Fortunato Marco, Chandraiahgari Chandrakanth Reddy, De Bellis Giovanni, Ballirano Paolo, Sarto Francesca, Tamburrano Alessio, Sarto Maria Sabrina
Department of Astronautical, Electrical and Energy Engineering, Sapienza University of Rome, Via Eudossiana 18, 00184 Rome, Italy.
Research Center for Nanotechnology Applied to Engineering of Sapienza (CNIS), SNNLab, Sapienza University of Rome, Piazzale Aldo Moro, 5, 00185 Rome, Italy.
Nanomaterials (Basel). 2018 Sep 19;8(9):743. doi: 10.3390/nano8090743.
Novel polymer-based piezoelectric nanocomposites with enhanced electromechanical properties open new opportunities for the development of wearable energy harvesters and sensors. This paper investigates how the dissolution of different types of hexahydrate metal salts affects -phase content and piezoelectric response (d) at nano- and macroscales of polyvinylidene fluoride (PVDF) nanocomposite films. The strongest enhancement of the piezoresponse is observed in PVDF nanocomposites processed with Mg(NO₃)₂⋅6H₂O. The increased piezoresponse is attributed to the synergistic effect of the dipole moment associated with the nucleation of the electroactive phase and with the electrostatic interaction between the CF₂ group of PVDF and the dissolved salt through hydrogen bonding. The combination of nanofillers like graphene nanoplatelets or zinc oxide nanorods with the hexahydrate salt dissolution in PVDF results in a dramatic reduction of d, because the nanofiller assumes a competitive role with respect to H-bond formation between PVDF and the dissolved metal salt. The measured peak value of d reaches the local value of 13.49 pm/V, with an average of 8.88 pm/V over an area of 1 cm². The proposed selection of metal salt enables low-cost production of piezoelectric PVDF nanocomposite films, without electrical poling or mechanical stretching, offering new opportunities for the development of devices for energy harvesting and wearable sensors.
具有增强机电性能的新型聚合物基压电纳米复合材料为可穿戴能量收集器和传感器的发展开辟了新机遇。本文研究了不同类型六水合金属盐的溶解如何影响聚偏氟乙烯(PVDF)纳米复合薄膜在纳米和宏观尺度上的β相含量和压电响应(d)。在用Mg(NO₃)₂⋅6H₂O处理的PVDF纳米复合材料中观察到压电响应的最强增强。压电响应的增加归因于与电活性相成核相关的偶极矩以及PVDF的CF₂基团与溶解盐之间通过氢键的静电相互作用的协同效应。在PVDF中,石墨烯纳米片或氧化锌纳米棒等纳米填料与六水合盐溶解相结合会导致d显著降低,因为纳米填料在PVDF与溶解的金属盐之间的氢键形成方面起到了竞争作用。测得的d峰值达到局部值13.49 pm/V,在1 cm²的面积上平均为8.88 pm/V。所提出的金属盐选择能够低成本生产压电PVDF纳米复合薄膜,无需电场极化或机械拉伸,为能量收集和可穿戴传感器设备的发展提供了新机遇。