钯
催化作用
甲醇
二氧化碳
化学
乙醇
金属
无机化学
大气压力
碳纤维
一氧化碳
氧化物
材料科学
有机化学
复合数
复合材料
地质学
海洋学
作者
Francisco J. Caparrós,Lluís Soler,Marta D. Rossell,Inmaculada Angurell,L. Piccolo,Oriol Rossell,Jordi Llorca
出处
期刊:Chemcatchem
[Wiley]
日期:2018-04-12
卷期号:10 (11): 2365-2369
被引量:112
标识
DOI:10.1002/cctc.201800362
摘要
Abstract The hydrogenation of CO 2 into value‐added chemicals is one of the most investigated methods to reduce CO 2 emissions in the atmosphere and thereby contributes to a sustainable chemical industry. Whereas the catalytic hydrogenation of CO 2 into methanol and synthetic hydrocarbons is well established, the effective and selective transformation of CO 2 into higher alcohols is still challenging. Here, we show that Pd single atoms anchored on the surface of Fe 3 O 4 are very active for the hydrogenation of CO 2 to ethanol at 300 °C, even at atmospheric pressure. By comparing various Pd/MO x catalysts, we conclude that the metal–oxide interface has a strong influence on catalytic behavior.
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