Resonance-Activated Spin-Flipping for Efficient Organic Ultralong Room-Temperature Phosphorescence

© 2018 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

Bibliographische Detailangaben
Veröffentlicht in:Advanced materials (Deerfield Beach, Fla.). - 1998. - 30(2018), 44 vom: 05. Nov., Seite e1803856
1. Verfasser: Tao, Ye (VerfasserIn)
Weitere Verfasser: Chen, Runfeng, Li, Huanhuan, Yuan, Jie, Wan, Yifang, Jiang, He, Chen, Cailin, Si, Yubing, Zheng, Chao, Yang, Baocheng, Xing, Guichuan, Huang, Wei
Format: Online-Aufsatz
Sprache:English
Veröffentlicht: 2018
Zugriff auf das übergeordnete Werk:Advanced materials (Deerfield Beach, Fla.)
Schlagworte:Journal Article dynamic activation organic afterglow organic ultralong room-temperature phosphorescence resonance molecules spin-flipping
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520 |a Triplet-excited-state-involved photonic and electronic properties have attracted tremendous attention for next-generation technologies. To populate triplet states, facile intersystem crossing (ISC) for efficient exciton spin-flipping is crucial, but it remains challenging in organic molecules free of heavy atoms. Here, a new strategy is proposed to enhance the ISC of purely organic optoelectronic molecules using heteroatom-mediated resonance structures capable of promoting spin-flipping at large singlet-triplet splitting energies with the aid of the fluctuation of the state energy and n-orbital component upon self-adaptive resonance variation. Combined experimental and theoretical investigations confirm the key contributions of the resonance variation to the profoundly promoted spin-flipping with ISC rate up to ≈107 s-1 in the rationally designed NPX (X = O or S) resonance molecules. Importantly, efficient organic ultralong room-temperature phosphorescence (OURTP) with simultaneously elongated lifetime and improved efficiency results overcoming the intrinsic competition between the OURTP lifetime and efficiency. With the spectacular resonance-activated OURTP molecules, time-resolved and color-coded quick response code devices with multiple information encryptions are realized, demonstrating the fundamental significance of this approach in boosting ISC dynamically for advanced optoelectronic applications 
650 4 |a Journal Article 
650 4 |a dynamic activation 
650 4 |a organic afterglow 
650 4 |a organic ultralong room-temperature phosphorescence 
650 4 |a resonance molecules 
650 4 |a spin-flipping 
700 1 |a Chen, Runfeng  |e verfasserin  |4 aut 
700 1 |a Li, Huanhuan  |e verfasserin  |4 aut 
700 1 |a Yuan, Jie  |e verfasserin  |4 aut 
700 1 |a Wan, Yifang  |e verfasserin  |4 aut 
700 1 |a Jiang, He  |e verfasserin  |4 aut 
700 1 |a Chen, Cailin  |e verfasserin  |4 aut 
700 1 |a Si, Yubing  |e verfasserin  |4 aut 
700 1 |a Zheng, Chao  |e verfasserin  |4 aut 
700 1 |a Yang, Baocheng  |e verfasserin  |4 aut 
700 1 |a Xing, Guichuan  |e verfasserin  |4 aut 
700 1 |a Huang, Wei  |e verfasserin  |4 aut 
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773 1 8 |g volume:30  |g year:2018  |g number:44  |g day:05  |g month:11  |g pages:e1803856 
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