15,737 research outputs found

    Operator improvement for Ginsparg-Wilson fermions

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    The improvement of fermionic operators for Ginsparg-Wilson fermions is investigated. We present explicit formulae for improved Green's functions, which apply both on-shell and off-shell.Comment: 13 pages, Latex, 4 postscript figure

    Efficient quantum computation within a disordered Heisenberg spin-chain

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    We show that efficient quantum computation is possible using a disordered Heisenberg spin-chain with `always-on' couplings. Such disorder occurs naturally in nanofabricated systems. Considering a simple chain setup, we show that an arbitrary two-qubit gate can be implemented using just three relaxations of a controlled qubit, which amounts to switching the on-site energy terms at most twenty-one times.Comment: To appear in Phys. Rev.

    Semimetalic graphene in a modulated electric potential

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    The π\pi-electronic structure of graphene in the presence of a modulated electric potential is investigated by the tight-binding model. The low-energy electronic properties are strongly affected by the period and field strength. Such a field could modify the energy dispersions, destroy state degeneracy, and induce band-edge states. It should be noted that a modulated electric potential could make semiconducting graphene semimetallic, and that the onset period of such a transition relies on the field strength. There exist infinite Fermi-momentum states in sharply contrast with two crossing points (Dirac points) for graphene without external fields. The finite density of states (DOS) at the Fermi level means that there are free carriers, and, at the same time, the low DOS spectrum exhibits many prominent peaks, mainly owing to the band-edge states.Comment: 12pages, 5 figure

    Quenched chiral logarithms in lattice QCD with exact chiral symmetry

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    We examine quenched chiral logarithms in lattice QCD with overlap Dirac quark. For 100 gauge configurations generated with the Wilson gauge action at β=5.8 \beta = 5.8 on the 83×24 8^3 \times 24 lattice, we compute quenched quark propagators for 12 bare quark masses. The pion decay constant is extracted from the pion propagator, and from which the lattice spacing is determined to be 0.147 fm. The presence of quenched chiral logarithm in the pion mass is confirmed, and its coefficient is determined to be δ=0.203±0.014 \delta = 0.203 \pm 0.014 , in agreement with the theoretical estimate in quenched chiral perturbation theory. Further, we obtain the topological susceptibility of these 100 gauge configurations by measuring the index of the overlap Dirac operator. Using a formula due to exact chiral symmetry, we obtain the η′ \eta' mass in quenched chiral perturbation theory, mη′=(901±64) m_{\eta'} = (901 \pm 64) Mev, and an estimate of δ=0.197±0.027 \delta = 0.197 \pm 0.027 , which is in good agreement with that determined from the pion mass.Comment: 24 pages, 6 EPS figures; v2: some clarifications added, to appear in Physical Review

    Solutions of the Ginsparg-Wilson Relation

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    We analyze general solutions of the Ginsparg-Wilson relation for lattice Dirac operators and formulate a necessary condition for such operators to have non-zero index in the topologically nontrivial background gauge fields.Comment: 6 pages, latex, no figures, set T to 1 in eqs. (10)--(13

    Ceramic automotive Stirling engine study

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    A conceptual design study for a Ceramic Automotive Stirling Engine (CASE) is performed. Year 1990 structural ceramic technology is assumed. Structural and performance analyses of the conceptual design are performed as well as a manufacturing and cost analysis. The general conclusions from this study are that such an engine would be 10-26% more efficient over its performance map than the current metal Automotive Stirling Reference Engine (ASRE). Cost of such a ceramic engine is likely to be somewhat higher than that of the ASRE but engine cost is very sensitive to the ultimate cost of the high purity, ceramic powder raw materials required to fabricate high performance parts. When the design study is projected to the year 2000 technology, substantinal net efficiency improvements, on the order of 25 to 46% over the ASRE, are computed

    Dissociation of mitochondrial depolarization from cytochrome c release during apoptosis induced by photodynamic therapy

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    Photodynamic therapy (PDT) with the phthalocyanine photosensitizer Pc 4 induces rapid apoptosis in mouse lymphoma (LY-R) cells, initiating with the release of cytochrome c from mitochondria. It has been proposed that the opening of the mitochondrial membrane permeability transition pores, which results in the dissipation of the mitochondrial membrane potential (Δψm), is essential for the escape of cytochrome c from mitochondria into the cytosol as well as for apoptotic cell death. Therefore, we have assessed the correlation between the loss of Δψm and the release of cytochrome c following PDT. Treatment of LY-R cells with 300 nM Pc 4 and 60, 90 or 120 mJ/cm2of red light resulted in apoptosis of 80–90% of the cells, accompanied by >20-fold elevation in caspase-3-like activity within one h. At all 3 doses of PDT employed here, the majority of the cytochrome c was released from mitochondria at 15 min after irradiation, as determined by an immunohistochemical method. In contrast, the loss of Δψm following PDT, as monitored by the uptake of JC-1 or Rh-123, depended on the PDT dose and the post-treatment time. In spite of the release of cytochrome c at 15 min after each of the 3 doses, a corresponding loss of Δψm was observed only for those cells that received the highest dose of PDT. Virtually all cells that received one of the lower doses of PDT (300 nM Pc 4 plus 60 or 90 mJ/cm2) maintained normal Δψm. Hence, our results support the conclusion that the release of cytochrome c from mitochondria resulting from Pc 4-PDT-induced photodamage is independent of the loss of Δψm. Therefore, it is important to consider a range of doses of this or other apoptotic stimuli in deciphering the relationship of metabolic responses that contribute to apoptosis. © 2001 Cancer Research Campaign http://www.bjcancer.co
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