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11.
Disordered Sr2FeMoO6 shows a drastic reduction in saturation magnetization compared to highly ordered samples, moreover magnetization as a function of the temperature for different disordered samples shows qualitatively different behaviours. We investigate the origin of such diversity by performing spatially resolved photoemission spectroscopy on various disordered samples. Our results establish that extensive electronic inhomogeneity, arising most probably from an underlying chemical inhomogeneity in disordered samples, is responsible for the observed magnetic inhomogeneity. It is further pointed out that these inhomogeneities are connected with composition fluctuations of the type Sr2Fe1+x Mo1-x O6 with Fe-rich (x > 0) and Mo-rich (x < 0) regions. Dedicated to Prof J Gopalakrishnan on his 62nd birthday.  相似文献   
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Mesoporous polymer microspheres with gold (Au) nanoparticles inside their pores were prepared considering their surface functionality and porosity. The Au/polymer composite microspheres prepared were characterized by transmission electron microscope (TEM), X‐ray diffraction (XRD), and Brunauer–Emmett–Teller (BET) techniques. The results showed that the adsorption of Au nanoparticles could be increased by imparting the pore structure and surface‐functional groups into the supporting polymer microspheres (in this study, poly (ethylene glycol dimethacrylate‐co‐acrylonitrile) and poly (EGDMA‐co‐AN) system). Above all, from this study, it was established that the porosity of the polymer microspheres is the most important factor that determines the distribution and adsorption amount of face‐centered cubic (fcc) Au nanoparticles in the final products. Our study showed that the continuous adsorption of Au nanoparticles with the aid of the large surface area and surface interaction sites formed more favorably the Au/polymer composite microspheres. The BET measurements of Au/poly(EGDMA‐co‐AN) composite microspheres reveals that the adsorption of Au nanoparticles into the pores kept the pore structure intact and made it more porous. © 2004 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 42: 5627–5635, 2004  相似文献   
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Summary Single layers and layer systems on diverse substrates were measured by Total Reflection X-Ray Fluorescence (TXRF) spectrometry. The angular dependence of the fluorescence intensities at grazing incidence allows the elemental composition, density and thickness of the layers to be evaluated using model calculations.  相似文献   
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This paper provides exact and rigorous upper and lower bounds to the ground state energy of the Single Impurity Anderson Model in the limit of infiniteU. The upper bound approximates the ground state energy very well and the corresponding state may be used as a starting point for further investigations. The energy spectrum of the Single Impurity Anderson Model is calculated exactly for a special non-trivial model density of states describing the bare band electrons. All approaches introduced here are compared to this exact result and to other ground state energy calculations.  相似文献   
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The application, the advantage and limits of neutron monitoring techniques, such as Hf-monitors, fissile material accumulation and concentration monitors are being discussed. The active neutron counting technique applied to emptied pulsed extraction columns containing Hf-sieve plates allows conclusive answers as to the position of the plates in the columns. Pu-accumulations on Hf-sieve plates in pulsed extraction columns can be estimated within a factor of two, whereby the detection limit is about equal to or less than 1 g Pu/plate. Fissile material concentration changes of 1.1 g/l can be detected in the case of235U in solution and of 0.4 Pu/l if a239Pu/240Pu ratio of 4 to 1 is assumed.  相似文献   
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Ohne Zusammenfassung  相似文献   
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Induced ferroelectric S*C phases are formed by non-chiral SC host phases doped with chiral dipolar guest molecules. In those mixtures the spontaneous polarization Ps and the tilt angle Θ has been investigated as a function of the mole fraction xG of the chiral dopant. In most cases the reduced polarization P0 = PS/ sin Θ has been found to depend linearly on xG. The polarization power which is defined by δP=(∂P0/∂xGT is discussed in terms of the molecular structure of the chiral dopants. There are systems in which P0(xG) deviates positively from linearity. This behaviour can be understood by considering a local field correction to P0. By assuming a local field of Lorentz type a theoretical relation for P0(xG) has been derived which explains the experimental results. The effect of a local field is considerable if the transverse dipole moment and the polarizability of the chiral dopant are large.  相似文献   
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