Science.gov

Sample records for linked conducting polymers

  1. Conductive Polymers

    SciTech Connect

    Bohnert, G.W.

    2002-11-22

    Electroluminescent devices such as light-emitting diodes (LED) and high-energy density batteries. These new polymers offer cost savings, weight reduction, ease of processing, and inherent rugged design compared to conventional semiconductor materials. The photovoltaic industry has grown more than 30% during the past three years. Lightweight, flexible solar modules are being used by the U.S. Army and Marine Corps for field power units. LEDs historically used for indicator lights are now being investigated for general lighting to replace fluorescent and incandescent lights. These so-called solid-state lights are becoming more prevalent across the country since they produce efficient lighting with little heat generation. Conductive polymers are being sought for battery development as well. Considerable weight savings over conventional cathode materials used in secondary storage batteries make portable devices easier to carry and electric cars more efficient and nimble. Secondary battery sales represent an $8 billion industry annually. The purpose of the project was to synthesize and characterize conductive polymers. TRACE Photonics Inc. has researched critical issues which affect conductivity. Much of their work has focused on production of substituted poly(phenylenevinylene) compounds. These compounds exhibit greater solubility over the parent polyphenylenevinylene, making them easier to process. Alkoxy substituted groups evaluated during this study included: methoxy, propoxy, and heptyloxy. Synthesis routes for production of alkoxy-substituted poly phenylenevinylene were developed. Considerable emphasis was placed on final product yield and purity.

  2. Polymers that Conduct Electricity.

    ERIC Educational Resources Information Center

    Edelson, Edward

    1983-01-01

    Although polymers are regarded as electrical insulators, it was discovered that they can be made to conduct electricity. This discovery has opened vast new practical and theoretical areas for exploration by physicists and chemists. Research studies with these conducting polymers and charge-transfer salts as well as possible applications are…

  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. 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.

  5. 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.

  6. Discrete conductance switching in conducting polymer wires

    NASA Astrophysics Data System (ADS)

    He, H. X.; Li, X. L.; Tao, N. J.; Nagahara, L. A.; Amlani, I.; Tsui, R.

    2003-07-01

    Charge transport in conducting polymers (polyaniline and polypyrrole) bridged between two gold nanoelectrodes separated with a nanoscale gap (varying from ˜1 nm to a few tens of nm was studied by controlling the polymer redox states electrochemically. In sharp contrast to the macroscopic samples, the conductance switches abruptly between insulating (off) and conducting (on) states like a telegraphic signal. The time durations of the on and off states depend on the potential of the nanoelectrodes, indicating the important role of the redox states in the signal. We attribute the telegraphic signal to the fluctuation between the insulating reduced state and conducting oxidized state of the polymer, which rises as electrons trap into the oxidized state and escape from the reduced state.

  7. Conductive polymer-based material

    SciTech Connect

    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.

  8. Conducting Polymer 3D Microelectrodes

    PubMed Central

    Sasso, Luigi; Vazquez, Patricia; Vedarethinam, Indumathi; Castillo-León, Jaime; Emnéus, Jenny; Svendsen, Winnie E.

    2010-01-01

    Conducting polymer 3D microelectrodes have been fabricated for possible future neurological applications. A combination of micro-fabrication techniques and chemical polymerization methods has been used to create pillar electrodes in polyaniline and polypyrrole. The thin polymer films obtained showed uniformity and good adhesion to both horizontal and vertical surfaces. Electrodes in combination with metal/conducting polymer materials have been characterized by cyclic voltammetry and the presence of the conducting polymer film has shown to increase the electrochemical activity when compared with electrodes coated with only metal. An electrochemical characterization of gold/polypyrrole electrodes showed exceptional electrochemical behavior and activity. PC12 cells were finally cultured on the investigated materials as a preliminary biocompatibility assessment. These results show that the described electrodes are possibly suitable for future in-vitro neurological measurements. PMID:22163508

  9. 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)

  10. 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)

  11. 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.

  12. 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.

  13. 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.

  14. 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.

  15. 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.

  16. 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.

  17. 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.

  18. Highly cross-linked nanoporous polymers

    DOEpatents

    Steckle, Jr., Warren P.; Apen, Paul G.; Mitchell, Michael A.

    1997-01-01

    Condensation polymerization followed by a supercritical extraction step can be used to obtain highly cross-linked nanoporous polymers with high surface area, controlled pore sizes and rigid structural integrity. The invention polymers are useful for applications requiring separation membranes.

  19. Highly cross-linked nanoporous polymers

    DOEpatents

    Steckle, Jr., Warren P.; Apen, Paul G.; Mitchell, Michael A.

    1998-01-01

    Condensation polymerization followed by a supercritical extraction step can be used to obtain highly cross-linked nanoporous polymers with high surface area, controlled pore sizes and rigid structural integrity. The invention polymers are useful for applications requiring separation membranes.

  20. 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.

  1. 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.

  2. Direct writing of conducting polymers.

    PubMed

    Aydemir, Nihan; Parcell, James; Laslau, Cosmin; Nieuwoudt, Michel; Williams, David E; Travas-Sejdic, Jadranka

    2013-08-01

    Described herein is a new printing method-direct writing of conducting polymers (CPs)-based on pipette-tip localized continuous electrochemical growth. A single barrel micropipette containing a metal wire (Pt) is filled with a mixture of monomer, supporting electrolyte, and an appropriate solvent. A droplet at the tip of the pipette contacts the substrate, which becomes the working electrode of a micro-electrochemical cell confined to the tip droplet and the pipette. The metallic wire in the pipette acts as both counter and reference electrode. Electropolymerization forms the CP on the working electrode in a pattern controlled by the movement of the pipette. In this study, various width poly(pyrrole) 2D and 3D structures are extruded and characterized in terms of microcyclic voltammetry, Raman spectroscopy, and scanning electron microscopy. PMID:23857715

  3. Direct writing of conducting polymers.

    PubMed

    Aydemir, Nihan; Parcell, James; Laslau, Cosmin; Nieuwoudt, Michel; Williams, David E; Travas-Sejdic, Jadranka

    2013-08-01

    Described herein is a new printing method-direct writing of conducting polymers (CPs)-based on pipette-tip localized continuous electrochemical growth. A single barrel micropipette containing a metal wire (Pt) is filled with a mixture of monomer, supporting electrolyte, and an appropriate solvent. A droplet at the tip of the pipette contacts the substrate, which becomes the working electrode of a micro-electrochemical cell confined to the tip droplet and the pipette. The metallic wire in the pipette acts as both counter and reference electrode. Electropolymerization forms the CP on the working electrode in a pattern controlled by the movement of the pipette. In this study, various width poly(pyrrole) 2D and 3D structures are extruded and characterized in terms of microcyclic voltammetry, Raman spectroscopy, and scanning electron microscopy.

  4. 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.

  5. Thermal conductivity and multiferroics of electroactive polymers and polymer composites

    NASA Astrophysics Data System (ADS)

    Jin, Jiezhu

    /m˙K, greatly affected by the phonon-phonon scattering and phonon boundary scattering. When the films are thicker than 130 nm, heat capacity also plays an important role in thermal conduction in polyaniline. The same technique is extended to measure the electrical and thermal conductivity of 55 nm thick polyaniline thin films doped with different levels of camphorsulfonic acid. Results indicate that the effect of the doping level (camphorsulfonic acid/polyaniline ratio) is more pronounced on electrical conductivity than on thermal conductivity, thereby greatly affecting their ratio that determines the thermoelectric efficiency. At the 60% doping level, polyaniline thin film exhibits the maximum electrical and thermal conductivity due to the formation of mostly delocalized polaron structures. It is suggested that polarons are the charge carriers responsible for the electrical conduction, while phonons play a dominant role in the heat conduction in doped polyaniline thin films. Multiferroic materials combine unusual elastic, magnetic and electric properties, and have promising applications in many areas, such as sensors, transducers and read/write memory devices. For strain-mediated multiferroic ME composites, their ME effect are generated as a product property of the piezoelectric phase and magnetostrictive phase. In this dissertation, new multiferroic composites are developed and presented. One of them is based on chain-end cross-linked ferroelectric poly(vinylidene fluoride-co-trifluoroethylene) (PVDF-TrFE). With a low dc bias magnetic field, the ME coefficient of this composite is 17.7 V/cm Oe at non-resonance and 383 V/cm Oe at resonance, well above the reported ME voltage coefficient of polymer based ME composite in current literature. ME composite based on poly(vinylidene fluoride-co-hexafluoropropylene) P(VDF-HFP) are also developed in this dissertation. Crystalline beta phase structure in P(VDF-HFP) is produced by uniaxially stretching of pre-melted and quenched films

  6. 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.

  7. 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.

  8. Highly cross-linked nanoporous polymers

    DOEpatents

    Steckle, W.P. Jr.; Apen, P.G.; Mitchell, M.A.

    1998-01-20

    Condensation polymerization followed by a supercritical extraction step can be used to obtain highly cross-linked nanoporous polymers with high surface area, controlled pore sizes and rigid structural integrity. The invention polymers are useful for applications requiring separation membranes. 1 fig.

  9. 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.

  10. 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.

  11. Nanostructured conductive polymers for advanced energy storage.

    PubMed

    Shi, Ye; Peng, Lele; Ding, Yu; Zhao, Yu; Yu, Guihua

    2015-10-01

    Conductive polymers combine the attractive properties associated with conventional polymers and unique electronic properties of metals or semiconductors. Recently, nanostructured conductive polymers have aroused considerable research interest owing to their unique properties over their bulk counterparts, such as large surface areas and shortened pathways for charge/mass transport, which make them promising candidates for broad applications in energy conversion and storage, sensors, actuators, and biomedical devices. Numerous synthetic strategies have been developed to obtain various conductive polymer nanostructures, and high-performance devices based on these nanostructured conductive polymers have been realized. This Tutorial review describes the synthesis and characteristics of different conductive polymer nanostructures; presents the representative applications of nanostructured conductive polymers as active electrode materials for electrochemical capacitors and lithium-ion batteries and new perspectives of functional materials for next-generation high-energy batteries, meanwhile discusses the general design rules, advantages, and limitations of nanostructured conductive polymers in the energy storage field; and provides new insights into future directions.

  12. 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.

  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. 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.

  15. 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.

  16. 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.

  17. 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.

  18. Thiazolothiazole-linked porous organic polymers

    SciTech Connect

    Zhu, Xiang; Tian, Chengcheng; Jin, Tian; Wang, Jitong; Mahurin, Shannon Mark; Mei, Wenwen; Xiong, Yan; Hu, Jun; Feng, Xinliang; Liu, Honglai; Dai, Sheng

    2014-10-07

    In this study, thiazolothiazole-linked porous organic polymers have been synthesized from a facile catalyst-free condensation reaction between aldehydes and dithiooxamide under solvothermal conditions. The resultant porous frameworks exhibit a highly selective uptake of CO2 over N2 under ambient conditions.

  19. Thiazolothiazole-linked porous organic polymers

    DOE PAGESBeta

    Zhu, Xiang; Tian, Chengcheng; Jin, Tian; Wang, Jitong; Mahurin, Shannon Mark; Mei, Wenwen; Xiong, Yan; Hu, Jun; Feng, Xinliang; Liu, Honglai; et al

    2014-10-07

    In this study, thiazolothiazole-linked porous organic polymers have been synthesized from a facile catalyst-free condensation reaction between aldehydes and dithiooxamide under solvothermal conditions. The resultant porous frameworks exhibit a highly selective uptake of CO2 over N2 under ambient conditions.

  20. 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.

  1. 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.

  2. 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

  3. 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.

  4. 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.

  5. 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.

  6. 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.

  7. 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.

  8. 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.

  9. 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.

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

    SciTech Connect

    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.

  11. Maskless electrodeposited contact for conducting polymer nanowires

    NASA Astrophysics Data System (ADS)

    Hangarter, Carlos M.; Bangar, Mangesh; Hernandez, Sandra C.; Chen, Wilfred; Deshusses, Marc A.; Mulchandani, Ashok; Myung, Nosang V.

    2008-02-01

    This letter reports a simple and scalable method to create mechanical joints and electrical contacts of conducting polymer nanowires to electrodes by selective maskless metal electrodeposition on electrodes. This is an attractive route for contacting nanowires as it bypasses harsh processing conditions of conventional methods. The electrodeposition conditions and initial resistance of the nanowires were found to have a significant impact on the selective maskless deposition. Different dopants were also investigated to understand the polymer reduction during cathodic deposition of metal. A single dodecyl sulfate doped polypyrrole nanowire with maskless electrodeposited nickel contacts was shown to have improved sensitivity toward ammonia gas.

  12. 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.

  13. 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.

  14. Conducting polymers are simultaneous sensing actuators

    NASA Astrophysics Data System (ADS)

    Córdova, Fransisco G.; Ismail, Yahya A.; Martinez, Jose G.; Al Harrasi, Ahmad S.; Otero, Toribio F.

