Science.gov

Sample records for intrinsically conducting polymer

  1. Intrinsic electrical conductivity of nanostructured metal-organic polymer chains

    PubMed Central

    Hermosa, Cristina; Vicente Álvarez, Jose; Azani, Mohammad-Reza; Gómez-García, Carlos J.; Fritz, Michelle; Soler, Jose M.; Gómez-Herrero, Julio; Gómez-Navarro, Cristina; Zamora, Félix

    2013-01-01

    One-dimensional conductive polymers are attractive materials because of their potential in flexible and transparent electronics. Despite years of research, on the macro- and nano-scale, structural disorder represents the major hurdle in achieving high conductivities. Here we report measurements of highly ordered metal-organic nanoribbons, whose intrinsic (defect-free) conductivity is found to be 104 S m−1, three orders of magnitude higher than that of our macroscopic crystals. This magnitude is preserved for distances as large as 300 nm. Above this length, the presence of structural defects (~ 0.5%) gives rise to an inter-fibre-mediated charge transport similar to that of macroscopic crystals. We provide the first direct experimental evidence of the gapless electronic structure predicted for these compounds. Our results postulate metal-organic molecular wires as good metallic interconnectors in nanodevices. PMID:23591876

  2. Intrinsically Conductive Polymer Fibers from Thermoplastic trans-1,4-Polyisoprene.

    PubMed

    Han, Peng; Zhang, Xiaohong; Qiao, Jinliang

    2016-05-17

    Herein, we report a new strategy to prepare conductive polymer fibers to overcome the insurmountable weakness of current conductive polymer fibers. First, special thermoplastic polymers are processed into polymer fibers using a conventional melt-spinning process, and then the nonconductive polymer fibers are converted into intrinsically conductive polymer fibers. Using this new strategy, intrinsically conductive polymer fibers have been prepared by melt spinning low-cost thermoplastic trans-1,4-polyisoprene and doping with iodine, which can be as fine as 0.01 mm, and the resistivity can be as low as 10(-2) Ω m. Moreover, it has been found that drawing can improve the orientation of trans-1,4-polyisoprene crystals in the fibers and, thus, the conductivity of the conductive polymer fibers. Therefore, conductive fibers with excellent conductivities can be prepared by large drawing ratios before doping. Such conductive polymer fibers with low cost could be used in textile, clothing, packing, and other fields, which would benefit both industry and daily life. The newly developed method also allows one to produce conductive polymers of any shape besides fibers for antistatic or conductive applications. PMID:27135825

  3. Thermally conductive polymers

    NASA Technical Reports Server (NTRS)

    Byrd, N. R.; Jenkins, R. K.; Lister, J. L. (Inventor)

    1971-01-01

    A thermally conductive polymer is provided having physical and chemical properties suited to use as a medium for potting electrical components. The polymer is prepared from hydroquinone, phenol, and formaldehyde, by conventional procedures employed for the preparation of phenol-formaldehyde resins. While the proportions of the monomers can be varied, a preferred polymer is formed from the monomers in a 1:1:2.4 molar or ratio of hydroquinone:phenol:formaldehyde.

  4. Advancing polymers of intrinsic microporosity by mechanochemistry

    DOE PAGESBeta

    Zhang, Pengfei; Jiang, Xueguang; Wan, Shun; Dai, Sheng

    2015-02-20

    Herein, we report a fast (15 min) and solvent-free mechanochemical approach to construct polymers of intrinsic microporosity (PIMs) with high molecular mass and low polydispersity by solid grinding. The enhanced reaction efficiency results from the instantaneous frictional heating and continuous exposure of active sites within those solid reactants.

  5. Water soluble conductive polymers

    SciTech Connect

    Aldissi, M.

    1989-11-14

    This patent describes polymers which are soluble in water and are electrically conductive. The monomer repeat unit is a thiophene or pyrrole molecule having an alkyl group substituted for the hydrogen atom located in the beta position of the thiophene or pyrrole ring and having a surfactant molecule at the end of the alkyl chain. Polymers of this class having 8 or more carbon atoms in the alkyl chain exhibit liquid crystalline behavior, resulting in high electrical anisotropy. The monomer-to-monomer bonds are located between the carbon atoms which are adjacent to the sulfur or nitrogen atoms. The number of carbon atoms in the alkyl group may vary from 1 to 20 carbon atoms. The surfactant molecule consists of a sulfonate group, or a sulfate group, or a carboxylate group, and hydrogen or an alkali metal. Negative ions from a supporting electrolyte which may be used in the electrochemical synthesis of a polymer may be incorporated into the polymer during the synthesis and serve as a dopant to increase the conductivity.

  6. Conducting polymer ultracapacitor

    DOEpatents

    Shi, Steven Z.; Davey, John R.; Gottesfeld, Shimshon; Ren, Xiaoming

    2002-01-01

    A sealed ultracapacitor assembly is formed with first and second electrodes of first and second conducting polymers electrodeposited on porous carbon paper substrates, where the first and second electrodes each define first and second exterior surfaces and first and second opposing surfaces. First and second current collector plates are bonded to the first and second exterior surfaces, respectively. A porous membrane separates the first and second opposing surfaces, with a liquid electrolyte impregnating the insulating membrane. A gasket formed of a thermoplastic material surrounds the first and second electrodes and seals between the first and second current collector plates for containing the liquid electrolyte.

  7. Electrical conduction in polymer dielectrics

    NASA Technical Reports Server (NTRS)

    Cotts, D. B.

    1985-01-01

    The use of polymer dielectrics with moderate resistivities could reduce or eliminate problems associated with spacecraft charging. The processes responsible for conduction and the properties of electroactive polymers are reviewed, and correlations drawn between molecular structure and electrical conductivity. These structure-property relationships led to the development of several new electroactive polymer compositions and the identification of several systems that have the requisite thermal, mechanical, environmental and electrical properties for use in spacecraft.

  8. Conductive polymer-based material

    DOEpatents

    McDonald, William F.; Koren, Amy B.; Dourado, Sunil K.; Dulebohn, Joel I.; Hanchar, Robert J.

    2007-04-17

    Disclosed are polymer-based coatings and materials comprising (i) a polymeric composition including a polymer having side chains along a backbone forming the polymer, at least two of the side chains being substituted with a heteroatom selected from oxygen, nitrogen, sulfur, and phosphorus and combinations thereof; and (ii) a plurality of metal species distributed within the polymer. At least a portion of the heteroatoms may form part of a chelation complex with some or all of the metal species. In many embodiments, the metal species are present in a sufficient concentration to provide a conductive material, e.g., as a conductive coating on a substrate. The conductive materials may be useful as the thin film conducting or semi-conducting layers in organic electronic devices such as organic electroluminescent devices and organic thin film transistors.

  9. Nanostructured conducting polymers for energy applications: towards a sustainable platform

    NASA Astrophysics Data System (ADS)

    Ghosh, Srabanti; Maiyalagan, Thandavarayan; Basu, Rajendra N.

    2016-03-01

    Recently, there has been tremendous progress in the field of nanodimensional conducting polymers with the objective of tuning the intrinsic properties of the polymer and the potential to be efficient, biocompatible, inexpensive, and solution processable. Compared with bulk conducting polymers, conducting polymer nanostructures possess a high electrical conductivity, large surface area, short path length for ion transport and superior electrochemical activity which make them suitable for energy storage and conversion applications. The current status of polymer nanostructure fabrication and characterization is reviewed in detail. The present review includes syntheses, a deeper understanding of the principles underlying the electronic behavior of size and shape tunable polymer nanostructures, characterization tools and analysis of composites. Finally, a detailed discussion of their effectiveness and perspectives in energy storage and solar light harvesting is presented. In brief, a broad overview on the synthesis and possible applications of conducting polymer nanostructures in energy domains such as fuel cells, photocatalysis, supercapacitors and rechargeable batteries is described.

  10. Nanostructured conducting polymers for energy applications: towards a sustainable platform.

    PubMed

    Ghosh, Srabanti; Maiyalagan, Thandavarayan; Basu, Rajendra N

    2016-04-01

    Recently, there has been tremendous progress in the field of nanodimensional conducting polymers with the objective of tuning the intrinsic properties of the polymer and the potential to be efficient, biocompatible, inexpensive, and solution processable. Compared with bulk conducting polymers, conducting polymer nanostructures possess a high electrical conductivity, large surface area, short path length for ion transport and superior electrochemical activity which make them suitable for energy storage and conversion applications. The current status of polymer nanostructure fabrication and characterization is reviewed in detail. The present review includes syntheses, a deeper understanding of the principles underlying the electronic behavior of size and shape tunable polymer nanostructures, characterization tools and analysis of composites. Finally, a detailed discussion of their effectiveness and perspectives in energy storage and solar light harvesting is presented. In brief, a broad overview on the synthesis and possible applications of conducting polymer nanostructures in energy domains such as fuel cells, photocatalysis, supercapacitors and rechargeable batteries is described. PMID:26980404

  11. Conductive polymer coatings for anodes in aqueous electrowinning

    NASA Astrophysics Data System (ADS)

    Alfantazi, A. M.; Moskalyk, R. R.

    2003-07-01

    This article discusses the potential application of electrically conductive polymers as protective coatings for permanent lead anodes employed in aqueous electrowinning processes. Also presented are results from a preliminary study of the performance of two intrinsically conductive polymers (polyaniline and poly 3,4,5-trifluorophenylthiophene [TFPT]) under mild copper electrowinning conditions as conductive and protective coatings on anodic surfaces. The laboratory results indicated that using lead alloy anodes coated with TFPT merits continued research.

  12. Electrically conductive polymer concrete overlays

    NASA Astrophysics Data System (ADS)

    Fontana, J. J.; Webster, R. P.

    1984-08-01

    The use of cathodic protection to prevent the corrosion of reinforcing steel in concrete structures has been well established. Application of a durable, skid-resistant electrically conductive polymer concrete overlay would advance the use of cathodic protection for the highway industry. Laboratory studies indicate that electrically conductive polymer concrete overlays using conductive fillers, such as calcined coke breeze, in conjunction with polyester or vinyl ester resins have resistivities of 1 to 10 ohm-cm. Both multiple-layer and premixed mortar-type overlays were made. Shear bond strengths of the conductive overlays to concrete substrates vary from 600 to 1300 psi, with the premixed overlays having bond strengths 50 to 100% higher than the multiple-layer overlays.

  13. The Workshop on Conductive Polymers: Final Report

    DOE R&D Accomplishments Database

    1985-10-01

    Reports are made by groups on: polyacetylene, polyphenylene, polyaniline, and related systems; molecular, crystallographic, and defect structures in conducting polymers; heterocyclic polymers; synthesis of new and improved conducting polymers; future applications possibilities for conducting polymers; and challenges for improved understanding of properties. (DLC)

  14. The workshop on conductive polymers: Final report

    SciTech Connect

    Not Available

    1985-01-01

    Reports are made by groups on: polyacetylene, polyphenylene, polyaniline, and related systems; molecular, crystallographic, and defect structures in conducting polymers; heterocyclic polymers; synthesis of new and improved conducting polymers; future applications possibilities for conducting polymers; and challenges for improved understanding of properties. (DLC)

  15. Water-soluble conductive polymers

    DOEpatents

    Aldissi, M.

    1988-02-12

    Polymers which are soluble in water and are electrically conductive. The monomer repeat unit is a thiophene or pyrrole molecule having an alkyl group substituted for the hydrogen atom located in the beta position of the thiophene or pyrrole ring and having a surfactant molecule at the end of the alkyl chain. Polymers of this class having 8 or more carbon atoms in the alkyl chain exhibit liquid crystalline behavior, resulting in high electrical anisotropy. The monomer-to-monomer bonds are located between the carbon atoms which are adjacent to the sulfur or nitrogen atoms. The number of carbon atoms in the alkyl group may vary from 1 to 20 carbon atoms. The surfactant molecule consists of a sulfonate group, or a sulfate group, or a carboxylate group, and hydrogen or an alkali metal. Negative ions from a supporting electrolyte which may be used in the electrochemical synthesis of a polymer may be incorporated into the polymer during the synthesis and serve as a dopant to increase the conductivity.

  16. Water-soluble conductive polymers

    DOEpatents

    Aldissi, Mahmoud

    1989-01-01

    Polymers which are soluble in water and are electrically conductive. The monomer repeat unit is a thiophene or pyrrole molecule having an alkyl group substituted for the hydrogen atom located in the beta position of the thiophene or pyrrole ring and having a surfactant molecule at the end of the alkyl chain. Polymers of this class having 8 or more carbon atoms in the alkyl chain exhibit liquid crystalline behavior, resulting in high electrical anisotropy. The monomer-to-monomer bonds are located between the carbon atoms which are adjacent to the sulfur or nitrogen atoms. The number of carbon atoms in the alkyl group may vary from 1 to 20 carbon atoms. The surfactant molecule consists of a sulfonate group, or a sulfate group, or a carboxylate group, and hydrogen or an alkali metal. Negative ions from a supporting electrolyte which may be used in the electrochemical synthesis of a polymer may be incorporated into the polymer during the synthesis and serve as a dopant to increase the conductivity.

  17. Water-soluble conductive polymers

    DOEpatents

    Aldissi, Mahmoud

    1990-01-01

    Polymers which are soluble in water and are electrically conductive. The monomer repeat unit is a thiophene or pyrrole molecule having an alkyl group substituted for the hydrogen atom located in the beta position of the thiophene or pyrrole ring and having a surfactant molecule at the end of the alkyl chain. Polymers of this class having 8 or more carbon atoms in the alkyl chain exhibit liquid crystalline behavior, resulting in high electrical anisotropy. The monomer-to-monomer bonds are located between the carbon atoms which are adjacent to the sulfur or nitrogen atoms. The number of carbon atoms in the alkyl group may vary from 1 to 20 carbon atoms. The surfactant molecule consists of a sulfonate group, or a sulfate group, or a carboxylate group, and hydrogen or an alkali metal. Negative ions from a supporting electrolyte which may be used in the electrochemical synthesis of a polymer may be incorporated into the polymer during the synthesis and serve as a dopant to increase the conductivity.

  18. Water-soluble conductive polymers

    SciTech Connect

    Aldissi, M.

    1990-05-29

    This patent describes polymers which are soluble in water and are electrically conductive. The monomer repeat unit is a thiophene or pyrrole molecule having an alkyl group substituted for the hydrogen atom located in the beta position of the thiophene or pyrrole ring and having a surfactant molecule at the end of the alkyl chain. Polymers of this class having 8 or more carbon atoms in the alkyl chain exhibit liquid crystalline behavior, resulting in high electrical anisotropy. The monomer-to-monomer bonds are located between the carbon atoms which are adjacent to the sulfur or nitrogen atoms. The number of carbon atoms in the alkyl group may vary from 1 to 20 carbon atoms. The surfactant molecule consists of a sulfonate group, or a sulfate group, or a carboxylate group, and hydrogen or an alkali metal. Negative ions from a supporting electrolyte which may be used in the electrochemical synthesis of a polymer may be incorporated into the polymer during the synthesis and serve as a dopant to increase the conductivity.

  19. Electrically conductive polymer concrete coatings

    DOEpatents

    Fontana, J.J.; Elling, D.; Reams, W.

    1988-05-26

    A sprayable electrically conductive polymer concrete coating for vertical and overhead applications is described. The coating is permeable yet has low electrical resistivity (<10 ohm-cm), good bond strength to concrete substrates, and good weatherability. A preferred formulation contains about 60 wt% calcined coke breeze, 40 wt% vinyl ester resin with 3.5 wt% modified bentonite clay. Such formulations apply evenly and provide enough rigidity for vertical or overhead structures so there is no drip or sag. 4 tabs.

  20. Electrically conductive polymer concrete coatings

    DOEpatents

    Fontana, J.J.; Elling, D.; Reams, W.

    1990-03-13

    A sprayable electrically conductive polymer concrete coating for vertical d overhead applications is described. The coating is permeable yet has low electrical resistivity (<10 ohm-cm), good bond strength to concrete substrates, and good weatherability. A preferred formulation contains about 60 wt % calcined coke breeze, 40 wt % vinyl ester with 3.5 wt % modified bentonite clay. Such formulations apply evenly and provide enough rigidity for vertical or overhead structures so there is no drip or sag.

  1. Electrically conductive polymer concrete coatings

    DOEpatents

    Fontana, Jack J.; Elling, David; Reams, Walter

    1990-01-01

    A sprayable electrically conductive polymer concrete coating for vertical d overhead applications is described. The coating is permeable yet has low electrical resistivity (<10 ohm-cm), good bond strength to concrete substrates, and good weatherability. A preferred formulation contains about 60 wt % calcined coke breeze, 40 wt % vinyl ester with 3.5 wt % modified bentonite clay. Such formulations apply evenly and provide enough rigidity for vertical or overhead structures so there is no drip or sag.

  2. Comparing proton conductivity of polymer electrolytes by percent conducting volume

    SciTech Connect

    Kim, Yu Seung; Pivovar, Bryan

    2009-01-01

    Proton conductivity of sulfonated polymers plays a key role in polymer electrolyte membrane fuel cells. Mass based water uptake and ion exchange capacity of sulfonated polymers have been failed to correlating their proton conductivity. In this paper, we report a length scale parameter, percent conductivity volume, which is rather simply obtained from the chemical structure of polymer to compare proton conductivity of wholly aromatic sulfonated polymer perflurosulfonic acid. Morphology effect on proton conductivity at lower RH conditions is discussed using the percent conductivity volume parameter.

  3. Conducting polymer based electrochemical biosensors.

    PubMed

    Aydemir, Nihan; Malmström, Jenny; Travas-Sejdic, Jadranka

    2016-03-28

    Conducting polymer (CP)-based electrochemical biosensors have gained great attention as such biosensor platforms are easy and cost-effective to fabricate, and provide a direct electrical readout for the presence of biological analytes with high sensitivity and selectivity. CP materials themselves are both sensing elements and transducers of the biological recognition event at the same time, simplifying sensor designs. This review summarizes the advances in electrochemical biosensors based on CPs. Recognition probe immobilisation techniques, transduction mechanisms and detection of various target biomolecules have been discussed in detail. Efforts to miniaturize CP-based electrochemical biosensors and fabrication of sensor arrays are also briefly reviewed. PMID:26948182

  4. Electrically conducting polymers for aerospace applications

    NASA Technical Reports Server (NTRS)

    Meador, Mary Ann B.; Gaier, James R.; Good, Brian S.; Sharp, G. R.; Meador, Michael A.

    1991-01-01

    Current research on electrically conducting polymers from 1974 to the present is reviewed focusing on the development of materials for aeronautic and space applications. Problems discussed include extended pi-systems, pyrolytic polymers, charge-transfer systems, conductive matrix resins for composite materials, and prospects for the use of conducting polymers in space photovoltaics.

  5. Electronically conductive polymer composites and microstructures

    SciTech Connect

    Van Dyke, L.S.

    1993-01-01

    Composites of electronically conductive polymers with insulating host materials are investigated. A template synthesis method was developed for the production of electronically conductive polymer microstructures. In template synthesis the pores of a porous host membrane act as templates for the polymerization of a conductive polymer. The template synthetic method can be used to form either solid microfibrils or hollow microtubules. The electrochemical properties of conductive polymers produced via the template synthesis method are superior to those of conventionally synthesized conductive polymers. Electronically conductive polymers are used to impart conductivity to non-conductive materials. Two different approaches are used. First, thin film composites of conductive polymers with fluoropolymers are made by the polymerization of conductive polymers onto fluoropolymer films. Modification of the fluoropolymer surface prior to conductive polymer polymerization is necessary to obtain good adhesion between the two materials. The difference in adhesion of the conductive polymer to the modified and unmodified fluoropolymer surfaces can be used to pattern the conductive polymer coating. Patterning of the conductive polymer coating can alternatively be done via UV laser ablation of the conductive polymer. The second method by which conductive polymers were used to impart conductivity to an insulating polymer was via the formation of a graft copolymer. In this approach, heterocyclic monomers grafted to an insulating polyphosphazene backbone were polymerized to yield semiconductive materials. Finally the measurement of electrolyte concentration in polypyrrole and the effects of hydroxide anion on the electrochemical and electrical properties of polypyrrole are described. It is shown that treatment of polypyrrole with hydroxide anion increases the potential window over which polypyrrole is a good electronic conductor.

  6. Advances in inherently conducting polymers

    SciTech Connect

    Aldissi, M.

    1987-09-01

    The discovery of polyacetylene as the prototype material led to extensive research on its synythesis and characterization. The techniques that emerged as the most important and promising ones are those that dealt with molecular orientation and that resulted in conductivities almost as high as that of copper. The study of dozens of other materials followed. Interest in conducting polymers stems from their nonclassical optical and electronic properties as well as their potential technological applications. However, some of the factors currently limiting their use are the lack of long-term stability and the need to develop conventional low-cost techniques for easy processing. Therefore, research was extended toward solving these problems, and progress has been recently made in that direction. The synthesis of new materials such as stable and easily processable alkylthiophenes, water-soluble polymers, and multicomponent systems, including copolymers and composites, constitutes an important step forward in the area of synthetic metals. However, a full understanding of materials chemistry and properties requires more work in the years to come. Although, few small-scale applications have proven to be successful, long-term stability and applicability tests are needed before their commercial use becomes reality.

  7. Flexible conductive polymer polarizer designed for a chemical tag

    NASA Astrophysics Data System (ADS)

    Washburn, C. M.; Jones, J. C.; Vigil, S. R.; Finnegan, P. S.; Boye, R. R.; Hunker, J. D.; Scrymgeour, D. A.; Dirk, S. M.; Hance, B. G.; Strong, J. M.; Massey, L. M.; Brumbach, M. T.

    2013-03-01

    Conductive polymers with high solids loading (> 40wt.%) are challenging to pattern to single micron feature sizes and require unique techniques or templates to mold the material. The development of a conductive polymer optical tag is discussed for identifying the presence of hydrofluoric acid (HF) and leverages free standing silicon fins as a template utilizing deep reactive ion etching (DRIE) techniques will be discussed. This work is aimed towards a future flexible conductive polymer tag to be transferred via adhesive or epoxy for a novel sensor surface. The advantage to this technique over wafer thinning is a higher throughput of device manufacture without damage to the silicon fins or polymer due to chemical-mechanical interactions or added protective layers. The gratings consist of a high spatial frequency (1.15 μm pitch) grating consisting of lines of conductive polymer and lines of silicon which are free standing. A novel running bond pattern aims to minimize the intrinsic stress and allows the conductive polymer to infiltrate without distorting the template. The polymer conductivity mechanism has been designed to break down under a chemical binding to fluorine; changing its conductivity upon exposure, and results in a change in the polarization response. The use of the polarization response makes the signal more robust to intensity fluctuations in the background or interrogation system. Additionally, the use of optical interrogation allows for standoff detection in instances where hazardous conditions may be present. Examples of material and device responses will be shown and directions for further investigation are discussed.

  8. Conducting Polymers for Neutron Detection

    SciTech Connect

    Kimblin, Clare; Miller, Kirk; Vogel, Bob; Quam, Bill; McHugh, Harry; Anthony, Glen; Mike, Grover

    2007-12-01

    Conjugated polymers have emerged as an attractive technology for large-area electronic applications. As organic semiconductors, they can be used to make large-area arrays of diodes or transistors using fabrication techniques developed for polymer coatings, such as spraying and screen-printing. We have demonstrated both neutron and alpha detection using diodes made from conjugated polymers and have done preliminary work to integrate a boron carbide layer into the conventional polymer device structure to capture thermal neutrons. The polymer devices appear to be insensitive to gamma rays, due to their small physical thickness and low atomic number.

  9. Mixed ionic and electronic conductivity in polymers

    SciTech Connect

    Shriver, D.F.

    1990-06-01

    The conductivity of iodine-containing polymers was investigated and conductivity along polyiodide chains is implicated by the concentration dependence of the conductivity data and spectroscopic measurements. On the theoretical side, entropy based models were developed to describe ion motion in polymers.

  10. Nanostructured polymer membranes for proton conduction

    DOEpatents

    Balsara, Nitash Pervez; Park, Moon Jeong

    2013-06-18

    Polymers having an improved ability to entrain water are characterized, in some embodiments, by unusual humidity-induced phase transitions. The described polymers (e.g., hydrophilically functionalized block copolymers) have a disordered state and one or more ordered states (e.g., a lamellar state, a gyroid state, etc.). In one aspect, the polymers are capable of undergoing a disorder-to-order transition while the polymer is exposed to an increasing temperature at a constant relative humidity. In some aspects the polymer includes a plurality of portions, wherein a first portion forms proton-conductive channels within the membrane and wherein the channels have a width of less than about 6 nm. The described polymers are capable of entraining and preserving water at high temperature and low humidity. Surprisingly, in some embodiments, the polymers are capable of entraining greater amounts of water with the increase of temperature. The polymers can be used in Polymer Electrolyte Membranes in fuel cells.

  11. Ionic conduction in polymer composite electrolytes

    NASA Astrophysics Data System (ADS)

    Dam, Tapabrata; Tripathy, Satya N.; Paluch, M.; Jena, S.; Pradhan, D. K.

    2016-05-01

    Conductivity and structural relaxation has been explored from modulus and dielectric loss formalisms respectively for a series of polymer composite electrolytes with zirconia as filler. The temperature dependence of conductivity followed Vogel-Tamman-Fulcher (VTF) behavior, which suggested a close correlation between conductivity and the segmental relaxation process in polymer electrolytes. Vogel temperature (T0) plays significant role in ion conduction process in these kind of materials.

  12. Biochemical synthesis of water soluble conducting polymers

    NASA Astrophysics Data System (ADS)

    Bruno, Ferdinando F.; Bernabei, Manuele

    2016-05-01

    An efficient biomimetic route for the synthesis of conducting polymers/copolymers complexed with lignin sulfonate and sodium (polystyrenesulfonate) (SPS) will be presented. This polyelectrolyte assisted PEG-hematin or horseradish peroxidase catalyzed polymerization of pyrrole (PYR), 3,4 ethyldioxithiophene (EDOT) and aniline has provided a route to synthesize water-soluble conducting polymers/copolymers under acidic conditions. The UV-vis, FTIR, conductivity and cyclic voltammetry studies for the polymers/copolymer complex indicated the presence of a thermally stable and electroactive polymers. Moreover, the use of water-soluble templates, used as well as dopants, provided a unique combination of properties such as high electronic conductivity, and processability. These polymers/copolymers are nowadays tested/evaluated for antirust features on airplanes and helicopters. However, other electronic applications, such as photovoltaics, for transparent conductive polyaniline, actuators, for polypyrrole, and antistatic films, for polyEDOT, will be proposed.

  13. Morphology in electrochemically grown conducting polymer films

    DOEpatents

    Rubinstein, Israel; Gottesfeld, Shimshon; Sabatani, Eyal

    1992-01-01

    A conducting polymer film with an improved space filling is formed on a metal electrode surface. A self-assembling monolayer is formed directly on the metal surface where the monolayer has a first functional group that binds to the metal surface and a second chemical group that forms a chemical bonding site for molecules forming the conducting polymer. The conducting polymer is then conventioonally deposited by electrochemical deposition. In one example, a conducting film of polyaniline is formed on a gold electrode surface with an intermediate monolayer of p-aminothiophenol.

  14. Morphology in electrochemically grown conducting polymer films

    DOEpatents

    Rubinstein, I.; Gottesfeld, S.; Sabatani, E.

    1992-04-28

    A conducting polymer film with an improved space filling is formed on a metal electrode surface. A self-assembling monolayer is formed directly on the metal surface where the monolayer has a first functional group that binds to the metal surface and a second chemical group that forms a chemical bonding site for molecules forming the conducting polymer. The conducting polymer is then conventionally deposited by electrochemical deposition. In one example, a conducting film of polyaniline is formed on a gold electrode surface with an intermediate monolayer of p-aminothiophenol. 2 figs.

  15. Dual function conducting polymer diodes

    DOEpatents

    Heeger, Alan J.; Yu, Gang

    1996-01-01

    Dual function diodes based on conjugated organic polymer active layers are disclosed. When positively biased the diodes function as light emitters. When negatively biased they are highly efficient photodiodes. Methods of preparation and use of these diodes in displays and input/output devices are also disclosed.

  16. Electronically conducting polymers with silver grains

    NASA Technical Reports Server (NTRS)

    Murphy, Oliver J. (Inventor); Hitchens, G. Duncan (Inventor); Hodko, Dolibor (Inventor)

    1999-01-01

    The present invention provides electronically conducting polymer films formed from photosensitive formulations of pyrrole and an electron acceptor that have been selectively exposed to UV light, laser light, or electron beams. The formulations may include photoinitiators, flexibilizers, solvents and the like. These solutions can be used in applications including printed circuit boards and through-hole plating and enable direct metallization processes on non-conducting substrates. After forming the conductive polymer patterns, a printed wiring board can be formed by sensitizing the polymer with palladium and electrolytically depositing copper.

  17. Application of conducting polymers to electroanalysis

    SciTech Connect

    Josowicz, M.A.

    1994-04-01

    Conducting polymers can be used as sensitive layers in chemical microsensors leading to new applications of theses devices. They offer the potential for developing material properties that are critical to the sensor sensitivity, selectivity and fabrication. The advantages and limitations of the use of thin polymer layers in electrochemical sensors are discussed.

  18. Conductance tomography of conductive filaments in intrinsic silicon-rich silica RRAM.

    PubMed

    Buckwell, Mark; Montesi, Luca; Hudziak, Stephen; Mehonic, Adnan; Kenyon, Anthony J

    2015-11-21

    We present results from an imaging study of filamentary conduction in silicon suboxide resistive RAM devices. We used a conductive atomic force microscope to etch through devices while measuring current, allowing us to produce tomograms of conductive filaments. To our knowledge this is the first report of such measurements in an intrinsic resistance switching material. PMID:26482563

  19. Engineering thermal conductivity in polymer blends

    NASA Astrophysics Data System (ADS)

    Rashidi, Vahid; Coyle, Eleanor; Kieffer, John; Pipe, Kevin

    Weak inter-chain bonding in polymers is believed to be a bottleneck for both thermal conductivity and mechanical strength. Most polymers have low thermal conductivity (~0.1 W/mK), hindering their performance in applications for which thermal management is critical (e.g., electronics packaging). In this work, we use computational methods to study how hydrogen bonding between polymer chains as well as water content can be used to engineer thermal transport in bulk polymers. We examine how changes in the number of hydrogen bonds, chain elongation, density, and vibrational density of states correlate with changes in thermal conductivity for polymer blends composed of different relative constituent fractions. We also consider the effects of bond strength, tacticity, and polymer chain mass. For certain blend fractions, we observe large increases in thermal conductivity, and we analyze these increases in terms of modifications to chain chemistry (e.g., inter-chain bonding) and chain morphology (e.g., chain alignment and radius of gyration). We observe that increasing the number of hydrogen bonds in the system results in better packing as well as better chain alignment and elongation that contribute to enhanced thermal conductivity. The Air Force Office of Scientific Research, Grant No. FA9550-14-1-0010.

  20. Electrically conductive and redox electroactive organic polymers

    SciTech Connect

    Reynolds, J.R.; Balanda, P.B.; Sotzing, G.A.

    1995-12-01

    We describe new fully conjugated bis(pyrrol-2-yl)arylene and bis(3,4-dioxyethylenethiophene)arylene monomers which electropolymerize at low potentials avoiding degradative side reactions to yield highly stable redox switchable polymers. We outline the properties of DOET polymers which exhibit low electronic band gaps allowing for the formation of conducting complexes with a high degree of optical transmission of visible light and show their electrochromic properties. Finally, we discuss the properties of polymers containing electron donor molecules as an integral part of the polymer backbone and as pendant substituents. These donor molecules have been chosen due to their propensity to form metallic, and in some instances superconducting, crystalline complexes and suggest these properties can be extended to highly processible organic polymers.

  1. Conducting polymer membranes as intelligent separation systems

    SciTech Connect

    Price, W.E.; Wallace, G.G.

    1994-12-31

    Conducting electroactive polymers such as polypyrroles, are emerging as excellent materials in which to base a generic technology for the development of intelligent material systems. They are easy to make and many different chemistries may be built in during synthesis by varying the polymer(s) used and the counterions incorporated. However, the unique feature about them is that they have dynamic chemical and physical properties which may be manipulated via changing the redox states after synthesis. This paper illustrates their potential using recent work on developing a new electro-membrane separation technology using free-standing polypyrrole films. These systems are shown to be capable of a high degree of permselectivity and controllable transport that may be turned on and off by application of potential to the conducting polymer membrane.

  2. On the high conductivity of nonconjugated polymers

    SciTech Connect

    Lachinov, A. N. Kornilov, V. M.; Zagurenko, T. G.; Zherebov, A. Yu.

