三碘化物
钙钛矿(结构)
量子点
光致发光
X射线光电子能谱
材料科学
量子产额
纳米晶
三辛基氧化膦
纳米技术
光谱学
化学
化学工程
光电子学
物理化学
结晶学
光学
物理
有机化学
色素敏化染料
萃取(化学)
电极
电解质
工程类
量子力学
荧光
作者
Chang Lü,Hui Li,Kathy Kolodziejski,Chaochao Dun,Wenxiao Huang,David Carroll,Scott M. Geyer
出处
期刊:Nano Research
[Springer Science+Business Media]
日期:2017-07-12
卷期号:11 (2): 762-768
被引量:111
标识
DOI:10.1007/s12274-017-1685-1
摘要
In recent years, significant attention has been paid to perovskite materials. In particular, lead triiodide-based perovskites have exhibited superb optoelectronic properties. Enhancing the stability of these materials is an essential step towards large-scale applications. In this study, by simply adding trioctylphosphine (TOP) as part of the post-synthesis treatment, we significantly enhance the stability of CsPbI3 quantum dots (QDs) in the solution phase, which otherwise decay rapidly in hours. For CsPbI3 QDs treated with TOP, the absorption and photoluminescence emission properties are unchanged over the course of weeks, and the quantum yield remains almost constant at 30% even after 1 month. The morphologies of both treated and untreated QDs are initially cubic; however, the treated QDs largely maintain their initial size and shape, while the untreated ones lose size uniformity, which is a sign of degradation. Infrared spectroscopy and X-ray photoelectron spectroscopy confirm the presence of P in the TOP-treated QDs. We insights that help to resolve the intrinsic instability issue of triiodide perovskite materials and devices.
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