New perspectives for triplet-triplet annihilation based photon upconversion using all-organic energy donor & acceptor chromophores

被引:51
|
作者
Manna, Manoj K. [1 ]
Shokri, Siamak [1 ]
Wiederrecht, Gary P. [2 ]
Gosztola, David J. [2 ]
Ayitou, A. Jean-Luc [1 ]
机构
[1] IIT, Dept Chem, 3101 S Dearborn St South, Chicago, IL 60616 USA
[2] Argonne Natl Lab, Ctr Nanoscale Mat, 9700 S Cass Ave, Argonne, IL 60439 USA
基金
美国国家科学基金会;
关键词
EXCITED-STATE; LOW-POWER; HIGHLY EFFICIENT; DELAYED FLUORESCENCE; PERYLENE DIIMIDES; LIGHT; SENSITIZER; DERIVATIVES; BODIPY; RED;
D O I
10.1039/c8cc01553h
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
It is recognized that metal organic complexes that serve as sensitizers can present various degrees of challenges viz. synthesis and stability for photonic applications such as triplet-triplet annihilation based photon upconversion (TTA-PUC). Presently, researchers, including our group, are turning their attention toward purely organic triplet sensitizers, which can be handled more easily for photon management science. In this review, we surveyed recently developed all-organic chromophoric systems that were devised and used for TTA-PUC research. Knowing that TTA-PUC research has mainly been focused on the design and synthesis of the triplet sensitizers, we detailed the underlying photophysics and thermodynamics that served as the starting point for the synthesis of the purely organic chromophores in question. Accordingly, this review details triplet sensitizers that operate on (i) spin-orbit coupling or heavy atom effect, (ii) Baird-type aromaticity and antiaromaticity, (iii) open-shell characteristics or doublet excited state and (iv) thermally activated delayed fluorescence.
引用
收藏
页码:5809 / 5818
页数:10
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