4.7 Article

Metal-organic frameworks Co3[Co(CN)6]2: A promising candidate for dramatically reinforcing the piezoelectric activity of PVDF

期刊

COMPOSITES SCIENCE AND TECHNOLOGY
卷 196, 期 -, 页码 -

出版社

ELSEVIER SCI LTD
DOI: 10.1016/j.compscitech.2020.108232

关键词

Poly(vinylidene fluoride); Metal-organic frameworks; Co-3[Co(CN)(6)](2); Piezoelectricity

资金

  1. National Natural Science Foundation of China [51905149]
  2. Fundamental Research Funds for the Central Universities [2019B16214]
  3. Nantong Science and Technology Bureau [JC2019003, JC2019086]

向作者/读者索取更多资源

Over decades, the exploration of poly(vinylidene fluoride) (PVDF) based composites with outstanding piezoelectric activity has gained great popularity and interest from diverse research communities because of their potential in realizing flexible sensors and energy harvesters. Herein, in this work, we reported a novel high performance PVDF based piezoelectric composites containing Metal-organic frameworks (MOF) Co-3[Co(CN)(6)](2). The ultra-high specific surface area and unique open framework nanostructure of Co-3[Co(CN)(6)](2) demonstrated to be efficient in inducing strong interfacial coupling effect within PVDF, resulting in piezoelectricity enhancement. Moreover, the redox behavior of metal ions in Co-3[Co(CN)(6)](2 )which provides pathway for electrons, was anticipated to further hardness the interfacial coupling effect and consequently piezoelectric reinforcing effect. Upon an addition of 0.6 wt% Co-3[Co(CN)(6)](2), the piezoelectric response of composites reached the maximum, i.e. a d(33) and a d(31) of 37 pC/N and 33 pC/N, respectively, which are both almost double those of PVDF. Furthermore, the resultant composites exhibited superior electromechanical coupling factor k(31) up to 0.135 while that of pure PVDF was only 0.078. For the first time, we present the applicability of MOF as a new class of reinforcing fillers for piezoelectric composites, providing a new perspective to develop PVDF based composites with superior piezoelectric response.

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