    2013-04-01

    Conducting polymers are soft, wet and reactive gels capable of mimicking biological functions. They are the electrochemomechanical actuators having the ability to sense the surrounding variables simultaneously. The sensing and actuating signals are sent/received back through the same two connecting wires in these materials. The sensing ability is a general property of all conducting polymers arises from the unique electrochemical reaction taking place in them. This sensing ability is verified for two different conducting polymers here - for an electrochemically generated polypyrrole triple layer bending actuator exchanging cations and for a chemically generated polytoluidine linear actuator exchanging anions. The configuration of the polypyrrole actuator device corresponds to polypyrrole-dodecyl benzene sulfonate (pPy-DBS) film/tape/ pPy-DBS film in which the film on one side of the triple layer is acted as anode and the film on the other side acted as cathode simultaneously, and the films interchanged their role when move in the opposite direction. The polytoluidine linear actuator was fabricated using a hydrgel microfiber through in situ chemical polymerization. The sensing characteristics of these two actuators were studied as a function of their working conditions: applied current, electrolyte concentration and temperature in aqueous electrolytes. The chronopotentiometric responses were studied by applying square electrical currents for a specified time. For the pPy actuator it was set to produce angular movement of +/- 45° by the free end of the actuator, consuming constant charges of 60 mC. In both the actuators the evolution of the muscle potential along the electrical current cycle was found to be a function of chemical and physical variables acting on the polymer reaction rates: electrolyte concentration, temperature or driving electrical current. The muscle potential evolved decreases with increasing electrolyte concentrations, increasing temperatures or

  15. 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.

  16. 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.

  17. 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.

  18. 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.

  19. 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.

  20. 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

  1. Optimizing end-group cross-linking polymer electrolytes for fuel cell applications

    SciTech Connect

    Kim, Yu Seung; Lee, Kwan Soo; Jeong, Myung - Hwan; Lee, Jae - Suk

    2009-01-01

    This paper demonstrates the optimization of proton conductivity and water uptake for cross-linkable polymer electrolytes through synthesis and characterization of end-group cross-linkable sulfonated poly(arylene ether) copolymers (ESF-BPs). The extent of reaction of cross-linking was controlled by reaction time resulting in a series of polymers with two, independent tunable parameters, degree of sulfonation (DS) and degree of cross-linking (DC). For the polymers presented, cross-linking improved proton conductivity while reducing water uptake, an uncommon trend in polymer electrolytes where water is critical for proton conduction. Other trends relating to changes are reported and the results yield insight into the role of DS and DC and how to optimize electrochemical properties and performance of polymer electrolytes through these tunable parameters. Select polymer electrolytes were tested in fuel cells where performance and durability with accelerated relative humidity cycling were compared with Nafion{reg_sign}.

  2. 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

  3. 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.

  4. Electrochemical Analysis of Conducting Polymer Thin Films

    PubMed Central

    Vyas, Ritesh N.; Wang, Bin

    2010-01-01

    Polyelectrolyte multilayers built via the layer-by-layer (LbL) method has been one of the most promising systems in the field of materials science. Layered structures can be constructed by the adsorption of various polyelectrolyte species onto the surface of a solid or liquid material by means of electrostatic interaction. The thickness of the adsorbed layers can be tuned precisely in the nanometer range. Stable, semiconducting thin films are interesting research subjects. We use a conducting polymer, poly(p-phenylene vinylene) (PPV), in the preparation of a stable thin film via the LbL method. Cyclic voltammetry and electrochemical impedance spectroscopy have been used to characterize the ionic conductivity of the PPV multilayer films. The ionic conductivity of the films has been found to be dependent on the polymerization temperature. The film conductivity can be fitted to a modified Randle’s circuit. The circuit equivalent calculations are performed to provide the diffusion coefficient values. PMID:20480052

  5. 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

  6. Electrochemical relaxation at electrically conducting polymers

    NASA Astrophysics Data System (ADS)

    Nateghi, M. R.; zarandi, M. B.

    2008-08-01

    In this study, slow relaxation (SR) associated with the electroreduction of polyaniline (PAn) films during polarization to high cathodic potentials was investigated by cyclic voltammetry technique. Anodic voltammetric currents were used as experimental variable to indicate the relaxation occurring in PAn films deposited electrochemically on the Pt electrode surface. The dependence of SR on polymer film thickness, waiting potential, and mobility of the doped anion was investigated. Percolation threshold potential for heteropolyanion doped PAn was estimated to be between 150 and 200 mV depending on polymer thickness on the electrode surface. A new model of the conducting to insulating conversion is described by the percolation theory and mobility gap changes during the process.

  7. 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.

  8. 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.

  9. 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.

  10. 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.

  11. Cross-Linking Aromatic Polymers With Ionizing Radiation

    NASA Technical Reports Server (NTRS)

    Bell, Vernon L.; Havens, Stephen J.

    1987-01-01

    Resistance to heat and solvents increased. Certain aromatic polymers containing radiation-sensitive methylene groups cross-linked through methylene groups upon exposure to ionizing radiation. Cross-linked polymers resistant to most organic solvents and generally more resistant to high temperatures, with less tendency to creep under load. No significant embrittlement of parts fabricated from these polymers when degree of cross-linking, as controlled by irradiation dose, kept at moderate level.

  12. 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).

  13. 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.

  14. Enzyme linked immunoassay with stabilized polymer saccharide enzyme conjugates

    DOEpatents

    Callstrom, M.R.; Bednarski, M.D.; Gruber, P.R.

    1997-11-25

    An improvement in enzyme linked immunoassays is disclosed wherein the enzyme is in the form of a water soluble polymer saccharide conjugate which is stable in hostile environments. The conjugate comprises the enzyme which is linked to the polymer at multiple points through saccharide linker groups. 19 figs.

  15. Enzyme linked immunoassay with stabilized polymer saccharide enzyme conjugates

    DOEpatents

    Callstrom, Matthew R.; Bednarski, Mark D.; Gruber, Patrick R.

    1997-01-01

    An improvement in enzyme linked immunoassays is disclosed wherein the enzyme is in the form of a water soluble polymer saccharide conjugate which is stable in hostile environments. The conjugate comprises the enzyme which is linked to the polymer at multiple points through saccharide linker groups.

  16. Photogeneration of polaron pairs in conducting polymers

    NASA Astrophysics Data System (ADS)

    Conwell, E. M.; Mizes, H. A.

    1995-03-01

    It is usually assumed that when photogeneration in a conducting polymer results in an electron and hole on separate chains they form negative and positive polarons that can move independently of each other. We show, on the basis of the small carrier yield per photon seen in picosecond photoconductivity, the different behavior of photoinduced absorption (PA) in dilute solution and thin films, and the spectral distribution of the PA in thin films, that photogenerated positive and negative polarons in poly(p-phenylene vinylene), polythiophene, and polyacetylene are, for the most part, bound in pairs by their Coulomb attraction. We also show that PA data give evidence for a gap of 2.8 eV, and thus an exciton binding energy of 0.4 eV, in poly(p-phenylene vinylene).

  17. Chemical synthesis of chiral conducting polymers

    SciTech Connect

    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.

  18. Chemical synthesis of chiral conducting polymers

    SciTech Connect

    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.

  19. Improved thermally conducting electron transfer polymers

    NASA Technical Reports Server (NTRS)

    Jenkins, R. K.; Byrd, N. R.; Lister, J. L.

    1972-01-01

    Development of polymers with improved heat transfer coefficients for use in encapsulating electronic modules is discussed. Chemical reactions for synthesizing the polymers are described and thermodynamic and physical properties are analyzed.

  20. 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.

  1. 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

  2. Electrochemical post-functionalization of conducting polymers.

    PubMed

    Inagi, Shinsuke; Fuchigami, Toshio

    2014-05-01

    This article summarizes recent progress in the post-functionalization of conjugated polymers by electrochemical methods. These electrochemical polymer reactions typically proceed via electrochemical doping of a conjugated polymer film, followed by chemical transformation. Examples include the quantitative oxidative fluorination of polyfluorenes and oxidative halogenation of polythiophenes, as well as the reductive hydrogenation of polyfluorenones. The degree of functionalization, otherwise known as the reaction ratio, can be controlled by varying the charge passed through the polymer, allowing the optoelectronic properties of the conjugated polymers to be tailored. Wireless bipolar electrodes with an in-plane potential distribution are also useful with regard to the electrochemical doping and reaction of conjugated polymers and allow the synthesis of films exhibiting composition gradients. Such bipolar electrochemistry can induce multiple reaction sites during electrochemical polymer reactions.

  3. 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.

  4. 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.

  5. 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.

  6. 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.

  7. 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.

  8. Anion-Conducting Polymer, Composition, and Membrane

    DOEpatents

    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.

  9. 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.

  10. 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.

  11. EFFECTS OF TRITIUM GAS EXPOSURE ON ELECTRICALLY CONDUCTING POLYMERS

    SciTech Connect

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

    2009-12-16

    main backbone chain, or by protonation of the imine groups [de Acevedo, 1999]. There are several types of radiation sensors commercially available, including ionization chambers, geiger counters, proportional counters, scintillators and solid state detectors. Each type has advantages, although many of these sensors require expensive electronics for signal amplification, are large and bulky, have limited battery life or require expensive materials for fabrication. A radiation sensor constructed of a polymeric material could be flexible, light, and the geometry designed to suit the application. Very simple and inexpensive electronics would be necessary to measure the change in conductivity with exposure to radiation and provide an alarm system when a set change of conductivity occurs in the sensor that corresponds to a predetermined radiation dose having been absorbed by the polymer. The advantages of using a polymeric sensor of this type rather than those currently in use are the flexibility of sensor geometry and relatively low cost. It is anticipated that these sensors can be made small enough for glovebox applications or have the ability to monitor the air tritium levels in places where a traditional monitor cannot be placed. There have been a few studies on the changes in conductivity of polyaniline specifically for radiation detection [de Acevedo, 1999; Lima Pacheco, 2003], but there have been no reports on the effects of tritium (beta radiation) on conducting polymers, such as polyaniline or polythiophene. The direct implementation of conducting polymers as radiation sensor materials has not yet been commercialized due to differing responses with total dose, dose rate, etc. Some have reported a large increase in the surface conductivity with radiation dose while others report a marked decrease in conductive properties; these differing observations may reflect the competing mechanisms of chain scission and cross-linking. However, it is clear that the radiation dose

  12. 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.

  13. Proton Conductive Nanosheets Formed by Alignment of Metallo-Supramolecular Polymers.

    PubMed

    Pandey, Rakesh K; Rana, Utpal; Chakraborty, Chanchal; Moriyama, Satoshi; Higuchi, Masayoshi

    2016-06-01

    Linear Fe(II)-based metallo-supramolecular polymer chains were precisely aligned by the simple replacement of the counteranion with an N,N'-bis(4-benzosulfonic acid)perylene-3,4,9,10-tetracarboxylbisimide (PSA) dianion, which linked the polymer chains strongly. A parallel alignment of the polymer chains promoted by the PSA dianions yielded nanosheets formation. The nanosheets' structure was analyzed with FESEM, HRTEM, UV-vis, and XRD in detail. The nanosheets showed more than 5 times higher proton conductivity than the original polymer due to the smooth ionic conduction through the aligned polymer chains. The complex impedance plot with two semicircles also suggested the presence of grain boundaries in the polymer nanosheets. PMID:27164027

  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. 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.

  16. Nanostructured conducting polymer hydrogels for energy storage applications.

    PubMed

    Shi, Ye; Peng, Lele; Yu, Guihua

    2015-08-14

    Conducting polymer hydrogels are emerging as a promising class of polymeric materials for various technological applications, especially for energy storage devices due to their unique combination of advantageous features of conventional polymers and organic conductors. To overcome the drawbacks of conventional synthesis, new synthetic routes in which acid molecules are adopted as both crosslinkers and dopants have been developed for conducting polymer hydrogels with unique 3D hierarchical porous nanostructures, resulting in high electrical conductivity, large surface area, structural tunability and hierarchical porosity for rapid mass/charge transport. The newly developed conducting polymer hydrogels exhibit high performance when applied as active electrode materials for electrochemical capacitors or as functional binder materials for high-energy lithium-ion batteries. This feature article summarizes the synthesis of conducting polymer hydrogels, presents their applications in energy storage, and discusses further opportunities and challenges.

  17. 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

  18. 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.

  19. Low-Thermal-Conduction Links For Silicon Sensors

    NASA Technical Reports Server (NTRS)

    Mott, D. Brent

    1991-01-01

    Simple method of texturing surface of silicon reduces thermal conductivities of links in silicon x-ray calorimeters and infrared bolometers. Gives links high density of phonon scattering sites reducing conduction of heat. Links made shorter and more robust. Used in making x-ray calorimeters and infrared bolometers. Applicable to any microelectronic device in which high degree of thermal isolation needed.

