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Artykuły w czasopismach na temat "Resonant Raman Effect"

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Wurth, W. "Resonant Auger Raman effect for adsorbates". Applied Physics A: Materials Science & Processing 65, nr 2 (1.08.1997): 155–58. http://dx.doi.org/10.1007/s003390050558.

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Iwazumi, T., K. Kobayashi, S. Kishimoto, T. Nakamura, S. Nanao, D. Ohsawa, R. Katano i Y. Isozumi. "Magnetic resonance effect in x-ray resonant Raman scattering". Physical Review B 56, nr 22 (1.12.1997): R14267—R14270. http://dx.doi.org/10.1103/physrevb.56.r14267.

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Zhong, Qing-Hu, Yu Wu, Yun-Chang Xiao, Liang-Bin Hu i Rui-Qiang Wang. "The influence of size effect on interface phonons in core-shell quantum dot: a resonant Raman study". Modern Physics Letters B 28, nr 21 (20.08.2014): 1450172. http://dx.doi.org/10.1142/s0217984914501723.

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In this paper, the interface phonons in a core-shell quantum dot are theoretically studied by a resonant Raman scattering (RRS) process. Fröhlich electron–phonon interaction is considered in the framework of the dielectric continuum approach. The Raman peaks are found to be sensitive to the size of strongly confined shell. The shift of the Raman resonant peaks is a consequence of the change of observed dispersion of the phonon frequency. The Raman intensity changes in the system with shell thickness, originating from the competition between the spacial distribution of electron wave function and the number of phonons joining in the RRS process. The analysis of the Raman spectra gives a physical explanation to the size-selective nature of the Raman process and some experimental results.
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Medel-Ruiz, C. I., H. Pérez Ladrón de Guevara, J. R. Molina-Contreras i C. Frausto-Reyes. "Fano effect in resonant Raman spectrum of CdTe". Solid State Communications 312 (maj 2020): 113895. http://dx.doi.org/10.1016/j.ssc.2020.113895.

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Gołasa, Katarzyna, Magdalena Grzeszczyk, Maciej R. Molas, Małgorzata Zinkiewicz, Karol Nogajewski, Marek Potemski, Andrzej Wysmołek i Adam Babiński. "Anomalous Raman Scattering In Few Monolayer MoTe2". MRS Advances 2, nr 29 (2017): 1539–44. http://dx.doi.org/10.1557/adv.2017.39.

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ABSTRACTThe effect of temperature (5K to 300K) on the Raman scattering due to A1g/A1’ modes associated with the out-of-plane vibrations in bilayer (2L) and trilayer (3L) MoTe2 is investigated. The temperature evolution of the modes critically depends on the flake thickness. The A1g mode intensity in 2L MoTe2 observed with λ=632.8 nm light excitation decreases with decreasing temperature down to 220K and the mode vanishes from the Stokes scattering spectrum in the temperature range between 160K and 220K. The peak recovers at lower temperatures and at T=5K it becomes three times more intense that at room temperature. Similar non-monotonic intensity evolution is observed for the A1’ mode in 3L MoTe2 in which tellurium atoms in all three layers vibrate in-phase. On the contrary, the intensity of the other out-of-plane Raman-active mode in which vibrations of tellurium atoms in the central layer of 3L MoTe2 are shifted by 180° with respect to vibrations in outer layers, only weakly depends on temperature.The observed quenching of the out-of-plane modes in the Raman scattering in thin MoTe2 layers is related to the destructive interference of the resonant- and the non-resonant contributions to the Raman scattering. The resonance with the M point of the Brillouin zone in few-layers of MoTe2 is considered. Effects related to the resonant quenching of the in-phase out-of-plane mode are discussed.
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LEE, HYUN C. "RESONANT RAMAN SCATTERING OF QUANTUM WIRE IN STRONG MAGNETIC FIELD". International Journal of Modern Physics B 13, nr 17 (10.07.1999): 2275–83. http://dx.doi.org/10.1142/s0217979299002381.

