YaXi Zhang, Jin Liang, Li Zhang, FengYuan Zou, YunFeng Li, ZiQuan Zeng, Tian Lei, Guang Yang
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In 1.0 M KOH electrolyte, the MXene@ZnCoP/NF heterostructure exhibits exceptional HER performance, achieving a low overpotential of 15 mV at 10 mA cm<sup>−2</sup>, 64 mV at 50 mA cm<sup>−2</sup>, 214 mV at 500 mA cm<sup>−2</sup>, and a Tafel slope of 86.0 mV dec<sup>−1</sup>, indicative of rapid reaction kinetics. Furthermore, the catalyst demonstrates industrial-grade durability, maintaining stable operation for 65 h at 500 mA cm<sup>−2</sup> without significant degradation. When integrated into a full-cell electrolyzer with RuO<sub>2</sub>/NF as the anode (RuO<sub>2</sub>/NF ||MXene@ZnCoP/NF), the system requires only 1.53 V to deliver a current density of 10 mA cm<sup>−2</sup>, surpassing the performance of the noble metal system Pt-C/NF||RuO<sub>2</sub>/NF (1.61 V). This highlights its potential as a cost-effective alternative to noble metal-based electrocatalysts for scalable hydrogen production. The enhanced catalytic performance can be primarily attributed to the synergistic interplay of three key factors: the superior conductivity provided by MXene-engineered NF substrates, the Zn doping-induced crystalline-to-amorphous phase reconstruction, and the morphological transformation from micrometer-scale architectures to nanoscale structures. This study proposes an innovative “substrate–structure–composition” synergistic strategy that establishes a new paradigm for designing highly efficient non-noble metal HER electrocatalysts, thereby propelling the scalable industrial implementation of electrocatalytic water splitting for hydrogen production.</p><h3>Graphical abstract</h3>\n<div><figure><div><div><picture><source><img></source></picture></div></div></figure></div></div>","PeriodicalId":645,"journal":{"name":"Journal of Materials Science","volume":"60 38","pages":"17781 - 17795"},"PeriodicalIF":3.9000,"publicationDate":"2025-09-20","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Zn-driven amorphous CoP on MXene-modified Ni foam: phase engineering for efficient hydrogen evolution catalysis\",\"authors\":\"YaXi Zhang, Jin Liang, Li Zhang, FengYuan Zou, YunFeng Li, ZiQuan Zeng, Tian Lei, Guang Yang\",\"doi\":\"10.1007/s10853-025-11504-2\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><p>As a clean energy carrier, hydrogen necessitates efficient production via cost-effective, highly active non-noble metal electrocatalysts. 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引用次数: 0
摘要
氢作为一种清洁的能源载体,必须通过高性价比、高活性的非贵金属电催化剂进行高效生产。在此,我们通过协同衬底工程和成分调制,证明了一种锌掺杂CoP异质结构催化剂锚定在mxene工程泡沫镍(MXene@ZnCoP/NF)上。该设计实现了卓越的碱性析氢反应(HER)活性和优越的整体水分解效率。在1.0 M KOH电解质中,MXene@ZnCoP/NF异质结构表现出优异的HER性能,在10 mA cm - 2时达到15 mV的过电位,在50 mA cm - 2时达到64 mV,在500 mA cm - 2时达到214 mV, Tafel斜率为86.0 mV dec - 1,表明反应动力学快速。此外,该催化剂具有工业级的耐久性,在500毫安厘米−2下保持65小时的稳定运行,没有明显的降解。当集成到以RuO2/NF作为阳极(RuO2/NF ||MXene@ZnCoP/NF)的全电池电解槽中时,该系统仅需要1.53 V就能提供10 mA cm - 2的电流密度,超过贵金属系统Pt-C/NF||RuO2/NF (1.61 V)的性能。这凸显了它作为贵金属基电催化剂的一种具有成本效益的可扩展制氢替代品的潜力。催化性能的增强主要归因于三个关键因素的协同相互作用:mxene工程NF衬底提供的优越导电性,Zn掺杂诱导的晶体到非晶相的重建以及从微米级结构到纳米级结构的形态转变。本研究提出了一种创新的“基质-结构-成分”协同策略,为设计高效的非贵金属HER电催化剂建立了新的范例,从而推动了电催化水裂解制氢的可扩展工业实施。图形抽象
Zn-driven amorphous CoP on MXene-modified Ni foam: phase engineering for efficient hydrogen evolution catalysis
As a clean energy carrier, hydrogen necessitates efficient production via cost-effective, highly active non-noble metal electrocatalysts. Herein, we demonstrate a Zn-doped CoP heterostructure catalyst anchored on MXene-engineered nickel foam (MXene@ZnCoP/NF) through synergistic substrate engineering and compositional modulation. This design achieves exceptional alkaline hydrogen evolution reaction (HER) activity and superior overall water splitting efficiency. In 1.0 M KOH electrolyte, the MXene@ZnCoP/NF heterostructure exhibits exceptional HER performance, achieving a low overpotential of 15 mV at 10 mA cm−2, 64 mV at 50 mA cm−2, 214 mV at 500 mA cm−2, and a Tafel slope of 86.0 mV dec−1, indicative of rapid reaction kinetics. Furthermore, the catalyst demonstrates industrial-grade durability, maintaining stable operation for 65 h at 500 mA cm−2 without significant degradation. When integrated into a full-cell electrolyzer with RuO2/NF as the anode (RuO2/NF ||MXene@ZnCoP/NF), the system requires only 1.53 V to deliver a current density of 10 mA cm−2, surpassing the performance of the noble metal system Pt-C/NF||RuO2/NF (1.61 V). This highlights its potential as a cost-effective alternative to noble metal-based electrocatalysts for scalable hydrogen production. The enhanced catalytic performance can be primarily attributed to the synergistic interplay of three key factors: the superior conductivity provided by MXene-engineered NF substrates, the Zn doping-induced crystalline-to-amorphous phase reconstruction, and the morphological transformation from micrometer-scale architectures to nanoscale structures. This study proposes an innovative “substrate–structure–composition” synergistic strategy that establishes a new paradigm for designing highly efficient non-noble metal HER electrocatalysts, thereby propelling the scalable industrial implementation of electrocatalytic water splitting for hydrogen production.
期刊介绍:
The Journal of Materials Science publishes reviews, full-length papers, and short Communications recording original research results on, or techniques for studying the relationship between structure, properties, and uses of materials. The subjects are seen from international and interdisciplinary perspectives covering areas including metals, ceramics, glasses, polymers, electrical materials, composite materials, fibers, nanostructured materials, nanocomposites, and biological and biomedical materials. The Journal of Materials Science is now firmly established as the leading source of primary communication for scientists investigating the structure and properties of all engineering materials.