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Articles de revues sur le sujet "Static and time resolved spectroscopies"
Niedzwiedzki, Dariusz M., Mojgan Kouhnavard, Yifan Diao, Julio M. D'Arcy et Pratim Biswas. « Spectroscopic investigations of electron and hole dynamics in MAPbBr3 perovskite film and carrier extraction to PEDOT hole transport layer ». Physical Chemistry Chemical Physics 23, no 23 (2021) : 13011–22. http://dx.doi.org/10.1039/d1cp00658d.
Texte intégralCurtright, Aimee E., et James K. McCusker. « Static and Time-Resolved Spectroscopic Studies of Low-Symmetry Ru(II) Polypyridyl Complexes ». Journal of Physical Chemistry A 103, no 35 (septembre 1999) : 7032–41. http://dx.doi.org/10.1021/jp9919415.
Texte intégralRastogi, Vinay, Usha Rao, Shivanand Chaurasia, Chakkalakkal Davis Sijoy, Vinayak Mishra, Shashank Chaturvedi et Mukul Narayan Deo. « Time-Resolved Vibrational Spectroscopy of Polytetrafluoroethylene Under Laser-Shock Compression ». Applied Spectroscopy 71, no 12 (11 août 2017) : 2643–52. http://dx.doi.org/10.1177/0003702817726542.
Texte intégralThekku Veedu, Sreevidya. « Ultrafast Dynamical Study Using Time-resolved Laue Diffraction ». Acta Crystallographica Section A Foundations and Advances 70, a1 (5 août 2014) : C766. http://dx.doi.org/10.1107/s205327331409233x.
Texte intégralMottin, Stephane, Canh Tran-Minh, Pierre Laporte, Raymond Cespuglio et Michel Jouvet. « Fiber-Optic Time-Resolved Fluorescence Sensor for in Vitro Serotonin Determination ». Applied Spectroscopy 47, no 5 (mai 1993) : 590–97. http://dx.doi.org/10.1366/0003702934067180.
Texte intégralSciortino, Alice, Roberto Pecorella, Marco Cannas et Fabrizio Messina. « Effect of Halogen Ions on the Photocycle of Fluorescent Carbon Nanodots ». C — Journal of Carbon Research 5, no 4 (24 octobre 2019) : 64. http://dx.doi.org/10.3390/c5040064.
Texte intégralNoda, Isao, A. E. Dowrey et Curtis Marcott. « A Spectrometer for Measuring Time-Resolved Infrared Linear Dichroism Induced by a Small-Amplitude Oscillatory Strain ». Applied Spectroscopy 42, no 2 (février 1988) : 203–16. http://dx.doi.org/10.1366/0003702884428310.
Texte intégralAbraham, Suja, et Vellaichamy Parthasarathy. « INTERACTION OF COPPER OXIDE NANOPARTICLES WITH BOVINE SERUM ALBUMIN BY SPECTROSCOPIC STUDIES ». International Journal of Pharmacy and Pharmaceutical Sciences 10, no 5 (1 mai 2018) : 35. http://dx.doi.org/10.22159/ijpps.2018v10i5.24877.
Texte intégralRao, Usha, Shivanand Chaurasia, C. D. Sijoy, Vinayak Mishra et M. N. Deo. « In Situ Raman Spectroscopic Studies of Liquid Carbon Tetrachloride (CCl4) Under Static and Laser-Driven Shock Compression ». Applied Spectroscopy 73, no 12 (12 août 2019) : 1420–27. http://dx.doi.org/10.1177/0003702819856372.
Texte intégralChinnathambi, Shanmugavel, Subramani Karthikeyan, Devadasan Velmurugan, Nobutaka Hanagata, Prakasarao Aruna et Singaravelu Ganesan. « Investigations on the Interactions of 5-Fluorouracil with Herring Sperm DNA : Steady State/Time Resolved and Molecular Modeling Studies ». Biophysical Reviews and Letters 10, no 02 (juin 2015) : 115–33. http://dx.doi.org/10.1142/s1793048015500034.
