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

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)...

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Bibliographic Details
Published in:Dyes and pigments 2021-04, Vol.188, p.109249, Article 109249
Main Authors: Chen, Zhen, Dai, Chenghu, Zhou, Qian, Du, Huitian, Fan, Jihui, Han, Shenghao, Zhang, Chuang, Pang, Zhiyong
Format: Article
Language:English
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Summary: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 ~6.9 nm for two-photon excited exciplex formation is obtained. •A strategy for TADF exciplex-based two-photon-excited fluorescence was proposed.•Enhanced upconverted fluorescence was observed in films of D-A exciplex.•The mechanisms of enhanced upconverted fluorescence in TADF exciplex was explained.•A maximum D-A distance of ~6.9 nm for two-photon excited exciplex formation was obtained.
ISSN:0143-7208
1873-3743
DOI:10.1016/j.dyepig.2021.109249