Explores hole transfer dynamics in perovskite nanocrystals, suggesting enhanced efficiency for solar cells.
Over the past decade, lead halide perovskites have shown an excellent promise for photovoltaic applications. To maximize their efficiency, understanding the electron/hole separation and transfer processes is crucial. A key focus is identifying effective hole acceptors; our research explores the hole acceptor ability of CuBr with various bromide‐based green‐emitting APbBr 3 (A = FA, MA, Cs) perovskite nanocrystals (NCs). We observed significant photoluminescence (PL) quenching and fast PL decay in the presence of CuBr, indicating a strong interaction between the two species. The energy levels of the NCs align with CuBr’s HOMO–LUMO levels, and ultrafast pump–probe experiments reveal quick hole transfer from photoexcited APbBr 3 NCs to CuBr, with time constants of 100 ps for FAPbBr 3 , 125 ps for CsPbBr 3 , and 176 ps for MAPbBr 3 NCs. This rapid hole extraction is attributed to the strong CuBr anchoring on the NCs surface, highlighting how a simple halide salt can enhance charge carrier transfer and advance the development of affordable solar cells.
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Gautam et al. (2026) studied this question.
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