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  • 1
    Electronic Resource
    Electronic Resource
    Oxford, UK : Blackwell Publishing Ltd
    Annals of the New York Academy of Sciences 588 (1990), S. 0 
    ISSN: 1749-6632
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Natural Sciences in General
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    Analytical chemistry 53 (1981), S. 2157-2158 
    ISSN: 1520-6882
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    The @journal of organic chemistry 48 (1983), S. 2555-2557 
    ISSN: 1520-6904
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    The @journal of organic chemistry 41 (1976), S. 1939-1943 
    ISSN: 1520-6904
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    The @journal of physical chemistry 〈Washington, DC〉 94 (1990), S. 8025-8028 
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology , Physics
    Type of Medium: Electronic Resource
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  • 6
    Electronic Resource
    Electronic Resource
    [S.l.] : American Institute of Physics (AIP)
    Journal of Applied Physics 69 (1991), S. 7723-7726 
    ISSN: 1089-7550
    Source: AIP Digital Archive
    Topics: Physics
    Notes: Composite samples of PrBa2Cu3O7-GdBa2Cu3O7 have been fabricated with the nominal GdBa2Cu3O7 volume fraction φ ranging from 0.00 to 1.00. Resistivity and magnetization measurements performed on the samples are interpreted in terms of sample structure composed of GdBa2Cu3O7 and PrBa2Cu3O7 grains embedded in a Gd1−xPrxBa2Cu3O7 matrix. The Pr concentration x as a function of φ is established by inferring it from the superconducting transition temperature Tc. In particular, both the resistivities and magnetizations show drastic changes when φ exceeds about 0.6. This is the value of φ at which x first exceeds a critical value of about 0.5 and where the Gd1−xPrxBa2Cu3O7 matrix first superconducts. The Gd1−xPrxBa2Cu3O7 phase is presumably formed during the high temperature (900 °C) firing process which results in mutual substitution between the Gd and Pr atoms.
    Type of Medium: Electronic Resource
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  • 7
    Electronic Resource
    Electronic Resource
    [S.l.] : American Institute of Physics (AIP)
    Journal of Applied Physics 73 (1993), S. 5871-5873 
    ISSN: 1089-7550
    Source: AIP Digital Archive
    Topics: Physics
    Notes: The pressure effect on the superconducting transition temperature (dTc/dP) has been measured for Dy1−xPrxBa2Cu3O7−δ with x=0, 0.02, 0.05, 0.1, 0.15, 0.2, and 0.3. Although the Tc suppression by Pr is in a different fashion for Y1−xPrxBa2Cu3O7−δ and Dy1−xPrxBa2Cu3O7−δ, the dTc/dP is similar in these two systems, with respect to x. The measured dTc/dP is positive at small x but becomes negative for x≥0.2 which is associated with the pressure effect on the normal-state resistivity (1/R)(dR/dP). The positive (1/R)(dR/dP) at x≥0.2 indicates that the number of carriers is decreasing under pressure and it supports the picture of hole localization through the hybridization of Pr-4f and O-2p bands. The mechanical pressure has a negative effect on Tc for x≥0.2, but chemical pressure has a positive effect on Tc according to the results of chemical substitution. This suggests that the large R (=rare earth element) may possibly reduce the Pr-O distance, and increase the hybridization of Pr-4f and O-2p bands.
    Type of Medium: Electronic Resource
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  • 8
    Electronic Resource
    Electronic Resource
    [S.l.] : American Institute of Physics (AIP)
    Journal of Applied Physics 69 (1991), S. 6701-6703 
    ISSN: 1089-7550
    Source: AIP Digital Archive
    Topics: Physics
    Notes: Persistent photoconductivity (PPC) mechanisms, as well as the similarities and the differences of PPC properties in II-VI and III-V semiconductor alloys have been investigated. The potential applications based on PPC phenomenon in these two kinds of materials are discussed. We have observed that PPC induced in a II-VI mixed crystal by visible (above band gap) illumination can be quenched by long wavelength infrared radiation even at room temperature, which further supports our interpretation that PPC in II-VI mixed crystals is caused by random local potential fluctuations induced by compositional fluctuations. A newly developed infrared detector based on the PPC infrared quenching property of II-VI semiconductor alloys is also reported.
    Type of Medium: Electronic Resource
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  • 9
    Electronic Resource
    Electronic Resource
    [S.l.] : American Institute of Physics (AIP)
    Journal of Applied Physics 68 (1990), S. 985-993 
    ISSN: 1089-7550
    Source: AIP Digital Archive
    Topics: Physics
    Notes: The transition character of paraelectric-to-ferroelectric phase transition and its relation to lattice soft-mode behavior in the solid solutions of (Ba,Sr)TiO3, (Ba,Ca)TiO3, Ba(Ti,Zr)O3, and Ba(Ti,Sn)O3 were investigated by the measurements of dielectric constants in the temperature range from −30 to 150 °C, and x-ray line breadth of 100, 110, and 111 Bragg reflections at temperatures above the transition point. From the result of dielectric measurement, it was found that the specimens containing Ti-site substituents have shown a diffuse phase transition character, whereas those having Ba-site substituents have preserved a sharp phase transition. It was also noted from the change of line breath of Bragg reflections that for the solutions of Ba(Ti,Zr)O3 and Ba(Ti,Sn)O3, the high dynamic strain at the 〈1 0 0〉 axis, induced from the soft-mode of lattice vibration, become repressed when a large amount of solutes is contained, but for the solutions of (Ba,Sr)TiO3 and (Ba,Ca)TiO3, it is recovered at temperatures near the transition point. Moreover, the dynamic strain at the 〈1 1 1〉 axis can be rapidly repressed by the addition of Ti-site substituents. The different effects on the dynamic strains are attributed to the disparate distortions of oxygen octahedra in the perovskite lattice, induced by the solutes of different site substitution. It is also believed that the influence on the soft-mode of lattice vibration has caused the different phase transition characters of the four BaTiO3 solid solutions.
    Type of Medium: Electronic Resource
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  • 10
    Electronic Resource
    Electronic Resource
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 90 (1989), S. 5135-5145 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: The existence of Cu overlayers on O/W(110) and CO/W(110) was investigated using thermal desorption, work function, UPS, XPS, and energy loss measurements. It was shown that these layers exist and have very different properties from O/Cu/W(110) and CO/Cu/W(110), respectively. The most striking fact is that the work function at Cu monolayer coverage (slightly higher in the case of CO/W(110), probably because of Cu second layer formation and gaps in the first Cu layer) is almost that of Cu1/W(110) regardless of the underlying adsorbate. HeI UPS spectra show a Cu d-band structure even at Cu submonolayer coverages for Cu/O/W and for Cu1/CO/W(110). A loss peak at 4.64 eV was found for both systems [and for Cu8/W(110)] at θCu≥0.2 for O/W(110), and at θCu≥0.6 for CO/W(110). This is tentatively interpreted as a Cu interband transition. Unexpectedly small shifts in Cu2p3/2 and O1s binding energies were found under all conditions; the reasons for the virtual absence of shifts are not understood. The main conclusion of this work is that overlayers of Cu on top of other adsorbates show metallic properties even at submonolayer Cu coverages.
    Type of Medium: Electronic Resource
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