Letteratura scientifica selezionata sul tema "Electronic spectroscopies"
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Articoli di riviste sul tema "Electronic spectroscopies":
KOBAYASHI, NAGAO. "Theoretical interpretation of spectroscopic data". Journal of Porphyrins and Phthalocyanines 04, n. 04 (giugno 2000): 377–79. http://dx.doi.org/10.1002/(sici)1099-1409(200006/07)4:4<377::aid-jpp236>3.0.co;2-3.
Oliver, Thomas A. A. "Recent advances in multidimensional ultrafast spectroscopy". Royal Society Open Science 5, n. 1 (gennaio 2018): 171425. http://dx.doi.org/10.1098/rsos.171425.
Dessau, Dan, Zahid Hussain e Z. Q. Qiu. "Workshop on Spectroscopies of Electronic Materials". Synchrotron Radiation News 15, n. 1 (gennaio 2002): 13–14. http://dx.doi.org/10.1080/08940880208602925.
Busca, G., G. Martra e A. Zecchina. "Characterisation by vibrational and electronic spectroscopies". Catalysis Today 56, n. 4 (marzo 2000): 361–70. http://dx.doi.org/10.1016/s0920-5861(99)00296-5.
Biswas, Somnath, JunWoo Kim, Xinzi Zhang e Gregory D. Scholes. "Coherent Two-Dimensional and Broadband Electronic Spectroscopies". Chemical Reviews 122, n. 3 (17 gennaio 2022): 4257–321. http://dx.doi.org/10.1021/acs.chemrev.1c00623.
Pen, H. F., M. Abbate, A. Fuijmori, Y. Tokura, H. Eisaki, S. Uchida e G. A. Sawatzky. "Electronic structure ofY1−xCaxVO3studied by high-energy spectroscopies". Physical Review B 59, n. 11 (15 marzo 1999): 7422–32. http://dx.doi.org/10.1103/physrevb.59.7422.
Fujisawa, M., S. Suga, T. Mizokawa, A. Fujimori e K. Sato. "Electronic structures ofCuFeS2andCuAl0.9Fe0.1S2studied by electron and optical spectroscopies". Physical Review B 49, n. 11 (15 marzo 1994): 7155–64. http://dx.doi.org/10.1103/physrevb.49.7155.
Le F�vre, P., H. Magnan, K. Hricovini, D. Chandesris, J. Vogel, V. Formoso, T. Eickhoff e W. Drube. "Ce Electronic Structure Studied by Resonant Electron Spectroscopies". physica status solidi (b) 215, n. 1 (settembre 1999): 617–23. http://dx.doi.org/10.1002/(sici)1521-3951(199909)215:1<617::aid-pssb617>3.0.co;2-c.
Hawrylak, P., A. Wojs, D. J. Lockwood, P. D. Wang, C. M. Sotomayor Torres, A. Pinczuk e B. S. Dennis. "Optical spectroscopies of electronic excitations in quantum dots". Surface Science 361-362 (luglio 1996): 774–77. http://dx.doi.org/10.1016/0039-6028(96)00531-6.
Khalifi, Mohammed El, Fabien Picaud e Mohamed Bizi. "Electronic and optical properties of CeO2 from first principles calculations". Analytical Methods 8, n. 25 (2016): 5045–52. http://dx.doi.org/10.1039/c6ay00374e.
Tesi sul tema "Electronic spectroscopies":
Li, Xin. "Theoretical studies on electronic structure and x-ray spectroscopies of 2D materials". Doctoral thesis, KTH, Teoretisk kemi och biologi, 2016. http://urn.kb.se/resolve?urn=urn:nbn:se:kth:diva-185683.
QC 20160425
Lindblad, Andreas. "A Treatise on the Geometric and Electronic Structure of Clusters : Investigated by Synchrotron Radiation Based Electron Spectroscopies". Doctoral thesis, Uppsala University, Department of Physics and Materials Science, 2008. http://urn.kb.se/resolve?urn=urn:nbn:se:uu:diva-8463.
Clusters are finite ensembles of atoms or molecules with sizes in the nanometer regime (i.e. nanoparticles). This thesis present results on the geometric and electronic structure of homogeneous and heterogeneous combinations of atoms and molecules. The systems have been studied with synchrotron radiation and valence, core and Auger electron spectroscopic techniques.
