Luminescence and decay behaviors of Tb-doped yttrium silicate

2001 ◽  
Vol 16 (3) ◽  
pp. 881-889 ◽  
Author(s):  
Yoon Young Choi ◽  
Kee-Sun Sohn ◽  
Hee Dong Park ◽  
Se Young Choi
Keyword(s):  
Energy Transfer ◽  
Charge Transfer Band ◽  
Diffuse Reflectance Spectrum ◽  
Cross Relaxation ◽  
Rate Equations ◽  
Excitation Spectra ◽  
Multipolar Interaction ◽  
Broad Absorption Band ◽  
Direct Quenching ◽  
Yttrium Silicate

The photoluminescence of terbium-activated yttrium silicate with the general formula Y2−XTbxSiO5 was investigated as a function of Tb3+ concentration. Especially, the main attention was focused on the 5D3 fluorescence and its energy transfer behavior. The emission and excitation spectra were measured in terms of Tb3+ concentration. The diffuse reflectance spectrum was also measured in the range from VUV to UV. As a result, yttrium silicate was found to have a broad absorption band extended from the VUV to UV range. The concentration quenching was investigated in terms of luminance and decay time both for 5D3 and 5D4 fluorescence. The energy transfer was also investigated by analyzing the decay curve of 5D3 emission on the basis of the multipolar interaction. The decay curves of 5D3 emission, for which well-known cross-relaxation has been accepted as a main factor, were analyzed by Inokuti and Hirayama's formula on the basis of the direct quenching scheme. Furthermore, the rate equations including a newly proposed quenching scheme were taken into consideration. The rate equations accept the emission quenching as due to the cross-relaxation from 5D3 or 4 to some upper levels such as 7D and the charge-transfer band.

Yb3+ to Er3+ energy transfer and rate-equations formalism in the eye safe laser material Yb:Er:Ca2Al2SiO7

1996 ◽  
Vol 6 (4) ◽  
pp. 267-274 ◽  
Author(s):  
B. Simondi-Teisseire ◽  
B. Viana ◽  
D. Vivien ◽  
A.M. Lejus
Keyword(s):  
Energy Transfer ◽  
Rate Equations ◽  
Laser Material

scholarly journals Процессы передачи энергии в эвлитите Sr-=SUB=-3-=/SUB=-Y(PO-=SUB=-4-=/SUB=-)-=SUB=-3-=/SUB=-, по отдельности и одновременно легированном ионами Tb-=SUP=-3+-=/SUP=- и Tm-=SUP=-3+-=/SUP=-

2022 ◽  
Vol 130 (1) ◽  
pp. 99
Author(s):  
Xiaowu Hu ◽  
Fabio Piccinelli ◽  
Marco Bettinelli
Keyword(s):  
Energy Transfer ◽  
Optical Spectroscopy ◽  
Emission Spectra ◽  
Cross Relaxation ◽  
Transfer Efficiency ◽  
Relaxation Processes ◽  
Donor Concentration ◽  
Acceptor Concentration ◽  
Transfer Processes ◽  
Double Phosphate

In this work the optical spectroscopy and the energy transfer processes involving the Tb3+and Tm3+ ions, have been studied in eulytite double phosphate hosts of the type Sr3Y(PO4)3 doped with various amounts of the two Ln ions. It has been found that several energy transfer and cross-relaxation processes are active in this class of materials, upon excitation in the 5D4 level of Tb, and in the 1G4 one of Tm. In particular, a Tb→Tm transfer of excitation has been found to quench strongly the 5D4 level of Tb. This process occurs with a transfer efficiency increasing from 0.08 to 0.62, for a donor concentration of 2 mol%, and an acceptor concentration increasing from 2 to 15 mol%. The emission spectra are strongly affected by the presence of Tb⟷Tm energy transfer, and Tm→Tm cross relaxation processes.

scholarly journals Synthesis and Luminescent Properties of Eu3+/Tb3+ Rare Earth Ions Doped Li2SrSiO4 Phosphors

