材料科学
量子点
光降解
光致发光
光谱学
钙钛矿(结构)
量子产额
傅里叶变换红外光谱
超快激光光谱学
悬空债券
猝灭(荧光)
吸收(声学)
吸收光谱法
光化学
纳米技术
光电子学
荧光
化学工程
光学
化学
光催化
催化作用
硅
生物化学
量子力学
复合材料
工程类
物理
作者
Rui An,Fengying Zhang,Xianshao Zou,Yingying Tang,Mingli Liang,I. V. Oshchapovskyy,Yuchen Liu,Alireza Honarfar,Yunqian Zhong,Chuanshuai Li,Huifang Geng,Junsheng Chen,Sophie E. Canton,Tõnu Pullerits,Kaibo Zheng
标识
DOI:10.1021/acsami.8b14480
摘要
All-inorganic CsPbI3 perovskite quantum dots (QDs) have attracted intense attention for their successful application in photovoltaics (PVs) and optoelectronics that are enabled by their superior absorption capability and great photoluminescence (PL) properties. However, their photostability remains a practical bottleneck and further optimization is highly desirable. Here, we studied the photostability of as-obtained colloidal CsPbI3 QDs suspended in hexane. We found that light illumination does induce photodegradation of CsPbI3 QDs. Steady-state spectroscopy, X-ray diffraction, Fourier transform infrared spectroscopy, transmission electron microscopy, and transient absorption spectroscopy verified that light illumination leads to detachment of the capping agent, collapse of the CsPbI3 QD surface, and finally aggregation of surface Pb0. Both dangling bonds containing surface and Pb0 serve as trap states causing PL quenching with a dramatic decrease of PL quantum yield. Our work provides a detailed insight about the correlation between the structural and photophysical consequences of the photodegradation process in CsPbI3 QDs and may lead to the optimization of such QDs toward device applications.
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