2001
DOI: 10.1023/a:1007020731786
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Cited by 35 publications
(8 citation statements)
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“…Assuming that the effective stimulated emission cross-section, r em,eff =r em ) r ex , at the peak amplified spontaneous emission wavelength (k TWL,max =550 nm) is equal to the to stimulated emission cross-section, r em , at this wavelength ðr em ¼ 8:6 Â 10 À17 cm 2 Þ; i.e. neglecting the excited-state absorption r ex , then the experimental laser threshold requires a gain length of ' gain ¼ 10 lm (calculated by use of Equations (11) and (12d) in Holzer et al (2001)). For a smaller effective stimulated emission cross-section the gain length has to be correspondingly longer.…”
Section: Discussionmentioning
confidence: 99%
See 1 more Smart Citation
“…Assuming that the effective stimulated emission cross-section, r em,eff =r em ) r ex , at the peak amplified spontaneous emission wavelength (k TWL,max =550 nm) is equal to the to stimulated emission cross-section, r em , at this wavelength ðr em ¼ 8:6 Â 10 À17 cm 2 Þ; i.e. neglecting the excited-state absorption r ex , then the experimental laser threshold requires a gain length of ' gain ¼ 10 lm (calculated by use of Equations (11) and (12d) in Holzer et al (2001)). For a smaller effective stimulated emission cross-section the gain length has to be correspondingly longer.…”
Section: Discussionmentioning
confidence: 99%
“…The size of the luminophore, i.e. of the emitting chromophore (emitting singlet exciton) expressed by the number m em of repeat units forming a coherently emitting entity, is extracted from the ratio of the repeat unit based Strickler-Berg radiative lifetime (Strickler and Berg 1962;Birks and Dyson 1963), s rad,RU , to the experimentally determined radiative lifetime, s rad =s F // F , according to (Holzer et al 2001) m em =s rad,RU /s rad , where s F and / F are the fluorescence lifetime and the fluorescence quantum yield, respectively.…”
Section: Photo-physical and Lasing Characterisation Of A Ppv Neat Filmmentioning
confidence: 99%
“…In order to understand the origin of higher threshold than other organic materials, an absorption cross‐section (Figure S2(b)) was estimated by the following relationship and absorption spectrum (Figure S2(a)): τ = nσd ( τ : optical density, n : molecular density, σ : absorption cross‐section, d : crystal thickness). Although the in‐plane long molecular axis of the BP1T‐CN allows for efficient optical excitation, the effective absorption cross‐section per molecule at the pumping wavelength (<10 ‐18 cm 2 ) is smaller than the values (10 ‐17 –10 ‐16 cm 2 ) reported for other organic materials . The smaller σ gave rise to the higher threshold.…”
mentioning
confidence: 87%
“…15. The photon lifetime ph , can be expressed as a function of the group velocity and a loss factor combining absorption and scattering of photons, ph =1/͑V gr · ␣ loss ͒, where ␣ loss represents the losses from the resonator including both absorption and scattering of the photons.…”
Section: Subpicosecond Pulses From a Gain-switched Polymer Distributementioning
confidence: 99%