Copper-ceria solid solution with improved catalytic activity for hydrogenation of CO2 to CH3OH

被引:57
|
作者
Yang, Bin [1 ]
Deng, Wei [1 ]
Guo, Limin [1 ]
Ishihara, Tatsumi [2 ,3 ]
机构
[1] Huazhong Univ Sci & Technol, Sch Environm Sci & Engn, Wuhan 430074, Hubei, Peoples R China
[2] Kyushu Univ, Int Inst Carbon Neutral Energy Res, Nishi Ku, 744 Motooka, Fukuoka 8190395, Japan
[3] Kyushu Univ, Fac Engn, Dept Appl Chem, Nishi Ku, 744 Motooka, Fukuoka 8190395, Japan
基金
国家重点研发计划; 中国国家自然科学基金;
关键词
Copper-ceria; Solid solution; CO2; hydrogenation; Methanol; Active site; METHANOL SYNTHESIS; CU/ZNO/AL2O3; CATALYSTS; SURFACE-AREA; OXIDATION; H-2; IDENTIFICATION; CHEMISORPTION; INTERFACE; TOLUENE; SITES;
D O I
10.1016/S1872-2067(20)63605-1
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
A copper-ceria solid solution and ceria-supported copper catalysts were prepared and used for the catalytic hydrogenation of CO2 to CH3OH. According to site-specific classification and quantitative analyses (X-ray diffraction, Raman spectroscopy, X-ray photoelectron spectroscopy, H-2 temperature-programmed reduction, and CO adsorption), the interfaces of the prepared catalysts were classified as Cu incorporated into ceria (Cu-Ov-Cex), dispersed CuO (D-CuO-CeO2), and bulk CuO (B-CuO-CeO2) over the CeO2 surface. These results, together with those of activity tests, showed that the Cu-Ov-Cex species was closely related to the CO2 hydrogenation activity and resulted in a much higher turnover frequency of CH3OH production than that observed with the D-CuO-CeO2 and B-CuO-CeO2 species. Thus, the copper-ceria solid solution exhibited improved activity due to the higher Cu-Ov-Cex fraction. (c) 2020, Dalian Institute of Chemical Physics, Chinese Academy of Sciences. Published by Elsevier B.V. All rights reserved.
引用
收藏
页码:1348 / 1359
页数:12
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