http://www.cnr.it/ontology/cnr/individuo/prodotto/ID34192
Time-Resolved Stimulated Emission Spectroscopy in the Ultrashort Domain Through Pump-Probe Experiments (Articolo in rivista)
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- Label
- Time-Resolved Stimulated Emission Spectroscopy in the Ultrashort Domain Through Pump-Probe Experiments (Articolo in rivista) (literal)
- Anno
- 2007-01-01T00:00:00+01:00 (literal)
- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#doi
- 10.1016/j.apsusc.2007.09.040 (literal)
- Alternative label
S. Orlando, A. Paladini, L. Guidoni, A. Santagata, G.P. Parisi, P. Villani, R. Teghil, A. De Bonis, A. Galasso, A. Giardini (2007)
Time-Resolved Stimulated Emission Spectroscopy in the Ultrashort Domain Through Pump-Probe Experiments
in Applied surface science; ELSEVIER SCIENCE BV, PO BOX 211, 1000 AE AMSTERDAM, NETHERLANDS, AMSTERDAM (Paesi Bassi)
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- S. Orlando, A. Paladini, L. Guidoni, A. Santagata, G.P. Parisi, P. Villani, R. Teghil, A. De Bonis, A. Galasso, A. Giardini (literal)
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- http://www.sciencedirect.com/science/article/pii/S0169433207013402 (literal)
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- Univ Roma La Sapienza, Dipartimento Chim, 00185 Rome, Italy
CNR - IMIP UOS Potenza, 85050 Tito, Italy
Univ Paris 07, CNRS, Mat & Phenomenes Quant UMR 7162, Paris 7, France
Univ Basilicata, Dipartimento Chim, 85100 Potenza, Italy (literal)
- Titolo
- Time-Resolved Stimulated Emission Spectroscopy in the Ultrashort Domain Through Pump-Probe Experiments (literal)
- Abstract
- The photoemission properties of fluorescent chromophores have a widespread application in many fields ranging from chemical-physics and biology to organic light emitting devices. These systems usually display high fluorescence conversion efficiency, which makes them suitable for transient/gain experiments also in liquid solutions, thin films and eventually in protein environments.
Pump and probe methods have been widely employed for wavelength-resolved spectroscopy in the subpicosecond time scale. In our group, we have recently assembled a new experimental setup for pump and probe spectroscopy: preliminary tests on the Rhodamine B dye in ethanol have been performed in order to optimize the setup. The dynamic response of photoinduced changes of the chromophore dispersed into a suitable solvent has been studied with a subpicosecond time resolution.
The optically prepared initial state of the Rhodamine B in ethanol solution appears to evolve on a timescale of few picoseconds into a successive state, which could be attributed to an intramolecular charge transfer state.
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