State-resolved exciton dynamics in quantum dots

被引:1
作者
Kambhampati, Patanjali [1 ]
机构
[1] McGill Univ, Dept Chem, Montreal, PQ H3A 2K6, Canada
来源
PHYSICAL CHEMISTRY OF INTERFACES AND NANOMATERIALS IX | 2010年 / 7758卷
关键词
quantum dot; nanocrystal; exciton; multi-exciton; hot electron; Auger relaxation; multiple exciton generation; SEMICONDUCTOR NANOCRYSTALS; OPTICAL GAIN; CLUSTERS;
D O I
10.1117/12.862016
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
The elementary excitation in semiconductor quantum dots is the exciton, an excited electron-hole pair. The size and geometry of the dot confines the exciton thereby yielding quantum confinement effects. The simplest examples of size quantization effects include the spectrum of single exciton states which dominate the linear absorption spectrum and the Stokes shift for the spontaneous photoluminescence spectrum. Here, we report on our recent results exploring the structure and dynamics of both single excitons and multi-excitons in colloidal CdSe quantum dots using femtosecond state-resolved pump/probe spectroscopy. These experiments have revealed tremendous insight into the relaxation pathways of hot excitons, new aspects of exciton-phonon interactions, and in the first observation of the electronic structure of multi-excitons.
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页数:9
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