3,458 research outputs found

    Quark Loop Contributions to Neutron, Deuteron, and Mercury EDMs from Supersymmetry without R parity

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    We present a detailed analysis of the neutron, deuteron and mercury electric dipole moment from supersymmetry without R parity, focusing on the quark-scalar loop contributions. Being proportional to top Yukawa and top mass, such contributions are often large. Analytical expressions illustrating the explicit role of the R-parity violating parameters are given following perturbative diagonalization of mass-squared matrices for the scalars. Dominant contributions come from the combinations Biλij1B_i \lambda^{\prime}_{ij1} for which we obtain robust bounds. It turns out that neutron and deuteron EDMs receive much stronger contributions than mercury EDM and any null result at the future deuteron EDM experiment or Los Alamos neutron EDM experiment can lead to extra-ordinary constraints on RPV parameter space. Even if R-parity violating couplings are real, CKM phase does induce RPV contribution and for some cases such a contribution is as strong as contribution from phases in the R-parity violating couplings.Hence, we have bounds directly on Biλij1|B_i \lambda^{\prime}_{ij1}| even if the RPV parameters are all real. Interestingly, even if slepton mass and/or μ0\mu_0 is as high as 1 TeV, it still leads to neutron EDM that is an order of magnitude larger than the sensitivity at Los Alamos experiment. Since the results are not much sensitive to tanβ\tan \beta, our constraints will survive even if other observables tighten the constraints on tanβ\tan \beta.Comment: 16 pages, 10 figures, accepted for publication in Physical Review

    Charge transfer in nanocrystalline-Au/ZnO nanorods investigated by x-ray spectroscopy and scanning photoelectron microscopy

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    [[abstract]]O K- and Zn and Au L3-edge x-ray absorption near-edge structure (XANES), x-ray emission spectroscopy (XES), and scanning photoelectron microscopy (SPEM) are performed to investigate the electronic structure of ZnO nanorods with nanocrystalline (nc)-Au particles grown on the surfaces. The XANES spectra of nc-Au/ZnO nanorods reveal the decrease of the number of both O 2p and Zn 4s/3d unoccupied states with the increase of the nc-Au particle size. The number of Au 6s/5d unoccupied states increases when the size of nc-Au particle decreases, indicating that the deposition of nc-Au particles on the surface of ZnO nanorods promotes charge transfer from the ZnO nanorods to nc-Au particles. Excitation energy dependent XES and SPEM spectra show that the number of electrons in the valence band of O 2p-Zn 4sp hybridized states decreases as the nc-Au particle size increases, revealing that more electrons are excited from the valence band to the conduction band of ZnO nanorods and the storage of electrons in nc-Au particles.[[journaltype]]國外[[incitationindex]]SCI[[cooperationtype]]國內[[booktype]]紙本[[countrycodes]]US

    Electronic structure of ZnO nanorods studied by angle-dependent x-ray absorption spectroscopy and scanning photoelectron microscopy

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    [[abstract]]Angle-dependent x-ray absorption near-edge structure (XANES) and scanning photoelectron microscopy measurements were performed to differentiate local electronic structures at the tips and sidewalls of highly aligned ZnO nanorods. The overall intensity of the O K-edge XANES spectra is greatly enhanced for small photon incident angles. In contrast, the overall intensity of the Zn K-edge XANES is much less sensitive to the photon incident angle. Both valence-band photoemission and O K-edge XANES spectra show substantial enhancement of O 2p derived states near the valence band maximum and conduction band minimum, respectively. The spatially resolved Zn 3d core level spectra from tip and sidewall regions show the lack of chemical shift. All the results consistently suggest that the tip surfaces of the highly aligned ZnO nanorods are terminated by O ions and the nanorods are oriented in the [0001¯] direction. © 2004 American Institute of Physics.[[notice]]補正完畢[[booktype]]紙本[[booktype]]電子

    Electronic structure of the carbon nanotube tips studied by x-ray-absorption spectroscopy and scanning photoelectron microscopy

