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Sean T. Holmes

Publications and source records attributed to Sean T. Holmes.

2 recordsLinked to original sources

Emergent Atomic Scale Polarisation Vortices in BaTiS3

Topological defects, such as vortices and skyrmions in magnetic and dipolar systems, can give rise to properties that are not observed in typical magnets and dielectrics. Here, we report the discovery of long-range ordered periodic dipole arrays of atomic-scale vortices and antivortices in the unconventional charge-density-wave (CDW) phase of BaTiS3, a quasi-1D chalcogenide. Synchrotron X-ray diffraction (XRD) reveals the presence of a multi-q ordering in BaTiS3 that confines vortex-vortex-antivortex polarisation triplets to the a-b plane with alternating handedness along the c-axis. The multi-q displacive distortions are characterised by three distinctive off-centre TiS6 configurations, whose ratios are independently confirmed by 47/49Ti solid-state nuclear magnetic resonance (SSNMR). Using first-principles calculations and phenomenological modelling, we show that the dipolar vortex unit cell in BaTiS3 arises from the coupling between multiple lattice instabilities arising from flat, soft phonon bands. This mechanism contrasts with classical dipolar textures in ferroelectric heterostructures that emerge from the competition between electrostatic and strain energies. The observation of dipolar vortices in BaTiS3 brings the ultimate scaling limit for real-space dipolar topological structures down to about a nanometre and unveils the intimate connection between crystal symmetry and real-space topology. Our work sets up zero-filling semiconducting materials with competing structural instabilities as a playground for realising and understanding quantum polarisation topologies.

cond-mat.mtrl-sci

Rietveld Refinement and NMR Crystallographic Investigations of Multicomponent Crystals Containing Alkali Metal Chlorides and Urea

New mechanochemical preparations of three multicomponent crystals (MCCs) of the form MCl:urea.nH2O (M = Li+, Na+, and Cs+) are reported. Their structures were determined by an NMR crystallography approach, combining Rietveld refinement of synchrotron powder X-ray diffraction data (PXRD), multinuclear (35Cl, 7Li, 23Na, and 133Cs) solid-state NMR (SSNMR) spectroscopy, and thermal analysis. Mechanochemical syntheses of the three MCCs, two of which are novel, are optimized for maximum yield and efficiency. 35Cl SSNMR is well-suited for the structural characterization of these MCCs since it is sensitive to subtle differences and/or changes in chloride ion environments, providing a powerful means of examining H...Cl-bonding environments. Alkali metal NMR is beneficial for identifying the number of unique magnetically and crystallographically distinct sites and enables facile detection of educts and/or impurities. In the case of NaCl:urea.H2O, 23Na MAS NMR spectra are key, both for identifying residual NaCl educt and for monitoring NaCl:urea.H2O degradation, which appears to proceed via an autocatalytic decomposition process driven by water (with a rate constant of k = 1.22x10-3 s-1). SSNMR and PXRD were used to inform the initial structural models. Following Rietveld refinement, the models were subjected to dispersion-corrected plane-wave DFT geometry optimizations and subsequent calculations of the 35Cl EFG tensors, which enable the refinement of hydrogen atom positions, as well as the exploration of their relationships to the local hydrogen bonding environments of the chloride ions and crystallographic symmetry elements.

cond-mat.mtrl-sci