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Alexander G. Squires

Publications and source records attributed to Alexander G. Squires.

3 recordsLinked to original sources

Revealing low-energy surfaces of multinary compounds by controlling surface coordination environments

When modeling surfaces of multinary compounds, conventional cleavage planes often cut through strongly bonded polyhedra, resulting in unphysical surface energies. Here, we introduce SALAMI (Symmetric Atomic Layers for Arbitrary Multinary Interfaces), a Python package that generates symmetric, charge-neutral, dipole-free, and low-energy slab models for multinary compounds. SALAMI performs combinatorial searches to selectively remove surface atoms and generate corrugated terminations that preserve optimal coordination environments. We applied this workflow to all symmetrically inequivalent crystallographic orientations with Miller indices up to 2 for two prototypical structures: the solid-state electrolyte Li3PS4 and the transparent conducting oxide ZnSb2O6. Density functional theory calculations reveal that Li3PS4 must preserve all PS4 units to achieve the minimum surface energy. For ZnSb2O6, low-energy surfaces are achieved by partial undercoordination of surface Sb atoms to SbO5 or SbO4 from the bulk SbO6, depending on the surface orientations. Compared to surface models generated with unconstrained coordination, applying constraints to achieve optimal local coordination environments significantly lowers surface energies, shrinking the volume of the predicted Wulff shape by approximately 20%. Our results demonstrate that meticulous control of local coordination environments is necessary for accurately predicting the surface energetics of multinary compounds.

cond-mat.mtrl-sci

doped: Python toolkit for robust and repeatable charged defect supercell calculations

Defects are a universal feature of crystalline solids, dictating the key properties and performance of many functional materials. Given their crucial importance yet inherent difficulty in measuring experimentally, computational methods (such as DFT and ML/classical force-fields) are widely used to predict defect behaviour at the atomic level and the resultant impact on macroscopic properties. Here we report doped, a Python package for the generation, pre-/post-processing, and analysis of defect supercell calculations. doped has been built to implement the defect simulation workflow in an efficient and user-friendly -- yet powerful and fully-flexible -- manner, with the goal of providing a robust general-purpose platform for conducting reproducible calculations of solid-state defect properties.

cond-mat.mtrl-sci

Anion-polarisation-directed short-range-order in antiperovskite Li$_2$FeSO

Short-range ordering in cation-disordered cathodes can have a significant effect on their electrochemical properties. Here, we characterise the cation short-range order in the antiperovskite cathode material Li$_2$FeSO, using density functional theory, Monte Carlo simulations, and synchrotron X-ray pair-distribution-function data. We predict partial short-range cation-ordering, characterised by favourable OLi$_4$Fe$_2$ oxygen coordination with a preference for polar cis-OLi$_4$Fe$_2$ over non-polar trans-OLi$_4$Fe$_2$ configurations. This preference for polar cation configurations produces long-range disorder, in agreement with experimental data. The predicted short-range-order preference contrasts with that for a simple point-charge model, which instead predicts preferential trans-OLi$_4$Fe$_2$ oxygen coordination and corresponding long-range crystallographic order. The absence of long-range order in Li$_2$FeSO can therefore be attributed to the relative stability of cis-OLi$_4$Fe$_2$ and other non-OLi$_4$Fe$_2$ oxygen-coordination motifs. We show that this effect is associated with the polarisation of oxide and sulfide anions in polar coordination environments, which stabilises these polar short-range cation orderings. We propose similar anion-polarisation-directed short-range-ordering may be present in other heterocationic materials that contain cations with different formal charges. Our analysis also illustrates the limitations of using simple point-charge models to predict the structure of cation-disordered materials, where other factors, such as anion polarisation, may play a critical role in directing both short- and long-range structural correlations.

cond-mat.mtrl-sci