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Abstract:

Energetics, structural features, polarity, and melting transitions in water clusters containing up to eight molecules were studied using ab initio methods and empirical force field models. Our quantum approach was based on density functional theory performed at the generalized gradient approximation level. For the specific case of (H2O)6, we selected five conformers of similar energy with different geometries and dipolar moments. For these cases, the cyclic arrangement was found to be the only nonpolar aggregate. For (H2O)8, the most stable structures corresponded to nonpolar, cubic-like, D2d and S4 conformers. Higher energy aggregates exhibit a large spectrum in their polarities. The static polarizability was found to be proportional to the size of the aggregates and presents a weak dependence with the number of hydrogen bonds. In order to examine the influence of thermal fluctuations on the aggregates, we have performed a series of classical molecular dynamics experiments from low temperature up to the melting transition using two different effective pseudopotentials: the TIP4P and MCY models. Minimum energy structures for both classical potentials were found to reproduce reasonably well the results obtained using ab initio methods. Isomerization and phase transitions were monitored by following changes in dipole moments, number of hydrogen bonds and Lindemann's parameter. For (H2O)6 and (H2O)8, the melting transitions were found at Tm≈50 and 160 K, respectively; for both aggregates, we observed premelting transitions between well differentiated conformers as well. © 1999 American Institute of Physics.

Registro:

Documento: Artículo
Título:Isomerization, melting, and polarity of model water clusters: (H2O)6 and (H2O)8
Autor:Rodriguez, J.
Filiación:Departamento de Química Inorgánica, Facultad de Ciencias Exactas y Naturales, Universidad de Buenos Aires Ciudad Universitaria, Pabellón II. (1428), Argentina
Palabras clave:Classical molecular dynamics; Classical potentials; Empirical force fields; Generalized gradient approximation level; Minimum-energy structures; Pre-melting transition; Static polarizabilities; Thermal fluctuations; Dipole moment; Hydrogen bonds; Isomerization; Isomers; Melting; Molecular dynamics; Aggregates
Año:1999
Volumen:110
Número:18
Página de inicio:9039
Página de fin:9047
DOI: http://dx.doi.org/10.1063/1.478824
Handle:http://hdl.handle.net/20.500.12110/paper_00219606_v110_n18_p9039_Rodriguez
Título revista:Journal of Chemical Physics
Título revista abreviado:J Chem Phys
ISSN:00219606
CODEN:JCPSA
PDF:https://bibliotecadigital.exactas.uba.ar/download/paper/paper_00219606_v110_n18_p9039_Rodriguez.pdf
Registro:https://bibliotecadigital.exactas.uba.ar/collection/paper/document/paper_00219606_v110_n18_p9039_Rodriguez

Referencias:

  • Kim, K.S., Dupuis, M., Lie, G.C., Clementi, E., (1986) Chem. Phys. Lett., 131, p. 451
  • Mhin, B.J., Kim, J., Lee, J.Y., Kim, K.S., (1993) J. Chem. Phys., 100, p. 4484

Citas:

---------- APA ----------
(1999) . Isomerization, melting, and polarity of model water clusters: (H2O)6 and (H2O)8. Journal of Chemical Physics, 110(18), 9039-9047.
http://dx.doi.org/10.1063/1.478824
---------- CHICAGO ----------
Rodriguez, J. "Isomerization, melting, and polarity of model water clusters: (H2O)6 and (H2O)8" . Journal of Chemical Physics 110, no. 18 (1999) : 9039-9047.
http://dx.doi.org/10.1063/1.478824
---------- MLA ----------
Rodriguez, J. "Isomerization, melting, and polarity of model water clusters: (H2O)6 and (H2O)8" . Journal of Chemical Physics, vol. 110, no. 18, 1999, pp. 9039-9047.
http://dx.doi.org/10.1063/1.478824
---------- VANCOUVER ----------
Rodriguez, J. Isomerization, melting, and polarity of model water clusters: (H2O)6 and (H2O)8. J Chem Phys. 1999;110(18):9039-9047.
http://dx.doi.org/10.1063/1.478824