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碳质辅助受限合成难熔高熵合金纳米复合材料及其在海水电解中的应用。

Carbonaceous-assisted confinement synthesis of refractory high-entropy alloy nanocomposites and their application for seawater electrolysis.

作者信息

Wang Xiaoming, Peng Qianqian, Zhang Xilin, Lv Xucheng, Wang Xin, Fu Yongzhu

机构信息

College of Chemistry and Center of Green Catalysis, Zhengzhou University, Zhengzhou 450001, PR China.

School of Physics, Henan Normal University, Xinxiang 453007, China.

出版信息

J Colloid Interface Sci. 2022 Feb;607(Pt 2):1580-1588. doi: 10.1016/j.jcis.2021.08.201. Epub 2021 Sep 10.

DOI:10.1016/j.jcis.2021.08.201
PMID:34587532
Abstract

Refractory high-entropy alloy nanocomposites (HEA-NPs) are important class of materials with unique structure and potential applications. Although several synthetic methods have been reported, developing novel routes to prepare nanoscale HEA-based catalysts facilely is still urgently desired. This work takes advantage of confinement assisted arc and plasma shock (APS) to prepare a series of HEA-NPs by regulating the type and proportion of metal precursors. The phase constitutes and morphology of the HEA-NPs are fully characterized. The prepared refractory HEA-NPs possesses five highly dispersed metal components, including titanium (Ti), niobium (Nb), tantalum (Ta), chromium (Cr), molybdenum (Mo) and simultaneously exhibits an uniform hexagonal morphology of nanocrystals. By taking advantage of its unique corrosion resistance, TiNbTaCrMo HEA-NPs can function as a promising candidate for electrocatalytic hydrogen evolution reaction (HER) in natural seawater. And its catalytic performance after alloying is significantly enhanced compared with the elemental metal. Theoretically, the promoted HER activity can be attributed to the strong adsorption for the various metal components in HEA-NPs caused by the upshifting d-band center close to the Fermi level. Furthermore, this confinement strategy can be further extended to synthesize other HEA-NPs. Our strategy provides a novel method to synthesize various HEA-NPs for further catalytic application.

摘要

难熔高熵合金纳米复合材料(HEA-NPs)是一类具有独特结构和潜在应用价值的重要材料。尽管已经报道了几种合成方法,但仍迫切需要开发新颖的路线来轻松制备基于纳米级HEA的催化剂。这项工作利用受限辅助电弧和等离子体冲击(APS),通过调节金属前驱体的类型和比例来制备一系列HEA-NPs。对HEA-NPs的相组成和形态进行了全面表征。所制备的难熔HEA-NPs拥有五个高度分散的金属组分,包括钛(Ti)、铌(Nb)、钽(Ta)、铬(Cr)、钼(Mo),并且同时呈现出均匀的六方纳米晶体形态。利用其独特的耐腐蚀性,TiNbTaCrMo HEA-NPs可作为天然海水电催化析氢反应(HER)的有前景候选物。并且与元素金属相比,其合金化后的催化性能显著增强。理论上,HER活性的提高可归因于靠近费米能级的d带中心上移导致HEA-NPs中各种金属组分的强吸附。此外,这种受限策略可进一步扩展以合成其他HEA-NPs。我们的策略为合成各种用于进一步催化应用的HEA-NPs提供了一种新方法。

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