability and color-tunable luminescent properties suggest that the developed material is a promising green-emitting phosphor candidate for optical devices. - Highlights: • A Color-tunable emitting phosphor Sr_2MgAl_2_2O_3_6:Tb"3"+ was prepared successfully via high-temperature solid-state reaction. • The photoluminescence of Sr_2MgAl_2_2O_3_6:Tb"3"+ shows highly thermal stable. • The cross-relaxation mechanism between the "5D_3 and "5D_4 emission was investigated and discussed.

Facile Template-Free Fabrication of the hollow sea cucumber-like TbF{sub 3} and luminescent properties

Energy Technology Data Exchange (ETDEWEB)

Gao, Yu, E-mail: gaoy777@126.com [College of Materials Science and Engineering, Shenyang University of Chemical Technology, Shenyang, 100142 (China); Shi, Shan; Fang, Qinghong; Yang, Feng [College of Materials Science and Engineering, Shenyang University of Chemical Technology, Shenyang, 100142 (China); Xu, Zhenhe [College of Applied Chemistry, Shenyang University of Chemical Technology, Shenyang, 100142 (China)

2014-12-15

Graphical abstract: Hollow sea cucumber-like TbF{sub 3} has been prepared via a facile hydrothermal route. The possible growth mechanism and the luminescent properties of the as-prepared sample have been discussed. - Highlights: • TbF3 particles were prepared by a facile hydrothermal route. • TbF3 product show strong green emission. • This method may be more widely applicable in the design of other rare-earth compounds. - Abstract: Hollow sea cucumber-like TbF{sub 3} was successfully fabricated by a self-assembled hydrothermal method. The crystal structure, morphology and photoluminescence properties of the as-prepared TbF{sub 3} crystals were investigated. The results revealed that the as-prepared TbF{sub 3} sample has orthorhombic structure and composed of monodispersed 3D hollow sea cucumber-like particles. The possible formation mechanism for sea cucumber-like TbF{sub 3} is presented in detail. Additionally, the as-prepared sample possesses property of down-conversion photoluminescence. The excitation spectrum of TbF{sub 3} sample was obtained by monitoring the emission of Tb{sup 3+} at 545 nm was composed of the characteristics f–f transition lines within the Tb{sup 3+} 4f{sup 8} configuration. Under the UV light irradiation, the emission spectrum exhibited four obvious lines centered at 491, 545, 588, and 620 nm, which was corresponding to the {sup 5}D{sub 4} → {sup 7}F{sub J} (J = 6, 5, 4, 3) transitions of the Tb{sup 3+} ions in the TbF{sub 3} nanoparticles.

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

Science.gov (United States)

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

2015-02-07

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

A comparative study on the luminescence properties of Ce3+/Tb3+ doped Gd-based host nanomaterials

Science.gov (United States)

Jadhao, Charushila Vasant; Rani, Barkha; Sahu, Niroj Kumar

2018-04-01

A comparative study on the crystal phases and their respective luminescence behaviour of Gd3+ based host materials such as GdPO4, GdF3, GdVO4 and Gd2O3 sensitized with 7at.% Ce3+ and activated with 5 at.% Tb3+ have been reported. The nanomaterials were prepared by polyol method using ethylene glycol as solvent and found to have different crystal structures such as monoclinic, orthorhombic, tetragonal and cubic phase. Clear characteristics emission from Tb3+ has been observed in all the samples when excited in the absorption wavelength of Ce3+ and Gd3+ (˜280 nm). Among all the above materials, intense emission of Tb3+ is found in GdPO4 followed by GdF3, Gd2O3 and GdVO4 respectively. The Tb3+ emission is strongly influenced by the energy transfer process and crystal structure of the host materials and hence this study will be important for choosing suitable materials for display devices and biomedical applications.

Integrated nanophotonic hubs based on ZnO-Tb(OH3/SiO2 nanocomposites

Directory of Open Access Journals (Sweden)

Lin Yu

2011-01-01

Full Text Available Abstract Optical integration is essential for practical application, but it remains unexplored for nanoscale devices. A newly designed nanocomposite based on ZnO semiconductor nanowires and Tb(OH3/SiO2 core/shell nanospheres has been synthesized and studied. The unique sea urchin-type morphology, bright and sharply visible emission bands of lanthanide, and large aspect ratio of ZnO crystalline nanotips make this novel composite an excellent signal receiver, waveguide, and emitter. The multifunctional composite of ZnO nanotips and Tb(OH3/SiO2 nanoparticles therefore can serve as an integrated nanophotonics hub. Moreover, the composite of ZnO nanotips deposited on a Tb(OH3/SiO2 photonic crystal can act as a directional light fountain, in which the confined radiation from Tb ions inside the photonic crystal can be well guided and escape through the ZnO nanotips. Therefore, the output emission arising from Tb ions is truly directional, and its intensity can be greatly enhanced. With highly enhanced lasing emissions in ZnO-Tb(OH3/SiO2 as well as SnO2-Tb(OH3/SiO2 nanocomposites, we demonstrate that our approach is extremely beneficial for the creation of low threshold and high-power nanolaser.

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

Energy Technology Data Exchange (ETDEWEB)

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

1975-01-01

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

Differential cellular recognition pattern to M. tuberculosis targets defined by IFN-γ and IL-17 production in blood from TB + patients from Honduras as compared to health care workers: TB and immune responses in patients from Honduras.

Science.gov (United States)

Alvarez-Corrales, Nancy; Ahmed, Raija K; Rodriguez, Carol A; Balaji, Kithiganahalli N; Rivera, Rebeca; Sompallae, Ramakrishna; Vudattu, Nalini K; Hoffner, Sven E; Zumla, Alimuddin; Pineda-Garcia, Lelany; Maeurer, Markus

2013-03-06

A better understanding of the quality of cellular immune responses directed against molecularly defined targets will guide the development of TB diagnostics and identification of molecularly defined, clinically relevant M.tb vaccine candidates. Recombinant proteins (n = 8) and peptide pools (n = 14) from M. tuberculosis (M.tb) targets were used to compare cellular immune responses defined by IFN-γ and IL-17 production using a Whole Blood Assay (WBA) in a cohort of 148 individuals, i.e. patients with TB + (n = 38), TB- individuals with other pulmonary diseases (n = 81) and individuals exposed to TB without evidence of clinical TB (health care workers, n = 29). M.tb antigens Rv2958c (glycosyltransferase), Rv2962c (mycolyltransferase), Rv1886c (Ag85B), Rv3804c (Ag85A), and the PPE family member Rv3347c were frequently recognized, defined by IFN-γ production, in blood from healthy individuals exposed to M.tb (health care workers). A different recognition pattern was found for IL-17 production in blood from M.tb exposed individuals responding to TB10.4 (Rv0288), Ag85B (Rv1886c) and the PPE family members Rv0978c and Rv1917c. The pattern of immune target recognition is different in regard to IFN-γ and IL-17 production to defined molecular M.tb targets in PBMCs from individuals frequently exposed to M.tb. The data represent the first mapping of cellular immune responses against M.tb targets in TB patients from Honduras.

Optical absorption, luminescence, and energy transfer processes studies for Dy3+/Tb3+-codoped borate glasses for solid-state lighting applications

Science.gov (United States)

Lakshminarayana, G.; Kaky, Kawa M.; Baki, S. O.; Lira, A.; Caldiño, U.; Kityk, I. V.; Mahdi, M. A.

2017-10-01

By using melt quenching technique, good optical quality singly doped Dy3+ or Tb3+ and Dy3+/Tb3+-codoped borate glasses were synthesized and studied by optical absorption, excitation, emission and decay lifetimes curve analysis. Following the absorption spectrum, the evaluated Judd-Ofelt (J-O) intensity parameters (Ωλ (λ = 2, 4 and 6)) were used to calculate the transition probability (AR), the branching ratio (βR), and the radiative lifetime (τR) for different luminescent transitions such as 4I15/2 → 6H15/2, 4F9/2 → 6H15/2, 4F9/2 → 6H13/2, 4F9/2 → 6H11/2 and 4F9/2 → 6H9/2,6F11/2 for the 0.5 mol % singly Dy3+-doped glass. The βR calculated (65%) indicates that for lasing applications, 4F9/2 → 6H13/2 emission transition is highly suitable. For all the Dy3+/Tb3+-codoped glasses, Tb3+: 5D3→7F6 emission decay lifetime curves are found to be non-exponential in nature for different concentrations of Dy3+ codoping. Using the Inokuti-Hirayama model, these nonexponential decay curves were analyzed to identify the nature of the energy transfer (ET) processes and here the electric dipole-dipole interaction is dominant for the ET. Based on the excitation and emission spectra and decay lifetimes curve analysis, the cross relaxation and ET processes between Dy3+ and Tb3+ were confirmed. For the 0.5 mol % Tb3+ and 2.0 mol % Dy3+-codoped glass, the evaluated Tb3+→Dy3+ ET efficiency (η) is found to be 45% under 369 nm excitation. Further, for Tb3+/Dy3+ -codoped glasses, an enhancement of Tb3+ green emission is observed up to 1.5 mol % Dy3+ codoping, and this is due to the non-radiative resonant ET from Dy3+ to Tb3+ upon 395 nm excitation. For singly 0.5 mol % Dy3+ or 0.5 mol % Tb3+-doped glass, the calculated color coordinates (x,y) and correlated color temperatures (CCT) represent the neutral white or warm white light regions, whereas Dy3+/Tb3+-codoped glasses (x,y) and CCT values fall in the yellowish green region with respect to the different Dy3

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

Energy Technology Data Exchange (ETDEWEB)

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

2017-06-15

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

Evaluation of optoelectronic response and Raman active modes in Tb{sup 3+} and Eu{sup 3+}-doped gadolinium oxide (Gd{sub 2}O{sub 3}) nanoparticle systems

Energy Technology Data Exchange (ETDEWEB)

Paul, Nibedita [National Institute of Technology Nagaland, Department of Physics, Dimapur, Nagaland (India); Tezpur University, Department of Physics, Tezpur, Assam (India); Mohanta, D. [Tezpur University, Department of Physics, Tezpur, Assam (India)

2016-09-15

Rare earth oxide (Tb{sup 3+}:Gd{sub 2}O{sub 3} and Eu{sup 3+}:Gd{sub 2}O{sub 3}) nanophosphors are exploited through spectroscopic and microscopic tools with special emphasis on D-F mediated radiative emission and Raman active vibrational modes. Powder X-ray diffraction measurements have revealed cubic crystal structure of the nanosystems and with an average crystallite size varying between ∝3.2 and 4.8 nm. Photoluminescence (PL) spectra of Tb{sup 3+} doped systems signify intense blue-green (∝490 nm) and green (∝544 nm) emissions mediated by {sup 5}D{sub 4} → {sup 7}F{sub 6} and {sup 5}D{sub 4} → {sup 7}F{sub 5} transitional events; respectively. In the PL responses of Eu{sup 3+} doped nanoparticle systems, we also identify magnetically-driven {sup 5}D{sub 0} → {sup 7}F{sub 1} (∝591 nm) and electrically driven {sup 5}D{sub 0} → {sup 7}F{sub 2} (∝619 nm) radiative features which seem to improve with increasing doping level. However, the magnitude of Judd-Ofelt (J-O) intensity parameters (Ω {sub 2,} {sub 4}), is significantly lowered for the high doping cases. Raman spectra of the undoped and RE doped systems exhibited several A{sub g} and F{sub g} modes in the range of Raman shift ∝100-600 cm{sup -1}. In the Raman spectra, the peaks located at ∝355 cm{sup -1} are assigned to the mixed mode of F{sub g} + A{sub g}, the line width of which was found to increase with RE doping. Moreover, owing to the enhanced defect concentration in the doped systems than its undoped counterpart, we anticipate a faster phonon relaxation and consequently, a suppression of phonon lifetime in the former case. (orig.)

A phosphor-free white light-emitting diode using In2O3 : Tb transparent conductive light converter

International Nuclear Information System (INIS)

Chen, Lung-Chien; Tien, Ching-Ho; Liao, Wei-Chian

2011-01-01

Tb-doped indium oxide (In 2 O 3 : Tb) films were deposited on a GaN-based near-ultraviolet (NUV) light-emitting diode (LED) as a transparent conductive light converter to form a white LED. The transmittance of the In 2 O 3 : Tb film (Tb at 10 wt%) exceeded 80% in visible light and the resistivity was 0.325 Ω cm. The In 2 O 3 : Tb transparent conductive light converter was also employed on GaN-based LEDs. GaN-based NUV-LEDs with In 2 O 3 : Tb film (Tb at 10 wt%) produced forward biases of 3.42 V at an injection current of 20 mA. With increasing temperature, increasing Tb 3+ concentration and increasing injection current from 20 to 100 mA, the chromaticity coordinates barely changed in the white light area. Therefore, the GaN-based NUV-LED with In 2 O 3 : Tb film had a stable white light colour, when temperature and injection current changed, and is suitable for solid-state lighting.

Development of Tb{sup 3+} activated gadolinium aluminate garnet (Gd{sub 3}Al{sub 5}O{sub 12}) as highly efficient green-emitting phosphors

Energy Technology Data Exchange (ETDEWEB)

Teng, Xin; Li, Jinkai, E-mail: mse_lijk@ujn.edu.cn; Duan, Guangbin; Liu, Zongming, E-mail: ost_liuzm@ujn.edu.cn

2016-11-15

The powder processing of (Gd{sub 1-x}Tb{sub x}){sub 3}Al{sub 5}O{sub 12} (GdAG:Tb{sup 3+}) solid solutions was achieved through precursor synthesized via carbonate precipitation, followed by calcination at 1500 °C. The performance of the GdAG:Tb{sup 3+} phosphors were characterized by the combined techniques of XRD, FE-SEM, HR-TEM, PLE/PL, and fluorescence decay analyses. Lower Tb{sup 3+} doping can stabilize the crystal structure of GdAG garnet against its thermal decomposition. The GdAG:Tb{sup 3+} phosphors with good dispersion and fairly uniform particle morphology exhibit a series of {sup 5}D{sub 4}–{sup 7}F{sub J} transitions of Tb{sup 3+} with strongest green emission at ~544 nm ({sup 5}D{sub 4}–{sup 7}F{sub 5} transitions of Tb{sup 3+}) under UV excitation at ~277 nm (4f{sup 8}−4f{sup 7}5d{sup 1} transition of Tb{sup 3+}). The later is overlapping with {sup 8}S{sub 7/2}–{sup 6}I{sub J} intra f–f transition of Gd{sup 3+} indirectly suggesting the existence of energy transfer from Gd{sup 3+} to Tb{sup 3+}. With the Gd{sup 3+}–Tb{sup 3+} energy transfer, higher Tb{sup 3+} emission and quantum efficiency than the well-known YAG:Tb{sup 3+} and LuAG:Tb{sup 3+} were obtained in the present work. The effects of Tb{sup 3+} content on luminescent property of the phosphor, especially PLE/PL properties, fluorescence lifetime and quantum efficient, were thoroughly investigated, which were also compared to those of Tb{sup 3+}-activated YAG and LuAG compounds. The CIE chromaticity coordinates and quenching concentration of GdAG:Tb{sup 3+} were determined to be (~0.37, ~0.56) and ~10 at%, respectively. Keeping the optimum Tb{sup 3+} content at ~10 at%, the (Gd{sub 0.9}Tb{sub 0.1})AG phosphor possesses high internal and external quantum efficiencies of ~88.7% and ~73.6% under ~277 nm excitation, respectively. Owing to its improved luminescent property and high theoretical density, the phosphors of (Gd{sub 1-x}Tb{sub x})AG garnet developed in the present work are

Photoluminescence and thermoluminescence properties of Tb{sup 3+} doped K{sub 3}Gd(PO{sub 4}){sub 2} nanophosphor

Energy Technology Data Exchange (ETDEWEB)

Gupta, Palvi; Bedyal, A.K. [School of Physics, Shri Mata Vaishno Devi University, Katra, 182320 Jammu and Kashmir (India); Kumar, Vinay, E-mail: vinaykdhiman@yahoo.com [School of Physics, Shri Mata Vaishno Devi University, Katra, 182320 Jammu and Kashmir (India); Department of Physics, University of the Free State, P.O. Box 339, Bloemfontein ZA9300 (South Africa); Khajuria, Y. [School of Physics, Shri Mata Vaishno Devi University, Katra, 182320 Jammu and Kashmir (India); Lochab, S.P. [Inter University Accelerator Centre, Anura Asaf Ali Marg, P. O. Box 10502, New Delhi 110067 (India); Pitale, S.S. [Crystal Technology Laboratory,TPD, Bhabha Atomic Research Centre Trombay, Mumbai 400085 (India); Department of Physics, University of the Free State, P.O. Box 339, Bloemfontein ZA9300 (South Africa); Ntwaeaborwa, O.M.; Swart, H.C. [Department of Physics, University of the Free State, P.O. Box 339, Bloemfontein ZA9300 (South Africa)

2014-12-15

Energy level diagram of Tb{sup 3+} ion in the K{sub 3}Gd(PO{sub 4}){sub 2} host lattice. - Highlights: • First time, a detailed TL and PL study on undoped and Tb{sup 3+} doped K{sub 3}Gd(PO{sub 4}){sub 2} nanophosphor. • Combustion method was employed to synthesize the Tb{sup 3+} doped K{sub 3}Gd(PO{sub 4}){sub 2} nanophosphor. • Mechanism of excitation and emission in undoped and Tb{sup 3+} doped K{sub 3}Gd(PO{sub 4}){sub 2} nanophosphor was given. - Abstract: Tb{sup 3+} doped nanoparticulate K{sub 3}Gd(PO{sub 4}){sub 2} phosphor was prepared by combustion method using urea as a fuel. The structure, optical and luminescent properties of the phosphor were studied by X-ray diffraction (XRD), scanning electron microscopy (SEM), diffuse reflectance spectroscopy (DRS), photoluminescence spectroscopy (PL), and thermoluminescence (TL) spectroscopy. In undoped K{sub 3}Gd(PO{sub 4}){sub 2}, the excitation and emission peaks at 273 nm and 323 nm belongs to the {sup 8}S{sub 7/2} → {sup 6}I{sub J(J=7/2)} and {sup 6}P{sub J(J=7/2)} → {sup 8} S{sub 7/2} transitions of Gd{sup 3+} while green emission was observed in the Tb{sup 3+} doped K{sub 3}Gd(PO{sub 4}){sub 2}. TL study was carried out after exposing the samples to γ-radiations (0.1–5 kGy) in the K{sub 3}Gd(PO{sub 4}){sub 2}:Tb{sup 3+} (1.5 mol%). The calculated kinetic parameters were compared with different methods. The band gap of the phosphor was estimated as 5.80 eV. The green shade of the Tb{sup 3+} ion with the CIE coordinates (x, y) as (0.29, 0.54) was in good agreement with the well known green phosphors.

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

International Nuclear Information System (INIS)

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

2009-01-01

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

Luminescence and surface properties of Tb3+ doped Sr3(VO4)2 nanophosphors

International Nuclear Information System (INIS)

Bedyal, A.K.; Kumar, Vinay; Sharma, Vishal

2013-01-01

In this paper, we present a detailed investigation of the luminescence and surface properties of Tb 3+ doped Sr 3 (VO 4 ) 2 nanocrystalline phosphors, synthesized by the combustion method. X-ray diffraction (XRD) peaks in the patterns corresponding to the reflection of rhombohedral pure phase of Sr 3 (VO 4 ) 2 . The average particle sizes have been found in the range of 30-34 nm. Scanning electron microscopy (SEM) indicated that an agglomerated peanut like morphology was obtained. Photoluminescence (PL) spectroscopy has been utilized to investigate the spectral properties of the phosphor. Under 237 nm excitation, it shows several bands centered at 487, 544, 588 and 624 nm, which result from 5 D 4 → 7 F J (J = 6, 5, 4 and 3) transitions of Tb 3+ , and the green emission band ( 5 D 4 → 7 F 5 ) located at 544 nm is dominant. The chemical states and homogeneous dopants' distribution in the host were analyzed with X-ray photoelectron spectroscopy (XPS) and time of flight-secondary ion mass spectroscopy (TOF-SIMS), respectively. A ToF-SIMS imaging shows an uniform distribution of Tb 3+ in the Sr 3 (VO 4 ) 2 . (author)

Optical spectroscopy and optical waveguide fabrication in Eu{sup 3+} and Eu{sup 3+}/Tb{sup 3+} doped zinc–sodium–aluminosilicate glasses

Energy Technology Data Exchange (ETDEWEB)

Caldiño, U., E-mail: cald@xanum.uam.mx [Departamento de Física, Universidad Autónoma Metropolitana-Iztapalapa, P.O. Box 55-534, 09340 México D.F. (Mexico); Speghini, A. [Dipartimento di Biotecnologie, Università di Verona and INSTM, UdR Verona, Strada Le Grazie 15, I-37314 Verona (Italy); Istituto di Fisica Applicata Nello Carrara, C.N.R., Via Madonna del Piano 10, 50019 Sesto Fiorentino (Firenze) (Italy); Berneschi, S. [Istituto di Fisica Applicata Nello Carrara, C.N.R., Via Madonna del Piano 10, 50019 Sesto Fiorentino (Firenze) (Italy); Bettinelli, M. [Dipartimento di Biotecnologie, Università di Verona and INSTM, UdR Verona, Strada Le Grazie 15, I-37314 Verona (Italy); Brenci, M. [Istituto di Fisica Applicata Nello Carrara, C.N.R., Via Madonna del Piano 10, 50019 Sesto Fiorentino (Firenze) (Italy); Pasquini, E. [Istituto di Fisica Applicata Nello Carrara, C.N.R., Via Madonna del Piano 10, 50019 Sesto Fiorentino (Firenze) (Italy); Dipartimento di Fisica e Astronomia, Università di Firenze, Via Sansone 1, 50019 Sesto Fiorentino (Firenze) (Italy); Pelli, S. [Istituto di Fisica Applicata Nello Carrara, C.N.R., Via Madonna del Piano 10, 50019 Sesto Fiorentino (Firenze) (Italy); Righini, G.C. [Istituto di Fisica Applicata Nello Carrara, C.N.R., Via Madonna del Piano 10, 50019 Sesto Fiorentino (Firenze) (Italy); Museo Storico della Fisica e Centro Studi e Ricerche “Enrico Fermi”, Piazza del Viminale 2, 00184 Roma (Italy)

2014-03-15

Optical and spectroscopic properties of 2.0% Eu(PO{sub 3}){sub 3} singly doped and 5.0% Tb(PO{sub 3}){sub 3}–2.0% Eu(PO{sub 3}){sub 3} codoped zinc–sodium–aluminosilicate glasses were investigated. Reddish-orange light emission, with x=0.64 and y=0.36 CIE1931 chromaticity coordinates, is obtained in the europium singly doped glass excited at 393 nm. Such chromaticity coordinates are close to those (0.67,0.33) standard of the National Television System Committee for the red phosphor. When the sodium–zinc–aluminosilicate glass is co-doped with Tb{sup 3+} and Eu{sup 3+}, reddish-orange light emission, with (0.61,0.37) CIE1931 chromaticity coordinates, is obtained upon Tb{sup 3+} excitation at 344 nm. This reddish-orange luminescence is generated mainly by {sup 5}D{sub 0}→{sup 7}F{sub 1} and {sup 5}D{sub 0} →{sup 7}F{sub 2} emissions of Eu{sup 3+}, europium being sensitized by terbium through a non-radiative energy transfer. From an analysis of the Tb{sup 3+} emission decay curves it is inferred that the Tb{sup 3+}→Eu{sup 3+} energy transfer might take place between Tb{sup 3+} and Eu{sup 3+} clusters through a short-range interaction mechanism, so that an electric dipole–quadrupole interaction appears to be the most probable transfer mechanism. The efficiency of this energy transfer is about 62% upon excitation at 344 nm. In the singly doped and codoped glasses multimode optical waveguides were successfully produced by Ag{sup +}–Na{sup +} ion exchange, and they could be characterized at various wavelengths. -- Highlights: • Reddish-orange light emission can be generated from Tb{sup 3+} and Eu{sup 3+} codoped zinc–sodium–aluminosilicate glasses excited at 344 nm. • The Eu{sup 3+} is sensitized by Tb{sup 3+} through a non-radiative energy transfer. • Highly multimode waveguides can be fabricated by diluted silver–sodium exchange. • This type of AlGaN LEDs pumped glass phosphors might be useful for generation of reddish-orange light.

