Probe exciplex structure of highly efficient thermally activated delayed fluorescence organic light emitting diodes
Tzu-Chieh Lin,
Monima Sarma,
Yi-Ting Chen,
Shih-Hung Liu,
Ke-Ting Lin,
Pin-Yi Chiang,
Wei-Tsung Chuang,
Yi-Chen Liu,
Hsiu-Fu Hsu,
Wen-Yi Hung (),
Wei-Chieh Tang,
Ken-Tsung Wong () and
Pi-Tai Chou ()
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Tzu-Chieh Lin: National Taiwan University
Monima Sarma: National Taiwan University
Yi-Ting Chen: National Taiwan University
Shih-Hung Liu: National Taiwan University
Ke-Ting Lin: National Taiwan Ocean University
Pin-Yi Chiang: National Taiwan Ocean University
Wei-Tsung Chuang: National Synchrotron Radiation Research Center
Yi-Chen Liu: Tamkang University
Hsiu-Fu Hsu: Tamkang University
Wen-Yi Hung: National Taiwan Ocean University
Wei-Chieh Tang: National Taiwan University
Ken-Tsung Wong: National Taiwan University
Pi-Tai Chou: National Taiwan University
Nature Communications, 2018, vol. 9, issue 1, 1-8
Abstract:
Abstract The lack of structural information impeded the access of efficient luminescence for the exciplex type thermally activated delayed fluorescence (TADF). We report here the pump-probe Step-Scan Fourier transform infrared spectra of exciplex composed of a carbazole-based electron donor (CN-Cz2) and 1,3,5-triazine-based electron acceptor (PO-T2T) codeposited as the solid film that gives intermolecular charge transfer (CT), TADF, and record-high exciplex type cyan organic light emitting diodes (external quantum efficiency: 16%). The transient infrared spectral assignment to the CT state is unambiguous due to its distinction from the local excited state of either the donor or the acceptor chromophore. Importantly, a broad absorption band centered at ~2060 cm−1 was observed and assigned to a polaron-pair absorption. Time-resolved kinetics lead us to conclude that CT excited states relax to a ground-state intermediate with a time constant of ~3 µs, followed by a structural relaxation to the original CN-Cz2:PO-T2T configuration within ~14 µs.
Date: 2018
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Persistent link: https://EconPapers.repec.org/RePEc:nat:natcom:v:9:y:2018:i:1:d:10.1038_s41467-018-05527-4
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DOI: 10.1038/s41467-018-05527-4
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