Literatura científica selecionada sobre o tema "Time-Resolved spectroscopie"
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Artigos de revistas sobre o assunto "Time-Resolved spectroscopie"
Yakovlev, V. "Time-resolved luminescence spectroscopy study of CsI:Eu crystal". Functional Materials 20, n.º 4 (25 de dezembro de 2013): 451–56. http://dx.doi.org/10.15407/fm20.04.451.
Texto completo da fonteLiu Fan, 刘璠, 姚旭日 Yao Xuri, 刘雪峰 Liu Xuefeng e 翟光杰 Zhai Guangjie. "基于压缩感知的单光子时间分辨成像光谱技术". Laser & Optoelectronics Progress 58, n.º 10 (2021): 1011016. http://dx.doi.org/10.3788/lop202158.1011016.
Texto completo da fonteGaft, Michael, Harold Seigel, Gerard Panczer e Renata Reisfeld. "Laser-induced time-resolved luminescence spectroscopy of Pb2+ in minerals". European Journal of Mineralogy 14, n.º 6 (25 de novembro de 2002): 1041–48. http://dx.doi.org/10.1127/0935-1221/2002/0014-1041.
Texto completo da fonteDAI Zijie, 戴子杰, 康黎星 KANG Lixing, 龚诚 GONG Cheng, 刘政 LIU Zheng e 刘伟伟 LIU Weiwei. "PtSe2薄膜的时间分辨太赫兹光谱特性研究(特邀)". ACTA PHOTONICA SINICA 50, n.º 8 (2021): 0850206. http://dx.doi.org/10.3788/gzxb20215008.0850206.
Texto completo da fonteQingli Zhou, Qingli Zhou, e Xicheng Zhang Xicheng Zhang. "Applications of time-resolved terahertz spectroscopy in ultrafast carrier dynamics (Invited Paper)". Chinese Optics Letters 9, n.º 11 (2011): 110006–9. http://dx.doi.org/10.3788/col201109.110006.
Texto completo da fonteZhang Tong, 张童, 刘东远 Liu Dongyuan e 高峰 Gao Feng. "基于MC模型和Nelder‑Mead单纯形算法的时域组织光谱学". Chinese Journal of Lasers 51, n.º 3 (2024): 0307203. http://dx.doi.org/10.3788/cjl231142.
Texto completo da fonteFabelinskii, Immanuil L. "Time-resolved spectroscopy". Uspekhi Fizicheskih Nauk 152, n.º 8 (1987): 722. http://dx.doi.org/10.3367/ufnr.0152.198708y.0722.
Texto completo da fonteFabelinskiĭ, Immanuil L. "Time-resolved spectroscopy". Soviet Physics Uspekhi 30, n.º 8 (31 de agosto de 1987): 755–56. http://dx.doi.org/10.1070/pu1987v030n08abeh002959.
Texto completo da fonteClark, R. J. H., R. E. Hester e T. L. Gustafson. "Time Resolved Spectroscopy". Vibrational Spectroscopy 1, n.º 1 (dezembro de 1990): 106–8. http://dx.doi.org/10.1016/0924-2031(90)80018-y.
Texto completo da fonteBeddard, G. S. "Time resolved spectroscopy". Spectrochimica Acta Part A: Molecular Spectroscopy 47, n.º 2 (janeiro de 1991): 311. http://dx.doi.org/10.1016/0584-8539(91)80104-q.
Texto completo da fonteTeses / dissertações sobre o assunto "Time-Resolved spectroscopie"
Hawecker, Jacques. "Terahertz time resolved spectroscopy of Intersubband Polaritons and Spintronic Emitters". Electronic Thesis or Diss., Sorbonne université, 2021. http://www.theses.fr/2021SORUS101.
