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Amund Ruud

Publications and source records attributed to Amund Ruud.

2 recordsLinked to original sources

Structural effects of liquid infiltration of 3Y-Zirconia with Sc, Mg and Y

The current work has investigated the effect of co-doping 3Y-Zirconia (3YSZ) with Sc, Mg and Y by wet infiltration. Pre-sintered discs of 3YSZ were immersed in diluted nitric acid solutions containing Sc, Mg or Y, and combinations of the three, trapping liquid within the porosities of the samples. Upon drying, the cations are maintained inside the pellet, making the basis for the co-doping. After sintering, mass increase confirms the co-doping effect and X-ray diffraction analysis show clear variations in atomic structure depending on the doping element. Rietveld refinements show that the wet-infiltrated samples contain the tetragonal t, t double prime and cubic c-phase in various fractions depending on the doping elements. Sc-infiltrated samples show a tendency to higher tetragonality, while the Mg-infiltrated sample obtained a single cubic phase. The multi-phase wet-infiltrated samples have a similar phase separation after sintering as 5Y-Zirconia (5YSZ), as calculated by the tetragonality deviation parameter. 3YSZ and 5YSZ sintered for 0 hours and 2 hours at 1500 degrees C show the effect of sintering time on the phase segregation. To evaluate the material properties in an application-based perspective, the Knoop hardness, translucency and grain size was measured. We conclude that liquid infiltration is a viable route to perform co-doping of Zirconia with various co-doping elements.

cond-mat.mtrl-sci

Pseudo-ternary LiBH4-LiCl-P2S5 system as structurally disordered bulk electrolyte for all-solid-state lithium batteries

The properties of the mixed system LiBH4 LiCl P2S5 are studied with respect to all-solid-state batteries. The studied material undergoes an amorphization upon heating above 601C, accompanied with increased Li+ conductivity beneficial for battery electrolyte applications. The measured ionic conductivity is 10-3 Scm-1 at room temperature with an activation energy of 0.40(2) eV after amorphization. Structural analysis and characterization of the material suggest that BH4 groups and PS4 may belong to the same molecular structure, where Cl ions interplay to accommodate the structural unit. Thanks to its conductivity, ductility and electrochemical stability (up to 5 V, Au vs. Li+/Li), this new electrolyte is successfully tested in battery cells operated with a cathode material (layered TiS2, theo. capacity 239 mAh g-1) and Li anode resulting in 93% capacity retention (10 cycles) and notable cycling stability under the current density 12 mA g-1 (0.05C-rate) at 501C. Further advanced characterisation by means of operando synchrotron X-ray diffraction in transmission mode contributes explicitly to a better understanding of the (de)lithiation processes of solid-state battery electrodes operated at moderate temperatures.

cond-mat.mtrl-sci