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
Atom(片上系统)
氧化物
材料科学
有机化学
复合材料
计算机科学
嵌入式系统
地质学
海洋学
复合数
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:101
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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