fabrication of a direct -scheme photocatalyst by immobilizing CdS quantum dots in the channels of graphene-hybridized and supported mesoporous titanium nanocrystals for high photocatalytic performance under visible light.

We report the considerable advantages of direct -scheme photocatalysts by immobilizing high-quality CdS quantum dots (QDs) in the channels of graphene-hybridized and supported mesoporous titania (GMT) nanocrystals (CdS@GMT/GR) under facile hydrothermal conditions. The photocatalysts have been characterized by XRD, PL, XPS, SEM, DRS, TEM, EIS, and N adsorption. CdS QDs primarily serve as photosensitizers with a unique pore-embedded structure for the effective utilization of the light source. This direct -scheme CdS@GMT/GR exhibits higher photocatalytic activity than CdS/GR, GMT/GR, or CdS@MT. In addition, the rate constant of CdS@GMT/GR-2 is approximately twice the sum of those of CdS@MT and GMT/GR, because GR played the role of hole-transporting and collection layer as well as the hybridization level formation in terms of hybridizing MT and serving as a support. Therefore, the GR content tunes the energy band, affects the surface area, and controls the interfacial hole transfer and collection rate of the direct -scheme system. Furthermore, CdS@GMT/GR retains its high performance in repeated photocatalytic processes. This can be attributed to the fact that GR prevents QDs from photocorrosion by means of the hole-transporting and collection effect. A possible reaction mechanism is proposed. This work provides a promising strategy for the construction of highly efficient visible-light-driven photocatalysts to reduce the growing menace of environmental pollution.