Unique Features of the Photocatalytic Reduction of H2O and CO2 by New Catalysts Based on the Analogues of CdS, Cd4P2X3 (X = Cl, Br, I)

Abstract

Photochemical reduction of H2O and CO2 has been investigated with a new family of catalysts of the formula Cd4P2X3 (X= Cl, Br, I), obtained by the complete aliovalent substitution of the sulfide ions in CdS by P and X (Cl, Br, I). Unlike CdS, the Cd4P2X3 compounds exhibit hydrogen evolution and CO2 reduction from water even in the absence of a sacrificial agent or a cocatalyst. Use of NixPy as the cocatalyst, enhances hydrogen evolution, reaching 3870 (apparent quantum yield (AQY) = 4.11) and 9258 (AQY = 9.83) μmol h-1 g-1, respectively, under artificial and natural (sunlight) irradiation, in the case of Cd4P2Br3/NixPy. Electrochemical and spectroscopic studies have been employed to understand the photocatalytic activity of this family of compounds. Unlike most of the semiconductor-based photocatalysts, Cd4P2X3 catalysts reduce CO2 to CO and CH4 in the absence of sacrificial-agent or cocatalyst using water as the electron source. CO, CH4, and H2 have been obtained with these catalysts under artificial as well as sun-light irradiation. First-principles, calculations have been carried out to understand the electronic structure and catalytic features of these new catalysts.