Giant anisotropy of magnetocaloric effect in TbMnO3 single crystals

Science.gov (United States)

Jin, Jin-Ling; Zhang, Xiang-Qun; Li, Guo-Ke; Cheng, Zhao-Hua; Zheng, Lin; Lu, Yi

2011-05-01

The magnetocaloric effect (MCE) in TbMnO3 single crystals was investigated by isothermal magnetization curves for the ab plane at low temperatures. Large magnetic entropy change, ΔSM = -18.0 J/kg K, and the refrigerant capacity, RC = 390.7 J/kg, are achieved near the ordering temperature of Tb3+ moment (TNTb) under 70 kOe along the a axis. Furthermore, the TbMnO3 single crystal exhibits a giant MCE anisotropy. The difference of ΔSMand RC between the a and b axes is field and temperature dependent, which reaches maximum values of 11.4 J/kg K and 304.1 J/kg, respectively. By taking magnetocrystalline anisotropy into account, the rotating ΔSMwithin the ab plane can be well simulated, indicating that the anisotropy of ΔSMis directly contributed from the magnetocrystalline anisotropy. Our finding for giant MCE anisotropy in TbMnO3 single crystals explores the possibility of using this material for magnetic refrigerators by rotating its magnetization vector rather than moving it in and out of the magnet.

Concentration effect on the spectroscopic behavior of Tb3+ ions in zinc phosphate glasses

International Nuclear Information System (INIS)

Kesavulu, C.R.; Almeida Silva, Anielle Christine; Dousti, M.R.; Dantas, Noelio Oliveira; Camargo, A.S.S. de; Catunda, Tomaz

2015-01-01

Zinc phosphate glasses (PZABPTb) in the compositional system: P 2 O 5 –ZnO–Al 2 O 3 –BaO–PbO doped with variable Tb 3+ concentrations (1–5 wt% Tb 2 O 3 ) were prepared and characterized through absorption, excitation, emission and intensity decay rate measurements. The Judd–Ofelt model has been adopted to evaluate the radiative properties of the 5 D 4 → 7 F 6–3 emission transitions. The effect of Tb 3+ ion concentration on the emissions from the 5 D 3,4 excited levels is discussed in detail. Analysis of the intensity decay curves corresponding to blue and green emissions from levels 5 D 3 and 5 D 4 , respectively, allowed determination of effective lifetimes, which confirmed the Tb 3+ ion concentration quenching of the blue emission in these glasses. The decay curves for the 5 D 3 level are found to be non-exponential in nature for all the studied concentrations due to ion–ion energy transfer through cross-relaxation. In an attempt to identify the origin of the energy transfer mechanism, the decay curves were well fitted to the Inokuti–Hirayama model for S=6, which indicates that the energy transfer process is of dipole–dipole type. The optical band gap energy (E opt ) has been evaluated taking into account the ultraviolet edge of absorption spectra. - Highlights: • Tb 3+ -doped zinc phosphate glasses have been prepared by melt quenching technique. • Spectroscopic parameters were evaluated using the Judd–Ofelt theory. • Effects of Tb 3+ concentration on luminescence of the glasses were studied. • Strong intense laser transition for Tb 3+ ion in PZABPTb glasses is 5 D 4 → 7 F 5 (0.54 μm). • PZABPTb glasses could be used in the development of green color display devices and solid state visible lasers

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

Science.gov (United States)

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

2011-01-03

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

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

Directory of Open Access Journals (Sweden)

Joel Moreno Palmerin

2011-09-01

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

Sol-hydrothermal synthesis and optical properties of Eu3+, Tb(3+)-codoped one-dimensional strontium germanate full color nano-phosphors.

Science.gov (United States)

Lin, Liangwu; Sun, Xinyuan; Jiang, Yao; He, Yuehui

2013-12-21

Novel near-UV and blue excited Eu(3+), Tb(3+)-codoped one dimensional strontium germanate full-color nano-phosphors have been successfully synthesized by a simple sol-hydrothermal method. The morphologies, internal structures, chemical constitution and optical properties of the resulting samples were characterized using FE-SEM, TEM, HRTEM, EDS, XRD, FTIR, XPS, PL and PLE spectroscopy and luminescence decay curves. The results suggested that the obtained Eu(3+), Tb(3+)-codoped strontium germanate nanowires are single crystal nanowires with a diameter ranging from 10 to 80 nm, average diameter of around 30 nm and the length ranging from tens to hundreds micrometers. The results of PL and PLE spectra indicated that the Eu(3+), Tb(3+)-codoped single crystal strontium germanate nanowires showed an intensive blue, blue-green, green, orange and red or green, orange and red light emission under excitation at 350-380 nm and 485 nm, respectively, which may attributed to the coexistent Eu(3+), Eu(2+) and Tb(3+) ions, and the defects located in the strontium germanate nanowires. A possible mechanism of energy transfer among the host, Eu(3+) and Tb(3+) ions was proposed. White-emission can be realized in a single-phase strontium germanate nanowire host by codoping with Tb(3+) and Eu(3+) ions. The Eu(3+), Tb(3+)-codoped one-dimensional strontium germanate full-color nano-phosphors have superior stability under electron bombardment. Because of their strong PL intensity, good CIE chromaticity and stability, the novel 1D strontium germanate full-color nano-phosphors have potential applications in W-LEDs.

Luminescence properties of Ce3+ and Tb3+ co-activated ZnAl2O4 phosphor

International Nuclear Information System (INIS)

Tshabalala, K.G.; Cho, S.-H.; Park, J.-K.; Pitale, Shreyas S.; Nagpure, I.M.; Kroon, R.E.; Swart, H.C.; Ntwaeaborwa, O.M.

2012-01-01

In this study, a solution combustion method was used to prepare green emitting Ce 3+ –Tb 3+ co-activated ZnAl 2 O 4 phosphor. The samples were annealed at 700 °C in air or hydrogen atmosphere to improve their crystallinity and optical properties. X-ray diffraction study confirmed that both as-prepared and post-preparation annealed samples crystallized in the well known cubic spinel structure of ZnAl 2 O 4 . An agglomeration of irregular platelet-like particles whose surfaces were encrusted with smaller spheroidal particles was confirmed by scanning electron microscopy (SEM). The fluorescence data collected from the annealed samples with different concentrations of Ce 3+ and Tb 3+ show the enhanced green emission at 543 nm associated with 5 D 4 → 7 F 5 transitions of Tb 3+ . The enhancement was attributed to energy transfer from Ce 3+ to Tb 3+ . Possible mechanism of energy transfer via a down conversion process is discussed. Furthermore, cathodoluminescence (CL) intensity degradation of this phosphor was also investigated and the degradation data suggest that the material was chemically stable and the CL intensity was also stable after 10 h of irradiation by a beam of high energy electrons.

Photoluminescence, energy transfer and tunable color of Ce(3+), Tb(3+) and Eu(2+) activated oxynitride phosphors with high brightness.

Science.gov (United States)

Lü, Wei; Huo, Jiansheng; Feng, Yang; Zhao, Shuang; You, Hongpeng

2016-06-21

New tuneable light-emitting Ca3Al8Si4O17N4:Ce(3+)/Tb(3+)/Eu(2+) oxynitride phosphors with high brightness have been prepared. When doped with trivalent cerium or divalent europium they present blue luminescence under UV excitation. The energy transfer from Ce(3+) to Tb(3+) and Ce(3+) to Eu(2+) ions is deduced from the spectral overlap between Ce(3+) emission and Tb(3+)/Eu(2+) excitation spectra. The energy-transfer efficiencies and corresponding mechanisms are discussed in detail, and the mechanisms of energy transfer from the Ce(3+) to Tb(3+) and Ce(3+) to Eu(2+) ions are demonstrated to be a dipole-quadrupole and dipole-dipole mechanism, respectively, by the Inokuti-Hirayama model. The International Commission on Illumination value of color tuneable emission as well as luminescence quantum yield (23.8-80.6%) can be tuned by controlling the content of Ce(3+), Tb(3+) and Eu(2+). All results suggest that they are suitable for UV light-emitting diode excitation.

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

International Nuclear Information System (INIS)

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

2015-01-01

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

Intense green emission from Tb3+- doped Teo2-Wo3-Geo2 glasses

Science.gov (United States)

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

2018-04-01

Tb3+ -doped oxyfluoro tellurite (TWGTb) glasses were prepared by conventional melt quenching technique. The Judd-Ofelt theory has been applied to evaluate the Ωλ (λ=2,4,6) intensity parameters. The TWGTb glasses exhibit 5D3 → 7F5-3 and 5D4 → 7F6-0 transitions when excited at 316 nm wavelength. The variation of intensity of 5D4 → 7F5 (Green) and 5D3 → 7F4 (Blue) transitions and the green to blue (IG/IB) intensity ratios were studied as a function of Tb3+ ions concentration. The laser characteristic parameters such as effective bandwidth (Δλeff), stimulated emission cross-section (σe), gain bandwidth (σe×Δλeff) and optical gain (σe×τR) were determined using the emission spectra and radiative parameters. The luminescence decay profiles exhibit single-exponential nature for all the samples. Based on the experimental results we suggest that the 1.0 mol% of Tb3+-doped TWGTb glass could be the suitable laser host materials to emit intense green luminescence at 545 nm.

Kinetic study of Tb/sup 3 +/(/sup 5/D/sub 3/) luminescence in phosphate glasses

Energy Technology Data Exchange (ETDEWEB)

Anisimov, V.A.; Dmitryuk, A.V.; Karapetyan, G.O.

1986-01-01

This paper presents precise determinations of the kinetics of terbium luminescence over a broad dynamic range, in order to refine the mechanism of concentration quenching of the Tb/sup 3 +/(/sup 5/D/sub 3/) luminescence in glasses. After establishing the mechanism of Tb/sup 3 +/(/sup 5/D/sub 3/) luminescence quenching by the iteration method, the authors determine the value of the parameter for an arbitrary concentration of the activator. Results of this study show that the mechanism of concentration quenching of luminescence is static dipole-dipole interaction of terbium ions.

Stimulated luminescence property of Zn(BO{sub 2}){sub 2}:TbCl{sub 3}

Energy Technology Data Exchange (ETDEWEB)

Cedillo, G.; Cruz Z, E. [UNAM, Instituto de Ciencias Nucleares, Circuito Exterior, Ciudad Universitaria, 04510 Mexico D. F. (Mexico); Garcia H, M. [UNAM, Instituto de Investigaciones en Materiales, Posgrado en Ciencia e Ingenieria de Materiales, Apdo. Postal 70-360, 04510 Mexico D. F. (Mexico); Marcazzo, J. [Instituto de Fisica Arroyo Seco / UNICEN, Gral. Pinto 399, 7000 Tandil, Buenos Aires (Argentina); Hernandez A, J. M.; Murrieta S, H., E-mail: ecruz@nucleares.unam.mx [UNAM, Instituto de Fisica, Apdo. Postal 20-364, 01000 Mexico D. F. (Mexico)

2015-10-15

Zinc borate, Zn(BO{sub 2}){sub 2}, doped with TbCl{sub 3} at different concentration (0.5-8 mol %) was synthesized. The polycrystalline samples were characterized by Scanning Electron Microscopy (Sem/EDS) and X-ray Diffraction. The X-ray difractrograms of the pure samples sintered at 750 and 800 degrees C shown the evidence of the Zn(BO{sub 2}){sub 2} has the body centered cubic (bcc) structure and a ZnB{sub 4}O{sub 7} primitive orthorhombic phase of the crystal system. The thermoluminescent (Tl) intensity was dependent on the thermal treatment (250-500 degrees C) and also on the impurity concentration. The glow curves show four glow peaks at about 82, 164, 251, and 331 degrees C when the Tb{sup 3+} doped zinc borate samples were exposed to gamma or beta radiation. The structure of the glow curves was analyzed by CGCD deconvolution method. The kinetics parameters (activation energy, frequency factor and the kinetic order) were calculated assuming the general order kinetics model describing accurately the Tl process. The glow peaks were overlapped and then the whole glow curve was considered for dosimetric characteristics measurements. The linear Tl response as a function of gamma and beta doses was performed using a {sup 60}Co irradiator and a {sup 90}Sr, respectively. Zinc borate with 8 mol % of impurity concentration exhibited an intense radio luminescent (Rl) emission. The Rl spectra show their maximum bands at 370, 490, 545 and 700 nm. The linear dose-response was between 2.2 c Gy and 27.7 Gy when the samples were exposed to beta radiation. These results suggest that the Tb -doped zinc borate material is a good phosphor for use in radiation dosimetry because its high Tl sensitivity to the ionizing radiation and good dose-response. (Author)

Tunable luminescence properties and energy transfer of Ba{sub 3}NaLa(PO{sub 4}){sub 3}F:Tb{sup 3+},Sm{sup 3+} phosphors with apatite structure

Energy Technology Data Exchange (ETDEWEB)

Liu, Haikun; Liao, Libing, E-mail: clayl@cugb.edu.cn; Chen, Jian; Guo, Qingfeng; Zhang, Yuanyuan; Mei, Lefu, E-mail: mlf@cugb.edu.cn

2016-01-15

Tb{sup 3+}–Sm{sup 3+} co-doped Ba{sub 3}NaLa(PO{sub 4}){sub 3}F phosphors with apatite structure have been prepared by a high temperature solid-state reaction, and their luminescence properties have been investigated in detail. The energy transfer (ET) mechanism was verified as the dipole–quadrupole mechanism, and the ET efficiency as well as the critical distance is also estimated. As a result of fine-tuning of the emission composition of the Tb{sup 3+} and Sm{sup 3+} ions, tunable luminescence properties can be realized by combining the emission of Tb{sup 3+} and Sm{sup 3+} in a single host lattice under UV light excitation. The emission color of the obtained phosphors can be modulated from green to yellow by controlling the doping content of the Sm{sup 3+} ions with the fixed Tb{sup 3+} content. Additional, as the temperature increases from RT to 150 °C, the PL intensities of Ba{sub 3}NaLa{sub 0.7}(PO{sub 4}){sub 3}F:0.10Tb{sup 3+},0.20Sm{sup 3+} decreased to 80.4% and 78.6% of the initial PL intensity, corresponding to the intensity of transition of Sm{sup 3+} and transition of Tb{sup 3+} in the Ba{sub 3}NaLa{sub 0.7}(PO{sub 4}){sub 3}F:0.10Tb{sup 3+},0.20Sm{sup 3+} phosphor, respectively. These results indicate the series of Ba{sub 3}NaLa{sub 1−x−y}(PO{sub 4}){sub 3}F:xTb{sup 3+},ySm{sup 3+} phosphors can be acted as a good candidate for the application in white light-emitting diodes. - Highlights: • Tb{sup 3+},Sm{sup 3+}-codoped Ba{sub 3}NaLa(PO{sub 4}){sub 3}F phosphors have been synthesized. • The emission color of the obtained phosphors can be modulated from green to red. • This phosphor has a good thermal stability.

Assessment of the influence of direct tobacco smoke on infection and active TB management.

Directory of Open Access Journals (Sweden)

Neus Altet

Full Text Available Smoking is a risk factor for tuberculosis (TB infection and disease progression. Tobacco smoking increases susceptibility to TB in a variety of ways, one of which is due to a reduction of the IFN-γ response. Consequently, an impaired immune response could affect performance of IFN-γ Release Assays (IGRAs.In the present study, we assess the impact of direct tobacco smoking on radiological manifestations, sputum conversion and immune response to Mycobacterium tuberculosis, analyzing IFN-γ secretion by IGRAs.A total of 525 participants were studied: (i 175 active pulmonary TB patients and (ii 350 individuals coming from contact tracing studies, 41 of whom were secondary TB cases. Clinical, radiological and microbiological data were collected. T-SPOT.TB and QFN-G-IT were processed according manufacturer's instructions.In smoking patients with active TB, QFN-G-IT (34.4% and T-SPOT.TB (19.5% had high frequencies of negative results. In addition, by means of an unconditional logistic regression, smoking was a main factor associated with IGRAs' false-negative results (aOR: 3.35; 95%CI:1.47-7.61; p<0.05. Smoking patients with active TB presented a high probability of having cavitary lesions (aOR: 1.88; 95%CI:1.02-3.46;p<0.05. Mean culture negativization (months ± standard deviation (SD was higher in smokers than in non-smokers (2.47±1.3 versus 1.69±1.4. Latent TB infection (LTBI was favored in smoking contacts, being a risk factor associated with infection (aOR: 11.57; 95%CI:5.97-22.41; p<0.00005. The IFN-γ response was significantly higher in non-smokers than in smokers. Smoking quantity and IFN-γ response analyzed by IGRAs were dose-dependent related.Smoking had a negative effect on radiological manifestations, delaying time of sputum conversion. Our data establish a link between tobacco smoking and TB due to a weakened IFN-γ response caused by direct tobacco smoke.

Use of QuantiFERON®-TB Gold in-tube culture supernatants for measurement of antibody responses.

Directory of Open Access Journals (Sweden)

Simon G Kimuda

Full Text Available QuantiFERON®-TB Gold in-tube (QFT-GIT supernatants may be important samples for use in assessment of anti-tuberculosis (TB antibodies when only limited volumes of blood can be collected and when a combination of antibody and cytokine measurements are required. These analytes, when used together, may also have the potential to differentiate active pulmonary TB (APTB from latent TB infection (LTBI. However, few studies have explored the use of QFT-GIT supernatants for investigations of antibody responses. This study determined the correlation and agreement between anti-CFP-10 and anti-ESAT-6 antibody concentrations in QFT-GIT nil supernatant and serum pairs from 68 TB household contacts. We also explored the ability of Mycobacterium tuberculosis (M.tb specific antibodies, or ratios of antibody to interferon gamma (IFN-γ in QFT-GIT supernatants, to differentiate 97 APTB cases from 58 individuals with LTBI. Sputum smear microscopy was used to define APTB, whereas the QFT-GIT and tuberculin skin test were used to define LTBI. There were strong and statistically significant correlations between anti-CFP-10 and anti-ESAT-6 antibodies in unstimulated QFT-GIT supernatants and sera (r = 0.89; p<0.0001 for both, and no significant differences in antibody concentration between them. Anti-CFP-10 & anti-ESAT-6 antibodies differentiated APTB from LTBI with sensitivities of 88.7% & 71.1% and specificities of 41.4% & 51.7% respectively. Anti-CFP-10 antibody/M.tb specific IFN-γ and anti-ESAT-6 antibody/M.tb specific IFN-γ ratios had sensitivities of 48.5% & 54.6% and specificities of 89.7% and 75.9% respectively. We conclude that QFT-GIT nil supernatants may be used in the place of sera when measuring antibody responses, reducing blood volumes needed for such investigations. Antibodies in QFT-GIT nil supernatants on their own discriminate APTB from LTBI with high sensitivity but have poor specificity, whereas the reverse is true when antibodies are used in

Energy transfer between Tb{sup 3+} and Eu{sup 3+} in co-doped Y{sub 2}O{sub 3} nanocrystals prepared by Pechini method

Energy Technology Data Exchange (ETDEWEB)

Back, M., E-mail: m.back@hotmail.it [Universita Ca' Foscari di Venezia and INSTM, Dipartimento di Scienze Molecolari e Nanosistemi (Italy); Boffelli, M. [Kyoto Institute of Technology and Research Institute for Nanoscience (Japan); Massari, A.; Marin, R. [Universita Ca' Foscari di Venezia and INSTM, Dipartimento di Scienze Molecolari e Nanosistemi (Italy); Enrichi, F. [Coordinamento Interuniversitario Veneto per le Nanotecnologie (CIVEN) (Italy); Riello, P., E-mail: riellop@unive.it [Universita Ca' Foscari di Venezia and INSTM, Dipartimento di Scienze Molecolari e Nanosistemi (Italy)

2013-07-15

Tb{sup 3+} and Eu{sup 3+} co-doped Y{sub 2}O{sub 3} nanoparticles with a volume-weighted average size of about 30 nm were synthesized via simple Pechini-type sol-gel process. The growth of monocrystalline nanoparticles is investigated via XRD and TEM analysis. The study of energy transfer between Tb{sup 3+} and Eu{sup 3+} ions was carried out by means of PL, PLE, and photoluminescence decay analyses. The energy transfer from Tb{sup 3+} to Eu{sup 3+} is efficient and we show how a resonant type via a dipole-dipole interaction is the most probable mechanism. We compared the energy-transfer efficiencies calculated from the intensities and from the lifetimes of {sup 5}D{sub 4}{yields}{sup 7}F{sub 5} transition of Tb, showing the presence of two populations of Tb, with different local surroundings, in the matrix. Furthermore, the critical distance between Tb{sup 3+} and Eu{sup 3+} ions has been calculated by means of different theories, from a new probabilistic approach based on the discretization of the theory of Chandrasekhar about the distribution of the nearest neighbors in a random distribution of particles, and from the PL data, suggesting a value of about 7 A.

