高性能析氢反应用生物质杂化电极的构建

Yajun Zou, Fan Yang, Yun Zhao, Wei Wang, Yanbo Wang, Dawei Wang, Haibin Wan
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引用次数: 0

摘要

电催化水裂解反应是一种可持续的大规模制氢方法,为能量转换提供了一条很有前景的途径。然而,电催化剂活性仍然是制约水电解系统能量转换效率的一个制约因素。在这项研究中,构建了一种三维分层异质结构电催化剂,该电催化剂由垂直排列的NiFe层状双氢氧化物(LDH)纳米片/Fe-NiSx纳米颗粒负载在生物质衍生的碳上。实验结果表明,该催化剂在碱性溶液中具有良好的电催化析氢活性和耐久性。该电极显示出电催化活性,需要169 mV的过电位才能在HER中提供目标10 mA•cm-2的电流密度;结合密度泛函理论的计算结果,催化剂独特的三维构型、碳微管支架的高导电性以及NiFe LDH与Fe-NiSx界面处的强耦合效应加速了电子/离子转移,进一步促进了析氢反应动力学。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Construction of Biomass-Derived Hybrid Electrodes for High-Performance Hydrogen Evolution Reaction
Electrocatalytic water splitting reaction is a sustainable method for producing hydrogen at a large scale, which provides a promising pathway for energy transition. However, electrocatalyst activity remains a limitation restricting the energy conversion efficiency of water electrolysis systems. In this study, a three-dimensional hierarchical heterostructure electrocatalyst with vertically aligned NiFe layered double hydroxides (LDH) nanoflakes/Fe-NiSx nanoparticles supported on biomass-derived carbons was constructed. The experimental results proved that the catalyst has good activity and duralibity toward electrocatalytic hydrogen evolution in alkaline solutions. The electrode exhibits an electrocatalytic activity requiring an overpotential of 169 mV for delivering a current density of targeted 10 mA•cm-2 in HER; catalytic activity does not decay significantly within 15 h. Combined with the calculation results of density functional theory, the unique three-dimensional configuration of the catalyst, the high conductivity of the carbon microtube support, and the strong coupling effect at the interface between NiFe LDH and Fe-NiSx accelerates electron/ion transfer, further facilitating the reaction kinetics of hydrogen evolution.
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