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Enhanced dielectric performance of poly(vinylidene fluoride)-based composites filled with hexadecylphosphonic acid functionalized nanometals
被引:2
作者:
Chen, Tian
[1
]
Wang, Song
[1
]
Shao, Peipei
[1
]
机构:
[1] Nanjing Univ Aeronaut & Astronaut, Coll Mat Sci & Technol, Nanjing 210016, Jiangsu, Peoples R China
基金:
中国国家自然科学基金;
关键词:
HIGH-PERMITTIVITY;
POLYMER;
CONSTANT;
SURFACE;
MONOLAYERS;
NANOTUBES;
PRESSURE;
GRAPHENE;
OXIDE;
FILM;
D O I:
10.1007/s10854-017-6679-y
中图分类号:
TM [电工技术];
TN [电子技术、通信技术];
学科分类号:
0808 ;
0809 ;
摘要:
Zero-dimensional nickel nanosphere (0-D NiNS), one-dimensional silver nanowire (1-D AgNW) and two-dimensional silver nanoplate (2-D AgNP) were prepared and studied as conductive nanofiller within flexible dielectric poly(vinylidene fluoride) (PVDF) matrix. Hexadecylphosphonic acid (HDPA) modifiers were functionalized onto the surface of those nanometals. X-ray photoelectron spectroscopy (XPS) verified the functionalization of organophosphonic acid surface modification agent. X-ray diffraction characterization (XRD) suggested the surface functionalization did not change the crystal structure of nanometals. The organic dielectric surface modified layer not only acted as interparticle barriers to prevent nanometals from direct connection but also produced excellent compatibility between the fillers and the polymer matrix and ensures the dispersion of fillers in the polymer matrix. Fourier transform infrared spectroscopy (FT-IR) spectra information indicated the increase of electro-active beta-phase of PVDF composites after doping of nanometals and surface functionalization of filler. Among all the PVDF composites, dielectric materials with HDPA functionalized AgNP as fillers have the best dielectric performance. The good dielectric performance could be triggered by relatively smaller size effect, parallel micro-capacitor microstructure, particular morphology and large-small nanosize co-doping way.
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页码:9387 / 9394
页数:8
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