Visible light-driven CO2 photoreduction by a Re(I) complex immobilized onto CuO/Nb2O5 heterojunctions

Gabriela N Silva; Leandro A Faustino; Lucas L Nascimento; Osmando F Lopes; Antonio Otavio T Patrocinio

doi:10.1063/5.0178945

Visible light-driven CO2 photoreduction by a Re(I) complex immobilized onto CuO/Nb2O5 heterojunctions

J Chem Phys. 2024 Jan 21;160(3):034701. doi: 10.1063/5.0178945.

Authors

Gabriela N Silva¹, Leandro A Faustino¹, Lucas L Nascimento¹, Osmando F Lopes¹, Antonio Otavio T Patrocinio¹

Affiliation

¹ Laboratory of Photochemistry and Materials Science, LAFOT-CM, Universidade Federal de Uberlândia, 38400-902 Uberlândia, MG, Brazil.

PMID: 38226823
DOI: 10.1063/5.0178945

Abstract

The immobilization of Re(I) complexes onto metal oxide surfaces presents an elegant strategy to enhance their stability and reusability toward photocatalytic CO2 reduction. In this study, the photocatalytic performance of fac-[ClRe(CO)3(dcbH2)], where dcbH2 = 4,4'-dicarboxylic acid-2,2'-bipyridine, anchored onto the surface of 1%m/m CuO/Nb2O5 was investigated. Following adsorption, the turnover number for CO production (TONCO) in DMF/TEOA increased significantly, from ten in solution to 370 under visible light irradiation, surpassing the TONCO observed for the complex onto pristine Nb2O5 or CuO surfaces. The CuO/Nb2O5 heterostructure allows for efficient electron injection by the Re(I) center, promoting efficient charge separation. At same time CuO clusters introduce a new absorption band above 550 nm that contributes for the photoreduction of the reaction intermediates, leading to a more efficient CO evolution and minimization of side reactions.