화학공학소재연구정보센터
Catalysis Today, Vol.356, 570-578, 2020
Electronic structure modulating for supported Rh catalysts toward CO2 methanation
Methanation of carbon dioxide is a promising approach to ameliorate greenhouse effect. Rhodium based catalysts have been intensively investigated due to its ability in cleavage of C-O bond, but the role of support in the catalysts was underestimated. In this regard, we explored the methanation of CO2 over Rh catalysts with three metal oxide supports (TiO2, Al2O3, and ZnO). It was found that Rh/TiO2 exhibited the highest catalytic activity with product yield of 455 mmol g(cat)-(1) h(-1) (CH4 and CO) at 370 degrees C and 2 MPa, which is 2 and 14 times higher than Rh/Al2O3 and Rh/ZnO, respectively. Moreover, the CH4 selectivity over Rh/TiO2 was higher than 95 %. The superior catalytic performance of Rh/TiO2 can be mainly attributed to its unique electronic structure associated with stronger Rh-TiO2 interaction and the existence of Ti3+ ions on TiO2.