Materials Map

Discover the materials research landscape. Find experts, partners, networks.

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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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Materials Map under construction

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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Naji, M.
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Kharytonau, Dzmitry S.

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in Cooperation with on an Cooperation-Score of 37%

Topics

Publications (4/4 displayed)

  • 2024Corrosion Inhibition of AZ31-xLi (x = 4, 8, 12) magnesium alloys in sodium chloride solutions by aqueous molybdate3citations
  • 2023Multisine impedimetric monitoring with an in-depth distribution of relaxation times analysis of WE43 and AZ31 magnesium alloys corrosion11citations
  • 2022Influence of CeO2 and TiO2 Particles on Physicochemical Properties of Composite Nickel Coatings Electrodeposited at Ambient Temperature11citations
  • 2022Improvement of La0.8Sr0.2MnO3−δ Cathode Material for Solid Oxide Fuel Cells by Addition of YFe0.5Co0.5O39citations

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Chart of shared publication
Kurilo, Irina I.
1 / 3 shared
Adamiec, Janusz
1 / 2 shared
Ryl, Jacek
3 / 19 shared
Skowron, Konrad
1 / 1 shared
Osipenk, Maria A.
1 / 1 shared
Paspelau, Andrei V.
1 / 1 shared
Kasach, Aliaksandr A.
1 / 1 shared
Dominów, Michał
1 / 1 shared
Prześniak-Welenc, Marta
1 / 2 shared
Osipenko, Maria A.
1 / 1 shared
Makarava, Iryna V.
2 / 11 shared
Kurilo, Irina
1 / 1 shared
Karczewski, Jakub
1 / 13 shared
Bilesan, Mohammad Reza
1 / 1 shared
Pelcastre, Leonardo
1 / 25 shared
Vuorinen, Esa
1 / 16 shared
Esmaeili, Mohammadamin
1 / 1 shared
Repo, Eveliina
1 / 5 shared
Górski, Miłosz
1 / 1 shared
Krzan, Marcel
1 / 11 shared
Komenda, Anna
1 / 1 shared
Zimowska, Małgorzata
1 / 5 shared
Mosiałek, Michał
1 / 5 shared
Chart of publication period
2024
2023
2022

Co-Authors (by relevance)

  • Kurilo, Irina I.
  • Adamiec, Janusz
  • Ryl, Jacek
  • Skowron, Konrad
  • Osipenk, Maria A.
  • Paspelau, Andrei V.
  • Kasach, Aliaksandr A.
  • Dominów, Michał
  • Prześniak-Welenc, Marta
  • Osipenko, Maria A.
  • Makarava, Iryna V.
  • Kurilo, Irina
  • Karczewski, Jakub
  • Bilesan, Mohammad Reza
  • Pelcastre, Leonardo
  • Vuorinen, Esa
  • Esmaeili, Mohammadamin
  • Repo, Eveliina
  • Górski, Miłosz
  • Krzan, Marcel
  • Komenda, Anna
  • Zimowska, Małgorzata
  • Mosiałek, Michał
OrganizationsLocationPeople

article

Improvement of La0.8Sr0.2MnO3−δ Cathode Material for Solid Oxide Fuel Cells by Addition of YFe0.5Co0.5O3

  • Górski, Miłosz
  • Krzan, Marcel
  • Komenda, Anna
  • Kharytonau, Dzmitry S.
  • Zimowska, Małgorzata
  • Mosiałek, Michał
Abstract

<jats:p>The high efficiency of solid oxide fuel cells with La0.8Sr0.2MnO3−δ (LSM) cathodes working in the range of 800–1000 °C, rapidly decreases below 800 °C. The goal of this study is to improve the properties of LSM cathodes working in the range of 500–800 °C by the addition of YFe0.5Co0.5O3 (YFC). Monophasic YFC is synthesized and sintered at 950 °C. Composite cathodes are prepared on Ce0.8Sm0.2O1.9 electrolyte disks using pastes containing YFC and LSM powders mixed in 0:1, 1:19, and 1:1 weight ratios denoted LSM, LSM1, and LSM1, respectively. X-ray diffraction patterns of tested composites reveal the presence of pure perovskite phases in samples sintered at 950 °C and the presence of Sr4Fe4O11, YMnO3, and La0.775Sr0.225MnO3.047 phases in samples sintered at 1100 °C. Electrochemical impedance spectroscopy reveals that polarization resistance increases from LSM1, by LSM, to LSM2. Differences in polarization resistance increase with decreasing operating temperatures because activation energy rises in the same order and equals to 1.33, 1.34, and 1.58 eV for LSM1, LSM, and LSM2, respectively. The lower polarization resistance of LSM1 electrodes is caused by the lower resistance associated with the charge transfer process.</jats:p>

Topics
  • perovskite
  • impedance spectroscopy
  • phase
  • x-ray diffraction
  • composite
  • activation