激子
飞秒
比克西顿
量子点
光激发
离域电子
硫系化合物
超短脉冲
材料科学
凝聚态物理
超快激光光谱学
化学物理
分子物理学
纳米技术
光电子学
物理
原子物理学
光学
激光器
激发态
量子力学
作者
Zhilong Zhang,Jooyoung Sung,Daniel T. W. Toolan,Sanyang Han,Raj Pandya,Michael P. Weir,James Xiao,Simon Dowland,Mengxia Liu,Anthony J. Ryan,Richard Jones,Shujuan Huang,Akshay Rao
出处
期刊:Nature Materials
[Springer Nature]
日期:2022-03-07
卷期号:21 (5): 533-539
被引量:48
标识
DOI:10.1038/s41563-022-01204-6
摘要
Quantum dot (QD) solids are an emerging platform for developing a range of optoelectronic devices. Thus, understanding exciton dynamics is essential towards developing and optimizing QD devices. Here, using transient absorption microscopy, we reveal the initial exciton dynamics in QDs with femtosecond timescales. We observe high exciton diffusivity (~102 cm2 s-1) in lead chalcogenide QDs within the first few hundred femtoseconds after photoexcitation followed by a transition to a slower regime (~10-1-1 cm2 s-1). QD solids with larger interdot distances exhibit higher initial diffusivity and a delayed transition to the slower regime, while higher QD packing density and heterogeneity accelerate this transition. The fast transport regime occurs only in materials with exciton Bohr radii much larger than the QD sizes, suggesting the transport of delocalized excitons in this regime and a transition to slower transport governed by exciton localization. These findings suggest routes to control the optoelectronic properties of QD solids.
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