三卤化物
纳米反应器
材料科学
纳米晶
钙钛矿(结构)
聚合物
卤化物
半导体
纳米技术
量子产额
光化学
化学工程
光电子学
化学
纳米颗粒
无机化学
光学
荧光
复合材料
物理
工程类
作者
Verena A. Hintermayr,Carola Lampe,Maximilian Löw,Janina Melanie Roemer,Willem Vanderlinden,Moritz Gramlich,Anton Böhm,Cornelia Sattler,Bert Nickel,Theobald Lohmüller,Alexander S. Urban
出处
期刊:Nano Letters
[American Chemical Society]
日期:2019-07-19
卷期号:19 (8): 4928-4933
被引量:71
标识
DOI:10.1021/acs.nanolett.9b00982
摘要
Halide perovskite nanocrystals (NCs) have shown impressive advances, exhibiting optical properties that outpace conventional semiconductor NCs, such as near-unity quantum yields and ultrafast radiative decay rates. Nevertheless, the NCs suffer even more from stability problems at ambient conditions and due to moisture than their bulk counterparts. Herein, we report a strategy of employing polymer micelles as nanoreactors for the synthesis of methylammonium lead trihalide perovskite NCs. Encapsulated by this polymer shell, the NCs display strong stability against water degradation and halide ion migration. Thin films comprising these NCs exhibit a more than 15-fold increase in lifespan in comparison to unprotected NCs in ambient conditions and even survive over 75 days of complete immersion in water. Furthermore, the NCs, which exhibit quantum yields of up to 63% and tunability of the emission wavelength throughout the visible range, show no signs of halide ion exchange. Additionally, heterostructures of MAPI and MAPBr NC layers exhibit efficient Förster resonance energy transfer (FRET), revealing a strategy for optoelectronic integration.
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