Constructing a dual-functional 0D/2D-3D PtO/ZnIn2S4 photocatalyst for phenylcarbinol oxidation and H2 production under visible light

The efficient harnessing of photoexcited charge carriers in photocatalytic systems is essential for addressing contemporary energy and environmental challenges; however, significant obstacles remain in achieving high conversion efficiencies. This study introduces a novel 0D/2D-3D PtO/ZnIn 2 S 4 (PtO/ZIS) heterostructure photocatalyst, engineered to boost the separation and transfer of photoexcited charge carriers and drive the selective oxidation of phenylcarbinol (BA), concurrently producing hydrogen (H 2 ) in mild reaction conditions. The optimized formulation of 1 % PtO/ZIS demonstrated remarkable photocatalytic capabilities, attaining an H 2 evolution rate of 43.1 mmol g −1 h −1 with a 90.6 % selectivity for benzaldehyde (BAD). The mechanism exploration confirmed the photoexcited electrons on ZIS transferred to PtO to react with hydrogen protons to generate H 2 . While the photoexcited holes located on ZIS were used to selectively oxidize BA into value-added fine chemicals. This photocatalytic system surpasses traditional hole scavengers, such as lactic acid and sodium sulfide/sodium sulfite systems, in H 2 production efficiency. This investigation delves into the synergistic mechanisms facilitating photogenerated carrier utilization, which provides pivotal insights for the advancement of photocatalysts capable of dual functionalities: high-value chemical synthesis and clean energy generation. • 0D/2D-3D dual-function photocatalyst PtO/ZnIn 2 S 4 was constructed. • Photogenerated charges were efficient separated and utilized completely. • Clear energy H 2 and fine chemical benzaldehyde were simultaneous obtained. • Mechanisms of dual-function photocatalysis were studied systematically.