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  • SERS study of the adsorption of gelatin at a copper electrode in sulfuric acid solution

    Author(s)
    BROWN, GM
    HOPE, GA
    Griffith University Author(s)
    Hope, Greg A.
    Year published
    1995
    Metadata
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    Abstract
    The adsorption of gelatin at a copper electrode in sulfuric acid solution has been investigated in situ by SERS spectroscopy. The adsorption of gelation at the copper electrode is supported by the presence of shoulder bands at 260 and 326 cm−1 in all SERS spectra for gelatin, which are assigned to Cu-N vibrational modes, indicative of molecular adsorption via the nitrogen-containing amino acid groups of the molecule. The adsorption of gelatin at the copper electrode is dependent on electrode potential and, furthermore, is accompanied by coadsorption of anion species. In electrolytes containing low chloride concentrations, ...
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    The adsorption of gelatin at a copper electrode in sulfuric acid solution has been investigated in situ by SERS spectroscopy. The adsorption of gelation at the copper electrode is supported by the presence of shoulder bands at 260 and 326 cm−1 in all SERS spectra for gelatin, which are assigned to Cu-N vibrational modes, indicative of molecular adsorption via the nitrogen-containing amino acid groups of the molecule. The adsorption of gelatin at the copper electrode is dependent on electrode potential and, furthermore, is accompanied by coadsorption of anion species. In electrolytes containing low chloride concentrations, halide coadsorption with gelatin occurs at less negative potentials, while sulfate is observed as the coadsorbed species at more negative potentials. In solutions of high chloride concentration, the halide ion is present on the electrode surface over the entire potential range investigated. Additionally, it is apparent that chloride may enhance the adsorption of gelatin at the electrode surface owing to an interaction between the surface adsorbed chloride and the amine groups of the gelatin molecule.
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    Journal Title
    Journal of Electroanalytical Chemistry
    Volume
    397
    Issue
    1-2
    DOI
    https://doi.org/10.1016/0022-0728(95)04159-3
    Subject
    Chemical sciences
    Publication URI
    http://hdl.handle.net/10072/120089
    Collection
    • Journal articles

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