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Literatura académica sobre el tema "Fluorescence de Poincaré"
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Artículos de revistas sobre el tema "Fluorescence de Poincaré"
Léger, A., P. Boissel y L. d’Hendecourt. "Predicted fluorescence mechanism in highly isolated molecules: The Poincaré fluorescence". Physical Review Letters 60, n.º 10 (7 de marzo de 1988): 921–24. http://dx.doi.org/10.1103/physrevlett.60.921.
Texto completoLEE, YI-KUEN, CHIANG SHIH, PATRICK TABELING y CHIH-MING HO. "Experimental study and nonlinear dynamic analysis of time-periodic micro chaotic mixers". Journal of Fluid Mechanics 575 (marzo de 2007): 425–48. http://dx.doi.org/10.1017/s0022112006004289.
Texto completoSOTIROPOULOS, FOTIS, DONALD R. WEBSTER y TAHIRIH C. LACKEY. "Experiments on Lagrangian transport in steady vortex-breakdown bubbles in a confined swirling flow". Journal of Fluid Mechanics 466 (10 de septiembre de 2002): 215–48. http://dx.doi.org/10.1017/s0022112002001271.
Texto completoFOUNTAIN, G. O., D. V. KHAKHAR, I. MEZIĆ y J. M. OTTINO. "Chaotic mixing in a bounded three-dimensional flow". Journal of Fluid Mechanics 417 (25 de agosto de 2000): 265–301. http://dx.doi.org/10.1017/s002211200000118x.
Texto completoTesis sobre el tema "Fluorescence de Poincaré"
Ji, Ming Chao. "Molecular relaxation dynamics of Anthracene cations studied in an electrostatic storage ring". Thesis, Lyon 1, 2015. http://www.theses.fr/2015LYO10051.
Texto completoThe polycyclic aromatic hydrocarbon (PAH) molecules have been considered as possible carrier of the unidentified infrared emission bands from the interstellar medium (ISM) for about thirty years. The cooling dynamics of the PAH molecules which is essential to estimate their photostability and therefore their lifetime and size distributions in the ISM, has attracted numerous theoretical and experimental studies. In recent years, electrostatic storage devices (ESD) became powerful tool to investigate the cooling regime of molecules and clusters in a large time range from microseconds to seconds. Generally speaking, the decay of the emitted neutral yields due to dissociation of molecular cations or electron detachment of anions in such experiments carries information on the internal energy of the stored molecular ions. In this thesis work, the cooling regimes of anthracene cations are studied by following the time evolution of the internal energy distribution (IED) of the stored anthracene cations. A spontaneous neutral yield curve obtained from the stored molecular ions as a function of the storage time shows three distinguishable regions. The three regions indicate different cooling regimes at corresponding storage time range, i.e., the dissociation mechanism of the molecule dominates at storage time t < 1 ms, quenching of the dissociation by radiative cooling processes occurs during 1 < t < 3 ms and radiative cooling governs at t > 3 ms
Ortega, Céline. "Dynamique de refroidissement du cation naphtalène dans un anneau de stockage électrostatique". Thesis, Lyon 1, 2015. http://www.theses.fr/2015LYO10086/document.
Texto completoThe study of Polycyclic Aromatic Hydrocarbons (PAH) has been of increasing interest during the last thirty years: their possible presence in the interstellar medium is commonly invoked to explain the observation of still unassigned IR emission bands. In this thesis, the cooling dynamics of the naphthalene cations C10H8 +, the smallest molecule of the PAH family, is studied in an electrostatic storage ring, the Mini-Ring. Particularly, we consider the two main cooling processes for naphthalene cation, the dissociation and photon emission. Naphthalene molecules are ionized in an electron cyclotron resonance source (ECR), accelerated to 12 keV and then injected and stored in the Mini-Ring for several milliseconds. The internal energy distribution of the stored ions is probed by laser induced dissociation using an excitation wavelength at 532 nm. The cooling dynamics of the photo-excited cations is observed by measuring the number of emitted neutrals as a function of time. The decay curve of the neutral signal is directly related to the internal energy distribution of the ions at the excitation time. This internal energy distribution can then be determined at various storage times by analyzing the decay curves using a code developed during this thesis. The time evolution of the internal energy distribution shows a fast cooling process characterized by a cooling rate increasing from 70 to 90 s−1 for internal energies from 5.9 to 6.8 eV. This fast cooling process can’t be explained by infrared photons emission. It is attributed to the "Poincaré fluorescence " which involves an inverse internal conversion process followed by the emission of a visible photon. This fluorescence from thermally excited electron or recurrent fluorescence was predicted more than 20 years ago, but has never been measured directly up to now. The measured cooling rates in this thesis provide indirect evidence of this process