Počet záznamů: 1  

Dielectric Properties of Water at Rutile and Graphite Surfaces: Effect of Molecular Structure

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    0439935 - ÚCHP 2015 RIV US eng J - Článek v odborném periodiku
    Pařez, Stanislav - Předota, Milan - Machesky, M.
    Dielectric Properties of Water at Rutile and Graphite Surfaces: Effect of Molecular Structure.
    Journal of Physical Chemistry C. Roč. 118, č. 9 (2014), s. 4818-4834. ISSN 1932-7447. E-ISSN 1932-7455
    Grant CEP: GA ČR GA13-09914S
    Grant ostatní: GA ČR(CZ) GA13-08651S; GA MŠMT(CZ) LM2010005
    Institucionální podpora: RVO:67985858
    Klíčová slova: electric double layer * dynamics simulations * interfacial water
    Kód oboru RIV: CF - Fyzikální chemie a teoretická chemie
    Impakt faktor: 4.772, rok: 2014

    The dielectric properties of interfacial water adjacent to the surfaces of hydrophobic graphite and the 110 surface of hydrophilic rutile (alpha-TiO2) are investigated by means of nonequilibrium molecular dynamics simulations. The dielectric behavior of water is found to arise from its local density and molecular polarizability in response to an external field, and can be rationalized in terms of the number and strength of water-surface and water-water H-bonds. The interplay of local density and polarizability leads to a particularly strong dielectric response, exceeding the external field, of the water layer directly contacting the surfaces, while the second layer exhibits a reduced response. Consequently, dielectric profiles near surfaces cannot be correctly described by implicit solvent models valid for bulk water. The overscreening response of the contact water layer has been observed in previous simulation studies and implies the local permittivity (dielectric constant) of that layer is negative. However, the negative permittivity of the contact water layer is counterbalanced by the positive permittivities of the surface depletion layer and the second water layer such that the calculated Stern layer capacitance is positive and compatible with experimental data. Moreover, the electrostatic potential profile matches well the profile calculated for an aqueous salt solution at the charged rutile (110) surface, thus supporting the water centric view of aqueous electrical double layers.
    Trvalý link: http://hdl.handle.net/11104/0243104

     
     
Počet záznamů: 1  

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