Page 170 - Polymer-based Nanocomposites for Energy and Environmental Applications
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144                Polymer-based Nanocomposites for Energy and Environmental Applications

               2
             r ψ rðÞ ¼  eε  1  X z i n i ∞ðÞe  z i eψ rðÞ=kT             (5.9)
                            i

         where ψ(r) is the potential distribution function varying with distance, r, from the sur-
         face of the nanoparticle, ε is the dielectric constant of the medium, k is the Boltzmann
         constant, and z i and n i (∞) are the valency and concentration of ionic species i in the
         bulk matrix, respectively. For a lower potential, the Debye-H€ uckel approximation can
         be represented given below:

             |z i eψ rðÞ=kT| < 1                                        (5.10)
         The solution of the Eq. (5.9) is simplified to Debye-H€ uckel form as shown below:

                                            1=2
                                           !
                              2e  2 X  2
                       kr
             ψ rðÞ ¼ ψ e  ;k ¼      z n i ∞ðÞ                           (5.11)
                     o
                                     i
                              εkT
                                   i
                                                       1
         where κ is the Debye-H€ uckel parameter in the units of m . The inverse of κ is called
         Debye length. The solution of Eq. (5.11) for a diffused double layer is given by the
         below equation:

                   z i eψ rðÞ    z i eψ oðÞ   kr
             tanh         ¼ tanh         e                              (5.12)
                    4kT            4kT
         Eq. (5.12) is also known as Gouy-Chapman equation, which represents the potential
         variation in the diffused part of the double layer starting from the Stern layer [153].
            Lewis argued that the properties of the polymer-filler interface would become
         dominant over the bulk properties of the constituents as the size of the filler particles
         decreases to the nanometer scale [35,167]. So, engineering the filler surface was a
         good idea to obtain better dispersion of the dielectric filler particles. Hence, the large
         surface area of the filler amplifies the unique interface properties in the nanodielectric.
         Sun et al. studied this concept experimentally on epoxy-/silica-based composites and
         explored the effect of the interface on the dielectric properties [13,176].


         5.2.5.2  Tanaka’s model
         This model explores the role of interface in defining the dielectric properties of the
         nanocomposites [34]. He found that a reduction in the internal field occurred on addi-
         tion of nanofiller due to the decrease in particle size [41]. As mentioned earlier, the
         large particle size causes greater field distortion and larger dielectric loss as compared
         with the nanocomposites. Further, the variation in the space charge distribution has
         been proposed to improve the dielectric behavior in the nanocomposites [177]. There
         is a significant reduction in charge accumulation on addition of a nanofiller, which
         reduces the breakdown at lower fields. Tanaka et al. presented a multicore model
         and discussed the interfacial structure and charge behavior (Fig. 5.5) [178].
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