Zheng Wang, Zhenhan Li, Yang Chao, Yu Cui, Xin-yu He, P. Liang, Chi Zhang, Zhonghua Zhang
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引用次数: 11
摘要
脱合金是制备纳米析氧反应(OER)催化剂的重要技术。在金属箔表面采用合金化-脱合金工艺制备自支撑型活性催化剂。本研究采用ga辅助合金化-脱合金策略,结合电氧化和杂原子掺杂制备了fe掺杂Ni(OH)2/Ni自支撑OER催化剂。通过控制反应扩散温度和时间,可以调节表面相组成和合金结构。优化后的O-Ni-Fe/200-3催化剂的过电位为318 mV,可激活10 mA cm-2电流密度,Tafel斜率为60.60 mV / dec1。催化剂的非原位表征证明,Fe掺杂促进了活性NiOOH的形成,这有助于优异的OER活性。本研究扩展了ga辅助合金化-脱合金策略,并证明了通过改变反应扩散条件来控制脱合金材料微观组织的可能性。
Dealloying-derived Fe-doped Ni(OH)2/Ni foils as self-supported oxygen evolution reaction catalysts
Dealloying has been an essential technique for developing nanostructured catalysts for the oxygen evolution reaction (OER). Self-supported active catalysts can be fabricated through an alloying-dealloying process on metal foil surfaces. This study uses a Ga-assisted alloying-dealloying strategy combined with electrooxidation and heteroatom doping to fabricate a Fe-doped Ni(OH)2/Ni self-supported OER catalyst. We find that the surface phase compositions and dealloyed structures can be adjusted by controlling the reaction-diffusion temperature and time. The optimized O-Ni-Fe/200-3 catalyst shows an overpotential of 318 mV to activate a 10 mA cm-2 current density with a Tafel slope of 60.60 mV dec-1. Ex-situ characterization of the catalyst proves that Fe doping promotes the formation of active NiOOH, which contributes to the excellent OER activity. This study extends the Ga-assisted alloying-dealloying strategy and demonstrates the possibility of controlling the microstructure of dealloyed materials by changing the reaction-diffusion conditions.