Tang Xiaolan, Yang Na, Li Zixiao, Cai Zhengwei, Dai Qiuying, Wang Hefeng, He Xun, Yao Yongchao, Li Tingshuai, Guo Jun, Niu Xiaobin, Sun Xuping
School of Materials and Energy, University of Electronic Science and Technology of China, Chengdu 611731 Sichuan, China.
College of Chemistry, Chemical Engineering and Materials Science, Shandong Normal University, Jinan 250014 Shandong, China.
J Colloid Interface Sci. 2025 Apr 15;684(Pt 2):64-72. doi: 10.1016/j.jcis.2025.01.106. Epub 2025 Jan 13.
Seawater splitting is increasingly recognized as a promising technique for hydrogen production, while the lack of good electrocatalysts and detrimental chlorine chemistry may hinder further development of this technology. Here, the interfacial engineering of manganese dioxide nanoparticles decorated on NiFe layered double hydroxide supported on nickel foam (MnO@NiFe LDH/NF) is reported, which works as a robust catalyst for alkaline seawater oxidation. Density functional theory calculations and experiment findings reveal that MnO@NiFe LDH/NF can selectively enrich OH and repel Cl in oxygen evolution reaction (OER). MnO@NiFe LDH/NF attains a current density of 1000 mA cm in alkaline seawater with an ultralow overpotential of only 313 mV. Furthermore, it can maintain stability at 1500 mA cm over 600 h. Further phosphidation of MnO@NiFe LDH/NF can create MnO@NiFeP/NF used in efficient hydrogen evolution reaction. Moreover, an anion exchange membrane electrolyzer with MnO@NiFe LDH/NF as the anode and MnO@NiFeP/NF as the cathode was also capable of seawater splitting at 500 mA cm for 100 h. This work offers light to develop effective and long-lasting electrocatalysts for seawater splitting.
海水分解作为一种有前景的制氢技术正日益受到认可,然而,缺乏良好的电催化剂以及有害的氯化学性质可能会阻碍该技术的进一步发展。在此,报道了在泡沫镍负载的镍铁层状双氢氧化物(MnO@NiFe LDH/NF)上装饰二氧化锰纳米颗粒的界面工程,其作为碱性海水氧化的稳健催化剂。密度泛函理论计算和实验结果表明,MnO@NiFe LDH/NF在析氧反应(OER)中能够选择性地富集OH并排斥Cl。MnO@NiFe LDH/NF在碱性海水中达到1000 mA cm的电流密度,过电位仅为313 mV,超低。此外,它在1500 mA cm下可保持600多小时的稳定性。对MnO@NiFe LDH/NF进一步磷化可制备用于高效析氢反应的MnO@NiFeP/NF。此外,以MnO@NiFe LDH/NF为阳极、MnO@NiFeP/NF为阴极的阴离子交换膜电解槽也能够在500 mA cm下进行100小时的海水分解。这项工作为开发用于海水分解的有效且持久的电催化剂提供了思路。