Conducting composites of polythiophene and polyfuran with acetylene black

Conducting composites of polythiophene (PTP) and polyfuran (PF) with acetylene black (AB) were prepared via chemical oxidative polymerization of thiophene and furan in a suspension of AB in CHCl₃ at room temperature using anhydrous FeCl₃ as the oxidant. Formation of PTP and PF and their subsequent incorporation in PTP–AB and PF–AB composite systems were confirmed by FTIR analysis. Scanning electron microscope analysis showed the presence of compact clusters of particles in both composites. Transmission electron micrographs of PTP–AB and PF–AB composites showed formation of globular polymer encapsulated AB particles with average diameters of the order of ～100 nm in both systems. Thermogravimetric analysis revealed that the overall thermal stability varied in the order: AB > PTP–AB > PTP and AB > PF–AB > PF. DC conductivity values for the PTP–AB and PF–AB composites were of the order of 10^?2 and 10^?3 S cm^?1, respectively. Copyright © 2004 Society of Chemical Industry     

Conducting composites of poly(N‐vinylcarbazole), polypyrrole,and polyaniline with 13X‐zeolite

N‐vinylcarbazole (NVC) was polymerized by 13X zeolite alone in melt (65°C) or in toluene (110°C) and a poly(N‐vinylcarbazole) (PNVC)‐13X composite was isolated. Composites of polypyrrole (PPY) and polyaniline(PANI) with 13X zeolite were prepared via polymerization of the respective monomers in the presence of dispersion of 13X zeolite in water (CuCl₂ oxidant) and in CHCl₃ (FeCl₃ oxidant) at an ambient temperature. The composites were characterized by Fourier transform infrared analyses. Scanning electron microscopic analyses of various composites indicated the formation of lumpy aggregates of irregular sizes distinct from the morphology of unmodified 13X zeolite. X‐ray diffraction analysis revealed some typical differences between the various composites, depending upon the nature of the polymer incorporated. Thermogravimetric analyses revealed the stability order as: 13X‐zeolite > polymer‐13X‐zeolite > polymer. PNVC‐13X composite was essentially a nonconductor, while PPY‐13X and PANI‐13X composites showed direct current conductivity in the order of 10^?4 S/cm in either system. However, the conductivity of PNVC‐ 13X composite could be improved to 10^?5 and 10^?6 S/cm by loading PPY and PANI, respectively. © 2006 Wiley Periodicals, Inc. J Appl Polym Sci 101: 913–921, 2006     

Evaluating the role of composition and local structure on alkali out-diffusion in glasses for thin-film solar cells

The presence of alkali ions has reportedly improved the performance of CIGS/CZTS–based thin-film solar cells. The out-diffusion of the alkali ion, in particular, Na, from the glass substrate offers a facile scalable route of supplying the alkali ions during the growth of the absorber layer. In this work, we demonstrate the diffusion of different alkali ions (Li/Na/K) from composition tuned glasses with intentionally incorporated excess alkali ions into a thin Mo film, typically used as a bottom electrode in solar cells. We also evaluate the physical, mechanical, and thermal properties of the glasses for suitability as a substrate in thin-film deposition. The out-diffusion of alkali ions to the overlayer is found to be critically influenced by the composition and the local structure of the glasses. The Na ions exhibit the highest extent of diffusion among the alkali ions present in glass substrates, while that for the K-ions is the lowest. For the glasses with mixed alkali ions, the presence of Li facilitated the out-diffusion of Na, whereas K ions appear to inhibit the same. Differently with the existing reports, we show that the activation energy and the presence of Ca ions as additional modifiers play a crucial role in the transport mechanism of the ions. In addition, the synthesized glasses exhibit hardness of the order 5-7 GPa, density ~2.55 g cm^-3. The glass transition temperature lies between 535 and 580°C and the coefficient of thermal expansion 8.5-10 ppm/K, which is highly suitable for use as substrates in thin-film solar cells.     

Comparing and aggregating partially resolved trees

Partially-resolved-that is, non-binary-trees arise frequently in the analysis of species evolution. Non-binary nodes, also called multifurcations, must be treated carefully, since they can be interpreted as reflecting either lack of information or actual evolutionary history. While several distance measures exist for comparing trees, none of them deal explicitly with this dichotomy. Here we introduce two kinds of distance measures between rooted and unrooted partially-resolved phylogenetic trees over the same set of species; the measures address multifurcations directly. For rooted trees, the measures are based on the topologies the input trees induce on triplets; that is, on three-element subsets of the set of species. For unrooted trees, the measures are based on quartets (four-element subsets). The first class of measures are parametric distances, where there is a parameter that weighs the difference between an unresolved triplet/quartet topology and a resolved one. The second class of measures are based on the Hausdorff distance, where each tree is viewed as a set of all possible ways in which the tree can be refined to eliminate unresolved nodes. We give efficient algorithms for computing parametric distances and give conditions under which Hausdorff distances can be calculated approximately in polynomial time. Additionally, we (i) derive the expected value of the parametric distance between two random trees, (ii) characterize the conditions under which parametric distances are near-metrics or metrics, (iii) study the computational and algorithmic properties of consensus tree methods based on the measures, and (iv) analyze the interrelationships among Hausdorff and parametric distances.     

