摘要
3D mesoporous black TiO 2-x /Ag nanosphere coupled with 2D g-C 3 N 4 sheet ternary heterojunctions are successfully fabricated through a facile evaporation-induced self-assembly (EISA) process and photodeposition method, followed by a mild calcination (350 °C) under an argon atmosphere after an in situ solid-state chemical reduction strategy. The resultant mesoporous black TiO 2-x /Ag/g-C 3 N 4 ternary heterojunctions with narrow band gap of ∼ 2.27 eV possess a relative high specific surface area of ∼ 100 m 2 g −1 , main pore size of 6.2 nm and the highest visible-light-driven photocatalytic property for degradation of methyl orange (97%) and methylene blue (99%). The apparent reaction rate constants (k) of mesoporous black TiO 2-x /Ag/g-C 3 N 4 for methyl orange and methylene blue are ∼ 9 and 11 times higher than that of pristine TiO 2 . The possible mechanism is proposed, and the excellent photocatalytic property can be ascribed to the introduction of Ti 3+ self-doping and g-C 3 N 4 , which favor the visible light absorption and the separation of electron-hole pairs, the surface plasma resonance effect of Ag nanoparticle, and the mesoporous networks offer more surface active sites.
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