铟
催化作用
氧化物
乙炔
烯烃
化学
选择性
氧气
光化学
多相催化
化学物理
材料科学
无机化学
有机化学
作者
Davide Albani,Marçal Capdevila‐Cortada,Gianvito Vilé,Sharon Mitchell,Oliver Martin,Núria López,Javier Pérez‐Ramírez
标识
DOI:10.1002/anie.201704999
摘要
Indium oxide catalyzes acetylene hydrogenation with high selectivity to ethylene (>85 %); even with a large excess of the alkene. In situ characterization reveals the formation of oxygen vacancies under reaction conditions, while an in depth theoretical analysis links the surface reduction with the creation of well-defined vacancies and surrounding In3 O5 ensembles, which are considered responsible for this outstanding catalytic function. This behavior, which differs from that of other common reducible oxides, originates from the presence of four crystallographically inequivalent oxygen sites in the indium oxide surface. These resulting ensembles are 1) stable against deactivation, 2) homogeneously and densely distributed, and 3) spatially isolated and confined against transport; thereby broadening the scope of oxides in hydrogenation catalysis.
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