Hard X-ray photon-in-photon-out spectroscopy with lifetime resolution - of XAS, XES, RIXSS and HERFD

被引:0
作者
Glatzel, P. [1 ]
Sikora, M. [1 ]
Eeckhout, S. G. [1 ]
Safonova, O. V. [1 ]
Smolentsev, G. [2 ]
Pirngruber, G. [3 ]
van Bokhoven, J. A. [3 ]
Grunwaldt, J. -D. [3 ]
Tromp, M. [4 ]
机构
[1] European Synchrotron Radiat Facil, BP 22,6 Rue Jules Horowitz, F-38043 Grenoble, France
[2] Rostov State Univ, Fac Phys, Rostov Na Donu, Russia
[3] Swiss Fed Inst Technol, Inst Chem & Bioengn, CH-8093 Zurich, Switzerland
[4] Univ Southampton, Sch Chem, Southampton S017 1BJ, Hants, England
来源
SYNCHROTRON RADIATION INSTRUMENTATION, PTS 1 AND 2 | 2007年 / 879卷
关键词
emission spectroscopy; coordination chemistry; electronic structure; EXAFS;
D O I
暂无
中图分类号
TH7 [仪器、仪表];
学科分类号
0804 ; 080401 ; 081102 ;
摘要
Spectroscopic techniques that aim to resolve the electronic configuration and local coordination of a central atom by detecting inner-shell radiative decays following photoexcitation using hard X-rays are presented. The experimental setup requires an X-ray spectrometer based on perfect crystal Bragg optics. The possibilities arising from non-resonant (X-Ray Emission Spectroscopy - XES) and resonant excitation (Resonant Inelastic X-Ray Scattering Spectroscopy - RIXSS, High-Energy-Resolution Fluorescence Detected (HERFD) XAS) are discussed when the instrumental energy broadenings of the primary (beamline) monochromator and the crystal spectrometer for x-ray emission detection are on the order of the core hole lifetimes of the intermediate and final electronic states. The small energy bandwidth in the emission detection yields line-sharpened absorption features. In transition metal compounds, electron-electron interactions as well as orbital splittings and fractional population can be revealed. Combination with EXAFS spectroscopy enables to extent the k-range beyond unwanted absorption edges in the sample that limit the EXAFS range in conventional absorption spectroscopy.
引用
收藏
页码:1731 / +
页数:2
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