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- W4318260225 startingPage "295" @default.
- W4318260225 abstract "In the 21st century, research into energy storage is receiving tremendous attention in the scientific community. Renewable energy sources and energy storage solutions are two main keys in the future global economy. Low-cost environmentally friendly with high-energy conversion and storage efficiency system is needed for the rapid development of electronic devices and vehicles, and also in pulsed power weapon systems. Among the different dielectric materials, relaxor ferroelectrics (RF) and antiferroelectrics (AFE) feature high-recoverable energy density and, for this reason, they are generally used in energy storage materials. Again, in a comparative study, AFE materials showed higher-energy density than RF due to double perovskite loops with negligible remanent polarization (Pr) and high maximum polarization (Pmax) in the former. In this respect, lead-free dielectrics have received importance and are worth investigating due to environmental issues. The association of metal ions with diverse radii can stimulate local electric fields and elastic fields that allow dispersing long-range ordering. The breakup of long-range ordering leads to the creation of polar nanoregions (PNRs) or nanodomains that are responsible for relaxation. The smaller size characteristics of PNRs provide extra apt to aligning and back switching the applied electric field and display thin P-E loops. In the P-E hysteresis study, slim characteristics reflected the relaxor characteristics of the material." @default.
- W4318260225 created "2023-01-28" @default.
- W4318260225 creator A5001433318 @default.
- W4318260225 creator A5025559053 @default.
- W4318260225 date "2023-01-01" @default.
- W4318260225 modified "2023-09-26" @default.
- W4318260225 title "Perovskite lead-free dielectric ceramics: Highly promising materials for energy storage applications" @default.
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- W4318260225 doi "https://doi.org/10.1016/b978-0-323-90586-2.00008-5" @default.
- W4318260225 hasPublicationYear "2023" @default.