Abdullah S. Abbas, Daniel Chabeda, Daniel Weinberg, David T. Limmer, Eran Rabani, A. Paul Alivisatos
{"title":"Non-Monotonic Size-Dependent Exciton Radiative Lifetime in CsPbBr3 Nanocrystals","authors":"Abdullah S. Abbas, Daniel Chabeda, Daniel Weinberg, David T. Limmer, Eran Rabani, A. Paul Alivisatos","doi":"arxiv-2409.06165","DOIUrl":null,"url":null,"abstract":"Lead-halide perovskite nanocrystals have recently emerged as desirable\noptical materials for applications such as coherent quantum light emitters and\nsolid-state laser cooling due to their short radiative lifetime and near-unity\nphotoluminescence quantum yield. Here, we investigate the effect of CsPbBr3\nnanocrystal size on the radiative lifetime under ambient conditions.\nHigh-quality nanocrystals, with monoexponential time-resolved photoluminescence\ndecay behaviors, unveil a non-monotonic trend in radiative lifetime. This\nnon-monotonicity appears to reflect a behavior common among II-VI (CdSe) and\nperovskites semiconducting nanocrystals. We find that large nanocrystals in the\nweak quantum confinement regime exhibit long radiative lifetimes due to a\nthermally accessible population of dim states. Small nanocrystals within the\nstrong quantum confinement regime, surprisingly, also show long radiative\nlifetimes, due however to a substantial reduction in oscillator strength.\nNanocrystals in the intermediate quantum confinement regime displays the\nshortest radiative lifetime, as their oscillator strength is enhanced relative\nto particles in the strong confinement regime, but do not have sufficient\nlow-lying dim states like the large particles to counteract this affect. These\nfindings shed light on the impact of nanocrystal size on radiative lifetime and\npave the way for tailored optical materials in various optical applications.","PeriodicalId":501137,"journal":{"name":"arXiv - PHYS - Mesoscale and Nanoscale Physics","volume":"175 1","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2024-09-10","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"arXiv - PHYS - Mesoscale and Nanoscale Physics","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/arxiv-2409.06165","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0
Abstract
Lead-halide perovskite nanocrystals have recently emerged as desirable
optical materials for applications such as coherent quantum light emitters and
solid-state laser cooling due to their short radiative lifetime and near-unity
photoluminescence quantum yield. Here, we investigate the effect of CsPbBr3
nanocrystal size on the radiative lifetime under ambient conditions.
High-quality nanocrystals, with monoexponential time-resolved photoluminescence
decay behaviors, unveil a non-monotonic trend in radiative lifetime. This
non-monotonicity appears to reflect a behavior common among II-VI (CdSe) and
perovskites semiconducting nanocrystals. We find that large nanocrystals in the
weak quantum confinement regime exhibit long radiative lifetimes due to a
thermally accessible population of dim states. Small nanocrystals within the
strong quantum confinement regime, surprisingly, also show long radiative
lifetimes, due however to a substantial reduction in oscillator strength.
Nanocrystals in the intermediate quantum confinement regime displays the
shortest radiative lifetime, as their oscillator strength is enhanced relative
to particles in the strong confinement regime, but do not have sufficient
low-lying dim states like the large particles to counteract this affect. These
findings shed light on the impact of nanocrystal size on radiative lifetime and
pave the way for tailored optical materials in various optical applications.