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Sample records for pump-probe spectroscopy experiments

  1. Development of an X-ray delay unit for correlation spectroscopy and pump-probe experiments

    Energy Technology Data Exchange (ETDEWEB)

    Roseker, Wojciech

    2008-07-15

    Probing condensed matter on time scales ranging from femtoseconds to nanoseconds will be one of the key topics for future X-ray Free Electron Laser (XFEL) sources. The accessible time windows are, however, compromised by the intrinsic time structure of the sources. One way to overcome this limitation is the usage of a time delay unit. A prototype device capable of splitting an X-ray pulse into two adjustable fractions, delaying one of them with the aim to perform X-ray Photon Correlation Spectroscopy and pump-probe type studies was designed and manufactured. The device utilizes eight perfect crystals in vertical 90 scattering geometry. Its performance has been verified with 8.39 keV and 12.4 keV Xrays at various synchrotron sources. The measured throughput of the device with a Si(333) monochromator at 8.39 keV under ambient conditions is 0.6%. The stability was verified at 12.4 keV and operation without realignment and feedback was possible for more than 30 minutes. Time delays up to 2.95 ns have been achieved. The highest resolution achieved in an experiment was 15.4 ps, a value entirely determined by the diagnostics system. The influence of the delay unit optics on the coherence properties of the beam was investigated by means of Fraunhofer diffraction and static speckle analysis. The obtained high fringe visibility and contrast values larger than 23% indicate the feasibility of performing coherence based experiments with the delay line. (orig.)

  2. Theoretical Simulations and Ultrafast Pump-probe Spectroscopy Experiments in Pigment-protein Photosynthetic Complexes

    Energy Technology Data Exchange (ETDEWEB)

    Buck, D. R. [Iowa State Univ., Ames, IA (United States)

    2000-09-12

    Theoretical simulations and ultrafast pump-probe laser spectroscopy experiments were used to study photosynthetic pigment-protein complexes and antennae found in green sulfur bacteria such as Prosthecochloris aestuarii, Chloroflexus aurantiacus, and Chlorobium tepidum. The work focused on understanding structure-function relationships in energy transfer processes in these complexes through experiments and trying to model that data as we tested our theoretical assumptions with calculations. Theoretical exciton calculations on tubular pigment aggregates yield electronic absorption spectra that are superimpositions of linear J-aggregate spectra. The electronic spectroscopy of BChl c/d/e antennae in light harvesting chlorosomes from Chloroflexus aurantiacus differs considerably from J-aggregate spectra. Strong symmetry breaking is needed if we hope to simulate the absorption spectra of the BChl c antenna. The theory for simulating absorption difference spectra in strongly coupled photosynthetic antenna is described, first for a relatively simple heterodimer, then for the general N-pigment system. The theory is applied to the Fenna-Matthews-Olson (FMO) BChl a protein trimers from Prosthecochloris aestuarii and then compared with experimental low-temperature absorption difference spectra of FMO trimers from Chlorobium tepidum. Circular dichroism spectra of the FMO trimer are unusually sensitive to diagonal energy disorder. Substantial differences occur between CD spectra in exciton simulations performed with and without realistic inhomogeneous distribution functions for the input pigment diagonal energies. Anisotropic absorption difference spectroscopy measurements are less consistent with 21-pigment trimer simulations than 7-pigment monomer simulations which assume that the laser-prepared states are localized within a subunit of the trimer. Experimental anisotropies from real samples likely arise from statistical averaging over states with diagonal energies shifted by

  3. Theoretical Simulations and Ultrafast Pump-probe Spectroscopy Experiments in Pigment-protein Photosynthetic Complexes

    Energy Technology Data Exchange (ETDEWEB)

    Buck, D.R.

    2000-09-12

    Theoretical simulations and ultrafast pump-probe laser spectroscopy experiments were used to study photosynthetic pigment-protein complexes and antennae found in green sulfur bacteria such as Prosthecochloris aestuarii, Chloroflexus aurantiacus, and Chlorobium tepidum. The work focused on understanding structure-function relationships in energy transfer processes in these complexes through experiments and trying to model that data as we tested our theoretical assumptions with calculations. Theoretical exciton calculations on tubular pigment aggregates yield electronic absorption spectra that are superimpositions of linear J-aggregate spectra. The electronic spectroscopy of BChl c/d/e antennae in light harvesting chlorosomes from Chloroflexus aurantiacus differs considerably from J-aggregate spectra. Strong symmetry breaking is needed if we hope to simulate the absorption spectra of the BChl c antenna. The theory for simulating absorption difference spectra in strongly coupled photosynthetic antenna is described, first for a relatively simple heterodimer, then for the general N-pigment system. The theory is applied to the Fenna-Matthews-Olson (FMO) BChl a protein trimers from Prosthecochloris aestuarii and then compared with experimental low-temperature absorption difference spectra of FMO trimers from Chlorobium tepidum. Circular dichroism spectra of the FMO trimer are unusually sensitive to diagonal energy disorder. Substantial differences occur between CD spectra in exciton simulations performed with and without realistic inhomogeneous distribution functions for the input pigment diagonal energies. Anisotropic absorption difference spectroscopy measurements are less consistent with 21-pigment trimer simulations than 7-pigment monomer simulations which assume that the laser-prepared states are localized within a subunit of the trimer. Experimental anisotropies from real samples likely arise from statistical averaging over states with diagonal energies shifted by

  4. Noisy pulses enhance temporal resolution in pump-probe spectroscopy

    CERN Document Server

    Meyer, Kristina; Raith, Philipp; Kaldun, Andreas; Jiang, Yuhai; Senftleben, Arne; Kurka, Moritz; Moshammer, Robert; Ullrich, Joachim; Pfeifer, Thomas

    2011-01-01

    Time-resolved measurements of quantum dynamics are based on the availability of controlled events (e.g. pump and probe pulses) that are shorter in duration than the typical evolution time scale of the dynamical processes to be observed. Here we introduce the concept of noise-enhanced pump-probe spectroscopy, allowing the measurement of dynamics significantly shorter than the average pulse duration by exploiting randomly varying, partially coherent light fields consisting of bunched colored noise. It is shown that statistically fluctuating fields can be superior by more than a factor of 10 to frequency-stabilized fields, with important implications for time-resolved pump-probe experiments at x-ray free-electron lasers (FELs) and, in general, for measurements at the frontiers of temporal resolution (e.g. attosecond spectroscopy). As an example application, the concept is used to explain the recent experimental observation of vibrational wave packet motion in a deuterium molecular ion on time scales shorter than...

  5. Superconducting detector dynamics studied by quantum pump-probe spectroscopy

    NARCIS (Netherlands)

    Heeres, R.W.; Zwiller, V.

    2012-01-01

    We explore the dynamics of superconducting single-photon detectors (SSPDs) on the picosecond time-scale using a correlated photon-pair source based on spontaneous parametric downconversion (SPDC), corresponding to a pump-probe experiment at the single-photon level. We show that the detector can oper

  6. Flexible attosecond beamline for high harmonic spectroscopy and XUV/near-IR pump probe experiments requiring long acquisition times

    Energy Technology Data Exchange (ETDEWEB)

    Weber, S. J., E-mail: sebastien.weber@cea.fr; Manschwetus, B.; Billon, M.; Bougeard, M.; Breger, P.; Géléoc, M.; Gruson, V.; Lin, N.; Ruchon, T.; Salières, P.; Carré, B. [Commissariat l’Energie Atomique, Laser, Interactions and Dynamics Laboratory (LIDyL), DSM/IRAMIS, CEA-Saclay, 91191 Gif sur Yvette (France); Böttcher, M.; Huetz, A.; Picard, Y. J. [ISMO, UMR 8214, Université Paris-Sud, Batiment 350, Orsay (France)

    2015-03-15

    We describe the versatile features of the attosecond beamline recently installed at CEA-Saclay on the PLFA kHz laser. It combines a fine and very complete set of diagnostics enabling high harmonic spectroscopy (HHS) through the advanced characterization of the amplitude, phase, and polarization of the harmonic emission. It also allows a variety of photo-ionization experiments using magnetic bottle and COLTRIMS (COLd Target Recoil Ion Momentum Microscopy) electron spectrometers that may be used simultaneously, thanks to a two-foci configuration. Using both passive and active stabilization, special care was paid to the long term stability of the system to allow, using both experimental approaches, time resolved studies with attosecond precision, typically over several hours of acquisition times. As an illustration, applications to multi-orbital HHS and electron-ion coincidence time resolved spectroscopy are presented.

  7. Coherence specific signal detection via chiral pump-probe spectroscopy.

    Science.gov (United States)

    Holdaway, David I H; Collini, Elisabetta; Olaya-Castro, Alexandra

    2016-05-21

    We examine transient circular dichroism (TRCD) spectroscopy as a technique to investigate signatures of exciton coherence dynamics under the influence of structured vibrational environments. We consider a pump-probe configuration with a linearly polarized pump and a circularly polarized probe, with a variable angle θ between the two directions of propagation. In our theoretical formalism the signal is decomposed in chiral and achiral doorway and window functions. Using this formalism, we show that the chiral doorway component, which beats during the population time, can be isolated by comparing signals with different values of θ. As in the majority of time-resolved pump-probe spectroscopy, the overall TRCD response shows signatures of both excited and ground state dynamics. However, we demonstrate that the chiral doorway function has only a weak ground state contribution, which can generally be neglected if an impulsive pump pulse is used. These findings suggest that the pump-probe configuration of optical TRCD in the impulsive limit has the potential to unambiguously probe quantum coherence beating in the excited state. We present numerical results for theoretical signals in an example dimer system.

  8. Controlling double ionization of atoms in pump-probe experiments

    CERN Document Server

    Bauch, S; Bonitz, M

    2010-01-01

    The ionization dynamics of a two-electron atom in an attosecond XUV-infrared pump-probe experiment is simulated by solving the time-dependent two-electron Schr\\"odinger equation. A dramatic change of the double ionization (DI) yield with variation of the pump-probe delay is reported and the governing role of electron-electron correlations is shown. The results allow for a direct control of the DI yield and of the relative strength of double and single ionization.

  9. Photo-induced absorption in the pump probe spectroscopy of single-walled carbon nanotubes

    Institute of Scientific and Technical Information of China (English)

    Zhu Zi-Peng

    2013-01-01

    Femtosecond pump probe spectroscopy is employed to study the photo-induced absorption feature in the singlewalled carbon nanotube transient spectrum.The two advantages of the experiment,a chirality enriched sample and tuning the pump wavelength to the resonance of a specific nanotube species,greatly facilitate the identification of the photoinduced absorption signal of one tube species.It is found that a photo-induced absorption feature is located at one radial breathing mode to the blue side of the Eii state.This finding prompts a new explanation for the origin of the photoinduced absorption:the transition from the ground state to a phonon coupled state near the Eii state.The explanation suggests a superposition mechanism of the photo-bleach and photo-induced absorption signals,which may serve as a key to the interpretation of the complex pump probe transient spectrum of carbon nanotubes.The finding sheds some light on the understanding of the complex non-radiative relaxation process and the electronic structure of single-walled carbon nanotubes.

  10. Time-resolved pump-probe experiments at the LCLS

    Energy Technology Data Exchange (ETDEWEB)

    Glownia, James; /SLAC /Stanford U., Appl. Phys. Dept.; Cryan, J.; /SLAC /Stanford U., Phys. Dept.; Andreasson, J.; /Uppsala U.; Belkacem, A.; /LBNL, Berkeley; Berrah, N.; /Western Michigan U.; Blaga, C.L.; /Ohio State U.; Bostedt, C.; Bozek, J.; /SLAC; DiMauro, L.F.; /Ohio State U.; Fang, L.; /Western Michigan U.; Frisch, J.; /SLAC; Gessner, O.; /LBNL; Guhr, M.; /SLAC; Hajdu, J.; /Uppsala U.; Hertlein, M.P.; /LBNL; Hoener, M.; /Western Michigan U. /LBNL; Huang, G.; Kornilov, O.; /LBNL; Marangos, J.P.; /Imperial Coll., London; March, A.M.; /Argonne; McFarland, B.K.; /SLAC /Stanford U., Phys. Dept. /SLAC /IRAMIS, Saclay /Stanford U., Phys. Dept. /Georgia Tech /Argonne /Kansas State U. /SLAC /Stanford U., Phys. Dept. /SLAC /Stanford U., Appl. Phys. Dept. /Stanford U., Appl. Phys. Dept. /SLAC /LBNL /Argonne /SLAC /SLAC /Stanford U., Appl. Phys. Dept. /Stanford U., Phys. Dept.

    2011-08-12

    The first time-resolved x-ray/optical pump-probe experiments at the SLAC Linac Coherent Light Source (LCLS) used a combination of feedback methods and post-analysis binning techniques to synchronize an ultrafast optical laser to the linac-based x-ray laser. Transient molecular nitrogen alignment revival features were resolved in time-dependent x-ray-induced fragmentation spectra. These alignment features were used to find the temporal overlap of the pump and probe pulses. The strong-field dissociation of x-ray generated quasi-bound molecular dications was used to establish the residual timing jitter. This analysis shows that the relative arrival time of the Ti:Sapphire laser and the x-ray pulses had a distribution with a standard deviation of approximately 120 fs. The largest contribution to the jitter noise spectrum was the locking of the laser oscillator to the reference RF of the accelerator, which suggests that simple technical improvements could reduce the jitter to better than 50 fs.

  11. Valley Carrier Dynamics in Monolayer Molybdenum Disulphide from Helicity Resolved Ultrafast Pump-probe Spectroscopy

    CERN Document Server

    Wang, Qinsheng; Li, Xiao; Qiu, Jun; Ji, Yanxin; Feng, Ji; Sun, Dong

    2013-01-01

    We investigate the valley related carrier dynamics in monolayer MoS2 using helicity resolved non-degenerate ultrafast pump-probe spectroscopy at the vicinity of the high-symmetry K point under the temperature down to 78 K. Monolayer MoS2 shows remarkable transient reflection signals, in stark contrast to bilayer and bulk MoS2 due to the enhancement of many-body effect at reduced dimensionality. The helicity resolved ultrafast time-resolved result shows that the valley polarization is preserved for only several ps before scattering process makes it undistinguishable. We suggest that the dynamical degradation of valley polarization is attributable primarily to the exciton trapping by defect states in the exfoliated MoS2 samples. Our experiment and a tight-binding model analysis also show that the perfect valley CD selectivity is fairly robust against disorder at the K point, but quickly decays from the high-symmetry point in the momentum space in the presence of disorder.

  12. Femtosecond pump-probe photoionization-photofragmentation spectroscopy of azobenzene cation

    Institute of Scientific and Technical Information of China (English)

    HO; JrWei

    2010-01-01

    We report the studies of ultrafast dynamics of azobenzene cations using femtosecond photoionization-photofragmentation spectroscopy. In our experiment,a femtosecond pump pulse first prepares an ensemble of azobenzene cations via photoionization of neutrals. A delayed probe pulse then brings the evolving ionic system to higher states that ultimately undergo ion fragmentation. The dynamics is followed by monitoring either the parent-ion depletion or fragment-ion formation as a function of the pump-probe delay time. The observed transients for azobenzene cations are characterized by a constant ion depletion modulated by a rapidly damped oscillatory signal with a period of about 1 ps. Theoretical calculations suggest that the oscillation arises from a vibration motion along the twisting inversion coordinate involving displacements in CNNC and phenyl-ring torsions. The oscillation is damped rapidly with a time constant of about 1.2 ps,suggesting that energy dissipation from the active mode to bath modes takes place on this time scale.

  13. Coherence and Relaxation in Potassium-Doped Helium Droplets Studied by Femtosecond Pump-Probe Spectroscopy

    Science.gov (United States)

    Stienkemeier, F.; Meier, F.; Hägele, A.; Lutz, H. O.; Schreiber, E.; Schulz, C. P.; Hertel, I. V.

    1999-09-01

    Superfluid helium droplets are doped with potassium atoms to form complexes in which the metal atom is weakly bound to the cluster surface. The dynamics of these systems upon electronic excitation of the metal atom is probed by means of femtosecond pump-probe spectroscopy. Alignment of the excited potassium p orbital parallel to the cluster surface leads to quantum interferences, the decay of which gives information on the ultrafast perturbation of the induced atomic coherence by the superfluid environment; exciting the p state aligned perpendicularly, the strong repulsive interaction with the helium surface comes into play and the response of the helium environment is followed in time.

  14. Ultra-broadband infrared pump-probe spectroscopy using synchrotron radiation and a tuneable pump

    Energy Technology Data Exchange (ETDEWEB)

    Carroll, Lee; Friedli, Peter; Stutz, Stefan; Sigg, Hans [Laboratory for Micro and Nanotechnology, Paul Scherrer Institut, CH-5232 Villigen PSI (Switzerland); Lerch, Philippe; Schneider, Joerg; Treyer, Daniel; Hunziker, Stephan [Swiss Light Source, Paul Scherrer Institut, CH-5232 Villigen PSI (Switzerland)

    2011-06-15

    Synchrotron infrared sources have become popular mainly because of their excellent broadband brilliance, which enables spectroscopically resolved spatial-mapping of stationary objects at the diffraction limit. In this article we focus on an often-neglected further advantage of such sources - their unique time-structure - to bring such broadband spectroscopy to the time domain, for studying dynamic phenomenon down to the 100 ps limit. We describe the ultra-broadband (12.5 to 1.1 {mu}m) Fourier transform pump-probe setup, for condensed matter transmission- and reflection-spectroscopy, installed at the X01DC infrared beam-line of the Swiss Light Source (SLS). The optical pump consists of a widely tuneable 100 ps 1 kHz laser system, covering 94% of the 16 to 1.1 {mu}m range. A thorough description of the system is given, including (i) the vector-modulator providing purely electronic tuning of the pump-probe overlap up to 1 ms with sub-ps time resolution, (ii) the 500 MHz data acquisition system interfaced with the experimental physics and industrial control system (EPICS) based SLS control system for consecutive pulse sampling, and (iii) the step-scan time-slice Fourier transform scheme for simultaneous recording of the dual-channel pumped, un-pumped, and difference spectra. The typical signal/noise ratio of a single interferogram in a 100 ps time slice is 300 (measured during one single 140 s TopUp period). This signal/noise ratio is comparable to that of existing gated Globar pump-probe Fourier transform spectroscopy, but brings up to four orders of magnitude better time resolution. To showcase the utility of broadband pump-probe spectroscopy, we investigate a Ge-on-Si material system similar to that in which optically pumped direct-gap lasing was recently reported. We show that the mid-infrared reflection-spectra can be used to determine the optically injected carrier density, while the mid- and near-infrared transmission-spectra can be used to separate the strong

  15. Ultra-broadband infrared pump-probe spectroscopy using synchrotron radiation and a tuneable pump.

    Science.gov (United States)

    Carroll, Lee; Friedli, Peter; Lerch, Philippe; Schneider, Jörg; Treyer, Daniel; Hunziker, Stephan; Stutz, Stefan; Sigg, Hans

    2011-06-01

    Synchrotron infrared sources have become popular mainly because of their excellent broadband brilliance, which enables spectroscopically resolved spatial-mapping of stationary objects at the diffraction limit. In this article we focus on an often-neglected further advantage of such sources - their unique time-structure - to bring such broadband spectroscopy to the time domain, for studying dynamic phenomenon down to the 100 ps limit. We describe the ultra-broadband (12.5 to 1.1 μm) Fourier transform pump-probe setup, for condensed matter transmission- and reflection-spectroscopy, installed at the X01DC infrared beam-line of the Swiss Light Source (SLS). The optical pump consists of a widely tuneable 100 ps 1 kHz laser system, covering 94% of the 16 to 1.1 μm range. A thorough description of the system is given, including (i) the vector-modulator providing purely electronic tuning of the pump-probe overlap up to 1 ms with sub-ps time resolution, (ii) the 500 MHz data acquisition system interfaced with the experimental physics and industrial control system (EPICS) based SLS control system for consecutive pulse sampling, and (iii) the step-scan time-slice Fourier transform scheme for simultaneous recording of the dual-channel pumped, un-pumped, and difference spectra. The typical signal/noise ratio of a single interferogram in a 100 ps time slice is 300 (measured during one single 140 s TopUp period). This signal/noise ratio is comparable to that of existing gated Globar pump-probe Fourier transform spectroscopy, but brings up to four orders of magnitude better time resolution. To showcase the utility of broadband pump-probe spectroscopy, we investigate a Ge-on-Si material system similar to that in which optically pumped direct-gap lasing was recently reported. We show that the mid-infrared reflection-spectra can be used to determine the optically injected carrier density, while the mid- and near-infrared transmission-spectra can be used to separate the strong pump

  16. Time-resolved pump-probe spectroscopy of intraband absorption by a semiconductor nanorod

    Science.gov (United States)

    Leonov, Mikhail Y.; Rukhlenko, Ivan D.; Baranov, Alexander V.; Fedorov, Anatoly V.

    2013-09-01

    We develop a theory of time-resolved pump-probe optical spectroscopy of intraband absorption of a probe pulse inside an anisotropic semiconductor nanorod. The absorption is preceded by the absorption of the pump pulse resonant to an interband transition. It is assumed that the resonantly exited states of the nanorod are interrelated via the relaxation induced by their interaction with a bath. We reveal the conditions for which the absorption of the probe's pulse is governed by a simple formula regardless of the pulse's shape. This formula is useful for the analysis of the experimental data containing information on the relaxation parameters of the nanorod's electronic subsystem.

  17. Extraction of carrier lifetime in Ge waveguides using pump probe spectroscopy

    Science.gov (United States)

    Srinivasan, S. A.; Pantouvaki, M.; Verheyen, P.; Lepage, G.; Absil, P.; Van Campenhout, J.; Van Thourhout, D.

    2016-05-01

    Carrier lifetimes in Ge-on-Si waveguides are deduced using time-resolved infrared transmission pump-probe spectroscopy. Dynamics of pump-induced excess carriers generated in waveguides with varying Ge thickness and width is probed using a CW laser. The lifetimes of these excess carriers strongly depend on the thickness and width of the waveguide due to defect assisted surface recombination. Interface recombination velocities of 0.975 × 104 cm/s and 1.45 × 104 cm/s were extracted for the Ge/Si and the Ge/SiO2 interfaces, respectively.

  18. Confocal ultrafast pump-probe spectroscopy: a new technique to explore nanoscale composites

    Science.gov (United States)

    Virgili, Tersilla; Grancini, Giulia; Molotokaite, Egle; Suarez-Lopez, Inma; Rajendran, Sai Kiran; Liscio, Andrea; Palermo, Vincenzo; Lanzani, Guglielmo; Polli, Dario; Cerullo, Giulio

    2012-03-01

    This article is devoted to the exploration of the benefits of a new ultrafast confocal pump-probe technique, able to study the photophysics of different structured materials with nanoscale resolution. This tool offers many advantages over standard stationary microscopy techniques because it directly interrogates excited state dynamics in molecules, providing access to both radiative and non-radiative deactivation processes at a local scale. In this paper we present a few different examples of its application to organic semiconductor systems. The first two are focussed on the study of the photophysics of phase-separated polymer blends: (i) a blue-emitting polyfluorene (PFO) in an inert matrix of PMMA and (ii) an electron donor polythiophene (P3HT) mixed with an electron acceptor fullerene derivative (PCBM). The experimental results on these samples demonstrate the capability of the technique to unveil peculiar interfacial dynamics at the border region between phase-segregated domains, which would be otherwise averaged out using conventional pump-probe spectroscopy. The third example is the study of the photophysics of isolated mesoscopic crystals of the PCBM molecule. Our ultrafast microscope could evidence the presence of two distinctive regions within the crystals. In particular, we could pinpoint for the first time areas within the crystals showing photobleaching/stimulated emission signals from a charge-transfer state.

  19. The retarding Bessel–Box—An electron-spectrometer designed for pump/probe experiments

    Energy Technology Data Exchange (ETDEWEB)

    Schiwietz, G., E-mail: schiwietz@helmholtz-berlin.de [Institut Methoden und Instrumentierung der Forschung mit Synchrotronstrahlung (FG-ISRR) and also former Division HMI/SF8, Helmholtz-Zentrum Berlin für Materialien und Energie GmbH, Hahn-Meitner-Platz 1, 14109 Berlin (Germany); Beye, M.; Kühn, D. [Institut Methoden und Instrumentierung der Forschung mit Synchrotronstrahlung (FG-ISRR) and also former Division HMI/SF8, Helmholtz-Zentrum Berlin für Materialien und Energie GmbH, Hahn-Meitner-Platz 1, 14109 Berlin (Germany); Xiao, G. [Institut Methoden und Instrumentierung der Forschung mit Synchrotronstrahlung (FG-ISRR) and also former Division HMI/SF8, Helmholtz-Zentrum Berlin für Materialien und Energie GmbH, Hahn-Meitner-Platz 1, 14109 Berlin (Germany); Institute of Modern Physics, PO Box 31, Lanzhou 730000 (China)

    2015-08-15

    Highlights: • A new electrostatic electron spectrometer has been developed and tested. • It yields high count rates for rapid NEXAFS, photo ionization or Auger scans. • It yields excellent intrinsic timing even without position-sensitive detector. • It is optimized for electron coincidences and femtosecond pump/probe-experiments. • It is insensitive to electron pile-up and light due to strong Laser fields. - Abstract: A new type of electrostatic electron spectrometer is developed, capable of particular sensitive measurements of energy spectra and time-of-flight distributions. This instrument is specifically designed and optimized for laser-pump/X-ray-probe measurements, where photo electrons or Auger electrons from surfaces, clusters, molecular or atomic targets are being measured with high time-resolution at an extremely low detection-noise level. The compact and robust cylinder-symmetrical system is a strongly improved Bessel–Box design, featuring electron retardation, a large detection solid-angle, about 100% electron transmission (gridless design) and excellent time-resolution. In this paper we describe the principle of operation of this type of spectrometer and various tests. We present quantitative results for electron measurements with different solid-state targets and two different electron-detection systems in comparison to electron-trajectory simulations inside the electrostatic spectrometer fields. Picosecond-pump/probe operation has been tested with high laser power and even the ability to work under femtosecond-pump-probe conditions with electron detection at the BESSY II slicing facility has been proven.

  20. Light Driven Energy Research at LCLS: Planned Pump-Probe X-ray Spectroscopy Studies on Photosynthetic Water Splitting

    Science.gov (United States)

    Bergmann, Uwe

    2010-02-01

    Arguably the most important chemical reaction on earth is the photosynthetic splitting of water to molecular oxygen by the Mn-containing oxygen-evolving complex (Mn-OEC) in the protein known as photosystem II (PSII). It is this reaction which has, over the course of some 3.8 billion years, gradually filled our atmosphere with O2 and consequently enabled and sustained the evolution of complex aerobic life. Coupled to the reduction of carbon dioxide, biological photosynthesis contributes foodstuffs for nutrition while recycling CO2 from the atmosphere and replacing it with O2. By utilizing sunlight to power these energy-requiring reactions, photosynthesis also serves as a model for addressing societal energy needs as we enter an era of diminishing fossil hydrocarbon resources. Understanding, at the molecular level, the dynamics and mechanism of how nature has solved this problem is of fundamental importance and could be critical to aid in the design of manufactured devices to accomplish the conversion of sunlight into useful electrochemical energy and transportable fuel in the foreseeable future. In order to understand the photosynthetic splitting of water by the Mn-OEC we need to be able to follow the reaction in real time at an atomic level. A powerful probe to study the electronic and molecular structure of the Mn-OEC is x-ray spectroscopy. Here, in particular x-ray emission spectroscopy (XES) has two crucial qualities for LCLS based time-dependent pump-probe studies of the Mn-OEC: a) it directly probes the Mn oxidation state and ligation, b) it can be performed with wavelength dispersive optics to avoid the necessity of scanning in pump probe experiments. Recent results and the planned time dependent experiments at LCLS will be discussed. )

  1. Theoretical description of pump/probe experiments in electron-mediated charge-density-wave insulators

    Science.gov (United States)

    Freericks, J. K.; Matveev, O. P.; Shen, Wen; Shvaika, A. M.; Devereaux, T. P.

    2017-03-01

    In this review, we develop the formalism employed to describe charge-density-wave insulators in pump/probe experiments that use ultrashort driving pulses of light. The theory emphasizes exact results in the simplest model for a charge-density-wave insulator (given by a noninteracting system with two bands and a gap) and employs nonequilibrium dynamical mean-field theory to solve the Falicov-Kimball model in its ordered phase. We show how to develop the formalism and how the solutions behave. Care is taken to describe the details behind these calculations and to show how to verify their accuracy via sum-rule constraints.

  2. Tunable IR/THz source for pump probe experiments at the European XFEL

    Science.gov (United States)

    Schneidmiller, E. A.; Yurkov, M. V.; Krasilnikov, M.; Stephan, F.

    2013-05-01

    We present a concept of an accelerator based source of powerful, coherent IR/THz radiation for pump-probe experiments at the European XFEL. The electron accelerator is similar to that operating at the PITZ facility. It consists of an rf gun and a warm accelerating section (energy up to 30 MeV). The radiation is generated in an APPLE-II type undulator, thus providing polarization control. Radiation with wavelength below 200 micrometers is generated using the mechanism of SASE FEL. Powerful coherent radiation with wavelength above 200 micrometers is generated in the undulator by a tailored (compressed) electron beam. Properties of the radiation are: wavelength range is 10 to 1000 micrometers (30 THz - 0.3 THz), radiation pulse energy is up to a few hundred microjoule, peak power is 10 to 100 MW, spectrum bandwidth is 2 - 3 %. Pump-probe experiments involving ultrashort electron pulses can be realized as well. The time structure of the THz source and x-ray FEL are perfectly matched since the THz source is based on the same technology as the injector of the European XFEL. A similar scheme can also be realized at LCLS, SACLA, or SWISS FEL with S-band rf accelerator technology.

  3. Towards pump-probe experiments of defect dynamics with short ion beam pulses

    Science.gov (United States)

    Schenkel, T.; Lidia, S. M.; Weis, C. D.; Waldron, W. L.; Schwartz, J.; Minor, A. M.; Hosemann, P.; Kwan, J. W.

    2013-11-01

    A novel, induction type linear accelerator, the Neutralized Drift Compression eXperiment (NDCX-II), is currently being commissioned at Berkeley Lab. This accelerator is designed to deliver intense (up to 3 × 1011 ions/pulse), 0.6 to ∼600 ns duration pulses of 0.05-1.2 MeV lithium ions at a rate of about 2 pulses per minute onto 1-10 mm scale target areas. When focused to mm-diameter spots, the beam is predicted to volumetrically heat micrometer thick foils to temperatures of ∼30,000 °K. At lower beam power densities, the short excitation pulse with tunable intensity and time profile enables pump-probe type studies of defect dynamics in a broad range of materials. We briefly describe the accelerator concept and design, present results from beam pulse shaping experiments and discuss examples of pump-probe type studies of defect dynamics following irradiation of materials with intense, short ion beam pulses from NDCX-II.

  4. Towards pump probe experiments of defect dynamics with short ion beam pulses

    Energy Technology Data Exchange (ETDEWEB)

    Schenkel, T. [Lawrence Berkeley National Laboratory (LBNL); Lidia, S. [Lawrence Berkeley National Laboratory (LBNL); Weis, C. D. [Lawrence Berkeley National Laboratory (LBNL); Waldron, W. L. [Lawrence Berkeley National Laboratory (LBNL); Schwartz, J. [Lawrence Berkeley National Laboratory (LBNL); Minor, Andrew [Lawrence Berkeley National Laboratory (LBNL); Hosemann, P [University of California, Berkeley; Kwan, J. W. [Lawrence Berkeley National Laboratory (LBNL)

    2013-01-01

    A novel, induction type linear accelerator, the Neutralized Drift Compression eXperiment (NDCX-II), is currently being commissioned at Berkeley Lab. This accelerator is designed to deliver intense (up to 3 1011 ions/pulse), 0.6 to 600 ns duration pulses of 0.05 1.2 MeV lithium ions at a rate of about 2 pulses per minute onto 1 10 mm scale target areas. When focused to mm-diameter spots, the beam is predicted to volumetrically heat micrometer thick foils to temperatures of 30,000 K. At lower beam power densities, the short excitation pulse with tunable intensity and time profile enables pump probe type studies of defect dynamics in a broad range of materials. We briefly describe the accelerator concept and design, present results from beam pulse shaping experiments and discuss examples of pump probe type studies of defect dynamics following irradiation of materials with intense, short ion beam pulses from NDCX-II.

  5. Plasma switch as a temporal overlap tool for pump-probe experiments at FEL facilities

    Science.gov (United States)

    Harmand, M.; Murphy, C. D.; Brown, C. R. D.; Cammarata, M.; Döppner, T.; Düsterer, S.; Fritz, D.; Förster, E.; Galtier, E.; Gaudin, J.; Glenzer, S. H.; Göde, S.; Gregori, G.; Hilbert, V.; Hochhaus, D.; Laarmann, T.; Lee, H. J.; Lemke, H.; Meiwes-Broer, K.-H.; Moinard, A.; Neumayer, P.; Przystawik, A.; Redlin, H.; Schulz, M.; Skruszewicz, S.; Tavella, F.; Tschentscher, T.; White, T.; Zastrau, U.; Toleikis, S.

    2012-08-01

    We have developed an easy-to-use and reliable timing tool to determine the arrival time of an optical laser and a free electron laser (FEL) pulses within the jitter limitation. This timing tool can be used from XUV to X-rays and exploits high FELs intensities. It uses a shadowgraph technique where we optically (at 800 nm) image a plasma created by an intense XUV or X-ray FEL pulse on a transparent sample (glass slide) directly placed at the pump - probe sample position. It is based on the physical principle that the optical properties of the material are drastically changed when its free electron density reaches the critical density. At this point the excited glass sample becomes opaque to the optical laser pulse. The ultra-short and intense XUV or X-ray FEL pulse ensures that a critical electron density can be reached via photoionization and subsequent collisional ionization within the XUV or X-ray FEL pulse duration or even faster. This technique allows to determine the relative arrival time between the optical laser and the FEL pulses in only few single shots with an accuracy mainly limited by the optical laser pulse duration and the jitter between the FEL and the optical laser. Considering the major interest in pump-probe experiments at FEL facilities in general, such a femtosecond resolution timing tool is of utmost importance.

  6. Retrieval of spectral and dynamic properties from two-dimensional infrared pump-probe experiments.

    Science.gov (United States)

    Chelli, Riccardo; Volkov, Victor V; Righini, Roberto

    2008-07-15

    We have developed a fitting algorithm able to extract spectral and dynamic properties of a three level oscillator from a two-dimensional infrared spectrum (2D-IR) detected in time resolved nonlinear experiments. Such properties go from the frequencies of the ground-to-first and first-to-second vibrational transitions (and hence anharmonicity) to the frequency-fluctuation correlation function. This last is represented through a general expression that allows one to approach the various strategies of modeling proposed in the literature. The model is based on the Kubo picture of stochastic fluctuations of the transition frequency as a result of perturbations by a fluctuating surrounding. To account for the line-shape broadening due to pump pulse spectral width in double-resonance measurements, we supply the fitting algorithm with the option to perform the convolution of the spectral signal with a Lorentzian function in the pump-frequency dimension. The algorithm is tested here on 2D-IR pump-probe spectra of a Gly-Ala dipeptide recorded at various pump-probe delay times. Speedup benchmarks have been performed on a small Beowulf cluster. The program is written in FORTRAN language for both serial and parallel architectures and is available free of charge to the interested reader.

  7. Characterization of optically excited semiconductors by phase-resolved pump-probe spectroscopy; Charakterisierung optisch angeregter Halbleiter mit phasenaufgeloester Pump-Probe-Spektroskopie

    Energy Technology Data Exchange (ETDEWEB)

    Seemann, M.

    2005-07-01

    This thesis aims to present new experimentally and theoretically verified statements about the many-body effects in thin Zinc Selenide layers and to discuss the various techniques applied in the experiments. Centred in this thesis is the investigation of ultrafast nonlinear effects in the response of thin Zinc Selenide layers on their optical excitation with ultrashort laser pulses. The experiments address the regime of quantum coherence and thermalisation of the excitation. In the energy range of the band gap the response is determined by the propagation of exciton polaritons in the samples. The dynamics of the interactions between the polaritons and the particles of the solid are investigated by conducting pump-probe experiments. This thesis extends and surpasses previous work in that the reflected light is completely analysed in its classical phase and amplitude. Thus all the information in the electromagnetic field in the temporal and spectral domain is available. It is found that especially not just the power spectrum of the reflected light is much structured but the spectral phase too. The spectral phase reflects directly the carrier-density dependent of the polariton dispersion while the temporal field, characterised by the beating of slowly propagating polaritons, does not show dramatic carrier-density depended changes. Phase resolved measurement of the reflected field is performed with the technique of Spectral Interferometry which is adapted to the experiment and tested on correctness. The measured electromagnetic fields are interpreted with classical and a semi-classical microscopic models. Further is shown how these results relate to recent microscopic quantum mechanical models. (orig.)

  8. Ultrafast pump-probe spectroscopy of the photoreceptor stentorins from the ciliate stentor coeruleus

    Energy Technology Data Exchange (ETDEWEB)

    Savikhin, S.; Struve, W.S. (Iowa State Univ., Ames, IA (United States)); Tao, N.; Song, P.S. (Univ. of Nebraska, Lincoln, NE (United States))

    1993-11-25

    Polarized absorption difference profiles have been obtained with 3-6-ps resolution between 565 and 630 nm for the chromoproteins stentorin I and stentorin II, isolated from the protozoan ciliate Stentor coeruleus. Control experiments were performed on hypericin and on the stentorin chromophore in methanol. The isotropic decays of stentorin I and the stentorin chromophore are dominated by components with lifetimes conservatively longer than 1 ns. Stentorin I, the stentorin chromophore, and hypericin all develop, within <5 ps, an intense excited-state absorption band that is blue-shifted from and polarized essentially perpendicular to the main long-wavelength absorption band. The presence of this excited-state absorption band is signaled by the appearance of strongly wavelength-dependent initial anisotropies r(0), which assume large positive as well as negative values (>0.4 and <[minus]0.2). To our knowledge, such anisotropies have not been reported in polarized pump-probe studies of rotational diffusion in solution or of energy-transfer kinetics in photosynthetic antennae. Hypericin itself exhibits 0.4-6-ps excited-state absorption decay kinetics, which are likely associated with intramolecular excited-state proton transfer. 19 refs., 8 figs., 5 tabs.

  9. Measurements of linear and circular birefringence in metals by femtosecond optical pump-probe spectroscopy

    CERN Document Server

    Wilks, R

    2002-01-01

    Optically induced transient linear and circular birefringence has been studied in three different materials: ferromagnetic Ni, semiconducting GaAs and the non-magnetic metal Al. A pump-probe experiment with sub-ps resolution was set up for this purpose. The time-resolved reflectivity, rotation and ellipticity of the reflected probe beam were recorded after pumping with light of variable helicity. In the Ni sample an ultrafast demagnetisation effect was observed and the variation of the rotation and ellipticity on sub-picosecond time scales was compared. Rotation and ellipticity were found to have a similar time dependence. In GaAs, optical orientation of spin was achieved and the subsequent spin relaxation was measured for different pump powers. Fitting of the optical rotation data has revealed the power dependence of the various decay constants. In the Al sample a small signal was observed that decays on ps time scales. This was attributed to a linear birefringence effect resulting from a cubic optical nonli...

  10. Discriminating Bio-aerosols from Non-Bio-aerosols in Real-Time by Pump-Probe Spectroscopy

    Science.gov (United States)

    Sousa, Gustavo; Gaulier, Geoffrey; Bonacina, Luigi; Wolf, Jean-Pierre

    2016-09-01

    The optical identification of bioaerosols in the atmosphere and its discrimination against combustion related particles is a major issue for real-time, field compatible instruments. In the present paper, we show that by embedding advanced pump-probe depletion spectroscopy schemes in a portable instrument, it is possible to discriminate amino acid containing airborne particles (bacteria, humic particles, etc.) from poly-cyclic aromatic hydrocarbon containing combustion particles (Diesel droplets, soot, vehicle exhausts) with high selectivity. Our real-time, multi-modal device provides, in addition to the pump-probe depletion information, fluorescence spectra (over 32 channels), fluorescence lifetime and Mie scattering patterns of each individually flowing particle in the probed air.

  11. Femtosecond pump probe spectroscopy for the study of energy transfer of light-harvesting complexes from extractions of spinach leaves

    Directory of Open Access Journals (Sweden)

    L. van Rensburg

    2010-01-01

    Full Text Available Measurements of ultrafast transient processes, of temporal durations in the picosecond and femtosecond regime, are made possible by femtosecond pump probe transient absorption spectroscopy. Such an ultrafast pump probe transient absorption setup has been implemented at the CSIR National Laser Centre and has been applied to investigate energy transfer processes in different parts of photosynthetic systems. In this paper we report on our first results obtained with Malachite green as a benchmark. Malachite green was chosen because the lifetime of its excited state is well known. We also present experimental results of the ultrafast energy transfer of light-harvesting complexes in samples prepared from spinach leaves. Various pump wavelengths in the range 600–680 nm were used; the probe was a white light continuum spanning 420–700 nm. The experimental setup is described in detail in this paper. Results obtained with these samples are consistent with those expected and achieved by other researchers in this field.

  12. Deducing fast electron density changes in randomly orientated uncrystallized biomolecules in a pump-probe experiment.

    Science.gov (United States)

    Pande, K; Schwander, P; Schmidt, M; Saldin, D K

    2014-07-17

    We propose a method for deducing time-resolved structural changes in uncrystallized biomolecules in solution. The method relies on measuring the angular correlations of the intensities, when averaged over a large number of diffraction patterns from randomly oriented biomolecules in solution in a liquid solvent. The experiment is somewhat like a pump-probe version of an experiment on small angle X-ray scattering, except that the data expected by the algorithm are not just the radial variation of the averaged intensities. The differences of these correlation functions as measured from a photoexcited and dark structure enable the direct calculation of the difference electron density with a knowledge of only the dark structure. We exploit a linear relation we derive between the difference in these correlation functions and the difference electron density, applicable for small structural changes.

  13. Pump-probe SAXS experiments on ultrafast demagnetization of magnetic multilayers

    Energy Technology Data Exchange (ETDEWEB)

    Pfau, B.; Schaffert, S.; Mohanty, J.; Geilhufe, J.; Flewett, S.; Eisebitt, S. [IOAP, Technische Universitaet Berlin (Germany); Buettner, F. [IOAP, Technische Universitaet Berlin (Germany); Paul Scherrer Institut, Villigen (Switzerland); Mueller, L.; Gutt, C.; Al-Shemmary, A.; Duesterer, S.; Redlin, H.; Gruebel, G. [HASYLAB, DESY, Hamburg (Germany); Vodungbo, B. [ENSTA ParisTech, Ecole Polytechnique, Palaiseau (France); Luening, J. [Universite Pierre et Marie Curie, Paris (France); Stickler, D.; Froemter, R.; Oepen, H.P. [Universitaet Hamburg (Germany); Schlotter, W.F. [LCLS, SLAC, Menlo Park (United States)

    2011-07-01

    We have investigated the ultrafast optical demagnetization of domain patterns in magnetic multilayers with perpendicular magnetic anisotropy in an infrared-pump x-ray-probe experiment. As a probe we used small angle x-ray scattering which, via x-ray magnetic circular dichroism at the Co M-edge, allows us to simultaneously obtain information on the magnitude of the local magnetization and the characteristic length scale of the magnetic domains. The free-electron laser source FLASH at Hamburg was tuned to deliver {lambda}=20.9nm x-ray pulses of approx. 25 fs duration which were synchronized to an infrared fs laser for pump-probe experiments with sub-ps time resolution. In addition to ultrafast demagnetization, we observe sub-ps structural changes of the magnetic domain configuration. Models to explain this ultrafast structural change will be discussed.

  14. Pump-Probe Spectroscopy and the Exciton Delocalization Length in Molecular Aggregates

    NARCIS (Netherlands)

    Bakalis, Lisette D.; Knoester, Jasper

    1999-01-01

    Using numerical simulations, we investigate to what extent the pump-probe spectrum can be used as a tool to determine the exciton delocalization length in disordered molecular (J) aggregates. We compare the delocalization length obtained through heuristic arguments from the spectral separation betwe

  15. A two-parameter nondiffusive heat conduction model for data analysis in pump-probe experiments

    Science.gov (United States)

    Ma, Yanbao

    2014-12-01

    Nondiffusive heat transfer has attracted intensive research interests in last 50 years because of its importance in fundamental physics and engineering applications. It has unique features that cannot be described by the Fourier law. However, current studies of nondiffusive heat transfer still focus on studying the effective thermal conductivity within the framework of the Fourier law due to a lack of a well-accepted replacement. Here, we show that nondiffusive heat conduction can be characterized by two inherent material properties: a diffusive thermal conductivity and a ballistic transport length. We also present a two-parameter heat conduction model and demonstrate its validity in different pump-probe experiments. This model not only offers new insights of nondiffusive heat conduction but also opens up new avenues for the studies of nondiffusive heat transfer outside the framework of the Fourier law.

  16. Generation of 8.5-fs pulses at 1.3 microm for ultrabroadband pump-probe spectroscopy.

    Science.gov (United States)

    Brida, Daniele; Bonora, Stefano; Manzoni, Cristian; Marangoni, Marco; Villoresi, Paolo; De Silvestri, Sandro; Cerullo, Giulio

    2009-07-20

    We report on a near-infrared non-collinear optical parametric amplifier (NOPA) based on periodically poled stoichiometric lithium tantalate. The NOPA generates muJ-energy pulses with spectrum spanning the 1-1.7 microm wavelength range, which are compressed to nearly transformlimited 8.5 fs duration by a deformable mirror. By synchronizing this source with a sub-10-fs visible NOPA, we demonstrate an unprecedented combination of temporal resolution and spectral coverage in two-colour pump-probe spectroscopy.

  17. Ultrafast time-resolved pump-probe spectroscopy of PYP by a sub-8 fs pulse laser at 400 nm.

    Science.gov (United States)

    Liu, Jun; Yabushita, Atsushi; Taniguchi, Seiji; Chosrowjan, Haik; Imamoto, Yasushi; Sueda, Keiichi; Miyanaga, Noriaki; Kobayashi, Takayoshi

    2013-05-01

    Impulsive excitation of molecular vibration is known to induce wave packets in both the ground state and excited state. Here, the ultrafast dynamics of PYP was studied by pump-probe spectroscopy using a sub-8 fs pulse laser at 400 nm. The broadband spectrum of the UV pulse allowed us to detect the pump-probe signal covering 360-440 nm. The dependence of the vibrational phase of the vibrational mode around 1155 cm(-1) on the probe photon energy was observed for the first time to our knowledge. The vibrational mode coupled to the electronic transition observed in the probe spectral ranges of 2.95-3.05 and 3.15-3.35 eV was attributed to the wave packets in the ground state and the excited state, respectively. The frequencies in the ground state and excited state were determined to be 1155 ± 1 and 1149 ± 1 cm(-1), respectively. The frequency difference is due to change after photoexcitation. This means a reduction of the bond strength associated with π-π* excitation, which is related to the molecular structure change associated with the primary isomerization process in the photocycle in PYP. Real-time vibrational modes at low frequency around 138, 179, 203, 260, and 317 cm(-1) were also observed and compared with the Raman spectrum for the assignment of the vibrational wave packet.

  18. Ultrafast pump-probe reflectance spectroscopy: Why sodium makes Cu(In,Ga)Se2 solar cells better

    KAUST Repository

    Eid, Jessica

    2015-04-14

    Although Cu(In,Ga)Se2 (CIGS) solar cells have the highest efficiency of any thin-film solar cell, especially when sodium is incorporated, the fundamental device properties of ultrafast carrier transport and recombination in such cells remain not fully understood. Here, we explore the dynamics of charge carriers in CIGS absorber layers with varying concentrations of Na by femtosecond (fs) broadband pump-probe reflectance spectroscopy with 120 fs time resolution. By analyzing the time-resolved transient spectra in a different time domain, we show that a small amount of Na integrated by NaF deposition on top of sputtered Cu(In,Ga) prior to selenization forms CIGS, which induces slower recombination of the excited carriers. Here, we provide direct evidence for the elongation of carrier lifetimes by incorporating Na into CIGS.

  19. An electro-optical timing diagnostic for pump-probe experiments at the free-electron laser in Hamburg FLASH

    Energy Technology Data Exchange (ETDEWEB)

    Azima, Armin

    2009-07-15

    Femtosecond pump-probe experiments have extensively been used to follow atomic and molecular motion in time. The very intense extreme ultraviolet XUV light of the Free electron LASer in Hamburg FLASH facility allows to investigate fundamental processes such as direct one or few photon inner shell ionizations. A supplementary Ti:Sapphire near infrared femtosecond laser system allows to perform two-color pump-probe experiments with FLASH involving intense laser fields of hugely different photon energies. Within this work a bunch arrival measurement system has been built, which assists these two-color pump-probe experiments to reduce the temporal jitter of FLASH and to increase the temporal resolution. The diagnostic is based upon an electro-optical detection scheme and measures the relative arrival time between the Ti:Sapphire femtosecond pulse and the electron bunch, which generates the self-amplified by stimulated emission SASE XUV pulse in the undulator section of FLASH. Key feature of the diagnostic is a 150 m long glass fiber pulse transport line, which inflicts non-linear dispersion. A dispersion control system to compensate for this higher order dispersion has been developed including the control and programming of a spatial light phase modulator. It was possible to transport a 90 fs FWHM short near infrared femtosecond laser pulse Fourier limited by the dispersion compensated glass fiber. The electro-optical signal induced by the FLASH electron bunch was generated, characterized and optimized. The signal features beside the designated bunch arrival timing capability the additional possibility to measure the longitudinal electron bunch density distribution of an arbitrary bunch of FLASH in a single shot with a temporal resolution of below 100 fs RMS. Timing and bunch analysis capabilities of the developed diagnostic have been cross-checked with other comparable diagnostics at FLASH like the transversal deflecting cavity structure named LOLA. Finally, the

  20. Inverting pump-probe spectroscopy for state tomography of excitonic systems.

    Science.gov (United States)

    Hoyer, Stephan; Whaley, K Birgitta

    2013-04-28

    We propose a two-step protocol for inverting ultrafast spectroscopy experiments on a molecular aggregate to extract the time-evolution of the excited state density matrix. The first step is a deconvolution of the experimental signal to determine a pump-dependent response function. The second step inverts this response function to obtain the quantum state of the system, given a model for how the system evolves following the probe interaction. We demonstrate this inversion analytically and numerically for a dimer model system, and evaluate the feasibility of scaling it to larger molecular aggregates such as photosynthetic protein-pigment complexes. Our scheme provides a direct alternative to the approach of determining all Hamiltonian parameters and then simulating excited state dynamics.

  1. Calculating time-resolved differential absorbance spectra for ultrafast pump-probe experiments with surface hopping trajectories

    Energy Technology Data Exchange (ETDEWEB)

    Petit, Andrew S.; Subotnik, Joseph E. [Department of Chemistry, University of Pennsylvania, 231 S. 34th Street, Philadelphia, Pennsylvania 19104 (United States)

    2014-10-21

    We report a surface hopping approach for modeling the full time- and frequency-resolved differential absorbance spectra (beyond the inhomogenous limit) obtained in ultrafast pump-probe experiments. In our approach, we combine dynamical information obtained from ensembles of classical trajectories propagated on the ground and on the excited potential energy surfaces to directly calculate optical response functions and hence spectral lineshapes. We demonstrate that our method is exact for the model problem of two shifted harmonic potentials with identical harmonic frequencies in the absence of electronic relaxation. We then consider a model three state system with electronic relaxation and show that our method is able to capture the effects of nonadiabatic excited state dynamics on the time-dependent differential absorbance spectra. Furthermore, by comparing our spectra against those spectra calculated with either an (1) inhomogenous expression, (2) ground-state Kubo theory, or (3) excited-state Kubo theory, we show that including dynamical information from both the ground and excited potential energy surfaces significantly improves the reliability of the semiclassical approximations. As such, our surface hopping method should find immediate use in modeling the time-dependent differential abosrbance spectra of ultrafast pump-probe experiments.

  2. In-Situ Probing Plasmonic Energy Transfer in Cu(In, Ga)Se2 Solar Cells by Ultrabroadband Femtosecond Pump-Probe Spectroscopy

    OpenAIRE

    Shih-Chen Chen; Kaung-Hsiung Wu; Jia-Xing Li; Atsushi Yabushita; Shih-Han Tang; Chih Wei Luo; Jenh-Yih Juang; Hao-Chung Kuo; Yu-Lun Chueh

    2015-01-01

    In this work, we demonstrated a viable experimental scheme for in-situ probing the effects of Au nanoparticles (NPs) incorporation on plasmonic energy transfer in Cu(In, Ga)Se2 (CIGS) solar cells by elaborately analyzing the lifetimes and zero moment for hot carrier relaxation with ultrabroadband femtosecond pump-probe spectroscopy. The signals of enhanced photobleach (PB) and waned photoinduced absorption (PIA) attributable to surface plasmon resonance (SPR) of Au NPs were in-situ probed in ...

  3. Optical pump-probe spectroscopy of photocarriers in rubrene single crystals

    Science.gov (United States)

    Tao, Shoichi; Matsuzaki, Hiroyuki; Uemura, Hirotaka; Yada, Hiroyuki; Uemura, Takafumi; Takeya, Jun; Hasegawa, Tatsuo; Okamoto, Hiroshi

    2011-02-01

    The photocarrier dynamics of rubrene, an organic molecular semiconductor, are investigated by transient absorption spectroscopy over a wide energy range (0.1-2.2 eV). By photoirradiation, we observed three kinds of absorption bands in the infrared region, which are attributable to induced absorptions of excitons, free carriers, and polarons. The results show that for photoirradiation with energies higher than ˜2.7 eV (˜0.4 eV higher than the lowest exciton energy), free carriers are photogenerated just after the photoirradiation. Some of those free carriers are stabilized as polarons and the others are relaxed to excitons. For the resonant excitation to the lowest-exciton, polarons can also be generated from the excitons. The temperature dependence of the decay dynamics of polarons reveals that polaron mobility increases with decreasing temperature, indicating bandlike transport of large polarons. Below 80 K, photocarriers are trapped by defects or impurities and their decay dynamics are dominated by the escape time from traps.

  4. Chirped seeded free-electron lasers: self-standing light sources for two-colour pump-probe experiments

    CERN Document Server

    De Ninno, Giovanni; Mahieu, Benoit

    2012-01-01

    We demonstrate the possibility to run a single-pass free-electron laser in a new dynamical regime, which can be exploited to perform two-colour pump-probe experiments in the VUV/X-ray domain, using the free-electron laser emission both as a pump and as a probe. The studied regime is induced by triggering the free-electron laser process with a powerful laser pulse, carrying a significant and adjustable frequency chirp. As a result, the emitted light is eventually split in two sub-pulses, whose spectral and temporal separations can be independently controlled. We provide a theoretical description of this phenomenon, which is found in good agreement with experiments performed on the FERMI@Elettra free-electron laser.

  5. Optical afterburner for an x-ray free electron laser as a tool for pump-probe experiments

    Directory of Open Access Journals (Sweden)

    E. L. Saldin

    2010-03-01

    Full Text Available We propose a new scheme for two-color operation of an x-ray self-amplified spontaneous emission free electron laser (SASE FEL. The scheme is based on an intrinsic feature of such a device: chaotic modulations of electron beam energy and energy spread on the scale of FEL coherence length are converted into large density modulations on the same scale with the help of a dispersion section, installed behind the x-ray undulator. Powerful radiation is then generated with the help of a dedicated radiator (like an undulator that selects a narrow spectral line, or one can simply use, for instance, broadband edge radiation. A typical radiation wavelength can be as short as a FEL coherence length, and can be redshifted by increasing the dispersion section strength. In practice it means the wavelength ranges from vacuum ultraviolet to infrared. The long-wavelength radiation pulse is naturally synchronized with the x-ray pulse and can be either directly used in pump-probe experiments or cross correlated with a high-power pulse from a conventional laser system. In this way experimenters overcome jitter problems and can perform pump-probe experiments with femtosecond resolution. Additional possibilities like on-line monitoring of x-ray pulse duration (making “optical replica” of an x-ray pulse are also discussed in the paper. The proposed scheme is very simple, cheap, and robust, and therefore can be easily realized in facilities like FLASH, European XFEL, LCLS, and SCSS.

  6. Ultrafast pump-probe spectroscopy of Zinc Phthalocynine (ZnPc) and light harvesting complex II (LHC II)

    CSIR Research Space (South Africa)

    Ombinda-Lemboumba, Saturnin

    2009-07-01

    Full Text Available The presentation discusses basic principles of pump-probe technique, possible transient absorption signals, LHC II and ZnPc, experimental setup, chirp measurement and correction methods. The results of the study, conclusion and future work are also...

  7. Time-resolved multi-mass ion imaging: Femtosecond UV-VUV pump-probe spectroscopy with the PImMS camera

    Science.gov (United States)

    Forbes, Ruaridh; Makhija, Varun; Veyrinas, Kévin; Stolow, Albert; Lee, Jason W. L.; Burt, Michael; Brouard, Mark; Vallance, Claire; Wilkinson, Iain; Lausten, Rune; Hockett, Paul

    2017-07-01

    The Pixel-Imaging Mass Spectrometry (PImMS) camera allows for 3D charged particle imaging measurements, in which the particle time-of-flight is recorded along with (x, y) position. Coupling the PImMS camera to an ultrafast pump-probe velocity-map imaging spectroscopy apparatus therefore provides a route to time-resolved multi-mass ion imaging, with both high count rates and large dynamic range, thus allowing for rapid measurements of complex photofragmentation dynamics. Furthermore, the use of vacuum ultraviolet wavelengths for the probe pulse allows for an enhanced observation window for the study of excited state molecular dynamics in small polyatomic molecules having relatively high ionization potentials. Herein, preliminary time-resolved multi-mass imaging results from C2F3I photolysis are presented. The experiments utilized femtosecond VUV and UV (160.8 nm and 267 nm) pump and probe laser pulses in order to demonstrate and explore this new time-resolved experimental ion imaging configuration. The data indicate the depth and power of this measurement modality, with a range of photofragments readily observed, and many indications of complex underlying wavepacket dynamics on the excited state(s) prepared.

  8. Low frequency dynamics of the nitrogenase MoFe protein via femtosecond pump probe spectroscopy - Observation of a candidate promoting vibration.

    Science.gov (United States)

    Maiuri, Margherita; Delfino, Ines; Cerullo, Giulio; Manzoni, Cristian; Pelmenschikov, Vladimir; Guo, Yisong; Wang, Hongxin; Gee, Leland B; Dapper, Christie H; Newton, William E; Cramer, Stephen P

    2015-12-01

    We have used femtosecond pump-probe spectroscopy (FPPS) to study the FeMo-cofactor within the nitrogenase (N2ase) MoFe protein from Azotobacter vinelandii. A sub-20-fs visible laser pulse was used to pump the sample to an excited electronic state, and a second sub-10-fs pulse was used to probe changes in transmission as a function of probe wavelength and delay time. The excited protein relaxes to the ground state with a ~1.2ps time constant. With the short laser pulse we coherently excited the vibrational modes associated with the FeMo-cofactor active site, which are then observed in the time domain. Superimposed on the relaxation dynamics, we distinguished a variety of oscillation frequencies with the strongest band peaks at ~84, 116, 189, and 226cm(-1). Comparison with data from nuclear resonance vibrational spectroscopy (NRVS) shows that the latter pair of signals comes predominantly from the FeMo-cofactor. The frequencies obtained from the FPPS experiment were interpreted with normal mode calculations using both an empirical force field (EFF) and density functional theory (DFT). The FPPS data were also compared with the first reported resonance Raman (RR) spectrum of the N2ase MoFe protein. This approach allows us to outline and assign vibrational modes having relevance to the catalytic activity of N2ase. In particular, the 226cm(-1) band is assigned as a potential 'promoting vibration' in the H-atom transfer (or proton-coupled electron transfer) processes that are an essential feature of N2ase catalysis. The results demonstrate that high-quality room-temperature solution data can be obtained on the MoFe protein by the FPPS technique and that these data provide added insight to the motions and possible operation of this protein and its catalytic prosthetic group. Copyright © 2015 Elsevier Inc. All rights reserved.

  9. Focal overlap gating in velocity map imaging to achieve high signal-to-noise ratio in photo-ion pump-probe experiments

    Science.gov (United States)

    Shivaram, Niranjan; Champenois, Elio G.; Cryan, James P.; Wright, Travis; Wingard, Taylor; Belkacem, Ali

    2016-12-01

    We demonstrate a technique in velocity map imaging (VMI) that allows spatial gating of the laser focal overlap region in time resolved pump-probe experiments. This significantly enhances signal-to-noise ratio by eliminating background signal arising outside the region of spatial overlap of pump and probe beams. This enhancement is achieved by tilting the laser beams with respect to the surface of the VMI electrodes which creates a gradient in flight time for particles born at different points along the beam. By suitably pulsing our microchannel plate detector, we can select particles born only where the laser beams overlap. This spatial gating in velocity map imaging can benefit nearly all photo-ion pump-probe VMI experiments especially when extreme-ultraviolet light or X-rays are involved which produce large background signals on their own.

  10. Focal overlap gating in velocity map imaging to achieve high signal-to-noise ratio in photo-ion pump-probe experiments

    CERN Document Server

    Shivaram, Niranjan; Cryan, James P; Wright, Travis W; Wingard, Taylor; Belkacem, Ali

    2016-01-01

    We demonstrate a new technique in velocity map imaging (VMI) that allows spatial gating of the laser focal overlap region in time resolved pump-probe experiments. This significantly enhances signal-to-noise ratio by eliminating background signal arising outside the region of spatial overlap of pump and probe beams. This enhancement is achieved by tilting the laser beams with respect to the surface of the VMI electrodes which creates a gradient in flight time for particles born at different points along the beam. By suitably pulsing our microchannel plate detector, we can select particles born only where the laser beams overlap. This spatial gating in velocity map imaging can benefit nearly all photoion pump-probe VMI experiments especially when extreme-ultraviolet (XUV) light or X-rays are involved which produce large background signals on their own.

  11. Gauge invariance in the theoretical description of time-resolved angle-resolved pump/probe photoemission spectroscopy

    Energy Technology Data Exchange (ETDEWEB)

    Freericks, J. K.; Krishnamurthy, H. R.; Sentef, M. A.; Devereaux, T. P.

    2015-10-01

    Nonequilibrium calculations in the presence of an electric field are usually performed in a gauge, and need to be transformed to reveal the gauge-invariant observables. In this work, we discuss the issue of gauge invariance in the context of time-resolved angle-resolved pump/probe photoemission. If the probe is applied while the pump is still on, one must ensure that the calculations of the observed photocurrent are gauge invariant. We also discuss the requirement of the photoemission signal to be positive and the relationship of this constraint to gauge invariance. We end by discussing some technical details related to the perturbative derivation of the photoemission spectra, which involve processes where the pump pulse photoexcites electrons due to nonequilibrium effects.

  12. Extended pump-probe Faraday rotation spectroscopy of the submicrosecond electron spin dynamics in n -type GaAs

    Science.gov (United States)

    Belykh, V. V.; Evers, E.; Yakovlev, D. R.; Fobbe, F.; Greilich, A.; Bayer, M.

    2016-12-01

    We develop an extended pump-probe Faraday rotation technique to study submicrosecond electron spin dynamics with picosecond time resolution in a wide range of magnetic fields. The electron spin dephasing time T2* and the longitudinal spin relaxation time T1, both approaching 250 ns in weak fields, are measured thereby in n -type bulk GaAs. By tailoring the pump pulse train through increasing the contained number of pulses, the buildup of resonant spin amplification is demonstrated for the electron spin polarization. The spin precession amplitude in high magnetic fields applied in the Voigt geometry shows a nonmonotonic dynamics deviating strongly from a monoexponential decay and revealing slow beatings. The beatings indicate a two spin component behavior with a g -factor difference of Δ g ˜4 ×10-4 , much smaller than the Δ g expected for free and donor-bound electrons. This g -factor variation indicates efficient, but incomplete spin exchange averaging.

  13. Near infrared ultrafast pump-probe spectroscopy with ZrF4-BaF2-LaF3-AlF3-NaF fiber supercontinuum

    Science.gov (United States)

    Fischbach, Stefan; Gorbach, Andrey V.; Di Nuzzo, Daniele; Da Como, Enrico

    2015-07-01

    We report on the performance of a setup designed for femtosecond pump-probe spectroscopy in the near infrared (NIR) spectral region. We generate a supercontinuum (SC) probe by coupling 140 fs light pulses at 1550 nm into a ZrF4-BaF2-LaF3-AlF3-NaF (ZBLAN) fiber. The combined high nonlinearity and transparency of the ZBLAN fluoride glass allows us to obtain a SC probe from 1 to 2.6 μm. The NIR pulses are used to demonstrate a proof of principle experiment probing the relaxation of photo induced excitations in a conjugated polymer:fullerene blend film. The results show the possibility to perform fibre based NIR SC femtosecond spectroscopy at >100 KHz repetition rate and using lasers with pulse energy just above 300 nJ.

  14. Multiple exciton generation in nano-crystals revisited: Consistent calculation of the yield based on pump-probe spectroscopy

    CERN Document Server

    Karki, Khadga J; Zheng, Kaibo; Zidek, Karel; Mousa, Abdelrazek; Abdellah, Mohamed A; Messing, Maria; Wallenberg, L Reine; Yartsev, Arkadi; Pullerits, Tonu

    2013-01-01

    Multiple exciton generation (MEG) is a process in which more than one exciton is generated upon the absorption of a high energy photon, typically higher than two times the band gap, in semiconductor nanocrystals. It can be observed experimentally using time resolved spectroscopy such as the transient absorption measurements. Quantification of the MEG yield is usu- ally done by assuming that the bi-exciton signal is twice the signal from a single exciton. Herein we show that this assumption is not always justified and may lead to significant errors in the estimated MEG yields. We develop a methodology to determine proper scaling factors to the signals from the transient absorption experiments. Using the methodology we find modest MEG yields in lead chalcogenide nanocrystals including the nanorods.

  15. Ultrafast pump-probe spectroscopy studies of CeO2 thin film deposited on Ni-W substrate by RF magnetron sputtering

    Science.gov (United States)

    Singh, Preetam; Srivatsa, K. M. K.; Jewariya, Mukesh

    2016-08-01

    This study presents the first investigation of rapid dynamical processes that occur in pure CeO2 thin film, using ultra fast pump-probe spectroscopy at room temperature. For this purpose we have used a single (200) oriented CeO2 film deposited on biaxially textured Ni-W substrate by RF magnetron sputtering technique. The ultrafast transient spectra show initial sharp rise transition followed by an exponential photon decay. This rise time is about 10 ps irrespective of the probe wavelengths range 500-800 nm. The initial decay constant (τ) at 500 nm probe wavelength is found to be 171 ps, while at 800 nm probe wavelength it is 107.5 ps. The ultrafast absorption spectra show two absorption peaks at 745 and 800 nm, and are attributed to the electronic transitions from 2F7/2-2F5/2 and 1S0-1F3 respectively. The relatively high intensity absorption peak at 745 nm indicates dominant f-f electronic transition. Further, the absorption peak at 745 nm splits into two distinct peaks with respect to delay time, and is attributed to the charge transfer in between Ce4+ and Ce3+ ions. These results indicate that CeO2 itself is a potential candidate and can be used for optical applications.

  16. Ultrashort laser ablation of metals: pump probe experiments, the role of ballistic electrons and the two-temperature model

    Science.gov (United States)

    Schmidt, V.; Husinsky, W.; Betz, G.

    2002-09-01

    The dynamics of laser ablation from metallic surfaces (Ag, Al, Fe and Ni) induced by the combined effect of two 30 fs sub-threshold laser pulses has been examined. In a pump-probe setup the yield of the emitted secondary ions and neutrals has been determined as a function of the delay between the two laser pulses. The instantaneous generation of highly excited (ballistic) electrons by the laser pulse and the thermal properties of the metal, which have been modified to be valid into the regime of high electron temperatures have been found to be determining factors for the ablation process. Unexpectedly, two distinct maxima for particle emission have been observed as a function of the time separation of the pump and the probe pulse. The energy relaxation is discussed within the frame of the two-temperature model (TTM) and it is shown that the measured behavior (in the time domain) of ablated particles can only be explained by taking into account a general expression for the thermal conductivity, valid for a wide range of electron temperatures and in addition a substantial role of hot, ballistic electrons.

  17. Pump-probe spectroscopy of J-aggregates : a way to measure intermolecular correlations in the frequency disorder

    NARCIS (Netherlands)

    Knoester, Jasper

    1994-01-01

    We show that two-color pump—probe experiments yield an ideal opportunity to obtain independent information on the size and the degree of intermolecular correlation of the frequency disorder in molecular J-aggregates. Our general approach is based on the motional narrowing treatment of the disorder a

  18. Ultrafast pump-probe spectroscopy in the UV-blue range with an extremely broad probe spectrum for the carrier relaxation study in an InGaN thin film with indium-rich nano-clusters.

    Science.gov (United States)

    Wang, Hsiang-Chen; Lu, Yen-Cheng; Chen, Cheng-Yen; Yang, C C

    2007-03-19

    We implement an extremely broad second-harmonic spectrum of about 90 nm in width based on a 7-fs mode-locked Ti:sapphire laser. This broadband second-harmonic signal is used as the probe in a non-degenerate pump-probe experiment to investigate the ultrafast carrier dynamics in wide band-gap semiconductors. To properly calibrate the pump-probe data, the time delays between the pump of a particular wavelength and the probes of various spectral portions are determined through the interferometry measurement and the dispersion calculation. To demonstrate the pump-probe experiment operation, we measure the carrier relaxation process from the excitation levels down to the free-carrier and the localized states in an InGaN thin-film sample, in which indium-rich nano-clusters exist to form the localized states. From the time-resolved differential transmission profiles at various spectral positions of an infinitesimal spectral width and the temporal evolution of probe spectrum, one can observe the following relaxation process: First, once carriers are excited, only a small portion of carriers relaxes into the free-carrier and localized states independently within 1 ps. Then, the major part of carriers starts to relax into the two groups of states not until several ps after excitation. Such a relaxation process does not seem to be cascading, i.e., relaxation into the localized states through the free-carrier states.

  19. Scheme for femtosecond-resolution pump-probe experiments at XFELs with two-color ten GW-level X-ray pulses

    CERN Document Server

    Geloni, Gianluca; Saldin, Evgeni

    2010-01-01

    This paper describes a scheme for pump-probe experiments that can be performed at LCLS and at the European XFEL and determines what additional hardware development will be required to bring these experiments to fruition. It is proposed to derive both pump and probe pulses from the same electron bunch, but from different parts of the tunable-gap baseline undulator. This eliminates the need for synchronization and cancels jitter problems. The method has the further advantage to make a wide frequency range accessible at high peak-power and high repetition-rate. An important feature of the proposed scheme is that the hardware requirement is minimal. Our technique is based in essence on the "fresh" bunch technique. For its implementation it is sufficient to substitute a single undulator module with short magnetic delay line, i.e. a weak magnetic chicane, which delays the electron bunch with respect to the SASE pulse of half of the bunch length in the linear stage of amplification. This installation does not pertur...

