The electrical conduction mechanisms of semicrystalline thermoplastic parylene C (-H(2)C-C(6)H(3)Cl-CH(2)-)(n) thin films were studied in large temperature and frequency regions. The alternative current (AC) electrical conduction in parylene C is governed by two processes which can be ascribed to a hopping transport mechanism: correlated barrier hopping (CBH) model at low [77-155 K] and high [473-533 K] temperature and the small polaron tunneling mechanism (SPTM) from 193 to 413 K within the framework of the universal law of dielectric response. The conduction mechanism is explained with the help of Elliot's theory, and the Elliot's parameters are determined. From frequency- and temperature-conductivity characteristics, the activation energy is found to be 1.27 eV for direct current (DC) conduction interpreted in terms of ionic conduction mechanism. The power law dependence of AC conductivity is interpreted in terms of electron hopping with a density N(E(F)) (~10(18) eV cm(-3)) over a 0.023-0.03 eV high barrier across a distance of 1.46-1.54 Å.

α , β, and γ relaxation mechanisms have been identified in semicrystalline (45% of crystallinity) parylene-C (–H2C–C6H3Cl–CH2–)n films. C–Cl bonds induce the β-relaxation and explain increase in the dielectric constant as the frequency decreases in usual temperatures of operation for devices incorporating parylene-C. At cryogenic temperature (<−20 °C), γ-relaxation is assigned to the local motions of phenyl groups. Both β and γ relaxation processes obey an Arrhenius law with activation energy Ea(β)=91.7 kJ/mole and Ea(γ)=8.68 kJ/mole. α-relaxation associated with cooperative segmental motions of the (–H2C–∅–CH2–)n chains is observed with a peak at 10−2 Hz for T=80 °C and follows a Vogel–Fulcher–Tamman–Hesse law.

This study focuses on electrowetting using two immmiscible liquids on a dielectric coating. It is demonstrated that low contact angle of oil on the hydrophobic surfaces is a key parameter to obtain a low hysteresis system, below 2 degrees . On the basis of these results, three aspects of the wetting properties have been studied: the influence of the surface hydrophobic properties, the design of the liquids according to the hydrophobic surface, and a graphical method to solve the Bartell-Osterhof equation and predict the wetting properties of two liquids on a surface. These results define clear design rules to obtain a low hysteresis system, useful for many applications from liquid lenses to displays and laboratory-on-a-chip.

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Dielectric and electrical properties correlated with the structure analysis have been studied on 27% semicrystalline parylene-N (-H2C-C6H4-CH2-)n thin films. Transition-phase, AC- and DC-conduction mechanisms, and the MW-interfacial polarization were identified in parylene N at high temperature by experimental and theoretical investigations. The dielectric analysis based on the dc conductivity highlights a temperature of 230 °C as a transition temperature from the α-form to the β1-form. This structure transition is accompanied by a modification on the DC-conduction mechanisms from ionic to electronic conduction in the α-form and the β1-form, respectively. The AC conduction mechanism is governed by the small polaron tunneling mechanism (SPTM) with WH,α = 0.23 eV and a tunneling distance of 7.71 Å in the α-form, while it becomes a correlated barrier-hopping (CBH) mechanism with a WM,β 1 = 0.52 eV in the β1-form. The imaginary part of the electrical modulus formalism obeys the Kohlrausch-Williams-Watt (KWW) model and shows the presence of the interfacial polarization effect. The theoretical Kohlrausch exponent (βKWW) confirms the existence of the transition phase on the parylene N in the vicinity of the 230 °C as deduced by the DC- and the AC-conduction parameters. The correlations between the experimental results and the theoretical models are very useful knowledge and tools for diverse parylene N applications at high temperature.