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The resonant Raman scattering of a quantum wire in a strong magnetic field is studied, focused on the effect of long range Coulomb interaction and the spin–charge separation. The energy–momentum dispersions of charge and spin excitation obtained from Raman cross-section show the characteristc cross-over behaviour induced by inter-edge Coulomb interaction. The "SPE" peak near resonance in polarized spectra becomes broad due to the momentum dependence of charge velocity. The broad peak in the depolarized spectra is shown to originate from the disparity between charge and spin excitation velocity.
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Kobayashi, Naoki, Takeshi Toriyama i Yoshiji Horikoshi. "Resonant Raman effect in thin‐layered AlAs‐GaAs superlattices". Applied Physics Letters 50, nr 25 (22.06.1987): 1811–13. http://dx.doi.org/10.1063/1.97705.

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Drube, W., i R. Treusch. "Photoemission study of the radiationless X-ray resonant Raman effect". Physica B: Condensed Matter 208-209 (marzec 1995): 33–34. http://dx.doi.org/10.1016/0921-4526(94)00626-7.

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Kukk, E., S. Aksela i H. Aksela. "Features of the Auger resonant Raman effect in experimental spectra". Physical Review A 53, nr 5 (1.05.1996): 3271–77. http://dx.doi.org/10.1103/physreva.53.3271.

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Ziemath, E. C., M. A. Aegerter, F. E. A. Melo, J. E. Moreira, J. Mendes Filho, M. S. S. Dantas i M. A. Pimenta. "Pre-resonant Raman effect of CrO42− in a metasilicate glass". Journal of Non-Crystalline Solids 194, nr 1-2 (styczeń 1996): 41–47. http://dx.doi.org/10.1016/0022-3093(95)00492-0.

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Rozprawy doktorskie na temat "Resonant Raman Effect"

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Feng, Yejun. "Exciton spectroscopy using non-resonant x-ray Raman scattering /". Thesis, Connect to this title online; UW restricted, 2003. http://hdl.handle.net/1773/9642.

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Tanaka, Tomoyoshi. "Resonance raman and surface enhanced raman studies of hemeproteins and model compounds". Diss., Georgia Institute of Technology, 1986. http://hdl.handle.net/1853/27678.

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Short, Billy Joe. "Ultraviolet resonance Raman enhancements in the detection of explosives". Thesis, Monterey, Calif. : Naval Postgraduate School, 2009. http://edocs.nps.edu/npspubs/scholarly/theses/2009/Jun/09Jun%5FShort.pdf.

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Thesis (M.S. in Applied Physics)--Naval Postgraduate School, June 2009.
Thesis Advisor(s): Smith, Craig F. "June 2009." Description based on title screen as viewed on 14 July 2009. Author(s) subject terms: Raman spectroscopy, standoff detection, high explosives, explosive detection, inelastic scattering, resonance Raman. Includes bibliographical references (p. 77-80). Also available in print.
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Rwere, Freeborn. "Resonance Raman studies of isotopically labeled heme proteins". [Milwaukee, Wis.] : e-Publications@Marquette, 2009. http://epublications.marquette.edu/dissertations_mu/22.

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Lin, Shun-hua. "Resonance raman studies of hemoproteins and model heme complexes". Diss., Georgia Institute of Technology, 1987. http://hdl.handle.net/1853/30311.

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BOURGEOIS, CHARIGOT MARIE-THERESE. "Diffusion raman resonnante et structure des etats moleculaires excites". Reims, 1988. http://www.theses.fr/1988REIMS013.

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Des modeles d'etude sont proposes et appliques a differentes especes moleculaires. Les modeles suivants, de complexite croissante, sont presentes: approximation de reflexion, approximation harmonique, potentiels de morse, modele analytique tridimensionnel incluant l'effet duschinsky. Ce dernier modele est applique au cas de l'ozone et etendu ensuite aux molecules rendues non symetriques par une substitution isotopique
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Foster, Catherine. "Resonance raman intensity analysis of chlorine dioxide in solution /". Thesis, Connect to this title online; UW restricted, 2000. http://hdl.handle.net/1773/11595.