  20. On the interpretation of negative birefringence observed in strong-field optical pump-probe experiments: high-order Kerr and plasma grating effects

    CERN Document Server

    Karras, G; Houzet, J; Hertz, E; Billard, F; Lavorel, B; Faucher, O

    2013-01-01

    The analysis of negative birefringence optically induced in major air components (Loriot et al., [1, 2]) is revisited in light of the recently reported plasma grating-induced phase-shift effect predicted for strong field pump-probe experiments (Wahlstrand and Milchberg, [3]). The nonlinear birefrin- gence induced by a short and intense laser pulse in argon is measured by femtosecond time-resolved polarimetry. The experiments are performed with degenerate colors, where the pump and probe beam share the same spectrum, or with two different colors and non-overlapping spectra. The in- terpretation of the experimental results is substantiated using a numerical 3D+1 model accounting for nonlinear propagation effects, cross-beam geometry of the interacting laser pulses, and detec- tion technique. The model also includes the ionization rate of argon and high-order Kerr indices introduced by Loriot et al. enabling to assess the contribution of both terms to the observed effect. The results show that the ionization-ind...

  1. A multi-MHz single-shot data acquisition scheme with high dynamic range: pump-probe X-ray experiments at synchrotrons.

    Science.gov (United States)

    Britz, Alexander; Assefa, Tadesse A; Galler, Andreas; Gawelda, Wojciech; Diez, Michael; Zalden, Peter; Khakhulin, Dmitry; Fernandes, Bruno; Gessler, Patrick; Sotoudi Namin, Hamed; Beckmann, Andreas; Harder, Manuel; Yavaş, Hasan; Bressler, Christian

    2016-11-01

    The technical implementation of a multi-MHz data acquisition scheme for laser-X-ray pump-probe experiments with pulse limited temporal resolution (100 ps) is presented. Such techniques are very attractive to benefit from the high-repetition rates of X-ray pulses delivered from advanced synchrotron radiation sources. Exploiting a synchronized 3.9 MHz laser excitation source, experiments in 60-bunch mode (7.8 MHz) at beamline P01 of the PETRA III storage ring are performed. Hereby molecular systems in liquid solutions are excited by the pulsed laser source and the total X-ray fluorescence yield (TFY) from the sample is recorded using silicon avalanche photodiode detectors (APDs). The subsequent digitizer card samples the APD signal traces in 0.5 ns steps with 12-bit resolution. These traces are then processed to deliver an integrated value for each recorded single X-ray pulse intensity and sorted into bins according to whether the laser excited the sample or not. For each subgroup the recorded single-shot values are averaged over ∼10(7) pulses to deliver a mean TFY value with its standard error for each data point, e.g. at a given X-ray probe energy. The sensitivity reaches down to the shot-noise limit, and signal-to-noise ratios approaching 1000 are achievable in only a few seconds collection time per data point. The dynamic range covers 100 photons pulse(-1) and is only technically limited by the utilized APD.

  2. Sub-Picosecond Tunable Hard X-Ray Undulator Source for Laser/X-Ray Pump-Probe Experiments

    Science.gov (United States)

    Ingold, G.; Beaud, P.; Johnson, S.; Streun, A.; Schmidt, T.; Abela, R.; Al-Adwan, A.; Abramsohn, D.; Böge, M.; Grolimund, D.; Keller, A.; Krasniqi, F.; Rivkin, L.; Rohrer, M.; Schilcher, T.; Schmidt, T.; Schlott, V.; Schulz, L.; van der Veen, F.; Zimoch, D.

    2007-01-01

    The FEMTO source under construction at the μXAS beamline is designed to enable tunable time-resolved laser/x-ray absorption and diffraction experiments in photochemistry and condensed matter with ps- and sub-ps resolution. The design takes advantage of (1) the highly stable operation of the SLS storage ring, (2) the reliable high harmonic operation of small gap, short period undulators to generate hard x-rays with energy 3-18 keV at 2.4 GeV beam energy, and (3) the progress in high power, high repetition rate fs solid-state laser technology to employ laser/e-beam `slicing' to reach a time resolution of ultimately 100 fs. The source will profit from the inherently synchronized pump (laser I: 100 fs, 2 mJ, 1 kHz) and probe (sliced X-rays, laser II: 50 fs, 5 mJ, 1 kHz) pulses, and from the excellent stability of the SLS storage ring which is operated in top-up mode and controlled by a fast orbit feedback (FOFB). Coherent radiation emitted at THz frequencies by the sliced 100 fs electron bunches will be monitored as on-line cross-correlation signal to keep the laser-electron beam interaction at optimum. The source is designed to provide at 8 keV (100 fs) a monochromized flux of 104 ph/s/0.01% bw (Si crystal monochromator) and 106 ph/s/1.5% bw (multilayer monochromator) at the sample. It is operated in parasitic mode using a hybrid bunch filling pattern. Because of the low intensity measurements are carried out repetitively over many shots using refreshing samples and gated detectors. `Diffraction gating' experiments will be used to characterize the sub-ps X-ray pulses.

  3. Ultrafast pump-probe dynamics of iron oxide based earth pigments for applications to ancient pottery manufacture

    Science.gov (United States)

    Villafana, Tana E.; Brown, William; Warren, Warren S.; Fischer, Martin

    2015-06-01

    We demonstrate that ultrafast pump-probe microscopy provides unique dynamics for natural iron oxide and iron hydroxide earth pigments, despite their chemical similarity. First, we conducted a pump-probe spectroscopy study on heat-treated hematite (the pure red iron oxide mineral) and found the pump-probe dynamics to be temperature dependent. Second, we investigated pottery fired under known conditions and observed firing dependent pump-probe dynamics. Finally, we imaged a New World potshard from the North Carolina Museum of Art. Our results indicate that pump-probe microscopy could be a useful tool in elucidating pottery manufacture.

  4. Ultrafast relaxation kinetics of the dark S{sub 1} state in all-trans-{beta}-carotene explored by one- and two-photon pump-probe spectroscopy

    Energy Technology Data Exchange (ETDEWEB)

    Kosumi, Daisuke, E-mail: kosumi@sci.osaka-cu.ac.jp [Department of Physics, Graduate School of Science, Tohoku University, 6-3 Aramaki-Aza-Aoba, Sendai 980-8578 (Japan); Abe, Kenta; Karasawa, Hiroshi [Department of Physics, Graduate School of Science, Tohoku University, 6-3 Aramaki-Aza-Aoba, Sendai 980-8578 (Japan); Fujiwara, Masazumi [Department of Physics, Graduate School of Science, Osaka City University, 3-3-138 Sugimoto, Sumiyoshi-ku, Osaka 558-8585 (Japan); Cogdell, Richard J. [Glasgow Biomedical Research Center, University of Glasgow, 120 University Place, Glasgow G12 8TA, Scotland (United Kingdom); Hashimoto, Hideki [Department of Physics, Graduate School of Science, Osaka City University, 3-3-138 Sugimoto, Sumiyoshi-ku, Osaka 558-8585 (Japan); JST/CREST, 4-1-8 Hon-chou, Kawaguchi, Saitama 332-0012 (Japan); Yoshizawa, Masayuki [Department of Physics, Graduate School of Science, Tohoku University, 6-3 Aramaki-Aza-Aoba, Sendai 980-8578 (Japan); JST/CREST, 4-1-8 Hon-chou, Kawaguchi, Saitama 332-0012 (Japan)

    2010-07-19

    Femtosecond one- and two-photon pump-probe dispersive spectroscopic measurements have been applied to the investigation of the vibrational relaxation kinetics of the dark S{sub 1} (2{sup 1}A{sub g}{sup -}) state in {beta}-carotene, combining a higher sensitive detection system with tunable visible and infrared excitation pulses. The two-photon excitation measurements enable the preferential detection of the dark S{sub 1} state. The tunable infrared excitation pulses allowed selective excitation to a different vibrational level of S{sub 1}. The S{sub 1} dynamics at early delay times depend strongly on excitation energy. A dependence of the initial S{sub 1} dynamics on excitation energy is discussed in term of the vibrational relaxation of S{sub 1}.

  5. Ultrafast and nanoscale plasmonic phenomena in exfoliated graphene revealed by infrared pump-probe nanoscopy.

    Science.gov (United States)

    Wagner, Martin; Fei, Zhe; McLeod, Alexander S; Rodin, Aleksandr S; Bao, Wenzhong; Iwinski, Eric G; Zhao, Zeng; Goldflam, Michael; Liu, Mengkun; Dominguez, Gerardo; Thiemens, Mark; Fogler, Michael M; Castro Neto, Antonio H; Lau, Chun Ning; Amarie, Sergiu; Keilmann, Fritz; Basov, D N

    2014-02-12

    Pump-probe spectroscopy is central for exploring ultrafast dynamics of fundamental excitations, collective modes, and energy transfer processes. Typically carried out using conventional diffraction-limited optics, pump-probe experiments inherently average over local chemical, compositional, and electronic inhomogeneities. Here, we circumvent this deficiency and introduce pump-probe infrared spectroscopy with ∼ 20 nm spatial resolution, far below the diffraction limit, which is accomplished using a scattering scanning near-field optical microscope (s-SNOM). This technique allows us to investigate exfoliated graphene single-layers on SiO2 at technologically significant mid-infrared (MIR) frequencies where the local optical conductivity becomes experimentally accessible through the excitation of surface plasmons via the s-SNOM tip. Optical pumping at near-infrared (NIR) frequencies prompts distinct changes in the plasmonic behavior on 200 fs time scales. The origin of the pump-induced, enhanced plasmonic response is identified as an increase in the effective electron temperature up to several thousand Kelvin, as deduced directly from the Drude weight associated with the plasmonic resonances.

  6. Comparison of vibrational dynamics between non-ionic and ionic vibrational probes in water: Experimental study with two-dimensional infrared and infrared pump-probe spectroscopies

    Science.gov (United States)

    Okuda, Masaki; Ohta, Kaoru; Tominaga, Keisuke

    2016-09-01

    Dynamics of the hydration structure around small vibrational probes have been extensively studied over the past few decades. However, we need to gain insight into how vibrational dynamics is affected by the molecular nature of the probe molecules in water. In this study, 2-nitro-5-thiocyanate benzoic acid (NTBA), which has an SCN group attached to an aromatic ring, and thiocyanate ion (SCN-) were used to investigate the vibrational dynamics of two vibrational probes, including vibrational frequency fluctuations and rotational relaxation. By performing two-dimensional infrared spectroscopic measurements, the vibrational frequency fluctuations of the SCN anti-stretching modes of these solutes were compared. The frequency-frequency time correlation function (FFTCF) of these solutes can be modeled by a delta function plus an exponential function and a constant. The FFTCF of NTBA was characterized by a time constant of 1.1 ps, which is similar to that of SCN-. Moreover, no component was longer than this constant. Consequently, the loss of the correlation in frequency fluctuations of the SCN anti-stretching mode of NTBA may be controlled by a mechanism similar to that of the ionic probe, which involves the hydrogen bonding dynamics of water. Polarization-controlled IR pump-probe measurements were performed for these vibrational probes in water to study the vibrational energy relaxation (VER) and reorientational relaxation processes. The VER rate of NTBA is much smaller than that of SCN-, which indicates that the intramolecular relaxation process is significant for VER of NTBA. Based on the rotational relaxation time of NTBA being shorter than that of SCN-, the internal rotational motion of the SCN group around the Cphenyl-S bond axis, where Cphenyl denotes a carbon atom of the aromatic ring to which the SCN group is attached, may play an important role in the anisotropic decay of NTBA in H2O.

  7. Dynamics of a Room Temperature Ionic Liquid in Supported Ionic Liquid Membranes vs the Bulk Liquid: 2D IR and Polarized IR Pump-Probe Experiments.

    Science.gov (United States)

    Shin, Jae Yoon; Yamada, Steven A; Fayer, Michael D

    2017-01-11

    Supported ionic liquid membranes (SILMs) are membranes that have ionic liquids impregnated in their pores. SILMs have been proposed for advanced carbon capture materials. Two-dimensional infrared (2D IR) and polarization selective IR pump-probe (PSPP) techniques were used to investigate the dynamics of reorientation and spectral diffusion of the linear triatomic anion, SeCN(-), in poly(ether sulfone) (PES) membranes and room-temperature ionic liquid (RTIL), 1-ethyl-3-methylimidazolium bis(trifluoromethylsulfonyl)imide (EmimNTf2). The dynamics in the bulk EmimNTf2 were compared to its dynamics in the SILM samples. Two PES membranes, PES200 and PES30, have pores with average sizes, ∼300 nm and ∼100 nm, respectively. Despite the relatively large pore sizes, the measurements reveal that the reorientation of SeCN(-) and the RTIL structural fluctuations are substantially slower in the SILMs than in the bulk liquid. The complete orientational randomization, slows from 136 ps in the bulk to 513 ps in the PES30. 2D IR measurements yield three time scales for structural spectral diffusion (SSD), that is, the time evolution of the liquid structure. The slowest decay constant increases from 140 ps in the bulk to 504 ps in the PES200 and increases further to 1660 ps in the PES30. The results suggest that changes at the interface propagate out and influence the RTIL structural dynamics even more than a hundred nanometers from the polymer surface. The differences between the IL dynamics in the bulk and in the membranes suggest that studies of bulk RTIL properties may be poor guides to their use in SILMs in carbon capture applications.

  8. Development and Implementation of an Ultrafast Vacuum-UV (8eV) Light Source for use in UV-VUV Pump Probe Experiments of Neutral Excited State Dynamics

    Science.gov (United States)

    Liu, Yusong; Horton, Spencer; Matsika, Spiridoula; Weinacht, Thomas

    2016-05-01

    Probing neutral excited state dynamics in polyatomic molecules with ultrafast laser systems enables us to study phenomena such as internal conversion, isomerization, intersystem crossing, and dissociation. Using the third harmonic (260 nm) and the fifth harmonic (156 nm) of our laser system we have developed an apparatus to perform pump-probe experiments for the study neutral excited state dynamics in various polyatomic molecules. The fifth harmonic of our laser system is generated through the four-wave-mixing process of k5 ω = 2k3 ω -kω performed with a non-collinear geometry in an argon gas cell. In several polyatomic molecular systems of interest a photon with 8 eV of energy gives us the unique ability to ionize from essentially anywhere along the excited state potential, but does not produce any ionization yield from the ground state. This enables us to measure excited state lifetimes without the photon energy becoming too low to ionize while the nuclear wave-packet is traveling on the excited state potential. We also have the advantage of working in the perturbative weak-field ionization regime. These experiments can also be directly compare to strong-field ionization experiments conducted with a UV-pump and an IR-probe conducted on the same molecules.

  9. Theory of Floquet band formation and local pseudospin textures in pump-probe photoemission of graphene.

    Science.gov (United States)

    Sentef, M A; Claassen, M; Kemper, A F; Moritz, B; Oka, T; Freericks, J K; Devereaux, T P

    2015-05-11

    Ultrafast materials science promises optical control of physical properties of solids. Continuous-wave circularly polarized laser driving was predicted to induce a light-matter coupled state with an energy gap and a quantum Hall effect, coined Floquet topological insulator. Whereas the envisioned Floquet topological insulator requires high-frequency pumping to obtain well-separated Floquet bands, a follow-up question regards the creation of Floquet-like states in graphene with realistic low-frequency laser pulses. Here we predict that short optical pulses attainable in experiments can lead to local spectral gaps and novel pseudospin textures in graphene. Pump-probe photoemission spectroscopy can track these states by measuring sizeable energy gaps and Floquet band formation on femtosecond time scales. Analysing band crossings and pseudospin textures near the Dirac points, we identify new states with optically induced nontrivial changes of sublattice mixing that leads to Berry curvature corrections of electrical transport and magnetization.

  10. Broadband sensitive pump-probe setup for ultrafast optical switching of photonic nanostructures and semiconductors

    NARCIS (Netherlands)

    Euser, T.G.; Harding, P.J.; Vos, Willem L.

    2009-01-01

    We describe an ultrafast time resolved pump-probe spectroscopy setup aimed at studying the switching of nanophotonic structures. Both femtosecond pump and probe pulses can be independently tuned over broad frequency range between 3850 and 21 050 cm−1. A broad pump scan range allows a large optical

  11. Invited Review Article: Pump-probe microscopy

    Energy Technology Data Exchange (ETDEWEB)

    Fischer, Martin C., E-mail: Martin.Fischer@duke.edu; Wilson, Jesse W.; Robles, Francisco E. [Department of Chemistry, Duke University, Durham, North Carolina 27708 (United States); Warren, Warren S. [Departments of Chemistry, Biomedical Engineering, Physics, and Radiology, Duke University, Durham, North Carolina 27708 (United States)

    2016-03-15

    Multiphoton microscopy has rapidly gained popularity in biomedical imaging and materials science because of its ability to provide three-dimensional images at high spatial and temporal resolution even in optically scattering environments. Currently the majority of commercial and home-built devices are based on two-photon fluorescence and harmonic generation contrast. These two contrast mechanisms are relatively easy to measure but can access only a limited range of endogenous targets. Recent developments in fast laser pulse generation, pulse shaping, and detection technology have made accessible a wide range of optical contrasts that utilize multiple pulses of different colors. Molecular excitation with multiple pulses offers a large number of adjustable parameters. For example, in two-pulse pump-probe microscopy, one can vary the wavelength of each excitation pulse, the detection wavelength, the timing between the excitation pulses, and the detection gating window after excitation. Such a large parameter space can provide much greater molecular specificity than existing single-color techniques and allow for structural and functional imaging without the need for exogenous dyes and labels, which might interfere with the system under study. In this review, we provide a tutorial overview, covering principles of pump-probe microscopy and experimental setup, challenges associated with signal detection and data processing, and an overview of applications.

  12. Pump-probe imaging of historical pigments used in paintings.

    Science.gov (United States)

    Samineni, Prathyush; deCruz, Adele; Villafaña, Tana E; Warren, Warren S; Fischer, Martin C

    2012-04-15

    A recently developed nonlinear optical pump-probe microscopy technique uses modulation transfer to sensitively extract excited-state dynamics of endogenous biological pigments, such as eumelanin and pheomelanin. In this work, we use this method to image and characterize several inorganic and organic pigments used in historical art. We show substantial differences in the near-IR pump-probe signatures from nominally similar pigments and suggest extensions to art restoration.

  13. Towards jitter-free pump-probe measurements at seeded free electron laser facilities.

    Science.gov (United States)

    Danailov, Miltcho B; Bencivenga, Filippo; Capotondi, Flavio; Casolari, Francesco; Cinquegrana, Paolo; Demidovich, Alexander; Giangrisostomi, Erika; Kiskinova, Maya P; Kurdi, Gabor; Manfredda, Michele; Masciovecchio, Claudio; Mincigrucci, Riccardo; Nikolov, Ivaylo P; Pedersoli, Emanuele; Principi, Emiliano; Sigalotti, Paolo

    2014-06-02

    X-ray free electron lasers (FEL) coupled with optical lasers have opened unprecedented opportunities for studying ultrafast dynamics in matter. The major challenge in pump-probe experiments using FEL and optical lasers is synchronizing the arrival time of the two pulses. Here we report a technique that benefits from the seeded-FEL scheme and uses the optical seed laser for nearly jitter-free pump-probe experiments. Timing jitter as small as 6 fs has been achieved and confirmed by measurements of FEL-induced transient reflectivity changes of Si3N4 using both collinear and non-collinear geometries. Planned improvements of the experimental set-up are expected to further reduce the timing jitter between the two pulses down to fs level.

  14. Alignment, vibronic level splitting, and coherent coupling effects on the pump-probe polarization anisotropy.

    Science.gov (United States)

    Smith, Eric R; Jonas, David M

    2011-04-28

    The pump-probe polarization anisotropy is computed for molecules with a nondegenerate ground state, two degenerate or nearly degenerate excited states with perpendicular transition dipoles, and no resonant excited-state absorption. Including finite pulse effects, the initial polarization anisotropy at zero pump-probe delay is predicted to be r(0) = 3/10 with coherent excitation. During pulse overlap, it is shown that the four-wave mixing classification of signal pathways as ground or excited state is not useful for pump-probe signals. Therefore, a reclassification useful for pump-probe experiments is proposed, and the coherent anisotropy is discussed in terms of a more general transition dipole and molecular axis alignment instead of experiment-dependent ground- versus excited-state pathways. Although coherent excitation enhances alignment of the transition dipole, the molecular axes are less aligned than for a single dipole transition, lowering the initial anisotropy. As the splitting between excited states increases beyond the laser bandwidth and absorption line width, the initial anisotropy increases from 3/10 to 4/10. Asymmetric vibrational coordinates that lift the degeneracy control the electronic energy gap and off-diagonal coupling between electronic states. These vibrations dephase coherence and equilibrate the populations of the (nearly) degenerate states, causing the anisotropy to decay (possibly with oscillations) to 1/10. Small amounts of asymmetric inhomogeneity (2 cm(-1)) cause rapid (130 fs) suppression of both vibrational and electronic anisotropy beats on the excited state, but not vibrational beats on the ground electronic state. Recent measurements of conical intersection dynamics in a silicon napthalocyanine revealed anisotropic quantum beats that had to be assigned to asymmetric vibrations on the ground electronic state only [Farrow, D. A.; J. Chem. Phys. 2008, 128, 144510]. Small environmental asymmetries likely explain the observed absence

  15. Excited state absorption spectroscopy of ZBLAN:Er3+ glass - Experiment and simulation

    Science.gov (United States)

    Piatkowski, D.; Wisniewski, K.; Rozanski, M.; Koepke, Cz.

    2009-08-01

    We present the excited state absorption (ESA) spectroscopy of ZBLAN:Er3+ glass. The experimental spectra were measured in broad spectral range (500-1800 nm) by the CW pump-probe technique. Judd-Ofelt (JO) approach was employed to interpret the results and to simulate the ESA spectra which were successfully confronted with the experiment. We also propose a systematic approach for prediction of various types of up-conversion mechanisms such as ESA up-conversion and photon avalanche (PA). Careful investigations were made to indicate possible up-conversion excitation channels in a wide spectral range, from 400 nm up to 2 μm.

  16. Photoacoustic pump-probe tomography of fluorophores in vivo using interleaved image acquisition for motion suppression

    Science.gov (United States)

    Märk, Julia; Wagener, Asja; Zhang, Edward; Laufer, Jan

    2017-01-01

    In fluorophores, the excited state lifetime can be modulated using pump-probe excitation. By generating photoacoustic (PA) signals using simultaneous and time-delayed pump and probe excitation pulses at fluences below the maximum permissible exposure, a modulation of the signal amplitude is observed in fluorophores but not in endogenous chromophores. This provides a highly specific contrast mechanism that can be used to recover the location of the fluorophore using difference imaging. The practical challenges in applying this method to in vivo PA tomography include the typically low concentrations of fluorescent contrast agents, and tissue motion. The former results in smaller PA signal amplitudes compared to those measured in blood, while the latter gives rise to difference image artefacts that compromise the unambiguous and potentially noise-limited detection of fluorescent contrast agents. To address this limitation, a method based on interleaved pump-probe image acquisition was developed. It relies on fast switching between simultaneous and time-delayed pump-probe excitation to acquire PA difference signals in quick succession, and to minimise the effects of tissue motion. The feasibility of this method is demonstrated in tissue phantoms and in initial experiments in vivo. PMID:28091571

  17. Photoacoustic pump-probe tomography of fluorophores in vivo using interleaved image acquisition for motion suppression

    Science.gov (United States)

    Märk, Julia; Wagener, Asja; Zhang, Edward; Laufer, Jan

    2017-01-01

    In fluorophores, the excited state lifetime can be modulated using pump-probe excitation. By generating photoacoustic (PA) signals using simultaneous and time-delayed pump and probe excitation pulses at fluences below the maximum permissible exposure, a modulation of the signal amplitude is observed in fluorophores but not in endogenous chromophores. This provides a highly specific contrast mechanism that can be used to recover the location of the fluorophore using difference imaging. The practical challenges in applying this method to in vivo PA tomography include the typically low concentrations of fluorescent contrast agents, and tissue motion. The former results in smaller PA signal amplitudes compared to those measured in blood, while the latter gives rise to difference image artefacts that compromise the unambiguous and potentially noise-limited detection of fluorescent contrast agents. To address this limitation, a method based on interleaved pump-probe image acquisition was developed. It relies on fast switching between simultaneous and time-delayed pump-probe excitation to acquire PA difference signals in quick succession, and to minimise the effects of tissue motion. The feasibility of this method is demonstrated in tissue phantoms and in initial experiments in vivo.

  18. Development of a Pump-Probe System using a Non-Coated ZnSe Beam Splitter Cube for an MIR-FEL

    CERN Document Server

    Heya, Manabu; Horiike, Hiroshi; Ishii, Katsonuri; Suzuki, Sachiko

    2004-01-01

    A pump-probe technique is essential for a proper understanding of laser interaction with tissue and material. Our pump-probe system divides the incident mid-infrared Free Electron Laser (MIR-FEL) into two beams with equal intensity, and crosses simultaneously the two incoming beams at the same position. One is for a pump beam, another is for a probe beam. Time-resolved absorption spectroscopy involving this technique gives us information on the vibrational dynamics of molecules. We have developed this system for an MIR-FEL using a non-coating ZnSe beam splitter cube. The beam splitter cube is composed of two ZnSe prisms in the shape like a trapezoid. The two pulses with equal intensity are generated due to Fresnel reflection and transmission at the boundary between two prisms, then are reflected due to total reflection at other side boundaries between each prism and air, and illuminate simultaneously the same spot. We have conducted a proof-of-concept of experiment of this system using an MIR-FEL. We showed t...

  19. Antihydrogen Experiment Gravity Interferometry Spectroscopy

    CERN Multimedia

    Tietje, I C; Trezzi, D; Dassa, L; Rienacker, B; Khalidova, O; Ferrari, G; Krasnicky, D; Perini, D; Cerchiari, G; Belov, A; Boscolo, I; Sacerdoti, M G; Ferragut, R O; Nedelec, P; Testera, G; Hinterberger, A; Al-qaradawi, I; Malbrunot, C L S; Brusa, R S; Prelz, F; Manuzio, G; Riccardi, C; Fontana, A; Genova, P; Haider, S; Haug, F; Turbabin, A; Castelli, F; Lagomarsino, V E; Doser, M; Penasa, L; Gninenko, S; Cataneo, F; Zenoni, A; Cabaret, L; Comparat, D P; Zmeskal, J; Scampoli, P; Nesteruk, K P; Dudarev, A; Kellerbauer, A G; Mariazzi, S; Fesel, J V; Carraro, C; Zavatarelli, S M

    The AEGIS experiment (Antihydrogen Experiment: Gravity, Interferometry, Spectroscopy) has the aim of carrying out the first measurement of the gravitational interaction of antimatter to a precision of 1%, by applying techniques from atomic physics, laser spectroscopy and interferometry to a beam of antihydrogen atoms. A further goal of the experiment is to carry out spectroscopy of the antihydrogen atoms in flight.

  20. Coherence specific signal detection via chiral pump-probe spectroscopy

    CERN Document Server

    Holdaway, David I H; Olaya-Castro, Alexandra

    2016-01-01

    We examine the transient circular dichroism as a technique to investigate exciton coherence signatures in structured vibrational environments. We consider multiple beam configurations, in terms of both direction and polarization, which provide independent contributions to the signal. We develop a formalism in terms of chiral doorway and windows contributions. Using this formalism we show that signals which beat during the population time can be isolated by comparing signals from configurations in which the angle between the pump and probe pulses is varied. The chiral doorway signal has only a weak ground state contribution, which can generally be neglected if a short pump pulse is used, allowing for unambiguous identification of quantum superpositions of exciton states.

  1. Broadband sensitive pump-probe setup for ultrafast optical switching of photonic nanostructures and semiconductors.

    Science.gov (United States)

    Euser, Tijmen G; Harding, Philip J; Vos, Willem L

    2009-07-01

    We describe an ultrafast time resolved pump-probe spectroscopy setup aimed at studying the switching of nanophotonic structures. Both femtosecond pump and probe pulses can be independently tuned over broad frequency range between 3850 and 21,050 cm(-1). A broad pump scan range allows a large optical penetration depth, while a broad probe scan range is crucial to study strongly photonic crystals. A new data acquisition method allows for sensitive pump-probe measurements, and corrects for fluctuations in probe intensity and pump stray light. We observe a tenfold improvement of the precision of the setup compared to laser fluctuations, allowing a measurement accuracy of better than DeltaR=0.07% in a 1 s measurement time. Demonstrations of the improved technique are presented for a bulk Si wafer, a three-dimensional Si inverse opal photonic bandgap crystal, and z-scan measurements of the two-photon absorption coefficient of Si, GaAs, and the three-photon absorption coefficient of GaP in the infrared wavelength range.

  2. Pump-probe microscopy of respiratory chain pigments: towards non-fluorescent label-free metabolic imaging

    Science.gov (United States)

    Domingue, Scott R.; Chicco, Adam J.; Bartels, Randy A.; Wilson, Jesse W.

    2017-02-01

    Current label-free metabolic microscopy techniques are limited to obtaining contrast from fluorescent molecules NAD(P)H and FAD+, and are unable to determine redox state along the mitochondrial respiratory chain itself. The respiratory chain electron carriers do not fluoresce, but some are heme proteins that have redox-dependent absorption spectra. The most prominent of these, cytochrome c, has been extensively characterized by transient absorption spectroscopy, which suggests that pump-probe measurements in the vicinity of 450 - 600 nm can provide strong contrast between its redox states. Motivated by the success of pump-probe microscopy targeting another heme protein, hemoglobin, we seek to extend the technique to the cytochromes, with the ultimate goal of dissecting respiratory chain function of individual cells in live tissue. To that end, we have developed a new optical system producing ultrafast, visible, independently-tunable pulse pairs via sum-frequency generation of nonlinearly broadened pulses in periodically-poled lithium niobate. The system is pumped by a homebuilt fiber-based oscillator/amplifier emitting 1060 nm pulses at 1.3 W (63 MHz repetition rate), and produces tunable pulses in the vicinity of 488 and 532 nm. Pump-probe spectroscopy of cytochrome c with this source reveals differences in excited-state absorption relaxation times between redox states. Though redox contrast is weak with this setup, we argue that this can be improved with a resonant galvo-scanning microscope. Moreover, pump-probe images were acquired of brown adipose tissue (which contains dense mitochondria), demonstrating label-free contrast from excited-state absorption in respiratory chain hemes.

  3. Pump-probe laser development for the European X-ray Free-Electron Laser facility

    Science.gov (United States)

    Lederer, Max J.; Pergament, Mikhail; Kellert, Martin; Mendez, Cruz

    2012-10-01

    The successful implementation of superconducting LINAC technology at the European XFEL will boost the time averaged X-RAY power density substantially above current values. In fact, the XFEL will operate at repetition rates of up to 4.5MHz. However, this high pulse rate occurs only during 600μs long bursts of 10Hz repetition rate, rendering up to 27000 pulses per second. Matching this peculiar burst mode operation is a requirement also for the pump-probe femtosecond laser used in experiments. There is currently no commercially available femtosecond laser technology offering this kind of output at close to mJ-level energies per pulse and sub-20fs pulse width. We will outline the scheme of the pump-probe laser currently under development at the European XFEL. The laser design is based on a noncollinear optical parametric amplifier (NOPA) which will be pumped by sub-picosecond pulses from a high power, frequency-doubled Yb:YAG slab amplifier, delivering up to 20kW of fundamental average power during a burst. The design aims at highest possible flexibility regarding intra-burst rep-rates and pulse energies. Also, the use of uncompressed as well as compressed NOPA pump pulses at fundamental wavelength will enhance the flexibility in experiments.

  4. Heterodyne pump-probe and four-wave mixing in semiconductor optical amplifiers using balanced lock-in detection

    DEFF Research Database (Denmark)

    Borri, Paola; Langbein, Wolfgang; Mørk, Jesper;

    1999-01-01

    We demonstrate a new detection scheme for pump-probe and four-wave mixing heterodyne experiments, using balanced detection and a dual-phase lock-in for spectral filtering. The technique allows the use of low repetition-rate laser systems, as is demonstrated on an InGaAsP/InP bulk optical amplifier...... at 1.53 mym. Ultrafast pump-induced changes in the amplitude and phase of the transmitted probe signal are simultaneously measured, going from small to large signal changes and with no need of an absolute phase calibration, showing the versatility and the sensitivity of this detection scheme....... The results for small perturbations are consistent with previous pump-probe experiments reported in literature. Time-resolved four-wave mixing in the absorption regime of the device is measured, and compared with numerical simulations, indicating a 100 fs dephasing time....

  5. Localized thin film damage sourced and monitored via pump-probe modulated thermoreflectance

    Science.gov (United States)

    Donovan, Brian F.; Tomko, John A.; Giri, Ashutosh; Olson, David H.; Braun, Jeffrey L.; Gaskins, John T.; Hopkins, Patrick E.

    2017-05-01

    Damage in the form of dewetting and delamination of thin films is a major concern in applications requiring micro- or nano-fabrication. In non-contact nanoscale characterization, optical interrogation must be kept to energies below damage thresholds in order to conduct measurements such as pump-probe spectroscopy. In this study, we show that the thermoreflectance of thin films can indicate the degree of film damage induced by a modulated optical heating source. By adjusting the absorbed power of the pump heating event, we identify the characteristics of the change in the thermoreflectance signal when leading up to and exceeding the damage threshold of gold films of varying thicknesses on glass substrates.

  6. Quantum Dynamics Simulations for Modeling Experimental Pump-Probe Measurements

    Science.gov (United States)

    Pearson, Brett; Nayyar, Sahil; Liss, Kyle; Weinacht, Thomas

    2016-05-01

    Time-resolved studies of quantum dynamics have benefited greatly from developments in ultrafast table-top and free electron lasers. Advances in computer software and hardware have lowered the barrier for performing calculations such that relatively simple simulations allow for direct comparison with experimental results. We describe here a set of quantum dynamics calculations in low-dimensional molecular systems. The calculations incorporate coupled electronic-nuclear dynamics, including two interactions with an applied field and nuclear wave packet propagation. The simulations were written and carried out by undergraduates as part of a senior research project, with the specific goal of allowing for detailed interpretation of experimental pump-probe data (in additional to the pedagogical value).

  7. Ablation of metals using ultrashort laser pulses in a pump-probe experiment dynamics of laser induced particle emission from metal surfaces on the femto and picosecond time scale

    CERN Document Server

    Schmidt, V

    2001-01-01

    The main part of this work deals with the dynamics of the laser ablation process of metals (Al, Ag, Fe and Ni) initiated by approx. 50 fs laser pulses. The phenomena have been investigated by interferometric time resolved pump and probe measurements. This work reports one of the first yield measurements of emitted singly charged ions and neutrals from a metal surface induced by laser light. The experiments have been performed using a two-pulse autocorrelation setup in which the differential yield of emitted metal ions is measured as a function of the temporal separation between a pair of excitation pulses with a reflectron-type time-of-flight (TOF) spectrometer. The intensity of each pulse is kept below the ablation threshold, thus only the combined interaction of both pulses causes particle emission. It must be pointed out, that the time information obtained in this way concerns only the initial excitation responsible for ablation, but does not yield information about the dynamics of the way this excitation ...

  8. Ultrafast pump-probe study of the excited-state charge-transfer dynamics in blue copper rusticyanin.

    Science.gov (United States)

    Bizzarri, Anna Rita; Brida, Daniele; Santini, Simona; Cerullo, Giulio; Cannistraro, Salvatore

    2012-04-12

    We have used femtosecond pump-probe spectroscopy to investigate the excited-state dynamics of the anticancer blue copper protein rusticyanin, by exciting its ligand to metal charge-transfer band with 25 fs pump pulses centered at 585 nm. The charge-transfer excited state decays exponentially to the ground state with a time constant of about 230 fs, and its recovery is modulated by coherent oscillations. The Fourier transform of the oscillatory component of the signal provides most of the vibrational modes obtained by means of conventional resonance Raman studies, in addition to the low frequency modes below 80 cm(-1) believed to reflect collective motions of biological relevance.

  9. Spin dynamics of electron with high excess energy in GaAs investigated by the simplified circularly dichromatic pump-probe model

    Science.gov (United States)

    Teng, L. H.; Mu, L. J.; Wang, X.

    2014-03-01

    Time-resolved circularly polarized pump-probe spectroscopy is used to study the spin dynamics of electron with high excess energy in bulk GaAs at room temperature, an abnormal phenomenon that the curve taken from co-helicity circularly polarized pump-probe beam drops below the curve taken from cross-helicity circularly polarized pump-probe beam is observed. With both the spin-dependent band-filling and band-gap renormalization effects being taken into account, a simplified circularly dichromatic pump-probe model is further developed, the model can be used to fit the scanning experimental traces to retrieve the spin relaxation time, carrier recombination time, intensity coefficient of spin-dependent band-filling and band-gap renormalization effects, etc. With the parameters retrieved from the experimental data, the physical origin of the spectrum reversal can be explained in detail, both of the spin-dependent band-filling and band-gap renormalization effects contribute to the reversal spectrum.

  10. Excitons recombination investigation in CdSe/ZnS quantum dots solutions by pump-probe technique

    Science.gov (United States)

    Kulagina, A. S.; Danilov, V. V.; Shilov, V. B.; Grigorenko, K. M.; Vlasov, V. V.; Ermolaeva, G. M.

    2017-07-01

    It reports results of the pump-probe experiment on colloidal solutions of semiconductor CdSe/ZnS quantum dots with 5 nm diameter for intense pulsed resonant excitation at 560 nm wavelength. The dependence of intensity of a transmitted probe pulse on time delay relative to the pump pulse was used to determine relaxation time τexc of excited excitons in the QDs. The intensity of nonlinear reducing of QDs solution transmittance served the reason to set it for pump pulse. We found that the excited states in the QDs recombine within 300 ps after interaction with a 20-ps pump pulse.

  11. Femtosecond pump-probe studies of actinic-wavelength dependence in aqueous chlorine dioxide photochemistry

    Science.gov (United States)

    Bixby, Teresa J.; Bolinger, Joshua C.; Patterson, Joshua D.; Reid, Philip J.

    2009-04-01

    The actinic or photolysis-wavelength dependence of aqueous chlorine dioxide (OClO) photochemistry is investigated using femtosecond pump-probe spectroscopy. Following photoexcitation at 310, 335, and 410 nm the photoinduced evolution in optical density is measured from the UV to the near IR. Analysis of the optical-density evolution illustrates that the quantum yield for atomic chlorine production (ΦCl) increases with actinic energy, with ΦCl=0.16±0.02 for 410 nm excitation and increasing to 0.25±0.01 and 0.54±0.10 for 335 and 310 nm excitations, respectively. Consistent with previous studies, the production of Cl occurs through two channels, with one channel corresponding to prompt (<5 ps) Cl formation and the other corresponding to the thermal decomposition of ClOO formed by OClO photoisomerization. The partitioning between Cl production channels is dependent on actinic energy, with prompt Cl production enhanced with an increase in actinic energy. Limited evidence is found for enhanced ClO production with an increase in actinic energy. Stimulated emission and excited-state absorption features associated with OClO populating the optically prepared A22 surface decrease with an increase in actinic energy suggesting that the excited-state decay dynamics are also actinic energy dependent. The studies presented here provide detailed information on the actinic-wavelength dependence of OClO photochemistry in aqueous solution.

  12. Pump-probe studies of radiation induced defects and formation of warm dense matter with pulsed ion beams

    Science.gov (United States)

    Schenkel, T.; Persaud, A.; Gua, H.; Seidl, P. A.; Waldron, W. L.; Gilson, E. P.; Kaganovich, I. D.; Davidson, R. C.; Friedman, A.; Barnard, J. J.; Minior, A. M.

    2014-10-01

    We report results from the 2nd generation Neutralized Drift Compression Experiment at Berkeley Lab. NDCX-II is a pulsed, linear induction accelerator designed to drive thin foils to warm dense matter (WDM) states with peak temperatures of ~ 1 eV using intense, short pulses of 1.2 MeV lithium ions. Tunability of the ion beam enables pump-probe studies of radiation effects in solids as a function of excitation density, from isolated collision cascades to the onset of phase-transitions and WDM. Ion channeling is an in situ diagnostic of damage evolution during ion pulses with a sensitivity of channeled ions tracks lattice disorder evolution with a resolution of ~ 1 ns using fast current measurements. We will discuss pump-probe experiments with pulsed ion beams and the development of diagnostics for WDM and multi-scale (ms to fs) access to the materials physics of collision cascades e.g. in fusion reactor materials. Work performed under auspices of the US DOE under Contract No. DE-AC02-05CH11231.

  13. Pump-probe model for the Kramers-Kronig relations in a laser

    CERN Document Server

    Yum, Honam

    2010-01-01

    In this paper, we study theoretically a pump-probe model for the Kramers-Kronig (KK) relations during laser operation. A laser gain medium at steady state becomes saturated and the lasing field experiences a flat gain equal to the cavity loss. A solution of the laser equations reveals that the lasing frequency experiences a dispersion that is linear over the allowed bandwidth. However, outside this band, the lasing stops, so that the dispersion is that of the unsaturated gain medium. The combined profile is therefore non-analytical, and cannot be explained in terms of the KK relations. In order to interpret this situation, it is important to consider carefully the physical basis of the KK relations and its connection to causality. We conclude that the KK relation is expected to apply only to an independent probe applied to the medium, which is under excitation by the pump producing the gain as well as the lasing mode. The absorption/gain and dispersion profiles are then analytical, and satisfy the KK-relation...

  14. Ultrafast Multiphoton Pump-probe Photoemission Excitation Pathways in Rutile TiO2(110)

    Energy Technology Data Exchange (ETDEWEB)

    Argondizzo, Adam; Cui, Xuefeng; Wang, Cong; Sun, Huijuan; Shang, Honghui; Zhao, Jin; Petek, Hrvoje

    2015-04-27

    We investigate the spectroscopy and photoinduced electron dynamics within the conduction band of reduced rutile TiO2(110) surface by multiphoton photoemission (mPP) spectroscopy with wavelength tunable ultrafast (!20 fs) laser pulse excitation. Tuning the mPP photon excitation energy between 2.9 and 4.6 eV reveals a nearly degenerate pair of new unoccupied states located at 2.73 ± 0.05 and 2.85 ± 0.05 eV above the Fermi level, which can be analyzed through the polarization and sample azimuthal orientation dependence of the mPP spectra. Based on the calculated electronic structure and optical transition moments, as well as related spectroscopic evidence, we assign these resonances to transitions between Ti 3d bands of nominally t2g and eg symmetry, which are split by crystal field. The initial states for the optical transition are the reduced Ti3+ states of t2g symmetry populated by formation oxygen vacancy defects, which exist within the band gap of TiO2. Furthermore,we studied the electron dynamics within the conduction band of TiO2 by three-dimensional time-resolved pump-probe interferometric mPP measurements. The spectroscopic and time-resolved studies reveal competition between 2PP and 3PP processes where the t2g-eg transitions in the 2PP process saturate, and are overtaken by the 3PP process initiated by the band-gap excitation from the valence band of TiO2.

  15. High Speed Pump-Probe Apparatus for Observation of Transitional Effects in Ultrafast Laser Micromachining Processes

    Directory of Open Access Journals (Sweden)

    Ilya Alexeev

    2015-12-01

    Full Text Available A pump-probe experimental approach has been shown to be a very efficient tool for the observation and analysis of various laser matter interaction effects. In those setups, synchronized laser pulses are used to create an event (pump and to simultaneously observe it (probe. In general, the physical effects that can be investigated with such an apparatus are restricted by the temporal resolution of the probe pulse and the observation window. The latter can be greatly extended by adjusting the pump-probe time delay under the assumption that the interaction process remains fairly reproducible. Unfortunately, this assumption becomes invalid in the case of high-repetition-rate ultrafast laser material processing, where the irradiation history strongly affects the ongoing interaction process. In this contribution, the authors present an extension of the pump-probe setup that allows to investigate transitional and dynamic effects present during ultrafast laser machining performed at high pulse repetition frequencies.

  16. Genuinely quantum effects in nonlinear spectroscopy: vacuum fluctuations and their induced superradiance

    CERN Document Server

    León-Montiel, R de J; Yuen-Zhou, Joel

    2016-01-01

    The classical or quantum nature of optical spectroscopy signals is a topic that has attracted great attention recently. Spectroscopic techniques have been classified as quantum or classical depending on the light-source used in their implementations. In this way, experiments performed with quantum light---such as entangled photon pairs---have been labeled as quantum spectroscopies, whereas those performed with coherent laser pulses are generally referred to as classical ones. In this work, we highlight the fact that typical laser-spectroscopy signals should sometimes be deemed quantum too, as they contain information about the quantum vacua of the modes that interact with the sample. Using a minimalistic model, namely frequency-integrated pump-probe spectroscopy, we demonstrate that vacuum contributions can be expressed as a correction term to the \\emph{classical} pump-probe signals, which scales linearly with the intensity of the pump field. Remarkably, we show that these vacuum contributions may not be negl...

  17. Heterodyne pump probe measurements of nonlinear dynamics in an indium phosphide photonic crystal cavity

    DEFF Research Database (Denmark)

    Heuck, Mikkel; Combrié, S.; Lehoucq, G.

    2013-01-01

    Using a sensitive two-color heterodyne pump-probe technique, we investigate the carrier dynamics of an InP photonic crystal nanocavity. The heterodyne technique provides unambiguous results for all wavelength configurations, including the degenerate case, which cannot be investigated with the wid...... with the widely used homodyne technique. A model based on coupled mode theory including two carrier distributions is introduced to account for the relaxation dynamics, which is assumed to be governed by both diffusion and recombination.......Using a sensitive two-color heterodyne pump-probe technique, we investigate the carrier dynamics of an InP photonic crystal nanocavity. The heterodyne technique provides unambiguous results for all wavelength configurations, including the degenerate case, which cannot be investigated...

  18. Comparing in vivo pump-probe and multiphoton fluorescence microscopy of melanoma and pigmented lesions

    Science.gov (United States)

    Wilson, Jesse W.; Degan, Simone; Gainey, Christina S.; Mitropoulos, Tanya; Simpson, Mary Jane; Zhang, Jennifer Y.; Warren, Warren S.

    2015-05-01

    We demonstrate a multimodal approach that combines a pump-probe with confocal reflectance and multiphoton autofluorescence microscopy. Pump-probe microscopy has been proven to be of great value in analyzing thin tissue sections of pigmented lesions, as it produces molecular contrast which is inaccessible by other means. However, the higher optical intensity required to overcome scattering in thick tissue leads to higher-order nonlinearities in the optical response of melanin (e.g., two-photon pump and one-photon probe) that present additional challenges for interpreting the data. We show that analysis of pigment composition in vivo must carefully account for signal terms that are nonlinear with respect to the pump and probe intensities. We find that pump-probe imaging gives useful contrast for pigmented structures over a large range of spatial scales (100 μm to 1 cm), making it a potentially useful tool for tracking the progression of pigmented lesions without the need to introduce exogenous contrast agents.

  19. Towards simultaneous measurements of electronic and structural properties in ultra-fast x-ray free electron laser absorption spectroscopy experiments.

    Science.gov (United States)

    Gaudin, J; Fourment, C; Cho, B I; Engelhorn, K; Galtier, E; Harmand, M; Leguay, P M; Lee, H J; Nagler, B; Nakatsutsumi, M; Ozkan, C; Störmer, M; Toleikis, S; Tschentscher, Th; Heimann, P A; Dorchies, F

    2014-04-17

    The rapidly growing ultrafast science with X-ray lasers unveils atomic scale processes with unprecedented time resolution bringing the so called "molecular movie" within reach. X-ray absorption spectroscopy is one of the most powerful x-ray techniques providing both local atomic order and electronic structure when coupled with ad-hoc theory. Collecting absorption spectra within few x-ray pulses is possible only in a dispersive setup. We demonstrate ultrafast time-resolved measurements of the LIII-edge x-ray absorption near-edge spectra of irreversibly laser excited Molybdenum using an average of only few x-ray pulses with a signal to noise ratio limited only by the saturation level of the detector. The simplicity of the experimental set-up makes this technique versatile and applicable for a wide range of pump-probe experiments, particularly in the case of non-reversible processes.

  20. Dynamic characterization of silicon nanowires using a terahertz optical asymmetric demultiplexer-based pump-probe scheme

    DEFF Research Database (Denmark)

    Ji, Hua; Cleary, C. S.; Dailey, J. M.;

    2012-01-01

    Dynamic phase and amplitude all-optical responses of silicon nanowires are characterized using a terahertz optical asymmetric demultiplexer (TOAD) based pump-probe scheme. Ultra-fast recovery is observed for moderate pump powers....

  1. Femtosecond spectroscopy on alkali-doped helium nanodroplets; Femtosekundenspektroskopie an alkalidotierten Helium-Nanotroepfchen

    Energy Technology Data Exchange (ETDEWEB)

    Claas, P.

    2006-01-15

    In the present thesis first studies on the short-time dynamics in alkali dimers and microclusters, which were bound on the surface of superfluid helium droplets, were presented. The experiments comprehended pump-probe measurements on the fs scale on the vibration dynamics on the dimers and on the fragmentation dynamics on the clusters. Generally by the studies it was shown that such extremely short slopes can also be observed on helium droplets by means of the femtosecond spectroscopy.

  2. Beware the two-beam coupling phase shift: Interpreting pump-probe measurements of the nonlinear refractive index

    CERN Document Server

    Wahlstrand, J K; McCole, E T; Cheng, Y -H; Palastro, J P; Levis, R J; Milchberg, H M

    2013-01-01

    Nonlinear optics experiments measuring phase shifts induced in a weak probe pulse by a strong pump pulse must account for coherent effects that only occur when the pump and probe pulses are temporally overlapped. It is well known that a weak probe beam experiences a greater phase shift from a strong pump beam than the pump beam induces on itself. The physical mechanism behind the enhanced phase shift is diffraction of pump light into the probe direction by a nonlinear refractive index grating produced by interference between the two beams. For an instantaneous third-order response, the effect of the grating is to simply double the probe phase shift, but when delayed nonlinearities are considered, the effect is more complex. A comprehensive treatment is given for both degenerate and nondegenerate pump-probe experiments in noble and diatomic gases. Results of numerical calculations are compared to a recent transient birefringence measurement [Loriot et al., Opt. Express 17, 13429 (2009)] and a recent spectral i...

  3. Diagnosis and staging of female genital tract melanocytic lesions using pump-probe microscopy (Conference Presentation)

    Science.gov (United States)

    Robles, Francisco E.; Selim, Maria A.; Warren, Warren S.

    2016-02-01

    Melanoma of the vulva is the second most common type of malignancy afflicting that organ. This disease caries poor prognosis, and shows tendencies to recur locally and develop distant metastases through hematogenous dissemination. Further, there exists significant clinical overlap between early-stage melanomas and melanotic macules, benign lesions that are believed to develop in about 10% of the general female population. In this work we apply a novel nonlinear optical method, pump-probe microscopy, to quantitatively analyze female genitalia tract melanocytic lesions. Pump-probe microscopy provides chemical information of endogenous pigments by probing their electronic excited state dynamics, with subcellular resolution. Using unstained biopsy sections from 31 patients, we find significant differences between melanin type and structure in tissue regions with invasive melanoma, melanoma in-situ and non-malignant melanocytic proliferations (e.g., nevi, melanocytic macules). The molecular images of non-malignant lesion have a well-organized structure, with relatively homogenous pigment chemistry, most often consistent with that of eumelanin with large aggregate size or void of metals, such as iron. On the other hand, pigment type and structure observed in melanomas in-situ and invasive melanomas is typically much more heterogeneous, with larger contributions from pheomelanin, melanins with larger metal content, and/or melanins with smaller aggregate size. Of most significance, clear differences can be observed between melanocytic macules and vulvar melanoma in-situ, which, as discussed above, can be difficult to clinically distinguish. This initial study demonstrates pump-probe microscopy's potential as an adjuvant diagnostic tool by revealing systematic chemical and morphological differences in melanin pigmentation among invasive melanoma, melanoma in-situ and non-malignant melanocytic lesions.

  4. Nonequilibrium Pump-Probe Photoexcitation as a Tool for Analyzing Unoccupied Equilibrium States of Correlated Electrons

    Science.gov (United States)

    Yamaji, Youhei; Imada, Masatoshi

    2016-09-01

    Relaxation of electrons in a Hubbard ring coupled to a dissipative bosonic bath is studied to simulate the pump-probe photoemission measurement. From this insight, we propose an experimental method of eliciting the unoccupied part of single-particle spectra at the equilibrium of doped Mott insulators. We reveal first that the effective temperatures of distribution functions and electronic spectra are different during the relaxation, which makes the frequently employed thermalization picture inappropriate. Contrary to the conventional analysis, we show that the unoccupied spectra at equilibrium can be detected as the states that relax faster.

  5. Pump-probe imaging of laser-induced periodic surface structures after ultrafast irradiation of Si

    Energy Technology Data Exchange (ETDEWEB)

    Murphy, Ryan D. [Applied Physics Program, University of Michigan, Ann Arbor, Michigan 48109 (United States); Torralva, Ben [Department of Atmospheric, Oceanic and Space Sciences, University of Michigan, Ann Arbor, Michigan 48109 (United States); Adams, David P. [Sandia National Laboratories, Albuquerque, New Mexico 87123 (United States); Yalisove, Steven M. [Department of Materials Science and Engineering, University of Michigan, Ann Arbor, Michigan 48109 (United States)

    2013-09-30

    Ultrafast pump-probe microscopy has been used to investigate laser-induced periodic surface structure (LIPSS) formation on polished Si surfaces. A crater forms on the surface after irradiation by a 150 fs laser pulse, and a second, subsequent pulse forms LIPSS within the crater. Sequentially delayed images show that LIPSS with a periodicity slightly less than the fundamental laser wavelength of 780 nm appear on Si surfaces ∼50 ps after arrival of the second pump laser pulse, well after the onset of melting. LIPSS are observed on the same timescale as material removal, suggesting that their formation involves material ejection.

  6. Pump-probe imaging of laser-induced periodic surface structures after ultrafast irradiation of Si

    Science.gov (United States)

    Murphy, Ryan D.; Torralva, Ben; Adams, David P.; Yalisove, Steven M.

    2013-09-01

    Ultrafast pump-probe microscopy has been used to investigate laser-induced periodic surface structure (LIPSS) formation on polished Si surfaces. A crater forms on the surface after irradiation by a 150 fs laser pulse, and a second, subsequent pulse forms LIPSS within the crater. Sequentially delayed images show that LIPSS with a periodicity slightly less than the fundamental laser wavelength of 780 nm appear on Si surfaces ˜50 ps after arrival of the second pump laser pulse, well after the onset of melting. LIPSS are observed on the same timescale as material removal, suggesting that their formation involves material ejection.

  7. Pump-probe differencing technique for cavity-enhanced, noise-canceling saturation laser spectroscopy

    CERN Document Server

    De Vine, G; Close, J D; Gray, M B; Vine, Glenn de; Clelland, David E. Mc; Close, John D.; Gray, Malcolm B.

    2004-01-01

    We present an experimental technique enabling mechanical-noise free, cavity-enhanced frequency measurements of an atomic transition and its hyperfine structure. We employ the 532nm frequency doubled output from a Nd:YAG laser and an iodine vapour cell. The cell is placed in a traveling-wave Fabry-Perot interferometer (FPI) with counter-propagating pump and probe beams. The FPI is locked using the Pound-Drever-Hall (PDH) technique. Mechanical noise is rejected by differencing pump and probe signals. In addition, this differenced error signal gives a sensitive measure of differential non-linearity within the FPI.

  8. Patterning effects in quantum dot amplifiers characterized through pump probe spectroscopy using two pump pulses

    DEFF Research Database (Denmark)

    Berg, Tommy Winther; Poel, Mike van der; Laemmlin, M.;

    2004-01-01

    Patterning effects at ultrahigh bitrates in quantum dot amplifiers are investigated by a novel experimental technique. Slow carrier dynamics in the excited states and wetting layer are found to limit the potential for ultrahigh-speed signal processing....

  9. Carrier dynamics in EuTiO3 films probed by femtosecond pump-probe spectroscopy

    Science.gov (United States)

    Li, Zhongguo; Zhao, Run; Li, Weiwei; Wang, Haiyan; Yang, Hao; Zhang, Xueru; Wang, Yuxiao; Wei, Tai-Huei; Song, Ying-Lin

    2015-03-01

    Recently, perovskite oxide EuTiO3 has attracted considerable attention due to its intriguing multiferroic properties. To gain a deeper understanding of its fascinating properties, it is essential to characterize the competing interactions between charge, lattice, spin, and orbital parameters. Here we present optical studies of the ultrafast carrier dynamics in EuTiO3 films grown on SrTiO3 substrates by probing photo-induced transient absorption (TA) in the weak excitation limit. All the signals were measured at room temperature. The transient curve of EuTiO3 exhibits a fast rise after photo excitation (approximately 2 ps) and a long decay component with time constant of several nanoseconds, which are attributed to carrier-phonon coupling and carrier recombination respectively. The absorption change of EuTiO3 near zero temporal delay is found to be quite different from the SrTiO3 substrates, implying carrier-phonon interactions differ distinctively between these two materials. Our results could be helpful to understand the microscopic interactions in perovskite oxide. The authors acknowledge the support of the National Natural Science Foundation of China.

  10. Mapping of wave packets in direct fragmentation via pump-probe frequency integrated fluorescence spectroscopy

    DEFF Research Database (Denmark)

    Engel, Volker; Henriksen, Niels Engholm

    2000-01-01

    We consider femtosecond excitation of a molecule to a dissociative electronic state. The quantum dynamics is recorded via delayed excitation to a higher electronic state and measurement of the total fluorescence from this state detected as a function of delay time. It is shown that the signal can...

  11. High P-T Thermal Conductivity of Periclase using an Ultrafast Pump-Probe Method

    Science.gov (United States)

    Dalton, D. A.; Goncharov, A. F.; Hsieh, W.; Cahill, D.

    2011-12-01

    Measurements of thermal conductivity were carried out on MgO at elevated pressures via a diamond anvil cell (DAC) at ambient and high temperatures. The time domain thermoreflectance (TDTR) technique is an optical pump-probe method for heating and probing the dynamics of thermal diffusion. Samples of MgO (~10 μm) coated with aluminum (~70 nm) are loaded into a diamond cell with argon as the pressure medium. Ambient temperature results are presented up to 60 GPa, while high P-T measurements were performed in a resistively heated cell up to 45 GPa and ~600 K, where ruby and SrB4O7:Sm2+ were used as P-T calibrants. The extrapolation of these results to conditions that are relevant to the mantle will be discussed.

  12. Energy Transfer in Isolated LHC Ⅱ Studied by Femtosecond Pump-Probe Technique

    Institute of Scientific and Technical Information of China (English)

    杨毅; 郭立俊; 刘源; 刘伟民; 朱荣毅; 钱士雄; 徐春和

    2003-01-01

    Excitation energy transfer in the isolated light-harvesting chlorophyll (Chl)-a/b protein complex of photosystem Ⅱ (LHC Ⅱ) was studied by the one-colour pump-probe technique with femtosecond time resolution. After exciting Chl-b by 638 nm beam, the dynamic behaviour shows that the ultrafast energy transfer from Chl-b at positions of B2, B3, and B5 to the corresponding Chl-a molecules in monomeric subunit of LHC Ⅱ is in the time scale of 230 fs. While with the excitation of Chl-a at 678 nm, the energy transfer between excitons of Chl-a molecules has the lifetime of about 370 fs, and two other slow decay components are due to the energy transfer between different Chl-a molecules in a monomeric subunit of LHC Ⅱ or in different subunits, or due to change of molecular conformation.

  13. Energy transfer in isolated LHC II studied by femtosecond pump-probe technique

    CERN Document Server

    Yang Yi; Liu Yuan; Liu Wei Min; Zhu Rong Yi; Qian Shi Xiong; Xu Chun He

    2003-01-01

    Excitation energy transfer in the isolated light-harvesting chlorophyll (Chl)-a/b protein complex of photosystem II (LHC II) was studied by the one-colour pump-probe technique with femtosecond time resolution. After exciting Chl-b by 638nm beam, the dynamic behaviour shows that the ultrafast energy transfer from Chl-b at positions of B2, B3, and B5 to the corresponding Chl-a molecules in monomeric subunit of LHC II is in the time scale of 230fs. While with the excitation of Chl-a at 678nm, the energy transfer between excitons of Chl-a molecules has the lifetime of about 370 fs, and two other slow decay components are due to the energy transfer between different Chl-a molecules in a monomeric subunit of LHC II or in different subunits, or due to change of molecular conformation. (20 refs).

  14. Analysis of the Thermo-Reflectivity Coefficient Influence Using Photothermal Pump-Probe Techniques.

    Science.gov (United States)

    Zanuto, Vitor S; Capeloto, Otávio A; Sandrini, Marcelo; Malacarne, Luis C; Astrath, Nelson G C; Bialkowski, Stephen E

    2016-11-18

    Recent improvements in the modeling of photo-induced thermo-optical-mechanical effects have broadened the application of photothermal techniques to a large class of solids and fluids. During laser excitation, changes in optical reflectivity due to temperature variation may affect the photothermal signal. In this study, the influence of the reflectivity change due to heating is analyzed for two pump-probe photothermal techniques, thermal lens and thermal mirror. A linear equation for the temperature dependence of the reflectivity is derived, and the solution is tested using optical properties of semi-transparent and opaque materials. For semi-transparent materials, the influence of the reflectivity change in photothermal signals is less than 0.01%, while for opaque materials it is lower than 3%.

  15. Experimental observation of pump-probe spectra of caesium D2 line with a vapour cell

    Institute of Scientific and Technical Information of China (English)

    Wang Yan-Hua; Yang Hai-Jing; Zhang Tian-Cai; Wang Jun-Min

    2005-01-01

    Pump-probe spectra of caesium D2 line are experimentally investigated in a Cs atomic vapour cell with copropagating orthogonal linearly-polarized pump and probe laser beams. Absorption-reduction dips duo to electromagnetically induced transparency (EIT) in multi-A-type Zeeman sublevels of 6 S1/2 F=3-6 P3/2 F'=2 hyperfine transition and absorption-enhanced peaks due to electromagnetically induced absorption (EIA) in 6 S1/2 F=4-6 P3/2 F'=5 hyperfine transition are demonstrated. With detuned pump beam abnormal sign-reversed signals inside the EIT dip and the EIA peak are clearly observed.

  16. Pulse accumulation, radial heat conduction, and anisotropic thermal conductivity in pump-probe transient thermoreflectance.

    Science.gov (United States)

    Schmidt, Aaron J; Chen, Xiaoyuan; Chen, Gang

    2008-11-01

    The relationship between pulse accumulation and radial heat conduction in pump-probe transient thermoreflectance (TTR) is explored. The results illustrate how pulse accumulation allows TTR to probe two thermal length scales simultaneously. In addition, the conditions under which radial transport effects are important are described. An analytical solution for anisotropic heat flow in layered structures is given, and a method for measuring both cross-plane and in-plane thermal conductivities of thermally anisotropic thin films is described. As verification, the technique is used to extract the cross-plane and in-plane thermal conductivities of highly ordered pyrolytic graphite. Results are found to be in good agreement with literature values.

  17. Pulsed laser noise analysis and pump-probe signal detection with a data acquisition card.

    Science.gov (United States)

    Werley, Christopher A; Teo, Stephanie M; Nelson, Keith A

    2011-12-01

    A photodiode and data acquisition card whose sampling clock is synchronized to the repetition rate of a laser are used to measure the energy of each laser pulse. Simple analysis of the data yields the noise spectrum from very low frequencies up to half the repetition rate and quantifies the pulse energy distribution. When two photodiodes for balanced detection are used in combination with an optical modulator, the technique is capable of detecting very weak pump-probe signals (ΔI/I(0) ~ 10(-5) at 1 kHz), with a sensitivity that is competitive with a lock-in amplifier. Detection with the data acquisition card is versatile and offers many advantages including full quantification of noise during each stage of signal processing, arbitrary digital filtering in silico after data collection is complete, direct readout of percent signal modulation, and easy adaptation for fast scanning of delay between pump and probe.

  18. Real-time ultrafast dynamics of dense, hot matter measured by pump-probe Doppler spectrometry

    Science.gov (United States)

    Lad, Amit D.; Mondal, S.; Narayanan, V.; Ahmed, Saima; Rajeev, P. P.; Robinson, A. P. L.; Pasley, J.; Kumar, G. Ravindra

    2010-08-01

    A detailed understanding of the critical surface motion of high intensity laser produced plasma is very crucial for understanding the interaction. We employ the two colour pump-probe technique to report the first ever femtosecond scale ultrafast dynamics measurement of the critical surface of a solid plasma produced by a relativistically intense, femtosecond pump laser beam (1018 W/cm2, 30 fs, 800 nm) on an aluminium target. We observe the Doppler shift of a time delayed probe laser beam (1012 W/cm2, 80 fs, 400 nm) up to delays of 30 ps. Such unravelling of dynamics has not been possible in earlier measurements, which typically used the self reflection of a powerful pump pulse. We observe time dependent red and blue shifts and measure their magnitudes to infer plasma expansion velocity and acceleration and thereby the plasma profile. Our results are very well reproduced by 1D hydrodynamic simulation (HYADES code).

  19. Exploring Extra Dimensions in Spectroscopy Experiments

    Institute of Scientific and Technical Information of China (English)

    LUO Feng; LIU Hong-Ya

    2006-01-01

    @@ We propose an idea in spectroscopy to search for extra spatial dimensions as well as to detect the possible deviation from Newton's inverse-square law at small scale, and we take high-Z hydrogenic systems and muonic atoms as illustrations. The relevant experiments might help to explore a more than two extra dimensions scenario in the brane world model proposed by Arkani-Hamed, Dimopoulos, Dvali (ADD) and to set constraints for fundamental parameters such as the size of extra dimensions.

  20. Disentangling Multichannel Photodissociation Dynamics in Acetone by Time-Resolved Photoelectron-Photoion Coincidence Spectroscopy.

    Science.gov (United States)

    Maierhofer, Paul; Bainschab, Markus; Thaler, Bernhard; Heim, Pascal; Ernst, Wolfgang E; Koch, Markus

    2016-08-18

    For the investigation of photoinduced dynamics in molecules with time-resolved pump-probe photoionization spectroscopy, it is essential to obtain unequivocal information about the fragmentation behavior induced by the laser pulses. We present time-resolved photoelectron-photoion coincidence (PEPICO) experiments to investigate the excited-state dynamics of isolated acetone molecules triggered by two-photon (269 nm) excitation. In the complex situation of different relaxation pathways, we unambiguously identify three distinct pump-probe ionization channels. The high selectivity of PEPICO detection allows us to observe the fragmentation behavior and to follow the time evolution of each channel separately. For channels leading to fragment ions, we quantitatively obtain the fragment-to-parent branching ratio and are able to determine experimentally whether dissociation occurs in the neutral molecule or in the parent ion. These results highlight the importance of coincidence detection for the interpretation of time-resolved photochemical relaxation and dissociation studies if multiple pathways are present.

  1. Exotic hadron spectroscopy at the LHCb experiment

    CERN Document Server

    Cowan, G A

    2016-01-01

    The LHCb experiment is designed to study the decays and properties of heavy flavoured hadrons produced in the forward region from proton-proton collisions at the CERN Large Hadron Collider. During Run 1, it has recorded the world's largest data sample of beauty and charm hadrons, enabling precise studies into the spectroscopy of such particles, including discoveries of new states and measurements of their masses, widths and quantum numbers. An overview of recent LHCb results in the area of exotic hadron spectroscopy is presented, focussing on the discovery of the first pentaquark states in the $\\Lambda_b^0 \\to J/\\psi p K^-$ channel and a search for them in the related $\\Lambda_b^0 \\to J/\\psi p\\pi^-$ mode. The LHCb non-confirmation of the D0 tetraquark candidate in the $B_s^0\\pi^+$ invariant mass spectrum is presented.

  2. A split-beam probe-pump-probe scheme for femtosecond time resolved protein X-ray crystallography

    Directory of Open Access Journals (Sweden)

    Jasper J. van Thor

    2015-01-01

    Full Text Available In order to exploit the femtosecond pulse duration of X-ray Free-Electron Lasers (XFEL operating in the hard X-ray regime for ultrafast time-resolved protein crystallography experiments, critical parameters that determine the crystallographic signal-to-noise (I/σI must be addressed. For single-crystal studies under low absorbed dose conditions, it has been shown that the intrinsic pulse intensity stability as well as mode structure and jitter of this structure, significantly affect the crystallographic signal-to-noise. Here, geometrical parameters are theoretically explored for a three-beam scheme: X-ray probe, optical pump, X-ray probe (or “probe-pump-probe” which will allow experimental determination of the photo-induced structure factor amplitude differences, ΔF, in a ratiometric manner, thereby internally referencing the intensity noise of the XFEL source. In addition to a non-collinear split-beam geometry which separates un-pumped and pumped diffraction patterns on an area detector, applying an additional convergence angle to both beams by focusing leads to integration over mosaic blocks in the case of well-ordered stationary protein crystals. Ray-tracing X-ray diffraction simulations are performed for an example using photoactive yellow protein crystals in order to explore the geometrical design parameters which would be needed. The specifications for an X-ray split and delay instrument that implements both an offset angle and focused beams are discussed, for implementation of a probe-pump-probe scheme at the European XFEL. We discuss possible extension of single crystal studies to serial femtosecond crystallography, particularly in view of the expected X-ray damage and ablation due to the first probe pulse.

  3. Photodissociation/photoionization processes of chlorobromomethane induced by femtosecond laser pulses with pump-probe scheme

    Institute of Scientific and Technical Information of China (English)

    ZHANG Feng; WEI ZhengRong; CAO ZhenZhou; ZHANG ChangHua; ZHANG Bing

    2008-01-01

    The photodissociation/photoionization processes of chlorobromomethane (CH2BrCl) induced by femtosecond laser pulses have been investigated using pump-probe scheme combined with the time-of-flight mass spectra. The dominate photoproducts are observed at different delay time of the pump (400 nm) and probe (800 nm) pulses and the corresponding time-dependence of them is obtained. The results show that the decaying time of the molecule CH2BrCl in the A-band is in the 100 fs. The decaying tendencies of the fragment ions (CH2Cl+ and CH2Br+) and the parent ion (CH2BrCl+) are almost the same and the relative ratios of the yields of them keep constant during the delay time of 0 to 150 fs. These facts suggest that the fragment ions come from the fragmentation of the parent ions in excited electronic states. The probabilities to form CH2Cl+ and CH2Br+ are obtained from the relative ratio of the ion intensity and are about 71.6% and 14.2%, respectively.

  4. Velocity anisotropy effect in pump-probe spectra of cesium in a micrometric thickness optical cell

    Science.gov (United States)

    Ghosh, P. N.; Mitra, S.; Ray, B.; Krasteva, A.; Slavov, D.; Todorov, P.; Cartaleva, S.