Melanocortin-3 receptors in the limbic system mediate feeding-related motivational responses during weight loss

Directory of Open Access Journals (Sweden)

Maria Mavrikaki

2016-07-01

Full Text Available Objective: Appetitive responses to weight loss are mediated by a nutrient-sensing neural network comprised of melanocortin neurons. The role of neural melanocortin-3 receptors (MC3R in mediating these responses is enigmatic. Mc3r knockout mice exhibit a paradoxical phenotype of obesity and reduced feeding-related behaviors in situations of nutrient scarcity. Here we examined whether MC3Rs expressed in mesolimbic neurons regulate feeding-related motivational responses. Methods: Interactions between Mc3r genotype, cognitive function and energy balance on food self-administration were assessed using operant conditioning with fixed- and progressive ratio (FR1/PR1 settings. Inhibition of Mc3r transcription by a loxP-flanked transcriptional blocker (TB in C57BL/6JN mice (Mc3rTB/TB was reversed in mesolimbic neurons using DAT-Cre (DAT-MC3R. Results: Caloric restriction (CR caused 10–15% weight loss and increased motivation to acquire food rewards during training sessions. c-Fos-expression in the nucleus accumbens was increased 1 h following food presentation. While exhibiting weight loss, total food self-administration, enhanced motivation to self-administer food rewards in training sessions held during CR and c-Fos-activation in the nucleus accumbens following re-feeding were all markedly attenuated in Mc3rTB/TB mice. In contrast, cognitive abilities were normal in Mc3rTB/TB mice. Total food self-administration during FR1 sessions was not rescued in DAT-MC3R mice, however enhanced motivational responses to self-administer food rewards in PR1 conditions were restored. The nutrient-partitioning phenotype observed with Mc3r-deficiency was not rescued in DAT-MC3R mice. Conclusions: Mesolimbic MC3Rs mediate enhanced motivational responses during CR. However, they are insufficient to restore normal caloric loading when food is presented during CR and do not affect metabolic conditions altering nutrient partitioning. Author Video: Author Video Watch what

First principles results on TbAl3(BO3)4: A promising magneto-optical material

KAUST Repository

Saeed, Y.

2011-11-21

The electronic and optical properties of TbAl3(BO3)4 are determined using density functional theory. The calculated total magnetic moment of 5.96 μB is close to the expected moment of Tb3+. The frequency dependent dielectric function, refractive index, extinction coefficient, absorption, optical reflectivity, and energy loss function are explained in terms of the transitions between the valence and conduction bands. We find very high Kerr angles for ultraviolet light and potential for extension, even into the visible range by band structure design.

First principles results on TbAl3(BO3)4: A promising magneto-optical material

KAUST Repository

Saeed, Y.; Singh, Nirpendra; Schwingenschlö gl, Udo

2011-01-01

The electronic and optical properties of TbAl3(BO3)4 are determined using density functional theory. The calculated total magnetic moment of 5.96 μB is close to the expected moment of Tb3+. The frequency dependent dielectric function, refractive index, extinction coefficient, absorption, optical reflectivity, and energy loss function are explained in terms of the transitions between the valence and conduction bands. We find very high Kerr angles for ultraviolet light and potential for extension, even into the visible range by band structure design.

Color tunable emission in Ce3+ and Tb3+ co-doped Ba2Ln(BO3)2Cl (Ln=Gd and Y) phosphors for white light-emitting diodes.

Science.gov (United States)

Zhang, Niumiao; Guo, Chongfeng; Jing, Heng; Jeong, Jung Hyun

2013-12-01

Ce(3+) and Tb(3+) co-doped Ba2Ln(BO3)2Cl (Ln=Y and Gd) green emitting phosphors were prepared by solid state reaction in reductive atmosphere. The emission and excitation spectra as well as luminescence decays were investigated, showing the occurrence of efficient energy transfer from Ce(3+) to Tb(3+) in this system. The phosphors exhibit both a blue emission from Ce(3+) and a green emission from Tb(3+) under near ultraviolet light excitation with 325-375 nm wavelength. Emission colors of phosphors could be tuned from deep blue through cyan to green by adjusting the Tb(3+) concentrations. The energy transfer efficiency and emission intensity of Ba2Y(BO3)2Cl:Ce(3+), Tb(3+) precede those of Ba2Gd(BO3)2Cl:Ce(3+), Tb(3+), and the sample Ba2Y(BO3)2Cl:0.03Ce(3+), 0.10Tb(3+) is the best candidate for n-UV LEDs. Copyright © 2013 Elsevier B.V. All rights reserved.

Immune TB Antibody Phage Display Library as a Tool To Study B Cell Immunity in TB Infections.

Science.gov (United States)

Hamidon, Nurul Hamizah; Suraiya, Siti; Sarmiento, Maria E; Acosta, Armando; Norazmi, Mohd Nor; Lim, Theam Soon

2018-03-01

B cells and in particular antibodies has always played second fiddle to cellular immunity in regard to tuberculosis (TB). However, recent studies has helped position humoral immunity especially antibodies back into the foray in relation to TB immunity. Therefore, the ability to correlate the natural antibody responses of infected individuals toward TB antigens would help strengthen this concept. Phage display is an intriguing approach that can be utilized to study antibody-mediated responses against a particular infection via harvesting the B cell repertoire from infected individuals. The development of disease-specific antibody libraries or immune libraries is useful to better understand antibody-mediated immune responses against specific disease antigens. This study describes the generation of an immune single-chain variable fragment (scFv) library derived from TB-infected individuals. The immune library with an estimated diversity of 10 9 independent clones was then applied for the identification of monoclonal antibodies against Mycobacterium tuberculosis α-crystalline as a model antigen. Biopanning of the library isolated three monoclonal antibodies with unique gene usage. This strengthens the role of antibodies in TB immunity in addition to the role played by cellular immunity. The developed library can be applied against other TB antigens and aid antibody-derived TB immunity studies in the future.

Crystal growth of Sm0.3Tb0.7FeO3 and spin reorientation transition in Sm1−xTbxFeO3 orthoferrite

International Nuclear Information System (INIS)

Wu, Anhua; Wang, Bo; Zhao, Xiangyang; Xie, Tao; Man, Peiwen; Su, Liangbi; Kalashnikova, A.M.; Pisarev, R.V.

2017-01-01

In this work, Sm 0.3 Tb 0.7 FeO 3 single crystal was successfully grown by optical floating zone method. Sm 0.3 Tb 0.7 FeO 3 samples with a-, b-, and c-orientation were manufactured by means of Laue photograph. Magnetic properties of Sm 0.3 Tb 0.7 FeO 3 single crystals are studied over a wide temperature range from 2 to 400 K. Spin reorientation transition from Γ 2 to Γ 4 are observed by means of the temperature dependence of magnetization It indicated the reorientation transition temperature of Sm 1−x Tb x FeO 3 single crystals is lowered with the contents of Tb contents rising based on this work and our previous works, thus the spin reorientation transition temperature can be adjusted through changing the compound in orthoferrites materials, which means that we can get orthoferrites single crystals with high magnetism property in various temperature through material design. - Highlights: • Sm 0.3 Tb 0.7 FeO 3 single crystals with various compounds were successfully grown by optical floating zone method. • The relation between SRT temperature and composition in Sm 1−x Tb x FeO 3 orthoferrite was indicated. • The spin reorientation transition temperature of Sm 1−x Tb x FeO 3 single crystals can be adjusted through changing the compound in orthoferrites materials.

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

International Nuclear Information System (INIS)

Flores, M.; Arroyo, R.

2003-01-01

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

Synthesis, structure, and photoluminescence properties of novel KBaSc2 (PO4 )3 :Ce(3+) /Eu(2+) /Tb(3+) phosphors for white-light-emitting diodes.

Science.gov (United States)

Jiao, Mengmeng; Lü, Wei; Shao, Baiqi; Zhao, Lingfei; You, Hongpeng

2015-08-24

A series of novel KBaSc2 (PO4 )3 :Ce(3+) /Eu(2+) /Tb(3+) phosphors are prepared using a solid-state reaction. X-ray diffraction analysis and Rietveld structure refinement are used to check the phase purity and crystal structure of the prepared samples. Ce(3+) - and Eu(2+) -doped phosphors both have broad excitation and emission bands, owing to the spin- and orbital-allowed electron transition between the 4f and 5d energy levels. By co-doping the KBaSc2 (PO4 )3 :Eu(2+) and KBaSc2 (PO4 )3 :Ce(3+) phosphors with Tb(3+) ions, tunable colors from blue to green can be obtained. The critical distance between the Eu(2+) and Tb(3+) ions is calculated by a concentration quenching method and the energy-transfer mechanism for Eu(2+) →Tb(3+) is studied by utilizing the Inokuti-Hirayama model. In addition, the quantum efficiencies of the prepared samples are measured. The results indicate that KBaSc2 (PO4 )3 :Eu(2+) ,Tb(3+) and KBaSc2 (PO4 )3 :Ce(3+) ,Tb(3+) phosphors might have potential applications in UV-excited white-light-emitting diodes. © 2015 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

Growth and magnetooptical properties of anisotropic TbF3 single crystals

Science.gov (United States)

Valiev, Uygun V.; Karimov, Denis N.; Burdick, Gary W.; Rakhimov, Rakhim; Pelenovich, Vasiliy O.; Fu, Dejun

2017-06-01

This paper investigates the Faraday effect and absorption and luminescence spectra of single-crystal TbF3 measured at 90 K and 300 K. The optical-quality single-phase TbF3 crystals (structural type β-YF3) were grown by the Bridgman technique. Faraday rotation angles were measured at remagnetization along the [100] crystallographic axis. Low temperature optical measurements were carried out along the [100] axis. "Quasi-doublet" sublevels with energy at 0 cm-1, 65 cm-1, and 190 cm-1, and also a singlet sublevel with energy at 114 cm-1 located in the ground 7F6 multiplet were determined from the low temperature luminescence spectra. The Van-Vleck behavior of the magnetic susceptibility χb can be satisfactorily explained by the magnetic mixing of wave functions belonging to the ground and first excited "quasi-doublet" sublevels at 0 and 65 cm-1, respectively. Analysis of the oscillation dependences of the rotation angle showed that the value of the natural birefringence (Δn ≈ 0.0186) remains nearly constant within the wavelength and temperature ranges under investigation. As the temperature decreases, we find significant increases in the oscillation amplitude of the rotation angle and in the Verdet constant V. The spectral dependences V(χ) are linear throughout the temperature range. The magnetooptical activity of TbF3 can be explained by means of the spin- and parity-allowed electric-dipole 4f → 5d transitions in the Tb3+ ions.

New Technology Changing The Face of Mobile Seismic Networks

Science.gov (United States)

Brisbourne, A.; Denton, P.; Seis-Uk

SEIS-UK, a seismic equipment pool and data management facility run by a consortium of four UK universities (Leicester, Leeds, Cambridge and Royal Holloway, London) completed its second phase in 2001. To compliment the existing broadband equipment pool, which has been deployed to full capacity to date, the consortium undertook a tender evaluation process for low-power, lightweight sensors and recorders, for use on both controlled source and passive seismic experiments. The preferred option, selected by the consortium, was the Guralp CMG-6TD system, with 150 systems ordered. The CMG-6TD system is a new concept in temporary seismic equipment. A 30s- 100Hz force-feedback sensor, integral 24bit digitiser and 3-4Gbyte of solid-state memory are all housed in a single unit. Use of the most recent technologies has kept the power consumption to below 1W and the weight to 3.5Kg per unit. The concept of the disk-swap procedure for obtaining data from the field has been usurped by a fast data download technique using firewire technology. This allows for rapid station servicing, essential when 150 stations are in use, and also ensures the environmental integrity of the system by removing the requirement for a disk access port and envi- ronmentally exposed data disk. The system therefore meets the criteria for controlled source and passive seismic experiments: (1) the single unit concept and low-weight is designed for rapid deployment on short-term projects; (2) the low power consumption reduces the power-supply requirements facilitating deployment; (3) the low self-noise and bandwidth of the sensor make it applicable to passive experiments involving nat- ural sources. Further to this acquisition process, in collaboration with external groups, the SEIS- UK data management procedures have been streamlined with the integration of the Guralp GCF format data into the PASSCAL PDB software. This allows for rapid dissemination of field data and the production of archive-ready datasets

Study on mechanism controlling {sup 5}D{sub 3}/{sup 5}D{sub 4}emissions of Tb{sup 3+} in glasses

Energy Technology Data Exchange (ETDEWEB)

Wang, Yang; Liu, Siyuan; Mao, Jiayi; Li, Xinxi; Li, Lei; Zeng, Huidan; Chen, Guorong, E-mail: grchen@ecust.edu.cn

2017-05-15

Tb{sup 3+} doped SiO{sub 2}-ZnO-BaO glasses are prepared by melting quenching method and their unique photoluminescent properties for the UV excitation are studied by using emission/excitation spectra and decay curves. Glasses in the composition (mol%) of 60SiO{sub 2}-xZnO-(40-x)BaO-0.2Tb{sup 3+}(x=30, 20, 10) show the strongest emission peaking at 436 nm which is different from majority of other reported work. Lower content of the free OH groups mainly contribute to this phenomenon due to the decreased probability of the multi-phonon aided non-radiative relaxation process from {sup 5}D{sub 3} to {sup 5}D{sub 4} energy levels of Tb{sup 3+} ions. The Tb{sup 3+} concentration also affects the {sup 5}D{sub 3}/{sup 5}D{sub 4} emissions as a result of the cross-relaxation effect on two nearby Tb{sup 3+} ions ({sup 5}D{sub 3}-{sup 5}D{sub 4}⇒{sup 7}F{sub 6}-{sup 7}F{sub 0}). Moreover, by adjusting Tb{sup 3+} concentration and/or ZnO/BaO concentration ratio of the host glass we obtained the adjustable emission with the required CIE chromaticity from blue to green, suggesting that the present Tb{sup 3+}-doped SiO{sub 2}-ZnO-BaO glasses are potential as blue/green dual-color luminescent materials for different applications.

Synthesis, characterization and property evaluation of Y substituted TbMnO3

International Nuclear Information System (INIS)

Shukla, Rakesh; Mandal, B.P.; Tyagi, A.K.; Chakraborty, Keka R.; Mukadam, M.D.; Yusuf, S.M.; Kaushik, S.D.; Siruguri, V.; Lawes, G.; Naik, R.; Akila, K.

2013-01-01

Tb 1-x Y x MnO 3 (x = 0.0 - 0.3) compounds were synthesized by gel-combustion method in stoichiometric ratio. Phase pure compounds were obtained in orthorhombic structure (space group Pnma). Specific heat measurements revealed anomalies in between at 2K and 50K. Variable temperature neutron diffraction measurements carried out on the x = 0.1 and x = 0.2 samples at 2 K showed short range ordering of Tb moments. For the samples x = 0.1 - 0.3, neutron diffraction data at 20K showed long range antiferromagnetic ordering of Mn moments with no mark of short ranged ordering of Tb moments at these temperatures. The samples showed pyroelectric alignment of electric dipole moments. Signatures of coupling between magnetic and electrical properties were revealed in this study. (author)

{sup 5}D{sub 3}{yields}{sup 7}F{sub J} emission of Tb doped sol-gel silica

Energy Technology Data Exchange (ETDEWEB)

Seed Ahmed, H.A.A.; Ntwaeaborwa, O.M.; Gusowski, M.A. [Department of Physics, University of the Free State, IB51, Box 339, Bloemfontein 9300 (South Africa); Botha, J.R. [Department of Physics, Nelson Mandela Metropolitan University, Box 77000, Port Elizabeth 6031 (South Africa); Kroon, R.E., E-mail: KroonRE@ufs.ac.za [Department of Physics, University of the Free State, IB51, Box 339, Bloemfontein 9300 (South Africa)

2012-05-15

Amorphous silica samples doped with 0.1 and 1 mol% of terbium (Tb) were synthesized by the sol-gel method. In addition to the green light associated with {sup 5}D{sub 4}{yields}{sup 7}F{sub J} transitions of Tb{sup 3+}, the sample containing 0.1 mol% also emitted blue light as a result of {sup 5}D{sub 3}{yields}{sup 7}F{sub J} transitions during photoluminescence (PL) measurements. As a result of concentration quenching this blue emission was not observed for the samples doped with the higher concentration (1 mol%). However the blue {sup 5}D{sub 3} {yields}{sup 7}F{sub J} emission was observed in the 1 mol% doped samples during cathodoluminescence (CL) measurements. Since a rough calculation indicated that the excitation rate in the CL system where the blue emission is observed may be similar to a laser PL system under conditions where the blue emission is not observed, the difference is attributed to the nature of the excitation sources. It is suggested that during the CL excitation incident electrons can reduce non-luminescent Tb{sup 4+} ions in the silica, substituting for Si{sup 4+} ions, to the excited (Tb{sup 3+}) Low-Asterisk state and that these are responsible for the blue emission, which does not occur during PL excitation.

Heightened vulnerability to MDR-TB epidemics after controlling drug-susceptible TB.

Directory of Open Access Journals (Sweden)

Jason D Bishai

2010-09-01

Full Text Available Prior infection with one strain TB has been linked with diminished likelihood of re-infection by a new strain. This paper attempts to determine the role of declining prevalence of drug-susceptible TB in enabling future epidemics of MDR-TB.A computer simulation of MDR-TB epidemics was developed using an agent-based model platform programmed in NetLogo (See http://mdr.tbtools.org/. Eighty-one scenarios were created, varying levels of treatment quality, diagnostic accuracy, microbial fitness cost, and the degree of immunogenicity elicited by drug-susceptible TB. Outcome measures were the number of independent MDR-TB cases per trial and the proportion of trials resulting in MDR-TB epidemics for a 500 year period after drug therapy for TB is introduced.MDR-TB epidemics propagated more extensively after TB prevalence had fallen. At a case detection rate of 75%, improving therapeutic compliance from 50% to 75% can reduce the probability of an epidemic from 45% to 15%. Paradoxically, improving the case-detection rate from 50% to 75% when compliance with DOT is constant at 75% increases the probability of MDR-TB epidemics from 3% to 45%.The ability of MDR-TB to spread depends on the prevalence of drug-susceptible TB. Immunologic protection conferred by exposure to drug-susceptible TB can be a crucial factor that prevents MDR-TB epidemics when TB treatment is poor. Any single population that successfully reduces its burden of drug-susceptible TB will have reduced herd immunity to externally or internally introduced strains of MDR-TB and can experience heightened vulnerability to an epidemic. Since countries with good TB control may be more vulnerable, their self interest dictates greater promotion of case detection and DOTS implementation in countries with poor control to control their risk of MDR-TB.

A potential green emitting citrate gel synthesized NaSrBO3:Tb3+ phosphor for display application

Science.gov (United States)

Bedyal, A. K.; Kumar, Vinay; Swart, H. C.

2018-04-01

A potential green emitting NaSrBO3:Tb3+ (1-9 mol%) phosphor was synthesized by a citrate gel combustion method. X-ray diffraction patterns confirmed the monoclinic phase of the phosphor. The phosphor emitted intense green emission under near-UV and electron excitation due to the characteristic transitions 5D4→7F6(488 nm),5D4→7F5(544 nm),5D4→7F4(586 nm) and 5D4→7F3(622 nm) of Tb3+ ions. The optimal molar concentration of Tb3+ ions was found to be 6 mol%, after that concentration quenching occurred. The dipole-dipole interaction was found to be accountable for energy transfer between the Tb3+ ions. X-ray photoelectron spectroscopy was carried out to analyze the chemical states of the elements and suggest that terbium was mostly presented in the (+3) valance state in the phosphor. The approximated Commission Internationale de l‧Eclairage coordinates for the PL (0.31, 0.61) and CL (0.33, 0.57) were found to be very close to the well-known green emitting phosphor. The obtained results suggest that the studied phosphor could be an ultimate choice for green emission in display applications.

