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Time-resolved X-ray absorption spectroelectrochemistry of redox active species in solution.
Cheaib, Khaled; Maurice, Baptiste; Mateo, Tiphaine; Halime, Zakaria; Lassalle-Kaiser, Benedikt.
Afiliação
  • Cheaib K; Institut de Chimie Moléculaire et des Matériaux d'Orsay (UMR CNRS 8182), Université Paris-Sud, Batiment 420, Rue du Doyen G. Poitou, 91405 Orsay, France.
  • Maurice B; Synchrotron SOLEIL, l'Orme des Merisiers, Saint-Aubin, 91191 Gif-sur-Yvette, France.
  • Mateo T; Synchrotron SOLEIL, l'Orme des Merisiers, Saint-Aubin, 91191 Gif-sur-Yvette, France.
  • Halime Z; Institut de Chimie Moléculaire et des Matériaux d'Orsay (UMR CNRS 8182), Université Paris-Sud, Batiment 420, Rue du Doyen G. Poitou, 91405 Orsay, France.
  • Lassalle-Kaiser B; Synchrotron SOLEIL, l'Orme des Merisiers, Saint-Aubin, 91191 Gif-sur-Yvette, France.
J Synchrotron Radiat ; 26(Pt 6): 1980-1985, 2019 Nov 01.
Article em En | MEDLINE | ID: mdl-31721743
Electrochemistry and electrocatalysis have been receiving increased attention recently due to their crucial contribution to electrical-to-chemical conversion systems. We describe here the development and operation of a new spectroelectrochemical transmission cell for time-resolved X-ray absorption spectroscopy of solutions. X-ray absorption spectra were recorded on the ROCK beamline of SOLEIL under constant and scanning potentials. Spectra were recorded at a frequency of 2 Hz during a cyclic voltammetry experiment performed on a 20 mM solution of FeIIICl3·6H2O at 20 mV s-1 scanning speed. Spectra with good signal-to-noise ratios were obtained when averaging ten spectra over 5 s, corresponding to a 100 mV potential range. A 90% conversion rate from Fe(III) to Fe(II) was spectroscopically demonstrated in cyclic voltammetry mode.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: J Synchrotron Radiat Ano de publicação: 2019 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: J Synchrotron Radiat Ano de publicação: 2019 Tipo de documento: Article