Position-selected cocatalyst modification on a Z-scheme Cd0.5Zn0.5S/NiTiO3 photocatalyst for boosted H2 evolution

Photocatalytic water splitting by semiconductors is a promising technology to produce clean H(2)fuel, but the efficiency is restrained seriously by the high overpotential of the H-2-evolution reaction together with the high recombination rate of photoinduced charges. To enhance H-2 production, it is highly desirable yet challenging to explore an efficient reductive cocatalyst and place it precisely on the right sites of the photocatalyst surface to work the proton reduction reaction exclusively. Herein, the metalloid NixP cocatalyst is exactly positioned on the Z-scheme Cd0.5Zn0.5S/NiTiO3 (CZS/NTO) heterostructure through a facile photodeposition strategy, which renders the cocatalyst form solely at the electron-collecting locations. It is revealed that the directional transfer of photoexcited electrons from Cd0.5Zn0.5S to NixP suppresses the quenching of charge carriers. Under visible light, the CZS/NTO hybrid loaded with the NixP cocatalyst exhibits an optimal H-2 yield rate of 1103 mu mol h(-1) (i.e., 27.57 mmol h(-1 )g(-1 )), which is about twofold of pristine CZS/NTO and comparable to the counterpart deposited with the Pt cocatalyst. Besides, the high apparent quantum yield (AQY) of 56% is reached at 400 nm. Further, the mechanisms of the cocatalyst formation and the H(2 )generation reaction are discussed in detail.