催化作用
纳米棒
化学
选择性
铜
空位缺陷
活化能
吸附
化学工程
反应机理
氧化还原
无机化学
材料科学
纳米技术
物理化学
结晶学
有机化学
工程类
作者
Lei Xue,Chunjuan Zhang,Jinfang Wu,Qiyuan Fan,Yang Liu,Yanxin Wu,Jiaxin Li,Heng Zhang,Fenrong Liu,Shanghong Zeng
标识
DOI:10.1016/j.apcatb.2021.120951
摘要
The determination of reaction mechanism for electrocatalytic CO2 reduction by experiments is still out of reach on copper catalyst, which limits its advance towards industrial implementation. Here, the Cu/CeO2 catalyst as paradigm was studied to validate the reaction intermediates and pathway. The Cu/CeO2 catalysts with different morphologies were synthesized, and it is discovered that the nanorod Cu/CeO2 catalyst exhibits high selectivity for CO2-to-CH4 with the highest turnover frequency for CH4 production among the samples. Detailed study indicates that the nanorod Cu/CeO2 possesses the largest electrochemically active surface area, higher proportion of O-vacancy sites, and better capability of CO2 adsorption and activation. The chemical nature above together contributes to its high activity. Theoretical calculations reveal that the doping of Cu into CeO2 can significantly lower the reaction energy barrier of *CO2 →*COOH and change the reaction pathway from *CHOH →*CH2OH to *CHOH →*CH, effectively improving the catalytic performance for CO2 electroreduction.
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