Dielectric Properties of Polymer-Particle Nanocomposites Influenced by Electronic Nature of Filler Surfaces

被引:109
作者
Siddabattuni, Sasidhar [1 ]
Schuman, Thomas P. [1 ]
Dogan, Fatih [2 ]
机构
[1] Missouri Univ Sci & Technol, Dept Chem, 400 W 11th St, Rolla, MO 65409 USA
[2] Missouri Univ Sci & Technol, Dept Mat Sci & Engn, Rolla, MO 65409 USA
基金
美国国家科学基金会;
关键词
interface; organophosphate; dielectric breakdown; permittivity; energy density; SELF-ASSEMBLED MONOLAYERS; BARIUM-TITANATE; BREAKDOWN STRENGTH; PERMITTIVITY; DENSITY; THIN; NANOPARTICLES; BEHAVIOR; SILICA; FILMS;
D O I
10.1021/am3030239
中图分类号
TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
The interface between the polymer and the particle has a critical role in altering the properties of a composite dielectric. Polymer-ceramic nanocomposites are promising dielectric materials for many electronic and power devices, combining the high dielectric constant of ceramic particles with the high dielectric breakdown strength of a polymer. Self-assembled monolayers of electron rich or electron poor organophosphate coupling groups were applied to affect the filler-polymer interface and investigate the role of this interface on composite behavior. The interface has potential to influence dielectric properties, in particular the leakage and breakdown resistance. The composite films synthesized from the modified filler particles dispersed into an epoxy polymer matrix were analyzed by dielectric spectroscopy, breakdown strength, and leakage current measurements. The data indicate that significant reduction in leakage currents and dielectric losses and improvement in dielectric breakdown strengths resulted when electropositive phenyl, electron-withdrawing functional groups were located at the polymer-particle interface. At a 30 vol % particle concentration, dielectric composite films yielded a maximum energy density of similar to 8 J.cm(-3) for TiO2-epoxy nanocomposites and similar to 9.5 J.cm(-3) for BaTiO3-epoxy nanocomposites.
引用
收藏
页码:1917 / 1927
页数:11
相关论文
共 59 条
  • [1] Thermal molecular motion in polystyrene thin and ultrathin films by dynamic viscoelastic measurement
    Akabori, Kei-ichi
    Tanaka, Keiji
    Nagamura, Toshihiko
    Takahara, Atsushi
    Kajiyama, Tisato
    [J]. JOURNAL OF CENTRAL SOUTH UNIVERSITY OF TECHNOLOGY, 2007, 14 (Suppl 1): : 346 - 349
  • [2] Polymer Composite and Nanocomposite Dielectric Materials for Pulse Power Energy Storage
    Barber, Peter
    Balasubramanian, Shiva
    Anguchamy, Yogesh
    Gong, Shushan
    Wibowo, Arief
    Gao, Hongsheng
    Ploehn, Harry J.
    zur Loye, Hans-Conrad
    [J]. MATERIALS, 2009, 2 (04) : 1697 - 1733
  • [3] Filamentary model of dielectric breakdown
    Blonkowski, S.
    [J]. JOURNAL OF APPLIED PHYSICS, 2010, 107 (08)
  • [4] Dynamics of adsorbed poly(methyl acrylate) and poly(methyl methacrylate) on silica
    Blum, FD
    Lin, WY
    Porter, CE
    [J]. COLLOID AND POLYMER SCIENCE, 2003, 281 (03) : 197 - 202
  • [5] DENSITY PROFILE OF TERMINALLY ADSORBED POLYMERS
    BLUM, FD
    SINHA, BR
    SCHWAB, FC
    [J]. MACROMOLECULES, 1990, 23 (15) : 3592 - 3598
  • [6] A rational consideration of space charge
    Boggs, S
    [J]. IEEE ELECTRICAL INSULATION MAGAZINE, 2004, 20 (04) : 22 - 27
  • [7] Finite difference simulations of permittivity and electric field statistics in ceramic-polymer composites for capacitor applications
    Calame, J. P.
    [J]. JOURNAL OF APPLIED PHYSICS, 2006, 99 (08)
  • [8] Carey F. A., 2007, ADV ORGANIC CHEM B
  • [9] Charton M., 1981, Progress in Physical Organic Chemistry, P119
  • [10] Low-voltage organic thin-film transistors with polymeric nanocomposite dielectrics
    Chen, Fang-Chung
    Chuang, Chiao-Shun
    Lin, Yung-Sheng
    Kung, Li-Jen
    Chen, Tung-Hsien
    Shieh, Han-Ping D.
    [J]. ORGANIC ELECTRONICS, 2006, 7 (05) : 435 - 439