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Kernohan, Edward Thomas Mark. "High resolution resonant Raman scattering in InP and GaAs". Thesis, University of Cambridge, 1996. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.364445.

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Rodriguez, Arturo A. (Arturo Angel). "Raman and NMR Relaxation Studies of Molecular Dynamics in Liquids". Thesis, North Texas State University, 1987. https://digital.library.unt.edu/ark:/67531/metadc330818/.

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Raman vibrational bands are sensitive to fluctuations in the molecular environment. Variations in the bandwidth and peak position can then be utilized to monitor molecular forces and interactions present in condense phases. Nuclear Magnetic Resonance (NMR) provides a convenient probe for the study of molecular reorientation in liquids since nuclear spin relaxation times are dependent on the details of molecular motion. Presented here is the solvent study of the Raman bandwidths and frequency displacements of the mode of the compounds CH3MCI3 (M = C, Si, Ge, Sn) in a number of solvents of widely varying molecular structure. Also, a detailed isotope dilution study of the modes in CH2CI2/CD2CI2 mixtures is presented. In this set of experiments, I observed broadening of the v1 mode of CH2C12 upon dilution,which is the first experimental observation of such behavior. The temperature-dependent carbon-13 relaxation times and nuclear Overhauser enhancements in neat dichloromethane were measured. In this study we found that the molecular reorientation of this molecule was highly anisotropic, but could be well characterized assuming quasi-symmetric top behavior. In addition, in order to gain a more complete understanding of the reorientational dynamics in dichloromethane, we analyzed the 13-C NMR relaxation of CH2CI2 both in "inert" solvents of differing viscosities and in interactive solvents of varying Lewis basicities. Various theoretical models were also applied in order to characterize dichloromethane1s reorientational dynamics.
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Kabagambe, Benjamin. "Spectroscopic investigation of proteins : UV resonance Raman studies of apomyoglobin /". Saarbrücken, Germany : VDM Verlag Dr. Müller, 2008. http://etd.library.pitt.edu/ETD/available/etd-10232007-094038.

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Thesis (M.S.)--University of Pittsburgh, Department of Chemistry, 2007.
Thesis advisor: Sanford A. Asher. Also available as an electronic book in PDF on the University of Pittsburgh Library Web site. Bibliography: p. 37-41.
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Książki na temat "Resonant Raman Effect"

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Derner, Harald. Untersuchungen über den Resonanz-Ramaneffekt an Anthracen, Naphthalin und p-nitro-p-dimethylamino-azobenzol. Freiburg [im Breisgau]: Hochschulverlag, 1986.

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Zucker, Jane Elisa. Raman scattering resonant with two-dimensional excitons in GaAs-AlGaAs heterostructures. 1985.

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Saito, R., A. Jorio, J. Jiang, K. Sasaki, G. Dresselhaus i M. S. Dresselhaus. Optical properties of carbon nanotubes and nanographene. Redaktorzy A. V. Narlikar i Y. Y. Fu. Oxford University Press, 2017. http://dx.doi.org/10.1093/oxfordhb/9780199533053.013.1.

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This article examines the optical properties of single-wall carbon nanotubes (SWNTs) and nanographene. It begins with an overview of the shape of graphene and nanotubes, along wit the use of Raman spectroscopy to study the structure and exciton physics of SWNTs. It then considers the basic definition of a carbon nanotube and graphene, focusing on the crystal structure of graphene and the electronic structure of SWNTs, before describing the experimental setup for confocal resonance Raman spectroscopy. It also discusses the process of resonance Raman scattering, double-resonance Raman scattering, and the Raman signals of a SWNT as well as the dispersion behavior of second-order Raman modes, the doping effect on the Kohn anomaly of phonons, and the elastic scattering of electrons and photons. The article concludes with an analysis of excitons in SWNTs and outlines future directions for research.
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Części książek na temat "Resonant Raman Effect"

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Kuzmany, H., i P. Knoll. "The Dispersion Effect of Resonance Raman Lines in trans-Polyacetylene". W Springer Series in Solid-State Sciences, 114–21. Berlin, Heidelberg: Springer Berlin Heidelberg, 1985. http://dx.doi.org/10.1007/978-3-642-82569-9_19.

