Solid state electrochemistry, X-ray powder diffraction, magnetic susceptibility, electron spin resonance, Mossbauer and diffuse reflectance spectroscopy of mixed iron(III)-cadmium(II) hexacyanoferrates

被引:47
作者
Zakharchuk, NF
Naumov, N
Stösser, R
Schröder, U
Scholz, F
Mehner, H
机构
[1] Russian Acad Sci, Siberian Branch, Inst Inorgan Chem, Novosibirsk 630090, Russia
[2] Humboldt Univ, Inst Chem, D-10115 Berlin, Germany
[3] Bundesanstalt Mat Prufung, D-14289 Berlin, Germany
关键词
solid state electrochemistry; Mossbauer; magnetic susceptibility; X-ray powder diffraction; iron(III)-cadmium(II) hexacyanoferrates;
D O I
10.1007/s100080050157
中图分类号
O646 [电化学、电解、磁化学];
学科分类号
081704 ;
摘要
Coprecipitates of Cd-II, K-I and Fe-III 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, Mossbauer 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 Cd-II and Fe-III 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 Kubellca-Munk function diminishes by more than 30%, indicating a tremendous decrease in iron(III)-iron(II) interaction.
引用
收藏
页码:264 / 276
页数:13
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