Ion-specific hydration structures revealed by SCAN-based ab initio simulations* Article Swipe
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· 2025
· Open Access
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· DOI: https://doi.org/10.1088/1674-1056/ae12d2
Hydrated ions play essential roles in diverse chemical and biological processes, yet accurately characterizing their hydration structures remains challenging due to delicate interplay of ion-water and water-water interactions. Here, we use ab initio molecular dynamics (AIMD) simulations based on the strongly constrained and appropriately normed (SCAN) exchange-correlation functional to systematically investigate the hydration structures of eight representative ions (Mg 2+ , Ca 2+ , Li + , Na + , K + , F - , Cl - , Br - ) in aqueous solution. Compared to the widely used Perdew-Burke-Ernzerhof (PBE) functional, SCAN substantially improves the description of solvent water by weakening the hydrogen-bond network and enhancing structural disorder, yielding results in closer agreement with experiments. SCAN modifies ionic hydration shells in an ion-specific manner, governed by ionic size and charge, and reproduces experimental hydration geometries especially well for intermediate-size monovalent ions (Na + , Cl - ). Moreover, SCAN consistently reduces the overpolarization of water molecules near ions. These improvements lead to more accurate and physically consistent hydration structures, highlighting SCAN’s utility for modeling complex aqueous systems and offering guidance for future studies of ionic solvation.
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Ion-specific hydration structures revealed by SCAN-based ab initio simulations*Work title
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articleOpenAlex work type
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enPrimary language
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2025Year of publication
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2025-10-14Full publication date if available
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Tiancheng Liang, Liying Zhou, Yun‐Heub Song, Xifan Wu, Limei XuList of authors in order
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https://doi.org/10.1088/1674-1056/ae12d2Publisher landing page
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