Authors: Lopez-Caballero, Patricia; Hauser, Andreas W.; de Lara-Castells, Maria Pilar

Contribution: Article

Journal: JOURNAL OF PHYSICAL CHEMISTRY C

Publication date: 2019/09/19

DOI: 10.1021/acs.jpcc.9b06620

Abstract: In this work, we explore the decomposition of CO, on unsupported and TiO2-supported Cu, clusters via computational modeling, using both finite cluster and periodic slab structures of the rutile TiO2(110) surface. While the energy needed for C = O bond breaking is already significantly reduced upon adsorption onto the unsupported metal catalyst (it drops from 7.8 to 1.3 eV), gas desorption before bond activation is still the inevitable outcome due to the remaining barrier height even at 0 K. However, when the Cu-5 cluster itself is supported on TiO2, reactant and product adsorption is strongly enhanced, the barrier for bond breaking is further reduced, and a spontaneous decomposition of the Molecule is predicted. This finding is linked to our previous work on charge-transfer processes in the Cu-5 TiO2 system triggered by solar photons, since a combination of both phenomena at suitable temperatures would allow for a photoinduced activation of CO2 by sunlight.