The first theme of the thesis is that of mixed clusters. It is shown that by varying the cluster production technique both structures that are close to that predicted by equilibrium considerations can be attained as well as far from equilibrium structures.
Electronic processes following ionization constitute the second theme. The post-collision interaction phenomenon, energy exchange between the photo- and the Auger electrons, is shown to be different in clusters of argon, krypton and xenon. A model is proposed that takes polarization screening in the final state into account. This result is of general character and should be applicable to the analysis of core level photoelectron and Auger electron spectra of insulating and semi-conducting bulk materials as well.
Interatomic Coloumbic Decay is a process that can occur in the condensed phases of weakly bonded systems. Results on the time-scale of the process in Ne clusters and mixed Ar/Ne clusters are herein discussed, as well observations of resonant contributions to the process. In analogy to Auger vis-à-vis Resonant Auger it is found that to the ICD process there is a corresponding Resonant ICD process possible. This has later been observed in other systems and by theoretical calculations as well in subsequent works by other groups.
Delocalization of dicationic valence final states in the hydrogen bonded ammonia clusters and aqueous ammonia has also been investigated by Auger electron spectroscopy. With those results it was possible to assign a previously observed feature in the Auger electron spectrum of solid ammonia.
Lee, Min-I. "Atomic structure, electronic states and relaxation dynamics in photovoltaic materials and interfaces from photoemission-related spectroscopies". Thesis, Université Paris-Saclay (ComUE), 2018. http://www.theses.fr/2018SACLS220/document.
The efficiency of the photovoltaic process depends on the electronic band structure of the active material and the charge carrier dynamics. In this thesis, we have studied how these issues are related to the atomic structure in materials for two different technologies of solar cells, namely silicon heterostructure solar cells, and hybrid organic-inorganic perovskite solar cells. In silicon heterostructure solar cells, we have analyzed the impact of defects on the electronic properties of amorphous silicon heterostructures (a-Si:H/a-SIC:H/c-Si) by core level and valence band spectroscopies. In particular, we have quantified the number of dangling bonds inside a-Si:H layer upon irradiation, we have identified the electronic states associated to them, and we have understood the transitions previously observed by photoluminescence. In perovskite solar cells, we have correlated the atomic structure, the electronic structure and the electronic dynamics for two- and three-dimensional hybrid organic-inorganic perovskites. We have used with this goal a whole panel of complementary techniques: X-ray diffraction, angle-resolved photoemission spectroscopy, inverse photoemission spectroscopy, and time-resolved two-photon photoemission. In the two-dimensional perovskite (C₆H₅C₂H₄NH₃)₂PbI₄, the valence and conduction bands have been determined experimentally and compared to spectral function simulations. In the three-dimensional perovskite CH₃NH₃PbI₃, we have again determined the band structure and simulated it. Very broad spectral features have been experimentally observed, which relax the optical transition conditions impacting in the solarcell efficiencies. In both experiments and calculations, we observe that the spectral weight follows a cubic periodicity while the system is structurally in the tetragonal phase. This apparent contradiction is explained by the band broadness, which hides the band folding of the tetragonal distortion. As for the relaxation dynamics, we have observed that the photoexcited carriers thermalize in a subpicosecond time scale through the coupling to organic cation vibrations. At longer timescales (10~100 picoseconds), the electron diffusion controls the dynamics. This dynamics is affected by the annealing-induced defects, which localize the photoexcited electrons for more than 300 picoseconds
Carleschi, Emanuela. "Electronic structure of transition metal and rare earth ions in complex materials by resonant core-level spectroscopies". Doctoral thesis, Università degli studi di Trieste, 2009. http://hdl.handle.net/10077/3061.
In the course of this thesis I present an experimental investigation into various strongly correlated transition metal and rare earth compounds using core-level spectroscopic techniques, which have augmented the understanding of the electronic properties of these different systems. I will discuss the orbital occupation and the symmetry of the states near the Fermi level, responsible for the variety of ground states shown by a variety of strongly correlated systems such as misfit cobaltates, strontium ruthenates, metallic manganese and rare earth compounds.
XXI Ciclo
1978
Tournier-Colletta, Cédric. "Etude par spectroscopies d'électrons d'interfaces métalliques et semiconductrices". Thesis, Nancy 1, 2011. http://www.theses.fr/2011NAN10109/document.
