Enhanced Metal‐Support Interactions Boost the Electrocatalytic Water Splitting of Supported Ruthenium Nanoparticles on a Ni3N/NiO Heterojunction at Industrial Current Density

Author:

Liu Rui1,Sun Mingzi2,Liu Xiangjian1,Lv Zunhang1,Yu Xinyu1,Wang Jinming1,Liu Yarong1,Li Liuhua1,Feng Xiao1,Yang Wenxiu1,Huang Bolong2,Wang Bo1ORCID

Affiliation:

1. Key Laboratory of Cluster Science Ministry of Education Beijing Key Laboratory of Photoelectronic/Electrophotonic Conversion Materials Advanced Technology Research Institute (Jinan) Advanced Research Institute of Multidisciplinary Science School of Chemistry and Chemical Engineering Beijing Institute of Technology No. 5, South Street, Zhongguancun, Haidian District Beijing 100081 China

2. Department of Applied Biology and Chemical Technology The Hong Kong Polytechnic University Hung Hom, Kowloon Hong Kong SAR China

Abstract

AbstractDeveloping highly efficient and stable hydrogen production catalysts for electrochemical water splitting (EWS) at industrial current densities remains a great challenge. Herein, we proposed a heterostructure‐induced‐strategy to optimize the metal‐support interaction (MSI) and the EWS activity of Ru‐Ni3N/NiO. Density functional theory (DFT) calculations firstly predicted that the Ni3N/NiO‐heterostructures can improve the structural stability, electronic distributions, and orbital coupling of Ru‐Ni3N/NiO compared to Ru‐Ni3N and Ru‐NiO, which accordingly decreases energy barriers and increases the electroactivity for EWS. As a proof‐of‐concept, the Ru‐Ni3N/NiO catalyst with a 2D Ni3N/NiO‐heterostructures nanosheet array, uniformly dispersed Ru nanoparticles, and strong MSI, was successfully constructed in the experiment, which exhibited excellent HER and OER activity with overpotentials of 190 mV and 385 mV at 1000 mA cm−2, respectively. Furthermore, the Ru‐Ni3N/NiO‐based EWS device can realize an industrial current density (1000 mA cm−2) at 1.74 V and 1.80 V under alkaline pure water and seawater conditions, respectively. Additionally, it also achieves a high durability of 1000 h (@ 500 mA cm−2) in alkaline pure water.

Funder

National Key Research and Development Program of China

National Natural Science Foundation of China

Publisher

Wiley

Subject

General Chemistry,Catalysis

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