Modulating Pt‐N/O Bonds on Co‐doped WO3 for Acid Electrocatalytic Hydrogen Evolution with Over 2000 h Operation

Author:

Chen Hengyi1,Yu Jidong1,Liu Lijia2,Gao Rui‐Ting1,Gao Zehua1,Yang Yang3,Chen Zhiqiang4,Zhan Sibo5,Liu Xianhu6,Zhang Xueyuan7,Dong Hongliang4,Wu Limin18,Wang Lei1ORCID

Affiliation:

1. College of Chemistry and Chemical Engineering College of Energy Material and Chemistry Inner Mongolia University Hohhot 010021 China

2. Department of Chemistry Western University 1151 Richmond Street London Ontario N6A5B7 Canada

3. NanoScience Technology Center Department of Materials Science and Engineering Department of Chemistry Renewable Energy and Chemical Transformation Cluster The Stephen W. Hawking Center for Microgravity Research and Education University of Central Florida Orlando FL 32826 USA

4. Center for High Pressure Science and Technology Advanced Research Shanghai 201203 China

5. Analysis Center of Agrobiology and Environmental Sciences Faculty of Agriculture Life and Environment Sciences Zhejiang University Hangzhou 310058 China

6. State Key Laboratory of Structural Analysis Optimization and CAE Software for Industrial Equipment National Engineering Research Center for Advanced Polymer Processing Technology Zhengzhou University Wenhua Road 97‐1 Zhengzhou 450002 China

7. School of Materials Science and Engineering China University of Petroleum (East China) Qingdao 266580 China

8. Department of Materials Science and State Key Laboratory of Molecular Engineering of Polymers Fudan University Shanghai 200433 China

Abstract

AbstractDeveloping durable electrocatalysts with high performance for hydrogen evolution reaction (HER) in acid conditions is of prime challenge for hydrogen production. Durability is of important prerequisite for catalyst application. Herein, this work constructs the Co‐doped WO3 loaded with Pt nanoparticles under ammonia treatment (Pt/N‐CoWO3) with the Pt‐N/O‐W interaction, which shows excellent activity and stability for acidic hydrogen production at industrial current density. The electronic structure of Pt species is modulated with enhanced Pt‐N/O bonding by Co doping, hence reinforcing the metal‐support interaction, and greatly enhancing the stability of the catalyst under high current density in acidic media. The resultant Pt/N‐CoWO3 catalyst exhibits the overpotentials of only 94 and 108 mV at high current densities of 1 and 2 A cm−2, respectively. More impressively, Pt/N‐CoWO3 delivers a record operation for acid electrocatalytic hydrogen evolution over 2000 h at 1 A cm−2, denoting its potential for catalyst applications at the industrial current density. This work opens a new avenue for developing Pt‐loading acidic HER catalysts for long‐term operation at ampere‐level current densities in acid conditions.

Funder

National Science and Technology Major Project

Publisher

Wiley

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