arXiv subjects

Gwenaëlle Rousse

Publications and source records attributed to Gwenaëlle Rousse.

4 recordsLinked to original sources

arXiv2026

One-dimensional self-organization of water molecules in proton conducting Andersson-Wadsley titanates

Layered alkali titanates with M 2 Ti 2 O 5 chemical formula (MTO, M=K,Rb) belonging to the Andersson-Wadsley perovskite family spontaneously incorporate water to form MTO.(H 2 O) x compounds, which exhibit superionic conductivity. At very low hydration x, scanning electron microscopy evidences one-dimensional heterogeneous patterns oriented along ___ b that are arranged in an orderly manner. At higher hydration, the material is observed to spontaneously exfoliate by creating (001) surfaces. Simulations carried out using Density Functional Theory reveal an ordered arrangement of the guest water molecules in Rb 2 Ti 2 O 5 , with strong hydrogen bonds between the water molecules and the apical oxygen of the host crystal. At low hydration x, the water molecules form self-organized one dimensional (1D) double chains along ___ b. Further increase of the water content leads to the creation of hydrated (001)-surfaces that are made of densely packed water chains in agreement with the infrared spectroscopy measurements. Rb 2 Ti 2 O 5 exhibits highly anisotropic proton conductivity, with respect to the crystal orientation, with super-ionic conductivity along ___ b reaching 3 mS/cm at room temperature after hydration. The combined observations and simulations suggest that these water chains are thus at the root of fast proton conduction, which is likely powered by a Grotthuss-like mechanism.

cond-mat.mtrl-sci↗

arXiv2021

Crystallographic and magnetic structures of the VI$_3$ and LiVI$_3$ van der Waals compounds

Two-dimensional (2D) layered magnetic materials are generating a great amount of interest for the next generation of electronic devices thanks to their remarkable properties associated to spin dynamics. The recently discovered layered VI$_3$ ferromagnetic phase belongs to this family, although a full understanding of its properties is limited by an ill-defined crystallographic structure. This is not any longer true. Here, we investigate the VI$_3$ crystal structure upon cooling using both synchrotron X-ray and neutron powder diffraction and provide structural models for the two structural transitions occurring at 76 K and 32 K. Moreover, we confirm by magnetic measurements that VI$_3$ becomes ferromagnetic at 50 K and discuss the difficulty of solving its full magnetic structure by neutrons. We equally determined the magnetic properties of our recently reported LiVI$_3$ phase, which is alike the well-known CrI$_3$ ferromagnetic phase in terms of electronic and crystallographic structures and found to our surprise an antiferromagnetic behavior with a Néel temperature of 12 K. Such a finding provides extra clues for a better understanding of magnetism in these low dimension compounds. Finally, the easiness of preparing novel Li-based 2D magnetic materials by chemical/electrochemical means opens wide the opportunity to design materials with exotic properties.

cond-mat.mtrl-sci↗

arXiv2019

Triplet excitations in the frustrated spin ladder Li$_2$Cu$_2$O(SO$_4$)$_2$

Magnetic excitations of the recently discovered frustrated spin-1/2 two-leg ladder system Li$_2$Cu$_2$O(SO$_4$)$_2$ are investigated using inelastic neutron scattering, magnetic susceptibility and infrared absorption measurements. Despite the presence of a magnetic dimerization concomitant with the tetragonal-to-triclinic structural distortion occurring below 125 K, neutron scattering experiments reveal the presence of dispersive triplet excitations above a spin gap of $Δ= 10.6$ meV at 1.5 K, a value consistent with the estimates extracted from magnetic susceptibility. The likely detection of these spin excitations in infrared spectroscopy is explained by invoking a dynamic Dzyaloshinskii-Moriya mechanism in which light is coupled to the dimer singlet-to-triplet transition through an optical phonon. These results are qualitatively explained by exact diagonalization and higher-order perturbation calculations carried out on the basis of the dimerized spin Hamiltonian derived from first-principles.

cond-mat.str-el↗

arXiv2018

Photoemission Fingerprints for Structural Identification of Titanium Dioxide Surfaces

The wealth of properties of titanium dioxide relies on its various polymorphs and on their mixtures coupled with a sensitivity to crystallographic orientations. It is therefore pivotal to set out methods that allow surface structural identification. We demonstrate herein the ability of photoemission spectroscopy to provide Ti LMV (V = valence) Auger templates to quantitatively analyze TiO$_2$ polymorphs. The Ti LMV decay reflects Ti 4sp-O 2p hybridizations that are intrinsic properties of TiO$_2$ phases and orientations. Ti LMV templates collected on rutile (110), anatase (101), and (100) single crystals allow for the quantitative analysis of mixed nanosized powders, which bridges the gap between surfaces of reference and complex materials. As a test bed, the anatase/rutile P25 is studied both as received and during the anatase-to-rutile transformation upon annealing. The agreement with X-ray diffraction measurements proves the reliability of the Auger analysis and highlights its ability to detect surface orientations.

cond-mat.mtrl-sci↗