Abstract
In this work, sol‐gel (SG) oxide films were formed by dip‐coating Pt substrates from Ni, Co, and mixed Ni‐Co sols. After withdrawing the substrate at a constant rate, the films were dried between 100 and 400°C for various periods of time (15 min to 1 h). Based primarily on the cyclic voltammetric behavior of the SG‐formed Ni‐Co films after drying at high temperatures, it is suggested that both the Ni and Co sites undergo redox reactions in 1 M NaOH solutions. This also explains the high charge efficiency and charge density of SG‐derived, Co‐containing Ni oxide films. Careful optimization of the experimental variables in the SG film preparation route indicated that the use of 50:50 Ni‐Co sols, a withdrawal rate of 6 cm/min, and drying at 250°C for 1 h yields films which display the highest charge density, the most rapid redox kinetics, and good stability to prolonged potential cycling. In addition, the charge capacity of the optimized 50:50 Ni‐Co SG oxide films can be increased further by the deposition of multilayers. The redox kinetics of the optimized coatings in 1 M NaOH solution were superior to those for Ni‐Co oxide films of comparable charges, but formed in other ways. Diminished reaction rates resulted when higher film drying temperatures were used (denser films) and when thicker, multilayered films were formed. © 2000 The Electrochemical Society. All rights reserved.
Talk to us
Join us for a 30 min session where you can share your feedback and ask us any queries you have
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.