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In-depth understandings of charge carrier transfer dynamics in any artificial catalytic system are of critical importance for the future design of highly efficient photocatalysts. Herein, we synthesized sub-monolayer ZnSe partial-shell coated CdSe/CdS core/shell quantum dots in a controlled fashion. The ZnSe decorated quantum dots were employed as a model catalyst for photogeneration of H2 under light illumination. Both theoretical calculations and experimental results unravel that the growth of ZnSe partial-shell would retard the photogenerated electron transfer, and meanwhile, accelerate the corresponding hole migration process during the H2 photogeneration reaction in the artificial photocatalytic system. As such, the performance of the relevant photocatalytic system can be modulated and optimized, and accordingly, a plausible underlying mechanism is rationalized. [ABSTRACT FROM AUTHOR]

Semiconductor quantum dots (QDs) have attracted tremendous attention in the field of photocatalysis, owing to their superior optoelectronic properties for photocatalytic reactions, including high absorption coefficients and long photogenerated carrier lifetimes. Herein, by choosing 2‐(3,4‐dimethoxyphenyl)‐3‐oxobutanenitrile as a model substrate, we demonstrate that the stereoselective (>99 %) C−C oxidative coupling reaction can be realized with a high product yield (99 %) using zwitterionic ligand capped CsPbBr3 perovskite QDs under visible light illumination. The reaction can be generalized to different starting materials with various substituents on the phenyl ring and varied functional moieties, producing stereoselective dl‐isomers. A radical mediated reaction pathway has been proposed. Our study provides a new way of stereoselective C−C oxidative coupling via a photocatalytic means using specially designed perovskite QDs. [ABSTRACT FROM AUTHOR]