Atomic Scale Engineering of Multivalence-State Palladium Photocatalyst for Transfer Hydrogenation with Water as a Proton Source.

Abstract

Hydrogenation reactions are fundamental in the fine chemical, pharmaceutical, and petrochemical industries, however heavily relying on H₂ gas at high temperatures and pressures, incurring large energy and carbon costs. Photocatalytic transfer hydrogenation, using water as a proton source, offers a greener alternative, but existing photocatalysts often suffer from modest yields, limited selectivity, and narrow substrate scope. Additionally, they often require co-activation, such as Mg-activated water or non-sustainable hydrogen feeds. Here, a photocatalyst is introduced that offers high yields and selectivities across a broad spectrum of organic compounds. The developed photocatalyst is a multivalence palladium superstructure with ultrasmall Pd⁰ nanoparticles enveloped by isolated Pd²⁺/Pd⁴⁺ atoms within a carbon-nitride matrix. Mechanistic studies reveal that the redox-flexible Pd single atoms, with triethylamine as an electronic modulator, attract photogenerated holes for water oxidation, while Pd⁰ nanoparticles facilitate hydrogen transfer to the unsaturated bonds of the organic molecules. The cooperative and dynamic behavior of Pd centers during catalysis, involving transitions among Pd⁺², Pd⁺³, and Pd⁺⁴ states, is validated using operando electron paramagnetic resonance spectroscopy. This multivalent palladium catalyst represents a conceptual advance in photocatalytic transfer hydrogenation with water as a hydrogen source, holding promise for sustainable hydrogenation processes in the chemical industry.