    2015-01-01

    The pump-probe spectra in a cell of micrometric thickness containing cesium vapor are reported. The line shape and nonlinear features observed in the case of fluorescence in the direction parallel to the cell windows and the transmission spectra observed along the propagation direction of the probe beam show considerable differences in the spectral profiles. We observed Electromagnetically Induced Transparency (EIT) and enhanced Velocity Selective Optical Pumping (VSOP) signals. Atoms moving nearly parallel to the windows and perpendicular to the collinear pump and probe beams will see much lower Doppler shift of incident frequencies and hence will lead to considerable narrowing of the Doppler background in the fluorescence spectra. The coherence decay rate is also low for such atoms as they do not meet with the cell walls. A theoretical model based on five level optical Bloch equations is used to simulate the spectra. The Doppler convolution includes all possible orientation of atomic velocities with respect to the laser beam direction. The simulated curves reproduce the observed sharp EIT peaks and enhanced broad VSOP signals for the closed probe transition in the fluorescence and absorption spectra. The observed effect of the light intensity and temperature change on the non-linear features is reproduced by the simulation.

  5. Temperature-dependent and pump-probe ellipsometric studies of TlInSe{sub 2}

    Energy Technology Data Exchange (ETDEWEB)

    Mamedov, Nazim [Institute of Physics, Azerbaijan National Academy of Science, Baku, AZ-1143 (Azerbaijan)], E-mail: n.mamedov@physics.ab.az; Wakita, Kazuki [Department of Electrical, Electronics and Computer Engineering, Chiba Institute of Technology, 2-17-1, Tsudanuma, Narashino 275-0016 (Japan); Shim, YongGu; Abe, Kouji; Ogushi, Naoki [Department of Physics and Electronics, Graduate School of Engineering, Osaka Prefecture University, 1-1 Gakuen-cho, Nakaku, Sakai 599-8531 (Japan)

    2008-12-31

    Temperature-dependent phase-modulated spectroscopic ellipsometry over the photon energies 1.5-5.5 eV and temperatures 300-400 K, as well as pump-probe single wavelength rotating-analyzer laser ellipsometry at photon energy 1.61 eV and pumping power-density up to 160 W/cm{sup 2} has been carried out on TlInSe{sub 2} that has a quasi one-dimensional crystalline structure and apparently undergoes an incommensurate phase transition with temperature. Refractive indices and extinction coefficients, as well as their variation with temperature and pumping power-density have been determined. The change of the surface profile under pumping has been disclosed. The reversibility of the effect has been confirmed by the dynamic reflectance examination. Obtained results are discussed in terms of thermal effects and incommensurate phase transition in TlInSe{sub 2}. It is proposed that a giant thermo-elastic effect and a soliton wave formation are behind the observed reversible change of the surface profile.

  6. Photoionization of NaK molecule with a double-well potential in femtosecond pump-probe pulse laser fields

    Institute of Scientific and Technical Information of China (English)

    Yu Jie; Wang Sen-Ming; Yuan Kai-Jun; Cong Shu-Lin

    2006-01-01

    The method of time-dependent quantum wave packet dynamics is used to calculate the femtosecond pump-probe photoelectron spectra and study the wave packet dynamic processes of the double-minimum potential state 61∑+ of NaK in intense laser fields. The evolutions of the wave packet and the photoelectron energy spectra with time and internuclear distance are described in detail. The wave packet dynamic information of the 61∑+ state can be extracted from the photoelectron energy spectra.

  7. Towards circularly polarized (sub-) femtosecond XUV pulses for ultrafast pump-probe experiments

    Energy Technology Data Exchange (ETDEWEB)

    Schmidt, Juergen; Chew, Soo Hoon; Kranjec, Mihael; Kleineberg, Ulf [LMU Muenchen, Physik-Department, Garching (Germany); Guggenmos, Alexander; Hofstetter, Michael [MPQ fuer Quantenoptik, Garching (Germany)

    2012-07-01

    Circularly polarized (CP) XUV radiation has been demonstrated to be a useful probe for the experimental investigation of electronic effects in magnetic materials such as magnetic circular dichroism, spin-polarized photoemission, magneto-optical Kerr-effect and others. On the laboratory scale, High Harmonic (HH) gas jet sources which inherently provide coherent and ultrashort linearly polarized XUV pulses in the sub-fs domain, suitable to study ultrafast dynamics, have emerged. In our setup we aim at incorporating in-house fabricated broadband transmission multilayer phase shifters into a laser driven 10kHz repetition rate HH Source in the 50-70eV photon energy range. To our knowledge only little investigation on such polarizers intended for use in HH radiation has been made so far. We examine our phase shifters regarding tunability of energy range, phase retardation, transmission efficiency and spectral bandwidth. For this purpose we use a home-made XUV flat-field spectrometer and a multilayer mirror based polarization analyzer. Combining the expected CP pulses with our TOF-PEEM and ARPES spectrometer will pave the way towards time resolved measurements of exchange-coupled electron dynamics.

  8. A novel electro-optical pump-probe system for bioelectromagnetic investigations

    Science.gov (United States)

    De Angelis, Annalisa; Couderc, Vincent; Leproux, Philippe; Labruyère, Alexis; Tonello, Alessandro; El Amari, Saad; Arnaud-Cormos, Delia; Leveque, Philippe

    2012-10-01

    In the area of bioelectromagnetic studies there is a growing interest to understand the mechanisms leading to nanosecond electric fields induced electroporation. Real-time imaging techniques at molecular level could probably bring further advances on how electric fields interact with living cells. However the investigations are limited by the present-day lack of these kinds of advanced instrumentations. In this context, we present an innovative electro-optical pump-probe system. The aim of our project is to provide a performing and compact device for electrical stimulation and multiplex Coherent anti-Stokes Raman Scattering (M-CARS) imaging of biological cells at once. The system consists of a 1064 nm sub-nanosecond laser source providing both a monochromatic pump and a polychromatic Stokes optical beam used in a CARS process, as well as the trigger beam for the optoelectronic switching-based electrical pulse generator. The polychromatic Stokes beam (from 600 to 1700 nm) results from a supercontinuum generation in a photonic crystal fiber (PCF). A detailed spectro-temporal characterization of such a broadband spectrum shows the impact of the nonlinear propagation in the fiber on the Stokes wave. Despite the temporal distortions observable on Stokes pulse profiles, their spectral synchronization with the pump pulse remains possible and efficient in the interesting region between 1100 nm and 1700 nm. The electrical stimulation device consists of a customized generator combining microstrip-line technology and laser-triggered photoconductive semiconductor switches. Our experimental characterization highlights the capability for such a generator to control the main pulse parameters (profile, amplitude and duration) and to be easily synchronized with the imaging system. We finally test and calibrate the system by means of a KDP crystal. The preliminary results suggest that this electro-optical system provides a suitable tool for real-time investigation of

  9. Vibrational dynamics of the CN stretching mode of [Ru(CN)6]4- in D2O studied by nonlinear infrared spectroscopy

    Institute of Scientific and Technical Information of China (English)

    Jumpei; TAYAMA; Motohiro; BANNO; Kaoru; OHTA; Keisuke; TOMINAGA

    2010-01-01

    We have studied vibrational dynamics of the T1u mode of the CN stretching mode of [Ru(CN)6 ]4- in D2O by infrared(IR) nonlinear spectroscopy such as an IR three-pulse photon echo experiment and polarization-sensitive IR pump-probe spectroscopy. The isotropic component of the pump-probe signal shows a bi-exponential decay with time constants of 0.8 ps and 20.8 ps. The fast and slow components correspond to the rapid equilibration between the T1u mode and the Raman active modes of the CN stretching mode and the vibrational population relaxation from the v=1 state of the T1u mode,respectively. Anisotropy of the pump-probe signal decays with a time constant of 3.1 ps,which is due to the time evolution of the superposition states of the triply degenerate T1u modes. Three pulse photon echo measurements showed that the time correlation function of the frequency fluctuation decays bi-exponentially with time constants of 80 fs and 1.4 ps. These time constants depend only on the solute and are independent of the solvent,whereas the amplitudes depend on both the solute and solvent.

  10. Nonlinear Spectroscopy of Rubidium: An Undergraduate Experiment

    Science.gov (United States)

    Jacques, V.; Hingant, B.; Allafort, A.; Pigeard, M.; Roch, J. F.

    2009-01-01

    In this paper, we describe two complementary nonlinear spectroscopy methods which both allow one to achieve Doppler-free spectra of atomic gases. First, saturated absorption spectroscopy is used to investigate the structure of the 5S[subscript 1/2] [right arrow] 5P[subscript 3/2] transition in rubidium. Using a slightly modified experimental…

  11. Bases for time-resolved probing of transient carrier dynamics by optical pump-probe scanning tunneling microscopy.

    Science.gov (United States)

    Yokota, Munenori; Yoshida, Shoji; Mera, Yutaka; Takeuchi, Osamu; Oigawa, Haruhiro; Shigekawa, Hidemi

    2013-10-07

    The tangled mechanism that produces optical pump-probe scanning tunneling microscopy spectra from semiconductors was analyzed by comparing model simulation data with experimental data. The nonlinearities reflected in the spectra, namely, the excitations generated by paired laser pulses with a delay time, the logarithmic relationship between carrier density and surface photovoltage (SPV), and the effect of the change in tunneling barrier height depending on SPV, were examined along with the delay-time-dependent integration process used in measurement. The optimum conditions required to realize reliable measurement, as well as the validity of the microscopy technique, were demonstrated for the first time.

  12. Technical brief: Pump-probe paradigm in an integrating cavity to study photodecomposition processes.

    Science.gov (United States)

    Gonzalez-Fernandez, Federico; Betts-Obregon, Brandi; Tsin, Andrew T; DeSa, Richard J

    2016-01-01

    flashes to be placed between scans. Exposure of the all-trans retinol to 366 nm flashes resulted in marked reduction in absorbance and a blue shift of the λmax. A white LED, despite its higher photon output, did not support all-trans retinol photolysis. Singular value decomposition (SVD) analysis revealed three spectral intermediates with mechanism, I -> II -> III. HPLC analysis of the reactants at the beginning and the conclusion of the light exposure confirmed the retinol photodecomposition. The highly reflecting cavity acts as a multipass cuvette that markedly increased the light path length and, thus, sensitivity. Triggering the LED during a dark period within the scan time allowed the actinic flashes to be interleafed between scans in a pump-probe paradigm. Furthermore, the entire sample was exposed to scan beam and actinic flashes, which is not possible in traditional spectrophotometers. Finally, the integrating cavity cuvette allowed use of turbid samples. SVD was useful for resolving spectral intermediates. Although the identity of the intermediates was not determined here, the ability to define molecular intermediates during photodecomposition reactions will allow future studies to isolate and identify the degradation products and determine the mechanism of light-induced retinoid degradation and that of retinoid-binding protein-mediated photoprotection.

  13. Retroreflecting polarization spectroscopy enabling miniaturization.

    Science.gov (United States)

    Groswasser, D; Waxman, A; Givon, M; Aviv, G; Japha, Y; Keil, M; Folman, R

    2009-09-01

    We describe and characterize alternative configurations for Doppler-free polarization spectroscopy. The suggested apparatus enables complete pump/probe beam overlap and allows substantial miniaturization. Its utility and performance for narrow linewidth, high-stability frequency locking is discussed for the /5S(1/2)F=2>-->/5P(3/2)F(')>D(2) transition in (87)Rb.

  14. "Pump-probe" atom-centered density matrix propagation studies to gauge anharmonicity and energy repartitioning in atmospheric reactive adducts: case study of the OH + isoprene and OH + butadiene reaction intermediates.

    Science.gov (United States)

    Pacheco, Alexander B; Dietrick, Scott M; Stevens, Philip S; Iyengar, Srinivasan S

    2012-04-26

    Time-resolved "pump-probe" ab initio molecular dynamics studies are constructed to probe the stability of reaction intermediates, the mechanism of energy transfer, and energy repartitioning, for moieties involved during the interaction of volatile organic compunds with hydroxyl radical. These systems are of prime importance in the atmosphere. Specifically, the stability of reaction intermediates of hydroxyl radical adducts to isoprene and butadiene molecules is used as a case study to develop novel computational techniques involving "pump-probe" ab initio molecular dynamics. Starting with the various possible hydroxyl radical adducts to isoprene and butadiene, select vibrational modes of each of the adducts are populated with excess energy to mimic the initial conditions of an experiment. The flow of energy into the remaining modes is then probed by subjecting the excited adducts to ab initio molecular dynamics simulations. It is found that the stability of the adducts arises directly due to the anhormonically driven coupling of the modes to facilitate repartitioning of the excess vibrational energy. This kind of vibrational repartitioning has a critical influence on the energy density.

  15. Construction of a magnetic bottle spectrometer and its application to pulse duration measurement of X-ray laser using a pump-probe method

    Directory of Open Access Journals (Sweden)

    S. Namba

    2015-11-01

    Full Text Available To characterize the temporal evolution of ultrashort X-ray pulses emitted by laser plasmas using a pump-probe method, a magnetic bottle time-of-flight electron spectrometer is constructed. The design is determined by numerical calculations of a mirror magnetic field and of the electron trajectory in a flight tube. The performance of the spectrometer is characterized by measuring the electron spectra of xenon atoms irradiated with a laser-driven plasma X-ray pulse. In addition, two-color above-threshold ionization (ATI experiment is conducted for measurement of the X-ray laser pulse duration, in which xenon atoms are simultaneously irradiated with an X-ray laser pump and an IR laser probe. The correlation in the intensity of the sideband spectra of the 4d inner-shell photoelectrons and in the time delay of the two laser pulses yields an X-ray pulse width of 5.7 ps, in good agreement with the value obtained using an X-ray streak camera.

  16. The influences of surface plasmons and thermal effects on femtosecond laser-induced subwavelength periodic ripples on Au film by pump-probe imaging

    Science.gov (United States)

    Zhou, Kan; Jia, Xin; Jia, Tianqing; Cheng, Ke; Cao, Kaiqiang; Zhang, Shian; Feng, Donghai; Sun, Zhenrong

    2017-03-01

    In this paper, the influences of surface plasmons and thermal effects on the formation of subwavelength periodic ripples on Au films irradiated by 800 nm femtosecond laser pulses were studied by collinear pump-probe imaging. The spatial and temporal resolutions of the experiment were 300 nm and 1 ps, respectively. No periodic ripples were observed on the Au film during ablation by the first pump pulse, but during ablation by the second pump pulse the appearance of transient ripples was evident from a delay time of hundreds of picoseconds to several nanoseconds. These ripples, however, were not retained after solidification. When the sample was immersed in water during ablation, however, the ripples were retained. It is proposed that, during the second laser pulse irradiation, the surface defects produced by the first pulse induced surface plasmon polaritons on the Au film, which caused a modulated energy deposition and the formation of transient ripples. The weak electron-phonon coupling and significant residual heat erase these ripples after the molten surface was solidified.

  17. Analysis of femtosecond laser ionization/dissociation of polyatomic molecule C6H10O form one-colour pump-probe measurement

    Institute of Scientific and Technical Information of China (English)

    Hu Fei-Fei; Zhou Sheng-Peng; Hu Zhan; Jin Ming-Xing; Zhang Dong-Dong; Wu Di; Cheng Xi-Hui; Jiang Dian-Wu; Diug Da-Jun

    2009-01-01

    This paper reports that a one-colour fs pump-probe measurement has been carried out for studying photoionization/photodissociation of cyclohexanone(CsH10O)in intense laser field.Two of the fragments from cyclohcxanone,C2H+3 and C3H+3,are studied under 800 nm laser pump-probe and the results obtained show similar time evolutions.It proposes a feasible model for analysing the experimental observations of the one-colour fs pump-probe measurement.The results demonstrate that as an intermediate product,the excited molecular parent ions play a very important role in photionization/photodissociation processes in intense laser field.

  18. Hadron spectroscopy in double pomeron exchange experiments

    Science.gov (United States)

    Albrow, Michael G.

    2017-03-01

    Central exclusive production in hadron-hadron collisions at high energies, for example p + p → p + X + p, where the + represents a large rapidity gap, is a valuable process for spectroscopy of mesonic states X. At collider energies the gaps can be large enough to be dominated by pomeron exchange, and then the quantum numbers of the state X are restricted. Isoscalar JPC = 0++ and 2++ mesons are selected, and our understanding of these spectra is incomplete. In particular, soft pomeron exchanges favor gluon-dominated states such as glueballs, which are expected in QCD but not yet well established. I will review some published data.

  19. Hadron Spectroscopy in Double Pomeron Exchange Experiments

    Energy Technology Data Exchange (ETDEWEB)

    Albrow, Michael [Fermilab

    2016-11-15

    Central exclusive production in hadron-hadron collisions at high energies, for example p + p -> p + X + p, where the "+" represents a large rapidity gap, is a valuable process for spectroscopy of mesonic states X. At collider energies the gaps can be large enough to be dominated by pomeron exchange, and then the quantum numbers of the state X are restricted. Isoscalar JPC = 0++ and 2++ mesons are selected, and our understanding of these spectra is incomplete. In particular, soft pomeron exchanges favor gluon-dominated states such as glueballs, which are expected in QCD but not yet well established. I will review some published data.

  20. Pump-probe reflectivity study of ultrafast dynamics of strongly correlated 5f electrons inUO2

    Energy Technology Data Exchange (ETDEWEB)

    Au, Yongqiang Q [Los Alamos National Laboratory; Taylor, Antoinette J [Los Alamos National Laboratory; Durakiewicz, Tomasz [Los Alamos National Laboratory; Rodriguez, George [Los Alamos National Laboratory

    2010-01-01

    5f electrons in the Mott insulator UO{sub 2} produce intriguing electronic states and dynamics, such as strong correlation and f-f excitations. We have performed femtosecond pump-probe reflectivity measurements on a single crystal UO{sub 2} at temperatures 5-300 K to study the ultrafast dynamics of photoexcited 5f electrons. The laser pulses at 400 nm pump 5 f electrons across the Mott gap, while those at 800 nm probe the pump-induced change of reflectivity. We find temperature-dependent excitation and relaxation processes and long-lived acoustic phonons, and extract picosecond risetimes and microsecond relaxation times at low temperatures. The observed slow relaxation is ascribed to the decay of Hubbard excitons formed by U{sup 3+}-U{sup 5+} pairs.

  1. Fabry-perot modes enhanced pump-probe coupling in gold micro-disk patterned ruby thin film

    Science.gov (United States)

    Kumari, Satchi; Khare, Alika; Gupta, Reema; Tomar, Monika; Gupta, Vinay

    2017-10-01

    Enhanced pump-probe coupling has been experimentally observed in epitaxial Ruby thin film patterned with equidistant gold micro-disks (∼100 μm), as compared to pure Ruby film. This has been attributed to Fabry-Perot and surface plasmon modes in Ruby/gold film. In case of S polarized pump and probe beam, Fabry-Perot modes leads to a two-wave mixing gain of ∼1.35. Moreover gain was ∼1.62 in P-polarization case, it has been attributed to coupling of Fabry-Perot and surface plasmon modes. Enhanced coupling for P-polarization can lead to improved nonlinear response in the thin film geometry. It can find applications in thin film based compact photonic devices.

  2. Pump-probe imaging of the fs-ps-ns dynamics during femtosecond laser Bessel beam drilling in PMMA.

    Science.gov (United States)

    Yu, Yanwu; Jiang, Lan; Cao, Qiang; Xia, Bo; Wang, Qingsong; Lu, Yongfeng

    2015-12-14

    A pump-probe shadowgraph imaging technique was used to reveal the femtosecond-picosecond-nanosecond multitimescale fundamentals of high-quality, high-aspect-ratio (up to 287:1) microhole drilling in poly-methyl-meth-acrylate (PMMA) by a single-shot femtosecond laser Bessel beam. The propagation of Bessel beam in PMMA (at 1.98 × 10⁸ m/s) and it induced cylindrical pressure wave expansion (at 3000-3950 m/s in radius) were observed during drilling processes. Also, it was unexpectedly found that the expansion of the cylindrical pressure wave in PMMA showed a linear relation with time and was insensitive to the laser energy fluctuation, quite different from the case in air. It was assumed that the energy insensitivity was due to the anisotropy of wave expansion in PMMA and the ambient air.

  3. Observation of femtosecond X-ray interactions with matter using an X-ray-X-ray pump-probe scheme.

    Science.gov (United States)

    Inoue, Ichiro; Inubushi, Yuichi; Sato, Takahiro; Tono, Kensuke; Katayama, Tetsuo; Kameshima, Takashi; Ogawa, Kanade; Togashi, Tadashi; Owada, Shigeki; Amemiya, Yoshiyuki; Tanaka, Takashi; Hara, Toru; Yabashi, Makina

    2016-02-01

    Resolution in the X-ray structure determination of noncrystalline samples has been limited to several tens of nanometers, because deep X-ray irradiation required for enhanced resolution causes radiation damage to samples. However, theoretical studies predict that the femtosecond (fs) durations of X-ray free-electron laser (XFEL) pulses make it possible to record scattering signals before the initiation of X-ray damage processes; thus, an ultraintense X-ray beam can be used beyond the conventional limit of radiation dose. Here, we verify this scenario by directly observing femtosecond X-ray damage processes in diamond irradiated with extraordinarily intense (∼10(19) W/cm(2)) XFEL pulses. An X-ray pump-probe diffraction scheme was developed in this study; tightly focused double-5-fs XFEL pulses with time separations ranging from sub-fs to 80 fs were used to excite (i.e., pump) the diamond and characterize (i.e., probe) the temporal changes of the crystalline structures through Bragg reflection. It was found that the pump and probe diffraction intensities remain almost constant for shorter time separations of the double pulse, whereas the probe diffraction intensities decreased after 20 fs following pump pulse irradiation due to the X-ray-induced atomic displacement. This result indicates that sub-10-fs XFEL pulses enable conductions of damageless structural determinations and supports the validity of the theoretical predictions of ultraintense X-ray-matter interactions. The X-ray pump-probe scheme demonstrated here would be effective for understanding ultraintense X-ray-matter interactions, which will greatly stimulate advanced XFEL applications, such as atomic structure determination of a single molecule and generation of exotic matters with high energy densities.

  4. "FluSpec": A Simulated Experiment in Fluorescence Spectroscopy

    Science.gov (United States)

    Bigger, Stephen W.; Bigger, Andrew S.; Ghiggino, Kenneth P.

    2014-01-01

    The "FluSpec" educational software package is a fully contained tutorial on the technique of fluorescence spectroscopy as well as a simulator on which experiments can be performed. The procedure for each of the experiments is also contained within the package along with example analyses of results that are obtained using the software.

  5. "FluSpec": A Simulated Experiment in Fluorescence Spectroscopy

    Science.gov (United States)

    Bigger, Stephen W.; Bigger, Andrew S.; Ghiggino, Kenneth P.

    2014-01-01

    The "FluSpec" educational software package is a fully contained tutorial on the technique of fluorescence spectroscopy as well as a simulator on which experiments can be performed. The procedure for each of the experiments is also contained within the package along with example analyses of results that are obtained using the software.

  6. The pump-probe coupling of matter wave packets to remote lattice states

    DEFF Research Database (Denmark)

    Sherson, Jacob F; Park, Sung Jong; Pedersen, Poul Lindholm;

    2012-01-01

    containing a Bose–Einstein condensate. The evolution of these wave packets is monitored in situ and their six-photon reflection at a band gap is observed. In direct analogy with pump–probe spectroscopy, a probe pulse allows for the resonant de-excitation of the wave packet into states localized around...

  7. Exciton Dynamics in LH1 and LH2 of Rhodopseudomonas Acidophila and Rhodobium Marinum Probed with Accumulated Photon Echo and Pump-Probe Measurements

    NARCIS (Netherlands)

    Lampoura, Stefania S.; Grondelle, Rienk van; Stokkum, Ivo H.M. van; Cogdell, Richard J.; Wiersma, Douwe A.; Duppen, Koos; van Stokkum, I.H.N.

    2000-01-01

    Exciton dynamics in the B850 and B875 bands of isolated complexes of Rhodopseudomonas acidophila (strain 10050 and 7050) and in the B875 band of isolated complexes of Rhodobium marinum were investigated by means of accumulated photon echo and pump-probe techniques at different temperatures and wavel

  8. A Dual-Colour Architecture for Pump-Probe Spectroscopy of Ultrafast Magnetization Dynamics in the Sub-10-femtosecond Range

    Science.gov (United States)

    Gonçalves, C. S.; Silva, A. S.; Navas, D.; Miranda, M.; Silva, F.; Crespo, H.; Schmool, D. S.

    2016-03-01

    Current time-resolution-limited dynamic measurements clearly show the need for improved techniques to access processes on the sub-10-femtosecond timescale. To access this regime, we have designed and constructed a state-of-the-art time-resolved magneto-optic Kerr effect apparatus, based on a new dual-color scheme, for the measurement of ultrafast demagnetization and precessional dynamics in magnetic materials. This system can operate well below the current temporal ranges reported in the literature, which typically lie in the region of around 50 fs and above. We have used a dual-colour scheme, based on ultra broadband hollow-core fibre and chirped mirror pulse compression techniques, to obtain unprecedented sub-8-fs pump and probe pulse durations at the sample plane. To demonstrate the capabilities of this system for ultrafast demagnetization and precessional dynamics studies, we have performed measurements in a ferrimagnetic GdFeCo thin film. Our study has shown that the magnetization shows a sudden drop within the first picosecond after the pump pulse, a fast recovery (remagnetization) within a few picoseconds, followed by a clear oscillation or precession during a slower magnetization recovery. Moreover, we have experimentally confirmed for the first time that a sub-10-fs pulse is able to efficiently excite a magnetic system such as GdFeCo.

  9. Structural dynamics of nitrosylruthenium isomeric complexes studied with steady-state and transient pump-probe infrared spectroscopies

    Science.gov (United States)

    Zhao, Yan; Yang, Fan; Wang, Jianru; Yu, Pengyun; Pan, Huifen; Wang, Hongfei; Wang, Jianping

    2016-09-01

    The characteristic nitrosyl stretching (NO) in the region of 1800-1900 cm- 1 was used to study the geometric and ligand effect on two nitrosylruthenium complexes, namely [Ru(OAc)(2QN)2NO] (QN = 2-chloro-8-quinolinol (H2cqn) or QN = 2-methyl-8-quinolinol (H2mqn)). The NO stretching frequency (νNO) was found in the following order: νcis-1 (2cqn) > νcis-2 (2cqn) > νcis-1 (2mqn) > νtrans (2mqn). The results exhibited a spectral sensitivity of the NO mode to both charge distribution and ligand arrangement, which was supported by ab initio computations and natural bond orbital (NBO) analyses. Further, the vibrational population of the vibrationally excited NO stretching mode was found to relax on the order of 7-10 ps, showing less than 30% variation from one isomer to another, which were explained on the basis of NO local structures and solute-solvent interactions in these isomeric nitrosylruthenium complexes.

  10. Tracing molecular dynamics at the femto-/atto-second boundary through extreme-ultraviolet pump-probe spectroscopy

    CERN Document Server

    Carpeggiani, P A; Palacios, A; Gray, D; Martín, F; Charalambidis, D

    2013-01-01

    Coherent light pulses of few to hundreds of femtoseconds (fs) duration have prolifically served the field of ultrafast phenomena. While fs pulses address mainly dynamics of nuclear motion in molecules or lattices in the gas, liquid or condensed matter phase, the advent of attosecond pulses has in recent years provided direct experimental access to ultrafast electron dynamics. However, there are processes involving nuclear motion in molecules and in particular coupled electronic and nuclear motion that possess few fs or even sub-fs dynamics. In the present work we have succeeded in addressing simultaneously vibrational and electronic dynamics in molecular Hydrogen. Utilizing a broadband extreme-ultraviolet (XUV) continuum the entire, Frank-Condon allowed spectrum of H2 is coherently excited. Vibrational, electronic and ionization 1fs scale dynamics are subsequently tracked by means of XUV-pump-XUV-probe measurements. These reflect the intrinsic molecular behavior as the XUV probe pulse hardly distorts the mole...

  11. Femtosecond pump probe spectroscopy for the study of energy transfer of light-harvesting complexes from extractions of spinach leaves

    CSIR Research Space (South Africa)

    Ombinda-Lemboumba, Saturnin

    2009-09-01

    Full Text Available :sapphire femtosecond oscillator (Coherent Mira 900-F), operating at a repetition rate of 76 MHz and pumped by the 5 W output of a continuous diode-pumped Nd:YVO4 laser (Coherent Verdi V5), produced pulses of approximately 130 fs duration, as measured by a home...

  12. Electron spectroscopy of carbon materials: experiment and theory

    Energy Technology Data Exchange (ETDEWEB)

    El-Barbary, A A [University of Sussex, School of Life Sciences, Falmer, Brighton, BN1 9QJ (United Kingdom); University of Ain-Shams, Faculty of Education, Department of Physics, Cairo (Egypt); Trasobares, S [Laboratoire de physique des Solides Batiment 510, Universite Paris Sud 91405, Orsay (France); Departamento de Ciencia de los Materiales Ingenieria Metalurgica Quimica Inorganica, Universidad de Cadiz, Apdo 40 Puerto Real, 11510-Cadiz (Spain); Ewels, C P [University of Sussex, School of Life Sciences, Falmer, Brighton, BN1 9QJ (United Kingdom); Stephan, O [Laboratoire de physique des Solides Batiment 510, Universite Paris Sud 91405, Orsay (France); Okotrub, A V [Nikolaev Institute of Inorganic Chemistry SB RAS, pr. Ak. Lavrentieva 3 (Russian Federation); Bulusheva, L G [Nikolaev Institute of Inorganic Chemistry SB RAS, pr. Ak. Lavrentieva 3 (Russian Federation); Fall, C J [ELCA Informatique SA, Avenue de la Harpe 22-24, CH-1000 Lausanne 13 (Switzerland); Heggie, M I [University of Sussex, School of Life Sciences, Falmer, Brighton, BN1 9QJ (United Kingdom)

    2006-02-22

    We present a comparative spectroscopic study of carbon as graphite, diamond and C{sub 60} using C1s K-edge electron energy-loss spectroscopy (EELS), X-ray emission spectroscopy, and theoretical modelling. The first principles calculations of these spectra are obtained in the local density approximation using a self-consistent Gaussian basis pseudo-potential method. Calculated spectra show excellent agreement with experiment and are able to discriminate not only between various carbon hybridisations but also local variation in environment. Core-hole effects on the calculated spectra are also investigated. For the first time, the EEL spectrum of carbyne is calculated.

  13. Ultrafast pump-probe microscopy reveals the mechanism of selective fs laser structuring of transparent thin films for maskless micropatterning

    Science.gov (United States)

    Rapp, Stephan; Rosenberger, Janosch; Domke, Matthias; Heise, Gerhard; Huber, Heinz P.; Schmidt, Michael

    2014-01-01

    Maskless patterning of biocompatible Ta2O5/Pt/glass sensor chips can be realized by ultra-short laser pulse ablation. At a fluence of 0.2 J/cm2, the thin Ta2O5 film is selectively lifted-off by indirectly-induced ablation at laser wavelenghts where the Ta2O5 is transparent and the Pt absorbing. This enables precise and very fast structuring. Here, 660 fs laser pulses at a center wavelength of 1053 nm are applied. The driving physical effects of this ablation mechanism are revealed by pump-probe microscopy. This technique allows the observation of the whole ablation process ranging temporally from femtoseconds to microseconds. An ultrafast heat-expansion in the absorbing Pt, initiating a shock-wave to the Ta2O5 within the first 10 ps, bulges the Ta2O5 film after some nanoseconds. Bulging velocities of 750 m/s are determined corresponding to an extreme acceleration of about 1010 g. Exceeding the stress limit in the Ta2O5 causes film disintegration after 50 ns. A model, describing essential reaction steps, is developed. This model is also applicable to other industrial important layer systems, where thin transparent films have to be removed.

  14. Mapping and controlling ultrafast dynamics of highly excited H2 molecules by VUV-IR pump-probe schemes

    Science.gov (United States)

    Sturm, F. P.; Tong, X. M.; Palacios, A.; Wright, T. W.; Zalyubovskaya, I.; Ray, D.; Shivaram, N.; Martín, F.; Belkacem, A.; Ranitovic, P.; Weber, Th.

    2017-01-01

    We used ultrashort femtosecond vacuum ultraviolet (VUV) and infrared (IR) pulses in a pump-probe scheme to map the dynamics and nonequilibrium dissociation channels of excited neutral H2 molecules. A nuclear wave packet is created in the B Σ+1u state of the neutral H2 molecule by absorption of the ninth harmonic of the driving infrared laser field. Due to the large stretching amplitude of the molecule excited in the B Σ+1u electronic state, the effective H2+ ionization potential changes significantly as the nuclear wave packet vibrates in the bound, highly electronically and vibrationally excited B potential-energy curve. We probed such dynamics by ionizing the excited neutral molecule using time-delayed VUV-or-IR radiation. We identified the nonequilibrium dissociation channels by utilizing three-dimensional momentum imaging of the ion fragments. We found that different dissociation channels can be controlled, to some extent, by changing the IR laser intensity and by choosing the wavelength of the probe laser light. Furthermore, we concluded that even in a benchmark molecular system such as H2*, the interpretation of the nonequilibrium multiphoton and multicolor ionization processes is still a challenging task, requiring intricate theoretical analysis.

  15. Ultrafast spectroscopy of quasiparticle dynamics in cuprate superconductors

    Energy Technology Data Exchange (ETDEWEB)

    Li, Wei [National Laboratory of Solid State Microstructures and Department of Physics, Nanjing University, Nanjing 210093 (China); Zhang, Chunfeng, E-mail: cfzhang@nju.edu.cn [National Laboratory of Solid State Microstructures and Department of Physics, Nanjing University, Nanjing 210093 (China); Wang, Xiaoyong [National Laboratory of Solid State Microstructures and Department of Physics, Nanjing University, Nanjing 210093 (China); Chakhalian, Jak, E-mail: jchakhal@uark.edu [Department of Physics, University of Arkansas, Fayetteville, AR 72701 (United States); Xiao, Min, E-mail: mxiao@uark.edu [National Laboratory of Solid State Microstructures and Department of Physics, Nanjing University, Nanjing 210093 (China); Department of Physics, University of Arkansas, Fayetteville, AR 72701 (United States)

    2015-02-15

    Ultrafast pump-probe spectroscopy is a powerful tool to study the nonequilibrium dynamics in high-Tc cuprate superconductors. The photo-induced quasiparticle (QP) dynamics revealed by pump-probe spectroscopy are sensitive to the near-Fermi level electronic structures. Here we review several selected examples to illustrate the enduring challenges including pairing glue, phase separation, and phase transitions in cuprate superconductors. We also present the data obtained on thin films of YBa{sub 2}Cu{sub 3}O{sub 7−δ} in connection to these issues. - Highlights: • This paper reviews recent ultrafast spectroscopic study on cuprates. • Dynamics related to pairing glues and phase separations are summarized. • Mid-IR pulses enhance the coherent transport in underdoped cuprates. • Pump-probe data on the quasiparticle dynamics in YBCO films are presented.

  16. Analysis Tools for Next-Generation Hadron Spectroscopy Experiments

    CERN Document Server

    Battaglieri, M; Celentano, A; Chung, S -U; D'Angelo, A; De Vita, R; Döring, M; Dudek, J; Eidelman, S; Fegan, S; Ferretti, J; Fox, G; Galata, G; Garcia-Tecocoatzi, H; Glazier, D I; Grube, B; Hanhart, C; Hoferichter, M; Hughes, S M; Ireland, D G; Ketzer, B; Klein, F J; Kubis, B; Liu, B; Masjuan, P; Mathieu, V; McKinnon, B; Mitchell, R; Nerling, F; Paul, S; Pelaez, J R; Rademacker, J; Rizzo, A; Salgado, C; Santopinto, E; Sarantsev, A V; Sato, T; Schlüter, T; da Silva, M L L; Stankovic, I; Strakovsky, I; Szczepaniak, A; Vassallo, A; Walford, N K; Watts, D P; Zana, L

    2014-01-01

    The series of workshops on New Partial-Wave Analysis Tools for Next-Generation Hadron Spectroscopy Experiments was initiated with the ATHOS 2012 meeting, which took place in Camogli, Italy, June 20-22, 2012. It was followed by ATHOS 2013 in Kloster Seeon near Munich, Germany, May 21-24, 2013. The third, ATHOS3, meeting is planned for April 13-17, 2015 at The George Washington University Virginia Science and Technology Campus, USA. The workshops focus on the development of amplitude analysis tools for meson and baryon spectroscopy, and complement other programs in hadron spectroscopy organized in the recent past including the INT-JLab Workshop on Hadron Spectroscopy in Seattle in 2009, the International Workshop on Amplitude Analysis in Hadron Spectroscopy at the ECT*-Trento in 2011, the School on Amplitude Analysis in Modern Physics in Bad Honnef in 2011, the Jefferson Lab Advanced Study Institute Summer School in 2012, and the School on Concepts of Modern Amplitude Analysis Techniques in Flecken-Zechlin near...

  17. Simulation of force spectroscopy experiments on galacturonic acid oligomers.

    Directory of Open Access Journals (Sweden)

    Justyna Cybulska

    Full Text Available Pectins, forming a matrix for cellulose and hemicellulose, determine the mechanics of plant cell walls. They undergo salient structural changes during their development. In the presence of divalent cations, usually calcium, pectins can form gel-like structures. Because of their importance they have been the subject of many force spectroscopy experiments, which have examined the conformational changes and molecular tensions due to external forces. The most abundant unit present in the pectin backbone is polygalacturonic acid. Unfortunately, experimental force spectroscopy on polygalacturonic acid molecules is still not a trivial task. The mechanism of the single-molecule response to external forces can be inferred by theoretical methods. Therefore, in this work we simulated such force spectroscopy experiments using the Enforced Geometry Optimization (EGO method. We examined the oligomeric (up to hexamer structures of α-D-galacturonic acid exposed to external stretching forces. The EGO simulation of the force spectroscopy appropriately reproduced the experimental course of the enforced conformational transition: chair →inverted chair via the twisted boat conformation(s in the pyranose ring of α-D-galacturonic acid. Additionally, our theoretical approach also allowed to determine the minimum oligomer size adequate for the description of nano-mechanical properties of (poly-α-D-galacturonic acid.

  18. Simulation of force spectroscopy experiments on galacturonic acid oligomers.

    Science.gov (United States)

    Cybulska, Justyna; Brzyska, Agnieszka; Zdunek, Artur; Woliński, Krzysztof

    2014-01-01

    Pectins, forming a matrix for cellulose and hemicellulose, determine the mechanics of plant cell walls. They undergo salient structural changes during their development. In the presence of divalent cations, usually calcium, pectins can form gel-like structures. Because of their importance they have been the subject of many force spectroscopy experiments, which have examined the conformational changes and molecular tensions due to external forces. The most abundant unit present in the pectin backbone is polygalacturonic acid. Unfortunately, experimental force spectroscopy on polygalacturonic acid molecules is still not a trivial task. The mechanism of the single-molecule response to external forces can be inferred by theoretical methods. Therefore, in this work we simulated such force spectroscopy experiments using the Enforced Geometry Optimization (EGO) method. We examined the oligomeric (up to hexamer) structures of α-D-galacturonic acid exposed to external stretching forces. The EGO simulation of the force spectroscopy appropriately reproduced the experimental course of the enforced conformational transition: chair →inverted chair via the twisted boat conformation(s) in the pyranose ring of α-D-galacturonic acid. Additionally, our theoretical approach also allowed to determine the minimum oligomer size adequate for the description of nano-mechanical properties of (poly)-α-D-galacturonic acid.

  19. Calculations of Nonlinear Wave-Packet Interferometry Signals in the Pump-Probe Limit as Tests for Vibrational Control over Electronic Excitation Transfer

    CERN Document Server

    Biggs, Jason D

    2009-01-01

    The preceding paper describes a strategy for externally influencing the course of short-time electronic excitation transfer (EET) in molecular dimers and observing the process by nonlinear wave-packet interferometry (nl-WPI). Within a sample of isotropically oriented dimers having a specified internal geometry, a vibrational mode internal to the acceptor chromophore can be preferentially driven by electronically nonresonant impulsive stimulated Raman (or resonant infrared) excitation with a short polarized control pulse. A subsequent electronically resonant polarized pump then preferentially excites the donor, and EET ensues. Here we test both the control strategy and its spectroscopic investigation-with some sacrifice of amplitude-level detail-by calculating the pump-probe difference signal. That signal is the limiting case of the control-influenced nl-WPI signal in which the two pulses in the pump pulse-pair coincide, as do the two pulses in the probe pulse-pair. We present calculated pump-probe difference ...

  20. Electron spin dynamics of Ce3 + ions in YAG crystals studied by pulse-EPR and pump-probe Faraday rotation

    Science.gov (United States)

    Azamat, D. V.; Belykh, V. V.; Yakovlev, D. R.; Fobbe, F.; Feng, D. H.; Evers, E.; Jastrabik, L.; Dejneka, A.; Bayer, M.

    2017-08-01

    The spin relaxation dynamics of Ce3 + ions in heavily cerium-doped YAG crystals is studied using pulse-electron paramagnetic resonance and time-resolved pump-probe Faraday rotation. Both techniques address the 4 f ground state, while pump-probe Faraday rotation also provides access to the excited 5 d state. We measure a millisecond spin-lattice relaxation time T1, a microsecond spin coherence time T2, and a ˜10 ns inhomogeneous spin dephasing time T2* for the Ce3 + ground state at low temperatures. The spin-lattice relaxation of Ce3 + ions is due to modified Raman processes involving the optical phonon mode at ˜125 cm-1 . The relaxation at higher temperature goes through a first excited level of the 5/2 2F term at about ℏ ω ≈228 cm-1 . Effects provided by the hyperfine interaction of the Ce3 + with the 27Al nuclei are observed.

  1. Nodal Quasiparticle Meltdown in Ultra-High Resolution Pump-Probe Angle-Resolved Photoemission

    Energy Technology Data Exchange (ETDEWEB)

    Graf, Jeff; Jozwiak, Chris; Smallwood, Chris L.; Eisaki, H.; Kaindl, Robert A.; Lee, Dung-Hai; Lanzara, Alessandra

    2011-06-03

    High-T{sub c} cuprate superconductors are characterized by a strong momentum-dependent anisotropy between the low energy excitations along the Brillouin zone diagonal (nodal direction) and those along the Brillouin zone face (antinodal direction). Most obvious is the d-wave superconducting gap, with the largest magnitude found in the antinodal direction and no gap in the nodal direction. Additionally, while antin- odal quasiparticle excitations appear only below T{sub c}, superconductivity is thought to be indifferent to nodal excitations as they are regarded robust and insensitive to T{sub c}. Here we reveal an unexpected tie between nodal quasiparticles and superconductivity using high resolution time- and angle-resolved photoemission on optimally doped Bi{sub 2}Sr{sub 2}CaCu{sub 2}O{sub 8+{delta}} . We observe a suppression of the nodal quasiparticle spectral weight following pump laser excitation and measure its recovery dynamics. This suppression is dramatically enhanced in the superconducting state. These results reduce the nodal-antinodal dichotomy and challenge the conventional view of nodal excitation neutrality in superconductivity. The electronic structures of high-Tc cuprates are strongly momentum-dependent. This is one reason why the momentum-resolved technique of angle-resolved photoemission spectroscopy (ARPES) has been a central tool in the field of high-temperature superconductivity. For example, coherent low energy excitations with momenta near the Brillouin zone face, or antinodal quasiparticles (QPs), are only observed below T{sub c} and have been linked to superfluid density. They have therefore been the primary focus of ARPES studies. In contrast, nodal QPs, with momenta along the Brillouin zone diagonal, have received less attention and are usually regarded as largely immune to the superconducting transition because they seem insensitive to perturbations such as disorder, doping, isotope exchange, charge ordering, and temperature. Clearly

  2. Nodal Quasiparticle Meltdown in Ultra-High Resolution Pump-Probe Angle-Resolved Photoemission

    Energy Technology Data Exchange (ETDEWEB)

    Graf, Jeff; Jozwiak, Chris; Smallwood, Chris L.; Eisaki, H.; Kaindl, Robert A.; Lee, Dung-Hai; Lanzara, Alessandra

    2011-06-03

    High-T{sub c} cuprate superconductors are characterized by a strong momentum-dependent anisotropy between the low energy excitations along the Brillouin zone diagonal (nodal direction) and those along the Brillouin zone face (antinodal direction). Most obvious is the d-wave superconducting gap, with the largest magnitude found in the antinodal direction and no gap in the nodal direction. Additionally, while antin- odal quasiparticle excitations appear only below T{sub c}, superconductivity is thought to be indifferent to nodal excitations as they are regarded robust and insensitive to T{sub c}. Here we reveal an unexpected tie between nodal quasiparticles and superconductivity using high resolution time- and angle-resolved photoemission on optimally doped Bi{sub 2}Sr{sub 2}CaCu{sub 2}O{sub 8+{delta}} . We observe a suppression of the nodal quasiparticle spectral weight following pump laser excitation and measure its recovery dynamics. This suppression is dramatically enhanced in the superconducting state. These results reduce the nodal-antinodal dichotomy and challenge the conventional view of nodal excitation neutrality in superconductivity. The electronic structures of high-Tc cuprates are strongly momentum-dependent. This is one reason why the momentum-resolved technique of angle-resolved photoemission spectroscopy (ARPES) has been a central tool in the field of high-temperature superconductivity. For example, coherent low energy excitations with momenta near the Brillouin zone face, or antinodal quasiparticles (QPs), are only observed below T{sub c} and have been linked to superfluid density. They have therefore been the primary focus of ARPES studies. In contrast, nodal QPs, with momenta along the Brillouin zone diagonal, have received less attention and are usually regarded as largely immune to the superconducting transition because they seem insensitive to perturbations such as disorder, doping, isotope exchange, charge ordering, and temperature. Clearly

  3. Two-wavelength pump-probe technique using single distributed feedback laser array to probe gain recovery of an erbium-doped fiber amplifier

    Science.gov (United States)

    Kuroda, Keiji; Yoshikuni, Yuzo

    2017-03-01

    We propose a two-wavelength pump-probe technique to probe the gain recovery characteristics of an erbium-doped fiber amplifier. The two-wavelength pulse pairs are generated through the direct modulation of a single distributed feedback laser array. The proposed technique allows us to measure the wavelength dependence of the recovery time after gain saturation is induced by a signal of the same wavelength.

  4. Accessing thermo-mechanical properties of semiconductors using a pump-probe surface displacement method

    Science.gov (United States)

    González-Borrero, P. P.; Lukasievicz, G. V. B.; Zanuto, V. S.; Astrath, N. G. C.; Malacarne, L. C.

    2017-05-01

    Description of the physical mechanism leading to laser induced thermal and electronic effects in semiconductors is crucial in both basic research and technological applications. In this paper, we present a thermal mirror technique to study the thermo-mechanical properties of semiconductors. A detailed theoretical investigation is presented, and the dominant effects are described in terms of the physical properties of the material. The effect of heat coupling between the sample and the surrounding fluid was taken into account and considerations on the time and spatial approximations to the photogenerated carriers profile were used to simplify the theoretical model. These approximations were then compared to numerical models and the results hold for high recombination rate semiconductors. Experiments were performed to validate the theoretical model, and the thermal diffusivity and photogenerated heat in the sample were determined. The values obtained for these properties were found to be in good agreement with literature.

  5. Validity Using Pump-Probe Pulses to Determine the Optical Response of Niobate Crystals

    Science.gov (United States)

    Liu, Huimin; Jia, Weiyi

    1997-01-01

    A variety of niobate crystals have found their places in nonlinear optical applications as well as in laser devices. In recent years much attention has been paid to study the ultrafast optical response in a variety of photorefractive crystals such as KTa(1-x)Nb(x)O3 and KNbO3 crystals, glasses, semiconductors and polymers for applications in optical switching, information processing, optical computing, and all-optical device systems. Third-order optical nonlinearity is the most important property for realization of all-optical switching. Therefore experiments have been performed on the third order susceptibility using a variety of techniques such as the third-order harmonic generation, EFISH and degenerate four-wave mixing(DFWM). The latter has been conducted with a variety of pump wavelengths and with nanosecond, picosecond and femtosecond pulses. Niobate crystals, such as potassium niobate KNbO3, potassium tantalate niobate KTN family (KTa(1-x)Nb(x)O3), strontium barium niobate SBN (Sr(x)Ba(1-x)Nb2O6) and potassium-sodium niobate SBN (KNSBN) are attractive due to their photorefractive properties for application in optical storage and processing. The pulsed probe experiments performed on theses materials have suggested two types of time responses. These responses have been associated with an coherent response due to Chi(sup 3), and a long lived component due to excited state population. Recent study of DFWM on KNbO3 and KTN family reveals that the long lived component of those crystals depends on the crystal orientation. A slowly decaying signal is observable when the grating vector K(sub g) is not perpendicular to the C-axis of those photorefractive crystals', otherwise the optical response signal would be only a narrow coherent peak with FWHM equal to the cross-correlation width of the write beam pulses. Based on this understanding, we study the photodynamical process of a variety of niobate crystals using DFWM in a Kg perpindicular to C geometry with a ps

  6. Baryon Spectroscopy - Recent Results from the CBELSA/TAPS Experiment

    CERN Document Server

    Hartmann, Jan

    2016-01-01

    One of the remaining challenges within the standard model is to gain a good understanding of QCD in the non-perturbative regime. One key step toward this aim is baryon spectroscopy, investigating the spectrum and the properties of baryon resonances. To get access to resonances with small $\\pi N$ partial width, photoproduction experiments provide essential information. In order to extract the contributing resonances, partial wave analyses need to be performed. Here, a complete experiment is required to unambiguously determine the contributing amplitudes. This involves the measurement of carefully chosen single and double polarization observables. The CBELSA/TAPS experiment with a longitudinally or transversely polarized target and an energy tagged, linearly or circularly polarized photon beam allows the measurement of a large set of polarization observables. Due to its good energy resolution, high detection efficiency for photons, and the nearly complete solid angle coverage it is ideally suited for the measur...

  7. Two-colour pump-probe experiments with a twin-pulse-seed extreme ultraviolet free-electron laser.

    Science.gov (United States)

    Allaria, E; Bencivenga, F; Borghes, R; Capotondi, F; Castronovo, D; Charalambous, P; Cinquegrana, P; Danailov, M B; De Ninno, G; Demidovich, A; Di Mitri, S; Diviacco, B; Fausti, D; Fawley, W M; Ferrari, E; Froehlich, L; Gauthier, D; Gessini, A; Giannessi, L; Ivanov, R; Kiskinova, M; Kurdi, G; Mahieu, B; Mahne, N; Nikolov, I; Masciovecchio, C; Pedersoli, E; Penco, G; Raimondi, L; Serpico, C; Sigalotti, P; Spampinati, S; Spezzani, C; Svetina, C; Trovò, M; Zangrando, M

    2013-01-01

    Exploring the dynamics of matter driven to extreme non-equilibrium states by an intense ultrashort X-ray pulse is becoming reality, thanks to the advent of free-electron laser technology that allows development of different schemes for probing the response at variable time delay with a second pulse. Here we report the generation of two-colour extreme ultraviolet pulses of controlled wavelengths, intensity and timing by seeding of high-gain harmonic generation free-electron laser with multiple independent laser pulses. The potential of this new scheme is demonstrated by the time evolution of a titanium-grating diffraction pattern, tuning the two coherent pulses to the titanium M-resonance and varying their intensities. This reveals that an intense pulse induces abrupt pattern changes on a time scale shorter than hydrodynamic expansion and ablation. This result exemplifies the essential capabilities of the jitter-free multiple-colour free-electron laser pulse sequences to study evolving states of matter with element sensitivity.

  8. Multidimensional X-Ray Spectroscopy of Valence and Core Excitations in Cysteine

    CERN Document Server

    Biggs, Jason D; Healion, Daniel; Mukamel, Shaul

    2013-01-01

    Several nonlinear spectroscopy experiments which employ broadband x-ray pulses to probe the coupling between localized core and delocalized valence excitation are simulated for the amino acid cysteine at the K-edges of oxygen and nitrogen and the K and L-edges of sulfur. We focus on two dimensional (2D) and 3D signals generated by two- and three-pulse stimulated x-ray Raman spectroscopy (SXRS) with frequency-dispersed probe. We show how the four-pulse x-ray signals $\\boldsymbol{k}_\\mathrm{I}=-\\boldsymbol{k}_1+\\boldsymbol{k}_2+\\boldsymbol{k}_3$ and $\\boldsymbol{k}_\\mathrm{II}=\\boldsymbol{k}_1-\\boldsymbol{k}_2+\\boldsymbol{k}_3$ can give new 3D insight into the SXRS signals. The coupling between valence- and core-excited states can be visualized in three dimensional plots, revealing the origin of the polarizability that controls the simpler pump-probe SXRS signals.

  9. Dynamic force spectroscopy on multiple bonds: experiments and model

    CERN Document Server

    Erdmann, T; Nassoy, P; Schwarz, U S

    2007-01-01

    We probe the dynamic strength of multiple biotin-streptavidin adhesion bonds under linear loading using the biomembrane force probe setup for dynamic force spectroscopy. Measured rupture force histograms are compared to results from a master equation model for the stochastic dynamics of bond rupture under load. This allows us to extract the distribution of the number of initially closed bonds. We also extract the molecular parameters of the adhesion bonds, in good agreement with earlier results from single bond experiments. Our analysis shows that the peaks in the measured histograms are not simple multiples of the single bond values, but follow from a superposition procedure which generates different peak positions.

  10. TIME-RESOLVED INFRARED SPECTROSCOPY IN THE U121R BEAMLINE AT THE NSLS

    Energy Technology Data Exchange (ETDEWEB)

    CARR,G.L.; LAVEIGNE,J.D.; LOBO,R.P.S.M.; REITZE,D.H.; TANNER,D.B.

    1999-07-19

    A facility for performing time-resolved infrared spectroscopy has been developed at the NSLS, primarily at beamline U12IR. The pulsed IR light from the synchrotron is used to perform pump-probe spectroscopy. The authors present here a description of the facility and results for the relaxation of photoexcitations in both a semiconductor and superconductor.

  11. A Simple LIBS (Laser-Induced Breakdown Spectroscopy) Laboratory Experiment to Introduce Undergraduates to Calibration Functions and Atomic Spectroscopy

    Science.gov (United States)

    Chinni, Rosemarie C.

    2012-01-01

    This laboratory experiment introduces students to a different type of atomic spectroscopy: laser-induced breakdown spectroscopy (LIBS). LIBS uses a laser-generated spark to excite the sample; once excited, the elemental emission is spectrally resolved and detected. The students use LIBS to analyze a series of standard synthetic silicate samples…

  12. A Simple LIBS (Laser-Induced Breakdown Spectroscopy) Laboratory Experiment to Introduce Undergraduates to Calibration Functions and Atomic Spectroscopy

    Science.gov (United States)

    Chinni, Rosemarie C.

    2012-01-01

    This laboratory experiment introduces students to a different type of atomic spectroscopy: laser-induced breakdown spectroscopy (LIBS). LIBS uses a laser-generated spark to excite the sample; once excited, the elemental emission is spectrally resolved and detected. The students use LIBS to analyze a series of standard synthetic silicate samples…

  13. Single Molecule Spectroscopy of Monomeric LHCII: Experiment and Theory

    CERN Document Server

    Malý, Pavel; van Grondelle, Rienk; Mančal, Tomáš

    2015-01-01

    We derive approximate equations of motion for excited state dynamics of a multilevel open quantum system weakly interacting with light to describe fluorescence detected single molecule spectra. Based on the Frenkel exciton theory, we construct a model for the chlorophyll part of the LHCII complex of higher plants and its interaction with previously proposed excitation quencher in the form of the lutein molecule Lut 1. The resulting description is valid over a broad range of timescales relevant for single molecule spectroscopy, i.e. from ps to minutes. Validity of these equations is demonstrated by comparing simulations of ensemble and single-molecule spectra of monomeric LHCII with experiments. Using a conformational change of the LHCII protein as a switching mechanism, the intensity and spectral time traces of individual LHCII complexes are simulated, and the experimental statistical distributions are reproduced. Based on our model, it is shown that with reasonable assumptions about its interaction with chlo...

  14. Modelling multi-pulse population dynamics from ultrafast spectroscopy.

    Directory of Open Access Journals (Sweden)

    Luuk J G W van Wilderen

    modelling is essential to model and resolve the details of physical behaviour of populations in ultrafast spectroscopy such as pump-probe, pump-dump-probe and pump-repump-probe experiments.

  15. A Bloch equation approach to intensity dependent optical spectra of light harvesting complex II: excitation dependence of light harvesting complex II pump-probe spectra.

    Science.gov (United States)

    Richter, Marten; Renger, Thomas; Knorr, Andreas

    2008-01-01

    On the basis of the recent progress in the resolution of the structure of the antenna light harvesting complex II (LHC II) of the photosystem II, we propose a microscopically motivated theory to predict excitation intensity-dependent spectra. We show that optical Bloch equations provide the means to include all 2( N ) excited states of an oligomer complex of N coupled two-level systems and analyze the effects of Pauli Blocking and exciton-exciton annihilation on pump-probe spectra. We use LHC Bloch equations for 14 Coulomb coupled two-level systems, which describe the S (0) and S (1) level of every chlorophyll molecule. All parameter introduced into the Hamiltonian are based on microscopic structure and a quantum chemical model. The derived Bloch equations describe not only linear absorption but also the intensity dependence of optical spectra in a regime where the interplay of Pauli Blocking effects as well as exciton-exciton annihilation effects are important. As an example, pump-probe spectra are discussed. The observed saturation of the spectra for high intensities can be viewed as a relaxation channel blockade on short time scales due to Pauli blocking. The theoretical investigation is useful for the interpretation of the experimental data, if the experimental conditions exceed the low intensity pump limit and effects like strong Pauli Blocking and exciton-exciton annihilation need to be considered. These effects become important when multiple excitations are generated by the pump pulse in the complex.

  16. HELIOS—A laboratory based on high-order harmonic generation of extreme ultraviolet photons for time-resolved spectroscopy

    Energy Technology Data Exchange (ETDEWEB)

    Plogmaker, S., E-mail: Stefan.Plogmaker@physics.uu.se, E-mail: Joachim.Terschluesen@physics.uu.se, E-mail: Johan.Soderstrom@physics.uu.se; Terschlüsen, J. A., E-mail: Stefan.Plogmaker@physics.uu.se, E-mail: Joachim.Terschluesen@physics.uu.se, E-mail: Johan.Soderstrom@physics.uu.se; Krebs, N.; Svanqvist, M.; Forsberg, J.; Cappel, U. B.; Rubensson, J.-E.; Siegbahn, H.; Söderström, J., E-mail: Stefan.Plogmaker@physics.uu.se, E-mail: Joachim.Terschluesen@physics.uu.se, E-mail: Johan.Soderstrom@physics.uu.se [Department of Physics and Astronomy, Molecular and Condensed Matter Physics, Uppsala University, P.O. Box 516, 75120 Uppsala (Sweden)

    2015-12-15

    In this paper, we present the HELIOS (High Energy Laser Induced Overtone Source) laboratory, an in-house high-order harmonic generation facility which generates extreme ultraviolet (XUV) photon pulses in the range of 15-70 eV with monochromatized XUV pulse lengths below 35 fs. HELIOS is a source for time-resolved pump-probe/two-color spectroscopy in the sub-50 fs range, which can be operated at 5 kHz or 10 kHz. An optical parametric amplifier is available for pump-probe experiments with wavelengths ranging from 240 nm to 20 000 nm. The produced XUV radiation is monochromatized by a grating in the so-called off-plane mount. Together with overall design parameters, first monochromatized spectra are shown with an intensity of 2 ⋅ 10{sup 10} photons/s (at 5 kHz) in the 29th harmonic, after the monochromator. The XUV pulse duration is measured to be <25 fs after monochromatization.

  17. HELIOS—A laboratory based on high-order harmonic generation of extreme ultraviolet photons for time-resolved spectroscopy

    Science.gov (United States)

    Plogmaker, S.; Terschlüsen, J. A.; Krebs, N.; Svanqvist, M.; Forsberg, J.; Cappel, U. B.; Rubensson, J.-E.; Siegbahn, H.; Söderström, J.

    2015-12-01

    In this paper, we present the HELIOS (High Energy Laser Induced Overtone Source) laboratory, an in-house high-order harmonic generation facility which generates extreme ultraviolet (XUV) photon pulses in the range of 15-70 eV with monochromatized XUV pulse lengths below 35 fs. HELIOS is a source for time-resolved pump-probe/two-color spectroscopy in the sub-50 fs range, which can be operated at 5 kHz or 10 kHz. An optical parametric amplifier is available for pump-probe experiments with wavelengths ranging from 240 nm to 20 000 nm. The produced XUV radiation is monochromatized by a grating in the so-called off-plane mount. Together with overall design parameters, first monochromatized spectra are shown with an intensity of 2 ṡ 1010 photons/s (at 5 kHz) in the 29th harmonic, after the monochromator. The XUV pulse duration is measured to be <25 fs after monochromatization.

  18. HELIOS--A laboratory based on high-order harmonic generation of extreme ultraviolet photons for time-resolved spectroscopy.

    Science.gov (United States)

    Plogmaker, S; Terschlüsen, J A; Krebs, N; Svanqvist, M; Forsberg, J; Cappel, U B; Rubensson, J-E; Siegbahn, H; Söderström, J

    2015-12-01

    In this paper, we present the HELIOS (High Energy Laser Induced Overtone Source) laboratory, an in-house high-order harmonic generation facility which generates extreme ultraviolet (XUV) photon pulses in the range of 15-70 eV with monochromatized XUV pulse lengths below 35 fs. HELIOS is a source for time-resolved pump-probe/two-color spectroscopy in the sub-50 fs range, which can be operated at 5 kHz or 10 kHz. An optical parametric amplifier is available for pump-probe experiments with wavelengths ranging from 240 nm to 20,000 nm. The produced XUV radiation is monochromatized by a grating in the so-called off-plane mount. Together with overall design parameters, first monochromatized spectra are shown with an intensity of 2 ⋅ 10(10) photons/s (at 5 kHz) in the 29th harmonic, after the monochromator. The XUV pulse duration is measured to be <25 fs after monochromatization.

  19. Modeling Orbital Gamma-Ray Spectroscopy Experiments at Carbonaceous Asteroids

    CERN Document Server

    Lim, Lucy F; Evans, Larry G; Parsons, Ann M; Zolensky, Michael E; Boynton, William V

    2016-01-01

    To evaluate the feasibility of measuring differences in bulk composition among carbonaceous meteorite parent bodies from an asteroid or comet orbiter, we present the results of a performance simulation of an orbital gamma-ray spectroscopy ("GRS") experiment in a Dawn-like orbit around spherical model asteroids with a range of carbonaceous compositions. The orbital altitude was held equal to the asteroid radius for 4.5 months. Both the asteroid gamma-ray spectrum and the spacecraft background flux were calculated using the MCNPX Monte-Carlo code. GRS is sensitive to depths below the optical surface (to ~20--50 cm depth depending on material density). This technique can therefore measure underlying compositions beneath a sulfur-depleted (e.g., Nittler et al. 2001) or desiccated surface layer. We find that 3\\sigma\\ uncertainties of under 1 wt% are achievable for H, C, O, Si, S, Fe, and Cl for five carbonaceous meteorite compositions using the heritage Mars Odyssey GRS design in a spacecraft- deck-mounted configu...

  20. Modeling orbital gamma-ray spectroscopy experiments at carbonaceous asteroids

    Science.gov (United States)

    Lim, Lucy F.; Starr, Richard D.; Evans, Larry G.; Parsons, Ann M.; Zolensky, Michael E.; Boynton, William V.

    2017-01-01

    To evaluate the feasibility of measuring differences in bulk composition among carbonaceous meteorite parent bodies from an asteroid or comet orbiter, we present the results of a performance simulation of an orbital gamma-ray spectroscopy (GRS) experiment in a Dawn-like orbit around spherical model asteroids with a range of carbonaceous compositions. The orbital altitude was held equal to the asteroid radius for 4.5 months. Both the asteroid gamma-ray spectrum and the spacecraft background flux were calculated using the MCNPX Monte-Carlo code. GRS is sensitive to depths below the optical surface (to ≈20-50 cm depth depending on material density). This technique can therefore measure underlying compositions beneath a sulfur-depleted (e.g., Nittler et al.) or desiccated surface layer. We find that 3σ uncertainties of under 1 wt% are achievable for H, C, O, Si, S, Fe, and Cl for five carbonaceous meteorite compositions using the heritage Mars Odyssey GRS design in a spacecraft-deck-mounted configuration at the Odyssey end-of-mission energy resolution, FWHM = 5.7 keV at 1332 keV. The calculated compositional uncertainties are smaller than the compositional differences between carbonaceous chondrite subclasses.

  1. Intercomparison of the comparative reactivity method (CRM) and pump-probe technique for measuring total OH reactivity in an urban environment

    Science.gov (United States)

    Hansen, R. F.; Blocquet, M.; Schoemaecker, C.; Léonardis, T.; Locoge, N.; Fittschen, C.; Hanoune, B.; Stevens, P. S.; Sinha, V.; Dusanter, S.

    2015-10-01

    The investigation of hydroxyl radical (OH) chemistry during intensive field campaigns has led to the development of several techniques dedicated to ambient measurements of total OH reactivity, which is the inverse of the OH lifetime. Three techniques are currently used during field campaigns, including the total OH loss rate method, the pump-probe method, and the comparative reactivity method. However, no formal intercomparison of these techniques has been published so far, and there is a need to ensure that measurements of total OH reactivity are consistent among the different techniques. An intercomparison of two OH reactivity instruments, one based on the comparative reactivity method (CRM) and the other based on the pump-probe method, was performed in October 2012 in a NOx-rich environment, which is known to be challenging for the CRM technique. This study presents an extensive description of the two instruments, the CRM instrument from Mines Douai (MD-CRM) and the pump-probe instrument from the University of Lille (UL-FAGE), and highlights instrumental issues associated with the two techniques. It was found that the CRM instrument used in this study underestimates ambient OH reactivity by approximately 20 % due to the photolysis of volatile organic compounds (VOCs) inside the sampling reactor; this value is dependent on the position of the lamp within the reactor. However, this issue can easily be fixed, and the photolysis of VOCs was successfully reduced to a negligible level after this intercomparison campaign. The UL-FAGE instrument may also underestimate ambient OH reactivity due to the difficulty to accurately measure the instrumental zero. It was found that the measurements are likely biased by approximately 2 s-1, due to impurities in humid zero air. Two weeks of ambient sampling indicate that the measurements performed by the two OH reactivity instruments are in agreement, within the measurement uncertainties for each instrument, for NOx mixing ratios

  2. Coherent optical spectroscopy in a biological semiconductor quantum dot-DNA hybrid system

    Science.gov (United States)

    2012-01-01

    We theoretically investigate coherent optical spectroscopy of a biological semiconductor quantum dot (QD) coupled to DNA molecules. Coupling with DNAs, the linear optical responses of the peptide QDs will be enhanced significantly in the simultaneous presence of two optical fields. Based on this technique, we propose a scheme to measure the vibrational frequency of DNA and the coupling strength between peptide QD and DNA in all-optical domain. Distinct with metallic quantum dot, biological QD is non-toxic and pollution-free to environment, which will contribute to clinical medicine experiments. This article leads people to know more about the optical behaviors of DNAs-quantum dot system, with the currently popular pump-probe technique. PMID:22340277

  3. Coherent optical spectroscopy in a biological semiconductor quantum dot-DNA hybrid system.

    Science.gov (United States)

    Li, Jin-Jin; Zhu, Ka-Di

    2012-02-16

    We theoretically investigate coherent optical spectroscopy of a biological semiconductor quantum dot (QD) coupled to DNA molecules. Coupling with DNAs, the linear optical responses of the peptide QDs will be enhanced significantly in the simultaneous presence of two optical fields. Based on this technique, we propose a scheme to measure the vibrational frequency of DNA and the coupling strength between peptide QD and DNA in all-optical domain. Distinct with metallic quantum dot, biological QD is non-toxic and pollution-free to environment, which will contribute to clinical medicine experiments. This article leads people to know more about the optical behaviors of DNAs-quantum dot system, with the currently popular pump-probe technique.

  4. New perspectives in the ultrafast spectroscopy of many-body excitations in correlated materials

    Science.gov (United States)

    Giannetti, C.

    2016-03-01

    Ultrafast spectroscopies constitute a fundamental tool to investigate the dynamics of non-equilibrium many-body states in correlated materials. Two-pulses (pump-probe) experiments have shed new light on the interplay between high-energy electronic excitations and the emerging low-energy properties, such as superconductivity and charge order, in many interesting materials. Here we will review some recent results on copper oxides and we will propose the use of high-resolution multi-dimensional techniques to investigate the decoherence processes of optical excitations in these systems. This novel piece of information is expected to open a new route toward the understanding of the fundamental interactions that lead to the exotic electronic and magnetic properties of correlated materials.

  5. Signals for Lorentz and CPT Violation in Atomic Spectroscopy Experiments and Other Systems

    CERN Document Server

    Vargas, Arnaldo J

    2016-01-01

    The prospects of studying nonminimal operators for Lorentz violation using spectroscopy experiments with light atoms and muon spin-precession experiments are presented. Possible improvements on bounds on minimal and nonminimal operators for Lorentz violation are discussed.

  6. Enquiry-Based Learning: Experiences of First Year Chemistry Students Learning Spectroscopy

    Science.gov (United States)

    Lucas, Timothy; Rowley, Natalie M.

    2011-01-01

    We explored the experiences of first year chemistry students of an Enquiry-Based Learning (EBL) approach to learning spectroscopy. An investigation of how students' perceived confidences changed as a result of their experience of using EBL in the spectroscopy course was carried out. Changes in the students' perceived confidence, both in their…

  7. Enquiry-Based Learning: Experiences of First Year Chemistry Students Learning Spectroscopy

    Science.gov (United States)

    Lucas, Timothy; Rowley, Natalie M.

    2011-01-01

    We explored the experiences of first year chemistry students of an Enquiry-Based Learning (EBL) approach to learning spectroscopy. An investigation of how students' perceived confidences changed as a result of their experience of using EBL in the spectroscopy course was carried out. Changes in the students' perceived confidence, both in their…

  8. Nonlinear Optical Spectroscopy of Excited States in Polyfluorene

    CERN Document Server

    Tong, M; Vardeny, Z V

    2006-01-01

    We used a variety of nonlinear optical (NLO) spectroscopies to study the singlet excited states order, and primary photoexcitations in polyfluorene; an important blue emitting p-conjugated polymer. The polarized NLO spectroscopies include ultrafast pump-probe photomodulation, two-photon absorption, and electroabsorption. For completeness we also measured the linear absorption and photoluminescence spectra. We found that the primary photoexcitations in polyfluorene are singlet excitons.

  9. Continuum probe two-dimensional electronic spectroscopy of the photosystem II reaction center

    Directory of Open Access Journals (Sweden)

    Ogilvie J. P.