Texte intégralThèses sur le sujet "Static and time resolved spectroscopies"
Capogrosso, Valentina. « Dimensionality and ordering effects on the electronic structure of low dimensional strongly correlated electron transition metal oxides ». Doctoral thesis, Università degli studi di Trieste, 2013. http://hdl.handle.net/10077/8587.
Texte intégralNel vasto scenario dei materiali fortemente correlati gli ossidi dei metalli di transizione hanno attratto enorme interesse a causa delle loro interessanti proprietà fisiche, come ad esempio, la superconduttività nei cuprati e la magnetoresistenza gigante nelle manganiti. In particolare, il mio interesse è stato rivolto ad una specifica classe di materiali, per i quali la dimensionalità è il parametro più importante. Le attività sperimentali sono state focalizzate verso due sistemi: la manganite Pr0.5Ca1.5MnO4 dopata a metà e a strato singolo (hd-PCMO) e la famiglia dei rutenati Srn+1RunO3n+1 (n=1,2,3). Entrambi questi sistemi esibiscono fenomeni affascinanti strettamente legati ad una complicata interazione tra i gradi di libertà del reticolo cristallino, di spin, di carica, ed orbitale, dove la dimensionalità cristallina gioca un ruolo cruciale. Con il mio progetto di dottorato ho studiato alcune proprietà dei materiali sopracitati per mezzo di spettroscopie con raggi X, come l’emissione risonante di raggi X (RXES) e l’assorbimento di raggi X (XAS) statico e risolto in tempo. Tutte le misure sono state condotte utilizzando la linea di luce BACH (linea di luce per dicroismo avanzato) dell’anello di accumulazione Elettra della Elettra-Sincrotrone Trieste. Il sistema hd-PCMO presenta una transizione di ordinamento di carica ed orbitale (CO-O) ad una temperatura TCO relativamente elevate, i.e. 340 K, accompagnata da una distorsione strutturale ortorombica, dove i portatori di carica fortemente correlati eg del Mn si ordinano in sotto-reticoli cristallografici separati (stato di carica ordinato) con un carattere orbitale specifico (stato di ordinamento orbitale). Inoltre, hd-PCMO presenta anche una risposta reticolare anomala ad una temperatura 20 K sopra la temperatura di Neél TN, che è associata ad un inatteso accoppiamento spin-reticolo. Poiché mancava uno studio degli stati elettronici non occupati del PCMO, misure dipendenti dalla temperatura per mezzo del dicroismo lineare (XLD) sono state realizzate alle soglie K dell’ossigeno e L3 del Mn al fine di spiegare il ruolo della topologia orbitale dei Mn 3d – O 2p. I dati sperimentali, supportati da calcoli ab-initio LDA+U, ci danno informazioni sulla ridistribuzione di carica e sui cambiamenti delle p-DOS alla transizione CO-O e a quella antiferromagnetica (AFM). I risultati ottenuti mostrano che l’interazione competitiva tra la distorsione locale atomica, necessaria per permettere l’ordinamento CO, e le dinamiche di carica del meccanismo di hopping regolano lo stato orbitale dei portatori di carica. Inoltre, sulla base di studi teorici che predicono la formazione di fasi orbitali e strutturali transienti “nascoste” per mezzo della stimolazione ottica, abbiamo studiato le DOS non occupate dello stato metastabile indotto otticamente nel PCMO per mezzo della XAS risolta in tempo, che offre uno strumento unico per misurare le DOS proiettate in sito ed in simmetria degli stati metastabili della materia. Le misure XAS risolte in tempo alla soglia K dell’ossigeno sono state realizzate per mezzo di un nuovo apparato sperimentale disponibile a BACH, che si basa su un laser Ti:zaffiro (impulsi di pompa) con tasso di ripetizione variabile sincronizzato con gli impulsi a 500 MHz dei raggi X (impulsi di sonda). L’evoluzione temporale degli spettri XAS attraverso la transizione CO-O fotoindotta otticamente risulta differente rispetto alle misure XAS adiabatiche, dimostrando l’esistenza di una “fase nascosta” fotoindotta nel PCMO, la cui natura è ancora sconosciuta. I rutenati Srn+1RunO3n+1 (n=1,2,3) sono emersi come una famiglia importante di peroschiti a causa dell’evoluzione inattesa e senza precedenti dal comportamento anisotropico ferro- o metamagnetico del Sr4Ru3O10 (n=3) dipendente dalla direzione del