retour à l'accueil

Laboratoire d'Electrochimie Moleculaire, LEM, Paris

UMR CNRS - Université Paris Diderot - Paris France

   
 
Master Frontiers in Chemistry | UFR de Chimie - Université Paris Diderot - Paris 7 CNRS - Institut de chimie Université de Paris Master Chimie Sorbonne Paris Cité UFR de Chimie - Université Paris Diderot - Paris 7 CNRS - Institut de chimie
 |   Ecole Doctorale 388  |    Master Frontiers in Chemistry   |   C'Nano IdF   |   Respore  |
Université Paris Diderot
Université de Paris CNRS, Centre National de la Recherche Scientifique
 
 


Le LEM - Publications: Abstracts

Publication 730

J. Phys. Chem. C , 117 (33),17073-17077, 2013
DOI:10.1021/jp405134a
   
doi

Monometallic cobalt-trisglyoximato complexes as precatalysts for catalytic H2 evolution in water

Sanae El Ghachtouli, Maxime Fournier, Stéphanie Cherdo, Régis Guillot, Marie-France Charlot, Elodie Anxolabéhère-Mallart, Marc Robert, and Ally Aukauloo

Institut de Chimie Moléculaire et des Matériaux d’Orsay, UMR-CNRS 8182, Université de Paris-Sud XI, F-91405, Orsay, France
Univ Paris Diderot, Sorbonne Paris Cité, Laboratoire d’Electrochimie Moléculaire, UMR 7591 CNRS, 15 rue Jean-Antoine de Baïf, F-75205 Paris Cedex 13, France
CEA, iBiTec-S, Service de Bioénergétique Biologie Structurale et Mécanismes (SB2SM), F-91191, Gif-sur-Yvette, France

Electrochemical investigation on differently substituted boron-caped and glyoximato-strapped ligands of cobalt clathrochelate complexes in the presence of acid revealed the formation of cobalt-based nanoparticles at the surface of the electrode. The potential for the electrochemical deposition is a function of the chemical nature of the substituents. The overpotential for the catalytic proton reduction of the resulting cobalt particles at pH 7 was found to be 700 mV less negative than on the bare carbon electrode for a geometric current density of 5 mA/cm2

 
   
 
© 2005 LEM CréditsContactVenir au LEM