167,640 research outputs found

    Pressure effect on the in-plane magnetic penetration depth in YBa_2Cu_4O_8

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    We report a study of the pressure effect (PE) on the in-plane magnetic field penetration depth lambda_{ab} in YBa_2Cu_4O_8 by means of Meissner fraction measurements. A pronounced PE on lambda_{ab}^{-2}(0) was observed with a maximum relative shift of \Delta\lambda^{-2}_{ab}/\lambda^{-2}_{ab}= 44(3)% at a pressure of 10.2 kbar. It arises from the pressure dependence of the effective in-plane charge carrier mass and pressure induced charge carrier transfer from the CuO chains to the superconducting CuO_2 planes. The present results imply that the charge carriers in YBa_2Cu_4O_8 are coupled to the lattice.Comment: 4pages 3 figure

    Bending rigidity of stiff polyelectrolyte chains: Single chain and a bundle of multichains

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    We study the bending rigidity of highly charged stiff polyelectrolytes, for both a single chain and many chains forming a bundle. A theory is developed to account for the interplay between competitive binding of counterions and charge correlations in softening the polyelectrolyte (PE) chains. The presence of even a small concentration of multivalent counterions leads to a dramatic reduction in the bending rigidity of the chains that are nominally stiffened by the repulsion between their backbone charges. The variation of the bending rigidity as a function of f0f_{0}, the fraction of charged monomers on the chain, does not exhibits simple scaling behavior; it grows with increasing f0f_{0} below a critical value of f0f_{0}. Beyond the critical value, however, the chain becomes softer as f0f_{0} increases. The bending rigidity also exhibits intriguing dependence on the concentration of multivalent counterion n2n_{2}; for highly charged PEs, the bending rigidity decreases as n2n_2 increases from zero, while it increases with increasing n2n_{2} beyond a certain value of n2n_{2}. When polyelectrolyte chains form a NN-loop condensate (e.g., a toroidal bundle formed by NN turns (winds) of the chain), the inter-loop coupling further softens the condensate, resulting in the bending free energy of the condensate that scales as NN for large NN.Comment: 11 pages, 2 figure

    Improving Photoelectron Counting and Particle Identification in Scintillation Detectors with Bayesian Techniques

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    Many current and future dark matter and neutrino detectors are designed to measure scintillation light with a large array of photomultiplier tubes (PMTs). The energy resolution and particle identification capabilities of these detectors depend in part on the ability to accurately identify individual photoelectrons in PMT waveforms despite large variability in pulse amplitudes and pulse pileup. We describe a Bayesian technique that can identify the times of individual photoelectrons in a sampled PMT waveform without deconvolution, even when pileup is present. To demonstrate the technique, we apply it to the general problem of particle identification in single-phase liquid argon dark matter detectors. Using the output of the Bayesian photoelectron counting algorithm described in this paper, we construct several test statistics for rejection of backgrounds for dark matter searches in argon. Compared to simpler methods based on either observed charge or peak finding, the photoelectron counting technique improves both energy resolution and particle identification of low energy events in calibration data from the DEAP-1 detector and simulation of the larger MiniCLEAN dark matter detector.Comment: 16 pages, 16 figure

    Effective Electrostatic Interactions in Suspensions of Polyelectrolyte Brush-Coated Colloids

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    Effective electrostatic interactions between colloidal particles, coated with polyelectrolyte brushes and suspended in an electrolyte solvent, are described via linear response theory. The inner cores of the macroions are modeled as hard spheres, the outer brushes as spherical shells of continuously distributed charge, the microions (counterions and salt ions) as point charges, and the solvent as a dielectric continuum. The multi-component mixture of macroions and microions is formally mapped onto an equivalent one-component suspension by integrating out from the partition function the microion degrees of freedom. Applying second-order perturbation theory and a random phase approximation, analytical expressions are derived for the effective pair interaction and a one-body volume energy, which is a natural by-product of the one-component reduction. The combination of an inner core and an outer shell, respectively impenetrable and penetrable to microions, allows the interactions between macroions to be tuned by varying the core diameter and brush thickness. In the limiting cases of vanishing core diameter and vanishing shell thickness, the interactions reduce to those derived previously for star polyelectrolytes and charged colloids, respectively.Comment: 20 pages, 5 figures, Phys. Rev. E (in press

    In-situ characterization of the Hamamatsu R5912-HQE photomultiplier tubes used in the DEAP-3600 experiment

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    The Hamamatsu R5912-HQE photomultiplier-tube (PMT) is a novel high-quantum efficiency PMT. It is currently used in the DEAP-3600 dark matter detector and is of significant interest for future dark matter and neutrino experiments where high signal yields are needed. We report on the methods developed for in-situ characterization and monitoring of DEAP's 255 R5912-HQE PMTs. This includes a detailed discussion of typical measured single-photoelectron charge distributions, correlated noise (afterpulsing), dark noise, double, and late pulsing characteristics. The characterization is performed during the detector commissioning phase using laser light injected through a light diffusing sphere and during normal detector operation using LED light injected through optical fibres

    Neutral and Charged Polymers at Interfaces

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    Chain-like macromolecules (polymers) show characteristic adsorption properties due to their flexibility and internal degrees of freedom, when attracted to surfaces and interfaces. In this review we discuss concepts and features that are relevant to the adsorption of neutral and charged polymers at equilibrium, including the type of polymer/surface interaction, the solvent quality, the characteristics of the surface, and the polymer structure. We pay special attention to the case of charged polymers (polyelectrolytes) that have a special importance due to their water solubility. We present a summary of recent progress in this rapidly evolving field. Because many experimental studies are performed with rather stiff biopolymers, we discuss in detail the case of semi-flexible polymers in addition to flexible ones. We first review the behavior of neutral and charged chains in solution. Then, the adsorption of a single polymer chain is considered. Next, the adsorption and depletion processes in the many-chain case are reviewed. Profiles, changes in the surface tension and polymer surface excess are presented. Mean-field and corrections due to fluctuations and lateral correlations are discussed. The force of interaction between two adsorbed layers, which is important in understanding colloidal stability, is characterized. The behavior of grafted polymers is also reviewed, both for neutral and charged polymer brushes.Comment: a review: 130 pages, 30 ps figures; final form, added reference

    Polyelectrolyte multilayer formation: electrostatics and short-range interactions

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    We investigate the phenomenon of multilayer formation via layer-by-layer deposition of alternating charge polyelectrolytes. Using mean-field theory, we find that a strong short-range attraction between the two types of polymer chains is essential for the formation of multilayers. The dependence of the required short-range attraction on the polymer charge fraction and salt concentration is calculated. For weak short-range attraction between any two adjacent layers, the adsorbed amount (per added layer) decays as the distance from the surface increases, until the chains stop adsorbing altogether. For strong short-range attraction, the adsorbed amount per layer increases after an initial decrease, and finally it stabilizes in the form of a polyelectrolyte multilayer that can be repeated many times.Comment: 8 pages, 7 figure
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