Researchers have made efforts to develop high-productivity photocatalysts for photocatalytic hydrogen production to reduce the problem of a lack of energy. Bulk semiconductor photocatalysts mainly endure particular limitations, such as low visible light application, a quick recombination rate of electron-hole pairs, and poor photocatalytic efficiency. The major challenge is to improve solar-light-driven heterostructure photocatalysts that are highly active and stable under the photocatalytic system. In this study, the proposed nano-heterojunction exhibits a great capacity for hydrogen production (871.2 μmol g-1 h-1), which is over 8.1-fold and 12.3-fold higher than that of the bare MoS2 and bare α-Fe2O3 samples, respectively. It is demonstrated that the MoS2/α-Fe2O3 heterojunction gives rise to an enhanced visible light response and accelerated photoinduced charge carrier separation. This work provides an improved visible light absorption efficiency and a narrowed energy band gap, and presents a "highway" for electron-hole pairs to promote transfer and inhibit the combination of photoinduced charge carriers for the utilization of nano-heterojunction photocatalysts in the field of hydrogen production.
Keywords: MoS2/α-Fe2O3; heterojunction; photocatalytic hydrogen evolution (PHE).