Interfacial Effect on Dielectric Properties of Polymer Nanocomposites Filled with Core/Shell-Structured Particles

Novel polymer nanocomposites were prepared by solution processing with core/shell structured nanoparticles (carbonaceous shell coating on silver cores) as fillers. The organic carbonaceous shells act as interlayers between the Ag cores as well as with the polymer matrix. It is shown that the electri...

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Bibliographic Details
Published in:Advanced functional materials Vol. 17; no. 14; pp. 2405 - 2410
Main Authors: Shen, Y., Lin, Y. H., Nan, C.-W.
Format: Journal Article
Language:English
Published: Weinheim WILEY-VCH Verlag 24-09-2007
WILEY‐VCH Verlag
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Summary:Novel polymer nanocomposites were prepared by solution processing with core/shell structured nanoparticles (carbonaceous shell coating on silver cores) as fillers. The organic carbonaceous shells act as interlayers between the Ag cores as well as with the polymer matrix. It is shown that the electrical properties of the interlayers play a dominative role in determining the dielectric behavior of the nanocomposites. Insulating interlayers reduce the tunnel current between neighboring Ag cores by causing potential barriers, endowing the nanocomposites with stable and high dielectric constants and low dielectric loss. Furthermore, the stable dielectric constants of the nanocomposites could be tuned by adjusting the thickness of the interlayers. Increasing the conductivity of the interlayers lowers the potential barriers, making the dielectric behavior of the nanocomposites more similar to that of conventional percolative composites. Polymer nanocomposites were prepared with Ag@C core/shell nanoparticles as fillers. The shell acts as an interlayer between metal cores, and its electrical properties play a dominative role in determining the dielectric behavior of the nanocomposites (see figure, which shows the effect of Ag@C volume fraction f on the dielectric constant ϵ of the composite).
Bibliography:istex:265AF3CDFD520C79C5B811DCC597A4FD426F1DFE
This work was supported by the Ministry of Science and Technology of China (Grant No. 2002CB613303) and the NSF of China (Grant No. 50621201).
NSF of China - No. 50621201
ark:/67375/WNG-R6SFKM5M-9
Ministry of Science and Technology of China - No. 2002CB613303
ArticleID:ADFM200700200
ObjectType-Article-2
SourceType-Scholarly Journals-1
ObjectType-Feature-1
content type line 23
ISSN:1616-301X
1616-3028
DOI:10.1002/adfm.200700200