In situ infrared (FTIR) study of the borohydride oxidation reaction

Autor: Marian Chatenet, Françoise Hahn, Christophe Coutanceau, B. Molina Concha
Přispěvatelé: Laboratoire d'Electrochimie et de Physico-chimie des Matériaux et des Interfaces (LEPMI ), Institut de Chimie du CNRS (INC)-Institut National Polytechnique de Grenoble (INPG)-Institut polytechnique de Grenoble - Grenoble Institute of Technology (Grenoble INP )-Université Joseph Fourier - Grenoble 1 (UJF)-Université Savoie Mont Blanc (USMB [Université de Savoie] [Université de Chambéry])-Centre National de la Recherche Scientifique (CNRS), Laboratoire de catalyse en chimie organique (LACCO), Université de Poitiers-Centre National de la Recherche Scientifique (CNRS)-Institut de Chimie du CNRS (INC)
Jazyk: angličtina
Rok vydání: 2009
Předmět:
Zdroj: Electrochemistry Communications, Vol 11, Iss 1, Pp 223-226 (2009)
Electrochemistry Communications
Electrochemistry Communications, Elsevier, 2009, 11 (1), pp. 223-226. ⟨10.1016/j.elecom.2008.11.018⟩
ISSN: 1388-2481
DOI: 10.1016/j.elecom.2008.11.018⟩
Popis: International audience; The direct borohydride fuel cell (DBFC) is an interesting alternative for the electrochemical power generation at lower temperatures due to its high anode theoretical specific capacity(5 A h g−1). However, the borohydride oxidation reaction (BOR) is a very complex eight-electron reaction, influenced by the nature of the electrode material (catalytic or not with respect to BH4− hydrolysis), the ratio [BH4−][OH−] and the temperature. In order to understand the BOR mechanism, we performed in situ infrared reflectance spectroscopy measurements (SPAIRS technique) in 1 M NaOH/1 M NaBH4with the aim to study intermediate reactions occurring on a gold electrode (a poor BH4− hydrolysis catalyst). We monitored several bands in B–H (1184 cm−1) and B–O bond regions (1326 and 1415 cm−1), appearing sequentially with increasing electrode polarisation. Thanks to these experimental findings, we propose possible initial elementary steps for the BOR.
Databáze: OpenAIRE