2018 ◽  
Vol 1 (1) ◽  
Author(s):  
Kaitao Yu ◽  
Lifang Wei ◽  
Jiaqi Shen
Keyword(s):  
Charge Transfer ◽  
Charge Transfer Band ◽  
Emission Spectra ◽  
Luminescent Properties ◽  
Rare Earth Ions ◽  
Luminescent Materials ◽  
Excitation Spectra ◽  
Solid State Method ◽  
X Ray ◽  
Uv Visible

The series of luminescent materials of Eu3 +, Tb3 + doped Li2SrSiO4 were synthesized by a high-temperature solid-state method. The phase purity of the samples was measured by X-ray powder diffraction (XRD). The luminescent properties of the samples were studied by UV-visible excitation spectra and emission spectra The It is found that the strong absorption of Eu3 + doped Li2-xSr1-xEuxSiO4 is from the 250 ~ 290 nm charge transfer band of Eu3 + and the 7F0 → 5L6 absorption transition of 393 nm. The strongest emission of the emission spectra at 393 nm is 614 nm and 701 nm, respectively, from the 5D0 → 7F2 and 5D0 → 7F4 transitions of Eu3 +. Tb3 + doped sample Li2-xSr1-xTb xSiO4 excitation spectrum is mainly composed of Tb3 + ion fd transition and charge transfer band composed of broadband, the strongest absorption at 269 nm, the emission of the main emission of 5D4 → 7F5 transition (542 nm).

VUV-Photoluminescence Properties of (Gd, La)2O2CO3: Eu3+

2014 ◽  
Vol 1052 ◽  
pp. 203-206
Author(s):  
Zhi Long Wang ◽  
Shi Qin Wang ◽  
Nin Yao ◽  
Xing Min Wei
Keyword(s):  
Charge Transfer ◽  
Vacuum Ultraviolet ◽  
Charge Transfer Band ◽  
Broad Band ◽  
Photoluminescence Properties ◽  
Flux Method ◽  
Excitation Spectra ◽  
Red Emission ◽  
Ultraviolet Excitation

(Gd,La)2-x O2CO3:Eux3+(0.01 ≤x≤0.04) were synthesized via a flux method at 400°C, and their photoluminescence properties under vacuum ultraviolet (VUV) excitation were examined. The excitation spectra showed two bands in the region from 125 nm to 300 nm, the first band centered at 190 nm was ascribed to absorption of related CO32- complex, and the second broad band centered at 246nm and 278nm in Gd2O2CO3:Eu3+ was ascribed to the charge transfer band of O2-→ Eu3+. Series samples exhibited red emission at around 611 nm under vacuum ultraviolet excitation corresponding to the 5D0→ 7F2.transition of Eu3+.

Changes of Excitation Spectra of in vivo Chlorophyll Fluorescence during Induction of Photosynthesis

1993 ◽  
Vol 48 (1-2) ◽  
pp. 46-51 ◽  
Author(s):  
Wieslaw I. Gruszecki ◽  
Zbigniew Krupa
Keyword(s):  
Energy Transfer ◽  
Chlorophyll Fluorescence ◽  
Quantum Yield ◽  
Dark Adaptation ◽  
Fluorescence Quantum Yield ◽  
Excitation Energy Transfer ◽  
Reaction Centers ◽  
Excitation Spectra ◽  
In Vivo Chlorophyll Fluorescence

Excitation spectra of chlorophyll fluorescence from intact rye leaves were registered at different steps of the induction of photosynthesis after dark adaptation. Analysis of these spectra indicates that at least two processes related to spectroscopic features are responsible for a fluorescence quenching. The first one, active during the first 100 s of illumination, was interpreted to consists in an overall decrease of the fluorescence quantum yield of antenna pigments and chlorophylls, in particular close to the reaction centers. The second type of a fluorescence decrease (between 100 s and 300 s of illumination) was found to be in large extent related to decrease of the rate of an excitation energy transfer between accessory xanthophyll pigments and chlorophylls emitting fluorescence. This latter molecular mechanism is discussed as being related to violaxanthin availability to de-epoxidation in the xanthophyll cycle.

