CsPbBr3微晶体中深能级阱的近红外发光

IF 4.6 2区 化学 Q2 CHEMISTRY, PHYSICAL The Journal of Physical Chemistry Letters Pub Date : 2025-03-31 DOI:10.1021/acs.jpclett.5c00545
Jonathan Vandenwijngaerden, Bapi Pradhan, Bob Van Hout, Eduard Fron, Yasuyuki Araki, Xianjun Zhang, Yutaka Shibata, Dario Santantonio, Roger Bresoli-Obach, Santi Nonell, Haifeng Yuan, Jialiang Xu, Mark Van der Auweraer, Maarten Roeffaers, Johan Hofkens, Hiroshi Fukumura, Elke Debroye
{"title":"CsPbBr3微晶体中深能级阱的近红外发光","authors":"Jonathan Vandenwijngaerden, Bapi Pradhan, Bob Van Hout, Eduard Fron, Yasuyuki Araki, Xianjun Zhang, Yutaka Shibata, Dario Santantonio, Roger Bresoli-Obach, Santi Nonell, Haifeng Yuan, Jialiang Xu, Mark Van der Auweraer, Maarten Roeffaers, Johan Hofkens, Hiroshi Fukumura, Elke Debroye","doi":"10.1021/acs.jpclett.5c00545","DOIUrl":null,"url":null,"abstract":"In this study, we report the first observation of a near-infrared (NIR) emission band from all-inorganic CsPbBr<sub>3</sub> and CsPb(Br/Cl)<sub>3</sub> perovskite microcrystals. By means of temperature- and power-dependent NIR and visible luminescence spectroscopy, we demonstrate that a fraction of the excited states in these materials relax through radiative transitions involving traps located deep within the band gap, leading to broadband NIR emission. The quantum yield of this deep trap emission is quantitatively determined for the first time and amounts to approximately 0.3% at room temperature. Furthermore, by examining the picosecond-to-nanosecond dynamics of the excited states, using time-resolved luminescence spectroscopy, we observe that the population of NIR initial states occurs on a 660 ps time scale, consistent with the capture of free carriers by deep trap sites. Hence, this work deepens our fundamental understanding of previously unexplored recombination channels in metal halide perovskite microcrystals.","PeriodicalId":62,"journal":{"name":"The Journal of Physical Chemistry Letters","volume":"4 1","pages":""},"PeriodicalIF":4.6000,"publicationDate":"2025-03-31","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"NIR Luminescence from Deep-Level Traps in CsPbBr3 Microcrystals\",\"authors\":\"Jonathan Vandenwijngaerden, Bapi Pradhan, Bob Van Hout, Eduard Fron, Yasuyuki Araki, Xianjun Zhang, Yutaka Shibata, Dario Santantonio, Roger Bresoli-Obach, Santi Nonell, Haifeng Yuan, Jialiang Xu, Mark Van der Auweraer, Maarten Roeffaers, Johan Hofkens, Hiroshi Fukumura, Elke Debroye\",\"doi\":\"10.1021/acs.jpclett.5c00545\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"In this study, we report the first observation of a near-infrared (NIR) emission band from all-inorganic CsPbBr<sub>3</sub> and CsPb(Br/Cl)<sub>3</sub> perovskite microcrystals. By means of temperature- and power-dependent NIR and visible luminescence spectroscopy, we demonstrate that a fraction of the excited states in these materials relax through radiative transitions involving traps located deep within the band gap, leading to broadband NIR emission. The quantum yield of this deep trap emission is quantitatively determined for the first time and amounts to approximately 0.3% at room temperature. Furthermore, by examining the picosecond-to-nanosecond dynamics of the excited states, using time-resolved luminescence spectroscopy, we observe that the population of NIR initial states occurs on a 660 ps time scale, consistent with the capture of free carriers by deep trap sites. Hence, this work deepens our fundamental understanding of previously unexplored recombination channels in metal halide perovskite microcrystals.\",\"PeriodicalId\":62,\"journal\":{\"name\":\"The Journal of Physical Chemistry Letters\",\"volume\":\"4 1\",\"pages\":\"\"},\"PeriodicalIF\":4.6000,\"publicationDate\":\"2025-03-31\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"The Journal of Physical Chemistry Letters\",\"FirstCategoryId\":\"1\",\"ListUrlMain\":\"https://doi.org/10.1021/acs.jpclett.5c00545\",\"RegionNum\":2,\"RegionCategory\":\"化学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q2\",\"JCRName\":\"CHEMISTRY, PHYSICAL\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"The Journal of Physical Chemistry Letters","FirstCategoryId":"1","ListUrlMain":"https://doi.org/10.1021/acs.jpclett.5c00545","RegionNum":2,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"CHEMISTRY, PHYSICAL","Score":null,"Total":0}
引用次数: 0

摘要

在这项研究中,我们首次观察到全无机CsPbBr3和CsPb(Br/Cl)3钙钛矿微晶体的近红外(NIR)发射带。通过温度和功率相关的近红外光谱和可见发光光谱,我们证明了这些材料中的一部分激发态通过位于带隙深处的陷阱的辐射跃迁而松弛,从而导致宽带近红外发射。首次定量确定了该深阱发射的量子产率,在室温下约为0.3%。此外,通过使用时间分辨发光光谱分析激发态的皮秒到纳秒动态,我们观察到近红外初始态的分布发生在660 ps的时间尺度上,与深阱位置捕获自由载流子一致。因此,这项工作加深了我们对金属卤化物钙钛矿微晶体中以前未探索的复合通道的基本理解。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

摘要图片

查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
NIR Luminescence from Deep-Level Traps in CsPbBr3 Microcrystals
In this study, we report the first observation of a near-infrared (NIR) emission band from all-inorganic CsPbBr3 and CsPb(Br/Cl)3 perovskite microcrystals. By means of temperature- and power-dependent NIR and visible luminescence spectroscopy, we demonstrate that a fraction of the excited states in these materials relax through radiative transitions involving traps located deep within the band gap, leading to broadband NIR emission. The quantum yield of this deep trap emission is quantitatively determined for the first time and amounts to approximately 0.3% at room temperature. Furthermore, by examining the picosecond-to-nanosecond dynamics of the excited states, using time-resolved luminescence spectroscopy, we observe that the population of NIR initial states occurs on a 660 ps time scale, consistent with the capture of free carriers by deep trap sites. Hence, this work deepens our fundamental understanding of previously unexplored recombination channels in metal halide perovskite microcrystals.
求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
来源期刊
The Journal of Physical Chemistry Letters
The Journal of Physical Chemistry Letters CHEMISTRY, PHYSICAL-NANOSCIENCE & NANOTECHNOLOGY
CiteScore
9.60
自引率
7.00%
发文量
1519
审稿时长
1.6 months
期刊介绍: The Journal of Physical Chemistry (JPC) Letters is devoted to reporting new and original experimental and theoretical basic research of interest to physical chemists, biophysical chemists, chemical physicists, physicists, material scientists, and engineers. An important criterion for acceptance is that the paper reports a significant scientific advance and/or physical insight such that rapid publication is essential. Two issues of JPC Letters are published each month.
期刊最新文献
Atomic Force Microscopy Captures Light-Induced Higher-Order Structural Dynamics in Photosystem II Supercomplexes. Predicting Complete Basis Set Limit Quasiparticle Energies from Triple-ζ Calculations How Crystal Size and Number Steer Asymmetric Crystallization Direct Experimental Evidence for Reverse Internal Conversion in the Relaxation Pathway of the Excited Anions Profiling the Electron Trap States of II-VI Chalcogenide Colloidal Quantum Dots.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1