Materials Map

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The Materials Map is an open tool for improving networking and interdisciplinary exchange within materials research. It enables cross-database search for cooperation and network partners and discovering of the research landscape.

The dashboard provides detailed information about the selected scientist, e.g. publications. The dashboard can be filtered and shows the relationship to co-authors in different diagrams. In addition, a link is provided to find contact information.

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The Materials Map is still under development. In its current state, it is only based on one single data source and, thus, incomplete and contains duplicates. We are working on incorporating new open data sources like ORCID to improve the quality and the timeliness of our data. We will update Materials Map as soon as possible and kindly ask for your patience.

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in Cooperation with on an Cooperation-Score of 37%

Topics

Publications (1/1 displayed)

  • 2009Valence-tautomeric RbMnFe Prussian blue analogues8citations

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Chart of shared publication
Salmon, Lionel
1 / 17 shared
Van Koningsbruggen, Petra
1 / 6 shared
Vertelman, Esther J. M.
1 / 3 shared
Bousseksou, Azzedine
1 / 35 shared
Cobo, Saioa
1 / 8 shared
Molnár, Gábor
1 / 32 shared
Chart of publication period
2009

Co-Authors (by relevance)

  • Salmon, Lionel
  • Van Koningsbruggen, Petra
  • Vertelman, Esther J. M.
  • Bousseksou, Azzedine
  • Cobo, Saioa
  • Molnár, Gábor
OrganizationsLocationPeople

article

Valence-tautomeric RbMnFe Prussian blue analogues

  • Murgui, Carlos B.
  • Salmon, Lionel
  • Van Koningsbruggen, Petra
  • Vertelman, Esther J. M.
  • Bousseksou, Azzedine
  • Cobo, Saioa
  • Molnár, Gábor
Abstract

Three different stoichiometric forms of RbMn[Fe(CN) ]y·zHO [x = 0.96, y = 0.98, z = 0.75 (1); x = 0.94, y = 0.88, z = 2.17 (2); x = 0.61, y = 0.86, z = 2.71 (3)] Prussian blue analogues were synthesized and investigated by magnetic, calorimetric, Raman spectroscopic, X-ray diffraction, and Fe Mössbauer spectroscopic methods. Compounds 1 and 2 show a hysteresis loop between the high-temperature (HT) Fe(S = 1/2)-CN-Mn(S = 5/2) and the low-temperature (LT) Fe(S = 0)-CN-Mn(S = 2) forms of 61 and 135 K width centered at 273 and 215 K, respectively, whereas the third compound remains in the HT phase down to 5 K. The splitting of the quadrupolar doublets in the Fe Mössbauer spectra reveal the electron-transfer-active centers. Refinement of the X-ray powder diffraction profiles shows that electron-transfer-active materials have the majority of the Rb ions on only one of the two possible interstitial sites, whereas nonelectron-transfer-active materials have the Rb ions equally distributed. Moreover, the stability of the compounds with time and following heat treatment is also discussed.

Topics
  • impedance spectroscopy
  • compound
  • phase
  • x-ray diffraction
  • interstitial