ArticleNature communications2024
Microsecond triplet emission from organic chromophore-transition metal dichalcogenide hybrids via through-space spin orbit proximity effect.
Article in Nature communications, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.
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Who cites it
3 citing papers in PubMed.
- Lanthanide-doped nanocrystals enable organic room-temperature phosphorescence in solution through direct triplet excitation.Nature chemistry · 2026Article
- Reversible color switching of bright phosphorescence in purely organic materials for advanced data encryption.Nature communications · 2026Article
- Synthesis of Elastic Metallic Nickel by Solvent-Ligand-Mediated Reductive Assembly.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2025Article
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Authors and funding
14 authors.
Funding
Abstract
Efficient light generation from triplet states of organic molecules has been a hot yet demanding topic in academia and the display industry. Herein, we propose a strategy for developing triplet emitter by creating heterostructures of organic chromophores and transition metal dichalcogenides (TMDs). These heterostructures emit microsecond phosphorescence at room temperature, while their organic chromophores intrinsically exhibit millisecond phosphorescence under vibration dissipation-free conditions. This enhancement in phosphorescence is indicative of significantly enhanced spin-orbit coupling efficiency through coupling with TMDs. Through detailed studies on these hybrids from various perspectives, we elucidate key features of each component essential for generating microsecond triplet emission, including 2H-TMDs with heavy transition metals and aromatic carbonyl with an ortho-hydroxy group. Our intriguing findings open avenues for exploring the universal applicability of fast and stable hybrid triplet emitters.
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Registered trials
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