کد مقاله | کد نشریه | سال انتشار | مقاله انگلیسی | نسخه تمام متن |
---|---|---|---|---|
218063 | 463180 | 2016 | 9 صفحه PDF | دانلود رایگان |
• FDS adsorbs weakly on Au with Au–S distances longer than those for TU and thioureate.
• Physisorbed FDS dissociates homolytically to yield adsorbed thioureate.
• Some adsorbed thioureate species are reduced to adsorbed thiourea.
• Dosing conditions influence the rate of formation of adsorbed thiourea.
• The thiourea/thioureate adsorbate ratio depends on the applied potential.
The adsorption and reactivity of formamidine disulfide (FDS) were studied at gold single crystal and thin film electrodes in perchloric acid solutions and the results of cyclic voltammetry and in situ infrared spectroscopy (SNIFTIR and ATR-SEIRAS) experiments compared with those previously obtained with thiourea (TU). In addition, optimized geometries and theoretical harmonic vibrational frequencies were obtained for adsorbed FDS, TU and thioureate from plane-wave DFT calculations using periodic surface models. These results were compared in the case of TU and thioureate to those previously obtained with a model Au cluster surface with (111) orientation. In the case of FDS, weak adsorption takes place with the S–S bond essentially parallel to the metal surface. No specific bands for adsorbed FDS can be identified in the experimental ATR-SEIRA spectra. These latter spectra suggest that adsorbed thioureate species are spontaneously formed upon dissociative adsorption of FDS when dosing this molecule at open circuit. Some of the adsorbed thioureate species undergo reductive protonation giving rise to a mixed adlayer formed by adsorbed thioureate and thiourea in a surface process which is faster when a controlled potential of 0.70 V is applied. In agreement with the observations reported when dosing TU, the ratio between TU and thioureate adsorbates is found to depend on the electrode potential, being higher for potentials close to the hydrogen evolution limit and decreasing for higher potential values.
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Journal: Journal of Electroanalytical Chemistry - Volume 764, 1 March 2016, Pages 79–87