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March 2, 2026Inorganic Chemistry2 citations

Coordination Induction-Enhanced Thermally Activated Delayed Fluorescence for Silver(I) Complexes

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JJJi-Hui JiaDZDeng-chao ZhangYJYu-Bing Jiang

Key Points

  • The aim is to enhance the efficiency of TADF emitters through silver(I) coordination in D-A-type compounds.
  • Synthesize donor-acceptor type nitrogen-containing complexes with silver(I) coordination.
  • Evaluate energy-level structure and emission efficiency.
  • Measure photoluminescent quantum yield and lifetimes in PMMA films.
  • Complex 1 achieves a photoluminescent quantum yield (PLQY) of 98% with a short emission lifetime.
  • Complex 2 achieves a PLQY of 46%, indicating varying efficiency based on coordination environment.
  • Coordination reduces the energy gap between singlet and triplet states, enhancing TADF performance.

Abstract

Donor-acceptor (D-A) type nitrogen-containing compounds represent a key class of materials for constructing thermally activated delayed fluorescence (TADF) emitters. Achieving high-efficiency emission is the first issue in designing D-A-type TADF materials, particularly for applications in doped organic light-emitting diodes. Coordination-induced delayed fluorescence provides an effective strategy to regulate energy levels in these TADF materials, enabling efficient intramolecular ligand charge transfer (ILCT)-type emission. Moreover, metal coordination induces critical improvements, including enhanced spin-orbit coupling effect and shortened radiative lifetimes. Herein, we modulate the energy-level structure of yellow-emitting D-A-type hybrid fluorescence-TADF molecules via Ag(I) coordination, obtaining two Ag(I) complexes exhibiting ILCT-type emission. The coordination environment tunes the energy levels and reduces ΔEST, leading to a sharp enhancement in hybrid fluorescence-TADF performance. When doped in PMMA films, complex 1 achieves a PLQY of 98% (τF = 134 ns; τTADF = 2.7 μs), while complex 2 shows a PLQY of 46% (τF = 70.7 ns; τTADF = 2.0 μs). This work establishes a robust strategy to design novel TADF-active metal complexes.

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Cite This Study

Jia et al. (2026) studied this question.

synapsesocial.com/papers/69a52de5f1e85e5c73bf120chttps://doi.org/10.1021/acs.inorgchem.5c05430
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