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Terner, James, Andrew J. Sitter i John R. Shifflett. "Resonance Raman Spectroscopic Characterization of the Oxidation of the Horseradish Peroxidase Active Site". W Charge and Field Effects in Biosystems—2, 31–42. Boston, MA: Springer US, 1989. http://dx.doi.org/10.1007/978-1-4613-0557-6_4.

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Palaniappan, V., Ann M. Sullivan, Melissa M. Fitzgerald, John R. Shifflett i James Terner. "Resonance Raman Spectroscopy with Near Ultraviolet Excitation of Peroxidase Intermediates in High Oxidation States". W Charge and Field Effects in Biosystems—3, 349–63. Boston, MA: Birkhäuser Boston, 1992. http://dx.doi.org/10.1007/978-1-4615-9837-4_29.

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Anderton, C. L., R. E. Hester i J. N. Moore. "A Resonance Raman Spectroscopic Study of Polarity Effects in Mutant Myoglobins". W Spectroscopy of Biological Molecules, 243–44. Dordrecht: Springer Netherlands, 1995. http://dx.doi.org/10.1007/978-94-011-0371-8_109.

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Nechaev, V. V., i G. N. Ten. "Vibronic Coupling Effects in the Resonance Raman and Absorption Spectra of Adenine". W Spectroscopy of Biological Molecules, 301–2. Dordrecht: Springer Netherlands, 1995. http://dx.doi.org/10.1007/978-94-011-0371-8_134.

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Rospendowski, Bernard N., Vicki L. Schlegel, Randall E. Holt i Therese M. Cotton. "Surface-Enhanced Resonance Raman Scattering from Cytochromes Cand P-450 on Bare and Phospholipid-Coated Silver Substrates". W Charge and Field Effects in Biosystems—2, 43–58. Boston, MA: Springer US, 1989. http://dx.doi.org/10.1007/978-1-4613-0557-6_5.

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Lagant, P., i G. Vergoten. "Effects of Solvation on the Ultraviolet Resonance Raman Intensities of PI-Electrons Systems:". W Fifth International Conference on the Spectroscopy of Biological Molecules, 17–18. Dordrecht: Springer Netherlands, 1993. http://dx.doi.org/10.1007/978-94-011-1934-4_4.

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Moore, J. N., P. Matousek, A. W. Parker, W. T. Toner, M. Towrie i R. E. Hester. "Mode-Specific Effects in the Picosecond Resonance-Raman Spectra of Trans-Stilbene Solutions". W Springer Proceedings in Physics, 89–94. Berlin, Heidelberg: Springer Berlin Heidelberg, 1994. http://dx.doi.org/10.1007/978-3-642-85060-8_22.

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Ziegler, L. D. "Resonance Raman Studies of CH3I Sub-Picosecond Mode-Specific Photodissociation and Radiation-Induced Pure Dephasing Effects". W Springer Proceedings in Physics, 214–15. Berlin, Heidelberg: Springer Berlin Heidelberg, 1992. http://dx.doi.org/10.1007/978-3-642-84771-4_63.

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Ivanov, Victor G. "Interference Effects in the Resonant Raman Scattering from the Apical Oxygen Vibrations in the Ortho-II Phase of YBa2Cu3Ox". W ACS Symposium Series, 120–30. Washington, DC: American Chemical Society, 1999. http://dx.doi.org/10.1021/bk-1999-0730.ch008.

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Streszczenia konferencji na temat "Resonant Raman Effect"

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Bobbs, Bradley, i Charles Warner. "Raman-resonant four-wave mixing and energy transfer". W OSA Annual Meeting. Washington, D.C.: Optica Publishing Group, 1987. http://dx.doi.org/10.1364/oam.1987.thpo5.

