选择性
催化作用
固溶体
氧化物
甲醇
离解(化学)
材料科学
氢
异构化
金属
化学工程
无机化学
物理化学
化学
有机化学
工程类
作者
Jijie Wang,Chizhou Tang,Guanna Li,Zhe Han,Zelong Li,Hailong Liu,Cheng Feng,Can Li
出处
期刊:ACS Catalysis
[American Chemical Society]
日期:2019-10-04
卷期号:9 (11): 10253-10259
被引量:179
标识
DOI:10.1021/acscatal.9b03449
摘要
Hydrogenation of CO2 to methanol utilizing the hydrogen from renewable energy sources offers a promising way to reduce CO2 emissions through the CO2 utilization as a carbon source. However, it is a challenge to convert CO2 to methanol with high activity and high methanol selectivity. Herein, we report a class of metal-oxide solid-solution catalysts: MaZrOx (Ma = Cd, Ga), which show a methanol selectivity up to 80% with the CO2 single pass conversion reaching 4.3%–12.4% under the reaction conditions of H2/CO2 = 3/1, 24 000 h–1, 5 MPa. Structural and electronic characterizations combined with denisty functional theory calculations suggest that the Ma and Zr components in MaZrOx (Ma = Cd, Ga) solid-solution catalysts show a strong synergetic effect, which enhances the H2 heterolytic dissociation and results in high activity and high methanol selectivity. The solid-solution catalyst with dual metal oxide components offers an approach for the selective hydrogenation of CO2 to chemicals.
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