campo magnetico, all’ aumentato paramagnetismo di Pauli vicino all’ordinamento magnetico del Sr3Ru2O7 (n=2) e, infine, alla superconduttività a bassa temperature in Sr2RuO4 (n=1). Nonostante vengano riportati numerosi studi sulle proprietà strutturali e magnetiche di questi composti, l’evoluzione delle strutture elettroniche occupate e non occupate non è stata investigata in dettaglio. Quindi, la dipendenza delle strutture elettroniche e l’ibridizzazione degli stati 2p dell’ossigeno sono state investigate combinando la spettroscopia XAS alla soglia K dell’ossigeno (transizione 2p-1s) dipendente dalla polarizzazione e la spettroscopia RXES. Una sezione del capitolo 3 è dedicata ad illustrare un setup sperimentale sviluppato recentemente per esperimenti XAS risolti in tempo sfruttando la struttura temporale “multibunch” dell’anello di accumulazione del sincrotrone. Sfruttando le potenzialità di questo setup, la transizione di superficie semiconduttore-metallo nel germanio cristallino è stata fotoindotta ed il set completo di dati viene discusso. Lo schema della mia tesi di dottorato è il seguente. Il primo capitolo presenta una panoramica dell’intero lavoro. Il secondo capitolo è diviso in due sezioni. La prima sezione introduce il lettore alla fisica orbitale ed alle transizioni di fase elettroniche nei metalli di transizione a ridotta dimensionalità, con un excursus sullo stato dell’arte dei composti 3d del manganese e la famiglia 4d dei rutenati. L’intento della seconda sezione è quello di spiegare l’importanza delle tecniche spettroscopiche nei raggi X molli come strumenti per investigare le proprietà elettroniche dei solidi. La descrizione delle spettroscopie XAS e RXES vengono riviste più in dettaglio nel capitolo 3, che include anche la descrizione dell’apparato sperimentale della beamline BACH e del laboratorio T-ReX al Sincrotrone Elettra. Il capitolo 4 è dedicato alla teoria funzionale di densità (DFT) ed alla approssimazione locale di densità più U (LDA+U) ed ai dettagli del modello del sistema hd-PCMO. Il capitolo 5, che presenta i casi studiati, è diviso in due sezioni: il caso del PCMO, che include le misure XAS statiche e risolte in tempo, ed il caso della serie Ruddlesden-Popper dei rutenati di Sr investigate per mezzo della RXES. Nel capitolo finale vengono presentati i commenti finali su questo lavoro.
In the vast scenario of strongly correlated-electron materials transition-metal oxides have attracted enormous interest because of their interesting physical properties, including for example, superconductivity in cuprates and colossal magnetoresistance in manganites. In particular, my interest was directed to a particular class of materials, whose dimensionality is the most defining material parameter. With my Ph.D. project I deepened into some physical properties of these materials by means of core-levels spectroscopies such as resonant x ray emission (RXES) and static and time-resolved x ray absorption (XAS). All the measurements have been carried out at the beamline BACH (Beamline for Advanced diCHroism) at the Elettra light source facility in Trieste. The experimental activities focused on two case-study systems: the single layered half-doped Pr0.5Ca1.5MnO4 (hd-PCMO) and the layered Srn+1RunO3n+1 (n=1,2,3) family. Both these systems exhibit fascinating phenomena intimately related to a complicated interplay between the crystal lattice, spin, charge, and orbital degrees of freedom, where crystal dimensionality plays a crucial role. hd-PCMO exhibits a charge-orbital ordering (CO-O) transition at a remarkably high TCO, slightly above room temperature, accompanied by an orthorhombic structural distortion, where the strongly correlated Mn eg charge carriers order onto separate crystallographic sub-lattices (charge-ordered state) with a specific orbital character (orbital ordered state). Furthermore, hd-PCMO also displays an anomalous lattice response at temperatures 20K above the Neél temperature TN, which is associated to an unexpected spin-lattice coupling. Since a study of the PCMO unoccupied electronic states was lacking, temperature dependence measurements by XAS