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    [[abstract]]Angle-dependent x-ray absorption near edge structure (XANES) and scanning photoelectron microscopy (SPEM) measurements have been performed to differentiate local electronic structures of the tips and sidewalls of highly aligned carbon nanotubes. The intensities of both π∗- and σ∗-band C K-edge XANES features are found to be significantly enhanced at the tip. SPEM results also show that the tips have a larger density of states and a higher C 1s binding energy than those of sidewalls. The increase of the tip XANES and SPEM intensities are quite uniform over an energy range wider than 10 eV in contrast to earlier finding that the enhancement is only near the Fermi level.[[booktype]]紙本[[booktype]]電子

    Diameter dependence of the electronic structure of ZnO nanorods determined by x-ray absorption spectroscopy and scanning photoelectron microscopy

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    [[abstract]]O K-, Zn L3, and K-edges x-ray absorption near-edge structure (XANES) spectra and scanning photoelectron microscopy (SPEM) spectra were obtained for ZnO nanorods with various diameters. The analysis of the XANES spectra revealed increased numbers of O 2p and Zn 4p unoccupied states with the downsizing of the nanorods, which reflects the enhancement of surface states when the diameter is decreased. Valence-band photoemission spectra show a significant narrowing of the valence band for the 45 nm diameter nanorod. The Zn 3d intensities in the Zn 3d SPEM spectra are drastically diminished for all nanorods as compared to the ZnO reference film, which can be interpreted as a reduction in density of itinerant final states or in transition probability.[[notice]]補正完畢[[incitationindex]]SCI[[booktype]]紙

    Angle-dependent x-ray absorption spectroscopy study of Zn-doped GaN

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    [[abstract]]As-grown and Zn-implanted wurtzite GaN samples have been studied by angle-dependent x-ray absorption near edge structure (XANES) measurements at the N and Ga K-edges and the Ga L3-edge. The angle dependence of the XANES spectra shows that the Ga–N bonds lying in the bilayer have lower energies than bonds along the c-axis, which can be attributed to the polar nature of the GaN film. The comparison of the Ga L3-edge XANES spectra of as-grown and Zn-doped GaN reveals significant dopant induced enhancement of near-edge Ga d-derived states. © 2002 American Institute of Physics.[[journaltype]]國外[[incitationindex]]SCI[[booktype]]紙本[[countrycodes]]US

    Ultrasonic Flaw Classification Using a Quasi-Pulse-Echo Technique

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    In solving ultrasonic flaw characterization problems, flaw type information is often needed in order to pursue succeeding tasks such as flaw sizing. In a typical inspection, the interaction of the incident ultrasonic pulse with the flaw results in a series of signal trains. A variety of signal features are extracted from these flaw signals and then used as the basis for the classification process. This classification process is made difficult by the large number of possible scattered waves. For example, typical ultrasonic signals from a planar crack-like defect consist of reflected responses, surface traveling waves, edge diffracted waves and head wave components. For a volumetric void-like defect, the returned signal pattern similarly contains reflected waves of the same mode as well as mode-converted reflections and “creeping” waves. However, in pulse-echo testing a fundamental difference exists between a crack-like flaw and a volumetric flaw that can be used for classification purposes. This difference is reflected in the fact that a significant mode-converted diffracted wave component can exist for a crack-like defect (Fig. 1(a)) which does not exist in pulse-echo testing for a volumetric defect (Fig.1(b))

    Tumor Angiogenesis as a Target for Dietary Cancer Prevention

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    Between 2000 and 2050, the number of new cancer patients diagnosed annually is expected to double, with an accompanying increase in treatment costs of more than $80 billion over just the next decade. Efficacious strategies for cancer prevention will therefore be vital for improving patients' quality of life and reducing healthcare costs. Judah Folkman first proposed antiangiogenesis as a strategy for preventing dormant microtumors from progressing to invasive cancer. Although antiangiogenic drugs are now available for many advanced malignancies (colorectal, lung, breast, kidney, liver, brain, thyroid, neuroendocrine, multiple myeloma, myelodysplastic syndrome), cost and toxicity considerations preclude their broad use for cancer prevention. Potent antiangiogenic molecules have now been identified in dietary sources, suggesting that a rationally designed antiangiogenic diet could provide a safe, widely available, and novel strategy for preventing cancer. This paper presents the scientific, epidemiologic, and clinical evidence supporting the role of an antiangiogenic diet for cancer prevention
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