Li Mingxu, Chu Genjie, Gao Jiyun, Ye Xiaolei, Hou Ming, Guo Shenghui, Li Yunchuan, Zhou Ziqi, Yang Li, Briois Pascal
Faculty of Metallurgical and Energy Engineering, Kunming University of Science and Technology, Kunming, 650093, China.
State Key Laboratory of Complex Nonferrous Metal Resources Clean Utilization, Faculty of Metallurgical and Energy Engineering, Kunming University of Science and Technology, Kunming, 650093, China.
Sci Rep. 2025 Jan 22;15(1):2862. doi: 10.1038/s41598-025-87104-6.
Seawater electrolysis is an ideal technology for obtaining clean energy-green hydrogen. Developing efficient bifunctional catalysts is crucial for hydrogen production through direct seawater electrolysis. Currently, metal substrates loaded with active catalysts are widely employed as electrodes for seawater electrolysis. However, the challenge of metal corrosion cannot be ignored. In this work, the boron-doped diamond (BDD) with excellent corrosion resistance was explored as a substrate for loading active catalysts in seawater electrolysis. A step-by-step electrodeposition method was used to fabricate the FeCoS/Ni/BDD electrode, effectively addressing the poor adhesion of the FeCoS active layer to the BDD substrate. The resulting electrode demonstrated interesting bifunctional catalytic performance, achieving oxygen evolution reaction (OER) and hydrogen evolution reaction (HER) overpotentials of 425 mV and 360 mV, respectively, in alkaline simulated seawater (1 M KOH and 3.5 wt% NaCl) at a current density of 100 mA cm. Furthermore, by increasing the KOH concentration in the alkaline simulated seawater to 3 M, the OER and HER overpotentials of the electrode significantly decreased to 383 and 300 mV, respectively. This work offers a novel approach for utilizing BDD substrates in the design of corrosion-resistant electrodes for alkaline seawater electrolysis.
海水电解是获取清洁能源——绿色氢能的理想技术。开发高效的双功能催化剂对于通过直接海水电解制氢至关重要。目前,负载活性催化剂的金属基底被广泛用作海水电解电极。然而,金属腐蚀问题不容忽视。在这项工作中,具有优异耐腐蚀性的硼掺杂金刚石(BDD)被探索用作海水电解中负载活性催化剂的基底。采用分步电沉积法制备了FeCoS/Ni/BDD电极,有效解决了FeCoS活性层与BDD基底结合力差的问题。所得电极表现出有趣的双功能催化性能,在碱性模拟海水(1 M KOH和3.5 wt% NaCl)中,电流密度为100 mA cm时,析氧反应(OER)和析氢反应(HER)的过电位分别为425 mV和360 mV。此外,通过将碱性模拟海水中的KOH浓度提高到3 M,电极的OER和HER过电位分别显著降低到383和300 mV。这项工作为在碱性海水电解耐腐蚀电极设计中利用BDD基底提供了一种新方法。