131 research outputs found

    Static and dynamic magnetic properties of densely packed magnetic nanowire arrays

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    PublishedJournal ArticleThe static and dynamic magnetic properties of magnetic nanowire arrays with high packing density (>0.4) and wire diameter much greater than the exchange length have been studied by static and time-resolved magneto-optical Kerr effect measurements and micromagnetic simulations. The nanowires were formed by electrodeposition within a nanoporous template such that their symmetry axes lay normal to the plane of the substrate. A quantitative and systematic investigation has been made of the static and dynamic properties of the array, which lie between the limiting cases of a single wire and a continuous ferromagnetic thin film. In particular, the competition between anisotropies associated with the shape of the individual nanowires and that of the array as a whole has been studied. Measured and simulated hysteresis loops are largely anhysteretic with zero remanence, and the micromagnetic configuration is such that the net magnetization vanishes in directions orthogonal to the applied field. Simulations of the remanent state reveal antiferromagnetic alignment of the magnetization in adjacent nanowires and the formation of vortex flux closure structures at the ends of each nanowire. The excitation spectra obtained from experiment and micromagnetic simulations are in qualitative agreement for magnetic fields applied both parallel and perpendicular to the axes of the nanowires. For the field parallel to the nanowire axes, there is also good quantitative agreement between experiment and simulation. The resonant frequencies are initially found to decrease as the applied field is increased from remanence. This is the result of a change of mode profile within the plane of the array from nonuniform to uniform as the ground state evolves with increasing applied field. Quantitative differences between experimental and simulated spectra are observed when the field is applied perpendicular to the nanowire axes. The dependence of the magnetic excitation spectra upon the array packing density is explored, and dispersion curves for spin waves propagating within the array parallel to the nanowire axis are presented. Finally, a tunneling of end modes through the middle region of the nanowires was observed. The tunneling is more efficient for wires forming densely packed arrays, as a result of the extended penetration of the dynamic demagnetizing fields into the middle of the wires and due to the lowering of the tunneling barrier by the static demagnetizing field of the array. © 2013 American Physical Society.The authors gratefully acknowledge the assistance of V.-A. Antohe and S. Tuilard with sample fabrication and M. Dvornik, M. Franchin, and H. Fangohr with micromagnetic simulations. The financial support from the European Community’s Seventh Framework Programme (FP7/2007-2013) under Grant Agreements No. 212257 MASTER (fabrication and experiment) and No. 233552 DYNAMAG (simulations) is gratefully acknowledged. We also gratefully acknowledge financial support from a UKIERI-DST standard research award (Grants No. SA 07-021 and No. DST/INT/UKIERI/SA/P- 2/2008) for travel between S. N. B. N. C. B. S., India, and the University of Exeter, United Kingdom. Finally, V.V.K. gratefully acknowledges funding received from the U.K. Engineering and Physical Sciences Research Council Project No. EP/E055087/1

    Salmonella-Induced Mucosal Lectin RegIIIÎČ Kills Competing Gut Microbiota

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    Intestinal inflammation induces alterations of the gut microbiota and promotes overgrowth of the enteric pathogen Salmonella enterica by largely unknown mechanisms. Here, we identified a host factor involved in this process. Specifically, the C-type lectin RegIIIÎČ is strongly upregulated during mucosal infection and released into the gut lumen. In vitro, RegIIIÎČ kills diverse commensal gut bacteria but not Salmonella enterica subspecies I serovar Typhimurium (S. Typhimurium). Protection of the pathogen was attributable to its specific cell envelope structure. Co-infection experiments with an avirulent S. Typhimurium mutant and a RegIIIÎČ-sensitive commensal E. coli strain demonstrated that feeding of RegIIIÎČ was sufficient for suppressing commensals in the absence of all other changes inflicted by mucosal disease. These data suggest that RegIIIÎČ production by the host can promote S. Typhimurium infection by eliminating inhibitory gut microbiota

    Palladium nanoparticles supported on fluorine-doped tin oxide as an efficient heterogeneous catalyst for Suzuki coupling and 4-nitrophenol reduction

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    Immobilization of palladium nanoparticles onto the fluorine-doped tin oxide (FTO) as support Pd/FTO, resulted in a highly active heterogeneous catalyst for Suzuki-Miyaura cross-coupling reactions and 4-nitrophenol reduction. The Pd/FTO catalyst has been synthesized by immobilization of palladium nanoparticles onto FTO via a simple impregnation method. ICP-MS analysis confirmed that there is 0.11 mmol/g of palladium was loaded successfully on FTO support. The crystallinity, morphologies, compositions and surface properties of Pd/FTO were fully characterized by various techniques. It was further examined for its catalytic activity and robustness in Suzuki coupling reaction with different aryl halides and solvents. The yields obtained from Suzuki coupling reactions were basically over 80%. The prepared catalyst was also tested on mild reaction such as reduction of 4-nitrophenol (4-NP) to 4-aminophenol (4-AP). Pd/FTO catalyst exhibited high catalytic activity towards 4-NP reduction with a rate constant of 1.776 min(-1) and turnover frequency (TOF) value of 29.1 hr(-1). The findings revealed that Pd/FTO also maintained its high stability for five consecutive runs in Suzuki reactions and 4-NP reductions. The catalyst showed excellent catalytic activities by using a small amount of Pd/FTO for the Suzuki coupling reaction and 4-NP reduction

    The Microbiota Mediates Pathogen Clearance from the Gut Lumen after Non-Typhoidal Salmonella Diarrhea

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    Many enteropathogenic bacteria target the mammalian gut. The mechanisms protecting the host from infection are poorly understood. We have studied the protective functions of secretory antibodies (sIgA) and the microbiota, using a mouse model for S. typhimurium diarrhea. This pathogen is a common cause of diarrhea in humans world-wide. S. typhimurium (S. tmatt, sseD) causes a self-limiting gut infection in streptomycin-treated mice. After 40 days, all animals had overcome the disease, developed a sIgA response, and most had cleared the pathogen from the gut lumen. sIgA limited pathogen access to the mucosal surface and protected from gut inflammation in challenge infections. This protection was O-antigen specific, as demonstrated with pathogens lacking the S. typhimurium O-antigen (wbaP, S. enteritidis) and sIgA-deficient mice (TCRÎČ−/−ή−/−, JH−/−, IgA−/−, pIgR−/−). Surprisingly, sIgA-deficiency did not affect the kinetics of pathogen clearance from the gut lumen. Instead, this was mediated by the microbiota. This was confirmed using ‘L-mice’ which harbor a low complexity gut flora, lack colonization resistance and develop a normal sIgA response, but fail to clear S. tmatt from the gut lumen. In these mice, pathogen clearance was achieved by transferring a normal complex microbiota. Thus, besides colonization resistance ( = pathogen blockage by an intact microbiota), the microbiota mediates a second, novel protective function, i.e. pathogen clearance. Here, the normal microbiota re-grows from a state of depletion and disturbed composition and gradually clears even very high pathogen loads from the gut lumen, a site inaccessible to most “classical” immune effector mechanisms. In conclusion, sIgA and microbiota serve complementary protective functions. The microbiota confers colonization resistance and mediates pathogen clearance in primary infections, while sIgA protects from disease if the host re-encounters the same pathogen. This has implications for curing S. typhimurium diarrhea and for preventing transmission
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