Luo Langli, Nian Yao, Wang Shuangbao, Dong Zejian, He Yang, Han You, Wang Chongmin
Institute of Molecular Plus, Tianjin Key Laboratory of Molecular Optoelectronic Sciences, Department of Chemistry, Tianjin University, 92 Weijin Road, Tianjin, 300072, China.
School of Chemical Engineering and Technology, Tianjin University and Collaborative Innovation Center of Chemical Science and Chemical Engineering (Tianjin), Tianjin, 300350, China.
Angew Chem Int Ed Engl. 2020 Feb 3;59(6):2505-2509. doi: 10.1002/anie.201915024. Epub 2019 Dec 30.
By using in situ aberration-corrected environmental transmission electron microscopy, for the first time at atomic level, the dynamic evolution of the Cu surface is captured during CO oxidation. Under reaction conditions, the Cu surface is activated, typically involving 2-3 atomic layers with the formation of a reversible metastable phase that only exists during catalytic reactions. The distinctive role of CO and O in the surface activation is revealed, which features CO exposure to lead to surface roughening and consequently formation of low-coordinated Cu atoms, while O exposure induces a quasi-crystalline CuOx phase. Supported by DFT calculations, it is shown that crystalline CuOx reversibly transforms into the amorphous phase, acting as an active species to facilitate the interaction of gas reactants and catalyzing CO oxidation.
通过使用原位像差校正环境透射电子显微镜,首次在原子水平上捕捉到了CO氧化过程中Cu表面的动态演变。在反应条件下,Cu表面被激活,通常涉及2至3个原子层,并形成仅在催化反应期间存在的可逆亚稳相。揭示了CO和O在表面激活中的独特作用,其特征是CO暴露导致表面粗糙化并因此形成低配位的Cu原子,而O暴露诱导准晶CuOx相。在DFT计算的支持下,结果表明结晶CuOx可逆地转变为非晶相,作为促进气体反应物相互作用并催化CO氧化的活性物种。