Abstract
The dependence of the a‐c response of iridium oxide films upon thickness, potential, and pH was explored in sulfuric and perchloric acid solutions. For concentrations greater than 0.1M, the response function closely resembled that for an injection process diffusively spreading from one interface throughout the film. The response time shifted by a factor of 105 with the potential drop across the film. A porous film model is suggested in which response is determined by the mobility of reduced lattice sites, the diffusion coefficient being controlled by a hydrogen ion exchange current within the pores.
Published Version
Talk to us
Join us for a 30 min session where you can share your feedback and ask us any queries you have
Schedule a callDisclaimer: 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.
