Precisely Modulating the Photosensitization Efficiency of Transition-Metal Chalcogenide Quantum Dots toward Solar Water Oxidation.

Precisely modulating the spatial charge migration/separation constitutes the central issue in dictating the solar conversion efficiency of photoelectrochemical (PEC) cells, whereas it still remains a grand challenge. Here, we conceptually demonstrate the construction of hierarchically ordered metal oxide (MO)/transition-metal chalcogenide quantum dots (TMC QDs) multilayered heterostructured photoanodes, that is, MO/[TMC QDs(+)/TMC QDs(-)] (TMC QDs: CdTe, CdSe, CdS), by a simple and general bottom-up self-assembly route. Tailor-made intrinsically oppositely charged TMC QDs are alternately deposited on the highly ordered MO via a generic ligand-triggered electrostatic interaction to craft heterostructured photoanodes. The charge-transfer pathway stimulated by the photosensitization of TMC QDs is finely tuned by the assembly sequence. The advantageous multilayered nanoarchitecture renders the MO/[TMC QDs(+)/TMC QDs(-)] photoanodes exhibit substantially enhanced PEC performances under light irradiation, owing to the applicable energy-level configuration and peculiar combination fashion between building blocks and considerably boosted interfacial charge separation resulting from generating spatial tandem charge transport. Furthermore, photosensitization efficiency comparison among TMC QDs is comprehensively performed with PEC mechanisms elucidated.