Polymeric Nanofibers with Ultrahigh Piezoelectricity via Self -Orientation of Nanocrystals

被引:160
作者
Liu, Xia [1 ,2 ]
Ma, Jing [3 ]
Wu, Xiaoming [1 ,2 ]
Lin, Liwei [4 ]
Wang, Xiaohong [1 ,2 ]
机构
[1] Tsinghua Univ, Inst Microelect, Beijing 100084, Peoples R China
[2] Tsinghua Univ, Tsinghua Natl Lab Informat Sci & Technol, Beijing 100084, Peoples R China
[3] Tsinghua Univ, Sch Mat Sci & Engn, Beijing 100084, Peoples R China
[4] Univ Calif Berkeley, Dept Mech Engn, Berkeley, CA 94720 USA
基金
中国国家自然科学基金;
关键词
PVDF/GO nanofiber; core shell; piezoelectricity; self; -orientation; ss-phase; piezoresponse force microscopy; PIEZORESPONSE FORCE MICROSCOPY; POLY(VINYLIDENE FLUORIDE); COMPOSITE NANOFIBERS; BETA-PHASE; PVDF; POLYMORPHISM; COEFFICIENT; FABRICATION; REDUCTION; DEVICES;
D O I
10.1021/acsnano.6b07961
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Piezoelectricity in macromolecule polymers has been gaining immense attention, particularly for applications in biocompatible, implantable, and flexible electronic devices. This paper introduces core shell-structured piezoelectric polyvinylidene fluoride (PVDF) nanofibers chemically wrapped by graphene oxide (GO) lamellae (PVDF/GO nanofibers), in which the polar ss-phase nanocrystals are formed and uniaxially self -oriented by the synergistic effect of mechanical stretching, high -voltage alignment, and chemical interactions. The ss-phase orientation of the PVDF/GO nanofibers along their axes is observed at atomic scale through high resolution transmission electron microscopy, and the ss-phase content is found to be 88.5%. The piezoelectric properties of the PVDF/GO nanofibers are investigated in terms of piezoresponse mapping, local hysteresis loops, and polarization reversal by advanced piezoresponse force microscopy. The PVDF/GO nanofibers show a desirable out -of-plane piezoelectric constant (d33) of 93.75 pm WI (at 1.0 wt % GO addition), which is 426% higher than that of the conventional pure PVDF nanofibers. The mechanism behind this dramatic enhancement in piezoelectricity is elucidated by three-dimensional molecular modeling.
引用
收藏
页码:1901 / 1910
页数:10
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