Texto completo da fonteThe terahertz (THz) domain provides a rich playground for many practical and fundamental applications, where the low energy of THz photons permits to probe novel light-matter interactions. This work investigates two recent and emerging scientific areas where ultrafast THz spectroscopy can be used as a probe of fundamental phenomena, as well as potentially enabling the conception of new THz sources. In the first case, ultrafast THz spintronics are studied where ultrafast excitations of spintronic heterojunctions result in efficient pulse generation. These structures consist of nanometer thick ferromagnetic - heavy metal junctions, where an optically generated spin-charge in the former is converted to a charge-current in the latter via the Inverse Spin Hall Effect. Beyond these metal-based junctions, ultrafast THz spintronics based on “quantum” materials is also investigated, where THz pulses are generated using quantum phenomena such as the Inverse Edelstein Effect in Topological Insulators, shown to be a promising research direction. The second subject area is focused on THz intersubband polaritons, quasi-particles that emerge from the strong light-matter coupling of a THz photonic cavity and an intersubband transition. Here we are interested in the bosonic nature of the intersubband polaritons, as a long-term aim of realizing a novel THz laser based on Bose-Einstein condensation. In this work, we investigate resonant narrowband pumping of a polariton branch and probe using spectrally broad THz pulses. This shows strong indications of nonlinear effects and potential signatures of scattering processes that could eventually lead to the demonstration of THz polaritonic gain. Finally, to support our work in the above subject areas, technological developments were made in existing THz sources. This included high power THz photoconductive switches using cavities, which permitted the first demonstrations of real time THz imaging with such devices, and high power THz quantum cascade lasers as narrowband laser pumps
Gaury, Benoit. "Emerging concepts in time-resolved quantum nanoelectronics". Thesis, Grenoble, 2014. http://www.theses.fr/2014GRENY026/document.
Texto completo da fonteWith the recent technical progress, single electron sources have moved fromtheory to the lab. Conceptually new types of experiments where one probesdirectly the internal quantum dynamics of the devices are within grasp. In thisthesis we develop the analytical and numerical tools for handling suchsituations. The simulations require appropriate spatial resolution for thesystems, and simulated times long enough so that one can probe their internalcharacteristic times. So far the standard theoretical approach used to treatsuch problems numerically---known as Keldysh or NEGF (Non Equilibrium Green'sFunctions) formalism---has not been very successful mainly because of aprohibitive computational cost. We propose a reformulation of the NEGFtechnique in terms of the electronic wave functions of the system in anenergy--time representation. The numerical algorithm we obtain scales nowlinearly with the simulated time and the volume of the system, and makessimulation of systems with $10^5-10^6$ atoms/sites feasible. We leverage thistool to propose new intriguing effects and experiments. In particular weintroduce the concept of dynamical modification of interference pattern of aquantum system. For instance, we show that when raising a DC voltage $V$ to anelectronic interferometer, the transient current responseoscillates as $cos(eVt/hbar)$. We expect a wealth of new effects whennanoelectronic circuits are probed fast enough. The tools and conceptsdeveloped in this work shall play a key role in the analysis and proposal ofupcoming experiments
Weis, Mateusz. "Growth and spectroscopic studies (continuous and time-resolved) of ultrathin films of topological insulators". Thesis, Le Mans, 2019. http://www.theses.fr/2019LEMA1001.
Texto completo da fonteTopological insulators (TI) are one of the critical elements for the new generation of electronics and spintronics devices. Such as charge-to-spin current conversion gates or Dirac fermions based nanometer scale Schottky diodes. When reduced just too a few single layers or exposed to additional doping, TI begins to show a dramatic effect that changes the electronic structure and in consequence dynamics of carriers and phonons. In order to describe those behaviors, I used advanced high-vacuum cluster with MBE to produce ultrathin films of Bi2Te3. The samples were grown on a muscovite mica substrate. The monocrystalline structure of the film was confirmed with both LEED and RHEED measurements, and the complementary studies of electronic structure focused on the analysis of the valence band and core levels. The femtosecond pump-probe spectroscopy has been used to excite the hot carriers and generate coherent optical phonons within Bi2Te3 nanostructures and observe it in the time domain.In this thesis, I reveal an evident modification of the out-of-equilibrium carriers and phonons dynamics when extreme thickness or doping modify the BT layer. Performed experimental optical measurement integrate both bulk and surface electrons, but nonnegligible surface carriers contribution still gives a strong response. This continuous and time-domain investigation provides new insight into physical properties of topological insulators and shows that downscaling the topological insulators properties and their interaction with metallic interfaces have to be taken into account for potential TIs based spintronic devices
Skilitsi, Anastasia Ioanna. "Applications of time-resolved spectroscopy for microenvironment sensing and biomolecular interactions studies". Thesis, Strasbourg, 2017. http://www.theses.fr/2017STRAE029/document.
