In Situ Fast Construction of Ni3S4/FeS Catalysts on 3D Foam Structure Achieving Stable Large‐Current‐Density Water Oxidation

Author:

Tan Pingping123,Wu Yuanke4,Tan Yangyang1,Xiang Yang1,Zhou Liyuan1,Han Ning3,Jiang Yinzhu25,Bao Shu‐Juan1,Zhang Xuan23ORCID

Affiliation:

1. School of Materials and Energy Southwest University Chongqing 400715 P. R. China

2. ZJU‐Hangzhou Global Scientific and Technological Innovation Centre Zhejiang University Hangzhou 311200 P. R. China

3. Department of Materials Engineering KU Leuven Kasteelpark Arenberg 44, bus 2450 Heverlee B‐3001 Belgium

4. State Key Laboratory of Materials Processing and Die and Mould Technology School of Materials Science and Engineering Huazhong University of Science and Technology Wuhan 430074 P. R. China

5. School of Materials Science and Engineering Zhejiang University Hangzhou 310027 P. R. China

Abstract

AbstractBy increasing the content of Ni3+, the catalytic activity of nickel‐based catalysts for the oxygen evolution reaction (OER), which is still problematic with current synthesis routes, can be increased. Herein, a Ni3+‐rich of Ni3S4/FeS on FeNi Foam (Ni3S4/FeS@FNF) via anodic electrodeposition to direct obtain high valence metal ions for OER catalyst is presented. XPS showed that the introduction of Fe not only further increased the Ni3+ concentration in Ni3S4/FeS to 95.02%, but also inhibited the dissolution of NiOOH by up to seven times. Furthermore, the OER kinetics is enhanced by the combination of the inner Ni3S4/FeS heterostructures and the electrochemically induced surface layers of oxides/hydroxides. Ni3S4/FeS@FNF shows the most excellent OER activity with a low Tafel slope of 11.2 mV dec−1 and overpotentials of 196 and 445 mV at current densities of 10 and 1400 mA cm−2, respectively. Furthermore, the Ni3S4/FeS@FNF catalyst can be operated stably at 1500 mA cm−2 for 200 h without significant performance degradation. In conclusion, this work has significantly increased the high activity Ni3+ content in nickel‐based OER electrocatalysts through an anodic electrodeposition strategy. The preparation process is time‐saving and mature, which is expected to be applied in large‐scale industrialization.

Funder

National Natural Science Foundation of China

Publisher

Wiley

Subject

Biomaterials,Biotechnology,General Materials Science,General Chemistry

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