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基于非晶/晶体Fe-NiS异质结构的铁掺杂及界面工程用于高稳定性和动力学加速的水分解

Iron doping and interface engineering on amorphous/crystalline Fe-NiS heterostructures toward high-stability and kinetically accelerated water splitting.

作者信息

Li Jiaxin, Lv Yan, Wu Xueyan, Zhao Kenan, Guo Jixi, He Binhai, Jia Dianzeng

机构信息

State Key Laboratory of Chemistry and Utilization of Carbon Based Energy Resources; College of Chemistry, Xinjiang University, Urumqi, 830017, Xinjiang, PR China.

State Key Laboratory of Chemistry and Utilization of Carbon Based Energy Resources; College of Chemistry, Xinjiang University, Urumqi, 830017, Xinjiang, PR China.

出版信息

J Colloid Interface Sci. 2023 Nov 15;650(Pt B):1086-1096. doi: 10.1016/j.jcis.2023.07.070. Epub 2023 Jul 13.

DOI:10.1016/j.jcis.2023.07.070
PMID:37463534
Abstract

It is very important to develop transition metal-based electrocatalysts with excellent activity, high stability and low-cost for overall water splitting. In this work, the Fe-doped NiS/NF amorphous/crystalline heterostructure nanoarrays (Fe-NiS/NF) was synthesized by a simple one-step method. The resulting hierarchically structured nanoarrays offer the advantages of large surface area, high structural void fraction and accessible internal surfaces. These advantages not only furnish additional catalytically active sites, but also enhance the stability of the structure and effectively accelerate mass diffusion and charge transport. Experimental and characterization results indicate that Fe doping increases the electrical conductivity of amorphous/crystalline NiS/NF, and the NiS-NiS heterojunctions evoke interfacial charge rearrangement and optimize the adsorption free energy of the intermediates, which allows the catalyst to exhibit low overpotential and superior electrocatalytic activity. Especially, the overpotentials of hydrogen evolution reaction (HER) and oxygen evolution reaction (OER) of Fe-NiS/NF at 10 mA cm in an alkaline environment are 102.4 and 230.5 mV, respectively. When applied as a bifunctional catalyst for overall water splitting, it requires only 1.45 V cell voltage to deliver a current density of 10 mA cm, which is preferable to the all-noble metal Pt/C || IrO electrocatalyst (1.62 mV @ 10 mA cm). In addition, Fe-NiS/NF has excellent stability, and there is no obvious degradation after 96 h continuous operation at a current density of 100 mA cm. This work affords insights into the application of doping strategies and crystalline/amorphous synergistic modulation of the electrocatalytic activity of transition metal-based catalysts in energy conversion systems.

摘要

开发具有优异活性、高稳定性和低成本的用于全水分解的过渡金属基电催化剂非常重要。在这项工作中,通过简单的一步法合成了Fe掺杂的NiS/NF非晶/晶体异质结构纳米阵列(Fe-NiS/NF)。所得的分层结构纳米阵列具有大表面积、高结构孔隙率和可及内表面的优点。这些优点不仅提供了额外的催化活性位点,还增强了结构的稳定性,并有效地加速了质量扩散和电荷传输。实验和表征结果表明,Fe掺杂提高了非晶/晶体NiS/NF的电导率,并且NiS-NiS异质结引起界面电荷重排并优化了中间体的吸附自由能,这使得催化剂表现出低过电位和优异的电催化活性。特别是,在碱性环境中,Fe-NiS/NF在10 mA cm时的析氢反应(HER)和析氧反应(OER)过电位分别为102.4和230.5 mV。当用作全水分解的双功能催化剂时,在10 mA cm的电流密度下仅需要1.45 V的电池电压,这优于全贵金属Pt/C||IrO电催化剂(在10 mA cm时为1.62 mV)。此外,Fe-NiS/NF具有优异的稳定性,在100 mA cm的电流密度下连续运行96 h后没有明显降解。这项工作为掺杂策略的应用以及过渡金属基催化剂在能量转换系统中的电催化活性的晶体/非晶协同调制提供了见解。

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