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  • Immobilized microparticles  (1)
  • Iron(III)-cadmium(II) hexacyanoferrates  (1)
  • Springer  (2)
  • American Physical Society
  • American Physical Society (APS)
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  • Springer  (2)
  • American Physical Society
  • American Physical Society (APS)
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  • 1
    ISSN: 1433-0768
    Keywords: Key words Solid state electrochemistry ; Mössbauer ; Magnetic susceptibility ; X-ray powder diffraction ; Iron(III)-cadmium(II) hexacyanoferrates
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract Coprecipitates of CdII, KI and FeIII with hexacyanoferrate ions [Fe(CN)6]4− have been studied by solid-state electrochemistry (voltammetry of immobilized microparticles), magnetic susceptibility measurements, X-ray powder diffraction, electron spin resonance, Mössbauer and diffuse reflectance spectroscopy. Most suprisingly, all experimental results point to the formation of a continuous series of complex mixed phases without the formation of phase mixtures. Although CdII and FeIII ions differ too much in their ionic radii to allow the formation of simple substitution mixed hexacyanoferrates, they are capable of forming different kinds of complex insertion and substitution mixed crystals because of the zeolitic structure of both the iron and the cadmium hexacyanoferrate. Low cadmium concentrations can be found in the zeolitic cavities of iron hexacyanoferrate (Prussian blue), and they start to widen the lattice and facilitate, at higher concentrations, the direct substitution of high-spin iron(III) ions by cadmium ions. In cases of an excess of cadmium, the formation of cadmium hexacyanoferrate with iron(III) ions in the interstitials of the zeolitic structure is observed. These mixed phases show strong charge transfer bands in the visible range and have the appearance of “diluted” Prussian blue. For the first time, this indicates that the charge transfer between the carbon-coordinated low-spin iron(II) ions and the high-spin iron(III) ions can also occur when the latter are situated in the cavities of a host hexacyanoferrate. In Prussian blue the interstitial iron(III) ions are responsible for a very strong charge transfer interaction between the low-spin iron(II) ions and the nitrogen-coordinated high-spin iron(III) ions. Upon substitution of the very small amount of interstitial iron(III) ions in Prussian blue by potassium and cadmium ions the Kubelka-Munk function diminishes by more than 30%, indicating a tremendous decrease in iron(III)-iron(II) interaction.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Springer
    Journal of solid state electrochemistry 4 (1999), S. 17-23 
    ISSN: 1433-0768
    Keywords: Key words Lithium nickelate ; Solid state electrochemisty ; Proton intercalation ; Voltammetry ; Immobilized microparticles
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract Lithium nickelate was synthesized by self-propagating high-temperature combustion. The electrochemical behaviour of the product was studied by cyclic voltammetry of microparticles immobilized on the surface of graphite electrodes. Whereas numerous previous studies have dealt with non-aqueous electrolyte solutions, here the behaviour of lithium nickelate in contact with aqueous electrolyte solutions was investigated. It could be shown that protons are intercalating upon reduction of the Ni(III) to Ni(II) and deintercalating upon oxidation. This insertion electrochemistry is chemically reversible. Within 1600 oxidation-reduction cycles, the response diminished only by about 10%. Scanning electron microscopy reveals a considerable recrystallization during the electrochemical cycles. Energy dispersive X-ray detection proved that no metal cations are intercalating. The electrochemical system is accessible only in very alkaline solutions as it shifts to more positive values with decreasing pH.
    Type of Medium: Electronic Resource
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