4.8 Article

TADF-Type Organic Afterglow

期刊

ANGEWANDTE CHEMIE-INTERNATIONAL EDITION
卷 60, 期 31, 页码 17138-17147

出版社

WILEY-V C H VERLAG GMBH
DOI: 10.1002/anie.202105628

关键词

afterglow; organic materials; phosphorescence; thermally activated delayed fluorescence; triplet excited state

资金

  1. Shanghai Scientific and Technological Innovation Project [20QA1411600, 20ZR1469200]
  2. Hundred Talents Program from Shanghai Institute of Organic Chemistry [Y121078]
  3. Shanghai Municipal Human Resources and Social Security Bureau [Y3400419C0]

向作者/读者索取更多资源

A highly efficient dopant-matrix afterglow system utilizing the TADF mechanism has been developed to achieve afterglow quantum yields of 60-70%. By designing compounds with multiple electron-donating groups and selecting matrices that interact with the excited states of the dopants, the afterglow materials exhibit excellent performance and potential applications in bioimaging.
We report a highly efficient dopant-matrix afterglow system enabled by TADF mechanism to realize afterglow quantum yields of 60-70%, which features a moderate rate constant for reverse intersystem crossing (kRISC) to simultaneously improve afterglow quantum yields and maintain afterglow emission lifetime. Difluoroboron beta-diketonate (BF2bdk) compounds are designed with multiple electron-donating groups to possess moderate kRISC values and are selected as luminescent dopants. The matrices with carbonyl functional groups such as phenyl benzoate (PhB) have been found to interact with and perturb BF2bdk excited states by dipole-dipole interactions and thus enhance the intersystem crossing of BF2bdk excited states. Through dopant-matrix collaboration, the efficient TADF-type afterglow materials have been achieved to exhibit excellent processability into desired shapes and large-area films by melt casting, as well as aqueous afterglow dispersions for potential bioimaging applications.

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