铜
催化作用
锰
一氧化碳
Atom(片上系统)
金属
氧化还原
过渡金属
化学
氧气
氧气储存
无机化学
有机化学
计算机科学
生物化学
嵌入式系统
作者
Mingzhu Jiang,Jing Chen,Yanxia Gao,Xuelong Lv,Dongxu Yan,Hongpeng Jia
标识
DOI:10.1002/chem.202100442
摘要
Abstract The interaction between Cu and Mn has been used to immobilize the Cu single‐atom on MnO 2 surface by redox‐driven hydrolysis. Comprehensive structure and property characterizations demonstrate that the existence of an Cu−Mn interaction on the catalyst surface can effectively restrain the aggregation of Cu single atoms and improve carbon monoxide (CO) oxidation activity. The interaction of forming the Cu−O−Mn entity is beneficial for CO catalytic activity as the migration of reactive oxygen species and the coordination effect of active centers accelerate the reaction. In particular, 3%‐Cu 1 /MnO 2 shows an oxygen storage capacity (OSC) value (342.75 μmol/g) more than ten times that of pure MnO 2 (27.79 μmol/g) and has high CO catalytic activity ( T 90% =80 °C), it can maintain CO conversion of 95 % after 15 cycles. This work offers a reliable method for synthesizing Cu single‐atom catalysts and deepens understanding of the interaction effect between single transition metal atoms and supports that can improve the catalytic activity of CO oxidation.
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