Purely organic near-infrared afterglow systems based on a triplet excimer donor
An efficient near-infrared (NIR) afterglow emission at over 750 nm is highly valuable for the advanced detection technology. Herein, a new kind of organic NIR afterglow system with persistent emission (0.16 s) at 808 nm is prepared by using a red room temperature phosphorescence (RTP) excimer as a d...
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Published in | Journal of materials chemistry. C, Materials for optical and electronic devices Vol. 12; no. 11; pp. 3924 - 393 |
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Main Authors | , , , , , , , , , |
Format | Journal Article |
Language | English |
Published |
Cambridge
Royal Society of Chemistry
14.03.2024
|
Subjects | |
Online Access | Get full text |
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Summary: | An efficient near-infrared (NIR) afterglow emission at over 750 nm is highly valuable for the advanced detection technology. Herein, a new kind of organic NIR afterglow system with persistent emission (0.16 s) at 808 nm is prepared by using a red room temperature phosphorescence (RTP) excimer as a donor and a NIR dye cyanine 7 (Cy7) as an acceptor. In the pyren-1-ylboronic acid@poly(vinyl alcohol) (PYB@PVA) system, its red persistent RTP emission at over 590 nm is proved to be derived from the triplet excimer of PYB. So, the bright NIR afterglow is achieved
via
only a single triplet-to-singlet Förster-resonance energy transfer process between PYB@PVA and Cy7. Moreover, PYB
2
@PVA with more triplet excimers is beneficial to improve NIR emission intensity with a quantum yield of 1.6%. This work demonstrates that exploiting triplet excimers is meaningful to develop purely organic red or NIR afterglow materials with the emission at a long wavelength.
A kind of NIR afterglow with a lifetime of 0.16 s at 808 nm was prepared using triplet excimer (PVB@PVA) as the donor. PYB
2
@PVA containing more excimers is beneficial to improve luminescence of Cy7 acceptor
via
a triplet-to-singlet energy transfer. |
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Bibliography: | Electronic supplementary information (ESI) available. See DOI https://doi.org/10.1039/d3tc04708c |
ISSN: | 2050-7526 2050-7534 |
DOI: | 10.1039/d3tc04708c |