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María Teresa Fernández-Díaz

Researcher at Spanish National Research Council

Publications -  179
Citations -  3654

María Teresa Fernández-Díaz is an academic researcher from Spanish National Research Council. The author has contributed to research in topics: Neutron diffraction & Crystal structure. The author has an hindex of 29, co-authored 179 publications receiving 2897 citations. Previous affiliations of María Teresa Fernández-Díaz include Complutense University of Madrid & Carlos III Health Institute.

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Lithium Distribution in Aluminum-Free Cubic Li7La3Zr2O12

TL;DR: In this paper, the authors determined Li sites and occupancies by neutron diffraction of cubic Al-free Li7La3Zr2O12 cubic formwork, with half of tetrahedral sites vacant and long-range ordered.
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Na-doped ruthenium perovskite electrocatalysts with improved oxygen evolution activity and durability in acidic media

TL;DR: Sodium doping of strontium ruthenate is shown to improve the catalytic durability while maintaining a high O2 evolution activity and illustrates how high OER activity and durability can be simultaneously engineered by chemical doping of perovskites.
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Metal-insulator transitions, structural and microstructural evolution of rnio3 (r = sm, eu, gd, dy, ho, y) perovskites : evidence for room-temperature charge disproportionation in monoclinic honio3 and ynio3

TL;DR: In this article, the authors show that the distortion of the orthorhombic perovskite progressively increases along the series, leading for the smallest Ho3+ and Y3+ cations to a subtle monoclinic distortion (space group P21/n) which implies the splitting of the Ni positions in the crystal.
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Evolution of the Magnetic Structure of Hexagonal HoMnO3 from Neutron Powder Diffraction Data

TL;DR: In this paper, a hexagonal, nonperovskite HoMnO3 oxide, containing a triangular arrangement of Mn3+ cations, has been prepared in polycrystalline form by the thermal decomposition of metal citrates.
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On the Location of Li+ Cations in the Fast Li‐Cation Conductor La0.5Li0.5TiO3 Perovskite

TL;DR: The unusual coordination and the partially unoccupied sublattice (occupancy factors 1/6 and (1/2) for Li and La, respectively) account for the high mobility of the Li(+) cations.