Electroactive polymers (EAPs) can behave as actuators, changing their shape in response to electrical stimulation. EAPs that are controlled by external electric fields--referred to here as field-type EAPs--include ferroelectric polymers, electrostrictive polymers, dielectric elastomers and liquid crystal polymers. Field-type EAPs can exhibit fast response speeds, low hysteresis and strain levels far above those of traditional piezoelectric materials, with elastic energy densities even higher than those of piezoceramics. However, these polymers also require a high field (>70 V micro m(-1)) to generate such high elastic energy densities (>0.1 J cm(-3); refs 4, 5, 9, 10). Here we report a new class of all-organic field-type EAP composites, which can exhibit high elastic energy densities induced by an electric field of only 13 V micro m(-1). The composites are fabricated from an organic filler material possessing very high dielectric constant dispersed in an electrostrictive polymer matrix. The composites can exhibit high net dielectric constants while retaining the flexibility of the matrix. These all-organic actuators could find applications as artificial muscles, 'smart skins' for drag reduction, and in microfluidic systems for drug delivery.
A ceramic-powder polymer composite, making use of a relaxor ferroelectric polymer that has a high room-temperature dielectric constant as the matrix, is developed. The experimental data show that the dielectric constant of the composites with Pb(Mg1/3Nb2/3)O3–PbTiO3 powders can reach more than 250 with weak temperature dependence. In addition, the composites under a proper preparation procedure exhibit a high breakdown field strength (>120 MV/m), leading to a maximum energy storage density of more than 15 J/cm3. Experimental results also indicate that the high electron irradiation does not have much effect on the dielectric behavior of Pb(Mg1/3Nb2/3)O3–PbTiO3 powders, possibly due to the relaxor nature of the ceramic.
A series of novel hybrid poly(acetoxylstyrene-co-isobutylstyryl-POSS)s (PAS−POSS) and
poly(vinylpyrrolidone-co-isobutylstyryl-POSS)s (PVP−POSS) are synthesized and characterized. The POSS
content in these hybrids can be controlled by varying the monomer feed ratio. The polyhedral
oligosilsesquoixane (POSS) moiety can effectively increase the T
g of the resultant organic/inorganic hybrid
polymer at a relatively high POSS content and produce the hybrid copolymer with narrower molecular
weight distribution. The FTIR spectra are used to investigate the structure−property relationship of
these hybrid polymers, and the T
g enhancement mechanism is discussed in detail.
Addition of an astutely selected third monomer to poly(vinylidene fluoride–trifluoroethylene) (P(VDF‐TrFE))‐based polymers can significantly improve their electromechanical response. This is demonstrated here for the terpolymer containing 1,1‐chlorofluoroethylene as the third monomer, which effectively reduces the all‐trans conformation in the polymer, and thus enhances the molecular conformational changes that accompany the polarization response under an external electric field.
This letter reports the ferroelectric and electromechanical properties of a class of ferroelectric polymer, poly(vinylidene-fluoride–trifluoroethylene–chlorotrifluoroethylene) terpolymer, which exhibits a slim polarization hysteresis loop and a high electrostrictive strain at room temperature. The dielectric and polarization behaviors of this terpolymer are typical of the ferroelectric relaxor. The x-ray and Fourier transform infrared results reveal that the random incorporation of bulky chlorotrifluoroethylene (CTFE) ter-monomers into polymer chains causes disordering of the ferroelectric phase. Furthermore, CTFE also acts as random defect fields which randomize the inter- and intrachain polar coupling, resulting in the observed ferroelectric relaxor behavior.
Spatio-temporal growth of isotactic polystyrene single crystals during isothermal crystallization has been investigated theoretically based on the phase field model by solving temporal evolution of a nonconserved phase order parameter coupled with a heat conduction equation. In the description of the total free energy, an asymmetric double-well local free energy density has been adopted to represent the metastable melt and the stable solid crystal. Unlike the small molecule systems, polymer crystallization rarely reaches thermodynamic equilibrium; most polymer crystals are kinetically stabilized in some metastable states. To capture various metastable polymer crystals, the phase field crystal order parameter at the solidification potential has been treated to be supercooling dependent such that it can assume an intermediate value between zero (melt) and unity (perfect crystal), reflecting imperfect polycrystalline nature of polymer crystals. Two-dimensional simulations exhibit various single crystal morphologies of isotactic polystyrene crystals such as faceted hexagonal patterns transforming to nonfaceted snowflakes with increasing supercooling. Of particular interest is that heat liberation from the crystallizing front influences the curvature of the crystal-melt interface, leading to directional growth of lamellar tips and side branches. The landscape of these morphological textures has been established as a function of anisotropy of surface energy and supercooling. With increasing supercooling and decreasing anisotropy, the hexagonal single crystal transforms to the dense lamellar branching morphology in conformity with the experimental findings.
The soluble poly(methyl methacrylate-co-octavinyl-polyhedral oligomeric silsesquioxane) (PMMA-POSS) hybrid nanocomposites with improved T g and high thermal stability were synthesized by common free radical polymerization and characterized using FTIR, high-resolution 1 H NMR, 29 Si NMR, GPC, DSC, and TGA. The POSS contents in the nanocomposites were determined based on FTIR spectrum, revealing that it can be effectively adjusted by varying the feed ratio of POSS in the hybrid composites. On the basis of the 1 H NMR analysis, the number of the reacted vinyl groups on each POSS molecules was determined to be about 6-8. The DSC and TGA measurements indicated that the hybrid nanocomposites had higher T g and better thermal properties than the pure PMMA homopolymer. The T g increase mechanism was investigated using FTIR, displaying that the dipole-dipole interaction between PMMA and POSS also plays very important role to the T g improvement besides the molecular motion hindrance from the hybrid structure. The thermal stability enhances with increase of POSS content, which is mainly attributed to the incorporation of nanoscale inorganic POSS uniformly dispersed at molecular level.
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