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When nonlinear four-wave mixing (FWM) is resonant with a Raman transition, it causes coupling between lightwaves separated by two Raman frequency shifts. This coupling is manifested in effects such as Raman gain suppression, higher-order Stokes generation, and coherent Raman spectroscopies (e.g., CARS). An understanding of these effects, however, has been impeded by a widespread misconception that Raman-resonant FWM does not transfer energy between the lightwaves and the medium. The equations for the photon densities at each light frequency show that, in actuality, two medium excitations are created or destroyed for each photon produced by FWM. This point may be further clarified by consideration of the driving nonlinear polarization and by comparisons with broadband Raman conversion and nonresonant FWM. The Raman gain suppression effect may be understood qualitatively in terms of destructive interference between FWM and the usual stimulated Raman process.
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Schelokov, R. V., i V. V. Yatsishen. "Calculation of intensity of a resonant Raman effect by organic molecules". W SPIE Proceedings, redaktor Vadim E. Privalov. SPIE, 2006. http://dx.doi.org/10.1117/12.677681.

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Karagodova, Tamara Y. "Calculation of nonlinear resonant Raman effect cross sections in intense laser and magnetic fields". W Photonics West '96, redaktorzy Mool C. Gupta, William J. Kozlovsky i David C. MacPherson. SPIE, 1996. http://dx.doi.org/10.1117/12.239692.

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Bobbs, Bradley, J. A. Goldstone i Michael M. Johnson. "Angle-tuned multiline stimulated Raman scattering". W OSA Annual Meeting. Washington, D.C.: Optica Publishing Group, 1988. http://dx.doi.org/10.1364/oam.1988.mr26.

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The stimulated Raman scattering gain of a multiline pump laser spanning a sufficiently wide spectral range is significantly reduced from that of a narrowband laser. This is due to destructive interference between the narrowband Raman effect and the Raman-resonant four-wave mixing effect which couples the lines together. However, this interference can be constrained to be always constructive by angle tuning of the pump and Stokes seed input beams to satisfy a phase matching condition for the four-wave mixing. The narrowband Raman gain will then be obtained. Calculations for a two-line XeF laser in a Raman conversion cell show that submilliradian beam angles can shorten the required cell length by factors of ~2, while loosening the pump intensity variation tolerance by an order of magnitude. Calculations for lasers with wider spectra indicate the potential for much larger gain increases and cell length reductions.
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Silvestri, Markus R., Peter D. Persans i John Schroeder. "Pressure-tuned spectroscopy of II–VI semiconducting nanocrystals". W OSA Annual Meeting. Washington, D.C.: Optica Publishing Group, 1993. http://dx.doi.org/10.1364/oam.1993.thvv.1.

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Here CdSxSe1-x nanocrystals were studied and characterized by resonant Raman scattering, low frequency inelastic scattering, pressure tuned Raman scattering and photoluminescence. Ordinary Raman scattering and low frequency inelastic scattering were used for composition and size characterization. In the photoluminescence spectra we found that the deep defects where symbatic for compositions in the range close to CdS. For intermediate compositions down to CdSe no marked change in the defect peak positions were observed. This behavior is similar to the bulk case.1 Also the pressure coefficients in our measurements reflected this peculiarity. Resonant Raman scattering at different pressures was applied to examine the electron phonon interaction in the framework of the one dimensional configuration model. We found that the coupling strength (Huang-Rhys parameter) is larger than expected from theory and might indicate an extrinsic effect such as a point defect.2 The pressure dependence of the coupling was also compared with bulk CdS calculated from phonon replicas of the green defect line 3 and we found the same tendency of weakening with pressure. In the case of nanocrystals we were able to observe this beyond the phase transition point of bulk due to their higher stability or superpressure effects.
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Harris, T. D. "Fluorescence of molecules near small metal particles". W International Laser Science Conference. Washington, D.C.: Optica Publishing Group, 1986. http://dx.doi.org/10.1364/ils.1986.tue2.