This thesis is devoted to the electronic properties of low-dimensional systems based on metal and semiconducting materials. The first part deals with the Shockley state confinement in Ag(111) nanostructures, by means of very-low temperature (5 K) STM/STS measurements. We study the electronic structure and spatial distribution of the confined modes. Then the discrete nature of the electronic spectrum allows one to yield the quasiparticule lifetime. A Fermi-liquid behaviour is evidenced and we show that the dominant decay mechanism is attributed to the electron-phonon coupling. The extrinsic contribution arising from the partial confinement of the electronic wave is obtained as well. A scaling law with the nanostructure width is demonstrated, from which we deduce a higher reflection amplitude than in monoatomic islands. In the second part of the thesis, we study semiconducting ultra-thin films produced by alkali (K, Rb, Cs) deposition on the Si(111):B-[root of]3 surface. This work solves the controversy concerning the ground state of this system, and especially the nature of the 2[root of]3 surface recontruction obtained at saturation coverage. Prior understanding of the crystallographic structure allows to elucidate the electronic properties. We show that a one-electron picture, leading to a band insulator scenario, gives a good description of the system, in spite of strong polaronic effects. This conclusion results from an in-depth, combined study of complementary techniques (LEED, ARPES, XPS, STM/STS and DFT calculations)
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.
Nel 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
Gallo, Erik. "Modification of the electronic structure of catalytic active transition-metal centers upon molecular adsorption : an XAS/XES study". Thesis, Rennes 1, 2013. http://www.theses.fr/2013REN1S054/document.
The purpose of this research project was to apply advanced X-ray based spectroscopic techniques for investigating the electronic structure of transition metals within catalysts and molecular sieves under in-situ conditions. Thus, the first chapter of the thesis, "X-Ray Spectroscopy: an Overview " briefly presents the spectroscopic techniques available at ID26, beamline of the European Synchrotron Radiation Facility (Grenoble) where all the measurements reported in this work have been obtained. In the second chapter, "Study of the Electronic structure of the Ti-sites in TS-1 using hard X-ray spectroscopy", it is reported the electronic characterization of the Ti centres in titanium silicalite-1 (TS-1), that is a relevant catalyst employed in industrial plants worldwide. The chapter shows that the combination of X-ray absorption and X-ray emission spectroscopy with quantum mechanical calculations is effective to obtain important insights on the electronic structure of the Ti-centres under in-situ conditions. The third chapter entitled “Identification of the Ti-Ligands in Silica Supported Ziegler-Natta Catalyst by X- Ray Emission Spectroscopy" presents the study of a variant of the Ziegler-Natta catalyst. The chapter discusses the interpretation of the valence emission lines within the theoretical framework provided by the density functional theory (DFT) and proposes possible models for the Ti-ligand-environment. The fourth chapter, entitled "Observing the dd-Excitations in CPO-27-Ni using Resonant Inelastic X-ray Scattering", concludes the main part of the thesis. It presents the application of resonant inelastic X-ray scattering (RIXS) for obtaining the crystal field excitations of the Ni ions within nickel oxide and within a Ni- metal-organic-framework (CPO-27-Ni). The chapter briefly describes the different theoretical approaches that can be used for the interpretation of the spectral features and discusses the adsorption of probe molecules like H2O, CO and H2S on the Ni centres of CPO-27-Ni. The last chapter (Chapter five) drawn a series of conclusions concerning the performed investigations and indicates possible future research directions. In Appendix A entitled "Pump and Probe Time Resolved Experiments at ID26" it is reported the description of the experimental setup co-developed and co-realized by the candidate for time resolved experiments. The appendix also accounts for the scientific outcome of the performed pump and probe measurements. The curriculum vitae and the publications list of the candidate are respectively reported in Appendix B and C
Mahjoub, Mohamed Aymen. "Contributions aux études quantitatives par spectroscopies électroniques (EPES et XPS) : Applications aux surfaces nanostructurées". Thesis, Clermont-Ferrand 2, 2016. http://www.theses.fr/2016CLF22666/document.
