1s2p resonant inelastic X-ray scattering of iron oxides

被引:105
|
作者
de Groot, FMF
Glatzel, P
Bergmann, U
van Aken, PA
Barrea, RA
Klemme, S
Hävecker, M
Knop-Gericke, A
Heijboer, WM
Weckhuysen, BM
机构
[1] Univ Utrecht, Debye Inst, Dept Inorgan Chem & Catalysis, NL-3584 CA Utrecht, Netherlands
[2] European Synchrotron Radiat Facil, F-38043 Grenoble, France
[3] Stanford Synchrotron Radiat Lab, Menlo Pk, CA 94025 USA
[4] Tech Univ Darmstadt, Inst Angew Geowissensch, D-64287 Darmstadt, Germany
[5] Argonne Natl Lab, Adv Photon Source, Argonne, IL 60439 USA
[6] Heidelberg Univ, Inst Mineral, D-69120 Heidelberg, Germany
[7] Max Planck Gesell, Fritz Haber Inst, D-14195 Berlin, Germany
来源
JOURNAL OF PHYSICAL CHEMISTRY B | 2005年 / 109卷 / 44期
关键词
D O I
10.1021/jp054006s
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
1s2p resonant inelastic X-ray scattering (RTXS) spectroscopy has been measured for a series of iron oxides, including octahedral and tetrahedral Fe-II and Fe-III systems. Their spectral shapes have been analyzed and explained using crystal-field multiplet simulations. The RIXS planes and the K-edge and L-edge X-ray absorption spectra related to these RIXS planes will be discussed with respect to their analytical opportunities. It is concluded that the full power and possibilities of 1s2p RIXS needs an overall resolution of 0.3 eV. This will yield a technique with more detailed information than K-edge and L-edge X-ray absorption combined, obtained in a single experiment. Another major advantage is that 1s2p RIXS involves only hard X-rays, and experiments under essentially any condition and on any system are feasible.
引用
收藏
页码:20751 / 20762
页数:12
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