47,750 research outputs found

    Semi-Finite Forms of Bilateral Basic Hypergeometric Series

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    We show that several classical bilateral summation and transformation formulas have semi-finite forms. We obtain these semi-finite forms from unilateral summation and transformation formulas. Our method can be applied to derive Ramanujan's 1ψ1_1\psi_1 summation, Bailey's 2ψ2_2\psi_2 transformations, and Bailey's 6ψ6_6\psi_6 summation.Comment: 8 pages. accepted by Proc. Amer. Math. So

    Calibration of the Pulsed Electroacoustic Technique in the Presence of Trapped Charge

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    The influence of pulse voltage on the accuracy of charge density distribution in the pulsed electroacoustic technique (PEA) is discussed. It is shown that significant error can be introduced if a low dc voltage and high pulse voltage are used to calibrate charge density. However, our main focus in the present paper is to deal with one of the practical situations where space charge exists in the material prior to any measurements. The conventional calibration method can no longer be used to calibrate charge density due to the interference by the charge on the electrode induced by space charge. A method has been proposed which is based on two measurements. Firstly, the sample containing charge is measured without any applied voltage. The second measurement is carried out with a small external applied voltage. The applied voltage should be small enough so there is no disturbance of the existing charge in the sample. The difference of the two measurements can be used for calibration. An additional advantage of the proposed method avoids the influence of the pulse voltage on calibration and therefore gives a more accurate representation of space charge. The proposed method has been validated

    Spherical to deformed shape transition in the nucleon-pair shell model

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    A study of the shape transition from spherical to axially deformed nuclei in the even Ce isotopes using the nucleon-pair approximation of the shell model is reported. As long as the structure of the dominant collective pairs is determined using a microscopic framework appropriate to deformed nuclei, the model is able to produce a shape transition. However, the resulting transition is too rapid, with nuclei that should be transitional being fairly well deformed, perhaps reflecting the need to maintain several pairs with each angular momentum.Comment: 7 pages, 5 figure

    Residual proton-neutron interactions and the NpNnN_{\rm p} N_{\rm n} scheme

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    We investigate the correlation between integrated proton-neutron interactions obtained by using the up-to-date experimental data of binding energies and the NpNnN_{\rm p} N_{\rm n}, the product of valence proton number and valence neutron number with respect to the nearest doubly closed nucleus. We make corrections on a previously suggested formula for the integrated proton-neutron interaction. Our results demonstrate a nice, nearly linear, correlation between the integrated p-n interaction and NpNnN_{\rm p} N_{\rm n}, which provides us with a firm foundation of the applicability of the NpNnN_{\rm p} N_{\rm n} scheme to nuclei far from the stability line.Comment: four pages, three figures, Physical Review C, in pres

    Faulhaber's Theorem on Power Sums

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    We observe that the classical Faulhaber's theorem on sums of odd powers also holds for an arbitrary arithmetic progression, namely, the odd power sums of any arithmetic progression a+b,a+2b,...,a+nba+b, a+2b, ..., a+nb is a polynomial in na+n(n+1)b/2na+n(n+1)b/2. While this assertion can be deduced from the original Fauhalber's theorem, we give an alternative formula in terms of the Bernoulli polynomials. Moreover, by utilizing the central factorial numbers as in the approach of Knuth, we derive formulas for rr-fold sums of powers without resorting to the notion of rr-reflexive functions. We also provide formulas for the rr-fold alternating sums of powers in terms of Euler polynomials.Comment: 12 pages, revised version, to appear in Discrete Mathematic

    Local Spin Susceptibility of the S=1/2 Kagome Lattice in ZnCu3(OD)6Cl2

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    We report single-crystal 2-D NMR investigation of the nearly ideal spin S=1/2 kagome lattice ZnCu3(OD)6Cl2. We successfully identify 2-D NMR signals originating from the nearest-neighbors of Cu2+ defects occupying Zn sites. From the 2-D Knight shift measurements, we demonstrate that weakly interacting Cu2+ spins at these defects cause the large Curie-Weiss enhancement toward T=0 commonly observed in the bulk susceptibility data. We estimate the intrinsic spin susceptibility of the kagome planes by subtracting defect contributions, and explore several scenarios.Comment: 4 figures; published in PR-B Rapid Communication

    The structure of electronic polarization and its strain dependence

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    The \phi(\kpp)\sim \kpp relation is called polarization structure. By density functional calculations, we study the polarization structure in ferroelectric perovskite PbTiO3_3, revealing (1) the \kpp point that contributes most to the electronic polarization, (2) the magnitude of bandwidth, and (3) subtle curvature of polarization dispersion. We also investigate how polarization structure in PbTiO3_3 is modified by compressive inplane strains. The bandwidth of polarization dispersion in PbTiO3_3 is shown to exhibit an unusual decline, though the total polarization is enhanced. As another outcome of this study, we formulate an analytical scheme for the purpose of identifying what determine the polarization structure at arbitrary \kpp points by means of Wannier functions. We find that \phi(\kpp) is determined by two competing factors: one is the overlaps between neighboring Wannier functions within the plane {\it perpendicular} to the polarization direction, and the other is the localization length {\it parallel} to the polarization direction. Inplane strain increases the former while decreases the latter, causing interesting non-monotonous effects on polarization structure. Finally, polarization dispersion in another paradigm ferroelectric BaTiO3_3 is discussed and compared with that of PbTiO3_3.Comment: 5 Figure
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