Abstract
The control of excited states and related emissive properties of gold(III) complexes mainly depends on the modulation of intramolecular electronic interactions among gold(III) metal center, chelating ligands and/or peripheral groups. However, luminescent gold(III) systems based on intermolecular electronic interactions have never been explored. Here we report a series of proof-of-concept gold(III) exciplexes using a simple gold(III) complex, AuDPPy, as an electron acceptor. The emissive properties of gold(III) exciplexes can be regulated by combining AuDPPy with different donors. Inspiringly, these gold(III) exciplexes have donor-dependent emission mechanisms: dominant phosphorescence or dual radiative channels of thermally activated delayed fluorescence (TADF) and phosphorescence. Consequently, these gold(III) exciplexes deliver green-to-red electroluminescence with external quantum efficiencies (EQEs) of up to 10.1%. More importantly, using these gold(III) exciplexes to host multi-resonance TADF emitters results in narrowband yellow, orange, and deep-red electroluminescence with high EQEs of 23.5%, 24.4%, and 27.4%, respectively, competitive to the highest values for gold(III) OLEDs in similar color gamut.
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Acknowledgements
This work was supported by the National Natural Science Foundation of China (52022071, 52130308) and Shenzhen Fundamental Research Program (JCYJ20190808151209557, ZDSYS20210-623091813040). The authors wish to acknowledge the supercomputing system in the Supercomputing Center of Wuhan University for numerical calculations.
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Zhan, L., Chen, T., Zhong, C. et al. Luminescent gold(III) exciplexes enable efficient multicolor electroluminescence. Sci. China Chem. 66, 3213–3222 (2023). https://doi.org/10.1007/s11426-023-1546-5
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DOI: https://doi.org/10.1007/s11426-023-1546-5