    2006-04-15

    The mechanism of charge transfer in a metal-electroactive polymer-metal structure has been experimentally studied near the threshold of the uniaxial-pressure-induced transition into a high-conductivity state in the polymer. The dynamics of the I-V curve is investigated as a function of the applied pressure. The data obtained are analyzed in terms of the model of injection currents using the concepts of possible scanning of a quasi-Fermi level near an injection level. Our estimates suggest that a narrow band made of deep trap states located near the Fermi level forms in the polymer film in the pretransition pressure range. In the immediate vicinity of the transition range, a narrow band of coherent charge transfer appears from these states; this band can be responsible for the high metal-type conductivity of thin polymer films, which has been repeatedly observed by many researchers.

  3. Mixed ionic and electronic conductivity in polymers

    SciTech Connect

    Shriver, D.F.

    1991-06-01

    New polymer films were synthesized that are mixed ionic-electronic conductors. Preliminary ion transport measurements have been made on these materials in the reduced state where electronic conductivity is negligible. We also have made preliminary measurements of switching times for these materials. Theoretical studies have been performed ion pairing in insulating and electronically conducting films.

  4. Liquid crystal-templated conducting organic polymers

    DOEpatents

    Stupp, Samuel I.; Hulvat, James F.

    2004-01-20

    A method of preparing a conductive polymeric film, includes providing a liquid crystal phase comprising a plurality of hydrophobic cores, the phase on a substrate, introducing a hydrophobic component to the phase, the component a conductive polymer precursor, and applying an electric potential across the liquid crystal phase, the potential sufficient to polymerize the said precursor.

  5. Increasing the conductivity of crystalline polymer electrolytes.

    PubMed

    Christie, Alasdair M; Lilley, Scott J; Staunton, Edward; Andreev, Yuri G; Bruce, Peter G

    2005-01-01

    Polymer electrolytes consist of salts dissolved in polymers (for example, polyethylene oxide, PEO), and represent a unique class of solid coordination compounds. They have potential applications in a diverse range of all-solid-state devices, such as rechargeable lithium batteries, flexible electrochromic displays and smart windows. For 30 years, attention was focused on amorphous polymer electrolytes in the belief that crystalline polymer:salt complexes were insulators. This view has been overturned recently by demonstrating ionic conductivity in the crystalline complexes PEO6:LiXF6 (X = P, As, Sb); however, the conductivities were relatively low. Here we demonstrate an increase of 1.5 orders of magnitude in the conductivity of these materials by replacing a small proportion of the XF6- anions in the crystal structure with isovalent N(SO2CF3)2- ions. We suggest that the larger and more irregularly shaped anions disrupt the potential around the Li+ ions, thus enhancing the ionic conductivity in a manner somewhat analogous to the AgBr(1-x)I(x) ionic conductors. The demonstration that doping strategies can enhance the conductivity of crystalline polymer electrolytes represents a significant advance towards the technological exploitation of such materials. PMID:15635406

  6. Temperature dependence of conductivity measurement for conducting polymer

    NASA Astrophysics Data System (ADS)

    Gutierrez, Leandro; Duran, Jesus; Isah, Anne; Albers, Patrick; McDougall, Michael; Wang, Weining

    2014-03-01

    Conducting polymer-based solar cells are the newest generation solar cells. While research on this area has been progressing, the efficiency is still low because certain important parameters of the solar cell are still not well understood. It is of interest to study the temperature dependence of the solar cell parameters, such as conductivity of the polymer, open circuit voltage, and reverse saturation current to gain a better understanding on the solar cells. In this work, we report our temperature dependence of conductivity measurement using our in-house temperature-varying apparatus. In this project, we designed and built a temperature varying apparatus using a thermoelectric cooler module which gives enough temperature range as we need and costs much less than a cryostat. The set-up of the apparatus will be discussed. Temperature dependence of conductivity measurements for PEDOT:PSS films with different room-temperature conductivity will be compared and discussed. NJSGC-NASA Fellowship grant

  7. Conducting polymers: Synthesis and industrial applications

    SciTech Connect

    Gottesfeld, S.

    1995-05-01

    The Conducting Polymer project funded by the AIM Materials Program is developing new methods for the synthesis of electronically conducting polymers and is evaluating new industrial applications for these materials which will result in significant reductions in energy usage or industrial waste. The applications specifically addressed during FY 1994 are electrochemical capacitors and membranes for gas separation. As an active material in electrochemical capacitors, conducting polymers have the potential of storing large amounts of electrical energy in low cost materials. Such devices are needed in electronics for power failure back-up and peak power, in power supplies for filtering, and in electric vehicles for peak power and load leveling. As a gas electrically adapt the membrane for specific gas combinations. Potential energy savings in the US. for this application are estimated at 1 to 3 quads/yr.

  8. Conducting polymers: Synthesis and industrial applications

    SciTech Connect

    Gottesfeld, S.

    1997-04-01

    The Conducting Polymer project funded by the AIM Program has developed new methods for the synthesis of conducting polymers and evaluated new industrial applications for these materials which will result in significant reductions in energy usage or industrial waste. The applications specifically addressed during FY 1996 included two ongoing efforts on membranes for gas separation and on electrochemical capacitors and a third new application: electrochemical reactors (ECRs) based on polymeric electrolytes. As a gas separation membrane, conducting polymers offer high selectivity and the potential to chemically or electrically adapt the membrane for specific gas combinations. Potential energy savings in the US for this application are estimated at 1 to 3 quads/yr. As an active material in electrochemical capacitors, electronically conducting polymers have the potential of storing large amounts of electric energy in low cost materials. Potential energy savings estimated at 1 quad/yr would result from introduction of electrochemical capacitors as energy storage devices in power trains of electric and hybrid vehicles, once such vehicles reach 20% of the total transportation market in the US. In the chlor-alkali industry, electrochemical reactors based on polymer electrolyte membranes consume around 1 % of the total electric power in the US. A new activity, started in FY 1996, is devoted to energy efficient ECRs. In the case of the chlor-alkali industry, energy savings as high as 50% seem possible with the novel ECR technology demonstrated by the author in 1996.

  9. Conductance tomography of conductive filaments in intrinsic silicon-rich silica RRAM

    NASA Astrophysics Data System (ADS)

    Buckwell, Mark; Montesi, Luca; Hudziak, Stephen; Mehonic, Adnan; Kenyon, Anthony J.

    2015-10-01

    We present results from an imaging study of filamentary conduction in silicon suboxide resistive RAM devices. We used a conductive atomic force microscope to etch through devices while measuring current, allowing us to produce tomograms of conductive filaments. To our knowledge this is the first report of such measurements in an intrinsic resistance switching material.We present results from an imaging study of filamentary conduction in silicon suboxide resistive RAM devices. We used a conductive atomic force microscope to etch through devices while measuring current, allowing us to produce tomograms of conductive filaments. To our knowledge this is the first report of such measurements in an intrinsic resistance switching material. Electronic supplementary information (ESI) available. See DOI: 10.1039/c5nr04982b

  10. Designing conducting polymers using genetic algorithms

    NASA Astrophysics Data System (ADS)

    Giro, R.; Cyrillo, M.; Galvão, D. S.

    2002-11-01

    We have developed a new methodology to design conducting polymers with pre-specified properties. The methodology is based on the use of genetic algorithms (GAs) coupled to Negative Factor Counting technique. We present the results for a case study of polyanilines, one of the most important families of conducting polymers. The methodology proved to be able of generating automatic solutions for the problem of determining the optimum relative concentration for binary and ternary disordered polyaniline alloys exhibiting metallic properties. The methodology is completely general and can be used to design new classes of materials.

  11. Conductivity of carbon nanotube polymer composites

    SciTech Connect

    Wescott, J T; Kung, P; Maiti, A

    2006-11-20

    Dissipative Particle Dynamics (DPD) simulations were used to investigate methods of controlling the assembly of percolating networks of carbon nanotubes (CNTs) in thin films of block copolymer melts. For suitably chosen polymers the CNTs were found to spontaneously self-assemble into topologically interesting patterns. The mesoscale morphology was projected onto a finite-element grid and the electrical conductivity of the films computed. The conductivity displayed non-monotonic behavior as a function of relative polymer fractions in the melt. Results are compared and contrasted with CNT dispersion in small-molecule fluids and mixtures.

  12. Structural and Electrical Study of Conducting Polymers

    NASA Astrophysics Data System (ADS)

    Shaktawat, Vinodini; Dixit, Manasvi; Saxena, N. S.; Sharma, Kananbala

    2010-06-01

    Pure and oxalic acid doped conducting polymers (polyaniline and polypyrrole) were chemically synthesized using ammonium persulfate (APS) as an oxidant. These samples were characterized through Scanning Electron Microscopy (SEM), which provides information about the surface topography of polymers. I-V characteristics have been recorded at room temperature as well as in the temperature range from 313 K to 463 K. So obtained characteristic curves were found to be linear. Temperature dependence of conductivity suggests a semiconducting nature in polyaniline samples with increase in temperature, whereas oxalic acid doped polypyrrole sample suggests a transition from semiconducting to metallic nature with the increase of temperature.

  13. Conducting polymer for high power ultracapacitor

    DOEpatents

    Shi, Steven Z.; Gottesfeld, Shimshon

    2002-01-01

    In accordance with the purposes of the present invention, as embodied and broadly described herein, the present invention is directed to an electrode having a conducting polymer active material for use in an ultracapacitor. The conducting polymer active material is electropolymerized onto a carbon paper substrate from a mixed solution of a dimer of (3,3' bithiophene) (BT) and a monomer that is selected from the group of thiophenes derived in the 3-position, having an aryl group attached to thiophene in the 3-position or having aryl and alkly groups independently attached to thiophene in the 3 and 4 positions.

  14. Conducting polymers as corrosion resistant coatings

    SciTech Connect

    Wrobleski, D.A.; Benicewicz, B.C.

    1994-09-01

    Although the majority of top coatings used for corrosion protection are electrically insulating, previous workers have proposed using an electrically active barrier for corrosion control. The most effective corrosion resistant undercoatings in use today are based on chromium compounds. Coatings based on other materials will need to replace these coatings by the turn of the century because of environmental and health concerns. For this reason the authors have begun an investigation of the use of conducting polymers as corrosion resistant coatings as an alternative to metal-based coatings. Conducting polymers have long been considered to be unsuitable for commercial processing, hindering their use for practical applications. Research in the field of electrically conducting polymers has recently produced a number of polymers such as polyaniline and its derivatives which are readily soluble in common organic solvents. The authors coating system, consisting of a conducting polyaniline primer layer, topcoated with epoxy or polyurethane, has been evaluated for corrosion resistance on mild steel substrates. In this paper, the authors report the results of laboratory testing under acidic and saline conditions and the results of testing in the severe launch environment at the Beach Testing Facility at Kennedy Space Center. The launch environment consists of exposure to corrosive HCl exhaust fumes and the salt spray from the Atlantic Ocean.

  15. Ionic Conduction Mechanism of Polymer Gel Electrolytes

    NASA Astrophysics Data System (ADS)

    Saito, Yuria; Kataoka, Hiroshi

    2002-12-01

    Carrier migration mechanism of polymer gel electrolyte for lithium secondary batteries was investigated through the dynamic behavior of diffusion coefficient and conductivity. The gel prepared with PEO showed a homogeneous structure with any fraction of the electrolyte solution. The diffusion coefficient of the ionic species decreased with the increase in the polymer fraction in the gel. Cation migration is closely associated with the polymer, showing the reduced activation energy for diffusion with polymer in contrast to the increasing feature of the activation energy of the anion diffusion. The PVDF-gel electrolytes have a solid solubility limit due to the swelling saturation. The excess solution was then trapped in the cavities of the swollen polymer network. As a result, the diffusion showed two components. One is the fast migration of the carriers similar to that in the solution and the other is the relatively slow migration in the swollen region. The latter was influenced by the polymer due to the physical blocking and chemical interactive effects.

  16. Mechanically stiff, electrically conductive composites of polymers and carbon nanotubes

    DOEpatents

    Worsley, Marcus A.; Kucheyev, Sergei O.; Baumann, Theodore F.; Kuntz, Joshua D.; Satcher, Jr., Joe H.; Hamza, Alex V.

    2015-07-21

    Using SWNT-CA as scaffolds to fabricate stiff, highly conductive polymer (PDMS) composites. The SWNT-CA is immersing in a polymer resin to produce a SWNT-CA infiltrated with a polymer resin. The SWNT-CA infiltrated with a polymer resin is cured to produce the stiff and electrically conductive composite of carbon nanotube aerogel and polymer.

  17. Ion-Conducting Organic/Inorganic Polymers

    NASA Technical Reports Server (NTRS)

    Kinder, James D.; Meador, Mary Ann B.

    2007-01-01

    Ion-conducting polymers that are hybrids of organic and inorganic moieties and that are suitable for forming into solid-electrolyte membranes have been invented in an effort to improve upon the polymeric materials that have been used previously for such membranes. Examples of the prior materials include perfluorosulfonic acid-based formulations, polybenzimidazoles, sulfonated polyetherketone, sulfonated naphthalenic polyimides, and polyethylene oxide (PEO)-based formulations. Relative to the prior materials, the polymers of the present invention offer greater dimensional stability, greater ease of formation into mechanically resilient films, and acceptably high ionic conductivities over wider temperature ranges. Devices in which films made of these ion-conducting organic/inorganic polymers could be used include fuel cells, lithium batteries, chemical sensors, electrochemical capacitors, electrochromic windows and display devices, and analog memory devices. The synthesis of a polymer of this type (see Figure 1) starts with a reaction between an epoxide-functionalized alkoxysilane and a diamine. The product of this reaction is polymerized by hydrolysis and condensation of the alkoxysilane group, producing a molecular network that contains both organic and inorganic (silica) links. The silica in the network contributes to the ionic conductivity and to the desired thermal and mechanical properties. Examples of other diamines that have been used in the reaction sequence of Figure 1 are shown in Figure 2. One can use any of these diamines or any combination of them in proportions chosen to impart desired properties to the finished product. Alternatively or in addition, one could similarly vary the functionality of the alkoxysilane to obtain desired properties. The variety of available alkoxysilanes and diamines thus affords flexibility to optimize the organic/inorganic polymer for a given application.

  18. Structure and Conductivity of Semiconducting Polymer Hydrogels.

    PubMed

    Huber, Rachel C; Ferreira, Amy S; Aguirre, Jordan C; Kilbride, Daniel; Toso, Daniel B; Mayoral, Kenny; Zhou, Z Hong; Kopidakis, Nikos; Rubin, Yves; Schwartz, Benjamin J; Mason, Thomas G; Tolbert, Sarah H

    2016-07-01

    Poly(fluorene-alt-thiophene) (PFT) is a conjugated polyelectrolyte that self-assembles into rod-like micelles in water, with the conjugated polymer backbone running along the length of the micelle. At modest concentrations (∼10 mg/mL in aqueous solutions), PFT forms hydrogels, and this work focuses on understanding the structure and intermolecular interactions in those gel networks. The network structure can be directly visualized using cryo electron microscopy. Oscillatory rheology studies further tell us about connectivity within the gel network, and the data are consistent with a picture where polymer chains bridge between micelles to hold the network together. Addition of tetrahydrofuran (THF) to the gels breaks those connections, but once the THF is removed, the gel becomes stronger than it was before, presumably due to the creation of a more interconnected nanoscale architecture. Small polymer oligomers can also passivate the bridging polymer chains, breaking connections between micelles and dramatically weakening the hydrogel network. Fits to solution-phase small-angle X-ray scattering data using a Dammin bead model support the hypothesis of a bridging connection between PFT micelles, even in dilute aqueous solutions. Finally, time-resolved microwave conductivity measurements on dried samples show an increase in carrier mobility after THF annealing of the PFT gel, likely due to increased connectivity within the polymer network. PMID:27079171

  19. Effects of compatability on the conductivity of conducting polymer blends

    SciTech Connect

    Liu, Mingjun; Nowak, C.K.; Gregory, R.V.

    1995-12-01

    The electrical conductivity of chemically synthesized polyaniline (PANI) blends with nylon 6,6 and polystyrene was measured. The conductivities of the top and bottom of the films cast from blend solutions were found to differ. This effect was most pronounced at low percent loadings of PANI. The maximum difference in conductivity between two sides of the same film was found to be five orders of magnitude in the case of a 5% PANI blend with polystyrene. In this case the conductive polymer appears to be rich on one side of the film rather than more homogeneously dispersed on both sides. SEM provides evidence for the formation of a percolation cluster on one side of the film which is most notable in polystyrene blends. X-ray and FTIR indicated that greater interaction between PANI and nylon 6,6 than PANI and polystyrene. It is proposed that the magnitude of the variation in conductivity between the two sides of the film depends on the compatibility of the conducting and insulating host polymers.

  20. Electrochemical evaluation of the p-Si/conducting polymer interfacial properties

    NASA Technical Reports Server (NTRS)

    Nagasubramanian, G.; Distefano, S.; Moacanin, J.

    1988-01-01

    Results are presented from an experimental investigation of the contact resistance and interfacial properties of a p-Si/conducting polymer interface for solar cell applications. The electronic character of the polymer/semiconductor function is determined by studying the electrochemical behavior of both poly(isothianapthene) (PITN) and polypyrrole (PP) in an acetonitrile solution on p-silicon electrodes. The results obtained indicate that while PITN is intrinsically more conductive than PP, neither passivates surface states nor forms ohmic contact.

  1. Actuator device utilizing a conductive polymer gel

    DOEpatents

    Chinn, Douglas A.; Irvin, David J.

    2004-02-03

    A valve actuator based on a conductive polymer gel is disclosed. A nonconductive housing is provided having two separate chambers separated by a porous frit. The conductive polymer is held in one chamber and an electrolyte solution, used as a source of charged ions, is held in the second chamber. The ends of the housing a sealed with a flexible elastomer. The polymer gel is further provide with electrodes with which to apply an electrical potential across the gel in order to initiate an oxidation reaction which in turn drives anions across the porous frit and into the polymer gel, swelling the volume of the gel and simultaneously contracting the volume of the electrolyte solution. Because the two end chambers are sealed the flexible elastomer expands or contracts with the chamber volume change. By manipulating the potential across the gel the motion of the elastomer can be controlled to act as a "gate" to open or close a fluid channel and thereby control flow through that channel.

  2. Scattering and physical aging in intrinsically microporous polymers

    NASA Astrophysics Data System (ADS)

    McDermott, Amanda Grace

    Polymers of intrinsic microporosity (PIMs) form glassy, rigid membranes featuring a large concentration of pores smaller than 1 nm, a large internal surface area, and high gas permeability and selectivity. Porosity in these materials---closely related to free volume--- arises from an unusual chain structure combining rigid segments with sites of contortion. Linear PIMs can be easily solution-cast into films whose interconnected networks of micropores can be exploited for applications such as gas separation and storage. Like other glasses, though, PIMs are subject to physical aging: a slow increase in density over time. This is accompanied by a decrease in permeability that reduces their performance as gas separation membranes. Several characterization methods are routinely employed to measure the structural properties of microporous materials, but none are as widely available and as easily applied to film samples with varied sample histories as small- and wide-angle X-ray scattering (SAXS and WAXS). Although it is possible to derive useful information such as surface areas and pore sizes from the scattering patterns of many porous materials, scattering from PIMs includes some unusual features whose interpretation is not readily apparent. In this work, a robust interpretation of PIM SAXS and WAXS features is developed with support from molecular dynamics simulations. The sensitivity of these patterns to time, temperature and film thickness is shown to be qualitatively consistent with physical aging, demonstrating that high-free-volume, porous polymeric glasses present a unique opportunity to study structural changes during physical aging using scattering methods. Models for extracting quantitative information about changes in the sizes and volume fraction of pores are also explored. Although quantitative interpretation of scattering patterns remains challenging, results of the aging study suggest that there may be two distinct mechanisms of aging in PIMs. Several

  3. Ion conducting organic/inorganic hybrid polymers

    NASA Technical Reports Server (NTRS)

    Meador, Maryann B. (Inventor); Kinder, James D. (Inventor)

    2010-01-01

    This invention relates to a series of organic/inorganic hybrid polymers that are easy to fabricate into dimensionally stable films with good ion-conductivity over a wide range of temperatures for use in a variety of applications. The polymers are prepared by the reaction of amines, preferably diamines and mixtures thereof with monoamines with epoxy-functionalized alkoxysilanes. The products of the reaction are polymerized by hydrolysis of the alkoxysilane groups to produce an organic-containing silica network. Suitable functionality introduced into the amine and alkoxysilane groups produce solid polymeric membranes which conduct ions for use in fuel cells, high-performance solid state batteries, chemical sensors, electrochemical capacitors, electro-chromic windows or displays, analog memory devices and the like.

  4. Gas Sensors Based on Conducting Polymers

    PubMed Central

    Bai, Hua; Shi, Gaoquan

    2007-01-01

    The gas sensors fabricated by using conducting polymers such as polyaniline (PAni), polypyrrole (PPy) and poly (3,4-ethylenedioxythiophene) (PEDOT) as the active layers have been reviewed. This review discusses the sensing mechanism and configurations of the sensors. The factors that affect the performances of the gas sensors are also addressed. The disadvantages of the sensors and a brief prospect in this research field are discussed at the end of the review.

  5. The Organic Chemistry of Conducting Polymers

    SciTech Connect

    Tolbert, Laren Malcolm

    2014-12-01

    For the last several years, we have examined the fundamental principles of conduction in one-dimensional systems, i.e., molecular “wires”. It is, of course, widely recognized that such systems, as components of electronically conductive materials, function in a two- and three-dimensional milieu. Thus interchain hopping and grain-boundary resistivity are limiting conductivity factors in highly conductive materials, and overall conductivity is a function of through-chain and boundary hopping. We have given considerable attention to the basic principles underlying charge transport (the “rules of the game”) in two-dimensional systems by using model systems which allow direct observation of such processes, including the examination of tunneling and hopping as components of charge transfer. In related work, we have spent considerable effort on the chemistry of conjugated heteropolymers, most especially polythiophens, with the aim of using these most efficient of readily available electroactive polymers in photovoltaic devices.

  6. Bulk limited conduction in electroluminescent polymer devices

    NASA Astrophysics Data System (ADS)

    Campbell, A. J.; Weaver, M. S.; Lidzey, D. G.; Bradley, D. D. C.

    1998-12-01

    The current-voltage (J-V) characteristics of ITO/polymer film/Al or Au structures of poly(phenylene vinylene) (PPV) and a dialkoxy PPV copolymer have been recorded for a range of different film thickness d and temperatures T. At high applied bias all the characteristics can be fitted over a given range to a power law J=KVm, where m increases with decreasing T, log(K) is proportional to m, and K is proportional to d-α m, where α˜2 (ITO/polymer film/Al devices) and ˜1 (ITO/polymer film/Au devices). Different single carrier space charge limited conduction theories have been used to try and explain this behavior. The analytical theory in which the carrier density is decreased by an exponential trap distribution lying below effectively isoelectronic transport states is in good agreement, but cannot explain the thickness dependence of the ITO/polymer film/Au devices and can be criticized as being physically unreasonable. A numerical analysis in which the mobility has the field and temperature dependence found for hopping transport in disordered systems is also in good agreement, but can only fit a small range of J and cannot explain the magnitude of K, the temperature dependence of m or the abrupt change in slope in the J-V characteristics with increasing bias. Mixed models are equally good but cannot explain the deviations from experiment. We consider that further experimental studies of carrier mobilities and the nature of the traps present in such materials is required to distinguish between these models and resolve the nature of bulk limited conduction in conjugated polymers.

  7. Interfacial charge transfer behavior of conducting polymers as contact electrode for semiconductor devices

    NASA Astrophysics Data System (ADS)

    Kawakita, Jin; Fujikawa, Yuki; Nagata, Takahiro; Chikyow, Toyohiro

    2016-04-01

    As an alternative contact electrode material to metals, which is necessary for downsized semiconductor devices in 10 nm processes, an intrinsically conducting polymer was studied in terms of its interfacial charge-transfer behavior with an inorganic semiconductor. Polypyrrole as the conducting polymer was formed using an electrochemical technique on an oxide semiconductor and its electronic properties were evaluated using scanning probe microscopy. The experimental results showed that an ohmic contact was observed dynamically at local positions, although a Schottky barrier was expected in the static electronic state over the measurement area. From this research, the conducting polymer was found to be promising as a contact electrode.

  8. Synthesis and characterization of soluble conducting polymers and conducting adhesives

    NASA Astrophysics Data System (ADS)

    Oztemiz, Serhan

    With the demanding nature of the technology today, scientists are looking for new materials in order to decrease the cost, increase the efficiency of the use of the materials, and decrease time-consuming steps in order to increase the speed of production. New materials are being studied to decrease the weight of cars, planes and space vehicles; surface properties are being modified to decrease the drag coefficient; new technologies are being introduced for speeding up applications in production and assembly lines. In this research we address the needs of different technological applications from a conductivity perspective. In the first part of the thesis, the synthesis of soluble conducting polymers in order to make them more processable for potential electronic and photovoltaic applications is presented. Soluble conducting polymers of 3-hexylthiophene, 3-octylthiophene, 3-decylthiophene and 3-dodecylthiophene were synthesized electrochemically and thus, doped during synthesis. It was found that the conductivities; molecular weights and degrees of polymerization of the polymers strongly depend on the side chain's length. The substitution of alkyl side chains decreases the reactivity of the growing chain, and with an increasing side-chain length, all of these properties show a decrease. The hexyl substituent, being the shortest of the four side chains, causes the least distortion in the background, has the highest conjugation, and has the highest shift in the UV spectrum when it polymerizes. As the length of the side chain increases, the shift in the UV spectrum decreases, too. Decrease in the pi-stacking, conjugation and delocalization decreases the conductivity. This gives the material an opportunity to be used in photovoltaic applications. In the second part of the thesis, a conducting adhesive formulation that eliminates the need for heat or other expensive and rather bothersome application methods to activate the adhesive is investigated. Using the quick

  9. Tactile sensors based on conductive polymers

    NASA Astrophysics Data System (ADS)

    Castellanos-Ramos, Julian; Navas-Gonzalez, Rafael; Macicior, Haritz; Ochoteco, Estibalitz; Vidal-Verdú, Fernando

    2009-05-01

    This paper presents results from a few tactile sensors we have designed and fabricated. These sensors are based on a common approach that consists of placing a sheet of piezoresistive material on the top of a set of electrodes. If a force is exerted against the surface of the so obtained sensor, the contact area between the electrodes and the piezoresistive material changes. Therefore, the resistance at the interface changes. This is exploited as transconduction principle to measure forces and build advanced tactile sensors. For this purpose, we use a thin film of conductive polymers as the piezoresistive material. Specifically, a conductive water-based ink of these polymers is deposited by spin coating on a flexible plastic sheet, giving as a result a smooth, homogeneous and conducting thin film on it. The main interest in this procedure is it is cheap and it allows the fabrication of flexible and low cost tactile sensors. In this work we present results from sensors made with two technologies. First, we have used a Printed Circuit Board technology to fabricate the set of electrodes and addressing tracks. Then we have placed the flexible plastic sheet with the conductive polymer film on them to obtain the sensor. The result is a simple, flexible tactile sensor. In addition to these sensors on PCB, we have proposed, designed and fabricated sensors with a screen printing technology. In this case, the set of electrodes and addressing tracks are made by printing an ink based on silver nanoparticles. There is a very interesting difference with the other sensors, that consists of the use of an elastomer as insulation material between conductive layers. Besides of its role as insulator, this elastomer allows the modification of the force versus resistance relationship. It also improves the dynamic response of the sensor because it implements a restoration force that helps the sensor to relax quicker when the force is taken off.

  10. Conducting polymer electrodes for auditory brainstem implants

    PubMed Central

    Guex, Amélie A.; Vachicouras, Nicolas; Hight, Ariel E.; Brown, M. Christian; Lee, Daniel J.; Lacour, Stéphanie P.

    2015-01-01

    The auditory brainstem implant (ABI) restores hearing in patients with damaged auditory nerves. One of the main ideas to improve the efficacy of ABIs is to increase spatial specificity of stimulation, in order to minimize extra-auditory side-effects and to maximize the tonotopy of stimulation. This study reports on the development of a microfabricated conformable electrode array with small (100 μm diameter) electrode sites. The latter are coated with a conducting polymer, PEDOT:PSS, to offer high charge injection properties and to safely stimulate the auditory system with small stimulation sites. We report on the design and fabrication of the polymer implant, and characterize the coatings in physiological conditions in vitro and under mechanical deformation. We characterize the coating electrochemically and during bending tests. We present a proof of principle experiment where the auditory system is efficiently activated by the flexible polymeric interface in a rat model. These results demonstrate the potential of using conducting polymer coatings on small electrode sites for electrochemically safe and efficient stimulation of the central auditory system. PMID:26207184

  11. Single conducting polymer nanowire based conductometric sensors

    NASA Astrophysics Data System (ADS)

    Bangar, Mangesh Ashok

    The detection of toxic chemicals, gases or biological agents at very low concentrations with high sensitivity and selectivity has been subject of immense interest. Sensors employing electrical signal readout as transduction mechanism offer easy, label-free detection of target analyte in real-time. Traditional thin film sensors inherently suffered through loss of sensitivity due to current shunting across the charge depleted/added region upon analyte binding to the sensor surface, due to their large cross sectional area. This limitation was overcome by use of nanostructure such as nanowire/tube as transducer where current shunting during sensing was almost eliminated. Due to their benign chemical/electrochemical fabrication route along with excellent electrical properties and biocompatibility, conducting polymers offer cost-effective alternative over other nanostructures. Biggest obstacle in using these nanostructures is lack of easy, scalable and cost-effective way of assembling these nanostructures on prefabricated micropatterns for device fabrication. In this dissertation, three different approaches have been taken to fabricate individual or array of single conducting polymer (and metal) nanowire based devices and using polymer by itself or after functionalization with appropriate recognition molecule they have been applied for gas and biochemical detection. In the first approach electrochemical fabrication of multisegmented nanowires with middle functional Ppy segment along with ferromagnetic nickel (Ni) and end gold segments for better electrical contact was studied. This multi-layered nanowires were used along with ferromagnetic contact electrode for controlled magnetic assembly of nanowires into devices and were used for ammonia gas sensing. The second approach uses conducting polymer, polypyrrole (Ppy) nanowires using simple electrophoretic alignment and maskless electrodeposition to anchor nanowire which were further functionalized with antibodies against

  12. Synthesis of novel electrically conducting polymers: Potential conducting Langmuir-Blodgett films and conducting polymers on defined surfaces

    NASA Technical Reports Server (NTRS)

    Zimmer, Hans

    1993-01-01

    Based on previous results involving thiophene derived electrically conducting polymers in which it was shown that thiophene, 3-substituted thiophenes, furans, and certain oligomers of these compounds showed electrical conductivity after polymerization. The conductivity was in the order of up to 500 S/cm. In addition, these polymers showed conductivity without being doped and most of all they were practically inert toward ambient conditions. They even could be used in aqueous media. With these findings as a guide, a number of 3-long-chain-substituted thiophenes and 1-substituted-3-long-chain substituted pyrrols were synthesized as monomers for potential polymeric electrically conducting Langmuir-Blodgett films.

  13. Electrochemical characterization of aminated acrylic conducting polymer

    NASA Astrophysics Data System (ADS)

    Rashid, Norma Mohammad; Heng, Lee Yook; Ling, Tan Ling

    2015-09-01

    New attempt has been made to synthesize aminated acrylic conducting polymer (AACP) using precursor of phenylvinylsulfoxide (PVS). The process was conducted via the integration of microemulsion and photopolymerization techniques. It has been utilized for covalent immobilization of amino groups by the adding of N-achryiloxisuccinimide (NAS). Thermal eliminating of benzene sulfenic acids from PVS has been done at 250 °C to form electroactive polyacetylene (PA) segment. Characterization of AACP has been conducted using fourier transform infrared (FTIR), scanning electron microscopy (SEM) and linear sweep cyclic voltammetry (CV). A range of 0.3-1.25μm particle size obtained from SEM characterization. A quasi-reversible system performed as shown in electrochemical study.

  14. Electrochemical characterization of aminated acrylic conducting polymer

    SciTech Connect

    Rashid, Norma Mohammad; Heng, Lee Yook; Ling, Tan Ling

    2015-09-25

    New attempt has been made to synthesize aminated acrylic conducting polymer (AACP) using precursor of phenylvinylsulfoxide (PVS). The process was conducted via the integration of microemulsion and photopolymerization techniques. It has been utilized for covalent immobilization of amino groups by the adding of N-achryiloxisuccinimide (NAS). Thermal eliminating of benzene sulfenic acids from PVS has been done at 250 °C to form electroactive polyacetylene (PA) segment. Characterization of AACP has been conducted using fourier transform infrared (FTIR), scanning electron microscopy (SEM) and linear sweep cyclic voltammetry (CV). A range of 0.3-1.25μm particle size obtained from SEM characterization. A quasi-reversible system performed as shown in electrochemical study.

