量子产额
光致发光
钙钛矿(结构)
钝化
量子点
材料科学
配体(生物化学)
溶剂
纳米技术
化学工程
化学
光电子学
有机化学
光学
物理
荧光
工程类
生物化学
受体
图层(电子)
作者
Fengjun Chun,Binbin Zhang,Yuchen Li,Wen Li,Meilin Xie,Xiaodong Peng,Cheng Yan,Zi Chen,Haitao Zhang,Weiqing Yang
标识
DOI:10.1016/j.cej.2020.125715
摘要
Methyl-ammonium lead iodide (MAPbI3) perovskite quantum dots (QDs) have emerged as a promising material for photoelectronic, however, they usually suffer intrinsically from the environmental instability and low photoluminescence quantum yield (PLQY), which will seriously impede their commercial applications. Here, we report an internal-external combination strategy by lowering the dose of good solvent and reducing the chain length of amine ligand to simultaneously enhance the air stability and PLQY of MAPbI3 QDs. The low-dose solvent can effectively reduce internal iodine vacancies defects and external residual solvent molecules, meanwhile, the faster and denser assembly of nimble short-chain (SC) ligand on the MAPbI3 QDs surface can helpfully enhance the external surface passivation. As a result, compared to MAPbI3 QDs synthesized by traditional ligand-assisted reprecipitation (LARP) method, the air stability and PLQY of which are improved by more than four orders of magnitude (from a few minutes to dozens of days) and nearly two times (from 42% to 80%) prepared by our strategy. Besides, this strategy can widely tune the color of MAPbX3 (X = Cl, Br, I) QDs from 388 to 735 nm through regulating components. This internal-external combination strategy can provide some beneficial enlightenment for preparing long-term air-stable hybrid perovskite QDs with high PLQY, which drastically driving their commercial applications.
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