Transition Metal Chalcogenides/Nonconjugated Polymer Artificial Photosystems for Photoredox Catalysis

Surface charge transfer doping (SCTD) has been established as an efficient strategy to achieve strong electronic coupling interactions between semiconductors and dopants, which lead to highly efficient electron transport over semiconductors. Herein, we report a facile, easily accessible, and effective SCTD strategy to exquisitely modulate the interfacial charge transfer over transition metal chalcogenides (TMCs: CdS, Zn0.5Cd0.5S, CdIn2S4, and ZnIn2S4) through surface modification with a nonconjugated polymer, poly(dimethyldiallylammonium chloride) (PDDA). We provide evidence that PDDA, as a surface electron transfer acceptor, can be used to enable rapid, directional, and tunable charge transfer along with an optimal charge lifetime over TMCs in photoredox catalysis because of the high-efficiency electron-trapping property of quaternary ammonium functional groups in the molecular structure of PDDA. The thus-assembled PDDA-encapsulated TMC composite artificial photosystems demonstrate significantly enhanced and versatile photoredox catalytic activities toward visible-light-responsive photocatalytic reduction of aromatic nitro compounds, photocatalytic oxidation of aromatic alcohols, and photocatalytic H2 production, wherein the ultrathin PDDA layer accelerates the interfacial charge transport and separation rate over TMC substrates. Moreover, it was evidenced that such an interface engineering strategy is general for a collection of TMCs. Our work will provide conceptual insights into nonconjugated polymer-based artificial photosystems for optimizing solar energy utilization.