A cation exchange resin from poly(N-vinyl carbazole)

Poly(N-vinyl carbazole) was sulfonated with different sulfonating agents and ion exchange capacities of the resins produced were evaluated. A maximum capacity of 4.5 meq · g^?1 of dry resin was realized when sulfonation was done with 98.8% H₂SO⁴ at 30°C for 10 h. The pH titration curves reveal the nature of a strong monofunctional cation exchanger with a pK value of 2.2. The resin exhibits a moderate rate of exchange with NaCl and is thermally stable up to ca. 250°C.     

Machining feature-based similarity assessment algorithms for prismatic machined parts

This paper presents algorithms for identifying machined parts in a database that are similar to a given query part based on machining features. In this paper we only consider parts that are machined on 3-axis machining centers. We utilize reduced feature vectors consisting of machining feature access directions, feature types, feature volumes, feature dimensional tolerances and feature group cardinality as a basis for assessing shape similarity. We have defined a distance function between two sets of reduced feature vectors to assess the similarity between them from the machining effort point of view. To assess the similarity between the two parts, one set of reduced feature vectors is transformed in space using rigid body transformations with respect to the other set such that the distance between them is minimized. The distance between the two sets of aligned reduced feature vectors is used as a measure of similarity between the two parts. The existing machined parts are rank ordered based on the value of the distance with respect to the query part. The cost of previously machined parts that have a very small distance from the query part can be used as a basis for estimating the cost of machining the new part.     

Polymerization of pyrrole by isopolymetallates of vanadium/molybdenum and preparation of a polypyrrole–molybdenum blues nanocomposite

Oxidative polymerization of pyrrole (PY) was achieved in high yield (>90 %) by adding the monomer directly to isopolyvanadate (IPV) and isopolymolybdate (IPMo) solutions at selected pH. In the case of the IPV solution instantaneous precipitation of a black mass was obtained while in the IPMo solution in situ precipitation of polypyrrole (PPY) onto molybdenum blues (MB) formed through reduction of IPMo by PY resulting in a PPY‐encapsulated MB nanocomposite (PPY–MB). Formation of PPY was confirmed from Fourier‐transform infrared (FTIR) and thermogravimetric (TG) analyses. Transmission electron microscope (TEM) photographs for the composite revealed the formation of spherical particles of average size ≈75 nm. Scanning electron microscope (SEM) analyses showed the distinctive morphological patterns for PPY and PPY–MB composite. The direct current conductivity values for PPY prepared by IPV, IPMo and PPY–MB were of the order of 10^?2, 10^?4 and 10^?6 S cm^?1, respectively. Copyright © 2004 Society of Chemical Industry     

Growth and characterizations of dual ion beam sputtered CIGS thin films for photovoltaic applications

The growth of CIGS thin films on soda-lime glass substrates at different substrate temperatures by dual ion beam sputtering system in a single-step route from a single quaternary sputtering target with the composition of Cu (In_0.70 Ga_0.30) Se₂ was reported. The effects of the substrate temperature on structural, optical, morphological and electrical properties of CIGS films were investigated. Stoichiometry of one such film was investigated by X-ray photoelectron spectroscopy. All CIGS films had demonstrated a strong (112) orientation located at 2θ ~26.70^o, which indicated the chalcopyrite structure of films. The value of full-width at half-maximum of (112) peak was reduced from 0.58° to 0.19° and crystallite size was enlarged from 14.98 to 43.05 nm as growth temperature was increased from 100 to 400 °C. However, atomic force microscope results showed a smooth and uniform surface at lower growth temperature and the surface roughness was observed to increase with increasing growth temperature. Hall measurements exhibited the minimum film resistivity of 0.09 Ω cm with a hole concentration of 2.42 × 10¹⁸ cm^?3 and mobility of 28.60 cm² V^?1 s^?1 for CIGS film grown at 100 °C. Film absorption coefficient was found to enhance nominally from 1 × 10⁵ to 2.3 × 10⁵ cm^?1 with increasing growth temperature from 100 to 400 °C.     

Preparation,characterization and dielectric behaviour of some yttrium doped strontium stannates

Samples of Sr_{(1− 3x/2)}YxSnO₃ are prepared by usual solid state reaction route. X- ray diffraction studies confirm the formation of single cubic perovskite single phase. The dielectric constant and dielectric loss at 1 kHz were measured in the temperature range from room temperature up to -150†C. The dielectric constant decreases and losses increase with increased yttrium content in the samples. The percentage porosity and unit cell parameters are also calculated for the samples.