甲醛
扫描隧道显微镜
金红石
分子
化学
结晶学
化学物理
材料科学
纳米技术
有机化学
作者
Ke Zhu,Yaobiao Xia,Miru Tang,Zhi‐Tao Wang,Bryan Jan,Igor Lyubinetsky,Qingfeng Ge,Zdenek Dohnálek,Kenneth T. Park,Zhenrong Zhang
标识
DOI:10.1021/acs.jpcc.5b04781
摘要
Direct imaging of site-specific reactions of individual molecules as a function of temperature has been a long-sought goal in molecular science. Here, we report the direct visualization of molecular coupling of formaldehyde on reduced rutile TiO2(110) surfaces as we track the same set of molecules using scanning tunneling microscopy (STM) when the temperature is increased from 75 to 170 K. Our previous study showed that formaldehyde preferably adsorbs at bridging-bonded oxygen (Ob) vacancy (VO) defect site. Herein, images from the same area as the temperature is increased show that VO-bound formaldehyde couples with Ti-bound formaldehyde forming a diolate intermediate. Consequently, exposure of formaldehyde at room temperature leads to diolate as the majority species on the surface, and no VO-bound formaldehyde is observed. The diolate species are the key reaction intermediates in the formation of ethylene reported in previous ensemble-averaged studies.
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