量子点
化学
激子
俄歇效应
超快激光光谱学
玻尔半径
光谱学
吸收(声学)
猝灭(荧光)
多激子产生
分子物理学
光电子学
原子物理学
螺旋钻
荧光
物理
光学
凝聚态物理
量子力学
作者
Gaoyuan Yang,Liu Leo Liu,Shuang Shi,Xin Zhang,Ying Liang,Guijie Liang
标识
DOI:10.1002/jccs.202100161
摘要
Abstract As closely related to exciton quenching, Auger recombination (AR) is very important to colloidal semiconductor quantum dots (QDs) in applications such as lasing, solar energy conversion, and light‐emitting diodes. It is beneficial to understand the kinetic mechanism of AR. In this article, colloidal CdSe QDs with a narrow range of diameters, 2.7, 2.5, 2.3, 2.2, and 2.0 nm, are synthesized by adequately modulating the reaction temperature and time during hot injection synthesis. With sizes less than the Bohr exciton radius, the resultant collision probability differs for various CdSe QDs attributed to the varying extent of the spatial confinement effect. To analyze the bi‐exciton AR in these QDs, the ultrafast time‐resolved absorption spectrum is utilized to derive the bi‐exciton lifetime ( τ BX ) in high precision as a function of QD size. The τ BX varying with volume ( V ) obeys the universal scaling law; that is, τ BX = γV . In our experiments, the scaling factor γ is 1.649 ± 0.097 ps/nm 3 . This study could provide further insight for understanding the theory of the AR process and rational design of optoelectronic devices based on colloidal QDs.
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