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  • 1
    Electronic Resource
    Electronic Resource
    [S.l.] : International Union of Crystallography (IUCr)
    Acta crystallographica 38 (1982), S. 177-186 
    ISSN: 1600-5724
    Source: Crystallography Journals Online : IUCR Backfile Archive 1948-2001
    Topics: Chemistry and Pharmacology , Geosciences , Physics
    Notes: The A-cation-deficient perovskite, Th0.25NbO3, i.e. ThNb4O12, when slowly cooled from the melt, presents an interesting hierarchy of ordering phenomena. The associated diffraction effects have been studied with electron microscopy/diffraction and X-ray diffraction techniques. Three main types of ordering processes occur, with different degrees of long-range order. A primary ordering of thorium atoms into alternate (001)p planes of A-cation sites (cell ap × bp × 2cp, P4/mmm) exhibits well-established long-range ordering. A secondary ordering of thorium atoms within the (001)p planes (cell 3\sqrt{2\alpha_{p}} × \sqrt{2b_{p}} × 4cp, Immm) is short range in nature and gives rise to superlattice reflections in the form of diffuse rods directed along g(110)p and g(\bar 110)p. The length of the rods corresponds to correlation lengths of only 20-30 Å between {110}p planes of thorium atoms, and the thorium/ vacancy ordering is adequately described by a sinusoidal modulation model, with accompanying modulated displacements of niobium and oxygen atoms. Thirdly, a system of octahedral tilts about [110]p or [\bar 110]p axes is described by a cell \sqrt{2\alpha _{p}} × \sqrt{2b_{p}} × 2cp, Pmam. Independent models for thorium/ vacancy ordering and octahedral tilts have been refined with the intensities of the corresponding groups of satellites measured from precession photographs. The complete model for ThNb4O12 can be described in the unit cell 3\sqrt{2\alpha _{p}} × \sqrt{2b_{p}} × 4cp, P2mm. The superlattice reflections arising from the octahedral tilts are split into groups of four satellites in the form of crosses, owing to microdomain formation in ThNb4O12, with domain boundaries parallel to (100)p and (010)p and with average widths of 2̃5 Å.
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  • 2
    Electronic Resource
    Electronic Resource
    [S.l.] : International Union of Crystallography (IUCr)
    Acta crystallographica 38 (1982), S. 753-761 
    ISSN: 1600-5724
    Source: Crystallography Journals Online : IUCR Backfile Archive 1948-2001
    Topics: Chemistry and Pharmacology , Geosciences , Physics
    Notes: Electron diffraction/microscopy and X-ray diffraction techniques have been used to study the thorium/ vacancy ordering and microdomain structures of quenched and slow-cooled samples of the A-cation deficient perovskite-related phase ThNb4O12. In both types of samples, there is primary ordering of thorium atoms into the cuboctahedral sites in alternate (001)p layers. The quenched and slow-cooled samples have different secondary orderings of thorium atoms and vacancies in the occupied (001)p layers. In the quenched samples, the thorium atoms and vacancies are ordered in alternate rows parallel to [100]p and [010]p. Short segments (20-50 Å) of the two orientation variants are statistically distributed in a type of tweed pattern, separated by boundaries that are aligned predominantly parallel to (110)p and ({\bar 1}10)p. In the slow-cooled samples, the ordering of columns of thorium atoms and vacancies parallel to [110]p or [{\bar 1}10]p occurs in microdomains, with domain boundaries parallel to (100)p and (010)p and with average separations of 6ap, 6bp ≡ 24 Å. The domains corresponding to the two orientations of thorium columns form a checkerboard pattern of two interpenetrating sets of corner-shared squares. In either set, the ordering of columns is propagated along diagonal rows of corner-shared domains, but there is no correlation between adjacent rows. The NbO6 octahedra are tilted about the [110]p and [{\bar 1}10]p axes, parallel to the thorium-column orientations, and the domain boundaries act as mirror-twin planes for the octahedral tilt systems. This periodic change in the tilt-axis orientation gives rise to characteristic clusters of split superlattice spots in the diffraction patterns for ThNb4O12. Optical transform methods were used to check the validity of microdomain models for both the quenched and the slow-cooled samples.
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  • 3
    Electronic Resource
    Electronic Resource
    [S.l.] : American Institute of Physics (AIP)
    Journal of Applied Physics 72 (1992), S. 1164-1171 
    ISSN: 1089-7550
    Source: AIP Digital Archive
    Topics: Physics
    Notes: Well-separated magnetic particles (∼1 μm size) of Nd2Fe14B alloy are successfully crystallized using an oxygen-reduction-diffusion process. In this process suitable mixtures of Nd2O3, Fe, and B precursor powders were sintered (at 900–1000 °C for 1–3 h) with finely dispersed calcium granules (reducing agent) and anhydrous CaCl2 under a pure argon atmosphere. The crystallization of promisingly small alloy particles in this reaction is analyzed by studying the microstructure and by x-ray diffractometry of reaction products before and after washing away the oxidized calcium and other by-product impurities using fresh water. It is shown that during the crystallization process, the alloy crystals grow in a matrix of oxidized calcium with CaCl2 and possibly unoxidized calcium left in the reaction (if the reaction takes place with an excess calcium). Since oxidized calcium is a thermally highly rigid material (mp∼2580 °C), it controls large-grain growth of the alloy by slowing down diffusion of the reaction species on sintering at such a low temperature Ts≤950 °C for a few hours. When washed with water, oxidized calcium is dissolved with other by-product impurities and results in a loose powder of separated crystallized Nd2Fe14B alloy particles.
