催化作用
选择性
氧气
空位缺陷
金属
化学
氧化物
纳米颗粒
化学工程
纳米技术
化学物理
光化学
材料科学
结晶学
有机化学
工程类
作者
Juan Li,Lin Zhang,Xingda An,Kai Feng,Xuchun Wang,Jiari He,Yang Huang,Jingjing Liu,Liang Zhang,Binhang Yan,Chaoran Li,Chaoran Li,Le He
出处
期刊:Angewandte Chemie
[Wiley]
日期:2024-05-14
卷期号:63 (31): e202407025-e202407025
被引量:53
标识
DOI:10.1002/anie.202407025
摘要
Abstract The adsorbate‐mediated strong metal‐support interaction (A‐SMSI) offers a reversible means of altering the selectivity of supported metal catalysts, thereby providing a powerful tool for facile modulation of catalytic performance. However, the fundamental understanding of A‐SMSI remains inadequate and methods for tuning A‐SMSI are still in their nascent stages, impeding its stabilization under reaction conditions. Here, we report that the initial concentration of oxygen vacancy in oxide supports plays a key role in tuning the A‐SMSI between Ru nanoparticles and defected titania (TiO 2‐x ). Based on this new understanding, we demonstrate the in situ formation of A‐SMSI under reaction conditions, obviating the typically required CO 2 ‐rich pretreatment. The as‐formed A‐SMSI layer exhibits remarkable stability at various temperatures, enabling excellent activity, selectivity and long‐term stability in catalyzing the reverse water gas‐shift reaction. This study deepens the understanding of the A‐SMSI and the ability to stabilize A‐SMSI under reaction conditions represents a key step for practical catalytic applications.
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