Water Gas Shift Reaction Catalyzed by Rhodium-Manganese Oxide Cluster Anions

被引:7
作者
Chen, Jiao-Jiao [1 ,2 ]
Li, Xiao-Na [1 ,2 ]
Liu, Qing-Yu [1 ,2 ]
Wei, Gong-Ping [1 ,2 ,3 ]
Yang, Yuan [1 ,2 ,3 ]
Li, Zi-Yu [1 ,2 ]
He, Sheng-Gui [1 ,2 ,3 ]
机构
[1] Chinese Acad Sci, Inst Chem, State Key Lab Struct Chem Unstable & Stable Speci, Beijing 100190, Peoples R China
[2] CAS Res Educ Ctr Excellence Mol Sci, Beijing Natl Lab Mol Sci, Beijing 100190, Peoples R China
[3] Univ Chinese Acad Sci, Beijing 100049, Peoples R China
基金
中国博士后科学基金; 中国国家自然科学基金;
关键词
HYDROGEN-ATOM TRANSFER; CO OXIDATION; TEMPERATURE; GOLD; SIZE; MOLYBDENUM; MECHANISMS; INTERFACE; EVOLUTION; INSIGHTS;
D O I
10.1021/acs.jpclett.1c02267
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
Fundamental understanding of the nature of active sites in real-life water gas shift (WGS) catalysts that can convert CO and H2O into CO2 and H-2 is crucial to engineer related catalysts performing under ambient conditions. Herein, we identified that the WGS reaction can be, in principle, catalyzed by rhodium-manganese oxide clusters Rh2MnO1,2- in the gas phase at room temperature. This is the first example of the construction of such a potential catalysis in cluster science because it is challenging to discover clusters that can abstract the oxygen from H2O and then supply the anchored oxygen to oxidize CO. The WGS reaction was characterized by mass spectrometry, photoelectron spectroscopy, and quantum-chemical calculations. The coordinated oxygen in Rh2MnO1,2- is paramount for the generation of an electron-rich Mn+-Rh- bond that is critical to capture and reduce H2O and giving rise to a polarized Rh+-Rh- bond that functions as the real redox center to drive the WGS reaction.
引用
收藏
页码:8513 / 8520
页数:8
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