Potassium electrochemical optimization of the MoS2 catalytic hydrogen evolution reaction performance†

IF 4.3 2区 化学 Q2 CHEMISTRY, MULTIDISCIPLINARY
Sizhuo Feng , Yan Tu , Qingfeng Zhang , Lingbin Xie , Shujuan Liu , Longlu Wang , Qiang Zhao
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引用次数: 0

Abstract

This study presents a flexible self-supporting C@MoSx@pCNF electrode, prepared via potassium electrochemical intercalation, which fragments MoS2 into smaller, amorphous nanoparticles. The amorphous MoSx shows enhanced active sites and superior hydrophilic/aerophobic properties. The electrode demonstrates excellent HER performance with a low overpotential of 51 mV at 10 mA cm−2 and a Tafel slope of 77 mV dec−1, offering a new strategy for improving MoS2 catalysis.
二硫化钼催化析氢反应性能的钾电化学优化
过渡金属二硫化物,特别是二硫化钼(MoS2)因其资源丰富、成本低、催化活性高等特点而日益受到人们的关注。然而,诸如团聚、导电性差和低活性位点密度等挑战限制了它们在析氢反应(HER)中的应用。本研究提出了一种柔性自支撑催化电极C@MoSx@pCNF,该电极是通过钾电化学插层制备的。这种方法将包裹在导电碳中的二硫化钼纳米片分解成更小的片层,将其转化为非晶结构。与结晶MoS2相比,无定形MoSx表现出活性位点增加,超亲水性和超疏水性增强。在酸性条件下,C@MoSx@pCNF电极在电流密度为10 mA cm-2、Tafel斜率为77 mV dec1时的过电位为51 mV,突出了其优异的HER性能,为提高MoS2的催化效率提供了新的途径。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Chemical Communications
Chemical Communications 化学-化学综合
CiteScore
8.60
自引率
4.10%
发文量
2705
审稿时长
1.4 months
期刊介绍: ChemComm (Chemical Communications) is renowned as the fastest publisher of articles providing information on new avenues of research, drawn from all the world''s major areas of chemical research.
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