Co₃O₄/BiVO₄ Heterostructures for Photochemical Water Oxidation: The Role of Synthesis Parameters and Preparation Route for the Physico-Chemical Properties and the Catalytic Activity

Abstract

The synthesis conditions of the semiconductor BiVO4 have marked influence on its physicochemical and photocatalytic properties. In this work, a pH-controlled co-precipitation route was systematically investigated. Special attention was paid to the pH value during co-precipitation and co-precipitate post-treatment. In a sacrificial photocatalytic water oxidation test, the highest activity was observed for a sample precipitated at pH = 1 and 70 °C, which was post treated at 600 °C in air for 3 h after washing and drying. The activity was further improved by another 90% by the addition of the Co3O4-based co-catalyst. Good synergy between semiconductor and co-catalyst was obtained for the deposition of pre-formed nanoparticles at a loading of 0.1 w% (physical impregnation). The effects of different synthesis conditions of the semiconductor and impregnation method for the co-catalyst on the structure, morphology and optical properties of the catalysts were investigated by PXRD, SEM, UV-vis spectroscopy, and TEM, while the water oxidation activity was compared in the dark and with the aid of visible light using cerium (IV) or silver (I) as sacrificial agents, respectively, with the aim of establishing structure-activity correlations. The roles of semiconductor particle anisotropy and co-catalyst particle distribution for optimal photo-activity in the oxygen evolution reaction are discussed.