linear dichroism (XLD) have been performed at the O-K and Mn-L3 thresholds in order to elucidate the role of Mn 3d - O 2p orbital topology. The experimental data, supported by ab-initio LDA+U, shed light on the charge redistribution and p-DOS changes at the CO-O and antiferromagnetic (AFM) transitions. The results obtained show that the competitive interplay between the local atomic distortion, necessary for accomodating the CO-ordering, and the charge dynamics of the hopping mechanism regulates the orbital state of the charge carriers. Furthermore, on the basis of theoretical studies that predict the formation of transient “hidden” orbital and structural phases by optical stimulation, we have studied the unoccupied DOS of the optically induced metastable state in PCMO by means of time resolved XAS, which offers a unique tool to measure site and symmetry projected DOS of metastable states in matter. Tr-XAS measurements at the O-K edge have been carried out by means of a novel experimental apparatus available at BACH, which is based on a variable repetition rate Ti:sapphire laser (pump pulse) synchronized with the ∼ 500 MHz X-ray photon pulses (probe pulses). The time evolution of the XAS lineshapes across the optically photoinduced CO-O transition results different respect to the adiabatic XAS measurements, demonstrating the existence of a photoinduced “hidden phase” in PCMO, whose nature is still unknown. The layered Srn+1RunO3n+1 (n=1,2,3) have emerged as an important family of perovskites because of the unexpected and unprecedented evolution from anisotropic ferro- or metamagnetic behavior of Sr4Ru3O10 (n=3) dependent on the direction of the magnetic field, enhanced Pauli paramagnetism close to magnetic order of Sr3Ru2O7 (n=2) and, finally, to low-temperature superconductivity in Sr2RuO4 (n=1). Although numerous studies have been reported on the structural and magnetic properties of these compounds, the evolution of the occupied and unoccupied electronic structures were not investigated in detail. Thus, the dependence of electronic structures and the hybridization of O 2p states have been investigated by combining polarization dependent O K (2p-1s transition) XAS and RXES spectroscopies. A section of the chapter 3 is dedicated to illustrate a newly developed experimental setup for time-resolved XAS experiments by exploiting the multibunch time structure of a synchrotron storage ring. By exploiting the capabilities of this setup, the surface semiconductor-metal transition in crystalline germanium has been photoinduced and the complete set of data discussed. The outline of my Ph.D. thesis is the following. The first chapter presents an overview of the entire work. The second chapter is divided into two sections. The first section introduces the reader into the orbital physics and the electronic phase transitions in low dimensional transition metal oxides, with an excursus on the state of the art of 3d manganese compounds and the family of 4d Ruthenates. The second section is aimed to explain the importance of soft x-ray spectroscopic techniques as tools to investigate the electronic properties of solids. The description of XAS and RXES are reviewed in more details in chapter 3, which includes also the description of the experimental apparatus of BACH beamline and T-ReX lab at the Elettra synchrotron light source. Chapter 4 is dedicated to the Density Functional Theory (DFT) and Local Density Approximation plus U (LDA+U) theories and to the details of the modelling of the hd-PCMO system. Chapter 5, which presents the cases studied, is divided into two sections: the case of PCMO, including static and time resolved XAS measurements, and the case of Ruddlesden-Popper series of Sr Ruthenates investigated by means of RXES. In the final chapter the concluding remarks on this work are presented.
XXV Ciclo
1983
Pemasiri, Karunananda. « Investigation of zincblende, wurtzite, and mixed phase InP nanowires by photocurrent, photoluminescence and time-resolved photoluminescence spectroscopies ». University of Cincinnati / OhioLINK, 2013. http://rave.ohiolink.edu/etdc/view?acc_num=ucin1377873494.