    2013-03-01

    Full Text Available We report two-dimensional electronic spectroscopy of the photosystem II reaction center, collected in the pump-probe geometry employing a continuum probe. This enables observation of ion bands that report on intermediates in the charge separation process.

  10. Probing spin-vibronic dynamics using femtosecond X-ray spectroscopy

    DEFF Research Database (Denmark)

    Penfold, T. J.; Pápai, Mátyás Imre; Rozgonyi, T.;

    2016-01-01

    Ultrafast pump-probe spectroscopy within the X-ray regime is now possible owing to the development of X-ray Free Electrons Lasers (X-FELs) and is opening new opportunities for the direct probing of femtosecond evolution of the nuclei, the electronic and spin degrees of freedom. In this contributi...

  11. Two-Copy Wavelength Conversion of an 80 Gbit/s Serial Data Signal Using Cross-Phase Modulation in a Silicon Nanowire and Detailed Pump-Probe Characterisation

    DEFF Research Database (Denmark)

    Ji, Hua; Cleary, C. S.; Dailey, J. M.;

    2012-01-01

    We experimentally demonstrate 80 Gbit/s wavelength conversion to two copies by simultaneously extracting the blue- and red-shifted sidebands from XPM in a silicon nanowire. Bit error rates of 10-9 with only ~2 dB power penalty is achieved for both sidebands. Detailed pump-probe characterisation r...

  12. Toward Femtosecond X-ray Spectroscopy at the Advanced Light Source

    Energy Technology Data Exchange (ETDEWEB)

    Chong, Henry Herng Wei

    2004-04-16

    The realization of tunable, ultrashort pulse x-ray sources promises to open new venues of science and to shed new light on long-standing problems in condensed matter physics and chemistry. Fundamentally new information can now be accessed. Used in a pump-probe spectroscopy, ultrashort x-ray pulses provide a means to monitor atomic rearrangement and changes in electronic structure in condensed-matter and chemical systems on the physically-limiting time-scales of atomic motion. This opens the way for the study of fast structural dynamics and the role they play in phase transitions, chemical reactions and the emergence of exotic properties in materials with strongly interacting degrees of freedom. The ultrashort pulse x-ray source developed at the Advanced Light Source at the Lawrence Berkeley Laboratory is based on electron slicing in storage rings, and generates {approx}100 femtosecond pulses of synchrotron radiation spanning wavelengths from the far-infrared to the hard x-ray region of the electromagnetic spectrum. The tunability of the source allows for the adaptation of a broad range of static x-ray spectroscopies to useful pump-probe measurements. Initial experiments are attempted on transition metal complexes that exhibit relatively large structural changes upon photo-excitation and which have excited-state evolution determined by strongly interacting structural, electronic and magnetic degrees of freedom. Specifically, iron(II) complexes undergo a spin-crossover transition upon optical irradiation. The dynamics of the transition involve a metal-to-ligand charge transfer, a {Delta}S=2 change in magnetic moment and 10% bond dilation in the first coordination shell of the iron. Studies of the electronic dynamics are studied with time-resolved optical absorption measurements. The current progress of time-resolved structural studies to complete the picture of the spin-crossover transition is presented.

  13. Toward Femtosecond X-ray Spectroscopy at the Advanced Light Source

    Energy Technology Data Exchange (ETDEWEB)

    Chong, Henry Herng Wei [Univ. of California, Berkeley, CA (United States)

    2004-01-01

    The realization of tunable, ultrashort pulse x-ray sources promises to open new venues of science and to shed new light on long-standing problems in condensed matter physics and chemistry. Fundamentally new information can now be accessed. Used in a pump-probe spectroscopy, ultrashort x-ray pulses provide a means to monitor atomic rearrangement and changes in electronic structure in condensed-matter and chemical systems on the physically-limiting time-scales of atomic motion. This opens the way for the study of fast structural dynamics and the role they play in phase transitions, chemical reactions and the emergence of exotic properties in materials with strongly interacting degrees of freedom. The ultrashort pulse x-ray source developed at the Advanced Light Source at the Lawrence Berkeley Laboratory is based on electron slicing in storage rings, and generates ~100 femtosecond pulses of synchrotron radiation spanning wavelengths from the far-infrared to the hard x-ray region of the electromagnetic spectrum. The tunability of the source allows for the adaptation of a broad range of static x-ray spectroscopies to useful pump-probe measurements. Initial experiments are attempted on transition metal complexes that exhibit relatively large structural changes upon photo-excitation and which have excited-state evolution determined by strongly interacting structural, electronic and magnetic degrees of freedom. Specifically, iron(II) complexes undergo a spin-crossover transition upon optical irradiation. The dynamics of the transition involve a metal-to-ligand charge transfer, a ΔS=2 change in magnetic moment and 10% bond dilation in the first coordination shell of the iron. Studies of the electronic dynamics are studied with time-resolved optical absorption measurements. The current progress of time-resolved structural studies to complete the picture of the spin-crossover transition is presented.

  14. All-fiber hydrogen sensor based on stimulated Raman gain spectroscopy with a 1550 nm hollow-core fiber

    CERN Document Server

    Yang, Fan

    2016-01-01

    We report a highly sensitive all-fiber hydrogen sensor based on continuous-wave stimulated Raman gain spectroscopy with a hollow-core photonic crystal fiber operating around 1550 nm. A pump-probe configuration is used, in which the frequency difference between the pump and the probe lasers is tuned to the S0(0) transition of para-hydrogen with a Raman shift of 354 cm-1. Preliminary experiments demonstrate a detection limit down to 17 ppm with a 250 s averaging time, and further improvement is possible. The all-fiber configuration operating in the telecommunication wavelength band would enable cost-effective and compact sensors for high sensitivity and high-resolution trace analysis.

  15. CdS and Cd-Free Buffer Layers on Solution Phase Grown Cu2ZnSn(SxSe1- x)4 :Band Alignments and Electronic Structure Determined with Femtosecond Ultraviolet Photoemission Spectroscopy

    Energy Technology Data Exchange (ETDEWEB)

    Haight, Richard; Barkhouse, Aaron; Wang, Wei; Yu, Luo; Shao, Xiaoyan; Mitzi, David; Hiroi, Homare; Sugimoto, Hiroki

    2013-12-02

    The heterojunctions formed between solution phase grown Cu2ZnSn(SxSe1- x)4(CZTS,Se) and a number of important buffer materials including CdS, ZnS, ZnO, and In2S3, were studied using femtosecond ultraviolet photoemission spectroscopy (fs-UPS) and photovoltage spectroscopy. With this approach we extract the magnitude and direction of the CZTS,Se band bending, locate the Fermi level within the band gaps of absorber and buffer and measure the absorber/buffer band offsets under flatband conditions. We will also discuss two-color pump/probe experiments in which the band bending in the buffer layer can be independently determined. Finally, studies of the bare CZTS,Se surface will be discussed including our observation of mid-gap Fermi level pinning and its relation to Voc limitations and bulk defects.

  16. Antiprotonic atom formation and spectroscopy-ASACUSA experiment at CERN-AD

    CERN Document Server

    Widmann, E

    1999-01-01

    This talk describes the experiments on atomic spectroscopy and atomic collisions as proposed by the ASACUSA collaboration for the forthcoming AD facility at CERN. They consist of high-precision spectroscopy of antiprotonic atoms, the study of anti-protonic atom formation processes, and stopping power and ionization measurements in low-pressure gases. (18 refs).

  17. Spectroscopy

    Energy Technology Data Exchange (ETDEWEB)

    Hellman, Hal

    1968-01-01

    This booklet discusses spectroscopy, the study of absorption of radiation by matter, including X-ray, gamma-ray, microwave, mass spectroscopy, as well as others. Spectroscopy has produced more fundamental information to the study of the detailed structure of matter than any other tools.

  18. Retrieving the susceptibility from time-resolved terahertz experiments

    NARCIS (Netherlands)

    Schins, J.M.; Hendry, E.; Bonn, M.; Muller, H.G.

    2007-01-01

    We present an analytical expression for the observed signal in time- and phase-resolved pump-probe studies, with particular emphasis on terahertz time-domain spectroscopy. Maxwell’s equations are solved for the response of damped, harmonic oscillators to a driving probe field in the perturbative reg

  19. X-Ray Emission Spectrometer Design with Single-Shot Pump-Probe and Resonant Excitation Capabilities

    Energy Technology Data Exchange (ETDEWEB)

    Spoth, Katherine; /SUNY, Buffalo /SLAC

    2012-08-28

    Core-level spectroscopy in the soft X-ray regime is a powerful tool for the study of chemical bonding processes. The ultrafast, ultrabright X-ray pulses generated by the Linac Coherent Light Source (LCLS) allow these reactions to be studied in greater detail than ever before. In this study, we investigated a conceptual design of a spectrometer for the LCLS with imaging in the non-dispersive direction. This would allow single-shot collection of X-ray emission spectroscopy (XES) measurements with varying laser pump X-ray probe delay or a variation of incoming X-ray energy over the illuminated area of the sample. Ray-tracing simulations were used to demonstrate how the components of the spectrometer affect its performance, allowing a determination of the optimal final design. These simulations showed that the spectrometer's non-dispersive focusing is extremely sensitive to the size of the sample footprint; the spectrometer is not able to image a footprint width larger than one millimeter with the required resolution. This is compatible with a single shot scheme that maps out the laser pump X-ray probe delay in the non-dispersive direction as well as resonant XES applications at normal incidence. However, the current capabilities of the Soft X-Ray (SXR) beamline at the LCLS do not produce the required energy range in a small enough sample footprint, hindering the single shot resonant XES application at SXR for chemical dynamics studies at surfaces. If an upgraded or future beamline at LCLS is developed with lower monochromator energy dispersion the width can be made small enough at the required energy range to be imaged by this spectrometer design.

  20. Spectroscopy

    CERN Document Server

    Walker, S

    1976-01-01

    The three volumes of Spectroscopy constitute the one comprehensive text available on the principles, practice and applications of spectroscopy. By giving full accounts of those spectroscopic techniques only recently introduced into student courses - such as Mössbauer spectroscopy and photoelectron spectroscopy - in addition to those techniques long recognised as being essential in chemistry teaching - sucha as e.s.r. and infrared spectroscopy - the book caters for the complete requirements of undergraduate students and at the same time provides a sound introduction to special topics for graduate students.

  1. Optical detection system using time structure of UVSOR for combined laser-SR experiments

    CERN Document Server

    Azuma, J; Tsujibayashi, T; Itoh, M; Watanabe, M; Arimoto, O; Nakanishi, S; Itoh, H; Kamada, M

    2001-01-01

    A new TAC-MCA detection system has been developed for combined laser-SR spectroscopy such as two-photon excitation or pump-probe experiments in the VUV region. In order to improve the signal to noise ratio, the time structure under partial-filling operation of UVSOR is utilized together with this detection system. In our experiment, where the two-photon excitation efficiency of laser and SR is more important than the time resolution, a pulse stretching technique using optical fiber is applied to the output pulse of a CW mode-locked Ti : sapphire laser. The usefulness of the present system is successfully demonstrated by observing luminescence signals from the two-photon-excited core state in BaF sub 2 crystals.

  2. In situ ALD experiments with synchrotron radiation photoelectron spectroscopy

    Science.gov (United States)

    Tallarida, Massimo; Schmeisser, Dieter

    2012-07-01

    In this contribution, we describe some features of atomic layer deposition (ALD) investigated by means of synchrotron radiation photoelemission spectroscopy (SR-PES). In particular, we show how the surface sensitivity of SR-PES combined with the in situ nature of our investigations can point out interactions between the substrate and ALD precursors. We observed changes on all substrates investigated, included Si, GaAs, Ru and their surface oxides. These interactions are extremely important during the first ALD cycles and induce modifications in the substrate, which might lead to its functionality enhancement.

  3. PEANUT experiment in NQR spectroscopy for I=3/2.

    Science.gov (United States)

    Sinyavsky, Nikolay; Dolinenkov, Philip; Maćkowiak, Mariusz

    2012-01-01

    The experiment with phase inversion and phase-inverted echo-amplitude detected nutation (PEANUT) was introduced in the nuclear quadrupole resonance (NQR). Formulas were obtained describing the NQR (I=3/2) experiment. Exemplary experiments are provided confirming the predicted particularities of the PEANUT spectra in NQR Cl-35. It is proposed to apply the method for the purpose of determination the asymmetry parameter of the electric field gradient (EFG) tensor in powders with the help of the analysis of PEANUT interferograms. Application of two-dimensional PEANUT experiments, in which the nutation frequencies correlate with the resonance NQR frequencies, can substantially simplify the interpretation of complex spectra.

  4. Hydrogen spectroscopy with a Lamb-shift polarimeter. An alternative approach towards anti-hydrogen spectroscopy experiments

    Energy Technology Data Exchange (ETDEWEB)

    Westig, M.P. [I. Physikalisches Institut, Univ. zu Koln (Germany); Westig, M.P.; Engels, R.; Grigoryev, K.; Mikirtytchiants, M.; Rathmann, F.; Schug, G.; Stroher, H. [Institut fur Kernphysik and Julich Center for Hadron Physics, Forschungszentrum Julich GmbH, Julich (Germany); Grigoryev, K.; Mikirtytchiants, M.; Vasilyev, A. [Petersburg Nuclear Physics Institute, Gatchina (Russian Federation); Paetz gen Schieck, H. [Institut fur Kernphysik, Univ. zu Koln (Germany)

    2010-03-15

    A Lamb-shift polarimeter, which has been built for a fast determination of the polarization of protons and deuterons of an atomic-beam source and which is frequently used in the ANKE experiment at COSY-Juelich, is shown to be an excellent device for atomic-spectroscopy measurements of metastable hydrogen isotopes. It is demonstrated that magnetic and electric dipole transitions in hydrogen can be measured as a function of the external magnetic field, giving access to the full Breit-Rabi diagram for the 2{sup 2}S{sub 1/2} and the 2{sup 2}P{sub 1/2} states. This will allow the study of hyperfine structure, g factors and the classical Lamb shift. Although the data are not yet competitive with state-of-the-art measurements, the potential of the method is enormous, including a possible application to anti-hydrogen spectroscopy. (authors)

  5. Hydrogen Spectroscopy with a Lamb-shift Polarimeter - An Alternative Approach Towards Anti-Hydrogen Spectroscopy Experiments

    CERN Document Server

    Westig, M P; Grigoryev, K; Mikirtytchiants, M; Rathmann, F; Schieck, H Paetz gen; Schug, G; Vasilyev, A; Ströher, H; 10.1140/epjd/e2010-00016-9

    2011-01-01

    A Lamb-shift polarimeter, which has been built for a fast determination of the polarization of protons and deuterons of an atomic-beam source and which is frequently used in the ANKE experiment at COSY-J\\"ulich, is shown to be an excellent device for atomic-spectroscopy measurements of metastable hydrogen isotopes. It is demonstrated that magnetic and electric dipole transitions in hydrogen can be measured as a function of the external magnetic field, giving access to the full Breit-Rabi diagram for the $2^2S_{1/2}$ and the $2^2P_{1/2}$ states. This will allow the study of hyperfine structure, $g$ factors and the classical Lamb shift. Although the data are not yet competitive with state-of-the-art measurements, the potential of the method is enormous, including a possible application to anti-hydrogen spectroscopy.

  6. Resonance Raman Spectroscopy of Beta-Carotene and Lycopene: A Physical Chemistry Experiment.

    Science.gov (United States)

    Hoskins, L. C.

    1984-01-01

    Discusses the theory of resonance Raman (RR) spectroscopy as it applies to beta-carotene and lycopene pigments (found in tomatoes and carrots, respectively). Also discusses an experiment which demonstrates the theoretical principles involved. The experiment has been tested over a three-year period and has received excellent acceptance by physical…

  7. The HKS experiment on Lambda--hypernuclear spectroscopy via electroproduction at JLab

    Energy Technology Data Exchange (ETDEWEB)

    Tang, Liguang; Yuan, Lulin; Acha Quimper, Armando; Ahmidouch, Abdellah; Androic, Darko; Asaturyan, Arshak; Asaturyan, Razmik; Baker, O.; Baturin, Pavlo; Benmokhtar, Fatiha; Bosted, Peter; Carlini, Roger; Chen, X.; Christy, Michael; Cole, Leon; Danagoulian, Samuel; Daniel, AJI; Dharmawardane, Kahanawita; Egiyan, Kim; Elaasar, Mostafa; Ent, Rolf; Fenker, Howard; Fujii, Yu; Furic, Miroslav; Gan, Liping; Gaskell, David; Gasparian, Ashot; Gibson, Edward; Gueye, Paul; Halkyard, Rebekah; Hashimoto, Osamu; Hashimoto, Osamu; Honda, D.; Horn, Tanja; Hu, Bitao; Hu, S.; Hungerford, Ed; Ispiryan, Mikayel; Johnston, Kathleen; Jones, Mark; Kalantarians, Narbe; Kaneta, M.; Kato, F.; Kato, Seigo; Kawama, Daisuke; Keppel, Cynthia; Li, Y.; Luo, Wei; Mack, David; Margaryan, Amur; Marikyan, Gagik; Maruyama, Nayuta; Matsumura, Akihiko; Miyoshi, Toshinobu; Mkrtchyan, Arthur; Mkrtchyan, Hamlet; Nakamura, Satoshi; Navasardyan, Tigran; Niculescu, Gabriel; Niculescu, Maria-Ioana; Nomura, Hiroshi; Nonaka, Kenichi; Ohtani, Atsushi; Okayasu, Yuichi; Pamela, Priscilla; Perez, Naipy; Petkovic, Tomislav; Randeniya, Kapugodage; Reinhold, Joerg; Rivera Castillo, Roberto; Roche, Julie; Rodriguez, Victor; Sato, Yoshinori; Seva, Tomislav; Simicevic, Neven; Smith, Gregory; Sumihama, Mizuki; Song, Yujun; Tadevosyan, Vardan; Takahashi, Toshiyuki; Tamura, Hirokazu; Tvaskis, Vladas; Vulcan, William; Wang, B.; Wells, Stephen; Wood, Stephen; Yan, Chen; Zamkochian, S.

    2008-06-01

    The HKS (Jlab E01-011) experiment on spectroscopy of Lambda-hypernuclei using (e,e'K+) reaction was successfully carried out in 2005. This paper gives a brief description of the experiment and its technique and shows some of the preliminary spectra that are still under analysis.

  8. Development of a multipurpose vacuum chamber for serial optical and diffraction experiments with free electron laser radiation

    Energy Technology Data Exchange (ETDEWEB)

    Rajkovic, I.; Hallmann, J.; Gruebel, S.; More, R.; Quevedo, W.; Petri, M.; Techert, S. [Department of Structural Dynamics of (Bio)chemical Systems, Max Planck Institute for Biophysical Chemistry, 37070 Goettingen (Germany)

    2010-04-15

    In this paper we present a development of a multipurpose vacuum chamber which primal function is to be used in pump/probe experiments with free electron laser (FEL) radiation. The chamber is constructed for serial diffraction and serial spectroscopy allowing a fast exchange of samples during the measurement process. For the fast exchange of samples, liquid jet systems are used. Both applications, utilizing soft x-ray FEL pulses as pump and optical laser pulses as probe and vice versa are documented. Experiments with solid samples as well as the liquid jet samples are presented. When working with liquid jets, a system of automatically refilled liquid traps for capturing liquids has been developed in order to ensure stable vacuum conditions. Differential pumping stages are placed in between the FEL beamline and the experimental chamber so that working pressure in the chamber can be up to four orders of magnitude higher than the pressure in the FEL beamline.

  9. Initial Active MHD Spectroscopy Experiments on Alcator C-MOD

    Science.gov (United States)

    Schmittdiel, D. A.; Snipes, J. A.; Granetz, R. S.; Parker, R. R.; Wolfe, S. M.; Fasoli, A.

    2002-11-01

    The Active MHD Spectroscopy system is a new diagnostic on C-MOD that will be used to study low frequency MHD modes and TAE's present at high B_tor, n_e, and Te ˜= T_i. The present system consists of two antennas, power amplifiers, and an impedance matching network. Each antenna is 15 × 25 cm with five turns, an inductance of ˜10 μH, and is covered by boron nitride tiles. The two antennas are placed at the same toroidal location, symmetrically above and below the midplane. Each antenna is driven by a ˜1 kW power amplifier in the range of 1 kHz - 1 MHz with an expected antenna current ˜10 A, which will produce a vacuum field of ˜0.5 G at the q = 1.5 surface. This diagnostic is designed to excite high n ( ˜20) stable TAE's and initial results regarding their frequency, mode structure, and damping rate will be presented. Evolution of these modes could also provide information on the q profile to compare with MSE measurements, which will be important for planned lower hybrid current drive operation in 2003.

  10. New results in meson spectroscopy from the crystal barrel experiment

    Energy Technology Data Exchange (ETDEWEB)

    Meyer, C.A. [Carnegie Mellon Univ., Pittsburgh, PA (United States)

    1994-04-01

    Recent observations by the Crystal Barrel experiment of two scalar resonances, f{sub o}(1365) and a{sub o}(1450) have allowed the authors to clarify the members of the scalar nonet. In addition, a third scalar, f{sub o}(1500), appears to be supernumerary, and is a candidate for the scalar glueball expected near 1500 MeV.

  11. Ultrafast optical spectroscopy of the lowest energy excitations in the Mott insulator compound YVO3 : Evidence for Hubbard-type excitons

    NARCIS (Netherlands)

    Novelli, Fabio; Fausti, Daniele; Reul, Julia; Cilento, Federico; van Loosdrecht, Paul H. M.; Nugroho, Agung A.; Palstra, Thomas T. M.; Grueninger, Markus; Parmigiani, Fulvio

    2012-01-01

    Revealing the nature of charge excitations in strongly correlated electron systems is crucial to understanding their exotic properties. Here we use broadband ultrafast pump-probe spectroscopy in the visible range to study low-energy transitions across the Mott-Hubbard gap in the orbitally ordered in

  12. Spectroscopy

    DEFF Research Database (Denmark)

    Berg, Rolf W.

    This introductory booklet covers the basics of molecular spectroscopy, infrared and Raman methods, instrumental considerations, symmetry analysis of molecules, group theory and selection rules, as well as assignments of fundamental vibrational modes in molecules.......This introductory booklet covers the basics of molecular spectroscopy, infrared and Raman methods, instrumental considerations, symmetry analysis of molecules, group theory and selection rules, as well as assignments of fundamental vibrational modes in molecules....

  13. TESIS experiment on EUV imaging spectroscopy of the Sun

    Science.gov (United States)

    Kuzin, S. V.; Bogachev, S. A.; Zhitnik, I. A.; Pertsov, A. A.; Ignatiev, A. P.; Mitrofanov, A. M.; Slemzin, V. A.; Shestov, S. V.; Sukhodrev, N. K.; Bugaenko, O. I.

    2009-03-01

    TESIS is a set of solar imaging instruments in development by the Lebedev Physical Institute of the Russian Academy of Science, to be launched aboard the Russian spacecraft CORONAS-PHOTON in December 2008. The main goal of TESIS is to provide complex observations of solar active phenomena from the transition region to the inner and outer solar corona with high spatial, spectral and temporal resolution in the EUV and Soft X-ray spectral bands. TESIS includes five unique space instruments: the MgXII Imaging Spectroheliometer (MISH) with spherical bent crystal mirror, for observations of the Sun in the monochromatic MgXII 8.42 Å line; the EUV Spectoheliometer (EUSH) with grazing incidence difraction grating, for the registration of the full solar disc in monochromatic lines of the spectral band 280-330 Å; two Full-disk EUV Telescopes (FET) with multilayer mirrors covering the band 130-136 and 290-320 Å; and the Solar EUV Coronagraph (SEC), based on the Ritchey-Chretien scheme, to observe the inner and outer solar corona from 0.2 to 4 solar radii in spectral band 290-320 Å. TESIS experiment will start at the rising phase of the 24th cycle of solar activity. With the advanced capabilities of its instruments, TESIS will help better understand the physics of solar flares and high-energy phenomena and provide new data on parameters of solar plasma in the temperature range 10-10K. This paper gives a brief description of the experiment, its equipment, and its scientific objectives.

  14. Determination of Calcium in Cereal with Flame Atomic Absorption Spectroscopy: An Experiment for a Quantitative Methods of Analysis Course

    Science.gov (United States)

    Bazzi, Ali; Kreuz, Bette; Fischer, Jeffrey

    2004-01-01

    An experiment for determination of calcium in cereal using two-increment standard addition method in conjunction with flame atomic absorption spectroscopy (FAAS) is demonstrated. The experiment is intended to introduce students to the principles of atomic absorption spectroscopy giving them hands on experience using quantitative methods of…

  15. Quantum-beat Auger spectroscopy

    CERN Document Server

    Zhang, Song Bin

    2015-01-01

    The concept of nonlinear quantum-beat pump-probe Auger spectroscopy is introduced by discussing a relatively simple four-level model system. We consider a coherent wave packet involving two low-lying states that was prepared by an appropriate pump pulse. This wave packet is subsequently probed by a weak, time-delayed probe pulse with nearly resonant coupling to a core-excited state of the atomic or molecular system. The resonant Auger spectra are then studied as a function of the duration of the probe pulse and the time delay. With a bandwidth of the probe pulse approaching the energy spread of the wave packet, the Auger yields and spectra show quantum beats as a function of pump-probe delay. An analytic theory for the quantum-beat Auger spectroscopy will be presented, which allows for the reconstruction of the wave packet by analyzing the delaydependent Auger spectra. The possibility of extending this method to a more complex manifold of electronic and vibrational energy levels is also discussed.

  16. Perspective: Electrospray photoelectron spectroscopy: From multiply-charged anions to ultracold anions

    Energy Technology Data Exchange (ETDEWEB)

    Wang, Lai-Sheng, E-mail: Lai-Sheng-Wang@brown.edu [Department of Chemistry, Brown University, Providence, Rhode Island 02912 (United States)

    2015-07-28

    Electrospray ionization (ESI) has become an essential tool in chemical physics and physical chemistry for the production of novel molecular ions from solution samples for a variety of spectroscopic experiments. ESI was used to produce free multiply-charged anions (MCAs) for photoelectron spectroscopy (PES) in the late 1990 s, allowing many interesting properties of this class of exotic species to be investigated. Free MCAs are characterized by strong intramolecular Coulomb repulsions, which create a repulsive Coulomb barrier (RCB) for electron emission. The RCB endows many fascinating properties to MCAs, giving rise to meta-stable anions with negative electron binding energies. Recent development in the PES of MCAs includes photoelectron imaging to examine the influence of the RCB on the electron emission dynamics, pump-probe experiments to examine electron tunneling through the RCB, and isomer-specific experiments by coupling PES with ion mobility for biological MCAs. The development of a cryogenically cooled Paul trap has led to much better resolved PE spectra for MCAs by creating vibrationally cold anions from the room temperature ESI source. Recent advances in coupling the cryogenic Paul trap with PE imaging have allowed high-resolution PE spectra to be obtained for singly charged anions produced by ESI. In particular, the observation of dipole-bound excited states has made it possible to conduct vibrational autodetachment spectroscopy and resonant PES, which yield much richer vibrational spectroscopic information for dipolar free radicals than traditional PES.

  17. Femtosecond Raman induced polarization spectroscopy studies of coherent rotational dynamics in molecular fluids

    Energy Technology Data Exchange (ETDEWEB)

    Morgen, Michael Mark [Univ. of California, Berkeley, CA (United States). Dept. of Chemistry

    1997-05-01

    We develop a polarization-sensitive femtosecond pump probe technique, Raman induced polarization spectroscopy (RIPS), to study coherent rotation in molecular fluids. By observing the collisional dephasing of the coherently prepared rotational states, we are able to extract information concerning the effects of molecular interactions on the rotational motion. The technique is quite sensitive because of the zero background detection method, and is also versatile due to its nonresonant nature.

  18. Multidimensional resonance raman spectroscopy by six-wave mixing in the deep UV

    Science.gov (United States)

    Molesky, Brian P.; Giokas, Paul G.; Guo, Zhenkun; Moran, Andrew M.

    2014-09-01

    Two-dimensional (2D) resonance Raman spectroscopies hold great potential for uncovering photoinduced relaxation processes in molecules but are not yet widely applied because of technical challenges. Here, we describe a newly developed 2D resonance Raman experiment operational at the third-harmonic of a Titanium-Sapphire laser. High-sensitivity and rapid data acquisition are achieved by combining spectral interferometry with a background-free (six-pulse) laser beam geometry. The third-harmonic laser pulses are generated in a filament produced by the fundamental and second-harmonic pulses in neon gas at pressures up to 35 atm. The capabilities of the setup are demonstrated by probing ground-state wavepacket motions in triiodide. The information provided by the experiment is explored with two different representations of the signal. In one representation, Fourier transforms are carried out with respect to the two experimentally controlled delay times to obtain a 2D Raman spectrum. Further insights are derived in a second representation by dispersing the signal pulse in a spectrometer. It is shown that, as in traditional pump-probe experiments, the six-wave mixing signal spectrum encodes the wavepacket's position by way of the (time-evolving) emission frequency. Anharmonicity additionally induces dynamics in the vibrational resonance frequency. In all cases, the experimental signals are compared to model calculations based on a cumulant expansion approach. This study suggests that multi-dimensional resonance Raman spectroscopies conducted on systems with Franck-Condon active modes are fairly immune to many of the technical issues that challenge off-resonant 2D Raman spectroscopies (e.g., third-order cascades) and photon-echo experiments in the deep UV (e.g., coherence spikes). The development of higher-order nonlinear spectroscopies operational in the deep UV is motivated by studies of biological systems and elementary organic photochemistries.

  19. Broadband Velocity Modulation Spectroscopy of Molecular Ions for Use in the Jila Electron Edm Experiment

    Science.gov (United States)

    Gresh, Daniel N.; Cossel, Kevin C.; Cornell, Eric A.; Ye, Jun

    2013-06-01

    The JILA electron electric dipole moment (eEDM) experiment will use a low-lying, metastable ^3Δ_1 state in trapped molecular ions of HfF^+ or ThF^+. Prior to this work, the low-lying states of these molecules had been investigated by PFI-ZEKE spectroscopy. However, there were no detailed studies of the electronic structure. The recently developed technique of frequency comb velocity modulation spectroscopy (VMS) provides broad-bandwidth, high-resolution, ion-sensitive spectroscopy, allowing the acquisition of 150 cm^{-1} of continuous spectra in 30 minutes over 1500 simultaneous channels. By supplementing this technique with cw-laser VMS, we have investigated the electronic structure of HfF^+ in the frequency range of 9950 to 14600 cm^{-1}, accurately fitting and assigning 16 rovibronic transitions involving 8 different electronic states including the X^1Σ^+ and a^3Δ_1 states. In addition, an observed ^3Π_{0+} state with coupling to both the X and a states has been used in the actual eEDM experiment to coherently transfer population from the rovibronic ground state of HfF^+ to the eEDM science state. Furthermore, we report on current efforts of applying frequency comb VMS at 700 - 900 nm to the study of ThF^+, which has a lower energy ^3Δ_1 state and a greater effective electric field, and will provide increased sensitivity for a measurement of the eEDM. A. E. Leanhardt et. al., Journal of Molecular Spectroscopy 270, 1-25 (2011). B. J. Barker, I. O. Antonov, M. C. Heaven, K. A. Peterson, Journal of Chemical Physics 136, 104305 (2012). L. C. Sinclair, K. C. Cossel, T. Coffey, J. Ye, E. A. Cornell, Physical Review Letters 107, 093002 (2011). K.C. Cossel et. al., Chemical Physics Letters 546, 1-11 (2012).

  20. Perspectives for neutron and gamma spectroscopy in high power laser driven experiments at ELI-NP

    Science.gov (United States)

    Negoita, F.; Gugiu, M.; Petrascu, H.; Petrone, C.; Pietreanu, D.; Fuchs, J.; Chen, S.; Higginson, D.; Vassura, L.; Hannachi, F.; Tarisien, M.; Versteegen, M.; Antici, P.; Balabanski, D.; Balascuta, S.; Cernaianu, M.; Dancus, I.; Gales, S.; Neagu, L.; Petcu, C.; Risca, M.; Toma, M.; Turcu, E.; Ursescu, D.

    2015-02-01

    The measurement of energy spectra of neutrons and gamma rays emitted by nuclei, together with charge particles spectroscopy, are the main tools for understanding nuclear phenomena occurring also in high power laser driven experiments. However, the large number of particles emitted in a very short time, in particular the strong X-rays flash produced in laser-target interaction, impose adaptation of technique currently used in nuclear physics experiment at accelerator based facilities. These aspects are discussed (Section 1) in the context of proposed studies at high power laser system of ELI-NP. Preliminary results from two experiments performed at Titan (LLNL) and ELFIE (LULI) facilities using plastic scintillators for neutron detection (Section 2) and LaBr3(Ce) scintillators for gamma detection (Section 3) are presented demonstrating the capabilities and the limitations of the employed methods. Possible improvements of these spectroscopic methods and their proposed implementation at ELI-NP will be discussed as well in the last section.

  1. A position sensitive silicon detector for AEgIS (Antimatter Experiment: Gravity, Interferometry, Spectroscopy)

    CERN Multimedia

    Gligorova, A

    2014-01-01

    The AEḡIS experiment (Antimatter Experiment: Gravity, Interferometry, Spectroscopy) is located at the Antiproton Decelerator (AD) at CERN and studies antimatter. The main goal of the AEḡIS experiment is to carry out the first measurement of the gravitational acceleration for antimatter in Earth’s gravitational field to a 1% relative precision. Such a measurement would test the Weak Equivalence Principle (WEP) of Einstein’s General Relativity. The gravitational acceleration for antihydrogen will be determined using a set of gravity measurement gratings (Moiré deflectometer) and a position sensitive detector. The vertical shift due to gravity of the falling antihydrogen atoms will be detected with a silicon strip detector, where the annihilation of antihydrogen will take place. This poster presents part of the development process of this detector.

  2. Ultrafast Optical Spectroscopy of Unbundled Single-Walled Carbon Nanotubes

    Science.gov (United States)

    Ostojic, G.; Zaric, S.; Kono, J.; Strano, M. S.; Moore, V. C.; Hauge, R. H.; Smalley, R. E.

    2004-03-01

    Single-walled carbon nanotubes (SWNTs) are currently under intensive investigation due to both interesting physical properties and possible applications. Owing to the recently developed method for separating bundled tubes [1], it is now possible to explore the true one-dimensional (1D) properties of SWNTs. We have used degenerate and nondegerenerate pump-probe measurements to probe the relaxation of photogenerated carriers in micelle suspended nanotubes prepared by this method. Degenerate pump-probe experiments in a wide range of the two lowest transition energies of semiconducting SWNTs show two distinct relaxation regimes. A fast relaxation component (0.3-1.2 ps) is always present whereas a slow component (5-20 ps) is resonantly enhanced whenever the pump photon energy coincides with an interband absorption peak. We attributed the fast relaxation to intraband carrier relaxation towards the band edge and the slow one to interband relaxation. Nondegenerate pump-probe experiments were performed to elucidate the details of these processes. [1] M. J. O'Connell et al., Science 297, 593 (2002). This work was supported by the Robert A. Welch Foundation (through Grant No. C-1509), the Texas Advanced Technology Program (through Project No. 003604-0001-2001), and the National Science Foundation CAREER Award (through Grant No. DMR-0134058).

  3. Finite-difference time-domain analysis of time-resolved terahertz spectroscopy experiments

    DEFF Research Database (Denmark)

    Larsen, Casper; Cooke, David G.; Jepsen, Peter Uhd

    2011-01-01

    In this paper we report on the numerical analysis of a time-resolved terahertz (THz) spectroscopy experiment using a modified finite-difference time-domain method. Using this method, we show that ultrafast carrier dynamics can be extracted with a time resolution smaller than the duration of the THz...... probe pulse and can be determined solely by the pump pulse duration. Our method is found to reproduce complicated two-dimensional transient conductivity maps exceedingly well, demonstrating the power of the time-domain numerical method for extracting ultrafast and dynamic transport parameters from time...

  4. Energy landscape investigation by wavelet transform analysis of atomic force spectroscopy data in a biorecognition experiment.

    Science.gov (United States)

    Bizzarri, Anna Rita

    2016-01-01

    Force fluctuations recorded in an atomic force spectroscopy experiment, during the approach of a tip functionalized with biotin towards a substrate charged with avidin, have been analyzed by a wavelet transform. The observation of strong transient changes only when a specific biorecognition process between the partners takes place suggests a drastic modulation of the force fluctuations when biomolecules recognize each other. Such an analysis allows to investigate the peculiar features of a biorecognition process. These results are discussed in connection with the possible role of energy minima explored by biomolecules during the biorecognition process.

  5. Nanopuller-open data acquisition platform for AFM force spectroscopy experiments.

    Science.gov (United States)

    Pawlak, Konrad; Strzelecki, Janusz

    2016-05-01

    Atomic Force Microscope (AFM) is a widely used tool in force spectroscopy studies. Presently, this instrument is accessible from numerous vendors, albeit commercial solutions are expensive and almost always hardware and software closed. Approaches for open setups were published, as with modern low cost and readily available piezoelectric actuators, data acquisition interfaces and optoelectronic components building such force spectroscopy AFM is relatively easy. However, suitable software to control such laboratory made instrument was not released. Developing it in the lab requires significant time and effort. Our Nanopuller software described in this paper is intended to eliminate this obstacle. With only minimum adjustments this program can be used to control and acquire data with any suitable National Instruments universal digital/analog interface and piezoelectric actuator analog controller, giving significant freedom and flexibility in designing force spectroscopy experiment. Since the full code, written in a graphical LabVIEW environment is available, our Nanopuller can be easily customized. In this paper we describe the program and test its performance in controlling different setups. Successful and accurate force curve acquisition for standard samples (single molecules of I27O reference titin polyprotein and DNA as well as red blood cells) is shown.

  6. Synthesizing and Characterizing Graphene via Raman Spectroscopy: An Upper-Level Undergraduate Experiment That Exposes Students to Raman Spectroscopy and a 2D Nanomaterial

    Science.gov (United States)

    Parobek, David; Shenoy, Ganesh; Zhou, Feng; Peng, Zhenbo; Ward, Michelle; Liu, Haitao

    2016-01-01

    In this upper-level undergraduate experiment, students utilize micro-Raman spectroscopy to characterize graphene prepared by mechanical exfoliation and chemical vapor deposition (CVD). The mechanically exfoliated samples are prepared by the students while CVD graphene can be purchased or obtained through outside sources. Owing to the intense Raman…

  7. Ultrafast supercontinuum fiber-laser based pump-probe scanning MOKE microscope for the investigation of electron spin dynamics in semiconductors at cryogenic temperatures with picosecond time and micrometer spatial resolution

    CERN Document Server

    Henn, T; Ossau, W; Molenkamp, L W; Biermann, K; Santos, P V

    2013-01-01

    We describe a two-color pump-probe scanning magneto-optical Kerr effect (MOKE) microscope which we have developed to investigate electron spin phenomena in semiconductors at cryogenic temperatures with picosecond time and micrometer spatial resolution. The key innovation of our microscope is the usage of an ultrafast `white light' supercontinuum fiber-laser source which provides access to the whole visible and near-infrared spectral range. Our Kerr microscope allows for the independent selection of the excitation and detection energy while avoiding the necessity to synchronize the pulse trains of two separate picosecond laser systems. The ability to independently tune the pump and probe wavelength enables the investigation of the influence of excitation energy on the optically induced electron spin dynamics in semiconductors. We demonstrate picosecond real-space imaging of the diffusive expansion of optically excited electron spin packets in a (110) GaAs quantum well sample to illustrate the capabilities of t...

  8. An open source/real-time atomic force microscope architecture to perform customizable force spectroscopy experiments.

    Science.gov (United States)

    Materassi, Donatello; Baschieri, Paolo; Tiribilli, Bruno; Zuccheri, Giampaolo; Samorì, Bruno

    2009-08-01

    We describe the realization of an atomic force microscope architecture designed to perform customizable experiments in a flexible and automatic way. Novel technological contributions are given by the software implementation platform (RTAI-LINUX), which is free and open source, and from a functional point of view, by the implementation of hard real-time control algorithms. Some other technical solutions such as a new way to estimate the optical lever constant are described as well. The adoption of this architecture provides many degrees of freedom in the device behavior and, furthermore, allows one to obtain a flexible experimental instrument at a relatively low cost. In particular, we show how such a system has been employed to obtain measures in sophisticated single-molecule force spectroscopy experiments [Fernandez and Li, Science 303, 1674 (2004)]. Experimental results on proteins already studied using the same methodologies are provided in order to show the reliability of the measure system.

  9. Control of stopping position of radioactive ion beam in superfluid helium for laser spectroscopy experiments

    Energy Technology Data Exchange (ETDEWEB)

    Yang, X.F., E-mail: yangxf@ribf.riken.jp [School of Physics, Peking University, Chengfu Road, Haidian District, Beijing 100871 (China); RIKEN Nishina Center, 2-1 Hirosawa, Wako, Saitama 351-0198 (Japan); Furukawa, T. [Dept. of Physics, Tokyo Metropolitan University, 1-1 Minami-Osawa, Hachioji, Tokyo 192-0397 (Japan); Wakui, T. [Cyclotron and Radioisotope Center Tohoku University, 6-3 Aoba, Aramaki, Aoba-ku, Sendai, Miyagi 980-8578 (Japan); Imamura, K. [Dept. of Physics, Meiji University, 1-1-1 Higashi-Mita, Tama-ku, Kawasaki, Kanagawa 214-8571 (Japan); Tetsuka, H. [Dept. of Physics, Tokyo Gakugei University, 4-1-1 Nukuikitamachi, Koganei, Tokyo 184-8501 (Japan); Fujita, T. [Dept. of Physics, Osaka University, 1-1 Machikaneyama, Toyonaka, Osaka 560-0043 (Japan); Yamaguchi, Y. [Dept. of Physics, Meiji University, 1-1-1 Higashi-Mita, Tama-ku, Kawasaki, Kanagawa 214-8571 (Japan); Tsutsui, Y. [Dept. of Physics, Tokyo Gakugei University, 4-1-1 Nukuikitamachi, Koganei, Tokyo 184-8501 (Japan); Mitsuya, Y. [Dept. of Physics, Meiji University, 1-1-1 Higashi-Mita, Tama-ku, Kawasaki, Kanagawa 214-8571 (Japan); Ichikawa, Y. [Dept. of Physics, Tokyo Institute of Technology, 2-12-1 O-Okayama, Meguro, Tokyo152-8551 (Japan); Ishibashi, Y. [RIKEN Nishina Center, 2-1 Hirosawa, Wako, Saitama 351-0198 (Japan); Dept. of Physics, University of Tsukuba, 1-1-1 Tennodai, Tsukuba, Ibaraki 305-8571 (Japan); Yoshida, N.; Shirai, H. [Dept. of Physics, Tokyo Institute of Technology, 2-12-1 O-Okayama, Meguro, Tokyo152-8551 (Japan); Ebara, Y.; Hayasaka, M. [Dept. of Physics, Tokyo Gakugei University, 4-1-1 Nukuikitamachi, Koganei, Tokyo 184-8501 (Japan); Arai, S.; Muramoto, S. [Dept. of Physics, Meiji University, 1-1-1 Higashi-Mita, Tama-ku, Kawasaki, Kanagawa 214-8571 (Japan); Hatakeyama, A. [Dept. of Applied Physics, Tokyo University of Agriculture and Technology, 2-24-16 Naka-cho, Koganei, Tokyo 184-8588 (Japan); Wada, M.; Sonoda, T. [RIKEN Nishina Center, 2-1 Hirosawa, Wako, Saitama 351-0198 (Japan); and others

    2013-12-15

    In order to investigate the structure of exotic nuclei with extremely low yields by measuring nuclear spins and moments, a new laser spectroscopy technique – “OROCHI” (Optical Radioisotopes Observation in Condensed Helium as Ion-catcher) has been proposed in recent years. The feasibility of this technique has been demonstrated by means of a considerable amount of offline and online studies of various atoms in superfluid helium. For in-situ laser spectroscopy of atoms in He II, trapping atoms in the observation region of laser is a key step. Therefore, a method which enables us to trap accelerated atoms at a precise position in He II is highly needed for performing experiment. In this work, a technique making use of a degrader, two plastic scintillators and a photon detection system is established for checking the stopping position of beam based on the LISE++ calculation. The method has been tested and verified by on-line experiments with the {sup 84,85,87}Rb beam. Details of the experimental setup, working procedure and testing results of this method are presented.

  10. Rotational coherence spectroscopy at FLASH. Toward dynamic studies in nanosuperfluids

    Energy Technology Data Exchange (ETDEWEB)

    Kickermann, Andreas

    2013-07-15

    The field of molecular physics, which is focusing on molecular motion in the transition states of physical, chemical, and biological changes, is a wide-spread research area. It strives to reveal the structural and functional properties of molecules, the chemical bonds between atoms and the time evolution. Many processes occurring in nature upon electronic excitation proceed on the ultrafast femtosecond timescale and can be triggered by modern ultrashort femtosecond-laser sources under laboratory conditions. In the present thesis pump-probe studies were performed to follow molecular motion using ultrashort light pulses in the nanometer wavelength range provided by an XUV freeelectron laser (FEL). In detail, alignment of molecular species in space under field-free conditions was investigated. In the specific case of rotational wave packets in molecules the rotational dynamics shows characteristic temporal features, which contain a wealth of information on molecular structure and give insight into molecular coupling mechanisms, i.e. rotational constants and transition frequencies. Within this thesis, Rotational Coherence Spectroscopy (RCS) reveals wave-packet motion observed by subsequent Coulomb explosion of Raman excited carbon monoxide, which results in a time-dependent asymmetry of spatial fragmentation patterns. With the method presented here, the time resolution to elucidate the fast dynamics of strong couplings can be pushed toward a single rotational period even for the fastest rotors. This is due to large pump-probe delays with small subpicosecond step size. This kind of spectroscopy can also be expanded to molecular species, which are not accessible by other powerful spectroscopic methods, such as Fourier-transform microwave spectroscopy (FTMW). Furthermore, it allows to measure weak molecular couplings on a long timescale (large pump-probe delays), e.g. couplings of molecules in a solution or molecules dissolved in quantum fluids. This is valuable to

  11. Kinetics of Hydrolysis of Acetic Anhydride by In-Situ FTIR Spectroscopy: An Experiment for the Undergraduate Laboratory

    Science.gov (United States)

    Haji, Shaker; Erkey, Can

    2005-01-01

    A reaction kinetics experiment for the chemical engineering undergraduate laboratory course was developed in which in-situ Fourier Transfer Infrared spectroscopy was used to measure reactant and product concentrations. The kinetics of the hydrolysis of acetic anhydride was determined by experiments carried out in a batch reactor. The results…

  12. Nanopuller-open data acquisition platform for AFM force spectroscopy experiments

    Energy Technology Data Exchange (ETDEWEB)

    Pawlak, Konrad; Strzelecki, Janusz

    2016-05-15

    Atomic Force Microscope (AFM) is a widely used tool in force spectroscopy studies. Presently, this instrument is accessible from numerous vendors, albeit commercial solutions are expensive and almost always hardware and software closed. Approaches for open setups were published, as with modern low cost and readily available piezoelectric actuators, data acquisition interfaces and optoelectronic components building such force spectroscopy AFM is relatively easy. However, suitable software to control such laboratory made instrument was not released. Developing it in the lab requires significant time and effort. Our Nanopuller software described in this paper is intended to eliminate this obstacle. With only minimum adjustments this program can be used to control and acquire data with any suitable National Instruments universal digital/analog interface and piezoelectric actuator analog controller, giving significant freedom and flexibility in designing force spectroscopy experiment. Since the full code, written in a graphical LabVIEW environment is available, our Nanopuller can be easily customized. In this paper we describe the program and test its performance in controlling different setups. Successful and accurate force curve acquisition for standard samples (single molecules of I27O reference titin polyprotein and DNA as well as red blood cells) is shown. - Highlights: • We created open data acquisition software for performing Atomic Force Microscopy force measurements with custom laboratory made setups. • The software allows large flexibility in atomic force microscope design with minimum adjustment necessary. • The software is written in LabVIEW, allowing easy customization. • We successfully tested the program on two different hardware configurations by stretching single macromolecules and indenting cells.

  13. Spectroscopy of intraband optical transitions in anisotropic semiconductor nanocrystals

    Science.gov (United States)

    Turkov, Vadim K.; Baimuratov, Anvar S.; Rukhlenko, Ivan D.; Baranov, Alexander V.; Fedorov, Anatoly V.

    2013-09-01

    We propose a new type of optical spectroscopy of anisotropic semiconductor nanocrystals, which is based on the welldeveloped stationary pump-probe technique, where the pump and probe fields are absorbed upon, respectively, interband and intraband transitions of the nanocrystals' electronic subsystem. We develop a general theory of intraband absorption based on the density matrix formalism. This theory can be applied to study degenerate eigenstates of electrons in semiconductor nanocrystals of different shapes and dimentions. We demonstrate that the angular dependence of intraband absorption by nonspherical nanocrystals enables investigating their shape and orientation, as well as the symmetry of quantum states excited by the probe field and selection rules of electronic transitions.

  14. Visible photodissociation spectroscopy of PAH cations and derivatives in the PIRENEA experiment

    CERN Document Server

    Useli-Bacchitta, F; Mulas, G; Malloci, G; Toublanc, D; Joblin, C; 10.1016/j.chemphys.2010.03.012

    2010-01-01

    The electronic spectra of gas-phase cationic polycyclic aromatic hydrocarbons (PAHs), trapped in the Fourier Transform Ion Cyclotron Resonance cell of the PIRENEA experiment, have been measured by multiphoton dissociation spectroscopy in the 430-480 nm spectral range using the radiation of a mid-band optical parametric oscillator laser. We present here the spectra recorded for different species of increasing size, namely the pyrene cation (C16H10+), the 1-methylpyrene cation (CH3-C16H9+), the coronene cation (C24H12+), and its dehydrogenated derivative C24H10+. The experimental results are interpreted with the help of time-dependent density functional theory calculations and analysed using spectral information on the same species obtained from matrix isolation spectroscopy data. A kinetic Monte Carlo code has also been used, in the case of pyrene and coronene cations, to estimate the absorption cross-sections of the measured electronic transitions. Gas-phase spectra of highly reactive species such as dehydrog...

  15. Multi-fiber strains measured by micro-Raman spectroscopy: Principles and experiments

    Science.gov (United States)

    Lei, Zhenkun; Wang, Yunfeng; Qin, Fuyong; Qiu, Wei; Bai, Ruixiang; Chen, Xiaogang

    2016-02-01

    Based on widely used axial strain measurement method of Kevlar single fiber, an original theoretical model and measurement principle of application of micro-Raman spectroscopy to multi-fiber strains in a fiber bundle were established. The relationship between the nominal Raman shift of fiber bundle and the multi-fiber strains was deduced. The proposed principle for multi-fiber strains measurement is consistent with two special cases: single fiber deformation and multi-fiber deformation under equal strain. It is found experimentally that the distribution of Raman scattering intensity of a Kevlar 49 fiber as a function of distance between a fiber and the laser spot center follows a Gaussian function. Combining the Raman-shift/strain relationship of the Kevlar 49 single fiber and the uniaxial tension measured by micro-Raman spectroscopy, the Raman shift as a function of strain was obtained. Then the Raman peak at 1610 cm-1 for the Kevlar 49 fiber was fitted to a Lorentzian function and the FWHM showed a quadratic increase with the fiber strain. Finally, a dual-fiber tensile experiment was performed to verify the adequacy of the Raman technique for the measurement of multi-fiber strains.

  16. Simulating systematic errors in X-ray absorption spectroscopy experiments: Sample and beam effects

    Energy Technology Data Exchange (ETDEWEB)

    Curis, Emmanuel [Laboratoire de Biomathematiques, Faculte de Pharmacie, Universite Rene, Descartes (Paris V)-4, Avenue de l' Observatoire, 75006 Paris (France)]. E-mail: emmanuel.curis@univ-paris5.fr; Osan, Janos [KFKI Atomic Energy Research Institute (AEKI)-P.O. Box 49, H-1525 Budapest (Hungary); Falkenberg, Gerald [Hamburger Synchrotronstrahlungslabor (HASYLAB), Deutsches Elektronen-Synchrotron (DESY)-Notkestrasse 85, 22607 Hamburg (Germany); Benazeth, Simone [Laboratoire de Biomathematiques, Faculte de Pharmacie, Universite Rene, Descartes (Paris V)-4, Avenue de l' Observatoire, 75006 Paris (France); Laboratoire d' Utilisation du Rayonnement Electromagnetique (LURE)-Ba-hat timent 209D, Campus d' Orsay, 91406 Orsay (France); Toeroek, Szabina [KFKI Atomic Energy Research Institute (AEKI)-P.O. Box 49, H-1525 Budapest (Hungary)

    2005-07-15

    The article presents an analytical model to simulate experimental imperfections in the realization of an X-ray absorption spectroscopy experiment, performed in transmission or fluorescence mode. Distinction is made between sources of systematic errors on a time-scale basis, to select the more appropriate model for their handling. For short time-scale, statistical models are the most suited. For large time-scale, the model is developed for sample and beam imperfections: mainly sample inhomogeneity, sample self-absorption, beam achromaticity. The ability of this model to reproduce the effects of these imperfections is exemplified, and the model is validated on real samples. Various potential application fields of the model are then presented.

  17. A synthetic diagnostic for beam emission spectroscopy in the helically symmetric experiment stellarator

    Science.gov (United States)

    Dobbins, T. J.; Kumar, S. T. A.; Anderson, D. T.

    2016-11-01

    The Helically Symmetric Experiment (HSX) has a number of active spectroscopy diagnostics. Due to the relatively large beam width compared to the plasma minor radius, it is difficult to achieve good spatial resolution at the core of the HSX plasma. This is due to the fact that the optical sightline cuts through many flux surfaces with varying field vectors within the beam. In order to compare the experimental results with theoretical models it is important to accurately model the beam width effects. A synthetic diagnostic has been developed for this purpose. This synthetic diagnostic calculates the effect of spot size and beam width on the measurements of quantities of interest, including radial electric field, flow velocity, and Stark polarization.

  18. Different mechanisms of action of antimicrobial peptides: insights from fluorescence spectroscopy experiments and molecular dynamics simulations.

    Science.gov (United States)

    Bocchinfuso, Gianfranco; Palleschi, Antonio; Orioni, Barbara; Grande, Giacinto; Formaggio, Fernando; Toniolo, Claudio; Park, Yoonkyung; Hahm, Kyung-Soo; Stella, Lorenzo

    2009-09-01

    Most antimicrobial peptides exert their activity by interacting with bacterial membranes, thus perturbing their permeability. They are investigated as a possible solution to the insurgence of bacteria resistant to the presently available antibiotic drugs. However, several different models have been proposed for their mechanism of membrane perturbation, and the molecular details of this process are still debated. Here, we compare fluorescence spectroscopy experiments and molecular dynamics (MD) simulations regarding the association with lipid bilayers and lipid perturbation for two different amphiphilic helical antimicrobial peptides, PMAP-23 and trichogin GA IV. PMAP-23, a cationic peptide member of the cathelicidin family, is considered to induce membrane permeability according to the Shai-Matsuzaki-Huang "carpet" model, while trichogin GA IV is a neutral peptide, member of the peptaibol family. Although several lines of evidence suggest a "barrel-stave" mechanism of pore formation for the latter peptide, its length is only half the normal thickness of a lipid bilayer. Both fluorescence spectroscopy experiments and MD simulations indicated that PMAP-23 associates with membranes close to their surface and parallel to it, and in this arrangement it causes a severe perturbation to the bilayer, both regarding its surface tension and lipid order. By contrast, trichogin GA IV can undergo a transition from a surface-bound state to a transmembrane orientation. In the first arrangement, it does not cause any strong membrane perturbation, while in the second orientation it might be able to span the bilayer from one side to the other, despite its relatively short length, by causing a significant thinning of the membrane.

  19. Optimization of identity operation in NMR spectroscopy via genetic algorithm: Application to the TEDOR experiment

    Science.gov (United States)

    Manu, V. S.; Veglia, Gianluigi

    2016-12-01

    Identity operation in the form of π pulses is widely used in NMR spectroscopy. For an isolated single spin system, a sequence of even number of π pulses performs an identity operation, leaving the spin state essentially unaltered. For multi-spin systems, trains of π pulses with appropriate phases and time delays modulate the spin Hamiltonian to perform operations such as decoupling and recoupling. However, experimental imperfections often jeopardize the outcome, leading to severe losses in sensitivity. Here, we demonstrate that a newly designed Genetic Algorithm (GA) is able to optimize a train of π pulses, resulting in a robust identity operation. As proof-of-concept, we optimized the recoupling sequence in the transferred-echo double-resonance (TEDOR) pulse sequence, a key experiment in biological magic angle spinning (MAS) solid-state NMR for measuring multiple carbon-nitrogen distances. The GA modified TEDOR (GMO-TEDOR) experiment with improved recoupling efficiency results in a net gain of sensitivity up to 28% as tested on a uniformly 13C, 15N labeled microcrystalline ubiquitin sample. The robust identity operation achieved via GA paves the way for the optimization of several other pulse sequences used for both solid- and liquid-state NMR used for decoupling, recoupling, and relaxation experiments.

  20. Serial Femtosecond Crystallography and Ultrafast Absorption Spectroscopy of the Photoswitchable Fluorescent Protein IrisFP.

    Science.gov (United States)

    Colletier, Jacques-Philippe; Sliwa, Michel; Gallat, François-Xavier; Sugahara, Michihiro; Guillon, Virginia; Schirò, Giorgio; Coquelle, Nicolas; Woodhouse, Joyce; Roux, Laure; Gotthard, Guillaume; Royant, Antoine; Uriarte, Lucas Martinez; Ruckebusch, Cyril; Joti, Yasumasa; Byrdin, Martin; Mizohata, Eiichi; Nango, Eriko; Tanaka, Tomoyuki; Tono, Kensuke; Yabashi, Makina; Adam, Virgile; Cammarata, Marco; Schlichting, Ilme; Bourgeois, Dominique; Weik, Martin

    2016-03-03

    Reversibly photoswitchable fluorescent proteins find growing applications in cell biology, yet mechanistic details, in particular on the ultrafast photochemical time scale, remain unknown. We employed time-resolved pump-probe absorption spectroscopy on the reversibly photoswitchable fluorescent protein IrisFP in solution to study photoswitching from the nonfluorescent (off) to the fluorescent (on) state. Evidence is provided for the existence of several intermediate states on the pico- and microsecond time scales that are attributed to chromophore isomerization and proton transfer, respectively. Kinetic modeling favors a sequential mechanism with the existence of two excited state intermediates with lifetimes of 2 and 15 ps, the second of which controls the photoswitching quantum yield. In order to support that IrisFP is suited for time-resolved experiments aiming at a structural characterization of these ps intermediates, we used serial femtosecond crystallography at an X-ray free electron laser and solved the structure of IrisFP in its on state. Sample consumption was minimized by embedding crystals in mineral grease, in which they remain photoswitchable. Our spectroscopic and structural results pave the way for time-resolved serial femtosecond crystallography aiming at characterizing the structure of ultrafast intermediates in reversibly photoswitchable fluorescent proteins.

  1. The CORONAS-Photon/TESIS experiment on EUV imaging spectroscopy of the Sun

    Science.gov (United States)

    Kuzin, S.; Zhitnik, I.; Bogachev, S.; Bugaenko, O.; Ignat'ev, A.; Mitrofanov, A.; Perzov, A.; Shestov, S.; Slemzin, V.; Suhodrev, N.

    The new experiment TESIS is developent for russian CORONAS-Photon mission launch is planned on the end of 2007 The experiment is aimed on the study of activity of the Sun in the phases of minimum rise and maximum of 24 th cycle of Solar activity by the method of XUV imaging spectroscopy The method is based on the registration full-Sun monochromatic images with high spatial and temporal resolution The scientific tasks of the experiment are i Investigation dynamic processes in corona flares CME etc with high spatial up to 1 and temporal up to 1 second resolution ii determination of the main plasma parameters like plasma electron and ion density and temperature differential emission measure etc iii study of the processes of appearance and development large scale long-life magnetic structures in the solar corona study of the fluency of this structures on the global activity of the corona iv study of the mechanisms of energy accumulation and release in the solar flares and mechanisms of transformation of this energy into the heating of the plasma and kinematics energy To get the information for this studies the TESIS will register full-Sun images in narrow spectral intervals and the monochromatic lines of HeII SiXI FeXXI-FeXXIII MgXII ions The instrument includes 5 independent channels 2 telescopes for 304 and 132 A wide-field 2 5 degrees coronograph 280-330A and 8 42 A spectroheliographs The detailed description of the TESIS experiment and the instrument is presented

  2. Pump laser-induced space-charge effects in HHG-driven time- and angle-resolved photoelectron spectroscopy

    Science.gov (United States)

    Oloff, L.-P.; Hanff, K.; Stange, A.; Rohde, G.; Diekmann, F.; Bauer, M.; Rossnagel, K.

    2016-06-01

    With the advent of ultrashort-pulsed extreme ultraviolet sources, such as free-electron lasers or high-harmonic-generation (HHG) sources, a new research field for photoelectron spectroscopy has opened up in terms of femtosecond time-resolved pump-probe experiments. The impact of the high peak brilliance of these novel sources on photoemission spectra, so-called vacuum space-charge effects caused by the Coulomb interaction among the photoemitted probe electrons, has been studied extensively. However, possible distortions of the energy and momentum distributions of the probe photoelectrons caused by the low photon energy pump pulse due to the nonlinear emission of electrons have not been studied in detail yet. Here, we systematically investigate these pump laser-induced space-charge effects in a HHG-based experiment for the test case of highly oriented pyrolytic graphite. Specifically, we determine how the key parameters of the pump pulse—the excitation density, wavelength, spot size, and emitted electron energy distribution—affect the measured time-dependent energy and momentum distributions of the probe photoelectrons. The results are well reproduced by a simple mean-field model, which could open a path for the correction of pump laser-induced space-charge effects and thus toward probing ultrafast electron dynamics in strongly excited materials.

  3. Development of PID counter for charmed baryon spectroscopy experiment at J-PARC

    Energy Technology Data Exchange (ETDEWEB)

    Yamaga, T. [Research Center for Nuclear Physics (RCNP), Osaka University, 10-1, Mihogaoka, Ibaraki-shi, Osaka 567-0047 (Japan); Ishikawa, T. [ELPH, Tohoku University, 1-2-1, Mikamine, Taihaku-ku, Sendai-shi, Miyagi (Japan); Miyachi, Y. [Department of Physics, Yamagata University, 1-4-12, Shirakawa-cho, Yamagata-shi, Yamagata 990-8560 (Japan); Morino, Y. [RIKEN Nishina Center, RIKEN, 2-1, Hirosawa, Wako-shi, Saitama 351-0198 (Japan); Nakano, T.; Noumi, H. [Research Center for Nuclear Physics (RCNP), Osaka University, 10-1, Mihogaoka, Ibaraki-shi, Osaka 567-0047 (Japan); Ozawa, K. [KEK, 1-1, Oho, Tsukuba-shi, Ibaraki 305-0801 (Japan); Shirotori, K.; Sugaya, Y. [Research Center for Nuclear Physics (RCNP), Osaka University, 10-1, Mihogaoka, Ibaraki-shi, Osaka 567-0047 (Japan); Tanida, K. [Department of Physics and Astronomy, Seoul National University, Seoul 151-747 (Korea, Republic of)

    2014-12-01

    We have proposed an experiment for studying charmed baryons via the p(π{sup −},D{sup ⁎−}) reaction at the J-PARC high-momentum beam line. Charmed baryons will be measured by a missing mass method. Scattered D{sup ⁎−} will be reconstructed by detecting its decay chain of D{sup ⁎−}→D{sup ¯0}π{sup −}→K{sup +}π{sup −}π{sup −}. We designed a Ring Imaging Cherenkov (RICH) counter with two radiators, aerogel and C{sub 4}F{sub 10} of refractive indices 1.04 and 1.00137, respectively, in order to identify pions and kaons in a wide momentum range from 2 to 16 GeV/c. Spherical mirrors will be used to focus Cherenkov photons to the photon sensor alloys. The performance of the designed RICH counter is evaluated by a Monte-Carlo simulation based on GEANT4. Detection efficiency for scattered particles averaged over π and K is found to be 99%. Wrong particle identification ratios of pions and protons to kaons are 0.1% and 0.14%, respectively. The background level in the inclusive p(π{sup −},D{sup ⁎−}) spectrum increases only 5% due to the wrong identifications. - Highlights: • We design the PID counter for using charmed baryon spectroscopy experiment at JPARC. • The designed PID counter was studied with GEANT4 simulation and expected particle distribution in the experiment. • The estimated efficiency of pion and kaon is about 99% and wrong ID ratio is small enough.

  4. Temperature and Electron Density Determination on Laser-Induced Breakdown Spectroscopy (LIBS) Plasmas: A Physical Chemistry Experiment

    Science.gov (United States)

    Najarian, Maya L.; Chinni, Rosemarie C.

    2013-01-01

    This laboratory is designed for physical chemistry students to gain experience using laser-induced breakdown spectroscopy (LIBS) in understanding plasma diagnostics. LIBS uses a high-powered laser that is focused on the sample causing a plasma to form. The emission of this plasma is then spectrally resolved and detected. Temperature and electron…

  5. Temperature and Electron Density Determination on Laser-Induced Breakdown Spectroscopy (LIBS) Plasmas: A Physical Chemistry Experiment

    Science.gov (United States)

    Najarian, Maya L.; Chinni, Rosemarie C.

    2013-01-01

    This laboratory is designed for physical chemistry students to gain experience using laser-induced breakdown spectroscopy (LIBS) in understanding plasma diagnostics. LIBS uses a high-powered laser that is focused on the sample causing a plasma to form. The emission of this plasma is then spectrally resolved and detected. Temperature and electron…

  6. Pressure-dependent DLTS (Deep Level Transient Spectroscopy) experiments on Si-doped AlGaAs

    Energy Technology Data Exchange (ETDEWEB)

    Farmer, J.W.; Hjalmarson, H.P.; Samara, G.A.

    1987-01-01

    Pressure dependent Deep Level Transient Spectroscopy (DLTS) experiments are used to measure the properties of the deep donors (DX-centers) responsible for the persistent photoconductivity effect in Si-doped AlGaAs. The sample dependence of the DLTS spectra shows evidence for a defect complex involved in the DX-center. 9 refs., 4 figs.

  7. Pressure-dependent DLTS (Deep Level Transient Spectroscopy) experiments on Si-doped AlGaAs

    Science.gov (United States)

    Farmer, J. W.; Hjalmarson, H. P.; Samara, G. A.

    Pressure dependent Deep Level Transient Spectroscopy (DLTS) experiments are used to measure the properties of the deep donors (DX-centers) responsible for the persistent photoconductivity effect in Si-doped AlGaAs. The sample dependence of the DLTS spectra shows evidence for a defect complex involved in the DX-center.

  8. Two-color femtosecond experiments by use of two independently tunable Ti:sapphire lasers with a sample-and-hold switch.

    Science.gov (United States)

    Sohn, J Y; Ahn, Y H; Yee, K J; Kim, D S

    1999-09-20

    We performed femtosecond two-color experiments (four-wave mixing and pump probe) using two independently tunable, partially synchronized femtosecond lasers. Despite the fact that the jitter is of the order of 5-10 ps, the time resolution is limited only by the pulse width when a homemade sample-and-hold switch is used.

  9. Development of a pump-probe facility with sub-picosecond time resolution combining a high-power ultraviolet regenerative FEL amplifier and a soft X-ray SASE FEL

    CERN Document Server

    Faatz, B; Feldhaus, J; Krzywinski, J; Pflüger, J; Rossbach, J; Saldin, E L; Schneidmiller, E A; Yurkov, M V

    2001-01-01

    This paper presents the conceptual design of a high power radiation source with laser-like characteristics in the ultraviolet spectral range at the TESLA Test Facility (TTF). The concept is based on the generation of radiation in a regenerative FEL amplifier (RAFEL). The RAFEL described in this paper covers a wavelength range of 200-400 nm and provides 200 fs pulses with 2 mJ of optical energy per pulse. The linac operates at 1% duty factor and the average output radiation power exceeds 100 W. The RAFEL will be driven by the spent electron beam leaving the soft X-ray FEL, thus providing minimal interference between these two devices. The RAFEL output radiation has the same time structure as the X-ray FEL and the UV pulses are naturally synchronized with the soft X-ray pulses from the TTF FEL. Therefore, it should be possible to achieve synchronization close to the duration of the radiation pulses (200 fs) for pump-probe techniques using either an UV pulse as a pump and soft X-ray pulse as a probe, or vice ver...

  10. Photo-stability of Super-hydrogenated PAHs Determined by Action Spectroscopy Experiments

    Science.gov (United States)

    Wolf, M.; Kiefer, H. V.; Langeland, J.; Andersen, L. H.; Zettergren, H.; Schmidt, H. T.; Cederquist, H.; Stockett, M. H.

    2016-11-01

    We have investigated the photo-stability of pristine and super-hydrogenated pyrene cations ({{{C}}}16{{{H}}}10+m+,m=0,6,{{}} {{or}} {{}}16) by means of gas-phase action spectroscopy. Optical absorption spectra and photo-induced dissociation mass spectra are presented. By measuring the yield of mass-selected photo-fragment ions as a function of laser pulse intensity, the number of photons (and hence the energy) needed for fragmentation of the carbon backbone was determined. Backbone fragmentation of pristine pyrene ions ({{{C}}}16{{{H}}}10+) requires absorption of three photons of energy just below 3 eV, whereas super-hydrogenated hexahydropyrene (C16H{}16+) must absorb two such photons and fully hydrogenated hexadecahydropyrene (C16H{}26+) only a single photon. These results are consistent with previously reported dissociation energies for these ions. Our experiments clearly demonstrate that the increased heat capacity from the additional hydrogen atoms does not compensate for the weakening of the carbon backbone when pyrene is hydrogenated. In photodissociation regions, super-hydrogenated Polycyclic Aromatic Hydrocarbons (PAHs) have been proposed to serve as catalysts for H2 formation. Our results indicate that carbon backbone fragmentation may be a serious competitor to H2 formation at least for small hydrogenated PAHs like pyrene.

  11. Photo-stability of super-hydrogenated PAHs determined by action spectroscopy experiments

    CERN Document Server

    Wolf, M; Langeland, J; Andersen, L H; Zettergren, H; Schmidt, H T; Cederquist, H; Stockett, M H

    2016-01-01

    We have investigated the photo-stability of pristine and super-hydrogenated pyrene cations C$_{16}$H$_{10+m}^+, m = 0,6, \\mathrm{\\ or\\ } 16$) by means of gas-phase action spectroscopy. Optical absorption spectra and photo-induced dissociation mass spectra are presented. By measuring the yield of mass-selected photo-fragment ions as a function of laser pulse intensity, the number of photons (and hence the energy) needed for fragmentation of the carbon backbone was determined. Backbone fragmentation of pristine pyrene ions (C$_{16}$H$_{10}^+$) requires absorption of three photons of energy just below 3 eV, whereas super-hydrogenated hexahydropyrene (C$_{16}$H$_{16}^+$) must absorb two such photons and fully hydrogenated hexadecahydropyrene (C$_{16}$H$_{26}^+$) only a single photon. These results are consistent with previously reported dissociation energies for these ions. Our experiments clearly demonstrate that the increased heat capacity from the additional hydrogen atoms does not compensate for the weakening...