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  • 4
    Electronic Resource
    Electronic Resource
    [S.l.] : American Institute of Physics (AIP)
    Journal of Applied Physics 76 (1994), S. 1992-1994 
    ISSN: 1089-7550
    Source: AIP Digital Archive
    Topics: Physics
    Notes: An optical band-gap shrinkage was found in highly transparent and conducting thin films deposited by the Pyrosol process. The narrowing appears at carrier concentrations which are consistent with a metal-semiconductor transition. The gap-shrinkage dependence on carrier concentration is consistent with the model proposed by P. E. Schmid [Phys. Rev. B 23, 5531 (1981)] for Si:As and Si:B.
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  • 5
    ISSN: 1089-7550
    Source: AIP Digital Archive
    Topics: Physics
    Notes: Rare-earth alkaline earth substitute manganites perovskites, Ln1−xAx2+MnO3 (A=Ca, Sr, Ba, Pb), have retained considerable attention in regard to their colossal magnetoresistance coefficient for compositions in the range 0.1≤x≤0.4. Compounds where A2+ cations replaced monovalent A+ cations such as K+ Ag+, etc., have been known for a long time1 and have even been tested as oxidation catalysts for exhaust gazes of internal combustion engines. Surprisingly enough, however, they have given rise to very little investigation as potential giant MR candidates. Preliminary structural features (cell distortions), magnetic and electric properties versus temperature are presented for the series of compounds of general composition La1−xAx+Mn1−2x3+Mn2x4+O3, where A+=Rb, K, Na, Ag, Tl, Cu, and Li. Lanthanum can be partly or totally replaced by Pr, Nd or other rare-earth cations or yttrium. Most of the phases of the lanthanum subseries are rhombohedral (R-3c) and ferromagnetic. Curie temperatures are strongly dependent on x, with a maximum around 330 K for Na, K, or Ag. A sharp decrease of the resistivity is observed just below the Curie temperature, accompanied by a very steep increase of the spontaneous magnetization, uncharacteristic of a conventional Brillouin-type curve. This may be related to a first-order crystallographic transition accompanying the isolant–metal transition. The average magnetic moment of Mn is about 3.55 μB at 20 K for the composition La0.8K0.2MnO3. Preliminary magnetoresistance measurements on bulk ceramic samples display a MR effect of the same amplitude as the case of the alkaline earth substituted La manganites. © 1997 American Institute of Physics.
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  • 6
    Electronic Resource
    Electronic Resource
    [S.l.] : American Institute of Physics (AIP)
    Journal of Applied Physics 64 (1988), S. 780-786 
    ISSN: 1089-7550
    Source: AIP Digital Archive
    Topics: Physics
    Notes: Strongly coercive films of γFe2O3-Fe3O4 solid solution [xFe8/3O4-(1−x)Fe3O4] have been deposited using a new pyrolysis technique. The magnetic and crystallographic properties of nonoxidized Fe3O4 (x=0) and completely oxidized γFe2O3 (x=1) films are shown to be closely related to the planar stress present in the films. An x-ray method is proposed for the study of the iron oxide film stress. The different results are applied to understand the origin of the strong coercive force of partially oxidized solid solution films.
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  • 7
    Electronic Resource
    Electronic Resource
    Woodbury, NY : American Institute of Physics (AIP)
    Applied Physics Letters 61 (1992), S. 613-615 
    ISSN: 1077-3118
    Source: AIP Digital Archive
    Topics: Physics
    Notes: Finely divided loose Nd2Fe14BHx, x≤5, hydride powder (particle size ≤1 μm is synthesized by washing Nd2Fe14B crystallites embedded in calcium and other by-products (during a reduction-diffusion-reaction performed using excess calcium) in water. The calcium reacts thereby with the water and produces, Ca+H2O(large-closed-square)CaO+H2, native hydrogen, which very intimately reacts the alloy and forms the hydrided alloy. The particles are passivated forming a thin but rather hydrogen proof (and probably amorphous) layer of oxide and hydroxide species on the surface. Consequently, peculiarly, they are stable, stand against high corrosion, and can be stored in laboratory air atmosphere at room temperature for extended periods of time with no apparent further loss in structural or magnetic properties.
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  • 8
    Electronic Resource
    Electronic Resource
    Amsterdam : Elsevier
    Journal of Crystal Growth 66 (1984), S. 257-261 
    ISSN: 0022-0248
    Source: Elsevier Journal Backfiles on ScienceDirect 1907 - 2002
    Topics: Chemistry and Pharmacology , Geosciences , Physics
    Type of Medium: Electronic Resource
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  • 9
    Electronic Resource
    Electronic Resource
    Amsterdam : Elsevier
    Solid State Communications 8 (1970), S. 1583-1587 
    ISSN: 0038-1098
    Source: Elsevier Journal Backfiles on ScienceDirect 1907 - 2002
    Topics: Physics
    Type of Medium: Electronic Resource
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  • 10
    Electronic Resource
    Electronic Resource
    Copenhagen : International Union of Crystallography (IUCr)
    Applied crystallography online 1 (1968), S. 318-319 
    ISSN: 1600-5767
    Source: Crystallography Journals Online : IUCR Backfile Archive 1948-2001
    Topics: Geosciences , Physics
    Notes: Huntite structure compounds with the formula REFe3B4O12 (RE = La3+, Nd3+, Sm3+, Eu3+, Gd3+, Tb3+, Dy3+, Ho3+ and Y3+) have been synthesized. X-ray powder diffraction patterns and cell parameter data are reported. The infrared spectrum confirms the triangular coordination of boron in these compounds.
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