Room-temperature white and color-tunable afterglow by manipulating multi-mode triplet emissions
Herein, we succeed in achieving room-temperature persistent white afterglow by manipulating multi-mode triplet emissions from a single purely organic phosphorescence molecule. Two D-A-A′-D type organic isomers p DCzPyCN and o DCzPyCN are designed and synthesized, with two carbazolyls as the donors a...
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Veröffentlicht in: | Journal of materials chemistry. C, Materials for optical and electronic devices Materials for optical and electronic devices, 2021-01, Vol.9 (9), p.3257-3263 |
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Format: | Artikel |
Sprache: | eng |
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Zusammenfassung: | Herein, we succeed in achieving room-temperature persistent white afterglow by manipulating multi-mode triplet emissions from a single purely organic phosphorescence molecule. Two D-A-A′-D type organic isomers
p
DCzPyCN and
o
DCzPyCN are designed and synthesized, with two carbazolyls as the donors and pyridine and a cyanogroup as the acceptors. Amazingly,
o
DCzPyCN and
p
DCzPyCN manifest white afterglow and green afterglow at room temperature, which lasts for over 3 s and 2 s, respectively. The white afterglow of
o
DCzPyCN is made up of thermally activated delayed fluorescence (TADF) (455 nm, ∼90 ms), distinguishable thermally activated delayed phosphorescence (TADP) (483 nm) and organic ultralong phosphorescence (OURTP) from the intermolecular interaction-stabilized triplet state (T
1
*) (542 nm and 592 nm, ∼240 ms). The calculated CIE
x
,
y
chromaticity coordinates are (0.30, 0.35) in the white-light zone. The green afterglow of
p
DCzPyCN contains TADF (475 nm, ∼51 ms), TADP from the lowest molecular triplet state (T
1
) released from T
1
* (490 nm, ∼55 ms), and weak T
1
* emission (542 nm and 592 nm, ∼46 ms and ∼49 ms). Fascinatingly, both isomers adopt the unique multi-mode triplet emission mechanism but different emission components play a leading role in the final afterglow for each isomer, leading to the different afterglow colors. Single crystal analyses and TD-DFT calculations evidence the T
1
* phosphorescence. Temperature-dependent experiments validate the TADF and TADP of
p
DCzPyCN and
o
DCzPyCN. To the best of our knowledge, this is the first time that the afterglow color has been tuned and single component white afterglow has been finally realized by manipulating multi-mode triplet emissions. This work will help gain deep insight into the mechanism for organic afterglow and extend its application scope.
Two isomers
p
DCzPyCN and
o
DCzPyCN are designed and synthesized. Amazingly,
o
DCzPyCN manifest white afterglow at room temperature. This is the first time that single-component white afterglow has finally been realized. |
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ISSN: | 2050-7526 2050-7534 |
DOI: | 10.1039/d0tc05816e |