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

Energy Technology Data Exchange (ETDEWEB)

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

2003-07-01

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

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

Energy Technology Data Exchange (ETDEWEB)

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

2017-06-15

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

Low temperature synthesis, characterization and tunable optical properties of Eu3+, Tb3+ doped CaMoO4 nanoparticles

International Nuclear Information System (INIS)

Sharma, K. Gayatri; Singh, Th. Prasanta; Singh, N. Rajmuhon

2014-01-01

Highlights: • Red and green nanophosphors of CaMoO 4 :Eu 3+ and Tb 3+ were synthesized via an ethylene glycol route at very low temperature. • The prepared nanoparticles have tetragonal structure. • The luminescence properties of the nanoparticles are also studied extensively. • CIE chromaticity coordinates of the phosphors are also studied. • The blue-green emission of host could be easily tuned to red or green by varying the dopant ion used in the host. - Abstract: CaMoO 4 doped with Eu 3+ and Tb 3+ nanoparticles are obtained using ethylene glycol as the solvent. The synthesis has been carried out at 130 °C temperature. The XRD patterns reveal that all the doped samples are well assigned to the scheelite structure of the CaMoO 4 phase. Upon excitation by ultraviolet radiation, the CaMoO 4 :Eu 3+ , Tb 3+ phosphors show the characteristic emission lines of Eu 3+ and Tb 3+ . For Eu 3+ doped samples, red emission dominates over other transitions and for Tb 3+ doped, green emission is the predominant one. The blue-green emission of the host could be easily tuned to red and green by doping with activator ions. The emission intensity is also dependent on the concentration of the dopant ions. The prepared nanoparticles could find applications in LEDs and other optical devices

Photon up-conversion production in Tb{sup 3+}–Yb{sup 3+} co-doped CaF{sub 2} phosphors prepared by combustion synthesis

Energy Technology Data Exchange (ETDEWEB)

Rakov, Nikifor, E-mail: nikifor.gomez@univasf.edu.br [PG—Ciência dos Materiais, Universidade Federal do Vale do São Francisco, 48902-300 Juazeiro, BA (Brazil); Guimarães, Renato B. [Instituto de Física, Universidade Federal Fluminense, 24210-346 Niterói, RJ (Brazil); Maciel, Glauco S., E-mail: glauco@if.uff.br [Instituto de Física, Universidade Federal Fluminense, 24210-346 Niterói, RJ (Brazil)

2016-02-15

Graphical abstract: Up-conversion luminescence from Tb{sup 3+} obtained by energy transfer from Yb{sup 3+} pairs in CaF{sub 2} powder prepared by combustion synthesis. - Highlights: • Calcium fluoride (CaF{sub 2}) powders were prepared by combustion synthesis. • Rare-earth ions doped in this material were found in interstitial sites. • Cooperative up-conversion was observed in Tb{sup 3+}:Yb{sup 3+}:CaF{sub 2} powder. • Energy transfer between Tb{sup 3+} and pairs of Yb{sup 3+} was analyzed using rate equations. - Abstract: Calcium fluoride (CaF{sub 2}) crystalline powders were successfully prepared by the combustion synthesis method. The powder material containing luminescent rare-earth ions, more specifically terbium (Tb{sup 3+}) and ytterbium (Yb{sup 3+}), was studied by X-ray diffraction, scanning electronic microscopy and optical spectroscopy. These ions are allocated in charge compensated interstitial positions of tetragonal (C{sub 4v}) and trigonal (C{sub 3v}) symmetry sites of the cubic (O{sub h}) CaF{sub 2} lattice. Up-conversion (UC) luminescence in Tb{sup 3+} was achieved using a low power diode laser operating at 975 nm. Tb{sup 3+} is insensitive to near-infrared radiation but UC can be achieved via energy transfer from pairs of Yb{sup 3+} ions to Tb{sup 3+} ions. The UC luminescence dynamics of Tb{sup 3+} was used to study the energy transfer mechanism.

Structural and optical properties of Tb and Na-Tb co-doped Ca3V2O8 phosphors prepared by sol-gel process

Science.gov (United States)

Parab, Shambhu S.; Salker, A. V.

2018-01-01

A malic acid assisted sol-gel route was successfully employed to prepare two distinct series of green emitting Ca3V2O8 phosphors. In the first series, Tb was solely doped whereas in the second series Na and Tb were doped simultaneously in the Ca3V2O8 crystal lattice. X-ray diffraction studies proved the utility of adopted preparative method by confirming the monophasic formation of all compounds from both the series. Spectral analysis like Raman spectroscopy, UV-DRS were undertaken to analyse the local structure, crystallinity and absorptive characteristics. XPS validated the presence of desired oxidation states of all the elements present. Finally, photoluminescence studies were done to elucidate the scope of prepared compounds as green emitting phosphors and also to understand the effect of both doping schemes on the luminescence. Intense green emission was observed in both the cases. Tb concentration of 0.08 was found to be optimum in case of Tb singly doped compounds whereas Tb = 0.12 showed highest intensity among the Na-Tb co-doped samples. Moreover, a red shift in the excitation wavelength was observed after Na doping signifying a change in the local electronic environment which in turn has affected the luminescence pattern. Local crystallinity and vacancy concentrations were found to have a major say on the emission intensities.

Optical investigation of Tb3+-doped Y2O3 nanocrystals prepared by Pechini-type sol–gel process

International Nuclear Information System (INIS)

Back, M.; Massari, A.; Boffelli, M.; Gonella, F.; Riello, P.; Cristofori, D.; Riccò, R.; Enrichi, F.

2012-01-01

We report an optical study of Tb 3+ -doped Y 2 O 3 nanocrystals synthesized by Pechini-type sol–gel method. The particles are investigated in terms of size and morphology by means of X-ray diffraction and transmission electron microscopy analysis. It is shown how the simple Pechini method allows for the growth of monocrystalline nanoparticles with a volume-weighted average size of about 30 nm. The optical properties of Tb 3+ in the host lattice are studied in terms of PL, PLE, and lifetimes. Moreover, a correlation between the type of decay curves, the emission and excitation bands' shapes, and the site location of the emitting Tb 3+ in the host material Y 2 O 3 is proposed.

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

Science.gov (United States)

Xia, Zhiguo; Wu, Weiwei

2013-09-28

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

Temperature dependent emission characteristics of monoclinic YBO{sub 3}: Eu{sup 3+}/Tb{sup 3+} phosphor

Energy Technology Data Exchange (ETDEWEB)

Sharma, Suchinder K., E-mail: suchindersharma@gmail.com [AMO-Physics Division, Physical Research Laboratory, Navrangpura, Ahmedabad 380009 (India); Malik, M. Manzar [Department of Physics, Maulana Azad National Institute of Technology (MANIT), Bhopal (India)

2016-05-15

YBO{sub 3}:Eu{sup 3+}/Tb{sup 3+} phosphor samples synthesized by modified combustion method are studied in the present work using powder X-ray diffraction, UV–visible absorption spectroscopy, X-ray excited luminescence spectroscopy and optical parametric oscillator (OPO) based laser excited emission spectroscopy. The temperature dependence of luminescence emission is also studied. The structural analysis suggests that the samples possess monoclinic structure with C2/c space group. The emission maximum was excitation wavelength dependent and prominent emission was observed at 593 nm (241 nm excitation) and 613 nm (300 nm excitation) for YBO{sub 3}:Eu{sup 3+} samples. The prominent magnetic/ electric (593/613 nm) dipole-moment allowed transitions are attributed to the presence of Eu{sup 3+} at different sites. For YBO{sub 3}:Tb{sup 3+} phosphor, 543 nm emission was prominent and had no impact of the cite symmetry. The increase in PL intensity in Eu{sup 3+} doped samples above 225 K is associated with the carrier mobility. An energy level scheme showing the positions of the 4f and 5d energy levels of all divalent and trivalent lanthanide ions relative to the valence and conduction band of the YBO{sub 3} has been constructed opening the possibility of using YBO{sub 3} for other interesting applications. - Highlights: • Synthesis of YBO{sub 3} by modified combustion method using glycine as fuel. • Crystallization in monoclinic phase (rarely investigated). • Eu and Tb doping and investigation of temperature dependent PL. • VRBE diagram generated in YBO{sub 3} to develop new optical materials.

Stop TB in My Lifetime: A Call for a World Free of TB - World TB Day 2013

Centers for Disease Control (CDC) Podcasts

2012-03-12

In this podcast Dr. Kenneth Castro, Director of the Division of Tuberculosis Elimination, discusses World TB Day, the 2013 slogan and theme.  Created: 3/12/2012 by National Center for HIV/AIDS, Viral Hepatitis, STD, and TB Prevention (NCHHSTP).   Date Released: 3/13/2012.

Broadband Seismometer at 2500m Depth in the Mediterranean Sea

Science.gov (United States)

Deschamps, A.; Hello, Y.; Charvis, P.; Dugué, M.; Bertin, V.; Valdy, P.; Le van Suu, A.; Real, D.

2003-04-01

In the frame of the ANTARES project, devoted to solar neutrinos detection across a large (0.1 km3) water volume located in deep sea, sea bottom facilities were developed at a depth of 2500m. Power supply, instrumentation control and data transmission have been implemented offshore Toulon (France) through a 43km long marine cable. A broadband seismological sensor has been installed among the instrumentation to control of physical and chemical environment of the neutrino detectors. The instrument was designed by Guralp Systems on the basis of CMG-3T seismometer (band-pass 120s-50hz) connected to a CMG DM24 digitizer for mechanical control and signal digitisation. Seismometer was inserted in titanium housing which fulfil the safety requirements of deployment operation. Control of CMG DM24 through asynchronous RS232 serial line was implemented in the ANTARES acquisition software running on the sea bottom. An interface running at the surface allows control and storage of the data. In January, the sensor was launched with the ANTARES instrumental line. In a second step the sensor has been slightly moved away from the ANTARES structure (60m), partly buried in the ground, roughly levelled and oriented by the IFREMER submarine Nautile. During the same operation the instrumentation line was connected to the power supply and data acquisition control. Masses of the seismometer were unlocked from the surface. Data are now continuously collected from Toulon and transmitted to Geosciences Azur in quasi real time. After a test period of 3 months, the sensor should be recovered for upgrades. For the final deployment (10 years), the ANTARES time control signal should be used to synchronise the sensor internal clock. This is the first real time broadband seismometer deployed in Europe and it will increase, in the future, our capability of marine earthquake detection in the area.

Ce decay curves in Ce, Tb co-doped LaF3 and the energy transfer mechanism

International Nuclear Information System (INIS)

Kroon, R.E.; Swart, H.C.; Ntwaeaborwa, O.M.; Seed Ahmed, H.A.A.

2014-01-01

Energy transfer phenomena can play an important role in the development of luminescent materials, and hosts co-doped with Ce 3+ and Tb 3+ ions continue to be actively studied. Several recent reports on Ce, Tb co-doped phosphors suggest different mechanisms for the energy transfer from Ce 3+ to Tb 3+ ions and further study is required to reach consensus on the mechanism or to understand why different mechanisms dominate in different hosts. A more direct method of analysis is proposed to distinguish between the different types of multipole energy transfer mechanisms. When applied to Ce, Tb co-doped LaF 3 , the experimental data shows a poor match to any of these models but is consistent with energy transfer through the exchange mechanism. The decay curves of Ce emission in Ce, Tb co-doped LaF 3 were also studied to obtain further insight on the energy transfer mechanism. Although the decrease in lifetime with increasing Tb concentration shows that energy transfer occurs through a non-radiative mechanism, the form of the decay curves does not correspond to what is expected for energy transfer via multipole interactions.

Enhancement of the up-conversion luminescence from NaYF{sub 4}:Yb{sup 3+},Tb{sup 3+}

Energy Technology Data Exchange (ETDEWEB)

Hölsä, Jorma, E-mail: jholsa@utu.fi [University of Turku, Department of Chemistry, FI-20014 Turku (Finland); Turku University Centre for Materials and Surfaces (MatSurf), Turku (Finland); Universidade de São Paulo, Instituto de Química, São Paulo-SP (Brazil); Laihinen, Tero [University of Turku, Department of Chemistry, FI-20014 Turku (Finland); Laamanen, Taneli; Lastusaari, Mika [University of Turku, Department of Chemistry, FI-20014 Turku (Finland); Turku University Centre for Materials and Surfaces (MatSurf), Turku (Finland); Pihlgren, Laura [University of Turku, Department of Chemistry, FI-20014 Turku (Finland); Graduate School of Materials Research (GSMR), Turku (Finland); Rodrigues, Lucas C.V. [University of Turku, Department of Chemistry, FI-20014 Turku (Finland); Universidade de São Paulo, Instituto de Química, São Paulo-SP (Brazil); Soukka, Tero [University of Turku, Department of Biochemistry, FI-20014 Turku (Finland)

2014-04-15

The synthesis conditions of the Yb{sup 3+} and Tb{sup 3+} co-doped NaYF{sub 4} were optimized by reducing the number of washings to include only ethanol. The avoidance of the loss of amorphous NaF prior to post-annealing of the as-prepared materials resulted in the enhancement of the otherwise rather weak up-conversion from Tb{sup 3+} by 1–2 orders of magnitude. At the same time, the temperature of formation of the hexagonal NaRF{sub 4} phase with high up-conversion could be lowered by 100 °C down to 350 °C. This improvement in up-conversion was concluded to result from the better stoichiometry of the material without washing with water. The deficit of Na{sup +} would result in the excess of fluoride which, although not as fatal to the luminescence as the fluoride vacancies, has serious implications to the up-conversion intensity. A further enhancement in the up-conversion luminescence was observed to be due to the Er{sup 3+} ion impurity frequently associated with high-concentration Yb{sup 3+} materials. The mechanism involving the unintentional Er{sup 3+} sensitizer and the resonance energy transfer in the Yb{sup 3+}–Er{sup 3+}–Tb{sup 3+} co-doped NaYF{sub 4} were discussed based on the energy level schemes of the Yb{sup 3+}, Er{sup 3+}, and Tb{sup 3+} ions in NaYF{sub 4}.

Supporting clinical management of the difficult-to-treat TB cases: the ERS-WHO TB Consilium

Directory of Open Access Journals (Sweden)

Lia D’Ambrosio

2015-03-01

The primary objective of the ERS/WHO TB Consilium is to provide clinical consultation for drug-resistant TB and other difficult-to-treat TB cases, including co-infection with HIV and paediatric cases. Through technical guidance to clinicians managing complex TB cases, the main contribution and outcome of the initiative will be a public health response aimed at achieving correct treatment of affected patients and preventing further development of drug resistance. The Consilum's secondary objective is to ensure monitoring and evaluation of clinical practices on the ground (diagnosis, treatment and prevention.

Combustion synthesis and optical properties of Oxy-borate phosphors YCa4O(BO3)3:RE3+ (RE = Eu3+, Tb3+) under UV, VUV excitation

International Nuclear Information System (INIS)

Ingle, J.T.; Gawande, A.B.; Sonekar, R.P.; Omanwar, S.K.; Wang, Yuhua; Zhao, Lei

2014-01-01

Graphical abstract: VUV Photoluminescence of YCa 4 O(BO 3 ) 3 : Eu 3+ and YCa 4 O(BO 3 ) 3 : Tb 3+ for PDPs applications. Highlights: • Inorganic Oxy-borate phosphors YCa 4 O(BO 3 ) 3 :Eu 3+ ,Tb 3+ was synthesized by novel solution combustion synthesis. • This single host produces efficient and intense Red and Green color for display applications. • Good agreement with CIE co-ordinates as prescribes by NTCL, for flat panel, PDP display color. • Synthesized materials were characterized using powder XRD, FE-SEM, UV and VUV Spectophotometer. -- Abstract: The inorganic Oxy-borate host phosphors YCa 4 O(BO 3 ) 3 :RE 3+ (RE = Eu 3+ ,Tb 3+ ) were synthesized by a novel solution combustion technique. The synthesis is based on the exothermic reaction between the fuel (Urea) and Oxidizer (Ammonium nitrate). The heat generated in reaction is use for auto combustion of precursors. The structures of the prepared samples were confirmed by powder XRD technique. The photoluminescence properties of the powder samples were investigated under UV and VUV excitation; “The phosphor YCa 4 O(BO 3 ) 3 :Eu 3+ and YCa 4 O(BO 3 ) 3 :Tb 3+ shows strong absorption in UV and VUV region and exhibits intense red and green emission upon excited by 254 nm UV and 147 nm VUV radiation”

Synchrotron diffraction characterization of nanostructured KY3F10:Tb

International Nuclear Information System (INIS)

Ichikawa, Rodrigo U.; Teixeira, Maria I.; Ranieri, Izilda M.; Martinez, Luis G.; Linhares, Horacio M.S.M.D.; Turrillas, Xavier

2015-01-01

Nanostructured rare-earth fluorides materials are being intensively studied recently due to their potential applications in high-dose dosimetry. Particularly, nanostructured Tb-doped KY 3 F 10 has shown satisfactory results to be used in this area. In the present work, the structure and microstructure of KY 3 F 10 :Tb was investigated by means of X-ray synchrotron diffraction. One of the samples was analyzed as synthesized and another after a heat treatment. Rietveld refinement of synchrotron diffraction data was applied to obtain cell parameters, atomic positions and atomic displacement factors and the results were compared to values found in literature. X-ray line profile analysis methods were applied to determine mean crystallite sizes and their distribution. (author)

Analysis of host responses to Mycobacterium tuberculosis antigens in a multi-site study of subjects with different TB and HIV infection states in sub-Saharan Africa.

Directory of Open Access Journals (Sweden)

Jayne S Sutherland

Full Text Available Tuberculosis (TB remains a global health threat with 9 million new cases and 1.4 million deaths per year. In order to develop a protective vaccine, we need to define the antigens expressed by Mycobacterium tuberculosis (Mtb, which are relevant to protective immunity in high-endemic areas.We analysed responses to 23 Mtb antigens in a total of 1247 subjects with different HIV and TB status across 5 geographically diverse sites in Africa (South Africa, The Gambia, Ethiopia, Malawi and Uganda. We used a 7-day whole blood assay followed by IFN-γ ELISA on the supernatants. Antigens included PPD, ESAT-6 and Ag85B (dominant antigens together with novel resuscitation-promoting factors (rpf, reactivation proteins, latency (Mtb DosR regulon-encoded antigens, starvation-induced antigens and secreted antigens.There was variation between sites in responses to the antigens, presumably due to underlying genetic and environmental differences. When results from all sites were combined, HIV- subjects with active TB showed significantly lower responses compared to both TST(- and TST(+ contacts to latency antigens (Rv0569, Rv1733, Rv1735, Rv1737 and the rpf Rv0867; whilst responses to ESAT-6/CFP-10 fusion protein (EC, PPD, Rv2029, TB10.3, and TB10.4 were significantly higher in TST(+ contacts (LTBI compared to TB and TST(- contacts fewer differences were seen in subjects with HIV co-infection, with responses to the mitogen PHA significantly lower in subjects with active TB compared to those with LTBI and no difference with any antigen.Our multi-site study design for testing novel Mtb antigens revealed promising antigens for future vaccine development. The IFN-γ ELISA is a cheap and useful tool for screening potential antigenicity in subjects with different ethnic backgrounds and across a spectrum of TB and HIV infection states. Analysis of cytokines other than IFN-γ is currently on-going to determine correlates of protection, which may be useful for vaccine

Concentration effect on the spectroscopic behavior of Tb{sup 3+} ions in zinc phosphate glasses

Energy Technology Data Exchange (ETDEWEB)

Kesavulu, C.R., E-mail: crkesavulu2005@gmail.com [Instituto de Fisica de São Carlos, Universidade de São Paulo, Avenida Trabalhador Sãocarlense 400, São Carlos, SP (Brazil); Almeida Silva, Anielle Christine [Laboratorio de Novos Materials Isolantes e Semicondutores (LNMIS), Instituto de Física, Universidade Federal de Uberândia, MG (Brazil); Dousti, M.R. [Instituto de Fisica de São Carlos, Universidade de São Paulo, Avenida Trabalhador Sãocarlense 400, São Carlos, SP (Brazil); Dantas, Noelio Oliveira [Laboratorio de Novos Materials Isolantes e Semicondutores (LNMIS), Instituto de Física, Universidade Federal de Uberândia, MG (Brazil); Camargo, A.S.S. de; Catunda, Tomaz [Instituto de Fisica de São Carlos, Universidade de São Paulo, Avenida Trabalhador Sãocarlense 400, São Carlos, SP (Brazil)

2015-09-15

Zinc phosphate glasses (PZABPTb) in the compositional system: P{sub 2}O{sub 5}–ZnO–Al{sub 2}O{sub 3}–BaO–PbO doped with variable Tb{sup 3+} concentrations (1–5 wt% Tb{sub 2}O{sub 3}) were prepared and characterized through absorption, excitation, emission and intensity decay rate measurements. The Judd–Ofelt model has been adopted to evaluate the radiative properties of the {sup 5}D{sub 4}→{sup 7}F{sub 6–3} emission transitions. The effect of Tb{sup 3+} ion concentration on the emissions from the {sup 5}D{sub 3,4} excited levels is discussed in detail. Analysis of the intensity decay curves corresponding to blue and green emissions from levels {sup 5}D{sub 3} and {sup 5}D{sub 4}, respectively, allowed determination of effective lifetimes, which confirmed the Tb{sup 3+} ion concentration quenching of the blue emission in these glasses. The decay curves for the {sup 5}D{sub 3} level are found to be non-exponential in nature for all the studied concentrations due to ion–ion energy transfer through cross-relaxation. In an attempt to identify the origin of the energy transfer mechanism, the decay curves were well fitted to the Inokuti–Hirayama model for S=6, which indicates that the energy transfer process is of dipole–dipole type. The optical band gap energy (E{sub opt}) has been evaluated taking into account the ultraviolet edge of absorption spectra. - Highlights: • Tb{sup 3+}-doped zinc phosphate glasses have been prepared by melt quenching technique. • Spectroscopic parameters were evaluated using the Judd–Ofelt theory. • Effects of Tb{sup 3+} concentration on luminescence of the glasses were studied. • Strong intense laser transition for Tb{sup 3+} ion in PZABPTb glasses is {sup 5}D{sub 4}→{sup 7}F{sub 5} (0.54 μm). • PZABPTb glasses could be used in the development of green color display devices and solid state visible lasers.

