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  • Articles  (2)
  • Diffuse reflectance spectrometry  (1)
  • Key words Solid state electrochemistry  (1)
  • 1995-1999  (2)
  • 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 1 (1997), S. 62-67 
    ISSN: 1433-0768
    Keywords: Key wordsSpectroelectrochemistry ; Diffuse reflectance spectrometry ; Solid state electrochemistry ; Voltammetry ; Microscopy
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract An instrumental setup is described which allows electrochemical measurements to be performed with solid particles immobilized on the surface of a graphite electrode with in situ recording of diffuse reflectance spectra under an incident light microscope. The instrument used includes a special electrochemical cell and a microscope which is interfaced by a light␣guide to a transputer-integrated photodiode-array spectrometer allowing measurements ranging from 320 to 950 nm with a resolution of 3.2 nm/pixel and a PC-interfaced potentiostat. The 0R0 geometry of the optical arrangement and the use of crossed polarization filters for blocking specular reflectance makes it possible to use the Kubelka-Munk function for quantifying the optical measurements. The above instrument has been used for the study of the electrochromic system of solid silver octacyanomolybdate(IV/V) adjacent to a silver nitrate solution. The in situ diffuse reflec tance spectroelectrochemical measurements prove that the electrochemical reaction starts at the graphite/sample interface and then advances into the bulk of the sample towards the sample/electrolyte interface. The ratios Red:Ox determined by spectrometry and chronocoulometry as a function of electrode potentials are identical.
    Type of Medium: Electronic Resource
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