Enhanced two-photon-excited fluorescence from electron donor-acceptor exciplex

被引:18
|
作者
Chen, Zhen [1 ]
Dai, Chenghu [1 ]
Zhou, Qian [1 ]
Du, Huitian [1 ]
Fan, Jihui [1 ]
Han, Shenghao [1 ]
Zhang, Chuang [2 ]
Pang, Zhiyong [1 ]
机构
[1] Shandong Univ, Sch Microelect, State Key Lab Crystal Mat, Jinan 250100, Peoples R China
[2] Chinese Acad Sci, Inst Chem, Beijing 100190, Peoples R China
基金
中国国家自然科学基金;
关键词
Exciplex; Thermally activated delayed fluorescence; Two-photon absorption; Upconversion; LIGHT-EMITTING-DIODES; CHARGE-TRANSFER INTERACTIONS; TRANSFER STATES; ABSORPTION; DESIGN; EFFICIENCY; EMITTERS; CHANNEL; OLEDS;
D O I
10.1016/j.dyepig.2021.109249
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
Exciplex-based thermally activated delayed fluorescence (TADF) materials show long luminescence lifetimes and high quantum efficiency by converting the non-radiative triplets into the radiative singlets. Here, strong upconverted fluorescence from the amorphous thin films of TADF donor-acceptor (D-A) exciplexes is observed under near-infrared excitation. The spectroscopic studies demonstrate that the enhanced upconversion in exciplex emission combines a series of excited state processes including the two-photon absorption (TPA) of donors and the TADF of D-A pairs. The comparison between donor-only and D-A systems indicates that the upconversion is greatly facilitated by the energy harvesting mechanisms existing in the exciplex-based TADF materials. The results reveal the formation mechanism of exciplex excited-states following the two-photon excitation in D-A blends, and consequently the potentials of exciplex materials in nonlinear optics applications. Moreover, a maximum D-A distance of similar to 6.9 nm for two-photon excited exciplex formation is obtained.
引用
收藏
页数:7
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