Hydrothermal synthesis of 4ZnO·B2O3·H2O:Ln3 + (Ln = Eu, Tb) phosphors: Morphology-tunable and luminescence properties

Science.gov (United States)

Cao, Shiwei; Jiao, Yang; Han, Weifang; Ge, Chunhua; Song, Bo; Wang, Jie; Zhang, Xiangdong

2018-02-01

4ZnO·B2O3·H2O:Ln3 + (Ln = Eu, Tb) phosphors with different morphologies have been successfully synthesized via one-step hydrothermal method through regulating the molar amount of Eu3 + and Tb3 +. Comprehensive scanning electron microscopy (SEM), X-ray diffraction (XRD) Fourier transform infrared spectrum (FT-IR) and inductively coupled plasma atomic emission spectrometer (ICP-AES) characterizations all confirm that obtained products are 4ZnO·B2O3·H2O:Ln3 + (Ln = Eu, Tb). The experimental results displayed that the morphology and photoluminescence of compounds is regularly changed with increased the molar amount of rare earth ions. For the Eu3 +-doped, Tb3 +-doped and Eu3 +/Tb3 + co-doped 4ZnO·B2O3·H2O phosphors of morphologies, the rod-like structures gradually changed to flower-like structures, fine wire-like structure and hybrid structure, respectively. To their photoluminescence, the Eu3 + shows a red emission (615 nm); the Tb3 + shows a green emission (545 nm); for the Eu3 +/Tb3 + co-doped 4ZnO·B2O3·H2O phosphors, a combination of blue (5d-4f of Eu2 +), green (5D4-7F5 of Tb3 +) and red (5D0-7F2 of Eu3 +) emissions emerges to achieve white emission. In addition, the energy transfer among Eu3 +, Eu2 + and Tb3 + ions was also discussed.

The effects of Tb 3+ doping concentration on luminescence ...

Indian Academy of Sciences (India)

BaF2 phosphor; crystal structure; luminescence properties; X-ray diffraction; concentration quenching. 1. Introduction ... reported that the particle size, shape, crystallinity, etc., sig- nificantly ... Figure 3 shows the excitation and emission spectra of sam- ple with 4 ... gies obtained earlier.9,10 The ground term of the Tb3+ ion is.

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

Science.gov (United States)

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

2018-05-01

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

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

Science.gov (United States)

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

2013-12-02

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

Tunable emission and the systematic study on energy-transfer properties of Ce{sup 3+}- and Tb{sup 3+}-co-doped Sr{sub 3}(PO{sub 4}){sub 2} phosphors

Energy Technology Data Exchange (ETDEWEB)

Liu, Zhijun [Guangzhou Maritime Institute, Department of Shipping Engineering, Guangzhou (China)

2015-09-15

An emitting color tunable phosphor Sr{sub 3}(PO{sub 4}){sub 2}:Ce{sup 3+}, Tb{sup 3+} was synthesized by the traditional high-temperature solid-state reaction method. The photoluminescence and energy-transfer (ET) properties of Ce{sup 3+}- and Tb{sup 3+}-doped Sr{sub 3}(PO{sub 4}){sub 2} host were studied in detail. The obtained phosphors show both a blue emission from Ce{sup 3+} and a yellowish green emission from Tb{sup 3+} with considerable intensity under ultraviolet (UV) excitation (∝311 nm). When the content of Ce{sup 3+} was fixed at 0.03, the emission chromaticity coordinates could be adjusted from blue to green region by tuning the contents of Tb{sup 3+} ions with the aid of ET process. The critical distance between Ce{sup 3+} and Tb{sup 3+} is 14.69 A. The ET mechanism from Ce{sup 3+} to Tb{sup 3+} ions was identified with dipole-dipole interaction. The obtained phosphor exhibits a strong excitation in UV spectral region and high-efficient ET from Ce{sup 3+} to Tb{sup 3+} ions. It may find applications as a green light-emitting UV-convertible phosphor in white LED devices. (orig.)

Eu3+/Tb3+-doped La2O2CO3/La2O3 nano/microcrystals with multiform morphologies: facile synthesis, growth mechanism, and luminescence properties.

Science.gov (United States)

Li, Guogang; Peng, Chong; Zhang, Cuimiao; Xu, Zhenhe; Shang, Mengmeng; Yang, Dongmei; Kang, Xiaojiao; Wang, Wenxin; Li, Chunxia; Cheng, Ziyong; Lin, Jun

2010-11-15

LaCO(3)OH nano/microcrystals with a variety of morphologies/sizes including nanoflakes, microflowers, nano/microrhombuses, two-double microhexagrams sandwichlike microspindles, and peach-nucleus-shaped microcrystals have been synthesized via a facile homogeneous precipitation route under mild conditions. A series of controlled experiments indicate that the pH values in the initial reaction systems, carbon sources, and simple ions (NH(4)(+) and Na(+)) were responsible for the shape determination of the LaCO(3)OH products. A possible formation mechanism for these products with diverse architectures has been presented. After annealing at suitable temperatures, LaCO(3)OH was easily converted to La(2)O(2)CO(3) and La(2)O(3) with the initial morphologies. A systematic study on the photoluminescence and cathodoluminescence properties of Eu(3+)- or Tb(3+)-doped La(2)O(2)CO(3)/La(2)O(3) samples has been performed in detail. The excitation and site-selective emission spectra were recorded to investigate the microstructure, site symmetry, and difference in the (5)D(0) → (7)F(2) transition of Eu(3+) ions in La(2)O(2)CO(3) and La(2)O(3) host lattices. In addition, the dependence of the luminescent intensity on the morphology for the as-prepared La(2)O(2)CO(3)/La(2)O(3):Ln(3+) (Ln = Eu, Tb) samples has been investigated. The ability of generating diverse morphologies and multiemitting colors for different rare-earth activator ion (Ln = Eu, Tb) doped La(2)O(2)CO(3)/La(2)O(3) nano/microstructures provides a great opportunity for the systematic evaluation of morphology-dependent luminescence properties, as well as the full exploration of their application in many types of color display fields.

Synthesis, luminescence, and energy-transfer properties of β-Na2Ca4(PO4)2(SiO4):A (A = Eu(2+), Dy(3+), Ce(3+)/Tb(3+)) phosphors.

Science.gov (United States)

Li, Kai; Shang, Mengmeng; Geng, Dongling; Lian, Hongzhou; Zhang, Yang; Fan, Jian; Lin, Jun

2014-07-07

A series of β-Na2Ca4(PO4)2(SiO4) (β-NCPS):A (A = Eu(2+), Dy(3+), Ce(3+)/Tb(3+)) phosphors were prepared via a high-temperature solid-state reaction route. The X-ray diffraction, Fourier transform infrared, photoluminescence (PL), cathodoluminescence (CL) properties, fluorescent lifetimes, and absolute quantum yield were exploited to characterize the samples. Under UV radiation, the β-NCPS:Eu(2+) phosphors present bright green emissions, and the β-NCPS:Ce(3+) phosphors show strong blue emissions, which are attributed to their 4f(6)5d(1) → 4f(7) and 5d-4f allowed transitions, respectively. The β-NCPS:Ce(3+), Tb(3+) phosphors display intense tunable color from blue to green and high absolute quantum yields (81% for β-NCPS:0.12Ce(3+) and 83% for β-NCPS:0.12Ce(3+), 0.08Tb(3+)) when excited at 365 nm. Simultaneously, the energy transfer from Ce(3+) to Tb(3+) ions is deduced from the spectral overlap between Ce(3+) emission and Tb(3+) excitation spectra and demonstrated by the change of emission spectra and decay lifetimes. Moreover, the energy-transfer mechanism from Ce(3+) to Tb(3+) ions is confirmed to be exchange interaction according to the discussion of expression from Dexter and Reisfeld. Under a low-voltage electron-beam excitation, the β-NCPS:A (A = Eu(2+), Dy(3+), Ce(3+)/Tb(3+)) phosphors exhibit their characteristic emissions, and the emission profiles of β-NCPS:Ce(3+),Tb(3+) phosphors are obviously different from those of the PL spectra; this difference might be ascribed to their different luminescence mechanisms. These results in PL and CL properties suggest that β-NCPS:A (A = Eu(2+), Dy(3+), Ce(3+)/Tb(3+)) phosphors are potential candidates for solid-state lighting and field-emission displays.

Facile controlled synthesis different morphologies of LuBO3:Ln3+ (Ln = Eu, Tb) phosphors and tunable luminescent properties

International Nuclear Information System (INIS)

Leng, Zhihua; Xiong, Hailong; Li, Linlin; Zhang, Nannan; Liu, Yali; Gan, Shucai

2015-01-01

Sphere-like and cauliflower-like hexagonal-vaterite LuBO 3 have been successfully synthesized for the first time via a chemical conversion route using Lu(OH)CO 3 colloid spheres as sacrificial precursor and H 3 BO 3 as boron source without any additional surfactant. FTIR analysis provides an additional evidence of the formation of vaterite-type LuBO 3 in this method. It was found that, an appropriate amount ethanol in the hydrothermal process has a great effect on the products' morphology and crystallinity. Time-dependent experiments indicate that the formation of LuBO 3 crystals went through a two-stage growth process, which involves a fast nucleation of primary particles followed by a slow aggregation and crystallization of primary particles. An investigation on the photoluminescence (PL) properties of LuBO 3 :Eu 3+ phosphors with different morphologies indicates that their PL intensity are dependent on their crystallinity. The effect of Eu 3+ and Tb 3+ doping concentration on PL intensity were also investigated and the quenching concentration of LuBO 3 :Eu 3+ and LuBO 3 :Tb 3+ is 0.25 and 0.20, respectively. Moreover, for Eu 3+ /Tb 3+ doped LuBO 3 phosphors, the color tones can be tuned from green, through green–yellow and yellow, and then to red by simply adjusting the relative doping concentrations of the Tb 3+ and Eu 3+ ions. - Highlights: • Sphere-like and cauliflower-like LuBO 3 were obtained by a conversion route. • This method used Lu(OH)CO 3 and H 3 BO 3 as the precursors for the first time. • Ethanol can control the products' morphology, crystallinity and PL intensity. • The emitting color tones vary with Tb 3+ /Eu 3+ doped concentration

Treatment: Latent TB Infection (LTBI) and TB Disease

Science.gov (United States)

... Adverse Events TB Treatment of Persons Living with HIV TB Treatment and Pregnancy TB Treatment for Children Drug-Resistant TB Research TB Epidemiologic Studies Consortium Research Projects Publications TB Trials Consortium Study ...

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

Energy Technology Data Exchange (ETDEWEB)

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

2016-10-15

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

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

Energy Technology Data Exchange (ETDEWEB)

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

2016-02-15

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

Synthesis and tunable luminescence properties of Eu2+ and Tb3+-activated Na2Ca4(PO4)3F phosphors based on energy transfer

International Nuclear Information System (INIS)

Zhou, Jun; Xia, Zhiguo; You, Hongpeng; Shen, Kai; Yang, Mengxia; Liao, Libing

2013-01-01

A series of color-tunable blue–green emitting Na 2 Ca 4 (PO 4 ) 3 F:Eu 2+ ,Tb 3+ phosphors were prepared by a high temperature solid-state reaction. Their luminescence properties reveal that there is an efficient energy transfer from Eu 2+ to Tb 3+ ions via a dipole–quadrupole mechanism where Eu 2+ ions exhibit a strong excitation band in near ultraviolet (UV) region, matching well with the dominant emission band of near UV (350–420 nm) LED chips, and Eu 2+ and Tb 3+ ions can give characteristic blue and green emission light. The varied color of the phosphors from blue to green can be achieved by properly tuning the relative ratio of Eu 2+ to Tb 3+ dopant through the energy transfer from Eu 2+ to Tb 3+ ions. Thermal quenching luminescence results reveal that Na 2 Ca 4 (PO 4 ) 3 F:Eu 2+ ,Tb 3+ exhibits good thermal stability. These results demonstrate that Tb 3+ ion with low 4f–4f absorption efficiency in near UV region can play the role of an activator in narrow green-emitting phosphor through efficient energy feeding by allowing 4f–5d absorption of Eu 2+ with high oscillator strength. The present Eu 2+ –Tb 3+ codoped Na 2 Ca 4 (PO 4 ) 3 F phosphor will have potential application for the near UV white LEDs. - Highlights: ► Color-tunable blue–green Na 2 Ca 4 (PO 4 ) 3 F:Eu 2+ ,Tb 3+ phosphors were prepared. ► Eu 2+ –Tb 3+ energy transfer process and mechanism discussed. ► Thermal quenching properties of blue and green phosphors were studied.

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

International Nuclear Information System (INIS)

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

2016-01-01

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

Thermoluminescence properties of Al{sub 2}O{sub 3}:Tb nanoparticles irradiated by gamma rays and 85 MeV C{sup 6+} ion beam

Energy Technology Data Exchange (ETDEWEB)

Salah, Numan, E-mail: nsalah@kau.edu.sa [Center of Nanotechnology, King Abdulaziz University, Jeddah 21589 (Saudi Arabia); Alharbi, Najlaa D. [Sciences Faculty for Girls, King Abdulaziz University, Jeddah 21589 (Saudi Arabia); Habib, Sami S. [Center of Nanotechnology, King Abdulaziz University, Jeddah 21589 (Saudi Arabia); Lochab, S.P. [Inter-University Accelerator Centre, Aruna Asaf Ali Marg, New Delhi 110067 (India)

2015-11-15

Carbon ions beam is recently recognized as an ideal cancer treatment modality, because of its excellent local tumor control. These ions have a high relative biological effectiveness resulting from high linear energy transfer (LET) and their sharp Bragg peak. However, the dose of those energetic ions needs to be measured with great precision using a proper dosimeter. Aluminum Oxide (Al{sub 2}O{sub 3}) is a highly luminescent phosphor widely used for radiation dosimetry using thermoluminesence (TL) technique. In this work nanoparticles of this material activated by different elements like Eu, Tb, Dy, Cu and Ag were evaluated for their TL response to gamma rays irradiation. Tb doped sample is found to be the most sensitive sample, which could be selected for exposure to 85 MeV C{sup 6+} ion beam in the fluence range 10{sup 9}–10{sup 13} ions/cm{sup 2}. The obtained result shows that C ion beam irradiated sample has a simple glow curve structure with a prominent glow peak at around 230 °C. This glow curve has a dosimetric peak better than those induced by gamma rays. This glow peak exhibits a linear response in the range 10{sup 9}–10{sup 11} ions/cm{sup 2}, corresponding to the equivalent absorbed doses 0.285–28.5 kGy. The absorbed doses, penetration depths and main energy loss were calculated using TRIM code based on the Monte Carlo simulation. The wide linear response of Al{sub 2}O{sub 3}:Tb nanoparticles along with the low fading makes this low cost nanomaterial a good candidate for C ion beam dosimetry. - Highlights: • Nanoparticles of Al{sub 2}O{sub 3} doped with Eu, Tb, Dy, Cu and Ag were synthesised. • They were evaluated for their TL response to gamma rays and C ion beam irradiation. • Tb doped sample is the most sensitive sample to gamma rays. • Al{sub 2}O{sub 3}:Tb was exposed to 85 MeV C{sup 6+} ion beam in the fluence range 10{sup 9}-10{sup 13} ions/cm{sup 2}. • The glow peak induced by C ions has a linear response in the range 10{sup 9

Paclitaxel conjugated Fe{sub 3}O{sub 4}@LaF{sub 3}:Ce{sup 3+},Tb{sup 3+} nanoparticles as bifunctional targeting carriers for Cancer theranostics application

Energy Technology Data Exchange (ETDEWEB)

Mangaiyarkarasi, Rajendiran; Chinnathambi, Shanmugavel; Karthikeyan, Subramani; Aruna, Prakasarao; Ganesan, Singaravelu, E-mail: sganesan@annauniv.edu

2016-02-01

The bi-functional Chitosan functionalized magnetite doped luminescent rare earth nanoparticles (Fe{sub 3}O{sub 4}@LaF{sub 3}: Ce{sup 3+},Tb{sup 3+}/chi NPs) as a carrier of paclitaxel (PTX) drug was designed using a co-precipitation and facile direct precipitation method. The synthesized nanoparticles are spherical in shape with a typical diameter of 19–37 nm respectively. They are water soluble, super paramagnetic and biocompatible, in which the amino groups on the nanoparticles surface are used for the conjugation with an anticancer drug, paclitaxel. The nature of PTX binding with Fe{sub 3}O{sub 4}@LaF{sub 3}: Ce{sup 3+},Tb{sup 3+}/chi nanoparticles were studied using X-ray diffraction, vibrating sample magnetometer and scanning electron micrograph. The nature of interactions between PTX and Fe{sub 3}O{sub 4}@LaF{sub 3}: Ce{sup 3+},Tb{sup 3+}/chi NPs due to complex formation were conceded out by various spectroscopic methods viz., UV–visible, steady state and excited state fluorescence spectroscopy. The photo-physical characterization reveals that the adsorption and release of PTX from Fe{sub 3}O{sub 4}@LaF{sub 3}:Tb{sup 3+}/chi nanoparticles is quicker when compared with other nanoparticles and also confirms that this may be due to the hydrogen bond formation between the hydroxyl group of drug and amino group of nanoparticles respectively. The maximum loading capacity and entrapment efficiency of 83.69% and 80.51% were attained at a ratio of 5:8 of PTX and Fe{sub 3}O{sub 4}@LaF{sub 3}: Ce{sup 3+},Tb{sup 3+}/chi NPs respectively. In addition with that, antitumoral activity study of PTX conjugated Fe{sub 3}O{sub 4}@LaF{sub 3}:Tb{sup 3+}/chi nanoparticles exhibits increased cytotoxic effects on A549 lung cancer cell lines than that of unconjugated PTX. - Highlights: • Fe{sub 3}O{sub 4}@LaF{sub 3}: Ce{sup 3+},Tb{sup 3+}/chi nanoparticles as a carrier of paclitaxel. • These particles are water soluble, super paramagnetic and biocompatible. • The maximum

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

Science.gov (United States)

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

2018-06-01

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

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.

Ca8Mg(SiO4)4Cl2:Ce3+, Tb3+: A potential single-phased phosphor for white-light-emitting diodes

International Nuclear Information System (INIS)

Zhu Ge; Wang Yuhua; Ci Zhipeng; Liu Bitao; Shi Yurong; Xin Shuangyu

2012-01-01

A single-phased white-light-emitting phosphor Ca 8 Mg(SiO 4 ) 4 Cl 2 :Ce 3+ , Tb 3+ (CMSC:Ce 3+ , Tb 3+ ) is synthesized by a high temperature solid-state reaction method, and its photoluminescence properties are investigated. The obtained phosphor exhibits a strong excitation band between 250 and 410 nm, matching well with the dominant emission band of a UV light-emitting-diode (LED) chip. Energy transfer from Ce 3+ to Tb 3+ ions has been investigated and demonstrated to be a resonant type via a dipole–dipole mechanism. The energy transfer efficiency as well as the critical distance is also estimated. Furthermore, the phosphors can generate light from yellow-green through white and eventually to blue by properly tuning the relative ratio of Ce 3+ to Tb 3+ ions grounded on the principle of energy transfer. The results show that this phosphor has potential applications as a single-phased phosphor for UV white-light LEDs. - Highlights: ► The luminescence properties of Ca 8 Mg(SiO 4 ) 4 Cl 2 :Ce 3+ , Tb 3+ were investigated for the first time. ► The strong absorption of phosphors matches well with the emission band of UV LED chips. ► The energy transfer from Ce 3+ to Tb 3+ in Ca 8 Mg(SiO 4 ) 4 Cl 2 was investigated in detail. ► The white light (CIE=(0.29, 0.34)) is generated by tuning the relative ratio of Ce 3+ to Tb 3+ .

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

International Nuclear Information System (INIS)

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

2013-01-01

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

Recombinant ESAT-6-CFP10 Fusion Protein Induction of Th1/Th2 Cytokines and FoxP3 Expressing Treg Cells in Pulmonary TB.

Directory of Open Access Journals (Sweden)

Dolly Jackson-Sillah

Full Text Available Early secretory antigenic target 6 (ESAT-6 and culture filtrate protein 10 (CFP-10 are Mycobacterium tuberculosis (Mtb-specific antigens that are secreted by actively metabolising bacteria and contribute to the virulence of the bacteria. Their ability to induce Treg and Th2 responses, particularly during the first two weeks of treatment, has not been comprehensively examined to date. The purpose of this work was to characterise Th1, Th2 and Treg responses to rESAT-6-CFP10 fusion protein in TB patients before and during the intensive phase of treatment and in healthy M.bovis BCG vaccinated donors.Forty-six newly diagnosed, HIV-negative, smear-positive pulmonary TB patients and 20 healthy donors were recruited in the UK and Ghana. Their peripheral blood mononuclear cells (PBMC were used in ex vivo ELISPOT and in vitro cultures to identify immunological parameters of interest.The study confirmed that protective immune responses to rESAT-6-CFP10 are impaired in active TB but improved during treatment: circulating antigen-specific IL-4-producing T-cells were increased in untreated TB but declined by two weeks of treatment while the circulating antigen-specific IFN-γ producing T cells which showed a transient rise at one week of treatment, persisted at baseline levels at two months of treatment. In vitro T cell proliferation and IFN-γ production were reduced, while IL-4 and CD4(+FoxP3(+CD25(hi cell expression were increased in response to rESAT-6-CFP10 fusion protein in untreated TB. These responses were reversed during early treatment of TB.These observations support further investigations into the possible utility of these parameters as markers of active disease and favourable treatment outcomes.

