Constructing Asymmetric Charge Polarized NiCo Prussian Blue Analogue for Promoted Electrocatalytic Methanol to Formate Conversion

Author:

Lin Yunxiang1,Wang Yan‐ge1,Li Xiaoyu1,Zhao Jiahui1,Liu Hengjie2,Wu Chuanqiang1,Yang Li13,Li Guang1,Qi Zeming2,Shan Lei1,Jiang Yong45,Song Li26ORCID

Affiliation:

1. Institutes of Physical Science and Information Technology School of Materials Science and Engineering Leibniz International Joint Research Center of Materials Sciences of Anhui Province Center of High Magnetic Fields and Free Electron Lasers Information Meterials and Intelligent Sensing Laboratory of Anhui Province Anhui University Hefei 230601 China

2. National Synchrotron Radiation Laboratory University of Science and Technology of China Hefei 230029 China

3. Helmholtz‐Zentrum Dresden‐Rossendorf Bautzner Landstrasse 400 01328 Dresden Germany

4. School of Materials Science and Engineering University of Science and Technology Beijing Beijing 100083 China

5. School of Electronic and Information Engineering Tiangong University Tianjin 300387 China

6. Zhejiang Institute of Photonelectronics Jinhua Zhejiang 321004 China

Abstract

AbstractThe highly selective electrochemical conversion of methanol to formate is of great significance for various clean energy devices, but understanding the structure‐to‐property relationship remains unclear. Here, the asymmetric charge polarized NiCo prussian blue analogue (NiCo PBA‐100) is reported to exhibit remarkable catalytic performance with high current density (210 mA cm−2 @1.65 V vs RHE) and Faraday efficiency (over 90%). Meanwhile, the hybrid water splitting and Zinc–methanol‐battery assembled by NiCo PBA‐100 display the promoted performance with decent stability. X‐ray absorption spectroscopy (XAS) and operando Raman spectroscopy indicate that the asymmetric charge polarization in NiCo PBA leads to more unoccupied states of Ni and occupied states of Co, thereby facilitating the rapid transformation of the high‐active catalytic centers. Density functional theory calculations combining operando Fourier transform infrared spectroscopy demonstrate that the final reconstructed catalyst derived by NiCo PBA‐100 exhibits rearranged d band properties along with a lowered energy barrier of the rate‐determining step and favors the desired formate production.

Funder

National Key Research and Development Program of China

National Natural Science Foundation of China

Fundamental Research Funds for the Central Universities

Natural Science Foundation of Anhui Province

Publisher

Wiley

Subject

Biomaterials,Biotechnology,General Materials Science,General Chemistry

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