Texto completo da fonteIn the context of the present thesis, UV-Vis time-resolved spectroscopy was applied targeting the photophysics investigation of different environmentally sensitive molecular systems, but also as a biosensing approach to reveal molecular interactions or structural dynamics on much slower time scales (sec to min), using droplet microfluidics triggering structural relaxation through out-of-equilibrium initial conditions. I thus investigated on a three-axis-target spanning from 1) the in-depth investigation of the emissive properties of biosensors in order to allow their quantitative use in biomolecular interaction studies, to 2) the development of an original experimental approach to enable resolving the structural relaxation kinetics of an out-of-equilibrium distribution of biomolecular structures, and finally 3) the technological application of time resolved fluorescence for precise, rapid, cost effective, biomolecular interaction assays, appealing both for academic and industrial arenas
Bhuckory, Shashi. "Quantum dots and upconverting nanoparticles : Bioconjugation and time-resolved multiplexed FRET spectroscopy for cancer diagnostics". Thesis, Université Paris-Saclay (ComUE), 2016. http://www.theses.fr/2016SACLS447/document.
Texto completo da fonteCombining high sensitivity with simultaneous analysis of numerous biomarkers (multiplexing) is an essential requirement for significantly improving the field of biomedical diagnostics. Such progresses would allow earlier diagnosis, which is required for numerous diseases such as cancer or cardiac diseases. FRET-immunoassays are based on biomolecular recognition events that occur between biomarkers and two specific antibodies conjugated with different fluorophores. The spatial proximity of the two fluorophores can lead to Förster resonance energy transfer (FRET), which can be detected for biomarker quantification. To date, such assays are established using lanthanide complexes as FRET donors and fluorescence dyes as FRET acceptors. However, these assays do not provide sufficient multiplexing capability due to spectral overlap, when several acceptor dyes are used. This project aims at exploiting the exceptional photophysical properties of terbium complexes (Tb) and semiconductor quantum dots (QDs) to provide ultrasensitive multiplexed FRETimmunoassays. We also studied the optical and morphological properties of novel core and core/shell upconverting nanoparticles doped with ytterbium (Yb) and erbium (Er) ions as possible FRET-donors for biosensing
Zhang, Zailan. "Electronic structures, quasi-particle and gap dynamics in copper oxides superconductors using Time and Angle Resolved Photoemission Spectroscopy". Electronic Thesis or Diss., Paris 6, 2017. https://accesdistant.sorbonne-universite.fr/login?url=https://theses-intra.sorbonne-universite.fr/2017PA066126.pdf.
