激子
比克西顿
量子点
飞秒
分子物理学
钙钛矿(结构)
谱线
吸收光谱法
吸收(声学)
带隙
光致发光
材料科学
原子物理学
化学
凝聚态物理
物理
激光器
光电子学
光学
结晶学
量子力学
作者
Anja Barfüßer,Sebastian Rieger,Arun K. Dey,Ahmet Tosun,Quinten A. Akkerman,Tushar Debnath,Jochen Feldmann
出处
期刊:Nano Letters
[American Chemical Society]
日期:2022-10-17
卷期号:22 (22): 8810-8817
被引量:6
标识
DOI:10.1021/acs.nanolett.2c02223
摘要
Quantum dots (QDs) offer unique physical properties and novel application possibilities like single-photon emitters for quantum technologies. While strongly confined III-V and II-VI QDs have been studied extensively, their complex valence band structure often limits clear observations of individual transitions. In recently emerged lead-halide perovskites, band degeneracies are absent around the bandgap reducing the complexity of optical spectra. We show that for spherical-like CsPbBr3 QDs with diameters >6 nm, excitons confine with respect to their center-of-mass motion leading to well-pronounced resonances in their absorption spectra. Optical pumping of the lowest-confined exciton with femtosecond laser pulses not only bleaches all excitons but also reveals a series of distinct induced absorption resonances which we attribute to exciton-to-biexciton transitions and are red-shifted by the biexciton binding energy (∼40 meV). The temporal dynamics of the bleached excitons further support our exciton confinement model. Our study provides the first insight into confined excitons in CsPbBr3 QDs and gives a detailed understanding of their linear and nonlinear optical spectra.
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