Effective Hydrogen Evolution of Nickel–Molybdenum–Phosphide Electrodeposited Nickel Foam Electrode

IF 2.3 4区 化学 Q3 CHEMISTRY, PHYSICAL
Yi Xiong, Wei Zeng, Azmain Akib Akash, Yun Tang, Dong Wei, Huihong Liu, Sakil Mahmud
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引用次数: 0

Abstract

This study introduces an electrocatalyst composed of nickel-molybdenum-phosphide (NiMoP) supported on nickel foam (NiF), which has been synthesized using a straightforward two-step electrodeposition method intended for enhancing the efficiency of the hydrogen evolution reaction (HER) in alkaline environments. The addition of Mo and P, in contrast to traditional Ni-based catalysts, creates a synergistic electronic effect that considerably improves HER kinetics. The enhanced NiMoP/NiF catalyst demonstrates an impressively low overpotential of 171 mV at 10 mA cm⁻² and 376 mV at 100 mA․cm⁻², surpassing the performance of Ni/NiF (η10 = 229 mV) and NiMo/NiF (η10 = 181 mV). In comparison to current NiMoP systems, our catalyst exhibits superior catalytic activity, stability, and charge transfer efficiency. The electrochemical analysis indicates a Tafel slope of 119.98 mV․dec⁻¹, which supports a Volmer-controlled hydrogen evolution reaction mechanism characterized by enhanced water dissociation. The structural and compositional analysis demonstrates that Mo improves the electronic structure of Ni, whereas P increases water affinity and electrochemical surface area (Cdl = 3.18 mF·cm⁻²), which is almost four times higher than that of pristine NiF. The catalyst exhibits remarkable stability throughout 2000 cycles and shows reliable performance in multi-step chronopotentiometry evaluations. This study presents an economical, long-lasting, and scalable electrocatalyst for hydrogen evolution reaction, serving as a viable substitute for noble-metal-based systems in the pursuit of sustainable hydrogen production.

Graphical abstract

镍-磷化钼-泡沫镍电沉积电极的有效析氢
本研究介绍了一种由泡沫镍(NiF)支撑的磷化镍钼(NiMoP)组成的电催化剂,该电催化剂采用简单的两步电沉积法合成,旨在提高碱性环境下析氢反应(HER)的效率。与传统的镍基催化剂相比,Mo和P的加入产生了协同电子效应,大大提高了HER动力学。强化后的NiMoP/NiF催化剂在10 mA cm⁻²时的过电位为171 mV,在100 mA cm⁻²时的过电位为376 mV,超过了Ni/NiF (η10 = 229 mV)和NiMo/NiF (η10 = 181 mV)的过电位。与现有的NiMoP系统相比,我们的催化剂具有更好的催化活性、稳定性和电荷转移效率。电化学分析表明,Tafel斜率为119.98 mV . dec - 1,支持volmer控制的以水解离增强为特征的析氢反应机制。结构和成分分析表明,Mo改善了Ni的电子结构,而P增加了Ni的亲水性和电化学表面积(Cdl = 3.18 mF·cm⁻²),几乎是原始NiF的4倍。催化剂在2000次循环中表现出显著的稳定性,并在多步计时电位测定评估中表现出可靠的性能。本研究提出了一种经济、持久、可扩展的析氢电催化剂,在追求可持续制氢的过程中,可以作为贵金属基系统的可行替代品。图形抽象
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Catalysis Letters
Catalysis Letters 化学-物理化学
CiteScore
5.70
自引率
3.60%
发文量
327
审稿时长
1 months
期刊介绍: Catalysis Letters aim is the rapid publication of outstanding and high-impact original research articles in catalysis. The scope of the journal covers a broad range of topics in all fields of both applied and theoretical catalysis, including heterogeneous, homogeneous and biocatalysis. The high-quality original research articles published in Catalysis Letters are subject to rigorous peer review. Accepted papers are published online first and subsequently in print issues. All contributions must include a graphical abstract. Manuscripts should be written in English and the responsibility lies with the authors to ensure that they are grammatically and linguistically correct. Authors for whom English is not the working language are encouraged to consider using a professional language-editing service before submitting their manuscripts.
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