Universidad de Burgos Repositorio Repositorio
Por favor, use este identificador para citar o enlazar este ítem: http://hdl.handle.net/10259/4332

Ver estadísticas de uso
Título : Adsorption of choline benzoate ionic liquid on graphene, silicene, germanene and boron-nitride nanosheets: a DFT perspective
Autor : García Moreno, Gregorio J.
Atilhan, Mert
Aparicio Martínez, Santiago
Publicado en: Physical Chemistry Chemical Physics. 2015, V. 17, n. 25, p. 16315-16326
Editorial : Royal Society of Chemistry
Fecha de publicación : jul-2015
Resumen : The adsorption of choline benzoate ([CH][BE]) ionic liquid (IL) on the surface of different hexagonal nanosheets has been studied using Density Functional Theory (DFT) methods. For this, the interaction mechanism, binding energies and electronic structure of [CH][BE] ionic liquid on four types of nanosheets, i.e., graphene, silicene, germanene and boron-nitride, were estimated and compared. The adsorption of [CH][BE] ionic liquid on different nanosheets is mainly featured by van der Waals forces, leading to strong benzoate ion–surface π-stacking. Likewise, there is also an important charge transfer from the anion to the sheet. The electronic structure analysis shows that Si- and Ge-based sheets lead to the largest changes in the HOMO and LUMO levels of choline benzoate. This paper provides new insights into the capability of DFT methods to provide useful information about the adsorption of ionic liquids on nanosheets and how ionic liquid features could be tuned through the adsorption on the suitable nanosheet.
URI : http://hdl.handle.net/10259/4332
Versión del editor: http://dx.doi.org/10.1039/C5CP02432C
Aparece en las colecciones: Artículos AdF

Ficheros en este ítem:

Fichero Descripción Tamaño Formato
García-PCCP_2015-25.pdf3,61 MBAdobe PDFVisualizar/Abrir

Los ítems del Repositorio Institucional de la Universidad de Burgos están protegidos por copyright, con todos los derechos reservados, a menos que se indique lo contrario.

 

Valid XHTML 1.0! DSpace Software Copyright © 2002-2008 MIT and Hewlett-Packard - Sobre DSpace