等离子体子
催化作用
离解(化学)
光化学
氧气
氧化还原
材料科学
反应机理
机制(生物学)
热电子
热的
化学物理
光催化
化学
电子
化学工程
纳米技术
光电子学
无机化学
物理化学
物理
有机化学
气象学
工程类
量子力学
作者
Ke Wang,Mengyu Cao,Jiangbo Lu,Ying Lü,Cher Hon Lau,Ying Zheng,Xianfeng Fan
标识
DOI:10.1016/j.apcatb.2021.120341
摘要
Using solar energy to promote the thermocatalytic CO2 conversion is a promising way to reduce the energy consumption and increase the sustainability. Au/TiO2 is known for its good catalytic activity in both thermo- and photo- catalytic CO2 conversion, however both the reaction mechanisms in dark and in photo-thermo coupled reaction condition remain unclear. In this work, the operando isotope-labelled spectroscopic and computational analyses are combined to clarify these mechanisms. The redox mechanism that CO2 direct dissociation at the oxygen vacancy (VO) is found as the main reaction pathway of CO2 hydrogenation over Au/TiO2. The plasmonic enhancement mechanism is proven to be the hot electrons facilitated VO generation at interface. The clear understandings of reaction pathway and plasmonic enhancement mechanism are helpful for the future design of photo-thermal CO2 conversion catalysts.
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