  12. Understanding Multiferroic Hexagonal Manganites by Static and Ultrafast Optical Spectroscopy

    Directory of Open Access Journals (Sweden)

    Yu Ting Wang

    2013-01-01

    Full Text Available Multiferroic hexagonal manganites ReMnO3 studied by optics are reviewed. Their electronic structures were revealed by static linear and nonlinear spectra. Two transitions located at ~1.7 eV and ~2.3 eV have been observed and attributed to the interband transitions from the lower-lying Mn3+dxy/dx2-y2 and dxz/dyz states to the Mn3+d3z2-r2 state, respectively. These so-called d-d transitions exhibit a blueshift as decreasing temperatures and an extra blueshift near TN. This dramatic change indicates that the magnetic ordering seriously influences the electronic structure. On the other hand, the ultrafast optical pump-probe spectroscopy has provided the important information on spin-charge coupling and spin-lattice coupling. Because of the strongly correlation between electronic structure and magnetic ordering, the amplitude of the initial rising component in ΔR/R shows striking changes at the vicinity of TN. Moreover, the coherent optical and acoustic phonons were observed on optical pump-probe spectroscopy. Both the amplitude and dephasing time of coherent phonons also exhibit significant changes at TN, which provide the evidence for spin-lattice interaction in these intriguing materials.

  13. Synthesis and Resolution of the Atropisomeric 1,1'-Bi-2-Naphthol: An Experiment in Organic Synthesis and 2-D NMR Spectroscopy

    Science.gov (United States)

    Mak, Kendrew K. W.

    2004-01-01

    NMR spectroscopy is presented. It is seen that the experiment regarding the synthesis and resolution of 1,1'-Bi-2-naphtol presents a good experiment for teaching organic synthesis and NMR spectroscopy and provides a strategy for obtaining enantiopure compounds from achiral starting materials.

  14. Synthesis and Resolution of the Atropisomeric 1,1'-Bi-2-Naphthol: An Experiment in Organic Synthesis and 2-D NMR Spectroscopy

    Science.gov (United States)

    Mak, Kendrew K. W.

    2004-01-01

    NMR spectroscopy is presented. It is seen that the experiment regarding the synthesis and resolution of 1,1'-Bi-2-naphtol presents a good experiment for teaching organic synthesis and NMR spectroscopy and provides a strategy for obtaining enantiopure compounds from achiral starting materials.

  15. Polarization-enhanced absorption spectroscopy for laser stabilization.

    Science.gov (United States)

    Kunz, Paul D; Heavner, Thomas P; Jefferts, Steven R

    2013-11-20

    We demonstrate a variation of pump-probe spectroscopy that is particularly useful for laser frequency stabilization. The polarization-enhanced absorption spectroscopy (POLEAS) signal provides a significant improvement in signal-to-noise ratio over saturated absorption spectroscopy (SAS) for the important and commonly used atomic cycling transitions. The improvements can directly increase the short-term stability of a laser frequency lock, given sufficient servo loop bandwidth. The long-term stability of the POLEAS method, which is limited by environmental sensitivities, is comparable to that of SAS. The POLEAS signal is automatically Doppler-free, without requiring a separate Doppler subtraction beam, and lends itself to straightforward compact packaging. Finally, by increasing the amplitude of the desired (cycling) peak, while reducing the amplitude of all other peaks in the manifold, the POLEAS method eases the implementation of laser auto-locking schemes.

  16. Optical and Microwave Spectroscopy of Transient Metal-Containing Molecules

    Science.gov (United States)

    Steimle, Timothy

    2016-06-01

    Small metal containing molecules are ideal venues for testing Fundamental Physics, investigating relativistic effects, and modelling spin-orbit induced unimolecular dynamics. Electronic spectroscopy is an effective method for probing these phenomena because such spectra are readily recorded at the natural linewidth limited resolution and accuracy of 0.0001 wn. The information garnered includes fine and hyperfine interactions, magnetic and electric dipoles, and dynamics. With this in mind, three examples from our recent (unpublished) studies will be highlighted. SiHD: Long ago Duxbury et al. developed a semi-quantitative model invoking Renner-Teller and spin-orbit coupling of the tilde{a}3B{1}, tilde{X}1A1, and tilde{A}1B1, states to explain the observed local perturbations and anomalous radiative lifetimes in the visible spectrum. More recently, the tilde{a}3B1 to tilde{A}1B1 intersystem crossing has been modeled using both semi-classical transition state theory and quantum trajectory surface hopping dynamics. Here we investigate the effects of the reduced symmetry of SiHD on the spectroscopy and dynamics using 2D spectroscopy. Rotationally resolved lines in the origin tilde{X}1A'→ tilde{A}1A" band are assigned to both c-type transitions and additional axis-switching induced transitions. AuO and AuS: The observed markedly different bonding of thiols and alcohols to gold clusters should be traceable to the difference in Au-O and Au-S bonding. To investigate this difference we have used optical Stark and Zeeman spectroscopy to determine the permanent electric dipole moments and magnetic g-factors. The results are rationalized using simple m.o. correlation diagrams and compared to ab initio predictions. TaN: TaN is the best candidate to search for a T,P- violating nuclear magnetic quadrupole moment. Here we report on the optical 2D, Stark, and Zeeman spectra, and our efforts to record the pure rotational spectrum using the separated field pump/probe microwave

  17. Experiments with the High Resolution Kaon Spectrometer at Jlab Hall C and the New Spectroscopy of ^12_Lambda B Hypernuclei

    Energy Technology Data Exchange (ETDEWEB)

    Tang, Liguang; Chen, Chunhua; Gogami, Toshiyuki; Kawama, Daisuke; Han, Yuncheng; Yuan, Lulin; Matsumura, Akihiko; Okayasu, Yuichi; Seva, Tomislav; Rodriguez, Victor; Baturin, Pavlo; Acha Quimper, Armando; Achenbach, Carsten; Ahmidouch, Abdellah; Albayrak, Ibrahim; Androic, Darko; Asaturyan, Arshak; Asaturyan, Razmik; Ates, Ozgur; Badui, Rafael; Baker, Oliver; Benmokhtar, Fatiha; Boeglin, Werner; Bono, Jason; Bosted, Peter; Brash, Edward; Carter, Philip; Carlini, Roger; Chiba, Atsushi; Christy, Michael; Cole, Leon; Dalton, Mark; Danagoulian, Samuel; Daniel, Aji; De Leo, Raffaele; Dharmawardane, Kahanawita; Doi, Daisuke; Egiyan, Kim; Elaasar, Mostafa; Ent, Rolf; Fenker, Howard; Fujii, Yu; Furic, Miroslav; Gabrielyan, Marianna; Gan, Liping; Garibaldi, Franco; Gaskell, David; Gasparian, Ashot; Gibson, Edward; Gueye, Paul; Hashimoto, Osamu; Honda, D; Horn, Tanja; Hu, Bitao; Hungerford, Ed; Jayalath, Chandana; Jones, Mark; Johnston, Kathleen; Kalantarians, Narbe; Kanda, Hiroki; Kaneta, M; Kato, F; Kato, Seigo; Kawai, Masaharu; Keppel, Cynthia; Khanal, Hari; Kohl, M; Kramer, Laird; Lan, Kejian; Li, Ya; Habarakada Liyanage, Anusha; Luo, Wei; Mack, David; Maeda, Kazushige; Malace, Simona; Margaryan, Amur; Marikyan, Gagik; Markowitz, Pete; Maruta, Tomofumi; Maruyama, Nayuta; Maxwell, Victor; Millener, David; Miyoshi, Toshinobu; Mkrtchyan, Arthur; Mkrtchyan, Hamlet; Motoba, Toshio; Nagao, Sho; Nakamura, Satoshi; Narayan, Amrendra; Neville, Casey; Niculescu, Gabriel; Niculescu, Maria; Nunez, Angel; Nuruzzaman, nfn; Nomura, Hiroshi; Nonaka, Kenichi; Ohtani, Atsushi; Oyamada, Masamichi; Perez, Naipy; Petkovic, Tomislav; Pochodzalla, J; Qiu, Xiyu; Randeniya, Kapugodage; Raue, Brian; Reinhold, Joerg; Rivera, R; Roche, Julie; Samanta, Chhanda; Sato, Yoshinori; Sawatzky, Bradley; Segbefia, Edwin; Schott, Diane; Shichijo, Ayako; Simicevic, Neven; Smith, Gregory; Song, Yushou; Sumihama, Mizuki; Tadevosyan, Vardan; Takahashi, Toshiyuki; Taniya, Naotaka; Tsukada, Kyo; Tvaskis, Vladas; Veilleux, Micah; Vulcan, William; Wells, Steven; Wesselmann, Frank; Wood, Stephen; Yamamoto, Taku; Yan, Chen; Ye, Z; Yokota, Kosuke; Zhamkochyan, Simon; Zhu, Lingyan

    2014-09-01

    Since the pioneering experiment, E89-009 studying hypernuclear spectroscopy using the $(e,e^{\\prime}K^+)$ reaction was completed, two additional experiments, E01-011 and E05-115, were performed at Jefferson Lab. These later experiments used a modified experimental design, the "Tilt Method", to dramatically suppress the large electromagnetic background, and allowed for a substantial increase in luminosity. Additionally, a new kaon spectrometer, HKS (E01-011), a new electron spectrometer, HES, and a new splitting magnet were added to produce precision, high-resolution hypernuclear spectroscopy. These two experiments, E01-011 and E05-115, resulted in two new data sets, producing sub-MeV energy resolution in the spectra of ${}^{7}_{\\Lambda}\\text{He}$, ${}^{12}_{\\Lambda}\\text{B}$ and ${}^{28}_{\\Lambda} \\text{Al}$ and ${}^{7}_{\\Lambda}\\text{He}$, ${}^{10}_{\\Lambda}\\text{Be}$, ${}^{12}_{\\Lambda}\\text{B}$ and ${}^{52}_{\\Lambda}\\text{V}$. All three experiments obtained a ${}^{12}_{\\Lambda}\\text{B}$, spectrum, which is the most characteristic $p$-shell hypernucleus and is commonly used for calibration. Independent analyses of these different experiments demonstrate excellent consistency and provide the clearest level structure to date of this hypernucleus as produced by the $(e,e^{\\prime}K^+)$ reaction. This paper presents details of these experiments, and the extraction and analysis of the observed ${}^{12}_{\\Lambda}\\text{B}$ spectrum.

  18. Far-Ir Spectroscopy of Neutral Gas Phase Peptides: Signatures from Combined Experiments and Simulations

    Science.gov (United States)

    Mahé, Jérôme; Gaigeot, Marie-Pierre; Bakker, Daniël; Jaeqx, Sander; Rijs, Anouk

    2016-06-01

    Within the past two decades, action vibrational spectroscopy has become an almost routine experimental method to probe the structures of molecules and clusters in the gas phase (neutral and ions). Such experiments are mainly performed in the 1000-4000 wn fingerprint regions. Though successful in many respects, these spectral domains can be however restrictive in the information provided, and sometimes reach limitations for unravelling structures without ambiguity. In a collaborative work with the group of Dr A.M. Rijs (FELIX laboratory, Radbout University, The Netherlands) we have launched a new strategy where the far-IR/Tera-Hertz domain (100-800 wn domain) is experimentally probed for neutral gas phase molecules. Our group in Paris apply finite temperature DFT-based molecular dynamics (DFT-MD) simulations in order to unravel the complex signatures arising in the far-IR domain, and provide an unambiguous assignment both of the structural conformation of the gas phase molecules (taking into account the experimental conditions) and an understanding of the spectral signatures/fingerprints. We will discuss our experimental and theoretical investigations on two neutral peptides in the 100-800 wn far-IR spectral domain, i.e. Z-Ala6 and PheGly dipeptide, that represent two systems which definitive conformational assignment was not possible without the far IR signatures. We will also present our very recent results on the Phe-X peptide series, where X stands for Gly, Ala, Pro, Val, Ser, Cys, combining experiments and DFT-MD simulations, providing a detailed understanding of the vibrational fingerprints in the far-IR domain. In all exemples, we will show how DFT-MD simulations is the proper theoretical tool to account for vibrational anharmonicities and mode couplings, of prime importance in the far-IR domain. References : J. Mahé, S. Jaeqx, A.M. Rijs, M.P. Gaigeot, Phys. Chem. Chem. Phys., 17 :25905 (2015) S. Jaeqx, J. Oomens, A. Cimas, M.P. Gaigeot, A.M. Rijs, Angew

  19. Complex Roles of Solution Chemistry on Graphene Oxide Coagulation onto Titanium Dioxide: Batch Experiments, Spectroscopy Analysis and Theoretical Calculation

    OpenAIRE

    Shujun Yu; Xiangxue Wang; Rui Zhang; Tongtong Yang; Yuejie Ai; Tao Wen; Wei Huang; Tasawar Hayat; Ahmed Alsaedi; Xiangke Wang

    2017-01-01

    Although graphene oxide (GO) has been used in multidisciplinary areas due to its excellent physicochemical properties, its environmental behavior and fate are still largely unclear. In this study, batch experiments, spectroscopy analysis and theoretical calculations were addressed to promote a more comprehensive understanding toward the coagulation behavior of GO onto TiO2 under various environmental conditions (pH, co-existing ions, temperature, etc.). The results indicated that neutral pH w...

  20. 2D IR spectroscopy with phase-locked pulse pairs from a birefringent delay line.

    Science.gov (United States)

    Réhault, Julien; Maiuri, Margherita; Manzoni, Cristian; Brida, Daniele; Helbing, Jan; Cerullo, Giulio

    2014-04-21

    We introduce a new scheme for two-dimensional IR spectroscopy in the partially collinear pump-probe geometry. Translating birefringent wedges allow generating phase-locked pump pulses with exceptional phase stability, in a simple and compact setup. A He-Ne tracking scheme permits to scan continuously the acquisition time. For a proof-of-principle demonstration we use lithium niobate, which allows operation up to 5 μm. Exploiting the inherent perpendicular polarizations of the two pump pulses, we also demonstrate signal enhancement and scattering suppression.

  1. Two-dimensional electronic spectroscopy in the ultraviolet by a birefringent delay line.

    Science.gov (United States)

    Borrego-Varillas, Rocio; Oriana, Aurelio; Ganzer, Lucia; Trifonov, Anton; Buchvarov, Ivan; Manzoni, Cristian; Cerullo, Giulio

    2016-12-12

    We introduce a 2D electronic spectroscopy setup in the UV spectral range in the partially collinear pump-probe geometry. The required interferometrically phase-locked few-optical-cycle UV pulse pair is generated by combining a passive birefringent interferometer in the visible and nonlinear phase transfer. This is achieved by sum-frequency generation between the phase-locked visible pulse pair and narrowband infrared pulses. We demonstrate a pair of 16-fs, 330-nm pulses whose delay is interferometrically stable with an accuracy better than λ/450. 2DUV maps of pyrene solution probed in the UV and visible spectral ranges are demonstrated.

  2. Polarization spectroscopy and magnetically-induced dichroism of the potassium D2 lines

    CERN Document Server

    Pahwa, K; Goldwin, J

    2012-01-01

    We study modulation-free methods for producing sub-Doppler, dispersive line shapes for laser stabilization near the potassium D2 transitions at 767 nm. Polarization spectroscopy is performed and a comparison is made between the use of a mirror or beam splitter for aligning the counter-propagating pump and probe beams. Conventional magnetically-induced dichroism is found to suffer from a small dispersion and large background offset. We therefore introduce a modified scheme, using two spatially separated pump-probe beam pairs. Finally we compare our results to methods using phase modulation and heterodyne detection.

  3. Rapid and economical data acquisition in ultrafast frequency-resolved spectroscopy using choppers and a microcontroller.

    Science.gov (United States)

    Guo, Liang; Monahan, Daniele M; Fleming, Graham

    2016-08-08

    Spectrometers and cameras are used in ultrafast spectroscopy to achieve high resolution in both time and frequency domains. Frequency-resolved signals from the camera pixels cannot be processed by common lock-in amplifiers, which have only a limited number of input channels. Here we demonstrate a rapid and economical method that achieves the function of a lock-in amplifier using mechanical choppers and a programmable microcontroller. We demonstrate the method's effectiveness by performing a frequency-resolved pump-probe measurement on the dye Nile Blue in solution.

  4. The HKS Experiments at JLab Hall C and the New Spectroscopy of ${}^{12}_{\\Lambda}\\text{B}$ Hypernuclei

    CERN Document Server

    Tang, L; Gogami, T; Kawama, D; Han, Y; Yuan, L; Matsumura, A; Okayasu, Y; Seva, T; Rodriguez, V M; Baturin, P; Acha, A; Achenbach, P; Ahmidouch, A; Albayrak, I; Androic, D; Asaturyan, A; Asaturyan, R; Ates, O; Badui, R; Baker, O K; Benmokhtar, F; Boeglin, W; Bono, J; Bosted, P; Brash, E; Carter, P; Carlini, R; Chiba, A; Christy, M; Cole, L; Dalton, M; Danagoulian, S; Daniel, A; De Leo, R; Dharmawardane, V; Doi, D; Egiyan, K; Elaasar, M; Ent, R; Fenker, H; Fujii, Y; Furic, M; Gabrielyan, M; Gan, L; Garibaldi, F; Gaskell, D; Gasparian, A; Gibson, E F; Gueye, P; Hashimoto, O; Honda, D; Horn, T; Hu, B; Hungerford, Ed V; Jayalath, C; Jones, M; Johnston, K; Kalantarians, N; Kanda, H; Kaneta, M; Kato, F; Kato, S; Kawai, M; Keppel, C; Khanal, H; Kohl, M; Kramer, L; Lan, K J; Li, Y; Liyanage, A; Luo, W; Mack, D; Maeda, K; Malace, S; Margaryan, A; Marikyan, G; Markowitz, P; Maruta, T; Maruyama, N; Maxwell, V; Millener, D J; Miyoshi, T; Mkrtchyan, A; Mkrtchyan, H; Motoba, T; Nagao, S; Nakamura, S N; Narayan, A; Neville, C; Niculescu, G; Niculescu, M I; Nunez, A; Nuruzzaman,; Nomura, H; Nonaka, K; Ohtani, A; Oyamada, M; Perez, N; Petkovic, T; Pochodzalla, J; Qiu, X; Randeniya, S; Raue, B; Reinhold, J; Rivera, R; Roche, J; Samanta, C; Sato, Y; Sawatzky, B; Segbefia, E K; Schott, D; Shichijo, A; Simicevic, N; Smith, G; Song, Y; Sumihama, M; Tadevosyan, V; Takahashi, T; Taniya, N; Tsukada, K; Tvaskis, V; Veilleux, M; Vulcan, W; Wells, S; Wesselmann, F R; Wood, S A; Yamamoto, T; Yan, C; Ye, Z; Yokota, K; Zhamkochyan, S; Zhu, L

    2014-01-01

    Since the pioneering experiment, E89-009 studying hypernuclear spectroscopy using the $(e,e^{\\prime}K^+)$ reaction was completed, two additional experiments, E01-011 and E05-115, were performed at Jefferson Lab. These later experiments used a modified experimental design, the "Tilt Method", to dramatically suppress the large electromagnetic background, and allowed for a substantial increase in luminosity. Additionally, a new kaon spectrometer, HKS (E01-011), a new electron spectrometer, HES, and a new splitting magnet were added to produce precision, high-resolution hypernuclear spectroscopy. These two experiments, E01-011 and E05-115, resulted in two new data sets, producing sub-MeV energy resolution in the spectra of ${}^{7}_{\\Lambda}\\text{He}$, ${}^{12}_{\\Lambda}\\text{B}$ and ${}^{28}_{\\Lambda}\\text{Al}$ and ${}^{7}_{\\Lambda}\\text{He}$, ${}^{10}_{\\Lambda}\\text{Be}$, ${}^{12}_{\\Lambda}\\text{B}$ and ${}^{52}_{\\Lambda}\\text{V}$. All three experiments obtained a ${}^{12}_{\\Lambda}\\text{B}$, spectrum, which is ...

  5. COMPLIS experiments: COllaboration for spectroscopy Measurements using a Pulsed Laser Ion Source

    Energy Technology Data Exchange (ETDEWEB)

    Sauvage, J. [IN2P3-CNRS, Institut de Physique Nucleaire (France); Boos, N. [Universitaet Mainz, Institut fuer Physik (Germany); Cabaret, L. [Laboratoire AimeCotton (France); Crawford, J.E. [McGill University, Physics Department (Canada); Duong, H.T. [Laboratoire AimeCotton (France); Genevey, J. [IN2P3-CNRS, Institut des Sciences Nucleaires (France); Girod, M. [Commissariat al' Energie Atomique, Service de Physique Nucleaire (France); Huber, G. [Universitaet Mainz, Institut fuer Physik (Germany); Ibrahim, F. [IN2P3-CNRS, Institut de Physique Nucleaire (France); Krieg, M. [Universitaet Mainz, Institut fuer Physik (Germany); Le Blanc, F. [IN2P3-CNRS, Institut de Physique Nucleaire (France); Lee, J.K.P. [McGill University, Physics Department (Canada); Libert, J. [Centre d' Etudes Nucleaires de Bordeaux Gradignan (France); Lunney, D.; Obert, J.; Oms, J. [IN2P3-CNRS, Institut de Physique Nucleaire (France); Peru, S. [Commissariat al' Energie Atomique, Service de Physique Nucleaire (France); Pinard, J. [Laboratoire AimeCotton (France); Putaux, J.C.; Roussiere, B. [IN2P3-CNRS, Institut de Physique Nucleaire (France)] (and others)

    2000-12-15

    Laser spectroscopy measurements have been carried out on very neutron-deficient isotopes of Au, Pt and Ir, produced as daughter elements from a Hg ISOLDE beam. For these transitional region nuclides, the hyperfine structure (HFS) and isotope shift (IS) were measured by Resonance Ionization Spectroscopy (RIS). Magnetic moments {mu}, spectroscopic quadrupole moments Q{sub s} and changes of the nuclear mean square charge radius {delta}along isotopic series have been extracted. For some results, a detailed comparison with theoretical predictions is presented.

  6. Rapid screening of wheat bran contaminated by deoxynivalenol mycotoxin using Raman spectroscopy: a preliminary experiment

    Science.gov (United States)

    Mignani, A. G.; Ciaccheri, L.; Mencaglia, A. A.; De Girolamo, A.; Lippolis, V.; Pascale, M.

    2016-05-01

    Deoxynivalenol (DON) is a mycotoxin frequently occurring in cereals and derived products, and regulated in many countries. Raman spectroscopy performed using optical fibers, with excitation at 1064 nm and a dispersive detection scheme, was utilized to analyze wheat bran samples naturally contaminated with DON. A multivariate processing of the spectroscopic data allowed to distinguish two classes of contamination, with DON below and above 400 μg/kg, respectively. Only one highly contaminated sample was misclassified. This preliminary result demonstrates the potential of Raman spectroscopy as a useful analytical tool for the non-destructive and rapid analysis of mycotoxins in food.

  7. Applications and results of X-ray spectroscopy in implosion experiments on the National Ignition Facility

    Science.gov (United States)

    Epstein, R.; Regan, S. P.; Hammel, B. A.; Suter, L. J.; Scott, H. A.; Barrios, M. A.; Bradley, D. K.; Callahan, D. A.; Cerjan, C.; Collins, G. W.; Dixit, S. N.; Döppner, T.; Edwards, M. J.; Farley, D. R.; Fournier, K. B.; Glenn, S.; Glenzer, S. H.; Golovkin, I. E.; Hamza, A.; Hicks, D. G.; Izumi, N.; Jones, O. S.; Key, M. H.; Kilkenny, J. D.; Kline, J. L.; Kyrala, G. A.; Landen, O. L.; Ma, T.; MacFarlane, J. J.; Mackinnon, A. J.; Mancini, R. C.; McCrory, R. L.; Meyerhofer, D. D.; Meezan, N. B.; Nikroo, A.; Park, H.-S.; Patel, P. K.; Ralph, J. E.; Remington, B. A.; Sangster, T. C.; Smalyuk, V. A.; Springer, P. T.; Town, R. P. J.; Tucker, J. L.

    2017-03-01

    Current inertial confinement fusion experiments on the National Ignition Facility (NIF) [G. H. Miller, E. I. Moses, and C. R. Wuest, Opt. Eng. 43, 2841 (2004)] are attempting to demonstrate thermonuclear ignition using x-ray drive by imploding spherical targets containing hydrogen-isotope fuel in the form of a thin cryogenic layer surrounding a central volume of fuel vapor [J. Lindl, Phys. Plasmas 2, 3933 (1995)]. The fuel is contained within a plastic ablator layer with small concentrations of one or more mid-Z elements, e.g., Ge or Cu. The capsule implodes, driven by intense x-ray emission from the inner surface of a hohlraum enclosure irradiated by the NIF laser, and fusion reactions occur in the central hot spot near the time of peak compression. Ignition will occur if the hot spot within the compressed fuel layer attains a high-enough areal density to retain enough of the reaction product energy to reach nuclear reaction temperatures within the inertial hydrodynamic disassembly time of the fuel mass [J. Lindl, Phys. Plasmas 2, 3933 (1995)]. The primary purpose of the ablator dopants is to shield the ablator surface adjacent to the DT ice from heating by the hohlraum x-ray drive [S. W. Haan et al., Phys. Plasmas 18, 051001 (2011)]. Simulations predicted that these dopants would produce characteristic K-shell emission if ablator material mixed into the hot spot [B. A. Hammel et al., High Energy Density Phys. 6, 171 (2010)]. In NIF ignition experiments, emission and absorption features from these dopants appear in x-ray spectra measured with the hot-spot x-ray spectrometer in Supersnout II [S. P. Regan et al., "Hot-Spot X-Ray Spectrometer for the National Ignition Facility," to be submitted to Review of Scientific Instruments]. These include K-shell emission lines from the hot spot (driven primarily by inner-shell collisional ionization and dielectronic recombination) and photoionization edges, fluorescence, and absorption lines caused by the absorption of the

  8. Innovation and optimization of a method of pump-probe polarimetry with pulsed laser beams in view of a precise measurement of parity violation in atomic cesium; Innovation et optimisation d'une methode de polarimetrie pompe-sonde avec des faisceaux laser impulsionnels en vue d'une mesure precise de violation de la parite dans l'atome de cesium

    Energy Technology Data Exchange (ETDEWEB)

    Chauvat, D

    1997-10-15

    While Parity Violation (PV) experiments on highly forbidden transitions have been using detection of fluorescence signals; our experiment uses a pump-probe scheme to detect the PV signal directly on a transmitted probe beam. A pulsed laser beam of linear polarisation {epsilon}{sub 1} excites the atoms on the 6S-7S cesium transition in a colinear electric field E || k(ex). The probe beam (k(pr) || k(ex)) of linear polarisation {epsilon}{sub 2} tuned to the transition 7S-6P(3/2) is amplified. The small asymmetry ({approx} 10{sup -6}) in the gain that depends on the handedness of the tri-hedron (E, {epsilon}{sub 1}, {epsilon}{sub 2}) is the manifestation of the PV effect. This is measured as an E-odd apparent rotation of the plane of polarization of the probe beam; using balanced mode polarimetry. New criteria of selection have been devised, that allow us to distinguish the true PV-signal against fake rotations due to electromagnetic interferences, geometrical effects, polarization imperfections, or stray transverse electric and magnetic fields. These selection criteria exploit the symmetry of the PV-rotation - linear dichroism - and the revolution symmetry of the experiment. Using these criteria it is not only possible to reject fake signals, but also to elucidate the underlying physical mechanisms and to measure the relevant defects of the apparatus. The present signal-to-noise ratio allows embarking in PV measurements to reach the 10% statistical accuracy. A 1% measurement still requires improvements. Two methods have been demonstrated. The first one exploits the amplification of the asymmetry at high gain - one major advantage provided by our detection method based on stimulated emission. The second method uses both a much higher incident intensity and a special dichroic component which magnifies tiny polarization rotations. (author)

  9. Fifth-order Raman spectroscopy of liquid benzene : Experiment and theory

    NARCIS (Netherlands)

    Milne, C. J.; Li, Y. L.; Jansen, T. L. C.; Huang, L.; Miller, R. J. D.

    2006-01-01

    The heterodyned fifth-order Raman response of liquid benzene has been measured and characterized by exploiting the passive-phase stabilization of diffractive optics. This result builds on our previous work with liquid carbon disulfide and extends the spectroscopy to a new liquid for the first time.

  10. Fifth-order Raman spectroscopy of liquid benzene : Experiment and theory

    NARCIS (Netherlands)

    Milne, C. J.; Li, Y. L.; Jansen, T. L. C.; Huang, L.; Miller, R. J. D.

    2006-01-01

    The heterodyned fifth-order Raman response of liquid benzene has been measured and characterized by exploiting the passive-phase stabilization of diffractive optics. This result builds on our previous work with liquid carbon disulfide and extends the spectroscopy to a new liquid for the first time.

  11. Preliminary design of laser-induced breakdown spectroscopy for proto-Material Plasma Exposure eXperiment.

    Science.gov (United States)

    Shaw, G; Martin, M Z; Martin, R; Biewer, T M

    2014-11-01

    Laser-induced breakdown spectroscopy (LIBS) is a technique for measuring surface matter composition. LIBS is performed by focusing laser radiation onto a target surface, ablating the surface, forming a plasma, and analyzing the light produced. LIBS surface analysis is a possible diagnostic for characterizing plasma-facing materials in ITER. Oak Ridge National Laboratory has enabled the initial installation of a laser-induced breakdown spectroscopy diagnostic on the prototype Material-Plasma Exposure eXperiment (Proto-MPEX), which strives to mimic the conditions found at the surface of the ITER divertor. This paper will discuss the LIBS implementation on Proto-MPEX, preliminary design of the fiber optic LIBS collection probe, and the expected results.

  12. Examining Electron-Boson Coupling Using Time-Resolved Spectroscopy

    Energy Technology Data Exchange (ETDEWEB)

    Sentef, Michael; Kemper, Alexander F.; Moritz, Brian; Freericks, James K.; Shen, Zhi-Xun; Devereaux, Thomas P.

    2013-12-26

    Nonequilibrium pump-probe time-domain spectroscopies can become an important tool to disentangle degrees of freedom whose coupling leads to broad structures in the frequency domain. Here, using the time-resolved solution of a model photoexcited electron-phonon system, we show that the relaxational dynamics are directly governed by the equilibrium self-energy so that the phonon frequency sets a window for “slow” versus “fast” recovery. The overall temporal structure of this relaxation spectroscopy allows for a reliable and quantitative extraction of the electron-phonon coupling strength without requiring an effective temperature model or making strong assumptions about the underlying bare electronic band dispersion.

  13. Multiplexed sub-Doppler spectroscopy with an optical frequency comb

    CERN Document Server

    Long, David A; Plusquellic, David F; Hodges, Joseph T

    2016-01-01

    An optical frequency comb generated with an electro-optic phase modulator and a chirped radiofrequency waveform is used to perform saturation and pump-probe spectroscopy on the $D_1$ and $D_2$ transitions of atomic potassium. With a comb tooth spacing of 200 kHz and an optical bandwidth of 2 GHz the hyperfine transitions can be simultaneously observed. Interferograms are recorded in as little as 5 $\\mu$s (a timescale corresponding to the inverse of the comb tooth spacing). Importantly, the sub-Doppler features can be measured as long as the laser carrier frequency lies within the Doppler profile, thus removing the need for slow scanning or a priori knowledge of the frequencies of the sub-Doppler features. Sub-Doppler optical frequency comb spectroscopy has the potential to dramatically reduce acquisition times and allow for rapid and accurate assignment of complex molecular and atomic spectra which are presently intractable.

  14. Real-time observation of vibrational quantum beat in condensed phase by 20 fs time-resolved spectroscopy%凝聚相分子振动量子拍的20fs时间分辨光谱实时观测

    Institute of Scientific and Technical Information of China (English)

    王云鹏; 王专; 翁羽翔

    2012-01-01

    Impulsive coherent vibrational spectroscopy is a kind of time-resolved spectroscopy methodology with a pulse duration of the femtosecond laser shorter than the molecular vibrational period. Usually, it is based on pump-probe technique and is utilized to real-time observation of the molecular vibrational dynamics coupled to the electronic ground or excited state. We have built an impulsive coherent vibrational spectroscopy setup based on a sub-20 fs, 550 to 700 nm tunable non-collinear optical parametric amplifier and performed pump-probe experiment with an Oxazine 720 methanol solution as the sample. Two vibrational quantum beats with frequency of 592 and 678 cm-1 were observed and the corresponding vibrational periods are 56.3 and 49.2 fs respectively.%冲击相干振动光谱是以脉冲宽度比分子振动周期短的飞秒激光作为激发光源的一种光谱学实验方法,通常是以泵浦-探测实验装置为基础,可以实时观测与电子基态或激发态相耦合的分子振动动力学过程.中国科学院物理研究所以小于20 fs,550~700 nm光谱范围内可调谐的非共线光参量放大器为光源,建立了一套冲击相干振动光谱学实验装置,并以染料分子Oxazine 720的甲醇溶液为样品进行了实验测试.实验中样品被泵浦光脉冲激发后在电子基态形成振动波包,并观测到振动波包在电子势能曲面上运动所形成的振动量子拍信号.经分析有两个分子振动模式被激发,其振动频率分别为592与678cm-1,所对应的振动周期分别为56.3与49.2 fs.

  15. Performance of new solid state {gamma}-detectors in {sup 57}Fe Moessbauer spectroscopy experiments

    Energy Technology Data Exchange (ETDEWEB)

    Dellmann, Til; Klauss, Hans-Henning [Institute of Solid State Physics, TU Dresden (Germany)

    2011-07-01

    Usually, proportional counter tubes are used in {sup 57}Fe Moessbauer spectroscopy for the detection of the 14.4 keV transition line. % and further signal processing. The recent developement of Si-based solid state detectors led to commercially available drift detectors (SDD) and high purity PiN diodes without the necessity of cooling with liquid nitrogen. First applications of SDD detectors in the analysis of minerals are already highly promising. In this talk, we present a detailed comparison between the three detector types and their use in Moessbauer spectroscopy using a standard absorber-source-combination (metallic iron with a 2.0 GBq {sup 57}Co/Rh source) in absorbtion geometry. Starting with the definition of a global efficiency function, which optimises the goodness of a Moessbauer spectrum and thus the required measurement time, we examined the influence of the intrinsic detector parameters on the global efficiency.

  16. An effective method for trapping ion beams in superfluid helium for laser spectroscopy experiments

    Directory of Open Access Journals (Sweden)

    Yang X.F

    2014-03-01

    Full Text Available A novel laser spectroscopy technique -“OROCHI” (Optical Radioisotopes Observation in Condensed Helium as Ion-catcher has been proposed. This method aimed to investigate the structure of exotic nuclei systematically by measuring nuclear spins and moments. For in-situ laser spectroscopy of atoms in He II, a method to trap atoms precisely at the observation region of laser is highly needed. In this work, a setup composed of a degrader, two plastic scintillators and a photon detection system is further tested and verified for adjusting and checking the stopping position of 84–87Rb beam. Details of the current setup, experimental results using this method are presented.

  17. Ultra-fast X-ray absorption spectroscopy for the study of matter in transient regime; Spectroscopie d'absorption ultra-rapide de rayonnement X pour l'etude de la matiere en regime transitoire

    Energy Technology Data Exchange (ETDEWEB)

    Lecherbourg, L

    2007-12-15

    In this work, we study the physics of dense matter, plasmas or solids, using X-ray absorption spectroscopy. Through the use of sources produced by laser-matter interaction, we have measured the absorption spectra of aluminum and bromine plasmas, as well as those of vanadium dioxide (VO{sub 2}). The measurement of absorption coefficients allows us to probe the dense matter and to study its properties. The experiments are carried out following the same principle: they use the same experimental set-up, called pump-probe. When the matter is dense, the absorption properties of an atom are modified by the surrounding environment. In a plasma, it is mainly the bound- bound transitions which are altered: the shapes of those spectral rays are modified. In a solid, the position of the neighbouring atoms in relation to the absorbing atom modify the structure of absorption levels (bound-free transition). The study of this structure allows us to measure the parameters of the material, and provides information such as the state of the electronic band or the interatomic gaps. The experiments carried out at the LULI have allowed us to probe plasmas in the relatively unknown regime of the Warm Dense Matter. One of the key parameters is that the plasma is characterised independently (FDI diagnostic). It allows for a better comparison of the measured absorption against a calculation made with the numerical model OPA-S. The experiments carried out at INRS have led to the realisation of an experimental system having the characteristics which allow the study of the dynamics of solids showing ultra-fast phase transition. For those experiments, we have used vanadium dioxide as a model system allowing us to test the feasibility of the method. (author)

  18. A Simple Bioconjugate Attachment Protocol for Use in Single Molecule Force Spectroscopy Experiments Based on Mixed Self-Assembled Monolayers

    Directory of Open Access Journals (Sweden)

    Myriam Ouberai

    2012-10-01

    Full Text Available Single molecule force spectroscopy is a technique that can be used to probe the interaction force between individual biomolecular species. We focus our attention on the tip and sample coupling chemistry, which is crucial to these experiments. We utilised a novel approach of mixed self-assembled monolayers of alkanethiols in conjunction with a heterobifunctional crosslinker. The effectiveness of the protocol is demonstrated by probing the biotin-avidin interaction. We measured unbinding forces comparable to previously reported values measured at similar loading rates. Specificity tests also demonstrated a significant decrease in recognition after blocking with free avidin.

  19. Water-anion hydrogen bonding dynamics: Ultrafast IR experiments and simulations

    Science.gov (United States)

    Yamada, Steven A.; Thompson, Ward H.; Fayer, Michael D.

    2017-06-01

    Many of water's remarkable properties arise from its tendency to form an intricate and robust hydrogen bond network. Understanding the dynamics that govern this network is fundamental to elucidating the behavior of pure water and water in biological and physical systems. In ultrafast nonlinear infrared experiments, the accessible time scales are limited by water's rapid vibrational relaxation (1.8 ps for dilute HOD in H2O), precluding interrogation of slow hydrogen bond evolution in non-bulk systems. Here, hydrogen bonding dynamics in bulk D2O were studied from the perspective of the much longer lived (36.2 ps) CN stretch mode of selenocyanate (SeCN-) using polarization selective pump-probe (PSPP) experiments, two-dimensional infrared (2D IR) vibrational echo spectroscopy, and molecular dynamics simulations. The simulations make use of the empirical frequency mapping approach, applied to SeCN- for the first time. The PSPP experiments and simulations show that the orientational correlation function decays via fast (2.0 ps) restricted angular diffusion (wobbling-in-a-cone) and complete orientational diffusive randomization (4.5 ps). Spectral diffusion, quantified in terms of the frequency-frequency correlation function, occurs on two time scales. The initial 0.6 ps time scale is attributed to small length and angle fluctuations of the hydrogen bonds between water and SeCN-. The second 1.4 ps measured time scale, identical to that for HOD in bulk D2O, reports on the collective reorganization of the water hydrogen bond network around the anion. The experiments and simulations provide details of the anion-water hydrogen bonding and demonstrate that SeCN- is a reliable vibrational probe of the ultrafast spectroscopy of water.

  20. 利用脉冲激光技术研究哺乳动物碳氧血红蛋白光解量子产率%Quantum yields in photolyses of mammalian carboxy-hemoglobin studied by pulsed laser pump-probe technique

    Institute of Scientific and Technical Information of China (English)

    赵瑾瑜; 渠敏; 李家璜; 张铮; 张淑仪; 水修基; 杨跃涛; 华子春

    2011-01-01

    本文利用脉冲光解法测量了哺乳动物碳氧血红蛋白的光解反应的量子产率.脉冲光解法是利用一束波长为532 nm、脉冲宽度为8 ns、重复频率为10 Hz的脉冲激光照射碳氧血红蛋白溶液,使其发生光解反应.考虑到碳氧血红蛋白溶液和其光解产物脱氧血红蛋白的光吸收系数不同,可利用另一束波长为432 nm的连续激光检测溶液在光解前、后的透射率的变化,以测定溶液的光解量子产率.利用此实验系统,对人、猪、牛、马和兔等5种哺乳动物的碳氧血红蛋白的光解量子产率进行了测量和研究,结果表明,不同物种的光解量子产率各不相同,其中猪、牛、马的碳氧血红蛋白的光解量子产率很接近,兔的碳氧血红蛋白的光解量子产率与其他物种的差异最大.最后,对测量的结果从血红蛋白的氨基酸序列、氢键和盐桥排布、四级结构等方面进行了分析与讨论.%Hemoglobin (Hb) as the allosteric protein, in photo-dissociations of liganded Hb has been studied widely. The mechanisms describing the cooperative binding of CO and other ligands to hemoglobins has been the subject of extensive studies as an important fundamental problem for a long time. In this paper, the quantum yields in photolyses of carboxy-hemoglobins (HbCO) of mammals, such as human,pig, bovine, horse and rabbit, are investigated by the optical pump-probe technique, in which the quantum yield is defined as the molecular number of photoproduct species divided by the absorbed photon number. In the optical pump-probe technique, the HbCO of the mammals are irradiated by a pulsed pumping laser beam with the wavelength 532 nm, pulse width 8 ns and the repetition frequency 10 Hz, then the HbCO is photo-dissociated.Meanwhile, another continuous optical beam with the wavelength 432 nm is used as a probe beam to detect the absorbance change induced by the photo-dissociation before and after the laser pulse illuminating

  1. Flexible digital signal processing architecture for narrowband and spread-spectrum lock-in detection in multiphoton microscopy and time-resolved spectroscopy.

    Science.gov (United States)

    Wilson, Jesse W; Park, Jong Kang; Warren, Warren S; Fischer, Martin C

    2015-03-01

    The lock-in amplifier is a critical component in many different types of experiments, because of its ability to reduce spurious or environmental noise components by restricting detection to a single frequency and phase. One example application is pump-probe microscopy, a multiphoton technique that leverages excited-state dynamics for imaging contrast. With this application in mind, we present here the design and implementation of a high-speed lock-in amplifier on the field-programmable gate array (FPGA) coprocessor of a data acquisition board. The most important advantage is the inherent ability to filter signals based on more complex modulation patterns. As an example, we use the flexibility of the FPGA approach to enable a novel pump-probe detection scheme based on spread-spectrum communications techniques.

  2. Técnica de bombeio e prova para medidas de absorção de estado excitado e de emissão estimulada, em materiais sólidos dopados com íons terras raras Pump-probe technique for excited state absorption and stimulated emission measurements in rare earth ion doped solid materials

    Directory of Open Access Journals (Sweden)

    Andrea Simone Stucchi de Camargo

    2008-01-01

    Full Text Available Rare earth ion doped solid state materials are the most important active media of near-infrared and visible lasers and other photonic devices. In these ions, the occurrence of Excited State Absorptions (ESA, from long lived electronic levels, is commonplace. Since ESA can deeply affect the efficiencies of the rare earth emissions, evaluation of these transitions cross sections is of greatest importance in predicting the potential applications of a given material. In this paper a detailed description of the pump-probe technique for ESA measurements is presented, with a review of several examples of applications in Nd3+, Tm3+ and Er3+ doped materials.

  3. Development and data analysis of a position detector for AE$\\bar{g}$IS (Antimatter Experiment: Gravity, Interferometry, Spectroscopy)

    CERN Document Server

    Gligorova, Angela; Doser, Michael; Pacifico, Nicola

    2015-03-13

    AE$\\mathrm{\\bar{g}}$IS (Antimatter Experiment: Gravity, Interferometry, Spectroscopy) is an antimatter experiment based at CERN, the European Organization for Nuclear Research, whose goal is to carry out the first direct measurement of the Earth’s gravitational acceleration on antimatter. The outcome of such measurement would be the first precision test of the Weak Equivalence Principle in a completely new area. According to WEP, all bodies fall with the same acceleration regardless of their mass and composition. AE$\\mathrm{\\bar{g}}$IS will attempt to achieve its aim by measuring the gravitational acceleration ($\\bar{g}$) for antihydrogen with 1$\\%$ relative precision. The first step towards the final goal is the formation of a pulsed, cold antihydrogen beam, which will be performed by a charge exchange reaction between laser excited (Rydberg) positronium and cold (100 mK) antiprotons. The antihydrogen atoms will be accelerated by an inhomogeneous electric field (Stark acceleration) to form a beam whose fr...

  4. Modeling the high-energy electronic state manifold of adenine: Calibration for nonlinear electronic spectroscopy

    Energy Technology Data Exchange (ETDEWEB)

    Nenov, Artur, E-mail: Artur.Nenov@unibo.it; Giussani, Angelo; Segarra-Martí, Javier; Jaiswal, Vishal K. [Dipartimento di Chimica “G. Ciamician,” Università di Bologna, Via Selmi 2, IT-40126 Bologna (Italy); Rivalta, Ivan [Université de Lyon, CNRS, Institut de Chimie de Lyon, École Normale Supérieure de Lyon, 46 Allée d’Italie, F-69364 Lyon Cedex 07 (France); Cerullo, Giulio [Dipartimento di Fisica, Politecnico di Milano, IFN-CNR, Piazza Leonardo Da Vinci 32, IT-20133 Milano (Italy); Mukamel, Shaul [Department of Chemistry, University of California, Irvine, California 92697-2025 (United States); Garavelli, Marco, E-mail: marco.garavelli@unibo.it, E-mail: marco.garavelli@ens-lyon.fr [Dipartimento di Chimica “G. Ciamician,” Università di Bologna, Via Selmi 2, IT-40126 Bologna (Italy); Université de Lyon, CNRS, Institut de Chimie de Lyon, École Normale Supérieure de Lyon, 46 Allée d’Italie, F-69364 Lyon Cedex 07 (France)

    2015-06-07

    Pump-probe electronic spectroscopy using femtosecond laser pulses has evolved into a standard tool for tracking ultrafast excited state dynamics. Its two-dimensional (2D) counterpart is becoming an increasingly available and promising technique for resolving many of the limitations of pump-probe caused by spectral congestion. The ability to simulate pump-probe and 2D spectra from ab initio computations would allow one to link mechanistic observables like molecular motions and the making/breaking of chemical bonds to experimental observables like excited state lifetimes and quantum yields. From a theoretical standpoint, the characterization of the electronic transitions in the visible (Vis)/ultraviolet (UV), which are excited via the interaction of a molecular system with the incoming pump/probe pulses, translates into the determination of a computationally challenging number of excited states (going over 100) even for small/medium sized systems. A protocol is therefore required to evaluate the fluctuations of spectral properties like transition energies and dipole moments as a function of the computational parameters and to estimate the effect of these fluctuations on the transient spectral appearance. In the present contribution such a protocol is presented within the framework of complete and restricted active space self-consistent field theory and its second-order perturbation theory extensions. The electronic excited states of adenine have been carefully characterized through a previously presented computational recipe [Nenov et al., Comput. Theor. Chem. 1040–1041, 295-303 (2014)]. A wise reduction of the level of theory has then been performed in order to obtain a computationally less demanding approach that is still able to reproduce the characteristic features of the reference data. Foreseeing the potentiality of 2D electronic spectroscopy to track polynucleotide ground and excited state dynamics, and in particular its expected ability to provide

  5. Confocal X-ray fluorescence micro-spectroscopy experiment in tilted geometry

    Energy Technology Data Exchange (ETDEWEB)

    Czyzycki, Mateusz, E-mail: Mateusz.Czyzycki@desy.de [DESY Photon Science, Notkestr. 85, D-22607 Hamburg (Germany); AGH University of Science and Technology, Faculty of Physics and Applied Computer Science, Al. A. Mickiewicza 30, 30-059 Krakow (Poland); Wrobel, Pawel; Lankosz, Marek [AGH University of Science and Technology, Faculty of Physics and Applied Computer Science, Al. A. Mickiewicza 30, 30-059 Krakow (Poland)

    2014-07-01

    This paper provides a generalized mathematical model to describe the intensity of primary X-ray fluorescence radiation collected in the tilted confocal geometry mode, where the collimating optics is rotated over an angle relative to a horizontal plane. The influence of newly introduced terms, which take into account the tilted geometry mode, is discussed. The model is verified with a multi-layer test sample scanned in depth. It is proved that for low-Z matrices, the rotation of the detection channel does not induce any significant differences in a reconstruction of the thickness and chemical composition of layers, so that it may safely be ignored. - Highlights: • A mathematical model for confocal XRF spectroscopy in tilted geometry was derived. • Tilted geometry influenced the analytical capabilities of XRF instrument slightly. • Thickness and the chemical composition of multi-layers were determined.

  6. Excited state absorption spectroscopy of ZBLAN:Ho{sup 3+} glass-experiment and simulation

    Energy Technology Data Exchange (ETDEWEB)

    Piatkowski, D; Wisniewski, K; Rozanski, M; Koepke, Cz [Institute of Physics, Nicolaus Copernicus University, Grudziadzka 5/7, 87-100 Torun (Poland); Kaczkan, M; Klimczak, M; Piramidowicz, R; Malinowski, M [Institute of Microelectronics and Optoelectronics, Koszykowa 75, 00-662 Warsaw (Poland)], E-mail: dapi@fizyka.umk.pl

    2008-04-16

    The excited state absorption (ESA) spectra of ZBLAN glass activated by trivalent holmium ions have been measured in a wide spectral range (550-1750 nm) and simulated using such theoretical tools as the Judd-Ofelt formalism and McCumber theory of stimulated emission. We also propose a systematic approach for prediction of various types of up-conversion mechanisms in a given type of material. Experimental results on ESA up-conversion processes in ZBLAN:Ho{sup 3+} under red and infrared laser excitation, which confirm theoretical analysis, are presented. The optical linewidths were studied using high resolution laser spectroscopy at low temperatures and the existence of different crystallographic sites for Ho{sup 3+} ions was revealed.

  7. Excited state absorption spectroscopy of ZBLAN:Ho3+ glass—experiment and simulation

    Science.gov (United States)

    Piatkowski, D.; Wisniewski, K.; Rozanski, M.; Koepke, Cz; Kaczkan, M.; Klimczak, M.; Piramidowicz, R.; Malinowski, M.

    2008-04-01

    The excited state absorption (ESA) spectra of ZBLAN glass activated by trivalent holmium ions have been measured in a wide spectral range (550-1750 nm) and simulated using such theoretical tools as the Judd-Ofelt formalism and McCumber theory of stimulated emission. We also propose a systematic approach for prediction of various types of up-conversion mechanisms in a given type of material. Experimental results on ESA up-conversion processes in ZBLAN:Ho3+ under red and infrared laser excitation, which confirm theoretical analysis, are presented. The optical linewidths were studied using high resolution laser spectroscopy at low temperatures and the existence of different crystallographic sites for Ho3+ ions was revealed.

  8. Preparation of a Cobalt(II) Cage: An Undergraduate Laboratory Experiment That Produces a ParaSHIFT Agent for Magnetic Resonance Spectroscopy

    Science.gov (United States)

    Burns, Patrick J.; Tsitovich, Pavel B.; Morrow, Janet R.

    2016-01-01

    Laboratory experiments that demonstrate the effect of paramagnetic complexes on chemical shifts and relaxation times of protons are a useful way to introduce magnetic resonance spectroscopy (MRS) probes or magnetic resonance imaging (MRI) contrast agents. In this undergraduate inorganic chemistry experiment, a paramagnetic Co(II) cage complex is…

  9. Characterization of Shock Effects in Calcite by Raman Spectroscopy: Results of Experiments

    Science.gov (United States)

    Bell, M. S.

    2016-01-01

    Carbonates comprise approx. 20% by volume of present day Earth's sedimentary rocks and store most of the terrestrial CO2 inventory. Some of the oldest meta-sedimentary rocks found on Earth contain abundant carbonate from which impact-induced release of CO2 could have played a role in the formation and evolution of the atmosphere. Carbonates are also present in the target materials for approx. 30% of all terrestrial impact structures including large impacts such as Chicxulub which happened to occur at a location with extraordinarily thick platform carbonate 3-6 km deep. The impact release of CO2 from carbonates can cause global warming as a result of the well-known greenhouse effect and have subsequent effects on climate and biota. Therefore, the shock behavior of calcite is important in understanding the Cretaceous-Paleogene event and other impacts with carbonate-bearing sediments in their target(s) such as Mars and some asteroids. A comprehensive survey utilizing a variety of techniques to characterize the effects manifest in Calcite (Iceland Spar) experimentally shocked to 60.8 GPa has been completed. Results of analysis by Raman Spectroscopy are reported here.

  10. Structures of cycloserine and 2-oxazolidinone probed by X-ray photoelectron spectroscopy: theory and experiment.

    Science.gov (United States)

    Ahmed, Marawan; Wang, Feng; Acres, Robert G; Prince, Kevin C

    2014-05-22

    The electronic structures and properties of 2-oxazolidinone and the related compound cycloserine (CS) have been investigated using theoretical calculations and core and valence photoelectron spectroscopy. Isomerization of the central oxazolidine heterocycle and the addition of an amino group yield cycloserine. Theory correctly predicts the C, N, and O 1s core spectra, and additionally, we report theoretical natural bond orbital (NBO) charges. The valence ionization energies are also in agreement with theory and previous measurements. Although the lowest binding energy part of the spectra of the two compounds shows superficial similarities, further analysis of the charge densities of the frontier orbitals indicates substantial reorganization of the wave functions as a result of isomerization. The highest occupied molecular orbital (HOMO) of CS shows leading carbonyl π character with contributions from other heavy (non-H) atoms in the molecule, while the HOMO of 2-oxazolidinone (OX2) has leading nitrogen, carbon, and oxygen pπ characters. The present study further theoretically predicts bond resonance effects of the compounds, evidence for which is provided by our experimental measurements and published crystallographic data.

  11. Extensive Frequency Comb Velocity Modulation Spectroscopy of ThF^+ for Use in the Jila Electron Edm Experiment

    Science.gov (United States)

    Gresh, Dan; Cossel, Kevin; Ye, Jun; Cornell, Eric

    2014-06-01

    The metastable ^3Δ_1 state in trapped HfF^+ is being used for an ongoing measurement of the electron electric dipole moment (eEDM) ThF^+, which has a larger effective electric field and a longer-lived ^3Δ_1 state, offers increased sensitivity for an eEDM measurement. Recently, the Heaven group has spectroscopically studied the low-lying states of ThF^+. However, to date there is no detailed information available about technically-accessible laser transitions in the near-infrared region of the spectrum, which are necessary for state preparation and detection in an eEDM experiment. By applying the technique of frequency comb velocity modulation spectroscopy (VMS) to ThF^+ we can acquire 150 cm-1 of continuous, ion-sensitive spectra with 150 MHz resolution in 25 minutes. Here, we report on extensive broadband, high-resolution survey spectroscopy of ThF^+ in the near-IR where we have observed and accurately fit several rovibronic transitions. In addition, we have observed and characterized numerous rovibronic transitions from an unknown thoriated species of molecular ions. H. Loh, K. C. Cossel, M. C. Grau, K.-K. Ni, E. R. Meyer, J. L. Bohn, J. Ye, E. A. Cornell, Science 342, 1220 (2013). B. J. Barker, I. O. Antonov, M. C. Heaven, K. A. Peterson, J. Chem. Phys. 136, 104305 (2012). L. C. Sinclair, K. C. Cossel, T. Coffey, J. Ye, E. A. Cornell, PRL 107, 093002 (2011).

  12. Preliminary approach to neutron instrument selection at ESS-Bilbao based on experience at ISIS molecular spectroscopy group

    Energy Technology Data Exchange (ETDEWEB)

    Vicente Bueno, J. P. de

    2014-07-01

    Collaborative efforts between the Neutronics and Target Design Group at the Instituto de Fusion Nuclear and the Molecular Spectroscopy Group at the ISIS Pulsed Neutron and Muon Source date back to 2012 in the context of the ESS-Bilbao project. The rationale for these joint activities was twofold, namely: to assess the realm of applicability of the low-energy neutron source proposed by ESS-Bilbao; and to explore instrument capabilities for pulsed-neutron techniques in the range 0.05-3 ms, a time range where ESS-Bilbao and ISIS could offer a significant degree of synergy and complementarity. As part of this collaboration, J.P. de Vicente has spent a three-month period within the ISIS Molecular Spectroscopy Group, to gain hands-on experience on the practical aspects of neutron-instrument design and the requisite neutron-transport simulations. Building upon these previous works, the primary aim of this report is to provide a self contained discussion of general criteria for instrument selection at ESS-Bilbao, the first accelerator-driven, low-energy neutron source designed in Spain. (Author)

  13. Quantitative Investigations of Biodiesel Fuel Using Infrared Spectroscopy: An Instrumental Analysis Experiment for Undergraduate Chemistry Students

    Science.gov (United States)

    Ault, Andrew P.; Pomeroy, Robert

    2012-01-01

    Biodiesel has gained attention in recent years as a renewable fuel source due to its reduced greenhouse gas and particulate emissions, and it can be produced within the United States. A laboratory experiment designed for students in an upper-division undergraduate laboratory is described to study biodiesel production and biodiesel mixing with…

  14. Quantitative Investigations of Biodiesel Fuel Using Infrared Spectroscopy: An Instrumental Analysis Experiment for Undergraduate Chemistry Students

    Science.gov (United States)

    Ault, Andrew P.; Pomeroy, Robert

    2012-01-01

    Biodiesel has gained attention in recent years as a renewable fuel source due to its reduced greenhouse gas and particulate emissions, and it can be produced within the United States. A laboratory experiment designed for students in an upper-division undergraduate laboratory is described to study biodiesel production and biodiesel mixing with…

  15. Pump-dump-probe and pump-repump-probe ultrafast spectroscopy resolves cross section of an early ground state intermediate and stimulated emission in the photoreactions of the Pr ground state of the cyanobacterial phytochrome Cph1.

    Science.gov (United States)

    Fitzpatrick, Ann E; Lincoln, Craig N; van Wilderen, Luuk J G W; van Thor, Jasper J

    2012-01-26

    The primary photoreactions of the red absorbing ground state (Pr) of the cyanobacterial phytochrome Cph1 from Synechocystis PCC 6803 involve C15═C16 Z-E photoisomerization of its phycocyanobilin chromophore. The first observable product intermediate in pump-probe measurements of the photocycle, "Lumi-R", is formed with picosecond kinetics and involves excited state decay reactions that have 3 and 14 ps time constants. Here, we have studied the photochemical formation of the Lumi-R intermediate using multipulse picosecond visible spectroscopy. Pump-dump-probe (PDP) and pump-repump-probe (PRP) experiments were carried out by employing two femtosecond visible pulses with 1, 14, and 160 ps delays, together with a broadband dispersive visible probe. The time delays between the two excitation pulses have been selected to allow interaction with the dominant (3 and 14 ps) kinetic phases of Lumi-R formation. The frequency dependence of the PDP and PRP amplitudes was investigated at 620, 640, 660, and 680 nm, covering excited state absorption (λ(max) = 620 nm), ground state absorption (λ(max) = 660 nm), and stimulated emission (λ(max) = 680 nm) cross sections. Experimental double difference transient absorbance signals (ΔΔOD), from the PDP and PRP measurements, required corrections to remove contributions from ground state repumping. The sensitivity of the resulting ΔΔOD signals was systematically investigated for possible connectivity schemes and photochemical parameters. When applying a homogeneous (sequentially decaying) connectivity scheme in both the 3 and 14 ps kinetic phases, evidence for repumping of an intermediate that has an electronic ground state configuration (GSI) is taken from the dump-induced S1 formation with 620, 640, and 660 nm wavelengths and 1 and 14 ps repump delays. Evidence for repumping a GSI is also seen, for the same excitation wavelengths, when imposing a target connectivity scheme proposed in the literature for the 1 ps repump delay. In

  16. Feasibility study of performing high precision gamma spectroscopy of {lambda}{lambda} hypernuclei in the anti PANDA experiment

    Energy Technology Data Exchange (ETDEWEB)

    Sanchez-Lorente, Alicia

    2010-09-30

    Hypernuclear research will be one of the main topics addressed by the anti PANDA experiment at the planned Facility for Antiproton and Ion Research anti FAIR. Thanks to the use of stored anti p beams, copious production of double {lambda} hypernuclei is expected at the anti PANDA experiment, which will enable high precision {gamma} spectroscopy of such nuclei for the first time. At anti PANDA excited states of {xi}{sup -} hypernuclei will be used as a basis for the formation of double {lambda} hypernuclei. For their detection, a devoted hypernuclear detector setup is planned. This setup consists of a primary nuclear target for the production of {xi}{sup -}+ anti {xi} pairs, a secondary active target for the hypernuclei formation and the identification of associated decay products and a germanium array detector to perform {gamma} spectroscopy. In the present work, the feasibility of performing high precision {gamma} spectroscopy of double {lambda} hypernuclei at the anti PANDA experiment has been studied by means of a Monte Carlo simulation. For this issue, the designing and simulation of the devoted detector setup as well as of the mechanism to produce double {lambda} hypernuclei have been optimized together with the performance of the whole system. In addition, the production yields of double hypernuclei in excitedparticle stable states have been evaluated within a statistical decay model. A strategy for the unique assignment of various newly observed {gamma}-transitions to specific double hypernuclei has been successfully implemented by combining the predicted energy spectra of each target with the measurement of two pion momenta from the subsequent weak decays of a double hypernucleus. Indeed, based on these Monte Carlo simulation, the analysis of the statistical decay of {sup 13}{sub {lambda}}{sub {lambda}}B has been performed. As result, three {gamma}-transitions associated to the double hypernuclei {sup 11}{sub {lambda}}{sub {lambda}}Be and to the single

  17. Highlights from the COMPASS experiment at CERN -- Hadron spectroscopy and excitations

    CERN Document Server

    Nerling, Frank

    2016-01-01

    The COMPASS experiment at the CERN-SPS studies the spectrum and the structure of hadrons by scattering high energy hadrons and polarised muons off various fixed targets. Recent results for the hadron programme comprise highlights from different topics. A selective overview is given and, among others, the following results are discussed. The precise determination of the pion polarisability, a long standing puzzle that has been solved now, is presented as well as measurements of radiative widths. The observation of a new narrow axial-vector state, the $a_1(1420)$, as well as deeper insights into the exotic $1^{-+}$-wave, which is under study since decades by several experiments, are discussed and further, the search for the charmonium-like exotic $Z_c(3900)$ state in the COMPASS data is covered.

  18. Highlights from the COMPASS experiment at CERN. Hadron spectroscopy and excitations

    Science.gov (United States)

    Nerling, Frank

    2016-11-01

    The COMPASS experiment at the CERN-SPS studies the spectrum and the structure of hadrons by scattering high energy hadrons and polarised muons off various fixed targets. Recent results for the hadron programme comprise highlights from different topics. A selective overview is given and, among others, the following results are discussed. The precise determination of the pion polarisability, a long standing puzzle that has been solved now, is presented as well as measurements of radiative widths. The observation of a new narrow axial-vector state, the a1(1420), as well as deeper insights into the exotic 1-+-wave, which is under study since decades by several experiments, are discussed and further, the search for the charmonium-like exotic Zc(3900) state in the COMPASS data is covered.

  19. Two-dimensional electronic spectroscopy with birefringent wedges

    Energy Technology Data Exchange (ETDEWEB)

    Réhault, Julien; Maiuri, Margherita; Oriana, Aurelio; Cerullo, Giulio [IFN-CNR, Dipartimento di Fisica, Politecnico di Milano, Piazza Leonardo da Vinci 32, 20133 Milano (Italy)

    2014-12-15

    We present a simple experimental setup for performing two-dimensional (2D) electronic spectroscopy in the partially collinear pump-probe geometry. The setup uses a sequence of birefringent wedges to create and delay a pair of phase-locked, collinear pump pulses, with extremely high phase stability and reproducibility. Continuous delay scanning is possible without any active stabilization or position tracking, and allows to record rapidly and easily 2D spectra. The setup works over a broad spectral range from the ultraviolet to the near-IR, it is compatible with few-optical-cycle pulses and can be easily reconfigured to two-colour operation. A simple method for scattering suppression is also introduced. As a proof of principle, we present degenerate and two-color 2D spectra of the light-harvesting complex 1 of purple bacteria.

  20. Revisiting the Young's double slit experiment for background-free nonlinear Raman spectroscopy and microscopy.

    Science.gov (United States)

    Gachet, David; Brustlein, Sophie; Rigneault, Hervé

    2010-05-28

    In the Young's double slit experiment, the spatial shift of the interference pattern projected onto a screen is directly related to the phase difference between the fields diffracted by the two slits. We apply this property to fields emitted by nonlinear processes and thus demonstrate background-free coherent anti-Stokes Raman scattering microscopy near an axial interface between a resonant and a nonresonant medium. This method is relevant to remove the nonresonant background in other coherent resonant processes.

  1. Optical Spectroscopy

    DEFF Research Database (Denmark)

    Thyrhaug, Erling

    The work presented in this thesis is broadly concerned with how complexation reactions and molecular motion can be characterized with the standard techniques in optical spectroscopy. The thesis aims to show a relatively broad range of methods for probing physico-chemical properties in fluorophore...... containing systems and are characterized using techniques in optical spectroscopy. Of the standard techniques in optical spectroscopy, particular attention has been paid to those based on time-resolved measurements and polarization, which is reflected in the experiment design in the projects. Not all...... reactions by optical spectroscopy. In project 1 simple steady-state absorption and fluorescence spectroscopy is used to determine the stoichiometries and equilibrium constants in the inclusion complex formation between cyclodextrins and derivatives of the water-insoluble oligo(phenylene vinylene) in aqueous...

  2. Hyperfine spectroscopy of muonic hydrogen and the PSI Lamb shift experiment

    Energy Technology Data Exchange (ETDEWEB)

    Adamczak, Andrzej [Institute of Nuclear Physics, Polish Academy of Sciences, ul. Radzikowskiego 152, 31-342 Krakow (Poland); Bakalov, Dimitar, E-mail: dbakalov@inrne.bas.bg [Institute for Nuclear Research and Nuclear Energy, Bulgarian Academy of Sciences, Tsarigradsko chaussee 72, Sofia 1784 (Bulgaria); Stoychev, Lyubomir [Istituto Nazionale di Fisica Nucleare, Sezione di Trieste, Via A. Valerio 2, 34127 Trieste (Italy); The Abdus Salam International Centre for Theoretical Physics, Strada Costiera 11, 34014 Trieste (Italy); Vacchi, Andrea [Istituto Nazionale di Fisica Nucleare, Sezione di Trieste, Via A. Valerio 2, 34127 Trieste (Italy)

    2012-06-15

    The recent Lamb shift experiment at PSI and the discussions about the incompatibility of the proton radii extracted using different methods have revived the interest in the measurement of the hyperfine splitting of the ground state in muonic hydrogen. We summarize the existing experimental ideas for this measurement and analyze quantitatively the main methodological difficulties, expected to be related to the required power of the IR laser source, the signal-to-noise ratio and other systematic factors. An elaborate model is developed to estimate the statistical uncertainty of the experimental value of the hyperfine splitting.

  3. Baryon Spectroscopy - Recent results from the Crystal Barrel Experiment at ELSA -*

    Directory of Open Access Journals (Sweden)

    Schmidt C.

    2010-04-01

    Full Text Available To understand the spectrum and the properties of baryon resonances, the CBELSA/TAPS experiment investigates the photoproduction off the nucleon using linearly, circularly polarized or unpolarized photons impinging on a polarized or unpolarized target. Preliminary results on first double polarization observables have been obtained for the reactions $vec{gamma}{p}$ → pπ0 and $vec{gamma}{p}$ → pη using both circular and linear polarized photons on a longitudinally polarized target. This data will finally provide important information for the partial wave analyzes used to extract the resonances from the data.

  4. Hole-Burning Spectroscopy on Excitonically Coupled Pigments in Proteins: Theory Meets Experiment.

    Science.gov (United States)

    Adolphs, Julian; Berrer, Manuel; Renger, Thomas

    2016-03-09

    A theory for the calculation of resonant and nonresonant hole-burning (HB) spectra of pigment-protein complexes is presented and applied to the water-soluble chlorophyll-binding protein (WSCP) from cauliflower. The theory is based on a non-Markovian line shape theory ( Renger and Marcus J. Chem. Phys. 2002 , 116 , 9997 ) and includes exciton delocalization, vibrational sidebands, and lifetime broadening. An earlier approach by Reppert ( J. Phys. Chem. Lett. 2011 , 2 , 2716 ) is found to describe nonresonant HB spectra only. Here we present a theory that can be used for a quantitative description of HB data for both nonresonant and resonant burning conditions. We find that it is important to take into account the excess energy of the excitation in the HB process. Whereas excitation of the zero-phonon transition of the lowest exciton state, that is, resonant burning allows the protein to access only its conformational substates in the neighborhood of the preburn state, any higher excitation gives the protein full access to all conformations present in the original inhomogeneous ensemble. Application of the theory to recombinant WSCP from cauliflower, reconstituted with chlorophyll a or chlorophyll b, gives excellent agreement with experimental data by Pieper et al. ( J. Phys. Chem. B 2011 , 115 , 4053 ) and allows us to obtain an upper bound of the lifetime of the upper exciton state directly from the HB experiments in agreement with lifetimes measured recently in time domain 2D experiments by Alster et al. ( J. Phys. Chem. B 2014 , 118 , 3524 ).

  5. Polarization shaping in the mid-IR and polarization-based balanced heterodyne detection with application to 2D IR spectroscopy.

    Science.gov (United States)

    Middleton, Chris T; Strasfeld, David B; Zanni, Martin T

    2009-08-17

    We demonstrate amplitude, phase and polarization shaping of femtosecond mid-IR pulses using a germanium acousto-optical modulator by independently shaping the frequency-dependent amplitudes and phases of two orthogonally polarized pulses which are then collinearly overlapped using a wire-grid polarizer. We use a feedback loop to set and stabilize the relative phase of the orthogonal pulses. We have also used a wire-grid polarizer to implement polarization-based balanced heterodyne detection for improved signal-to-noise of 2D IR spectra collected in a pump-probe geometry. Applications include coherent control of molecular vibrations and improvements in multidimensional IR spectroscopy.

  6. Structural Studies of Phycobiliproteins from Spirulina: Combining Spectroscopy, Thermodynamics, and Molecular Modeling in an Undergraduate Biochemistry Experiment

    Science.gov (United States)

    Taylor, Ann T. S.; Feller, Scott E.