  15. Conducting Polymers and Their Hybrids as Organic Thermoelectric Materials

    NASA Astrophysics Data System (ADS)

    Toshima, Naoki; Ichikawa, Shoko

    2015-01-01

    Conducting polymers have received much attention recently as organic thermoelectric materials, because of such advantages as plentiful resources, easy synthesis, easy processing, low cost, low thermal conductivity, and easy fabrication of flexible, light, and printable devices with large area. Many reports on organic thermoelectric materials have recently been published. We have studied conducting polymers as organic thermoelectric materials since 1999. During these investigations, we found that the thermal conductivity of conducting polymers did not increase even though electrical conductivity increased; this was a major advantage of conducting polymers as organic thermoelectric materials. We also observed that molecular alignment was one of the most important factors for improvement of the thermoelectric performance of conducting polymers. Stretching of conducting polymers or their precursors was one of the most common techniques used to achieve good molecular alignment. Recently, alignment of the clusters of conducting polymers by treatment with solvents has been proposed as a means of achieving high electrical conductivity. Hybridization of conducting polymers with inorganic nanoparticles has also been found to improve thermoelectric performance. Here we present a brief history and discuss recent progress of research on conducting polymers as organic thermoelectric materials, and describe the techniques used to improve thermoelectric performance by treatment of conducting polymers with solvents and hybridization of conducting polymers with Bi2Te3 and gold nanoparticles.

  16. Electropolymerized Conducting Polymers as Glucose Sensors

    NASA Astrophysics Data System (ADS)

    Sadik, Omowunmi A.; Brenda, Sharin; Joasil, Patrick; Lord, John

    1999-07-01

    Conducting polymers are of considerable interest. Their electrochemical synthesis requires only inexpensive starting materials and low-cost equipment. This paper presents a laboratory-based experiment for possible inclusion in the undergraduate instrumental analysis laboratory curriculum. The objectives are to perform cyclic voltammetry on electropolymerized conducting polymers, to observe the effects of various parameters on the voltammogram obtained, and to perform quantitative analysis of glucose. In a typical experiment, glucose oxidase enzyme (GOx) was immobilized at an electrode surface by the electropolymerization of pyrrole from an aqueous solution containing the enzyme. The chemical activity of the immobilized GOx was evaluated by indirectly monitoring glucose oxidation using the electropolymerized PPy-modified electrode. The amount of glucose present was then determined by observing the rate at which hydrogen peroxide was produced. The magnitude of the current was linearly proportional to the concentration of glucose over the range 1 x 10-3 to 5 x 10-5M. The limit of detection was estimated at 3 times the background noise, 8 x 10-5 M glucose. The Michaelis-Menten parameters, Km and Vmax, were calculated to be approximately 1.5 x 10-3 M and 10-9 m/s, respectively, comparable with values cited in literature. This experiment illustrates the fundamental electrochemical and biosensor concepts. It reinforces the underlying principles of dynamic electrochemistry and illustrates the potential of using conducting polymers for analytical applications. The simple low-cost procedure employed should be attractive for undergraduate research projects, particularly in departments with modest means.

  17. Conductive inks for metalization in integrated polymer microsystems

    DOEpatents

    Davidson, James Courtney; Krulevitch, Peter A.; Maghribi, Mariam N.; Benett, William J.; Hamilton, Julie K.; Tovar, Armando R.

    2006-02-28

    A system of metalization in an integrated polymer microsystem. A flexible polymer substrate is provided and conductive ink is applied to the substrate. In one embodiment the flexible polymer substrate is silicone. In another embodiment the flexible polymer substrate comprises poly(dimethylsiloxane).

  18. Catalytic synthesis of metal crystals using conductive polymers

    DOEpatents

    Wang, Hsing-Lin; Li, Wenguang

    2008-01-15

    A method of forming metal nanoparticles using a polymer colloid that includes at least one conductive polymer and at least one polyelectrolyte. Metal ions are reduced in water by the conductive polymer to produce the nanoparticles, which may be then incorporated in the colloidal structure to form a colloid composite. The method can also be used to separate selected metal ions from aqueous solutions.

  19. Intrinsic bond strength of metal films on polymer substrates

    NASA Technical Reports Server (NTRS)

    Wheeler, Donald R.; Osaki, Hiroyuki

    1990-01-01

    A semiquantitative method for the measurement of the intrinsic bond strength between elastic substrates and elastic films that fail by brittle fracture is described. Measurements on a polyethylene terephthalate (PET)-Ni couple were used to verify the essential features of the analysis. It was found that the interfacial shear strength of Ni on PET doubled after ion etching.

  20. Conducting polymer actuators: From basic concepts to proprioceptive systems

    NASA Astrophysics Data System (ADS)

    Martinez Gil, Jose Gabriel

    Designers and engineers have been dreaming for decades of motors sensing, by themselves, working and surrounding conditions, as biological muscles do originating proprioception. Here bilayer full polymeric artificial muscles were checked up to very high cathodic potential limits (-2.5 V) in aqueous solution by cyclic voltammetry. The electrochemical driven exchange of ions from the conducting polymer film, and the concomitant Faradaic bending movement of the muscle, takes place in the full studied potential range. The presence of trapped counterion after deep reduction was corroborated by EDX determinations giving quite high electronic conductivity to the device. The large bending movement was used as a tool to quantify the amount of water exchanged per reaction unit (exchanged electron or ion). The potential evolutions of self-supported films of conducting polymers or conducting polymers (polypyrrole, polyaniline) coating different microfibers, during its oxidation/reduction senses working mechanical, thermal, chemical or electrical variables. The evolution of the muscle potential from electrochemical artificial muscles based on electroactive materials such as intrinsically conducting polymers and driven by constant currents senses, while working, any variation of the mechanical (trailed mass, obstacles, pressure, strain or stress), thermal or chemical conditions of work. One physically uniform artificial muscle includes one electrochemical motor and several sensors working simultaneously under the same driving reaction. Actuating (current and charge) and sensing (potential and energy) magnitudes are present, simultaneously, in the only two connecting wires and can be read by the computer at any time. From basic polymeric, mechanical and electrochemical principles a physicochemical equation describing artificial proprioception has been developed. It includes and describes, simultaneously, the evolution of the muscle potential during actuation as a function of the

  1. Chemical synthesis of chiral conducting polymers

    DOEpatents

    Wang, Hsing-Lin; Li, Wenguang

    2009-01-13

    An process of forming a chiral conducting polymer, e.g., polyaniline, is provided including reacting a monomer, e.g., an aniline monomer, in the presence of a chiral dopant acid to produce a first reaction mixture by addition of a solution including a first portion of an oxidizing agent, the first portion of oxidizing agent characterized as insufficient to allow complete reaction of the monomer, and further reacting the first reaction mixture in the presence of the chiral dopant acid by addition of a solution including a second portion of the oxidizing agent, the second portion of oxidizing agent characterized as insufficient to allow complete reaction of the monomer, and repeating the reaction by addition of further portions of the oxidizing agent until the monomer reaction is complete to produce a chiral conducting polymer, e.g., polyaniline. A preferred process includes addition of a catalyst during the reaction, the catalyst selected from among the group consisting of phenylene diamine, aniline oligomers and amino-capped aniline oligomers and metal salts.The processes of the present invention further provide a resultant polyaniline product having a chirality level defined by a molar ellipticity of from about 40.times.10.sup.3 degree-cm.sup.2/decimole to about 700.times.10.sup.3 degree-cm.sup.2/decimole. The processes of the present invention further provide a resultant polyaniline product having a nanofiber structure with a diameter of from about 30 nanometers to about 120 nanometers and from about 1 micron to about 5 microns in length.

  2. Chemical synthesis of chiral conducting polymers

    DOEpatents

    Wang, Hsing-Lin; Li, Wenguang

    2006-07-11

    An process of forming a chiral conducting polymer, e.g., polyaniline, is provided including reacting a monomer, e.g., an aniline monomer, in the presence of a chiral dopant acid to produce a first reaction mixture by addition of a solution including a first portion of an oxidizing agent, the first portion of oxidizing agent characterized as insufficient to allow complete reaction of the monomer, and further reacting the first reaction mixture in the presence of the chiral dopant acid by addition of a solution including a second portion of the oxidizing agent, the second portion of oxidizing agent characterized as insufficient to allow complete reaction of the monomer, and repeating the reaction by addition of further portions of the oxidizing agent until the monomer reaction is complete to produce a chiral conducting polymer, e.g., polyaniline. A preferred process includes addition of a catalyst during the reaction, the catalyst selected from among the group consisting of phenylene diamine, aniline oligomers and amino-capped aniline oligomers and metal salts. The processes of the present invention further provide a resultant polyaniline product having a chirality level defined by a molar ellipticity of from about 40.times.103 degree-cm2/decimole to about 700.times.103 degree-cm2/decimole. The processes of the present invention further provide a resultant polyaniline product having a nanofiber structure with a diameter of from about 30 nanometers to about 120 nanometers and from about 1 micron to about 5 microns in length.

  3. Conducting Polymer Nanostructures: Template Synthesis and Applications in Energy Storage

    PubMed Central

    Pan, Lijia; Qiu, Hao; Dou, Chunmeng; Li, Yun; Pu, Lin; Xu, Jianbin; Shi, Yi

    2010-01-01

    Conducting polymer nanostructures have received increasing attention in both fundamental research and various application fields in recent decades. Compared with bulk conducting polymers, conducting polymer nanostructures are expected to display improved performance in energy storage because of the unique properties arising from their nanoscaled size: high electrical conductivity, large surface area, short path lengths for the transport of ions, and high electrochemical activity. Template methods are emerging for a sort of facile, efficient, and highly controllable synthesis of conducting polymer nanostructures. This paper reviews template synthesis routes for conducting polymer nanostructures, including soft and hard template methods, as well as its mechanisms. The application of conducting polymer mesostructures in energy storage devices, such as supercapacitors and rechargeable batteries, are discussed. PMID:20717527

  4. Intrinsically Microporous Polymer Retains Porosity in Vacuum Thermolysis to Electroactive Heterocarbon.

    PubMed

    Rong, Yuanyang; He, Daping; Sanchez-Fernandez, Adrian; Evans, Craig; Edler, Karen J; Malpass-Evans, Richard; Carta, Mariolino; McKeown, Neil B; Clarke, Tomos J; Taylor, Stuart H; Wain, Andrew J; Mitchels, John M; Marken, Frank

    2015-11-10

    Vacuum carbonization of organic precursors usually causes considerable structural damage and collapse of morphological features. However, for a polymer with intrinsic microporosity (PIM-EA-TB with a Brunauer-Emmet-Teller (BET) surface area of 1027 m(2)g(-1)), it is shown here that the rigidity of the molecular backbone is retained even during 500 °C vacuum carbonization, yielding a novel type of microporous heterocarbon (either as powder or as thin film membrane) with properties between those of a conducting polymer and those of a carbon. After carbonization, the scanning electron microscopy (SEM) morphology and the small-angle X-ray scattering (SAXS) Guinier radius remain largely unchanged as does the cumulative pore volume. However, the BET surface area is decreased to 242 m(2)g(-1), but microporosity is considerably increased. The new material is shown to exhibit noticeable electrochemical features including two pH-dependent capacitance domains switching from ca. 33 Fg(-1) (when oxidized) to ca. 147 Fg(-1) (when reduced), a low electron transfer reactivity toward oxygen and hydrogen peroxide, and a four-point-probe resistivity (dry) of approximately 40 MΩ/square for a 1-2 μm thick film. PMID:26496244

  5. Chemical anchoring of organic conducting polymers to semiconducting surfaces

    DOEpatents

    Frank, Arthur J.; Honda, Kenji

    1984-01-01

    According to the present invention, an improved method of coating electrodes with conductive polymer films and/or preselected catalysts is provided. The charge-conductive polymer is covalently or coordinatively attached to the electrode surface to strengthen the adhesion characteristics of the polymer to the electrode surface or to improve charge-conductive properties between the conductive polymer and the electrode surface. Covalent or coordinative attachment is achieved by a number of alternative methods including covalently or coordinatively attaching the desired monomer to the electrode by means of a suitable coupling reagent and, thereafter, electrochemically polymerizing the monomer in situ.

  6. Chemical anchoring of organic conducting polymers to semiconducting surfaces

    DOEpatents

    Frank, A.J.; Honda, K.

    1984-01-01

    According to the present invention, an improved method of coating electrodes with conductive polymer films and/or preselected catalysts is provided. The charge conductive polymer is covalently or coordinatively attached to the electrode surface to strengthen the adhesion characteristics of the polymer to the electrode surface or to improve charge conductive properties between the conductive polymer and the electrode surface. Covalent or coordinative attachment is achieved by a number of alternative methods including covalently or coordinatively attaching the desired monomer to the electrode by means of a suitable coupling reagent and, thereafter, electrochemically polymerizing the monomer in situ.

  7. Electrochemical Impedance Spectroscopy of Conductive Polymer Coatings

    NASA Technical Reports Server (NTRS)

    Calle, Luz Marina; MacDowell, Louis G.

    1996-01-01

    Electrochemical impedance spectroscopy (EIS) was used to investigate the corrosion protection performance of twenty nine proprietary conductive polymer coatings for cold rolled steel under immersion in 3.55 percent NaCl. Corrosion potential as well as Bode plots of the data were obtained for each coating after one hour immersion, All coatings, with the exception of one, have a corrosion potential that is higher in the positive direction than the corrosion potential of bare steel under the same conditions. Group A consisted of twenty one coatings with Bode plots indicative of the capacitive behavior characteristic of barrier coatings. An equivalent circuit consisting of a capacitor in series with a resistor simulated the experimental EIS data for these coatings very well. Group B consisted of eight coatings that exhibited EIS spectra showing an inflection point which indicates that two time constants are present. This may be caused by an electrochemical process taking place which could be indicitive of coating failing. These coatings have a lower impedance that those in Group A.

  8. Conduction and trapping in electroluminescent polymer devices

    NASA Astrophysics Data System (ADS)

    Campbell, Alasdair J.; Weaver, Michael S.; Lidzey, David G.; Bradley, Donal D. C.; Werner, Ekkehard; Bruetting, Wolfgang; Schwoerer, Markus

    1998-12-01

    The current-voltage characteristics of ITO/polymer film/Al or Au devices of poly(phenylene vinylene) (PPV) and a dialkoxy PPV copolymer can be fitted at high applied bias to a power law of the form J equals KVm where m increases with decreasing temperature, log(K) is proportional to m, and K is proportional to d-(alpha m) where d is the film thickness and (alpha) is a constant. (alpha) 2 and 1 for the Al and Au cathode devices respectively. Different single carrier space charge limited conduction (SCLC) theories, including either an exponential trap distribution or a hopping transport field and temperature dependent mobility, are used to try and explain this behavior. Both models are in good agreement with the general experimental results, but can also be criticized on a number of specific issues.Mixed SCLC models and the effect of dispersive transport are also explored. It is concluded that carrier mobility and trap measurements are required to distinguish between these models. To this end, initial trap measurements of ITO/PPV/Al devices using deep level transient spectroscopy (DLTS) are reported. Very deep positive carrier transport with emptying times > 4 minutes have been detected. The non-exponential DLTS transients have been successfully modeled on an isoelectronic trap level emptying to a Gaussian distribution of transport states, with a trap depth and density of 0.8eV and 4 by 1016 cm-3 respectively.

  9. Proton Conducting Polymer Electrolyte Based on Pva-Pan

    NASA Astrophysics Data System (ADS)

    Devi, S. Siva; Selvasekarapandian, S.; Rajeswari, N.; Genova, F. Kingslin Mary; Karthikeyan, S.; Raja, C. Sanjeevi

    2013-07-01

    Proton conducting polymer electrolytes based on blend polymer using Poly Vinyl Alcohol (PVA) and Poly Acrylo Nitrile (PAN) doped with ammonium nitrate have been prepared by solution casting method. The highest conductivity at room temperature (305K) has been found to be 1.8×10-3 S cm-1 for 15 mole % NH4NO3 doped PVA-PAN system. X ray Diffraction pattern of the doped and the undoped blend polymer electrolyte confirms the amorphous nature of blend polymer, when salt is added. The complex formation between the blend polymer and the salt has been confirmed by Fourier transform infrared spectroscopy.

  10. Anion-conducting polymer, composition, and membrane

    DOEpatents

    Pivovar, Bryan S.; Thorn, David L.

    2011-11-22

    Anion-conducing polymers and membranes with enhanced stability to aqueous alkali include a polymer backbone with attached sulfonium, phosphazenium, phosphazene, and guanidinium residues. Compositions also with enhanced stability to aqueous alkali include a support embedded with sulfonium, phosphazenium, and guanidinium salts.

  11. Anion-Conducting Polymer, Composition, and Membrane

    SciTech Connect

    Pivovar, Bryan S.; Thorn, David L.

    2008-10-21

    Anion-conducing polymers and membranes with enhanced stability to aqueous alkali include a polymer backbone with attached sulfonium, phosphazenium, phosphazene, and guanidinium residues. Compositions also with enhanced stability to aqueous alkali include a support embedded with sulfonium, phosphazenium, and guanidinium salts.

  12. Anion-conducting polymer, composition, and membrane

    DOEpatents

    Pivovar, Bryan S.; Thorn, David L.

    2010-12-07

    Anion-conducing polymers and membranes with enhanced stability to aqueous alkali include a polymer backbone with attached sulfonium, phosphazenium, phosphazene, and guanidinium residues. Compositions also with enhanced stability to aqueous alkali include a support embedded with sulfonium, phosphazenium, and guanidinium salts.

  13. Anion-conducting polymer, composition, and membrane

    DOEpatents

    Pivovar, Bryan S.; Thorn, David L.

    2009-09-01

    Anion-conducing polymers and membranes with enhanced stability to aqueous alkali include a polymer backbone with attached sulfonium, phosphazenium, phosphazene, and guanidinium residues. Compositions also with enhanced stability to aqueous alkali include a support embedded with sulfonium, phosphazenium, and guanidinium salts.

  14. Conducting polymer supported bilayer lipid membrane reconstituted with alamethicin

    NASA Astrophysics Data System (ADS)

    Zhang, Hao; Salinas, Sergio; Baba Sundaresan, Vishnu

    2011-09-01

    Ionic electroactive polymers and bioderived materials have been independently demonstrated as actuators, sensors and energy harvesting devices. In an electroactive polymer, the applied electric field between the cathode and anode drives ion transport between the electrodes, impregnated electrolyte and the bulk of the polymer to generate force and displacement. Similarly, in a bioderived material an input stimulus (electrical, chemoelectrical or chemical) applied across the protein in a bilayer lipid membrane (BLM) displaces ions across the membrane barrier and enables sensing and actuation functions. This paper presents a novel architecture for a device that integrates the ionic function of an electroactive polymer and a bioderived material into a thin-film laminated device combining their unique advantages. A conducting polymer (PPy(DBS)) is used as the electroactive polymer and alamethicin-bound bilayer lipid membrane is used as the bioderived material in the thin-film laminated device. Owing to the configuration of the laminated device, the protein regulates the ionic concentration in the conducting polymer and regulates the electrochemical doping/undoping process in the polymer. By electrically connecting the conducting polymer across its thickness, this arrangement provides a mechanism external to the polymer besides electrical field that can control the electrical, mechanical and/or optical properties of the conducting polymer. This paper also presents the fabrication and characterization of the integrated ionic device and presents a template for the development of a novel category of electroactive ionic devices.

  15. Highly Conductive Anion-Exchange Membranes from Microporous Tröger's Base Polymers.

    PubMed

    Yang, Zhengjin; Guo, Rui; Malpass-Evans, Richard; Carta, Mariolino; McKeown, Neil B; Guiver, Michael D; Wu, Liang; Xu, Tongwen

    2016-09-12

    The development of polymeric anion-exchange membranes (AEMs) combining high ion conductivity and long-term stability is a major challenge for materials chemistry. AEMs with regularly distributed fixed cationic groups, based on the formation of microporous polymers containing the V-shape rigid Tröger's base units, are reported for the first time. Despite their simple preparation, which involves only two synthetic steps using commercially available precursors, the polymers provide AEMs with exceptional hydroxide conductivity at relatively low ion-exchange capacity, as well as a high swelling resistance and chemical stability. An unprecedented hydroxide conductivity of 164.4 mS cm(-1) is obtained at a relatively a low ion-exchange capacity of 0.82 mmol g(-1) under optimal operating conditions. The exceptional anion conductivity appears related to the intrinsic microporosity of the charged polymer matrix, which facilitates rapid anion transport. PMID:27505421

  16. Development of a New Monomer for the Synthesis of Intrinsic Antimicrobial Polymers with Enhanced Material Properties.

    PubMed

    Brodkorb, Florian; Fischer, Björn; Kalbfleisch, Katrin; Robers, Oliver; Braun, Carina; Dohlen, Sophia; Kreyenschmidt, Judith; Lorenz, Reinhard; Kreyenschmidt, Martin

    2015-01-01

    The use of biocidal compounds in polymers is steadily increasing because it is one solution to the need for safety and hygiene. It is possible to incorporate an antimicrobial moiety to a polymer. These polymers are referred to as intrinsic antimicrobial. The biocidal action results from contact of the polymer to the microorganisms, with no release of active molecules. This is particularly important in critical fields like food technology, medicine and ventilation technology, where migration or leaching is crucial and undesirable. The isomers N-(1,1-dimethylethyl)-4-ethenyl-benzenamine and N-(1,1-dimethyl-ethyl)-3-ethenyl-benzenamine (TBAMS) are novel (Co-)Monomers for intrinsic anti-microbial polymers. The secondary amines were prepared and polymerized to the corresponding water insoluble polymer. The antimicrobial activity was analyzed by the test method JIS Z 2801:2000. Investigations revealed a high antimicrobial activity against Staphylococcus aureus and Escherichia coli with a reduction level of >4.5 log10 units. Furthermore, scanning electron microscopy (SEM) of E. coli. in contact with the polymer indicates a bactericidal action which is caused by disruption of the bacteria cell membranes, leading to lysis of the cells. PMID:26305247

  17. Development of a New Monomer for the Synthesis of Intrinsic Antimicrobial Polymers with Enhanced Material Properties

    PubMed Central

    Brodkorb, Florian; Fischer, Björn; Kalbfleisch, Katrin; Robers, Oliver; Braun, Carina; Dohlen, Sophia; Kreyenschmidt, Judith; Lorenz, Reinhard; Kreyenschmidt, Martin

    2015-01-01

    The use of biocidal compounds in polymers is steadily increasing because it is one solution to the need for safety and hygiene. It is possible to incorporate an antimicrobial moiety to a polymer. These polymers are referred to as intrinsic antimicrobial. The biocidal action results from contact of the polymer to the microorganisms, with no release of active molecules. This is particularly important in critical fields like food technology, medicine and ventilation technology, where migration or leaching is crucial and undesirable. The isomers N-(1,1-dimethylethyl)-4-ethenyl-benzenamine and N-(1,1-dimethyl-ethyl)-3-ethenyl-benzenamine (TBAMS) are novel (Co-)Monomers for intrinsic anti-microbial polymers. The secondary amines were prepared and polymerized to the corresponding water insoluble polymer. The antimicrobial activity was analyzed by the test method JIS Z 2801:2000. Investigations revealed a high antimicrobial activity against Staphylococcus aureus and Escherichia coli with a reduction level of >4.5 log10 units. Furthermore, scanning electron microscopy (SEM) of E. coli. in contact with the polymer indicates a bactericidal action which is caused by disruption of the bacteria cell membranes, leading to lysis of the cells. PMID:26305247

  18. Proton-Conducting Magnetic Coordination Polymers.

    PubMed

    Biswas, Soumava; Jena, Himanshu Sekhar; Sanda, Suresh; Konar, Sanjit

    2015-09-21

    Three isostructural lanthanide-based two- dimensional coordination polymers (CPs) {[Ln2(L)3(H2O)2]n⋅2n CH3OH)⋅2n H2O} (Ln=Gd(3+) (1), Tb(3+) (2), Dy(3+) (3); H2L=cyclobutane-1,1-dicarboxylic acid) were synthesized by using a low molecular weight dicarboxylate ligand and characterized. Single-crystal structure analysis showed that in complexes 1-3 lanthanide centers are connected by μ3-bridging cyclobutanedicarboxylate ligands along the c axis to form a rod-shaped infinite 1D coordination chain, which is further linked with nearby chains by μ4-connected cyclobutanedicarboxylate ligands to form 2D CPs in the bc plane. Viewing the packing of the complexes down the b axis reveals that the lattice methanol molecules are located in the interlayer space between the adjacent 2D layers and form H-bonds with lattice and coordinated water molecules to form 1D chains. Magnetic properties of complexes 1-3 were thoroughly investigated. Complex 1 exhibits dominant ferromagnetic interaction between two nearby gadolinium centers and also acts as a cryogenic magnetic refrigerant having a significant magnetic entropy change of -ΔSm=32.8 J kg(-1) K(-1) for ΔH=7 T at 4 K (calculated from isothermal magnetization data). Complex 3 shows slow relaxation of magnetization below 10 K. Impedance analysis revealed that the complexes show humidity-dependent proton conductivity (σ=1.5×10(-5) S cm(-1) for 1, σ=2.07×10(-4) S cm(-1) for 2, and σ=1.1×10(-3) S cm(-1) for 3) at elevated temperature (>75 °C). They retain the conductivity for up to 10 h at high temperature and high humidity. Furthermore, the proton conductivity results were correlated with the number of water molecules from the water-vapor adsorption measurements. Water-vapor adsorption studies showed hysteretic and two-step water vapor adsorption (182,000 μL g(-1) for 1, 184,000 μL g(-1) for 2, and 1,874,000 μL g(-1) for 3) in the experimental pressure range. Simulation of

  19. Electrically Conductive Metal Nanowire Polymer Nanocomposites

    NASA Astrophysics Data System (ADS)

    Luo, Xiaoxiong

    This thesis investigates electrically conductive polymer nanocomposites formulated with metal nanowires for electrostatic discharge and electromagnetic interference shielding. Copper nanowires (CuNWs) of an average length of 1.98 mum and diameter of 25 +/- 4 nm were synthesized. The oxidation reaction of the CuNWs in air can be divided into two stages at weight of 111.2% on TGA curves. The isoconversional activation energies determined by Starink method were used to fit the different master plots. Johnson-Mehl-Avrami (JMA) equation gave the best fit. The surface atoms of the CuNWs are the sites for the random nucleation and the crystallite strain in the CuNWs is the driving force for the growth of nuclei mechanism during the oxidation process. To improve the anti-oxidation properties of the CuNWs, silver was coated onto the surface of the CuNWs in Ag-amine solution. The prepared silver coated CuNWs (AgCuNWs) with silver content of 66.52 wt. %, diameter of 28--33 nm exhibited improved anti-oxidation behavior. The electrical resistivity of the AgCuNW/low density polyethylene (LDPE) nanocomposites is lower than that of the CuNW/LDPE nanocomposites with the same volume percentage of fillers. The nanocomposites formulated with CuNWs and polyethylenes (PEs) were compared to study the different interaction between the CuNWs and the different types of PE matrices. The electrical conductivity of the different PE matrices filled with the same concentrations of CuNWs correlated well with the level of the CuNW dispersion. The intermolecular force and entanglement resulting from the different macromolecular structures such as molecular weight and branching played an important role in the dispersion, electrical properties and rheological behaviour of the CuNW/PE nanocomposites. Ferromagnetic polycrystalline nickel nanowires (NiNWs) were synthesized with uniform diameter of ca. 38 nm and an average length of 2.68 mum. The NiNW linear low density polyethylene (LLDPE

  20. Applications of conducting polymers: robotic fins and other devices

    NASA Astrophysics Data System (ADS)

    Tangorra, James L.; Anquetil, Patrick A.; Weideman, Nathan S.; Fofonoff, Timothy; Hunter, Ian W.

    2007-04-01

    Conducting polymers are becoming viable engineering materials and are gradually being integrated into a wide range of devices. Parallel efforts conducted to characterize their electromechanical behavior, understand the factors that affect actuation performance, mechanically process films, and address the engineering obstacles that must be overcome to generate the forces and displacements required in real-world applications have made it possible to begin using conducting polymers in devices that cannot be made optimal using traditional actuators and materials. The use of conducting polymers has allowed us to take better advantage of biological architectures for robotic applications and has enabled us to pursue the development of novel sensors, motors, and medical diagnostic technologies. This paper uses the application of conducting polymer actuators to a biorobotic fin for unmanned undersea vehicles (UUVs) as a vehicle for discussing the efforts in our laboratory to develop conducting polymers into a suite of useful actuators and engineering components.

  1. Intrinsic response of polymer liquid crystals in photochemical phase transition

    SciTech Connect

    Ikeda, Tomiki; Sasaki, Takeo; Kim, Haengboo )

    1991-01-24

    Time-resolved measurements were performed on the photochemically induced isothermal phase transition of polymer liquid crystals (PLC) with mesogenic side chains of phenyl benzoate (PAPB3) and cyanobiphenyl (PACB3) under conditions wherein the photochemical reaction of the doped photoresponsive molecule (4-butyl-4-{prime}-methoxyazobenzene, BMAB) was completed within {approximately} 10 ns, and the subsequent phase transition of the matrix PLC from nematic (N) to isotropic (I) state was followed by time-resolved measurements of the birefringence of the system. Formation of a sufficient amount of the cis isomer of BMAB with a single pulse of a laser lowered the N-I phase transition temperature of the mixture, inducing the N-I phase transition of PLCs isothermally in a time range of {approximately} 200 ms. This time range is comparable to that of low molecular weight liquid crystals, indicating that suppression in mobility of mesogens in PLCs does not affect significantly the thermodynamically controlled process.

  2. Conducting polymer/clay nanocomposites and their applications.

    PubMed

    Fang, Fei Fei; Choi, Hyoung Jin; Joo, Jinsoo

    2008-04-01

    This review aims at reporting on interesting and potential aspects of conducting polymer/clay nanocomposites with regard to their preparation, characteristics and engineering applications. Various conducting polymers such as polyaniline, polypyrrole and copolyaniline are introduced and three different preparation methods of synthesizing conducting polymer/clay nanocomposites are being emphasized. Morphological features, structure characteristics and thermal degradation behavior are explained based on SEM/TEM images, XRD pattern analyses and TGA/DSC graphs, respectively. Attentions are also being paid on conductive/magnetic performances as well as two potential applications in anti-corrosion coating and electrorheological (ER) fluids. PMID:18572558

  3. Improved morphology in electrochemically grown conducting polymer films

    SciTech Connect

    Rubinstein, I.; Gottesfeld, S.; Sabatani, E.

    1990-12-31

    A conducting polymer film with an improved space filling is formed on a metal electrode surface. A self-assembling monolayer is formed directly on the metal surface where the monolayer has a first functional group that binds to the metal surface and a second chemical group that forms a chemical bonding site for molecules forming the conducting polymer. The conducting polymer is then conventionally deposited by electrochemical deposition. In one example, a conducting film of polyaniline is formed on a gold electrode surface with an intermediate monolayer of p-aminothiophenol.

  4. Nuclear alkylated pyridine aldehyde polymers and conductive compositions thereof

    NASA Technical Reports Server (NTRS)

    Rembaum, A.; Singer, S. (Inventor)

    1970-01-01

    A thermally stable, relatively conductive polymer was disclosed. The polymer was synthesized by condensing in the presence of catalyst a 2, 4, or 6 nuclear alklylated 2, 3, or 4 pyridine aldehyde or quaternary derivatives thereof to form a polymer. The pyridine groups were liked by olefinic groups between 2-4, 2-6, 2-3, 3-4, 3-6 or 4-6 positions. Conductive compositions were prepared by dissolving the quaternary polymer and an organic charge transfer complexing agent such as TCNQ in a mutual solvent such as methanol.