Texte intégralVillamil, Franco Carolina. « Ultrafast dynamics of excitons and charge carriers in colloidal perovskite nanostructures studied by time-resolved optical spectroscopies ». Thesis, université Paris-Saclay, 2020. http://www.theses.fr/2020UPASF012.
Texte intégralHalide perovskites have emerged as very promising photoactive materials due to their outstanding optoelectronic properties combined with low-cost processability. In spite of their successful implementation in photovoltaic or light-emitting devices, a deep understanding of the dynamics of relaxation and recombination is still missing in order to enhance the device performances. This thesis focuses on the study of two major fundamental processes occurring in colloidal halide perovskite nanostructures: the hot charge carrier/exciton relaxation (“cooling”), after excitation above the optical bandgap, and the non-radiative Auger recombination, taking place after high-fluence or high-photon energy excitation. In particular, time-resolved photoluminescence and femtosecond transient absorption spectroscopy were used to investigate the confinement and composition effects in strongly confined two-dimensional (2D) lead iodide perovskite nanoplatelets (NPLs), that were synthesized following the development and optimizations of colloidal methods. For the investigation of the cooling dynamics, a global analysis method based on single value decomposition was used, where the temporal evolution of the spectral lineshapes was modeled with a sequential kinetic scheme. This method was succesfully applied to effectively describe the continuous energy relaxation in weakly-confined thick FAPbI₃ nanoplates (FA=formamidinium) and allowed disantangleting the hot phonon bottleneck from the Auger reheating effects at high excitation fluence. Furthermore, the global analysis was essential to investigate the cooling dynamics in strongly confined 2D NPLs presenting large Stark effects and discrete excitonic band-edge transition far away from the continuum of states (exciton binding energy in several hundreds of meV). As in the weakly confined samples, the cooling rate of the NPLs decreases with the excitation fluence. However, it is faster in more-strongly confined samples, evidencing the absence of an intrinsic phonon bottleneck. Furthermore, the cooling rate and its evolution with the exciton density were found independent of the nature of the internal cations (FA, MA=methylammonium and Cs=cesium). However, when comparing with the rate measured in 2D layered perovskite thin film with equivalent quantum well thickness, the results strongly suggest a role of the surface ligands in the possibility to release the excess energy to the surrounding environment. This ligand-mediated relaxation mechanism becomes dominent in the thinner NPL samples with enhanced exciton/ligand vibrational mode coupling. Then, the multiple exciton recombination dominated by non-radiative Auger recombination (AR) was studied in the strongly-confined 2D perovskite NPLs. Due to the large asymmetric geometry and the limited exciton wavefunction delocalization, the AR rate strongly depends on the exciton density via the initial average inter-exciton distance. At low fluence, this distance is in several tens of nanometers such as the AR is limited by the exciton diffusion in the 2D plane. It thus occurs on a timescale of several hundreds of picoseconds and depends on the sample dimensionality (thickness and lateral sizes). In contrast, high excitation fluences produce “overlapping” excitons with inter-exciton distances of only a few times the exciton Bohr radius, resulting in AR times of less than 10 ps and independent of the NPL composition nor geometry. Finally, the exciton population dynamics of 2D NPLs after excitation in the ultraviolet was measured. The strong dependence of the AR with the inter-exciton distance allows the identification of multiple exciton generation (MEG), which involves the reaction of “geminate biexcitons” produced by the absorption of a single high-energy photon
Hussain, Abid [Verfasser], et Nils [Akademischer Betreuer] Huse. « Theory and computation of time-resolved spectroscopies for molecular systems in complex environments / Abid Hussain ; Betreuer : Nils Huse ». Hamburg : Staats- und Universitätsbibliothek Hamburg, 2017. http://d-nb.info/1137323701/34.
Texte intégralMiki, Takeshi [Verfasser], et Marcus [Akademischer Betreuer] Motzkus. « Third- and Fifth-order Nonlinear Time-resolved Spectroscopies for Ultrafast Molecular Dynamics in Carotenoids / Takeshi Miki ; Betreuer : Marcus Motzkus ». Heidelberg : Universitätsbibliothek Heidelberg, 2017. http://d-nb.info/1180986385/34.
