TY - JOUR
T1 - Novel polymer ferroelectric behavior via crystal isomorphism and the nanoconfinement effect
AU - Yang, Lianyun
AU - Li, Xinyu
AU - Allahyarov, Elshad
AU - Taylor, Philip L.
AU - Zhang, Q. M.
AU - Zhu, Lei
N1 - Funding Information:
Lei Zhu is currently an Associate Professor of Macromolecular Science and Engineering at Case Western Reserve University. He received his B.S. degree in Materials Chemistry in 1993 and M.S. degree in Polymer Chemistry and Physics in 1996 from Fudan University. He earned his Ph.D. degree in Polymer Science in 2000 from the University of Akron. After two-year post-doctoral experience at University of Akron, he joined Institute of Materials Science and Department of Chemical, Materials and Biomolecular Engineering at University of Connecticut, as an Assistant Professor. In 2009, he moved to Case Western Reserve University. He is recipient of National Science Foundation (NSF) Career Award, 3M Non-tenured Faculty Award, and DuPont Young Professor Award. His research interests include high-k polymer and polymer–inorganic hybrid materials for electrical applications, development of artificial antibody as nanomedicines, and supramolecular self-assembly of supermolecules and polymers. He is author and co-author of ∼100 refereed journal publications and 5 book chapters.
Funding Information:
LZ and QMZ thank the Army Research Office (ARO, W911NF-11-1-0534 ) for supporting this work. LZ also acknowledges support from the Office of Naval Research (ONR, N00014-05-1-0338 ) and National Science Foundation (NSF, DMR-0907580 ). PLT acknowledges support from the Petroleum Research Fund of the American Chemical Society (PRF# 51995-ND7 ). The authors are indebted to Professors Donald Schuele and Jerome Lando at Case Western Reserve University and Professor Takeo Furukawa at Tokyo University of Science for helpful discussions.
PY - 2013/3/22
Y1 - 2013/3/22
N2 - In contrast to the comprehensive understanding of novel ferroelectric [i.e., relaxor ferroelectric (RFE) and antiferroelectric] behavior in ceramics, RFE and double-hysteresis-loop (DHL) behavior in crystalline ferroelectric polymers have only been studied in the past fifteen years. A number of applications such as electrostriction, electric energy storage, and electrocaloric cooling have been realized by utilizing these novel ferroelectric properties. Nonetheless, fundamental understanding behind these novel ferroelectric behaviors is still missing for polymers. In this feature article, we intend to unravel the basic physics via systematic studies of poly(vinylidene fluoride-co-trifluoroethylene) [P(VDF-TrFE)]-based terpolymers, electron-beam (e-beam) irradiated P(VDF-TrFE) copolymers, and PVDF graft copolymers. It is found that both the crystal internal structure and the crystal-amorphous interaction are important for achieving the RFE and DHL behaviors. For the crystal internal structure effect, dipole switching with reduced friction and nanodomain formation by pinning the polymer chains are essential, and they can be achieved through crystal repeating-unit isomorphism (i.e., defect modification). Physical pinning [e.g., in P(VDF-TrFE)-based terpolymers] induces a reversible, electric field-induced RFE↔FE phase transition and thus the DHL behavior, whereas chemical pinning [e.g., in e-beam irradiated P(VDF-TrFE)] results in the RFE behavior. Finally, the crystal-amorphous interaction (or the nanoconfinement effect) results in a competition between the polarization and depolarization local fields. When the depolarization field becomes stronger than the polarization field, a DHL behavior is observed. Obviously, the physics for ferroelectric polymers is different from that for ceramics/liquid crystals and can be largely attributed to the long-chain nature of semicrystalline polymers. This understanding will help us to design new ferroelectric polymers with improved properties and/or better applications.
AB - In contrast to the comprehensive understanding of novel ferroelectric [i.e., relaxor ferroelectric (RFE) and antiferroelectric] behavior in ceramics, RFE and double-hysteresis-loop (DHL) behavior in crystalline ferroelectric polymers have only been studied in the past fifteen years. A number of applications such as electrostriction, electric energy storage, and electrocaloric cooling have been realized by utilizing these novel ferroelectric properties. Nonetheless, fundamental understanding behind these novel ferroelectric behaviors is still missing for polymers. In this feature article, we intend to unravel the basic physics via systematic studies of poly(vinylidene fluoride-co-trifluoroethylene) [P(VDF-TrFE)]-based terpolymers, electron-beam (e-beam) irradiated P(VDF-TrFE) copolymers, and PVDF graft copolymers. It is found that both the crystal internal structure and the crystal-amorphous interaction are important for achieving the RFE and DHL behaviors. For the crystal internal structure effect, dipole switching with reduced friction and nanodomain formation by pinning the polymer chains are essential, and they can be achieved through crystal repeating-unit isomorphism (i.e., defect modification). Physical pinning [e.g., in P(VDF-TrFE)-based terpolymers] induces a reversible, electric field-induced RFE↔FE phase transition and thus the DHL behavior, whereas chemical pinning [e.g., in e-beam irradiated P(VDF-TrFE)] results in the RFE behavior. Finally, the crystal-amorphous interaction (or the nanoconfinement effect) results in a competition between the polarization and depolarization local fields. When the depolarization field becomes stronger than the polarization field, a DHL behavior is observed. Obviously, the physics for ferroelectric polymers is different from that for ceramics/liquid crystals and can be largely attributed to the long-chain nature of semicrystalline polymers. This understanding will help us to design new ferroelectric polymers with improved properties and/or better applications.
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U2 - 10.1016/j.polymer.2013.01.035
DO - 10.1016/j.polymer.2013.01.035
M3 - Review article
AN - SCOPUS:84874935679
SN - 0032-3861
VL - 54
SP - 1709
EP - 1728
JO - Polymer
JF - Polymer
IS - 7
ER -