Enhancement of Catalytic Activity via Inevitable Reconstruction of the Ni–Mo Interface for Alkaline Hydrogen Oxidation

Author:

Song Xiaoyun1,Yang Qimei1,Chen Zebi1,Zou Kaisheng1,Xie Zhenyang1,Ding Wei1ORCID,Wei Zidong1ORCID

Affiliation:

1. State Key Laboratory of Advanced Chemical Power Sources (SKL‐ACPS) School of Chemistry and Chemical Engineering Center of Advanced Electrochemical Energy (CAEE) Institute of Advanced Interdisciplinary Studies Chongqing University Chongqing 400044 China

Abstract

AbstractThe inevitable oxidation of nickel‐metal‐based catalysts exposed to the air will lead to instability and poor reproducibility of a catalytic interface, which is usually ignored and greatly hinders their application for the catalysis of alkaline hydrogen oxidation. The details on the formation of a world‐class nickel‐based HOR catalyst Ni3‐MoOx/C‐500 are reported via an interfacial reconstruction triggered by passive oxidation upon air exposure. Interfacial reconstruction, initiated with various Ni–Mo metal ratios and annealing temperature, can fine‐tune the Ni–Mo interface with an increased work function and a reduced d‐band center. The optimized Ni3‐MoOx/C exhibits a record high mass activity of 102.8 mA mgNi−1, a top‐level exchange current density of 76.5 µA cmNi−2, and exceptional resistance to CO poisoning at 1000 ppm CO for hours. The catalyzed alkaline exchange membrane fuel cell exhibits a maximum power output of 600 mW cm−2 and excellent stability, ranking it as one of the most active non‐precious metals HOR catalysts to date.

Funder

Key Technologies Research and Development Program

National Natural Science Foundation of China

Natural Science Foundation of Chongqing Municipality

Publisher

Wiley

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