4.8 Article

Dipole-Dipole Interaction Management for Efficient Blue Thermally Activated Delayed Fluorescence Diodes

Journal

CHEM
Volume 4, Issue 9, Pages 2154-2167

Publisher

CELL PRESS
DOI: 10.1016/j.chempr.2018.06.005

Keywords

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Funding

  1. Changjiang Scholar Program of Chinese Ministry of Education [Q2016208]
  2. National Natural Science Foundation of China [21672056, 61605042, 21602048]
  3. Science and Technology Bureau of Heilongjiang Province [JC2015002]
  4. National Postdoctoral Program for Innovative Talents [BX201600048]
  5. Harbin Science and Technology Bureau [2015RAYXJ008]

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Thermally activated delayed fluorescence (TADF) diodes have emerged in recent years. However, blue devices still suffer from low luminance and serious efficiency roll-off, partially because of the utilization of unipolar host materials, which can suppress interaction-induced quenching at the cost of carrier flux unbalance. Herein, we demonstrate that the strong host excited-state dipole field can significantly worsen exciton quenching of blue TADF dopants through hostdopant dipole-dipole interactions. To integrate low excited-state polarity and ambipolar characteristics, we developed a donor-s-acceptor host with dramatically reduced excited-state dipole moments by one order of magnitude to only similar to 2 Debye, which gave rise to state-of-the-art external quantum efficiency beyond 20% from its devices, as well as record-low roll-off. Comparison between the device efficiencies of the hosts and various excited-state polarities revealed that the suppression of dipole-dipole interaction-induced quenching is the primary determinant of device performance for ambipolar blue TADF hosts.

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