  5. Conductive polymers: towards a smart biomaterial for tissue engineering.

    PubMed

    Balint, Richard; Cassidy, Nigel J; Cartmell, Sarah H

    2014-06-01

    Developing stimulus-responsive biomaterials with easy-to-tailor properties is a highly desired goal of the tissue engineering community. A novel type of electroactive biomaterial, the conductive polymer, promises to become one such material. Conductive polymers are already used in fuel cells, computer displays and microsurgical tools, and are now finding applications in the field of biomaterials. These versatile polymers can be synthesised alone, as hydrogels, combined into composites or electrospun into microfibres. They can be created to be biocompatible and biodegradable. Their physical properties can easily be optimized for a specific application through binding biologically important molecules into the polymer using one of the many available methods for their functionalization. Their conductive nature allows cells or tissue cultured upon them to be stimulated, the polymers' own physical properties to be influenced post-synthesis and the drugs bound in them released, through the application of an electrical signal. It is thus little wonder that these polymers are becoming very important materials for biosensors, neural implants, drug delivery devices and tissue engineering scaffolds. Focusing mainly on polypyrrole, polyaniline and poly(3,4-ethylenedioxythiophene), we review conductive polymers from the perspective of tissue engineering. The basic properties of conductive polymers, their chemical and electrochemical synthesis, the phenomena underlying their conductivity and the ways to tailor their properties (functionalization, composites, etc.) are discussed. PMID:24556448

  6. Raising the conductivity of crystalline polymer electrolytes by aliovalent doping.

    PubMed

    Zhang, Chuhong; Staunton, Edward; Andreev, Yuri G; Bruce, Peter G

    2005-12-28

    Polymer electrolytes, salts dissolved in solid polymers, hold the key to realizing all solid-state devices such as rechargeable lithium batteries, electrochromic displays, or SMART windows. For 25 years conductivity was believed to be confined to amorphous polymer electrolytes, all crystalline polymer electrolytes were thought to be insulators. However, recent results have demonstrated conductivity in crystalline polymer electrolytes, although the levels at room temperature are too low for application. Here we show, for the first time, that it is possible to raise significantly the level of ionic conductivity by aliovalent doping. The conductivity may be raised by 1.5 orders of magnitude if the SbF6- ion in the crystalline conductor poly(ethylene oxide)6:LiSbF6 is replaced by less than 5 mol % SiF6(2-), thus introducing additional, mobile, Li+ ions into the structure to maintain electroneutrality. PMID:16366585

  7. Mechanoassisted Synthesis of Sulfonated Covalent Organic Frameworks with High Intrinsic Proton Conductivity.

    PubMed

    Peng, Yongwu; Xu, Guodong; Hu, Zhigang; Cheng, Youdong; Chi, Chenglong; Yuan, Daqiang; Cheng, Hansong; Zhao, Dan

    2016-07-20

    It is challenging to introduce pendent sulfonic acid groups into modularly built crystalline porous frameworks for intrinsic proton conduction. Herein, we report the mechanoassisted synthesis of two sulfonated covalent organic frameworks (COFs) possessing one-dimensional nanoporous channels decorated with pendent sulfonic acid groups. These COFs exhibit high intrinsic proton conductivity as high as 3.96 × 10(-2) S cm(-1) with long-term stability at ambient temperature and 97% relative humidity (RH). In addition, they were blended with nonconductive polyvinylidene fluoride (PVDF) affording a series of mixed-matrix membranes (MMMs) with proton conductivity up to 1.58 × 10(-2) S cm(-1) and low activation energy of 0.21 eV suggesting the Grotthuss mechanism for proton conduction. Our study has demonstrated the high intrinsic proton conductivity of COFs shedding lights on their wide applications in proton exchange membranes. PMID:27385672

  8. Conducting polymer as smart interfaces for cultured neurons

    NASA Astrophysics Data System (ADS)

    Ahluwalia, Arti; Mauricio, Ines; Mazzoldi, Alberto; Serra, Giorgio; Bianchi, Francesca

    2005-05-01

    This work is part of a research project aimed at realising conducting polymer matrices for interfacing with cultured neurons. The polymer matrix has a dual function, one as a medium for recording electrical activity; the other is chemical stimulation through the release of bioactive molecules. In this work we use poly-3-hexylthiophene as a conducting polymer matrix. To test the polymer"s ability to release molecules upon the application of a potential it was doped with glutamate (GA). GA is an important neurotransmitter, and its controlled release can be important in several medical and tissue engineering applications. Diffusional and controlled release of GA from the polymer were assessed. Biocompatibility of the samples was evaluated at each stage using neuroblastoma cell cultures.

  9. Thermophysical Properties of Polymer Materials with High Thermal Conductivity

    NASA Astrophysics Data System (ADS)

    Lebedev, S. M.; Gefle, O. S.; Dneprovskii, S. N.; Amitov, E. T.

    2015-06-01

    Results of studies on the main thermophysical properties of new thermally conductive polymer materials are presented. It is shown that modification of polymer dielectrics by micron-sized fillers allows thermally conductive materials with thermal conductivity not less than 2 W/(m K) to be produced, which makes it possible to use such materials as cooling elements of various electrical engineering and semiconductor equipment and devices.

  10. Transmitter function of synapse-structure system using conducting polymer

    NASA Astrophysics Data System (ADS)

    Fujii, Masaharu; Machiya, Yuka; Ihori, Haruo

    2012-04-01

    Conducting polymers with neuron-like pattern has been polymerized by controlling polymerization conditions. These conducting polymers have been connected each other to prepare network. If the synapse function can be added to the network, artificial neural network is prepared by conducting polymer. In this paper, we consider the transmitter function using synapse-structure conducting polymer. It consists of three parts: primary circuit as presynaptic terminal, space as synaptic cleft and secondary circuit as postsynaptic structure. Dopant in conducting polymer works as neurotransmitter. Migration as well as diffusion is also considered for dopant ion to transit the space/cleft. When signals from the primary circuit came at the end of the primary circuit in electrolyte solution, the current in the secondary circuit increased because the released dopant ion transited the cleft and entered another conducting polymer. When two primary circuits was used, the current in the secondary circuit increased higher than one primary circuit. This means the synapse-structured conducting polymer system can be use as logical circuit.

  11. The application of conducting polymers to a biorobotic fin propulsor

    NASA Astrophysics Data System (ADS)

    Tangorra, James; Anquetil, Patrick; Fofonoff, Timothy; Chen, Angela; DelZio, Mike; Hunter, Ian

    2007-06-01

    Conducting polymer actuators based on polypyrrole are being developed for use in biorobotic fins that are designed to create and control forces like the pectoral fin of the bluegill sunfish (Lepomis macrochirus). It is envisioned that trilayer bending actuators will be used within, and as, the fin's webbing to create a highly controllable, shape morphing, flexible fin surface, and that linear conducting polymer actuators will be used to actuate the bases of the fin's fin-rays, like an agonist-antagonist muscle pair, and control the fin's stiffness. For this application, trilayer bending actuators were used successfully to reproduce the cupping motion of the sunfish pectoral fin by controlling the curvature of the fin's surface and the motion of its dorsal and ventral edges. However, the speed of these large polymer films was slow, and must be increased if the fin's shape is to be modulated synchronously with the fin's flapping motion. Free standing linear conducting polymer films can generate large stresses and strains, but there are many engineering obstacles that must be resolved in order to create linear polymer actuators that generate simultaneously the forces, displacements and actuation rates required by the fin. We present two approaches that are being used to solve the engineering challenges involved in utilizing conducting polymer linear actuators: the manufacture of long, uniform ribbons of polymer and gold film, and the parallel actuation of multiple conducting polymer films.

  12. Layered conductive polymer on nylon membrane templates for high performance, thin-film supercapacitor electrodes

    NASA Astrophysics Data System (ADS)

    Shi, HaoTian Harvey; Naguib, Hani E.

    2016-04-01

    Flexible Thin-film Electrochemical Capacitors (ECs) are emerging technology that plays an important role as energy supply for various electronics system for both present era and the future. Intrinsically conductive polymers (ICPs) are promising pseudo-capacitive materials as they feature both good electrical conductivity and high specific capacitance. This study focuses on the construction and characterization of ultra-high surface area porous electrodes based on coating of nano-sized conductive polymer materials on nylon membrane templates. Herein, a novel nano-engineered electrode material based on nylon membranes was presented, which allows the creation of super-capacitor devices that is capable of delivering competitive performance, while maintaining desirable mechanical characteristics. With the formation of a highly conductive network with the polyaniline nano-layer, the electrical conductivity was also increased dramatically to facilitate the charge transfer process. Cyclic voltammetry and specific capacitance results showed promising application of this type of composite materials for future smart textile applications.

  13. Research Trends of Soft Actuators based on Electroactive Polymers and Conducting Polymers

    NASA Astrophysics Data System (ADS)

    Kaneto, K.

    2016-04-01

    Artificial muscles (or soft actuators) based on electroactive polymers (EAPs) are attractive power sources to drive human-like robots in place of electrical motor, because they are quiet, powerful, light weight and compact. Among EAPs for soft actuators, conducting polymers are superior in strain, stress, deformation form and driving voltage compared with the other EAPs. In this paper, the research trends of EAPs and conducting polymers are reviewed by retrieval of the papers and patents. The research activity of EAP actuators showed the maximum around 2010 and somehow declining now days. The reasons for the reducing activity are found to be partly due to problems of conducting polymer actuators for the practical application. The unique characteristics of conducting polymer actuators are mentioned in terms of the basic mechanisms of actuation, creeping, training effect and shape retention under high tensile loads. The issues and limitation of conducting polymer soft actuators are discussed.

  14. Making Conductive Polymers By Arc Tracking

    NASA Technical Reports Server (NTRS)

    Daech, Alfred F.

    1992-01-01

    Experimental technique for fabrication of electrically conductive polymeric filaments based on arc tracking, in which electrical arc creates conductive carbon track in material that initially was insulator. Electrically conductive polymeric structures made by arc tracking aligned along wire on which formed. Alignment particularly suited to high conductivity and desirable in materials intended for testing as candidate superconductors.

  15. Predoped conductive polymers as battery electrode materials

    SciTech Connect

    Jow, T.R.; Shacklette, L.W.

    1989-02-14

    An improved battery is described. The anode consists of one or more conjugated backbone polymers and one or more electroactive materials selected from the group consisting of metals which alloy with alkali metals and alkali metal cation inserting material. The electrolyte consists of an organic solvent and an alkali-metal salt. There is also a cathode alkali-metal cations from the electrolyte being inserted into the anode as a metal alloy or as an inserted ion in the alkali metal cation inserting material during the charging of the battery; the improvement comprises an anode in which the conjugated backbone polymers contained in the anode have been predoped with one or more alkali metal cations to the reduced state prior to incorporation of the anode into the battery.

  16. Ionically conducting polymers: Principles and properties of solid electrolytes

    SciTech Connect

    Skotheim, T.; Okamoto, Y.

    1987-01-01

    The recent success in developing rechargeable lithium batteries incorporating polyether-based electrolytes has led to the anticipation of a wider use of polymer electrolytes in a host of different applications. The polymers with the best combinations of solvation power, conductivity and electrochemical stability are all based on either PEO or polymers incorporating a high density of EO units. PEO-based electrolytes still yield the highest conductivities at elevated temperatures (approx.100/sup 0/C) when it is completely amorphous. What has emerged during the last ten years of research on polymer electrolytes is the central importance of the amorphous state for high conductivity, where the ion mobility is governed by the mobility associated with a low glass transition temperature. The difference between polymer and liquid electrolytes is that in the former the solvating part does not migrate with the ions. There is, however, still some controversy concerning the nature of the ionic species, i.e. whether the salt is present in the form of associated ions. The intensive research of the last few years has led to a far better understanding of these polymer-ion complexes. Several different types of solvating polymers have been developed, in particular single ion conductors, which represent much of the future of ion conducting polymer research. 36 refs.

  17. Conducting polymer nanofibers: Synthesis, properties and applications

    NASA Astrophysics Data System (ADS)

    Huang, Jiaxing

    An interfacial polymerization method is described which enables the synthesis of polyaniline nanofibers with diameters tunable from 30 to 120 nm. This synthesis is template-free and readily scalable and can be applied to polyaniline derivatives and other conjugated polymers. Mechanistic studies reveal that nanofibers form naturally during the chemical oxidative polymerization of aniline in water without the need for any template, functional molecule or seed. In conventional polymerization, nanofibers are subject to secondary growth of amorphous particles which leads to irregularly shaped agglomerates. The key to producing pure nanofibers is to suppress secondary growth. This has been achieved with interfacial polymerization where the interface separates nanofiber formation from secondary growth and also by using rapidly mixed reactions where the initiator molecules are consumed before secondary growth begins. Polyaniline nanofibers dramatically enhance many applications of conventional polyaniline, such as in chemical sensors. Here, the small diameter, high surface area and water dispersibility of the nanofibers enable improved sensor performance and new sensing mechanisms. The nanofibers can also serve as a template to grow inorganic/polyaniline nanocomposites. Polyaniline nanofibers with 1--5 nm gold nanoparticles possess exciting applications such as in electronic non-volatile memory devices. Additionally, a novel flash welding technique for the nanofibers has been invented. A photographic camera flash sets off cross-linking reactions that can be used to make asymmetric polymer membranes, form patterned nanofiber films and create polymer based nanocomposites.

  18. Electropolymerized Conducting Polymer as Actuator and Sensor Device

    ERIC Educational Resources Information Center

    Cortes, Maria T.; Moreno, Juan C.

    2005-01-01

    A study demonstrates the potential application of conducting polymers to convert electrical energy into mechanical energy at low voltage or current. The performance of the device is explained using electrochemistry and solid-state chemistry.

  19. Interfacial ionic and electronic conductivity in polymers

    SciTech Connect

    Shriver, D.F.

    1989-06-01

    New phosphazen-based ((NP(OR){sub x}(OC{sub 2}H{sub 4}SO{sub 3}Na){sub 2-x}){sub n}) single ion conductors were synthesized based on a polyphosphazene backbone and short-chain polyether sidechains, some of which are terminated with tetraalkylammonium groups. These materials are good anion conductors at room temperature. Related cation conductors were also prepared and characterized. Effects of interionic attractive interactions on the diffusion of a tracer were investigated theoretically. The results are relevant to ion pairing and trapping in polymer electrolytes.

  20. Conducting Polymer Electrodes for Gel Electrophoresis

    PubMed Central

    Bengtsson, Katarina; Nilsson, Sara; Robinson, Nathaniel D.

    2014-01-01

    In nearly all cases, electrophoresis in gels is driven via the electrolysis of water at the electrodes, where the process consumes water and produces electrochemical by-products. We have previously demonstrated that π-conjugated polymers such as poly(3,4-ethylenedioxythiophene) (PEDOT) can be placed between traditional metal electrodes and an electrolyte to mitigate electrolysis in liquid (capillary electroosmosis/electrophoresis) systems. In this report, we extend our previous result to gel electrophoresis, and show that electrodes containing PEDOT can be used with a commercial polyacrylamide gel electrophoresis system with minimal impact to the resulting gel image or the ionic transport measured during a separation. PMID:24586761

  1. Sensors employing Functionalized Conducting Polymer Thin Film Transistors

    NASA Astrophysics Data System (ADS)

    Tanese, M. C.; Torsi, L.; Cioffi, N.; Sabbatini, L.; Zambonin, P. G.

    2003-12-01

    Functionalized conducting polymers are employed as active layers in sensors with a thin film transistor (TFT) device structure. Such devices can work as multi-parameter sensors with responses that are fast, repeatable and reversible at room temperature. In this work, a strategy is proposed to enhance the chemical selectivity of organic TFT sensors, by selecting active layers that are made of conducting polymers bearing chemically different substituents. A modulation of the devices sensitivity towards analytes such as alcohols and ketones is demonstrated.

  2. Characterisation of Proton Conducting Polymer Electrolyte Based on Pan

    NASA Astrophysics Data System (ADS)

    Nithya, S.; Selvasekarapandian, S.; Rajeswari, N.; Sikkanthar, S.; Karthikeyan, S.; Sanjeeviraja, C.

    2013-07-01

    The polymer electrolytes composed of polyacrylonitrile (PAN) with various concentration of ammonium nitrare (NH4NO3) salt have been prepared by solution casting method, using DMF as solvent. The increase in amorphous nature of the polymer electrolytes has been confirmed by Xray diffraction analysis. The complex formation between polymer and dissociated salt has been confirmed by Fourier transform infrared spectroscopy. From the Ac impedance spectroscopic analysis, the ionic conductivity of 20 mol% NH4NO3 doped polymer complex has been found to be 2.742 × 10-6 S cm-1 at room temperature. The conductivity has been increased when the temperature is increased. The activation energy of 20 mol% NH4NO3 doped polymer electrolyte was calculated using Arrhenius plot and it has been found to be 0.58 eV. The dielectric permitivitty (ɛ*) and electric modulus (m*) have been discussed.

  3. Li conductivity in siloxane-based polymer electrolytes

    NASA Astrophysics Data System (ADS)

    Stacy, Eric; Fan, Fei; Feng, Hongbo; Gainaru, Catalin; Mays, Jimmy; Sokolov, Alexei

    Polymer electrolytes containing lithium ions are ideal candidates for electrochemical devices and energy storage applications. Understanding their ionic transport mechanism is the key for rational designing of highly conductive polymer matrices. Complementing dielectric spectroscopy investigations by results from rheology and differential scanning calorimetry we focused on the interplay between dynamics of lithium ions and the polymer matrix based on polysiloxane backbone. Our results demonstrate that the conductivity and the degree of decoupling between ion dynamics and structural relaxation depend strongly not only on the ions concentration, but also on the polarity and size of the polymeric side-groups. Chemical Science Division, Oak Ridge National Laboratory, Oak Ridge, Tennessee 37831, United States.

  4. Enhancement of CO2 Affinity in a Polymer of Intrinsic Microporosity by Amine Modification

    PubMed Central

    2014-01-01

    Nitrile groups in the polymer of intrinsic microporosity PIM-1 were reduced to primary amines using borane complexes. In adsorption experiments, the novel amine–PIM-1 showed higher CO2 uptake and higher CO2/N2 sorption selectivity than the parent polymer, with very evident dual-mode sorption behavior. In gas permeation with six light gases, the individual contributions of solubility and diffusion to the overall permeability was determined via time-lag analysis. The high CO2 affinity drastically restricts diffusion at low pressures and lowers CO2 permeability compared to the parent PIM-1. Furthermore, the size-sieving properties of the polymer are increased, which can be attributed to a higher stiffness of the system arising from hydrogen bonding of the amine groups. Thus, for the H2/CO2 gas pair, whereas PIM-1 favors CO2, amine–PIM-1 shows permselectivity toward H2, breaking the Robeson 2008 upper bound. PMID:24860196

  5. Characterization of intrinsic and induced lateral conduction in space dielectric materials

    SciTech Connect

    Hanna, R.; Paulmier, T. Belhaj, M.; Dirassen, B.; Payan, D.; Balcon, N.

    2014-02-14

    Characterization of lateral charge carrier conduction in space dielectrics is of high importance for the prediction of charging behavior and electrostatic discharges on satellites. In the present paper, a new experimental approach for the analysis of surface conduction, which is not well understood and characterized in the literature, is established and discussed. Though this method, based on the use of two Kelvin probes, we have been able to discriminate between lateral and bulk charge transports and to reveal the presence of an intrinsic lateral conductivity on Teflon{sup ®} FEP irradiated with low energy electron beam. We demonstrated that lateral intrinsic conductivity is enhanced when incident current density increases and when approaching the sample surface. The experimental results are analyzed through trapping/detrapping and hopping models. Depending on radiation configuration mode, we have revealed as well the presence of a lateral conductivity that is enhanced by radiation ionization processes, and explained as well with a trapping/recombination model.

  6. Method of forming electronically conducting polymers on conducting and nonconducting substrates

    NASA Technical Reports Server (NTRS)

    Murphy, Oliver J. (Inventor); Hitchens, G. Duncan (Inventor); Hodko, Dalibor (Inventor); Clarke, Eric T. (Inventor); Miller, David L. (Inventor); Parker, Donald L. (Inventor)

    2001-01-01

    The present invention provides electronically conducting polymer films formed from photosensitive formulations of pyrrole and an electron acceptor that have been selectively exposed to UV light, laser light, or electron beams. The formulations may include photoinitiators, flexibilizers, solvents and the like. These solutions can be used in applications including printed circuit boards and through-hole plating and enable direct metallization processes on non-conducting substrates. After forming the conductive polymer patterns, a printed wiring board can be formed by sensitizing the polymer with palladium and electrolytically depositing copper.

  7. UV-induced surface electrical conductivity jump of polymer nanocomposites

    SciTech Connect

    Chen Guangxin; Miyauchi, Masahiro; Shimizu, Hiroshi

    2008-05-19

    A method of improving the electrical conductivity of polymer nanocomposites under UV irradiation was described. An anatase TiO{sub 2}-grafted carbon nanotube could function as a conductive filler and a photocatalyst when it compounds with a poly(L-lactide) to produce a composite. After UV irradiation, the decomposition of the polymer only occurred on the surface of a poly(L-lactide)/TiO{sub 2} grafted carbon nanotube composite and not on bulk, resulting in an electrical conductivity jump as high as six orders of magnitude.

  8. Mediating conducting polymer growth within hydrogels by controlling nucleation

    NASA Astrophysics Data System (ADS)

    Patton, A. J.; Green, R. A.; Poole-Warren, L. A.

    2015-01-01

    This study examines the efficacy of primary and secondary nucleation for electrochemical polymerisation of conductive polymers within poly(vinyl alcohol) methacrylate hydrogels. The two methods of nucleation investigated were a primary heterogeneous mechanism via introduction of conductive bulk metallic glass (Mg64Zn30Ca5Na1) particles and a secondary mechanism via introduction of "pre-polymerised" conducting polymer within the hydrogel (PEDOT:PSS). Evidence of nucleation was not seen in the bulk metallic glass loaded gels, however, the PEDOT:PSS loaded gels produced charge storage capacities over 15 mC/cm2 when sufficient polymer was loaded. These studies support the hypothesis that secondary nucleation is an efficient approach to producing stand-alone conducting hydrogels.

  9. Phase diagram of hopping conduction mechanisms in polymer nanofiber network

    SciTech Connect

    Li, Jeng-Ting; Lu, Yu-Cheng; Jiang, Shiau-Bin; Zhong, Yuan-Liang; Yeh, Jui-Ming

    2015-12-07

    Network formation by nanofiber crosslinking is usually in polymer materials as application in organic semiconductor devices. Electron hopping transport mechanisms depend on polymer morphology in network. Conducting polymers morphology in a random network structure is modeled by a quasi-one-dimensional system coupled of chains or fibers. We observe the varying hopping conduction mechanisms in the polyaniline nanofibers of the random network structure. The average diameter d of the nanofibers is varied from approximately 10 to 100 nm. The different dominant hopping mechanisms including Efros-Shklovskii variable-range hopping (VRH), Mott VRH, and nearest-neighbor hopping are dependent on temperature range and d in crossover changes. The result of this study is first presented in a phase diagram of hopping conduction mechanisms based on the theories of the random network model. The hopping conduction mechanism is unlike in normal semiconductor materials.

  10. Rapid synthesis of flexible conductive polymer nanocomposite films

    NASA Astrophysics Data System (ADS)

    Blattmann, C. O.; Sotiriou, G. A.; Pratsinis, S. E.

    2015-03-01

    Polymer nanocomposite films with nanoparticle-specific properties are sought out in novel functional materials and miniaturized devices for electronic and biomedical applications. Sensors, capacitors, actuators, displays, circuit boards, solar cells, electromagnetic shields and medical electrodes rely on flexible, electrically conductive layers or films. Scalable synthesis of such nanocomposite films, however, remains a challenge. Here, flame aerosol deposition of metallic nanosliver onto bare or polymer-coated glass substrates followed by polymer spin-coating on them leads to rapid synthesis of flexible, free-standing, electrically conductive nanocomposite films. Their electrical conductivity is determined during their preparation and depends on substrate composition and nanosilver deposition duration. Accordingly, thin (<500 nm) and flexible nanocomposite films are made having conductivity equivalent to metals (e.g. 5 × 104 S cm-1), even during repetitive bending.

  11. Rapid synthesis of flexible conductive polymer nanocomposite films.

    PubMed

    Blattmann, C O; Sotiriou, G A; Pratsinis, S E

    2015-03-27

    Polymer nanocomposite films with nanoparticle-specific properties are sought out in novel functional materials and miniaturized devices for electronic and biomedical applications. Sensors, capacitors, actuators, displays, circuit boards, solar cells, electromagnetic shields and medical electrodes rely on flexible, electrically conductive layers or films. Scalable synthesis of such nanocomposite films, however, remains a challenge. Here, flame aerosol deposition of metallic nanosliver onto bare or polymer-coated glass substrates followed by polymer spin-coating on them leads to rapid synthesis of flexible, free-standing, electrically conductive nanocomposite films. Their electrical conductivity is determined during their preparation and depends on substrate composition and nanosilver deposition duration. Accordingly, thin (<500 nm) and flexible nanocomposite films are made having conductivity equivalent to metals (e.g. 5  × 10(4) S cm(-1)), even during repetitive bending. PMID:25736387

  12. Polymer electrolyte membranes with exceptional conductivity anisotropy via holographic polymerization

    NASA Astrophysics Data System (ADS)

    Smith, Derrick M.; Cheng, Shan; Wang, Wenda; Bunning, Timothy J.; Li, Christopher Y.

    2014-12-01

    Polymer electrolyte membranes using an ionic liquid as electrolyte with an ionic conductivity anisotropy of ∼5000 have been fabricated using a holographic polymerization nanomanufacturing technique. The resultant structure is referred to as holographic polymer electrolyte membranes (hPEMs), which are comprised of alternating nanolayers of a room temperature ionic liquid and crosslinked polymer resin, confirmed under TEM imaging. These hPEMs also show no reduction in room temperature conductivity with respect to the loaded ionic liquid when characterized in the plane of ionic liquid nanolayers. At elevated temperatures with the optimal electrolyte volume loading, calculation shows that the free ion concentration is higher than the pure ionic liquid, suggesting that the photopolymer dual-functionalizes as a loadbearing scaffold and an ion-complexing agent, allowing for more ions to participate in charge transfer. These hPEMs provide a promising solution to decoupling mechanical enhancement and ion transport in polymer electrolyte membranes.

  13. Mixed-ionic and electronic conductivity in polymers

    SciTech Connect

    Ratner, M.A.; Shriver, D.F.

    1991-01-01

    The aim in this portion of the research is to prepare new electroactive films with high ion mobility, and to characterize the transport properties of these materials. The classic conducting polymers, polyacetylene, polythiophene, and polypyrrole have dense structures that prevent rapid redox switching because of the low diffusivity of ions. The objective is to modify the last two polymers with pendant polyethers, which should greatly improve ion transport.

  14. Synthesis of novel metallocenes: Asymmetric hydrogenation catalysts to conductive polymers

    SciTech Connect

    Erickson, M.S.

    1992-01-01

    The goal of this research was to synthesize conductive polymers based on repeating ferrocene units. During the course of this study, the design of the conductive polymers evolved from the initial model based on [open quotes]stacked[open quotes] ferrocenes where ethano bridged cyclophentadienyl rings are linked by iron(II), to the latest ferrocene-diene model where ferrocene units were linked by double bonds. In the pursuit of these elusive monomers, attempts at their synthesis led down dead-end routes, even though new molecules were synthesized. Some of these dead-end routes, even though new molecules were synthesized. All the work reported in this dissertation had the eventual goal of synthesizing potential monomers for ferrocene conductive polymers. This dissertation is divided into three chapters. Chapter one describes the attempted synthesis of thiophene derivatives where a cyclopentadienyl ring is fused to the [c]-face. Although the target molecule was never synthesized, a convenient and safe new synthesis of 3,4-dibromo=2,5-dimethyl thiophene was developed along with the synthesis and full characterization of 3-bromo-4-trimethylsilyl-2,5-dimethylthiophene. Chapter two describes the design of asymmetric hydrogenation catalysts and the convenient synthesis of chiral titanocene derivatives. Chapter three summarizes the history of the attempts to prepare ferrocene containing conductive polymers and describes the synthesis of ferrocenophenes and diethano bridged bis(cyclophentadienyl) compounds for use as monomeric precursors to conductive polymers based on repeating ferrocene units.

  15. Electrical characterization of proton conducting polymer electrolyte based on bio polymer with acid dopant

    NASA Astrophysics Data System (ADS)

    Kalaiselvimary, J.; Pradeepa, P.; Sowmya, G.; Edwinraj, S.; Prabhu, M. Ramesh

    2016-05-01

    This study describes the biodegradable acid doped films composed of chitosan and Perchloric acid with different ratios (2.5 wt %, 5 wt %, 7.5 wt %, 10 wt %) was prepared by the solution casting technique. The temperature dependence of the proton conductivity of complex electrolytes obeys the Arrhenius relationship. Proton conductivity of the prepared polymer electrolyte of the bio polymer with acid doped was measured to be approximately 5.90 × 10-4 Scm-1. The dielectric data were analyzed using Complex impedance Z*, Dielectric loss ɛ', Tangent loss for prepared polymer electrolyte membrane with the highest conductivity samples at various temperature.

  16. Modeling and Extraction of Parasitic Thermal Conductance and Intrinsic Model Parameters of Thermoelectric Modules

    NASA Astrophysics Data System (ADS)

    Sim, Minseob; Park, Hyunbin; Kim, Shiho

    2015-11-01

    We have presented both modeling and a method for extracting parasitic thermal conductance as well as intrinsic device parameters of a thermoelectric module based on information readily available in vendor datasheets. An equivalent circuit model that is compatible with circuit simulators is derived, followed by a methodology for extracting both intrinsic and parasitic model parameters. For the first time, the effective thermal resistance of the ceramic and copper interconnect layers of the thermoelectric module is extracted using only parameters listed in vendor datasheets. In the experimental condition, including under condition of varying electric current, the parameters extracted from the model accurately reproduce the performance of commercial thermoelectric modules.

  17. A Conducting Polymer Film Stronger Than Aluminum

    NASA Astrophysics Data System (ADS)

    Shi, Gaoquan; Jin, Shi; Xue, Gi; Li, Cun

    1995-02-01

    Polythiophene (Pth) was electrochemically deposited onto stainless steel substrate from freshly distilled boron fluoride-ethyl ether containing 10 millimoles of thiophene per liter. The free-standing Pth film obtained at an applied potential of 1.3 volts (versus Ag/AgCl) had a conductivity of 48.7 siemens per centimeter. Its tensile strength (1200 to 1300 kilograms per square centimeter) was greater than that of aluminium (1000 to 1100 kilograms per square centimeter). This Pth film behaves like a metal sheet and can be easily cut into various structures with a knife or a pair of scissors.

  18. Corrosion resistant coatings from conducting polymers

    SciTech Connect

    Wrobleski, D.A.; Benicewicz, B.C.; Thompson, K.G.; Bryan, C.J.

    1993-12-01

    Cr-based corrosion resistant undercoatings will have to be replaced because of environmental and health concerns. A coating system of a conducting polyaniline primer layer topcoated with epoxy or polyurethane, is being evaluated for corrosion resistance on mild steel in 0.1 M HCl or in a marine setting. Results of both laboratory and Beach Site testing indicate that this coating is very effective; even when the coatings are scratched to expose bare metal, the coated samples show very little signs of corrosion in the exposed area. 3 figs, 6 refs.

  19. Preparation of Conducting Polymers by Electrochemical Methods and Demonstration of a Polymer Battery

    ERIC Educational Resources Information Center

    Goto, Hiromasa; Yoneyama, Hiroyuki; Togashi, Fumihiro; Ohta, Reina; Tsujimoto, Akitsu; Kita, Eiji; Ohshima, Ken-ichi

    2008-01-01

    The electrochemical polymerization of aniline and pyrrole, and demonstrations of electrochromism and the polymer battery effect, are presented as demonstrations suitable for high school and introductory chemistry at the university level. These demonstrations promote student interest in the electrochemical preparation of conducting polymers, where…

  20. DNA-sensors based on functionalized conducting polymers and quantum dots

    NASA Astrophysics Data System (ADS)

    Kjällman, Tanja; Peng, Hui; Travas-Sejdic, Jadranka; Soeller, Christian

    2007-12-01

    The availability of rapid and specific biosensors is of great importance for many areas of biomedical research and modern biotechnology. This includes a need for DNA sensors where the progress of molecular biology demands routine detection of minute concentrations of specific gene fragments. A promising alternative approach to traditional DNA essays utilizes novel smart materials, including conducting polymers and nanostructured materials such as quantum dots. We have constructed a number of DNA sensors based on smart materials that allow rapid one-step detection of unlabeled DNA fragments with high specificity. These sensors are based on functionalized conducting polymers derived from polypyrrole (PPy) and poly(p-phenylenevinylene) (PPV). PPy based sensors provide intrinsic electrical readout via cyclic voltammetry and electrochemical impedance spectroscopy. The performance of these sensors is compared to a novel self-assembled monolayer-PNA construct on a gold electrode. Characterization of the novel PNA based sensor shows that it has comparable performance to the PPy based sensors and can also be read out effectively using AC cyclic voltammetry. Complementary to such solid substrate sensors we have developed a novel optical DNA essay based on a new PPV derived cationic conducting polymer. DNA detection in this essay results from sample dependent fluorescence resonance energy transfer changes between the cationic conducting polymer and Cy3 labeled probe oligonucleotides. As an alternative to such fluorochrome based sensors we discuss the use of inorganic nanocrystals ('quantum dots') and present data from water soluble CdTe quantum dots synthesized in an aqueous environment.