This thesis focuses on the development of new in-situ methods of characterization based on the electron spectroscopies (XPS and EPES) coupled with theoretical calculations obtained through Monte-Carlo simulations in order to perform very precise quantitative studies. The first part of this thesis was devoted to quantitative studies of XPS and MM-EPES measurements. Firstly, the correction function of a hemispherical analyzer (HSA) which is a combination of the analysis area (A) and the transmission (T) was determined using a new method based on the elastic images. For the first time, the dependence of A on the kinetic energy of electrons was highlighted. Using this function, an in-situ method based on the combination of XPS and MM-EPES modeling was setting up. This method was used to determine the organization of gold film deposed on oxidized silicon substrate. Measurements show that this method is able to determine surface parameters when the microscopy techniques do not give any information in the case of a small quantity of gold deposit (less than 2 nm). The second part of this work was directed towards developing a new generation of microscopy called MM-EPEM which is based on the detection of elastic electrons. The stages required to obtain these images are well described and optimized here. The MM-EPEM images processing was used to study gold growth on different substrates. This technique is a non-destructive method and allows the operator to construct chemical tomography and to determine the nano-organization of the surface
Darsey, Gary Paul. "The electronic structure of methyl-substituted ferrocenes and early transition metal bent metallocenes by gas phase ultraviolet and X-ray photoelectron spectroscopies". Diss., The University of Arizona, 1988. http://hdl.handle.net/10150/184473.
KELLOGG, GLEN EUGENE. "ELECTRONIC FACTORS OF CARBON - HYDROGEN AND DOUBLE-BONDED CARBON BOND ACTIVATION: EXPERIMENTAL INFORMATION FROM ULTRAVIOLET AND X-RAY PHOTOELECTRON SPECTROSCOPIES (CORE, VALENCE, OLEFIN)". Diss., The University of Arizona, 1985. http://hdl.handle.net/10150/188067.
Libri sul tema "Electronic spectroscopies":
A, Balzarotti, Guizzetti G e Stella A, a cura di. Highlights on spectroscopies of semiconductors and insulators: Castro Marina, Italy, September 1987. Singapore: World Scientific, 1989.
Wolfgang, Domcke, Yarkony David e Köppel Horst, a cura di. Conical intersections: Electronic structure, dynamics & spectroscopy. River Edge, NJ: World Scientific, 2004.
Hughes, H. P., e H. I. Starnberg. Electron spectroscopies applied to low-dimensional structures. New York: Kluwer Academic, 2002.
M, Loew Leslie, a cura di. Spectroscopic membrane probes. Boca Raton, Fla: CRC Press, 1988.
Baldassare, Di Bartolo, Gambarota Giulio e NATO Advanced Study Institute on Ultrafast Dynamics of Quantum Systems: Physical Processes and Spectroscopic Techniques (1997 : Erice, Italy), a cura di. Ultrafast dynamics of quantum systems: Physical processes and spectroscopic techniques. New York: Plenum Press, 1998.
Nowicki, Marek. Zastosowanie efektów dyfrakcyjnych elektronów pierwotnych i wtórnych w badaniach strukturalnych. Wrocław: Wydawn. Uniwersytetu Wrocławskiego, 2003.
1942-, Thompson Michael, a cura di. Auger electron spectroscopy. New York: Wiley, 1985.
Long, Edward R. Spectroscopic comparison of effects of electron radiation on mechanical properties of two polyimides. [Washington, DC]: National Aeronautics and Space Administration, Scientific and Technical Information Branch, 1987.
Uchida, Masaki. Spectroscopic Study on Charge-Spin-Orbital Coupled Phenomena in Mott-Transition Oxides. Tokyo: Springer Japan, 2013.
Scottish, Universities Summer School in Physics (40th 1992 Dundee Scotland). Quantitative microbeam analysis: Proceedings of the Fortieth Scottish Universities Summer School in Physics, Dundee, August 1992. Bristol: The School, 1993.
Capitoli di libri sul tema "Electronic spectroscopies":
Colliex, Christian. "Investigation of Local Electronic Properties in Solids by Transmission Electron Energy Loss Spectroscopy". In Core Level Spectroscopies for Magnetic Phenomena, 213–33. Boston, MA: Springer US, 1995. http://dx.doi.org/10.1007/978-1-4757-9871-5_13.
Jentoft, Friederike C. "Electronic Spectroscopy: Ultra Violet-Visible and near IR Spectroscopies". In Characterization of Solid Materials and Heterogeneous Catalysts, 89–147. Weinheim, Germany: Wiley-VCH Verlag GmbH & Co. KGaA, 2012. http://dx.doi.org/10.1002/9783527645329.ch3.
