Temperature and frequency dependence of microwave conductivity of isotropic reticulate doped polymers

Frequency dependence of conductivity for reticulate doped systems is observed at room temperature only around 1 GHz and even so it is relatively weak. The temperature dependence of conductivity is characteristic of the CT complex used and not of the polymer matrix. For the system containing TTF-TCNQ, for which the d.c. conductivity has a maximum at c. 230 K (i.e. metal-like behaviour at higher temperatures), this maximum becomes more pronounced and shifts towards lower temperatures with increasing frequency in the GHz range. The temperature dependence of the microwave conductivity is weaker than that of the d.c. conductivity. Such behaviour can be described by a modified Maxwell-Wagner model if an appropriate shape factor for the conducting inclusions is introduced, and if a relatively high conductivity of the continuous phase is assumed. We conclude that charge-carrier transport in reticulate doped polymers is not controlled by insulating barriers. The disorder within microcrystals plays a fundamental role, while the CT complex crystalline network is continuous in spite of very low concentration

Poly(vinyl methyl ether) hydrogels at temperatures below the freezing point of water - molecular interactions and states of water

Water interacting with a polymer reveals a number of properties very different to bulk water. These interactions lead to the redistribution of hydrogen bonds in water. It results in modification of thermodynamic properties of water and the molecular dynamics of water. That kind of water is particularly well observable at temperatures below the freezing point of water, when the bulk water crystallizes. In this work, we determine the amount of water bound to the polymer and of the so-called pre-melting water in poly(vinyl methyl ether) hydrogels with the use of Raman spectroscopy, dielectric spectroscopy, and calorimetry. This analysis allows us to compare various physical properties of the bulk and the premelting water. We also postulate the molecular mechanism responsible for the pre-melting of part of water in poly(vinyl methyl ether) hydrogels. We suggest that above −60 °C, the first segmental motions of the polymer chain are activated, which trigger the process of the pre-melting

Poly(vinyl methyl ether) hydrogels at temperatures below the freezing point of water - molecular interactions and states of water

Water interacting with a polymer reveals a number of properties very different to bulk water. These interactions lead to the redistribution of hydrogen bonds in water. It results in modification of thermodynamic properties of water and the molecular dynamics of water. That kind of water is particularly well observable at temperatures below the freezing point of water, when the bulk water crystallizes. In this work, we determine the amount of water bound to the polymer and of the so-called pre-melting water in poly(vinyl methyl ether) hydrogels with the use of Raman spectroscopy, dielectric spectroscopy, and calorimetry. This analysis allows us to compare various physical properties of the bulk and the premelting water. We also postulate the molecular mechanism responsible for the pre-melting of part of water in poly(vinyl methyl ether) hydrogels. We suggest that above −60 °C, the first segmental motions of the polymer chain are activated, which trigger the process of the pre-melting

Persistent photoexcitation effect on the poly(3-hexylthiophene) film: Impedance measurement and modeling

International audienceWe report on the equivalent circuit modeling of the relaxation behavior of an optically excited thick poly(3-hexylthiophene) (P3HT) film by means of impedance spectroscopy. Fabricated metal-semiconductor-metal devices with Au electrodes showed a nearly perfect ohmic behavior under ambient conditions. Impedance measurements on illuminated P3HT device showed a dramatical decrease of the impedance modulus under illumination and very slow relaxation to the initial state. Impedance-frequency data obtained during relaxation could not be explained by a simple parallel resistance-capacitance circuit but it could be best fitted by incorporating a constant-phase element instead of a normal capacitance. By observing the variation of the circuit parameters, it is found that the relaxation process is dominated by slow recombination (elimination) of the excess photogenerated carriers, which is confirmed by the time-varying photoconductivity of the device

Synthesis and Characterization of Low Loss Dielectric Ceramics Prepared from Composite of Titanate Nanosheets with Barium Ions

We report a strategy for preparing barium titanate precursor, being the composite of titanate nanosheets (TN) with barium ions (Ba-TN), which subjected to step sintering allows obtaining TiO2 rich barium titanate ceramics of stoichiometry BaTi4O9 or Ba2Ti9O20. These compounds are important in modern electronics due to their required dielectric properties and grains’ size that can be preserved in nanometric range. The morphology studies, structural characterization, and dielectric investigations were performed simultaneously in each step of Ba-TN calcinations in order to properly characterize type of obtained ceramic, its grains’ morphology, and dielectric properties. The Ba-TN precursor can be sintered at given temperatures, so that its dielectric permittivity can be tuned between 25 and 42 with controlled temperature coefficients that change from negative 32 ppm/°C for Ba-TN sintered at 900°C up to positive 37 ppm/°C after calcination at 1300°C. XRD analysis and Raman investigations performed for the Ba-TN in the temperature range of 900÷1250°C showed that below 1100°C we obtained as a main phase BaTi4O9, whereas the higher calcinations temperature transformed Ba-TN into Ba2Ti9O20. Taking into account trend of device miniaturization and nanoscopic size requirements, temperatures of 900°C and 1100°C seem to be an optimal condition for Ba-TN precursor calcinations that guarantee the satisfactory value of dielectric permittivity (ε=26 and 32) and ceramic grains with a mean size of ~180 nm and ~550 nm, respectively

Evolution of structure and relaxations in glassy polymers due to aging

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Parylene C as a versatile dielectric material for organic field-effect transistors

An emerging new technology, organic electronics, is approaching the stage of large-scale industrial application. This is due to a remarkable progress in synthesis of a variety of organic semiconductors, allowing one to design and to fabricate, so far on a laboratory scale, different organic electronic devices of satisfactory performance. However, a complete technology requires upgrading of fabrication procedures of all elements of electronic devices and circuits, which not only comprise active layers, but also electrodes, dielectrics, insulators, substrates and protecting/encapsulating coatings. In this review, poly(chloro-para-xylylene) known as Parylene C, which appears to become a versatile supporting material especially suitable for applications in flexible organic electronics, is presented. A synthesis and basic properties of Parylene C are described, followed by several examples of use of parylenes as substrates, dielectrics, insulators, or protecting materials in the construction of organic field-effect transistors

Evolution of structure and relaxations in glassy polymers due to aging

International audienc