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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Roelsgaard, Martin

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Aarhus University

in Cooperation with on an Cooperation-Score of 37%

Topics

Publications (11/11 displayed)

  • 2023Operando X-ray scattering study of segmented thermoelectric Zn$_4$Sb$_3$4citations
  • 2023Operando X-ray scattering study of segmented thermoelectric Zn 4 Sb 34citations
  • 2023Operando X-ray scattering study of segmented thermoelectric Zn4Sb34citations
  • 2021Structural evolution in thermoelectric zinc antimonide thin films studied by in situ X-ray scattering techniques4citations
  • 2020Autocatalytic Formation of High-Entropy Alloy Nanoparticles95citations
  • 2020Mapping the redox chemistry of common solvents in solvothermal synthesis through in situ X-ray diffraction14citations
  • 2020Mapping the redox chemistry of common solvents in solvothermal synthesis through: In situ X-ray diffraction14citations
  • 2020Maximizing the Catalytically Active {001} Facets on Anatase Nanoparticles13citations
  • 2020Maximizing the Catalytically Active {001} Facets on Anatase Nanoparticles13citations
  • 2016The hydrothermal synthesis, crystal structure and electrochemical properties of MnSb 2 O 49citations
  • 2016The hydrothermal synthesis, crystal structure and electrochemical properties of MnSb2O49citations

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Iversen, Bo Brummerstedt
6 / 28 shared
Christensen, Rasmus
1 / 3 shared
Thorup, Peter Skjoett
1 / 1 shared
Christensen, Rasmus Stubkjær
1 / 3 shared
Thorup, Peter Skjøtt
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Christensen, Rasmus
1 / 2 shared
Dippel, Ann-Christin
1 / 29 shared
Jensen, Kirsten Marie Ørnsbjerg
1 / 6 shared
Zhang, Jiawei
1 / 6 shared
Song, Lirong
1 / 1 shared
Blichfeld, Anders Bank
1 / 3 shared
Søndergaard-Pedersen, Frederik
5 / 5 shared
Bondesgaard, Martin
1 / 9 shared
Broge, Nils L. N.
1 / 1 shared
Broge, Nils Lau Nyborg
4 / 10 shared
Hassing-Hansen, Xenia
2 / 2 shared
Yu, Jinlong
2 / 2 shared
Iversen, Bo B.
1 / 31 shared
Søndergaard, Martin
2 / 5 shared
Nørby, Peter
2 / 7 shared
Eikeland, Espen
2 / 4 shared
Chart of publication period
2023
2021
2020
2016

Co-Authors (by relevance)

  • Iversen, Bo Brummerstedt
  • Christensen, Rasmus
  • Thorup, Peter Skjoett
  • Christensen, Rasmus Stubkjær
  • Thorup, Peter Skjøtt
  • Christensen, Rasmus
  • Dippel, Ann-Christin
  • Jensen, Kirsten Marie Ørnsbjerg
  • Zhang, Jiawei
  • Song, Lirong
  • Blichfeld, Anders Bank
  • Søndergaard-Pedersen, Frederik
  • Bondesgaard, Martin
  • Broge, Nils L. N.
  • Broge, Nils Lau Nyborg
  • Hassing-Hansen, Xenia
  • Yu, Jinlong
  • Iversen, Bo B.
  • Søndergaard, Martin
  • Nørby, Peter
  • Eikeland, Espen
OrganizationsLocationPeople

article

The hydrothermal synthesis, crystal structure and electrochemical properties of MnSb2O4

  • Søndergaard, Martin
  • Roelsgaard, Martin
  • Nørby, Peter
  • Eikeland, Espen
Abstract

<p>Phase pure polycrystalline MnSb<sub>2</sub>O<sub>4</sub> was synthesised under hydrothermal conditions. Impurities formed outside a narrow range of pH and metal stoichiometric ratios. The structure and its temperature dependence was studied based on multi-temperature conventional single crystal X-ray diffraction (SC-XRD) and high resolution synchrotron powder X-ray diffraction (PXRD). At low temperature (100-300 K) the lattice parameters expanded linearly with thermal expansion coefficients of α<sub>a,300 K</sub> = 8(1) × 10<sup>-6</sup> K<sup>-1</sup> and α<sub>c,300 K</sub> = 7.2(2) × 10<sup>-6</sup> K<sup>-1</sup>. At high temperature an irreversible annealing effect was observed. Modelling the atomic displacement parameters based on the single crystal X-ray diffraction data gives a Debye temperature of 267(3) K for MnSb<sub>2</sub>O<sub>4</sub>. When heated in an oxygen-rich atmosphere MnSb<sub>2</sub>O<sub>4</sub> oxidises above 800 K and it decomposes at 975 K under inert conditions. Electrochemical measurements displayed similar behaviour to the isostructural CoSb<sub>2</sub>O<sub>4</sub>, with reversible alloying-dealloying of Li<sub>x</sub>Sb after the first cycle with a reversible capacity of 337 mAh g<sup>-1</sup> at the 2<sup>nd</sup> cycle, which degraded to c. 100 mAh g<sup>-1</sup> after 30 cycles.</p>

Topics
  • single crystal X-ray diffraction
  • single crystal
  • phase
  • Oxygen
  • powder X-ray diffraction
  • thermal expansion
  • annealing