Exchange coupling in P(VDF-TrFE) copolymer based all-organic composites with giant electrostriction

被引:124
作者
Li, JY [1 ]
机构
[1] Univ Nebraska, Dept Mech Engn, Lincoln, NE 68588 USA
关键词
D O I
10.1103/PhysRevLett.90.217601
中图分类号
O4 [物理学];
学科分类号
0702 ;
摘要
In this Letter, we discuss the dramatically enhanced electrostriction and dielectric constant in an all-organic composite consisting of polyvinylidene fluoride trifluoroethylene [P(VDF-TrFE)] copolymer matrix and copper-phthalocyanine (CuPc) particles, which could not be explained by traditional composite theory. Using a Landau-type potential energy combined with energy minimization, we demonstrate that the dramatic property enhancement is due to the exchange coupling between the dielectrically hard P(VDF-TrFE) and dielectrically soft CuPc, which becomes dominant when the heterogeneity size of the composite is comparable to the exchange length. The exchange coupling is a very effective mechanism for the enhancement of functional properties in ferroelectric and dielectric systems, and its variation with various material parameters is demonstrated and discussed.
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