Carbon Dioxide Conversion to Methanol over Size-Selected Cu4 Clusters at Low Pressures
Author(s) -
Cong Liu,
Yang Bing,
Eric C. Tyo,
Sönke Seifert,
Janae DeBartolo,
Bernd von Issendorff,
Peter Zapol,
Štefan Vajda,
Larry A. Curtiss
Publication year - 2015
Publication title -
journal of the american chemical society
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 7.115
H-Index - 612
eISSN - 1520-5126
pISSN - 0002-7863
DOI - 10.1021/jacs.5b03668
Subject(s) - chemistry , catalysis , methanol , carbon dioxide , atmospheric pressure , ambient pressure , hydrogen , carbon monoxide , chemical engineering , inorganic chemistry , analytical chemistry (journal) , photochemistry , organic chemistry , thermodynamics , oceanography , physics , engineering , geology
The activation of CO2 and its hydrogenation to methanol are of much interest as a way to utilize captured CO2. Here, we investigate the use of size-selected Cu4 clusters supported on Al2O3 thin films for CO2 reduction in the presence of hydrogen. The catalytic activity was measured under near-atmospheric reaction conditions with a low CO2 partial pressure, and the oxidation state of the clusters was investigated by in situ grazing incidence X-ray absorption spectroscopy. The results indicate that size-selected Cu4 clusters are the most active low-pressure catalyst for catalytic CO2 conversion to CH3OH. Density functional theory calculations reveal that Cu4 clusters have a low activation barrier for conversion of CO2 to CH3OH. This study suggests that small Cu clusters may be excellent and efficient catalysts for the recycling of released CO2.
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