  1. Statistical analysis of intrinsic and extrinsic coupling losses for step-index polymer optical fibers.

    PubMed

    Werzinger, Stefan; Bunge, Christian-Alexander

    2015-08-24

    The intrinsic and extrinsic coupling losses of step-index polymer optical fibers are statistically examined by Monte Carlo simulations. In contrast to most existing models that linearly scale individual losses, a comprehensive analytic coupling loss model is used that also considers the interdependencies between mismatches in numerical aperture and core diameter, as well as radial and longitudinal offsets. As a typical example, the coupling losses of A4a.2 step-index multimode fibers are analyzed for an equilibrium mode distribution. The results show considerably less conservative coupling loss estimations than with traditional models, improving link power budgeting. PMID:26368203

  2. Ion-Conducting Polymer Films as Chemical Sensors

    SciTech Connect

    Hughes, R.C.; Patel, S.V.; Pfeifer, K.B.; Yelton, W.G.

    1999-05-03

    Solid Polymer Electrolytes (SPE) are widely used in batteries and fuel cells because of the high ionic conductivity that can be achieved at room temperature. The ions are usually Li or protons, although other ions can be shown to conduct in these polymer films. There has been very little work on using these films as chemical sensors. We have found that thin films of polymers like polyethyleneoxide (PEO) are very sensitive to low concentrations of volatile organic compounds (VOCS) like common solvents. We will present impedance spectroscopy of PEO films in the frequency range 0.01 Hz to 1 MHz for different concentrations of VOCS. We find that the measurement frequency is important for distinguishing ionic conductivity from the double layer capacitance and parasitic capacitances.

  3. Sequence heuristics to encode phase behaviour in intrinsically disordered protein polymers.

    PubMed

    Quiroz, Felipe García; Chilkoti, Ashutosh

    2015-11-01

    Proteins and synthetic polymers that undergo aqueous phase transitions mediate self-assembly in nature and in man-made material systems. Yet little is known about how the phase behaviour of a protein is encoded in its amino acid sequence. Here, by synthesizing intrinsically disordered, repeat proteins to test motifs that we hypothesized would encode phase behaviour, we show that the proteins can be designed to exhibit tunable lower or upper critical solution temperature (LCST and UCST, respectively) transitions in physiological solutions. We also show that mutation of key residues at the repeat level abolishes phase behaviour or encodes an orthogonal transition. Furthermore, we provide heuristics to identify, at the proteome level, proteins that might exhibit phase behaviour and to design novel protein polymers consisting of biologically active peptide repeats that exhibit LCST or UCST transitions. These findings set the foundation for the prediction and encoding of phase behaviour at the sequence level. PMID:26390327

  4. Sequence heuristics to encode phase behaviour in intrinsically disordered protein polymers

    NASA Astrophysics Data System (ADS)

    Quiroz, Felipe García; Chilkoti, Ashutosh

    2015-11-01

    Proteins and synthetic polymers that undergo aqueous phase transitions mediate self-assembly in nature and in man-made material systems. Yet little is known about how the phase behaviour of a protein is encoded in its amino acid sequence. Here, by synthesizing intrinsically disordered, repeat proteins to test motifs that we hypothesized would encode phase behaviour, we show that the proteins can be designed to exhibit tunable lower or upper critical solution temperature (LCST and UCST, respectively) transitions in physiological solutions. We also show that mutation of key residues at the repeat level abolishes phase behaviour or encodes an orthogonal transition. Furthermore, we provide heuristics to identify, at the proteome level, proteins that might exhibit phase behaviour and to design novel protein polymers consisting of biologically active peptide repeats that exhibit LCST or UCST transitions. These findings set the foundation for the prediction and encoding of phase behaviour at the sequence level.

  5. Sequence heuristics to encode phase behaviour in intrinsically disordered protein polymers

    PubMed Central

    Quiroz, Felipe García; Chilkoti, Ashutosh

    2015-01-01

    Proteins and synthetic polymers that undergo aqueous phase transitions mediate self-assembly in nature and in man-made material systems. Yet little is known about how the phase behaviour of a protein is encoded in its amino acid sequence. Here, by synthesizing intrinsically disordered, repeat proteins to test motifs that we hypothesized would encode phase behaviour, we show that the proteins can be designed to exhibit tunable lower or upper critical solution temperature (LCST and UCST, respectively) transitions in physiological solutions. We also show that mutation of key residues at the repeat level abolishes phase behaviour or encodes an orthogonal transition. Furthermore, we provide heuristics to identify, at the proteome level, proteins that might exhibit phase behaviour and to design novel protein polymers consisting of biologically active peptide repeats that exhibit LCST or UCST transitions. These findings set the foundation for the prediction and encoding of phase behaviour at the sequence level. PMID:26390327

  6. Controlled thermal oxidative crosslinking of polymers of intrinsic microporosity towards tunable molecular sieve membranes

    NASA Astrophysics Data System (ADS)

    Song, Qilei; Cao, Shuai; Pritchard, Robyn H.; Ghalei, Behnam; Al-Muhtaseb, Shaheen A.; Terentjev, Eugene M.; Cheetham, Anthony K.; Sivaniah, Easan

    2014-09-01

    Organic open frameworks with well-defined micropore (pore dimensions below 2 nm) structure are attractive next-generation materials for gas sorption, storage, catalysis and molecular level separations. Polymers of intrinsic microporosity (PIMs) represent a paradigm shift in conceptualizing molecular sieves from conventional ordered frameworks to disordered frameworks with heterogeneous distributions of microporosity. PIMs contain interconnected regions of micropores with high gas permeability but with a level of heterogeneity that compromises their molecular selectivity. Here we report controllable thermal oxidative crosslinking of PIMs by heat treatment in the presence of trace amounts of oxygen. The resulting covalently crosslinked networks are thermally and chemically stable, mechanically flexible and have remarkable selectivity at permeability that is three orders of magnitude higher than commercial polymeric membranes. This study demonstrates that controlled thermochemical reactions can delicately tune the topological structure of channels and pores within microporous polymers and their molecular sieving properties.

  7. Corrosion-protective coatings from electrically conducting polymers

    SciTech Connect

    Thompson, K.G.; Bryan, C.J.; Benicewicz, B.C.; Wrobleski, D.A.

    1991-12-31

    In a joint research effort involving the Kennedy Space Center and the Los Alamos National Laboratory, electrically conductive polymer coatings have been developed as corrosion-protective coatings for metal surfaces. At the Kennedy Space Center, the launch environment consists of marine, severe solar, and intermittent high acid/elevated temperature conditions. Electrically conductive polymer coatings have been developed which impart corrosion resistance to mild steel when exposed to saline and acidic environments. Such coatings also seem to promote corrosion resistance in areas of mild steel where scratches exist in the protective coating. Such coatings appear promising for many commercial applications.

  8. Corrosion-protective coatings from electrically conducting polymers

    NASA Technical Reports Server (NTRS)

    Thompson, Karen Gebert; Bryan, Coleman J.; Benicewicz, Brian C.; Wrobleski, Debra A.

    1991-01-01

    In a joint effort between NASA Kennedy and LANL, electrically conductive polymer coatings were developed as corrosion protective coatings for metal surfaces. At NASA Kennedy, the launch environment consist of marine, severe solar, and intermittent high acid and/or elevated temperature conditions. Electrically conductive polymer coatings were developed which impart corrosion resistance to mild steel when exposed to saline and acidic environments. Such coatings also seem to promote corrosion resistance in areas of mild steel where scratches exist in the protective coating. Such coatings appear promising for many commercial applications.

  9. Controlling PbS nanocrystal aggregation in conducting polymers.

    PubMed

    Warner, Jamie H; Watt, Andrew A R; Tilley, Richard D

    2005-10-01

    PbS nanocrystals were synthesized directly in the conducting polymer, poly(3-hexylthiophene-2,5-diyl). Transmission electron microscopy shows that the PbS nanocrystals are faceted and relatively uniform in size with a mean size of 10 nm. FFT analysis of the atomic lattice planes observed in TEM and selected area electron diffraction confirm that the nanocrystals have the PbS rock salt structure. The synthesis conditions are explored to show control over the aggregation of PbS nanocrystals in the thiophene conducting polymer. PMID:20818021

  10. Chemical sensors using peptide-functionalized conducting polymer nanojunction arrays

    NASA Astrophysics Data System (ADS)

    Aguilar, Alvaro Díaz; Forzani, Erica S.; Li, Xiulan; Tao, Nongjian; Nagahara, Larry A.; Amlani, Islamshah; Tsui, Raymond

    2005-11-01

    We demonstrate a heavy metal-ion sensor for drinking water analysis using a conducting polymer nanojunction array. Each nanojunction is formed by bridging a pair of nanoelectrodes separated with a small gap (<60nm) with electrodeposited peptide-modified polyanilines. The signal transduction mechanism of the sensor is based on the change in the nanojunction conductance as a result of polymer conformational changes induced by the metal-ion chelating peptide. The nanojunction sensor allows real-time detection of Cu2+ and Ni2+ at ppt range.

  11. Thin film conductive polymer for microactuator and micromuscle applications

    SciTech Connect

    Lee, A.P.; Hong, K.; Trevino, J.; Northrup, M.A.

    1994-04-14

    Conductive polymer/polyimide bimorphic microcantilevers have been actuated vertically (out-of-plane) upon the volumetric changes induced by electrochemical doping of the polymer. The microcantilevers that are 200-500 {mu}m in length and 50-100 {mu}m in width can be fully extended from a circularly-curled geometry, and thus generate more than 100 {mu}m displacement. Dynamically the microcantilevers have been driven as fast as 1.2 Hz and the polymer was stable for over a week stored in air and light. Residual stresses in the polymer film is estimated to be as high as 254 MPa, and actuation stresses are as high as 50 MPa.

  12. Proton Ion Conducting Polymer Electrolyte Pan: NH4PF6

    NASA Astrophysics Data System (ADS)

    Sikkanthar, S.; Karthikeyan, S.; Rajeswari, N.; Selvasekarapandian, S.; Sanjeeviraja, C.

    2013-07-01

    Polymer electrolytes are an important class of materials and have been used in high energy batteries, fuel cells, gas sensors, display devices etc. PAN based polymer electrolyte films doped with ammonium hexafluorophosphate (NH4PF6) has been prepared by the solution casting method. The prepared films have been investigated by different techniques such as XRD, FTIR and AC Impedance spectroscopy. XRD studies reveal the amorphous nature of the polymer blend-salt complexes. The FTIR analysis confirms the complex formation of the polymer with salt. From the AC Impedance spectroscopy, the maximum proton conductivity at room temperature has been found to be 3.98×10-4 S cm-1 for 20 mol% salt doped electrolyte.

  13. Bioreceptor-conducting polymer multilayer assemblies for biosensing

    NASA Astrophysics Data System (ADS)

    Samuelson, Lynne A.; Alva, Shridhara; Kumar, Jayant; Kaplan, David L.; Tripathy, Sukant K.

    1998-04-01

    This research focuses on the organized integration of biological receptors and polymers into thin film architectures for biosensing applications. Layer-by-layer electrostatic adsorption was used for the first time to form alternating protein-conducting polymer multilayers. The light-harvesting, phycobiliproteins and the enzyme, alkaline phosphatase were the bioreceptors investigated and sulfonated polystyrene, poly(diallyl dimethyl ammonium chloride) and a new enzymatically polymerized, water soluble, polyaniline were the polymer counterions used for deposition. Spectroscopic characterization was used to determine both multilayer formation and biosensing function of the final bioreceptor-polymer assemblies. These techniques have proven to be simple, chemically mild, and versatile and are expected to find application in the fabrication of ultrathin films for biosensors, opto- electronic devices and biomedical applications.

  14. Slow Conductances Could Underlie Intrinsic Phase-Maintaining Properties of Isolated Lobster (Panulirus interruptus) Pyloric Neurons

    PubMed Central

    Hooper, Scott L.; Buchman, Einat; Weaver, Adam L.; Thuma, Jeffrey B.; Hobbs, Kevin H.

    2009-01-01

    The rhythmic pyloric network of the lobster stomatogastric system approximately maintains phase (that is, the burst durations and durations between the bursts of its neurons change proportionally) when network cycle period is altered by current injection into the network pacemaker (Hooper, 1997a,b). When isolated from the network and driven by rhythmic hyperpolarizing current pulses, the delay to firing after each pulse of at least one network neuron type (Pyloric, PY) varies in a phase-maintaining manner when cycle period is varied (Hooper, 1998). These variations require PY neurons to have intrinsic mechanisms that respond to changes in neuron activity on time scales at least as long as two seconds. Slowly activating and deactivating conductances could provide such a mechanism. We tested this possibility by building models containing various slow conductances. This work showed that such conductances could indeed support intrinsic phase-maintenance and we show here results for one such conductance, a slow potassium conductance. These conductances supported phase maintenance because their mean activation level changed, hence altering neuron post-inhibition firing delay, when the rhythmic input to the neuron changed. Switching the sign of the dependence of slow conductance activation and deactivation on membrane potential resulted in neuron delays switching to change in an anti-phase maintaining manner. These data suggest that slow conductances or similar slow processes such as changes in intracellular Ca2+ concentration could underlie phase maintenance in pyloric network neurons. PMID:19211890

  15. Electrically Conductive Multiphase Polymer Blend Carbon-Based Composites

    NASA Astrophysics Data System (ADS)

    Brigandi, Paul James

    The use of multiphase polymer blends provides unique morphologies and properties to reduce the percolation concentration and increase conductivity of carbon-based polymer composites. These systems offer improved conductivity, temperature stability and selective distribution of the conductive filler through unique morphologies at significantly lower conductive filler concentration. In this work, the kinetic and thermodynamic effects on a series of multiphase conductive polymer composites were investigated. The polymer blend phase morphology, filler distribution, electrical conductivity, and rheological properties of CB-filled PP/PMMA/EAA conductive polymer composites were determined. Thermodynamic and kinetic parameters were found to influence the morphology development and final composite properties. The morphology and CB distribution were found to be kinetically driven when annealed for a short period of time following the shear-intensive mixing process, whereas the three-phase polymer blend morphology is driven by thermodynamics when given sufficient time under high temperature annealing conditions in the melt state. At short annealing times, the CB distribution was influenced by the compounding sequence where the CB was added after being premixed with one of the polymer phases or directly added to the three phase polymer melt, but again was thermodynamically driven at longer annealing times with the CB migrating to the EAA phase. The resistivity was found to decrease by a statistically significant amount to similar levels for all of the composite systems with increasing annealing time, providing evidence of gradual phase coalescence to a tri-continuous morphology and CB migration. The addition of CB via the PP and EAA masterbatch results in significantly faster percolation and lower resistivity compared to when added direct to the system during compounding after 30 minutes annealing by a statistically significant amount. Dynamic oscillatory shear rheology using

  16. Fabrication, Modelling and Application of Conductive Polymer Composites

    NASA Astrophysics Data System (ADS)

    Price, Aaron David

    Electroactive polymers (EAP) are an emerging branch of smart materials that possess the capability to change shape in the presence of an electric field. Opportunities for the advancement of knowledge were identified in the branch of EAP consisting of inherently electrically conductive polymers. This dissertation explores methods by which the unique properties of composite materials having conductive polymers as a constituent may be exploited. Chapter 3 describes the blending of polyaniline with conventional thermoplastics. Processing these polyblends into foams yielded a porous conductive material. The effect of blend composition and processing parameters on the resulting porous morphology and electrical conductivity was investigated. These findings represent the first systematic study of porous conductive polymer blends. In Chapter 4, multilayer electroactive polymer actuators consisting of polypyrrole films electropolymerized on a passive polymer membrane core were harnessed as actuators. The membrane is vital in the transport of ionic species and largely dictates the stiffness of the layered configuration. The impact of the mechanical properties of the membrane on the actuation response of polypyrrole-based trilayer bending actuators was investigated. Candidate materials with distinct morphologies were identified and their mechanical properties were evaluated. These results indicated that polyvinylidene difluoride membranes were superior to the other candidates. An electrochemical synthesis procedure was proposed, and the design of a novel polymerization vessel was reported. These facilities were utilized to prepare actuators under a variety of synthesis conditions to investigate the impact of conductive polymer morphology on the electromechanical response. Characterization techniques were implemented to quantitatively assess physical and electrochemical properties of the layered composite. Chapter 5 proposes a new unified multiphysics model that captures the

  17. Tunable Nanopatterning of Conductive Polymers via Electrohydrodynamic Lithography.

    PubMed

    Rickard, Jonathan James Stanley; Farrer, Ian; Goldberg Oppenheimer, Pola

    2016-03-22

    An increasing number of technologies require the fabrication of conductive structures on a broad range of scales and over large areas. Here, we introduce advanced yet simple electrohydrodynamic lithography (EHL) for patterning conductive polymers directly on a substrate with high fidelity. We illustrate the generality of this robust, low-cost method by structuring thin polypyrrole films via electric-field-induced instabilities, yielding well-defined conductive structures with feature sizes ranging from tens of micrometers to hundreds of nanometers. Exploitation of a conductive polymer induces free charge suppression of the field in the polymer film, paving the way for accessing scale sizes in the low submicron range. We show the feasibility of the polypyrrole-based structures for field-effect transistor devices. Controlled EHL pattering of conductive polymer structures at the micro and nano scale demonstrated in this study combined with the possibility of effectively tuning the dimensions of the tailor-made architectures might herald a route toward various submicron device applications in supercapacitors, photovoltaics, sensors, and electronic displays. PMID:26905779

  18. Tunable Nanopatterning of Conductive Polymers via Electrohydrodynamic Lithography

    PubMed Central

    2016-01-01

    An increasing number of technologies require the fabrication of conductive structures on a broad range of scales and over large areas. Here, we introduce advanced yet simple electrohydrodynamic lithography (EHL) for patterning conductive polymers directly on a substrate with high fidelity. We illustrate the generality of this robust, low-cost method by structuring thin polypyrrole films via electric-field-induced instabilities, yielding well-defined conductive structures with feature sizes ranging from tens of micrometers to hundreds of nanometers. Exploitation of a conductive polymer induces free charge suppression of the field in the polymer film, paving the way for accessing scale sizes in the low submicron range. We show the feasibility of the polypyrrole-based structures for field-effect transistor devices. Controlled EHL pattering of conductive polymer structures at the micro and nano scale demonstrated in this study combined with the possibility of effectively tuning the dimensions of the tailor-made architectures might herald a route toward various submicron device applications in supercapacitors, photovoltaics, sensors, and electronic displays. PMID:26905779

  19. Advanced Proton Conducting Polymer Electrolytes for Electrochemical Capacitors

    NASA Astrophysics Data System (ADS)

    Gao, Han

    Research on solid electrochemical energy storage devices aims to provide high performance, low cost, and safe operation solutions for emerging applications from flexible consumer electronics to microelectronics. Polymer electrolytes, minimizing device sealing and liquid electrolyte leakage, are key enablers for these next-generation technologies. In this thesis, a novel proton-conducing polymer electrolyte system has been developed using heteropolyacids (HPAs) and polyvinyl alcohol for electrochemical capacitors. A thorough understanding of proton conduction mechanisms of HPAs together with the interactions among HPAs, additives, and polymer framework has been developed. Structure and chemical bonding of the electrolytes have been studied extensively to identify and elucidate key attributes affecting the electrolyte properties. Numerical models describing the proton conduction mechanism have been applied to differentiate those attributes. The performance optimization of the polymer electrolytes through additives, polymer structural modifications, and synthesis of alternative HPAs has achieved several important milestones, including: (a) high proton mobility and proton density; (b) good ion accessibility at electrode/electrolyte interface; (c) wide electrochemical stability window; and (d) good environmental stability. Specifically, high proton mobility has been addressed by cross-linking the polymer framework to improve the water storage capability at normal-to-high humidity conditions (e.g. 50-80% RH) as well as by incorporating nano-fillers to enhance the water retention at normal humidity levels (e.g. 30-60% RH). High proton density has been reached by utilizing additional proton donors (i.e. acidic plasticizers) and by developing different HPAs. Good ion accessibility has been achieved through addition of plasticizers. Electrochemical stability window of the electrolyte system has also been investigated and expanded by utilizing HPAs with different heteroatoms

  20. Polymer scaling laws of unfolded and intrinsically disordered proteins quantified with single-molecule spectroscopy

    PubMed Central

    Hofmann, Hagen; Soranno, Andrea; Borgia, Alessandro; Gast, Klaus; Nettels, Daniel; Schuler, Benjamin

    2012-01-01

    The dimensions of unfolded and intrinsically disordered proteins are highly dependent on their amino acid composition and solution conditions, especially salt and denaturant concentration. However, the quantitative implications of this behavior have remained unclear, largely because the effective theta-state, the central reference point for the underlying polymer collapse transition, has eluded experimental determination. Here, we used single-molecule fluorescence spectroscopy and two-focus correlation spectroscopy to determine the theta points for six different proteins. While the scaling exponents of all proteins converge to 0.62 ± 0.03 at high denaturant concentrations, as expected for a polymer in good solvent, the scaling regime in water strongly depends on sequence composition. The resulting average scaling exponent of 0.46 ± 0.05 for the four foldable protein sequences in our study suggests that the aqueous cellular milieu is close to effective theta conditions for unfolded proteins. In contrast, two intrinsically disordered proteins do not reach the Θ-point under any of our solvent conditions, which may reflect the optimization of their expanded state for the interactions with cellular partners. Sequence analyses based on our results imply that foldable sequences with more compact unfolded states are a more recent result of protein evolution. PMID:22984159

  1. Blends of a Polymer of Intrinsic Microporosity and Partially Sulfonated Polyphenylenesulfone for Gas Separation.

    PubMed

    Yong, Wai Fen; Lee, Zhi Kang; Chung, Tai-Shung; Weber, Martin; Staudt, Claudia; Maletzko, Christian

    2016-08-01

    Polyphenylenesulfone (PPSU) and sulfonated polyphenylenesulfone (sPPSU) are widely used for liquid separations in the medical and food industries. However, their potential applications for gas separation have not been studied extensively owing to their low intrinsic gas permeability. We report here for the first time that blending with sPPSU can significantly improve the gas separation performance of highly permeable polymers of intrinsic microporosity (PIMs), specifically PIM-1, because of the strong molecular interactions of the sulfonic acid groups of sPPSU with CO2 and O2 . In addition, a novel co-solvent system has been discovered to overcome the immiscibility of these polymers. The presence of a higher degree of sulfonation in sPPSU results in better gas separation performance of the blend membranes close to or above the Robeson upper bound lines for O2 /N2 , CO2 /N2 and CO2 /CH4 separations. Interestingly, the blend membranes have comparable gas selectivity to sPPSU even though their sPPSU content is only 5-20 wt %. Moreover, they also display improved anti-plasticization properties up to 30 atm (3 MPa) using a binary CO2 /CH4 feed gas. The newly developed PIM-1/sPPSU membranes are potential candidates for air separation, natural gas separation, and CO2 capture. PMID:27332951

  2. Electrically conducting novel polymer films containing pi-stacks

    NASA Astrophysics Data System (ADS)

    Duan, Robert Gang

    1997-12-01

    The primary focus of this thesis is to expand our knowledge of ion radicals of π-dimers and π- stacks in solutions and apply these insights in the development and understanding of new electrically conducting polymers. Two types of the conducting polymers were investigated. The first is the conducting polymer composites embedded with π-stacks of ion radicals. Flexible and air stable n-typed conducting thin films were prepared from imide/poly(vinyl alcohol) aqueous solutions. Conducting thin films of terthiophene/poly(methyl methacrylate) were cast from hexafluoro-2-propanol. Effects of casting conditions on the morphology and conductivity of the films were investigated. These films were fully characterized by UV- vis, NIR, IR, XRD, SEM and ESR. In the second type of conducting polymer system, PAMAM dendrimers generation 1 through 5 were peripherally modified with cationically substituted naphthalene diimide anion radicals. NMR, UV, IR, CV and Elemental Analysis were used to characterize modified dendrimers. Reduction with sodium dithionite in solution showed anion radicals were aggregated into π-dimers and π- stacks. Formamide was used to cast conducting dendrimer films. ESCA, SEM and optical microscope were used to study the composition and the morphology of the films. XRD showed complete amorphous nature of these films. NIR revealed that the π-stack aggregation depend strongly on the casting temperature and the degree of reduction. Four- probe co-liner conductivity of the films is on the order of 10-2 to 10-1/ S/ cm-1. ESR and conductivity measurements also revealed the isotropic nature of the conductivity. Conductivity/humidity relationship was discovered by accidental breathing over the films. Using a home-made controlled humidity device and PACERTM hygrometer, the conductivity of the films can be varied quickly and reversibly within two orders of a magnitude. This phenomenon was probed with NIR, XRD and quartz crystal microbalance techniques. These

  3. Direct measurement of ion mobility in a conducting polymer.

    PubMed

    Stavrinidou, Eleni; Leleux, Pierre; Rajaona, Harizo; Khodagholy, Dion; Rivnay, Jonathan; Lindau, Manfred; Sanaur, Sébastien; Malliaras, George G

    2013-08-27

    Using planar junctions between the conducting polymer PEDOT:PSS and various electrolytes, it is possible to inject common ions and directly observe their transit through the film. The 1D geometry of the experiment allows a straightforward estimate of the ion drift mobilities. PMID:23784809

  4. Wearable Keyboard Using Conducting Polymer Electrodes on Textiles.

    PubMed

    Takamatsu, Seiichi; Lonjaret, Thomas; Ismailova, Esma; Masuda, Atsuji; Itoh, Toshihiro; Malliaras, George G

    2016-06-01

    A wearable keyboard is demonstrated in which conducting polymer electrodes on a knitted textile sense tactile input as changes in capacitance. The use of a knitted textile as a substrate endows stretchability and compatibility to large-area formats, paving the way for a new type of wearable human-machine interface. PMID:26618790

  5. Robust solid polymer electrolyte for conducting IPN actuators

    NASA Astrophysics Data System (ADS)

    Festin, Nicolas; Maziz, Ali; Plesse, Cédric; Teyssié, Dominique; Chevrot, Claude; Vidal, Frédéric

    2013-10-01

    Interpenetrating polymer networks (IPNs) based on nitrile butadiene rubber (NBR) as first component and poly(ethylene oxide) (PEO) as second component were synthesized and used as a solid polymer electrolyte film in the design of a mechanically robust conducting IPN actuator. IPN mechanical properties and morphologies were mainly investigated by dynamic mechanical analysis and transmission electron microscopy. For 1-ethyl-3-methylimidazolium bis-(trifluoromethylsulfonyl)-imide (EMITFSI) swollen IPNs, conductivity values are close to 1 × 10-3 S cm-1 at 25 ° C. Conducting IPN actuators have been synthesized by chemical polymerization of 3,4-ethylenedioxythiophene (EDOT) within the PEO/NBR IPN. A pseudo-trilayer configuration has been obtained with PEO/NBR IPN sandwiched between two interpenetrated PEDOT electrodes. The robust conducting IPN actuators showed a free strain of 2.4% and a blocking force of 30 mN for a low applied potential of ±2 V.

  6. Functionalised hybrid materials of conducting polymers with individual wool fibers.

    PubMed

    Kelly, Fern M; Johnston, James H; Borrmann, Thomas; Richardson, Michael J

    2008-04-01

    Composites of natural protein materials, such as merino wool, with the conducting polymers polypyrrole (PPy) and polyaniline (PAn) have been successfully synthesised. In doing so, hybrid materials have been produced in which the mechanical strength and flexibility of the fibers is retained whilst also incorporating the desired chemical and electrical properties of the polymer. Scanning electron microscopy shows PPy coatings to comprise individual polymer spheres, approximately 100 to 150 nm in diameter. The average size of the polymer spheres of PAn was observed to be approximately 50 to 100 nm in diameter. These spheres fuse together in a continuous sheet to coat the fibers in their entirety. The reduction of silver ions to silver metal nanoparticles onto the redox active polymer surface has also been successful and thus imparts anti-microbial properties to the hybrid materials. This gives rise to further applications requiring the inhibition of microbial growth. The chemical and physical characterisation of such products has been undertaken through scanning electron microscopy (SEM), energy dispersive spectroscopy (EDS), electrical conductivity, cyclic voltammetry, X-ray photoelectron spectroscopy (XPS) and the testing of their anti-microbial activity. PMID:18572600

  7. Simulation of conductivity of polymer films on metal surface

    NASA Astrophysics Data System (ADS)

    Maksimova, O. G.; Maksimov, A. V.; Baidganov, A. R.

    2015-09-01

    In this paper, protective properties of polymer films are analyzed. The simulation is performed by means of the Monte-Carlo method on the basis of three-dimensional lattice model of polymer system with orientational interactions [1]. Initially, configuration of polymer system is calculated by the Metropolis algorithm taking into account the characteristics of the internal structure (constants of intermolecular interactions etc.), temperature regime and metal quality. Further, for the study of conductivity, the motion of charged particles within the proposed lattice model is investigated on the basis of the calculated configuration. The interaction energy of the oxygen atom with eight neighboring links of polymer chains and electric double layer on the metallic surface is accounted. The direction of movement of charged particles is calculated by the Monte-Carlo method according to the energy advantage of its position. This method allows to calculate the number of charged particles passing through the polymer film and reaching the metal sheet surface. The dependences of conductivity on temperature, film thickness, and distance between molecular layers are obtained. It is shown that there is an optimum density for the given film thickness at which it possesses protective properties. The adequacy of the developed mathematical models and calculated dependences are verified by comparison with laboratory data and production testing.

  8. Theoretical studies of optics and charge transport in organic conducting oligomers and polymers: Rational design of improved transparent and conducting polymers

    NASA Astrophysics Data System (ADS)

    Hutchison, Geoffrey Rogers

    Theoretical studies on a variety of oligo- and polyheterocycles elucidate their optical and charge transport properties, suggesting new, improved transparent conductive polymers. First-principles calculations provide accurate methodologies for predicting both optical band gaps of neutral and cationic oligomers and intrinsic charge transfer rates. Multidimensional analysis reveals important motifs in chemical tailorability of oligoheterocycle optical and charge transport properties. The results suggest new directions for design of novel materials. Using both finite oligomer and infinite polymer calculations, the optical band gaps in polyheterocycles follow a modified particle-in-a-box formalism, scaling approximately as 1/N (where N is the number of monomer units) in short chains, saturating for long chains. Calculations demonstrate that band structure changes upon heteroatom substitution, (e.g., from polythiophene to polypyrrole) derive from heteroatom electron affinity. Further investigation of chemical variability in substituted oligoheterocycles using multidimensional statistics reveals the interplay between heteroatom and substituent in correlations between structure and redox/optical properties of neutral and cationic species. A linear correlation between band gaps of neutral and cationic species upon oxidation of conjugated oligomers, shows redshifts of optical absorption for most species and blueshifts for small band gap species. Interstrand charge-transport studies focus on two contributors to hopping-style charge transfer rates: internal reorganization energy and the electronic coupling matrix element. Statistical analysis of chemical variability of reorganization energies in oligoheterocycles proves the importance of reorganization energy in determining intrinsic charge transfer rates (e.g., charge mobility in unsubstituted oligothiophenes). Computed bandwidths across several oligothiophene crystal packing motifs show similar electron and hole bandwidths

  9. Functionalized carbon nanotubes mixed matrix membranes of polymers of intrinsic microporosity for gas separation

    PubMed Central

    2012-01-01

    The present work reports on the gas transport behavior of mixed matrix membranes (MMM) which were prepared from multi-walled carbon nanotubes (MWCNTs) and dispersed within polymers of intrinsic microporosity (PIM-1) matrix. The MWCNTs were chemically functionalized with poly(ethylene glycol) (PEG) for a better dispersion in the polymer matrix. MMM-incorporating functionalized MWCNTs (f-MWCNTs) were fabricated by dip-coating method using microporous polyacrylonitrile membrane as a support and were characterized for gas separation performance. Gas permeation measurements show that MMM incorporated with pristine or functionalized MWCNTs exhibited improved gas separation performance compared to pure PIM-1. The f-MWCNTs MMM show better performance in terms of permeance and selectivity in comparison to pristine MWCNTs. The gas permeances of the derived MMM are increased to approximately 50% without sacrificing the selectivity at 2 wt.% of f-MWCNTs' loading. The PEG groups on the MWCNTs have strong interaction with CO2 which increases the solubility of polar gas and limit the solubility of nonpolar gas, which is advantageous for CO2/N2 selectivity. The addition of f-MWCNTs inside the polymer matrix also improved the long-term gas transport stability of MMM in comparison with PIM-1. The high permeance, selectivity, and long term stability of the fabricated MMM suggest that the reported approach can be utilized in practical gas separation technology. PMID:22953751

  10. Electrical conductivity studies on individual conjugated polymer nanowires: two-probe and four-probe results.

    PubMed

    Long, Yunze; Duvail, Jeanluc; Li, Mengmeng; Gu, Changzhi; Liu, Zongwen; Ringer, Simon P

    2009-01-01

    Two- and four-probe electrical measurements on individual conjugated polymer nanowires with different diameters ranging from 20 to 190 nm have been performed to study their conductivity and nanocontact resistance. The two-probe results reveal that all the measured polymer nanowires with different diameters are semiconducting. However, the four-probe results show that the measured polymer nanowires with diameters of 190, 95-100, 35-40 and 20-25 nm are lying in the insulating, critical, metallic and insulting regimes of metal-insulator transition, respectively. The 35-40 nm nanowire displays a metal-insulator transition at around 35 K. In addition, it was found that the nanocontact resistance is in the magnitude of 104Ω at room temperature, which is comparable to the intrinsic resistance of the nanowires. These results demonstrate that four-probe electrical measurement is necessary to explore the intrinsic electronic transport properties of isolated nanowires, especially in the case of metallic nanowires, because the metallic nature of the measured nanowires may be coved by the nanocontact resistance that cannot be excluded by a two-probe technique. PMID:20652139

  11. New secondary batteries utilizing electronically conductive polymer cathodes

    NASA Technical Reports Server (NTRS)

    Martin, Charles R.; White, Ralph E.

