Abstract

The transformation characterization of Ni(OH)2/NiOOH in Ni-Pt films was investigated using an electrochemical quartz crystal microbalance (EQCM) in an alkaline electrolyte under various experiment conditions. The Ni-Pt films were prepared by electro-deposition on gold-coated quartz crystal chips. When cyclic voltammetry (CV) was performed continually, the OHions diffused into the Ni-Pt film to form Ni(OH)2. The transformation from mixed type Ni(OH)2/NiOOH to � -Ni(OH)2/� -NiOOH occurred gradually. The phase transformation of Ni(OH)2/NiOOH was strongly affected by the composition, deposited weight, and aging conditions of the Ni-Pt films. The results show that high Pt content or high deposited weight of Ni-Pt films postponed the transformation to the � -Ni(OH)2/� -NiOOH phase. � -Ni(OH)2 was directly formed by dipping fresh Ni-Pt films in KOH solution while mixed type Ni(OH)2 was obtained after aging fresh Ni-Pt films in humid O2 atmosphere. These two pre-aging conditions accelerate the phase transformation of Ni(OH)2/NiOOH into � -Ni(OH)2/� -NiOOH. After 1050 and 2100 cycles of the electro-oxidation process of ethanol, the Ni(OH)2 phase in Ni-Pt films still remained in a � -Ni(OH)2-like phase with some � -Ni(OH)2. The well-defined � -Ni(OH)2 phase that formed in the Ni-Pt film after 1050 cycles of CV was more stable in a KOH solution than in a humid O2 atmosphere at room temperature. Ni-Pt films were also evaluated as a sensing element for an ethanol sensor. (doi:10.2320/matertrans.M2010079)

Full Text
Paper version not known

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 call

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.