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231224s2016 xx |||||o 00| ||eng c |
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|a 10.1002/adma.201602604
|2 doi
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|a eng
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| 100 |
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|a Xu, Shen
|e verfasserin
|4 aut
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|a Excited State Modulation for Organic Afterglow
|b Materials and Applications
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|c 2016
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|a Text
|b txt
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|a ƒaComputermedien
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|a Date Completed 17.07.2018
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|a Date Revised 01.10.2020
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|a published: Print-Electronic
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|a Citation Status PubMed-not-MEDLINE
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|a © 2016 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.
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|a Organic afterglow materials, developed recently by breaking through the difficulties in modulating ultrafast-decayed excited states, exhibit ultralong-lived emission for persistent luminescence with lifetimes of several orders of magnitude longer than traditional fluorescent and phosphorescent emissions at room temperature. Their exceptional properties, namely ultralong luminescent lifetime, large Stokes shifts, facile excited state transformation, and environmentally sensitive emission, have led to a diverse range of advanced optoelectronic applications. Here, the organic afterglow is reviewed from the perspective of fundamental concepts on both phenomenon and mechanism, examining the technical challenges in relation to excited state tuning and lifetime elongation. In particular, the advances in material design strategies that afford a large variety of organic afterglow materials for a broad utility in optoelectronics including lighting and displays, anti-counterfeiting, optical recording, chemical sensors and bio-imaging are highlighted
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|a Journal Article
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|a excited-state modulation
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|a organic afterglow
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|a organic persistent luminescence
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|a time-resolved optic applications
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|a ultralong luminescence lifetimes
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|a Chen, Runfeng
|e verfasserin
|4 aut
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|a Zheng, Chao
|e verfasserin
|4 aut
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| 700 |
1 |
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|a Huang, Wei
|e verfasserin
|4 aut
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|t Advanced materials (Deerfield Beach, Fla.)
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|g 28(2016), 45 vom: 15. Dez., Seite 9920-9940
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|g volume:28
|g year:2016
|g number:45
|g day:15
|g month:12
|g pages:9920-9940
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|u http://dx.doi.org/10.1002/adma.201602604
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