    2002-12-01

    Molecular modeling provides a powerful mechanism for students to connect molecular-level structural changes with macroscopically observable properties. We describe an experiment that integrates spectroscopy, thermodynamics, and molecular modeling into a single activity examining structural changes in phycobiliproteins upon denaturation with urea. Phycobiliproteins contain a covalently attached chromophore, phycocyanobilin, which is constrained in a planar conformation by the folded protein. Upon denaturation of the protein, the chromophore undergoes a conformational change, leading to a significant alteration of the absorption spectrum. By measuring the absorbance at 625 nm as a function of urea concentration, the free energy of unfolding can be determined. Students determine the dihedral angles in the chromophore and map the contacts between protein and chromophore using Protein Explorer, a structure visualization program freely available on the Internet. The change in absorption wavelength can be related to the difference between the LUMO and HOMO energies, obtained using PC Spartan Pro, for the chromophore in the folded and unfolded phycobiliprotein. This experiment could be used in a physical chemistry class in a curriculum that integrates biochemistry throughout the course work as well as in a traditional biochemistry course. Featured on the Cover

  7. Monte Carlo simulation of X-ray imaging and spectroscopy experiments using quadric geometry and variance reduction techniques

    Science.gov (United States)

    Golosio, Bruno; Schoonjans, Tom; Brunetti, Antonio; Oliva, Piernicola; Masala, Giovanni Luca

    2014-03-01

    The simulation of X-ray imaging experiments is often performed using deterministic codes, which can be relatively fast and easy to use. However, such codes are generally not suitable for the simulation of even slightly more complex experimental conditions, involving, for instance, first-order or higher-order scattering, X-ray fluorescence emissions, or more complex geometries, particularly for experiments that combine spatial resolution with spectral information. In such cases, simulations are often performed using codes based on the Monte Carlo method. In a simple Monte Carlo approach, the interaction position of an X-ray photon and the state of the photon after an interaction are obtained simply according to the theoretical probability distributions. This approach may be quite inefficient because the final channels of interest may include only a limited region of space or photons produced by a rare interaction, e.g., fluorescent emission from elements with very low concentrations. In the field of X-ray fluorescence spectroscopy, this problem has been solved by combining the Monte Carlo method with variance reduction techniques, which can reduce the computation time by several orders of magnitude. In this work, we present a C++ code for the general simulation of X-ray imaging and spectroscopy experiments, based on the application of the Monte Carlo method in combination with variance reduction techniques, with a description of sample geometry based on quadric surfaces. We describe the benefits of the object-oriented approach in terms of code maintenance, the flexibility of the program for the simulation of different experimental conditions and the possibility of easily adding new modules. Sample applications in the fields of X-ray imaging and X-ray spectroscopy are discussed. Catalogue identifier: AERO_v1_0 Program summary URL:http://cpc.cs.qub.ac.uk/summaries/AERO_v1_0.html Program obtainable from: CPC Program Library, Queen’s University, Belfast, N. Ireland

  8. Schlieren, Phase-Contrast, and Spectroscopy Diagnostics for the LBNL HIF Plasma Channel Experiment

    Science.gov (United States)

    Ponce, D. M.; Niemann, C.; Fessenden, T. J.; Leemans, W.; Vandersloot, K.; Dahlbacka, G.; Yu, S. S.; Sharp, W. M.; Tauschwitz, A.

    1999-11-01

    The LBNL Plasma Channel experiment has demonstrated stable 42-cm Z-pinch discharge plasma channels with peak currents in excess of 50 kA for a 7 torr nitrogen, 30 kV discharge. These channels offer the possibility of transporting heavy-ion beams for inertial fusion. We postulate that the stability of these channels resides in the existance of a neutral-gas density depresion created by a pre-pulse discharge before the main capacitor bank discharge is created. Here, we present the results and experimental diagnostics setup used for the study of the pre-pulse and main bank channels. Observation of both the plasma and neutral gas dynamics is achieved. Schlieren, Zernike's phase-contrast, and spectroscopic techniques are used. Preliminary Schlieren results show a gas shockwave moving radially at a rate of ≈ 10^6 mm/sec as a result of the fast and localized deposited energy during the evolution of the pre-pulse channel. This data will be used to validate simulation codes (BUCKY and CYCLOPS).

  9. Ultrafast XUV spectroscopy: Unveiling the nature of electronic couplings in molecular dynamics

    Science.gov (United States)

    Timmers, Henry Robert

    Molecules are traditionally treated quantum mechanically using the Born-Oppenheimer formalism. In this formalism, different electronic states of the molecule are treated independently. However, most photo-initiated phenomena occurring in nature are driven by the couplings between different electronic states in both isolated molecules and molecular aggregates, and therefore occur beyond the Born-Oppenheimer formalism. These couplings are relevant in reactions relating to the perception of vision in the human eye, the oxidative damage and repair of DNA, the harvesting of light in photosynthesis, and the transfer of charge across large chains of molecules. While these reaction dynamics have traditionally been studied with visible and ultraviolet spectroscopy, attosecond XUV pulses formed through the process of high harmonic generation form a perfect tool for probing coupled electronic dynamics in molecules. In this thesis, I will present our work in using ultrafast, XUV spectroscopy to study these dynamics in molecules of increasing complexity. We begin by probing the relaxation dynamics of superexcited states in diatomic O 2. These states can relax via two types of electronic couplings, either through autoionization or neutral dissociation. We find that our pump-probe scheme can disentangle the two relaxation mechanisms and independently measure their contributing lifetimes. Next, we present our work in observing a coherent electron hole wavepacket initiated by the ionization of polyatomic CO 2 near a conical intersection. The electron-nuclear couplings near the conical intersection drive the electron hole between different orbital configurations. We find that we can not only measure the lifetime of quantum coherence in the electron hole wavepacket, but also control its evolution with a strong, infrared probing field. Finally, we propose an experiment to observe the migration of an electron hole across iodobenzene on the few-femtosecond timescale. We present

  10. Prospects for laser spectroscopy of highly charged ions with high-harmonic XUV and soft x-ray sources

    Science.gov (United States)

    Rothhardt, J.; Hädrich, S.; Demmler, S.; Krebs, M.; Winters, D. F. A.; Kühl, Th; Stöhlker, Th; Limpert, J.; Tünnermann, A.

    2015-11-01

    We present novel high photon flux XUV and soft x-ray sources based on high harmonic generation (HHG). The sources employ femtosecond fiber lasers, which can be operated at very high (MHz) repetition rate and average power (>100 W). HHG with such lasers results in ˜1013 photons s-1 within a single harmonic line at ˜40 nm (˜30 eV) wavelength, a photon flux comparable to what is typically available at synchrotron beam lines. In addition, resonant enhancement of HHG can result in narrow-band harmonics with high spectral purity—well suited for precision spectroscopy. These novel light sources will enable seminal studies on electronic transitions in highly-charged ions. For example, at the experimental storage ring 2s1/2-2p1/2 transitions in Li-like ions can be excited up to Z = 47 (˜100 eV transition energy), which provides unique sensitivity to quantum electro-dynamical effects and nuclear corrections. We estimate fluorescence count rates of the order of tens per second, which would enable studies on short-lived isotopes as well. In combination with the Doppler up-shift available in head-on excitation at future heavy-ion storage rings, such as the high energy storage ring, even multi-keV transitions can potentially be excited. Pump-probe experiments with femtosecond resolution could also be feasible and access the lifetime of short-lived excited states, thus providing novel benchmarks for atomic structure theory.

  11. Determination of Fe Content of Some Food Items by Flame Atomic Absorption Spectroscopy (FAAS): A Guided-Inquiry Learning Experience in Instrumental Analysis Laboratory

    Science.gov (United States)

    Fakayode, Sayo O.; King, Angela G.; Yakubu, Mamudu; Mohammed, Abdul K.; Pollard, David A.

    2012-01-01

    This article presents a guided-inquiry (GI) hands-on determination of Fe in food samples including plantains, spinach, lima beans, oatmeal, Frosted Flakes cereal (generic), tilapia fish, and chicken using flame atomic absorption spectroscopy (FAAS). The utility of the GI experiment, which is part of an instrumental analysis laboratory course,…

  12. Design of experiments-based monitoring of critical quality attributes for the spray-drying process of insulin by NIR spectroscopy

    DEFF Research Database (Denmark)

    Maltesen, Morten Jonas; van de Weert, Marco; Grohganz, Holger

    2012-01-01

    Moisture content and aerodynamic particle size are critical quality attributes for spray-dried protein formulations. In this study, spray-dried insulin powders intended for pulmonary delivery were produced applying design of experiments methodology. Near infrared spectroscopy (NIR) in combination...

  13. Optical manipulation of a multilevel nuclear spin in ZnO: Master equation and experiment

    Science.gov (United States)

    Buß, J. H.; Rudolph, J.; Wassner, T. A.; Eickhoff, M.; Hägele, D.

    2016-04-01

    We demonstrate the dynamics and optical control of a large quantum mechanical solid state spin system consisting of a donor electron spin strongly coupled to the 9/2 nuclear spin of 115In in the semiconductor ZnO. Comparison of electron spin dynamics observed by time-resolved pump-probe spectroscopy with density matrix theory reveals nuclear spin pumping via optically oriented electron spins, coherent spin-spin interaction, and quantization effects of the ten nuclear spin levels. Modulation of the optical electron spin orientation at frequencies above 1 MHz gives evidence for fast optical manipulation of the nuclear spin state.

  14. Complex Roles of Solution Chemistry on Graphene Oxide Coagulation onto Titanium Dioxide: Batch Experiments, Spectroscopy Analysis and Theoretical Calculation

    Science.gov (United States)

    Yu, Shujun; Wang, Xiangxue; Zhang, Rui; Yang, Tongtong; Ai, Yuejie; Wen, Tao; Huang, Wei; Hayat, Tasawar; Alsaedi, Ahmed; Wang, Xiangke

    2017-01-01

    Although graphene oxide (GO) has been used in multidisciplinary areas due to its excellent physicochemical properties, its environmental behavior and fate are still largely unclear. In this study, batch experiments, spectroscopy analysis and theoretical calculations were addressed to promote a more comprehensive understanding toward the coagulation behavior of GO onto TiO2 under various environmental conditions (pH, co-existing ions, temperature, etc.). The results indicated that neutral pH was beneficial to the removal of GO due to the electrostatic interaction. The presence of cations accelerated GO coagulation significantly owing to the influence of electrical double layer compression. On the contrary, the presence of anions improved the stability of GO primarily because of electrostatic repulsion and steric hindrance. Results of XRD, FTIR and XPS analysis indicated that the coagulation of GO on TiO2 was mainly dominated by electrostatic interactions and hydrogen bonds, which were further evidenced by DFT calculations. The high binding energy further indicated the stability of GO + TiO2 system, suggesting that TiO2 can be used as an effective coagulant for the efficient elimination and coagulation of GO from aqueous solutions. These findings might likely lead to a better understanding of the migration and transformation of carbon nanomaterials in the natural environment.

  15. AIDA: A 16-channel amplifier ASIC to read out the advanced implantation detector array for experiments in nuclear decay spectroscopy

    Energy Technology Data Exchange (ETDEWEB)

    Braga, D. [STFC Rutherford Appleton Laboratory, Didcot, OX11 0QX (United Kingdom); Coleman-Smith, P. J. [STFC Daresbury Laboratory, Warrington WA4 4AD (United Kingdom); Davinson, T. [Dept. of Physics and Astronomy, Univ. of Edinburgh, Edinburgh EH9 3JZ (United Kingdom); Lazarus, I. H. [STFC Daresbury Laboratory, Warrington WA4 4AD (United Kingdom); Page, R. D. [Dept. of Physics, Univ. of Liverpool, Oliver Lodge Laboratory, Liverpool L69 7ZE (United Kingdom); Thomas, S. [STFC Rutherford Appleton Laboratory, Didcot, OX11 0QX (United Kingdom)

    2011-07-01

    We have designed a read-out ASIC for nuclear decay spectroscopy as part of the AIDA project - the Advanced Implantation Detector Array. AIDA will be installed in experiments at the Facility for Antiproton and Ion Research in GSI, Darmstadt. The AIDA ASIC will measure the signals when unstable nuclei are implanted into the detector, followed by the much smaller signals when the nuclei subsequently decay. Implant energies can be as high as 20 GeV; decay products need to be measured down to 25 keV within just a few microseconds of the initial implants. The ASIC uses two amplifiers per detector channel, one covering the 20 GeV dynamic range, the other selectable over a 20 MeV or 1 GeV range. The amplifiers are linked together by bypass transistors which are normally switched off. The arrival of a large signal causes saturation of the low-energy amplifier and a fluctuation of the input voltage, which activates the link to the high-energy amplifier. The bypass transistors switch on and the input charge is integrated by the high-energy amplifier. The signal is shaped and stored by a peak-hold, then read out on a multiplexed output. Control logic resets the amplifiers and bypass circuit, allowing the low-energy amplifier to measure the subsequent decay signal. We present simulations and test results, demonstrating the AIDA ASIC operation over a wide range of input signals. (authors)

  16. Mm-Wave Spectroscopy and Determination of the Radiative Branching Ratios of 11BH for Laser Cooling Experiments

    Science.gov (United States)

    Truppe, Stefan; Holland, Darren; Hendricks, Richard James; Hinds, Ed; Tarbutt, Michael

    2014-06-01

    We aim to slow a supersonic, molecular beam of 11BH using a Zeeman slower and subsequently cool the molecules to sub-millikelvin temperatures in a magneto-optical trap. Most molecules are not suitable for direct laser cooling because the presence of rotational and vibrational degrees of freedom means there is no closed-cycle transition which is necessary to scatter a large number of photons. As was pointed out by Di Rosa, there exists a class of molecules for which the excitation of vibrational modes is suppressed due to highly diagonal Franck-Condon factors. Furthermore, Stuhl et al. showed that angular momentum selection rules can be used to suppress leakage to undesired rotational states. Here we present a measurement of the radiative branching ratios of the A^1Π→ X^1Σ transition in 11BH - a necessary step towards subsequent laser cooling experiments. We also perform high-resolution mm-wave spectroscopy of the J'=1← J=0 rotational transition in the X^1Σ (v=0) state near 708 GHz. From this measurement we derive new, accurate hyper fine constants and compare these to theoretical descriptions. The measured branching ratios suggest that it is possible to laser cool 11BH molecules close to the recoil temperature of 4 μK using three laser frequencies only. M. D. Di Rosa, The European Physical Journal D, 31, 395, 2004 B. K. Stuhl et al., Physical Review Letters, 101, 243002, 2008

  17. Photo-Physical Behaviour of CdSe Nanocrystals/Bis(dithiocarbamate) Linker Multilayered Hybrid Systems.

    Science.gov (United States)

    Vercelli, B; Angella, G; Virgili, T; López Suarez, I; Pasini, M

    2015-05-01

    Multilayered films composed by CdSe Nanocrystals (NCs) interlinked by ethylene-1,2-bis(dithiocarbamate) or adipate anions were prepared on ITO glass via layer-by-layer alternation. The films were analyzed by UV-vis, TEM, Photoluminescence (PL) emission and Pump-Probe spectroscopy. While the PL emission of the two samples present no differences, femtosecond Pump-probe experiments reveal an higher charge generation efficiency in bis(dithiocarbamate) based films than in dicarboxylate ones.

  18. ATR-FTIR Spectroscopy in the Undergraduate Chemistry Laboratory: Part II--A Physical Chemistry Laboratory Experiment on Surface Adsorption

    Science.gov (United States)

    Schuttlefield, Jennifer D.; Larsen, Sarah C.; Grassian, Vicki H.

    2008-01-01

    Attenuated total reflectance-Fourier transform infrared (ATR-FTIR) spectroscopy is a useful technique for measuring the infrared spectra of solids and liquids as well as probing adsorption on particle surfaces. The use of FTIR-ATR spectroscopy in organic and inorganic chemistry laboratory courses as well as in undergraduate research was presented…

  19. Time-resolved soft X-ray core-level photoemission spectroscopy at 880 °C using the pulsed laser and synchrotron radiation and the pulse heating current

    Science.gov (United States)

    Abukawa, T.; Yamamoto, S.; Yukawa, R.; Kanzaki, S.; Mukojima, K.; Matsuda, I.

    2017-02-01

    We developed a time-resolved photoemission spectroscopy system for tracking the temporal variation in an electronic state of a heated sample. Our pump-probe method used laser and synchrotron radiation pulses on a silicon surface that was heated by a synchronized pulse current that did not interfere with the measurements. The transient surface photovoltage effect on the Si 2p core spectra was measured from room temperature to 880 °C and was found to be consistent with the thermal carrier distributions in silicon crystals at the corresponding temperatures. This versatile technique may have applications studying molecular dynamics on high temperature surfaces such as in catalytic reactions.

  20. Near-field reflection backscattering apertureless optical microscopy: Application to spectroscopy experiments on opaque samples, comparison between lock-in and digital photon counting detection techniques

    Energy Technology Data Exchange (ETDEWEB)

    Diziain, S. [Institut Charles Delaunay, CNRS FRE 2848, Laboratoire de Nanotechnologie et d' Instrumentation Optique, Universite de technologie de Troyes, 12 rue Marie Curie, BP 2060, 10010 Troyes cedex (France); Bijeon, J.-L. [Institut Charles Delaunay, CNRS FRE 2848, Laboratoire de Nanotechnologie et d' Instrumentation Optique, Universite de technologie de Troyes, 12 rue Marie Curie, BP 2060, 10010 Troyes cedex (France)]. E-mail: bijeon@utt.fr; Adam, P.-M. [Institut Charles Delaunay, CNRS FRE 2848, Laboratoire de Nanotechnologie et d' Instrumentation Optique, Universite de technologie de Troyes, 12 rue Marie Curie, BP 2060, 10010 Troyes cedex (France); Lamy de la Chapelle, M. [Institut Charles Delaunay, CNRS FRE 2848, Laboratoire de Nanotechnologie et d' Instrumentation Optique, Universite de technologie de Troyes, 12 rue Marie Curie, BP 2060, 10010 Troyes cedex (France); Thomas, B. [Institut Charles Delaunay, CNRS FRE 2848, Laboratoire de Nanotechnologie et d' Instrumentation Optique, Universite de technologie de Troyes, 12 rue Marie Curie, BP 2060, 10010 Troyes cedex (France); Deturche, R. [Institut Charles Delaunay, CNRS FRE 2848, Laboratoire de Nanotechnologie et d' Instrumentation Optique, Universite de technologie de Troyes, 12 rue Marie Curie, BP 2060, 10010 Troyes cedex (France); Royer, P. [Institut Charles Delaunay, CNRS FRE 2848, Laboratoire de Nanotechnologie et d' Instrumentation Optique, Universite de technologie de Troyes, 12 rue Marie Curie, BP 2060, 10010 Troyes cedex (France)

    2007-01-15

    An apertureless scanning near-field optical microscope (ASNOM) in reflection backscattering configuration is designed to conduct spectroscopic experiments on opaque samples constituted of latex beads. The ASNOM proposed takes advantage of the depth-discrimination properties of confocal microscopes to efficiently extract the near-field optical signal. Given their importance in a spectroscopic experiment, we systematically compare the lock-in and synchronous photon counting detection methods. Some results of Rayleigh's scattering in the near field of the test samples are used to illustrate the possibilities of this technique for reflection backscattering spectroscopy.

  1. Determination of structural topology of a membrane protein in lipid bilayers using polarization optimized experiments (POE) for static and MAS solid state NMR spectroscopy.

    Science.gov (United States)

    Mote, Kaustubh R; Gopinath, T; Veglia, Gianluigi

    2013-10-01

    The low sensitivity inherent to both the static and magic angle spinning techniques of solid-state NMR (ssNMR) spectroscopy has thus far limited the routine application of multidimensional experiments to determine the structure of membrane proteins in lipid bilayers. Here, we demonstrate the advantage of using a recently developed class of experiments, polarization optimized experiments, for both static and MAS spectroscopy to achieve higher sensitivity and substantial time-savings for 2D and 3D experiments. We used sarcolipin, a single pass membrane protein, reconstituted in oriented bicelles (for oriented ssNMR) and multilamellar vesicles (for MAS ssNMR) as a benchmark. The restraints derived by these experiments are then combined into a hybrid energy function to allow simultaneous determination of structure and topology. The resulting structural ensemble converged to a helical conformation with a backbone RMSD ~0.44 Å, a tilt angle of 24° ± 1°, and an azimuthal angle of 55° ± 6°. This work represents a crucial first step toward obtaining high-resolution structures of large membrane proteins using combined multidimensional oriented solid-state NMR and magic angle spinning solid-state NMR.

  2. Determination of structural topology of a membrane protein in lipid bilayers using polarization optimized experiments (POE) for static and MAS solid state NMR spectroscopy

    Energy Technology Data Exchange (ETDEWEB)

    Mote, Kaustubh R. [University of Minnesota, Department of Chemistry (United States); Gopinath, T. [University of Minnesota, Department of Biochemistry, Molecular Biology and Biophysics (United States); Veglia, Gianluigi, E-mail: vegli001@umn.edu [University of Minnesota, Department of Chemistry (United States)

    2013-10-15

    The low sensitivity inherent to both the static and magic angle spinning techniques of solid-state NMR (ssNMR) spectroscopy has thus far limited the routine application of multidimensional experiments to determine the structure of membrane proteins in lipid bilayers. Here, we demonstrate the advantage of using a recently developed class of experiments, polarization optimized experiments, for both static and MAS spectroscopy to achieve higher sensitivity and substantial time-savings for 2D and 3D experiments. We used sarcolipin, a single pass membrane protein, reconstituted in oriented bicelles (for oriented ssNMR) and multilamellar vesicles (for MAS ssNMR) as a benchmark. The restraints derived by these experiments are then combined into a hybrid energy function to allow simultaneous determination of structure and topology. The resulting structural ensemble converged to a helical conformation with a backbone RMSD {approx}0.44 A, a tilt angle of 24 Degree-Sign {+-} 1 Degree-Sign , and an azimuthal angle of 55 Degree-Sign {+-} 6 Degree-Sign . This work represents a crucial first step toward obtaining high-resolution structures of large membrane proteins using combined multidimensional oriented solid-state NMR and magic angle spinning solid-state NMR.

  3. Surface-Enhanced Resonance Raman Scattering and Visible Extinction Spectroscopy of Copper Chlorophyllin: An Upper Level Chemistry Experiment

    Science.gov (United States)

    Schnitzer, Cheryl S.; Reim, Candace Lawson; Sirois, John J.; House, Paul G.

    2010-01-01

    Advanced chemistry students are introduced to surface-enhanced resonance Raman scattering (SERRS) by studying how sodium copper chlorophyllin (CuChl) adsorbs onto silver colloids (CuChl/Ag) as a function of pH. Using both SERRS and visible extinction spectroscopy, the extent of CuChl adsorption and colloidal aggregation are monitored. Initially at…

  4. Surface-Enhanced Resonance Raman Scattering and Visible Extinction Spectroscopy of Copper Chlorophyllin: An Upper Level Chemistry Experiment

    Science.gov (United States)

    Schnitzer, Cheryl S.; Reim, Candace Lawson; Sirois, John J.; House, Paul G.

    2010-01-01

    Advanced chemistry students are introduced to surface-enhanced resonance Raman scattering (SERRS) by studying how sodium copper chlorophyllin (CuChl) adsorbs onto silver colloids (CuChl/Ag) as a function of pH. Using both SERRS and visible extinction spectroscopy, the extent of CuChl adsorption and colloidal aggregation are monitored. Initially at…

  5. In vivo 1H spectroscopy of the human brain at 1.5 tesla. Preliminary experience at a clinical installation

    DEFF Research Database (Denmark)

    Henriksen, O; Larsson, H; Jensen, K M

    1990-01-01

    In vivo localized water suppressed proton spectroscopy of human brain was carried out on 15 healthy volunteers and 2 patients suffering from a brain tumour and an infarction, respectively. The measurements were performed on a whole body MR system, operating at 1.5 tesla using the stimulated echo...

  6. Femtosecond Spectroscopy of Electron-Lattice Coupling in LuMnO3

    Science.gov (United States)

    Lou, Shitao

    2005-03-01

    Hexagonal manganite LuMnO3 is a ferroelectric (Tc 900 K) and strongly frustrated antiferromagnetic (TN 90 K) crystal. Strong coupling between lattice, electronic, and magnetic degrees of freedom make it a promissing electronic material. We have used femtosecond pump-probe spectroscopy to observe the interaction of electron excitation and lattice vibration in real time. Optical excitation at a sharp absorption peak at 800 nm corresponding to a Mn d(x^2-y^2),(xy)->d(3z^2-r^2)transition served as the primary excitation step. Reflectivity changes as a function of delay time reveal electronic relaxation and coherent oscillations of several optical phonon modes. Electron and phonon excitation and relaxation dynamics were studied using different polarization geometries and symmetry analysis. The interaction mechanisms of photons, electrons, and coherent phonons are discussed.

  7. Sub-nanosecond, time-resolved, broadband infrared spectroscopy using synchrotron radiation

    CERN Document Server

    Lobo, R; Reitze, D H; Tanner, D B; Carr, G L

    2001-01-01

    A facility for sub-nanosecond time-resolved (pump-probe) infrared spectroscopy has been developed at the National Synchrotron Light Source of Brookhaven National Laboratory. A mode-locked Ti:sapphire laser produces 2 ps duration, tunable near-IR pump pulses synchronized to probe pulses from a synchrotron storage ring. The facility is unique on account of the broadband infrared from the synchrotron, which allows the entire spectral range from 2 cm-1 (0.25 meV) to 20,000 cm-1 (2.5 eV) to be probed. A temporal resolution of 200 ps, limited by the infrared synchrotron-pulse duration, is achieved. A maximum time delay of 170 ns is available without gating the infrared detector. To illustrate the performance of the facility, a measurement of electron-hole recombination dynamics for an HgCdTe semiconductor film in the far- and mid infrared range is presented.

  8. Astronomical Spectroscopy

    CERN Document Server

    Massey, Philip

    2010-01-01

    Spectroscopy is one of the most important tools that an astronomer has for studying the universe. This chapter begins by discussing the basics, including the different types of optical spectrographs, with extension to the ultraviolet and the near-infrared. Emphasis is given to the fundamentals of how spectrographs are used, and the trade-offs involved in designing an observational experiment. It then covers observing and reduction techniques, noting that some of the standard practices of flat-fielding often actually degrade the quality of the data rather than improve it. Although the focus is on point sources, spatially resolved spectroscopy of extended sources is also briefly discussed. Discussion of differential extinction, the impact of crowding, multi-object techniques, optimal extractions, flat-fielding considerations, and determining radial velocities and velocity dispersions provide the spectroscopist with the fundamentals needed to obtain the best data. Finally the chapter combines the previous materi...

  9. Free-Electron Laser Wavelength-Selective Materials Alteration and Photoexcitation Spectroscopy

    Science.gov (United States)

    Tolk, Norman.

    1996-10-01

    -H stretch vibrational mode in chemical vapor deposited (CVD) diamond. The surface C-H stretch vibrational lifetime is believed to play a role in the efficiency of the vibrationally-assisted ablation, and a pump-probe experiment is now under way to measure the lifetime. The extension of this approach to tissue ablation will also be discussed. We gratefully acknowledge support by ONR under Grants N00014-91-J-4040 and N00014-91-C-0109.

  10. Nonlinear photothermal mid-infrared spectroscopy

    Science.gov (United States)

    Totachawattana, Atcha; Erramilli, Shyamsunder; Sander, Michelle Y.

    2016-10-01

    Mid-infrared photothermal spectroscopy is a pump-probe technique for label-free and non-destructive sample characterization by targeting intrinsic vibrational modes. In this method, the mid-infrared pump beam excites a temperature-induced change in the refractive index of the sample. This laser-induced change in the refractive index is measured by a near-infrared probe laser using lock-in detection. At increased pump powers, emerging nonlinear phenomena not previously demonstrated in other mid-infrared techniques are observed. Nonlinear study of a 6 μm-thick 4-Octyl-4'-Cyanobiphenyl (8CB) liquid crystal sample is conducted by targeting the C=C stretching band at 1606 cm-1. At high pump powers, nonlinear signal enhancement and multiple pitchfork bifurcations of the spectral features are observed. An explanation of the nonlinear peak splitting is provided by the formation of bubbles in the sample at high pump powers. The discontinuous refractive index across the bubble interface results in a decrease in the forward scatter of the probe beam. This effect can be recorded as a bifurcation of the absorption peak in the photothermal spectrum. These nonlinear effects are not present in direct measurements of the mid-infrared beam. Evolution of the nonlinear photothermal spectrum of 8CB liquid crystal with increasing pump power shows enhancement of the absorption peak at 1606 cm-1. Multiple pitchfork bifurcations and spectral narrowing of the photothermal spectrum are demonstrated. This novel nonlinear regime presents potential for improved spectral resolution as well as a new regime for sample characterization in mid-infrared photothermal spectroscopy.

  11. The radio waves and thermal electrostatic noise spectroscopy (SORBET) experiment on BEPICOLOMBO/MMO/PWI: Scientific objectives and performance

    Science.gov (United States)

    Moncuquet, M.; Matsumoto, H.; Bougeret, J.-L.; Blomberg, L. G.; Issautier, K.; Kasaba, Y.; Kojima, H.; Maksimovic, M.; Meyer-Vernet, N.; Zarka, P.

    2006-01-01

    SORBET ( Spectroscopie des Ondes Radio and du Bruit Electrostatique Thermique) is a radio HF spectrometer designed for the radio and Plasma Waves Instrument onboard BepiColombo/Mercury Magnetospheric Orbiter (MMO), which performs remote and in situ measurements of waves (electromagnetic and electrostatic). Technically, SORBET includes a plasma wave spectrometer, with two E-field inputs from the two perpendicular electric antennas and one B-field input from a search coil, in the range 2.5-640 kHz. This frequency band includes the local gyrofrequency and plasma frequency expected on most part of the MMO orbits. SORBET also includes a higher frequency radio receiver for remote sensing in the range 500 kHz-10.2 MHz. Owing to its capabilities, SORBET will be able to address the following scientific objectives: High resolution mapping (˜30 km) of electron density and temperature in the solar wind and in the Hermean magnetosphere and exo-ionosphere, via the technique of Quasi-Thermal Noise (QTN) spectroscopy. These QTN measurements will be determinant for the dynamic modeling of the magnetosphere and will provide a fundamental input for the chemistry of cold ionized species (Na, K, O, …) in Mercury's environment. Detection and study of Hermean radio emissions, including possible cyclotron emissions (up to ˜10-20 kHz) from mildly energetic electrons in most highly magnetized (polar?) regions, and possible synchrotron radiation (up to a few MHz?) from more energetic electrons. Monitoring of solar radio emissions up to ˜10 MHz in order to create a solar activity index from the view point of Mercury, allowing to correlate it with the Hermean magnetospheric response. We especially discuss the capabilities of SORBET for performing the QTN spectroscopy in Mercury's magnetosphere, using the two electric dipole antennas equipping MMO, called MEFISTO and WPT.

  12. High-speed stimulated Brillouin scattering spectroscopy at 780 nm

    Directory of Open Access Journals (Sweden)

    Itay Remer

    2016-09-01

    Full Text Available We demonstrate a high-speed stimulated Brillouin scattering (SBS spectroscopy system that is able to acquire stimulated Brillouin gain point-spectra in water samples and Intralipid tissue phantoms over 2 GHz within 10 ms and 100 ms, respectively, showing a 10-100 fold increase in acquisition rates over current frequency-domain SBS spectrometers. This improvement was accomplished by integrating an ultra-narrowband hot rubidium-85 vapor notch filter in a simplified frequency-domain SBS spectrometer comprising nearly counter-propagating continuous-wave pump-probe light at 780 nm and conventional single-modulation lock-in detection. The optical notch filter significantly suppressed stray pump light, enabling detection of stimulated Brillouin gain spectra with substantially improved acquisition times at adequate signal-to-noise ratios (∼25 dB in water samples and ∼15 dB in tissue phantoms. These results represent an important step towards the use of SBS spectroscopy for high-speed measurements of Brillouin gain resonances in scattering and non-scattering samples.

  13. Application of a protocol for magnetic resonance spectroscopy of adrenal glands: an experiment with over 100 cases.

    Science.gov (United States)

    Melo, Homero José de Farias E; Goldman, Suzan M; Szejnfeld, Jacob; Faria, Juliano F; Huayllas, Martha K P; Andreoni, Cássio; Kater, Cláudio E

    2014-01-01

    To evaluate a protocol for two-dimensional (2D) hydrogen proton (1H) magnetic resonance spectroscopy (MRS) (Siemens Medical Systems; Erlangen, Germany) in the detection of adrenal nodules and differentiation between benign and malignant masses (adenomas, pheochromocytomas, carcinomas and metastases). A total of 118 patients (36 men; 82 women) (mean age: 57.3 ± 13.3 years) presenting with 138 adrenal nodules/masses were prospectively assessed. A multivoxel system was utilized with a 2D point-resolved spectroscopy/chemical shift imaging sequence. The following ratios were calculated: choline (Cho)/creatine (Cr), 4.0-4.3/Cr, lipid (Lip)/Cr, Cho/Lip and lactate (Lac)/Cr. 2D-1H-MRS was successful in 123 (89.13%) lesions. Sensitivity and specificity values observed for the ratios and cutoff points were the following: Cho/Cr ≥ 1.2, 100% sensitivity, 98.2% specificity (differences between adenomas/pheochromocytomas and carcinomas/ metastases); 4.0-4.3 ppm/Cr ≥ 1.5, 92.3% sensitivity, 96.9% specificity (differences between carcinomas/pheochromocytomas and adenomas/metastases); Lac/Cr ≤ -7.449, 90.9% sensitivity and 77.8% specificity (differences between pheochromocytomas and carcinomas/adenomas). Information provided by 2D-1H-MRS were effective and allowed for the differentiation between adrenal masses and nodules in most cases of lesions with > 1.0 cm in diameter.

  14. Theoretical study of molecular vibrations in electron momentum spectroscopy experiments on furan: An analytical versus a molecular dynamical approach

    Energy Technology Data Exchange (ETDEWEB)

    Morini, Filippo; Deleuze, Michael S., E-mail: michael.deleuze@uhasselt.be [Center of Molecular and Materials Modelling, Hasselt University, Agoralaan Gebouw D, B-3590 Diepenbeek (Belgium); Watanabe, Noboru; Takahashi, Masahiko [Institute of Multidisciplinary Research for Advanced Materials, Tohoku University, Sendai 980-8577 (Japan)

    2015-03-07

    The influence of thermally induced nuclear dynamics (molecular vibrations) in the initial electronic ground state on the valence orbital momentum profiles of furan has been theoretically investigated using two different approaches. The first of these approaches employs the principles of Born-Oppenheimer molecular dynamics, whereas the so-called harmonic analytical quantum mechanical approach resorts to an analytical decomposition of contributions arising from quantized harmonic vibrational eigenstates. In spite of their intrinsic differences, the two approaches enable consistent insights into the electron momentum distributions inferred from new measurements employing electron momentum spectroscopy and an electron impact energy of 1.2 keV. Both approaches point out in particular an appreciable influence of a few specific molecular vibrations of A{sub 1} symmetry on the 9a{sub 1} momentum profile, which can be unravelled from considerations on the symmetry characteristics of orbitals and their energy spacing.

  15. Laser spectroscopy of short-lived radionuclides in an ion trap: MIRACLS’ proof-of-principle experiment

    CERN Document Server

    Maier, Franziska Maria

    2017-01-01

    Since 1978 Collinear Laser Spectroscopy is done at COLLAPS [1], which is located at ISOLDE,CERN’sfacilityforsynthesizingradioactiveions,toexplorethenuclearshell structure of the most exotic atomic nuclides far away from stability. At COLLAPS a laser beam is overlapped with a radioactive ion beam. If the wavelength of the laser corresponds to the energy difference of the electronic transitions, the laser excites the ions. The excited ions decay back to the ionic ground state and emit fluorescence photons that can be detected with photomultiplier tubes (PMTs). By measuring the hyperfine structure of the involved ionic states one obtains information about the nuclear spin, the nuclear magnetic dipole moment and the nuclear electric quadrupole moment. This hyperfine splitting is caused by the interaction of the bound electrons withtheatomicnucleus. Theelectronsinduceanelectromagneticfieldattheplaceof the nucleus that interacts with the electromagnetic nuclear moments and the nuclear spin. By calculating th...

  16. Femtosecond time-resolved photoelectron spectroscopy with a vacuum-ultraviolet photon source based on laser high-order harmonic generation.

    Science.gov (United States)

    Wernet, Philippe; Gaudin, Jérôme; Godehusen, Kai; Schwarzkopf, Olaf; Eberhardt, Wolfgang

    2011-06-01

    A laser-based tabletop approach to femtosecond time-resolved photoelectron spectroscopy with photons in the vacuum-ultraviolet (VUV) energy range is described. The femtosecond VUV pulses are produced by high-order harmonic generation (HHG) of an amplified femtosecond Ti:sapphire laser system. Two generations of the same setup and results from photoelectron spectroscopy in the gas phase are discussed. In both generations, a toroidal grating monochromator was used to select one harmonic in the photon energy range of 20-30 eV. The first generation of the setup was used to perform photoelectron spectroscopy in the gas phase to determine the bandwidth of the source. We find that our HHG source has a bandwidth of 140 ± 40 meV. The second and current generation is optimized for femtosecond pump-probe photoelectron spectroscopy with high flux and a small spot size at the sample of the femtosecond probe pulses. The VUV radiation is focused into the interaction region with a toroidal mirror to a spot smaller than 100 × 100 μm(2) and the flux amounts to 10(10) photons/s at the sample at a repetition rate of 1 kHz. The duration of the monochromatized VUV pulses is determined to be 120 fs resulting in an overall pump-probe time resolution of 135 ± 5 fs. We show how this setup can be used to map the transient valence electronic structure in molecular dissociation. © 2011 American Institute of Physics

  17. Nonlinear optics in germanium mid-infrared fiber material: Detuning oscillations in femtosecond mid-infrared spectroscopy

    Directory of Open Access Journals (Sweden)

    M. Ordu

    2017-09-01

    Full Text Available Germanium optical fibers hold great promise in extending semiconductor photonics into the fundamentally important mid-infrared region of the electromagnetic spectrum. The demonstration of nonlinear response in fabricated Ge fiber samples is a key step in the development of mid-infrared fiber materials. Here we report the observation of detuning oscillations in a germanium fiber in the mid-infrared region using femtosecond dispersed pump-probe spectroscopy. Detuning oscillations are observed in the frequency-resolved response when mid-infrared pump and probe pulses are overlapped in a fiber segment. The oscillations arise from the nonlinear frequency resolved nonlinear (χ(3 response in the germanium semiconductor. Our work represents the first observation of coherent oscillations in the emerging field of germanium mid-infrared fiber optics.

  18. Ultrafast Structural Fluctuations of Myoglobin-Bound Thiocyanate and Selenocyanate Ions Measured with Two-Dimensional Infrared Photon Echo Spectroscopy.

    Science.gov (United States)

    Maj, Michał; Kwak, Kyungwon; Cho, Minhaeng

    2015-11-16

    Structural dynamics within the distal cavity of myoglobin protein is investigated using 2D-IR and IR pump-probe spectroscopy of the N≡C stretch modes of heme-bound thiocyanate and selenocyanate ions. Although myoglobin-bound thiocyanate group shows a doublet in its IR absorption spectrum, no cross peaks originating from chemical exchange between the two components are observed in the time-resolved 2D IR spectra within the experimental time window. Frequency-frequency correlation functions of the two studied anionic ligands are obtained by means of a few different analysis approaches; these functions were then used to elucidate the differences in structural fluctuation around ligand, ligand-protein interactions, and the degree of structural heterogeneity within the hydrophobic pocket of these myoglobin complexes.

  19. Ultrafast differential transmission spectroscopy of excitonic transitions in InGaN/GaN multiple quantum wells

    Science.gov (United States)

    Chen, Fei; Cheung, M. C.; Sweeney, Paul M.; Kirkey, W. D.; Furis, M.; Cartwright, A. N.

    2003-04-01

    Room-temperature carrier dynamics in InGaN/GaN multiple quantum wells are studied by employing ultrafast pump-probe spectroscopy. Specifically, the observed differential spectral signatures are characteristic of changes in the absorption coefficient through both a reduction of the quantum-confined Stark shift due to the photoinduced in-well field screening (low carrier densities) and excitonic absorption quenching (high carrier densities). The comparison of the differential absorption spectra at different injected carrier densities allows us to separate field screening from excitonic bleaching. The estimated in-well field at the transition point between field screening and excitonic bleaching is consistent with the theoretical value of the piezoelectric field in the strained InGaN well.

  20. X-ray imaging and imaging spectroscopy of fusion plasmas and light-source experiments with spherical optics and pixel array detectors

    Science.gov (United States)

    Hill, K. W.; Bitter, M.; Delgado-Aparicio, L.; Pablant, N. A.; Beiersdorfer, P.; Sanchez del Rio, M.; Zhang, L.

    2012-10-01

    High resolution (λ/Δλ ~10,000) 1D imaging x-ray spectroscopy using a spherically bent crystal and a 2D hybrid pixelarray detector (PAD) is used world wide for Doppler measurements of ion-temperature (Ti) and plasma flow-velocityprofiles in magnetic confinement fusion (MCF) plasmas. Meter sized plasmas are diagnosed with cm spatial resolution and 10 ms time resolution. This concept can also be used as a diagnostic of small sources, such as inertial confinement fusion (ICF) plasmas and targets on x-ray light source beam lines, with spatial resolution of microns. A new concept of using matched pairs of spherically bent crystals for monochromatic stigmatic 2D x-ray imaging of mm sized sources offers the possibility of spatial resolution of microns and large solid angle, relative to that achieved with pinhole imaging. Other potential applications of the 2D imaging schemes include x-ray lithography and x-ray microscopy for biological and materials science research. Measurements from MFE plasmas, as well as laboratory experiments and ray tracing computations validating the 1D imaging spectroscopy and 2D x-ray imaging techniques will be presented.

  1. Gas-phase peptide structures unraveled by far-IR spectroscopy: combining IR-UV ion-dip experiments with Born-Oppenheimer molecular dynamics simulations.

    Science.gov (United States)

    Jaeqx, Sander; Oomens, Jos; Cimas, Alvaro; Gaigeot, Marie-Pierre; Rijs, Anouk M

    2014-04-01

    Vibrational spectroscopy provides an important probe of the three-dimensional structures of peptides. With increasing size, these IR spectra become very complex and to extract structural information, comparison with theoretical spectra is essential. Harmonic DFT calculations have become a common workhorse for predicting vibrational frequencies of small neutral and ionized gaseous peptides. Although the far-IR region (IR spectra of peptides. Here, Born-Oppenheimer molecular dynamics (BOMD) is applied to predict the far-IR signatures of two γ-turn peptides. Combining experiments and simulations, far-IR spectra can provide structural information on gas-phase peptides superior to that extracted from mid-IR and amide A features.

  2. Fluorescence correlation spectroscopy experiments to quantify free diffusion coefficients in reaction-diffusion systems: The case of Ca2 + and its dyes

    Science.gov (United States)

    Sigaut, Lorena; Villarruel, Cecilia; Ponce, María Laura; Ponce Dawson, Silvina

    2017-06-01

    Many cell signaling pathways involve the diffusion of messengers that bind and unbind to and from intracellular components. Quantifying their net transport rate under different conditions then requires having separate estimates of their free diffusion coefficient and binding or unbinding rates. In this paper, we show how performing sets of fluorescence correlation spectroscopy (FCS) experiments under different conditions, it is possible to quantify free diffusion coefficients and on and off rates of reaction-diffusion systems. We develop the theory and present a practical implementation for the case of the universal second messenger, calcium (Ca2 +) and single-wavelength dyes that increase their fluorescence upon Ca2 + binding. We validate the approach with experiments performed in aqueous solutions containing Ca2 + and Fluo4 dextran (both in its high and low affinity versions). Performing FCS experiments with tetramethylrhodamine-dextran in Xenopus laevis oocytes, we infer the corresponding free diffusion coefficients in the cytosol of these cells. Our approach can be extended to other physiologically relevant reaction-diffusion systems to quantify biophysical parameters that determine the dynamics of various variables of interest.

  3. Setting up the photoluminescence laboratory at ISOLDE & Perturbed Angular Correlation spectroscopy for BIO physics experiments using radioactive ions

    CERN Document Server

    Savva, Giannis

    2016-01-01

    The proposed project I was assigned was to set up the photoluminescence (PL) laboratory at ISOLDE, under the supervision of Karl Johnston. My first week at CERN coincided with the run of a BIO physics experiment using radioactive Hg(II) ions in which I also participated under the supervision of Stavroula Pallada. This gave me the opportunity to work in two projects during my stay at CERN and in the present report I describe briefly my contribution to them.

  4. VIS-NIR Imaging Spectroscopy of Mercury's Surface: SIMBIO-SYS/VIHI Experiment Onboard the BepiColombo

    Science.gov (United States)

    Capaccioni, Fabrizio; de Sanctis, Maria Cristina; Filacchione, Gianrico; Piccioni, Giuseppe; Ammannito, Eleonora; Tommasi, Leonardo; Ficai Veltroni, Iacopo; Cosi, Massimo; Debei, Stefano; Calamai, Luciano; Flamini, Enrico

    2010-07-01

    The Visible and Infrared Hyperspectral Imager (VIHI) is one of the three optical heads of the Spectrometers and Imagers for MPO BepiColombo Integrated Observatory SYStem (SIMBIO-SYS) experiment onboard European Space Agency's BepiColombo cornerstone mission to Mercury. The other two optical heads of SIMBIO-SYS are a stereo camera and a high-resolution image camera. The experiment is designed to scan the Hermean surface from a polar orbit with the three channels to map the physical, morphological, tectonic, and compositional properties of the planet. The main scientific objectives of SIMBIO-SYS are the study of Mercury's surface geology and stratigraphy, the surface composition, the regolith properties, the crustal differentiation, impact, and volcanic processes. The VIHI experiment uses a high-performance optical layout (Schmidt telescope and spectrometer in Littrow configuration) which allows investigating the 400-2000 nm spectral range with 256 spectral channels (6.25 nm/band sampling). The instrument has an instrument field of view (FOV) of 250 microrad corresponding to a spatial scale of about 100 m/pixel at periherm and 375 m at apoherm. The instrument operates in pushbroom configuration, sampling the surface of Mercury with an FOV of 64 x 0.25 mrad. The main technical challenges of this experiment are focal-plane design (cadmium-mercury-telluride thinned to improve the efficiency at visible wavelengths), short dwell time (from about 40 ms at equator to about 100 ms at poles), thermal control, mechanical miniaturization, radiation hardening, high data rate, and compression. A description of the internal calibration unit concept and functionalities is given.

  5. Ultrafast optical beam deflection in a pump probe configuration

    Science.gov (United States)

    Liang, Lingliang; Tian, Jinshou; Wang, Tao; Wu, Shengli; Li, Fuli; Wang, Junfeng; Gao, Guilong

    2016-09-01

    Propagation of a signal beam in an AlGaAs/GaAs waveguide multiple-prism light deflector is theoretically investigated by solving the scalar Helmholtz equation to obtain the dependences of the temporal and spatial resolvable characteristics of the ultrafast deflector on the material dispersion of GaAs including group velocity dispersion and angular dispersion, interface reflection, and interface scattering of multiple-prism deflector. Furthermore, we experimentally confirm that, in this ultrafast beam deflection device, the deflecting angle of the signal light beam is linear with the pump fluence and the temporal resolution of the ultrafast deflection is 10 ps. Our results show that the improvement of the temporal and spatial resolvable performances is possible by properly choosing the structural parameters and enhancing the quality of the device. Project supported by the National Natural Science Foundation of China (Grant Nos. 11274377 and 61176006) and the State Major Research Equipment Project, China (Grant No. ZDY2011-2).

  6. Optical pump-probe microscopy for biomedicine and art conservation

    Science.gov (United States)

    Fischer, Martin

    2013-03-01

    Nonlinear optical microscopy can provide contrast in highly heterogeneous media and a wide range of applications has emerged, primarily in biology, medicine, and materials science. Compared to linear microscopy methods, the localized nature of nonlinear interactions leads to high spatial resolution, optical sectioning, and larger possible imaging depth in scattering media. However, nonlinear contrast (other than fluorescence, harmonic generation or CARS) is generally difficult to measure because it is overwhelmed by the large background of detected illumination light. This background can be suppressed by using femtosecond pulse or pulse train shaping to encode nonlinear interactions in background-free regions of the frequency spectrum. We have developed this shaping technology to study novel intrinsic structural and molecular contrast in biological tissue, generally using less power than a laser pointer. For example we have recently been able to sensitively measure detailed transient absorption dynamics of melanin sub-types in a variety of skin lesions, showing clinically relevant differences of melanin type and distribution between cancerous and benign tissue.[1] Recently we have also applied this technology to paint samples and to historic artwork in order to provide detailed, depth-resolved pigment identification. Initial studies in different inorganic and organic pigments have shown a rich and pigment-specific nonlinear absorption signature.[2] Some pigments, for example lapis lazuli (natural ultramarine), even show marked differences in signal depending on its geographic origin and on age, demonstrating the potential of this technique to determine authenticity, provenance, technology of manufacture, or state of preservation of historic works of art.

  7. Magnetoencephalography with a two-color pump probe atomic magnetometer.

    Energy Technology Data Exchange (ETDEWEB)

    Johnson, Cort N.

    2010-07-01

    The authors have detected magnetic fields from the human brain with a compact, fiber-coupled rubidium spin-exchange-relaxation-free magnetometer. Optical pumping is performed on the D1 transition and Faraday rotation is measured on the D2 transition. The beams share an optical axis, with dichroic optics preparing beam polarizations appropriately. A sensitivity of <5 fT/{radical}Hz is achieved. Evoked responses resulting from median nerve and auditory stimulation were recorded with the atomic magnetometer. Recordings were validated by comparison with those taken by a commercial magnetoencephalography system. The design is amenable to arraying sensors around the head, providing a framework for noncryogenic, whole-head magnetoencephalography.

  8. Femtosecond pump-probe studies of zinc phthalocynine in DMSO

    CSIR Research Space (South Africa)

    Ombinda-Lemboumba, Saturnin

    2010-09-01

    Full Text Available Phthalocyanines are new class of photosensitiser used for photodynamic therapy. These drugs are used to treat small and superficial tumours. In recent years, a particular attention has been given to phthalocyanine in order to search suitable...

  9. White Light Pump-Probe Photothermal Mirror Spectrophotometer

    Science.gov (United States)

    Hlaing, May; Marcano, Aristides

    2016-05-01

    We develop a new kind of spectrophotometer based on the photothermal mirror effect. The absorption of a focused tunable pump light by first atomic layers of the sample's surface generates a nanometric surface distortion or bump of thermal origin. A probe beam of light of fixed wavelength and with spot dimensions much larger than the pump beam's spot is used to test this thermal distortion. Changes in the wave-front of the reflected probe beam yields changes of the diffraction pattern of the reflected beam at the far field which can be used to produce a signal proportional to the amount of released heat. Tuning of the wavelength of the pump field generates a photothermal mirror spectrum. As tunable pump source we use the light from a Xenon arc-lamp filtered using a series of interference filter. This way we generate tunable pump light in the spectral region of 370-730 nm with a HWHM of 5 nm and power density of the order of tens of microwatts per nanometer. We obtain photothermal mirror spectra of metallic surfaces and other non-transparent samples. We show that these spectra are fundamentally different from the usual reflectance spectra which measure the percentage of the total of the total energy reflected by the surface.

  10. Monitoring of tritium purity during long-term circulation in the KATRIN test experiment LOOPINO using laser Raman spectroscopy

    CERN Document Server

    Fischer, Sebastian; Schlösser, Magnus; Bornschein, Beate; Drexlin, Guido; Priester, Florian; Lewis, Richard J; Telle, Helmut H

    2012-01-01

    The gas circulation loop LOOPINO has been set up and commissioned at Tritium Laboratory Karlsruhe (TLK) to perform Raman measurements of circulating tritium mixtures under conditions similar to the inner loop system of the neutrino-mass experiment KATRIN, which is currently under construction. A custom-made interface is used to connect the tritium containing measurement cell, located inside a glove box, with the Raman setup standing on the outside. A tritium sample (purity > 95%, 20 kPa total pressure) was circulated in LOOPINO for more than three weeks with a total throughput of 770 g of tritium. Compositional changes in the sample and the formation of tritiated and deuterated methanes CT_(4-n)X_n (X=H,D; n=0,1) were observed. Both effects are caused by hydrogen isotope exchange reactions and gas-wall interactions, due to tritium {\\beta} decay. A precision of 0.1% was achieved for the monitoring of the T_2 Q_1-branch, which fulfills the requirements for the KATRIN experiment and demonstrates the feasibility ...

  11. Femtosecond Spectroscopy of LuMnO3

    Science.gov (United States)

    Lou, Shitao; Zimmermann, Frank M.; Bartynski, Robert A.; Hur, Namjun; Cheong, Sang-Wook

    2006-03-01

    Hexagonal LuMnO3 manganite is a ferroelectric and strongly frustrated antiferromagnetic crystal. Strong coupling between lattice, electronic, and magnetic degrees of freedom makes it a promising electronic material. We have used femtosecond pump-probe spectroscopy to study the interaction of electron excitations with lattice vibrations in real time. Optical excitation of a Mn d(x^2-y^2),(xy)->d(3z^2-r^2)transition served as the primary excitation step. With both pump and probe beam polarization perpendicular to the c axis, the probe reflectivity shows a sharp drop due to saturation of the transition, recovering on a timescale of 1 ps. We also observed displacive excitation of a coherent optical phonon vibration at 3.6 THz, which is assigned to an A1 symmetry mode involving Lu ion motion along the c axis. This mode was excited in longitudinal (LO) and transverse mode (TO) geometries. While the LO-TO frequency splitting is small (<0.1 THz), a remarkable phase reversal of the reflectivity curve was observed. This is attributed to a large linear electro-optic effect (Pockels effect), induced by the THz electric field associated with the LO mode.

  12. In vivo (31)P magnetic resonance spectroscopy of the human liver at 7 T: an initial experience.

    Science.gov (United States)

    Chmelik, Marek; Považan, Michal; Krššák, Martin; Gruber, Stephan; Tkačov, Martin; Trattnig, Siegfried; Bogner, Wolfgang

    2014-04-01

    Phosphorus ((31) P) MRS is a powerful tool for the non-invasive investigation of human liver metabolism. Four in vivo (31) P localization approaches (single voxel image selected in vivo spectroscopy (3D-ISIS), slab selective 1D-ISIS, 2D chemical shift imaging (CSI), and 3D-CSI) with different voxel volumes and acquisition times were demonstrated in nine healthy volunteers. Localization techniques provided comparable signal-to-noise ratios normalized for voxel volume and acquisition time differences, Cramer-Rao lower bounds (8.7 ± 3.3%1D-ISIS , 7.6 ± 2.5%3D-ISIS , 8.6 ± 4.2%2D-CSI , 10.3 ± 2.7%3D-CSI ), and linewidths (50 ± 24 Hz1D-ISIS , 34 ± 10 Hz3D-ISIS , 33 ± 10 Hz2D-CSI , 34 ± 11 Hz3D-CSI ). Longitudinal (T1 ) relaxation times of human liver metabolites at 7 T were assessed by 1D-ISIS inversion recovery in the same volunteers (n = 9). T1 relaxation times of hepatic (31) P metabolites at 7 T were the following: phosphorylethanolamine - 4.41 ± 1.55 s; phosphorylcholine - 3.74 ± 1.31 s; inorganic phosphate - 0.70 ± 0.33 s; glycerol 3-phosphorylethanolamine - 6.19 ± 0.91 s; glycerol 3-phosphorylcholine - 5.94 ± 0.73 s; γ-adenosine triphosphate (ATP) - 0.50 ± 0.08 s; α-ATP - 0.46 ± 0.07 s; β-ATP - 0.56 ± 0.07 s. The improved spectral resolution at 7 T enabled separation of resonances in the phosphomonoester and phosphodiester spectral region as well as nicotinamide adenine dinucleotide and uridine diphosphoglucose signals. An additional resonance at 2.06 ppm previously assigned to phosphoenolpyruvate or phosphatidylcholine is also detectable. These are the first (31) P metabolite relaxation time measurements at 7 T in human liver, and they will help in the exploration of new, exciting questions in metabolic research with 7 T MR. Copyright © 2014 John Wiley & Sons, Ltd.

  13. Quantitative ATP synthesis in human liver measured by localized 31P spectroscopy using the magnetization transfer experiment.

    Science.gov (United States)

    Schmid, A I; Chmelík, M; Szendroedi, J; Krssák, M; Brehm, A; Moser, E; Roden, M

    2008-06-01

    The liver plays a central role in intermediate metabolism. Accumulation of liver fat (steatosis) predisposes to various liver diseases. Steatosis and abnormal muscle energy metabolism are found in insulin-resistant and type-2 diabetic states. To examine hepatic energy metabolism, we measured hepatocellular lipid content, using proton MRS, and rates of hepatic ATP synthesis in vivo, using the 31P magnetization transfer experiment. A suitable localization scheme was developed and applied to the measurements of longitudinal relaxation times (T1) in six healthy volunteers and the ATP-synthesis experiment in nine healthy volunteers. Liver 31P spectra were modelled and quantified successfully using a time domain fit and the AMARES (advanced method for accurate, robust and efficient spectral fitting of MRS data with use of prior knowledge) algorithm describing the essential components of the dataset. The measured T1 relaxation times are comparable to values reported previously at lower field strengths. All nine subjects in whom saturation transfer was measured had low hepatocellular lipid content (1.5 +/- 0.2% MR signal; mean +/- SEM). The exchange rate constant (k) obtained was 0.30 +/- 0.02 s(-1), and the rate of ATP synthesis was 29.5 +/- 1.8 mM/min. The measured rate of ATP synthesis is about three times higher than in human skeletal muscle and human visual cortex, but only about half of that measured in perfused rat liver. In conclusion, 31P MRS at 3 T provides sufficient sensitivity to detect magnetization transfer effects and can therefore be used to assess ATP synthesis in human liver.

  14. UV-visible spectroscopy of macrocyclic alkyl, nitrosyl and halide complexes of cobalt and rhodium. Experiment and calculation.

    Science.gov (United States)

    Hull, Emily A; West, Aaron C; Pestovsky, Oleg; Kristian, Kathleen E; Ellern, Arkady; Dunne, James F; Carraher, Jack M; Bakac, Andreja; Windus, Theresa L

    2015-02-28

    Transition metal complexes (NH3)5CoX(2+) (X = CH3, Cl) and L(H2O)MX(2+), where M = Rh or Co, X = CH3, NO, or Cl, and L is a macrocyclic N4 ligand are examined by both experiment and computation to better understand their electronic spectra and associated photochemistry. Specifically, irradiation into weak visible bands of nitrosyl and alkyl complexes (NH3)5CoCH3(2+) and L(H2O)M(III)X(2+) (X = CH3 or NO) leads to photohomolysis that generates the divalent metal complex and ˙CH3 or ˙NO, respectively. On the other hand, when X = halide or NO2, visible light photolysis leads to dissociation of X(-) and/or cis/trans isomerization. Computations show that visible bands for alkyl and nitrosyl complexes involve transitions from M-X bonding orbitals and/or metal d orbitals to M-X antibonding orbitals. In contrast, complexes with X = Cl or NO2 exhibit only d-d bands in the visible, so that homolytic cleavage of the M-X bond requires UV photolysis. UV-Vis spectra are not significantly dependent on the structure of the equatorial ligands, as shown by similar spectral features for (NH3)5CoCH3(2+) and L(1)(H2O)CoCH3(2+).

  15. Photoelectron spectroscopy at a free-electron laser. Investigation of space-charge effects in angle-resolved and core-level spectroscopy and realizaton of a time-resolved core-level photoemission experiment

    Energy Technology Data Exchange (ETDEWEB)

    Marczynski-Buehlow, Martin

    2012-01-30

    The free-electron laser (FEL) in Hamburg (FLASH) is a very interesting light source with which to perform photoelectron spectroscopy (PES) experiments. Its special characteristics include highly intense photon pulses (up to 100 J/pulse), a photon energy range of 30 eV to 1500 eV, transverse coherence as well as pulse durations of some ten femtoseconds. Especially in terms of time-resolved PES (TRPES), the deeper lying core levels can be reached with photon energies up to 1500 eV with acceptable intensity now and, therefore, element-specific, time-resolved core-level PES (XPS) is feasible at FLASH. During the work of this thesis various experimental setups were constructed in order to realize angle-resolved (ARPES), core-level (XPS) as well as time-resolved PES experiments at the plane grating monochromator beamline PG2 at FLASH. Existing as well as newly developed systems for online monitoring of FEL pulse intensities and generating spatial and temporal overlap of FEL and optical laser pulses for time-resolved experiments are successfully integrated into the experimental setup for PES. In order to understand space-charge effects (SCEs) in PES and, therefore, being able to handle those effects in future experiments using highly intense and pulsed photon sources, the origin of energetic broadenings and shifts in photoelectron spectra are studied by means of a molecular dynamic N-body simulation using a modified Treecode Algorithm for sufficiently fast and accurate calculations. It turned out that the most influencing parameter is the ''linear electron density'' - the ratio of the number of photoelectrons to the diameter of the illuminated spot on the sample. Furthermore, the simulations could reproduce the observations described in the literature fairly well. Some rules of thumb for XPS and ARPES measurements could be deduced from the simulations. Experimentally, SCEs are investigated by means of ARPES as well as XPS measurements as a function of

  16. Sorption of Eu(III)/Cm(III) on Ca-montmorillonite and Na-illite. Part 1: Batch sorption and time-resolved laser fluorescence spectroscopy experiments

    Science.gov (United States)

    Rabung, Th.; Pierret, M. C.; Bauer, A.; Geckeis, H.; Bradbury, M. H.; Baeyens, B.

    2005-12-01

    Sorption of Cm(III) and Eu(III) at trace concentrations onto Ca-montmorillonite (SWy-1) and Na-illite (Illite du Puy) has been studied under anaerobic conditions by batch sorption experiments and time-resolved laser fluorescence spectroscopy (TRLFS). Comparison of the results from spectroscopic and batch sorption experiments with Cm and Eu indicates the existence of outer-sphere complexes at pH 5 for both clay minerals. Five H 2O/OH - molecules remain in the first metal ion coordination sphere of the sorbed Eu/Cm. Measured fluorescence lifetimes of sorbed Eu/Cm and peak deconvolution of Cm-spectra are consistent with the formation of surface complexes of the form ≡S-O-Eu/Cm(OH) x(2-x)(H 2O) 5-x. At pH ≥ 12 Cm becomes incorporated into a surface precipitate at the Ca-montmorillonite surface presumably composed of Ca(OH) 2 or calcium silicate hydrate. A dramatic shift of the fluorescence emission band by more than 20 nm and a clear increase in the fluorescence lifetime suggests the almost complete displacement of coordinated H 2O and OH -. The pH dependent Eu sorption data obtained in batch experiments are consistent with spectroscopic data on Eu and Cm within experimental uncertainties thus demonstrating the validity of Eu as a homologue for trivalent actinides. Parameterization of a two-site protolysis nonelectrostatic surface complexation and cation exchange model using the batch sorption data and spectroscopic results is discussed in Part 2 of this work.

  17. Enhancing the sensitivity of mid-IR quantum cascade laser-based cavity-enhanced absorption spectroscopy using RF current perturbation.

    Science.gov (United States)

    Manfred, Katherine M; Kirkbride, James M R; Ciaffoni, Luca; Peverall, Robert; Ritchie, Grant A D

    2014-12-15

    The sensitivity of mid-IR quantum cascade laser (QCL) off-axis cavity-enhanced absorption spectroscopy (CEAS), often limited by cavity mode structure and diffraction losses, was enhanced by applying a broadband RF noise to the laser current. A pump-probe measurement demonstrated that the addition of bandwidth-limited white noise effectively increased the laser linewidth, thereby reducing mode structure associated with CEAS. The broadband noise source offers a more sensitive, more robust alternative to applying single-frequency noise to the laser. Analysis of CEAS measurements of a CO(2) absorption feature at 1890  cm(-1) averaged over 100 ms yielded a minimum detectable absorption of 5.5×10(-3)  Hz(-1/2) in the presence of broadband RF perturbation, nearly a tenfold improvement over the unperturbed regime. The short acquisition time makes this technique suitable for breath applications requiring breath-by-breath gas concentration information.

  18. Light, Molecules, Action: Using Ultrafast Uv-Visible and X-Ray Spectroscopy to Probe Excited State Dynamics in Photoactive Molecules

    Science.gov (United States)

    Sension, R. J.

    2017-06-01

    Light provides a versatile energy source capable of precise manipulation of material systems on size scales ranging from molecular to macroscopic. Photochemistry provides the means for transforming light energy from photon to process via movement of charge, a change in shape, a change in size, or the cleavage of a bond. Photochemistry produces action. In the work to be presented here ultrafast UV-Visible pump-probe, and pump-repump-probe methods have been used to probe the excited state dynamics of stilbene-based molecular motors, cyclohexadiene-based switches, and polyene-based photoacids. Both ultrafast UV-Visible and X-ray absorption spectroscopies have been applied to the study of cobalamin (vitamin B_{12}) based compounds. Optical measurements provide precise characterization of spectroscopic signatures of the intermediate species on the S_{1} surface, while time-resolved XANES spectra at the Co K-edge probe the structural changes that accompany these transformations.

  19. Non-resonant wavelength modulation saturation spectroscopy in acetylene-filled hollow-core photonic bandgap fibres applied to modulation-free laser diode stabilisation.

    Science.gov (United States)

    Pineda-Vadillo, Pablo; Lynch, Michael; Charlton, Christy; Donegan, John F; Weldon, Vincent

    2009-12-07

    In this paper the application of Wavelength Modulation (WM) techniques to non-resonant saturation spectroscopy in acetylene-filled Hollow-Core Photonic Bandgap Fibres (HC-PBFs) and modulation-free Laser Diode (LD) frequency stabilisation is investigated. In the first part WM techniques are applied to non-resonant pump-probe saturation of acetylene overtone rotational transitions in a HC-PBF. A high-power DFB chip-on-carrier mounted LD is used in conjunction with a tuneable External Cavity Laser (ECL) and the main saturation parameters are characterized. In the second part a novel feedback system to stabilize the DFB emission wavelength based on the WM saturation results is implemented. Modulation-free locking of the DFB laser frequency to the narrow linewidth saturation feature is achieved for both constant and variable LD temperatures.

  20. Vibrational spectroscopy

    Science.gov (United States)

    Umesh P. Agarwal; Rajai Atalla

    2010-01-01

    Vibrational spectroscopy is an important tool in modern chemistry. In the past two decades, thanks to significant improvements in instrumentation and the development of new interpretive tools, it has become increasingly important for studies of lignin. This chapter presents the three important instrumental methods-Raman spectroscopy, infrared (IR) spectroscopy, and...

  1. Terahertz spectroscopy

    DEFF Research Database (Denmark)

    Jepsen, Peter Uhd

    2009-01-01

    In this presentation I will review methods for spectroscopy in the THz range, with special emphasis on the practical implementation of the technique known ad THz time-domain spectroscopy (THz-TDS). THz-TDS has revived the old field of far-infrared spectroscopy, and enabled a wealth of new...... activities that promise commercial potential for spectroscopic applications in the THz range. This will be illustrated with examples of spectroscopy of liquids inside their bottles as well as sensitive, quantitative spectroscopy in waveguides....

  2. Magnetic resonance spectroscopy imaging in the diagnosis of prostate cancer: initial experience; Espectroscopia por ressonancia magnetica no diagnostico do cancer de prostata: experiencia inicial

    Energy Technology Data Exchange (ETDEWEB)

    Melo, Homero Jose de Farias e [Universidade Federal de Sao Paulo (UNIFESP/EPM), SP (Brazil). Escola Paulista de Medicina. Ciencias Radiologicas]. E-mail: homero.ddi@epm.br; Szejnfeld, Denis [Universidade Federal de Sao Paulo (UNIFESP/EPM), Sp (Brazil). Dept. de Diagnostico por Imagem. Setor de Ressonancia Magnetica; Paiva, Cristiano Silveira [Universidade Federal do Amazonas (UFAM), Manaus, AM (Brazil); Abdala, Nitamar [Universidade Federal de Sao Paulo (UNIFESP/EPM), SP (Brazil). Dept. de Diagnostico por Imagem. Setor de Neuroradiologia; Arruda, Homero Oliveira de [Hospital do Servidor Publico Estadual de Sao Paulo (IAMSPE), SP (Brazil); Goldman, Suzan Menasce; Szejnfeld, Jacob [Universidade Federal de Sao Paulo (UNIFESP/EPM), Sp (Brazil). Escola Paulista de Medicina. Dept. de Diagnostico por Imagem

    2009-01-15

    Objective: to report an experiment involving the introduction of a protocol utilizing commercially available three-dimensional 1H magnetic resonance spectroscopy imaging (3D 1H MRSI) method in patients diagnosed with prostatic tumors under suspicion of neoplasm. Materials and methods: forty-one patients in the age range between 51 and 80 years (mean, 67 years) were prospectively evaluated. The patients were divided into two groups: patients with one or more biopsies negative for cancer and high specific-prostatic antigen levels (group A), and patients with cancer confirmed by biopsy (group B). The determination of the target area (group A) or the known cancer extent (group B) was based on magnetic resonance imaging and MRSI studies. Results: the specificity of MRSI in the diagnosis of prostate cancer was lower than the specificity reported in the literature (about 47%). On the other hand, for tumor staging, it corresponded to the specificity reported in the literature. Conclusion: the introduction and standardization of 3D 1H MRSI has allowed the obtention of a presumable diagnosis of prostate cancer, by a combined analysis of magnetic resonance imaging and metabolic data from 3D 1H MRSI. (author)

  3. Fine-pitch CdTe detector for hard X-ray imaging and spectroscopy of the Sun with the FOXSI rocket experiment

    Science.gov (United States)

    Ishikawa, Shin-nosuke; Katsuragawa, Miho; Watanabe, Shin; Uchida, Yuusuke; Takeda, Shin'ichiro; Takahashi, Tadayuki; Saito, Shinya; Glesener, Lindsay; Buitrago-Casas, Juan Camilo; Krucker, Säm.; Christe, Steven

    2016-07-01

    We have developed a fine-pitch hard X-ray (HXR) detector using a cadmium telluride (CdTe) semiconductor for imaging and spectroscopy for the second launch of the Focusing Optics Solar X-ray Imager (FOXSI). FOXSI is a rocket experiment to perform high sensitivity HXR observations from 4 to 15 keV using the new technique of HXR focusing optics. The focal plane detector requires -30°C). Double-sided silicon strip detectors were used for the first FOXSI flight in 2012 to meet these criteria. To improve the detectors' efficiency (66% at 15 keV for the silicon detectors) and position resolution of 75 μm for the second launch, we fabricated double-sided CdTe strip detectors with a position resolution of 60 μm and almost 100% efficiency for the FOXSI energy range. The sensitive area is 7.67 mm × 7.67 mm, corresponding to the field of view of 791'' × 791''. An energy resolution of 1 keV (FWHM) and low-energy threshold of ≈4 keV were achieved in laboratory calibrations. The second launch of FOXSI was performed on 11 December 2014, and images from the Sun were successfully obtained with the CdTe detector. Therefore, we successfully demonstrated the detector concept and the usefulness of this technique for future HXR observations of the Sun.

