A molecular dynamics study of the nonlinear ...
Type de document :
Article dans une revue scientifique: Article original
DOI :
PMID :
URL permanente :
Titre :
A molecular dynamics study of the nonlinear spectra and structure of charged (101) quartz/water interfaces.
Auteur(s) :
Smirnov, Konstantin [Auteur]
Laboratoire Avancé de Spectroscopie pour les Intéractions la Réactivité et l'Environnement (LASIRE) - UMR 8516
Laboratoire Avancé de Spectroscopie pour les Intéractions la Réactivité et l'Environnement (LASIRE) - UMR 8516
Titre de la revue :
Physical Chemistry Chemical Physics
Nom court de la revue :
Phys Chem Chem Phys
Date de publication :
2022-10-19
ISSN :
1463-9084
Discipline(s) HAL :
Chimie/Chimie théorique et/ou physique
Résumé en anglais : [en]
The relationship between the nonlinear spectra and the structure of charged (101) α-quartz/water interfaces was investigated by classical molecular dynamics simulations. The results of the simulations show that the layered ...
Lire la suite >The relationship between the nonlinear spectra and the structure of charged (101) α-quartz/water interfaces was investigated by classical molecular dynamics simulations. The results of the simulations show that the layered organization of interfacial water is only slightly perturbed by the surface charge and the ionic strength of the aqueous phase. Molecules next to the surface, in a bonded interfacial layer (BIL), tend to direct one of their OH bonds towards the surface, while the water orientation further from the surface, in a diffuse layer (DL), is essentially isotropic. A Stern layer of solvated cations is built up already on a neutral surface and the deprotonation of silanols leads to the formation of an inner Helmholtz plane of cations directly interacting with the SiO− surface sites. A flip of the molecular orientation in the DL could be inferred from the analysis of the structural characteristics of concentrated NaCl solution in contact with a highly charged surface. The computed spectra of χ(2) susceptibility show a double band structure typical of the spectra of silica/water interfaces and the calculations reproduce the experimentally observed variation of the spectral intensity with the pH of the liquid phase. The analysis of results suggests that the behaviour stems from the interplay between the orientational and induced components of the χ(2) susceptibility of the BIL and DL. The dependence of the Im[χ(2)] spectra of the BIL on the surface charge yields the spectrum of H2O molecules directly interacting with SiO− sites. The spectrum is in excellent agreement with the experimental spectrum of the topmost water of a silica/water interface [Urashima et al., J. Phys. Chem. Lett., 2018, 9, 4109].Lire moins >
Lire la suite >The relationship between the nonlinear spectra and the structure of charged (101) α-quartz/water interfaces was investigated by classical molecular dynamics simulations. The results of the simulations show that the layered organization of interfacial water is only slightly perturbed by the surface charge and the ionic strength of the aqueous phase. Molecules next to the surface, in a bonded interfacial layer (BIL), tend to direct one of their OH bonds towards the surface, while the water orientation further from the surface, in a diffuse layer (DL), is essentially isotropic. A Stern layer of solvated cations is built up already on a neutral surface and the deprotonation of silanols leads to the formation of an inner Helmholtz plane of cations directly interacting with the SiO− surface sites. A flip of the molecular orientation in the DL could be inferred from the analysis of the structural characteristics of concentrated NaCl solution in contact with a highly charged surface. The computed spectra of χ(2) susceptibility show a double band structure typical of the spectra of silica/water interfaces and the calculations reproduce the experimentally observed variation of the spectral intensity with the pH of the liquid phase. The analysis of results suggests that the behaviour stems from the interplay between the orientational and induced components of the χ(2) susceptibility of the BIL and DL. The dependence of the Im[χ(2)] spectra of the BIL on the surface charge yields the spectrum of H2O molecules directly interacting with SiO− sites. The spectrum is in excellent agreement with the experimental spectrum of the topmost water of a silica/water interface [Urashima et al., J. Phys. Chem. Lett., 2018, 9, 4109].Lire moins >
Langue :
Anglais
Comité de lecture :
Oui
Audience :
Internationale
Vulgarisation :
Non
Établissement(s) :
Université de Lille
CNRS
CNRS
Collections :
Date de dépôt :
2024-02-28T22:18:24Z
2024-03-19T15:29:36Z
2024-03-19T15:29:36Z
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