Cross-relaxation energy transfer between the Er3+ ions in vitreous arsenic chalcogenide

2019 ◽  
Vol 33 (28) ◽  
pp. 1950348
Author(s):  
S. Q. Asadullayeva ◽  
Q. Y. Eyyubov
Keyword(s):  
Energy Transfer ◽  
Relaxation Process ◽  
Luminescence Intensity ◽  
Near Infrared ◽  
Cross Relaxation ◽  
Relaxation Energy ◽  
Infrared Luminescence ◽  
Cross Relaxation Process ◽  
The Cross ◽  
Activator Ions

In this paper, we study widely investigated photoluminescent properties of [Formula: see text] compounds in the near-infrared ranges. The increase of the infrared luminescence intensity with increasing [Formula: see text] concentration can be attributed to the cross-relaxation process between the activator ions.

scholarly journals PYRENE EMISSION FROM MONOLAYERS "CLICKED" ONTO QUARTZ

2013 ◽  
Vol 01 (01) ◽  
pp. 1250007
Author(s):  
HONGYAN SONG ◽  
SERGEY GORELIK ◽  
JONATHAN HOBLEY ◽  
JIEXUN LI ◽  
AÏCHA BOUDHAR ◽  
...  
Keyword(s):  
Photoelectron Spectroscopy ◽  
Surface Coverage ◽  
Charge Transfer Band ◽  
Photophysical Properties ◽  
High Surface ◽  
Excimer Emission ◽  
Excitation Spectra ◽  
Visible Absorption ◽  
Molecular Monolayers ◽  
A Charge

A series of quartz surfaces were modified with a series of crosslinkers and functional groups in order to obtain an azide-terminated monolayer, which was then used to immobilize pyrene onto the surface via alkyne-azide "click" chemistry. During the course of the immobilization, different ratios of tert-butyl diphenyl chlorosilane were used to control the distribution and hence the photophysical properties of the pyrene on the surface. The preparative surface reactions and photophysical properties were investigated with contact angle, X-ray photoelectron spectroscopy, UV-visible absorption and emission spectroscopy. High surface coverage was achieved of just under 1molecule per nm2. At this coverage all emission from the pyrene was in the form of excimer emission. Excimer emission dominated at all surface coverages greater than 0.45 molecules per nm2. Below this coverage the monomer emission could also be observed. The conclusions that can be drawn are important for understanding the interactions of neighboring molecules in molecular monolayers. Our results suggest that at high surface coverage a substantial number of the pyrene molecules are already close enough to their neighbors that pairs of them can be directly excited to form excimer with no requirement for diffusion. This can be stated because the long wavelength end of the pyrene absorption and excitation spectra show a broad tail that is assigned to a charge transfer band resulting from an electron being directly transferred from a ground state pyrene to a neighboring pyrene molecule. Furthermore, absorption spectra shifts also indicate that the pyrene molecules undergo some interactions on the surface when they are closely packed.

Study on UV Excitation Properties of Y2O3:Ln3+ (Ln = Eu3+ or Tb3+) Luminescent Nanomaterials

2008 ◽  
Vol 8 (3) ◽  
pp. 1443-1448 ◽  
Author(s):  
Qingyu Meng ◽  
Baojiu Chen ◽  
Xiaoxia Zhao ◽  
Xiaojun Wang ◽  
Wu Xu
Keyword(s):  
Particle Size ◽  
Charge Transfer ◽  
Charge Transfer Band ◽  
Emission Spectra ◽  
X Ray Diffraction ◽  
Bulk Materials ◽  
Excitation Spectra ◽  
X Ray ◽  
Long Wavelength ◽  
Uv Excitation

Y2O3:Ln3+ (Ln = Eu or Tb) nanocrystals with different Ln3+ doping concentrations and average sizes were prepared by chemical self-combustion. The corresponding bulk materials with various doping concentrations were obtained by annealing the nanomaterials at high temperature. The emission spectra, excitation spectra, and X-ray diffraction spectra were used in this study. It was found that the charge transfer band of Y2O3:Eu3+ red-shifted as particle size decreased, and the charge transfer band in the 5-nm particles obviously broadened toward the long wavelength. It was also found that the profile of excitation spectra corresponding to the 4f5d (4f8 → 4f75d1) transition changed a lot with the variation of the particle size. The dependence of the excitation spectra of Y2O3:Ln3+ on particle size was investigated.

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