  4. Fine-pitch CdTe detector for hard X-ray imaging and spectroscopy of the Sun with the FOXSI rocket experiment

    CERN Document Server

    Ishikawa, S; Watanabe, S; Uchida, Y; Takeda, S; Takahashi, T; Saito, S; Glesener, L; Buitrago-Casas, J C; Krucker, S; Christe, S

    2016-01-01

    We have developed a fine-pitch hard X-ray (HXR) detector using a cadmium telluride (CdTe) semiconductor for imaging and spectroscopy for the second launch of the Focusing Optics Solar X-ray Imager (FOXSI). FOXSI is a rocket experiment to perform high sensitivity HXR observations from 4-15 keV using the new technique of HXR focusing optics. The focal plane detector requires -30 C). Double-sided silicon strip detectors were used for the first FOXSI flight in 2012 to meet these criteria. To improve the detectors' efficiency (66 at 15 keV for the silicon detectors) and position resolution of 75 um for the second launch, we fabricated double-sided CdTe strip detectors with a position resolution of 60 um and almost 100 % efficiency for the FOXSI energy range. The sensitive area is 7.67 mm x 7.67 mm, corresponding to the field of view of 791'' x 791''. An energy resolution of about 1 keV (FWHM) and low energy threshold of 4 keV were achieved in laboratory calibrations. The second launch of FOXSI was performed on De...

  5. Cooperative photo-induced effects: from photo-magnetism under continuous irradiation to ultra-fast phenomena - study through optical spectroscopy and X-ray diffraction; Effets photo-induits cooperatifs: du photomagnetisme sous irradiation continue aux phenomenes ultrarapides - etude par spectroscopie optique et diffraction X

    Energy Technology Data Exchange (ETDEWEB)

    Glijer, D

    2006-12-15

    The control with ultra-short laser pulses of the collective and concerted transformation of molecules driving a macroscopic state switching on an ultra-fast time scale in solid state opens new prospects in materials science. The goal is to realize at the material level what happens at the molecular level in femto-chemistry. These processes are highly cooperative and highly non-linear, leading to self-amplification and self-organization within the material, a so-called photo-induced phase transition with a new long range order (structural, magnetic, ferroelectric,...). Two families of molecular compounds have been studied here: first of all, spin transition materials changing from a diamagnetic state over to a paramagnetic state under the effect of temperature or under continuous laser excitation. It concerns photo-active molecular bi-stability prototype materials in solid state, whose switching has been studied during X-ray diffraction, optical reflectivity and magnetism experiments. Then we have studied charge-transfer molecular systems, prototype compounds for ultrafast photo-induced phase transitions: insulator-metal, neutral-ionic....As well as ultrafast optical experiments, time-resolved X ray crystallography is a key technique in order to follow at the atomic level the different steps of the photo-induced transformation and thus to observe the involved mechanisms. We have underlined a process of photo-formation of one-dimensional nano-domains of lattice-relaxed charge-transfer excitations, governing the photo-induced phase transition of the molecular charge-transfer complex TTF-CA by the first time-resolved diffuse scattering measurements. Moreover, a new femtosecond laser-plasma source and a optical pump-probe spectroscopy set-up with a highly sensitive detecting system have been developed in this work. The results presented here will be an illustration of the present scientific challenges existing on the one hand with the development of projects of major

  6. Development of a single-shot CCD-based data acquisition system for time-resolved X-ray photoelectron spectroscopy at an X-ray free-electron laser facility.

    Science.gov (United States)

    Oura, Masaki; Wagai, Tatsuya; Chainani, Ashish; Miyawaki, Jun; Sato, Hiromi; Matsunami, Masaharu; Eguchi, Ritsuko; Kiss, Takayuki; Yamaguchi, Takashi; Nakatani, Yasuhiro; Togashi, Tadashi; Katayama, Tetsuo; Ogawa, Kanade; Yabashi, Makina; Tanaka, Yoshihito; Kohmura, Yoshiki; Tamasaku, Kenji; Shin, Shik; Ishikawa, Tetsuya

    2014-01-01

    In order to utilize high-brilliance photon sources, such as X-ray free-electron lasers (XFELs), for advanced time-resolved photoelectron spectroscopy (TR-PES), a single-shot CCD-based data acquisition system combined with a high-resolution hemispherical electron energy analyzer has been developed. The system's design enables it to be controlled by an external trigger signal for single-shot pump-probe-type TR-PES. The basic performance of the system is demonstrated with an offline test, followed by online core-level photoelectron and Auger electron spectroscopy in 'single-shot image', 'shot-to-shot image (image-to-image storage or block storage)' and `shot-to-shot sweep' modes at soft X-ray undulator beamline BL17SU of SPring-8. In the offline test the typical repetition rate for image-to-image storage mode has been confirmed to be about 15 Hz using a conventional pulse-generator. The function for correcting the shot-to-shot intensity fluctuations of the exciting photon beam, an important requirement for the TR-PES experiments at FEL sources, has been successfully tested at BL17SU by measuring Au 4f photoelectrons with intentionally controlled photon flux. The system has also been applied to hard X-ray PES (HAXPES) in `ordinary sweep' mode as well as shot-to-shot image mode at the 27 m-long undulator beamline BL19LXU of SPring-8 and also at the SACLA XFEL facility. The XFEL-induced Ti 1s core-level spectrum of La-doped SrTiO3 is reported as a function of incident power density. The Ti 1s core-level spectrum obtained at low power density is consistent with the spectrum obtained using the synchrotron source. At high power densities the Ti 1s core-level spectra show space-charge effects which are analysed using a known mean-field model for ultrafast electron packet propagation. The results successfully confirm the capability of the present data acquisition system for carrying out the core-level HAXPES studies of condensed matter induced by the XFEL.

  7. Using Raman Spectroscopy and Surface-Enhanced Raman Scattering to Identify Colorants in Art: An Experiment for an Upper-Division Chemistry Laboratory

    Science.gov (United States)

    Mayhew, Hannah E.; Frano, Kristen A.; Svoboda, Shelley A.; Wustholz, Kristin L.

    2015-01-01

    Surface-enhanced Raman scattering (SERS) studies of art represent an attractive way to introduce undergraduate students to concepts in nanoscience, vibrational spectroscopy, and instrumental analysis. Here, we present an undergraduate analytical or physical chemistry laboratory wherein a combination of normal Raman and SERS spectroscopy is used to…

  8. Using Raman Spectroscopy and Surface-Enhanced Raman Scattering to Identify Colorants in Art: An Experiment for an Upper-Division Chemistry Laboratory

    Science.gov (United States)

    Mayhew, Hannah E.; Frano, Kristen A.; Svoboda, Shelley A.; Wustholz, Kristin L.

    2015-01-01

    Surface-enhanced Raman scattering (SERS) studies of art represent an attractive way to introduce undergraduate students to concepts in nanoscience, vibrational spectroscopy, and instrumental analysis. Here, we present an undergraduate analytical or physical chemistry laboratory wherein a combination of normal Raman and SERS spectroscopy is used to…

  9. In vivo 1H-spectroscopy of human intracranial tumors at 1.5 tesla. Preliminary experience at a clinical installation

    DEFF Research Database (Denmark)

    Henriksen, O; Wieslander, S; Gjerris, F

    1991-01-01

    Magnetic resonance spectroscopy (MRS) may contribute to the characterization of intracranial tumors in vivo. Volume selective water suppressed proton spectroscopy offers the possibility to study a number of metabolites in the brain including choline (CHO), creatinine/phosphocreatinine (CR/PCR), N...

  10. In vivo 1H-spectroscopy of human intracranial tumors at 1.5 tesla. Preliminary experience at a clinical installation

    DEFF Research Database (Denmark)

    Henriksen, O; Wieslander, S; Gjerris, F

    1991-01-01

    Magnetic resonance spectroscopy (MRS) may contribute to the characterization of intracranial tumors in vivo. Volume selective water suppressed proton spectroscopy offers the possibility to study a number of metabolites in the brain including choline (CHO), creatinine/phosphocreatinine (CR/PCR), N....... However, further research is warranted before a definite conclusion can be drawn....

  11. Sub-nanosecond time-resolved ambient-pressure X-ray photoelectron spectroscopy setup for pulsed and constant wave X-ray light sources.

    Science.gov (United States)

    Shavorskiy, Andrey; Neppl, Stefan; Slaughter, Daniel S; Cryan, James P; Siefermann, Katrin R; Weise, Fabian; Lin, Ming-Fu; Bacellar, Camila; Ziemkiewicz, Michael P; Zegkinoglou, Ioannis; Fraund, Matthew W; Khurmi, Champak; Hertlein, Marcus P; Wright, Travis W; Huse, Nils; Schoenlein, Robert W; Tyliszczak, Tolek; Coslovich, Giacomo; Robinson, Joseph; Kaindl, Robert A; Rude, Bruce S; Ölsner, Andreas; Mähl, Sven; Bluhm, Hendrik; Gessner, Oliver

    2014-09-01

    An apparatus for sub-nanosecond time-resolved ambient-pressure X-ray photoelectron spectroscopy studies with pulsed and constant wave X-ray light sources is presented. A differentially pumped hemispherical electron analyzer is equipped with a delay-line detector that simultaneously records the position and arrival time of every single electron at the exit aperture of the hemisphere with ~0.1 mm spatial resolution and ~150 ps temporal accuracy. The kinetic energies of the photoelectrons are encoded in the hit positions along the dispersive axis of the two-dimensional detector. Pump-probe time-delays are provided by the electron arrival times relative to the pump pulse timing. An average time-resolution of (780 ± 20) ps (FWHM) is demonstrated for a hemisphere pass energy E(p) = 150 eV and an electron kinetic energy range KE = 503-508 eV. The time-resolution of the setup is limited by the electron time-of-flight (TOF) spread related to the electron trajectory distribution within the analyzer hemisphere and within the electrostatic lens system that images the interaction volume onto the hemisphere entrance slit. The TOF spread for electrons with KE = 430 eV varies between ~9 ns at a pass energy of 50 eV and ~1 ns at pass energies between 200 eV and 400 eV. The correlation between the retarding ratio and the TOF spread is evaluated by means of both analytical descriptions of the electron trajectories within the analyzer hemisphere and computer simulations of the entire trajectories including the electrostatic lens system. In agreement with previous studies, we find that the by far dominant contribution to the TOF spread is acquired within the hemisphere. However, both experiment and computer simulations show that the lens system indirectly affects the time resolution of the setup to a significant extent by inducing a strong dependence of the angular spread of electron trajectories entering the hemisphere on the retarding ratio. The scaling of the angular spread with

  12. A Versatile Setup for Ultrafast Broadband Optical Spectroscopy of Coherent Collective Modes in Strongly Correlated Quantum Systems

    CERN Document Server

    Baldini, Edoardo; Borroni, Simone; Arrell, Christopher; van Mourik, Frank; Carbone, Fabrizio

    2016-01-01

    A femtosecond pump-probe setup is described that is optimised for broadband transient reflectivity experiments on solid samples over a wide range of temperatures. By combining a temporal resolution of 45 fs and a broad detection range between 1.75 and 2.85 eV, this apparatus can provide insightful information on the interplay between coherent collective modes and high-energy electronic excitations, which is one of the distinctive characteristics of strongly interacting and correlated quantum systems. The use of a single-shot readout CMOS array detector at frame rates up to 10 kHz allows to resolve coherent oscillations with amplitudes below 10$^{-4}$ in $\\Delta$R/R. We demonstrate the operation of this setup on the prototypical charge-transfer insulator La$_2$CuO$_4$, revealing the presence of coherent optical phonons with frequencies as high as 13 THz.

  13. Direct Visualization of Exciton Reequilibration in the LH1 and LH2 Complexes of Rhodobacter sphaeroides by Multipulse Spectroscopy

    Science.gov (United States)

    Cohen Stuart, Thomas A.; Vengris, Mikas; Novoderezhkin, Vladimir I.; Cogdell, Richard J.; Hunter, C. Neil; van Grondelle, Rienk

    2011-01-01

    The dynamics of the excited states of the light-harvesting complexes LH1 and LH2 of Rhodobacter sphaeroides are governed, mainly, by the excitonic nature of these ring-systems. In a pump-dump-probe experiment, the first pulse promotes LH1 or LH2 to its excited state and the second pulse dumps a portion of the excited state. By selective dumping, we can disentangle the dynamics normally hidden in the excited-state manifold. We find that by using this multiple-excitation technique we can visualize a 400-fs reequilibration reflecting relaxation between the two lowest exciton states that cannot be directly explored by conventional pump-probe. An oscillatory feature is observed within the exciton reequilibration, which is attributed to a coherent motion of a vibrational wavepacket with a period of ∼150 fs. Our disordered exciton model allows a quantitative interpretation of the observed reequilibration processes occurring in these antennas. PMID:21539791

  14. Direct Visualization of Exciton Reequilibration in the LH1 and LH2 Complexes of Rhodobacter sphaeroides by Multipulse Spectroscopy

    Energy Technology Data Exchange (ETDEWEB)

    Stuart, Thomas A. Cohen [Free Univ. of Amsterdam (Netherlands); Vengris, Mikas [Vilnius Univ. (Lithuania); Novoderezhkin, Vladimir I. [A.N. Belozersky Inst. of Physico-Chemical Biology, Moscow State Univ. (Russia); Cogdell, Richard J. [Microbial Photosynthesis Laboratory, Glasgow Biomedical Research Centre, Univ. of Glasgow (United Kingdom); Hunter, C. Neil [Department of Molecular Biology and Biotechnology, Univ. of Sheffield, (United Kingdom); van Grondelle, Rienk [Free Univ. of Amsterdam (Netherlands)

    2011-01-01

    The dynamics of the excited states of the light-harvesting complexes LH1 and LH2 of Rhodobacter sphaeroides are governed, mainly, by the excitonic nature of these ring-systems. In a pump-dump-probe experiment, the first pulse promotes LH1 or LH2 to its excited state and the second pulse dumps a portion of the excited state. By selective dumping, we can disentangle the dynamics normally hidden in the excited-state manifold. We find that by using this multiple-excitation technique we can visualize a 400-fs reequilibration reflecting relaxation between the two lowest exciton states that cannot be directly explored by conventional pump-probe. An oscillatory feature is observed within the exciton reequilibration, which is attributed to a coherent motion of a vibrational wavepacket with a period of ~150 fs. Our disordered exciton model allows a quantitative interpretation of the observed reequilibration processes occurring in these antennas.

  15. "Solvent Effects" in 1H NMR Spectroscopy.

    Science.gov (United States)

    Cavaleiro, Jose A. S.

    1987-01-01

    Describes a simple undergraduate experiment in chemistry dealing with the "solvent effects" in nuclear magnetic resonance (NMR) spectroscopy. Stresses the importance of having students learn NMR spectroscopy as a tool in analytical chemistry. (TW)

  16. Electronic spectroscopies

    NARCIS (Netherlands)

    Weckhuysen, B.M.; Schoonheydt, R.A.

    2000-01-01

    Diffuse reflectance spectroscopy (DRS) in the ultraviolet, visible and near-infrared region is a versatile spectroscopic technique, as both d-d and charge transfer transitions of supported TMI can be probed. One of the advantages of electronic spectroscopy is that the obtained information is

  17. Tuning non-equilibrium superconductors with lasers

    Energy Technology Data Exchange (ETDEWEB)

    Sentef, Michael A.; Kollath, Corinna [HISKP, University of Bonn, Nussallee 14-16, D-53115 Bonn (Germany); Kemper, Alexander F. [LBL Berkeley (United States); Georges, Antoine [Ecole Polytechnique and College de France, Paris (France)

    2015-07-01

    The study of the real-time dynamics dynamics of solids perturbed by short laser pulses is an intriguing opportunity of ultrafast materials science. Previous theoretical work on pump-probe photoemission spectroscopy revealed spectroscopic signatures of electron-boson coupling, which are reminiscent of features observed in recent pump-probe photoemission experiments on cuprate superconductors. Here we investigate the ordered state of electron-boson mediated superconductors subject to laser driving using Migdal-Eliashberg theory on the Kadanoff-Baym-Keldysh contour. We extract the characteristic time scales on which the non-equilibrium superconductor reacts to the perturbation, and their relation to the coupling boson and the underlying order.

  18. Excited-state intramolecular hydrogen transfer (ESIHT) of 1,8-Dihydroxy-9,10-anthraquinone (DHAQ) characterized by ultrafast electronic and vibrational spectroscopy and computational modeling

    KAUST Repository

    Mohammed, Omar F.

    2014-05-01

    We combine ultrafast electronic and vibrational spectroscopy and computational modeling to investigate the photoinduced excited-state intramolecular hydrogen-transfer dynamics in 1,8-dihydroxy-9,10-anthraquinone (DHAQ) in tetrachloroethene, acetonitrile, dimethyl sulfoxide, and methanol. We analyze the electronic excited states of DHAQ with various possible hydrogen-bonding schemes and provide a general description of the electronic excited-state dynamics based on a systematic analysis of femtosecond UV/vis and UV/IR pump-probe spectroscopic data. Upon photoabsorption at 400 nm, the S 2 electronic excited state is initially populated, followed by a rapid equilibration within 150 fs through population transfer to the S 1 state where DHAQ exhibits ESIHT dynamics. In this equilibration process, the excited-state population is distributed between the 9,10-quinone (S2) and 1,10-quinone (S1) states while undergoing vibrational energy redistribution, vibrational cooling, and solvation dynamics on the 0.1-50 ps time scale. Transient UV/vis pump-probe data in methanol also suggest additional relaxation dynamics on the subnanosecond time scale, which we tentatively ascribe to hydrogen bond dynamics of DHAQ with the protic solvent, affecting the equilibrium population dynamics within the S2 and S1 electronic excited states. Ultimately, the two excited singlet states decay with a solvent-dependent time constant ranging from 139 to 210 ps. The concomitant electronic ground-state recovery is, however, only partial because a large fraction of the population relaxes to the first triplet state. From the similarity of the time scales involved, we conjecture that the solvent plays a crucial role in breaking the intramolecular hydrogen bond of DHAQ during the S2/S1 relaxation to either the ground or triplet state. © 2014 American Chemical Society.

  19. Laser spectroscopy of protonium

    CERN Document Server

    Hayano, R S

    1999-01-01

    High-precision laser spectroscopy of protonium (pp) is one of the future experiments being considered by ASACUSA collaboration at CERN AD. A possible scheme to produce protonium in vacuum and to detect laser transitions is presented, and implications of reaching high precision are discussed. (7 refs).

  20. Laser spectroscopy

    CERN Document Server

    Demtröder, Wolfgang

    Keeping abreast of the latest techniques and applications, this new edition of the standard reference and graduate text on laser spectroscopy has been completely revised and expanded. While the general concept is unchanged, the new edition features a broad array of new material, e.g., ultrafast lasers (atto- and femto-second lasers) and parametric oscillators, coherent matter waves, Doppler-free Fourier spectroscopy with optical frequency combs, interference spectroscopy, quantum optics, the interferometric detection of gravitational waves and still more applications in chemical analysis, medical diagnostics, and engineering.

  1. The light meson spectroscopy program

    Directory of Open Access Journals (Sweden)

    Smith Elton S.

    2014-06-01

    Full Text Available Recent discoveries of a number of unexpected new charmomium-like meson states at the BaBar and Belle B-factories have demonstrated how little is still known about meson spectroscopy. In this talk we will review recent highlights of the light quark spectroscopy from collider and fixed target experiments.

  2. The light meson spectroscopy program

    Energy Technology Data Exchange (ETDEWEB)

    Smith, Elton S. [JLAB

    2014-06-01

    Recent discoveries of a number of unexpected new charmomium-like meson states at the BaBar and Belle B-factories have demonstrated how little is still known about meson spectroscopy. In this talk we will review recent highlights of the light quark spectroscopy from collider and fixed target experiments.

  3. Fluorescence spectroscopy

    DEFF Research Database (Denmark)

    Bagatolli, Luis

    2016-01-01

    Fluorescence spectroscopy is a powerful experimental tool used by scientists from many disciplines. During the last decades there have been important developments on distinct fluorescence methods, particularly those related to the study of biological phenomena. This chapter discusses...

  4. Modeling of coherent ultrafast magneto-optical experiments: Light-induced molecular mean-field model

    Energy Technology Data Exchange (ETDEWEB)

    Hinschberger, Y. [Instituto de Física dos Materiais da Universidade do Porto, Departamento de Física et Astronomia, Rua do campo Alegre, 687, 4169-007 Porto (Portugal); Hervieux, P.-A. [Institut de Physique et Chimie des Matériaux de Strasbourg, Université de Strasbourg, CNRS UMR 7504 BP 43 - F-67034 Strasbourg Cedex 2 (France)

    2015-12-28

    We present calculations which aim to describe coherent ultrafast magneto-optical effects observed in time-resolved pump-probe experiments. Our approach is based on a nonlinear semi-classical Drude-Voigt model and is used to interpret experiments performed on nickel ferromagnetic thin film. Within this framework, a phenomenological light-induced coherent molecular mean-field depending on the polarizations of the pump and probe pulses is proposed whose microscopic origin is related to a spin-orbit coupling involving the electron spins of the material sample and the electric field of the laser pulses. Theoretical predictions are compared to available experimental data. The model successfully reproduces the observed experimental trends and gives meaningful insight into the understanding of magneto-optical rotation behavior in the ultrafast regime. Theoretical predictions for further experimental studies are also proposed.

  5. ROLE OF SINGLE VOXEL PROTON MAGNETIC RESONANCE SPECTROSCOPY ON A 3 TESLA MR SCANNER IN CHARACTERISING BREAST LESIONS- A TERTIARY CARE CENTRE EXPERIENCE IN EASTERN INDIA

    Directory of Open Access Journals (Sweden)

    Archana Singh

    2016-12-01

    Full Text Available BACKGROUND To evaluate whether the detection of choline-containing compounds in single voxel MR spectroscopy of breast lesions can differentiate between benign and malignant breast lesions. MATERIALS AND METHODS This prospective observational study included 99 breast lesions in 77 patients (between 18 and 86 years age who underwent 3T breast MRI including proton MR spectroscopy before biopsy. Following dynamic contrast-enhanced study, single voxel, water and fat suppressed proton MR spectroscopy was performed. The position and size of the Volume of Interest (VOI was placed so as to include the enhancing part of the lesion and excluding as much as possible the nonenhancing gland parenchyma, adjoining fat or necrotic part of the lesion. Choline peak at 3.2 ppm was qualitatively evaluated. MRI BIRADS scoring was done for each lesion. Sensitivity and specificity of the (1 H-MRS were calculated. Final histopathological diagnosis was taken as the gold standard. RESULTS According to histopathology, 53 lesions were malignant and 46 were benign. The qualitative approach based on presence or absence of choline peak yielded 88.68% [95% CI 76.97% to 95.73%] sensitivity and 76.09% [95% CI 61.23 to 87.41%] specificity for differentiating malignant and benign lesions (p<0.0001. CONCLUSION In vivo proton, MR spectroscopy can be used as an adjunctive tool for characterising breast lesions. However, the detection of choline-containing compounds is not specific for malignancy. Benign breast lesions may also demonstrate choline peak.

  6. Birge-Sponer Estimation of the C-H Bond Dissociation Energy in Chloroform Using Infrared, Near-Infrared, and Visible Absorption Spectroscopy: An Experiment in Physical Chemistry

    Science.gov (United States)

    Myrick, M. L.; Greer, A. E.; Nieuwland, A. A.; Priore, R. J.; Scaffidi, J.; Andreatta, Danielle; Colavita, Paula

    2008-01-01

    The fundamental and overtone vibrational absorption spectroscopy of the C-H unit in CHCl[subscript 3] is measured for transitions from the v = 0 energy level to v = 1 through v = 5 energy levels. The energies of the transitions exhibit a linearly-decreasing spacing between adjacent vibrational levels as the vibrational quantum number increases.…

  7. Precision Muonium Spectroscopy

    CERN Document Server

    Jungmann, Klaus P

    2016-01-01

    The muonium atom is the purely leptonic bound state of a positive muon and an electron. It has a lifetime of 2.2 $\\mu$s. The absence of any known internal structure provides for precision experiments to test fundamental physics theories and to determine accurate values of fundamental constants. In particular groun dstate hyperfine structure transitions can be measured by microwave spectroscopy to deliver the muon magnetic moment. The frequency of the 1s-2s transition in the hydrogen-like atom can be determined with laser spectroscopy to obtain the muon mass. With such measurements fundamental physical interactions, in particular Quantum Electrodynamics, can also be tested at highest precision. The results are important input parameters for experiments on the muon magnetic anomaly. The simplicity of the atom enables further precise experiments, such as a search for muonium-antimuonium conversion for testing charged lepton number conservation and searches for possible antigravity of muons and dark matter.

  8. Precision Muonium Spectroscopy

    Science.gov (United States)

    Jungmann, Klaus P.

    2016-09-01

    The muonium atom is the purely leptonic bound state of a positive muon and an electron. It has a lifetime of 2.2 µs. The absence of any known internal structure provides for precision experiments to test fundamental physics theories and to determine accurate values of fundamental constants. In particular ground state hyperfine structure transitions can be measured by microwave spectroscopy to deliver the muon magnetic moment. The frequency of the 1s-2s transition in the hydrogen-like atom can be determined with laser spectroscopy to obtain the muon mass. With such measurements fundamental physical interactions, in particular quantum electrodynamics, can also be tested at highest precision. The results are important input parameters for experiments on the muon magnetic anomaly. The simplicity of the atom enables further precise experiments, such as a search for muonium-antimuonium conversion for testing charged lepton number conservation and searches for possible antigravity of muons and dark matter.

  9. {sup 31}P magnetic resonance spectroscopy to measure in vivo cardiac energetics in normal myocardium and hypertrophic cardiomyopathy: Experiences at 3 T

    Energy Technology Data Exchange (ETDEWEB)

    Shivu, Ganesh Nallur [Department of Cardiovascular Medicine, University of Birmingham, Vincent Drive, Edgbaston, Birmingham B15 2TT (United Kingdom)], E-mail: drgani23@gmail.com; Abozguia, Khalid; Phan, Thanh Trung; Ahmed, Ibrar [Department of Cardiovascular Medicine, University of Birmingham, Vincent Drive, Edgbaston, Birmingham B15 2TT (United Kingdom); Henning, Anke [Institute for Biomedical Engineering, University and ETH Zurich, Gloriastrasse 35, CH-8092, Zurich CH ETZ F97 (Switzerland); Frenneaux, Michael [Department of Cardiovascular Medicine, University of Birmingham, Vincent Drive, Edgbaston, Birmingham B15 2TT (United Kingdom)

    2010-02-15

    Background: {sup 31}P magnetic resonance spectroscopy (MRS) allows measurement of in vivo high-energy phosphate kinetics in the myocardium. While traditionally {sup 31}P cardiac spectroscopy is performed at 1.5 T, cardiac MRS at higher field strength can theoretically increase signal to noise ratio (SNR) and spectral resolution therefore improving sensitivity and specificity of the cardiac spectra. The reproducibility and feasibility of performing cardiac spectroscopy at 3 T is presented here in this study in healthy volunteers and patients with hypertrophic cardiomyopathy. Methods: Cardiac spectroscopy was performed using a Phillips 3T Achieva scanner in 37 healthy volunteers and 26 patients with hypertrophic cardiomyopathy (HCM) to test the feasibility of the protocol. To test the reproducibility a single volunteer was scanned eight times on separate occasions. A single voxel {sup 31}P MRS was performed using Image Selected In vivo Spectroscopy (ISIS) volume localization. Results: The mean phosphocreatine/adenosine triphosphate (PCr/ATP) ratio of the eight measurements performed on one individual was 2.11 {+-} 0.25. Bland Altman plots showed a variance of 12% in the measurement of PCr/ATP ratios. The PCr/ATP ratio was significantly reduced in HCM patients compared to controls, 1.42 {+-} 0.51 and 2.11 {+-} 0.57, respectively, P < 0.0001. (All results are expressed as mean {+-} standard deviation). Conclusions: Here we demonstrate that cardiac {sup 31}P MRS at 3 T is a reliable method of measuring in vivo high-energy phosphate kinetics in the myocardium for clinical studies and diagnostics. Based on our data an impairment of cardiac energetic state in patients with hypertrophic cardiomyopathy is indisputable.

  10. Electron Spectroscopy

    Science.gov (United States)

    Siegbahn, Kai

    Wilhelm Conrad Röntgen's discovery of X radiation in 1895 in Wörzburg resulted in an immediate break-through not only in physics but also in Society, the latter mainly because of its sensational radiological applications. Within a short time it furthermore indirectly led to the discovery of radioactivity by Henri Becquerel. The discovery of X radiation opened the gate to modern atomic physics, and radioactivity to nuclear physics. Later on, the discovery of X-ray diffraction by Laue, Friedrich and Knipping in 1912 initiated the field of X-ray spectroscopy with its fundamental contributions to atomic and crystal structures. Secondary electrons were early observed in the scattered radiation when X-rays were hitting a sample. The development of the corresponding electron spectroscopy had to wait a much longer time for its maturity. A survey of electron spectroscopy is presented.

  11. Modeling the Effect of Polychromatic Light in Quantitative Absorbance Spectroscopy

    Science.gov (United States)

    Smith, Rachel; Cantrell, Kevin

    2007-01-01

    Laboratory experiment is conducted to give the students practical experience with the principles of electronic absorbance spectroscopy. This straightforward approach creates a powerful tool for exploring many of the aspects of quantitative absorbance spectroscopy.

  12. Dynamics of water and hydrated protons in confinement

    NARCIS (Netherlands)

    Liu, L.

    2015-01-01

    In this thesis the dynamics of water and hydrated protons in confinement has been studied using nonlinear spectroscopy methods, including IR pump-probe spectroscopy and vibrational sum frequency generation spectroscopy (VSFG spectroscopy). Using the IR pump-probe spectroscopy, we first investigated

  13. Charge generation in organic solar cell materials studied by terahertz spectroscopy

    KAUST Repository

    Scarongella, M.

    2015-09-09

    We have investigated the photophysics in neat films of conjugated polymer PBDTTPD and its blend with PCBM using terahertz time-domain spectroscopy. This material has very high efficiency when used in organic solar cells. We were able to identify a THz signature for bound excitons in neat PBDTTPD films, pointing to important delocalization in those excitons. Then, we investigated the nature and local mobility (orders of magnitude higher than bulk mobility) of charges in the PBDTTPPD:PCBM blend as a function of excitation wavelength, fluence and pump-probe time delay. At low pump fluence (no bimolecular recombination phenomena), we were able to observe prompt and delayed charge generation components, the latter originating from excitons created in neat polymer domains which, thanks to delocalization, could reach the PCBM interface and dissociate to charges on a time scale of 1 ps. The nature of the photogenerated charges did not change between 0.5 ps and 800 ps after photo-excitation, which indicated that the excitons split directly into relatively free charges on an ultrafast time scale. © (2015) COPYRIGHT Society of Photo-Optical Instrumentation Engineers (SPIE). Downloading of the abstract is permitted for personal use only.

  14. Conductivity of ZnO nanowires, nanoparticles, and thin films using time-resolved terahertz spectroscopy.

    Science.gov (United States)

    Baxter, Jason B; Schmuttenmaer, Charles A

    2006-12-21

    The terahertz absorption coefficient, index of refraction, and conductivity of nanostructured ZnO have been determined using time-resolved terahertz spectroscopy, a noncontact optical probe. ZnO properties were measured directly for thin films and were extracted from measurements of nanowire arrays and mesoporous nanoparticle films by applying Bruggeman effective medium theory to the composite samples. Annealing significantly reduces the intrinsic carrier concentration in the ZnO films and nanowires, which were grown by chemical bath deposition. The complex-valued, frequency-dependent photoconductivities for all morphologies were found to be similar at short pump-probe delay times. Fits using the Drude-Smith model show that films have the highest mobility, followed by nanowires and then nanoparticles, and that annealing the ZnO increases its mobility. Time constants for decay of photoinjected electron density in films are twice as long as those in nanowires and more than 5 times those for nanoparticles due to increased electron interaction with interfaces and grain boundaries in the smaller-grained materials. Implications for electron transport in dye-sensitized solar cells are discussed.

  15. Chiroptical Spectroscopy

    Science.gov (United States)

    Gurst, Jerome E.

    1995-09-01

    A brief review of the literature, and Chemical and Engineering News in particular, reveals that the determination and use of optical activity is of increasing importance in today's commercial and research laboratories. The classical technique is to measure [alpha]D using a manual or recording polarimeter to provide a single value, the specific rotation at 589 nm. A spectropolarimeter can be used to determine optical activity through the UV-Visible spectrum (Optical Rotatory Dispersion [ORD]). At wavelengths far removed from electronic absorption bands, optical activity arises from circular birefringence, or the difference in the refractive index for left- and right-circularly polarized light; i.e., nL - nR does not equal zero for chiral materials. If the optical activity is measured through an absorption band, complex behavior is observed (a Cotton Effect curve). At an absorption band, chiral materials exhibit circular dichroism (CD), or a difference in the absorption of left- and right-circularly polarized light; epsilon L minus epsilon R does not equal zero. If the spectropolarimeter is set for the measurement of CD spectra, one observes what appears to be a UV-Vis spectrum except that some absorption bands are positive while others may be negative. Just as enantiomers have specific rotations that are equal and opposite at 589 nm (sodium D line), rotations are equal and opposite at all wavelengths, and CD measurements are equal and opposite at all wavelengths. Figure 1 shows the ORD curves for the enantiomeric carvones while Figure 2 contains the CD curves. The enantiomer of carvone that has the positive [alpha]D is obtained from caraway seeds and is known to have the S-configuration while the R-enantiomer is found in spearmint oil. Figure 1. ORD of S-(+)- and R-(-)-carvones Figure 2. CD of S-(+)- and R-(-)-carvones While little can be done to correlate stereochemistry with [alpha]D values, chiroptical spectroscopy (ORD and/or CD) often can be used to assign

  16. Raman spectroscopy

    Science.gov (United States)

    Raman spectroscopy has gained increased use and importance in recent years for accurate and precise detection of physical and chemical properties of food materials, due to the greater specificity and sensitivity of Raman techniques over other analytical techniques. This book chapter presents Raman s...

  17. Modern Spectroscopy

    Science.gov (United States)

    Barrow, Gordon M.

    1970-01-01

    Presents the basic ideas of modern spectroscopy. Both the angular momenta and wave-nature approaches to the determination of energy level patterns for atomic and molecular systems are discussed. The interpretation of spectra, based on atomic and molecular models, is considered. (LC)

  18. Wide-bandgap nonlinear crystal LiGaSsub>2sub> for femtosecond mid-infrared spectroscopy with chirped-pulse upconversion.

    Science.gov (United States)

    Nakamura, Ryosuke; Inagaki, Yoshizumi; Hata, Hidefumi; Hamada, Norio; Umemura, Nobuhiro; Kamimura, Tomosumi

    2016-11-20

    Femtosecond time-resolved mid-infrared (MIR) spectroscopy based on chirped-pulse upconversion is a promising method for observing molecular vibrational dynamics. A quantitative study on nonlinear media for upconversion is still essential for wide applications, particularly at the frequencies below 2000  cm-1. We evaluate wide-bandgap nonlinear crystals of Li-containing ternary chalcogenides based on their performance as the upconversion medium for femtosecond MIR spectroscopy. The upconversion efficiency is measured as a function of the MIR pulse frequency and the chirped pulse energy. LiGaSsub>2sub> is found to be an efficient crystal for the upconversion of MIR pulses in a wide frequency range of 1100-2700  cm-1, especially below 2000  cm-1. By using LiGaSsub>2sub> as an efficient upconversion crystal, we develop a MIR pump-probe spectroscopy system with a spectral resolution of 2.5  cm-1, a time resolution of 0.2 ps, and a probe window of 120  cm-1. Vibrational relaxation dynamics of CO stretching modes of Mnsub>2sub>(CO)sub>10sub> in cyclohexane and bovine serum albumin in Dsub>2sub>O are demonstrated with a high signal-to-noise ratio.

  19. Spectroscopy of neutral radium

    Energy Technology Data Exchange (ETDEWEB)

    Mol, Aran; De, Subhadeep; Jungmann, Klaus; Wilschut, Hans; Willmann, Lorenz [KVI, University of Groningen, Groningen (Netherlands)

    2008-07-01

    The heavy alkaline earth atoms radium is uniquely sensitive towards parity and time reversal symmetry violations due to a large enhancement of an intrinsic permanent electric dipole moment of the nucleous or the electron. Furthermore, radium is sensitive to atomic parity violation and the nuclear anapole moment. To prepare such experiments spectroscopy of relevant atomic states need to be done. At a later stage we will build a neutral atom trap for radium. We have built an atomic beam of the short lived isotope {sup 225}Ra with a flux of several 10{sup 4} atoms/sec. We are preparing the laser spectroscopy using this beam setup. In the preparation for efficient laser cooling and trapping we have successfully trapped barium, which is similar in it's requirements for laser cooling. The techniques which we have developed with barium can be used to trap rare radium isotopes. We report on the progress of the experiments.

  20. Grain Spectroscopy

    Science.gov (United States)

    Allamandola, L. J.

    1992-01-01

    Our fundamental knowledge of interstellar grain composition has grown substantially during the past two decades thanks to significant advances in two areas: astronomical infrared spectroscopy and laboratory astrophysics. The opening of the mid-infrared, the spectral range from 4000-400 cm(sup -1) (2.5-25 microns), to spectroscopic study has been critical to this progress because spectroscopy in this region reveals more about a materials molecular composition and structure than any other physical property. Infrared spectra which are diagnostic of interstellar grain composition fall into two categories: absorption spectra of the dense and diffuse interstellar media, and emission spectra from UV-Vis rich dusty regions. The former will be presented in some detail, with the latter only very briefly mentioned. This paper summarized what we have learned from these spectra and presents 'doorway' references into the literature. Detailed reviews of many aspects of interstellar dust are given.

  1. Picosecond time-resolved laser pump/X-ray probe experiments using a gated single-photon-counting area detector

    DEFF Research Database (Denmark)

    Ejdrup, T.; Lemke, H.T.; Haldrup, Martin Kristoffer

    2009-01-01

    . The capability of the gated PILATUS detector to selectively detect the signal from a given X-ray pulse in 24 bunch mode at the APS storage ring is demonstrated. A test experiment performed on polycrystalline organic thin films of [alpha]-perylene illustrates the possibility of reaching an X-ray pulse duration......The recent developments in X-ray detectors have opened new possibilities in the area of time-resolved pump/probe X-ray experiments; this article presents the novel use of a PILATUS detector to achieve X-ray pulse duration limited time-resolution at the Advanced Photon Source (APS), USA...... limited time-resolution of 60 ps using the gated PILATUS detector. This is the first demonstration of X-ray pulse duration limited data recorded using an area detector without the use of a mechanical chopper array at the beamline....

  2. Plasma polarization spectroscopy

    Energy Technology Data Exchange (ETDEWEB)

    Fujimoto, Takashi; Iwamae, Atsushi (eds.) [Kyoto Univ. (Japan). Dept. of Mechanical Engineering and Science

    2008-07-01

    Plasma Polarization Spectroscopy (PPS) is now becoming a standard diagnostic technique for working with laboratory plasmas. This new area needs a comprehensive framework, both experimental and theoretical. This book reviews the historical development of PPS, develops a general theoretical formulation to deal with this phenomenon, along with an overview of relevant cross sections, and reports on laboratory experiments so far performed. It also includes various facets that are interesting from this standpoint, e.g. X-ray lasers and effects of microwave irradiation. It also offers a timely discussion of instrumentation that is quite important in a practical PPS experiment. (orig.)

  3. Measuring Heterogeneous Reaction Rates with ATR-FTIR Spectroscopy to Evaluate Chemical Fates in an Atmospheric Environment: A Physical Chemistry and Environmental Chemistry Laboratory Experiment

    Science.gov (United States)

    Roberts, Jason E.; Zeng, Guang; Maron, Marta K.; Mach, Mindy; Dwebi, Iman; Liu, Yong

    2016-01-01

    This paper reports an undergraduate laboratory experiment to measure heterogeneous liquid/gas reaction kinetics (ozone-oleic acid and ozone-phenothrin) using a flow reactor coupled to an attenuated total reflectance-Fourier transform infrared (ATR-FTIR) spectrometer. The experiment is specially designed for an upper-level undergraduate Physical…

  4. Diels-Alder Cycloadditions: A MORE Experiment in the Organic Laboratory Including a Diene Identification Exercise Involving NMR Spectroscopy and Molecular Modeling

    Science.gov (United States)

    Shaw, Roosevelt; Severin, Ashika; Balfour, Miguel; Nettles, Columbus

    2005-01-01

    Two Diels-Alder reactions are described that are suitable for a MORE (microwave-induced organic reaction enhanced) experiment in the organic chemistry laboratory course. A second experiment in which the splitting patterns of the vinyl protons in the nuclear magnetic resonance (NMR) spectra of two MORE adducts are used in conjunction with molecular…

  5. Measuring Heterogeneous Reaction Rates with ATR-FTIR Spectroscopy to Evaluate Chemical Fates in an Atmospheric Environment: A Physical Chemistry and Environmental Chemistry Laboratory Experiment

    Science.gov (United States)

    Roberts, Jason E.; Zeng, Guang; Maron, Marta K.; Mach, Mindy; Dwebi, Iman; Liu, Yong

    2016-01-01

    This paper reports an undergraduate laboratory experiment to measure heterogeneous liquid/gas reaction kinetics (ozone-oleic acid and ozone-phenothrin) using a flow reactor coupled to an attenuated total reflectance-Fourier transform infrared (ATR-FTIR) spectrometer. The experiment is specially designed for an upper-level undergraduate Physical…

  6. Near-ultraviolet Incoherent Broadband Cavity Enhanced Absorption Spectroscopy for OClO and CH20 in Cl-initiated Photooxidation Experiment

    Institute of Scientific and Technical Information of China (English)

    Mei-li Dong; Wei-xiong Zhao; Ming-qiang Huang; Wei-dong Chen; Chang-jin Hu; Xue-jun Gu; Shi-xin Pei

    2013-01-01

    Chlorine dioxide (OClO) is an important indicator for Cl-activation.The monitoring of OClO appears to be crucial for understanding the chemistry of Cl-initialed oxidation and its impact on air quality in polluted coastal regions and industrialized areas.We report the development of a Xe arc lamp based near-ultraviolet (335-375 nm) incoherent broadband cavity enhanced absorption spectroscopy (IBBCEAS) spectrometer for quantitative assessment of OClO in an atmospheric simulation chamber.The important intermediate compound CH2O,and other key atmospheric trace species (NO2) were also simultaneously measured.The instrumental performance shows a strong potential of this kind of IBBCEAS instrument for field and laboratory studies of atmospheric halogen chemistry.

  7. Nuclear spectroscopy

    CERN Document Server

    Ajzenberg-Selove, Fay

    1960-01-01

    Nuclear Spectroscopy, Part B focuses on the ways in which experimental data may be analyzed to furnish information about nuclear parameters and nuclear models in terms of which the data are interpreted.This book discusses the elastic and inelastic potential scattering amplitudes, role of beta decay in nuclear physics, and general selection rules for electromagnetic transitions. The nuclear shell model, fundamental coupling procedure, vibrational spectra, and empirical determination of the complex potential are also covered. This publication is suitable for graduate students preparing for exper

  8. Laser spectroscopy

    CERN Document Server

    Demtröder, Wolfgang

    2008-01-01

    Keeping abreast of the latest techniques and applications, this new edition of the standard reference and graduate text on laser spectroscopy has been completely revised and expanded. While the general concept is unchanged, the new edition features a broad array of new material, e.g., frequency doubling in external cavities, reliable cw-parametric oscillators, tunable narrow-band UV sources, more sensitive detection techniques, tunable femtosecond and sub-femtosecond lasers (X-ray region and the attosecond range), control of atomic and molecular excitations, frequency combs able to synchronize independent femtosecond lasers, coherent matter waves, and still more applications in chemical analysis, medical diagnostics, and engineering.

  9. Use of d-3He proton spectroscopy as a diagnostic of shell rho r in capsule implosion experiments with approximately 0.2 NIF scale high temperature Hohlraums at Omega.

    Science.gov (United States)

    Delamater, N D; Wilson, D C; Kyrala, G A; Seifter, A; Hoffman, N M; Dodd, E; Singleton, R; Glebov, V; Stoeckl, C; Li, C K; Petrasso, R; Frenje, J

    2008-10-01

    We present the calculations and preliminary results from experiments on the Omega laser facility using d-(3)He filled plastic capsule implosions in gold Hohlraums. These experiments aim to develop a technique to measure shell rho r and capsule unablated mass with proton spectroscopy and will be applied to future National Ignition Facility (NIF) experiments with ignition scale capsules. The Omega Hohlraums are 1900 microm length x 1200 microm diameter and have a 70% laser entrance hole. This is approximately a 0.2 NIF scale ignition Hohlraum and reaches temperatures of 265-275 eV similar to those during the peak of the NIF drive. These capsules can be used as a diagnostic of shell rho r, since the d-(3)He gas fill produces 14.7 MeV protons in the implosion, which escape through the shell and produce a proton spectrum that depends on the integrated rho r of the remaining shell mass. The neutron yield, proton yield, and spectra change with capsule shell thickness as the unablated mass or remaining capsule rho r changes. Proton stopping models are used to infer shell unablated mass and shell rho r from the proton spectra measured with different filter thicknesses. The experiment is well modeled with respect to Hohlraum energetics, neutron yields, and x-ray imploded core image size, but there are discrepancies between the observed and simulated proton spectra.

  10. Time-resolved thermal lens spectroscopy with a single-pulsed laser excitation beam: an analytical model for dual-beam mode-mismatched experiments.

    Science.gov (United States)

    Sabaeian, Mohammad; Rezaei, Hamidreza; Ghalambor-Dezfouli, Abdolmohammad

    2017-02-01

    Pulsed laser beam excitations are more commonly used in thermal lens spectroscopy (TLS) than continuous-wave (CW) ones, because CW excitations limit the measurement to linear absorption processes [J. Opt. A5, 256 (2003)]. In this work, we present a new and full analytical model for a single-pulsed laser excitation dual-beam mode-mismatched TLS for low absorption solid-state and liquid samples. Our model has been based on a new solution of time-dependent heat equation for a finite-radius cylindrical sample exposed to a single-pulsed excitation laser beam. For low absorbent samples, unlike previous models, all aberration terms associated in the thermal lens were taken into account in Fresnel integration. Besides, the model provides a full analytical mathematical expression for the temperature rise, normalized signal intensity, and Z-scan photothermal lens signal. The model was confirmed with experimental data of distilled deionized water with excellent agreement. Therefore, the model allows us to extract thermo-optical properties of samples in an analytical and more accurate way.

  11. Measuring the Silver Composition of Nanocolloids by Inductively Coupled Plasma-Optical Emission Spectroscopy: A Laboratory Experiment for Chemistry and Engineering Students

    Science.gov (United States)

    Brittle, Seth W.; Baker, Joshua D.; Dorney, Kevin M.; Dagher, Jessica M.; Ebrahimian, Tala; Higgins, Steven R.; Pavel Sizemore, Ioana E.

    2015-01-01

    The increased worldwide exploitation of nanomaterials has reinforced the importance of introducing nanoscale aspects into the undergraduate and graduate curriculum. To meet this need, a novel nano-laboratory module was developed and successfully performed by science and engineering students. The main goal of the experiment was to accurately…

  12. What Is the True Color of Fresh Meat? A Biophysical Undergraduate Laboratory Experiment Investigating the Effects of Ligand Binding on Myoglobin Using Optical, EPR, and NMR Spectroscopy

    Science.gov (United States)

    Linenberger, Kimberly; Bretz, Stacey Lowery; Crowder, Michael W.; McCarrick, Robert; Lorigan, Gary A.; Tierney, David L.

    2011-01-01

    With an increased focus on integrated upper-level laboratories, we present an experiment integrating concepts from inorganic, biological, and physical chemistry content areas. Students investigate the effects of ligand strength on the spectroscopic properties of the heme center in myoglobin using UV-vis, [superscript 1]H NMR, and EPR…

  13. Hydrothermal Synthesis and Characterization of a Metal-Organic Framework by Thermogravimetric Analysis, Powder X-Ray Diffraction, and Infrared Spectroscopy: An Integrative Inorganic Chemistry Experiment

    Science.gov (United States)

    Crane, Johanna L.; Anderson, Kelly E.; Conway, Samantha G.

    2015-01-01

    This advanced undergraduate laboratory experiment involves the synthesis and characterization of a metal-organic framework with microporous channels that are held intact via hydrogen bonding of the coordinated water molecules. The hydrothermal synthesis of Co[subscript 3](BTC)[subscript 2]·12H[subscript 2]O (BTC = 1,3,5-benzene tricarboxylic acid)…

  14. Hydrothermal Synthesis and Characterization of a Metal-Organic Framework by Thermogravimetric Analysis, Powder X-Ray Diffraction, and Infrared Spectroscopy: An Integrative Inorganic Chemistry Experiment

    Science.gov (United States)

    Crane, Johanna L.; Anderson, Kelly E.; Conway, Samantha G.

    2015-01-01

    This advanced undergraduate laboratory experiment involves the synthesis and characterization of a metal-organic framework with microporous channels that are held intact via hydrogen bonding of the coordinated water molecules. The hydrothermal synthesis of Co[subscript 3](BTC)[subscript 2]·12H[subscript 2]O (BTC = 1,3,5-benzene tricarboxylic acid)…

  15. What Is the True Color of Fresh Meat? A Biophysical Undergraduate Laboratory Experiment Investigating the Effects of Ligand Binding on Myoglobin Using Optical, EPR, and NMR Spectroscopy

    Science.gov (United States)

    Linenberger, Kimberly; Bretz, Stacey Lowery; Crowder, Michael W.; McCarrick, Robert; Lorigan, Gary A.; Tierney, David L.

    2011-01-01

    With an increased focus on integrated upper-level laboratories, we present an experiment integrating concepts from inorganic, biological, and physical chemistry content areas. Students investigate the effects of ligand strength on the spectroscopic properties of the heme center in myoglobin using UV-vis, [superscript 1]H NMR, and EPR…

  16. (U) Implementation and demonstration of a time-resolved pyrometry/spectroscopy capability in shock compression experiments on metal oxide powders

    Energy Technology Data Exchange (ETDEWEB)

    Goodwin, Peter Marvin [Los Alamos National Lab. (LANL), Los Alamos, NM (United States); Lang, Jr., John Michael [Los Alamos National Lab. (LANL), Los Alamos, NM (United States); Dattelbaum, Dana Mcgraw [Los Alamos National Lab. (LANL), Los Alamos, NM (United States); Scharff, Robert Jason [Los Alamos National Lab. (LANL), Los Alamos, NM (United States)

    2015-04-08

    Temperature is notably the most difficult quantity to measure in shock compression experiments; however, it is critical for accurately constraining theoretical or tabular equations of state. Until now, the temperature achieved during the shock loading of porous materials could only be calculated. The technique presented in this report measures, for the first time, the shocked temperature of porous systems.

  17. On the determination of plasma electron number density from Stark broadened hydrogen Balmer series lines in Laser-Induced Breakdown Spectroscopy experiments

    Energy Technology Data Exchange (ETDEWEB)

    Pardini, L., E-mail: loren.pard@gmail.com [Istituto di Chimica dei Composti Organometallici del CNR, Area della Ricerca del CNR di Pisa, Via G. Moruzzi 1, 56124 Pisa (Italy); Legnaioli, S.; Lorenzetti, G.; Palleschi, V. [Istituto di Chimica dei Composti Organometallici del CNR, Area della Ricerca del CNR di Pisa, Via G. Moruzzi 1, 56124 Pisa (Italy); Gaudiuso, R.; De Giacomo, A. [Dipartimento di Chimica, Università di Bari, Via Orabona 4, 70126 Bari (Italy); Diaz Pace, D.M. [Instituto de Física ‘Arroyo Seco’, Facultad de Ciencias Exactas, Paraje Arroyo Seco, B7000GHG Tandil (Argentina); Anabitarte Garcia, F. [Photonic Engineering Group, Universidad de Cantabria, Edificio I+D+iTelecomunicación, Dpto. TEISA, 39005 Santander (Spain); Holanda Cavalcanti, G. de [Institute of Physics, Universidade Federal Fluminense, UFF, Campus da Praia Vermelha, Av. Gal Milton Tavares de Souza, Gragoatá, 24310 240 Niterói, RJ (Brazil); Parigger, C. [University of Tennessee Space Institute, 411 B. H. Goethert Parkway, Tullahoma, TN 37388-9700 (United States)

    2013-10-01

    In this work, different theories for the determination of the electron density in Laser-Induced Breakdown Spectroscopy (LIBS) utilizing the emission lines belonging to the hydrogen Balmer series have been investigated. The plasmas were generated by a Nd:Yag laser (1064 nm) pulsed irradiation of pure hydrogen gas at a pressure of 2 · 10{sup 4} Pa. H{sub α}, Η{sub β}, Η{sub γ}, Η{sub δ}, and H{sub ε} Balmer lines were recorded at different delay times after the laser pulse. The plasma electron density was evaluated through the measurement of the Stark broadenings and the experimental results were compared with the predictions of three theories (the Standard Theory as developed by Kepple and Griem, the Advanced Generalized Theory by Oks et al., and the method discussed by Gigosos et al.) that are commonly employed for plasma diagnostics and that describe LIBS plasmas at different levels of approximations. A simple formula for pure hydrogen plasma in thermal equilibrium was also proposed to infer plasma electron density using the H{sub α} line. The results obtained showed that at high hydrogen concentration, the H{sub α} line is affected by considerable self-absorption. In this case, it is preferable to use the H{sub β} line for a reliable calculation of the electron density. - Highlights: • We evaluated the electron density in LIPs utilizing the hydrogen Balmer series. • Plasmas were generated by a Nd:Yag laser (1064 nm) on pure hydrogen gas. • We show that at high hydrogen concentration, H{sub b}eta line is preferable than H{sub a}lpha. • We propose a formula to derive the plasma electron density using the H{sub a}lpha line.

  18. Non-invasive measurement of right atrial pressure by near-infrared spectroscopy: preliminary experience. A report from the SICA-HF study.

    Science.gov (United States)

    Pellicori, Pierpaolo; Clark, Andrew L; Kallvikbacka-Bennett, Anna; Zhang, Jufen; Urbinati, Alessia; Monzo, Luca; Dierckx, Riet; Anker, Stefan D; Cleland, John G F

    2017-07-01

    To assess the clinical value of measuring right atrial pressure (RAP) using near-infrared spectroscopy (NIRS) in patients with chronic heart failure (CHF). RAP was measured non-invasively using NIRS over the external jugular vein (Venus 1000, Mespere LifeSciences, Canada) in ambulatory patients with CHF enrolled in the Studies Investigating Co-morbidities Aggravating Heart Failure (SICA-HF) programme. Comparing 243 patients with CHF (mean age 71 years; mean left ventricular ejection fraction (LVEF) 45%, median NT-proBNP 788 ng/L) to 49 controls (NT-proBNP ≤125 ng/L), RAP was 7 [interquartile range (IQR) 4-11] mmHg vs. 4 (IQR 3-8) mmHg (P < 0.001). Those with RAP ≥10 mmHg (n = 75) were older, had more severe clinical congestion and renal dysfunction, higher plasma NT-proBNP, larger left atrial volume, higher systolic pulmonary pressure and were more often in atrial fibrillation but their LVEF was similar to patients with lower RAP. During a median follow-up of 595 (IQR: 492-714) days, 49 patients (20%) died or were hospitalized for worsening CHF. Compared with patients with RAP ≤5 mmHg, those with RAP ≥10 mmHg had a greater risk of an event (hazard ratio 2.38, 95% confidence interval 1.19-4.75, P = 0.014). RAP measured by NIRS predicted outcome, competing with NT-proBNP in multivariable models. Measuring RAP using NIRS identifies ambulatory patients with CHF who have more severe congestion and a worse outcome. The device might be a useful objective method of monitoring RAP, especially for those inexperienced in eliciting physical signs or when measurement of natriuretic peptides is not immediately available. © 2017 The Authors. European Journal of Heart Failure © 2017 European Society of Cardiology.

  19. Hydrogenation Reactions of CO and CO2: New Insights through In Situ X-ray Spectroscopy and Chemical Transient Kinetics Experiments on Cobalt Catalysts

    Science.gov (United States)

    Ralston, Walter Thomas

    The catalytic hydrogenations of CO and CO2 to more useful chemicals is not only beneficial in producing more valuable products and reducing dependence on fossil fuels, but present a scientific challenge in how to control the selectivity of these reactions. Using colloidal chemistry techniques, a high level of control over the synthesis of nanomaterials can be achieved, and by exploiting this fact a simple model system can be realized to understand the reaction of CO and CO2 on a molecular level. Specifically, this dissertation focuses on understanding cobalt materials for the conversion of CO and CO2 into more useful, valuable chemicals. Colloidally prepared cobalt nanoparticles with a narrow size distribution were supported in mesoporous SiO2 and TiO2 to study the effect of the support on the Co catalyzed hydrogenation of CO and CO2. The 10nm Co/SiO2 and Co/TiO2 catalysts were tested for CO and CO2 hydrogenation at 5 bar with a ratio to hydrogen of 1:2 and 1:3, respectively. In addition, the effect of Co oxidation state was studied by using different reduction pretreatment temperatures (250°C and 450°C). The results showed that for both hydrogenation reactions, Co/TiO2 had a high activity at both reduction temperatures compared to Co/SiO2. However, unlike Co/SiO2 which showed higher activity after 450°C reduction, Co/TiO2 had a higher activity after reduction at 250°C. Through synchrotron x-ray spectroscopy, it was concluded that the TiO2 was wetting the Co particle at higher reduction temperatures and dewetting at lower reduction temperatures. In addition to the wetting, CoO was observed to be the surface species on Co/TiO2 catalyst after reduction at low temperatures, which catalyzed both CO and CO2 hydrogenation reactions with higher activity than the Co metal obtained after reduction at 450°C. Classical steady-state measurements are limited in so much as they are often unable to provide information on individual reaction steps in complex reaction pathways

  20. Mid-infrared picosecond pump-dump-probe and pump-repump-probe experiments to resolve a ground-state intermediate in cyanobacterial phytochrome Cph1.

    Science.gov (United States)

    van Wilderen, Luuk J G W; Clark, Ian P; Towrie, Michael; van Thor, Jasper J

    2009-12-24

    -state structure of the ZZZ configuration of the linear tetrapyrrole chromophore. The dump-induced absorption decays with time constants of 5 and 19 ps to the Pr ground state. Employing a dump pulse at 14 ps results in an instantaneous decrease of the absorption of the 1608 cm(-1) band, indicating repumping of the GSI. The dump-induced absorption recovers back to the GSI with a 6 ps lifetime. A spectral similarity is observed between the 6 ps phase in the dump experiment and the 3 ps component found in the two-pulse pump-probe measurement. Combined with the dominance of ground-state absorption bands in the dump-induced spectrum, this indicates the presence of a GSI, which is additionally characterized by previously unidentified induced absorption at 1710 and 1570-80 cm(-1). The metastable photoproduct Lumi-R, which is in the electronic ground state and populated at 500 ps after excitation of Pr, is highly efficiently repumped into the Pr ground state with the power density used. After repumping, Lumi-R is not recovered on the 500 ps time scale of the experiment and is distinct from the GSI of Pr since it is not associated with its characteristic induced absorption at 1710 and 1570-80 cm(-1).

  1. Dark Matter Velocity Spectroscopy.

    Science.gov (United States)

    Speckhard, Eric G; Ng, Kenny C Y; Beacom, John F; Laha, Ranjan

    2016-01-22

    Dark matter decays or annihilations that produce linelike spectra may be smoking-gun signals. However, even such distinctive signatures can be mimicked by astrophysical or instrumental causes. We show that velocity spectroscopy-the measurement of energy shifts induced by relative motion of source and observer-can separate these three causes with minimal theoretical uncertainties. The principal obstacle has been energy resolution, but upcoming experiments will have the precision needed. As an example, we show that the imminent Astro-H mission can use Milky Way observations to separate possible causes of the 3.5-keV line. We discuss other applications.

  2. Dark Matter Velocity Spectroscopy

    CERN Document Server

    Speckhard, Eric G; Beacom, John F; Laha, Ranjan

    2016-01-01

    Dark matter decays or annihilations that produce line-like spectra may be smoking-gun signals. However, even such distinctive signatures can be mimicked by astrophysical or instrumental causes. We show that velocity spectroscopy-the measurement of energy shifts induced by relative motion of source and observer-can separate these three causes with minimal theoretical uncertainties. The principal obstacle has been energy resolution, but upcoming and proposed experiments will make significant improvements. As an example, we show that the imminent Astro-H mission can use Milky Way observations to separate possible causes of the 3.5-keV line. We discuss other applications.

  3. Layman friendly spectroscopy

    Science.gov (United States)

    Sentic, Stipo; Sessions, Sharon

    Affordable consumer grade spectroscopes (e.g. SCiO, Qualcomm Tricorder XPRIZE) are becoming more available to the general public. We introduce the concepts of spectroscopy to the public and K12 students and motivate them to delve deeper into spectroscopy in a dramatic participatory presentation and play. We use diffraction gratings, lasers, and light sources of different spectral properties to provide a direct experience of spectroscopy techniques. Finally, we invite the audience to build their own spectroscope--utilizing the APS SpectraSnapp cell phone application--and study light sources surrounding them in everyday life. We recontextualize the stigma that science is hard (e.g. ``Math, Science Popular Until Students Realize They're Hard,'' The Wall Street Journal) by presenting the material in such a way that it demonstrates the scientific method, and aiming to make failure an impersonal scientific tool--rather than a measure of one's ability, which is often a reason for shying away from science. We will present lessons we have learned in doing our outreach to audiences of different ages. This work is funded by the APS Outreach Grant ``Captain, we have matter matters!'' We thank New Mexico Tech Physics Department and Physics Club for help and technical equipment.

  4. Biomolecular EPR spectroscopy

    CERN Document Server

    Hagen, Wilfred Raymond

    2008-01-01

    Comprehensive, Up-to-Date Coverage of Spectroscopy Theory and its Applications to Biological SystemsAlthough a multitude of books have been published about spectroscopy, most of them only occasionally refer to biological systems and the specific problems of biomolecular EPR (bioEPR). Biomolecular EPR Spectroscopy provides a practical introduction to bioEPR and demonstrates how this remarkable tool allows researchers to delve into the structural, functional, and analytical analysis of paramagnetic molecules found in the biochemistry of all species on the planet. A Must-Have Reference in an Intrinsically Multidisciplinary FieldThis authoritative reference seamlessly covers all important bioEPR applications, including low-spin and high-spin metalloproteins, spin traps and spin lables, interaction between active sites, and redox systems. It is loaded with practical tricks as well as do's and don'ts that are based on the author's 30 years of experience in the field. The book also comes with an unprecedented set of...

  5. Theory of spin dynamics of magnetic adatoms traced by time-resolved scanning tunneling spectroscopy

    CERN Document Server

    Schüler, Michael; Berakdar, Jamal

    2012-01-01

    The inelastic scanning tunneling microscopy (STM) has been shown recently (Loth et al. Science 329, 1628 (2010)) to be extendable as to access the nanosecond, spin-resolved dynamics of magnetic adatoms and molecules. Here we analyze theoretically this novel tool by considering the time-resolved spin dynamics of a single adsorbed Fe atom excited by a tunneling current pulse from a spin-polarized STM tip. The adatom spin-configuration can be controlled and probed by applying voltage pulses between the substrate and the spin-polarized STM tip. We demonstrate how, in a pump-probe manner, the relaxation dynamics of the sample spin is manifested in the spin-dependent tunneling current. Our model calculations are based on the scattering theory in a wave-packet formulation. The scheme is nonpertubative and hence, is valid for all voltages. The numerical results for the tunneling probability and the conductance are contrasted with the prediction of simple analytical models and compared with experiments.

  6. Phosphorus dynamics in Swedish agricultural soils as influenced by fertilization and mineralogical properties: Insights gained from batch experiments and XANES spectroscopy.

    Science.gov (United States)

    Eriksson, Ann Kristin; Hesterberg, Dean; Klysubun, Wantana; Gustafsson, Jon Petter

    2016-10-01

    The soil chemistry of phosphorus (P) is important for understanding the processes governing plant availability as well as the risk of environmental losses of P. The objective of this research was to investigate both the speciation and the pH-dependent solubility patterns of P in clayey agricultural soils in relation to soil mineralogy and fertilization history. The study focused on soil samples from six fields that were subjected to different P fertilization regimes for periods of 45 to 57years. Soil P speciation was analyzed by P K-edge XANES spectroscopy and chemical fractionation, sorption isotherms were constructed, and dissolved P was measured as a function of pH. The XANES fitting results showed that organic P and P adsorbed to Fe and Al (hydr)oxides were common P constituents in all soils. Calcium phosphates were identified in five of six soil samples. The XANES results also indicated an increase in P adsorbed to Al and to a lesser extent Fe (hydr)oxides as a result of fertilization. Moreover, the fluorescence intensity from the P K-edge XANES analysis was most strongly correlated with HCl-digestible P (r=0.81***). Consistent with the XANES analysis, laboratory sorption isotherm models showed that the Freundlich sorption coefficient (KF) was most closely related to oxalate-extractable Al. Greater proportions of Ca phosphate in two of the heavily fertilized soils in combination with enhanced PO4 solubilization upon sample acidification indicated neoformation of Ca-phosphate precipitates. The results for the unfertilized soil samples generally showed a minimum in dissolved PO4 between pH6.5 and 7.5, with increases particularly at lower pH. This behavior can be explained either by the dissolution of Al-hydroxide-type sorbents or Ca phosphates at lower pH. In fertilized soils, there was no consistent trend in pH-dependent solubilization of P, with a complex relationship to solid-phase speciation. To conclude, inorganic P species changed most dynamically in

  7. Spectroscopy of transient neutral species via negative ion photoelectron spectroscopy

    Energy Technology Data Exchange (ETDEWEB)

    Weaver, A.

    1991-12-01

    Negative ion photoelectron spectroscopy has been used to study two types of transient neutral species: bound free radicals (NO{sub 2} and NO{sub 3}) and unstable neutral species ([IHI] and [FH{sub 2}]). The negative ion time-of-flight photoelectron spectrometer used for these experiments is described in detail.

  8. Spectroscopy of transient neutral species via negative ion photoelectron spectroscopy

    Energy Technology Data Exchange (ETDEWEB)

    Weaver, A.

    1991-12-01

    Negative ion photoelectron spectroscopy has been used to study two types of transient neutral species: bound free radicals (NO{sub 2} and NO{sub 3}) and unstable neutral species ((IHI) and (FH{sub 2})). The negative ion time-of-flight photoelectron spectrometer used for these experiments is described in detail.

  9. SIMP spectroscopy

    Energy Technology Data Exchange (ETDEWEB)

    Hochberg, Yonit [Ernest Orlando Lawrence Berkeley National Laboratory, University of California,Berkeley, CA 94720 (United States); Department of Physics, University of California,Berkeley, CA 94720 (United States); Kuflik, Eric [Department of Physics, LEPP, Cornell University,Ithaca NY 14853 (United States); Murayama, Hitoshi [Ernest Orlando Lawrence Berkeley National Laboratory, University of California,Berkeley, CA 94720 (United States); Department of Physics, University of California,Berkeley, CA 94720 (United States); Kavli Institute for the Physics and Mathematics of the Universe (WPI),University of Tokyo Institutes for Advanced Study, University of Tokyo,Kashiwa 277-8583 (Japan); Center for Japanese Studies, University of California,Berkeley, CA 94720 (United States)

    2016-05-16

    We study the interactions between strongly interacting massive particle dark matter and the Standard Model via a massive vector boson that is kinetically mixed with the hypercharge gauge boson. The relic abundance is set by 3→2 self-interactions of the dark matter, while the interactions with the vector mediator enable kinetic equilibrium between the dark and visible sectors. We show that a wide range of parameters is phenomenologically viable and can be probed in various ways. Astrophysical and cosmological constraints are evaded due to the p-wave nature of dark matter annihilation into visible particles, while direct detection methods using electron recoils can be sensitive to parts of the parameter space. In addition, we propose performing spectroscopy of the strongly coupled dark sector at e{sup +}e{sup −} colliders, where the energy of a mono-photon can track the resonance structure of the dark sector. Alternatively, some resonances may decay back into Standard Model leptons or jets, realizing ‘hidden valley’ phenomenology at the LHC and ILC in a concrete fashion.

  10. X-ray Absorption Spectroscopy and Coherent X-ray Diffraction Imaging for Time-Resolved Investigation of the Biological Complexes: Computer Modelling towards the XFEL Experiment

    Science.gov (United States)

    Bugaev, A. L.; Guda, A. A.; Yefanov, O. M.; Lorenz, U.; Soldatov, A. V.; Vartanyants, I. A.

    2016-05-01

    The development of the next generation synchrotron radiation sources - free electron lasers - is approaching to become an effective tool for the time-resolved experiments aimed to solve actual problems in various fields such as chemistry’ biology’ medicine’ etc. In order to demonstrate’ how these experiments may be performed for the real systems to obtain information at the atomic and macromolecular levels’ we have performed a molecular dynamics computer simulation combined with quantum chemistry calculations for the human phosphoglycerate kinase enzyme with Mg containing substrate. The simulated structures were used to calculate coherent X-ray diffraction patterns’ reflecting the conformational state of the enzyme, and Mg K-edge X-ray absorption spectra, which depend on the local structure of the substrate. These two techniques give complementary information making such an approach highly effective for time-resolved investigation of various biological complexes, such as metalloproteins or enzymes with metal-containing substrate, to obtain information about both metal-containing active site or substrate and the atomic structure of each conformation.

  11. Workshop on heavy hadron spectroscopy

    CERN Document Server

    2017-01-01

    The recent developments in heavy hadron spectroscopy at LHCb have shown that LHCb has a unique potential in the field, combining hadronic production mechanisms to a powerful identification system. In this short workshop we focus on the recent results from LHCb and theoretical developments with attention to the future perspectives, in the context of the potential of current and future experiments.

  12. Spectroscopy of radium

    Energy Technology Data Exchange (ETDEWEB)

    Mol, Aran; De, Subhadeep; Dammalapati, Umakanth; Jungmann, Klaus; Willmann, Lorenz [Kernfysisch Versneller Instituut, Rijksuniversiteit Groningen (Netherlands)

    2007-07-01

    Radium has been identified as a potential candidate for experiment al searches for violations of fundamental symmetries like parity (P), time reversal (T) and charge conjugation. In particular is shows a high sensitivity to T a nd P violating permanent electric dipole moments and also to atomic parity viola tion effects. This sensitivity arises from the unique atomic level scheme of rad ium. In the course of the setup of such experiments we need to improve the experimental data on radium. Within the TRI{mu}P (Trapped Radioactive Isotopes: microlaboratories for fundamental Physics) facility at KVI, we are setting up an radioactive atomic beam of {sup 225}Ra and the laser system for performing the spectroscopy. This is guided closely by the requirements for experimental searches for symmetry violating effect.

