Experimental and theoretical study of AC electrical conduction mechanisms of semicrystalline parylene C thin films.

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.

Chemical vapor deposition synthesis of carbon nanotube-graphene nanosheet hybrids and their application in polymer composites.

Both carbon nanotubes (CNTs) and graphene nanosheets (GNs) have potential applications in polymer composites. Combining them may induce a synergistic effect on enhancing the properties of composites. Herein, CNT-GN 3D hybrids were prepared by liquid injection chemical vapor deposition through a spray containing both carbon feedstocks and catalyst precursors. Vertically aligned CNTs were self-organized on the GNs. The morphology of hybrids could be well controlled as a function of the synthesis parameters. The unique 3D geometry of the CNT-GN hybrids provided composites with a higher electrical conductivity as compared to composites solely reinforced by CNTs or GNs. However, the thermal stability of the neat poly(vinylidene fluoride) matrix was found to decrease upon the addition of these hybrid fillers.

Flexible MnO nanoparticle-anchored N-doped porous carbon nanofiber interlayers for superior performance lithium metal anodes.

The mounting requirements for electric apparatus and vehicles stimulate the rapid progress of energy storage systems. Lithium (Li) metal is regarded as one of the most prospective anodes for high-performance cells. However, the uneven dendrite growth is one of the primary conundrums that hampers the use of the Li metal anode in rechargeable Li batteries. Achieving even Li deposition is crucial to solve this concern. In this study, a stable interlayer based on electrospun flexible MnO nanoparticle/nitrogen (N)-doped (polyimide) PI-based porous carbon nanofiber (MnO-PCNF) films was effectively prepared via electrospinning and in situ growth of MnO to reduce the growth of Li dendrites. It is revealed that the attraction of implanted MnO towards Li, the lithiophilic nature of N dopants and the capillary force of porous architectures are beneficial to the preeminent Li wettability of the MnO-PCNF interlayer. Furthermore, the wettable, stable and conductive structure of the MnO-PCNF interlayer can be retained well, offering rapid charge transfer to Li redox reactions, reduced local current density during the cycling process and homogeneous distribution of deposited Li. Consequently, anodes with MnO-PCNF interlayers can relieve the volume change and inhibit the growth of Li dendrites, demonstrating a remarkable lifetime for lithium metal cells at high current.

Nanocomposite-parylene C thin films with high dielectric constant and low losses for future organic electronic devices.

Nanocomposite-parylene C (NCPC) thin films were deposited with a new technique based on the combination of chemical vapor deposition (CVD) for parylene C deposition and RF-magnetron sputtering for silver deposition. This method yields good dispersion of Ag-containing nanoparticles inside the parylene C polymer matrix. Film composition and structure were studied by using several techniques. It was found that the plasma generated by the RF-magnetron reactor modifies the film density as well as the degree of crystallinity and the size of parylene C crystallites. Moreover, silver is incorporated in the parylene matrix as an oxide phase. The average size of the Ag oxide nanoparticles is lower than 20 nm and influences the roughness of the NCPC films. Samples with various contents and sizes of silver-oxide nanoparticles were investigated by broadband dielectric spectroscopy (BDS) in view of their final application. It was found that both the content and the size of the nanoparticles influence the value of the dielectric constant and the frequency-dependence of the permittivity. In particular, ß-relaxation is affected by the addition of nanoparticles as well as the dissipation factor, which is even improved. A dielectric constant of 5 ± 1 with a dissipation factor of less than 0.045 in the range from 0.1 Hz to 1 MHz is obtained for a 2.7 µm thick NCPC with 3.8% Ag content. This study provides guidance for future NCPC materials for insulating gates in organic field-effect transistors (OFETs) and advanced electronic applications.