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Small particles and rough surfaces of certain metals are known to give anomalously high electric fields when illuminated with radiation resonant with the plasmon oscillation of these structures. The most widely publicized manifestation of the high field is the surface enhanced Raman effect. Equally dramatic but less well known is the large change in radiative and nonradiative rates for molecules near these structures. A reduction of fluorescence life time of 104 with no loss in quantum efficiency has been reported. This fast radiative rate has been used to give recovery in quantum yield of 103 for heavily quenched fluorophor. We present further studies on the extent to which radiative and non-radiative rates can be controlled using metal particle substrates. Self-quenching, surface treatment, scattering, and the difficult engineering associated with this method are discussed. Prospects for large scale production of substrates and application of the effect to quantitative fluorescence analysis is assessed. The direction of future study required to realize in practice the large demonstrated effects is presented.
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Namura, Kyoko, i Motofumi Suzuki. "Marangoni Flow in Microfluidics Controlled by Laser Heating of Gold Nanoisland Films". W JSAP-OSA Joint Symposia. Washington, D.C.: Optica Publishing Group, 2017. http://dx.doi.org/10.1364/jsap.2017.8p_a410_6.

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Gold nanoparticles absorb light efficiently at their resonant frequency and convert it to heat within several picoseconds. Strong laser irradiation onto those gold nanoparticles enables us to heat the surrounding materials locally and rapidly, which has been reported to be useful for cancer therapy, ultrasonic generation, microfluidic control, and so on. Because the gold nanoparticles can also act as sensing platforms for such as Raman spectroscopy under laser irradiation, development of the microfluidic control method with laser heating of gold nanoparticles is desirable to meet the requirements in lab-on-a-chip devices. Here, we present microfluidic manipulation techniques based on Marangoni effect controlled by laser heating of gold nanoisland films and our most recent outcomes.
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Garmire, E., F. Karpushko, A. Kost i C. M. Yang. "Band-edge surface transient diffraction". W OSA Annual Meeting. Washington, D.C.: Optica Publishing Group, 1990. http://dx.doi.org/10.1364/oam.1990.fi2.

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As much as 25% self-diffraction has been observed at the surface of n-GaAs:Te when two pumps (and a weak probe) intersect with an internal angle of 0.15 rad in the Raman–Nath regime. The photoinduced gratings decayed in less than 100 ps. The diffraction efficiency was nearly independent of sample thickness (40 μm and 350 μm), and careful investigation has shown that the diffraction arose primarily at the surface and was resonant just below the band edge. It is proposed that band-bending at the surface states causes increased absorption and results in a sheet of optically induced charge. The faster diffusion of electrons relative to holes allows a transient charge separation to a distance of one diffusion length (1 μm). As a result, a space-charge field is formed (Dember field) that can cause an index change through the Franz–Keldysh effect. The resulting transient grating can cause the large observed diffraction. This new BEST effect has potential for optical-switching applications.
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Pandey, Rishikesh, Siva Umapathy, P. M. Champion i L. D. Ziegler. "Understanding Solvent Effect on Thioxanthone Using Time Resolved Resonance Raman Spectroscopy". W XXII INTERNATIONAL CONFERENCE ON RAMAN SPECTROSCOPY. AIP, 2010. http://dx.doi.org/10.1063/1.3482392.

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Moreira, E. C., G. D. Saraiva, A. G. Souza Filho, G. Braunstein, H. Muramatsu, Y. A. Kim, M. Endo, M. S. Dresselhaus, P. M. Champion i L. D. Ziegler. "Ion implantation effect on Resonance Raman spectroscopy of double-wall carbon nanotubes". W XXII INTERNATIONAL CONFERENCE ON RAMAN SPECTROSCOPY. AIP, 2010. http://dx.doi.org/10.1063/1.3482620.

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Raporty organizacyjne na temat "Resonant Raman Effect"

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Barrett, T. W. Inverse Faraday Effect in Hemoglobin Detected by Raman Spectroscopy: An Example of Magnetic Resonance Raman Activity. Fort Belvoir, VA: Defense Technical Information Center, czerwiec 1985. http://dx.doi.org/10.21236/ada159806.

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