Abstract
In this paper, a series of Co(3)O(4)-Ag photocatalysts with different Ag loadings were synthesized by facile hydrothermal and in situ photoreduction methods and fully characterized by XRD, SEM, TEM, FTIR spectroscopy, XPS, UV-vis and PL techniques. The catalysts were used for the degradation of methyl orange (MO). Compared with the pure Co(3)O(4) catalyst, the Co(3)O(4)-Ag catalysts showed better activity; among these, the Co(3)O(4)-Ag-0.3 catalyst demonstrated the most efficient activity with 96.4% degradation efficiency after 30 h UV light irradiation and high degradation efficiency of 99.1% after 6 h visible light irradiation. According to the corresponding dynamics study under UV light irradiation, the photocatalytic efficiency of Co(3)O(4)-Ag-0.3 was 2.72 times higher than that of Co(3)O(4) under identical reaction conditions. The excellent photocatalytic activity of Co(3)O(4)-Ag can be attributed to the synergistic effect of strong absorption under UV and visible light, reduced photoelectron and hole recombination rate, and decreased band gap due to Ag doping. Additionally, a possible reaction mechanism over the Co(3)O(4)-Ag photocatalysts was proposed and explained.