    1989-01-01

    The objectives of this project are to characterize the transport properties in electronically conductive polymers and to assess the utility of these films as cathodes in lithium/polymer secondary batteries. During this research period, progress has been made in a literature survey of the historical background, methods of preparation, the physical and chemical properties, and potential technological applications of polythiophene. Progress has also been made in the characterization of polypyrrole flat films and fibrillar films. Cyclic voltammetry and potential step chronocoulometry were used to gain information on peak currents and potentials switching reaction rates, charge capacity, and charge retention. Battery charge/discharge studies were also performed.

  12. The effect of macroscopic polarization on intrinsic and extrinsic thermal conductivities of AlN

    NASA Astrophysics Data System (ADS)

    Gedam, Vikas; Pansari, Anju; Sinha, Arvind Kumar; Sahoo, Bijay Kumar

    2015-03-01

    The effect of macroscopic polarization on thermal conductivity of bulk wurtzite AlN has been theoretically investigated. Our results show that macroscopic polarization modifies the phonon group velocity, Debye frequency and Debye temperature of the AlN. Using revised phonon velocity and Debye temperature, various phonon scattering rates and combined scattering rate are calculated as functions of the phonon frequency at room temperature. The intrinsic and extrinsic thermal conductivities of AlN have been estimated using these modified parameters. The theoretical analysis shows that up to a certain temperature the polarization effect acts as negative effect and reduces the intrinsic and extrinsic thermal conductivities. However, after this temperature both thermal conductivities are significantly enhanced. High phonon velocity and Debye temperature are the reason of this enhancement which happens due to the polarization effect. The revised thermal conductivities at room temperature are found to be increased by more than 20% in AlN due to macroscopic polarization phenomenon. The method we have developed can be taken into account during the simulation of heat transport in optoelectronic nitride devices to minimize the self heating processes.

  13. Electropolymerization on wireless electrodes towards conducting polymer microfibre networks

    NASA Astrophysics Data System (ADS)

    Koizumi, Yuki; Shida, Naoki; Ohira, Masato; Nishiyama, Hiroki; Tomita, Ikuyoshi; Inagi, Shinsuke

    2016-01-01

    Conducting polymers can be easily obtained by electrochemical oxidation of aromatic monomers on an electrode surface as a film state. To prepare conducting polymer fibres by electropolymerization, templates such as porous membranes are necessary in the conventional methods. Here we report the electropolymerization of 3,4-ethylenedioxythiophene and its derivatives by alternating current (AC)-bipolar electrolysis. Poly(3,4-ethylenedioxythiophene) (PEDOT) derivatives were found to propagate as a fibre form from the ends of Au wires used as bipolar electrodes (BPEs) parallel to an external electric field, without the use of templates. The effects of applied frequency and of the solvent on the morphology, growth rate and degree of branching of these PEDOT fibres were investigated. In addition, a chain-growth model for the formation of conductive material networks was also demonstrated.

  14. Conducting polymers at low temperatures and high magnetic fields

    SciTech Connect

    Clark, J.C.; Ihas, G.G.; Reghu, M.

    1995-11-01

    Advances in the synthesis of organic conducting polymer systems has increased the electrical conductivity of these systems by several orders of magnitude in the last decade. Several practical applications are envisioned for such systems, but a thorough understanding of the conduction mechanisms and identification of the charge carriers is lacking, making design and implementation for bulk synthesis difficult. In order to clarify our understanding of the electrical properties of these systems, the resistivity and magnetoresistivity of various polymers doped near the metal - insulator transition, such as polyaniline protonated by camphor sulfonic acid (PANi-CSA) and polypyrrole doped with PF{sub 6} (PPy-PF{sub 6}), have been studied down to 25 mK in magnetic fields up to 16 T.

  15. Electropolymerization on wireless electrodes towards conducting polymer microfibre networks

    PubMed Central

    Koizumi, Yuki; Shida, Naoki; Ohira, Masato; Nishiyama, Hiroki; Tomita, Ikuyoshi; Inagi, Shinsuke

    2016-01-01

    Conducting polymers can be easily obtained by electrochemical oxidation of aromatic monomers on an electrode surface as a film state. To prepare conducting polymer fibres by electropolymerization, templates such as porous membranes are necessary in the conventional methods. Here we report the electropolymerization of 3,4-ethylenedioxythiophene and its derivatives by alternating current (AC)-bipolar electrolysis. Poly(3,4-ethylenedioxythiophene) (PEDOT) derivatives were found to propagate as a fibre form from the ends of Au wires used as bipolar electrodes (BPEs) parallel to an external electric field, without the use of templates. The effects of applied frequency and of the solvent on the morphology, growth rate and degree of branching of these PEDOT fibres were investigated. In addition, a chain-growth model for the formation of conductive material networks was also demonstrated. PMID:26804140

  16. Electrically conductive, optically transparent polymer/carbon nanotube composites

    NASA Technical Reports Server (NTRS)

    Connell, John W. (Inventor); Smith, Jr., Joseph G. (Inventor); Harrison, Joycelyn S. (Inventor); Park, Cheol (Inventor); Watson, Kent A. (Inventor); Ounaies, Zoubeida (Inventor)

    2011-01-01

    The present invention is directed to the effective dispersion of carbon nanotubes (CNTs) into polymer matrices. The nanocomposites are prepared using polymer matrices and exhibit a unique combination of properties, most notably, high retention of optical transparency in the visible range (i.e., 400-800 nm), electrical conductivity, and high thermal stability. By appropriate selection of the matrix resin, additional properties such as vacuum ultraviolet radiation resistance, atomic oxygen resistance, high glass transition (T.sub.g) temperatures, and excellent toughness can be attained. The resulting nanocomposites can be used to fabricate or formulate a variety of articles such as coatings on a variety of substrates, films, foams, fibers, threads, adhesives and fiber coated prepreg. The properties of the nanocomposites can be adjusted by selection of the polymer matrix and CNT to fabricate articles that possess high optical transparency and antistatic behavior.

  17. Synthesis of polymer nanostructures with conductance switching properties

    DOEpatents

    Su, Kai; Nuraje, Nurxat; Zhang, Lingzhi; Matsui, Hiroshi; Yang, Nan Loh

    2015-03-03

    The present invention is directed to crystalline organic polymer nanoparticles comprising a conductive organic polymer; wherein the crystalline organic polymer nanoparticles have a size of from 10 nm to 200 nm and exhibits two current-voltage states: (1) a high resistance current-voltage state, and (2) a low resistance current-voltage state, wherein when a first positive threshold voltage (V.sub.th1) or higher positive voltage, or a second negative threshold voltage (V.sub.th2) or higher negative voltage is applied to the nanoparticle, the nanoparticle exhibits the low-resistance current-voltage state, and when a voltage less positive than the first positive threshold voltage or a voltage less negative than the second negative threshold voltage is applied to the nanoparticle, the nanoparticle exhibits the high-resistance current-voltage state. The present invention is also directed methods of manufacturing the nanoparticles using novel interfacial oxidative polymerization techniques.

  18. Mechanistic study of silver nanoparticle formation on conducting polymer surfaces.

    PubMed

    Mack, Nathan H; Bailey, James A; Doorn, Stephen K; Chen, Chien-An; Gau, Han-Mou; Xu, Ping; Williams, Darrick J; Akhadov, Elshan A; Wang, Hsing-Lin

    2011-04-19

    Conducting polymer (polyaniline) sheets are shown to be active substrates to promote the growth of nanostructured silver thin films with highly tunable morphologies. Using the spontaneous electroless deposition of silver, we show that a range of nanostructured metallic features can be controllably and reproducibly formed over large surface areas. The structural morphology of the resulting metal-polymer nanocomposite is demonstrated to be sensitive to experimental parameters such as ion concentration, temperature, and polymer processing and can range from densely packed oblate nanosheets to bulk crystalline metals. The deposition mechanisms are explained using a diffusion-limited aggregation (DLA) model to describe the semi-fractal-like growth of the metal nanostructures. We find these composite films to exhibit strong surface-enhanced Raman (SERS) activity, and the nanostructured features are optimized with respect to SERS activity using a self-assembled monolayer of mercapto-benzoic acid as a model Raman reporter. SERS enhancements are estimated to be on the order of 10(7). Through micro-Raman SERS mapping, these materials are shown to exhibit uniform SERS responses over macroscopic areas. These metal-polymer nanocomposites benefit from the underlying polymer's processability to yield SERS-active materials of almost limitless shape and size and show significant promise for future SERS-based sensing and detection schemes. PMID:21434643

  19. Stably Doped Conducting Polymer Nanoshells by Surface Initiated Polymerization.

    PubMed

    Li, Junwei; Yoon, Soon Joon; Hsieh, Bao-Yu; Tai, Wanyi; O'Donnell, Matthew; Gao, Xiaohu

    2015-12-01

    Despite broad applications ranging from electronics to biomedical sensing and imaging, a long-standing problem of conducting polymers is the poor resistance to dedoping, which directly affects their signature electrical and optical properties. This problem is particularly significant for biomedical uses because of fast leaching of dopant ions in physiological environments. Here, we describe a new approach to engineer multimodal core-shell nanoparticles with a stably doped conductive polymer shell in biological environments. It was achieved by making a densely packed polymer brush rather than changing its molecular structure. Polyaniline (PANI) was used as a model compound due to its concentrated near-infrared (NIR) absorption. It was grafted onto a magnetic nanoparticle via a polydopamine intermediate layer. Remarkably, at pH 7 its conductivity is ca. 2000× higher than conventional PANI nanoshells. Similarly, its NIR absorption is enhanced by 2 orders of magnitude, ideal for photothermal imaging and therapy. Another surprising finding is its nonfouling property, even outperforming polyethylene glycol. This platform technology is also expected to open exciting opportunities in engineering stable conductive materials for electronics, imaging, and sensing. PMID:26588215

  20. Carbon Nanotubes - Polymer Composites with Enhanced Conductivity using Functionalized Nanotubes

    NASA Astrophysics Data System (ADS)

    Ramasubramaniam, Rajagopal; Chen, Jian; Gupta, Rishi

    2003-03-01

    Individual carbon nanotubes show superior electrical, mechanical and thermal properties [1]. Composite materials using carbon nanotubes as fillers are predicted to show similar superior properties. However, realization of such composites has been plagued by poor dispersion of carbon nanotubes in solvents and in polymer matrices. We have developed a method to homogenously disperse carbon nanotubes in polymer matrices using functionalized nanotubes [2]. Thin films of functionalized single walled nanotubes (SWNT) - polystyrene composites and functionalized SWNT - polycarbonate composites were prepared using solution evaporation and spin coating. Both of the composites show several orders of magnitude increase in conductivity for less than 1 wt thresholds of the composites are less than 0.2 wt nanotubes. We attribute the enhanced conduction to the superior dispersion of the functionalized nanotubes in the polymer matrix and to the reduced nanotube waviness resulting from the rigid backbone of the conjugated polymer. References: [1]. R. H. Baughman, A. A. Zakhidov and W. A. de Heer, Science v297, p787 (2002); [2]. J. Chen, H. Liu, W. A. Weimer, M. D. Halls, D. H. Waldeck and G. C. Walker, J. Am. Chem. Soc. v124, p9034 (2002).

  1. Predicting permeability from the characteristic relaxation time and intrinsic formation factor of complex conductivity spectra

    NASA Astrophysics Data System (ADS)

    Revil, A.; Binley, A.; Mejus, L.; Kessouri, P.

    2015-08-01

    Low-frequency quadrature conductivity spectra of siliclastic materials exhibit typically a characteristic relaxation time, which either corresponds to the peak frequency of the phase or the quadrature conductivity or a typical corner frequency, at which the quadrature conductivity starts to decrease rapidly toward lower frequencies. This characteristic relaxation time can be combined with the (intrinsic) formation factor and a diffusion coefficient to predict the permeability to flow of porous materials at saturation. The intrinsic formation factor can either be determined at several salinities using an electrical conductivity model or at a single salinity using a relationship between the surface and quadrature conductivities. The diffusion coefficient entering into the relationship between the permeability, the characteristic relaxation time, and the formation factor takes only two distinct values for isothermal conditions. For pure silica, the diffusion coefficient of cations, like sodium or potassium, in the Stern layer is equal to the diffusion coefficient of these ions in the bulk pore water, indicating weak sorption of these couterions. For clayey materials and clean sands and sandstones whose surface have been exposed to alumina (possibly iron), the diffusion coefficient of the cations in the Stern layer appears to be 350 times smaller than the diffusion coefficient of the same cations in the pore water. These values are consistent with the values of the ionic mobilities used to determine the amplitude of the low and high-frequency quadrature conductivities and surface conductivity. The database used to test the model comprises a total of 202 samples. Our analysis reveals that permeability prediction with the proposed model is usually within an order of magnitude from the measured value above 0.1 mD. We also discuss the relationship between the different time constants that have been considered in previous works as characteristic relaxation time, including

  2. Does filler surface chemistry impact filler dispersion, polymer dynamics and conductivity in nanofilled solid polymer electrolytes?

    NASA Astrophysics Data System (ADS)

    Ganapatibhotla, Lalitha; Maranas, Janna

    2012-02-01

    We study the impact of nanofiller surface chemistry on filler dispersion, polymer dynamics and ionic conductivity in acidic α-Al2O3 filled PEO+LiClO4 solid polymer electrolytes (SPEs).SPEs are the key to light-weight and high energy density rechargeable Li ion batteries but suffer from low room temperature ionic conductivity. Addition of ceramic nanofillers improves conductivity of SPEs and their surface chemistry influences extent of conductivity enhancement. The ionic conductivity of acidic α-Al2O3 filled SPE is enhanced for salt concentrations at and below eutectic, while neutral γ-Al2O3 filler enhances conductivity only at eutectic composition. Li ion motion is coupled to segmental mobility of polymer and we study how this is affected by addition of α-Al2O3 using quasi-elastic neutron scattering. Aggregation extent of nanoparticles in SPE matrix, a less explored factor in filled SPEs, can affect segmental mobility of polymer. This can vary with surface chemistry of particles and we quantify this using small angle neutron scattering. All measurements are performed as a function of Li concentration, nanoparticle loading and temperature.

  3. Unusual Enhancement in Intrinsic Thermal Conductivity of Multilayer Graphene by Tensile Strains

    SciTech Connect

    Kuang, Youdi; Lindsay, Lucas R.; Huang, Baoling

    2015-01-01

    High basal plane thermal conductivity k of multi-layer graphene makes it promising for thermal management applications. Here we examine the effects of tensile strain on thermal transport in this system. Using a first principles Boltzmann-Peierls equation for phonon transport approach, we calculate the room-temperature in-plane lattice k of multi-layer graphene (up to four layers) and graphite under different isotropic tensile strains. The calculated in-plane k of graphite, finite mono-layer graphene and 3-layer graphene agree well with previous experiments. The dimensional transitions of the intrinsic k and the extent of the diffusive transport regime from mono-layer graphene to graphite are presented. We find a peak enhancement of intrinsic k for multi-layer graphene and graphite with increasing strain and the largest enhancement amplitude is about 40%. In contrast the calculated intrinsic k with tensile strain decreases for diamond and diverges for graphene, we show that the competition between the decreased mode heat capacities and the increased lifetimes of flexural phonons with increasing strain contribute to this k behavior. Similar k behavior is observed for 2-layer hexagonal boron nitride systems, suggesting that it is an inherent thermal transport property in multi-layer systems assembled of purely two dimensional atomic layers. This study provides insights into engineering k of multi-layer graphene and boron nitride by strain and into the nature of thermal transport in quasi-two-dimensional and highly anisotropic systems.

  4. Intrinsic signatures of polymer based fiber reinforced composite structures: An ultrasonic approach

    SciTech Connect

    Good, M.S.; Hansen, N.H.; Heasler, P.G.; Undem, H.A.; Fuller, J.L.; Skorpik, J.R.

    1993-09-01

    Combination of ultrasound, image comparison, and statistical analysis provide a method for acquiring a subsurface, intrinsic signature from polymer based, fiber-reinforced composites. Although materials properties are carefully controlled, localized fluctuations in the macrostructure and microstructure permit a basis for ultrasound and other NDE methods to read intrinsic signatures from a material. Under ideal conditions where a material signature is stable and has sufficient spatial features as a signature, an error rate on the order of one-out-of-a-million is feasible. A conclusion of an independent functional test performed on the laboratory prototype as it existed in June 1991 is that the system proved effective as a proof-of-concept system. An issue raised by the independent evaluation is that system performance is still at risk of factors relating to signature stability, particularly moisture absorption and material creep. System improvements made to mitigate noise sources identified by the independent evaluation include (1) implementation of a 3.0 {minus} 4.5 {mu}S software gate, (2) use of a RMS amplitude instead of the gated peak amplitude, and (3) optional use of a suction cup holder to facilitate reader alignment and scan consistency.

  5. Tunable Intrinsic Spin Hall Conductivities in Bi2(Se,Te)3 Topological Insulators

    NASA Astrophysics Data System (ADS)

    Şahin, Cüneyt; Flatté, Michael E.

    2015-03-01

    It has been recently shown by spin-transfer torque measurements that Bi2Se3 exhibits a very large spin Hall conductivity (SHC). It is expected that Bi2Te3, a topological insulator with similar crystal and band structures as well as large spin-orbit coupling, would also exhibit a giant SHC. In this study we have calculated intrinsic spin Hall conductivities of Bi2Se3andBi2Te3 topological insulators from a tight-binding Hamiltonian including two nearest-neighbor interactions. We have calculated the Berry curvature, used the Kubo formula in the static, clean limit and shown that both materials exhibit giant spin Hall conductivities, consistent with the results of Ref. 1 and larger than previously reported Bi1-xSbx alloys. The density of Berry curvature has also been computed from the full Brillouin zone in order to compute the dependence of the SHC in these materials on the Fermi energy. Finally we report the intrinsic SHC for Bi2(Se,Te)3 topological insulators, which changes dramatically with doping or gate voltage. This work was supported in part by C-SPIN, one of six centers of STARnet, a Semiconductor Research Corporation program, sponsored by MARCO and DARPA.

  6. Intrinsic conduction through topological surface states of insulating Bi2Te3 epitaxial thin films.

    PubMed

    Hoefer, Katharina; Becker, Christoph; Rata, Diana; Swanson, Jesse; Thalmeier, Peter; Tjeng, L H

    2014-10-21

    Topological insulators represent a novel state of matter with surface charge carriers having a massless Dirac dispersion and locked helical spin polarization. Many exciting experiments have been proposed by theory, yet their execution has been hampered by the extrinsic conductivity associated with the unavoidable presence of defects in Bi2Te3 and Bi2Se3 bulk single crystals, as well as impurities on their surfaces. Here we present the preparation of Bi2Te3 thin films that are insulating in the bulk and the four-point probe measurement of the conductivity of the Dirac states on surfaces that are intrinsically clean. The total amount of charge carriers in the experiment is of the order of 10(12) cm(-2) only, and mobilities up to 4,600 cm(2)/Vs have been observed. These values are achieved by carrying out the preparation, structural characterization, angle-resolved and X-ray photoemission analysis, and temperature-dependent four-point probe conductivity measurement all in situ under ultra-high-vacuum conditions. This experimental approach opens the way to prepare devices that can exploit the intrinsic topological properties of the Dirac surface states. PMID:25294928

  7. Intrinsic conduction through topological surface states of insulating Bi2Te3 epitaxial thin films

    PubMed Central

    Hoefer, Katharina; Becker, Christoph; Rata, Diana; Swanson, Jesse; Thalmeier, Peter; Tjeng, L. H.

    2014-01-01

    Topological insulators represent a novel state of matter with surface charge carriers having a massless Dirac dispersion and locked helical spin polarization. Many exciting experiments have been proposed by theory, yet their execution has been hampered by the extrinsic conductivity associated with the unavoidable presence of defects in Bi2Te3 and Bi2Se3 bulk single crystals, as well as impurities on their surfaces. Here we present the preparation of Bi2Te3 thin films that are insulating in the bulk and the four-point probe measurement of the conductivity of the Dirac states on surfaces that are intrinsically clean. The total amount of charge carriers in the experiment is of the order of 1012 cm−2 only, and mobilities up to 4,600 cm2/Vs have been observed. These values are achieved by carrying out the preparation, structural characterization, angle-resolved and X-ray photoemission analysis, and temperature-dependent four-point probe conductivity measurement all in situ under ultra-high-vacuum conditions. This experimental approach opens the way to prepare devices that can exploit the intrinsic topological properties of the Dirac surface states. PMID:25294928

  8. Intrinsic conductivity of carbon nanotubes and graphene sheets having a realistic geometry.

    PubMed

    Vargas-Lara, Fernando; Hassan, Ahmed M; Garboczi, Edward J; Douglas, Jack F

    2015-11-28

    The addition of carbon nanotubes (CNTs) and graphene sheets (GSs) into polymeric materials can greatly enhance the conductivity and alter the electromagnetic response of the resulting nanocomposite material. The extent of these property modifications strongly depends on the structural parameters describing the CNTs and GSs, such as their shape and size, as well as their degree of particle dispersion within the polymeric matrix. To model these property modifications in the dilute particle regime, we determine the leading transport virial coefficients describing the conductivity of CNT and GS composites using a combination of molecular dynamics, path-integral, and finite-element calculations. This approach allows for the treatment of the general situation in which the ratio between the conductivity of the nanoparticles and the polymer matrix is arbitrary so that insulating, semi-conductive, and conductive particles can be treated within a unified framework. We first generate ensembles of CNTs and GSs in the form of self-avoiding worm-like cylinders and perfectly flat and random sheet polymeric structures by using molecular dynamics simulation to model the geometrical shapes of these complex-shaped carbonaceous nanoparticles. We then use path-integral and finite element methods to calculate the electric and magnetic polarizability tensors (αE, αM) of the CNT and GS nanoparticles. These properties determine the conductivity virial coefficient σ in the conductive and insulating particle limits, which are required to estimate σ in the general case in which the conductivity contrast Δ between the nanoparticle and the polymer matrix is arbitrary. Finally, we propose approximate relationships for αE and αM that should be useful in materials design and characterization applications. PMID:26627970

  9. Intrinsic conductivity of carbon nanotubes and graphene sheets having a realistic geometry

    NASA Astrophysics Data System (ADS)

    Vargas-Lara, Fernando; Hassan, Ahmed M.; Garboczi, Edward J.; Douglas, Jack F.

    2015-11-01

    The addition of carbon nanotubes (CNTs) and graphene sheets (GSs) into polymeric materials can greatly enhance the conductivity and alter the electromagnetic response of the resulting nanocomposite material. The extent of these property modifications strongly depends on the structural parameters describing the CNTs and GSs, such as their shape and size, as well as their degree of particle dispersion within the polymeric matrix. To model these property modifications in the dilute particle regime, we determine the leading transport virial coefficients describing the conductivity of CNT and GS composites using a combination of molecular dynamics, path-integral, and finite-element calculations. This approach allows for the treatment of the general situation in which the ratio between the conductivity of the nanoparticles and the polymer matrix is arbitrary so that insulating, semi-conductive, and conductive particles can be treated within a unified framework. We first generate ensembles of CNTs and GSs in the form of self-avoiding worm-like cylinders and perfectly flat and random sheet polymeric structures by using molecular dynamics simulation to model the geometrical shapes of these complex-shaped carbonaceous nanoparticles. We then use path-integral and finite element methods to calculate the electric and magnetic polarizability tensors (αE, αM) of the CNT and GS nanoparticles. These properties determine the conductivity virial coefficient [" separators=" σ ] in the conductive and insulating particle limits, which are required to estimate [" separators=" σ ] in the general case in which the conductivity contrast Δ between the nanoparticle and the polymer matrix is arbitrary. Finally, we propose approximate relationships for αE and αM that should be useful in materials design and characterization applications.

  10. A practical multilayered conducting polymer actuator with scalable work output

    NASA Astrophysics Data System (ADS)

    Ikushima, Kimiya; John, Stephen; Yokoyama, Kazuo; Nagamitsu, Sachio

    2009-09-01

    Household assistance robots are expected to become more prominent in the future and will require inherently safe design. Conducting polymer-based artificial muscle actuators are one potential option for achieving this safety, as they are flexible, lightweight and can be driven using low input voltages, unlike electromagnetic motors; however, practical implementation also requires a scalable structure and stability in air. In this paper we propose and practically implement a multilayer conducting polymer actuator which could achieve these targets using polypyrrole film and ionic liquid-soaked separators. The practical work density of a nine-layer multilayer actuator was 1.4 kJ m-3 at 0.5 Hz, when the volumes of the electrolyte and counter electrodes were included, which approaches the performance of mammalian muscle. To achieve air stability, we analyzed the effect of air-stable ionic liquid gels on actuator displacement using finite element simulation and it was found that the majority of strain could be retained when the elastic modulus of the gel was kept below 3 kPa. As a result of this work, we have shown that multilayered conducting polymer actuators are a feasible idea for household robotics, as they provide a substantial practical work density in a compact structure and can be easily scaled as required.

  11. Microscopic mechanism of reinforcement and conductivity in polymer nanocomposite materials

    NASA Astrophysics Data System (ADS)

    Chang, Tae-Eun

    Modification of polymers by adding various nano-particles is an important method to obtain effective enhancement of materials properties. Within this class of materials, carbon nanotubes (CNT) are among the most studied materials for polymer reinforcement due to their extraordinary mechanical properties, superior thermal and electronic properties, and high aspect ratio. However, to unlock the potential of CNTs for applications, CNTs must be well dispersed in a polymer matrix and the microscopic mechanism of polymer reinforcement by CNTs must be understood. In this study, single-wall carbon nanotube (SWNT) composites with polypropylene (PP)-SWNT and polystyrene (PS)-SWNT were prepared and analyzed. Microscopic study of the mechanism of reinforcement and conductivity by SWNT included Raman spectroscopy, wide-angle X-ray diffraction (WAXD) and dielectric measurement. For PP-SWNT composites, tensile tests show a three times increase in the Young's modulus with addition of only 1 wt% SWNT, and much diminished increase of modulus with further increase in SWNT concentration. For PS-SWNT composites, well-dispersed SWNT/PS composite has been produced, using initial annealing of SWNT and optimum sonication conditions. The studies on the tangential mode in the Raman spectra and TEM indicated well-dispersed SWNTs in a PS matrix. We show that conductivity appears in composites already at very low concentrations, hinting at the formation of a 'percolative' network even below 0.5% of SWNT. The Raman studies for both composites show good transfer of the applied stress from the polymer matrices to SWNTs. However, no significant improvement of mechanical property is observed for PS-SWNT composites. The reason for only a slight increase of mechanical property remains unknown.

  12. EFFECTS OF TRITIUM GAS EXPOSURE ON ELECTRICALLY CONDUCTING POLYMERS

    SciTech Connect

    Kane, M.; Clark, E.; Lascola, R.

    2009-12-16

    Effects of beta (tritium) and gamma irradiation on the surface electrical conductivity of two types of conducting polymer films are documented to determine their potential use as a sensing and surveillance device for the tritium facility. It was shown that surface conductivity was significantly reduced by irradiation with both gamma and tritium gas. In order to compare the results from the two radiation sources, an approximate dose equivalence was calculated. The materials were also sensitive to small radiation doses (<10{sup 5} rad), showing that there is a measurable response to relatively small total doses of tritium gas. Spectroscopy was also used to confirm the mechanism by which this sensing device would operate in order to calibrate this sensor for potential use. It was determined that one material (polyaniline) was very sensitive to oxidation while the other material (PEDOT-PSS) was not. However, polyaniline provided the best response as a sensing material, and it is suggested that an oxygen-impermeable, radiation-transparent coating be applied to this material for future device prototype fabrication. A great deal of interest has developed in recent years in the area of conducting polymers due to the high levels of conductivity that can be achieved, some comparable to that of metals [Gerard 2002]. Additionally, the desirable physical and chemical properties of a polymer are retained and can be exploited for various applications, including light emitting diodes (LED), anti-static packaging, electronic coatings, and sensors. The electron transfer mechanism is generally accepted as one of electron 'hopping' through delocalized electrons in the conjugated backbone, although other mechanisms have been proposed based on the type of polymer and dopant [Inzelt 2000, Gerard 2002]. The conducting polymer polyaniline (PANi) is of particular interest because there are extensive studies on the modulation of the conductivity by changing either the oxidation state of the

  13. Electronically conductive polymer binder for lithium-ion battery electrode

    SciTech Connect

    Liu, Gao; Xun, Shidi; Battaglia, Vincent S; Zheng, Honghe

    2014-10-07

    A family of carboxylic acid group containing fluorene/fluorenon copolymers is disclosed as binders of silicon particles in the fabrication of negative electrodes for use with lithium ion batteries. These binders enable the use of silicon as an electrode material as they significantly improve the cycle-ability of silicon by preventing electrode degradation over time. In particular, these polymers, which become conductive on first charge, bind to the silicon particles of the electrode, are flexible so as to better accommodate the expansion and contraction of the electrode during charge/discharge, and being conductive promote the flow battery current.

  14. Better Proton-Conducting Polymers for Fuel-Cell Membranes

    NASA Technical Reports Server (NTRS)

    Narayan, Sri; Reddy, Prakash

    2012-01-01

    Polyoxyphenylene triazole sulfonic acid has been proposed as a basis for development of improved proton-conducting polymeric materials for solid-electrolyte membranes in hydrogen/air fuel cells. Heretofore, the proton-conducting membrane materials of choice have been exemplified by a family of perfluorosulfonic acid-based polymers (Nafion7 or equivalent). These materials are suitable for operation in the temperature of 75 to 85 C, but in order to reduce the sizes and/or increase the energy-conversion efficiencies of fuel-cell systems, it would be desirable to increase temperatures to as high as 120 C for transportation applications, and to as high as 180 C for stationary applications. However, at 120 C and at relative humidity values below 50 percent, the loss of water from perfluorosulfonic acid-based polymer membranes results in fuel-cell power densities too low to be of practical value. Therefore, membrane electrolyte materials that have usefully high proton conductivity in the temperature range of 180 C at low relative humidity and that do not rely on water for proton conduction at 180 C would be desirable. The proposed polyoxyphenylene triazole sulfonic acid-based materials have been conjectured to have these desirable properties. These materials would be free of volatile or mobile acid constituents. The generic molecular structure of these materials is intended to exploit the fact, demonstrated in previous research, that materials that contain ionizable acid and base groups covalently attached to thermally stable polymer backbones exhibit proton conduction even in the anhydrous state.

  15. Direct Assembly of Large Arrays of Oriented Conducting Polymer Nanowires

    SciTech Connect

    Liang, Liang; Liu, Jun; Windisch, Charles F.; Exarhos, Gregory J.; Lin, Yuehe

    2002-10-04

    Although oriented carbon nanotubes, oriented nanowires of metals, semiconductors and oxides have attracted wide attention, there have been few reports on oriented polymer nanostructures such as nanowires. In this paper we report the assembly of large arrays of oriented nanowires through controlled nucleation and growth during a stepwise electrochemical deposition process in which a large number of nuclei were first deposited on the substrate using a large current density. After the initial nucleation, the current density was reduced step by step to grow the oriented nanowires from the nucleation sites created in the first step. A very different morphology was also demonstrated by first depositing a monolayer of close-packed colloidal spheres using a similar step-wise deposition process. As a result, the polymer nanofibers grew from the spheres in a radial fashion and formed the continuous three-dimensional network of nanofibers in the film. The principles of control nucleation and growth in electrochemical deposition investigated in this paper should be applicable to other electrical conducting and electrochemical active materials, including metals and conducting oxides. We also hope the oriented electroactive polymer nanostructure will open the door for new applications, such as miniaturized biosensors.

