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Critical role of metal ions in surface engineering toward brightly luminescent and stable cesium lead bromide perovskite quantum dots

机译:金属离子在表面工程的关键作用对明亮发光稳定的铯溴化铅钙钛矿量子点

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摘要

The highly dynamic binding ligands on the surface of all-inorganic cesium lead halide perovskite quantum dots (PQDs), which can be easily lost or detached leading to a deterioration in the optical properties and stability, are one of the greatest challenges for the practical storage and application of PQDs. Herein, we report a facile metal ion-assisted ligand surface engineering strategy to synchronously boost the photoluminescence quantum yield and stability of CsPbBr3 PQDs by a sequential short-chain ligand (didodecyl dimethylammonium sulfide, DDA(+)-S2-) exchange and subsequent metal salt (In(Ac)(3)) treatment. From detailed characterization of the critical role of the metal ions, these enhancements were found to originate from the promoted ligand capping induced by the metal ions attached on the surface of the PQDs. Considering the shortened ligands and robust surface passivation, the modified CsPbBr3 PQDs exhibit drastically enhanced performance in an electroluminescent device. Our results have provided an insightful understanding of surface ligand engineering for high-quality and stable perovskite QDs and their effective optoelectronic applications.
机译:高度动态绑定表面配体all-inorganic铯的卤化铅钙钛矿量子点(PQDs),可以很容易丢失或分离导致恶化光学特性和稳定的一个实际存储和最大挑战PQDs中的应用。金属ion-assisted配体表面工程同步推进的策略光致发光量子产率和稳定的CsPbBr3 PQDs顺序短链配体(didodecyl dimethylammonium硫化,DDA (+) s2 -)交换和随后的金属盐((Ac) (3))治疗。关键作用的金属离子,这些增强被发现源自促进了配位金属离子引发的限制附加表面的PQDs。缩短配体和健壮的表面钝化,修改后的CsPbBr3 PQDs展览大大提高性能的电致发光装置。提供了一个深刻的理解配体工程高质量和稳定量子点钙钛矿及其有效的光电应用程序。

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