Green hydrogen and acetaldehyde production via photo-induced thermal dehydrogenation of bioethanol over a highly dispersed CuS/ TiO2 catalyst

The emergence of global warming issues has triggered the interest in producing carbon-neutral energy sources and fossil-based chemicals from affordable and renewable feedstocks (e.g., bio-ethanol). Herein, the synthesis of highly dispersed CuS/TiO 2 photothermal catalysts is reported for simultaneously converting ethanol into hydrogen and acetaldehyde under simulated sunlight. The catalyst achieved a hydrogen evolution rate of 51.61 mmol g −1 h −1 and an acetaldehyde production rate of 48.63 mmol g −1 h −1 , with a maximal acetaldehyde selectivity of 97% among carbon-containing products. Compared to pristine TiO 2 , the introduction of plasmonic CuS largely extended the light adsorption range and enhanced the photothermal performance, whilst the formation of heterojunction structure improved the charge transfer and separation efficiency. The density functional theory calculation results demonstrate that CuS/TiO 2 composite interfaces could significantly lower the activation energy of ethanol dehydrogenation reaction and improve hydrogen evolution reaction ability. This study provides deep insight into understanding and optimizing hot carrier dynamics in photothermal catalytic systems. • Novel CuS/TiO 2 catalyst for efficient ethanol dehydrogenation to co-produce hydrogen and acetaldehyde under mild conditions. • 0.05 CuS/TiO 2 achieved a H 2 evolution rate of 51.61 mmol g −1 h −1 and an acetaldehyde production rate of 48.63 mmol g −1 h −1 . • Synergistic effects of heterojunction and significant photothermal effect induced by CuS enhanced catalytic performance. • Reduced activation energy for ethanol dehydrogenation and improved H 2 evolution were achieved by CuS/TiO2 interface.