五元
化学
合金
相(物质)
金属
纳米技术
航程(航空)
化学工程
氢
耐久性
贵金属
大规模运输
可持续能源
表征(材料科学)
电子结构
晶体结构
X射线晶体学
作者
Sangmin Jeong,Anthony J. Branco,Porvajja Nagarajan,Connor S. Sullivan,Ji Hyeon,Silas W. Bollen,Noah Mason,Milinda AM Abeykoon,D. Olds,Michael B. Ross
摘要
High-entropy alloys (HEAs) provide uniquely tunable structural and electronic properties that enable robust electrocatalysis. While compositional manipulation of HEAs is well-known, systematically controlling the crystalline phase and morphology remains a challenge that could provide new avenues for controlling reactive sites and physical properties. Here, we show the preferential stabilization of mixed fcc/bcc to fcc phases by controlling the Au content in quinary AuPdFeCoNi HEA nanoparticles. This systematic structural and compositional control, when investigated with an ensemble of electronic, X-ray synchrotron, and surface techniques, allows us to identify the critical short- (few-Å) and medium- (6–10 Å) range structural motifs that deliver exceptional hydrogen evolution reaction (HER) catalysis. Specifically, these HEAs exhibit both outstanding durability (240 h) and high mass activity (50 A/mgPGM) normalized to noble metal content, outperforming commercial Pt/C (3.18 A/mgPGM). This structural control over HEA morphology, and its direct association with changes in specific metallic oxidation states and pair–pair atomic structural features, provides new means and strategies for finely designing robust and sustainable electrocatalysts with a majority nonprecious metal composition.
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