  20. 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.

  1. 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.

  2. 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.

  3. 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.

  4. 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

  5. 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.

  6. Unusually conductive carbon-inherently conducting polymer (ICP) composites: Synthesis and characterization

    NASA Astrophysics Data System (ADS)

    Bourdo, Shawn Edward

    Two groups of materials that have recently come to the forefront of research initiatives are carbon allotropes, especially nanotubes, and conducting polymers-more specifically inherently conducting polymers. The terms conducting polymers and inherently conducting polymers sometimes are used interchangeably without fully acknowledging a major difference in these terms. Conducting polymers (CPs) and inherently conducting polymers (ICPs) are both polymeric materials that conduct electricity, but the difference lies in how each of these materials conducts electricity. For CPs of the past, an electrically conductive filler such as metal particles, carbon black, or graphite would be blended into a polymer (insulator) allowing for the CP to carry an electric current. An ICP conducts electricity due to the intrinsic nature of its chemical structure. The two materials at the center of this research are graphite and polyaniline. For the first time, a composite between carbon allotropes (graphite) and an inherently conducting polymer (PANI) has exhibited an electrical conductivity greater than either of the two components. Both components have a plethora of potential applications and therefore the further investigation could lead to use of these composites in any number of technologies. Touted applications that use either conductive carbons or ICPs exist in a wide range of fields, including electromagnetic interference (EMI) shielding, radar evasion, low power rechargeable batteries, electrostatic dissipation (ESD) for anti-static textiles, electronic devices, light emitting diodes (LEDs), corrosion prevention, gas sensors, super capacitors, photovoltaic cells, and resistive heating. The main motivation for this research has been to investigate the connection between an observed increase in conductivity and structure of composites. Two main findings have resulted from the research as related to the observed increase in conductivity. The first was the structural evidence from

  7. Conducting polymers on microelectronic devices as tools for biological analyses.

    PubMed

    Livache, T; Bazin, H; Mathis, G

    1998-12-01

    In the field of biological analysis, the need for multiparametric analysis has prompted the development of supports bearing a series of biomolecules linked to a support in a precise location (addressed). To reach a high information density, miniaturization of this kind of support has to be carried out. We describe in this paper an approach involving the use of electro-conducting polymers such as polypyrrole. This technology is based on an electro-directed copolymerization of pyrrole and oligodeoxynucleotides (ODN) linked to a pyrrole residue. The process allows the grafting of the selected ODN at the surface of the successively addressed microelectrodes. In this way, the syntheses are carried out on 50 microm electrodes on passive chips or on active (multiplexed) chips bearing 48 or 128 gold microelectrodes, respectively. The detection of biological targets recognized by the biochip is carried out by using fluorescent tracers. This technology, involving prepurified materials precisely addressed, allows better reproducibility of the biochip preparation and, then, an easy interpretation of the fluorescence results. The versatility of this technology is illustrated by ODN or peptide copolymerizations leading to DNA chips or peptide chips, respectively. This would open the field for other biological interaction studies.

  8. 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.

  9. 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.

  10. Decoupling order and conductivity in doped conducting polymers.

    PubMed

    Mayevsky, David; Gann, Eliot; Garvey, Christopher J; McNeill, Christopher R; Winther-Jensen, Bjorn

    2016-07-28

    Herein it is demonstrated that the high level of interchain ordering of pEDOT is not necessary for the polymer to have efficient charge transport. Resistance and order are compared during the manufacturing process, where the polymerisation step and ordering step are decoupled as separate stages of the processing. GIWAXS experiments measuring interchain order are correlated to resistivity measurements at multiple stages of the manufacturing process on single films, and it is shown that for an individual film, where percolation is achieved, having a long range ordered system offers no reduction in resistance compared to having a highly disordered state of the same film. For this system, once the chains of pEDOT are formed, it is experimentally demonstrated that for percolation to be achieved, a remarkably low 4.5% volume fraction pEDOT is required. The apparent lack of necessity for significant interchain ordering allows for a meaningful measurement of development of the charge transport during the chemical polymerisation process. PMID:27374244

  11. Amine-functionalized polypyrrole: inherently cell adhesive conducting polymer

    PubMed Central

    Lee, Jae Y.; Schmidt, Christine E.

    2014-01-01

    Electrically conducting polymers have been recognized as novel biomaterials that can electrically communicate with biological systems. For their tissue engineering applications, conducting polymers 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 conducting polymers 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 conducting polymer substrates will be useful to achieve good cell adhesion and potentially electrically stimulate various cells. In addition, an amine functionality present on conducting polymers 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

  12. Multilayer structured polymer light emitting diodes with cross-linked polymer matrices

    NASA Astrophysics Data System (ADS)

    Zhou, Zhang-Lin; Sheng, Xia; Nauka, K.; Zhao, Lihua; Gibson, Gary; Lam, Sity; Yang, Chung Ching; Brug, James; Elder, Rich

    2010-01-01

    Currently, there is great interest in manufacturing multilayer polymer light emitting diode (PLED) structures via low-cost solution-based spin-casting or printing methods. The difficulty with this approach is that solvent from freshly deposited films often dissolves the underlying layers. This letter demonstrates that fully operational multilayer PLED structures can be fabricated via a solution process by embedding the hole transport material in cross-linked inert polymer matrices that protect the functional material while subsequent layers are deposited using the same solvent. The resulting devices exhibited greatly improved quantum efficiency compared with devices that did not employ cross-linked polymer matrices.

  13. 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.

  14. 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.

  15. 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.

  16. 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.

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

    NASA Astrophysics Data System (ADS)

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

    2015-12-01

    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.

  18. Preparation of Conductive Polymer Polyanilines for an Experiment for Students

    NASA Astrophysics Data System (ADS)

    Yano, Jun; Matsuzaki, Kiyoka; Ichimori, Hayato; Ito, Takeshi; Okano, Hiroshi; Osaki, Nobukazu

    For an organic and polymer chemistry experiment for students in university and college of technology, synthesis of conducting polymers was attempted. Three conductive polymers, polyaniline, poly (o-phenylenediamine) and poly (N-methylaniline) , were prepared by oxidative polymerizations of the corresponding monomers. Among four oxidizing agents, K2Cr2O7, KIO3, FeCl3 and (NH4) 2S2O8, (NH4) 2S2O8 was turned out to be the best oxidizing agent for the polymerizations. The polymerizing solutions gradually colored because of the formation of colored oligomers, which was monitored with the absorption spectra measured during the polymerizations. Since the time for experiment was limited, the molar ratio of [ (NH4) 2S2O8] to [monomer] was taken 2 : 1. The experiment was demonstrated in the organic and polymer chemistry experiments and was evaluated by students as well as teachers.

  19. Electronic structure calculations on helical conducting polymers.

    PubMed

    Ripoll, Juan D; Serna, Andrei; Guerra, Doris; Restrepo, Albeiro

    2010-10-21

    We present a study of the electronic structure and derived properties of polyfurane (PFu), polypyrrol (PPy), and polythiophene (PTh). Two spatial arrangements are considered: trans chain (tc-PFu, tc-PPy, tc-PTh) and cis α-helical (α-PFu, α-PPy, α-PTh). Even at the small sizes considered here, helical conformations appear to be stable. Band gaps of pure, undoped oligomers fall into the semiconductor range. Density of states (DOS) analysis suggest dense valence and conduction bands. Bond length alternation analysis predicts almost complete delocalization of the π clouds in all spatial arrangements. Doping with electron donors or electron-withdrawing impurities reduces all band gaps close to the metallic regime in addition to increasing the DOS for the valence and conduction bands.

  20. 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.

  1. Stabilization of zinc electrodes with a conducting polymer

    NASA Astrophysics Data System (ADS)

    Vatsalarani, J.; Geetha, S.; Trivedi, D. C.; Warrier, P. C.

    The reversibility of zinc anode in alkaline medium was enhanced by electrostatic deposition of a conducting polymer (polypyrrole). Electropolymerization of pyrrole onto zinc in aqueous medium using an organic acid as dopant is feasible and preferred as zinc is less corrosive in this medium. The structure of the polymer film was analyzed by FT-IR spectroscopy and scanning electron microscopy. The effect of the polypyrrole deposit on the zinc electrode was studied by cyclic voltammetry and charge-discharge cycling.

  2. 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.

  3. 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.

  4. Hybrid high-temperature superconductor/conducting polymer systems

    NASA Astrophysics Data System (ADS)

    Jones, Christopher Todd

    Hybrid systems of high-temperature superconductors and conducting polymers have been assembled and their properties assayed. Studies were conducted on several systems including bilayer thin film assemblies, particle composites, and intercalation materials. Crucial to the preparation of these ceramic/polymer composites is the availability of a pristine high-temperature superconductor surface and the identification of new synthetic methods that are capable of combining in an intimate manner these two different phases of electronic material. Surface corrosion and crystallographic orientation of the superconductor are found to be important variables which influence the polymer/cuprate charge transfer characteristics. To prepare many of the polymer composites described herein electrodeposition methods were employed. In this context, self-assembled monolayers were found to dramatically affect growth and the surface morphology of electrochemically deposited polypyrrole on bulk and thin film superconductors of YBasb2Cusb3Osb{7-x}. Conductivity experiments were performed to measure the temperature dependence of resistivity, superconducting transition temperature, and critical currents before and after polymer deposition as well as before and after polymer doping. Modulation of the transition temperature in superconducting/conducting polymer bilayer assemblies was accomplished by oxidative and reductive doping of the conducting polymer. These bilayer systems were used to create a "molecular switch" for lowering and raising the transition temperature of the superconductor. As another method for preparing composite polymer/superconductor structures, the intercalation of polypyrrole into the lattice of various Bi-Sr-Ca-Cu-O phases was accomplished by vapor phase exposure of iodine intercalated Bi-Sr-Ca-Cu-O with pyrrole monomer. X-ray powder diffraction was used to assess the structural changes which occur upon pyrrole exposure. Likewise, an increase of a 3.5 A in the distance

  5. 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…

  6. Vapour phase polymerisation of conducting and non-conducting polymers: a review.

    PubMed

    Lawal, Abdulazeez T; Wallace, Gordon G

    2014-02-01

    Vapour phase polymerisation (VPP) is a well established technique in which the monomer is introduced to an oxidant-coated substrate in vapour form. Polymerisation then takes place at the oxidant vapour interface. VPP is a technique that could be used to immobilise materials to the modified electrode surface. This review article concentrates on the VPP of conducting polymers such as Polypyrrole (PPy) polythiophen (PT) and polyaniline (PANi). VPP of conducting polymers and other non-conducting polymers have extensively been investigated. This review article is divided into three main parts as given in Table of contents related to the VPP process of some important conducting polymers such as PPy, PT, PANi and Poly(3,4-ethylenedioxythiophene). A total of 181 references are cited in this review article and it attempts to look into VPP from inception of the method till present day. PMID:24401395

  7. Studies on conducting polymer and conducting polymerinorganic composite electrodes prepared via a new cathodic polymerization method

    NASA Astrophysics Data System (ADS)

    Singh, Nikhilendra

    A novel approach for the electrodeposition of conducting polymers and conducting polymer-inorganic composite materials is presented. The approach shows that conducting polymers, such as polypyrrole (PPy) and poly(3,4-ethylenedioxythiophene) (PEDOT) can be electrodeposited by the application of a cathodic bias that generates an oxidizing agent, NO+, via the in-situ reduction of nitrate anions. This new cathodic polymerization method allows for the deposition of PPy and PEDOT as three dimensional, porous films composed of spherical polymer particles. The method is also suitable for the co-deposition of inorganic species producing conducting polymer-inorganic composite electrodes. Such composites are used as high surface area electrodes in Li-ion batteries, electrochemical hydrogen evolution and in the development of various other conducting polymer-inorganic composite electrodes. New Sn-PPy and Sb-PPy composite electrodes where Sn and Sb nanoparticles are well dispersed among the PPy framework are reported. These structures allow for decreased stress during expansion and contraction of the active material (Sn, Sb) during the alloying and de-alloying processes of a Li-ion battery anode, significantly alleviating the loss of active material due to pulverization processes. The new electrochemical synthesis mechanism allows for the fabrication of Sn-PPy and Sb-PPy composite electrodes directly from a conducting substrate and eliminates the use of binding materials and conducting carbon used in modern battery anodes, which significantly simplifies their fabrication procedures. Platinum (Pt) has long been identified as the most efficient catalyst for electrochemical water splitting, while nickel (Ni) is a cheaper, though less efficient alternative to Pt. A new morphology of PPy attained via the aforementioned cathodic deposition method allows for the use of minimal quantities of Pt and Ni dispersed over a very high surface area PPy substrate. These composite electrodes

  8. Nanostructure Titania Reinforced Conducting Polymer Composites

    NASA Astrophysics Data System (ADS)

    Kondawar, S. B.; Thakare, S. R.; Khati, V.; Bompilwar, S.