Doyen, G., D. Drakova e F. von Trentini. "Theoretical Aspects of Electronic Spectroscopies at (Adsorbate Covered) Surfaces". In Lectures on Surface Science, 154–68. Berlin, Heidelberg: Springer Berlin Heidelberg, 1987. http://dx.doi.org/10.1007/978-3-642-71723-9_28.
Zanni, Martin T. "Automated 2D infrared and electronic spectroscopies using pulse shaping". In Springer Series in Chemical Physics, 397–99. Berlin, Heidelberg: Springer Berlin Heidelberg, 2009. http://dx.doi.org/10.1007/978-3-540-95946-5_128.
Jaegermann, Wolfram, Andreas Klein e Christian Pettenkofer. "Electronic Properties of Van Der Waals-Epitaxy Films and Interfaces". In Electron Spectroscopies Applied to Low-Dimensional Materials, 317–402. Dordrecht: Springer Netherlands, 2002. http://dx.doi.org/10.1007/0-306-47126-4_7.
Parmigiani, Fulvio, e Luigi Sangaletti. "Electronic Correlations in the 3s Photoelectron Spectra of the Late Transition Metal Oxides". In Core Level Spectroscopies for Magnetic Phenomena, 249–64. Boston, MA: Springer US, 1995. http://dx.doi.org/10.1007/978-1-4757-9871-5_15.
Smulevich, Giulietta. "Electronic Absorption and Resonance Raman Spectroscopies to Investigate Heme Proteins". In Spectroscopy of Biological Molecules: Modern Trends, 83–84. Dordrecht: Springer Netherlands, 1997. http://dx.doi.org/10.1007/978-94-011-5622-6_35.
Mukamel, Shaul, Wei Min Zhang e Vladimir Chemyak. "Structure Determination of Antenna Complexes Using Two-Dimensional Femtosecond Electronic Spectroscopies". In Photosynthesis: Mechanisms and Effects, 3–8. Dordrecht: Springer Netherlands, 1998. http://dx.doi.org/10.1007/978-94-011-3953-3_1.
Sawatzky, G. A. "Electronic Structure of Transition Metal Compounds as Studied by High Energy Spectroscopies". In Springer Series in Solid-State Sciences, 99–124. Berlin, Heidelberg: Springer Berlin Heidelberg, 1988. http://dx.doi.org/10.1007/978-3-642-83437-0_9.
Conti, Irene, Matteo Bonfanti, Artur Nenov, Ivan Rivalta e Marco Garavelli. "Photo-Active Biological Molecular Materials: From Photoinduced Dynamics to Transient Electronic Spectroscopies". In Challenges and Advances in Computational Chemistry and Physics, 77–142. Cham: Springer International Publishing, 2020. http://dx.doi.org/10.1007/978-3-030-57721-6_2.
Atti di convegni sul tema "Electronic spectroscopies":
Garg, Manish. "Imaging electronic and atomic motion in molecules". In Enhanced Spectroscopies and Nanoimaging 2023, a cura di Prabhat Verma e Yung Doug Suh. SPIE, 2023. http://dx.doi.org/10.1117/12.2677254.
Myers, Anne B., e Alan E. Johnson. "Electronic and Vibrational Dephasing in Solution by Dynamic Symmetry Breaking". In International Conference on Ultrafast Phenomena. Washington, D.C.: Optica Publishing Group, 1996. http://dx.doi.org/10.1364/up.1996.fe.25.
Canel, E. "Theoretical Models for Photochromic Systems". In Spectral Hole-Burning and Related Spectroscopies: Science and Applications. Washington, D.C.: Optica Publishing Group, 1994. http://dx.doi.org/10.1364/shbs.1994.wd45.
Ikeda, Katsuyoshi. "Surface-enhanced Raman spectroscopy at electrified interfaces: electronic SERS and low-frequency vibrational SERS (Conference Presentation)". In Enhanced Spectroscopies and Nanoimaging 2022, a cura di Prabhat Verma e Yung Doug Suh. SPIE, 2022. http://dx.doi.org/10.1117/12.2634191.
Bawendi, Moungi G. "Size Dependent Spectroscopy of CdSe Nanocrystallites". In 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.
Small, G. J. "Applications of spectral hole-burning spectroscopies to the excited electronic states and transport dynamics of photosynthetic units". In Persistent Spectral Hole Burning: Science and Applications. Washington, D.C.: Optica Publishing Group, 1991. http://dx.doi.org/10.1364/pshb.1991.sb1.
