Highly active Pt/In2O3-ZrO2 catalyst for CO2 hydrogenation to methanol with enhanced CO tolerance: The effects of ZrO2

被引:97
作者
Sun, Kaihang [1 ]
Shen, Chenyang [1 ]
Zou, Rui [1 ]
Liu, Chang -jun [1 ,2 ]
机构
[1] Tianjin Univ, Sch Chem Engn & Technol, Tianjin 300350, Peoples R China
[2] Tianjin Univ, Collaborat Innovat Ctr Chem Sci & Engn, Tianjin 300072, Peoples R China
基金
中国国家自然科学基金;
关键词
CO2; hydrogenation; Methanol; CO tolerance; In2O3; Pt; Metal-support interaction; DFT study; SELECTIVE HYDROGENATION; OXIDE; DFT; DESIGN;
D O I
10.1016/j.apcatb.2022.122018
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
The supported Pt catalyst is normally not active for CO2 hydrogenation to methanol at the presence of CO. Herein, ZrO2 is added into Pt/In2O3 for CO2 hydrogenation to methanol with CO as a co-feed gas. High activity with enhanced CO tolerance is achieved on Pt/In2O3-ZrO2. For example, the space-time yield of methanol reaches 0.569 g(methanol) g(cat)(-1) h(-1 )at 300 degrees C and 5 MPa under feed gas containing 4% CO of 21,000 cm(3).h(-1)g(cat)(-1). With the addition of ZrO2, a stronger electron transfer occurs between Pt and the In2O3-ZrO2 solid solution support. This leads to weaker CO adsorption, which suppresses over-reduction of In2O3 and enhances CO tolerance of the Pt catalyst. The oxygen vacancy of In2O3 modified by ZrO2 promotes CO2 activation. The synergy between Zrmodified oxygen vacancy (In-O-v-Zr) and Pt catalyst facilitates methanol synthesis from CO2 hydrogenation via formate route. This is different from Pt/In2O3, which takes CO hydrogenation route.
引用
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页数:12
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