2002
DOI: 10.1016/s0009-2614(01)01343-4
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Exciton dissociation dynamics in a conjugated polymer containing aggregate states

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Cited by 40 publications
(17 citation statements)
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“…Conversely, the PFO NPs showed a QY value of 51.8%, which was lower than that of the free polymer chains in good solvent (63.1%). This reduction in emission efficiency was attributed to aggregation-induced depopulation of excitons resulting in quenching. , The QY of the as-prepared PFO NPs was higher than that reported for PFO NPs (40%), owing to residual THF in the mixture.…”
Section: Resultsmentioning
confidence: 74%
See 1 more Smart Citation
“…Conversely, the PFO NPs showed a QY value of 51.8%, which was lower than that of the free polymer chains in good solvent (63.1%). This reduction in emission efficiency was attributed to aggregation-induced depopulation of excitons resulting in quenching. , The QY of the as-prepared PFO NPs was higher than that reported for PFO NPs (40%), owing to residual THF in the mixture.…”
Section: Resultsmentioning
confidence: 74%
“…Furthermore, certain unique fluorescence properties, arising from the discrete structure of oligomers, show promise for applications in sensing, imaging, antibacterial agents, drug/gene delivery, and controlled release. Nevertheless, both conjugated polymers and oligomers suffer from aggregation-caused quenching (ACQ) when transferred from solution to a nanoparticle (NP) form or a solid film. This effect is attributed to aggregation-induced depopulation of excitons. , The ACQ problem greatly reduces the emission efficiency of such materials and restricts their applications in the solid state.…”
Section: Introductionmentioning
confidence: 99%
“…A key acquisition of these conjugated polymers is the capability of their nanoparticle formation resulting in increased dispersibility in water, low toxicity, and reduced sensitivity of the optical features to environmental changes such as thin film formation . However, the problem of significant decrease in the quantum yield (QY) after solution to nanoparticle (NP) and film transition, which is attributed to the aggregate-induced depopulation of the excitons, still persists and strongly restricts the use of conjugated polymers in solid film.…”
mentioning
confidence: 99%
“…Also, the presence of interchain coupled states induces an efficient energy transfer from higher energy intrachain singlet excitons to lower lying eigenstates that are delocalized over several polymer chains in intimate contact with each other (through dispersive relaxation processes). However, such aggregate-induced depopulation of the initially excited intrachain excitons also undesirably result in a significant red shift in the emission band, accompanied with a substantial reduction in the fluorescence quantum efficiency (Φ PL ) of typically more than 50% in the film state [7][8][9][10][11]. In this work, to address this problem, we propose and demonstrate the formation of organic nanoparticles (NPs) from π -conjugated polymers to exhibit higher fluorescence quantum efficiencies and reduced shifts in their emission bands in their NP films compared to their polymer thin films without forming NPs.…”
mentioning
confidence: 99%