Journal
JOURNAL OF PHYSICAL CHEMISTRY LETTERS
Volume 3, Issue 18, Pages 2653-2658Publisher
AMER CHEMICAL SOC
DOI: 10.1021/jz300932p
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Funding
- U.S. Department of Energy
- Lawrence Livermore National Laboratory [DE-AC52-07NA27344]
- DOE/CMCSN Structure and Dynamics of Water and Aqueous Solutions Collaborative Research Team
- Burroughs Wellcome Fund
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We investigated the structure of liquid water around cations (Na+) and anions (Cl-) confined inside of a (19,0) carbon nanotube with first-principles molecular dynamics and theoretical X-ray absorption spectroscopy (XAS). We found that the ions preferentially reside near the interface between the nanotube and the liquid. Upon confinement, the XAS signal of water molecules surrounding Na+ exhibits enhanced pre-edge and reduced post-edge features with respect to that of pure water, at variance with the solvation shell of Na+ in bulk water. Conversely, the first solvation shell of confined Cl- has a main-edge intensity comparable to that of bulk solvated Cl-, likely as a result of a high number of acceptor hydrogen bonds in the first solvation shell. Confined nonsolvating water molecules exhibit bulk-like or water-monomer-like properties, depending on whether they belong to core or interfacial layers, respectively.
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