Texte intégralHieke, Florian [Verfasser], et Wilfried [Akademischer Betreuer] Wurth. « Electronic Excitations in Solids Studied with Static and Time Resolved X-ray Spectroscopy / Florian Hieke ; Betreuer : Wilfried Wurth ». Hamburg : Staats- und Universitätsbibliothek Hamburg, 2017. http://d-nb.info/1129874826/34.
Texte intégralHua, Ying. « Structures auto-assemblées de guanines étudiées par spectroscopie optique résolue en temps ». Phd thesis, Université Paris Sud - Paris XI, 2013. http://tel.archives-ouvertes.fr/tel-00873695.
Texte intégralPaul, Rajsekhar [Verfasser], Josef [Akademischer Betreuer] Wachtveitl et C. Roy D. [Akademischer Betreuer] Lancaster. « From static difference to time-resolved spectroscopy of coupled electron and proton transfer in the quinol : fumarate reductase of Wolinella succinogenes / Rajsekhar Paul. Gutachter : Josef Wachtveitl ; C. Roy D. Lancaster ». Frankfurt am Main : Univ.-Bibliothek Frankfurt am Main, 2011. http://d-nb.info/1044195150/34.
Texte intégralKhadeeva, Liya. « Photo-isomerization and photo-induced NO release in ruthenium nitrosyl compounds ». Thesis, Rennes 1, 2016. http://www.theses.fr/2016REN1S067/document.
Texte intégralThis Ph. D. thesis is focused on the experimental study of two photo-induced processes observed in various [ML_5NO] complexes, where M=Fe, Ru, ..., L=CN, Cl, ... : (i) photo-isomerization, where the system goes from N-bound state (M-NO, stable GS state) to O-bound state (M-ON, metastable MSI state) and a second metastable state, 'side-on' MSII is observed during the inverse photo-transformation, MSI --> 'side-on' MSII --> GS; (ii) photo-induced release of NO° radical. The photo-isomerization is investigated in single crystals of [Ru(py)_4Cl(NO)](PF_6)_2.1/2H_2O compound by means of X-Ray diffraction, steady state visible and time-resolved UV-visible absorption spectroscopies. During these experiments we observed the evidence of a two-step photon absorption process (473 nm), we followed the dynamics of direct and inverse photo-switching by the evolution of lattice parameters and absorption in the visible range and we caracterised the structure of 'side-on' MSII state. The nature of MSII in the direct photo-switching, GS --> MSI, seems to be different from the 'side-on' configuration, however, we do not have a direct access to this state due to its low population. The role of water molecule in the unit cell of [Ru(py)_4Cl(NO)](PF_6)_2.1/2H_2O complex was tested by X-Ray diffraction studies on hydrated, dehydrated and rehydrated samples. The effect of sample dehydration on the unit cell parameters evolution and MSII species generation during the MSI --> MSII --> GS inverse photo-switching is presented. The photo-induced NO° release in trans-(Cl,Cl)[Ru^{II}(FT)Cl_2(NO)]PF_6 system in acetonitrile solution is studied by the UV-visible and mid-IR absorption spectroscopies, both steady state and time-resolved. By observing the ultra-fast dynamics of photo-transformation we evidenced a two-step photon absorption process (406 nm). The nature of intermediate state is discussed within the recent theoretical calculations and the photo-isomerization process
Bourhis, Kevin. « Photostructuration par laser infrarouge femtoseconde de verres photosensibles de phosphates de zinc, d'argent et de gallium ». Phd thesis, Université Sciences et Technologies - Bordeaux I, 2011. http://tel.archives-ouvertes.fr/tel-00661392.
Texte intégralChapitres de livres sur le sujet "Static and time resolved spectroscopies"
Kliger, David S., Eefei Chen et Robert A. Goldbeck. « Nanosecond Time-Resolved Natural and Magnetic Chiroptical Spectroscopies ». Dans Comprehensive Chiroptical Spectroscopy, 179–201. Hoboken, NJ, USA : John Wiley & Sons, Inc., 2012. http://dx.doi.org/10.1002/9781118120187.ch7.
