High-Energy-Resolution X-ray Absorption Spectroscopy for Identification of Reactive Surface Species on Supported Single-Site Iridium Catalysts

被引:36
|
作者
Hoffman, Adam S. [1 ,2 ]
Sokaras, Dimosthenis [2 ]
Zhang, Shengjie [3 ]
Debefve, Louise M. [1 ]
Fang, Chia-Yu [1 ,4 ]
Gallo, Alessandro [5 ,6 ]
Kroll, Thomas [2 ]
Dixon, David A. [3 ]
Bare, Simon R. [2 ]
Gates, Bruce C. [1 ]
机构
[1] Univ Calif Davis, Dept Chem Engn, Davis, CA 95616 USA
[2] SLAC Natl Accelerator Lab, Stanford Synchrotron Radiat Lightsource, Menlo Pk, CA 94025 USA
[3] Univ Alabama, Dept Chem, Box 870336, Tuscaloosa, AL 35487 USA
[4] Univ Calif Davis, Dept Mat Sci & Engn, Davis, CA 95616 USA
[5] Stanford Univ, Dept Chem Engn, Stanford, CA 94305 USA
[6] SLAC Natl Accelerator Lab, SUNCAT Ctr Interface Sci & Catalysis, Menlo Pk, CA 94025 USA
关键词
high-energy-resolution fluorescence detection; iridium; XANES; X-ray absorption spectroscopy; zeolites; XANES; FLUORESCENCE; ADSORPTION; REDUCTION; SPECTRA; ATOMS; PROBE; CO;
D O I
10.1002/chem.201701459
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
We report high-energy-resolution X-ray absorption spectroscopy detection of ethylene and CO ligands adsorbed on catalytically active iridium centers isolated on zeolite HY and on MgO supports. The data are supported by density functional theory and FEFF X-ray absorption near-edge modelling, together with infrared (IR) spectra. The results demonstrate that high-energy-resolution X-ray absorption spectra near the iridium L-III (2p(3/2)) edge provide clearly ascribable, distinctive signatures of the ethylene and CO ligands and illustrate effects of supports and other ligands. This X-ray absorption technique is markedly more sensitive than conventional IR spectroscopy for characterizing surface intermediates, and it is applicable to samples having low metal loadings and in reactive atmospheres and is expected to have an increasing role in catalysis research by facilitating the determination of mechanisms of solid-catalyzed reactions through identification of reaction intermediates in working catalysts.
引用
收藏
页码:14760 / 14768
页数:9
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