Solar hydrogen generation from organic substance using earth abundant CuS–NiO heterojunction semiconductor photocatalyst

This work explores the critical role of NiO co-catalyst assembled on the surface of a CuS primary photocatalyst which effectively improves interface properties and enhances solar-to-hydrogen production by prolonging lifetime of photo-excitons generated at the CuS surface. The nanoscale CuS/NiO heterojunction is formulated using hydrothermal and wet impregnation methods. The resultant CuS/NiO composite shows optical absorbance between 380 and 780 nm region. The type-II energetic structure formed at CuS/NiO heterojunction facilitates rapid charge separation and as a result, the CuS/NiO composite exhibits 13 folds higher photocatalytic water splitting performance than CuO and NiO. The champion CuO/NiO photocatalyst is first identified by screening the catalysts using a preliminary water splitting test reaction under natural Sunlight irradiation. After the optimization of the catalyst, it was further explored for enhanced photocatalytic hydrogen production using different organic substances dispersed in water (alcohols, amine and organic acids). The champion CuS/NiO catalyst (CPN-2) exhibited the photocatalytic hydrogen production rate of 52.3 mmol h^?1.g^?1_cat in the presence of lactic acid-based aqueous electrolyte and, it is superior than hydrogen production rate obtained in the presence of other organic substances (triethanolamine, glycerol, ethylene glycol, methanol) tested under identical experimental conditions. These results indicate that the energetic structure of CuS/NiO photocatalyst is favorable for photocatalytic oxidation or reforming of lactic acid. The oxidation of lactic acid contributes both protons and electrons for enhanced hydrogen generation as well as protects CuS from photocorrosion. The modification of surface property and energetic structure of CuS photocatalyst by the NiO co-catalyst improves photogenerated charge carrier separation and in turn enhances the solar-to-hydrogen generation efficiency. The recyclability tests showed the potential of CPN-2 photocatalyst for prolonged photocatalytic hydrogen production while continuous supply of lactic acid feedstock is available.     

Development of high quantum efficiency CdS/ZnS core/shell structured photocatalyst for the enhanced solar hydrogen evolution

Development of co-catalyst free, core/shell structured photocatalyst with ultra-thin shell is of great importance towards the stable and continuous hydrogen (H₂) production, where the shell prevents photo-corrosion of the core for longer stability with continuous H₂ generation. Accordingly, herein, we report a one-step, surfactant free hydrothermal process for synthesis of high-efficient CdS/ZnS core/shell structured catalyst for H₂ evolution under natural solar light. The structural and morphological characterizations using XRD and TEM techniques revealed the formation of phase pure CdS/ZnS system, with core and shell thickness of 395 and 15 nm, respectively. XPS studies revealed that the constituted elements in system exist in their native oxidation states, which indicated the stable structural integrity of the individual phase in the core/shell structure. The synergistic optical properties of CdS/ZnS showed the absorption edge around 500 nm and the decreased PL intensity indicated the improved charge recombination resistance in the system. The parametric studies such as synthesis time, core diameters and shell thickness optimization were conducted to study the formation kinetics of the core/shell structure and their photocatalytic efficiencies. Accordingly, the optimized core/shell catalyst showed around 763 and 2.4 folds superior activity when compared to the pristine CdS and ZnS, respectively. Further, the catalyst showed excellent stability for over 100 h with quantum efficiency of 8.78% under the irradiation of 20 W LED light at 420 nm. Based on the obtained results, the observed improved photocatalytic quantum efficiency could be ascribed to their synergistic effects of CdS and ZnS towards increased charge separation and spatial distributions of the carriers due to their core/shell configuration of the materials.