Recombinant ESAT-6-CFP10 Fusion Protein Induction of Th1/Th2 Cytokines and FoxP3 Expressing Treg Cells in Pulmonary TB.

Science.gov (United States)

Jackson-Sillah, Dolly; Cliff, Jacqueline M; Mensah, Gloria Ivy; Dickson, Emmanuel; Sowah, Sandra; Tetteh, John K A; Addo, Kwasi K; Ottenhoff, Tom H M; Bothamley, Graham; Dockrell, Hazel M

2013-01-01

Early secretory antigenic target 6 (ESAT-6) and culture filtrate protein 10 (CFP-10) are Mycobacterium tuberculosis (Mtb)-specific antigens that are secreted by actively metabolising bacteria and contribute to the virulence of the bacteria. Their ability to induce Treg and Th2 responses, particularly during the first two weeks of treatment, has not been comprehensively examined to date. The purpose of this work was to characterise Th1, Th2 and Treg responses to rESAT-6-CFP10 fusion protein in TB patients before and during the intensive phase of treatment and in healthy M.bovis BCG vaccinated donors. Forty-six newly diagnosed, HIV-negative, smear-positive pulmonary TB patients and 20 healthy donors were recruited in the UK and Ghana. Their peripheral blood mononuclear cells (PBMC) were used in ex vivo ELISPOT and in vitro cultures to identify immunological parameters of interest. The study confirmed that protective immune responses to rESAT-6-CFP10 are impaired in active TB but improved during treatment: circulating antigen-specific IL-4-producing T-cells were increased in untreated TB but declined by two weeks of treatment while the circulating antigen-specific IFN-γ producing T cells which showed a transient rise at one week of treatment, persisted at baseline levels at two months of treatment. In vitro T cell proliferation and IFN-γ production were reduced, while IL-4 and CD4(+)FoxP3(+)CD25(hi) cell expression were increased in response to rESAT-6-CFP10 fusion protein in untreated TB. These responses were reversed during early treatment of TB. These observations support further investigations into the possible utility of these parameters as markers of active disease and favourable treatment outcomes.

Estimation of Joule heating and its role in nonlinear electrical response of Tb0.5Sr0.5MnO3 single crystal

Science.gov (United States)

Nhalil, Hariharan; Elizabeth, Suja

2016-12-01

Highly non-linear I-V characteristics and apparent colossal electro-resistance were observed in non-charge ordered manganite Tb0.5Sr0.5MnO3 single crystal in low temperature transport measurements. Significant changes were noticed in top surface temperature of the sample as compared to its base while passing current at low temperature. By analyzing these variations, we realize that the change in surface temperature (ΔTsur) is too small to have caused by the strong negative differential resistance. A more accurate estimation of change in the sample temperature was made by back-calculating the sample temperature from the temperature variation of resistance (R-T) data (ΔTcal), which was found to be higher than ΔTsur. This result indicates that there are large thermal gradients across the sample. The experimentally derived ΔTcal is validated with the help of a simple theoretical model and estimation of Joule heating. Pulse measurements realize substantial reduction in Joule heating. With decrease in sample thickness, Joule heating effect is found to be reduced. Our studies reveal that Joule heating plays a major role in the nonlinear electrical response of Tb0.5Sr0.5MnO3. By careful management of the duty cycle and pulse current I-V measurements, Joule heating can be mitigated to a large extent.

Synthesis, crystal structure, optical and thermal properties of lanthanide hydrogen-polyphosphates Ln[H(PO3)4] (Ln = Tb, Dy, Ho).

Science.gov (United States)

Förg, Katharina; Höppe, Henning A

2015-11-28

Lanthanide hydrogen-polyphosphates Ln[H(PO3)4] (Ln = Tb, Dy, Ho) were synthesised as colourless (Ln = Tb, Dy) and light pink (Ln = Ho) crystalline powders by reaction of Tb4O7/Dy2O3/Ho2O3 with H3PO3 at 380 °C. All compounds crystallise isotypically (P2(1)/c (no. 14), Z = 4, a(Tb) = 1368.24(4) pm, b(Tb) = 710.42(2) pm, c(Tb) = 965.79(3) pm, β(Tb) = 101.200(1)°, 3112 data, 160 parameters, wR2 = 0.062, a(Ho) = 1363.34(5) pm, b(Ho) = 709.24(3) pm, c(Ho) = 959.07(4) pm, β(Ho) = 101.055(1)°, 1607 data, 158 parameters, wR2 = 0.058). The crystal structure comprises two different infinite helical chains of corner-sharing phosphate tetrahedra. In-between these chains the lanthanide ions are located, coordinated by seven oxygen atoms belonging to four different polyphosphate chains. Vibrational, UV/Vis and fluorescence spectra of Ln[H(PO3)4] (Ln = Tb, Dy, Ho) as well as Dy[H(PO3)4]:Ln (Ln = Ce, Eu) and the magnetic and thermal behaviour of Tb[H(PO3)4] are reported.

Label-Free Ag+ Detection by Enhancing DNA Sensitized Tb3+ Luminescence

Directory of Open Access Journals (Sweden)

Kimberly Kleinke

2016-08-01

Full Text Available In this work, the effect of Ag+ on DNA sensitized Tb3+ luminescence was studied initially using the Ag+-specific RNA-cleaving DNAzyme, Ag10c. While we expected to observe luminescence quenching by Ag+, a significant enhancement was produced. Based on this observation, simple DNA oligonucleotide homopolymers were used with systematically varied sequence and length. We discovered that both poly-G and poly-T DNA have a significant emission enhancement by Ag+, while the absolute intensity is stronger with the poly-G DNA, indicating that a G-quadruplex DNA is not required for this enhancement. Using the optimized length of the G7 DNA (an oligo constituted with seven guanines, Ag+ was measured with a detection limit of 57.6 nM. The signaling kinetics, G7 DNA conformation, and the binding affinity of Tb3+ to the DNA in the presence or absence of Ag+ are also studied to reveal the mechanism of emission enhancement. This observation is useful not only for label-free detection of Ag+, but also interesting for the rational design of new biosensors using Tb3+ luminescence.

Au@NaYF{sub 4}:Tb{sup 3+} core@shell nanostructures: Synthesis and construction of luminescence resonance energy transfer

Energy Technology Data Exchange (ETDEWEB)

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

2016-03-15

Luminescence resonance energy transfer (LRET) system can be constructed using NaYF{sub 4}:Tb{sup 3+} luminescence nanocrystals and gold nanoparticles (AuNPs) served as energy donor and acceptor, respectively. The AuNPs modified by cetyltrimethylammonium bromide (CTAB) were synthesized first and NaYF{sub 4}:Tb{sup 3+} shells encapsulated Au cores via a hydrothermal method. The synthesized materials were well characterized by X-ray diffraction (XRD), Fourier-transform infrared spectra (FT-IR), Transmission electron microscopy (TEM), X-ray photoelectron spectrum (XPS), UV–vis absorption spectra (UV–vis) and photoluminescence (PL) measurement. The results indicate that the synthesized Au@NaYF{sub 4}:Tb{sup 3+} core–shell nanoparticles have spherical morphology with a size of 80–90 nm and the shell layers of NaYF{sub 4}:Tb{sup 3+} nanocrystals have pure cubic structure. The luminescence properties of Au@NaYF{sub 4}:Tb{sup 3+} core–shell nanoparticles are same as those of NaYF{sub 4}:Tb{sup 3+} particles. The LRET process was realized using the core–shell nanoarchitectures due to the absorption spectrum of AuNPs matches well with the major emission peaks of Tb{sup 3+} ions. The LRET experiments have successfully verified the energy transfer between NaYF{sub 4}:Tb{sup 3+} nanocrystals and AuNPs. Additionally, the emission intensities of Tb{sup 3+} ions and the content of AuNPs exhibited a fair linear correlation.

TIME Impact - a new user-friendly tuberculosis (TB) model to inform TB policy decisions.

Science.gov (United States)

Houben, R M G J; Lalli, M; Sumner, T; Hamilton, M; Pedrazzoli, D; Bonsu, F; Hippner, P; Pillay, Y; Kimerling, M; Ahmedov, S; Pretorius, C; White, R G

2016-03-24

Tuberculosis (TB) is the leading cause of death from infectious disease worldwide, predominantly affecting low- and middle-income countries (LMICs), where resources are limited. As such, countries need to be able to choose the most efficient interventions for their respective setting. Mathematical models can be valuable tools to inform rational policy decisions and improve resource allocation, but are often unavailable or inaccessible for LMICs, particularly in TB. We developed TIME Impact, a user-friendly TB model that enables local capacity building and strengthens country-specific policy discussions to inform support funding applications at the (sub-)national level (e.g. Ministry of Finance) or to international donors (e.g. the Global Fund to Fight AIDS, Tuberculosis and Malaria).TIME Impact is an epidemiological transmission model nested in TIME, a set of TB modelling tools available for free download within the widely-used Spectrum software. The TIME Impact model reflects key aspects of the natural history of TB, with additional structure for HIV/ART, drug resistance, treatment history and age. TIME Impact enables national TB programmes (NTPs) and other TB policymakers to better understand their own TB epidemic, plan their response, apply for funding and evaluate the implementation of the response.The explicit aim of TIME Impact's user-friendly interface is to enable training of local and international TB experts towards independent use. During application of TIME Impact, close involvement of the NTPs and other local partners also builds critical understanding of the modelling methods, assumptions and limitations inherent to modelling. This is essential to generate broad country-level ownership of the modelling data inputs and results. In turn, it stimulates discussions and a review of the current evidence and assumptions, strengthening the decision-making process in general.TIME Impact has been effectively applied in a variety of settings. In South Africa, it

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.

Improved photoluminescence properties of a new green SrB2O4:Tb3+ phosphor by charge compensation

International Nuclear Information System (INIS)

Wu, Zhan-Chao; Wang, Ping; Liu, Jie; Li, Chao; Zhou, Wen-Hui; Kuang, Shao-Ping

2012-01-01

Highlights: ► New green-emitting SrB 2 O 4 :Tb 3+ phosphor was synthesized by solid-state reaction. ► Li + , Na + , and K + can all increase luminescent intensity of SrB 2 O 4 :Tb 3+ . ► Na + is the optimal charge compensator among Li + , Na + and K + . ► SrB 2 O 4 :Tb 3+ is a promising green phosphor for fabricating WLED. -- Abstract: A new green-emitting SrB 2 O 4 :Tb 3+ phosphor was synthesized by solid-state reaction. X-ray powder diffraction (XRD) analysis confirmed all the samples with orthorhombic formation of SrB 2 O 4 . The excitation spectra indicate the phosphor can be effectively excited by near ultraviolet (NUV) light, making it attractive as conversion phosphor for LED applications. The phosphor exhibits a bright green emission with the highest photoluminescence (PL) intensity at 544 nm excited by 378 nm light. The critical quenching concentration of Tb 3+ in SrB 2 O 4 :Tb 3+ is about 10 mol%. The effects of charge compensators (Li + , Na + , and K + ) on photoluminescence of SrB 2 O 4 :Tb 3+ were also studied. The results show that the emission intensity can be improved by all the three charge compensators and Na + is the optimal one for SrB 2 O 4 :Tb 3+ . All properties show that the phosphor is a promising green phosphor pumped by NUV InGaN chip for fabricating white light-emitting diodes (WLEDs).

A new series of borophosphate phosphor Cd{sub 3}BPO{sub 7}:M (M = Ce{sup 3+}, Tb{sup 3+}, Mn{sup 2+}) with tunable luminescence and energy transfer properties

Energy Technology Data Exchange (ETDEWEB)

Cao, Xiyu; Liu, Wei, E-mail: weiliu@ouc.edu.cn; Liu, Shuang; Cao, Lixin; Su, Ge; Gao, Rongjie; Jiang, Yu

2016-04-25

A new series of Cd{sub 3}BPO{sub 7}:M (M = Ce{sup 3+}, Tb{sup 3+}, Mn{sup 2+}) phosphors have been synthesized and characterized using X-ray powder diffraction as well as excitation and emission spectroscopy. Based on the Cd{sub 3}BPO{sub 7} host, the singly doping Ce{sup 3+}, Tb{sup 3+} and Mn{sup 2+} yield the blue, green and red-emitting phosphors respectively under the irradiation range from 270 to 300 nm UV. By appropriate tuning of Tb{sup 3+} or Mn{sup 2+} activator content, the emission color of the Cd{sub 3}BPO{sub 7}:Ce{sup 3+}/M (M = Tb{sup 3+} or Mn{sup 2+}) phosphors can be changed from blue to green or pink, respectively. Under UV excitation, the mixture of the as-prepared blue, green and red phosphors yields the warm white light, which exhibits their potential application as UV-convertible phosphors for WLEDs. - Highlights: • A new series of Cd{sub 3}BPO{sub 7}:M (M = Ce{sup 3+}, Tb{sup 3+}, Mn{sup 2+}) phosphors have been prepared. • The energy transfer from Ce{sup 3+} to Tb{sup 3+} is observed in Cd{sub 3}BPO{sub 7}:Ce{sup 3+}, Tb{sup 3+}. • Warm white light can be achieved by mixing physically the obtained tirphosphors.

tb diagnostics challenges of tb diagnosis and treatment in south africa

African Journals Online (AJOL)

2007-06-01

Jun 1, 2007 ... 45 currently provides treatment to 3 000 patients. Eighty-nine per cent of those accessing ART have symptomatic HIV disease. (WHO clinical stage 3 and 4) with a median CD4 cell count of. 95 cells/µl. More than 50% have a history of prior completed. TB treatment, 15% are on current TB treatment, 11% are.

Synthesis and photoluminescence properties of CaSixOy:Tb3+ phosphors prepared using solution-combustion method

CSIR Research Space (South Africa)

Dejene, FB

2011-07-01

Full Text Available Effect of Tb3+ ion concentrations on the structural and persistence luminescence properties of CaSixOy:Tb3+ crystals were evaluated using powders grown by the solution combustion technique. The XRD study indicates the change of phase from CaSiO3...

Tunable luminescence properties and efficient energy transfer in Eu2+, Tb3+ co-doped NaBaPO4

Directory of Open Access Journals (Sweden)

Qiuhong Zhang

2014-01-01

Full Text Available Eu2 + and Tb3+ singly doped and co-doped NaBaPO4 phosphors were synthesized by solid state reaction. The structure character, photoluminescence properties and the lifetime were investigated. The emission spectra of NaBaPO4:Eu2+, Tb3+, Na+ phosphor show both broad blue emission band and sharp green emission peaks. The energy transfer mechanism from Eu2+ to Tb3+ in NaBaPO4 host was discussed. The excitation spectra of NaBaPO4: Eu2+, Tb3+, Na+ phosphor show broad excitation band in the 250–400 nm range, which was in agreement with the near-ultraviolet (n-UV chip. The hue of the NaBaPO4: Eu2+, Tb3+, Na+ phosphors could be appropriately tuned by adjusting the contents of activators.

Favorable ultraviolet photoelectric effects in TbMnO3/Nb-SrTiO3 heterostructures

KAUST Repository

Jin, Kexin; Zhai, Y. X.; Li, Hui; Tian, Y. F.; Luo, B. C.; Wu, Tao

2014-01-01

The rectifying properties and ultraviolet photoelectric effects in TbMnO3/Nb-doped SrTiO3 heterostructures have been investigated. The ideality factors and the diffusion voltages obtained from the current-voltage curves nonlinearly decrease

Neutron diffraction and low temperature magnetization study of Tb0.8Y0.2MnO3

International Nuclear Information System (INIS)

Chakraborty, Keka R.; Mukadam, M.; Yusuf, S.M.; Shukla, R.; Tyagi, A.K.; Kaushik, S.D.; Siruguri, V.

2012-01-01

Multiferroic materials possess mutually correlated magnetic and electric order parameters which are suitable for device applications but scarcity of such materials and the separation of magnetic and electric ordering temperatures are a major hindrance in technological applications. TbMnO 3 is one of the material which is reported to have higher magnetoelectric coupling. Structurally, TbMnO 3 crystallizes in orthorhombically distorted perovskite structure (space group Pbnm). For TbMnO 3 , several reports are available in the literature which further modify the magnetoelectric coupling by selective doping or reducing the particle size to nano dimensions, or preparing thin films. Here, we study the effect of Y doping at Tb site in nanoparticle form in terms of crystal structure and magnetic properties. Nanoparticles of Tb 0.8 Y 0.2 MnO 3 were synthesized using the gel combustion technique. Crystal structure of this sample is studied at 300 K using neutron diffraction

Novel room temperature ionic liquid for fluorescence enhancement of Eu3+ and Tb3+

International Nuclear Information System (INIS)

Shyamala Devi, V.; Maji, S.; Viswanathan, K.S.

2011-01-01

The newly prepared ionic liquid, 1-butyl-3-methylimidazolium benzoate, ([bmim][BA]), was found to enhance the fluorescence of Eu 3+ and Tb 3+ . The fluorescence enhancement resulted from a sensitization of the lanthanide fluorescence by the benzoate anion of the ionic liquid, [bmim][BA], and a reduction in the non-radiative channels in the non-aqueous environment provided by the ionic liquid. However, the fluorescence enhancement of the lanthanides in the ionic liquid was limited due to the operation of the inner filter effect, which resulted from the strong absorption of the benzoate. The inner filter effect was minimized by observing the Eu 3+ fluorescence using a front face geometry and also by diluting the lanthanide-[bmim][BA] system, using another ionic liquid, 1-butyl-3-methylimidazolium bis(trifluoromethylsulfonyl)imide ([bmim][Tf 2 N]), as a solvent. In the case of Tb 3+ , the emission from the lanthanide was masked by the strong emission from the ionic liquid in the region 450-580 nm. The long lived Tb 3+ emission was therefore observed using delayed gated detection, where an appropriate delay was used to discriminate against the short lived emission from the ionic liquid. The large fluorescence enhancement due to ligand sensitized fluorescence observed with [bmim][BA] diluted in [bmim][Tf 2 N], leads to nanomolar detection of the lanthanides. This is, to the best of our knowledge, the first report of an ionic liquid being employed for ligand sensitized fluorescence enhancement of lanthanides. - Research highlights: →The use of an ionic liquid to enhance the fluorescence of lanthanides, Eu 3+ and Tb 3+ is discussed in this paper. → This study represents the first report of the use of a tailored ionic liquid for the purposes of fluorescence enhancement. → The fluorescence enhancement is achieved both a process of ligand sensitization, as well as reducing the non-radiative decay channels. → The first point is achieved by the use of an anion capable

Visible luminescence from highly textured Tb{sup 3+} doped RF sputtered zinc oxide films

Energy Technology Data Exchange (ETDEWEB)

Sreedharan, R. Sreeja; Krishnan, R. Reshmi; Bose, R. Jolly; Kavitha, V.S.; Suresh, S. [Department of Optoelectronics, University of Kerala, Thiruvananthapuram 695581, Kerala (India); Vinodkumar, R. [Department of Optoelectronics, University of Kerala, Thiruvananthapuram 695581, Kerala (India); Department of Physics, University College, Thiruvananthapuram, Kerala (India); Sudheer, S.K. [Department of Optoelectronics, University of Kerala, Thiruvananthapuram 695581, Kerala (India); Pillai, V.P. Mahadevan, E-mail: vpmpillai9@gmail.com [Department of Optoelectronics, University of Kerala, Thiruvananthapuram 695581, Kerala (India)

2017-04-15

Highly transparent, luminescent, c-axis oriented Tb{sup 3+} doped ZnO films are prepared by RF magnetron sputtering technique. The structural, morphological, optical and luminescence properties of these films are investigated as a function of Tb{sup 3+} doping concentration by X-ray diffraction (XRD), micro-Raman spectroscopy, atomic force microscopy (AFM), field emission scanning electron microscopy (FESEM), spectroscopic ellipsometry, UV-Visible spectroscopy and photoluminescence spectroscopy. The as-deposited films are found to be highly crystalline with wurtzite hexagonal phase of ZnO. The characteristic features of hexagonal wurtzite structure of ZnO, particularly the appearance of non-polar E{sub 2} modes are easily identified from the Raman spectra of the films. The surface morphology of the films revealed by FESEM and AFM images present a dense distribution of grains. The elemental analysis carried out using energy dispersive X-ray (EDX) spectra confirms the incorporation of Tb{sup 3+} ions in the ZnO lattice. The films are highly transparent in the visible region. Using ellipsometric analysis, the variation of refractive index, dielectric constant and thickness of the films are studied as a function of Tb{sup 3+} doping concentration. The photoluminescence spectra of the Tb{sup 3+} doped ZnO films recorded using an excitation radiation of wavelength 325 nm from a He-Cd laser exhibit visible luminescence ~430, 490, 516 and 542 nm. The origin of visible emissions ~490 and 542 nm in the doped films can be attributed to 5D{sub 4}→7F{sub 6} and 5D{sub 4}→7F{sub 5} transition of Tb{sup 3+} ion respectively. The intensity of the emission at 542 nm is found to be decreasing at higher doping concentration due to concentration quenching effect. The blue emission in the films can be attributed to the electron transition from shallow donor level formed by interstitial Zn atoms to the top of the valence band. The origin of the visible emission ~516 nm is attributed

Magnetic properties of multiferroic TbMnO{sub 3} doped with Al

Energy Technology Data Exchange (ETDEWEB)

Perez, F. [Centro de Ciencias de la Materia Condensada, Universidad Nacional Autonoma de Mexico, Km. 107.5 Carretera Tijuana-Ensenada, Ensenada, B.C. (Mexico); Escudero, R. [Instituto de Investigaciones en Materiales, Universidad Nacional Autonoma de Mexico, A. Postal 70-360, Mexico, D.F. 04510 (Mexico); Heiras, J.

