Junwei Sun , Xiaoming Li , Yue Wang , Juan Yang , Hongwei Luo , Xiaoyan Zhang , Junfeng Chen
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引用次数: 0
Abstract
As a cost-effective alternative to Pt-based catalysts, molybdenum carbide (MoC) exhibits considerable potential for catalysing hydrogen evolution reaction (HER) in both alkaline water electrolyzers and proton exchange membrane water electrolyzers. However, achieving ampere-level current densities at low overpotentials remains challenging for MoC-based electrocatalysts. In this study, we utilized electrospinning technology followed by a subsequent heat treatment to successfully synthesize monodisperse MoC nanoparticles (approximately 4.3 nm) embedded in carbon nanofibers. The resultant self-supporting one-dimensional molybdenum carbide@nitrogen-doped carbon nanofiber (MoC-A@NCNF), prepared with polyoxometalate anion (POM) and polyvinylpyrrolidone (PVP), exhibits excellent anti-aggregation behavior. Benefiting from its high specific surface area and one-dimensional conductive network structure, the MoC-A@NCNF displays outstanding hydrogen evolution reaction (HER) performance in both 1 M KOH and 0.5 M H2SO4, achieving overpotentials of 491 mV and 568 mV at a current density of 1 A cm−2, respectively. Furthermore, it exhibits exceptional electrochemical stability during prolonged HER testing under both acidic and alkaline conditions.
碳化钼(MoC)作为铂基催化剂的一种具有成本效益的替代品,在碱性水电解槽和质子交换膜水电解槽中催化氢进化反应(HER)方面具有相当大的潜力。然而,对于基于碳化钼的电催化剂来说,在低过电位下实现安培级的电流密度仍然具有挑战性。在本研究中,我们利用电纺丝技术,随后进行热处理,成功合成了嵌入碳纳米纤维的单分散 MoC 纳米颗粒(约 4.3 nm)。利用聚氧化金属阴离子(POM)和聚乙烯吡咯烷酮(PVP)制备的自支撑一维碳化钼@氮掺杂碳纳米纤维(MoC-A@NCNF)具有优异的抗聚集性能。得益于其高比表面积和一维导电网络结构,MoC-A@NCNF 在 1 M KOH 和 0.5 M H2SO4 中均表现出卓越的氢进化反应(HER)性能,在电流密度为 1 A cm-2 时,过电位分别达到 491 mV 和 568 mV。此外,在酸性和碱性条件下进行长时间的 HER 测试时,它还表现出卓越的电化学稳定性。
期刊介绍:
The Journal of Electroanalytical Chemistry is the foremost international journal devoted to the interdisciplinary subject of electrochemistry in all its aspects, theoretical as well as applied.
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