首页> 外文期刊>Journal of Molecular Structure >Optical spectroscopy of chromium doped deuterated (CH3)(2)NH2Al(SO4)(2)center dot 6H(2)O crystals
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Optical spectroscopy of chromium doped deuterated (CH3)(2)NH2Al(SO4)(2)center dot 6H(2)O crystals

机译:铬掺杂的氘(CH3)(2)NH2Al(SO4)(2)中心点6H(2)O晶体的光谱学

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摘要

Chromium doped, deuterated dimethylammonium aluminium sulfate hexahydrate (DDMAAS) crystals were investigated. The measurements of the photoluminescence spectra of these crystals at temperatures above and below its order-disorder phase transition (T-c(D) = 155.5 K) are reported. The temperature dependencies of the luminescence decay curves in a wide temperature range (from 5 to 190 K) were investigated. Results were compared with the data reported for dimethylammonium aluminium sulfate hexahydrate (DMAAS) crystal [1]. The lifetimes of the excited state at 5 K for DMAAS (the sample without deuterium), DDMAAS(1) and DDMAAS(2) were 30, 98 and 408 mus, respectively. Deuteration degree of the crystals were estimated from the FT-IR spectra and it amounted to 62 and 86% in DDMAAS(1) and DDMAAS(2), respectively. The dependence of the luminescence lifetimes on the degree of deuteration is non-linear. Based on these results the conclusions have been made on the influence of deuterium on the luminescence lifetime and its position in the crystal. The elongation of the luminescence lifetimes has been observed caused by the substitution of H atoms by D atoms, The shifting of the internal vibration energy to smaller values was noticed according to increase of deuterium concentration. The activation energy (E-a) was found as 2155 cm(-1). (C) 2000 Elsevier Science B.V. All rights reserved. [References: 10]
机译:研究了铬掺杂的氘代二甲基硫酸铝六水合物(DDMAAS)晶体。报道了在高于和低于其有序-无序相变(T-c(D)= 155.5 K)的温度下这些晶体的光致发光光谱的测量结果。研究了在宽温度范围(5至190 K)下发光衰减曲线的温度依赖性。将结果与报道的六水合二甲基硫酸铝铵(DMAAS)晶体的数据进行比较[1]。 DMAAS(不含氘的样品),DDMAAS(1)和DDMAAS(2)在5 K的激发态下的寿命分别为30、98和408 mus。从FT-IR光谱估计晶体的氘化程度,在DDMAAS(1)和DDMAAS(2)中分别达到62%和86%。发光寿命对氘化程度的依赖性是非线性的。基于这些结果,得出了氘对发光寿命及其在晶体中位置的影响的结论。观察到由于H原子被D原子取代而导致的发光寿命的延长。随着氘浓度的增加,内部振动能量向较小的值移动。发现活化能(E-a)为2155 cm(-1)。 (C)2000 Elsevier Science B.V.保留所有权利。 [参考:10]

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