    Composites of polyaniline with synthesized nanostructured titania (TiO2) and polyaniline with commercial TiO2 have been in situ synthesized by oxidative chemical polymerization method. Sulfuric acid was used as dopant during the polymerization process. Sol-gel precipitates of nanostructured titania were synthesized by hydrolyzing the mixture of titanium chloride (TiCl3) and colloidal transparent solution of starch. Composite materials were subjected for comparison to spectroscopic and X-ray diffraction analysis. Strong coupling/interaction of titania with the imine nitrogen in polyaniline confirmed by FTIR spectral analysis. XRD shows the composite of synthesized titania with polyaniline have broaden peak as compared to that of commercial titania with polyaniline indicating particle size in the range of nanometer scale which is supported by 40 nm particle size of the synthesized titania from TEM picture. Increase in conductivity with increasing temperature was observed in both the composite materials.

  9. Conducting polymers as active materials in electrochemical capacitors

    NASA Astrophysics Data System (ADS)

    Rudge, Andy; Davey, John; Raistrick, Ian; Gottesfeld, Shimshon; Ferraris, John P.

    Electronically conducting polymer represent an interesting clas of materials for use in electrochemical capacitors thanks to the combination of high capacitive energy density and low materials cost. Three generalized typed of electrochemical capacitors can be constructed using conducting polymers as active material, and in the third of these, which utilized conducting polymers that can be both n- and p-doped, energy densities of up to 39 Wh per kg of active material on both electrodes have been demonstrated. This energy density is obtained using poly-3-(4-fluorophenyl)-thiophene (PEPT) in an electrolyte of 1 M tetramethylammonium trifluoromethanesulfonate (TMATFMS) in acetonitrile. This unique system exhibits reversible n- and p-doping to high charge density in relatively thich films of the active polymer and a cell voltage exceeding 3 V in the fully charged state. Impedance data for both n- and p-doped PFPT suggest that high power densities can be obtained in electrochemical capacitors based on this active conducting polymer.

  10. Synthesis of conducting polymer nanospheres of high electrochemical activity.

    PubMed

    Kłucińska, Katarzyna; Jaworska, Ewa; Gryczan, Piotr; Maksymiuk, Krzysztof; Michalska, Agata

    2015-08-14

    We propose a novel approach to obtain conducting polymer nanoparticles with high electrochemical activity and a narrow size distribution. The method - templateless and seedless - uses polyacrylate microspheres to deliver the monomer for the polymerization reaction. Thus the obtained nanostructures have an active - unblocked - surface allowing fast charge/ion-exchange and the formation of stable suspensions in water. The obtained nanostructures have the potential to be applied in different fields ranging from conductive coatings and additives for increasing electronic conductivity, to electrochemical sensors.

  11. New Aptes Cross-linked Polymers from Poly(ethylene oxide)s and Cyanuric Chloride for Lithium Batteries

    NASA Technical Reports Server (NTRS)

    Tigelaar, Dean M.; Meador, Mary Ann B.; Kinder, James D.; Bennett, William R.

    2005-01-01

    A new series of polymer electrolytes for use as membranes for lithium batteries are described. Electrolytes were made by polymerization between cyanuric chloride and diamino-terminated poly(ethylene oxide)s, followed by cross-linking via a sol-gel process. Thermal analysis and lithium conductivity of freestanding polymer films were studied. The effects of several variables on conductivity were investigated, such as length of backbone PEO chain, length of branching PEO chain, extent of branching, extent of cross-linking, salt content, and salt counterion. Polymer films with the highest percentage of PEO were found to be the most conductive, with a maximum lithium conductivity of 3.9 x 10(exp -5) S/cm at 25 C. Addition of plasticizer to the dry polymers increased conductivity by an order of magnitude.

  12. Orienting semi-conducting π-conjugated polymers.

    PubMed

    Brinkmann, Martin; Hartmann, Lucia; Biniek, Laure; Tremel, Kim; Kayunkid, Navaphun

    2014-01-01

    The present review focuses on the recent progress made in thin film orientation of semi-conducting polymers with particular emphasis on methods using epitaxy and shear forces. The main results reported in this review deal with regioregular poly(3-alkylthiophene)s and poly(dialkylfluorenes). Correlations existing between processing conditions, macromolecular parameters and the resulting structures formed in thin films are underlined. It is shown that epitaxial orientation of semi-conducting polymers can generate a large palette of semi-crystalline and nanostructured morphologies by a subtle choice of the orienting substrates and growth conditions.

  13. 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.

  14. 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.

  15. 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

  16. 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.

  17. Improving conducting polymer electrochromic speeds and depositing aligned polymeric nanofibers by electrospinning process

    NASA Astrophysics Data System (ADS)

    Asemota, Chris I.

    The effects of film thickness and porosity on electrochromic switching time of conducting polymers was pursued to determine the morphology influence on ions transport during oxidation step of the redox process, affording sub-second or seconds switching times. Electrospinning technique provided non-woven nanofiber mats, while spin coating and electropolymerization of monomer (N3T) provided films. Porosity decreased as depositing method changed from electrospinning to spin coating. In electrochemical oxidation, the electrons leave the polymer at the metal electrode-polymer film interface, and counter ions arrive at the polaron-bipolaron sites left in the polymer, through polymer-electrolyte interface. Counter ion diffusion in conducting polymers are film thickness limited at increasing thickness and inability of ions to reach holes sites on the oxidizing polymer accounts for long switching speeds, introducing extensive and micro pores and high surface areas should lead to decreasing electrochromic switching speed to single digit time in seconds (for display and vision applications), while increasing the maximum optical switching contrast due to increased fiber mat thicknesses. Photolithographic patterning of nanofiber mats of the conducting polymer precursor having photo cross-linking unit was also explored. The photo-crosslinkable polymer was prepared by including norborene methacrylate (NMA) units to the polymer backbone during precursor polymerization, yielding a terpolymer poly(N3T-NA-NMA). The influence of photo crosslinking on electrochemical switching in conducting polymer nanofibers, and effect of developing parameters (solvent and time) on pattern transfer to the nanofiber mat was investigated and showed no influence on the electrochemical redox of the polymer. Solvents suitable for dissolving the polymer were investigated as developers with results showing non-differentiable pattern transfer for all suitable solvents, and no net preference to solvent choice

  18. 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.

  19. 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.

  20. 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

  1. 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

  2. Electrical conductivity of insulating polymer nanoscale layers: environmental effects.

    PubMed

    Bliznyuk, Valery; Galabura, Yuriy; Burtovyy, Ruslan; Karagani, Pranay; Lavrik, Nickolay; Luzinov, Igor

    2014-02-01

    As electronic devices are scaled down to submicron sizes, it has become critical to obtain uniform and robust insulating nanoscale polymer films. For that reason, we address the electrical properties of grafted polymer layers made of poly(glycidyl methacrylate), polyacrylic acid, poly(2-vinylpyridine), and polystyrene with thicknesses of 10-20 nm. It was found that layers insulating under normal ambient conditions can display a significant increase in conductivity as the environment changes. Namely, we demonstrated that the in-plane electrical conductivity of the polymer grafted layers can be changed by at least two orders of magnitude upon exposure to water or organic solvent vapors. Conductive properties of all polymer grafted films under study could also be significantly enhanced with an increase in temperature. The observed phenomenon makes possible the chemical design of polymer nanoscale layers with reduced or enhanced sensitivity to the anticipated change in environmental conditions. Finally, we demonstrated that the observed effects could be used in a micron-sized conductometric transducing scheme for the detection of volatile organic solvents.

  3. Hierarchically porous polymers from hyper-cross-linked block polymer precursors.

    PubMed

    Seo, Myungeun; Kim, Soobin; Oh, Jaehoon; Kim, Sun-Jung; Hillmyer, Marc A

    2015-01-21

    We report synthesis of hierarchically porous polymers (HPPs) consisting of micropores and well-defined 3D continuous mesopores by combination of hyper-cross-linking and block polymer self-assembly. Copolymerization of 4-vinylbenzyl chloride (VBzCl) with divinylbenzene (DVB) in the presence of polylactide (PLA) macro-chain-transfer agent produced a cross-linked block polymer precursor PLA-b-P(VBzCl-co-DVB) via reversible addition-fragmentation chain transfer polymerization. A nanoscopic bicontinuous morphology containing PLA and P(VBzCl-co-DVB) microdomains was obtained as a result of polymerization-induced microphase separation. While a basic treatment of the precursor selectively removed PLA to yield a reticulated mesoporous polymer, hyper-cross-linking of the precursor by FeCl3 generated micropores in the P(VBzCl-co-DVB) microdomain via Friedel-Crafts alkylation and simultaneously degraded PLA to produce the HPP containing micropores in the mesoporous framework. The mesopore size of the HPP could be precisely controlled from 6 to 15 nm by controlling the molar mass of PLA. We demonstrate acceleration in adsorption rate in the HPP compared to a hyper-cross-linked microporous polymer. PMID:25551291

  4. Tunable Nanopatterning of Conductive Polymers via Electrohydrodynamic Lithography.

    PubMed

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

    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

  5. 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

  6. Transport studies of conducting, semiconducting and photoconducting star polymers

    NASA Astrophysics Data System (ADS)

    Ferguson, John Baker

    Star polymers are studied for their transport properties in the highly conducting state doped with NOPF6 and iodine, the undoped semiconducting state and the photoconducting state. Doped star polymers exhibit variable range hopping of charge carriers. Transport dimensionality and conductivity depend intricately on the processing conditions for doping and casting films. The highest conducting diffusion doped film (room temperature conductivity 50 S/cm) exhibits 2-dimensional variable range for all doping levels. Polymers doped in solution, then cast to form films have 1.4 dimensional variable range hopping for the highest conducting samples with 10 S/cm at room temperature. The hopping dimensionality varies as the conductivity decreases. The doped star polymers remain on the insulator side of the insulator metal transition with localized carriers as revealed with Kramer-Kronig analysis. Optical and near infrared absorbance and photoluminescence reveal the core of the star polymers exist in a solid state solution of the arms with similar absorbance and luminescence for both solution and films. The arms retain the optical properties of their linear analogs indicating the core and arms do not interact quantum mechanically to produce a new state. Excitons created by absorption in the wider band gap cores rapidly migrate to the arms. Photoconductive time of flight mobility measurements reveal an almost field independent mobility at room temperature. This is due to a unique cancellation of on diagonal and off diagonal disorder in the Bassler disorder formalism. The cores introduce heterogeneous regions with a net lower mobility predicted by correlated disorder models. Space charge limited current reveals trap densities several orders of magnitude higher than the carrier density. Photovoltaic performance of star polymer and fullerene blend devices with both 20 nm and 100 nm thick layers are investigated. The thin devices have low open circuit voltages due to space charge

  7. Soft actuators based on conducting polymers: recent progress

    NASA Astrophysics Data System (ADS)

    Kaneto, Keiichi; Somekawa, H.; Takashima, Wataru

    2003-07-01

    Deformations of conducting polymer films, such as polyaniline, polypyrrole and polythiophene, induced by electrochemical oxidation and reduction are presented and discussed in terms of the mechanisms. Soft actuators with variety of motions such as bending stick, breathing ring and shouting lip utilizing polypyrrole films are demonstrated. A new operation method is proposed using electrodeposited polypyrrole films.

  8. 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

  9. 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.

  10. Investigation of anisotropic thermal transport in cross-linked polymers

    NASA Astrophysics Data System (ADS)

    Simavilla, David Nieto

    Thermal transport in lightly cross-linked polyisoprene and polybutadine subjected to uniaxial elongation is investigated experimentally. We employ two experimental techniques to assess the effect that deformation has on this class of materials. The first technique, which is based on Forced Rayleigh Scattering (FRS), allows us to measure the two independent components of the thermal diffusivity tensor as a function of deformation. These measurements along with independent measurements of the tensile stress and birefringence are used to evaluate the stress-thermal and stress-optic rules. The stress-thermal rule is found to be valid for the entire range of elongations applied. In contrast, the stress-optic rule fails for moderate to large stretch ratios. This suggests that the degree of anisotropy in thermal conductivity depends on both orientation and tension in polymer chain segments. The second technique, which is based on infrared thermography (IRT), allows us to measure anisotropy in thermal conductivity and strain induced changes in heat capacity. We validate this method measurements of anisotropic thermal conductivity by comparing them with those obtained using FRS. We find excellent agreement between the two techniques. Uncertainty in the infrared thermography method measurements is estimated to be about 2-5 %. The accuracy of the method and its potential application to non-transparent materials makes it a good alternative to extend current research on anisotropic thermal transport in polymeric materials. A second IRT application allows us to investigate the dependence of heat capacity on deformation. We find that heat capacity increases with stretch ratio in polyisoprene specimens under uniaxial extension. The deviation from the equilibrium value of heat capacity is consistent with an independent set of experiments comparing anisotropy in thermal diffusivity and conductivity employing FRS and IRT techniques. We identify finite extensibility and strain

  11. 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.

