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• W3200215972 endingPage "9168" @default.
• W3200215972 startingPage "9162" @default.
• W3200215972 abstract "The thermodynamic stability of water next to graphitic surfaces is of fundamental interest, as it underlies several natural phenomena and important industrial processes. It is commonly assumed that water wets graphite more than graphene due to increased, favorable van der Waals interactions between the interfacial water molecules with multiple carbon sheets. Here, we employed extensive computer simulations and analysis of the molecular correlation functions to show that the interfacial water thermodynamics is in fact dominated by surface entropy. We show that on graphite, destabilization of the interfacial hydrogen bond network leads to an overcompensating increase in population of low frequency translational and librational modes, which is ultimately responsible for the increased interfacial stability compared to graphene. The spectroscopic signature of this effect is an enhancement of the modes near 100 and 300 cm–1. This subtle interplay between entropy and surface binding may have important consideration for interpretations of various phenomena, including the hydrophobic effect." @default.
• W3200215972 created "2021-09-27" @default.
• W3200215972 creator A5035627473 @default.
• W3200215972 creator A5041947917 @default.
• W3200215972 date "2021-09-15" @default.
• W3200215972 modified "2023-10-16" @default.
• W3200215972 title "Entropic Stabilization of Water at Graphitic Interfaces" @default.
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• W3200215972 doi "https://doi.org/10.1021/acs.jpclett.1c02609" @default.
• W3200215972 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/34524831" @default.
• W3200215972 hasPublicationYear "2021" @default.
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