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在环境条件下,通过氧取代自发掺杂 MoS 单层的基面。

Spontaneous doping of the basal plane of MoS single layers through oxygen substitution under ambient conditions.

机构信息

Hungarian Academy of Sciences, Centre for Energy Research, Institute of Technical Physics and Materials Science, 2DNanoelectronics Lendület Research Group, Budapest, Hungary.

Hungarian Academy of Sciences, Centre for Energy Research, Institute for Energy Security and Environmental Safety, Surface Chemistry and Catalysis Department, Budapest, Hungary.

出版信息

Nat Chem. 2018 Dec;10(12):1246-1251. doi: 10.1038/s41557-018-0136-2. Epub 2018 Sep 17.

Abstract

The chemical inertness of the defect-free basal plane confers environmental stability to MoS single layers, but it also limits their chemical versatility and catalytic activity. The stability of pristine MoS basal plane against oxidation under ambient conditions is a widely accepted assumption however, here we report single-atom-level structural investigations that reveal that oxygen atoms spontaneously incorporate into the basal plane of MoS single layers during ambient exposure. The use of scanning tunnelling microscopy reveals a slow oxygen-substitution reaction, during which individual sulfur atoms are replaced one by one by oxygen, giving rise to solid-solution-type 2D MoSO crystals. Oxygen substitution sites present all over the basal plane act as single-atom reaction centres, substantially increasing the catalytic activity of the entire MoS basal plane for the electrochemical H evolution reaction.

摘要

无缺陷基面的化学惰性赋予了 MoS 单层环境稳定性,但也限制了它们的化学多功能性和催化活性。然而,人们普遍认为,原始 MoS 基面在环境条件下不易氧化,而我们在此报告的单原子级结构研究揭示,在环境暴露过程中,氧原子会自发地掺入 MoS 单层的基面中。扫描隧道显微镜的使用揭示了一个缓慢的氧取代反应,在此过程中,单个硫原子一个接一个地被氧取代,形成固溶体型二维 MoSO 晶体。整个基面的氧取代位作为单原子反应中心,极大地提高了电化学析氢反应中整个 MoS 基面的催化活性。

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