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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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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Dudek, Magdalena

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AGH University of Krakow

in Cooperation with on an Cooperation-Score of 37%

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Publications (6/6 displayed)

  • 2020Samples of Ba1−xSrxCe0.9Y0.1O3−δ, 0 < x < 0.1, with Improved Chemical Stability in CO2-H2 Gas-Involving Atmospheres as Potential Electrolytes for a Proton Ceramic Fuel Cell13citations
  • 2020Ionic Transport Properties of P2O5-SiO2 Glassy Protonic Composites Doped with Polymer and Inorganic Titanium-based Fillers5citations
  • 2019Utilisation of methylcellulose as a shaping agent in the fabrication of Ba0.95Ca0.05Ce0.9Y0.1O3 proton-conducting ceramic membranes via the gelcasting method5citations
  • 2016Influence of the Organophilisation Process on Properties of the Bentonite Filler and Mechanical Properties of the Clay/Epoxy Nanocomposites7citations
  • 2016Some observations on the synthesis and electrolytic properties of (Ba1-xCax) (M0.9Y0.1)O3, M = Ce, Zr-based samples modified with calcium9citations
  • 2013Synthetic preparation of proton conducting polyvinyl alcohol and TiO2-doped inorganic glasses for hydrogen fuel cell applications11citations

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Zabost, Dariusz
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Piszcz, Michał
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Żukowska, Grażyna
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Letmanowski, Rafał
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Siekierski, Maciej
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Wieczorek, Władysław
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Sasim, Elżbieta
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Struzik, Michał
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Mroczkowska-Szerszeń, Maja
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Co-Authors (by relevance)

  • Zabost, Dariusz
  • Piszcz, Michał
  • Żukowska, Grażyna
  • Letmanowski, Rafał
  • Siekierski, Maciej
  • Wieczorek, Władysław
  • Sasim, Elżbieta
  • Struzik, Michał
  • Mroczkowska-Szerszeń, Maja
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article

Some observations on the synthesis and electrolytic properties of (Ba1-xCax) (M0.9Y0.1)O3, M = Ce, Zr-based samples modified with calcium

  • Dudek, Magdalena
Abstract

<jats:title>Abstract</jats:title><jats:p>In this paper, the impact of partial substitution of calcium for barium in (Ba<jats:sub>1-x</jats:sub>Ca<jats:sub>x</jats:sub>) (M<jats:sub>0.9</jats:sub>Y<jats:sub>0.1</jats:sub>) O<jats:sub>3</jats:sub>, M = Ce, Zr on physicochemical properties of the powders and sintered samples was investigated. The powders, with various contents of calcium (x = 0, 0.02, 0.05, 0.1), were prepared by means of thermal decomposition of organometallic precursors containing EDTA. All of the BaCeO<jats:sub>3</jats:sub>-based powders synthesised at 1100 °C were monophasic with a rhombohedral structure, however, completely cubic BaZrO<jats:sub>3</jats:sub>-based solid solutions were obtained at 1200 °C. A study of the sinterability of BaZr<jats:sub>0.9</jats:sub>Y<jats:sub>0.1</jats:sub>O<jats:sub>3</jats:sub> and BaCe<jats:sub>0.9</jats:sub>Y<jats:sub>0.1</jats:sub>O<jats:sub>3</jats:sub>-based pellets was performed under non-isothermal conditions within a temperature range of 25 to 1200 °C. The partial substitution of barium for calcium in the (Ba<jats:sub>1-x</jats:sub>Ca<jats:sub>x</jats:sub>) (M<jats:sub>0.9</jats:sub>Y<jats:sub>0.1</jats:sub>) O<jats:sub>3</jats:sub>, M = Ce, Zr solid solution improved the sinterability of the samples in comparison to the initial BaCe<jats:sub>0.9</jats:sub>Y<jats:sub>0.1</jats:sub>O<jats:sub>3</jats:sub> or BaZr<jats:sub>0.9</jats:sub>Y<jats:sub>0.1</jats:sub>O<jats:sub>3</jats:sub>. The relative density of calcium-modified BaCe<jats:sub>0.9</jats:sub>Y<jats:sub>0.1</jats:sub>O<jats:sub>3</jats:sub>-based samples reached approximately 95 to 97 % after sintering at 1500 °C for 2 h in air. The same level of relative density was achieved after sintering calcium-modified BaZr<jats:sub>0.9</jats:sub>Y<jats:sub>0.1</jats:sub>O<jats:sub>3</jats:sub> at 1600 °C for 2 h. Analysis of the electrical conductivity from both series of investigated materials showed that the highest ionic conductivity, in air and wet 5 % H<jats:sub>2</jats:sub> in Ar, was attained for the compositions of x = 0.02 to 0.05 (Ba<jats:sub>1-x</jats:sub>Ca<jats:sub>x</jats:sub>)(M<jats:sub>0.9</jats:sub>Y<jats:sub>0.1</jats:sub>)O<jats:sub>3</jats:sub>, M = Zr, Ce. The oxygen reduction reaction on the interface Pt│BaM0.9Y0.1O3, M = Ce, Zr was investigated using Pt microelectrodes. Selected samples of (Ba<jats:sub>1-x</jats:sub>Ca<jats:sub>x</jats:sub>) (M<jats:sub>0.9</jats:sub>Y<jats:sub>0.1</jats:sub>)O<jats:sub>3</jats:sub>, M = Zr, Ce were tested as ceramic electrolytes in hydrogen-oxygen solid oxide fuel cells operating at temperatures of 700 to 850 °C.</jats:p>

Topics
  • density
  • Oxygen
  • Hydrogen
  • ceramic
  • Calcium
  • electrical conductivity
  • thermal decomposition
  • sintering
  • organometallic
  • Barium