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  • 1
    Electronic Resource
    Electronic Resource
    [S.l.] : American Institute of Physics (AIP)
    Journal of Applied Physics 87 (2000), S. 2003-2014 
    ISSN: 1089-7550
    Source: AIP Digital Archive
    Topics: Physics
    Notes: Time-resolved piezoelectric detection of wide-band ultrasonic transients induced by laser pulses in absorbing medium was studied. An optoacoustic transducer was developed for measuring the profiles of ultrasonic transients propagating in backward direction out of the laser-irradiated medium. For this purpose, an optical fiber for delivery of laser pulses to the surface of absorbing medium and a wide-band lithium niobate acoustic transducer were incorporated in one compact system, optoacoustic front surface transducer (OAFST). The transducer possesses temporal resolution (rise time) of 3.5 ns, low effective thermal noise pressure (10 Pa), and high sensitivity of piezoelectric detection (10 μV/Pa) over the ultrasonic frequency range from 1 to 100 MHz. Nd:YAG laser pulses at 355 nm were employed to generate distribution of acoustic sources in water solutions of potassium chromate with various concentrations. A temporal course of ultrasonic transients launched into an optically and acoustically transparent medium, coupled to the absorbing medium, was studied. Ultrasonic profiles experimentally measured at the site of laser irradiation were compared with profiles calculated using theoretical model. Experimental curves were in a good agreement with theoretical profiles. The backward detection mode permitted accurate reconstruction of the axial distribution of heat deposition in the laser-irradiated homogeneous or layered medium from the measured profiles. OAFST may become a useful modality for optoacoustic imaging in biological tissues and nondestructive evaluation of industrial materials. © 2000 American Institute of Physics.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Chichester [u.a.] : Wiley-Blackwell
    Surface and Interface Analysis 20 (1993), S. 949-954 
    ISSN: 0142-2421
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Physics
    Notes: Transmission Móssbauer spectra of binary coprecipitated nickel(II)-iron(III) hydroxides (molar ratios 9:1 and 4:1) are analysed and compared with the results of AES analyses of their surface composition. A correlation between the data of the above techniques has been noted, indicating a redistribution of the components (i.e. Ni and Fe) in the surface layers, the latter being enriched with iron(III) as compared to the bulk. The results obtained are in good agreement with an excellent electrocatalytic activity of composite Ni-Fe hydroxide systems towards anodic oxygen evolution in alkaline electrolytes, taking into account a distinctly exhibited ‘surface’ electrocatalytic effect of ferric species on the nickel hydroxide electrode in the anodic oxygen evolution process revealed previously. Transmission Móssbauer spectroscopy has been shown to be a highly effective probe sensitive both to various bulk and surface effects related to the solid phases studied.
    Additional Material: 3 Ill.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 107 (1997), S. 10288-10310 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: Analysis of the nuclear spin relaxation rates of lipid membranes provides a powerful means of studying the dynamics of these important biological representatives of soft matter. Here, temperature- and frequency-dependent 2H and 13C nuclear magnetic resonance (NMR) relaxation rates for vesicles and multilamellar dispersions of 1,2-dimyristoyl-sn-glycero-3-phosphocholine (DMPC) in the liquid–crystalline state have been fitted simultaneously to various dynamic models for different positions of the acyl chains. The data include 2H R1Z rates (Zeeman order of electric quadrupolar interaction) acquired at 12 external magnetic field strengths from 0.382 to 14.6 T, corresponding to a frequency range from ωD/2π=2.50–95.3 MHz; and 2H R1Q rates (quadrupolar order of electric quadrupolar interaction) at 15.3, 46.1, and 76.8 MHz. Moreover, 13C R1Z data (Zeeman order of magnetic dipolar interaction) for DMPC are included at six magnetic field strengths, ranging from 1.40 to 17.6 T, thereby enabling extension of the frequency range to effectively (ωC+ωH)/2π=938.7 MHz. Use of the generalized approach allows formulation of noncollective segmental and molecular diffusion models, as well as collective director fluctuation models, which were tested by fitting the 2H R1Z data at different frequencies and temperatures (30 °C and 50 °C). The corresponding 13C relaxation rates were predicted theoretically and compared to experiment, thus allowing one to unify the 13C and 2H NMR data for bilayer lipids in the fluid state. A further new aspect is that the spectral densities of motion have been explicitly calculated from the 2H R1Z and R1Q data at 40 °C. We conclude that the relaxation in fluid membrane bilayers is governed predominantly by relatively slow motions, which modulate the residual coupling remaining from faster local motions (order fluctuations). Only the molecular diffusion model, including an additional slow motional process, and the membrane deformation model describing three-dimensional collective fluctuations fit the 2H NMR data and predict the 13C NMR data in the MHz range. Orientational correlation functions have been calculated, which emphasizes the importance of NMR relaxation as a unique tool for investigating the dynamics of lipid bilayers and biological membranes. © 1997 American Institute of Physics.
