High resolution 1s core hole X-ray spectroscopy in 3d transition metal complexes - electronic and structural information

被引:792
|
作者
Glatzel, P
Bergmann, U
机构
[1] Stanford Synchrotron Radiat Lab, Stanford, CA 94309 USA
[2] Univ Utrecht, Dept Inorgan Chem & Catalysis, Debye Inst, NL-3584 CA Utrecht, Netherlands
基金
美国国家卫生研究院;
关键词
X-ray fluorescence; X-ray absorption; resonant inelastic X-ray scattering; 3d transition metal; multiplet theory; electronic structured; chemical bonding;
D O I
10.1016/j.ccr.2004.04.011
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
The creation of a 1s core hole in a 3d transition metal ion gives rise to an emission spectrum that can be recorded using a crystal analyzer. K shell X-ray spectroscopy using an analyser energy bandwidth of similar to 1eV is sensitive to electron-electron interactions and orbital splittings and preserves the advantages of the hard X-ray probe. We review recent developments in Kalpha and Kbeta spectroscopy and show how the chemical sensitivity of the fluorescence lines can be exploited for selective X-ray absorption studies. When the photo excitation energy is tuned close to the K edge threshold, the phenomenon known as X-ray resonant Raman or resonant inelastic X-ray scattering (RIXS) occurs. RIXS spectroscopy on 3d transition metals at the 1s resonances with lowest incident energies (K pre-edge) is a very recent technique. We discuss basic aspects and demonstrate with several examples its potential as a future routine spectroscopic tool. (C) 2004 Elsevier B.V. All rights reserved.
引用
收藏
页码:65 / 95
页数:31
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