物理吸附
化学吸附
范德瓦尔斯力
化学
分子
化学物理
吸附
过渡金属
一氧化碳
化学键
密度泛函理论
原子物理学
物理化学
计算化学
催化作用
有机化学
物理
作者
Fritz Huber,Julian Berwanger,S. Polesya,Sergiy Mankovsky,H. Ebert,Franz J. Gießibl
出处
期刊:Science
[American Association for the Advancement of Science (AAAS)]
日期:2019-10-11
卷期号:366 (6462): 235-238
被引量:77
标识
DOI:10.1126/science.aay3444
摘要
Surface molecules can transition from physisorption through weak van der Waals forces to a strongly bound chemisorption state by overcoming an energy barrier. We show that a carbon monoxide (CO) molecule adsorbed to the tip of an atomic force microscope enables a controlled observation of bond formation, including its potential transition from physisorption to chemisorption. During imaging of copper (Cu) and iron (Fe) adatoms on a Cu(111) surface, the CO was not chemically inert but transited through a physisorbed local energy minimum into a chemisorbed global minimum, and an energy barrier was seen for the Fe adatom. Density functional theory reveals that the transition occurs through a hybridization of the electronic states of the CO molecule mainly with s-, p z -, and d z2-type states of the Fe and Cu adatoms, leading to chemical bonding.
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