Electron Redistribution of Ru Site on MoO2@NiMoO4 Support for Efficient Ampere‐Level Current Density Electrolysis of Alkaline Seawater

Author:

Wang Lin12,Chen Yue2,Liu Yingnan2,Dai Qizhou3,Chen Zhengfei1,Yang Xiaoxuan2,Luo Yansong4,Li Zhongjian2,Yang Bin2,Zheng Menglian4,Lei Lecheng2,Hou Yang1256ORCID

Affiliation:

1. School of Biological and Chemical Engineering NingboTech University Ningbo 315100 China

2. Key Laboratory of Biomass Chemical Engineering of Ministry of Education College of Chemical and Biological Engineering Zhejiang University Hangzhou 310027 China

3. Institute of Environmental Biology and Catalysis College of Environment Zhejiang University of Technology Hangzhou 310014 China

4. Institute of Thermal Science and Power Systems School of Energy Engineering Zhejiang University Hangzhou 310027 China

5. Donghai Laboratory Zhoushan 316021 China

6. Institute of Zhejiang University‐Quzhou Quzhou 324000 China

Abstract

AbstractSeawater electrolysis is a promising but challenging strategy to generate carbon‐neutral hydrogen. A grand challenge for hydrogen evolution reaction (HER) from alkaline seawater electrolysis is the development of efficient and stable electrocatalysts to overcome the limitation of sluggish kinetics. Here, a 3D nanorod hybrid catalyst is reported, which comprises heterostructure MoO2@NiMoO4 supported Ru nanoparticles (Ru/ MoO2@NiMoO4) with a size of ≈5 nm. Benefitting from the effect of strongly coupled interaction, Ru/MoO2@NiMoO4 catalyst exhibits a remarkable alkaline seawater hydrogen evolution performance, featured by a low overpotential of 184 mV at a current density of 1.0 A cm−2, superior to commercial Pt/C (338 mV). Experimental observations demonstrate that the heterostructure MoO2@NiMoO4 as an electron‐accepting support makes the electron transfer from the Ru nanoparticles to MoO2, and thereby implements the electron redistribution of Ru site. Mechanistic analysis elucidates that the electron redistribution of active Ru site enhances the ability of hydrogen desorption, thereby promoting alkaline seawater HER kinetics and finally leading to a satisfactory catalysis performance at ampere‐level current density of alkaline seawater electrolysis.

Funder

National Natural Science Foundation of China

Fundamental Research Funds for the Central Universities

Publisher

Wiley

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