2022
DOI: 10.1002/adom.202102701
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Visible Light Activated Organic Room‐Temperature Phosphorescence Based on Triplet‐to‐Singlet Förster‐Resonance Energy Transfer

Abstract: Stimuli‐responsive room‐temperature phosphorescence (RTP) materials have drawn widespread attention in information encryption, sensors, and bio‐imaging. In this work, a photoactivated organic RTP material through triplet‐to‐singlet Förster‐resonance energy transfer (TS‐FRET) inhibited by visible‐light stimulation is reported. A stable phosphorescence energy donor and a fluorescent dye sensitive to visible light as the energy acceptor are doped into polyvinylpyrrolidone (PVP) polymer matrix to construct an amor… Show more

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Cited by 44 publications
(18 citation statements)
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“…On the other hand, in comparison with the gated‐emission spectra of Fluo/Rh6G/RhB‐codoped PVA films (λ ex = 360 nm; Figure S10A–C, Supporting Information), no obvious delayed fluorescence emissions are observed by directly exciting the Fluo/Rh6G/RhB‐codoped PVA films under the optimal excitation wavelength of acceptors (λ ex = 489/526/554 nm) or directly exciting the doping PVA films Fluo/Rh6G/RhB@PVA in the absence of a donor (λ ex = 360 nm; Figure S10D–F, Supporting Information). According to the previous works by Prof. Ma and Prof. George, [ 39,32 ] the gated‐excitation and gated‐emission spectra demonstrate that the persistently delayed fluorescence of energy acceptors is derived from the long‐lived triplet excitons of the energy donors via an efficient PRET mechanism.…”
Section: Resultsmentioning
confidence: 99%
“…On the other hand, in comparison with the gated‐emission spectra of Fluo/Rh6G/RhB‐codoped PVA films (λ ex = 360 nm; Figure S10A–C, Supporting Information), no obvious delayed fluorescence emissions are observed by directly exciting the Fluo/Rh6G/RhB‐codoped PVA films under the optimal excitation wavelength of acceptors (λ ex = 489/526/554 nm) or directly exciting the doping PVA films Fluo/Rh6G/RhB@PVA in the absence of a donor (λ ex = 360 nm; Figure S10D–F, Supporting Information). According to the previous works by Prof. Ma and Prof. George, [ 39,32 ] the gated‐excitation and gated‐emission spectra demonstrate that the persistently delayed fluorescence of energy acceptors is derived from the long‐lived triplet excitons of the energy donors via an efficient PRET mechanism.…”
Section: Resultsmentioning
confidence: 99%
“…Several visible-light photoswitches have already been applied as the basis of photoresponsive actuators, FETs, MOFs, and soft materials, and in photo-patterning, photopharmacology, and smart display materials. [71,72,[172][173][174][175][176][177][178][179][180] However, most switches still work within the 400-600 nm window, meaning their bioapplications remain rather limited to in vitro studies or in superficial organs (such as skin) due to the insufficient tissue penetration depth (< 1 mm). Therefore, the realization of photoswitches that operate in both directions with red and NIR light (650-1450 nm) is the essential next step for in vivo photocontrol.…”
Section: Discussionmentioning
confidence: 99%
“…Copyright 2021 Wiley-VCH GmbH. Part C is adapted/reproduced with permission from ref . Copyright 2022 Wiley-VCH GmbH.…”
mentioning
confidence: 99%
“…Based on the TS-energy transfer mechanism, in 2022, Ma et al developed a photo-stimuli responsive RTP material by employing polyvinylpyrrolidone (PVP) as the rigid matrix, compound 26 as the triplet energy donor, and compound 47 as the acceptor (Figure C) . Compound 47 has a good spectral overlap with phosphorescence emission of compound 26 , and an efficient TS-FRET process can occurr, which almost quenches the RTP emission of compound 26 at 470 nm.…”
mentioning
confidence: 99%