NuSTAR observations of the young, energetic radio pulsar PSR B1509-58

We report on Nuclear Spectroscopic Telescope Array (NuSTAR) hard X-ray observations of the young rotation-powered radio pulsar PSR B1509$-$58 in the supernova remnant MSH 15$-$52. We confirm the previously reported curvature in the hard X-ray spectrum, showing that a log parabolic model provides a statistically superior fit to the spectrum compared with the standard power law. The log parabolic model describes the NuSTAR data, as well as previously published gamma-ray data obtained with COMPTEL and AGILE, all together spanning 3 keV through 500 MeV. Our spectral modelling allows us to constrain the peak of the broadband high energy spectrum to be at 2.6$\pm$0.8 MeV, an improvement of nearly an order of magnitude in precision over previous measurements. In addition, we calculate NuSTAR spectra in 26 pulse phase bins and confirm previously reported variations of photon indices with phase. Finally, we measure the pulsed fraction of PSR B1509$-$58 in the hard X-ray energy band for the first time. Using the energy resolved pulsed fraction results, we estimate that the pulsar's off-pulse emission has a photon index value between 1.26 and 1.96. Our results support a model in which the pulsar's lack of GeV emission is due to viewing geometry, with the X-rays originating from synchrotron emission from secondary pairs in the magnetosphere.Comment: 10 pages, 8 figures, 6 tables, ApJ accepte

Pathwise solutions of SPDEs driven by Hölder-continuous integrators with exponent larger than 1/2 and random dynamical systems

This article is devoted to the existence and uniqueness of pathwise solutions to stochastic evolution equations, driven by a Hölder continuous function with Hölder exponent in (1/2, 1), and with nontrivial multiplicative noise. As a particular situation, we shall consider the case where the equation is driven by a fractional Brownian motion BH with Hurst parameter H > 1/2. In contrast to the article by Maslowski and Nualart, we present here an existence and uniqueness result in the space of H¨older continuous functions with values in a Hilbert space V. If the initial condition is in the latter space this forces us to consider solutions in a different space, which is a generalization of the H¨older continuous functions. That space of functions is appropriate to introduce a non-autonomous dynamical system generated by the corresponding solution to the equation. In fact, when choosing BH as the driving process, we shall prove that the dynamical system will turn out to be a random dynamical system, defined over the ergodic metric dynamical system generated by the infinite dimensional fractional Brownian motion.National Basic Research Program of ChinaNatural Science Foundation of Jiangsu ProvinceJiangsu Higher Education Committee of ChinaEuropean Funds for Regional DevelopmentMinisterio de Economía y Competitivida

Observation of spin-orbit magnetoresistance in metallic thin films on magnetic insulators

A magnetoresistance effect induced by the Rashba spin-orbit interaction was predicted, but not yet observed, in bilayers consisting of normal metal and ferromagnetic insulator. Here, we present an experimental observation of this new type of spin-orbit magnetoresistance (SOMR) effect in a bilayer structure Cu[Pt]/Y3Fe5O12 (YIG), where the Cu/YIG interface is decorated with nanosize Pt islands. This new MR is apparently not caused by the bulk spin-orbit interaction because of the negligible spin-orbit interaction in Cu and the discontinuity of the Pt islands. This SOMR disappears when the Pt islands are absent or located away from the Cu/YIG interface, therefore we can unambiguously ascribe it to the Rashba spin-orbit interaction at the interface enhanced by the Pt decoration. The numerical Boltzmann simulations are consistent with the experimental SOMR results in the angular dependence of magnetic field and the Cu thickness dependence. Our finding demonstrates the realization of the spin manipulation by interface engineering.Comment: 12 pages, 4 figures, 14 pages in supplementary. To appear on Science Advance

Deletions in the neuraminidase stalk region of H2N2 and H9N2 avian influenza virus subtypes do not affect postinfluenza secondary bacterial pneumonia

We investigated the synergism between influenza virus and Streptococcus pneumoniae, particularly the role of deletions in the stalk region of the neuraminidase (NA) of H2N2 and H9N2 avian influenza viruses. Deletions in the NA stalk (ΔNA) had no effect on NA activity or on the adherence of S. pneumoniae to virus-infected human alveolar epithelial (A549) and mouse lung adenoma (LA-4) cells, although it delayed virus elution from turkey red blood cells. Sequential S. pneumoniae infection of mice previously inoculated with isogenic recombinant H2N2 and H9N2 influenza viruses displayed severe pneumonia, elevated levels of intrapulmonary proinflammatory responses, and death. No differences between the WT and ΔNA mutant viruses were detected with respect to effects on postinfluenza pneumococcal pneumonia as measured by bacterial growth, lung inflammation, morbidity, mortality, and cytokine/chemokine concentrations. Differences were observed, however, in influenza virus-infected mice that were treated with oseltamivir prior to a challenge with S. pneumoniae. Under these circumstances, mice infected with ΔNA viruses were associated with a better prognosis following a secondary bacterial challenge. These data suggest that the H2N2 and H9N2 subtypes of avian influenza A viruses can contribute to secondary bacterial pneumonia and deletions in the NA stalk may modulate its outcome in the context of antiviral therapy. © 2012, American Society for Microbiology.Fil: Chockalingam, Ashok K.. University of Maryland; Estados UnidosFil: Hickman, Danielle. University of Maryland; Estados UnidosFil: Pena, Lindomar. University of Maryland; Estados UnidosFil: Ye, Jianqiang. University of Maryland; Estados UnidosFil: Ferrero, Andrea. University of Maryland; Estados UnidosFil: Echenique, Jose Ricardo. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Córdoba. Centro de Investigaciones en Bioquímica Clínica e Inmunología; ArgentinaFil: Chen, Hongjun. University of Maryland; Estados UnidosFil: Sutton, Troy. University of Maryland; Estados UnidosFil: Perez, Daniel R.. University of Maryland; Estados Unido

Two-dimensional g-C3N4/Ca2Nb2TaO10 nanosheet composites for efficient visible light photocatalytic hydrogen evolution

Scalable g-CN nanosheet powder catalyst was prepared by pyrolysis of dicyandiamide and ammonium chloride followed by ultra-sonication and freeze-drying. Nanosheet composite that combines the g-CN nanosheets and CaNbTaO nanosheets with various ratios were developed and applied as photocatalysts for solar hydrogen generation. Systematic studies reveal that the g-CN/CaNbTaO nanosheet composite with a mass ratio of 80:20 shows the best performance in photocatalytic H evolution under visible light-irradiation, which is more than 2.8 times out-performing bare g-CN bulk. The resulting nanosheets possess a high surface area of 96\ua0m/g, which provides abundance active sites for the photocatalytic activity. More importantly, the g-CN/CaNbTaO nanosheet composite shows efficient charge transfer kinetics at its interface, as evident by the photoluminescence measurement. The intimate interfacial connections and the synergistic effect between g-CN nanosheets and CaNbTaO nanosheets with cascading electrons are efficient in suppressing charge recombination and improving photocatalytic H evolution performance

Selective production of hydrogen peroxide and oxidation of hydrogen sulfide in an unbiased solar photoelectrochemical cell

A solar-to-chemical conversion process is demonstrated using a photoelectrochemical cell without external bias for selective oxidation of hydrogen sulfide (H2S) to produce hydrogen peroxide (H2O2) and sulfur (S). The process integrates two redox couples anthraquinone/anthrahydroquinone and I−/I3−, and conceptually illustrates the remediation of a waste product for producing valuable chemicals