2006
DOI: 10.1016/j.jlumin.2005.11.013
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Dual fluorescence and laser emissions from fluorescein-Na and eosin-B

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Cited by 26 publications
(14 citation statements)
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References 33 publications
(37 reference statements)
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“…In the DSSCs application, it is much of interests to concentrate in the visible solar spectrum. In addition, to that the molar extinction coefficient of EY equals 112,000 (cmM) -1 [39] which is greater than that of RB (106,000 (cmM) -1 ) [40] and much higher than that of EB (50620 (cmM) -1 ) [41], corresponding to π →π* transitions of conjugated molecules. This may explain the higher performance of DSSCs using EY above that using of other dyes.…”
Section: Photovoltaic Parametersmentioning
confidence: 99%
“…In the DSSCs application, it is much of interests to concentrate in the visible solar spectrum. In addition, to that the molar extinction coefficient of EY equals 112,000 (cmM) -1 [39] which is greater than that of RB (106,000 (cmM) -1 ) [40] and much higher than that of EB (50620 (cmM) -1 ) [41], corresponding to π →π* transitions of conjugated molecules. This may explain the higher performance of DSSCs using EY above that using of other dyes.…”
Section: Photovoltaic Parametersmentioning
confidence: 99%
“…Fluorescein powder does not exhibit luminescence properties; while in aqueous media the fluorescein dye is characterized by a bright yellow-green emission under blue excitation (fig. 3a) [5,26,27]. As shown in Fig 3b and c, a yellow green emission is recorded for HDL/fluorescein powder upon excitation at 450 nm, which is the wavelength corresponding to the emission of a commercial blue LED for a potential further association.…”
Section: Emission Spectra Interpretationmentioning
confidence: 91%
“…Despite the advance in the formulation of the ICT models, they have resulted to be insufficient for interpreting the dual emission of a large variety of fused-heterocyclic dyes and the generation of the CT state would seem to be associated with an ICT within the fused-heterocyclic ring, which is independent of the nature of exocyclic (D)- or (A)-groups. For example, mechanisms like TICT or PICT have been discarded for coumarins and quinolin-4­(1 H )-one dyes because its dual emission has not shown correlation with the restricted or free-motion nature of the exo-EDG at the benzo core. As a consequence, other non-ICT mechanisms like photo-induced electron transfer (PET) or formation of oligomers have been proposed for interpreting the dual emission of some fused heterocycles such as coumarins and rhodamines, respectively, , although these mechanisms seem to be restricted to interpret the dual emission of these mentioned molecular systems. However, it is interesting to highlight that most of these dual-emissive dyes are incompatible with the ICT models bearing a pseudo-aromatic ring in a rigid structure (Chart c), which opens the door to the occurrence of an ICT process dependent on the aromatization or partial aromatization of the pseudo-aromatic ring as an (A) moiety, which is a suitable process to stabilize the electronic distribution of the excited state and generate a stable charged state (CT).…”
Section: Introductionmentioning
confidence: 99%