4.7 Article

Charge transfer effects of ions at the liquid water/vapor interface

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JOURNAL OF CHEMICAL PHYSICS
卷 140, 期 18, 页码 -

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AMER INST PHYSICS
DOI: 10.1063/1.4874256

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资金

  1. National Science Foundation (NSF) [CHE-1301072]
  2. Louisiana Optical Network Institute (LONI)
  3. National Science Foundation under the NSF Experimental Program to Stimulate Competitive Research (EPSCoR) [EPS-1003897]
  4. Louisiana Board of Regents
  5. State of Louisiana Board of Regents
  6. Division Of Chemistry
  7. Direct For Mathematical & Physical Scien [1301072] Funding Source: National Science Foundation

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Charge transfer (CT), the movement of small amounts of electron density between non-bonded pairs, has been suggested as a driving force for a variety of physical processes. Herein, we examine the effect of CT on ion adsorption to the water liquid-vapor interface. Using a CT force field for molecular dynamics, we construct a potential of mean force (PMF) for Na+, K+, Cl-, and I-. The PMFs were produced with respect to an average interface and an instantaneous interface. An analysis of the PMF relative to the instantaneous surface reveals that the area in which the anions experience a free energy minimum is quite narrow, and the cations feel a steeply repulsive free energy near the interface. CT is seen to have only minor effects on the overall free energy profiles. However, the long-ranged effects of ions are highlighted by the CT model. Due to CT, the water molecules at the surface become charged, even when the ion is over 15 angstrom away from the surface. (C) 2014 AIP Publishing LLC.

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