Lin Gaoxin, Dong Anrui, Li Zhiheng, Li Wenlong, Cao Xing, Zhao Yilong, Wang Linqin, Sun Licheng
Center of Artificial Photosynthesis for Solar Fuels and Department of Chemistry, School of Science and Research Center for Industries of the Future, Westlake University, 600 Dunyu Road, Hangzhou, Zhejiang, 310030, China.
Institute of Natural Sciences, Westlake Institute for Advanced Study, 18 Shilongshan Road, Hangzhou, Zhejiang, 310024, China.
Adv Mater. 2025 Jul;37(30):e2507525. doi: 10.1002/adma.202507525. Epub 2025 May 16.
Noble metal-free electrodes for anion exchange membrane water electrolysis (AEM-WE) operating at high current densities are critical for sustainable hydrogen production. However, the massive amount of bubbles resulted in insufficient mass transfer and unevenly distributed local stress, which poses a major challenge in designing an efficient and robust hydrogen evolution catalyst. Herein, a facile chemical corrosion method is developed to synthesize an interlayer-anchored NiMo/MoO catalyst on a nickel foam (NF) substrate (NiMo/Int/NF) with high hydrogen evolution activity (overpotential of 80.2 ± 3.53 mV) and durability (stable for 5000 h) at 1000 mA cm in 1 m KOH. The interlayer tightly anchors the catalytic layer to the substrate, providing high compressive strength and strong adhesion to mitigate the bubble shock at a high current density. In situ Raman and X-ray diffraction analyses reveal that the heterostructural catalytic layer can accelerate the hydrogen evolution reaction with increased local pH and high component utilization. Using NiMo/Int/NF as the cathode, the assembled noble metal-free AEM-WE device exhibits a low cell voltage of 1.78 V at 1000 mA cm (significantly lower than that of a Pt/C-catalyzed cell (1.94 V)) while also showing excellent stability for 3000 h.
用于在高电流密度下运行的阴离子交换膜水电解(AEM-WE)的无贵金属电极对于可持续制氢至关重要。然而,大量气泡导致传质不足和局部应力分布不均,这在设计高效且耐用的析氢催化剂方面构成了重大挑战。在此,开发了一种简便的化学腐蚀方法,以在泡沫镍(NF)基底上合成一种层间锚定的NiMo/MoO催化剂(NiMo/Int/NF),该催化剂在1 m KOH中1000 mA cm²的电流密度下具有高析氢活性(过电位为80.2±3.53 mV)和耐久性(稳定5000小时)。中间层将催化层紧密锚定在基底上,提供高抗压强度和强附着力,以减轻高电流密度下的气泡冲击。原位拉曼和X射线衍射分析表明,异质结构催化层可通过提高局部pH值和高组分利用率来加速析氢反应。使用NiMo/Int/NF作为阴极,组装的无贵金属AEM-WE装置在1000 mA cm²时表现出1.78 V的低电池电压(明显低于Pt/C催化电池的1.94 V),同时在3000小时内也表现出优异的稳定性。