海水
膜
电解
材料科学
离子
化学工程
化学
电极
海洋学
电解质
地质学
生物化学
工程类
有机化学
物理化学
作者
Jiaqi Wang,Yue Liu,Ganceng Yang,Yanqing Jiao,Youming Dong,Chungui Tian,Haijing Yan,Honggang Fu
标识
DOI:10.1038/s41467-025-56639-7
摘要
Anion exchange membrane seawater electrolysis is vital for future large-scale green hydrogen production, however enduring a huge challenge that lacks high-stable oxygen evolution reaction electrocatalysts. Herein, we report a robust OER electrocatalyst for AEMSE by integrating MXene (Ti3C2) with NiFe sulfides ((Ni,Fe)S2@Ti3C2). The strong interaction between (Ni,Fe)S2 and Ti3C2 induces electron distribution to trigger lattice oxygen mechanism, improving the intrinsic activity, and particularly prohibits the dissolution of Fe species during OER process via the Ti-O-Fe bonding effectively, achieving notable stability. Furthermore, the good retention of sulfates and the abundant groups of Ti3C2 provide effective Cl- resistance. Accordingly, (Ni,Fe)S2@Ti3C2 achieves high OER activity (1.598 V@2 A cm-2) and long-term durability (1000 h) in seawater system. Furthermore, AEMSE with industrial current density (0.5 A cm-2) and durability (500 h) is achieved by (Ni,Fe)S2@Ti3C2 anode and Raney Ni cathode with electrolysis efficiency of 70% and energy consumption of 48.4 kWh kg-1 H2. The development of seawater electrolysis for green hydrogen production is crucial to addressing energy shortages. Here, the authors report that integrating NiFe sulfides with MXene enhances oxygen evolution reaction efficiency and stability, achieving 1000 hours of durability in seawater electrolysis.
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