电催化剂
格式化
催化作用
化学
密度泛函理论
电极
无机化学
物理化学
电化学
计算化学
有机化学
作者
Wenfu Xie,Hao Li,Guoqing Cui,Jianbo Li,Yuke Song,Shijin Li,Xin Zhang,Jin Yong Lee,Mingfei Shao,Min Wei
标识
DOI:10.1002/ange.202014655
摘要
Abstract The development of efficient electrocatalysts for the CO 2 reduction reaction (CO 2 RR) 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 CO 2 RR 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 CO 2 RR 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.
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