摘要
Perovskite quantum dots (PQDs) have garnered significant attention as promising gain media for laser applications due to their excellent optical properties. However, the dynamic binding behavior of conventional long-chain insulating ligands (oleic acid/oleylamine, OA/OAm) to QD surfaces inherently generates unfavorable defect states, exacerbating nonradiative recombination and fundamentally limiting their optoelectronic performance. In this work, we report a facile room-temperature synthetic strategy for high-performance CsPbBr3 PQDs by utilizing β-cyclodextrin (β-CD) instead of a mixed OA/OAm solution as a ligand. The β-CD-encapsulated CsPbBr3 PQDs present a maximum of 556% enhancement in photoluminescence (PL) intensity under an ambient environment compared to the OA/OAm-ligand counterparts. The pump power-dependent PL measurements reveal a 38% higher internal quantum efficiency, and further analysis based on a Bose–Einstein statistical model indicates a reduced defect density and superior excitonic recombination in such β-CD-modified PQDs. Additionally, by employing the PQDs as a gain medium, we successfully demonstrate a room-temperature single-mode surface-emitting laser with stable outputs and a low lasing threshold. This work not only presents a significant step forward in PQD synthesis and surface ligand engineering but also provides guidance for developing high-performance optoelectronic devices.
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