光致发光
钙钛矿(结构)
量子点
材料科学
半最大全宽
带隙
发光
量子产额
光电子学
纳米技术
光学
化学
结晶学
物理
荧光
作者
Shasha Li,Guanchen Liu,Qun Liu,Lanjian Nie,Guanpeng Yao,Fanming Zeng,Yaoting He,Weidong Xiang
出处
期刊:ACS Sustainable Chemistry & Engineering
[American Chemical Society]
日期:2020-07-08
被引量:7
标识
DOI:10.1021/acssuschemeng.0c03914
摘要
The instability of all-inorganic perovskites and poor understanding of the photoluminescence mechanisms have hindered their practical applications. While a large body of work on 3-D perovskite phases is available in the literature, the promising zero-dimensional (0-D) phase perovskite materials are still poorly understood. Herein, we report a new synthesis method for the production of 0-D Cs4PbBr6 perovskite quantum dots (QDs) in glass using a combination of Cs2CO3 concentration and heat-treatment temperature optimization. The differences in structure, morphology, and photoluminescence (PL) between the 0-D Cs4PbBr6 QDs and the 3-D CsPbBr3 QDs in glass were studied in detail. Cs4PbBr6 QD glass with high transmittance displayed a blue-shift PL emission centered at 503 nm, a narrow full width at half-maximum (fwhm, ∼20 nm), a high photoluminescence quantum yield (PLQY, ∼22%), and excellent long-term stability, thereby, advancing the study of these materials. It was demonstrated that Cs4PbBr6 displayed unique luminescent properties in correlation with the intrinsic defect states in the mid-band gap.
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