  16. Multidimensional conducting polymer nanotubes for ultrasensitive chemical nerve agent sensing.

    PubMed

    Kwon, Oh Seok; Park, Seon Joo; Lee, Jun Seop; Park, Eunyu; Kim, Taejoon; Park, Hyun-Woo; You, Sun Ah; Yoon, Hyeonseok; Jang, Jyongsik

    2012-06-13

    Tailoring the morphology of materials in the nanometer regime is vital to realizing enhanced device performance. Here, we demonstrate flexible nerve agent sensors, based on hydroxylated poly(3,4-ethylenedioxythiophene) (PEDOT) nanotubes (HPNTs) with surface substructures such as nanonodules (NNs) and nanorods (NRs). The surface substructures can be grown on a nanofiber surface by controlling critical synthetic conditions during vapor deposition polymerization (VDP) on the polymer nanotemplate, leading to the formation of multidimensional conducting polymer nanostructures. Hydroxyl groups are found to interact with the nerve agents. Representatively, the sensing response of dimethyl methylphosphonate (DMMP) as a simulant for sarin is highly sensitive and reversible from the aligned nanotubes. The minimum detection limit is as low as 10 ppt. Additionally, the sensor had excellent mechanical bendability and durability. PMID:22545863

  17. Unusual Enhancement in Intrinsic Thermal Conductivity of Multilayer Graphene by Tensile Strains

    DOE PAGESBeta

    Kuang, Youdi; Lindsay, Lucas R.; Huang, Baoling

    2015-01-01

    High basal plane thermal conductivity k of multi-layer graphene makes it promising for thermal management applications. Here we examine the effects of tensile strain on thermal transport in this system. Using a first principles Boltzmann-Peierls equation for phonon transport approach, we calculate the room-temperature in-plane lattice k of multi-layer graphene (up to four layers) and graphite under different isotropic tensile strains. The calculated in-plane k of graphite, finite mono-layer graphene and 3-layer graphene agree well with previous experiments. The dimensional transitions of the intrinsic k and the extent of the diffusive transport regime from mono-layer graphene to graphite are presented.more » We find a peak enhancement of intrinsic k for multi-layer graphene and graphite with increasing strain and the largest enhancement amplitude is about 40%. In contrast the calculated intrinsic k with tensile strain decreases for diamond and diverges for graphene, we show that the competition between the decreased mode heat capacities and the increased lifetimes of flexural phonons with increasing strain contribute to this k behavior. Similar k behavior is observed for 2-layer hexagonal boron nitride systems, suggesting that it is an inherent thermal transport property in multi-layer systems assembled of purely two dimensional atomic layers. This study provides insights into engineering k of multi-layer graphene and boron nitride by strain and into the nature of thermal transport in quasi-two-dimensional and highly anisotropic systems.« less

  18. Shear induced electrical behaviour of conductive polymer composites

    NASA Astrophysics Data System (ADS)

    Starý, Zdeněk; Krückel, Johannes; Schubert, Dirk W.

    2013-04-01

    The time-dependent electrical resistance of polymethylmethacrylate containing carbon black was measured under oscillatory shear in the molten state. The electrical signal was oscillating exactly at the doubled frequency of the oscillatory shear deformation. Moreover, the experimental results gave a hint to the development of conductive structures in polymer melts under shear deformation. It was shown that the flow induced destruction of conductive paths dominates over the flow induced build-up in the beginning of the shear deformations. However, for longer times both competitive effects reach a dynamic equilibrium and only the thermally induced build-up of pathways influences the changes in the composite resistance during the shear. Furthermore, the oscillating electrical response depends clearly on the deformation amplitude applied. A simple physical model describing the behaviour of conductive pathways under shear deformation was derived and utilized for the description of the experimental data.

  19. Pumping conductance, the intrinsic anomalous Hall effect, and statistics of topological invariants

    NASA Astrophysics Data System (ADS)

    Dahlhaus, Jan; Ilan, Roni; Freed, Daniel; Freedman, Michael; Moore, Joel E.

    2015-06-01

    The pumping conductance of a disordered two-dimensional Chern insulator scales with increasing size and fixed disorder strength to sharp plateau transitions at well-defined energies between ordinary and quantum Hall insulators. When the disorder strength is scaled to zero as system size increases, the "metallic" regime of fluctuating Chern numbers can extend over the whole band. A simple argument leads to a sort of weighted equipartition of Chern number over minibands in a finite system with periodic boundary conditions: even though there must be strong fluctuations between disorder realizations, the mean Chern number at a given energy is determined by the clean Berry curvature distribution, as in the intrinsic anomalous Hall effect formula for metals. This estimate is compared to numerical results using recently developed operator algebra methods, and indeed the dominant variation of average Chern number is explained by the intrinsic anomalous Hall formula. A mathematical appendix provides more precise definitions and a model for the full distribution of Chern numbers.

  20. Unusual Enhancement in Intrinsic Thermal Conductivity of Multilayer Graphene by Tensile Strains.

    PubMed

    Kuang, Youdi; Lindsay, Lucas; Huang, Baoling

    2015-09-01

    Using the Boltzmann-Peierls equation for phonon transport approach with the inputs of interatomic force constants from the self-consistent charge density functional tight binding method, we calculate the room-temperature in-plane lattice thermal conductivities k of multilayer graphene (up to four layers) and graphite under different isotropic tensile strains. The calculated in-plane k of graphite, finite monolayer graphene and 3-layer graphene agree well with previous experiments. For unstrained graphene systems, both the intrinsic k and the extent of the diffusive transport regime present a drastic dimensional transition in going from monolayer to 2-layer graphene and thereafter a gradual transition to the graphite limit. We find a peak enhancement of intrinsic k for multilayer graphene and graphite with increasing strain with the largest enhancement amplitude ∼40%. Competition between the decreased mode heat capacities and the increased lifetimes of flexural phonons with increasing strain contribute to this k behavior. Similar k behavior is observed for 2-layer hexagonal boron nitride systems. This study provides insights into engineering k of multilayer graphene and boron nitride by strain and into the nature of thermal transport in quasi-two-dimensional and highly anisotropic systems. PMID:26241731

  1. Hierarchical nanostructured conducting polymer hydrogel with high electrochemical activity

    PubMed Central

    Pan, Lijia; Yu, Guihua; Zhai, Dongyuan; Lee, Hye Ryoung; Zhao, Wenting; Liu, Nian; Wang, Huiliang; Tee, Benjamin C.-K.; Shi, Yi; Cui, Yi; Bao, Zhenan

    2012-01-01

    Conducting polymer hydrogels represent a unique class of materials that synergizes the advantageous features of hydrogels and organic conductors and have been used in many applications such as bioelectronics and energy storage devices. They are often synthesized by polymerizing conductive polymer monomer within a nonconducting hydrogel matrix, resulting in deterioration of their electrical properties. Here, we report a scalable and versatile synthesis of multifunctional polyaniline (PAni) hydrogel with excellent electronic conductivity and electrochemical properties. With high surface area and three-dimensional porous nanostructures, the PAni hydrogels demonstrated potential as high-performance supercapacitor electrodes with high specific capacitance (∼480 F·g-1), unprecedented rate capability, and cycling stability (∼83% capacitance retention after 10,000 cycles). The PAni hydrogels can also function as the active component of glucose oxidase sensors with fast response time (∼0.3 s) and superior sensitivity (∼16.7 μA·mM-1). The scalable synthesis and excellent electrode performance of the PAni hydrogel make it an attractive candidate for bioelectronics and future-generation energy storage electrodes. PMID:22645374

  2. Correlation between dimensional crossover and thermoelectric performance in conducting polymer

    NASA Astrophysics Data System (ADS)

    Jo, Junhyeon; Oh, In-Seon; Jin, Mi-Jin; Yoo, Jung-Woo

    Conjugated polymers are emerging as attractive thermoelectric materials, resulting from low thermal conductivity, easy process and variable potentials for change. Recently, there are significant improvements of the Seebeck coefficient (S) and electric conductivity (σ) in the conjugated polymers by adding chemical additives to reform its ordinary disordered structure system. However, the relation between thermoelectricity and charge transport in the system is not well understood, which gives us a new challenge to improve thermoelectricity in the organic system. Here, we studied thermoelectric performance of dimethyl sulfoxide (DMSO) doped poly(3,4-ethylenedioxythiophene)-poly(styrenesulfonate) (PEDOT:PSS) with adding variable amounts of fluorosurfactant Zonyl. The charge transport in this disordered system was analyzed within variable range hopping (VRH), which showed the change of hopping dimensionality with further molecular dopants. The morphological change and its effect on charge transport and thermoelectric performance were further investigated through AFM, XPS, etc. As a result, we found the optimal condition for increasing both the Seebeck coefficient and electric conductivity, resulting in a significant improvement for the power factor (S2 σ) .

  3. Synthesis and applications of electrically conducting polymer nanocomposites

    NASA Astrophysics Data System (ADS)

    Ku, Bon-Cheol

    This research focuses on the synthesis and applications of electrically conducting polymer nanocomposites through molecular self-assembly. Two different classes of polymers, polyaniline (PANI) and polyacetylenes have been synthesized by biomimetic catalysis and spontaneous polymerization method. For gas barrier materials, commercially available polymers, poly(allylamine hydrochloride) (PAH) and poly (acrylic acid) (PAA), have also been used and thermally cross-linked. The morphological, optical and electrical properties of amphiphilic polyacetylenes have been studied. Furthermore, barrier properties, permselectivity, pervaporation properties of polyacetylenes/aluminosilicate nanocomposites have been investigated. For processability and electrical properties of carbon nanotube and conducting polymers, substituted ionic polyacetylenes (SIPA) have been covalently incorporated onto single-walled carbon nanotubes (SWNT) using the "grafting-from" technique. In the first study, a nanocomposite film catalyst has been prepared by electrostatic layer-by-layer (ELBL) self-assembly of a polyelectrolyte and a biomimetic catalyst for synthesis of polyaniline. Poly(dimethyl diallylammonium chloride) (PDAC) and hematin have been used as polycation and counter anions, respectively. The absorption spectra by UV-vis-NIR spectroscopy showed that conductive form polyaniline was formed not only as a coating on the surface of the ELBL composites but was also formed in solution. Furthermore, it was found that the reaction rate was affected by pH and concentration of hematin in the multilayers. The feasibility of controlled desorption of hematin molecules from the LBL assembly was explored and demonstrated by changing the pH and hematin concentration. The polymerization rate of aniline in solution was enhanced with decreasing pH of the solutions due to increased desorption of hematin nanoparticles from the multilayers. These ELBL hematin assemblies demonstrated both a way to functionalize

  4. Fabrication and characterization of solid-state, conducting polymer actuators

    SciTech Connect

    Xie, J.; Sansinena, J. M.; Gao, J.; Wang, H. L.

    2004-01-01

    We report here the fabrication and characterization of solid-state, conducting polymer actuators. The electrochemical activity of polyaniline (PANI) thin film coated with solid-state polyelectrolyte is very similar to the polyaniline thin film in an aqueous solution. The solid-state actuator is adhere to a lever arm of an force transducer and the force generation is measured in real time. The force generated by the actuator is found to be length dependent. However, the overall torques generated by the actuators with different lengths remains essentially the same. The effect of stimulation signals such as voltage, current, on the bending angle and displacement is also studied using square wave potential.

  5. Cellular adhesion, proliferation and viability on conducting polymer substrates.

    PubMed

    del Valle, Luis J; Estrany, Francesc; Armelin, Elaine; Oliver, Ramón; Alemán, Carlos

    2008-12-01

    This work reports a comprehensive study about cell adhesion and proliferation on the surface of different electroactive substrates formed by pi-conjugated polymers. Biological assays were performed considering four different cellular lines: two epithelial and two fibroblasts. On the other hand, the electroactivity of the three conducting systems was determined in physiological conditions. Results indicate that the three substrates behave as a cellular matrix, even though compatibility with cells is larger for PPy and the 3-layered system. Furthermore, the three polymeric systems are electro-compatible with the cellular monolayers. PMID:18683167

  6. Enhancement in ionic conductivity on solid polymer electrolytes containing large conducting species

    NASA Astrophysics Data System (ADS)

    Praveen, D.; Damle, Ramakrishna

    2016-05-01

    Solid Polymer Electrolytes (SPEs) lack better conducting properties at ambient temperatures. Various methods to enhance their ionic conductivity like irradiation with swift heavy ions, γ-rays, swift electrons and quenching at low temperature etc., have been explored in the literature. Among these, one of the oldest methods is incorporation of different conducting species into the polymer matrix and/or addition of nano-sized inert particles into SPEs. Various new salts like LiBr, Mg(ClO4)2, NH4I etc., have already been tried in the past with some success. Also various nanoparticles like Al2O3, TiO2 etc., have been tried in the past. In this article, we have investigated an SPE containing Rubidium as a conducting species. Rubidium has a larger ionic size compared to lithium and sodium ions which have been investigated in the recent past. In the present article, we have investigated the conductivity of large sized conducting species and shown the enhancement in the ionic conductivity by addition of nano-sized inert particles.

  7. Smart conducting polymer composites having zero temperature coefficient of resistance

    NASA Astrophysics Data System (ADS)

    Chu, Kunmo; Lee, Sung-Chul; Lee, Sangeui; Kim, Dongearn; Moon, Changyoul; Park, Sung-Hoon

    2014-12-01

    Zero temperature coefficient of resistance (TCR) is essential for the precise control of temperature in heating element and sensor applications. Many studies have focused on developing zero-TCR systems with inorganic compounds; however, very few have dealt with developing zero-TCR systems with polymeric materials. Composite systems with a polymer matrix and a conducting filler show either a negative (NTC) or a positive temperature coefficient (PTC) of resistance, depending on several factors, e.g., the polymer nature and the filler shape. In this study, we developed a hybrid conducting zero-TCR composite having self-heating properties for thermal stability and reliable temperature control. The bi-layer composites consisted of a carbon nanotube (CNT)-based layer having an NTC of resistance and a carbon black (CB)-based layer having a PTC of resistance which was in direct contact with electrodes to stabilize the electrical resistance change during electric Joule heating. The composite showed nearly constant resistance values with less than 2% deviation of the normalized resistance until 200 °C. The CB layer worked both as a buffer and as a distributor layer against the current flow from an applied voltage. This behavior, which was confirmed both experimentally and theoretically, has been rarely reported for polymer-based composite systems.Zero temperature coefficient of resistance (TCR) is essential for the precise control of temperature in heating element and sensor applications. Many studies have focused on developing zero-TCR systems with inorganic compounds; however, very few have dealt with developing zero-TCR systems with polymeric materials. Composite systems with a polymer matrix and a conducting filler show either a negative (NTC) or a positive temperature coefficient (PTC) of resistance, depending on several factors, e.g., the polymer nature and the filler shape. In this study, we developed a hybrid conducting zero-TCR composite having self

  8. Varying the apparent conduction mechanism in polymer semiconductors

    NASA Astrophysics Data System (ADS)

    Bittle, Emily G.; Ro, Hyun Wook; Basham, James I.; Delongchamp, Dean; Gundlach, David; Jurchescu, Oana

    The weak van der Waals inter-molecular interactions in organic semiconductors (OSCs) result in large variations in transport behavior ranging from hopping to band-like. Accurately measuring and modelling charge transport is a prerequisite to establishing robust transport-microstructure correlations and developing predictive structure-function relationships for optimized materials design and processing. Field-effect transistors have become a favored test structure for parameterizing and benchmarking the electronic properties of OSCs due to their ease of fabrication, measurement, and possible use in commercial applications. However, correctly analyzing transistor current-voltage measurements to extract material properties has proven difficult, as parasitic effects influence the device electrical properties and mask intrinsic material properties. Here, we use impedance spectroscopy to evaluate the effects of contacts on device operation and extract the properties of the channel which we compare with conventional DC measurements. We apply this approach to model systems of the widely studied polymer regioregular poly(3-hexylthiophene-2,5-diyl) which we engineer through different solidification kinetics to achieve distinct, well characterized degrees of molecular order. When increasing the order we find that the transport changes from field enhanced to field independent. This study addresses the origins of transport behavior seen in OSCs while discerning non-linear contact effects from field dependent transport.

  9. Beta-adrenoceptor blockade and atrio-ventricular conduction in dogs. Role of intrinsic sympathomimetic activity.

    PubMed

    Giudicelli, J F; Lhoste, F

    1982-01-01

    1 Atrio-ventricular conduction and its modifications induced by six beta-adrenoceptor blocking agents and isoprenaline have been investigated in the anaesthetized dog using the extrastimulus technique and measuring atrial (AERP), nodal (NERP), global (GERP) effective refractory periods as well as global functional refractory period (GFRP). 2 When beta-adrenoceptor blockade was produced by (+/-)-propranolol (beta 1 + beta 2-adrenoceptor blockade) which is devoid of intrinsic sympathomimetic activity (ISA) but has membrane stabilizing effects (MSE), sotalol (beta 1 + beta 2-adrenoceptor blockade, no ISA, no MSE) and atenolol (beta 1-adrenoceptor blockade, no ISA, no MSE), all parameters were significantly increased. When beta-adrenoceptor blockade was achieved with pindolol (beta 1 + beta 2-adrenoceptor blockade) and practolol (beta 1-adrenoceptor blockade) which have ISA but no MSE, all parameters remained unchanged, as was also the case with (+)-propranolol, which has MSE but neither ISA nor beta-adrenolytic properties. 3 Isoprenaline at high doses significantly reduced the refractory periods but when infusion was stopped, marked but reversible conduction depression was observed. 4 It thus appears that beta-adrenoceptor blockade but not MSE is responsible for the onset of atrial and AV-conduction impairment and that ISA affords protection against this impairment. PMID:6125166

  10. Organic Molecules and Network Polymers of Intrinsic Microporosity: Structural Characterization via X-ray Scattering and Simulations

    NASA Astrophysics Data System (ADS)

    McDermott, Amanda G.; Abbott, Lauren J.; Del Regno, Annalaura; Msayib, Kadhum J.; Ghanem, Bader S.; Taylor, Rupert; Carta, Mariolino; McKeown, Neil B.; Budd, Peter M.; Siperstein, Flor R.; Colina, Coray M.; Runt, James

    2011-03-01

    Like polymers of intrinsic microporosity (PIMs), organic molecules of intrinsic microporosity (OMIMs) are glassy solids featuring a large concentration of pores smaller than 2 nm and large internal surface area as measured by gas sorption experiments. OMIMs are oligomers designed to fill space inefficiently, consisting of several rigid segments joined at one vertex to produce concave faces. Both X-ray scattering patterns and simulations provide insight into the packing geometry and short-range order of these molecules. We also discuss the interpretation of scattering patterns from two- and three-dimensional network PIMs. Supported by NSF/Materials World Network/EPSRC and the NSF Graduate Research Fellowship Program.

  11. Nanostructured conducting polymers for stiffness controlled cell adhesion

    NASA Astrophysics Data System (ADS)

    Moyen, Eric; Hama, Adel; Ismailova, Esma; Assaud, Loic; Malliaras, George; Hanbücken, Margrit; Owens, Roisin M.

    2016-02-01

    We propose a facile and reproducible method, based on ultra thin porous alumina membranes, to produce cm2 ordered arrays of nano-pores and nano-pillars on any kind of substrates. In particular our method enables the fabrication of conducting polymers nano-structures, such as poly[3,4-ethylenedioxythiophene]:poly[styrene sulfonate] (PEDOT:PSS). Here, we demonstrate the potential interest of those templates with controlled cell adhesion studies. The triggering of the eventual fate of the cell (proliferation, death, differentiation or migration) is mediated through chemical cues from the adsorbed proteins and physical cues such as surface energy, stiffness and topography. Interestingly, as well as through material properties, stiffness modifications can be induced by nano-topography, the ability of nano-pillars to bend defining an effective stiffness. By controlling the diameter, length, depth and material of the nano-structures, one can possibly tune the effective stiffness of a (nano) structured substrate. First results indicate a possible change in the fate of living cells on such nano-patterned devices, whether they are made of conducting polymer (soft material) or silicon (hard material).

  12. Rechargeable aluminum batteries with conducting polymers as positive electrodes.

    SciTech Connect

    Hudak, Nicholas S.

    2013-12-01

    This report is a summary of research results from an Early Career LDRD project con-ducted from January 2012 to December 2013 at Sandia National Laboratories. Demonstrated here is the use of conducting polymers as active materials in the posi-tive electrodes of rechargeable aluminum-based batteries operating at room tempera-ture. The battery chemistry is based on chloroaluminate ionic liquid electrolytes, which allow reversible stripping and plating of aluminum metal at the negative elec-trode. Characterization of electrochemically synthesized polypyrrole films revealed doping of the polymers with chloroaluminate anions, which is a quasi-reversible reac-tion that facilitates battery cycling. Stable galvanostatic cycling of polypyrrole and polythiophene cells was demonstrated, with capacities at near-theoretical levels (30-100 mAh g-1) and coulombic efficiencies approaching 100%. The energy density of a sealed sandwich-type cell with polythiophene at the positive electrode was estimated as 44 Wh kg-1, which is competitive with state-of-the-art battery chemistries for grid-scale energy storage.

  13. Tetraarylborate polymer networks as single-ion conducting solid electrolytes

    SciTech Connect

    Van Humbeck, Jeffrey F.; Aubrey, Michael L.; Alsbaiee, Alaaeddin; Ameloot, Rob; Coates, Geoffrey W.; Dichtel, William R.; Long, Jeffrey R.

    2015-06-23

    A new family of solid polymer electrolytes based upon anionic tetrakis(phenyl)borate tetrahedral nodes and linear bis-alkyne linkers is reported. Sonogashira polymerizations using tetrakis(4-iodophenyl)borate, tetrakis(4-iodo-2,3,5,6-tetrafluorophenyl)borate and tetrakis(4-bromo-2,3,5,6-tetrafluorophenyl)borate delivered highly cross-linked polymer networks with both 1,4-diethynylbeznene and a tri(ethylene glycol) substituted derivative. Promising initial conductivity metrics have been observed, including high room temperature conductivities (up to 2.7 × 10-4 S cm-1), moderate activation energies (0.25–0.28 eV), and high lithium ion transport numbers (up to tLi+ = 0.93). Initial investigations into the effects of important materials parameters such as bulk morphology, porosity, fluorination, and other chemical modification, provide starting design parameters for further development of this new class of solid electrolytes.

  14. Tetraarylborate polymer networks as single-ion conducting solid electrolytes

    DOE PAGESBeta

    Van Humbeck, Jeffrey F.; Aubrey, Michael L.; Alsbaiee, Alaaeddin; Ameloot, Rob; Coates, Geoffrey W.; Dichtel, William R.; Long, Jeffrey R.

    2015-06-23

    A new family of solid polymer electrolytes based upon anionic tetrakis(phenyl)borate tetrahedral nodes and linear bis-alkyne linkers is reported. Sonogashira polymerizations using tetrakis(4-iodophenyl)borate, tetrakis(4-iodo-2,3,5,6-tetrafluorophenyl)borate and tetrakis(4-bromo-2,3,5,6-tetrafluorophenyl)borate delivered highly cross-linked polymer networks with both 1,4-diethynylbeznene and a tri(ethylene glycol) substituted derivative. Promising initial conductivity metrics have been observed, including high room temperature conductivities (up to 2.7 × 10-4 S cm-1), moderate activation energies (0.25–0.28 eV), and high lithium ion transport numbers (up to tLi+ = 0.93). Initial investigations into the effects of important materials parameters such as bulk morphology, porosity, fluorination, and other chemical modification, provide starting design parameters for furthermore » development of this new class of solid electrolytes.« less

  15. Multiscale Modeling of Thermal Conductivity of Polymer/Carbon Nanocomposites

    NASA Technical Reports Server (NTRS)

    Clancy, Thomas C.; Frankland, Sarah-Jane V.; Hinkley, Jeffrey A.; Gates, Thomas S.

    2010-01-01

    Molecular dynamics simulation was used to estimate the interfacial thermal (Kapitza) resistance between nanoparticles and amorphous and crystalline polymer matrices. Bulk thermal conductivities of the nanocomposites were then estimated using an established effective medium approach. To study functionalization, oligomeric ethylene-vinyl alcohol copolymers were chemically bonded to a single wall carbon nanotube. The results, in a poly(ethylene-vinyl acetate) matrix, are similar to those obtained previously for grafted linear hydrocarbon chains. To study the effect of noncovalent functionalization, two types of polyethylene matrices. -- aligned (extended-chain crystalline) vs. amorphous (random coils) were modeled. Both matrices produced the same interfacial thermal resistance values. Finally, functionalization of edges and faces of plate-like graphite nanoparticles was found to be only modestly effective in reducing the interfacial thermal resistance and improving the composite thermal conductivity

  16. Electronically conductive polymer binder for lithium-ion battery electrode

    SciTech Connect

    Liu, Gao; Battaglia, Vincent S.; Park, Sang -Jae

    2015-10-06

    A family of carboxylic acid groups containing fluorene/fluorenon copolymers is disclosed as binders of silicon particles in the fabrication of negative electrodes for use with lithium ion batteries. Triethyleneoxide side chains provide improved adhesion to materials such as, graphite, silicon, silicon alloy, tin, tin alloy. These binders enable the use of silicon as an electrode material as they significantly improve the cycle-ability of silicon by preventing electrode degradation over time. In particular, these polymers, which become conductive on first charge, bind to the silicon particles of the electrode, are flexible so as to better accommodate the expansion and contraction of the electrode during charge/discharge, and being conductive promote the flow battery current.

  17. Electronically conductive polymer binder for lithium-ion battery electrode

    SciTech Connect

    Liu, Gao; Xun, Shidi; Battaglia, Vincent S.; Zheng, Honghe; Wu, Mingyan

    2015-07-07

    A family of carboxylic acid groups containing fluorene/fluorenon copolymers is disclosed as binders of silicon particles in the fabrication of negative electrodes for use with lithium ion batteries. Triethyleneoxide side chains provide improved adhesion to materials such as, graphite, silicon, silicon alloy, tin, tin alloy. These binders enable the use of silicon as an electrode material as they significantly improve the cycle-ability of silicon by preventing electrode degradation over time. In particular, these polymers, which become conductive on first charge, bind to the silicon particles of the electrode, are flexible so as to better accommodate the expansion and contraction of the electrode during charge/discharge, and being conductive promote the flow battery current.

  18. Formation of conductive polymers using nitrosyl ion as an oxidizing agent

    DOEpatents

    Choi, Kyoung-Shin; Jung, Yongju; Singh, Nikhilendra

    2016-06-07

    A method of forming a conductive polymer deposit on a substrate is disclosed. The method may include the steps of preparing a composition comprising monomers of the conductive polymer and a nitrosyl precursor, contacting the substrate with the composition so as to allow formation of nitrosyl ion on the exterior surface of the substrate, and allowing the monomer to polymerize into the conductive polymer, wherein the polymerization is initiated by the nitrosyl ion and the conductive polymer is deposited on the exterior surface of the substrate. The conductive polymer may be polypyrrole.

  19. A study on the stability of n-type conductive polymer

    NASA Astrophysics Data System (ADS)

    Onoda, M.

    2016-04-01

    Novel n-type conducting polymer, poly (p-methylpyridinium vinylene), PMePyV were synthesized by using the quaternization of poly (p-pyridyl vinylene), PPyV and several regiochemical consequences in this polymer were proposed. The electrical, optical, and electrochemical properties of n-type conductive polymer were observed. In addition, a possibility of a variety of functional applications of n-type conductive polymer was indicated.

  20. Intrinsic nanotwin effect on thermal boundary conductance in bulk and single-nanowire twinning superlattices

    NASA Astrophysics Data System (ADS)

    Porter, Aaron; Tran, Chan; Sansoz, Frederic

    2016-05-01

    Coherent twin boundaries form periodic lamellar twinning in a wide variety of semiconductor nanowires, and they are often viewed as near-perfect interfaces with reduced phonon and electron scattering behaviors. Such unique characteristics are of practical interest for high-performance thermoelectrics and optoelectronics; however, insufficient understanding of twin-size effects on thermal boundary resistance poses significant limitations for potential applications. Here, using atomistic simulations and ab initio calculations, we report direct computational observations showing a crossover from diffuse interface scattering to superlatticelike behavior for thermal transport across nanoscale twin boundaries present in prototypical bulk and nanowire Si examples. Intrinsic interface scattering is identified for twin periods ≥22.6 nm, but it also vanishes below this size to be replaced by ultrahigh Kapitza thermal conductances. Detailed analysis of vibrational modes shows that modeling twin boundaries as atomically thin 6 H -Si layers, rather than phonon scattering interfaces, provides an accurate description of effective cross-plane and in-plane thermal conductivities in twinning superlattices, as a function of the twin period thickness.

  1. Conductive polymer combined silk fiber bundle for bioelectrical signal recording.

    PubMed

    Tsukada, Shingo; Nakashima, Hiroshi; Torimitsu, Keiichi

    2012-01-01

    Electrode materials for recording biomedical signals, such as electrocardiography (ECG), electroencephalography (EEG) and evoked potentials data, are expected to be soft, hydrophilic and electroconductive to minimize the stress imposed on living tissue, especially during long-term monitoring. We have developed and characterized string-shaped electrodes made from conductive polymer with silk fiber bundles (thread), which offer a new biocompatible stress free interface with living tissue in both wet and dry conditions.An electroconductive polyelectrolyte, poly(3,4-ethylenedioxythiophene)-poly(styrenesulfonate) (PEDOT-PSS) was electrochemically combined with silk thread made from natural Bombyx mori. The polymer composite 280 µm thread exhibited a conductivity of 0.00117 S/cm (which corresponds to a DC resistance of 2.62 Mohm/cm). The addition of glycerol to the PEDOT-PSS silk thread improved the conductivity to 0.102 S/cm (20.6 kohm/cm). The wettability of PEDOT-PSS was controlled with glycerol, which improved its durability in water and washing cycles. The glycerol treated PEDOT-PSS silk thread showed a tensile strength of 1000 cN in both wet and dry states. Without using any electrolytes, pastes or solutions, the thread directly collects electrical signals from living tissue and transmits them through metal cables. ECG, EEG, and sensory evoked potential (SEP) signals were recorded from experimental animals by using this thread placed on the skin. PEDOT-PSS silk glycerol composite thread offers a new class of biocompatible electrodes in the field of biomedical and health promotion that does not induce stress in the subjects. PMID:22493670

  2. Conductive Polymer Combined Silk Fiber Bundle for Bioelectrical Signal Recording

    PubMed Central

    Tsukada, Shingo; Nakashima, Hiroshi; Torimitsu, Keiichi

    2012-01-01

    Electrode materials for recording biomedical signals, such as electrocardiography (ECG), electroencephalography (EEG) and evoked potentials data, are expected to be soft, hydrophilic and electroconductive to minimize the stress imposed on living tissue, especially during long-term monitoring. We have developed and characterized string-shaped electrodes made from conductive polymer with silk fiber bundles (thread), which offer a new biocompatible stress free interface with living tissue in both wet and dry conditions. An electroconductive polyelectrolyte, poly(3,4-ethylenedioxythiophene) -poly(styrenesulfonate) (PEDOT-PSS) was electrochemically combined with silk thread made from natural Bombyx mori. The polymer composite 280 µm thread exhibited a conductivity of 0.00117 S/cm (which corresponds to a DC resistance of 2.62 Mohm/cm). The addition of glycerol to the PEDOT-PSS silk thread improved the conductivity to 0.102 S/cm (20.6 kohm/cm). The wettability of PEDOT-PSS was controlled with glycerol, which improved its durability in water and washing cycles. The glycerol treated PEDOT-PSS silk thread showed a tensile strength of 1000 cN in both wet and dry states. Without using any electrolytes, pastes or solutions, the thread directly collects electrical signals from living tissue and transmits them through metal cables. ECG, EEG, and sensory evoked potential (SEP) signals were recorded from experimental animals by using this thread placed on the skin. PEDOT-PSS silk glycerol composite thread offers a new class of biocompatible electrodes in the field of biomedical and health promotion that does not induce stress in the subjects. PMID:22493670

  3. Conducting polymers on non-conducting substrates: Chemical coating processes and applications

    SciTech Connect

    Genies, E.M.

