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具有纯β晶体的双轴取向聚偏二氟乙烯中高极化率取向非晶部分增强的压电性。

Enhanced piezoelectricity from highly polarizable oriented amorphous fractions in biaxially oriented poly(vinylidene fluoride) with pure β crystals.

作者信息

Huang Yanfei, Rui Guanchun, Li Qiong, Allahyarov Elshad, Li Ruipeng, Fukuto Masafumi, Zhong Gan-Ji, Xu Jia-Zhuang, Li Zhong-Ming, Taylor Philip L, Zhu Lei

机构信息

College of Materials Science and Engineering, Shenzhen Key Laboratory of Polymer Science and Technology, Shenzhen University, 518055, Shenzhen, PR China.

Department of Macromolecular Science and Engineering, Case Western Reserve University, Cleveland, OH, 44106-7202, USA.

出版信息

Nat Commun. 2021 Jan 29;12(1):675. doi: 10.1038/s41467-020-20662-7.

Abstract

Piezoelectric polymers hold great potential for various electromechanical applications, but only show low performance, with |d | < 30 pC/N. We prepare a highly piezoelectric polymer (d = -62 pC/N) based on a biaxially oriented poly(vinylidene fluoride) (BOPVDF, crystallinity = 0.52). After unidirectional poling, macroscopically aligned samples with pure β crystals are achieved, which show a high spontaneous polarization (P) of 140 mC/m. Given the theoretical limit of P = 188 mC/m for the neat β crystal, the high P cannot be explained by the crystalline-amorphous two-phase model (i.e., P = 270 mC/m). Instead, we deduce that a significant amount (at least 0.25) of an oriented amorphous fraction (OAF) must be present between these two phases. Experimental data suggest that the mobile OAF resulted in the negative and high d for the poled BOPVDF. The plausibility of this conclusion is supported by molecular dynamics simulations.

摘要

压电聚合物在各种机电应用中具有巨大潜力,但目前性能较低,|d | < 30 pC/N。我们基于双轴取向聚偏二氟乙烯(BOPVDF,结晶度 = 0.52)制备了一种高性能压电聚合物(d = -62 pC/N)。单向极化后,获得了具有纯β晶体的宏观取向样品,其自发极化强度(P)高达140 mC/m。考虑到纯β晶体的P理论极限为188 mC/m,如此高的P无法用晶态-非晶两相模型来解释(即P = 270 mC/m)。相反,我们推断在这两个相之间必定存在大量(至少0.25)的取向非晶部分(OAF)。实验数据表明,取向非晶部分的移动性导致了极化后的BOPVDF具有负的且较高的d值。分子动力学模拟支持了这一结论的合理性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c087/7846586/4f9470e40f14/41467_2020_20662_Fig1_HTML.jpg

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