Texto completo da fonteThe superconductors of the copper-oxide family have been matter of extensive investigations and are still subject of fierce debates. After 30 years of research, some issues have been settled, whereas others remain controversial. The evolution of the superconducting order parameter with temperature and doping level is an exemplary case. In this thesis, we report a systematic Time resolved Angle Resolved PhotoEmission Spectroscopy (ARPES) study of the optimally doped Bi2Sr2CaCu2O8+δ to explore the possibility that an intense photoexcitation of the superconductor can generate a state with incoherent copper pairs and no superfluid density. The employed experimental methods allow us to measure the dynamics of non-equilibrium electrons and of the superconducting gap, providing complementary information to conventional ARPES and optical measurement. Our time resolved ARPES data of Bi2Sr2CaCu2O8+δ, report a momentum-dependent collapse of the superconducting gap upon photoexcitation. Interestingly, the QP relaxation develops a faster component at the threshold fluence F_pair where the gap has fully collapsed. The comparison between the F_pair and the F_phase extracted by tr-THz suggested the existence a fluence regime when the Cooper pairs have survived, but without holding superfluid current. A second major challenge in the physics of HTSCs is the poor understanding of the normal phase at high temperature. We also present the ARPES study of the near nodal pseudo-gap in La2-xBaxCuO4 (LBCO) to show a possible link with charge modulation (stripes). Our data show that the near nodal gap open below the LTT-LTO transition, which is linked to the formation of such modulations, instead of the one where spin modulations appear. The data show that the band structure of LBCO is affected by a renormalization setting in prior to the 70 meV kink. We were able to correlate this renormalization of the ARPES data to the region where the Cu-O bond-stretching mode soften, both in energy and momentum space
Nĕmec, Hynek. "Time-resolved terahertz spectroscopy applied to the investigation of magnetic materials and photonic structures". Grenoble INPG, 2006. http://www.theses.fr/2006INPG0020.
Texto completo da fonteTwo distinct branches of optics are combined in this work: Time-domain terahertz spectroscopy, and photonic structures. The works at first provides a survey of tools utilized for exploration of the terahertz region, and it en riches them by a method for simultaneous determination of dielectric and magnetic response of materials and metamaterials. Photonic structures operating in the terahertz range form the subject of the rest of this thesis. A periodically modulated dielectric waveguide is studied theoretically using a modal method: ThE band structure of guided and leaky modes is calculated and resonant modes are described. One-dimensional photonic crystals with a defect are then investigated in detail. Formation of defect modes is analyzed theoretically in a photonic crystal with a twinning defect. The analysis makes it possible to formulate requirements on a design of a structure with defect modes tunable by external parameters. Following these guidelines, we have successfully designed, fabricated and characterized photonic crystals with thermally tunable defect modes with relative tunability reaching 60 %
Lobato, Bailón Laura. "Internal dynamics of heme-based sensor proteins studied using advanced time-resolved optical spectroscopy". Palaiseau, Ecole polytechnique, 2013. http://pastel.archives-ouvertes.fr/pastel-00866894.
Texto completo da fonteHeme-proteins are involved in a large range of biological functions, including respiration, oxygen transport and xenobiotic detoxification. Importantly, bacterial heme-based sensor proteins exploit the ligation properties of heme to sense environmental gases. This thesis focuses on internal dynamics studies of the 6-coordinate heme-based gas sensor proteins CooA, from Rhodospirillum rubrum and DNR from Pseudomonas aeruginosa that are involved in adaptation of the metabolism of the organism to their environment. CooA and DNR, belonging to the important family of catabolite gene activator proteins, are transcription factors that bind DNA upon gas activation, thus enabling transcription of specific genes. Both sensor proteins are thought to undergo a large and delocalized conformational change upon binding of the physiological ligand to the heme (CO for CooA and NO for DNR). Here advanced optical spectroscopy techniques are used to investigate the mechanism and molecular pathway of activation/desactivation in this class of proteins. DNA-protein interactions were studied with steady-state and femtosecond ultrafast time resolved fluorescence techniques, using labeled DNA substrates. Physiological ligand-sensitive DNA binding in the nanomolar affinity range was deduced from anisotropy experiments. Quenching