    1996-01-01

    The presentation will be as follows: {emdash}Historical background {emdash}Oxidizing polymerization mechanism of heterocycles and aromatic compounds: the cases of pyrrole and anilin {emdash}The processes: solute, gas phase and from conducting polymer solutions {emdash}The substrates: glass, polymers, inorganic materials, textiles, powders. {emdash}Properties of coatings: {emdash}Chemical properties: redox, acid-base {emdash}Properties resulting from the polymer doping counter-ion {emdash}Physical properties: : optical, magnetic, conducting, microwave absorption {emdash}Stability {emdash}Applications: optics, microelectronics, sensors, electrochrome glasses, electromagnetic and antistatic shielding, military applications, packaging for electronic components, biocompat- ibility, plasturgy. {emdash}Commercial applications throughout the world. How to obtain these materials {emdash}Conclusions The examples will be taken from the results of our laboratory, those of CEA-Direction des Technologies Avanc{acute e}es{emdash}Centre d{close_quote}Etudes et de Recherche sur les Mat{acute e}riaux{emdash}Centre d{close_quote}Etudes Nucl{acute e}aires de Grenoble (Mssrs R. Jolly and J. C. Thi{acute e}blemont), from the Milliken Research Corp. (Dr. H. H. Kuhn), from the Zipperlin Kessler company (Dr. B. Wessling), from the Americhem company and from I.B.M. (Dr. M. Angelopoulos). {copyright} {ital 1996 American Institute of Physics.}

  4. Color combination of conductive polymers for black electrochromism.

    PubMed

    Shin, Haijin; Kim, Yuna; Bhuvana, Thiruvelu; Lee, Jiyea; Yang, Xu; Park, Cheolmin; Kim, Eunkyoung

    2012-01-01

    Conducting polymers that absorb three primary colors, red, green, and blue (RGB), were introduced with a yellow electrochromic polymer (Y) for the preparation of black electrochromic devices. Red poly(3-hexylthiophene) (P3HT) and blue poly(3,4-ethylenedioxythiophene) (PEDOT) were coated on one side of the electrode as a cathodically coloring electrochromic (EC) layer, while green poly(aniline-N-butylsulfonate) (PANBS) and yellow EC poly{[1,3-bis(9',9'-dihexylfluoren-20-yl)azulenyl]-alt-[2",7"-(9",9"-dihexylfluorenyl]} (PDHFA) were coated on the opposite electrode to complete a complementary EC device. The yellow PDHFA layer effectively compensated for absorption below 450 nm and above the 600 nm region, which was lacking in the RGB electrode. The resultant RGBY ECD provided a black color near the CIE black with L*, a*, and b* values of 32, -1.1, and 3.7, respectively, covering a broad absorption in the visible range in the colored state. The state of the black EC device was maintained, even after the electricity was turned off for 200 h, showing stable memory effect. PMID:22148317

  5. Amine-functionalized polypyrrole: Inherently cell adhesive conducting polymer.

    PubMed

    Lee, Jae Y; Schmidt, Christine E

    2015-06-01

    Electrically conducting polymers (CPs) have been recognized as novel biomaterials that can electrically communicate with biological systems. For their tissue engineering applications, CPs have been modified to promote cell adhesion for improved interactions between biomaterials and cells/tissues. Conventional approaches to improve cell adhesion involve the surface modification of CPs with biomolecules, such as physical adsorption of cell adhesive proteins and polycationic polymers, or their chemical immobilization; however, these approaches require additional multiple modification steps with expensive biomolecules. In this study, as a simple and effective alternative to such additional biomolecule treatment, we synthesized amine-functionalized polypyrrole (APPy) that inherently presents cell adhesion-supporting positive charges under physiological conditions. The synthesized APPy provides electrical activity in a moderate range and a hydrophilic surface compared to regular polypyrrole (PPy) homopolymers. Under both serum and serum-free conditions, APPy exhibited superior attachment of human dermal fibroblasts and Schwann cells compared to PPy homopolymer controls. Moreover, Schwann cell adhesion onto the APPy copolymer was at least similar to that on poly-l-lysine treated PPy controls. Our results indicate that amine-functionalized CP substrates will be useful to achieve good cell adhesion and potentially electrically stimulate various cells. In addition, amine functionality present on CPs can further serve as a novel and flexible platform to chemically tether various bioactive molecules, such as growth factors, antibodies, and chemical drugs. PMID:25294089

  6. Reciprocated suppression of polymer crystallization toward improved solid polymer electrolytes: Higher ion conductivity and tunable mechanical properties

    SciTech Connect

    Bi, Sheng; Sun, Che-Nan; Zawodzinski, Thomas A.; Ren, Fei; Keum, Jong Kahk; Ahn, Suk-Kyun; Li, Dawen; Chen, Jihua

    2015-08-06

    Solid polymer electrolytes based on lithium bis(trifluoromethanesulfonyl) imide and polymer matrix were extensively studied in the past due to their excellent potential in a broad range of energy related applications. Poly(vinylidene fluoride) (PVDF) and polyethylene oxide (PEO) are among the most examined polymer candidates as solid polymer electrolyte matrix. In this paper, we study the effect of reciprocated suppression of polymer crystallization in PVDF/PEO binary matrix on ion transport and mechanical properties of the resultant solid polymer electrolytes. With electron and X-ray diffractions as well as energy filtered transmission electron microscopy, we identify and examine the appropriate blending composition that is responsible for the diminishment of both PVDF and PEO crystallites. Laslty, a three-fold conductivity enhancement is achieved along with a highly tunable elastic modulus ranging from 20 to 200 MPa, which is expected to contribute toward future designs of solid polymer electrolytes with high room-temperature ion conductivities and mechanical flexibility.

  7. Conductive paper from lignocellulose wood microfibers coated with a nanocomposite of carbon nanotubes and conductive polymers

    NASA Astrophysics Data System (ADS)

    Agarwal, Mangilal; Xing, Qi; Shim, Bong Sup; Kotov, Nicholas; Varahramyan, Kody; Lvov, Yuri

    2009-05-01

    Composite nanocoating of poly(3,4-ethylenedioxythiophene)-poly(styrenesulfonate) (PEDOT-PSS) and aqueous dispersion of carbon nanotubes (CNT-PSS) on lignocellulose wood microfibers has been developed to make conductive microfibers and paper sheets. To construct the multilayers on wood microfibers, cationic poly(ethyleneimine) (PEI) has been used in alternate deposition with anionic conductive PEDOT-PSS and solubilized CNT-PSS. Using a Keithley microprobe measurement system, current-voltage measurements have been carried out on single composite microfibers after deposition of each layer to optimize the electrical properties of the coated microfibers. The conductivity of the resultant wood microfibers was in the range of 10-2-2 S cm-1 depending on the architecture of the coated layer. Further, the conductivity of the coated wood microfibers increased up to 20 S cm-1 by sandwiching multilayers of conductive co-polymer PEDOT-PSS with CNT-PSS through a polycation (PEI) interlayer. Moreover, paper hand sheets were manufactured from these coated wood microfibers with conductivity ranging from 1 to 20 S cm-1. A paper composite structure consisting of conductive/dielectric/conductive layers that acts as a capacitor has also been fabricated and is reported.

  8. Moving beyond mass-based parameters for conductivity analysis of sulfonated polymers

    SciTech Connect

    Kim, Yu Seung; Pivovar, Bryan

    2009-01-01

    Proton conductivity of polymer electrolytes is critical for fuel cells and has therefore been studied in significant detail. The conductivity of sulfonated polymers has been linked to material characteristics in order to elucidate trends. Mass based measurements based on water uptake and ion exchange capacity are two of the most common material characteristics used to make comparisons between polymer electrolytes, but have significant limitations when correlated to proton conductivity. These limitations arise in part because different polymers can have significantly different densities and conduction happens over length scales more appropriately represented by volume measurements rather than mass. Herein, we establish and review volume related parameters that can be used to compare proton conductivity of different polymer electrolytes. Morphological effects on proton conductivity are also considered. Finally, the impact of these phenomena on designing next generation sulfonated polymers for polymer electrolyte membrane fuel cells is discussed.

  9. Porous palladium coated conducting polymer nanoparticles for ultrasensitive hydrogen sensors.

    PubMed

    Lee, Jun Seop; Kim, Sung Gun; Cho, Sunghun; Jang, Jyongsik

    2015-12-28

    Hydrogen, a clean-burning fuel, is of key importance to various industrial applications, including fuel cells and in the aerospace and automotive industries. However, hydrogen gas is odorless, colorless, and highly flammable; thus appropriate safety protocol implementation and monitoring are essential. Highly sensitive hydrogen leak detection and surveillance sensor systems are needed; additionally, the ability to maintain uniformity through repetitive hydrogen sensing is becoming increasingly important. In this report, we detail the fabrication of porous palladium coated conducting polymer (3-carboxylate polypyrrole) nanoparticles (Pd@CPPys) to detect hydrogen gas. The Pd@CPPys are produced by means of facile alkyl functionalization and chemical reduction of a pristine 3-carboxylate polypyrrole nanoparticle-contained palladium precursor (PdCl(2)) solution. The resulting Pd@CPPy-based sensor electrode exhibits ultrahigh sensitivity (0.1 ppm) and stability toward hydrogen gas at room temperature due to the palladium sensing layer. PMID:26598964

  10. Conductive polymer-based microextraction methods: a review.

    PubMed

    Bagheri, Habib; Ayazi, Zahra; Naderi, Mehrnoush

    2013-03-12

    Conductive polymers (CPs) are classified as materials which exhibit highly reversible redox behavior and the unusual combined properties of metal and plastics. CPs, due to their multifunctionality, ease of synthesis and their stability, have attracted more attentions in different fields of research, including sample preparation. CPs along with several commercial hydrophilic sorbents, are alternative to the commercially available hydrophobic sorbents which despite their high specific surface areas, have poor interactions and retentions in the extraction of polar compounds. This review covers a general overview regarding the recent progress and new applications of CPs toward their synthesis and use in novel extraction and microextraction techniques including solid phase microextraction (SPME), electrochemically controlled solid-phase microextraction (EC-SPME) and other relevant techniques. Furthermore the contribution of nano-structured CPs in these methodologies is also reviewed. PMID:23452781

  11. Applications of conducting polymers and their issues in biomedical engineering

    PubMed Central

    Ravichandran, Rajeswari; Sundarrajan, Subramanian; Venugopal, Jayarama Reddy; Mukherjee, Shayanti; Ramakrishna, Seeram

    2010-01-01

    Conducting polymers (CPs) have attracted much interest as suitable matrices of biomolecules and have been used to enhance the stability, speed and sensitivity of various biomedical devices. Moreover, CPs are inexpensive, easy to synthesize and versatile because their properties can be readily modulated by (i) surface functionalization techniques and (ii) the use of a wide range of molecules that can be entrapped or used as dopants. This paper discusses the various surface modifications of the CP that can be employed in order to impart physico-chemical and biological guidance cues that promote cell adhesion/proliferation at the polymer–tissue interface. This ability of the CP to induce various cellular mechanisms widens its applications in medical fields and bioengineering. PMID:20610422

  12. PATTERN RECOGNITION STUDIES OF HALOGENATED ORGANIC COMPOUNDS USING CONDUCTING POLYMER SENSOR ARRAYS. (R825323)

    EPA Science Inventory

    Direct measurement of volatile and semivolatile halogenated organic compounds of environmental interest was carried out using arrays of conducting polymer sensors. Mathematical expressions of the sensor arrays using microscopic polymer network model is described. A classical, non...

  13. Strain sensing conductive polymer composites: Sensitivity and stability

    NASA Astrophysics Data System (ADS)

    Deng, Hua; Du, Rongni; Duan, Linyan; Fu, Qiang

    2016-03-01

    The effect of conductive network morphology and interfacial interaction on the strain sensing capability of conductive polymer composites (CPCs) is thought as crucial. Nevertheless, the stability in strain sensing behavior has barely been investigated. Herein, the resistivity-strain behavior in terms of stability and sensitivity of CPCs based on poly(styrene-butadiene-styrene) (SBS) containing multiwalled carbon nanotubes (MWCNTs) are studied. It is shown that the preparation method has an important influence on the resistivity-strain behavior of these CPCs. The sensitivity increases with decreasing filler content for both composites under linear uniaxial strain, showing higher strain sensitivity near the percolation threshold. A higher and wider range of sensitivities is obtained for melt mixed SBS/MWCNT. Meanwhile, resistivity downward drifting and shoulder peaks are shown for composites from melt mixing under dynamic strain. Interestingly, linear relationships and reversible resistivity in every cycle are observed for composites from solution mixing, showing good electromechanical consistency, stability and durability. From the TEM, rheology, SEM, SAXS, Raman microscopy and analytical modeling studies, the difference in morphology is thought to be responsible for such resistivity-strain behavior. As more disordered and less densely packed conductive networks in melt mixed CPCs are more easily destroyed under strain, evenly distributed and densely packed networks in solution mixed CPCs are more stable during cyclic stretching. Finally, different human motions have been detected using these CPCs, demonstrating the potential application of these CPCs as movement sensors.

  14. Understanding hopping transport and thermoelectric properties of conducting polymers

    NASA Astrophysics Data System (ADS)

    Ihnatsenka, S.; Crispin, X.; Zozoulenko, I. V.

    2015-07-01

    We calculate the conductivity σ and the Seebeck coefficient S for the phonon-assisted hopping transport in conducting polymers poly(3,4-ethylenedioxythiophene) or PEDOT, experimentally studied by Bubnova et al. [J. Am. Chem. Soc. 134, 16456 (2012)], 10.1021/ja305188r. We use the Monte Carlo technique as well as the semianalytical approach based on the transport energy concept. We demonstrate that both approaches show a good qualitative agreement for the concentration dependence of σ and S . At the same time, we find that the semianalytical approach is not in a position to describe the temperature dependence of the conductivity. We find that both Gaussian and exponential density of states (DOS) reproduce rather well the experimental data for the concentration dependence of σ and S giving similar fitting parameters of the theory. The obtained parameters correspond to a hopping model of localized quasiparticles extending over 2-3 monomer units with typical jumps over a distance of 3-4 units. The energetic disorder (broadening of the DOS) is estimated to be 0.1 eV. Using the Monte Carlo calculation we reproduce the activation behavior of the conductivity with the calculated activation energy close to the experimentally observed one. We find that for a low carrier concentration a number of free carriers contributing to the transport deviates strongly from the measured oxidation level. Possible reasons for this behavior are discussed. We also study the effect of the dimensionality on the charge transport by calculating the Seebeck coefficient and the conductivity for the cases of three-, two-, and one-dimensional motion.

  15. Intrinsic ultralow lattice thermal conductivity of the unfilled skutterudite FeSb3

    NASA Astrophysics Data System (ADS)

    Fu, Yuhao; Singh, David J.; Li, Wu; Zhang, Lijun

    2016-08-01

    It is generally accepted that unfilled skutterudites process high lattice thermal conductivity κl that can be efficiently reduced upon filling. Here by using first-principles Boltzmann-Peierls transport calculations, we find pure skutterudite of FeSb3 with no filler in fact has an intrinsic ultralow κl smaller than that of CoSb3 by one order of magnitude. The value is even smaller than those of most of the fully filled skutterudites. This finding means that with FeSb3 as a reference, filling does not necessarily lower κl. The ultralow κl of FeSb3 is a consequence of the overall softening of phonon spectrum, especially the lowering in frequency of optical phonon branches associated with the weakly bonded Sb4 rings. They overlap more with heat-carrying acoustic phonons and significantly increase the phase space for three-phonon anharmonic scattering processes. This provides an alternative non-filling-related mechanism for lowering the κl of skutterudites.

  16. Conducting polymer/polyimide-clay nanocomposite coatings for corrosion protection of AA-2024 alloy

    NASA Astrophysics Data System (ADS)

    Shah, Kunal G.

    Corrosion of metals is a major problem in the aerospace and automobile industry. The current methods of corrosion protection such as chromate conversion coatings are under increased scrutiny from the Environmental Protection Agency (EPA) due to their carcinogenic nature. Intrinsically conducting polymers (ICPs) like polyaniline and polypyrrole have been considered as a potential replacement for chromate conversion coatings and have been under investigation since past decade. The goal of this study is to replace the chromate conversion coating by an environmentally friendly organic coating. Poly (N-ethyl aniline) coating was electrodeposited as the primer layer and polyimide-clay nanocomposite was solution cast as the barrier layer on AA-2024 alloy. This study will provide a better understanding of the corrosion protection mechanism of the conducting polymer coating. Various characterization techniques such as infrared spectroscopy, cyclic voltammetry and scanning electron microscopy were used to study the formation, chemical structure and morphology of the coatings. Electrodeposition parameters like monomer concentration, applied current density and the reaction time were varied in order to optimize the properties of the conducting polymer coating. The corrosion performance of the primer coating was evaluated by DC polarization studies. It was found that poly (N-ethyl aniline) reduces from emeraldine to leucoemeraldine form; reducing the rate of cathodic reaction, which reduces the rate of corrosion of AA-2024 alloy. Polyimide-clay nanocomposite coating was solution cast on the conducting polymer primer layer for enhancing the barrier and corrosion properties of the coating system. The concentration of polyimide (10--25 vol%) and clay (0.1 and 1 wt%) were varied in the coating formulation to optimize the barrier properties of topcoat. X-ray diffraction showed that the intergallery clay distance decreased from 17.2 A to 11.79 A after immidization of polyimide

  17. Decoupling Ionic Conductivity from Structural Relaxation: A Way to Solid Polymer Electrolytes?

    SciTech Connect

    Agapov, Alexander L; Sokolov, Alexei P

    2011-01-01

    Using broadband dielectric spectroscopy, we studied the temperature dependence of ionic conductivity and structural relaxation in a number of polymers. We demonstrate that temperature dependence of ionic conductivity can be decoupled from structural relaxation in a material specific way. We show that the strength of the decoupling correlates with the steepness of the temperature dependence of structural relaxation in the polymer, i.e., with its fragility. We ascribe the observed result to stronger frustration in chain packing characteristic for more fragile polymers. We speculate that employment of more fragile polymers might lead to design of polymers with higher ionic conductivity.

  18. Soft capacitor fibers using conductive polymers for electronic textiles

    NASA Astrophysics Data System (ADS)

    Gu, Jian Feng; Gorgutsa, Stephan; Skorobogatiy, Maksim

    2010-11-01

    A novel, highly flexible, conductive polymer-based fiber with high electric capacitance is reported. In its cross section the fiber features a periodic sequence of hundreds of conductive and isolating plastic layers positioned around metallic electrodes. The fiber is fabricated using the fiber drawing method, where a multi-material macroscopic preform is drawn into a sub-millimeter capacitor fiber in a single fabrication step. Several kilometers of fibers can be obtained from a single preform with fiber diameters ranging between 500 and 1000 µm. A typical measured capacitance of our fibers is 60-100 nF m-1 and it is independent of the fiber diameter. Analysis of the fiber frequency response shows that in its simplest interrogation mode the capacitor fiber has a transverse resistance of 5 kΩ m L-1, which is inversely proportional to the fiber length L and is independent of the fiber diameter. Softness of the fiber materials, the absence of liquid electrolyte in the fiber structure, ease of scalability to large production volumes and high capacitance of our fibers make them interesting for various smart textile applications ranging from distributed sensing to energy storage.

  19. Polyaniline: a conductive polymer coating for durable nanospray emitters

    PubMed

    Maziarz; Lorenz; White; Wood

    2000-07-01

    Despite the tremendous sensitivity and lower sample requirements for nanospray vs. conventional electrospray, metallized nanospray emitters have suffered from one of two problems: low mechanical stability (leading to emitter failure) or lengthy, tedious production methods. Here, we describe a simple alternative to metallized tips using polyaniline (PANI), a synthetic polymer well known for its high conductivity, anticorrosion properties, antistatic properties, and mechanical stability. A simple method for coating borosilicate emitters (1.2 mm o.d.) pulled to fine tapers (4 +/- 1 microm) with water-soluble and xylene-soluble dispersions of conductive polyaniline (which allows for electrical contact at the emitter outlet) is described. The polyaniline-coated emitters show high durability and are resistant to electrical discharge, likely because of the thick (yet optically transparent) coatings; a single emitter can be used over a period of days for multiple samples with no visible indication of the destruction of the polyaniline coating. The optical transparency of the coating also allows the user to visualize the sample plug loaded into the emitter. Examples of nanospray using coatings of the water-soluble and xylene-soluble polyaniline dispersions are given. A comparison of PANI-coated and gold-coated nanospray emitters to conventional electrospray ionization (ESI) show that PANI-coated emitters provide similar enhanced sensitivity that gold-coated emitters exhibit vs. conventional ESI. PMID:10883822

  20. Conducting polymer composite materials for smart microwave windows

    NASA Astrophysics Data System (ADS)

    Barnes, Alan; Lees, K.; Wright, Peter V.; Chambers, Barry

    1999-07-01

    Samples of poly(aniline)-silver-polymer electrolyte particulate composites have been characterized at microwave frequencies when small d.c. electric fields are applied across them in both coaxial line and waveguide measurement test sets. The experimental data shows that the initial conductivity of the materials is dependent on the concentration of sliver metal and suggest that changes in resistance due to chemical switching take place, at least in part, in the manufacture of the composites. When silver is used as the electrodes, the experimental data show that changes in the slope of the cyclic voltammograms coincide with large changes in microwave reflectivity or transmission consistent with increasing conductivity of the composites when fields are applied. The reverse change occurs when the fields are removed. Measurements have shown that the composites are able to switch between the two impedance stats in times of less than one second for well over a million cycles with no apparent depreciation in material properties. Large area films have also been prepared and studied using the 'free space' technique.

  1. Highly Conductive, Stretchable, and Transparent Solid Polymer Electrolyte Membrane

    NASA Astrophysics Data System (ADS)

    He, Ruixuan; Echeverri, Mauricio; Kyu, Thein

    2014-03-01

    With the guidance of ternary phase diagrams, completely amorphous polymer electrolyte membranes (PEM) were successfully prepared by melt processing for lithium-ion battery. The PEM under consideration consisted of poly (ethylene glycol diacrylate) (PEGDA), succinonitrile (SCN) and Lithium bis(trifluoro-methane)sulfonamide (LiTFSI). After UV-crosslinking, the PEM is transparent and light-weight. Addition of SCN plastic crystal affords not only dissociation of the lithium salt, but also plasticization to the crosslinked PEGDA network. Of particular importance is the achievement of room-temperature ionic conductivity of ~10-3 S/cm, which is comparable to that of commercial liquid electrolyte. Higher ionic conductivities were achieved at elevated temperatures or with use of a moderately higher molecular weight of PEGDA. In terms of electrochemical and chemical stability, the PEM exhibited oxidative stability up to 5 V against lithium reference electrode. Stable interface behavior between the PEM and lithium electrode is also seen with ageing time. In the tensile tests, samples containing low molecular weight PEGDA are stiffer, whereas the high molecular weight PEGDA is stretchable up to 80% elongation. Supported by NSF-DMR 1161070.

  2. Conductivity and Stability of Photopolymerized Polymer Electrolyte Network

    NASA Astrophysics Data System (ADS)

    Kyu, Thein; He, Ruixuan; Chen, Yu-Ming; Mao, Jialin; Zhu, Yu; Kyu'S Group, , Dr.; Zhu'S Group Collaboration, , Dr.

    2014-03-01

    A melt-processing window has been identified within the wide isotropic region of the phase diagram of ternary blends consisting of poly (ethylene glycol diacrylate) (PEGDA), tetraethylene glycol dimethyl ether (TEGDME) and lithium bis(trifluoromethane) sulfonamide (LiTFSI). Upon UV-crosslinking of PEGDA in the isotropic window, the polymer electrolyte membrane (PEM) network thus formed is completely transparent and remains in the single phase without undergoing polymerization-induced phase separation or polymerization-induced crystallization. These PEM networks are solid albeit flexible and light-weight with safety and space saving attributes. The ionic conductivity as determined by AC impedance spectroscopy exhibited very high room-temperature ionic conductivity on the order of ~10-3 S/cm in several compositions, viz., 10/45/45, 20/40/40 and 30/35/35 PEGDA/TEGDME/LiTFSI networks. Cyclic voltammetry measurement of these solid-state PEM networks revealed excellent electrochemical stability against lithium reference electrode. The above study has been extended to the anode (graphite) and cathode (LiFePO4) half-cell configurations with lithium as counter electrode. Charge/discharge cycling behavior of these half cells will be discussed. Supported by NSF-DMR 1161070 and University of Akron.

  3. Synthesis of Conductive Nanofillers/Nanofibers and Electrical Properties of their Conductive Polymer Composites

    NASA Astrophysics Data System (ADS)

    Sarvi, Ali

    Thanks to their corrosion resistance, light weight, low cost, and ease of processing, electrically conducting polymer composites (CPCs) have received significant attention for the replacement of metals and inorganic materials for sensors, actuators, supercapacitors, and electromagnetic interference (EMI) shields. In this PhD thesis, high aspect ratio conductive nanofillers namely copper nanowires (CuNWs) and multiwall carbon nanotubes (MWCNTs) were coated with polyaniline (PANi) using solution mixing and in-situ polymerization method, respectively. Transmission electron microscopy (TEM) showed a smooth polyaniline nano-coating between 5--18 nm in thickness on the nanofillers' surface. The coating thickness and; consequently, electrical conductivity was controlled and tuned by polyaniline/aniline concentration in solution. Composites with tunable conductivity may be used as chemisensors, electronic pressure sensors and switches. Coated nanofillers demonstrated better dispersion in polystyrene (PS) and provided lower electrical percolation threshold. Dispersion of nanofillers in PS was investigated using rheological measurements and confirmed with electron micrographs and nano-scale images of CPCs. Polyaniline (PANi), when used as a coating layer, was able to attenuate electromagnetic (EM) waves via absorption and store electrical charges though pseudocapacitance mechanism. The dielectric measurements of MWCNT-PANi/PS composites showed one order of magnitude increase in real electrical permittivity compared to that of MWCNT/PS composites making them suitable for charge storage purposes. Incorporation of PANi also brought a new insight into conductive network formation mechanism in electrospun mats where the orientation of conductive high aspect ratio nanofillers is a major problem. Conductive nanofibers of poly(vinylidene fluoride) (PVDF) filled with coated multiwall carbon nanotubes (MWCNTs) were fabricated using electrospinning. These highly oriented PVDF

  4. Mixed ionic and electronic conductivity in polymers. Progress report, January 1, 1989--December 31, 1989

    SciTech Connect

    Shriver, D.F.

    1990-06-01

    The conductivity of iodine-containing polymers was investigated and conductivity along polyiodide chains is implicated by the concentration dependence of the conductivity data and spectroscopic measurements. On the theoretical side, entropy based models were developed to describe ion motion in polymers.

  5. Porous palladium coated conducting polymer nanoparticles for ultrasensitive hydrogen sensors

    NASA Astrophysics Data System (ADS)

    Lee, Jun Seop; Kim, Sung Gun; Cho, Sunghun; Jang, Jyongsik

    2015-12-01

    Hydrogen, a clean-burning fuel, is of key importance to various industrial applications, including fuel cells and in the aerospace and automotive industries. However, hydrogen gas is odorless, colorless, and highly flammable; thus appropriate safety protocol implementation and monitoring are essential. Highly sensitive hydrogen leak detection and surveillance sensor systems are needed; additionally, the ability to maintain uniformity through repetitive hydrogen sensing is becoming increasingly important. In this report, we detail the fabrication of porous palladium coated conducting polymer (3-carboxylate polypyrrole) nanoparticles (Pd@CPPys) to detect hydrogen gas. The Pd@CPPys are produced by means of facile alkyl functionalization and chemical reduction of a pristine 3-carboxylate polypyrrole nanoparticle-contained palladium precursor (PdCl2) solution. The resulting Pd@CPPy-based sensor electrode exhibits ultrahigh sensitivity (0.1 ppm) and stability toward hydrogen gas at room temperature due to the palladium sensing layer.Hydrogen, a clean-burning fuel, is of key importance to various industrial applications, including fuel cells and in the aerospace and automotive industries. However, hydrogen gas is odorless, colorless, and highly flammable; thus appropriate safety protocol implementation and monitoring are essential. Highly sensitive hydrogen leak detection and surveillance sensor systems are needed; additionally, the ability to maintain uniformity through repetitive hydrogen sensing is becoming increasingly important. In this report, we detail the fabrication of porous palladium coated conducting polymer (3-carboxylate polypyrrole) nanoparticles (Pd@CPPys) to detect hydrogen gas. The Pd@CPPys are produced by means of facile alkyl functionalization and chemical reduction of a pristine 3-carboxylate polypyrrole nanoparticle-contained palladium precursor (PdCl2) solution. The resulting Pd@CPPy-based sensor electrode exhibits ultrahigh sensitivity (0.1 ppm

  6. Proton conduction in Mo(VI)-based metallo-supramolecular polymers.

    PubMed

    Pandey, Rakesh K; Hossain, Md Delwar; Chakraborty, Chanchal; Moriyama, Satoshi; Higuchi, Masayoshi

    2015-07-14

    High proton conduction (8.5 × 10(-2) mS cm(-1)) was observed in a Mo(vi)-based metallo-supramolecular polymer with carboxylic acids at 95%RH. The integration of OH groups into the polymer was analysed using FTIR spectroscopy and found to be crucial for the proton transport in the polymer. PMID:26051550

  7. Rational design and synthesis of semi-conducting polymers.

    SciTech Connect

    Wong, Bryan Matthew; Reeder, Craig; Cordaro, Joseph Gabriel

    2010-12-01

    A rational approach was used to design polymeric materials for thin-film electronics applications, whereby theoretical modeling was used to determine synthetic targets. Time-dependent density functional theory calculations were used as a tool to predict the electrical properties of conjugated polymer systems. From these results, polymers with desirable energy levels and band-gaps were designed and synthesized. Measurements of optoelectronic properties were performed on the synthesized polymers and the results were compared to those of the theoretical model. From this work, the efficacy of the model was evaluated and new target polymers were identified.

  8. Molecular self-assembly of conducting polymer by Conducting Probe Technique in Atomic Force Microscope

    NASA Astrophysics Data System (ADS)

    Yamamoto, Shin-ichi; Ogawa, Kazufumi

    2007-04-01

    A polypyrrole derivative monolayer was investigated for the application as a wire. First, a pyrrole derivative monolayer was prepared by chemically adsorbing (self-assembling) monolayer (CAM) of 6-pyrrolylhexyl-12,12,12-trichloro-12- siladodecanoate (PEN) on a glass substrate. Then, the monolayer was polymerized in the presence of pure water by electrooxidation. The surface characterization of the molecular interaction was investigated by measuring the properties of CAMs attached to the glass substrate in the lateral direction. We formed PEN having polypyrrolyl groups, using Pt-patterned electrodes on glass surfaces and measured the conductance under a small bias voltage, using a conductive cantilever of atomic force microscopy (AFM). The polypyrrole derivative monolayer thus synthesized was covalently bonded to the glass substrate and showed conductivity as high as 3.05..103 S/cm after electro-oxidized. The method of preparing a conductive polymer monolayer by the combining chemical adsorption and electro-oxidation leads to a lot molecular wire to perpendicular to the Pt electrodes, and it is one of the key technologies for molecular devices.

  9. Electrochemical DNA Hybridization Sensors Based on Conducting Polymers

    PubMed Central

    Rahman, Md. Mahbubur; Li, Xiao-Bo; Lopa, Nasrin Siraj; Ahn, Sang Jung; Lee, Jae-Joon

    2015-01-01

    Conducting polymers (CPs) are a group of polymeric materials that have attracted considerable attention because of their unique electronic, chemical, and biochemical properties. This is reflected in their use in a wide range of potential applications, including light-emitting diodes, anti-static coating, electrochromic materials, solar cells, chemical sensors, biosensors, and drug-release systems. Electrochemical DNA sensors based on CPs can be used in numerous areas related to human health. This review summarizes the recent progress made in the development and use of CP-based electrochemical DNA hybridization sensors. We discuss the distinct properties of CPs with respect to their use in the immobilization of probe DNA on electrode surfaces, and we describe the immobilization techniques used for developing DNA hybridization sensors together with the various transduction methods employed. In the concluding part of this review, we present some of the challenges faced in the use of CP-based DNA hybridization sensors, as well as a future perspective. PMID:25664436

  10. Conductivity study and fourier transform infrared (FTIR) characterization of methyl cellulose solid polymer electrolyte with sodium iodide conducting ion

    SciTech Connect

    Abiddin, Jamal Farghali Bin Zainal; Ahmad, Azizah Hanom

    2015-08-28

    Sodium ion (Na{sup +}) based solid polymer electrolyte (SPE) has been prepared using solution cast technique with distilled water as solvent and Methylcellulose (MC) as a polymer host. Methylcellulose polymer was chosen as the polymer host due to the abundance of lone pair electrons in the carbonyl and C-O-C constituents, which in turn provide multiple hopping sites for the Na{sup +} conducting ions. Variable compositions of sodium iodide (NaI) salt were prepared to investigate the optimum MC-NaI weight ratio. Results from Electrical Impedance Spectroscopy (EIS) technique show that pure methylcellulose has a low conductivity of 3.61 × 10{sup −11} S/cm.The conductivity increases as NaI content increases up to optimum NaIcomposition of 40 wt%, which yields an average conductivity of 2.70 × 10{sup −5} S/cm.