Potential-induced acid-base chemistry of adsorbed species

Harlan Mantelli, Ricardo Martinez-Hincapie, Juan Feliu, Daniel Alberto Scherson

研究成果: Article

抜粋

The pKa of bicarbonate ion adsorbed on the surface of Pt(111), HCO3 (ads), in CO2 -saturated KClO4/HClO4 aqueous solutions has been determined by judicious application of a theoretical model originally proposed by Smith and White (Langmuir 1993, 9 (1), 1–3) to explain voltammetric features found for non-redox active alkyl chain monolayers bearing carboxylic moieties irreversibly bound to gold surfaces. The analysis herein presented relied on HCO3 -(ads) and CO3 2-(ads) coverages derived from in situ Fourier transform infrared spectroscopy measurements as a function of potential and pH reported by Martinez-Hincapie et al. (J. Phys. Chem. C 2016, 120 (29), 16191–16199), as input parameters, yielding a pKa for HCO3 (ads) of ca. 2.6 ± 0.2. This value is significantly smaller than that of HCO3 (aq) in bulk solutions, a phenomenon associated with the bonding of the species to the electrode surface, a factor that markedly modifies its acid base characteristics.

元の言語English
記事番号134793
ジャーナルElectrochimica Acta
324
DOI
出版物ステータスPublished - 2019 11 20

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ASJC Scopus subject areas

  • Chemical Engineering(all)
  • Electrochemistry

これを引用

Mantelli, H., Martinez-Hincapie, R., Feliu, J., & Scherson, D. A. (2019). Potential-induced acid-base chemistry of adsorbed species. Electrochimica Acta, 324, [134793]. https://doi.org/10.1016/j.electacta.2019.134793