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镁促进镍铁基电催化剂快速自重构以实现高效析氧

Magnesium-promoted rapid self-reconstruction of NiFe-based electrocatalysts toward efficient oxygen evolution.

作者信息

Jin Boxuan, Zhang Wenwen, Wei Shuaichong, Zhang Kai, Wang Hongyu, Liu Guihua, Li Jingde

机构信息

Tianjin Key Laboratory of Chemical Process Safety, School of Chemical Engineering and Technology, Hebei University of Technology, Tianjin 300130, China.

Tianjin Key Laboratory of Chemical Process Safety, School of Chemical Engineering and Technology, Hebei University of Technology, Tianjin 300130, China.

出版信息

J Colloid Interface Sci. 2025 Jan;677(Pt A):208-216. doi: 10.1016/j.jcis.2024.07.183. Epub 2024 Jul 23.

DOI:10.1016/j.jcis.2024.07.183
PMID:39089127
Abstract

The acceleration of active sites formation through surface reconstruction is widely acknowledged as the crucial factor in developing high-performance oxygen evolution reaction (OER) catalysts for water splitting. Herein, a simple one-step corrosion method and magnesium (Mg)-promoted strategy are reported to develop the NiFe-based catalyst with enhanced OER performance. The Mg is introduced in NiFe materials to preparate a "pre-catalyst" Mg-Ni/FeO. In-situ Raman shows that Mg doping would accelerate the self-reconstruction of Ni/FeO to form active NiOOH species during OER. In-situ infrared indicates that Mg doping benefits the formation of *OOH intermediate. Theoretical analysis further confirms that Mg doping can optimize the adsorption of oxygen intermediates, accelerating the OER kinetics. Accordingly, the Mg-Ni/FeO catalyst exhibits excellent OER performance with overpotential of 168 mV at 10 mA cm. The anion exchange membrane water electrolyzer achieved 200 mA cm at voltage of 1.53 V, showing excellent stability over 500 h as well. This work demonstrates the potential of Mg-promoted strategy in regulating the activity of transition metal-based OER electrocatalysts.

摘要

通过表面重构加速活性位点的形成被广泛认为是开发用于水分解的高性能析氧反应(OER)催化剂的关键因素。在此,报道了一种简单的一步腐蚀法和镁(Mg)促进策略来制备具有增强OER性能的镍铁基催化剂。将Mg引入镍铁材料中制备“预催化剂”Mg-Ni/FeO。原位拉曼光谱表明,Mg掺杂会加速Ni/FeO的自重构,在OER过程中形成活性NiOOH物种。原位红外光谱表明,Mg掺杂有利于*OOH中间体的形成。理论分析进一步证实,Mg掺杂可以优化氧中间体的吸附,加速OER动力学。因此,Mg-Ni/FeO催化剂表现出优异的OER性能,在10 mA cm时过电位为168 mV。阴离子交换膜水电解槽在1.53 V的电压下实现了200 mA cm的电流密度,并且在500 h以上也表现出优异的稳定性。这项工作展示了Mg促进策略在调节过渡金属基OER电催化剂活性方面的潜力。

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