6,615 research outputs found

    A novel boundary element method using surface conductive absorbers for full-wave analysis of 3-D nanophotonics

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    Fast surface integral equation (SIE) solvers seem to be ideal approaches for simulating 3-D nanophotonic devices, as these devices generate fields both in an interior channel and in the infinite exterior domain. However, many devices of interest, such as optical couplers, have channels that can not be terminated without generating reflections. Generating absorbers for these channels is a new problem for SIE methods, as the methods were initially developed for problems with finite surfaces. In this paper we show that the obvious approach for eliminating reflections, making the channel mildly conductive outside the domain of interest, is inaccurate. We describe a new method, in which the absorber has a gradually increasing surface conductivity; such an absorber can be easily incorporated in fast integral equation solvers. Numerical experiments from a surface-conductivity modified FFT-accelerated PMCHW-based solver are correlated with analytic results, demonstrating that this new method is orders of magnitude more effective than a volume absorber, and that the smoothness of the surface conductivity function determines the performance of the absorber. In particular, we show that the magnitude of the transition reflection is proportional to 1/L^(2d+2), where L is the absorber length and d is the order of the differentiability of the surface conductivity function.Comment: 10 page

    Ignition criteria for x-ray fast ignition inertial confinement fusion

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    The derivation of the ignition energy for fast ignition inertial confinement fusion is reviewed and one-dimensional simulations are used to produce a revised formula for the ignition energy of an isochoric central hot-spot, which accounts for variation in the radius of the hot-spot r_h as well as the density rho. The required energy may be as low as 1 kJ when rho*r_h ~ 0:36 g cm^-2; T ~ 20 keV, and rho greater or equal to 700 g cm^-2. Although there are many physical challenges to creating these conditions, a possible route to producing such a hot-spot is via a bright source of nonthermal soft x-rays. Further one-dimensional simulations are used to study the non-thermal soft x-ray heating of dense DT and it is found to offer the potential to significantly reduce hydrodynamic losses as compared to particle driven fast ignition due to the hotspot being heated supersonically in a layer-by-layer fashion. A sufficiently powerful soft x-ray source would be difficult to produce, but line emission from laser-produced-plasma is the most promising option

    Multi-Q mesoscale magnetism in CeAuSb2_2

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    We report the discovery of a field driven transition from a striped to woven Spin Density Wave (SDW) in the tetragonal heavy fermion compound CeAuSb2_2. Polarized along c\bf c, the sinusoidal SDW amplitude is 1.8(2) μB\mu_B/Ce for T≪TNT \ll T_N=6.25(10) K with wavevector q1=(η,η,12){\bf q}_{1}=( \eta, \eta, \frac{1}{2} ) (η=0.136(2)\eta=0.136(2)). For H∥c{\bf H}\parallel{\bf c}, harmonics appearing at 2q12{\bf q}_{1} evidence a striped magnetic texture below μ∘Hc1=2.78(1)\mu_\circ H_{c1}=2.78(1) T. Above Hc1H_{c1}, these are replaced by woven harmonics at q1+q2=(2η,0,0)+c∗{\bf q}_{1}+{\bf q}_2=(2\eta, 0, 0)+{\bf c}^* until μ∘Hc2=5.42(5)\mu_\circ H_{c2}=5.42(5) T, where satellites vanish and magnetization non-linearly approaches saturation at 1.64(2) μB\mu_B/Ce for μ∘H≈7\mu_\circ H\approx 7 T.Comment: 5 pages, 4 figure

    Secondary anionic phospholipid binding site and gating mechanism in Kir2.1 inward rectifier channels