Texte intégralKirkwood, Jason C., Christoph Scheurer, Tatsuya Minami, Vladimir Chernyak et Shaul Mukamel. « Energy funneling in the dendrimeric nanostar probed by time-resolved nonlinear spectroscopies ». Dans Ultrafast Phenomena XII, 610–12. Berlin, Heidelberg : Springer Berlin Heidelberg, 2001. http://dx.doi.org/10.1007/978-3-642-56546-5_180.
Texte intégralIto, Osamu. « Chapter 8. Electron-Transfer Processes of Fullerenes Studied with Time-Resolved Spectroscopies ». Dans Nanoscience & ; Nanotechnology Series, 270–328. Cambridge : Royal Society of Chemistry, 2011. http://dx.doi.org/10.1039/9781849732956-00270.
Texte intégralHarford, Jeff, et John M. Squire. « Static and Time-resolved X-ray Diffraction Studies of Fish Muscle ». Dans Molecular Mechanisms in Muscular Contraction, 287–320. London : Macmillan Education UK, 1990. http://dx.doi.org/10.1007/978-1-349-09814-9_10.
Texte intégralVenanzi, Mariano, Emanuela Gatto, Gianfranco Bocchinfuso, Antonio Palleschi, Lorenzo Stella, Chiara Baldini, Fernando Formaggio, Claudio Toniolo et Basilio Pispisa. « Monitoring Peptide Folding by Time-Resolved Spectroscopies : the Effect of a Single Gly to Aib Susbtitution ». Dans Advances in Experimental Medicine and Biology, 47–48. New York, NY : Springer New York, 2009. http://dx.doi.org/10.1007/978-0-387-73657-0_21.
Texte intégralMasotti, Lanfranco, Paolo Cavatorta, Arthur G. Szabo, Giorgio Farruggia et Giovanna Sartor. « Conformational Flexibility of the Polypeptide Hormone Bombesin : Time Resolved and Static Fluorescence Studies ». Dans Fluorescent Biomolecules, 173–93. Boston, MA : Springer US, 1989. http://dx.doi.org/10.1007/978-1-4684-5619-6_12.
Texte intégralHunter, D. B., W. P. Gates, P. M. Bertsch et K. M. Kemner. « Degradation of Tetraphenylboron at Hydrated Smectite Surfaces Studied by Time Resolved IR and X-ray Absorption Spectroscopies ». Dans ACS Symposium Series, 282–300. Washington, DC : American Chemical Society, 1999. http://dx.doi.org/10.1021/bk-1998-0715.ch014.
Texte intégralHienerwadel, Rainer, Eliane Nabedryk, Jacques Breton, Werner Kreutz et Werner Mäntele. « Time-Resolved Infrared and Static FTIR Studies of QA → QB Electron Transfer in Rhodopseudomonas Viridis Reaction Centers ». Dans The Photosynthetic Bacterial Reaction Center II, 163–72. Boston, MA : Springer US, 1992. http://dx.doi.org/10.1007/978-1-4615-3050-3_20.
Texte intégralDeveaud, B. « Time-Resolved Optical Spectroscopies ». Dans Encyclopedia of Condensed Matter Physics, 206–14. Elsevier, 2005. http://dx.doi.org/10.1016/b0-12-369401-9/00672-0.
Texte intégralGoldbeck, Robert A., et David S. Kliger. « [7] Nanosecond time-resolved absorption and polarization dichroism spectroscopies ». Dans Metallobiochemistry Part C : Spectroscopic and Physical Methods for Probing Metal Ion Environments in Metalloenzymes and Metalloproteins, 147–77. Elsevier, 1993. http://dx.doi.org/10.1016/0076-6879(93)26009-x.
Texte intégralActes de conférences sur le sujet "Static and time resolved spectroscopies"
Myers, Anne B., et Alan E. Johnson. « Electronic and Vibrational Dephasing in Solution by Dynamic Symmetry Breaking ». Dans International Conference on Ultrafast Phenomena. Washington, D.C. : Optica Publishing Group, 1996. http://dx.doi.org/10.1364/up.1996.fe.25.
