Luyu Liu , Xiang Ding , Jun Xiang , Haotian Qin , Siyuan Tang , Linlin Xu , Jianling Dong , Yin Yin , Nan Jiang , Xinchun Yang , Fuzhan Song
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Due to the synergistic interaction of multi-component, the obtained FeCoNi electrocatalysts exhibit an outstanding oxygen evolution reaction (OER) performance, requiring overpotential input of as low as 315, 353 and 402 mV to produce industrial-level current density of as high as 500, 1000 and 1500 mA cm<sup>−2</sup>, respectively, along with Tafel slope of 32 mV/dec in 1.0 M KOH electrolyte. In addition, the as-synthesized FeCoNi electrocatalysts represent an excellent performance toward electrocatalyzing seawater oxidation. In alkaline natural seawater electrolyte, FeCoNi could even produce an industrial current density of 1000 mA cm<sup>−2</sup> at overpotential input of 390 mV, representing high activity and corrosion-resistant in chloride environment of seawater. Remarkably, the rationally designed anode can stably operate for over 2000 h at an industrial-relevant current density of 500 mA cm<sup>−2</sup> in an alkaline electrolyze. In-situ Raman spectroscopy reveal Fe species could reconfigure electronic distribution, resulting in high-valent M (M = Co or Ni active sites) active sites for water oxidation in alkaline electrolyte. Moreover, Fe, as electron acceptor, could efficiently accelerate the charge transfer kinetics and build the high-efficient spatial charge separation for optimized valence band maximum and work function. Such a novel charge density reconfiguration not only facilitates the tensile lengthening of O–H bond, but also repulses undesirable anion adsorption, achieving a high-performance and robust water oxidation in alkaline electrolyte.</div></div>","PeriodicalId":325,"journal":{"name":"Fuel","volume":"406 ","pages":"Article 137084"},"PeriodicalIF":7.5000,"publicationDate":"2025-10-09","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Iron-induced charge density redistribution of medium entropy alloys for ampere-level seawater electrolysis\",\"authors\":\"Luyu Liu , Xiang Ding , Jun Xiang , Haotian Qin , Siyuan Tang , Linlin Xu , Jianling Dong , Yin Yin , Nan Jiang , Xinchun Yang , Fuzhan Song\",\"doi\":\"10.1016/j.fuel.2025.137084\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><div>Electrocatalytic seawater splitting into green hydrogen provides a promising strategy for clean and sustainable energy conversion. 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引用次数: 0
摘要
电催化海水分解成绿色氢为清洁和可持续的能源转换提供了有前途的策略。设计高性价比、高活性、高稳定性的电催化剂是实现工业规模碱性海水电解绿色制氢的关键。通过可行的电沉积策略,获得了一种经济高效的FeCoNi中熵合金电催化剂。由于多组分的协同作用,得到的FeCoNi电催化剂表现出出色的析氧反应(OER)性能,在1.0 M KOH电解质中,需要低至315、353和402 mV的过电位输入,分别产生高达500、1000和1500 mA cm−2的工业级电流密度,以及32 mV/dec的塔菲斜率。此外,所合成的FeCoNi电催化剂在电催化海水氧化方面表现出优异的性能。在碱性天然海水电解质中,FeCoNi在过电位输入为390 mV时甚至可以产生1000 mA cm−2的工业电流密度,在海水氯化物环境中具有较高的活性和耐腐蚀性。值得注意的是,在碱性电解液中,合理设计的阳极可以在工业相关电流密度为500 mA cm−2的情况下稳定工作2000小时以上。原位拉曼光谱显示,Fe可以重新配置电子分布,导致碱性电解质中水氧化的高价M (M = Co或Ni活性位点)活性位点。此外,Fe作为电子受体可以有效地加速电荷转移动力学,并建立高效的空间电荷分离,以优化价带最大值和功函数。这种新颖的电荷密度重构不仅有利于O-H键的拉伸延长,而且可以排斥不希望的阴离子吸附,从而在碱性电解质中实现高性能和稳健的水氧化。
Iron-induced charge density redistribution of medium entropy alloys for ampere-level seawater electrolysis
Electrocatalytic seawater splitting into green hydrogen provides a promising strategy for clean and sustainable energy conversion. Designing cost-effective electrocatalyst with high activity and robust stability is pivotal for achieving industrial-scale green hydrogen generation by alkaline seawater electrolysis. Herein, a cost-effective and high-performance FeCoNi medium-entropy alloys electrocatalyst was obtained via a feasible electrodeposition strategy. Due to the synergistic interaction of multi-component, the obtained FeCoNi electrocatalysts exhibit an outstanding oxygen evolution reaction (OER) performance, requiring overpotential input of as low as 315, 353 and 402 mV to produce industrial-level current density of as high as 500, 1000 and 1500 mA cm−2, respectively, along with Tafel slope of 32 mV/dec in 1.0 M KOH electrolyte. In addition, the as-synthesized FeCoNi electrocatalysts represent an excellent performance toward electrocatalyzing seawater oxidation. In alkaline natural seawater electrolyte, FeCoNi could even produce an industrial current density of 1000 mA cm−2 at overpotential input of 390 mV, representing high activity and corrosion-resistant in chloride environment of seawater. Remarkably, the rationally designed anode can stably operate for over 2000 h at an industrial-relevant current density of 500 mA cm−2 in an alkaline electrolyze. In-situ Raman spectroscopy reveal Fe species could reconfigure electronic distribution, resulting in high-valent M (M = Co or Ni active sites) active sites for water oxidation in alkaline electrolyte. Moreover, Fe, as electron acceptor, could efficiently accelerate the charge transfer kinetics and build the high-efficient spatial charge separation for optimized valence band maximum and work function. Such a novel charge density reconfiguration not only facilitates the tensile lengthening of O–H bond, but also repulses undesirable anion adsorption, achieving a high-performance and robust water oxidation in alkaline electrolyte.
期刊介绍:
The exploration of energy sources remains a critical matter of study. For the past nine decades, fuel has consistently held the forefront in primary research efforts within the field of energy science. This area of investigation encompasses a wide range of subjects, with a particular emphasis on emerging concerns like environmental factors and pollution.