通过氢氧化镍-镍外延界面加速水解离动力学,实现卓越的碱性制氢。

IF 9.4 1区 化学 Q1 CHEMISTRY, PHYSICAL
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引用次数: 0

摘要

通过构建适当的外延界面可以增强电催化剂的内在性能,其中调制的电子状态和吸附/解吸行为有利于提高电催化活性。在此,我们设计了以泡沫镍(Ni-Ni(OH)2/NF)为支撑的氢氧化镍外延界面,并在氢氧化镍纳米带表面外延生长镍纳米颗粒,用于碱性氢进化反应(HER)。值得注意的是,Ni-Ni(OH)2/NF 显示出卓越的碱性氢进化反应电催化活性(158 mV @ 100 mA cm-2)和强大的稳定性(在 200 mA cm-2 下连续测试 150 小时后活性保持率为 90%)。理论模拟显示,经过调整的界面电子结构和外延镍-氢氧化镍界面周围水的加速解离,使其具有高效的碱性氢演化电化学活性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Accelerated water dissociation kinetics by nickel-nickelous hydroxide epitaxial interfaces for superior alkaline hydrogen generation

Accelerated water dissociation kinetics by nickel-nickelous hydroxide epitaxial interfaces for superior alkaline hydrogen generation
The intrinsic performance of an electrocatalyst can be reinforced by constructing appropriate epitaxial interfaces, where the modulated electronic states and adsorption/desorption behaviors are conductive to enhancing electrocatalytic activity. Herein, nickel-nickelous hydroxide epitaxial interface supported on nickel foam (Ni-Ni(OH)2/NF) with epitaxial growth of nickel nanoparticles on the surface of nickelous hydroxide nanoribbons is devised for alkaline hydrogen evolution reaction (HER). Notably, the Ni-Ni(OH)2/NF reveals excellent electrocatalytic activity of alkaline HER (158 mV @ 100 mA cm−2), along with robust stability (90 % activity retention after 150 h continuous test at 200 mA cm−2). Theoretical simulations disclose the tuned interface electronic structure and accelerated water dissociation around the epitaxial nickel-nickelous hydroxide interface result in efficient electrochemical activity toward alkaline hydrogen evolution.
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来源期刊
CiteScore
16.10
自引率
7.10%
发文量
2568
审稿时长
2 months
期刊介绍: The Journal of Colloid and Interface Science publishes original research findings on the fundamental principles of colloid and interface science, as well as innovative applications in various fields. The criteria for publication include impact, quality, novelty, and originality. Emphasis: The journal emphasizes fundamental scientific innovation within the following categories: A.Colloidal Materials and Nanomaterials B.Soft Colloidal and Self-Assembly Systems C.Adsorption, Catalysis, and Electrochemistry D.Interfacial Processes, Capillarity, and Wetting E.Biomaterials and Nanomedicine F.Energy Conversion and Storage, and Environmental Technologies
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