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    Inwardly rectifying potassium (Kir) channels regulate multiple tissues. All Kir channels require interaction of phosphatidyl-4,5-bisphosphate (PIP(2)) at a crystallographically identified binding site, but an additional nonspecific secondary anionic phospholipid (PL(−)) is required to generate high PIP(2) sensitivity of Kir2 channel gating. The PL(−)-binding site and mechanism are yet to be elucidated. Here we report docking simulations that identify a putative PL(−)-binding site, adjacent to the PIP(2)-binding site, generated by two lysine residues from neighbouring subunits. When either lysine is mutated to cysteine (K64C and K219C), channel activity is significantly decreased in cells and in reconstituted liposomes. Directly tethering K64C to the membrane by modification with decyl-MTS generates high PIP(2) sensitivity in liposomes, even in the complete absence of PL(−)s. The results provide a coherent molecular mechanism whereby PL(−) interaction with a discrete binding site results in a conformational change that stabilizes the high-affinity PIP(2) activatory site

    A phase-field model of Hele-Shaw flows in the high viscosity contrast regime

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    A one-sided phase-field model is proposed to study the dynamics of unstable interfaces of Hele-Shaw flows in the high viscosity contrast regime. The corresponding macroscopic equations are obtained by means of an asymptotic expansion from the phase-field model. Numerical integrations of the phase-field model in a rectangular Hele-Shaw cell reproduce finger competition with the final evolution to a steady state finger the width of which goes to one half of the channel width as the velocity increases

    Long-term Evolution of Protostellar and Protoplanetary Disks. I. Outbursts

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    As an initial investigation into the long-term evolution of protostellar disks, we explore the conditions required to explain the large outbursts of disk accretion seen in some young stellar objects. We use one-dimensional time-dependent disk models with a phenomenological treatment of the magnetorotational instability (MRI) and gravitational torques to follow disk evolution over long timescales. Comparison with our previous two-dimensional disk model calculations (Zhu et al. 2009b, Z2009b) indicates that the neglect of radial effects and two-dimensional disk structure in the one-dimensional case makes only modest differences in the results; this allows us to use the simpler models to explore parameter space efficiently. We find that the mass infall rates typically estimated for low-mass protostars generally result in AU-scale disk accretion outbursts, as predicted by our previous analysis (Zhu et al. 2009a,Z2009a). We also confirm quasi-steady accretion behavior for high mass infall rates if the values of α\alpha-parameter for the magnetorotational instability is small, while at this high accretion rate convection from the thermal instability may lead to some variations. We further constrain the combinations of the α\alpha-parameter and the MRI critical temperature, which can reproduce observed outburst behavior. Our results suggest that dust sublimation may be connected with full activation of the MRI. This is consistent with the idea that small dust captures ions and electrons to suppress the MRI. In a later paper we will explore both long-term outburst and disk evolution with this model, allowing for infall from protostellar envelopes with differing angular momenta.Comment: Accepted to publish in Ap

    Synergy between a collagen IV mimetic peptide and a somatotropin-domain derived peptide as angiogenesis and lymphangiogenesis inhibitors

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    Angiogenesis is central to many physiological and pathological processes. Here we show two potent bioinformatically-identified peptides, one derived from collagen IV and translationally optimized, and one from a somatotropin domain-containing protein, synergize in angiogenesis and lymphangiogenesis assays including cell adhesion, migration and in vivo Matrigel plugs. Peptide-peptide combination therapies have recently been applied to diseases such as human immunodeficiency virus (HIV), but remain uncommon thus far in cancer, age-related macular degeneration and other angiogenesis-dependent diseases. Previous work from our group has shown that the collagen IV-derived peptide primarily binds β1 integrins, while the receptor for the somatotropin-derived peptide remains unknown. We investigate these peptides’ mechanisms of action and find both peptides affect the vascular endothelial growth factor (VEGF) pathway as well as focal adhesion kinase (FAK) by changes in phosphorylation level and total protein content. Blocking of FAK both through binding of β1 integrins and through inhibition of VEGFR2 accounts for the synergy we observe. Since resistance through activation of multiple signaling pathways is a central problem of anti-angiogenic therapies in diseases such as cancer, we suggest that peptide combinations such as these are an approach that should be considered as a means to sustain anti-angiogenic and anti-lymphangiogenic therapy and improve efficacy of treatment
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