2007-07-01

The synthesis, characterization, and magnetic properties of polycrystalline Tb{sub 1-x}Al{sub x}MnO{sub 3} with x=0.05 and 0.1 is reported. Samples were synthesized by the conventional solid state reaction method producing single phase compounds. Rietveld refinements indicate that Al substitutes Tb in the structure. Samples were highly porous with grain sizes up to {proportional_to}10 {mu}m. The magnetic measurements show a magnetic ordering, starting from antiferromagnetism, for the undoped sample, to a weak ferromagnetic phase coexisting with the antiferromagnetic phase for the two x values. The magnetic ordering is attributed to two different contributions of Mn and Tb sublattices. (copyright 2007 WILEY-VCH Verlag GmbH and Co. KGaA, Weinheim) (orig.)

New fluorophosphate glasses co-doped with Eu{sup 3+} and Tb{sup 3+} as candidates for generating tunable visible light

Energy Technology Data Exchange (ETDEWEB)

Queiroz, T.B. de, E-mail: thiago.branquinho-de-queiroz@uni-bayreuth.de [Physics Institute of São Carlos, University of São Paulo, 13566-590 São Carlos, SP (Brazil); Theoretical Physics IV, University of Bayreuth, 95440 Bayreuth (Germany); Botelho, M.B.S. [Physics Institute of São Carlos, University of São Paulo, 13566-590 São Carlos, SP (Brazil); University of Brasilia, 70910-900 Brasilia, DF (Brazil); Gonçalves, T.S.; Dousti, M. Reza [Physics Institute of São Carlos, University of São Paulo, 13566-590 São Carlos, SP (Brazil); Camargo, A.S.S. de, E-mail: andreasc@ifsc.usp.br [Physics Institute of São Carlos, University of São Paulo, 13566-590 São Carlos, SP (Brazil)

2015-10-25

A series of optically active Eu{sup 3+} and Tb{sup 3+} doped fluorophosphate glasses with compositions (BaF{sub 2}){sub 0.25}(SrF{sub 2}){sub 0.25}(AlF{sub 3}){sub 0.10}[Al(PO{sub 3}){sub 3}]{sub 0.20}(YF{sub 3}){sub 0.20-x}(EuF{sub 3} and/or TbF{sub 3}){sub x} (x = 0 to 0.04) was prepared and characterized by optical spectroscopy. While embedded in the oxyfluoride host, the cited rare earth (RE) ions exhibit improved spectroscopic properties such as longer excited state lifetimes than in oxide glasses and intense emissions in the red ({sup 5}D{sub 0} → {sup 7}F{sub 2}, Eu{sup 3+}), green and blue ({sup 5}D{sub 4} → {sup 7}F{sub 5} and {sup 5}D{sub 3},{sup 5}G{sub 6} → {sup 7}F{sub 5},{sup 7}F{sub 4}, Tb{sup 3+}) spectral regions. Based on this fact, co-doped samples can be designed with appropriate concentrations of these two ions and generate tunable and white light upon excitation with suitable wavelengths, dispensing the need for a third blue emitting RE ion. Four co-doped samples with equal amounts of EuF{sub 3} and TbF{sub 3} and total concentration of 0.3, 0.5, 1.0 and 1.5 mol% were tested. Their CIE chromaticity coordinates were calculated for various excitation wavelengths in the region from 350 to 360 nm allowing tuned emission from blue to red. The long lifetime values of the emitting levels in these co-doped samples (τ ≈ 3.1 ms for Eu{sup 3+5}D{sub 0}, and τ ≈ 4.0 ms for Tb{sup 3+5}D{sub 4}), associated with fairly high quantum yields (Q.Y. = 5–12%) of the samples indicate that these materials could be efficiently pumped by high power LEDs around 355 nm. - Highlights: • Fluorophosphate glasses doped with Eu{sup 3+} and Tb{sup 3+} and excellent optical properties. • Tunable visible emission and white emission in co-doped samples. • Rare earth bonding preference to fluoride rather than phosphate ions.

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

Science.gov (United States)

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

2016-03-01

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

Blue to bluish-green tunable phosphor Sr2LiSiO4F:Ce3+,Tb3+ and efficient energy transfer for near-ultraviolet light-emitting diodes

International Nuclear Information System (INIS)

Xie, Mubiao; Zeng, Lihua; Ye, TingLi; Yang, Xi; Zhu, Xianmei; Peng, Siyun; Lei, Lei

2014-01-01

Ce 3+ and Tb 3+ activated Sr 2 LiSiO 4 F phosphors were prepared by a solid state reaction technique at high temperature, and their ultraviolet (UV)-visible spectroscopic properties were investigated. Under ultraviolet light excitation, Ce 3+ -doped Sr 2 LiSiO 4 F phosphors emit blue light (420 nm), while Tb 3+ -doped phosphors show yellowish green emission. Efficient energy transfer from Ce 3+ to Tb 3+ ions in co-doped samples was confirmed in terms of corresponding excitation and emission spectra. The energy transfer mechanism between Ce 3+ and Tb 3+ was discussed and demonstrated to be dipole–dipole interaction in Sr 2 LiSiO 4 F:Ce 3+ ,Tb 3+ phosphors. Due to energy transfer from Ce 3+ to Tb 3+ , Ce 3+ and Tb 3+ co-doped Sr 2 LiSiO 4 F phosphors show intense absorption in near-UV region, and present tunable emission from blue to bluish green under 360 nm light excitation. The results indicate that these phosphors can be considered as candidates for white LEDs pumped by n-UV chips. (paper)

Faraday rotation and photoluminescence in heavily Tb(3+)-doped GeO2-B2O3-Al2O3-Ga2O3 glasses for fiber-integrated magneto-optics.

Science.gov (United States)

Gao, Guojun; Winterstein-Beckmann, Anja; Surzhenko, Oleksii; Dubs, Carsten; Dellith, Jan; Schmidt, Markus A; Wondraczek, Lothar

2015-03-10

We report on the magneto-optical (MO) properties of heavily Tb(3+)-doped GeO2-B2O3-Al2O3-Ga2O3 glasses towards fiber-integrated paramagnetic MO devices. For a Tb(3+) ion concentration of up to 9.7 × 10(21) cm(-3), the reported glass exhibits an absolute negative Faraday rotation of ~120 rad/T/m at 632.8 nm. The optimum spectral ratio between Verdet constant and light transmittance over the spectral window of 400-1500 nm is found for a Tb(3+) concentration of ~6.5 × 10(21) cm(-3). For this glass, the crystallization stability, expressed as the difference between glass transition temperature and onset temperature of melt crystallization exceeds 100 K, which is a prerequisite for fiber drawing. In addition, a high activation energy of crystallization is achieved at this composition. Optical absorption occurs in the NUV and blue spectral region, accompanied by Tb(3+) photoluminescence. In the heavily doped materials, a UV/blue-to-green photo-conversion gain of ~43% is achieved. The lifetime of photoluminescence is ~2.2 ms at a stimulated emission cross-section σem of ~1.1 × 10(-21) cm(2) for ~ 5.0 × 10(21) cm(-3) Tb(3+). This results in an optical gain parameter σem*τ of ~2.5 × 10(-24) cm(2)s, what could be of interest for implementation of a Tb(3+) fiber laser.

Faraday rotation and photoluminescence in heavily Tb3+-doped GeO2-B2O3-Al2O3-Ga2O3 glasses for fiber-integrated magneto-optics

Science.gov (United States)

Gao, Guojun; Winterstein-Beckmann, Anja; Surzhenko, Oleksii; Dubs, Carsten; Dellith, Jan; Schmidt, Markus A.; Wondraczek, Lothar

2015-01-01

We report on the magneto-optical (MO) properties of heavily Tb3+-doped GeO2-B2O3-Al2O3-Ga2O3 glasses towards fiber-integrated paramagnetic MO devices. For a Tb3+ ion concentration of up to 9.7 × 1021 cm−3, the reported glass exhibits an absolute negative Faraday rotation of ~120 rad/T/m at 632.8 nm. The optimum spectral ratio between Verdet constant and light transmittance over the spectral window of 400–1500 nm is found for a Tb3+ concentration of ~6.5 × 1021 cm−3. For this glass, the crystallization stability, expressed as the difference between glass transition temperature and onset temperature of melt crystallization exceeds 100 K, which is a prerequisite for fiber drawing. In addition, a high activation energy of crystallization is achieved at this composition. Optical absorption occurs in the NUV and blue spectral region, accompanied by Tb3+ photoluminescence. In the heavily doped materials, a UV/blue-to-green photo-conversion gain of ~43% is achieved. The lifetime of photoluminescence is ~2.2 ms at a stimulated emission cross-section σem of ~1.1 × 10−21 cm2 for ~ 5.0 × 1021 cm−3 Tb3+. This results in an optical gain parameter σem*τ of ~2.5 × 10−24 cm2s, what could be of interest for implementation of a Tb3+ fiber laser. PMID:25754819

Synthesis and characterization of pure and Tb/Cu doped Alq3 nanostructures

International Nuclear Information System (INIS)

Salah, Numan; Habib, Sami S.; Khan, Zishan H.; Alharbi, Najlaa D.

2013-01-01

Tris (8-hydroxyquinoline) aluminum (Alq 3 ) is an organic semiconductor molecule, widely used in optoelectronic devices. In this work we report on fabricating different nanostructures of Alq 3 and characterize them using different techniques. Nanostructured films of Alq 3 were grown using the physical vapor condensation and thermal-vapor transport methods. The as synthesized films were characterized by X-ray diffraction, scanning electron microscope, energy dispersive spectroscopy and absorption spectra. Nanoparticles and nanorods/nanowires are observed in the synthesized films. Tb and Cu doped Alq 3 films were also produced and studied for their photoluminescence (PL) properties. When the original powder sample of Alq 3 was excited by 378 nm, one broad PL emission band is observed at around 515 nm. The pure nanoparticles film shows similar band with a drastic increase in the intensity by a factor of 2. This has been attributed to the large specific surface area, which might has increased the absorption and then the quantum yields. The Tb and Cu doped films show also similar band with a slight shift in the peak position to the blue region, but with further enhancement in the peak intensity, particularly that of Cu. The PL intensity of Cu doped sample is around 1.5 times stronger than that of the pure Alq 3 nanoparticles. This remarkable result on obtaining highly luminescent nanomaterial based on Cu doped Alq 3 nanoparticles film might be useful for future organic light emitting diode display devices. -- Highlights: • Films of Alq 3 nanostructures were grown using different methods. • The PL intensity of Alq 3 in its nanostructure form is enhanced by a factor of 2. • This enhancement is attributed to the large specific surface area of the nanostructures. • Films of Alq 3 nanoparticles doped with Tb and Cu showed further PL enhancement. • The Tb and Cu ions could contribute to the PL intensity of the green band of Alq3

Concentration and wavelength dependent frequency downshifting photoluminescence from a Tb3+ doped yttria nano-phosphor: A photochromic phosphor

Science.gov (United States)

Yadav, Ram Sagar; Rai, Shyam Bahadur

2018-03-01

In this article, the Tb3+ doped Y2O3 nano-phosphor has been synthesized through solution combustion method. The structural measurements of the nano-phosphor have been carried out by X-ray diffraction (XRD), scanning electron microscopy (SEM) and transmission electron microscopy (TEM) techniques, which reveal nano-crystalline nature. The Fourier transform infrared (FTIR) measurements reveal the presence of different molecular species in the nano-phosphor. The UV-Vis-NIR absorption spectrum of the nano-phosphor shows large number of bands due to charge transfer band (CTB) and 4f-4f electronic transitions of Tb3+ ion. The Tb3+ doped Y2O3 nano-phosphor emits intense green downshifting photoluminescence centered at 543 nm due to 5D4 → 7F5 transition on excitation with 350 nm. The emission intensity of the nano-phosphor is optimized at 1.0 mol% concentration of Tb3+ ion. When the as-synthesized nano-phosphor is annealed at higher temperature the emission intensity of the nano-phosphor enhances upto 5 times. The enhancement in the emission intensity is due to an increase in crystallinity of the nano-phosphor, reduction in surface defects and optical quenching centers. The CIE diagram reveals that the Tb3+ doped nano-phosphor samples show the photochromic nature (color tunability) with a change in the concentration of Tb3+ ion and excitation wavelength. The lifetime measurement indicates an increase in the lifetime for the annealed sample. Thus, the Tb3+ doped Y2O3 nano-phosphor may be used in photochromic displays and photonic devices.

CD4 cell count recovery in HIV/TB co-infected patients versus TB uninfected HIV patients

Directory of Open Access Journals (Sweden)

Wanchu A

2010-10-01

Full Text Available Background: There is lack of data comparing the improvement in CD4 count following antitubercular (ATT and antiretroviral therapy (ART in patients presenting with Human Immunodeficiency Virus/Tuberculosis (HIV/TB dual infection compared with CD4 matched cohort of TB uninfected HIV patients initiated on ART. We sought to test the hypothesis; TB additionally contributes to reduction in CD4 count in HIV/TB co-infected patients and this would result in greater improvement in count following treatment compared with CD4 matched TB uninfected individuals. Materials and Methods: In a retrospective cohort study design we studied the change in CD4 cell counts in two groups of patients - those with CD4 cell count >100 cells / mm 3 (Group 1 and <100/mm 3 (Group 2 at presentation. In each group the change in CD4 cell count in dually infected patients following six-month ATT and ART was compared to cohorts of CD4 matched TB uninfected patients initiated on ART. Results: In Group 1 (52 patients dually infected subjects′ CD4 count improved from 150 cells/ mm 3 to 345 cells/mm 3 (P=0.001. In the control TB uninfected patients, the change was from 159 cells/mm 3 to 317 cells/mm 3 (P=0.001. Additional improvement in dually infected patients compared to the control group was not statistically significant (P=0.24. In Group 2 (65 patients dually infected subjects count improved from 49 cells/mm3 to 249 cells/mm 3 (P=0.001 where as in control TB uninfected patients improvement was from 50 cells/ mm 3 to 205 cells/mm 3 (P=0.001, there being statistically significant additional improvement in dually infected subjects (P=0.01. Conclusion: Greater increment in CD4 counts with ATT and ART in dually infected patients suggests that TB additionally influences the reduction of CD4 counts in HIV patients.

Narrow spectral emission CaMoO{sub 4}: Eu{sup 3+}, Dy{sup 3+}, Tb{sup 3+} phosphor crystals for white light emitting diodes

Energy Technology Data Exchange (ETDEWEB)

Khanna, A. [Smart Lighting Engineering Research Center, 110, 8th Street, Troy, New York, 12180 (United States); Electrical, Computer and Systems Engineering Department, Rensselaer Polytechnic Institute, 110, 8th Street, Troy, New York, 12180 (United States); Dutta, P.S., E-mail: duttap@rpi.edu [Smart Lighting Engineering Research Center, 110, 8th Street, Troy, New York, 12180 (United States); Electrical, Computer and Systems Engineering Department, Rensselaer Polytechnic Institute, 110, 8th Street, Troy, New York, 12180 (United States)

2013-02-15

Alkaline earth metal molybdates are promising candidates as a host material for high efficiency narrow spectral emission phosphors. These phosphors could potentially be used for the fabrication of phosphor-converted light emitting diodes (pc-LEDs). Phosphor crystals of calcium molybdate doped with rare earth dopant Ln{sup 3+}(Ln=Eu, Dy, Tb) grown using flux growth method have been shown to exhibit higher excitation efficiency than the powders synthesized by solid-state reaction process. Molybdenum (VI) oxide has been found to be a suitable flux for growing large size optically transparent high quality crystals at a temperature around 1100 Degree-Sign C. Using the excitation wavelengths of 465 nm, 454 nm and 489 nm for CaMoO{sub 4}: Eu{sup 3+}, CaMoO{sub 4}: Dy{sup 3+} and CaMoO{sub 4}: Tb{sup 3+}, respectively, intense emission lines at wavelengths of 615 nm, 575 nm and 550 nm were observed. The optimized doping concentrations of 12%, 2% and 5% for Eu{sup 3+}, Dy{sup 3+} and Tb{sup 3+}, respectively, provided the highest luminescence intensity. - Graphical Abstract: CaMoO{sub 4}: Eu{sup 3+} phosphor crystals grown using a molybdenum (VI) oxide flux exhibited around 1.5 times the emission intensity of powders obtained from solid-state reaction at the same synthesis temperature. These crystals were found to efficiently emit 615 nm red light when excited by near UV light up to a wavelength of 395 nm. Highlights: Black-Right-Pointing-Pointer CaMoO{sub 4}: Ln{sup 3+} (Ln=Eu{sup 3+}, Dy{sup 3+}, Tb{sup 3+}) phosphor crystals were successfully grown using high temperature flux (solutions) containing molybdenum (VI) oxide or lithium chloride. Black-Right-Pointing-Pointer Narrow spectral emission at 615 nm, 575 nm and 550 nm, respectively, was observed from CaMoO{sub 4}: Ln{sup 3+} (Ln=Eu{sup 3+}, Dy{sup 3+}, Tb{sup 3+}) phosphor crystals. Black-Right-Pointing-Pointer The optimized doping concentrations of Eu{sup 3+}, Dy{sup 3+}, Tb{sup 3+} in CaMoO{sub 4} for highest

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

Energy Technology Data Exchange (ETDEWEB)

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

2015-10-15

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

Physico-chemical characterization of terbium-161-chloride (161TbCl3) radioisotope from irradiated natural gadolinium oxide target

International Nuclear Information System (INIS)

Azmairit Aziz; Nana Suherman

2015-01-01

Currently cancer patients are increasing every year in Indonesia and become the third leading cause of death after heart disease and high blood pressure. Terbium-161 ( 161 Tb) is a low β- emitter (E β - = 0.155 MeV, T 1/2 = 6.9 d) and very similar to 177 Lu in terms of half-life, E β - energy and chemical properties.However, 161 Tb also ejects internal conversion electrons and Auger electrons which can provide a greater therapeutic effect than 177 Lu. Radioisotope of 161 Tb can be produced as a carrier-free for use in labeling of biomolecules as a targeted radiopharmaceutical for cancer therapy. 161 Tb was obtained through 160 Gd(n,γ) 161 Tb nuclear reaction by thermal neutron bombardment on 100 mg of natural gadolinium oxide target in RSG-G.A. Siwabessy at a thermal neutron flux of ~10 14 n.cm -2 .s -1 and followed by radiochemical separation of 161 Tb from Gd isotopes using extraction chromatography method. The physico-chemical characterization of 161 TbCl 3 solution was studied by determination of its radionuclide purity by means of a γ-rays spectrometry with HP-Ge detector coupled to a multichannel analyzer (MCA). Radiochemical purity was determined using paper chromatography and paper electrophoresis methods. The results showed that 161 TbCl 3 radioisotope has a pH of 2, radiochemical purity of 99.64 ± 0.34%, radionuclide purity of 99.69 ± 0.20%, specific activity and radioactive concentration at the end of irradiation (EOI) of 2.26 – 5.31 Ci/mg and 3.84 – 9.03 mCi/mL, respectively. 161 TbCl 3 solution stable for 3 weeks at room temperature with a radiochemical purity of 98.41 ± 0.42%. 161 TbCl 3 solution from irradiated natural gadolinium oxide target has the physico-chemical characteristic that meets the requirements for use as a precursor in preparation of radiopharmaceuticals. (author)

Highly Efficient Green-Emitting Phosphors Ba2Y5B5O17 with Low Thermal Quenching Due to Fast Energy Transfer from Ce3+ to Tb3.

Science.gov (United States)

Xiao, Yu; Hao, Zhendong; Zhang, Liangliang; Xiao, Wenge; Wu, Dan; Zhang, Xia; Pan, Guo-Hui; Luo, Yongshi; Zhang, Jiahua

2017-04-17

This paper demonstrates a highly thermally stable and efficient green-emitting Ba 2 Y 5 B 5 O 17 :Ce 3+ , Tb 3+ phosphor prepared by high-temperature solid-state reaction. The phosphor exhibits a blue emission band of Ce 3+ and green emission lines of Tb 3+ upon Ce 3+ excitation in the near-UV spectral region. The effect of Ce 3+ to Tb 3+ energy transfer on blue to green emission color tuning and on luminescence thermal stability is studied in the samples codoped with 1% Ce 3+ and various concentrations (0-40%) of Tb 3+ . The green emission of Tb 3+ upon Ce 3+ excitation at 150 °C can keep, on average, 92% of its intensity at room temperature, with the best one showing no intensity decreasing up to 210 °C for 30% Tb 3+ . Meanwhile, Ce 3+ emission intensity only keeps 42% on average at 150 °C. The high thermal stability of the green emission is attributed to suppression of Ce 3+ thermal de-excitation through fast energy transfer to Tb 3+ , which in the green-emitting excited states is highly thermally stable such that no lifetime shortening is observed with raising temperature to 210 °C. The predominant green emission is observed for Tb 3+ concentration of at least 10% due to efficient energy transfer with the transfer efficiency approaching 100% for 40% Tb 3+ . The internal and external quantum yield of the sample with Tb 3+ concentration of 20% can be as high as 76% and 55%, respectively. The green phosphor, thus, shows attractive performance for near-UV-based white-light-emitting diodes applications.

