Surface morphology effect on magnetoelectric response in P(VDF-TrFE)/nano-porous Ni binderless laminates

被引:1
作者
Song, Manseong [1 ]
Chang, Sang-Mok [1 ]
Yang, Su-Chul [1 ]
机构
[1] Dong A Univ, Dept Chem Engn BK21 FOUR, Busan, South Korea
来源
JOURNAL OF MATERIALS RESEARCH AND TECHNOLOGY-JMR&T | 2023年 / 24卷
基金
新加坡国家研究基金会;
关键词
Magnetoelectric voltage; Binderless laminate; Surface morphology; Electrochemical treatment; Piezoelectric phase; Magnetostrictive phase; NANOGENERATOR; COMPOSITES;
D O I
10.1016/j.jmrt.2023.04.186
中图分类号
T [工业技术];
学科分类号
08 ;
摘要
Owing to the widespread use of electronic devices, energy harvesting technologies have attracted enormous attention to fulfill the soaring energy demands. Considering this, a generator based on the magnetoelectric (ME) effect is proposed as a promising energy harvesting device. As one class of ME materials, polymer-based ME laminates consisting of piezoelectric (PE) and magnetostrictive (MS) phases convert magnetic fields to electric voltage by strain transfer between the PE and MS phases. Herein, P(VDF-TrFE)/nano-porous Ni (P/np-Ni) binderless laminates were designed to investigate the ME voltage in polymerbased ME laminates by regulating the surface morphology of MS substrate. To implement a binderless state, nano-porous Ni (np-Ni) substrates were prepared via an electrochemical treatment. The morphology of np-Ni substrates was electrochemically adjusted with different treatment conditions. As a result, from P/np-Ni binderless laminates, an optimal ME coefficient of 8.41 (& PLUSMN;1.00) mV/cm.Oe was achieved by a stable physical adhesion between the PE polymer and MS nano-porous structures. Moreover, the different ME voltage tendency according to interfacial morphology in the binderless laminates demonstrates the suitable interface configuration for polymer-based ME laminates as energy harvesting devices. & COPY; 2023 The Author(s). Published by Elsevier B.V. This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
引用
收藏
页码:6322 / 6333
页数:12
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