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Designing a heterojunction semiconductor is an efficient strategy to extend the light response of a photocatalyst to the visible range and thus improve photocatalytic activity. Starting with mesoporous anatase TiO 2 microspheres, mesoporous TiO 2 /g-C 3 N 4 microspheres were prepared via a facile nanocoating procedure, with the porous TiO 2 as the active supporting scaffold and g-C 3 N 4 (3 wt %) as the visible light sensitizer. Heterojunctions formed at the TiO 2 /g-C 3 N 4 interfaces separated photogenerated charges. The TiO 2 surface (64.4 m 2 g –1 ) was mostly covered by a photoactive g-C 3 N 4 layer, while the interconnected porous network featured a large pore volume (0.30 cm 3 g –1 ) for mass diffusion. The g-C 3 N 4 precursor, cyanamide, a nitrogen-rich molecule, also acted as a nitrogen source to form TiO 2– x N x . Substitution of N in the TiO 2 lattice triggered a visible light response due to an additional N level above the TiO 2 valence band that resulted in band gap narrowing to 1.5 eV. Compared with mesoporous g-C 3 N 4, the composite microspheres were 8.5 times more active in degrading phenol under visible light irradiation. A mechanism was proposed for the TiO 2 /g-C 3 N 4 heterojunction incorporated within the mesoporous structure that enhanced the photocatalytic properties.
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Wei et al. (2017) studied this question.
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