Exceptionally fast radiative decay of a dinuclear platinum complex through thermally activated delayed fluorescence.
Exceptionally fast radiative decay of a dinuclear platinum complex through thermally activated delayed fluorescence.
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DOI:
10.1039/d1sc00160d
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发表时间:
2021-03-22
期刊:
影响因子:
8.4
通讯作者:
Dias FB
中科院分区:
文献类型:
--
作者:
Pander P;Daniels R;Zaytsev AV;Horn A;Sil A;Penfold TJ;Williams JAG;Kozhevnikov VN;Dias FB
A novel dinuclear platinum(ii) complex featuring a ditopic, bis-tetradentate ligand has been prepared. The ligand offers each metal ion a planar O^N^C^N coordination environment, with the two metal ions bound to the nitrogen atoms of a bridging pyrimidine unit. The complex is brightly luminescent in the red region of the spectrum with a photoluminescence quantum yield of 83% in deoxygenated methylcyclohexane solution at ambient temperature, and shows a remarkably short excited state lifetime of 2.1 μs. These properties are the result of an unusually high radiative rate constant of around 4 × 105 s−1, a value which is comparable to that of the very best performing Ir(iii) complexes. This unusual behaviour is the result of efficient thermally activated reverse intersystem crossing, promoted by a small singlet–triplet energy difference of only 69 ± 3 meV. The complex was incorporated into solution-processed OLEDs achieving EQEmax = 7.4%. We believe this to be the first fully evidenced report of a Pt(ii) complex showing thermally activated delayed fluorescence (TADF) at room temperature, and indeed of a Pt(ii)-based delayed fluorescence emitter to be incorporated into an OLED. Efficient thermally activated delayed fluorescence (TADF) in a brightly luminescent diplatinum(ii) complex results in significant enhancement of the radiative decay rate.
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