Melt-Spun FeCrNiMoC0.3 High-Entropy Alloy Ribbons: Microstructure Refinement for Enhanced Bifunctional Alkaline Overall Water Splitting

IF 7.6 1区 化学 Q1 CHEMISTRY, MULTIDISCIPLINARY
Tong Zhang,Guanglong Li,Zhen Wen,Wei Zhang,Shulin Dong,Siruo Zhang,Yingdong Qu
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Abstract

Alkaline water electrolysis urgently requires scalable, binder-free integrated bulk electrodes with high activity and robust stability at high current densities. High-entropy alloys (HEAs) are promising candidates for such electrodes, but conventional as-cast HEAs generally suffer from coarse grains, which limits their electrocatalytic performance. Herein, FeCrNiMoC0.3 HEA ribbons were fabricated as integrated electrocatalysts via melt-spinning rapid solidification. This metallurgical treatment refines matrix grains to an average size of 135.7 nm, uniformly disperses nanoscale carbides, induces FCC lattice expansion, and drives directional charge transfer from Fe/Cr/Ni to Mo without altering the phase composition. In 1.0 M KOH, the melt-spun ribbons (MSRs) exhibit enhanced bifunctional electrocatalytic performance. At 10 mA cm–2, the MSR electrode delivers overpotentials of 218 mV for the oxygen evolution reaction (OER) and 81 mV for the hydrogen evolution reaction (HER), with Tafel slopes of 30.8 and 55.4 mV dec–1, respectively. The two-electrode overall water splitting achieves 500 mA cm–2 at 2.03 V and runs stably for over 500 h. Grain and carbide refinement, accompanied by electronic modulation, an enlarged electrochemically active surface area, and reduced charge transfer resistance, collectively accounts for the enhanced performance. This work provides a facile and scalable metallurgical strategy to optimize carbide-containing binder-free bulk HEAs and offers a reference for understanding the microstructure–activity relationship of bulk alloy electrodes for alkaline water electrolysis.

Abstract Image

熔体纺丝fecrnimo0.3高熵合金带:增强双功能碱性整体水分解的微观结构改进
碱水电解迫切需要可扩展的、无粘结剂的集成体电极,这些电极在高电流密度下具有高活性和强大的稳定性。高熵合金(HEAs)是这种电极的有希望的候选者,但传统的铸态HEAs通常存在粗大的晶粒,这限制了它们的电催化性能。采用熔融纺丝快速凝固法制备了FeCrNiMoC0.3 HEA带作为一体化电催化剂。这种冶金处理使基体晶粒细化到平均135.7 nm,均匀分散纳米级碳化物,诱导FCC晶格膨胀,并在不改变相组成的情况下驱动Fe/Cr/Ni向Mo的定向电荷转移。在1.0 M KOH条件下,熔融纺带(MSRs)表现出增强的双功能电催化性能。在10 mA cm-2下,MSR电极的析氧反应(OER)和析氢反应(HER)的过电位分别为218 mV和81 mV, Tafel斜率分别为30.8和55.4 mV / dec1。两电极整体水分解在2.03 V下达到500 mA cm-2,并稳定运行超过500小时。晶粒和碳化物的细化,伴随着电子调制,电化学活性表面积的扩大,电荷转移电阻的降低,共同导致了性能的增强。本研究为优化含碳化物无粘结剂大块HEAs提供了一种简便、可扩展的冶金策略,并为理解大块合金电极的显微结构-活性关系提供了参考。
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来源期刊
ACS Sustainable Chemistry & Engineering
ACS Sustainable Chemistry & Engineering CHEMISTRY, MULTIDISCIPLINARY-ENGINEERING, CHEMICAL
CiteScore
13.80
自引率
4.80%
发文量
1470
审稿时长
1.7 months
期刊介绍: ACS Sustainable Chemistry & Engineering is a prestigious weekly peer-reviewed scientific journal published by the American Chemical Society. Dedicated to advancing the principles of green chemistry and green engineering, it covers a wide array of research topics including green chemistry, green engineering, biomass, alternative energy, and life cycle assessment. The journal welcomes submissions in various formats, including Letters, Articles, Features, and Perspectives (Reviews), that address the challenges of sustainability in the chemical enterprise and contribute to the advancement of sustainable practices. Join us in shaping the future of sustainable chemistry and engineering.
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