Abstract
The adsorption of pyrazine on Au(111) and Ag(111) electrodes from aqueous solutions has been studied ex situ by X-ray photo-electron spectroscopy (XPS). The well known structure transition of pyrazine on Au(111) from flat to vertical is clearly reflected in a change in the N 1s binding energy, while no such change in orientation has been noted for pyrazine on Ag(111), for which a flat-lying molecule is assumed at all potentials. Furthermore, distinctly different electrochemical shifts for the N 1s level were observed for the two orientations in the case of pyrazine on Au(111). This suggests that the electrochemical shift of adsorbed molecules may be successfully employed for sensing the electrostatic potential variation inside the electrochemical double layer. The surface concentration of pyrazine on Au(111) as a function of potential has been determined from XPS intensities and is compared with coulometric data.
Talk to us
Join us for a 30 min session where you can share your feedback and ask us any queries you have
More From: Journal of the Chemical Society, Faraday Transactions
Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.