Small, G. J., N. R. S. Reddy e R. Jankowiak. "High Pressure Hole-Burning Studies of Transport Dynamics in Photosynthetic Protein Complex". In Spectral Hole-Burning and Related Spectroscopies: Science and Applications. Washington, D.C.: Optica Publishing Group, 1994. http://dx.doi.org/10.1364/shbs.1994.thd2.
Highstrete, Lt Clark, e John Wessel. "Intermolecular Interactions in the Fluorene Dimer". In High Resolution Spectroscopy. Washington, D.C.: Optica Publishing Group, 1993. http://dx.doi.org/10.1364/hrs.1993.pd9.
Vacha, Martin, Shinjiro Machida e Kazuyuki Horie. "Photochemical Hole Burning in the Soret Absorption Band of Zinc-tetrabenzoporphin Derivative by Two-photon Excitation". In Spectral Hole-Burning and Related Spectroscopies: Science and Applications. Washington, D.C.: Optica Publishing Group, 1994. http://dx.doi.org/10.1364/shbs.1994.thf2.
Naito, Hiroyoshi. "Modulation Spectroscopies for the Characterization of Electronic Properties in Organic Semiconductor Devices". In 2021 28th International Workshop on Active-Matrix Flatpanel Displays and Devices (AM-FPD). IEEE, 2021. http://dx.doi.org/10.23919/am-fpd52126.2021.9499130.
Rapporti di organizzazioni sul tema "Electronic spectroscopies":
Ogilvie, Jennifer P. Two-Dimensional Electronic Spectroscopies for Probing Electronic Structure and Charge Transfer: Applications to Photosystem II. Office of Scientific and Technical Information (OSTI), novembre 2016. http://dx.doi.org/10.2172/1333164.
Cooke, Stephen, A. Experimentally characterizing the electronic structures of f-electron systems using advanced high resolution Fourier transform microwave spectroscopies. Office of Scientific and Technical Information (OSTI), febbraio 2013. http://dx.doi.org/10.2172/1061478.
Walters, G. K., e F. B. Dunning. Application of spin-sensitive electron spectroscopies to investigations of electronic and magnetic properties of solid surfaces and epitaxial systems. Office of Scientific and Technical Information (OSTI), giugno 1992. http://dx.doi.org/10.2172/7113541.
Walters, G. K., e F. B. Dunning. Application of spin-sensitive electron spectroscopies to investigations of electronic and magnetic properties of solid surfaces and epitaxial systems. Office of Scientific and Technical Information (OSTI), aprile 1993. http://dx.doi.org/10.2172/6520905.
Morgan, M. A. Mapping of upper electronic reaction surfaces by tuned laser photolysis and by absorption and emission spectroscopies. Office of Scientific and Technical Information (OSTI), luglio 1989. http://dx.doi.org/10.2172/5655529.
Walters, G. K., e F. B. Dunning. Application of spin-sensitive electron spectroscopies to investigations of electronic and magnetic properties of solid surfaces and epitaxial systems. Progress report, 1 November 1993--31 October 1994. Office of Scientific and Technical Information (OSTI), maggio 1994. http://dx.doi.org/10.2172/10156526.
Walters, G. K., e F. B. Dunning. Application of spin-sensitive electron spectroscopies to investigations of electronic and magnetic properties of solid surfaces and epitaxial systems. Progress report, 1 November 1992--31 October 1993. Office of Scientific and Technical Information (OSTI), aprile 1993. http://dx.doi.org/10.2172/10156589.
Walters, G. K., e F. B. Dunning. Application of spin-sensitive electron spectroscopies to investigations of electronic and magnetic properties of solid surfaces and epitaxial systems. Progress report, 1 November 1991--31 October 1992. Office of Scientific and Technical Information (OSTI), giugno 1992. http://dx.doi.org/10.2172/10166548.
Gallagher, A. Spectroscopic diagnostics of electron-atom collisions. Office of Scientific and Technical Information (OSTI), gennaio 1991. http://dx.doi.org/10.2172/5957609.
Beechem, Iii, Thomas Edwin, Justin Raymond Serrano e Patrick E. Hopkins. Simultaneous electronic and lattice characterization using coupled femtosecond spectroscopic techniques. Office of Scientific and Technical Information (OSTI), settembre 2009. http://dx.doi.org/10.2172/1097197.