Ultrafast energy transfer from perovskite quantum dots to chromophore

被引:5
|
作者
Qin, Chaochao [1 ]
Li, Jie [1 ]
Song, Jian [1 ]
Ma, Shuhong [1 ]
Zhang, Jicai [1 ]
Jia, Guangrui [1 ]
Jiao, Zhaoyong [1 ]
Zhu, Zunlue [1 ]
Jiang, Yuhai [2 ]
Zhou, Zhongpo [1 ]
机构
[1] Henan Normal Univ, Henan Key Lab Infrared Mat & Spectrum Measures & A, Xinxiang 453007, Peoples R China
[2] ShanghaiTech Univ, Sch Phys Sci & Technol, Shanghai 201210, Peoples R China
基金
中国国家自然科学基金;
关键词
Energy transfer; Perovskite; Rhodamine B; Transient absorption spectra; Ultrafast carrier dynamics; ELECTRON-TRANSFER; NANOCRYSTALS; FORSTER;
D O I
10.1016/j.rinp.2023.106664
中图分类号
T [工业技术];
学科分类号
08 ;
摘要
Energy transfer plays an essential role in inorganic semiconductor nanocrystal-chromophore hybrids which show potential applications in light collection and emitting. The understanding of the fundamental mechanics of energy transfer processes is vital to enhance the performance of light-harvesting optoelectronic devices. Here we report the effect of varying donor sizes on energy transfer from perovskite nanocrystals to chromophore molecules. Both single energy transfer and triplet transfer mechanisms have been identified to occur between CsPbBr3 quantum dots linked to a Rhodamine B dye. The ease of adjusting optical properties via particle-size controlling provides a particular platform to accommodate excited-state couplings in perovskite-chromophore hybrids.
引用
收藏
页数:6
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