氧化物
金属
相(物质)
原子单位
材料科学
渗透(战争)
吸附
化学工程
化学物理
基质(水族馆)
动力学
化学反应
水蒸气
无机化学
化学
冶金
物理化学
有机化学
工程类
地质学
物理
海洋学
量子力学
生物化学
运筹学
作者
Zejian Dong,Qingye Ren,Shuangbao Wang,Lifeng Zhang,Langli Luo
标识
DOI:10.1021/acs.jpclett.1c02008
摘要
Metal oxidation initiates from surface adsorption to subsurface and bulk reaction through continuous interfacial phase transformation from metals to oxides. How the initial interfacial process affects the whole process of metal oxidation remains largely elusive because of the lack of direct observation of the evolving interface. Here, through in situ atomic-scale environmental TEM observations of Cu surface reaction in water vapor, we demonstrate that the interfacial strain between the substrate and growing oxide is coupled into the continuing chemical reaction that determines the reaction kinetics. Atomic imaging of the reaction process in real time reveals that the growing oxides could temporarily possess a disordered CuOx phase to lower its interfacial strain with Cu substrate and can transform to a crystalline Cu2O phase later. This flexibility of the oxide phase results from the strong chemomechanical coupling during the interfacial phase transformation, which enhances the oxide penetration into the metal under water vapor.
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