Sustainedly High‐Rate Electroreduction of CO2 to Multi‐Carbon Products on Nickel Oxygenate/Copper Interfacial Catalysts

Author:

Mao Xuejiao123,Chang Chun‐Wai4,Li Zhiguo123,Han Zishan123,Gao Jiachen123,Lyons Mason4,Sterbinsky George5,Guo Yong123,Zhang Bo123,Wang Yaogang123,Wang Xinyu123,Han Daliang123,Yang Quan‐Hong123,Feng Zhenxing4,Weng Zhe123

Affiliation:

1. Nanoyang Group, Tianjin Key Laboratory of Advanced Carbon and Electrochemical Energy Storage, School of Chemical Engineering and Technology, and Collaborative Innovation Center of Chemical Science and Engineering (Tianjin) Tianjin University Tianjin 300072 China

2. National Industry‐Education Integration Platform of Energy Storage Tianjin University Tianjin 300072 China

3. Haihe Laboratory of Sustainable Chemical Transformations Tianjin 300192 China

4. School of Chemical, Biological, and Environmental Engineering Oregon State University Corvallis OR 97331 USA

5. Advanced Photon Source Argonne National Laboratory Argonne IL 60439 USA

Abstract

AbstractCopper (Cu) is the most attractive electrocatalyst for CO2 reduction to multi‐carbon (C2+) products with high economic value in considerable amounts. However, the rational design of a structurally stable Cu‐based catalyst that can achieve high activity and stability towards C2+ products remain a grand challenge. Here, a highly stable nickel oxygenate/Cu electrocatalyst is developed with abundant NiOOH/Cu interfaces by in situ electrochemical reconstruction. The nickel oxygenate/Cu electrocatalyst achieves a superior Faradaic efficiency of 86.3 ± 3.0% and a record partial current density of 2085 A g−1 for C2+ products with long‐term stability. In situ experimental and theoretical studies demonstrates that the exceptional performance in generating C2+ products is attributed to the presence of the NiOOH/Cu interfaces which increase *CO coverage, lower energy barrier for *CO coupling and stabilize *OCCO simultaneously. This work provides new insights into the rational design of electrocatalysts to achieve stable and efficient electrocatalytic CO2 reduction capabilities.

Funder

National Natural Science Foundation of China

National Key Research and Development Program of China

Fundamental Research Funds for the Central Universities

Publisher

Wiley

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