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11.
We prove the converse of Raubenheimer and Rode's Banach algebra version of the Perron-Frobenius Theorem.

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The aim of this paper is to describe some results concerning the geometry of Lorentzian manifolds admitting Killing spinors. We prove that there are imaginary Killing spinors on simply connected Lorentzian Einstein–Sasaki manifolds. In the Riemannian case, an odd-dimensional complete simply connected manifold (of dimension n≠7) is Einstein–Sasaki if and only if it admits a non-trivial Killing spinor to . The analogous result does not hold in the Lorentzian case. We give an example of a non-Einstein Lorentzian manifold admitting an imaginary Killing spinor. A Lorentzian manifold admitting a real Killing spinor is at least locally a codimension one warped product with a special warping function. The fiber of the warped product is either a Riemannian manifold with a real or imaginary Killing spinor or with a parallel spinor, or it again is a Lorentzian manifold with a real Killing spinor. Conversely, all warped products of that form admit real Killing spinors.  相似文献   
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The exciton-exciton interaction is investigated for spatially indirect excitons in coupled quantum wells. The Hartree-Fock and Heitler-London approaches are improved by a full two-exciton calculation including the van der Waals effect. Using these potentials for the singlet and triplet channel, the two-body scattering matrix is calculated and employed to derive a modified relation between exciton density and blue shift. Such a relation is of central importance for gauging exciton densities on the way toward Bose condensation.  相似文献   
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We prove that the average order of the remainder in counting the number of points of a random lattice inside a disc of radius . Our proof is spectral in nature. Submitted: July 2001, Revised: August 2001, Revised: March 2002.  相似文献   
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We determine the limiting density of the zeroes of Heine–Stieltjes polynomials (or of any set of points satisfying the conclusion of Heine–Stieltjes Theorem) in the thermodynamic limit and use this to prove a strong law of large numbers for the zeroes.  相似文献   
20.
The single ion activity coefficients of hydrogen and chloride ions in aqueous HCl solutions have been estimated at 25°C at concentrations up to 1 mol-kg–1, using potentiometric measurements with ion-selective electrodes and appropriate calibration procedures. Two methods are described for an internal calibration of the electrodes in the extended Debye–Hückel concentration range. The results are compared to the conventional pH calibration with external buffer solutions. Since the latter calibration method does not account for the liquid junction potential E J which arises at the reference electrode, the resulting activity coefficients are quite different in HCl solutions of higher concentration. These differences between internal and external calibration decrease significantly, when a correction for E J is introduced into the conventional pH calibration. Hence, in solutions of higher ionic strength the accuracy of the conventional pH electrode calibration using buffer solutions is very limited, when exact H+ activities are required. The consistency of the results indicates that the liquid junction potentials in the examined systems calculated by the Henderson/Bates approximation are of reasonable precision.  相似文献   
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