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Lebegue, E., Brousse, T., Crosnier, O., Gaubicher, J. & Cougnon, C. (2012) Direct introduction of redox centers at activated carbon substrate based on acid-substituent-assisted diazotization. Electrochem. Commun. 25 124–127. 
Added by: Laurent Cournède (2016-03-10 21:28:38)
Type de référence: Article
DOI: 10.1016/j.elecom.2012.09.034
Numéro d'identification (ISBN etc.): 1388-2481
Clé BibTeX: Lebegue2012
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Catégories: ST2E
Mots-clés: activated carbon, Catechol, Chemical Grafting, Diazonium salt, Electrodes, energy, Supercapacitor, Surface, systems
Créateurs: Brousse, Cougnon, Crosnier, Gaubicher, Lebegue
Collection: Electrochem. Commun.
Consultations : 4/537
Indice de consultation : 4%
Indice de popularité : 1%
Résumé     
Redox properties have been imparted to activated carbon with a high degree of functionalization by chemical grafting of 2-amino-4,5-dimethoxybenzoic add in situ diazotized. The diazotization reaction was accomplished in the presence or in the absence of HCl for estimating the positive or negative effect of the carboxylic acid substituent on the grafting yield. Thermal gravimetric analysis, X-ray photoelectron spectroscopy and cyclic voltammetry experiments show that when the carboxylic acid group participates to the diazotization reaction. the grafting yield is improved and becomes even better than when the carboxylic group is not present, increasing the capacitance of pristine carbon electrode from 120 to 200 F/g. (C) 2012 Elsevier B.V. All rights reserved.
Added by: Laurent Cournède  
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