2011
DOI: 10.1016/j.jlumin.2011.05.043
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Characterization of the excimers of poly(N-vinylcarbazole) using TRANES

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Cited by 16 publications
(33 citation statements)
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References 39 publications
(77 reference statements)
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“…Observed spectral changes indicate dense packaging of carbazole moieties and formation of excimers with different stacking motifs. According to the literature data, the high-energy emission centered at ∼370 nm is ascribed to a partially overlapped structure, whereas the low-energy signal centered at ∼410 nm corresponds to a sandwich-like stacking (see insets in Figure ), where two carbazole molecules attain an eclipsed or fully overlapped arrangement. …”
Section: Resultsmentioning
confidence: 76%
“…Observed spectral changes indicate dense packaging of carbazole moieties and formation of excimers with different stacking motifs. According to the literature data, the high-energy emission centered at ∼370 nm is ascribed to a partially overlapped structure, whereas the low-energy signal centered at ∼410 nm corresponds to a sandwich-like stacking (see insets in Figure ), where two carbazole molecules attain an eclipsed or fully overlapped arrangement. …”
Section: Resultsmentioning
confidence: 76%
“…Looking at the reasonable disparity in the lifetime values for the lower and the higher energy emission bands, TRES spectra have been collected within the spectral range 300–550 nm at various selected time windows, as depicted in Figure A,C in EtOH and MCH, respectively. The spectral changes in TRES spectra at various time windows may occur because of the two or more emitting species or due to the different solvated cluster of single excited species. , To resolve this, we have opted for a model free extension of TRES, namely, TRANES by normalization of area under the time-resolved emission spectra. Panels B and D of Figure represent the TRANES spectra of anthril in EtOH and MCH, respectively, at different time windows. Isoemissive points (at 400 nm in EtOH and 389 nm in MCH) are observed in the TRANES spectra, revealing the coexistence of two conformers in the excited state.…”
Section: Results and Discussionmentioning
confidence: 99%
“…The emission at ∼380 nm (high energy excimer) is attributed to incompletely overlapped carbazole units while the emission at ∼405 nm (low energy excimer) is due to full overlapping. 44,45 The emission spectrum of PVK NPs shows that the intensity at 380 nm is lower than that at 405 nm. However when the PVK is dissolved in toluene (not nanoparticles), the trend is different; the emission intensity at 370 nm is higher than at 415 nm.…”
Section: Steady-state Studymentioning
confidence: 99%
“…However when the PVK is dissolved in toluene (not nanoparticles), the trend is different; the emission intensity at 370 nm is higher than at 415 nm. 45 Therefore, the excimer emission of the PVK NPs is coming mostly from the full overlapped excimers suggesting strong interactions between the carbazole units in the PVK NPs than in the toluene solution. Upon encapsulation of C153 (2.72 wt%) inside the PVK nanodomain, the emission of PVK is efficiently quenched (by 97% at the maximum of emission intensity), while the broad emission mainly comes from the trapped C153 (intensity maximum at 510 nm and no vibronic structure).…”
Section: Steady-state Studymentioning
confidence: 99%
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