  12. Structure, morphology and ionic conductivity of solid polymer electrolyte

    SciTech Connect

    Dey, Arup; Karan, S.; Dey, Ashis; De, S.K.

    2011-11-15

    Graphical abstract: Two-dimensional atomic force image of pure polyethylene oxide presents a crystallized network of regular spherulites developing spirals and branches of well distributed surface contours. Highlights: {yields} The incorporation of ceria significantly modifies the morphology of polyethylene oxide (PEO)-KI complex. {yields} The ionic conductivity increases by about two orders of magnitude by the addition of ceria nanoparticles. {yields} Ionic conductivity as a function of ceria concentration reveals two maxima. {yields} Grain boundary effect of nanofiller, strong Lewis acid-base interaction between PEO and nanosized ceria, change of conformation of PEO molecule and epitaxial effect of ceria nanoparticles control the ionic conductivity of composite polymer electrolyte. -- Abstract: Polyethylene oxide (PEO) complexed with potassium iodide (KI) is synthesized to investigate the ionic conductivity of alkaline based polymer electrolytes. The structural and morphological characterizations of the nanocomposite polymer electrolytes are performed by X-ray diffractometry (XRD), atomic force microscopy (AFM), differential scanning calorimetry (DSC) and Fourier transform infrared spectroscopy (FTIR) measurements. The ionic conductivity increases with the increase of KI concentration up to about 20 wt.%. The effect of nanosized ceria (CeO{sub 2} {approx} 10 nm) fillers on ionic conductivity in PEO-KI polymer electrolyte is also carried out, keeping PEO to KI wt.% ratio 80:20 and 85:15. The result reveals that the addition of ceria nanoparticles enhances the conductivity by two orders of magnitude. The presence of ceria at the highest concentration induces the same molecular environment within PEO chain as that of undoped PEO. Temperature dependence of ionic conductivity follows Arrhenius mechanism.

  13. Characteristics of aluminium solid electrolytic capacitors using a conducting polymer

    NASA Astrophysics Data System (ADS)

    Yamamoto, Hideo; Oshima, Masashi; Fukuda, Minoru; Isa, Isao; Yoshino, Katsumi

    In order to form an electrochemically polymerized polypyrrole film on an electrically insulated dielectric layer surface, a conductive precoating layer was first deposited, at the expense of electrical conductivity. Using the precoating layer as the anode, a polypyrrole layer was then deposited electrochemically in preparation for the fabrication of a solid electrolytic capacitor in which the composite conducting polymer layer was used as a solid electrolyte. Soluble polyaniline could be used as a conductive precoating layer as well as polypyrrole formed by chemical oxidizing polymerization. The capacitor using the composite solid electrolyte presented excellent impedance frequency and temperature characteristics; moreover, the solid electrolyte showed 'self-healing' and non-polar behaviour.

  14. Viscoelastic study of conducting polymers using quartz crystal microbalance

    NASA Astrophysics Data System (ADS)

    Bahrami Samani, Mehrdad; Whitten, Philip; Spinks, Geoffrey; Cook, Christopher

    2006-03-01

    Application of conducting polymers has been growing widely in different fields such as batteries, solar cells, capacitors and actuators. Mechanical properties of conducting polymers like flexibility, high power to mass ratio and high active strain make them potentially applicable to robotic and automation industries. Obviously, a dynamic model of the actuation phenomenon in conducting polymers is needed to study its controllability and also to optimize the mechanical performance. De Rossi and colleagues suggest treating the mechanical behaviour of conducting polymers separately from the viscoelastic structural model and electrochemical actuation [1]. But it has been observed that the effects of electrochemical actuation and diffusion of ions on the viscoelastic coefficients cannot be neglected in some conducting polymer actuators, as shown in [1]. In this paper, we present the effects of cyclic voltammetry actuation on shear modulus of polypyrrole in propylene carbonate and EMI.TSFI as measured by an electrochemical Quartz Crystal Microbalance (eQCM). The QCM consists basically of an AT-cut piezoelectric quartz crystal disc with metallic electrode films deposited on its faces. One face is exposed to the active medium. A driver circuit applies an AC signal to the electrodes, causing the crystal to oscillate in a shear mode, at a given resonance frequency. QCM has been routinely used for the determination of mass changes. Measured resonance frequency shifts are converted into mass changes by the wellknown Sauerbrey's equation. In this paper, we correlate the admittance output of QCM to the real shear modulus of polypyrrole. Then the results of the correlation which contains mechanical data are presented during actuation using two different types of electrolyte.

  15. Conducting transparent thin films based on Carbon Nanotubes — Conducting Polymers

    NASA Astrophysics Data System (ADS)

    Ferrer-Anglada, N.; Gomis, V.; El-Hachemi, Z.; Kaempgen, M.; Roth, S.

    2004-09-01

    The present work reports on the characterization and optimization of thin transparent and electrically conducting films (from 120 to 180 nm thick) based on single walled carbon nanotubes (CNT) and conducting polymers, polypyrrole (PPy) or polyaniline (PA). We obtained a number of different CNT-PPy doped with PTS or PF6 and CNT-PA under different parameters (electrodeposition time, density current or voltage) and analyzed the required properties, electrical conductivity and transparency, and other significant properties: Raman Spectroscopy, and AFM, from which we can estimate the film thickness. The electrochemical conditions for the polymer thin film deposition were studied in order to improve their conductivity and transparency. Compared to the well known transparent conducting oxides like ITO, the best of our composite thin films are from 10 to 100 times less conductive and highly transparent. As a great possibility, these conducting films could be prepared on a flexible substrate with a continuous deposition procedure.

  16. 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.

  17. Cationic polymers inhibit the conductance of lysenin channels.

    PubMed

    Fologea, Daniel; Krueger, Eric; Rossland, Steve; Bryant, Sheenah; Foss, Wylie; Clark, Tyler

    2013-01-01

    The pore-forming toxin lysenin self-assembles large and stable conductance channels in natural and artificial lipid membranes. The lysenin channels exhibit unique regulation capabilities, which open unexplored possibilities to control the transport of ions and molecules through artificial and natural lipid membranes. Our investigations demonstrate that the positively charged polymers polyethyleneimine and chitosan inhibit the conducting properties of lysenin channels inserted into planar lipid membranes. The preservation of the inhibitory effect following addition of charged polymers on either side of the supporting membrane suggests the presence of multiple binding sites within the channel's structure and a multistep inhibition mechanism that involves binding and trapping. Complete blockage of the binding sites with divalent cations prevents further inhibition in conductance induced by the addition of cationic polymers and supports the hypothesis that the binding sites are identical for both multivalent metal cations and charged polymers. The investigation at the single-channel level has shown distinct complete blockages of each of the inserted channels. These findings reveal key structural characteristics which may provide insight into lysenin's functionality while opening innovative approaches for the development of applications such as transient cell permeabilization and advanced drug delivery systems. PMID:24191139

  18. 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.

  19. COMMUNICATION: Electrochemical polymerization of conducting polymers in living neural tissue

    NASA Astrophysics Data System (ADS)

    Richardson-Burns, Sarah M.; Hendricks, Jeffrey L.; Martin, David C.

    2007-06-01

    A number of biomedical devices require extended electrical communication with surrounding tissue. Significant improvements in device performance would be achieved if it were possible to maintain communication with target cells despite the reactive, insulating scar tissue that forms at the device-tissue interface. Here, we report that the conducting polymer poly(3,4-ethylenedioxythiophene) (PEDOT) can be polymerized directly within living neural tissue resulting in an electrically conductive network that is integrated within the tissue. Nano and microscale PEDOT filaments extend out from electrode sites, presumably forming within extracellular spaces. The cloud of PEDOT filaments penetrates out into the tissue far enough that it should be possible to bypass fibrous scar tissue and contact surrounding healthy neurons. These electrically functional, diffuse conducting polymer networks grown directly within tissue signify a new paradigm for creating soft, low impedance implantable electrodes.

  20. 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

  1. 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.

  2. 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.

  3. Development of soluble ester-linked aldehyde polymers for proteomics.

    PubMed

    Beaudette, Patrick; Rossi, Nicholas A A; Huesgen, Pitter F; Yu, Xifei; Shenoi, Rajesh A; Doucet, Alain; Overall, Christopher M; Kizhakkedathu, Jayachandran N

    2011-09-01

    High molecular weight hyperbranched polyglycerol (HPG) was selected for development as a soluble polymer support for the targeted selection and release of primary-amine containing peptides from a complex mixture. HPG has been functionalized with ester-linked aldehyde groups that can bind primary-amine containing peptides via a reductive alkylation reaction. Once bound, the high molecular weight of the polymer facilitates separation from a complex peptide mixture by employing either a 30 kDa molecular weight cutoff membrane or precipitation in acetonitrile. Following the removal of unbound peptides and reagents, subsequent hydrolysis of the ester linker releases the bound peptide into solution for analysis by mass spectrometry. Released peptides retain the linker moiety and are therefore characteristically mass-shifted. Four water-soluble cleavable aldehyde polymers (CAP1, CAP2, CAP3, and CAP4) ranging in types of linker groups, length of the linker groups, have been prepared and characterized, each demonstrating the ability to selectively enrich and sequence primary-amine peptides from a complex human proteome containing blocked (dimethylated amine) and unblocked (primary amine) peptides. The polymers have very low nonspecific peptide-binding properties while possessing significantly more reactive groups per milligram of the support than commercially available resins. The polymers exhibit a range of reactivities and binding capacities that depend on the type of linker group between the aldehyde group and the polymer. Using various linker structures, we also probed the mechanism of the observed dehydration of hydrolyzed peptides during matrix-assisted laser desorption ionization time-of-flight mass spectrometry (MALDI-TOF MS) analysis.

  4. 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

  5. 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

  6. 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.

  7. Surface Modification of the Conducting Polymer, Polypyrrole, via Affinity Peptide**

    PubMed Central

    Nickels, Jonathan D.; Schmidt, Christine E.

    2012-01-01

    A novel strategy for affinity-based surface modification of the conducting polymer, polypyrrole, (PPy), has been developed. A 12-amino acid peptide (THRTSTLDYFVI, hereafter denoted T59) was previously identified via the phage display technique. This peptide non-covalently binds to the chlorine-doped conducting polymer polypyrrole (PPyCl). Studies have previously shown that conductive polymers have promising application in neural electrodes, sensors, and for improving regeneration and healing of peripheral nerves and other tissues. Thus, the strong and specific attachment of bio-active molecules to the surface of PPy using the T59 affinity peptide is an exciting new approach to enhance the bioactivity of electrically active materials for various biomedical applications. We demonstrate this by using T59 as a tether to modify PPyCl with the laminin fragment IKVAV to enhance cell interactions, as well as with the so-called stealth molecule poly(ethylene glycol; PEG) to decrease cell interactions. Using these two modification strategies, we were able to control cell attachment and neurite extension on the PPy surface, which is critical for different applications (i.e., the goal for tissue regeneration is to enhance cell interactions, whereas the goal for electrode and sensor applications is to reduce glial cell interactions and thus decrease scarring). Significantly, the conductivity of the PPyCl surface was unaffected by this surface modification technique, which is not the case with other methods that have been explored to surface modify conducting polymers. Finally, using subcutaneous implants, we confirmed that the PPyCl treated with the T59 peptide did not react in vivo differently than untreated PPyCl. PMID:23129217

  8. Surface modification of the conducting polymer, polypyrrole, via affinity peptide.

    PubMed

    Nickels, Jonathan D; Schmidt, Christine E

    2013-05-01

    A novel strategy for affinity-based surface modification of the conducting polymer, polypyrrole, (PPy), has been developed. A 12-amino acid peptide (THRTSTLDYFVI, hereafter denoted T59) was previously identified via the phage display technique. This peptide noncovalently binds to the chlorine-doped conducting polymer polypyrrole (PPyCl). Studies have previously shown that conductive polymers have promising application in neural electrodes, sensors, and for improving regeneration and healing of peripheral nerves and other tissues. Thus, the strong and specific attachment of bioactive molecules to the surface of PPy using the T59 affinity peptide is an exciting new approach to enhance the bioactivity of electrically active materials for various biomedical applications. We demonstrate this by using T59 as a tether to modify PPyCl with the laminin fragment IKVAV to enhance cell interactions, as well as with the so-called stealth molecule poly(ethylene glycol; PEG) to decrease cell interactions. Using these two modification strategies, we were able to control cell attachment and neurite extension on the PPy surface, which is critical for different applications (i.e., the goal for tissue regeneration is to enhance cell interactions, whereas the goal for electrode and sensor applications is to reduce glial cell interactions and thus decrease scarring). Significantly, the conductivity of the PPyCl surface was unaffected by this surface modification technique, which is not the case with other methods that have been explored to surface modify conducting polymers. Finally, using subcutaneous implants, we confirmed that the PPyCl treated with the T59 peptide did not react in vivo differently than untreated PPyCl. PMID:23129217

  9. 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.

