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The thermodynamic liquid-state anomalies and associated structural changes of the Stillinger-Weber family of liquids are mapped out as a function of the degree of tetrahedrality of the interaction potential, focusing in particular on tetrahedrality values suitable for modeling C, H2O, Si, Ge and Sn. We show that the density anomaly, associated with a rise in molar volume on isobaric cooling, emerges...
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