Affiliation:
1. School of Electronic Information and Electrical Engineering Shanghai Jiao Tong University Shanghai People's Republic of China
2. College of Biological Chemical Science and Engineering Jiaxing University Jiaxing China
3. Department of Chemical Engineering, School of Chemistry and Chemical Engineering Shanghai Jiao Tong University Shanghai China
4. Shanghai Blood Center Shanghai China
Abstract
AbstractHerein, we explore how OH groups on Pt/γ‐AlOOH and Pt/γ‐Al2O3 catalysts affect CO2 hydrogenation with H2 at temperatures from 250°C to 400°C. OH groups are abundant on γ‐AlOOH, but rare at Pt‐(γ‐AlOOH) interface which is the most favorable site for CO2 conversion on Pt/γ‐AlOOH. This makes CO2 hydrogenation on Pt/γ‐AlOOH form CO weakly bonding to γ‐AlOOH, which prefers to desorption from Pt/γ‐AlOOH rather than further conversion, thus enhancing CO production on Pt/γ‐AlOOH. Different from Pt/γ‐AlOOH, OH groups are abundant at Pt‐(γ‐Al2O3) interface which is the most favorable site for CO2 conversion on Pt/γ‐Al2O3. This promotes CO2 hydrogenation on Pt/γ‐Al2O3 to form CO strongly bonding to Pt, which prefers to further hydrogenation to CH4, and thereby increases CH4 selectivity on Pt/γ‐Al2O3. Therefore, the OH groups at metal‐support interface are crucial factor influencing product distribution, and must be considered seriously when fabricating catalysts.
Funder
National Natural Science Foundation of China
Subject
General Chemical Engineering,Environmental Engineering,Biotechnology
Cited by
6 articles.
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