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Multiphase photocatalysts Pt/Cd 1− x Zn x S/ZnO/Zn(OH) 2 , Pt/Cd 1− x Zn x S/ZnO, and Pt/Cd 1− x Zn x S/Zn(OH) 2 were synthesized by a new two-step technique. The photocatalysts were characterized by a wide range of experimental techniques: X-ray diffraction, high-resolution transmission electron microscopy combined with energy-dispersive X-ray spectroscopy, low-temperature N 2 adsorption/desorption, and UV/VIS spectroscopy. The photocatalytic activity was tested in a batch reactor in the reaction of H 2 evolution from aqueous solutions of ethanol under visible light irradiation ( λ > 420 nm). The highest achieved photocatalytic activity was 2256 μmol H 2 per gram of photocatalyst per hour; the highest quantum efficiency was 10.4%. The activity of Pt/Cd 1− x Zn x S/Zn(OH) 2 was higher than that of Pt/Cd 1− x Zn x S/ZnO/Zn(OH) 2 and Pt/Cd 1− x Zn x S/ZnO. The explanation of enhanced activity of zinc–cadmium sulfide/ε-zinc hydroxide based on quantum calculations was suggested. [ABSTRACT FROM AUTHOR]

Novel composite photocatalysts consisting of a cadmium and zinc sulfide solid solution (Cd 0.6 Zn 0.4 S) and zinc sulfide (ZnS) nanoparticles were successfully prepared by a simple hydrothermal treatment of suspended Cd 0.3 Zn 0.7 S at 120 °C. The as-obtained materials were characterized by X-ray diffraction, X-ray photoelectron spectroscopy, and UV-VIS diffuse reflection spectroscopy. The obtained photocatalysts were tested in the photocatalytic evolution of hydrogen from a Na 2 S/Na 2 SO 3 aqueous solution under visible light irradiation (λ = 450 nm). It is shown that the hydrothermal treatment of Cd 0.3 Zn 0.7 S at 120 °C increases the activity by a factor of 7.5 due to the phase transformations of the solid solution with the formation of the multiphase Cd 0.6 Zn 0.4 S/ZnS sample. The deposition of gold on the surface of Cd 0.6 Zn 0.4 S/ZnS leads to a further increase in activity: the achieved photocatalytic activity and quantum efficiency (450 nm) for 1%Au/Cd 0.6 Zn 0.4 S/ZnS are 17.4 mmol g−1 h−1 and 42.6%, respectively. This excellent performance is found to be attributable to the transformation of Cd 1-x Zn x S from the cubic to the hexagonal phase during the hydrothermal treatment. Additionally, photoelectrodes based on Cd 0.6 Zn 0.4 S/ZnS and FTO were synthesized and tested in a two-electrode cell. A high value of the photocurrent equal to 0.5 mA/cm2 is achieved for the Cd 0.6 Zn 0.4 S/ZnS/FTO electrode. An investigation by means of impedance spectroscopy reveals the longer lifetime of photogenerated charge carriers in the Cd 0.6 Zn 0.4 S/ZnS/FTO photoelectrode if to compare with Cd 0.3 Zn 0.7 S/FTO system. Image 1 • Au/Cd 0.6 Zn 0.4 S/ZnS photocatalysts were prepared via simple hydrothermal synthesis. • The highest value of the photocatalytic activity was 17.4 mmol H 2 per hour per gram. • The highest apparent quantum efficiency was 42.6% (450 nm). • Photocurrent 0.5 mA/cm2 was achieved for the Cd 0.6 Zn 0.4 S/ZnS/FTO electrode. [ABSTRACT FROM AUTHOR]