NiSn Atomic Pair on an Integrated Electrode for Synergistic Electrocatalytic CO2 Reduction

被引:212
作者
Xie, Wenfu [1 ]
Li, Hao [2 ]
Cui, Guoqing [1 ]
Li, Jianbo [1 ]
Song, Yuke [1 ]
Li, Shijin [1 ]
Zhang, Xin [1 ]
Lee, Jin Yong [2 ]
Shao, Mingfei [1 ]
Wei, Min [1 ]
机构
[1] Beijing Univ Chem Technol, State Key Lab Chem Resource Engn, Beijing 100029, Peoples R China
[2] Sungkyunkwan Univ, Dept Chem, Suwon 16419, South Korea
基金
中国国家自然科学基金; 北京市自然科学基金;
关键词
electrochemistry; carbon dioxide fixation; heterogeneous catalysis; reduction; structure elucidation; SELECTIVE ELECTROCHEMICAL REDUCTION; CARBON-DIOXIDE; ACTIVE-SITES; ELECTROREDUCTION; CATALYSTS;
D O I
10.1002/anie.202014655
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The development of efficient electrocatalysts for the CO2 reduction reaction (CO2RR) remains a challenge. Demonstrated here is a NiSn atomic-pair electrocatalyst (NiSn-APC) on a hierarchical integrated electrode, which exhibits a synergistic effect in simultaneously promoting the activity and selectivity of the CO2RR to formate. The NiSn atomic pair consists of adjacent Ni and Sn, each coordinated with four nitrogen atoms (N-4-Ni-Sn-N-4). The as-prepared NiSn-APC displays exceptional activity for the CO2RR to formate with a turnover frequency of 4752 h(-1), a formate productivity of 36.7 mol h(-1) g(Sn)(-1) and an utilization degree of active sites (57.9 %), which are superior to previously reported single-atomic catalysts. Both experimental data and density-functional theory calculations verify the electron redistribution of Sn imposed by adjacent Ni, which reduces the energy barrier of the *OCHO intermediate and makes this potential-determining step thermodynamically spontaneous. This synergistic catalysis provides a successful paradigm for rational design and preparation of atomic-pair electrocatalysts with enhanced performance.
引用
收藏
页码:7382 / 7388
页数:7
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