| Literature DB >> 33319448 |
Wenfu Xie1, Hao Li2, Guoqing Cui1, Jianbo Li1, Yuke Song1, Shijin Li1, Xin Zhang1, Jin Yong Lee2, Mingfei Shao1, Min Wei1.
Abstract
The development of efficient electrocatalysts for the CO2 reduction reaction (CO2 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 CO2 RR to formate. The NiSn atomic pair consists of adjacent Ni and Sn, each coordinated with four nitrogen atoms (N4 -Ni-Sn-N4 ). The as-prepared NiSn-APC displays exceptional activity for the CO2 RR to formate with a turnover frequency of 4752 h-1 , a formate productivity of 36.7 mol h-1 gSn -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.Entities:
Keywords: carbon dioxide fixation; electrochemistry; heterogeneous catalysis; reduction; structure elucidation
Year: 2021 PMID: 33319448 DOI: 10.1002/anie.202014655
Source DB: PubMed Journal: Angew Chem Int Ed Engl ISSN: 1433-7851 Impact factor: 15.336