Sayago-Carro Rocío, Barba-Nieto Irene, Gómez-Cerezo Natividad, Rodriguez José A, Fernández-García Marcos, Kubacka Anna
Instituto de Catálisis y Petroleoquímica, CSIC, C/Marie Curie 2, 28049 Madrid, Spain.
Escuela de Doctorado, Universidad Autónoma de Madrid, Ciudad Universitaria de Cantoblanco, C/ Francisco Tomás y Valiente, 1, 28049 Madrid, Spain.
ACS Appl Mater Interfaces. 2024 Nov 13;16(45):62131-62141. doi: 10.1021/acsami.4c14280. Epub 2024 Nov 4.
The valorization of CO is an important challenge within the current panorama, since this molecule is probably the main contributor to climate change. In this study, the synthesis of materials based on a nanostructured batonnet-type indium oxide is carried out. In them, different amounts of Co are introduced, varying between 2 and 8% mol. It is verified that the most active sample in the transformation of carbon dioxide to carbon monoxide contains 6 mol %. of Co. This sample's activity under dual excitation exceeds the thermal counterpart by more than 30%. After carrying out a complete physical and chemical characterization with the help of X-ray absorption spectroscopy and other techniques, it is shown that catalysts with amounts of cobalt equal to or below 4 mol % contain isolated single-atom species, while those with higher amounts of metal display a Co-Co interaction which triggers the evolution of the samples under reaction conditions. The optimum control of this Co-Co interaction and the nature of the final cobalt-containing species determine dual photothermal catalytic properties. This work establishes a structure-activity relationship to interpret the catalytic behavior of highly dispersed subnanometric cobalt species, and thus an avenue to optimize the photothermal valorization of carbon dioxide.