Unambiguous spectral characterization on triplet energy transfer from quantum dots mediated by hole transfer competing with other carrier dynamics

被引:2
|
作者
Wang, Lei [1 ]
Yang, Gaoyuan [1 ]
Zhang, Boyu [1 ,2 ]
Zhang, Xin [1 ]
Liu, Dezheng [1 ]
Liang, Ying [1 ]
Liang, Guijie [1 ]
机构
[1] Hubei Univ Arts & Sci, Hubei Key Lab Low Dimens Optoelect Mat & Devices, Xiangyang 441053, Peoples R China
[2] Chinese Acad Sci, Dalian Inst Chem Phys, State Key Lab Mol React Dynam, Dalian 116023, Peoples R China
基金
中国国家自然科学基金;
关键词
ULTRAFAST ELECTRON-TRANSFER; SINGLET-EXCITON-FISSION; CDSE NANOCRYSTALS; CHARGE-TRANSFER; SENSITIZATION; SURFACE; PHOTOCHEMISTRY; DISSOCIATION; DESIGN; STATES;
D O I
10.1364/OE.478579
中图分类号
O43 [光学];
学科分类号
070207 ; 0803 ;
摘要
Triplet generation by quantum dots (QDs)-sensitized molecules emerges great potential in many applications. However, the mechanism of triplet energy transfer (TET) is still fuzzy especially due to the complicated energy level alignment of QDs and molecules or trap states in QDs. Here, CdSe QDs and 5-tetracene carboxylic acid (TCA) molecules are selected as the triplet donor and acceptor, respectively, to form a TET system. By tuning the band gap of CdSe, the CdSe-TCA complex is exactly designed to present a Type-II like alignment of relative energetics. Coupling the transient absorption and time-resolved fluorescence spectra, all carrier dynamics is distinctly elucidated. Quantitative analysis demonstrates that hole transfer persisting for -2 ps outcompetes all other carrier dynamics such as electron trapping (-100 ps level), charge recombination (- 5 ns) and the so-called "back transfer charge recombination" (-50 ns), and thus leads to a hole-transfer-mediated TET process. The low TET yield (-34.0%) ascribed to electron behavior can be further improved if electron trapping and charge recombination are efficiently suppressed. The observation on distinguishable carrier dynamics attributed to legitimate design of energy level alignment facilitates a better understanding of the TET mechanism from QDs to molecules as well as further development of photoelectronic devices based on such TET systems.(c) 2022 Optica Publishing Group under the terms of the Optica Open Access Publishing Agreement
引用
收藏
页码:47440 / 47451
页数:12
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