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

Science.gov (United States)

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

2018-02-01

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

A novel KMgPO{sub 4}:Tb{sup 3+}(KMPT) phosphor for radiation dosimetry

Energy Technology Data Exchange (ETDEWEB)

Palan, C.B., E-mail: chetanpalan27@gmail.com [Department of Physics, Sant Gadge Baba Amravati University, Amravati 44602 (India); Bajaj, N.S. [Department of Physics, Toshniwal ACS College, Sengaon, Hingoli 431542 (India); Soni, A. [Radiological Physics and Advisory Division, Bhabha Atomic Research Centre, Mumbai 400094 (India); Omanwar, S.K. [Department of Physics, Sant Gadge Baba Amravati University, Amravati 44602 (India)

2016-08-15

The polycrystalline sample of KMgPO{sub 4}:Tb{sup 3+}(KMPT) phosphor was successfully synthesized by using solid state method. The X-ray powder diffraction, photoluminescence (PL) emission and excitation spectra, thermoluminescence (TL) and optically stimulated luminescence (OSL) were thoroughly measured. The PL spectra of as-prepared KMPT phosphor showed characteristic blue-green emission, when excited by 226 nm under UV excitation. The optimum PL intensity was observed at 0.01 mol concentration of Tb{sup 3+}ions and this phosphor used for remaining studies. The TL glow curve of KMPT phosphor consist two characterized peaks, which were deconvoluted and the kinetic parameters i.e. trap depth or activation energy, order of kinetic and frequency factor determined by using peak shape method. TL sensitivity of KMPT phosphors was found to be 10% than that of TL sensitivity of TLD-500 phosphor. The OSL sensitivity of KMPT was 0.92 times than OSL sensitivity of α-Al{sub 2}O{sub 3}:C phosphor. The OSL decay curve KMPT phosphor consist of three component having photoionization cross sections were found to be 0.26548×10{sup −17}, 0.220×10{sup −17}, 2.92×10{sup −17} cm{sup 2}. The KMPT phosphor showed linear dose response in range 100–6000 mGy and fading of KMPT phosphor was found to be 31% in 15 days. The Minimum detectable dose (MDD) was found to be 0.39 mGy with corresponding 3σ back ground. The phosphor shows good dosimetry properties such as sensitivity, dose response, MDD, Fading.

Preparation and photoluminescence characteristics of In(OH){sub 3}:xTb{sup 3+} obtained by Microwave-Assisted Hydrothermal method

Energy Technology Data Exchange (ETDEWEB)

Motta, F.V., E-mail: fabiana@ct.ufrn.br [DEMAT, CT, UFRN, Av. Sen. Salgado Filho 3000, CEP 59072-970 Natal, RN (Brazil); Marques, A.P.A. [UNIFESP, Rua Prof. Artur Riedel 275, CEP 09972-270 Diadema, SP (Brazil); Li, M.S. [IFSC, USP, Av. Trabalhador São Carlense 400, CEP 13566-590 São Carlos, SP (Brazil); Abreu, M.F.C. [LIEC, DQ, UFSCar, Via Washington Luiz, km 235, CEP 13565-905 São Carlos, SP (Brazil); Paskocimas, C.A.; Bomio, M.R.D. [DEMAT, CT, UFRN, Av. Sen. Salgado Filho 3000, CEP 59072-970 Natal, RN (Brazil); Souza, R.P. [DEP, CT, UFRN, Av. Sen. Salgado Filho 3000, CEP 59072-970 Natal, RN (Brazil); Varela, J.A. [LIEC, IQ, UNESP, Rua Francisco Degni s/n, CEP 14801-907 Araraquara, SP (Brazil); Longo, E. [LIEC, DQ, UFSCar, Via Washington Luiz, km 235, CEP 13565-905 São Carlos, SP (Brazil)

2013-03-15

Highlights: ► We report the preparation by Microwave-Hydrothermal method of In(OH){sub 3}:xTb{sup 3+}. ► Nanostructures were obtained at a low temperature. ► The crystallite size decreased with terbium doping level. ► The nucleation–dissolution–recrystallization mechanism is promoted by processing. ► This material is a highly promising candidate for photoluminescent applications. -- Abstract: Crystalline terbium-doped indium hydroxide structures were prepared by a rapid and efficient Microwave-Assisted Hydrothermal (MAH) method. Nanostructures were obtained at a low temperature. FE-SEM images confirm that these samples are composed of 3D nanostructures. XRD, optical diffuse reflectance and photoluminescence (PL) measurements were used to characterize the products. Emission spectra of terbium-doped indium hydroxide (In(OH){sub 3}:xTb{sup 3+}) samples under excitation (350.7 nm) presented broad band emission referent to the indium hydroxide matrix and {sup 5}D{sub 4} → {sup 7}F{sub 6}, {sup 5}D{sub 4} → {sup 7}F{sub 5}, {sup 5}D{sub 4} → {sup 7}F{sub 4}, and {sup 5}D{sub 4} → {sup 7}F{sub 3} terbium transitions at 495, 550, 590 and 627 nm, respectively. Relative intensities of the Tb{sup 3+} emissions increased as the concentration of this ion increased from 0, 1, 2, 4 and 8 mol%, of Tb{sup 3+}, but the luminescence is drastically quenched for the In(OH){sub 3} matrix.

Synthesis, structural and luminescent aspect of Tb3+ doped Sr2SnO4 phosphor

International Nuclear Information System (INIS)

Taikar, Deepak R.

2016-01-01

A novel green emitting, Tb 3+ doped Sr 2 SnO 4 phosphor was synthesized by the co-precipitation method and its photoluminescence characterization was performed. Sr 2 SnO 4 has an ordered tetragonal K 2 NiF 4 -type structure with space group I4/mmm. The structure of Sr 2 SnO 4 consists of SnO 6 octahedra. From the structure of Sr 2 SnO 4 , it was observed that the sites of Sn 4+ ions have inverse symmetry while the Sr 2+ ions have the low symmetry. X-ray powder diffraction (XRD) analysis confirmed the formation of Sr 2 SnO 4 :Tb 3+ . Photoluminescence measurements showed that the phosphor exhibited bright green emission at about 543 nm attributed to 5 D 4 à 7 F 5 transition of Tb 3+ ion under UV excitation. The emission spectra did not exhibit conventional blue emission peaks of Tb 3+ ions due to 5 D 3 → 7 F J transitions in the spectral region 350-470 nm. The excitation spectra indicate that this compound may be useful as a lamp phosphor. (author)

Structure of molten TbCl sub 3 measured by neutron diffraction

CERN Document Server

Martin, R A; Barnes, A C; Cuello, G J

2002-01-01

The total structure factor of molten TbCl sub 3 at 617 deg. C was measured by using neutron diffraction. The data are in agreement with results from previous experimental work but the use of a diffractometer having an extended reciprocal-space measurement window leads to improved resolution in real space. Significant discrepancies with the results obtained from recent molecular dynamics simulations carried out using a polarizable ion model, in which the interaction potentials were optimized to enhance agreement with previous diffraction data, are thereby highlighted. It is hence shown that there is considerable scope for the development of this model for TbCl sub 3 and for other trivalent metal halide systems spanning a wide range of ion size ratios. (letter to the editor)

Magnetic ordering and spin-reorientation transitions in TbCo3B2

International Nuclear Information System (INIS)

Dubman, Moshe; Caspi, El'ad N.; Ettedgui, Hanania; Keller, Lukas; Melamud, Mordechai; Shaked, Hagai

2005-01-01

The magnetic structure of the compound TbCo 3 B 2 has been studied in the temperature range 1.5 K≤T≤300 K by means of neutron powder diffraction, magnetization, magnetic ac susceptibility, and heat capacity measurements. The compound is of hexagonal symmetry and is paramagnetic at 300 K, undergoes a magnetic Co-Co ordering transition at ∼170 K, and a second magnetic Tb-Tb ordering transition at ∼30 K. The latter induces a spin-reorientation transition, in which the magnetic axis rotates from the c axis toward the basal plane. Below this transition a symmetry decrease (γ magnetostriction) sets in, leading to an orthorhombic distortion of the crystal lattice. The crystal and magnetic structures and interactions and their evolution with temperature are discussed using a microscopic physical model

Luminescence properties of Ce{sup 3+} and Tb{sup 3+} co-activated ZnAl{sub 2}O{sub 4} phosphor

Energy Technology Data Exchange (ETDEWEB)

Tshabalala, K.G. [Department of Physics, University of the Free State, Bloemfontein, ZA 9300 (South Africa); Cho, S.-H.; Park, J.-K. [Nano-Materials Center, Korea Institute of Science and Technology, Cheongryang, Seoul 130-650 (Korea, Republic of); Pitale, Shreyas S.; Nagpure, I.M.; Kroon, R.E.; Swart, H.C. [Department of Physics, University of the Free State, Bloemfontein, ZA 9300 (South Africa); Ntwaeaborwa, O.M., E-mail: ntwaeab@ufs.ac.za [Department of Physics, University of the Free State, Bloemfontein, ZA 9300 (South Africa)

2012-05-15

In this study, a solution combustion method was used to prepare green emitting Ce{sup 3+}-Tb{sup 3+} co-activated ZnAl{sub 2}O{sub 4} phosphor. The samples were annealed at 700 Degree-Sign C in air or hydrogen atmosphere to improve their crystallinity and optical properties. X-ray diffraction study confirmed that both as-prepared and post-preparation annealed samples crystallized in the well known cubic spinel structure of ZnAl{sub 2}O{sub 4}. An agglomeration of irregular platelet-like particles whose surfaces were encrusted with smaller spheroidal particles was confirmed by scanning electron microscopy (SEM). The fluorescence data collected from the annealed samples with different concentrations of Ce{sup 3+} and Tb{sup 3+} show the enhanced green emission at 543 nm associated with {sup 5}D{sub 4}{yields}{sup 7}F{sub 5} transitions of Tb{sup 3+}. The enhancement was attributed to energy transfer from Ce{sup 3+} to Tb{sup 3+}. Possible mechanism of energy transfer via a down conversion process is discussed. Furthermore, cathodoluminescence (CL) intensity degradation of this phosphor was also investigated and the degradation data suggest that the material was chemically stable and the CL intensity was also stable after 10 h of irradiation by a beam of high energy electrons.

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

Energy Technology Data Exchange (ETDEWEB)

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

2009-10-30

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

Magnetic properties of CaCu{sub 5}-type RNi{sub 3}TSi (R=Gd and Tb, T=Mn, Fe, Co and Cu) compounds

Energy Technology Data Exchange (ETDEWEB)

Morozkin, A.V., E-mail: morozkin@tech.chem.msu.ru [Department of Chemistry, Moscow State University, Leninskie Gory, House 1, Building 3, GSP-2, Moscow 119992 (Russian Federation); Knotko, A.V. [Department of Chemistry, Moscow State University, Leninskie Gory, House 1, Building 3, GSP-2, Moscow 119992 (Russian Federation); Yapaskurt, V.O. [Department of Petrology, Geological Faculty, Moscow State University, Leninskie Gory, Moscow 119992 (Russian Federation); Yao, Jinlei [Research Center for Solid State Physics and Materials, School of Mathematics and Physics, Suzhou University of Science and Technology, Suzhou 215009 (China); Yuan, Fang; Mozharivskyj, Y. [Department of Chemistry and Chemical Biology, McMaster University, 1280 Main Street West, Hamilton, Ontario, Canada L8S 4M1 (Canada); Nirmala, R. [Indian Institute of Technology Madras, Chennai 600036 (India); Quezado, S.; Malik, S.K. [Departamento de Física Teórica e Experimental, Universidade Federal do Rio Grande do Norte, Natal 59082-970 (Brazil)

2015-12-15

Magnetic properties and magnetocaloric effect of CaCu{sub 5}-type RNi{sub 3}TSi (R=Gd and Tb, T=Mn, Fe, Co and Cu) compounds have been investigated. Magnetic measurements of RNi{sub 3}TSi display the increasing of Curie temperature and the decreasing of magnetocaloric effect and saturated magnetic moment in the row of ‘RNi{sub 3}CuSi–RNi{sub 3}NiSi–RNi{sub 3}CoSi–RNi{sub 3}MnSi–RNi{sub 3}FeSi’. In contrast to GdNi{sub 3}{Mn, Fe, Co}Si, TbNi{sub 3}{Mn, Fe, Co}Si exhibit significant magnetic hysteresis. The coercive field increases from TbNi{sub 4}Si (~0.5 kOe) to TbNi{sub 3}CoSi (4 kOe), TbNi{sub 3}MnSi (13 kOe) and TbNi{sub 3}FeSi (16 kOe) in field of 50 kOe at 5 K, whereas TbNi{sub 3}CuSi exhibits a negligible coercive field. - Graphical abstract: Magnetic measurements of RNi{sub 3}TSi show the increasing of Curie temperature and the decreasing of magnetocaloric effect and saturated magnetic moment in the row of 'RNi{sub 3}CuSi–RNi{sub 3}NiSi–RNi{sub 3}CoSi–RNi{sub 3}MnSi–RNi{sub 3}FeSi'. In contrast to GdNi{sub 3}{Mn, Fe, Co}Si, TbNi{sub 3}{Mn, Fe, Co}Si exhibit significant magnetic hysteresis. The coercive field increases from TbNi{sub 4}Si (~0.5 kOe) to TbNi{sub 3}CoSi (4 kOe), TbNi{sub 3}MnSi (13 kOe) and TbNi{sub 3}FeSi (16 kOe) in field of 50 kOe at 5 K, whereas TbNi{sub 3}CuSi exhibits a negligible coercive field. - Highlights: • CaCu{sub 5}-type RNi{sub 3}TSi show ferromagnetic ordering (R=Gd, Tb, T=Mn–Co, Cu). • Curie point increases in ‘RNi{sub 3}CuSi–RNi{sub 3}NiSi–RNi{sub 3}CoSi–RNi{sub 3}MnSi–RNi{sub 3}FeSi’ row. • MCE decreases in ‘RNi{sub 3}CuSi–RNi{sub 3}NiSi–RNi{sub 3}CoSi–RNi{sub 3}MnSi–RNi{sub 3}FeSi’ row. • TbNi{sub 3}{Mn, Fe, Co}Si exhibit significant magnetic hysteresis. • The coercive field of TbNi{sub 3}MnSi and TbNi{sub 3}FeSi reach 13 kOe and 16 kOe at 5 K.

Energy transfer from triplet aromatic hydrocarbons to Tb3+ and Eu3+ in aqueous micellar solutions

International Nuclear Information System (INIS)

Almgren, M.; Grieser, F.; Thomas, J.K.

1979-01-01

The sensitization of Tb 3+ and Eu 3+ luminescence by energy transfer from aromatic triplet donors like naphthalene, bromonaphthalene, biphenyl, and phenanthrene in micellar sodium lauryl sulfate solution has been studied. Formal second-order rate constants for the energy transfer process in the micellar solutions were determined as 5 x 10 5 and 1.8 x 10 5 M -1 S -1 for transfer from biphenyl to Tb 3+ . The method of converting these rate constants to second-order constants pertaining to the micellar microenvironment is discussed; it is estimated that the transfer process at the micelles is charaterized by rate constants about one order of magnitude smaller than the formal ones. The transfer process is thus extremely slow. 7 figures

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

Energy Technology Data Exchange (ETDEWEB)

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

2017-04-15

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

Improved performance of P3HT:PCBM solar cells by both anode modification and short-wavelength energy utilization using Tb(aca)3phen

International Nuclear Information System (INIS)

Zhuo Zu-Liang; Wang Yong-Sheng; He Da-Wei; Fu Ming

2014-01-01

The performance of P3HT:PCBM solar cells was improved by anode modification using spin-coated Tb(aca) 3 phen ultrathin films. The modification of the Tb(aca) 3 phen ultrathin film between the indium tin oxide (ITO) anode and the PE-DOT:PSS layer resulted in a maximum power conversion efficiency (PCE) of 2.99% compared to 2.66% for the reference device, which was due to the increase in the short-circuit current density (J sc ). The PCE improvement could be attributed to the short-wavelength energy utilization and the optimized morphology of the active layers. Tb(aca) 3 phen with its strong down-conversion luminescence properties is suitable for the P3HT:PCBM blend active layer, and the absorption region of the ternary blend films is extended into the near ultraviolet region. Furthermore, the crystallization and the surface morphology of P3HT:PCBM films were improved with the Tb(aca) 3 phen ultrathin film. The ultraviolent—visible absorption spectra, atomic force microscope (AFM), and X-ray diffraction (XRD) of the films were investigated. Both anode modification and short-wavelength energy utilization using Tb(aca) 3 phen in P3HT:PCBM solar cells led to about a 12% PCE increase. (interdisciplinary physics and related areas of science and technology)

TB epidemiology: where are the young women? Know your tuberculosis epidemic, know your response.

Science.gov (United States)

Perumal, Rubeshan; Naidoo, Kogieleum; Padayatchi, Nesri

2018-03-27

The global predominance of tuberculosis in men has received significant attention. However, epidemiological studies now demonstrate that there is an increased representation of young women with tuberculosis, especially in high HIV burden settings where young women bear a disproportionate burden of HIV. The role of the HIV epidemic, as well as changes in behavioural, biological, and structural risk factors are explored as potential explanations for the increasing burden of tuberculosis in young women. As young women are particularly vulnerable to HIV infection in sub-Saharan Africa, it is unsurprising that the TB epidemic in this setting has become increasingly feminised. This age-sex trend of TB in South Africa is similar to WHO estimates for other countries with a high HIV prevalence where there are more female than male cases notified up to the age of 25 years. The high prevalence of anaemia of chronic disease in young women with HIV is an additional potential reason for their increased TB risk. The widespread use of injectable medroxyprogesterone acetate contraception, which has been shown to possess selective glucocorticoid effect and oestrogen suppression, in young women may be an important emerging biological risk factor for tuberculosis in young women. Behavioural factors such as alcohol use and tobacco smoking patterns are further factors which may be responsible for the narrowing of the sex gap in TB epidemiology. In comparison to the significantly higher alcohol consumption rates in men globally, there is a narrowing gap in alcohol consumption between the sexes in South Africa with alarming rates of alcohol abuse in young women. There is a similar narrowing of the tobacco smoking gap between the sexes in South Africa, with increasing smoking prevalence in young women. With nearly 70% of all TB patients being co-infected with HIV in our setting, it is not surprising that the age and sex distribution of TB is increasingly resembling the distribution of HIV

CTAB assisted hydrothermal preparation of YPO4:Tb3+ with controlled morphology, structure and enhanced photoluminescence

International Nuclear Information System (INIS)

Lai, Hua; Du, Ying; Zhao, Min; Sun, Kening; Yang, Lei

2014-01-01

Highlights: • A simple and convenient method toward fabrication of YPO 4 :Tb 3+ with controlled structures and morphologies was proposed. • The crucial role of CTAB during the fabrication process that acts as complexing reagent and inducing agent and the mechanism was discussed. • The addition of CTAB enhances the green emission in YPO 4 :Tb phosphors. -- Abstract: In this paper, we report a simple and convenient method toward fabrication of YPO 4 :Tb 3+ with controlled structures, morphologies and enhanced luminescent properties. By simply controlling the amount of the cetyltrimethyl ammonium bromide (CTAB) during the hydrothermal process, tetragonal YPO 4 :Tb 3+ and hexagonal YPO 4 ·0.8H 2 O:Tb 3+ with nanoparticle and olive-like nanoparticle can be obtained, respectively. Meanwhile, we find that the structures and morphologies can affect their luminescent properties obviously and the intensity of the samples with hexagonal phase is evidently higher than that with tetragonal phase. The variation of crystal structures, morphologies of the samples are ascribed to the crucial role of CTAB during the fabrication process that acts as complexing reagent and inducing agent and the mechanism was also discussed. We believe the method reported here will open a novel approach to rare earth phosphates with multiple structures

Is TB Testing Associated With Increased Blood Interferon-Gamma Levels?

Directory of Open Access Journals (Sweden)

Aideen E. Kennedy

2017-10-01

Full Text Available The Republic of Ireland reports a relatively low prevalence of Johne’s disease (JD compared to international counterparts. Postulated reasons for this include a lower average herd size and a grass-based production system. Ireland also engages in high levels of bovine tuberculosis (bTB testing. As interferon-gamma (IFN-γ is believed to play a key role in protecting against JD, it is our hypothesis that administration of purified protein derivative (PPD, as part of the bTB test, is associated with a systemic increase in IFN-γ production, which may potentially limit clinical progression of the disease. We studied 265 cows (202 Friesian and 63 “Non-Friesian,” e.g., JerseyX, Norwegian Red to assess IFN-γ levels and Mycobacterium avium subspecies paratuberculosis (MAP antibody response before and after the bTB test. As part of the compulsory annual bTB test, avian and bovine PPD were administered at two separate cervical sites. To assess IFN-γ production, blood samples were taken before and 72 h after PPD administration. MAP antibody response was assessed before and 10 days post-PPD administration. A significant increase in MAP antibody response was identified post-bTB compared to pre-bTB response (p < 0.001. Additionally, IFN-γ production significantly increased at the post-bTB time point (p < 0.001 compared to the pre-bTB test readings. This may indicate a beneficial effect of bTB testing in controlling JD.

Treatment Outcomes of Patients with Multidrug-Resistant Tuberculosis (MDR- TB) Compared with Non-MDR-TB Infections in Peninsular Malaysia.

Science.gov (United States)

Elmi, Omar Salad; Hasan, Habsah; Abdullah, Sarimah; Mat Jeab, Mat Zuki; Ba, Zilfalil; Naing, Nyi Nyi

2016-07-01

Treating patients with multidrug-resistant tuberculosis (MDR-TB) strains is more complicated, complex, toxic, expensive, than treating patients with susceptible TB strains. This study aims to compare the treatment outcomes and potential factors associated between patients with MDR-TB and non MDR TB infections in peninsular Malaysia. This study was a retrospective cohort study. Data were collected from the medical records of all registered MDR-TB patients and Non-MDR-TB patients at five TB hospitals in peninsular Malaysia from January 2010 to January 2014. A total of 314 subjects were studied, including 105 MDR-TB cases and 209 non-MDR-TB. After TB treatment, 24.8% of the MDR-TB patients and 17.7% of non MDR TB relapsed; 17.1% of the MDR-TB patients and 16.3% of non MDR TB defaulted from TB treatment. A significant difference seen in treatment success rate 17.1% for MDR-TB; 63.1% for non MDR TB (P history of TB treatment, and presence of HIV infection.