  10. Linking Atomistic and Mesoscale Simulations of Water Soluble Polymers

    NASA Astrophysics Data System (ADS)

    Jones, J. L.

    2003-03-01

    There exist a range of techniques for studying surfactants and polymers in the mesoscale regime. One of the challenges is to link mesoscale theories and simulations to other calculation methods which address different length scales of the system. We introduce some mesoscale methods of calculation for polymers and surfactants and then present a case study of where mesoscale modelling is used for mechanistic understanding, by linking the method to high throughput in-silico screening methods. We look at the adsorption onto silica of ethylene oxide (EO)/ propylene oxide (PO) block copolymers (lutrols) which have been modified by end-grafting of short, cationic dimethylamino ethyl methacrylate (DMAEMA)chains. Given that the silica surface is negatively charged, it is remarkable that in some circumstances, polymers with longercationic chains have a lower adsorption. The effect is attributed to a competition between strong adsorption of the cationic DMAEMA groups driven by electrostatics, and weaker adsorption of the more numerous EO groups. This then raises the question of how we produce the values for the mesoscale parameters in these models and in the second part of the talk we describe a calculation method for doing this for water soluble polymers. The most promising route, but notoriously costly, is based on free energy calculations at the atomistic level. Free energy calculations are computationally intensive in general, but in an aqueous system one is also faced with the additional problem of using complex continuum models and/or accurate interaction potentials for water. Here we show how potential of mean force (PMF)calculations offer a practical alternative which avoids these drawbacks, though one is still faced with extremely long simulations.

  11. Two-Dimensional Mesoscale-Ordered Conducting Polymers.

    PubMed

    Liu, Shaohua; Zhang, Jian; Dong, Renhao; Gordiichuk, Pavlo; Zhang, Tao; Zhuang, Xiaodong; Mai, Yiyong; Liu, Feng; Herrmann, Andreas; Feng, Xinliang

    2016-09-26

    Despite the availability of numerous two-dimensional (2D) materials with structural ordering at the atomic or molecular level, direct construction of mesoscale-ordered superstructures within a 2D monolayer remains an enormous challenge. Here, we report the synergic manipulation of two types of assemblies in different dimensions to achieve 2D conducting polymer nanosheets with structural ordering at the mesoscale. The supramolecular assemblies of amphipathic perfluorinated carboxylic acids and block co-polymers serve as 2D interfaces and meso-inducing moieties, respectively, which guide the polymerization of aniline into 2D, free-standing mesoporous conducting polymer nanosheets. Grazing-incidence small-angle X-ray scattering combined with various microscopy demonstrates that the resulting mesoscale-ordered nanosheets have hexagonal lattice with d-spacing of about 30 nm, customizable pore sizes of 7-18 nm and thicknesses of 13-45 nm, and high surface area. Such template-directed assembly produces polyaniline nanosheets with enhanced π-π stacking interactions, thereby resulting in anisotropic and record-high electrical conductivity of approximately 41 S cm(-1) for the pristine polyaniline nanosheet based film and approximately 188 S cm(-1) for the hydrochloric acid-doped counterpart. Our moldable approach creates a new family of mesoscale-ordered structures as well as opens avenues to the programmed assembly of multifunctional materials. PMID:27603275

  12. Two-Dimensional Mesoscale-Ordered Conducting Polymers.

    PubMed

    Liu, Shaohua; Zhang, Jian; Dong, Renhao; Gordiichuk, Pavlo; Zhang, Tao; Zhuang, Xiaodong; Mai, Yiyong; Liu, Feng; Herrmann, Andreas; Feng, Xinliang

    2016-09-26

    Despite the availability of numerous two-dimensional (2D) materials with structural ordering at the atomic or molecular level, direct construction of mesoscale-ordered superstructures within a 2D monolayer remains an enormous challenge. Here, we report the synergic manipulation of two types of assemblies in different dimensions to achieve 2D conducting polymer nanosheets with structural ordering at the mesoscale. The supramolecular assemblies of amphipathic perfluorinated carboxylic acids and block co-polymers serve as 2D interfaces and meso-inducing moieties, respectively, which guide the polymerization of aniline into 2D, free-standing mesoporous conducting polymer nanosheets. Grazing-incidence small-angle X-ray scattering combined with various microscopy demonstrates that the resulting mesoscale-ordered nanosheets have hexagonal lattice with d-spacing of about 30 nm, customizable pore sizes of 7-18 nm and thicknesses of 13-45 nm, and high surface area. Such template-directed assembly produces polyaniline nanosheets with enhanced π-π stacking interactions, thereby resulting in anisotropic and record-high electrical conductivity of approximately 41 S cm(-1) for the pristine polyaniline nanosheet based film and approximately 188 S cm(-1) for the hydrochloric acid-doped counterpart. Our moldable approach creates a new family of mesoscale-ordered structures as well as opens avenues to the programmed assembly of multifunctional materials.

  13. Conductivity and properties of polysiloxane-polyether cluster-LiTFSI networks as hybrid polymer electrolytes

    NASA Astrophysics Data System (ADS)

    Boaretto, Nicola; Joost, Christine; Seyfried, Mona; Vezzù, Keti; Di Noto, Vito

    2016-09-01

    This report describes the synthesis and the properties of a series of polymer electrolytes, composed of a hybrid inorganic-organic matrix doped with LiTFSI. The matrix is based on ring-like oligo-siloxane clusters, bearing pendant, partially cross-linked, polyether chains. The dependency of the thermo-mechanic and of the transport properties on several structural parameters, such as polyether chains' length, cross-linkers' concentration, and salt concentration is studied. Altogether, the materials show good thermo-mechanical and electrochemical stabilities, with conductivities reaching, at best, 8·10-5 S cm-1 at 30 °C. In conclusion, the cell performances of one representative sample are shown. The scope of this report is to analyze the correlations between structure and properties in networked and hybrid polymer electrolytes. This could help the design of optimized polymer electrolytes for application in lithium metal batteries.

  14. Functional Conducting Polymers via Thiol-ene Chemistry

    PubMed Central

    Feldman, Kathleen E.; Martin, David C.

    2012-01-01

    We demonstrate here that thiol-ene chemistry can be used to provide side-chain functionalized monomers based on 3,4-propylenedioxythiophene (ProDOT) containing ionic, neutral, hydrophobic, and hydrophilic side chains. All reactions gave high yields and purification could generally be accomplished through precipitation. These monomers were polymerized either chemically or electro-chemically to give soluble materials or conductive films, respectively. This strategy provides for facile tuning of the solubility, film surface chemistry, and film morphology of this class of conducting polymers. PMID:25585932

  15. 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.

  16. Ab-initio study of napthelene based conducting polymer

    SciTech Connect

    Ruhela, Ankur; Kanchan, Reena; Srivastava, Anurag; Sinha, O. P.

    2014-04-24

    In this paper, we have identified structural and electronic properties of conducting polymers by using DFT based ATK-VNL ab-initio tool. Naphthalene derivative structures were stabilized by varying the bond length between two atoms of the molecule C-N and C-C. We have also studied the molecular energy spectrum of naphthalene derivatives and found the HOMOLUMO for the same. A comparison of structural and electronic properties of naphthalene derivatives by attaching the functional group of amine, have been performed and found that they show good semi conducting properties.

  17. Conducting instant adhesives by grafting of silane polymer onto expanded graphite.

    PubMed

    Mondal, Titash; Bhowmick, Anil K; Krishnamoorti, Ramanan

    2014-09-24

    A "grafting to" methodology for the attachment of a silane based polymer (SG) onto functionalized graphitic platelets is demonstrated. The siloxy end groups of the modifier were further cross-linked without addition of any external curative. These sterically stabilized nanoplatelets with a high grafting density ensured complete screening of the attractive interparticle interactions. As a result, a better dispersion of platelets was observed compared to the physically mixed platelets in the polymer matrix (SUG). The larger size of the polymer tethered graphitic particles and the greater extent of heat liberated due to grafting resulted in a higher enthalpic contribution in the case of SG compared to SUG. This makes the formation of SG thermodynamically more favorable compared to SUG. Presence of a hierarchical spatial arrangement with a good dispersion of graphitic platelets was observed within the siloxane matrix in the case of SG compared to SUG. The nanoparticle tethered composite generated exhibited an "instant" conducting adhesive behavior. The adhesive properties of the SG were found to be increased due to grafting of graphitic platelets when compared with the neat polymer. Further, SG exhibited a conductive character whereas the neat polymer and SUG demonstrated an insulating character.

  18. Tunneling conductance of amine-linked alkyl chains.

    PubMed

    Prodan, Emil; Car, Roberto

    2008-06-01

    The tunneling transport theory developed in ref 9 (Phys. Rev. B 2007, 76, 115102) is applied to molecular devices made of alkyl chains linked to gold electrodes via amine groups. Using the analytic expression of the tunneling conductance derived in our previous work, we identify the key physical quantities that characterize the conductance of these devices. By investigating the transport characteristics of three devices, containing four, six, and eight methyl groups, we extract the dependence of the tunneling conductance on the chain's length, which is an exponential decay law in agreement with recent experimental data.

  19. Dimensionality and Localization of Electron States in Conducting Polymers

    NASA Astrophysics Data System (ADS)

    Wang, Zhao Hui

    The electron localization and the dimensionality of conducting polymers are studied by a variety of transport and magnetic techniques. Two model conducting polymer systems, the emeraldine salt form of polyaniline (PAN-ES) and one of its derivatives (POT-ES), are employed in the studies. The electron localization is increased with increasing one-dimensionality of a quasi-one-dimensional disordered system (Quasi-1d-DS). This concept is tested by studying electron localization in polyaniline (PAN) and its methyl ring-substituted derivative poly(o-toluidine) (POT). The experimental results showed greater electron localization in the HCl salt of POT than that of PAN, reflected in much smaller sigma_{DC}, sigma_{MW} and epsilon, increased Curie susceptibility and decreased Pauli-like susceptibility. The localization is attributed to the reduced interchain diffusion rate caused by decreased interchain coherence and increased interchain separation, both of which result from the presence of CH_3 on the C_6 rings. The T-dependences of lnsigma ~ -T^{-1/2} and S(T) ~ S_0 + B/T are interpreted as quasi-1d variable range hopping (VRH) between the nearest neighboring chains. Within the model, electric field (F) dependence of sigma(F)~{cal K}F^{1/2} with { cal K}~ T^{-1/2} can be understood. Charging energy limited tunneling model for granular metals and three-dimensional VRH model with a Coulomb gap are not consistent with the experiment. Other possible mechanisms for electron localization and the general implications for control of dimensionality and conductivity are discussed. The interchain coupling may change the dimensionality of electron states of conducting polymers. It is an open question if "metallic" polymers have one dimensional or three dimensional conduction states. We investigate this issue by studying the oriented polyaniline system. The thermopower, microwave dielectric constant and EPR data suggest that the electrons are three-dimensionally delocalized while the

  20. 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.

  1. Study of temperature dependence of thermal conductivity in cross-linked epoxies using molecular dynamics simulations with long range interactions

    NASA Astrophysics Data System (ADS)

    Kumar, A.; Sundararaghavan, V.; Browning, A. R.

    2014-03-01

    In this work, we demonstrate the use of the Green-Kubo integral of the heat flux autocorrelation function, incorporating long-range corrections to model the thermal conductivity versus temperature relationship of cross-linked polymers. The simulations were performed on a cross-linked epoxy made from DGEBA and a curing agent (diamino diphenyl sulfone) using a consistent valence force field (CVFF). A dendrimeric approach was utilized for building equilibrated cross-linked structures that allowed replication of the experimental dilatometric curve for the epoxy system. We demonstrate that the inclusion of a long-range correction within the Ewald/PPPM approach brings the results close to experimentally measured conductivity within an error of 10% while providing a good prediction of the relationship of thermal conductivity versus temperature. This method shows significant promise towards the computation of thermal conductivity from simulations even before synthesis of the polymer for purposes of materials by design.

  2. Conducting polymer nanofibers for high sensitivity detection of chemical analytes.

    NASA Astrophysics Data System (ADS)

    Kumar, Abhishek; Leshchiner, Ignaty; Nagarajan, Subhalakshmi; Nagarajan, Ramaswamy; Kumar, Jayant

    2008-03-01

    Possessing large surface area materials is vital for high sensitivity detection of analyte. We report a novel, inexpensive and simple technique to make high surface area sensing interfaces using electrospinning. Conducting polymers (CP) nanotubes were made by electrospinning a solution of a catalyst (ferric tosylate) along with poly (lactic acid), which is an environment friendly biodegradable polymer. Further vapor deposition polymerization of the monomer ethylenedioxy thiophene (EDOT) on the nanofiber surface yielded poly (EDOT) covered fibers. X-ray photo electron spectroscopy (XPS) study reveals the presence of PEDOT predominantly on the surface of nanofibers. Conducting nanotubes had been received by dissolving the polymer in the fiber core. By a similar technique we had covalently incorporated fluorescent dyes on the nanofiber surface. The materials obtained show promise as efficient sensing elements. UV-Vis characterization confirms the formation of PEDOT nanotubes and incorporation of chromophores on the fiber surface. The morphological characterization was carried out using scanning electron microscopy (SEM) and transmission electron microscopy (TEM).

