极化子
钙钛矿(结构)
量子点
光激发
激子
化学物理
材料科学
激发态
凝聚态物理
光致发光
纳米技术
物理
光电子学
化学
原子物理学
电子
量子力学
结晶学
作者
Juno Kim,Yuanze Xu,David Bain,Mingxing Li,Mircea Cotlet,Qiuming Yu,Andrew J. Musser
出处
期刊:ACS Nano
[American Chemical Society]
日期:2023-11-07
卷期号:17 (22): 23079-23093
被引量:1
标识
DOI:10.1021/acsnano.3c08748
摘要
The polaron is an essential photoexcitation that governs the unique optoelectronic properties of organic-inorganic hybrid halide perovskites, and it has been subject to extensive spectroscopic and theoretical investigation over the past decade. A crucial but underexplored question is how the nature of the photogenerated polarons is impacted by the microscopic perovskite structure and what functional properties this affects. To tackle this question, we chemically tuned the interactions between perovskite quantum dots (QDs) to rationally manipulate the polaron properties. Through a suite of time-resolved spectroscopies, we find that inter-QD interactions open an excited-state channel to form large polaron species, which exhibit enhanced spatial diffusion, slower hot polaron cooling, and a longer intrinsic lifetime. At the same time, polaronic excitons are formed in competition via localized band-edge states, exhibiting strong photoluminescence but are limited by shorter intrinsic lifetimes. This control of polaron type and function through tunable inter-QD interactions not only provides design principles for QD-based materials but also experimentally disentangles polaronic species in hybrid perovskite materials.
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