Chinese Journal of Catalysis ›› 2026, Vol. 89: 246-257.DOI: 10.1016/S1872-2067(26)65180-7

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High entropy engineering promoted active sites in layered double hydroxide for seawater oxygen evolution reaction

Peiran Chen,1, Luo Cheng,1, Congbao Guo, Yu He, Yangyang Liu, Yi Wang*(), Shuqin Song*()   

  1. The Key Laboratory of Low-carbon Chemistry & Energy Conservation of Guangdong Province, PCFM Laboratory, School of Materials Science and Engineering, School of Chemical Engineering and Technology, Sun Yat-sen University, Guangzhou 510275, Guangdong, China
  • Received:2026-04-01 Accepted:2026-05-07 Online:2026-10-18 Published:2026-09-01
  • Contact: *E-mail:wangyi76@mail.sysu.edu.cn(Y. Wang),stsssq@mail.sysu.edu.cn(S. Song).
  • About author:

    1 Contributed equally to this work.

  • Supported by:
    National Natural Science Foundation of China(22478450);National Natural Science Foundation of China(22478451);National Natural Science Foundation of China(22408408);National State Key Laboratory of Catalysis(2024SKL-A-013);Energy Revolution S&T Program of Yulin Innovation Institute of Clean Energy(E511030817);Guangdong Basic and Applied Basic Research Foundation(2021A1515010167);Guangdong Basic and Applied Basic Research Foundation(2022A1515011196);Guangzhou Key R&D Program/Plan Unveiled Flagship Project(20220602JBGS02);Guangzhou Basic and Applied Basic Research Project(202201011449);100 Talent Research Foundation of Sun Yat-sen University(76110-12230029)

Abstract:

Efficient oxygen-evolving electrodes that can operate under high-current-density alkaline water/seawater electrolysis are essential for practical hydrogen production, yet the simultaneous achievement of high activity, chloride tolerance, and long-term durability remains difficult for non-precious-metal catalysts. In this work, a binder-free high-entropy layered double hydroxide electrode has been successfully constructed by directly growing multimetal LDH nanosheets on nickel foam through a facile one-step hydrothermal process. The optimized quinary LDH, composed of five non-noble transition metals, namely Fe, Ni, Co, Zn, and Cr, is denoted as CoNiFeZnCr LDH@NF. Benefiting from the high-entropy multimetal coordination environment, this electrode exhibits superior OER performance compared with the corresponding binary, ternary, and quaternary LDH counterparts. In alkaline seawater, CoNiFeZnCr LDH@NF requires a low OER overpotential of 250 mV to reach 100 mA cm-2 and shows a Tafel slope of 66.93 mV dec-1. The electrode also maintains stable operation for 200 h at 100 mA cm-2, indicating strong resistance to seawater-induced degradation. Density functional theory calculations further reveal that the quinary high-entropy configuration optimizes the adsorption behavior of *O intermediates and lowers the energy barrier of the rate-determining OER step. The improved activity and durability are therefore attributed to the synergistic electronic and structural effects arising from the incorporation of Fe, Ni, Co, Zn, and Cr into the LDH framework. This study demonstrates a practical high-entropy engineering strategy for developing robust non-precious-metal OER electrodes toward seawater-relevant hydrogen production.

Key words: Layered double hydroxide, High entropy engineering, Seawater oxygen evolution reaction, Alkaline seawater electrolysis, Non-precious-metal catalyst