  3. Photodynamic Therapy with Blended Conducting Polymer/Fullerene Nanoparticle Photosensitizers.

    PubMed

    Doshi, Mona; Gesquiere, Andre J

    2015-10-28

    In this article a method for the fabrication and reproducible in-vitro evaluation of conducting polymer nanoparticles blended with fullerene as the next generation photosensitizers for Photodynamic Therapy (PDT) is reported. The nanoparticles are formed by hydrophobic interaction of the semiconducting polymer MEH-PPV (poly[2-methoxy-5-(2-ethylhexyloxy)-1,4-phenylenevinylene]) with the fullerene PCBM (phenyl-C61-butyric acid methyl ester) in the presence of a non-compatible solvent. MEH-PPV has a high extinction coefficient that leads to high rates of triplet formation, and efficient charge and energy transfer to the fullerene PCBM. The latter processes enhance the efficiency of the PDT system through fullerene assisted triplet and radical formation, and ultrafast deactivation of MEH-PPV excited stated. The results reported here show that this nanoparticle PDT sensitizing system is highly effective and shows unexpected specificity to cancer cell lines.

  4. 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

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

    PubMed

    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 10(4) 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.

  6. 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) .

  7. 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

  8. Conducting polymers in electrochemical sensing: factors influencing the electroanalytical signal.

    PubMed

    Tsakova, Vessela; Seeber, Renato

    2016-10-01

    The paper highlights the intrinsic role of the conducting polymers (CPs) in CP-based electrochemical sensing devices. The effects of specific parameters of the electrochemical synthesis and overall measurement protocol, such as nature of the solvent and doping ions, the characteristics of the electrochemical polymerisation procedure, the nature of the CP-carrying substrates, and the composition of the medium used for the electroanalytical measurement, are discussed in an attempt to provide guidelines necessary for optimisation of CP-based electrochemical sensing. The lesser stability of CPs is also addressed as one of the main possible drawbacks of these materials in comparison to inorganic-based sensors.

  9. 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.

  10. 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

  11. 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.

  12. 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

  13. Proton conducting, high modulus polymer electrolyte membranes by polymerization-induced microphase separation

    NASA Astrophysics Data System (ADS)

    Chopade, Sujay; Hillmyer, Marc; Lodge, Timothy

    Robust solid-state polymer electrolyte membranes (PEMs) are vital for designing next-generation lithium-ion batteries and high-temperature fuel cells. However, the performance of diblock polymer electrolytes is generally limited by poor mechanical stability and network defects in the conducting pathways. We present the in-situ preparation of robust cross-linked PEMs via polymerization-induced microphase separation, and incorporation of protic ionic liquid (IL) into one of the microphase separated domains. The facile design strategy involves a delicate balance between the controlled growth of polystyrene from a poly(ethylene oxide) macro-chain transfer agent (PEO-CTA) and simultaneous chemical cross-linking by divinylbenzene in the presence of IL. Small angle X-ray scattering and transmission electron microscopy confirmed the formation of a disordered structure with bicontinuous morphology and a characteristic domain size of order 20 nm. The long-range continuity of the PEO/protic IL conducting nanochannels and cross-linked polystyrene domains imparts high thermal and mechanical stability to the PEMs, with elastic modulus approaching 10 MPa and a high ionic conductivity of 15 mS/cm at 180 °C.

  14. Mechanically Strong, Polymer Cross-linked Aerogels (X-Aerogels)

    NASA Technical Reports Server (NTRS)

    Leventis, Nicholas

    2006-01-01

    Aerogels comprise a class of low-density, high porous solid objects consisting of dimensionally quasi-stable self-supported three-dimensional assemblies of nanoparticles. Aerogels are pursued because of properties above and beyond those of the individual nanoparticles, including low thermal conductivity, low dielectric constant and high acoustic impedance. Possible applications include thermal and vibration insulation, dielectrics for fast electronics, and hosting of functional guests for a wide variety of optical, chemical and electronic applications. Aerogels, however, are extremely fragile materials, hence they have found only limited application in some very specialized environments, for example as Cerenkov radiation detectors in certain types of nuclear reactors, aboard spacecraft as collectors of hypervelocity particles (refer to NASA's Stardust program) and as thermal insulators on planetary vehicles on Mars (refer to Sojourner Rover in 1997 and Spirit and Opportunity in 2004). Along these lines, the X-Aerogel is a new NASA-developed strong lightweight material that has resolved the fragility problem of traditional (native) aerogels. X-Aerogels are made by applying a conformal polymer coating on the surfaces of the skeletal nanoparticles of native aerogels (see Scanning Electron Micrographs). Since the relative amounts of the polymeric crosslinker and the backbone are comparable, X-Aerogels can be viewed either as aerogels modified by the templated accumulation of polymer on the skeletal nanoparticles, or as nanoporous polymers made by remplated casting of polymer on a nanostructured framework. The most striking feature of X-Aerogels is that for a nominal 3-fold increase in density (still a ultralighweight material), the mechanical strength can be up to 300 times higher than the strength of the underlying native aerogel. Thus, X-Aerogels combine a multiple of the specific compressive strength of steel, with the the thermal conductivity of styrofoam. X

  15. Electrical Conductivity in Polymer Blends/ Multiwall Carbon Nanotubes

    SciTech Connect

    Kulkarni, Ajit R.; Bose, Suryasarathi; Bhattacharyya, Arup R.

    2008-10-23

    Carbon nanotubes (CNT) based polymer composites have emerged as the future multifunctional materials in view of its exceptional mechanical, thermal and electrical properties. One of the major interests is to develop conductive polymer composites preferably at low concentration of CNT utilizing their high aspect ratio (L/D) for numerous applications, which include antistatic devices, capacitors and materials for EMI shielding. In this context, polymer blends have emerged as a potential candidate in lowering the percolation thresholds further by the utilization of 'double-percolation' which arises from the synergistic improvements in blend properties associated with the co-continuous morphology. Due to strong inter-tube van der Waals' forces, they often tend to aggregate and uniform dispersion remains a challenge. To overcome this challenge, we exploited sodium salt of 6-aminohexanoic acid (Na-AHA) which was able to assist in debundlling the multiwall carbon nanotubes (MWNT) through 'cation-{pi}' interactions during melt-mixing leading to percolative 'network-like' structure of MWNT within polyamide6 (PA6) phase in co-continuous PA6/acrylonitrile butadiene styrene (ABS) blends. The composite exhibited low electrical percolation thresholds of 0.25 wt% of MWNT, the lowest reported value in this system so far. Retention of 'network-like structure' in the solid state with significant refinement was observed even at lower MWNT concentration in presence Na-AHA, which was assessed through AC electrical conductivity measurements. Reactive coupling was found to be a dominant factor besides 'cation-{pi}' interactions in achieving low electrical percolation in PA6/ABS+MWNT composites.

  16. 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.

  17. All-Solid-State Conductive Polymer Miniaturized Reference Electrode

    NASA Astrophysics Data System (ADS)

    Chen, Chien Cheng; Chou, Jung Chuan

    2009-11-01

    A novel, stable, and all-solid-state miniaturized reference electrode (MRE) prepared by changing the properties of a conductive polymer for potentiometric applications is presented in this study. A monomer of a conductive polymer, pyrrole, was electrodeposited to form polypyrrole on an indium-tin oxide (ITO) glass at a DC power of 5 V. The difference of the solid-state MRE from the Ag/AgCl glass reference electrode is that the former requires no inner electrolyte and can be preserved without any storage solution (such as saturated KCl solution). In this study, the potentiometric characteristics of the solid-state MRE are investigated using the current-voltage (I-V) measurement system. The solid-state MRE exhibits sufficient stability and reproducibility in acid-base, sodium chloride, and potassium chloride solutions. Furthermore, the solid-state MRE can collocate successfully with H+-, Na+-, and K+-ion selective electrodes to measure H+, Na+, and K+ ion concentrations in acid-base, sodium chloride, and potassium chloride solutions, respectively.

  18. 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).

  19. 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.

  20. 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.

  1. 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

  2. Cross-linked Composite Gel Polymer Electrolyte using Mesoporous Methacrylate-Functionalized SiO2 Nanoparticles for Lithium-Ion Polymer Batteries

    PubMed Central

    Shin, Won-Kyung; Cho, Jinhyun; Kannan, Aravindaraj G.; Lee, Yoon-Sung; Kim, Dong-Won

    2016-01-01

    Liquid electrolytes composed of lithium salt in a mixture of organic solvents have been widely used for lithium-ion batteries. However, the high flammability of the organic solvents can lead to thermal runaway and explosions if the system is accidentally subjected to a short circuit or experiences local overheating. In this work, a cross-linked composite gel polymer electrolyte was prepared and applied to lithium-ion polymer cells as a safer and more reliable electrolyte. Mesoporous SiO2 nanoparticles containing reactive methacrylate groups as cross-linking sites were synthesized and dispersed into the fibrous polyacrylonitrile membrane. They directly reacted with gel electrolyte precursors containing tri(ethylene glycol) diacrylate, resulting in the formation of a cross-linked composite gel polymer electrolyte with high ionic conductivity and favorable interfacial characteristics. The mesoporous SiO2 particles also served as HF scavengers to reduce the HF content in the electrolyte at high temperature. As a result, the cycling performance of the lithium-ion polymer cells with cross-linked composite gel polymer electrolytes employing methacrylate-functionalized mesoporous SiO2 nanoparticles was remarkably improved at elevated temperatures. PMID:27189842

  3. Cross-linked Composite Gel Polymer Electrolyte using Mesoporous Methacrylate-Functionalized SiO2 Nanoparticles for Lithium-Ion Polymer Batteries

    NASA Astrophysics Data System (ADS)

    Shin, Won-Kyung; Cho, Jinhyun; Kannan, Aravindaraj G.; Lee, Yoon-Sung; Kim, Dong-Won

    2016-05-01

    Liquid electrolytes composed of lithium salt in a mixture of organic solvents have been widely used for lithium-ion batteries. However, the high flammability of the organic solvents can lead to thermal runaway and explosions if the system is accidentally subjected to a short circuit or experiences local overheating. In this work, a cross-linked composite gel polymer electrolyte was prepared and applied to lithium-ion polymer cells as a safer and more reliable electrolyte. Mesoporous SiO2 nanoparticles containing reactive methacrylate groups as cross-linking sites were synthesized and dispersed into the fibrous polyacrylonitrile membrane. They directly reacted with gel electrolyte precursors containing tri(ethylene glycol) diacrylate, resulting in the formation of a cross-linked composite gel polymer electrolyte with high ionic conductivity and favorable interfacial characteristics. The mesoporous SiO2 particles also served as HF scavengers to reduce the HF content in the electrolyte at high temperature. As a result, the cycling performance of the lithium-ion polymer cells with cross-linked composite gel polymer electrolytes employing methacrylate-functionalized mesoporous SiO2 nanoparticles was remarkably improved at elevated temperatures.

  4. Cross-linked Composite Gel Polymer Electrolyte using Mesoporous Methacrylate-Functionalized SiO2 Nanoparticles for Lithium-Ion Polymer Batteries.

    PubMed

    Shin, Won-Kyung; Cho, Jinhyun; Kannan, Aravindaraj G; Lee, Yoon-Sung; Kim, Dong-Won

    2016-01-01

    Liquid electrolytes composed of lithium salt in a mixture of organic solvents have been widely used for lithium-ion batteries. However, the high flammability of the organic solvents can lead to thermal runaway and explosions if the system is accidentally subjected to a short circuit or experiences local overheating. In this work, a cross-linked composite gel polymer electrolyte was prepared and applied to lithium-ion polymer cells as a safer and more reliable electrolyte. Mesoporous SiO2 nanoparticles containing reactive methacrylate groups as cross-linking sites were synthesized and dispersed into the fibrous polyacrylonitrile membrane. They directly reacted with gel electrolyte precursors containing tri(ethylene glycol) diacrylate, resulting in the formation of a cross-linked composite gel polymer electrolyte with high ionic conductivity and favorable interfacial characteristics. The mesoporous SiO2 particles also served as HF scavengers to reduce the HF content in the electrolyte at high temperature. As a result, the cycling performance of the lithium-ion polymer cells with cross-linked composite gel polymer electrolytes employing methacrylate-functionalized mesoporous SiO2 nanoparticles was remarkably improved at elevated temperatures. PMID:27189842

  5. 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.

