Abstract

The permittivity and power factor of ceramic barium titanate and barium titanate solid solutions have been measured as a function of time, starting from the time of cooling the material through the Curie point. Both parameters decrease linearly with log t over periods extending to several years. A theory is proposed which postulates that a large contribution is made to the permittivity by the motion of domain walls, and that the domain walls are gradually moved to more stable and less polarizable states by thermal agitation. A wide distribution of activation energies, reflecting the random character of obstacles to domain wall motion in a ceramic, yields the log t law. Domain walls moving over low-energy humps are considered responsible for the power factor decay.

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.