Texte intégralBawendi, Moungi G. « Size Dependent Spectroscopy of CdSe Nanocrystallites ». Dans Spectral Hole-Burning and Related Spectroscopies : Science and Applications. Washington, D.C. : Optica Publishing Group, 1994. http://dx.doi.org/10.1364/shbs.1994.fb1.
Texte intégralLong, J. P., B. S. Itchkawitz et M. N. Kabler. « Photoelectron Spectroscopy of Laser Excited Surfaces Using Synchrotron Radiation ». Dans High Resolution Fourier Transform Spectroscopy. Washington, D.C. : Optica Publishing Group, 1994. http://dx.doi.org/10.1364/hrfts.1994.wd2.
Texte intégralBressler, Christian. « Time-Resolved X-Ray Spectroscopies and Scattering ». Dans International Conference on Ultrafast Structural Dynamics. Washington, D.C. : OSA, 2012. http://dx.doi.org/10.1364/icusd.2012.iw2d.1.
Texte intégralGaft, M., L. Nagli et Arnold Gucsik. « Time-Resolved Laser Based Spectroscopies for Mineralogical Research and Applications ». Dans MICRO-RAMAN SPECTROSCOPY AND LUMINESCENCE STUDIES IN THE EARTH AND PLANETARY SCIENCES : Proceedings of the International Conference Spectroscopy 2009. AIP, 2009. http://dx.doi.org/10.1063/1.3222892.
Texte intégralXie, X. Sunney, et Robert C. Dunn. « Near-field Time-Resolved Fluorescence Spectroscopy of Single Molecules ». Dans Spectral Hole-Burning and Related Spectroscopies : Science and Applications. Washington, D.C. : Optica Publishing Group, 1994. http://dx.doi.org/10.1364/shbs.1994.fc2.
Texte intégralWooseok, Heo, Kim JunWoo, Lee Changmin et Joo Taiha. « Reaction dynamics by time-resolved wave packet spectroscopies & ; molecular dynamics simulation ». Dans Asian Spectroscopy Conference 2020. Institute of Advanced Studies, Nanyang Technological University, 2020. http://dx.doi.org/10.32655/asc_8-10_dec2020.36.
Texte intégralKoichi, Iwata. « Properties of lipid bilayer membranes examined with time-resolved fluorescence and Raman spectroscopies ». Dans Asian Spectroscopy Conference 2020. Institute of Advanced Studies, Nanyang Technological University, 2020. http://dx.doi.org/10.32655/asc_8-10_dec2020.1.
Texte intégralGoldbeck, Robert A., et David S. Kliger. « Nanosecond time-resolved polarization spectroscopies and applications to the study of protein function and folding ». Dans BiOS '98 International Biomedical Optics Symposium, sous la direction de Joseph R. Lakowicz et J. B. Alexander Ross. SPIE, 1998. http://dx.doi.org/10.1117/12.307069.
Texte intégralMatousek, P., A. W. Parker, P. F. Taday, W. T. Toner et M. Towrie. « Doubly Tunable Femtosecond Pulses Generated in the Visible using Optical Parametric Amplifiers for Time-resolved Spectroscopy ». Dans Laser Applications to Chemical and Environmental Analysis. Washington, D.C. : Optica Publishing Group, 1996. http://dx.doi.org/10.1364/lacea.1996.lwd.3.
Texte intégralRapports d'organisations sur le sujet "Static and time resolved spectroscopies"
Sandstrom, Donald R. Study of Chemical Systems in Static and Time Resolved Mode by X-ray Absorption Spectroscopy. Fort Belvoir, VA : Defense Technical Information Center, novembre 1989. http://dx.doi.org/10.21236/ada215383.
Texte intégralCrawford, Daniel. "Structure and dynamics in complex chemical systems : Gaining new insights through recent advances in time-resolved spectroscopies.” ACS Division of Physical Chemistry Symposium presented at the Fall National ACS Meeting in Boston, MA, August 2015. Office of Scientific and Technical Information (OSTI), septembre 2016. http://dx.doi.org/10.2172/1326393.
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