School of Environmental Science and Engineering, Shanghai Jiao Tong University, 800 Dongchuan Road, Shanghai 200240, China.
Nanoscale. 2019 Feb 7;11(6):2602-2607. doi: 10.1039/c8nr09350d.
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.
全无机铯铅卤钙钛矿量子点(PQDs)表面的高动态结合配体很容易丢失或脱离,导致光学性质和稳定性恶化,这是 PQDs 实际存储和应用的最大挑战之一。在此,我们报告了一种简便的金属离子辅助配体表面工程策略,通过顺序短链配体(二正十二烷基二甲基氯化铵硫代硫酸盐,DDA+-S2-)交换和随后的金属盐(In(Ac)3)处理,同时提高 CsPbBr3 PQDs 的光致发光量子产率和稳定性。通过对关键金属离子作用的详细表征,发现这些增强源于金属离子附着在 PQDs 表面上所引起的促进配体覆盖。考虑到缩短的配体和坚固的表面钝化,修饰后的 CsPbBr3 PQDs 在电致发光器件中表现出显著增强的性能。我们的研究结果为高质量和稳定的钙钛矿量子点的表面配体工程及其有效的光电应用提供了深入的认识。