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The electrooxidation of hydroxylamine, NH 2 OH, in 0.1 M phosphate buffer (PB, pH = 7) on Pt-, and Pd-modified Au electrodes prepared by galvanic displacement of underpotential deposited Cu, was investigated by electrochemical techniques and three and in situ vibrational probes, substrate-induced surface enhanced Raman scattering, SI-SERS, surface enhanced infrared absorption, SEIRAS, and Fourier transform infrared reflection-absorption, IRAS, spectroscopies. Analyses of the results obtained made it possible to identify at low overpotentials, solution phase (sol) and adsorbed (ads) nitric oxide, NO, as well as solution phase nitrous oxide, N 2 O. As the potential was increased, the peak(s) ascribed to NO(ads) gained in intensity and new features associated with NO 2 − (ads) and NO 2 − (sol) were clearly discerned. Further excursion toward higher potentials yielded an additional peak assigned to NO 2 (ads). This behavior is analogous to that found for bare Au electrodes in a potential region in which the metal is at least partially oxidized under otherwise the same experimental conditions. |
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