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具有高熵合金位点的介孔纳米球的定制设计用于高效氧化还原电催化

Tailored Design of Mesoporous Nanospheres with High Entropic Alloy Sites for Efficient Redox Electrocatalysis.

作者信息

Nandan Ravi, Nara Hiroki, Nam Ho Ngoc, Phung Quan Manh, Ngo Quynh Phuong, Na Jongbeom, Henzie Joel, Yamauchi Yusuke

机构信息

Research Center for Materials Nanoarchitectonics, National Institute for Materials Science (NIMS), 1-1 Namiki, Tsukuba, Ibaraki, 305-0044, Japan.

Waseda Research Institute for Science and Engineering, Waseda University, 3-4-1 Okubo, Shinjuku, Tokyo, 169-8555, Japan.

出版信息

Adv Sci (Weinh). 2024 Sep;11(35):e2402518. doi: 10.1002/advs.202402518. Epub 2024 Jul 19.

Abstract

High Entropy Alloys (HEAs) are a versatile material with unique properties, tailored for various applications. They enable pH-sensitive electrocatalytic transformations like hydrogen evolution reaction (HER) and hydrogen oxidation reactions (HOR) in alkaline media. Mesoporous nanostructures with high surface area are preferred for these electrochemical reactions, but designing mesoporous HEA sis challenging. To overcome this challenge, a low-temperature triblock copolymer-assisted wet-chemical approach is developed to produce mesoporous HEA nanospheres composed of PtPdRuMoNi systems with sufficient entropic mixing. Owing to active sites with inherent entropic effect, mesoporous features, and increased accessibility, optimized HEA nanospheres promote strong HER/HOR performance in alkaline medium. At 30 mV nominal overpotential, it exhibits a mass activity of ≈167 (HER) and 151 A g (HOR), far exceeding commercial Pt-C electrocatalysts (34 and 48 A g ) and many recently reported various alloys. The Mott-Schottky analysis reveals HEA nanospheres inherit high charge carrier density, positive flat band potential, and smaller charge transfer barrier, resulting in better activity and faster kinetics. This micelle-assisted synthetic enable the exploration of the compositional and configurational spaces of HEAs at relatively low temperature, while simultaneously facilitating the introduction of mesoporous nanostructures for a wide range of catalytic applications.

摘要

高熵合金(HEAs)是一种具有独特性能的多功能材料,适用于各种应用。它们能够实现pH敏感的电催化转化,如碱性介质中的析氢反应(HER)和氢氧化反应(HOR)。具有高表面积的介孔纳米结构对于这些电化学反应是优选的,但设计介孔高熵合金具有挑战性。为了克服这一挑战,开发了一种低温三嵌段共聚物辅助的湿化学方法,以制备由具有足够熵混合的PtPdRuMoNi体系组成的介孔高熵合金纳米球。由于具有固有熵效应的活性位点、介孔特征和增加了的可及性,优化后的高熵合金纳米球在碱性介质中促进了强大的HER/HOR性能。在30 mV的标称过电位下,它表现出约167(HER)和151 A g(HOR)的质量活性,远远超过商业Pt-C电催化剂(34和48 A g)以及许多最近报道的各种合金。莫特-肖特基分析表明,高熵合金纳米球具有高电荷载流子密度、正平带电位和较小的电荷转移势垒,从而具有更好的活性和更快的动力学。这种胶束辅助合成能够在相对较低的温度下探索高熵合金的组成和构型空间,同时促进介孔纳米结构的引入,以用于广泛的催化应用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3354/11425213/cbd727bfb2ea/ADVS-11-2402518-g007.jpg

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