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横向受限CdSe纳米片双激子结合能的增强

Enhancement of the Biexciton Binding Energy in Laterally Confined CdSe Nanoplatelets.

作者信息

Rodà Carmelita, Macias-Pinilla David F, Di Giacomo Alessio, Planelles Josep, Climente Juan I, Moreels Iwan

机构信息

Department of Chemistry, Ghent University, 9000 Gent, Belgium.

Department de Química Física i Analítica, Universitat Juame I, Av. Sos Baynat s/n, 12071, Castelló, Spain.

出版信息

Nano Lett. 2025 Sep 3;25(35):13251-13257. doi: 10.1021/acs.nanolett.5c03251. Epub 2025 Aug 19.

Abstract

Optical amplification in CdSe nanoplatelets (NPLs) has been linked to biexcitons with a large binding energy Δ, preventing dissociation at room temperature. While the exciton binding energy Δ has been studied extensively, Δ in colloidal NPLs is typically inferred using the 2D Haynes rule, Δ = 0.228·Δ. Systematic studies of Δ in CdSe NPLs with varying thicknesses and lateral dimensions are still lacking. Here, we used transient absorption spectroscopy to investigate Δ, through photoinduced biexciton absorption. Δ ranges between 40 and 55 meV and increases by 30% when reducing the width from 9 to 3 nm, while overall 3.5 ML NPLs have only 10% higher Δ compared to 4.5 ML NPLs. Fitting the linear absorbance spectra, we extracted Δ and demonstrate that the Δ/Δ ratio is substantially lower than 0.228. Results confirm that biexcitons in CdSe NPLs are stable at room temperature and have an increased Δ in laterally confined NPLs.

摘要

硒化镉纳米片(NPLs)中的光学放大与具有大结合能Δ的双激子有关,这使得双激子在室温下不会解离。虽然激子结合能Δ已得到广泛研究,但胶体NPLs中的Δ通常是使用二维海恩斯规则Δ = 0.228·Δ推断得出的。对于不同厚度和横向尺寸的硒化镉NPLs中的Δ,仍缺乏系统性研究。在此,我们通过光致双激子吸收,利用瞬态吸收光谱来研究Δ。Δ的范围在40至55毫电子伏特之间,当宽度从9纳米减小到3纳米时,Δ增加30%,而总体而言,3.5单层的NPLs的Δ仅比4.5单层的NPLs高10%。通过拟合线性吸收光谱,我们提取了Δ,并证明Δ/Δ比值远低于0.228。结果证实,硒化镉NPLs中的双激子在室温下是稳定的,并且在横向受限的NPLs中Δ会增加。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/aeb1/12412167/32cb78bd315e/nl5c03251_0001.jpg

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