Why Citrate Shapes Tetrahedral and Octahedral Colloidal Platinum Nanoparticles in Water
Por favor, use este identificador para citar o enlazar este ítem:
http://hdl.handle.net/10045/79215
Título: | Why Citrate Shapes Tetrahedral and Octahedral Colloidal Platinum Nanoparticles in Water |
---|---|
Autor/es: | Gisbert-González, José M. | Feliu, Juan M. | Ferre-Vilaplana, Adolfo | Herrero, Enrique |
Grupo/s de investigación o GITE: | Electroquímica de Superficies |
Centro, Departamento o Servicio: | Universidad de Alicante. Departamento de Química Física | Universidad de Alicante. Instituto Universitario de Electroquímica |
Palabras clave: | Citrate | Shape | Colloidal platinum nanoparticles | Water |
Área/s de conocimiento: | Química Física |
Fecha de publicación: | 26-jul-2018 |
Editor: | American Chemical Society |
Cita bibliográfica: | The Journal of Physical Chemistry C. 2018, 122(33): 19004-19014. doi:10.1021/acs.jpcc.8b05195 |
Resumen: | The performance of many advanced catalytic systems depends not only on the size and composition but also on the specific shape of the metal nanoparticles (NPs) from which they are assembled. In turn, the shape of colloidal NPs depends on the specific capping agent involved in their synthesis, though the mechanism is still poorly understood. Here, supported by electrochemical experiments, Fourier transform infrared spectra, and density functional theory calculations, on well-defined surfaces, we show how a specific capping agent determines the shape of colloidal NPs. Solvated citrate can become simultaneously adsorbed on the Pt(111) surface through three dehydrogenated carboxylic groups, with each one of them in bidentate configuration. On the other two basal planes, citrate can be adsorbed through only two of them. For this reason, under the synthesis conditions, citrate is more favorably adsorbed on the Pt(111) than on the other two basal planes of platinum. This adsorption behavior explains why colloidal platinum NPs of tetrahedral and octahedral shape are produced when citrate is used as the capping agent in water. The mechanism for citrate would also determine the shape of other pure face-centered cubic metals and can inspire the engineering of future capping agents. |
Patrocinador/es: | This work has been financially supported by the MCINN-FEDER (Spain) through project CTQ2016-76221-P. |
URI: | http://hdl.handle.net/10045/79215 |
ISSN: | 1932-7447 (Print) | 1932-7455 (Online) |
DOI: | 10.1021/acs.jpcc.8b05195 |
Idioma: | eng |
Tipo: | info:eu-repo/semantics/article |
Derechos: | © 2018 American Chemical Society |
Revisión científica: | si |
Versión del editor: | https://doi.org/10.1021/acs.jpcc.8b05195 |
Aparece en las colecciones: | INV - EQSUP - Artículos de Revistas |
Archivos en este ítem:
Archivo | Descripción | Tamaño | Formato | |
---|---|---|---|---|
2018_Gisbert_etal_JPhysChemC_final.pdf | Versión final (acceso restringido) | 2,08 MB | Adobe PDF | Abrir Solicitar una copia |
2018_Gisbert_etal_JPhysChemC_accepted.pdf | Accepted Manuscript (acceso abierto) | 790,63 kB | Adobe PDF | Abrir Vista previa |
Todos los documentos en RUA están protegidos por derechos de autor. Algunos derechos reservados.