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    The @journal of physical chemistry 〈Washington, DC〉 78 (1974), S. 203-207 
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology , Physics
    Type of Medium: Electronic Resource
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  • 5
    ISSN: 1520-4804
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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  • 6
    Electronic Resource
    Electronic Resource
    [S.l.] : American Institute of Physics (AIP)
    Journal of Applied Physics 76 (1994), S. 2918-2923 
    ISSN: 1089-7550
    Source: AIP Digital Archive
    Topics: Physics
    Notes: A quantum molecular dynamics study of the interface formation of the Al/GaAs(110) and In/GaAs(110) interfaces has been performed. It is found that, at very low coverages, both Al and In atoms chemisorb on threefold coordinated sites, bonded to two As atoms and one Ga atom. The metal atoms attract each other on the GaAs surface and tend to form islands. The electronic structure for one monolayer is found to be semiconducting for both In and Al. The results presented here are consistent with the temperature-dependent evolution of Fermi level from the very low metal coverage limit to the overlayer limit for the deposition of In and Al on GaAs(110).
    Type of Medium: Electronic Resource
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  • 7
    Electronic Resource
    Electronic Resource
    [S.l.] : American Institute of Physics (AIP)
    Journal of Applied Physics 78 (1995), S. 1281-1290 
    ISSN: 1089-7550
    Source: AIP Digital Archive
    Topics: Physics
    Notes: Pulsed laser ablation of aqueous medium irradiated under conditions of temporal confinement of thermal stress is described. Time-resolved measurements of laser-induced transient stress waves with simultaneous imaging of ablation process by laser-flash photography were performed. Stress transients induced in aqueous solution of K2CrO4 by ablative nanosecond laser pulses at 355 nm were studied by a broad-band lithium niobate acoustic transducer. Recoil momentum upon material ejection was measured from the temporal profiles of the acoustic transducer signal as a function of incident laser fluence. Cavitation bubbles produced in the irradiated volume during the tensile phase of thermoelastic stress were shown to drive material ejection at temperatures substantially below 100 °C. Experimental data are evident that nanosecond-pulse laser ablation of aqueous media (when temporal stress-confinement conditions are satisfied) include the following two main stages of material ejection: (1) ejection of water microdroplets due to expansion and rupture of subsurface cavitation bubbles; (2) ejection of liquid streams with substantial volume upon collapse of initial crater and large cavitation bubbles in the depth of irradiated volume (after coalescence of smaller bubbles). © 1995 American Institute of Physics.
