Journal
POLYMER COMPOSITES
Volume 44, Issue 4, Pages 2488-2499Publisher
WILEY
DOI: 10.1002/pc.27258
Keywords
dielectric properties; ferroelectricity; modification; nanocomposites; structure-property relations
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Polymer composite films were fabricated by embedding well-dispersed ZnO@APTES nanoflakes (0, 20, 30, 40, 50 vol%) into polyvinylidene fluoride (PVDF) matrix using a solution casting method. Surface modification and high aspect ratio morphology of ZnO@APTES enhanced the interfacial interaction between PVDF and ZnO, resulting in reduced dielectric loss and improved energy storage performance. The optimized loading of 30 vol% ZnO@APTES in PVDF showed an appreciable recoverable energy density of about 3.2 J/cm(3), indicating its potential application in energy storing portable devices.
Polymer composite films are ideal materials for advanced energy storage capacitor in electrical systems. Therefore herein, we fabricated a novel series of polyvinylidene fluoride (PVDF) based composites embedded with well dispersed ZnO@APTES {surface modified zinc oxide with (3-Aminopropyl) triethoxysilane (APTES)} nanoflake (0, 20, 30, 40, 50) vol% through solution casting method. Hydrothermally synthesized two-dimensional ZnO was pre-treated with H2O2 and surface modified with APTES for perfect distribution of nanoflake into PVDF matrix. Surface modification and high aspect ratio morphology of ZnO@APTES enhanced the interfacial interaction between organic PVDF and inorganic ZnO through reduction in heterogeneity between them. Surface functionalization reduced the dielectric loss and improved the overall energy storage performance. Investigation of electrical properties proclaimed incorporating 30 Vol% ZnO@APTES in PVDF as optimized loading due to its appreciable W-rec (recoverable energy density) about 3.2 J/cm(3). Relative comparison of the energy storage density (W-rec) of PVDF/ZnO@APTES (30) vol% with recent published works established its enhanced capacitive response and its future application in energy storing portable device.
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