of the fluorescence label by energy transfer to the native heme in the protein moiety of the complex was observed, and the rate of this process, reflecting the heme-substrate distance, was determined directly from the measured fluorescence decays. This observation opens the perspective of mapping out the global protein conformational changes using time-resolved FRET techniques. The primary processes in heme-based sensor switching mechanisms concern ligand binding and ligand dissociation from the heme. Femtosecond transient absorption experiments were performed in order to study the ligand dynamics in CooA and DNR in the vicinity of the heme. In DNR, upon photodissociation of NO, particularly fast and efficient geminate recombination was observed. This strongly strengthens the hypothesis that NO-sensors act as ligand traps. Also, the energetic barriers involved in CO migration have been determined in both sensor proteins by temperature dependence studies. All 6-coordinate heme-based sensor proteins that function via the exchange of an internal residue and the gas molecule as a heme ligand, display barrierless recombination and a thermally activated CO-escape out of the heme pocket. By contrast, the barrier for the CO-escape appears smaller or absent for 5-coordinate systems, as has been found for the mycobacterial heme-sensor DosT. These findings point to a general mechanism, where similar protein motions are required for both, ligand exchange and ligand escape. For reasons of comparison, the energetic barriers have also been studied in ligand binding variants of the electron transfer protein cytochrome c. Here, a more complex mechanism of multiple barriers in the ligand escape pathway was deduced. This feature is proposed to reflect the rather rigid nature of this non-sensor protein, which contains a 6-coordinate heme and is devoid of ligand entry pathways in the native state. Finally, the primary processes occurring in the wild type and mutant heme domains of the recently discovered oxygen sensor YddV from Escherichia coli were investigated. In particular, an important role in the ligand dynamics was elucidated for the distal tyrosine residue. This residue hydrogen bonds to heme-bound O2 and NO molecules and was found to have a remarkably discriminating effect: after respective dissociation from the heme, it strongly promotes O2 rebinding, but favors NO escape from the heme pocket
Zhang, Zailan. "Electronic structures, quasi-particle and gap dynamics in copper oxides superconductors using Time and Angle Resolved Photoemission Spectroscopy". Thesis, Paris 6, 2017. http://www.theses.fr/2017PA066126/document.
Texto completo da fonteThe superconductors of the copper-oxide family have been matter of extensive investigations and are still subject of fierce debates. After 30 years of research, some issues have been settled, whereas others remain controversial. The evolution of the superconducting order parameter with temperature and doping level is an exemplary case. In this thesis, we report a systematic Time resolved Angle Resolved PhotoEmission Spectroscopy (ARPES) study of the optimally doped Bi2Sr2CaCu2O8+δ to explore the possibility that an intense photoexcitation of the superconductor can generate a state with incoherent copper pairs and no superfluid density. The employed experimental methods allow us to measure the dynamics of non-equilibrium electrons and of the superconducting gap, providing complementary information to conventional ARPES and optical measurement. Our time resolved ARPES data of Bi2Sr2CaCu2O8+δ, report a momentum-dependent collapse of the superconducting gap upon photoexcitation. Interestingly, the QP relaxation develops a faster component at the threshold fluence F_pair where the gap has fully collapsed. The comparison between the F_pair and the F_phase extracted by tr-THz suggested the existence a fluence regime when the Cooper pairs have survived, but without holding superfluid current. A second major challenge in the physics of HTSCs is the poor understanding of the normal phase at high temperature. We also present the ARPES study of the near nodal pseudo-gap in La2-xBaxCuO4 (LBCO) to show a possible link with charge modulation (stripes). Our data show that the near nodal gap open below the LTT-LTO transition, which is linked to the formation of such modulations, instead of the one where spin modulations appear. The data show that the band structure of LBCO is affected by a renormalization setting in prior to the 70 meV kink. We were able to correlate this renormalization of the ARPES data to the region where the Cu-O bond-stretching mode soften, both in energy and momentum space
Morajkar, Pranay P. "Application of laser photolysis coupled to time resolved optical detection methods to study the kinetics and spectroscopy of atmospherically relevant species". Thesis, Lille 1, 2012. http://www.theses.fr/2012LIL10063/document.
