Robust and Corrosion‐Resistant Overall Water Splitting Electrode Enabled by Additive Manufacturing

Author:

Guo Binbin12,Lin Jie3,Mo Funian4,Ding Yihong3,Zeng Tianbiao3,Liang Haowen1,Wang Liping1,Chen Xiaoteng1,Mo Jiewen1,Li Dong‐sheng5,Yang Hui Ying2ORCID,Bai Jiaming1

Affiliation:

1. Shenzhen Key Laboratory for Additive Manufacturing of High‐performance Materials Department of Mechanical and Energy Engineering Southern University of Science and Technology Shenzhen 518055 P. R. China

2. Pillar of Engineering Product Development Singapore University of Technology and Design 8 Somapah Road Singapore 487372 Singapore

3. Key Laboratory of Carbon Materials of Zhejiang Province Wenzhou Key Lab of Advanced Energy Storage and Conversion Zhejiang Province Key Lab of Leather Engineering College of Chemistry and Materials Engineering Wenzhou University Wenzhou Zhejiang 325035 P. R. China

4. Shenzhen Key Laboratory of Flexible Printed Electronics Technology Center Harbin Institute of Technology Shenzhen 518055 P. R. China

5. College of Materials and Chemical Engineering Key Laboratory of Inorganic Nonmetallic Crystalline and Energy Conversion Materials China Three Gorges University Yichang 443002 P. R. China

Abstract

AbstractElectrolysis of water has emerged as a prominent area of research in recent years. As a promising catalyst support, copper foam is widely investigated for electrolytic water, yet the insufficient mechanical strength and corrosion resistance render it less suitable for harsh working conditions. To exploit high‐performance catalyst supports, various metal supports are comprehensively evaluated, and Ti6Al4V (Ti64) support exhibited outstanding compression and corrosion resistance. With this in mind, a 3D porous Ti64 catalyst support is fabricated using the selective laser sintering (SLM) 3D printing technology, and a conductive layer of nickel (Ni) is coated to increase the electrical conductivity and facilitate the deposition of catalysts. Subsequently, Co0.8Ni0.2(CO3)0.5(OH)·0.11H2O (CoNiCH) nanoneedles are deposited. The resulting porous Ti64/Ni/CoNiCH electrode displayed an impressive performance in the oxygen evolution reaction (OER) and reached 30 mA cm−2 at an overpotential of only 200 mV. Remarkably, even after being compressed at 15.04 MPa, no obvious structural deformation is observed, and the attenuation of its catalytic efficiency is negligible. Based on the computational analysis, the CoNiCH catalyst demonstrated superior catalytic activity at the Ni site in comparison to the Co site. Furthermore, the electrode reached 30 mA cm−2 at 1.75 V in full water splitting conditions and showed no significant performance degradation even after 60 h of continuous operation. This study presents an innovative approach to robust and corrosion‐resistant catalyst design.

Funder

National Key Research and Development Program of China

National Natural Science Foundation of China

Science, Technology and Innovation Commission of Shenzhen Municipality

Higher Education Discipline Innovation Project

Publisher

Wiley

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