发光
化学
水溶液
液氮
分析化学(期刊)
氮气
发射光谱
光谱学
荧光
离子
谱线
物理化学
材料科学
光学
物理
量子力学
有机化学
光电子学
色谱法
天文
作者
Akira Kirishima,Takaumi Kimura,Ryuji Nagaishi,Osamu Tochiyama
出处
期刊:Radiochimica Acta
[Oldenbourg Wissenschaftsverlag]
日期:2004-11-01
卷期号:92 (9-11): 705-710
被引量:31
标识
DOI:10.1524/ract.92.9.705.54971
摘要
Summary The luminescence spectra of U 4+ in aqueous solutions were observed in the UV-VIS region at ambient and liquid nitrogen temperatures. The excitation spectrum indicates that the luminescence is arising from the deexcitation of a 5 f electron at the 1 S 0 level and no other emissions of U 4+ in aqueous solutions were detected for other f – f transitions. All the luminescence peaks were assigned to the transitions from 1 S 0 to lower 5 f levels. To estimate the luminescence lifetime, luminescence decay curves were measured using time-resolved laser-induced fluorescence spectroscopy. At room temperature, the decay curve indicated that the lifetime was shorter than 20 ns. On the other hand, the frozen sample of U 4+ in aqueous solution at liquid nitrogen temperature showed the same emission spectrum as at room temperature and its lifetime was 149 ns in H 2 O system and 198 ns in D 2 O system. The longer lifetime at liquid nitrogen temperature made it possible to measure the spectrum of U 4+ at the concentration as low as 10 -6 M. The difference in the anion species (ClO 4 - , Cl - , SO 4 2- ) affected the structure of the emission spectrum to some extent.
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