    Type of Medium: Electronic Resource
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  • 8
    Electronic Resource
    Electronic Resource
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 112 (2000), S. 1413-1424 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: A coupled system of two molecules bearing spins of 1/2, which are allowed to diffuse relative to each other, is considered. By using a symmetry-adapted basis operator set, the overall density matrix equation is decoupled into two equations for the time-resolved isochromat components, the sum of which yields the observed signal. The appropriate stochastic Liouville equation is solved by a combination of eigenfunction expansion and finite-differences for the angular and radial relative motions, respectively. A full range of spectra from classic Pake patterns in the rigid limit to motionally narrowed Lorentzians is recovered. As an extension of the above approach, the solid-echo experiment is described in terms of the ensemble-averaged isochromats. Homogeneous transverse relaxation times (T2) as a function of the translational diffusion coefficient (DT) are obtained from simulating SECSY (spin-echo correlation spectroscopy) signals, which show distinct T2 minima vs DT. The present method of separating the quantum and stochastic classical variables constitutes a useful approach for treating multiquantum statistical systems, and it can be generalized to an arbitrary number of spins as shown in a companion paper. In the present study we obtained the usual linear dependence of T2 on DT in the motional narrowing (or Redfield) limit, whereas in the slow motional regime a DT−1/2 dependence is observed, consistent with studies of rotational diffusion. Varying the distance of maximum separation between the two spins (rmax) has virtually no effect on the location of the T2 minimum with respect to DT, implying that the onset of slow motion is essentially independent of rmax. © 2000 American Institute of Physics.
    Type of Medium: Electronic Resource
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  • 9
    Electronic Resource
    Electronic Resource
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 112 (2000), S. 1425-1443 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: The method utilized in Paper I [J. Chem. Phys. 112, 1413 (2000)] for treating the density matrix equation for a two-spin system in the presence of the dipolar interaction that is randomly modulated by translational diffusion, is extended to a many-body system of identical spins of 1/2. Generalized cumulant expansions are used, which allow one to take full advantage of the statistical independence of the motions of spins. In the high-temperature approximation (appropriate for dilute solutions), for a single nonselective pulse, the symmetry of the problem allows one to obtain a compact ordered binomial expression for the free-induction decay signal that is related to the two-particle solution, and it still contains the two spin-isochromat components. The latter are evaluated by solving the corresponding stochastic Liouville equation, which allows one to recover in a unified way the two limiting cases including Anderson's result for statistical broadening in a rigid lattice and the classical Torrey–Bloembergen–Redfield expression for the motional narrowing, as corrected by Hwang and Freed. The line shape expression in the thermodynamic limit, i.e., for large numbers of particles in a macroscopic volume, is obtained. It is found that the many-body dipolar line shapes are very close to Lorentzians over the entire motional range studied, with the linewidths proportional to the spin concentration, as predicted earlier for the limiting cases. Linewidths plotted versus the values of the translational diffusion coefficient clearly show the solid-state limit, the motional-narrowing limit, and the intermediate region. The method is extended to describe the behavior of the many-body system in a solid-echo sequence. This enables one to obtain the homogeneous T2's over the whole range of motions. A minimum in T2 is found at approximately the same value of translational diffusion coefficient as was found for the two-spin case in Paper I. © 2000 American Institute of Physics.
    Type of Medium: Electronic Resource
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  • 10
    Electronic Resource
    Electronic Resource
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 111 (1999), S. 4442-4452 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: Predictions of the diatomics-in-ionic-systems model for the variety of stationary points on the potential energy surfaces of the hydrogen fluoride clusters (HF)n (3≤n≤6) are compared to the results of ab initio MP2/6-311+G(2d,2p) calculations as well as to the results of the polarizable mechanics model of Hodges et al. [J. Phys. Chem. A 102, 2455 (1998)]. The diatomics-in-ionic-systems scheme which relies on the balanced treatment of neutral and ionic contributions to the electronic properties of polyatomic species within the diatomics-in-molecules theory takes into account here the mixing of the FH and F−H+ electronic states. The corresponding mixing coefficient serves as a single principal adjustable parameter of the model, finally selected by the reference value of the binding energy of (HF)3. It is shown that structures and energies of the main cyclic isomers are in a good agreement with the best estimates of Quack and Suhm [Conceptual Perspectives in Quantum Chemistry (Kluwer, Dordrecht, 1997)]. Every prediction of this model for the stationary points corresponding to 16 higher energy structures of (HF)n is confirmed by the MP2 ab initio data.© 1999 American Institute of Physics.
    Type of Medium: Electronic Resource
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