  13. Probing ice clouds by broadband mid-infrared extinction spectroscopy: case studies from ice nucleation experiments in the AIDA aerosol and cloud chamber

    Directory of Open Access Journals (Sweden)

    R. Wagner

    2006-01-01

    Full Text Available Series of infrared extinction spectra of ice crystals were recorded in the 6000–800 cm−1 wavenumber regime during expansion cooling experiments in the large aerosol and cloud chamber AIDA of Forschungszentrum Karlsruhe. Either supercooled sulphuric acid solution droplets or dry mineral dust particles were added as seed aerosols to initiate ice formation after having established ice supersaturated conditions inside the chamber. The various ice nucleation runs were conducted at temperatures between 237 and 195 K, leading to median sizes of the nucleated ice particles of 1–15 µm. The measured infrared spectra were fitted with reference spectra from T-matrix calculations to retrieve the number concentration as well as the number size distribution of the generated ice clouds. The precise evaluation of the time-dependent ice particle number concentrations, i.e., the rates of new ice particle formation, is of particular importance to quantitatively analyse the ice nucleation experiments in terms of nucleation rates and ice activation spectra. The ice particles were modelled as finite circular cylinders with aspect ratios ranging from 0.5 to 3.0. Benefiting from the comprehensive diagnostic tools for the characterisation of ice clouds which are available at the AIDA facility, the infrared retrieval results with regard to the ice particle number concentration could be compared to independent measurements with various optical particle counters. This provided a unique chance to quantitatively assess potential errors or solution ambiguities in the retrieval procedure which mainly originate from the difficulty to find an appropriate shape representation for the aspherical particle habits of the ice crystals. Based on these inter-comparisons, we demonstrate that there is no standard retrieval approach which can be routinely applied to all different experimental scenarios. In particular, the concept to account for the asphericity of the ice crystals

  14. Variable angle correlation spectroscopy

    Energy Technology Data Exchange (ETDEWEB)

    Lee, Y K [Univ. of California, Berkeley, CA (United States)

    1994-05-01

    In this dissertation, a novel nuclear magnetic resonance (NMR) technique, variable angle correlation spectroscopy (VACSY) is described and demonstrated with {sup 13}C nuclei in rapidly rotating samples. These experiments focus on one of the basic problems in solid state NMR: how to extract the wealth of information contained in the anisotropic component of the NMR signal while still maintaining spectral resolution. Analysis of the anisotropic spectral patterns from poly-crystalline systems reveal information concerning molecular structure and dynamics, yet in all but the simplest of systems, the overlap of spectral patterns from chemically distinct sites renders the spectral analysis difficult if not impossible. One solution to this problem is to perform multi-dimensional experiments where the high-resolution, isotropic spectrum in one dimension is correlated with the anisotropic spectral patterns in the other dimensions. The VACSY technique incorporates the angle between the spinner axis and the static magnetic field as an experimental parameter that may be incremented during the course of the experiment to help correlate the isotropic and anisotropic components of the spectrum. The two-dimensional version of the VACSY experiments is used to extract the chemical shift anisotropy tensor values from multi-site organic molecules, study molecular dynamics in the intermediate time regime, and to examine the ordering properties of partially oriented samples. The VACSY technique is then extended to three-dimensional experiments to study slow molecular reorientations in a multi-site polymer system.

  15. Building and analyzing models from data by stirred tank experiments for investigation of matrix effects caused by inorganic matrices and selection of internal standards in Inductively Coupled Plasma-Atomic Emission Spectroscopy

    Energy Technology Data Exchange (ETDEWEB)

    Grotti, Marco [Dipartimento di Chimica e Chimica Industriale, Via Dodecaneso 31, 16146 Genova (Italy)], E-mail: grotti@chimica.unige.it; Paredes, Eduardo; Maestre, Salvador; Todoli, Jose Luis [Departamento de Quimica Analitica, Nutricion y Bromatologia, Universidad de Alicante, 03080, Alicante (Spain)

    2008-05-15

    Interfering effects caused by inorganic matrices (inorganic acids as well as easily ionized elements) in inductively coupled plasma-atomic emission spectroscopy have been modeled by regression analysis of experimental data obtained using the 'stirred tank method'. The main components of the experimental set-up were a magnetically-stirred container and two peristaltic pumps. In this way the matrix composition was gradually and automatically varied, while the analyte concentration remained unchanged throughout the experiment. An inductively coupled plasma spectrometer with multichannel detection based on coupled charge device was used to simultaneously measure the emission signal at several wavelengths when the matrix concentration was modified. Up to 50 different concentrations were evaluated in a period of time of 10 min. Both single interfering species (nitric, hydrochloric and sulphuric acids, sodium and calcium) and different mixtures (aqua regia, sulfonitric mixture, sodium-calcium mixture and sodium-nitric acid mixture) were investigated. The dependence of the emission signal on acid concentration was well-fitted by logarithmic models. Conversely, for the easily ionized elements, 3-order polynomial models were more suitable to describe the trends. Then, the coefficients of these models were used as 'signatures' of the matrix-related signal variations and analyzed by principal component analysis. Similarities and differences among the emission lines were highlighted and discussed, providing a new insight into the interference phenomena, mainly with regards to the combined effect of concomitants. The combination of the huge amount of data obtained by the stirred tank method in a short period of time and the speed of analysis of principal component analysis provided a judicious means for the selection of the optimal internal standard in inductively coupled plasma-atomic emission spectroscopy.

  16. Study of the reaction between ammonium thiocyanate and Fe (II or Fe (III using infrared spectroscopy: an experiment of prebiotic chemistry

    Directory of Open Access Journals (Sweden)

    Dimas Augusto Morozin Zaia

    2010-09-01

    Full Text Available The prebiotic chemistry studies the reactions that could be played an important role on origins of life on Earth. However, these reactions should be carried out under conditions that existed on the prebiotic Earth. The laboratory experiments of heating substances in solid state could be corresponding to the following prebiotic environments: cooling lava from volcanoes on the ground and impact of meteorites or comets on the earth. The present study examined the reaction in solid state between ammonium thiocyanate and Fe (II or Fe (III. The samples were heated at 220 ºC in several different times (6 hours, 24 hours, 7 days. The most important finding of this work is that a reaction of oxidation-reduction is occurring between Fe (II and ammonium thiocyanate, the infrared spectrum of the reaction product ammonium thiocyanate/Fe (II showed a band that it is characteristic of ferricyanate. The infrared spectra also showed bands that they are characteristics of guanidine thiocyanate. Thus, the heating of ammonium thiocyanate with Fe (II in solid state is synthesizing guanidine thiocyanate and at the same time oxidizing Fe (II to Fe (III. The product of reaction between Fe (III and ammonium thiocyanate is guanidine thiocyanate. Fe (II and Fe (III are reacting with ammonium thiocyanate in different way.

  17. Spin-resolved photoelectron spectroscopy using femtosecond extreme ultraviolet light pulses from high-order harmonic generation

    Science.gov (United States)

    Plötzing, M.; Adam, R.; Weier, C.; Plucinski, L.; Eich, S.; Emmerich, S.; Rollinger, M.; Aeschlimann, M.; Mathias, S.; Schneider, C. M.

    2016-04-01

    The fundamental mechanism responsible for optically induced magnetization dynamics in ferromagnetic thin films has been under intense debate since almost two decades. Currently, numerous competing theoretical models are in strong need for a decisive experimental confirmation such as monitoring the triggered changes in the spin-dependent band structure on ultrashort time scales. Our approach explores the possibility of observing femtosecond band structure dynamics by giving access to extended parts of the Brillouin zone in a simultaneously time-, energy- and spin-resolved photoemission experiment. For this purpose, our setup uses a state-of-the-art, highly efficient spin detector and ultrashort, extreme ultraviolet light pulses created by laser-based high-order harmonic generation. In this paper, we present the setup and first spin-resolved spectra obtained with our experiment within an acquisition time short enough to allow pump-probe studies. Further, we characterize the influence of the excitation with femtosecond extreme ultraviolet pulses by comparing the results with data acquired using a continuous wave light source with similar photon energy. In addition, changes in the spectra induced by vacuum space-charge effects due to both the extreme ultraviolet probe- and near-infrared pump-pulses are studied by analyzing the resulting spectral distortions. The combination of energy resolution and electron count rate achieved in our setup confirms its suitability for spin-resolved studies of the band structure on ultrashort time scales.

  18. Ultrafast laser pump/x-ray probe experiments

    Energy Technology Data Exchange (ETDEWEB)

    Larsson, J.; Judd, E.; Schuck, P.J. [Univ. of California, Berkeley, CA (United States)] [and others

    1997-04-01

    In an ongoing project aimed at probing solids using x-rays obtained at the ALS synchrotron with a sub-picosecond time resolution following interactions with a 100 fs laser pulse, the authors have successfully performed pump-probe experiments limited by the temporal duration of ALS-pulse. They observe a drop in the diffraction efficiency following laser heating. They can attribute this to a disordering of the crystal. Studies with higher temporal resolution are required to determine the mechanism. The authors have also incorporated a low-jitter streakcamera as a diagnostic for observing time-dependant x-ray diffraction. The streakcamera triggered by a photoconductive switch was operated at kHz repetition rates. Using UV-pulses, the authors obtain a temporal response of 2 ps when averaging 5000 laser pulses. They demonstrate the ability to detect monochromatized x-ray radiation from a bend-magnet with the streak camera by measuring the pulse duration of a x-ray pulse to 70 ps. In conclusion, the authors show a rapid disordering of an InSb crystal. The resolution was determined by the duration of the ALS pulse. They also demonstrate that they can detect x-ray radiation from a synchrotron source with a temporal resolution of 2ps, by using an ultrafast x-ray streak camera. Their set-up will allow them to pursue laser pump/x-ray probe experiments to monitor structural changes in materials with ultrafast time resolution.

  19. Hypernuclear spectroscopy program at JLab Hall C

    Energy Technology Data Exchange (ETDEWEB)

    Hashimoto, Osamu; Hashimoto, Osamu; Nakamura, Satoshi; Acha Quimper, Armando; Ahmidouch, Abdellah; Androic, Darko; Asaturyan, Arshak; Asaturyan, Razmik; Baker, O.; Baturin, Pavlo; Benmokhtar, Fatiha; Bosted, Peter; Carlini, Roger; Chen, X.; Christy, Michael; Cole, Leon; Danagoulian, Samuel; Daniel, AJI; Dharmawardane, Kahanawita; Egiyan, Kim; Elaasar, Mostafa; Ent, Rolf; Fenker, Howard; Fujii, Yu; Furic, Miroslav; Gan, Liping; Gaskell, David; Gasparian, Ashot; Gibson, Edward; Gueye, Paul; Halkyard, Rebekah; Honda, D.; Horn, Tanja; Hu, Bitao; Hu, S.; Hungerford, Ed; Ispiryan, Mikayel; Johnston, Kathleen; Jones, Mark; Kalantarians, Narbe; Kaneta, M.; Kato, F.; Kato, Seigo; Kawama, Daisuke; Keppel, Cynthia; Li, Ya; Luo, Wei; Mack, David; Margaryan, Amur; Marikyan, Gagik; Maruyama, Nayuta; Matsumura, Akihiko; Miyoshi, Toshinobu; Mkrtchyan, Arthur; Mkrtchyan, Hamlet; Navasardyan, Tigran; Niculescu, Gabriel; Niculescu, Maria-Ioana; Nomura, Hiroshi; Nonaka, Kenichi; Ohtani, Atsushi; Okayasu, Yuichi; Pamela, Priscilla; Perez, Naipy; Petkovic, Tomislav; Randeniya, Kapugodage; Reinhold, Joerg; Rivera Castillo, Roberto; Roche, Julie; Rodriguez, Victor; Sato, Yoshinori; Seva, Tomislav; Tang, Liguang; Simicevic, Neven; Smith, Gregory; Sumihama, Mizuki; Song, Y.; Tadevosyan, Vardan; Takahashi, Toshiyuki; Tamura, Hirokazu; Tvaskis, Vladas; Vulcan, William; Wang, B.; Wells, Steven; Yan, Chen; Yuan, Lulin; Zamkochian, S.

    2008-05-01

    DOI: http://dx.doi.org/10.1016/j.nuclphysa.2008.01.029
    Hypernuclear production by the (e,e?K+) reaction has unique advantages in hypernuclear spectroscopy of the S=?1 regime. The second-generation spectroscopy experiment on 12C, 7Li and 28Si targets has been recently carried out at JLab Hall C with a new experimental configuration (Tilt method) and also using a new high-resolution kaon spectrometer (HKS). The experiment is described and preliminary results are presented together with the empasis of significance of the (e,e?K+) reaction for ? hypernuclear spectroscopy and its future prospects.

  20. Physics of ultracold Fermi gases revealed by spectroscopies

    Science.gov (United States)

    Törmä, Päivi

    2016-04-01

    This article provides a brief review of how various spectroscopies have been used to investitage many-body quantum phenomena in the context of ultracold Fermi gases. In particular, work done with RF spectroscopy, Bragg spectroscopy and lattice modulation spectroscopy is considered. The theoretical basis of these spectroscopies, namely linear response theory in the many-body quantum physics context is briefly presented. Experiments related to the BCS-BEC crossover, imbalanced Fermi gases, polarons, possible pseudogap and Fermi liquid behaviour and measuring the contact are discussed. Remaining open problems and goals in the field are sketched from the perspective how spectroscopies could contribute.

  1. Stark-assisted population control of coherent CS(2) 4f and 5p Rydberg wave packets studied by femtosecond time-resolved photoelectron spectroscopy.

    Science.gov (United States)

    Knappenberger, Kenneth L; Lerch, Eliza-Beth W; Wen, Patrick; Leone, Stephen R

    2007-09-28

    A two-color (3+1(')) pump-probe scheme is employed to investigate Rydberg wave packet dynamics in carbon disulfide (CS(2) (*)). The state superpositions are created within the 4f and 5p Rydberg manifolds by three photons of the 400 nm pump pulse, and their temporal evolution is monitored with femtosecond time-resolved photoelectron spectroscopy using an 800 nm ionizing probe pulse. The coherent behavior of the non-stationary superpositions are observed through wavepacket revivals upon ionization to either the upper (12) or lower (32) spin-orbit components of CS(2) (+). The results show clearly that the composition of the wavepacket can be efficiently controlled by the power density of the excitation pulse over a range from 500 GWcm(2) to 10 TWcm(2). The results are consistent with the anticipated ac-Stark shift for 400 nm light and demonstrate an effective method for population control in molecular systems. Moreover, it is shown that Rydberg wavepackets can be formed in CS(2) with excitation power densities up to 10 TWcm(2) without significant fragmentation. The exponential 1e population decay (T(1)) of specific excited Rydberg states are recovered by analysis of the coherent part of the signal. The dissociation lifetimes of these states are typically 1.5 ps. However, a region exhibiting a more rapid decay ( approximately 800 fs) is observed for states residing in the energy range of 74 450-74 550 cm(-1), suggestive of an enhanced surface crossing in this region.

  2. Note: application of a pixel-array area detector to simultaneous single crystal X-ray diffraction and X-ray absorption spectroscopy measurements.

    Science.gov (United States)

    Sun, Cheng-Jun; Zhang, Bangmin; Brewe, Dale L; Chen, Jing-Sheng; Chow, G M; Venkatesan, T; Heald, Steve M

    2014-04-01

    X-ray diffraction (XRD) and X-ray absorption spectroscopy (XAS) are two main x-ray techniques in synchrotron radiation facilities. In this Note, we present an experimental setup capable of performing simultaneous XRD and XAS measurements by the application of a pixel-array area detector. For XRD, the momentum transfer in specular diffraction was measured by scanning the X-ray energy with fixed incoming and outgoing x-ray angles. By selecting a small fixed region of the detector to collect the XRD signal, the rest of the area was available for collecting the x-ray fluorescence for XAS measurements. The simultaneous measurement of XRD and X-ray absorption near edge structure for Pr0.67Sr0.33MnO3 film was demonstrated as a proof of principle for future time-resolved pump-probe measurements. A static sample makes it easy to maintain an accurate overlap of the X-ray spot and laser pump beam.

  3. Time-resolved photoelectron spectroscopy of a dinuclear Pt(II) complex: Tunneling autodetachment from both singlet and triplet excited states of a molecular dianion

    Science.gov (United States)

    Winghart, Marc-Oliver; Yang, Ji-Ping; Vonderach, Matthias; Unterreiner, Andreas-Neil; Huang, Dao-Ling; Wang, Lai-Sheng; Kruppa, Sebastian; Riehn, Christoph; Kappes, Manfred M.

    2016-02-01

    Time-resolved pump-probe photoelectron spectroscopy has been used to study the relaxation dynamics of gaseous [Pt2(μ-P2O5H2)4 + 2H]2- after population of its first singlet excited state by 388 nm femtosecond laser irradiation. In contrast to the fluorescence and phosphorescence observed in condensed phase, a significant fraction of the photoexcited isolated dianions decays by electron loss to form the corresponding monoanions. Our transient photoelectron data reveal an ultrafast decay of the initially excited singlet 1A2u state and concomitant rise in population of the triplet 3A2u state, via sub-picosecond intersystem crossing (ISC). We find that both of the electronically excited states are metastably bound behind a repulsive Coulomb barrier and can decay via delayed autodetachment to yield electrons with characteristic kinetic energies. While excited state tunneling detachment (ESETD) from the singlet 1A2u state takes only a few picoseconds, ESETD from the triplet 3A2u state is much slower and proceeds on a time scale of hundreds of nanoseconds. The ISC rate in the gas phase is significantly higher than in solution, which can be rationalized in terms of changes to the energy dissipation mechanism in the absence of solvent molecules. [Pt2(μ-P2O5H2)4 + 2H]2- is the first example of a photoexcited multianion for which ESETD has been observed following ISC.

  4. Selective One-Dimensional Total Correlation Spectroscopy Nuclear Magnetic Resonance Experiments for a Rapid Identification of Minor Components in the Lipid Fraction of Milk and Dairy Products: Toward Spin Chromatography?

    Science.gov (United States)

    Papaemmanouil, Christina; Tsiafoulis, Constantinos G; Alivertis, Dimitrios; Tzamaloukas, Ouranios; Miltiadou, Despoina; Tzakos, Andreas G; Gerothanassis, Ioannis P

    2015-06-10

    We report a rapid, direct, and unequivocal spin-chromatographic separation and identification of minor components in the lipid fraction of milk and common dairy products with the use of selective one-dimensional (1D) total correlation spectroscopy (TOCSY) nuclear magnetic resonance (NMR) experiments. The method allows for the complete backbone spin-coupling network to be elucidated even in strongly overlapped regions and in the presence of major components from 4 × 10(2) to 3 × 10(3) stronger NMR signal intensities. The proposed spin-chromatography method does not require any derivatization steps for the lipid fraction, is selective with excellent resolution, is sensitive with quantitation capability, and compares favorably to two-dimensional (2D) TOCSY and gas chromatography-mass spectrometry (GC-MS) methods of analysis. The results of the present study demonstrated that the 1D TOCSY NMR spin-chromatography method can become a procedure of primary interest in food analysis and generally in complex mixture analysis.

  5. Soliton absorption spectroscopy

    CERN Document Server

    Kalashnikov, V L

    2010-01-01

    We analyze optical soliton propagation in the presence of weak absorption lines with much narrower linewidths as compared to the soliton spectrum width using the novel perturbation analysis technique based on an integral representation in the spectral domain. The stable soliton acquires spectral modulation that follows the associated index of refraction of the absorber. The model can be applied to ordinary soliton propagation and to an absorber inside a passively modelocked laser. In the latter case, a comparison with water vapor absorption in a femtosecond Cr:ZnSe laser yields a very good agreement with experiment. Compared to the conventional absorption measurement in a cell of the same length, the signal is increased by an order of magnitude. The obtained analytical expressions allow further improving of the sensitivity and spectroscopic accuracy making the soliton absorption spectroscopy a promising novel measurement technique.

  6. Analyzing Impedance Spectroscopy Results

    Institute of Scientific and Technical Information of China (English)

    Yoed Tsur; Sioma Baltianski

    2006-01-01

    In this contribution we briefly discuss several analysis techniques for impedance spectroscopy experiments. A number of different approaches, which differ even by the definition of the problem, are used in the literature. Some aimed towards finding an equivalent circuit. Others aimed towards finding directly dielectric properties of the material under an assumed model. Others towards finding distribution of relaxation times, either parametric or point-by point. No matter what the approach is, this will always be an ill-posed problem in the sense that there exist a large number of possible solutions that solve the problem (mathematically) equally well. Therefore some a-priori knowledge about the system must be used. In addition, we should remember that the ultimate goal is to get physical insight about the system.

  7. Nondiffusive thermal transport and prediction of the breakdown of Fourier's law in nanograting experiments

    Science.gov (United States)

    Qu, Zhengxian; Wang, Dadong; Ma, Yanbao

    2017-01-01

    An appropriate heat conduction model is indispensable for experimental data analysis in nanothermometry in order to extract parameters of interests and to achieve a fundamental understanding of phonon-mediated heat transfer in nanostructures and across interfaces. Recently, nanoscale periodic metallic gratings are used as a group of distributed heaters as well as transducers in nanothermometry. However, in this technique, there are coupled hotspot-size-dependent effective thermal conductivity (ETC) and hotspot-size-dependent thermal interface resistivity, which posts a challenge for experimental data analysis using Fourier's law that fails to extract both ETC and thermal interface resistivity simultaneously. To overcome this challenge, a novel two-parameter nondiffusive heat conduction (TPHC) model, which has been successfully applied to data analysis in different types of pump-probe experiments, is applied to analyze laser-induced nondiffusive heat transfer in nanoscale metallic grating experiments. Since the hotspot-size-dependent ETC is automatically captured by the TPHC model, the hotspot-size-dependent interface resistivity becomes the only parameter to be determined from experiments through data fitting. Thus, the hotspot-size-dependent thermal interface resistivity can be determined from experiments without the impact from the hotspot-size-dependent ETC. Currently, there is a lack of a criterion to predict when Fourier's law breaks down in nanoscale heat transfer. To fill this gap, a criterion based the TPHC model is identified to predict the valid range of Fourier's law, which is validated in both theoretical analyses and nanoscale metallic grating experiments.

  8. Analytical Spectroscopy Using Modular Systems

    Science.gov (United States)

    Patterson, Brian M.; Danielson, Neil D.; Lorigan, Gary A.; Sommer, André J.

    2003-12-01

    This article describes the development of three analytical spectroscopy experiments that compare the determination of salicylic acid (SA) content in aspirin tablets. The experiments are based on UV vis, fluorescence, and Raman spectroscopies and utilize modular spectroscopic components. Students assemble their own instruments, optimize them with respect to signal-to-noise, generate calibration curves, determine the SA content in retail aspirin tablets, and assign features in the respective spectra to functional groups within the active material. Using this approach in the discovery-based setting, the students gain invaluable insight into method-specific parameters, such as instrumental components, sample preparation, and analytical capability. In addition, the students learn the fundamentals of fiber optics and signal processing using the low-cost CCD based spectroscopic components.

  9. A theoretical analysis of the spin dynamics of magnetic adatoms traced by time-resolved scanning tunneling spectroscopy

    Science.gov (United States)

    Schüler, M.; Pavlyukh, Y.; Berakdar, J.

    2012-04-01

    Inelastic scanning tunneling microscopy (STM) has recently been shown (Loth et al 2010 Science 329 1628) to be extendable to access the nanosecond, spin-resolved dynamics of magnetic adatoms and molecules. Here we analyze this novel tool theoretically by considering the time-resolved spin dynamics of a single adsorbed Fe atom excited by a tunneling current pulse from a spin-polarized STM tip. The adatom spin configuration can be controlled and probed by applying voltage pulses between the substrate and the spin-polarized STM tip. We demonstrate how, in a pump-probe manner, the relaxation dynamics of the sample spin is manifested in the spin-dependent tunneling current. Our model calculations are based on the scattering theory in a wave-packet formulation. The scheme is non-perturbative and, hence, is valid for all voltages. The numerical results for the tunneling probability and the conductance are contrasted with the predictions of simple analytical models and compared with experiments.

  10. Transient absorption spectroscopy in biology using the Super-ACO storage ring FEL and the synchrotron radiation combination

    CERN Document Server

    Renault, E; De Ninno, G; Garzella, D; Hirsch, M; Nahon, L; Nutarelli, D

    2001-01-01

    The Super-ACO storage ring FEL, covering the UV range down to 300 nm with a high average power (300 mW at 350 nm) together with a high stability and long lifetime, is a unique tool for the performance of users applications. We present here the first pump-probe two color experiments on biological species using a storage ring FEL coupled to the synchrotron radiation. The intense UV pulse of the Super-ACO FEL is used to prepare a high initial concentration of chromophores in their first singlet electronic excited state. The nearby bending magnet synchrotron radiation provides, on the other hand a pulsed, white light continuum (UV-IR), naturally synchronized with the FEL pulses and used to probe the photochemical subsequent events and the associated transient species. We have demonstrated the feasibility with a dye molecule (POPOP) observing a two-color effect, signature of excited state absorption and a temporal signature with Acridine. Applications on various chromophores of biological interest are carried out,...

  11. Non-equilibrium Warm Dense Gold: Experiments and Simulations

    Science.gov (United States)

    Ng, Andrew

    2015-11-01

    This talk is an overview of a series of studies of non-equilibrium Warm Dense Matter using a broad range of measured properties of a single material, namely Au, as comprehensive benchmarks for theory. The measurements are made in fs-laser pump-probe experiments. For understanding lattice stability, our investigation reveals a solid phase at high energy density. This leads to the calculation of lattice dynamics using MD simulations and phonon hardening in DFT-MD simulations. For understanding electron transport in two-temperature states, AC conductivity is used to evaluate DFT-MD and Kubo-Greenwood calculations while DC conductivity is used to test Ziman calculations in a DFT average atom model. The electron density is also used to assess electronic structure calculations in DFT simulations. In our latest study of electron kinetics in states with a non-Fermi-Dirac distribution, three-body recombination is found to have a significant effect on electron thermalizaiton time. This is driving an effort to develop electron kinetics simulations using the Boltzmann equation method.

  12. Moessbauer spectroscopy with actinide elements

    Energy Technology Data Exchange (ETDEWEB)

    Potzel, W.; Moser, J.; Asch, L.; Kalvius, G.M. (Technische Univ. Muenchen, Garching (Germany, F.R.)

    1983-01-01

    Although formally equivalent to the lanthanide (4f) elements, the light actinides show a much more varied behaviour due to the larger spatial extent and ionizability of the 5f electrons. The application of Moessbauer spectroscopy for the determination of electronic properties of the actinides is outlined. Emphasis is put on high pressure Moessbauer experiments using the 60 keV transition in /sup 237/Np to study questions of delocalization of 5f electrons.

  13. Heavy quark production and spectroscopy

    Energy Technology Data Exchange (ETDEWEB)

    Appel, J.A.

    1993-11-01

    This review covers many new experimental results on heavy flavor production and spectroscopy. It also shows some of the increasingly improved theoretical understanding of results in light of basic perturbative QCD and heavy quark symmetry. At the same time, there are some remaining discrepancies among experiments as well as significant missing information on some of the anticipated lowest lying heavy quark states. Most interesting, perhaps, are some clearly measured production effects awaiting full explanation.

  14. Advances in atomic spectroscopy

    CERN Document Server

    Sneddon, J

    1997-01-01

    This series describes selected advances in the area of atomic spectroscopy. It is primarily intended for the reader who has a background in atmoic spectroscopy; suitable to the novice and expert. Although a widely used and accepted method for metal and non-metal analysis in a variety of complex samples, Advances in Atomic Spectroscopy covers a wide range of materials. Each Chapter will completely cover an area of atomic spectroscopy where rapid development has occurred.

  15. Basic molecular spectroscopy

    CERN Document Server

    Gorry, PA

    1985-01-01

    BASIC Molecular Spectroscopy discusses the utilization of the Beginner's All-purpose Symbolic Instruction Code (BASIC) programming language in molecular spectroscopy. The book is comprised of five chapters that provide an introduction to molecular spectroscopy through programs written in BASIC. The coverage of the text includes rotational spectra, vibrational spectra, and Raman and electronic spectra. The book will be of great use to students who are currently taking a course in molecular spectroscopy.

  16. Advances in atomic spectroscopy

    CERN Document Server

    Sneddon, J

    1995-01-01

    This series describes selected advances in the area of atomic spectroscopy. It is promarily intended for the reader who has a background in atmoic spectroscopy; suitable to the novice and expert. Although a widely used and accepted method for metal and non-metal analysis in a variety of complex samples, Advances in Atomic Spectroscopy covers a wide range of materials. Each Chapter will completely cover an area of atomic spectroscopy where rapid development has occurred.

  17. Symposium on atomic spectroscopy

    Energy Technology Data Exchange (ETDEWEB)

    1979-01-01

    Topics covered by the conference include: fast beam spectroscopy; astrophysical and other spectra; highly ionized spectroscopy; complex spectra; rydberg levels; fine structure, hyperfine structure and isotope shift; lineshapes; lifetimes, oscillator strengths and Einstein coefficients; and spectroscopy with lasers. Abstracts of the conference papers are presented. (GHT)

  18. Impact of a Vertically Polarized Undulator on LCLS Hard X-ray Experiments

    Energy Technology Data Exchange (ETDEWEB)

    Fritz, David [SLAC National Accelerator Lab., Menlo Park, CA (United States)

    2014-11-14

    The LCLS-II project will install two variable gap, horizontally polarized undulators into the LCLS undulator hall. One undulator is designed to produce soft x-rays spanning an energy range of 200-1250 eV (SXU) while the other is designed for the hard spectral range of 1-25 keV (HXU). The hard x-ray LCLS instruments (X-ray Pump- Probe [XPP], X-ray correlation Spectroscopy [XCS], Coherent X-ray Imaging [CXI], Matter in Extreme Conditions [MEC]) will be repurposed to operate on the HXU line while two new soft x-ray beamlines will be created for the SXU line. An alternate HXU undulator design is being considered that could provide advantages over the present design choice. In particular, the project team is collaborating with Argonne National Laboratory to develop a vertically polarized undulator (VPU). A 1-m prototype VPU device was successfully constructed this year and a full size prototype is in process. A decision to alter the project baseline, which is the construction of a horizontally polarized device, must be made in the coming weeks to not impact the present project schedule. Please note that a change to the soft x-ray undulator is not under discussion at the moment.

  19. Spectroscopy of Sound Transmission in Solid Samples

    Science.gov (United States)

    Campbell, Dean J.; Peterson, Joshua P.; Fitzjarrald, Tamara J.

    2013-01-01

    These laboratory experiments are designed to familiarize students with concepts of spectroscopy by using sound waves. Topics covered in these experiments include the structure of nitinol alloys and polymer chain stiffness as a function of structure and temperature. Generally, substances that are stiffer or have higher symmetry at the molecular…

  20. Spectroscopy of Sound Transmission in Solid Samples

    Science.gov (United States)

    Campbell, Dean J.; Peterson, Joshua P.; Fitzjarrald, Tamara J.

    2013-01-01

    These laboratory experiments are designed to familiarize students with concepts of spectroscopy by using sound waves. Topics covered in these experiments include the structure of nitinol alloys and polymer chain stiffness as a function of structure and temperature. Generally, substances that are stiffer or have higher symmetry at the molecular…

  1. Terahertz homodyne self-mixing transmission spectroscopy

    Energy Technology Data Exchange (ETDEWEB)

    Mohr, Till, E-mail: till.mohr@physik.tu-darmstadt.de; Breuer, Stefan; Blömer, Dominik; Patel, Sanketkumar; Schlosser, Malte; Birkl, Gerhard; Elsäßer, Wolfgang [Institute for Applied Physics, Technische Universität Darmstadt, Schlossgartenstr. 7, 64289 Darmstadt (Germany); Simonetta, Marcello [Dipartimento di Ingegneria Industriale e dell' Informazione, Università di Pavia, Via Ferrata 1, i-27100 Pavia (Italy); Deninger, Anselm [Toptica Photonics AG, Lochhamer Schlag 19, 82166 Gräfelfing (Germany); Giuliani, Guido [Dipartimento di Ingegneria Civile e Architettura, Università di Pavia, Via Ferrata 3, i-27100 Pavia (Italy)

    2015-02-09

    A compact homodyne self-mixing terahertz spectroscopy concept is experimentally investigated and confirmed by calculations. This method provides amplitude and phase information of the terahertz radiation emitted by a photoconductive antenna in a transmission experiment where a rotating chopper wheel serves as a feedback mirror. As a proof-of-principle experiment the frequency-dependent refractive index of Teflon is measured.

  2. Hands-on Force Spectroscopy: Weird Springs and Protein Folding

    Science.gov (United States)

    Euler, Manfred

    2008-01-01

    A force spectroscopy model experiment is presented using a low-cost tensile apparatus described earlier. Force-extension measurements of twisted rubber bands are obtained. They exhibit a complex nonlinear elastic behaviour that resembles atomic force spectroscopy investigations of molecules of titin, a muscle protein. The model experiments open up…

  3. Hadron Spectroscopy in COMPASS

    CERN Document Server

    Grube, Boris

    2012-01-01

    The COmmon Muon and Proton Apparatus for Structure and Spectroscopy (COMPASS) is a multi-purpose fixed-target experiment at the CERN Super Proton Synchrotron (SPS) aimed at studying the structure and spectrum of hadrons. In the naive Constituent Quark Model (CQM) mesons are bound states of quarks and antiquarks. QCD, however, predict the existence of hadrons beyond the CQM with exotic properties interpreted as excited glue (hybrids) or even pure gluonic bound states (glueballs). One main goal of COMPASS is to search for these states. Particularly interesting are so called spin-exotic mesons which have J^{PC} quantum numbers forbidden for ordinary q\\bar{q} states. Its large acceptance, high resolution, and high-rate capability make the COMPASS experiment an excellent device to study the spectrum of light-quark mesons in diffractive and central production reactions up to masses of about 2.5 GeV. COMPASS is able to measure final states with charged as well as neutral particles, so that resonances can be studied ...

  4. Meson spectroscopy at COMPASS

    Directory of Open Access Journals (Sweden)

    Grube Boris

    2016-01-01

    Full Text Available The goal of the COMPASS experiment at CERN is to study the structure and dynamics of hadrons. The two-stage spectrometer used by the experiment has large acceptance and covers a wide kinematic range for charged as well as neutral particles and can therefore measure a wide range of reactions. The spectroscopy of light mesons is performed with negative (mostly π− and positive (p, π+ hadron beams with a momentum of 190 GeV/c. The light-meson spectrum is measured in different final states produced in diffractive dissociation reactions with squared four-momentum transfer t to the target between 0.1 and 1.0 (GeV=c2. The flagship channel is the π−π−π+ final state, for which COMPASS has recorded the currently world’s largest data sample. These data not only allow to measure the properties of known resonances with high precision, but also to observe new states. Among these is a new axial-vector signal, the a1(1420, with unusual properties. Novel analysis techniques have been developed to extract also the amplitude of the π−π+ subsystem as a function of 3π mass from the data. The findings are confirmed by the analysis of the π−π0π0 final state.

  5. Meson Spectroscopy at COMPASS

    CERN Document Server

    Grube, Boris

    2016-11-29

    The goal of the COMPASS experiment at CERN is to study the structure and dynamics of hadrons. The two-stage spectrometer used by the experiment has large acceptance and covers a wide kinematic range for charged as well as neutral particles and can therefore measure a wide range of reactions. The spectroscopy of light mesons is performed with negative (mostly $\\pi^-$) and positive ($p$, $\\pi^+$) hadron beams with a momentum of 190 GeV/$c$. The light-meson spectrum is measured in different final states produced in diffractive dissociation reactions with squared four-momentum transfer $t$ to the target between 0.1 and 1.0 $(\\text{GeV}/c)^2$. The flagship channel is the $\\pi^-\\pi^-\\pi^+$ final state, for which COMPASS has recorded the currently world's largest data sample. These data not only allow to measure the properties of known resonances with high precision, but also to observe new states. Among these is a new axial-vector signal, the $a_1(1420)$, with unusual properties. Novel analysis techniques have been...

  6. Meson spectroscopy at COMPASS

    Science.gov (United States)

    Grube, Boris

    2016-11-01

    The goal of the COMPASS experiment at CERN is to study the structure and dynamics of hadrons. The two-stage spectrometer used by the experiment has large acceptance and covers a wide kinematic range for charged as well as neutral particles and can therefore measure a wide range of reactions. The spectroscopy of light mesons is performed with negative (mostly π-) and positive (p, π+) hadron beams with a momentum of 190 GeV/c. The light-meson spectrum is measured in different final states produced in diffractive dissociation reactions with squared four-momentum transfer t to the target between 0.1 and 1.0 (GeV=c)2. The flagship channel is the π-π-π+ final state, for which COMPASS has recorded the currently world's largest data sample. These data not only allow to measure the properties of known resonances with high precision, but also to observe new states. Among these is a new axial-vector signal, the a1(1420), with unusual properties. Novel analysis techniques have been developed to extract also the amplitude of the π-π+ subsystem as a function of 3π mass from the data. The findings are confirmed by the analysis of the π-π0π0 final state.

  7. Coherent Raman spectroscopy

    CERN Document Server

    Eesley, G L

    1981-01-01

    Coherent Raman Spectroscopy provides a unified and general account of the fundamental aspects of nonlinear Raman spectroscopy, also known as coherent Raman spectroscopy. The theoretical basis from which coherent Raman spectroscopy developed is described, along with its applications, utility, and implementation as well as advantages and disadvantages. Experimental data which typifies each technique is presented. This book is comprised of four chapters and opens with an overview of nonlinear optics and coherent Raman spectroscopy, followed by a discussion on nonlinear transfer function of matter

  8. Short-pulse, compressed ion beams at the Neutralized Drift Compression Experiment

    Science.gov (United States)

    Seidl, P. A.; Barnard, J. J.; Davidson, R. C.; Friedman, A.; Gilson, E. P.; Grote, D.; Ji, Q.; Kaganovich, I. D.; Persaud, A.; Waldron, W. L.; Schenkel, T.

    2016-05-01

    We have commenced experiments with intense short pulses of ion beams on the Neutralized Drift Compression Experiment (NDCX-II) at Lawrence Berkeley National Laboratory, with 1-mm beam spot size within 2.5 ns full-width at half maximum. The ion kinetic energy is 1.2 MeV. To enable the short pulse duration and mm-scale focal spot radius, the beam is neutralized in a 1.5-meter-long drift compression section following the last accelerator cell. A short-focal-length solenoid focuses the beam in the presence of the volumetric plasma that is near the target. In the accelerator, the line-charge density increases due to the velocity ramp imparted on the beam bunch. The scientific topics to be explored are warm dense matter, the dynamics of radiation damage in materials, and intense beam and beam-plasma physics including select topics of relevance to the development of heavy-ion drivers for inertial fusion energy. Below the transition to melting, the short beam pulses offer an opportunity to study the multi-scale dynamics of radiation-induced damage in materials with pump-probe experiments, and to stabilize novel metastable phases of materials when short-pulse heating is followed by rapid quenching. First experiments used a lithium ion source; a new plasma-based helium ion source shows much greater charge delivered to the target.

  9. Advances in atomic spectroscopy

    CERN Document Server

    Sneddon, J

    2000-01-01

    This fifth volume of the successful series Advances in Atomic Spectroscopy continues to discuss and investigate the area of atomic spectroscopy.It begins with a description of the use of various atomic spectroscopic methods and applications of speciation studies in atomic spectroscopy. The emphasis is on combining atomic spectroscopy with gas and liquid chromatography. In chapter two the authors describe new developments in tunable lasers and the impact they will have on atomic spectroscopy. The traditional methods of detection, such as photography and the photomultiplier, and how they are being replaced by new detectors is discussed in chapter three. The very active area of glow discharge atomic spectrometry is presented in chapter four where, after a brief introduction and historical review, the use of glow discharge lamps for atomic spectroscopy and mass spectrometry are discussed. Included in this discussion is geometry and radiofrequency power. The future of this source in atomic spectroscopy is also dis...

  10. A simple decay-spectroscopy station at CRIS-ISOLDE

    Science.gov (United States)

    Lynch, K. M.; Cocolios, T. E.; Althubiti, N.; Farooq-Smith, G. J.; Gins, W.; Smith, A. J.

    2017-02-01

    A new decay-spectroscopy station (DSS2.0) has been designed by the CRIS collaboration for use at the radioactive ion beam facility, ISOLDE. With the design optimised for both charged-particle and γ-ray detection, the DDS2.0 allows high-efficiency decay spectroscopy to be performed. The DSS2.0 complements the existing decay-spectroscopy system at the CRIS experiment, and together provide the ability to perform laser-assisted nuclear decay spectroscopy on both ground state and long-lived isomeric species. This paper describes the new decay-spectroscopy station and presents the characterisation studies that have recently been performed.

  11. Internal Conversion Process of Chlorophyll a in Solvents in Femtosecond Pump-Probe Laser Fields

    Institute of Scientific and Technical Information of China (English)

    Kai Niu; Li-qing Dong; Shu-lin Cong

    2008-01-01

    The internal conversion (IC) processes of chlorophyll a (chl-a) in solvents are studied based on the reduced density matrix theory. The IC times can be obtained by simulating the experimental fluorescence depletion spectra (FDS). The calculated IC times of chl-a in ethyl acetate, tetrahydrofuran and dimethyl formamide are 141, 147, and 241 fs, respectively. The oscillation feature of the FDS results from the forward and backward transfer of the population between coupled electronic states. The effects of diabatic coupling between two electronic states on the IC time and the FDS are described. The influence of molecule-reservoir coupling on the IC time is also investigated.

  12. Pump-probe measurements of the thermal conductivity tensor for materials lacking in-plane symmetry.

    Science.gov (United States)

    Feser, Joseph P; Liu, Jun; Cahill, David G

    2014-10-01

    We previously demonstrated an extension of time-domain thermoreflectance (TDTR) which utilizes offset pump and probe laser locations to measure in-plane thermal transport properties of multilayers. However, the technique was limited to systems of transversely isotropic materials studied using axisymmetric laser intensities. Here, we extend the mathematics so that data reduction can be performed on non-transversely isotropic systems. An analytic solution of the diffusion equation for an N-layer system is given, where each layer has a homogenous but otherwise arbitrary thermal conductivity tensor and the illuminating spots have arbitrary intensity profiles. As a demonstration, we use both TDTR and time-resolved magneto-optic Kerr effect measurements to obtain thermal conductivity tensor elements of α-SiO2. We show that the out-of-phase beam offset sweep has full-width half-maxima that contains nearly independent sensitivity to the in-plane thermal conductivity corresponding to the scanning direction. Also, we demonstrate a Nb-V alloy as a low thermal conductivity TDTR transducer layer that helps improve the accuracy of in-plane measurements.

  13. Interferometric pump-probe characterization of the nonlocal response of optically transparent ion implanted polymers

    Science.gov (United States)

    Stefanov, Ivan L.; Hadjichristov, Georgi B.

    2012-03-01

    Optical interferometric technique is applied to characterize the nonlocal response of optically transparent ion implanted polymers. The thermal nonlinearity of the ion-modified material in the near-surface region is induced by continuous wave (cw) laser irradiation at a relatively low intensity. The interferometry approach is demonstrated for a subsurface layer of a thickness of about 100 nm formed in bulk polymethylmethacrylate (PMMA) by implantation with silicon ions at an energy of 50 keV and fluence in the range 1014-1017 cm-2. The laser-induced thermooptic effect in this layer is finely probed by interferometric imaging. The interference phase distribution in the plane of the ion implanted layer is indicative for the thermal nonlinearity of the near-surface region of ion implanted optically transparent polymeric materials.

  14. Magnetoencephalography with a two-color pump-probe, fiber-coupled atomic magnetometer

    Science.gov (United States)

    Johnson, Cort; Schwindt, Peter D. D.; Weisend, Michael

    2010-12-01

    The authors have detected magnetic fields from the human brain with a compact, fiber-coupled rubidium spin-exchange-relaxation-free magnetometer. Optical pumping is performed on the D1 transition and Faraday rotation is measured on the D2 transition. The beams share an optical axis, with dichroic optics preparing beam polarizations appropriately. A sensitivity of magnetoencephalography system. The design is amenable to arraying sensors around the head, providing a framework for noncryogenic, whole-head magnetoencephalography.

  15. The pump-probe coupling of matter wave packets to remote lattice states

    DEFF Research Database (Denmark)

    Sherson, Jacob F; Park, Sung Jong; Pedersen, Poul Lindholm

    2012-01-01

    selected lattice sites at a long, controllable distance of more than 100 lattice sites from the main component. This precise control mechanism for ultra-cold atoms thus enables controlled quantum state preparation and splitting for quantum dynamics, metrology and simulation....

  16. Pulse laser photolysis of aqueous ozone in the microsecond range studied by time-resolved far-ultraviolet absorption spectroscopy.

    Science.gov (United States)

    Goto, Takeyoshi; Morisawa, Yusuke; Higashi, Noboru; Ikehata, Akifumi; Ozaki, Yukihiro

    2013-05-01

    Chemical dynamics of an ozone (O3) pulse-photolytic reaction in aqueous solutions were studied with pump-probe transient far-ultraviolet (FUV) absorption spectroscopy. With a nanosecond pulse laser of 266 nm as pump light, transient spectra of O3 aqueous solutions (78-480 μM, pH 2.5-11.3) were acquired in the time range from -50 to 50 μs in the wavelength region from 190 to 225 nm. The measured transient spectra were linearly decomposed into the molar absorption coefficients and the concentration-time profiles of constituted chemical components with a multivariate curve resolution method. From the dependences of the time-averaged concentrations for 20 μs of the constituted chemicals on the initial concentration of O3, it was found that the transient spectra involve the decomposition of O3 and the formation of hydrogen peroxide (H2O2) and a third component that is assigned to hydroxyl radical (OH) or perhydroxyl radical (HO2). Furthermore, the pH dependence of the time-averaged concentration of the third components indicates that HO2 is more probable than OH as the third component. The time-averaged concentration ratio of each chemical component to the initial O3 concentration depends on the pH conditions from -0.95 to -0.60 for O3, 0.98 to 1.2 for H2O2, 0.002 to 0.29 for OH, and 0.012 to 0.069 for HO2.

  17. Velocity-aligned Doppler spectroscopy

    Science.gov (United States)

    Xu, Z.; Koplitz, B.; Wittig, C.

    1989-03-01

    The use of velocity-aligned Doppler spectroscopy (VADS) to measure center-of-mass kinetic-energy distributions of nascent photofragments produced in pulsed-initiation photolysis/probe experiments is described and demonstrated. In VADS, pulsed photolysis and probe laser beams counterpropagate through the ionization region of a time-of-flight mass spectrometer. The theoretical principles of VADS and the mathematical interpretation of VADS data are explained and illustrated with diagrams; the experimental setup is described; and results for the photodissociation of HI, H2S, and NH3 are presented in graphs and characterized in detail. VADS is shown to give much higher kinetic-energy resolution than conventional Doppler spectroscopy.

  18. Spectroscopy of the Heaviest Elements

    Science.gov (United States)

    Clark, Roderick

    2009-10-01

    The specific ``magic'' proton and neutron numbers, representing major spherical shell gaps, beyond 208Pb are a matter of considerable debate. It is well established that nuclei near Z=100, N=152 (252Fm) have well-deformed prolate shapes. By performing prompt and delayed gamma-ray spectroscopy on deformed transfermium nuclei we can learn about the single-particle structure, shell gaps, pairing correlations, and excitation modes in the heaviest nuclei. After a brief overview of state-of-the-art measurements, I will describe recent results from experiments at the 88-Inch Cyclotron of the Lawrence Berkeley National Laboratory which use the Berkeley Gas-filled Separator (BGS). I will then discuss the prospects of a new generation of spectroscopy measurements on the heaviest elements when the BGS is used in conjunction with the GRETINA gamma--ray tracking array.

  19. Fundamentals of Protein NMR Spectroscopy

    CERN Document Server

    Rule, Gordon S

    2006-01-01

    NMR spectroscopy has proven to be a powerful technique to study the structure and dynamics of biological macromolecules. Fundamentals of Protein NMR Spectroscopy is a comprehensive textbook that guides the reader from a basic understanding of the phenomenological properties of magnetic resonance to the application and interpretation of modern multi-dimensional NMR experiments on 15N/13C-labeled proteins. Beginning with elementary quantum mechanics, a set of practical rules is presented and used to describe many commonly employed multi-dimensional, multi-nuclear NMR pulse sequences. A modular analysis of NMR pulse sequence building blocks also provides a basis for understanding and developing novel pulse programs. This text not only covers topics from chemical shift assignment to protein structure refinement, as well as the analysis of protein dynamics and chemical kinetics, but also provides a practical guide to many aspects of modern spectrometer hardware, sample preparation, experimental set-up, and data pr...

  20. Frequency Comb Velocity Modulation Spectroscopy

    Science.gov (United States)

    Cossel, Kevin C.; Sinclair, Laura C.; Coffey, Tyler; Cornell, Eric; Ye, Jun

    2011-06-01

    We have developed a novel technique for rapid ion-sensitive spectroscopy over a broad spectral bandwidth by combining the high sensitivity of velocity modulation spectroscopy (VMS) with the parallel nature and high frequency accuracy of cavity-enhanced direct frequency comb spectroscopy. Prior to this research, no techniques have been capable of high sensitivity velocity modulation spectroscopy on every parallel detection channel over such a broad spectral range. We have demonstrated the power of this technique by measuring the A^2Π_u - X^2Σ_g^+ (4,2) band of N_2^+ at 830 nm with an absorption sensitivity of 1×10-6 for each of 1500 simultaneous measurement channels spanning 150 Cm-1. A densely sampled spectrum consisting of interleaved measurements to achieve 75 MHz spacing is acquired in under an hour. This technique is ideally suited for high resolution survey spectroscopy of molecular ions with applications including chemical physics, astrochemistry, and precision measurement. Currently, this system is being used to map the electronic transitions of HfF^+ for the JILA electron electric dipole moment (eEDM) experiment. The JILA eEDM experiment uses trapped molecular ions to significantly increase the coherence time of the measurement in addition to utilizing the strong electric field enhancement available from molecules. Previous theoretical work has shown that the metastable ^3Δ_1 state in HfF^+ and ThF^+ provides high sensitivity to the eEDM and good cancellation of systematic effects; however, the electronic level structure of these species have not previously been measured, and the theoretical uncertainties are hundreds to thousands of wavenumbers. This necessitates broad-bandwidth, high-resolution survey spectroscopy provided by frequency comb VMS in the 700-900 nm spectral window. F. Adler, M. J. Thorpe, K. C. Cossel, and J. Ye. Annu. Rev. Anal. Chem. 3, 175-205 (2010) A. E. Leanhardt, et. al. arXiv:1008.2997v2 E. Meyer, J. L. Bohn, and M. P. Deskevich

  1. Ultrahigh spatiotemporal resolved spectroscopy

    Institute of Scientific and Technical Information of China (English)

    LI; Zhi

    2007-01-01

    We review the technique and research of the ultrahigh spatiotemporal resolved spectroscopy and its applications in the field of the ultrafast dynamics of mesoscopic systems and nanomaterials. Combining femtosecond time-resolved spectroscopy and scanning near-field optical microscopy (SNOM), we can obtain the spectra with ultrahigh temporal and spatial resolutions simultaneously. Some problems in doing so are discussed. Then we show the important applications of the ultrahigh spatiotemporal resolved spectroscopy with a few typical examples.……

  2. Ultrahigh spatiotemporal resolved spectroscopy

    Institute of Scientific and Technical Information of China (English)

    2007-01-01

    @@ We review the technique and research of the ultrahigh spatiotemporal resolved spectroscopy and its applications in the field of the ultrafast dynamics of mesoscopic systems and nanomaterials. Combining femtosecond time-resolved spectroscopy and scanning near-field optical microscopy (SNOM), we can obtain the spectra with ultrahigh temporal and spatial resolutions simultaneously. Some problems in doing so are discussed. Then we show the important applications of the ultrahigh spatiotemporal resolved spectroscopy with a few typical examples.

  3. Femtosecond linear and nonlinear spectroscopy of silicon, germanium, and silicon-germanium alloys

    Science.gov (United States)

    Hu, Xiaofeng

    The time-resolved optical response of optically thick Si 1-xGe x alloys across the entire compositional range (0 pump-probe experiment in which a femtosecond pump pulse excites carriers (electron-hole pairs) in the sample and a probe pulse measures the ultrafast carrier dynamics at fixed incident angle in reflection mode through ellipsometric optics. This technique permits the real and imaginary parts of the time-varying dielectric function ɛ1(t) + iɛ2(t) to be distinguished clearly. The temporal shape Δvarepsilon1(t) depends only mildly on alloy composition, and is accurately modeled in terms of the Drude contribution from a diffusing electron-hole plasma by numerically solved four coupled differential equations and Monte Carlo simulations. The evolution of Δvarepsilon2(t), on the other hand, varies widely with composition, and appears to reflect more complicated dynamic processes including nonequilibrium carrier-induced band renormalization, thermal band gap shrinkage by nonequilibrium phonons, interband absorption saturation, and inter-conduction band absorption. Si(001) and Si 1-xGe x alloys surfaces are studied by optical second harmonic (SH) spectra generated in reflection using Ti:Sapphire femtosecond laser pulses for SH photon energies 2.0 eV adsorption and hydrogen desorption during low temperature, ultrahigh vacuum chemical vapor deposition film growth on Si(001) and Ge(001) are investigated in- situ in real time by monitoring the instantaneous hydrogen coverage using optical second harmonic generation. A simple two-site adsorption model and first- order desorption are used to establish reactive sticking coefficients and to predict epitaxial growth rate. The reactive sticking coefficients are temperature independent for disilane and temperature dependence for silane between 740 and 900 K. Predicted growth rates for silane and disilane are in good agreement with published values.

  4. Spectroscopy for Dummies

    DEFF Research Database (Denmark)

    Lindvold, Lars René

    This presentation will give short introduction to the most pertinent topics of optical spectroscopy. The following topics will be discussed: • The origin of spectra in UV, VIS and IR spectral range • Spectroscopic methods like absorption, luminescence and Raman • Wavelength dispersive optical...... components • Materials for use optical spectroscopy • Spectrometer geometries • Detectors for use in spectrometer • Practical examples of optical spectroscopy The objective of this presentation is to give the audience a good feel for the range of possibilities that optical spectroscopy can provide....

  5. Advances in DUV spectroscopy

    DEFF Research Database (Denmark)

    Buchhave, Preben; Tidemand-Lichtenberg, Peter; Mogensen, Claus Tilsted

    The would-be advantages of deep UV (DUV) spectroscopy are well known, but the potential applications have so far not been fully realized due to technological limitations and, perhaps, lack of bright ideas. However, new components and new knowledge about DUV spectra and spectroscopic methods...... combined with increasing needs for solutions to practical problems in environmental protection, medicine and pollution monitoring promise a new era in DUV spectroscopy. Here we shall review the basis for DUV spectroscopy, both DUV fluorescence and DUV Raman spectroscopy, and describe recent advances...

  6. An ultrafast study of Zinc Phthalocyanine in DMSO

    CSIR Research Space (South Africa)

    Ombinda-Lemboumba, Saturnin

    2010-10-01

    Full Text Available The ultrafast dynamics of Zinc Phthalocyanine was studied using trasient absorption pump probe spectroscopy. Zinc Phthalocyanine was excited (pumped) at 672nm and probed by a white light continuum. The pump-probe technique used in this study...

  7. Meson Spectroscopy at COMPASS

    CERN Document Server

    Grube, Boris

    2015-01-01

    The COmmon Muon and Proton Apparatus for Structure and Spectroscopy (COMPASS) is a multi-purpose fixed-target experiment at the CERN Super Proton Synchrotron (SPS) aimed at studying the structure and spectrum of hadrons. The two-stage spectrometer has a good acceptance for charged as well as neutral particles over a wide kinematic range and thus allows to access a wide range of reactions. Light mesons are studied with negative (mostly $\\pi^-$) and positive ($p$, $\\pi^+$) hadron beams with a momentum of 190 GeV/$c$. The spectrum of light mesons is investigated in various final states produced in diffractive dissociation reactions at squared four-momentum transfers to the target between 0.1 and 1.0 $(\\text{GeV}/c)^2$. The flagship channel is the $\\pi^-\\pi^+\\pi^-$ final state, for which COMPASS has recorded the currently largest data sample. These data not only allow to measure the properties of known resonances with high precision, but also to search for new states. Among these is a new resonance-like signal, t...

  8. Laser spectroscopy of radium

    Energy Technology Data Exchange (ETDEWEB)

    Santra, Bodhaditya; Dammalapati, Umakanth; Jungmann, Klaus; Willmann, Lorenz [KVI, University of Groningen (Netherlands)

    2011-07-01

    Searches for permanent electric dipole moments (EDMs) of fundamental particles are sensitive probes of physics beyond the Standard Model. Fundamental EDMs can experience enhancements in atomic and molecular systems. In particular, isotopes of the heavy alkaline earth element radium exhibit the largest known enhancement factors for any atomic systems due to their atomic and nuclear structure. A sensitive search for EDMs will require an efficient use of the rare isotopes, which are available from radioactive sources or at rare isotope facilities like TRI{mu}P at KVI. Here, laser cooling and trapping methods play a crucial role. The main transitions from the ground state have been identified by laser spectroscopy. Nevertheless, the strongest cooling transitions 7s{sup 2} {sup 1}S{sub 0}-7s7p {sup 1}P{sub 1} suffers from strong leakage to metastable states, similar to the case of barium. We describe the experimental approach to determine the wavelength of the three needed repump transitions, which then will permit an efficient capture of radium atoms into a magneto optical trap.

  9. Meson spectroscopy with COMPASS

    CERN Document Server

    Nerling, Frank

    2011-01-01

    The COMPASS fixed-target experiment at CERN SPS is dedicated to the study of hadron structure and dynamics. In the physics programme using hadron beams, the focus is on the detection of new states, in particular the search for $J^{PC}$ exotic states and glueballs. After a short pilot run in 2004 (190 GeV/c negative pion beam, lead target), we started our hadron spectroscopy programme in 2008 by collecting an unprecedented statistics with a negative hadron beam (190 GeV/c) on a liquid hydrogen target. A similar amount of data with positive hadron beam (190 GeV/c) has been taken in 2009, as well as some additional data with negative beam on nuclear targets. The spectrometer features a large angular acceptance and high momentum resolution and also good coverage by electromagnetic calorimetry, crucial for the detection of final states involving $\\pi^0$ or $\\eta$. A first important result is the observation of a significant $J^{PC}$ spin exotic signal consistent with the disputed $\\pi_1(1600)$ in the pilot run dat...

  10. Critical Metadata for Spectroscopy Field Campaigns

    Directory of Open Access Journals (Sweden)

    Barbara A. Rasaiah

    2014-04-01

    Full Text Available A field spectroscopy metadata standard is defined as those data elements that explicitly document the spectroscopy dataset and field protocols, sampling strategies, instrument properties and environmental and logistical variables. Standards for field spectroscopy metadata affect the quality, completeness, reliability, and usability of datasets created in situ. Currently there is no standardized methodology for documentation of in situ spectroscopy data or metadata. This paper presents results of an international experiment comprising a web-based survey and expert panel evaluation that investigated critical metadata in field spectroscopy. The survey participants were a diverse group of scientists experienced in gathering spectroscopy data across a wide range of disciplines. Overall, respondents were in agreement about a core metadataset for generic campaign metadata, allowing for a prioritization of critical metadata elements to be proposed including those relating to viewing geometry, location, general target and sampling properties, illumination, instrument properties, reference standards, calibration, hyperspectral signal properties, atmospheric conditions, and general project details. Consensus was greatest among individual expert groups in specific application domains. The results allow the identification of a core set of metadata fields that enforce long term data storage and serve as a foundation for a metadata standard. This paper is part one in a series about the core elements of a robust and flexible field spectroscopy metadata standard.

  11. Towards laser spectroscopy of antihydrogen

    Energy Technology Data Exchange (ETDEWEB)

    Walz, J [CERN-EP/APE, CH-1211 Geneve (Switzerland); Fendel, P [Max-Planck-Institut fuer Quantenoptik, Hans-Kopfermann-Strasse 1, D-85748 Garching (Germany); Herrmann, M [Max-Planck-Institut fuer Quantenoptik, Hans-Kopfermann-Strasse 1, D-85748 Garching (Germany); Koenig, M [Max-Planck-Institut fuer Quantenoptik, Hans-Kopfermann-Strasse 1, D-85748 Garching (Germany); Pahl, A [Max-Planck-Institut fuer Quantenoptik, Hans-Kopfermann-Strasse 1, D-85748 Garching (Germany); Pittner, H [Max-Planck-Institut fuer Quantenoptik, Hans-Kopfermann-Strasse 1, D-85748 Garching (Germany); Schatz, B [Max-Planck-Institut fuer Quantenoptik, Hans-Kopfermann-Strasse 1, D-85748 Garching (Germany); Haensch, T W [Max-Planck-Institut fuer Quantenoptik, Hans-Kopfermann-Strasse 1, D-85748 Garching (Germany)

    2003-02-14

    Cold antihydrogen atoms in a magnetic trap will open up a fascinating field of very precise CPT tests by ultrahigh-resolution laser spectroscopy. Equally exciting is the prospect for experiments on the gravitational acceleration of antimatter. For both types of experiment it is of great importance to have antihydrogen as cold as possible. Laser cooling of antihydrogen can be done on the strong 1S-2P transition at Lyman-{alpha} (121.56 nm). The highest cooling efficiency, lowest temperature, and best magnetic sublevel selectivity is expected for continuous coherent radiation. We present an account of the first source for continuous coherent radiation at Lyman-{alpha} and discuss possible applications in experiments with antihydrogen.

  12. Metallomic EPR spectroscopy.

    Science.gov (United States)

    Hagen, Wilfred R

    2009-09-01

    Based on explicit definitions of biomolecular EPR spectroscopy and of the metallome, this tutorial review positions EPR in the field of metallomics as a unique method to study native, integrated systems of metallobiomolecular coordination complexes subject to external stimuli. The specific techniques of whole-system bioEPR spectroscopy are described and their historic, recent, and anticipated applications are discussed.

  13. Heterodyned holographic spectroscopy

    NARCIS (Netherlands)

    Douglas, NG

    1997-01-01

    In holographic spectroscopy an image of an interference pattern is projected onto a detector and transformed back to the input spectrum. The general characteristics are similar to those of Fourier transform spectroscopy, but the spectrum is obtained without scanning. In the heterodyned arrangement o

  14. Progress in field spectroscopy

    NARCIS (Netherlands)

    Milton, E.J.; Schaepman, M.E.; Anderson, K.; Kneubühler, M.; Fox, N.

    2009-01-01

    This paper reviews developments in the science of field spectroscopy, focusing on the last twenty years in particular. During this period field spectroscopy has become established as an important technique for characterising the reflectance of natural surfaces in situ, for supporting the vicarious c

  15. Quantum-limit spectroscopy

    CERN Document Server

    Ficek, Zbigniew

    2017-01-01

    This book covers the main ideas, methods, and recent developments of quantum-limit optical spectroscopy and applications to quantum information, resolution spectroscopy, measurements beyond quantum limits, measurement of decoherence, and entanglement. Quantum-limit spectroscopy lies at the frontier of current experimental and theoretical techniques, and is one of the areas of atomic spectroscopy where the quantization of the field is essential to predict and interpret the existing experimental results. Currently, there is an increasing interest in quantum and precision spectroscopy both theoretically and experimentally, due to significant progress in trapping and cooling of single atoms and ions. This progress allows one to explore in the most intimate detail the ways in which light interacts with atoms and to measure spectral properties and quantum effects with high precision. Moreover, it allows one to perform subtle tests of quantum mechanics on the single atom and single photon scale which were hardly eve...

  16. The spectroscopy of fission fragments

    Energy Technology Data Exchange (ETDEWEB)

    Phillips, W.R. [Department of Physics and Astronomy, University of Manchester, Manchester, M13 9PL (United Kingdom); Collaboration: La Direction des Sciences de la Matiere du CEA (FR); Le Fonds National de la Recherche Scientifique de Belgique (BE)

    1998-12-31

    High-resolution measurements on {gamma} rays from fission fragments have provided a rich source of information, unobtainable at the moment in any other way, on the spectroscopy of neutron-rich nuclei. In recent years important data have been obtained on the yrast- and near yrast-structure of neutron-rich fission fragments. We discuss the scope of measurements which can be made on prompt gamma rays from secondary fission fragments, the techniques used in the experiments and some results recently obtained. (author) 24 refs., 8 figs., 1 tab.

  17. Femtosecond Laser Spectroscopy of the Rhodopsin Photochromic Reaction: A Concept for Ultrafast Optical Molecular Switch Creation (Ultrafast Reversible Photoreaction of Rhodopsin

    Directory of Open Access Journals (Sweden)

    Olga Smitienko

    2014-11-01

    Full Text Available Ultrafast reverse photoreaction of visual pigment rhodopsin in the femtosecond time range at room temperature is demonstrated. Femtosecond two-pump probe experiments with a time resolution of 25 fs have been performed. The first рump pulse at 500 nm initiated cis-trans photoisomerization of rhodopsin chromophore, 11-cis retinal, which resulted in the formation of the primary ground-state photoproduct within a mere 200 fs. The second pump pulse at 620 nm with a varying delay of 200 to 3750 fs relative to the first рump pulse, initiated the reverse phototransition of the primary photoproduct to rhodopsin. The results of this photoconversion have been observed on the differential spectra obtained after the action of two pump pulses at a time delay of 100 ps. It was found that optical density decreased at 560 nm in the spectral region of bathorhodopsin absorption and increased at 480 nm, where rhodopsin absorbs. Rhodopsin photoswitching efficiency shows oscillations as a function of the time delay between two рump pulses. The quantum yield of reverse photoreaction initiated by the second pump pulse falls within the range 15% ± 1%. The molecular mechanism of the ultrafast reversible photoreaction of visual pigment rhodopsin may be used as a concept for the development of an ultrafast optical molecular switch.

  18. Strong influence of coadsorbate interaction on CO desorption dynamics on Ru(0001) probed by ultrafast x-ray spectroscopy and ab initio simulations

    Energy Technology Data Exchange (ETDEWEB)

    Xin, H. [SLAC National Accelerator Lab., Menlo Park, CA (United States); Stanford Univ., Stanford, CA (United States); LaRue, J. [SLAC National Accelerator Lab., Menlo Park, CA (United States); Oberg, H. [Stockholm Univ., Stockholm (Sweden); Beye, M. [SLAC National Accelerator Lab., Menlo Park, CA (United States); Helmholtz Zentrum Berlin fur Materialien und Energie GmbH, Berlin (Germany); Dell' Angela, M. [Univ. of Hamburg and Center for Free Electron Laser Science, Hamburg (Germany); Turner, J. J. [SLAC National Accelerator Lab., Menlo Park, CA (United States); Gladh, J. [Stockholm Univ., Stockholm (Sweden); Ng, M. L. [SLAC National Accelerator Lab., Menlo Park, CA (United States); Sellberg, J. A. [SLAC National Accelerator Lab., Menlo Park, CA (United States); Helmholtz Zentrum Berlin fur Materialien und Energie GmbH, Berlin (Germany); Kaya, S. [SLAC National Accelerator Lab., Menlo Park, CA (United States); Mercurio, G. [Univ. of Hamburg and Center for Free Electron Laser Science, Hamburg (Germany); Hieke, F. [Univ. of Hamburg and Center for Free Electron Laser Science, Hamburg (Germany); Nordlund, D. [SLAC National Accelerator Lab., Menlo Park, CA (United States); Schlotter, W. F. [SLAC National Accelerator Lab., Menlo Park, CA (United States); Dakovski, G. L. [SLAC National Accelerator Lab., Menlo Park, CA (United States); Minitti, M. P. [SLAC National Accelerator Lab., Menlo Park, CA (United States); Fohlisch, A. [Helmholtz Zentrum Berlin fur Materialien und Energie GmbH, Berlin (Germany); Univ. Potsdam, Potsdam (Germany); Wolf, M. [Fritz-Haber Institute of the Max-Planck-Society, Berlin (Germany); Wurth, W. [Univ. of Hamburg and Center for Free Electron Laser Science, Hamburg (Germany); DESY Photon Science, Hamburg (Germany); Ogasawara, H. [SLAC National Accelerator Lab., Menlo Park, CA (United States); Norskov, J. K. [SLAC National Accelerator Lab., Menlo Park, CA (United States); Stanford Univ., Stanford, CA (United States); Ostrom, H. [Stockholm Univ., Stockholm (Sweden); Pettersson, L. G. M. [Stockholm Univ., Stockholm (Sweden); Nilsson, A. [SLAC National Accelerator Lab., Menlo Park, CA (United States); Stockholm Univ., Stockholm (Sweden); Ablid-Pedersen, F. [SLAC National Accelerator Lab., Menlo Park, CA (United States)

    2015-04-16

    We show that coadsorbed oxygen atoms have a dramatic influence on the CO desorption dynamics from Ru(0001). In contrast to the precursor-mediated desorption mechanism on Ru(0001), the presence of surface oxygen modifies the electronic structure of Ru atoms such that CO desorption occurs predominantly via the direct pathway. This phenomenon is directly observed in an ultrafast pump-probe experiment using a soft x-ray free-electron laser to monitor the dynamic evolution of the valence electronic structure of the surface species. This is supported with the potential of mean force along the CO desorption path obtained from density-functional theory calculations. Charge density distribution and frozen-orbital analysis suggest that the oxygen-induced reduction of the Pauli repulsion, and consequent increase of the dative interaction between the CO 5σ and the charged Ru atom, is the electronic origin of the distinct desorption dynamics. Ab initio molecular dynamics simulations of CO desorption from Ru(0001) and oxygen-coadsorbed Ru(0001) provide further insights into the surface bond-breaking process.

  19. Mobile Raman spectroscopy in astrobiology research.

    Science.gov (United States)

    Vandenabeele, Peter; Jehlička, Jan

    2014-12-13

    Raman spectroscopy has proved to be a very useful technique in astrobiology research. Especially, working with mobile instrumentation during fieldwork can provide useful experiences in this field. In this work, we provide an overview of some important aspects of this research and, apart from defining different types of mobile Raman spectrometers, we highlight different reasons for this research. These include gathering experience and testing of mobile instruments, the selection of target molecules and to develop optimal data processing techniques for the identification of the spectra. We also identify the analytical techniques that it would be most appropriate to combine with Raman spectroscopy to maximize the obtained information and the synergy that exists with Raman spectroscopy research in other research areas, such as archaeometry and forensics.

  20. Real-time monitoring of bacterial and organic pollution in a water stream by fluorescence depletion spectroscopy

    Science.gov (United States)

    Gaulier, Geoffrey; Staedler, Davide; Sousa, Gustavo; Bonacina, Luigi; Wolf, Jean-Pierre

    2017-02-01

    We demonstrate an approach for a real-time, consumable-free optical system operating on a liquid jet which can be easily derived from the water distribution infrastructure. We apply a pump-probe scheme based on the acquisition and nanosecond manipulation of UV-excited fluorescence to increase the selective identification of bacterial against organic pollutants in water.