催化作用
X射线光电子能谱
电子顺磁共振
氧气
吸附
解吸
化学工程
无机化学
铜
分子
化学
物理化学
有机化学
核磁共振
工程类
物理
作者
Wei Chen,Jue Xu,Fajun Huang,Chaoying Zhao,Yingqiao Guan,Yarong Fang,Jinpeng Hu,Weiwei Yang,Zhu Luo,Yanbing Guo
标识
DOI:10.1016/j.apsusc.2023.156539
摘要
It is well documented that the existence of oxygen vacancies and active Cu species can improve CO oxidation activity over TiO2 substrate. Herein, TiO2-supported copper catalysts (CuOx/TiO2) with different ratio of oxygen vacancies (Ov) and Cu+ has been synthesized. The existence and amount of Ov and Cu+ species were characterized by transmission electron microscopy (TEM), X-ray photoelectron spectroscopy (XPS) and electron paramagnetic resonance spectrum (EPR). The synergetic effect between Cu+ and oxygen vacancies was investigated in terms of O2 temperature-programmed desorption (O2–TPD), H2 temperature-programmed reduction (H2–TPR) and in situ DRIFTS spectra. Cu+ is the adsorption site for CO molecules, the abundant Ov can significantly activate molecular oxygen, which effectively oxidize the adsorbed CO molecules. The most suitable ratio between Cu+ and Ov has been confirmed. The CuOx/TiO2(Cu+ rich) catalyst (51% Cu+, 26.3% Ov) shows superior CO oxidation activity (T90 = 136 °C) compared to CuOx/TiO2(Ov rich) catalyst (39% Cu+, 28.5% Ov, T90 > 350 °C). This work provides comprehensive investigation of the role for abundant oxygen vacancies and Cu+ in CO oxidation reactions.
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