Texto completo da fonteOH and HO2 radicals play a vital role in many oxidation processes in the atmosphere. Thedegradation of volatile organic compounds under tropospheric conditions is induced by reaction withhydroxyl radicals followed by the subsequent chemistry of the initial OH oxidation products with O2.This thesis deals with the kinetic study of some of these atmospherically relevant reactions to betterunderstand their oxidation mechanisms using experimental techniques such as laser photolysiscoupled to detection by Laser Induced Fluorescence (LIF, for OH), continuous wave- Cavity RingdownSpectroscopy (cw-CRDS, for HO2) and time resolved UV spectroscopy (UV, forHexamethylbenzene-OH adduct). Different chemical systems have been studied using the above techniques: 1) the reaction ofHO2 radicals with formaldehyde, 2) the 248 nm photolysis of acetaldehyde and 3) the OH initiatedoxidation of Hexamethyl benzene. In addition to this, the spectroscopic application of cw-CRDStechnique and UV spectroscopy has been used for the measurement of absorption cross section ofselected absorption lines of formaldehyde in the near infrared region and Hexamethylbenzene-OHadduct in the UV region respectively
Livros sobre o assunto "Time-Resolved spectroscopie"
1942-, Laubereau A., Stockburger M. 1929- e International Conference on TRVS (2nd : 1985 : Bayreuth, Germany and Bischofsgrün, Germany), eds. Time-resolved vibrational spectroscopy: Proceedings of the 2nd international conference, Emil-Warburg symposium, Bayreuth-Bischofsgrün, Fed. Rep. of Germany, June 3-7, 1985. Berlin: Springer-Verlag, 1985.
Encontre o texto completo da fonteWeinacht, Thomas C., e Brett J. Pearson. Time-Resolved Spectroscopy. Boca Raton : CRC Press, Taylor & Francis Group, 2019.: CRC Press, 2018. http://dx.doi.org/10.1201/9780429440823.
Texto completo da fonteH, Clark R. J., e Hester R. E. 1936-, eds. Time resolved spectroscopy. Chichester: Wiley, 1989.
Encontre o texto completo da fonteH, Clark R. J., e Hester R. E, eds. Time resolved spectroscopy. Chichester [England]: Wiley, 1989.
Encontre o texto completo da fonteBrückner, Volkmar. Applications of time-resolved optical spectroscopy. Leipzig: Akademische Verlagsgesellschaft Geest & Portig, 1990.
Encontre o texto completo da fonteBrückner, Volkmar. Applications of time-resolved optical spectroscopy. Amsterdam: Elsevier, 1990.
Encontre o texto completo da fonteBuckup, Tiago, e Jérémie Léonard, eds. Multidimensional Time-Resolved Spectroscopy. Cham: Springer International Publishing, 2019. http://dx.doi.org/10.1007/978-3-030-02478-9.
Texto completo da fonteLaubereau, Alfred, e Manfred Stockburger, eds. Time-Resolved Vibrational Spectroscopy. Berlin, Heidelberg: Springer Berlin Heidelberg, 1985. http://dx.doi.org/10.1007/978-3-642-47541-2.
Texto completo da fonteTakahashi, Hiroaki, ed. Time-Resolved Vibrational Spectroscopy V. Berlin, Heidelberg: Springer Berlin Heidelberg, 1992. http://dx.doi.org/10.1007/978-3-642-84771-4.
Texto completo da fonteLau, Albrecht, Wolfgang Werncke e Friedrich Siebert, eds. Time-Resolved Vibrational Spectroscopy VI. Berlin, Heidelberg: Springer Berlin Heidelberg, 1994. http://dx.doi.org/10.1007/978-3-642-85060-8.
Texto completo da fonteCapítulos de livros sobre o assunto "Time-Resolved spectroscopie"
Weinacht, Thomas C., e Brett J. Pearson. "Introduction". In Time-Resolved Spectroscopy, 3–10. Boca Raton : CRC Press, Taylor & Francis Group, 2019.: CRC Press, 2018. http://dx.doi.org/10.1201/9780429440823-1.
Texto completo da fonteWeinacht, Thomas C., e Brett J. Pearson. "Explicit Approach to N-D Dynamics". In Time-Resolved Spectroscopy, 185–204. Boca Raton : CRC Press, Taylor & Francis Group, 2019.: CRC Press, 2018. http://dx.doi.org/10.1201/9780429440823-10.
