催化作用
选择性
格式化
X射线光电子能谱
傅里叶变换红外光谱
甲醇
无机化学
高分辨率透射电子显微镜
吸附
材料科学
红外光谱学
化学
化学工程
物理化学
透射电子显微镜
纳米技术
有机化学
工程类
作者
Qian Chen,Shengyan Meng,Rui Liu,Xiaohan Zhai,Xinkui Wang,Li Wang,Hongchen Guo,Yanhui Yi
标识
DOI:10.1016/j.apcatb.2023.123422
摘要
Herein, we report a CuO-MgO/Beta catalyst, which exhibits 72.0% methanol selectivity with 8.5% CO2 conversion in plasma-catalytic CO2 hydrogenation at ambient conditions (30 °C and 0.1 MPa). The catalysts have been systematically characterized by XRD, H2-TPR, HRTEM, STEM, XPS, CO2-TPD and NH3-TPD to study the interaction between CuO and MgO, as well as physicochemical properties of the catalysts. Furthermore, in-situ Optical Emission Spectroscopy (OES) and in-situ Fourier Transform Infrared Spectroscopy (FTIR) were employed to investigate the active species in gas-phase and on catalyst surface. The excellent selectivity of the CuO-MgO/Beta catalyst is attributed to synergy between MgO and CuO species. The strong interaction between CuO and MgO leads to electron transfer from MgO to CuO, which is favorable for partially reduction of CuO to form Cu2O active sites. Furthermore, MgO strongly adsorb CO2 to form formate species, which suppresses CO generation and leads to CO2 hydrogenation through Formate pathway for CH3OH production.
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