手性(物理)
钙钛矿(结构)
不对称
圆极化
材料科学
光谱学
化学物理
纳米晶
极化(电化学)
分子物理学
辐射传输
发光
量子
凝聚态物理
激子
光电子学
联轴节(管道)
荧光
限制
发射光谱
线极化
荧光光谱法
光致发光
化学
作者
Yan Lv,Xueying Ma,Yao Xu,Jian Li,Wenheng Xu,Dawei Zhou,Congzhou Li,Fengrui Hu,Lin Wang,Xiaoyong Wang
出处
期刊:Nano Letters
[American Chemical Society]
日期:2025-12-10
卷期号:25 (51): 17962-17969
标识
DOI:10.1021/acs.nanolett.5c05385
摘要
Chiral ligand-functionalized perovskite nanocrystals (NCs) are promising sources of circularly polarized light, yet their intrinsic emissive behavior is often blurred by ensemble averaging, limiting mechanistic insights into chirality transfer. Here, by resolving individual emitters, single-NC spectroscopy unveils heterogeneity that complements ensemble measurements. Only a minority (∼22.2%) of NCs exhibit detectable chiroptical response, whereas rare emitters display circular polarization degrees approaching ∼48.0% while maintaining excellent single-photon purity of ∼95.0%. By disentangling fluorescence blinking and inhomogeneous broadening, we reveal that ligand chirality imprints distinct fingerprints on excitonic emission, including static energy splitting and dynamic asymmetry in radiative decay rates. These results provide direct evidence of the coupling between molecular chirality and NC band-edge emission states. Our findings underscore single-particle spectroscopy as an effective probe to identify emitter-specific behavior and offer fundamental insights for advancing chiral perovskite NCs toward efficient chiral quantum light sources.
科研通智能强力驱动
Strongly Powered by AbleSci AI