Texto completo da fonteWeinacht, Thomas C., e Brett J. Pearson. "Implicit Approaches to N-D Dynamics". In Time-Resolved Spectroscopy, 205–14. Boca Raton : CRC Press, Taylor & Francis Group, 2019.: CRC Press, 2018. http://dx.doi.org/10.1201/9780429440823-11.
Texto completo da fonteWeinacht, Thomas C., e Brett J. Pearson. "Incoherent Measurements in ND". In Time-Resolved Spectroscopy, 217–40. Boca Raton : CRC Press, Taylor & Francis Group, 2019.: CRC Press, 2018. http://dx.doi.org/10.1201/9780429440823-12.
Texto completo da fonteWeinacht, Thomas C., e Brett J. Pearson. "Coherent Optical Measurements in ND". In Time-Resolved Spectroscopy, 241–74. Boca Raton : CRC Press, Taylor & Francis Group, 2019.: CRC Press, 2018. http://dx.doi.org/10.1201/9780429440823-13.
Texto completo da fonteWeinacht, Thomas C., e Brett J. Pearson. "Coherent Diffractive Measurements in ND". In Time-Resolved Spectroscopy, 275–82. Boca Raton : CRC Press, Taylor & Francis Group, 2019.: CRC Press, 2018. http://dx.doi.org/10.1201/9780429440823-14.
Texto completo da fonteWeinacht, Thomas C., e Brett J. Pearson. "One System, Multiple Approaches". In Time-Resolved Spectroscopy, 283–96. Boca Raton : CRC Press, Taylor & Francis Group, 2019.: CRC Press, 2018. http://dx.doi.org/10.1201/9780429440823-15.
Texto completo da fonteWeinacht, Thomas C., e Brett J. Pearson. "Molecular Structure". In Time-Resolved Spectroscopy, 11–40. Boca Raton : CRC Press, Taylor & Francis Group, 2019.: CRC Press, 2018. http://dx.doi.org/10.1201/9780429440823-2.
Texto completo da fonteWeinacht, Thomas C., e Brett J. Pearson. "Light–Matter Interaction". In Time-Resolved Spectroscopy, 41–62. Boca Raton : CRC Press, Taylor & Francis Group, 2019.: CRC Press, 2018. http://dx.doi.org/10.1201/9780429440823-3.
Texto completo da fonteWeinacht, Thomas C., e Brett J. Pearson. "Introduction to Experimental Techniques". In Time-Resolved Spectroscopy, 63–72. Boca Raton : CRC Press, Taylor & Francis Group, 2019.: CRC Press, 2018. http://dx.doi.org/10.1201/9780429440823-4.
Texto completo da fonteTrabalhos de conferências sobre o assunto "Time-Resolved spectroscopie"
Svanberg, S. "Time-Resolved Spectroscopic Techniques in Laser Medicine". In International Conference on Ultrafast Phenomena. Washington, D.C.: Optica Publishing Group, 1994. http://dx.doi.org/10.1364/up.1994.fb.1.
Texto completo da fonteGraham, W. G. "Time resolved spectroscopy". In IEE Colloquium on Measurement and Plasma. IEE, 1997. http://dx.doi.org/10.1049/ic:19970517.
Texto completo da fonteBardeen, C. J., e C. V. Shank. "Solvent Dependence of the Femtosecond Three Pulse Photon Echo for LD690 in n-Alcohols." In International Conference on Ultrafast Phenomena. Washington, D.C.: Optica Publishing Group, 1994. http://dx.doi.org/10.1364/up.1994.thd.16.
Texto completo da fonteYe-xin, Shi, e Li Jiu-sheng. "Terahertz Spectroscopic measurements drinks by using time-resolved terahertz spectroscopy". In Advanced Spectroscopy and Applications. Washington, D.C.: OSA, 2017. http://dx.doi.org/10.1364/asa.2017.asu5a.3.
Texto completo da fonteWeidner, H., e R. E. Peale. "Improved Time-resolved Fourier Spectroscopy". In Fourier Transform Spectroscopy. Washington, D.C.: Optica Publishing Group, 2022. http://dx.doi.org/10.1364/fts.1997.ftub.3.
