钙钛矿(结构)
纳米晶
材料科学
纳米结构
胶束
卤化物
纳米技术
费斯特共振能量转移
化学工程
光电子学
化学
荧光
光学
无机化学
水溶液
物理化学
物理
工程类
作者
Michèle G. Greiner,Andreas Singldinger,Nina A. Henke,Carola Lampe,Ulrich Leo,Moritz Gramlich,Alexander S. Urban
出处
期刊:Nano Letters
[American Chemical Society]
日期:2022-08-08
卷期号:22 (16): 6709-6715
被引量:13
标识
DOI:10.1021/acs.nanolett.2c02108
摘要
Outstanding optoelectronic properties and a facile synthesis render halide perovskite nanocrystals (NCs) a promising material for nanostructure-based devices. However, the commercialization is hindered mainly by the lack of NC stability under ambient conditions and inefficient charge carrier injection. Here, we investigate solutions to both problems, employing methylammonium lead bromide (MAPbBr_3) NCs encapsulated in diblock copolymer core-shell micelles of tunable size. We confirm that the shell does not prohibit energy transfer, as FRET efficiencies between these NCs and 2D CsPbBr_3 nanoplatelets (NPLs) reach 73.6%. This value strongly correlates to the micelle size, with thicker shells displaying significantly reduced FRET efficiencies. Those high efficiencies come with a price, as the thinnest shells protect the encapsulated NCs less from environmentally induced degradation. Finding the sweet spot between efficiency and protection could lead to the realization of tailored energy funnels with enhanced carrier densities for high-power perovskite NC-based optoelectronic applications.
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