“…[1,8] However, the wide bandgap energy of TiO 2 (E g � 2.0-3.2 eV) and rapid recombination of photogenerated charge carriers limits its photocatalytic efficiency to only the UV range of light, which make up only about 3-5% of the whole solar light spectrum. [8] To extend the light absorption range, prolong the lifetimes of photoexcited electron-hole pairs and enhance the photocatalytic activity of TiO 2 , various strategies have been employed, such as surface modification, [10] bandgap engineering by doping with a transition metals (Cr, Mn, Co, Zn, Ni, Fe) [11][12][13] and non-metals (N, P, S, C, B, etc. ), [14][15][16][17] plasmonic coupling (Au, Ag, Pt and Pd) [18][19][20][21] and coupling with other semiconductors (ZnO, WO 3 , SrTiO 3 , SnO 2 , CdS, ZnS, CdSe, Cu 2 O and MoS 2 ).…”