卤化物
纳米晶
硫系化合物
钙钛矿(结构)
光伏
材料科学
铯
离子
发光
纳米技术
量子点
光电子学
化学
无机化学
光伏系统
结晶学
有机化学
生物
生态学
作者
Aidi Zhang,Chaoqing Dong,Jicun Ren
标识
DOI:10.1021/acs.jpcc.7b00343
摘要
Colloidal cesium lead halide nanocrystals (CsPbX3, where X = Cl, Br, and I) are newcomer optoelectronic materials and have been successfully utilized as bright light sources and high-efficiency photovoltaics due to their facial solution processability. However, detailed understanding of their fundamental chemistry and photophysics behavior are urgently required for utilizing the full potential of the perovskite nanocrystals. In this work, we described a simple and efficient approach for regulating the blinking behavior of the CsPbX3 nanocrystals through varying halide composition. We systematically investigated the ensemble and single-particle optical properties of the mixed-halide CsPbBrxI3–x and CsPbBr3–yIy nanocrystals via two different anion-exchange routes (Br– ions → I– ions and I– ions → Br– ions). The power-law fitting results demonstrated that both the "on" and "off" events of their fluorescence exhibited a similar power-law rule to those of the cadmium chalcogenide nanocrystals (e.g., CdSe nanocrystals). Under optimum conditions, the percentage of "non-blinking" CsPbBr3–yIy nanocrystals (the "on time" fraction >99% of the observation time) was about 71%. Furthermore, we observed that the blinking behavior of the perovskite nanocrystals also could be regulated by directly mixing two different perovskite nanocrystals. These findings will provide new insights in realizing the full potential of these substances in photovoltaic and optoelectronic applications.
科研通智能强力驱动
Strongly Powered by AbleSci AI