钙钛矿(结构)
兴奋剂
卤化物
存水弯(水管)
量子点
电荷(物理)
载流子
材料科学
化学物理
凝聚态物理
化学
光电子学
物理
无机化学
结晶学
量子力学
气象学
作者
Jie Meng,Zhenyun Lan,Mohamed Abdellah,Bin Yang,Susanne Mossin,Mingli Liang,Maria Naumova,Qi Shi,Sol Gutiérrez Álvarez,Yang Liu,Weihua Lin,Ivano E. Castelli,Sophie E. Canton,Tõnu Pullerits,Kaibo Zheng
标识
DOI:10.1021/acs.jpclett.0c01050
摘要
Transition-metal ion doping has been demonstrated to be effective for tuning the photoluminescence properties of perovskite quantum dots (QDs). However, it would inevitably introduce defects in the lattice. As the Mn concentration increases, the Mn dopant photoluminescence quantum yield (PLQY) first increases and then decreases. Herein the influence of the dopant and the defect states on the photophysics in Mn-doped CsPbCl3 QDs was studied by time-resolved spectroscopies, whereas the energy levels of the possible defect states were analyzed by density functional theory calculations. We reveal the formation of deep interstitials defects (Cli) by Mn2+ doping. The depopulation of initial QD exciton states is a competition between exciton-dopant energy transfer and defect trapping on an early time scale (
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