1988
DOI: 10.1016/0022-2313(88)90012-9
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Time-resolved synchrotron spectroscopy of exciton fluorescence in anthracene single crystals

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Cited by 10 publications
(5 citation statements)
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“…In more concentrated solutions, as well as on the water surface after long deposition times, the absolute intensity of the 380 nm peak begins to decrease, while the intensities of the other peaks continue to increase. This spectral shift can likely be attributed to self-association of anthracene: Crystalline anthracene does not fluoresce at 381 nm, and the greatest intensity shifts to the band at 420 nm, , as we see at high surface coverages on glass surfaces, and as others have observed on alumina and silica gel surfaces. , On ice, the fluorescence spectrum that we see even at the shortest deposition times resembles that of crystalline anthracene.…”
Section: Discussionsupporting
confidence: 69%
“…In more concentrated solutions, as well as on the water surface after long deposition times, the absolute intensity of the 380 nm peak begins to decrease, while the intensities of the other peaks continue to increase. This spectral shift can likely be attributed to self-association of anthracene: Crystalline anthracene does not fluoresce at 381 nm, and the greatest intensity shifts to the band at 420 nm, , as we see at high surface coverages on glass surfaces, and as others have observed on alumina and silica gel surfaces. , On ice, the fluorescence spectrum that we see even at the shortest deposition times resembles that of crystalline anthracene.…”
Section: Discussionsupporting
confidence: 69%
“…A single-exponential decay profile was observed, resulting in a lifetime of 2.21 ns that can be assigned to pure fluorescence emission. 35,36 The decay spectrum recorded at 650 nm shows a fluorescence emission with a decay time of 0.92 ns, in agreement with the emission arising from the π−π stacking in the film (Figure S4). Absolute photoluminescence quantum yields (PLQYs) of 97% and 17% were obtained for the dichloromethane solution and for the thin film (vacuum deposition at 10 −6 Torr) of bThBODIPY, respectively.…”
Section: ■ Introductionsupporting
confidence: 76%
“…The time period of pulsed radiation was about 176 ns and the width of each pulse was about 1.0 ns. The time-correlated single-photon counting technique was used, of which detail was already described elsewhere (Mitani et al, 1988). In this work, the fluorescence emitted from the samples was detected by a photomultiplier (Hamamatsu Photonics, R4129) through the filter (Toshiba, V-Y42).…”
Section: Time-correlated Single-photon Counting Measurement and Resultsmentioning
confidence: 99%