光致发光
材料科学
电介质
极化(电化学)
激发
纳米结构
各向异性
光电子学
极化度
光学
分子物理学
纳米技术
散射
化学
物理
量子力学
物理化学
作者
Juanzi Shi,I. Yu. Ryabov,Sudipta Seth,Pavel A. Frantsuzov,Safi Rafie-Zinedine,Andreas Walther,Maria E. Messing,Xian‐gang Wu,Wengao Lu,Haizheng Zhong,Ivan G. Scheblykin
出处
期刊:ACS Photonics
[American Chemical Society]
日期:2022-11-17
卷期号:9 (12): 3888-3898
被引量:3
标识
DOI:10.1021/acsphotonics.2c01150
摘要
High Resolution Image Download MS PowerPoint Slide The dielectric contrast effect is usually evoked to explain anisotropy of optical properties of elongated nanoobjects, for example, semiconductor nanowires. We applied two-dimensional polarization imaging microscopy to measure the polarization of photoluminescence (PL) excitation and PL intensity of nanoaggregates of in-situ formed MAPbBr 3 perovskite nanoparticles in a stretched polymeric matrix. Scanning electron microscopy images of these objects were also acquired to characterize their sizes and shapes. We find that individual perovskite aggregates with sizes of 100–300 nm often possess a PL excitation polarization degree as high as 0.5–0.9, which is up to three times higher than the polarization degree of absorption predicted by the dielectric contrast effect. Small aggregates of nanoparticles possess an emission polarization degree substantially higher than that of excitation. Computer simulations of many possible scenarios show that the dielectric contrast alone cannot quantitatively explain the polarization properties of the studied objects. We propose energy transfer to localized emitting sites and the dependence of PL yield on excitation power density as possible factors strongly influencing the polarization properties of PL emission and PL excitation, respectively.
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