Texto completo da fonteTavani, Marco. "Time resolved GRB spectroscopy". In The fifth huntsville gamma-ray burst symposium. AIP, 2000. http://dx.doi.org/10.1063/1.1361531.
Texto completo da fonteJacques, Steven L., e Stephen T. Flock. "Time-resolved reflectance spectroscopy". In Berlin - DL tentative, editado por Lars O. Svaasand. SPIE, 1991. http://dx.doi.org/10.1117/12.48185.
Texto completo da fonteGuelachvili, Guy. "High Information Time-Resolved Fourier Spectroscopy". In Fourier Transform Spectroscopy. Washington, D.C.: Optica Publishing Group, 1995. http://dx.doi.org/10.1364/fts.1995.ffc3.
Texto completo da fonteMyers, 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.
Texto completo da fonteWörner, Hans. "ATTOSECOND TIME-RESOLVED MOLECULAR SPECTROSCOPY". In 73rd International Symposium on Molecular Spectroscopy. Urbana, Illinois: University of Illinois at Urbana-Champaign, 2018. http://dx.doi.org/10.15278/isms.2018.ra04.
Texto completo da fonteRelatórios de organizações sobre o assunto "Time-Resolved spectroscopie"
Zhang, Yong-Hang. Time-Resolved IR Electroluminescence Spectroscopy System. Fort Belvoir, VA: Defense Technical Information Center, maio de 2006. http://dx.doi.org/10.21236/ada461015.
Texto completo da fonteCrim, F. F. Time-Resolved Photoisomerization Using Femtosecond Stimulated Raman Spectroscopy. Fort Belvoir, VA: Defense Technical Information Center, dezembro de 2009. http://dx.doi.org/10.21236/ada511313.
Texto completo da fonteAlfano, Robert R., e S. K. Gayen. Time-Resolved and Spectroscopic Three-Dimensional Optical Breast Tomography. Fort Belvoir, VA: Defense Technical Information Center, abril de 2008. http://dx.doi.org/10.21236/ada492472.
Texto completo da fonteAlfano, Robert R. Time-Resolved and Spectroscopic Three-Dimensional Optical Breast Tomography. Fort Belvoir, VA: Defense Technical Information Center, abril de 2006. http://dx.doi.org/10.21236/ada464218.
Texto completo da fonteKim, Dongho. Time- and Space-Resolved Spectroscopic Investigation on Pi-Conjugated Nanostructures. Fort Belvoir, VA: Defense Technical Information Center, março de 2013. http://dx.doi.org/10.21236/ada582490.
Texto completo da fonteSheps, Leonid, e David Chandler. Time-resolved broadband cavity-enhanced absorption spectroscopy for chemical kinetics. Office of Scientific and Technical Information (OSTI), abril de 2013. http://dx.doi.org/10.2172/1095949.
Texto completo da fonteMarjoribanks, R. Time-resolved spectroscopy of nonequilibrium ionization in laser-produced plasmas. Office of Scientific and Technical Information (OSTI), março de 1990. http://dx.doi.org/10.2172/7164582.
Texto completo da fonteKim, Dongho. Time- and Space-Resolved Spectroscopic Investigation on Pi-Conjugated Nanostructures - 2. Fort Belvoir, VA: Defense Technical Information Center, janeiro de 2016. http://dx.doi.org/10.21236/ada635074.
Texto completo da fonteSteel, Duncan G. Time Resolved Nano-Optical Spectroscopy of Coherently Excited Semiconductor Quantum Dots. Fort Belvoir, VA: Defense Technical Information Center, outubro de 2000. http://dx.doi.org/10.21236/ada386872.
Texto completo da fonteMizuno, Yoshiyuki. Time-Resolved Photoelectron Spectroscopy of Oxidation on the Ti(0001) Surface. Office of Scientific and Technical Information (OSTI), março de 2003. http://dx.doi.org/10.2172/812993.
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