Molecular structures of supported metal oxide catalysts under different environments

被引:333
作者
Bañares, MA
Wachs, IE
机构
[1] CSIC, Inst Catalisis & Petroleoquim, E-28049 Madrid, Spain
[2] Lehigh Univ, Zettlemoyer Ctr Surface Studies, Bethlehem, PA 18015 USA
[3] Lehigh Univ, Dept Chem Engn, Bethlehem, PA 18015 USA
关键词
D O I
10.1002/jrs.866
中图分类号
O433 [光谱学];
学科分类号
0703 ; 070302 ;
摘要
The use of in situ Raman spectroscopy to study the molecular structures of supported metal oxide catalysts under different environments is reviewed. The molecular structures under ambient (hydrated) and dehydrated conditions are presented. The effect of moisture at elevated temperatures is also presented and discussed with regard to its implications for catalytic phenomena. The molecular structural transformations during C-2-C-4 lower alkane (LPG) oxidation, methane oxidation, methanol oxidation and selective catalytic reduction of NO with NH3 reaction conditions are presented. In situ spectroscopy during catalytic reaction with simultaneous activity/selectivity measurement ('operando' spectroscopy) is emphasized owing to its contribution to the fundamental understanding of catalytic performance. The reducibility of the different surface metal oxide species, the relevance of surface coverage (surface monomeric vs polymeric species) and the specific oxide support are discussed when LPG, methane, methanol or hydrogen is the reducing agent. In situ Raman spectroscopy provides molecular-level information about the surface metal oxide species: structures, stability and transformations under different environments. In many cases, the use of complementary spectroscopic techniques results in a more complete understanding of the molecular structure - activity/selectivity relationships for supported metal oxide catalysts. Copyright (C) 2002 John Wiley Sons, Ltd.
引用
收藏
页码:359 / 380
页数:22
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