比克西顿
激子
俄歇效应
超快激光光谱学
钙钛矿(结构)
多激子产生
物理
红移
超短脉冲
化学物理
纳米晶
光谱学
螺旋钻
原子物理学
凝聚态物理
量子点
材料科学
分子物理学
化学
激光器
光电子学
光学
结晶学
量子力学
银河系
作者
J. Aneesh,Abhishek Swarnkar,Vikash Kumar Ravi,Rituraj Sharma,Angshuman Nag,K. V. Adarsh
标识
DOI:10.1021/acs.jpcc.7b00762
摘要
Exciton many-body interaction is the fundamental light–matter interaction that determines the optical response of the new class of colloidal perovskite nanocrystals of the general formula CsPbX3 [X = Cl, Br, or I]. However, the understanding of exciton many-body interactions manifested through the transient biexcitonic Stark effect at the early time scales and the Auger recombination process in this new class of materials still remains rather incomplete. In this Article, we studied the many-body exciton interactions under controlled conditions through ultrafast transient absorption spectroscopy. A large biexcitonic redshift ∼30 meV to the effect of hot excitations on the excitonic resonance is observed at the early time scales. From the fluence-dependent studies, it is evident that the samples have only single and biexciton lifetimes, suggesting that the band edges are 2-fold degenerate. This explicit experimental evidence for the exciton many-body interactions in CsPbBr3 nanocrystals provides a powerful tool to explore the development of their prospective applications in light-emitting devices, lasers, and solar cells.
科研通智能强力驱动
Strongly Powered by AbleSci AI