  6. Polymer Composition and Substrate Influences on the Adhesive Bonding of a Biomimetic, Cross-Linking Polymer

    PubMed Central

    Matos-Pérez, Cristina R.; White, James D.; Wilker, Jonathan J.

    2012-01-01

    Hierarchical biological materials such as bone, sea shells, and marine bioadhesives are providing inspiration for the assembly of synthetic molecules into complex structures. The adhesive system of marine mussels has been the focus of much attention in recent years. Several catechol-containing polymers are being developed to mimic the cross-linking of proteins containing 3,4-dihydroxyphenylalanine (DOPA) used by shellfish for sticking to rocks. Many of these biomimetic polymer systems have been shown to form surface coatings or hydrogels, however bulk adhesion is demonstrated less often. Developing adhesives requires addressing design issues including finding a good balance between cohesive and adhesive bonding interactions. Despite the growing number of mussel mimicking polymers, there has been little effort to generate structure-property relations and gain insights on what chemical traits give rise to the best glues. In this report, we examined the simplest of these biomimetic polymers, poly[(3,4-dihydroxystyrene)-co-styrene]. Pendant catechol groups (i.e., 3,4-dihydroxystyrene) were distributed throughout a polystyrene backbone. Several polymer derivatives were prepared, each with a different 3,4-dihyroxystyrene content. Bulk adhesion testing showed where the optimal middle ground of cohesive and adhesive bonding resides. Adhesive performance was benchmarked against commercial glues as well as the genuine material produced by live mussels. In the best case, bonding was similar to cyanoacrylate “Krazy” or “Super” glue. Performance was also examined using low (e.g., plastics) and high (e.g., metals, wood) energy surfaces. Adhesive bonding of poly[(3,4-dihydroxystyrene)-co-styrene] may be the strongest of reported mussel protein mimics. These insights should help us to design future biomimetic systems, thereby bringing us closer to development of bone cements, dental composites, and surgical glues. PMID:22582754

  7. 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

  8. 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

  9. Conducting-polymer-based radar-absorbing materials

    NASA Astrophysics Data System (ADS)

    Truong, Vo-Van; Turner, Ben D.; Muscat, Richard F.; Russo, M. S.

    1997-11-01

    The controllability of conductivity and the ease of manufacturing/coating of conducting polymers enable tailor- made dielectric loss components for radar absorbing materials (RAM). Different polypyrrole (PPy) based RAM, e.g. paint/rubber containing PPy powder and PPy coated structural phenolic foams with a gradient of impedance, have been examined. Reflection loss strongly depends on thickness and complex permittivity of the material. For a single layer material, the optimum values of the real part, (epsilon) ', and imaginary part, (epsilon) ", of the complex permittivity required to achieve a minimum reflectivity at a given sample thickness are found by theoretical calculations. The conductivity of the PPy powder is controlled to obtain RAM with lowest reflectivity according to the calculated optimum values of (epsilon) ' and (epsilon) ". A paint panel containing 2 wt% of the PPy powder with a thickness of 2.5 mm exhibits a reflectivity less than $minus 10 dB over 12 to 18 GHz. Blending and milling in the manufacturing process can destroy the original fibrous shape of PPy aggregates leading to low absorbing performances. PPy can be coated on rigid or flexible open cell foams to provide a lightweight broadband RAM. In particular, a coating technique on phenolic foams (12 - 15 mm thick) with a pore size of micrometer order has been developed to generate a gradient of conductivity across the foam thickness. The PPy coated foams are broadband RAM.

  10. Anhydrous Proton Conducting Polymer Electrolyte Membranes via Polymerization-Induced Microphase Separation.

    PubMed

    Chopade, Sujay A; So, Soonyong; Hillmyer, Marc A; Lodge, Timothy P

    2016-03-01

    Solid-state polymer electrolyte membranes (PEMs) exhibiting high ionic conductivity coupled with mechanical robustness and high thermal stability are vital for the design of next-generation lithium-ion batteries and high-temperature fuel cells. We present the in situ preparation of nanostructured PEMs incorporating a protic ionic liquid (IL) into one of the domains of a microphase-separated block copolymer created via polymerization-induced microphase separation. This facile, one-pot synthetic strategy transforms a homogeneous liquid precursor consisting of a poly(ethylene oxide) (PEO) macro-chain-transfer agent, styrene and divinylbenzene monomers, and protic IL into a robust and transparent monolith. The resulting PEMs exhibit a bicontinuous morphology comprising PEO/protic IL conducting pathways and highly cross-linked polystyrene (PS) domains. The cross-linked PS mechanical scaffold imparts thermal and mechanical stability to the PEMs, with an elastic modulus approaching 10 MPa at 180 °C, without sacrificing the ionic conductivity of the system. Crucially, the long-range continuity of the PEO/protic IL conducting nanochannels results in an outstanding ionic conductivity of 14 mS/cm at 180 °C. We posit that proton conduction in the protic IL occurs via the vehicular mechanism and the PEMs exhibit an average proton transference number of 0.7. This approach is very promising for the development of high-temperature, robust PEMs with excellent proton conductivities. PMID:26927732

  11. 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.

  12. 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.

  13. 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

  14. 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.

  15. Electromechanical Behavior of Carbon Nanotubes-Conducting Polymer Films

    NASA Astrophysics Data System (ADS)

    Kim, Cheol; Liu, Xinyun

    A relationship between strain and applied potential is derived for composite films consisting of single-wall carbon nanotubes (SWNTs) and conductive polymers (CPs). When it is derived, an electrochemical ionic approach is utilized to formulate the electromechanical actuation of the film actuator. This relationship can give us a direct understanding of actuation of the nanoactuator. The results show that the well-aligned SWNTs composite actuator can give good actuation responses and high actuating forces available. The actuation is found to be affected by both SWNTs and CPs components and the actuation of SWNTs component has two kinds of influences on that of the CPs component: reinforcement at the positive voltage and abatement at the negative voltage. Optimizations of SWNTs-CPs composite actuator may be achieved by using well-aligned nanotubes as well as choosing suitable electrolyte and an input voltage range.

  16. How to improve electrochemomechanical strain in conducting polymers

    NASA Astrophysics Data System (ADS)

    Kaneto, Keiichi; Takayanagi, Kohei; Tominaga, Kazuo; Takashima, Wataru

    2012-04-01

    We have been studying electrochemomechanical deformation (ECMD) of conducting polymers to realize artificial muscles or soft actuators, since 1992. For the practical application, i.e., strain, stress, response time, cycle stability and creep have to be improved to levels of demands. In this paper, some attempts to improve the strain are mentioned for polyaniline, polypyrrole and poly(3,4-ethylenedioxythiophene), PEDOT. Especially, PEDOT actuator was found to show novel features in ECMD under tensile loads. The actuation was driven by cation insertion upon reduction in any combination of electrolytes and solvents. Another interesting feature was that the actuation under tensile loads showed larger strain than that without tensile loads. These facts were explained with a model of helical confinement of anions during the electrodeposition and uniaxial alignment of helices by the electrochemical creep under tensile loads.

  17. Conducting Polymers for Neural Prosthetic and Neural Interface Applications.

    PubMed

    Green, Rylie; Abidian, Mohammad Reza

    2015-12-01

    Neural-interfacing devices are an artificial mechanism for restoring or supplementing the function of the nervous system, lost as a result of injury or disease. Conducting polymers (CPs) are gaining significant attention due to their capacity to meet the performance criteria of a number of neuronal therapies including recording and stimulating neural activity, the regeneration of neural tissue and the delivery of bioactive molecules for mediating device-tissue interactions. CPs form a flexible platform technology that enables the development of tailored materials for a range of neuronal diagnostic and treatment therapies. In this review, the application of CPs for neural prostheses and other neural interfacing devices is discussed, with a specific focus on neural recording, neural stimulation, neural regeneration, and therapeutic drug delivery.

  18. 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

  19. 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

  20. 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

  1. 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...

  2. 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.

  3. Complex impedance and conductivity of agar-based ion-conducting polymer electrolytes

    NASA Astrophysics Data System (ADS)

    Nwanya, A. C.; Amaechi, C. I.; Udounwa, A. E.; Osuji, R. U.; Maaza, M.; Ezema, F. I.

    2015-04-01

    Agar-based electrolyte standing films with different salts and weak acids as ion and proton conductors were prepared and characterized by X-ray diffraction, UV-visible spectrophotometry, photoluminescence emission spectroscopy and electrochemical impedance spectroscopy. The salts used are lithium perchlorate (LiClO4) and potassium perchlorate (KClO4), while the weak acids used are acetic acid (CH3COOH) and lactic acid (C3H6O3). The values of the ion conductivity obtained for the agar-based polymer films are 6.54 × 10-8, 9.12 × 10-8, 3.53 × 10-8, 2.24 × 10-8 S/cm for the agar/acetic acid, agar/lactic acid, agar/LiClO4 and agar/KClO4 polymer films, respectively. As a function of temperature, the ion conductivity exhibits an Arrhenius behavior and the estimated activation energy is ≈0.1 eV for all the samples. The samples depicted high values of dielectric permittivity toward low frequencies which is due mostly to electrode polarization effect. The samples showed very high transparency (85-98 %) in the visible region, and this high transparency is one of the major requirements for application in electrochromic devices (ECD). The values of conductivity and activation energy obtained indicate that the electrolytes are good materials for application in ECD.

  4. 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.

  5. 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.

  6. 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.

  7. 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.

  8. Designer coordination polymers: dimensional crossover architectures and proton conduction.

    PubMed

    Yamada, Teppei; Otsubo, Kazuya; Makiura, Rie; Kitagawa, Hiroshi

    2013-08-21

    Coordination polymers (CPs) have large degrees of freedom in framework compositions and in the structures and environment of the inner pores. This review focuses on the recent significant progress achieved by controlling these degrees of freedom. Two breakthroughs are reviewed for constructing sophisticated structures of CP frameworks, especially in dimensional crossover regions. The first is the synthesis of quasi one-dimensional halogen-bridged coordinative tubes by applying state-of-the-art techniques of coordination chemistry. The electronic state of the coordinative tube was studied by structural, spectroscopic and theoretical methods and found to be distinct from conventional one-dimensional systems. The second breakthrough is the achievement of a quasi-two-dimensional architecture by combining Langmuir-Blodgett and layer-by-layer methods. Two-dimensional LB CP films were prepared on liquid; the films were stacked layer by layer, and a crystalline quasi-two-dimensional structure was constructed. This review also covers the design of the environment of the inner pore, where hydrogen bond networks with various acidic sites were modified. By appropriate design of the hydrogen bond network, proton-conductive CPs are invented, which are summarized in this review. Types of proton donor sites are discussed and classified, and superprotonic conductive CPs were achieved in these investigations. These results will provide new strategies for constructing functional materials for smart devices.

  9. Development of multilayer conducting polymer actuator for power application

    NASA Astrophysics Data System (ADS)

    Ikushima, Kimiya; Kudoh, Yuji; Hiraoka, Maki; Yokoyama, Kazuo; Nagamitsu, Sachio

    2009-03-01

    In late years many kinds of home-use robot have been developed to assist elderly care and housework. Most of these robots are designed with conventional electromagnetic motors. For safety it is desirable to replace these electromagnetic motors with artificial muscle. However, an actuator for such a robot is required to have simple structure, low driving voltage, high stress generation, high durability, and operability in the air. No polymer actuator satisfying all these requirements has been realized yet. To meet these we took following two approaches focusing on conducting polymer actuators which can output high power in the air. (Approach 1) We have newly developed an actuator by multiply laminating ionic liquid infiltrated separators and polypyrrole films. Compared with conventional actuator that is driven in a bath of ionic liquid, the new actuator can greatly increase generated stress since the total sectional area is tremendously small. In our experiment, the new actuator consists of minimum unit with thickness of 128um and has work/weight ratio of 0.92J/kg by laminating 9 units in 0.5Hz driving condition. In addition, the driving experiment has shown a stable driving characteristic even for 10,000 cycles durability test. Furthermore, from our design consideration, it has been found that the work/weight ratio can be improved up to 8J/kg (1/8 of mammalian muscle of 64J/kg) in 0.1Hz by reducing the thickness of each unit to 30um. (Approach 2) In order to realize a simplified actuator structure in the air without sealing, we propose the use of ionic liquid gel. The actuation characteristic of suggested multilayered actuator using ionic liquid gel is simulated by computer. The result shows that performance degradation due to the use of ionic liquid gel is negligible small when ionic liquid gel with the elasticity of 3kPa or less is used. From above two results it is concluded that the proposed multilayerd actuator is promising for the future robotic applications

  10. 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

  11. 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

  12. 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.

  13. 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.

  14. 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

  15. Electroanalytical measurements without electrolytes: conducting polymers as probes for redox titration in non-conductive organic media.

    PubMed

    Lange, Ulrich; Mirsky, Vladimir M

    2012-09-26

    Electroanalytical methods have been applied only in conducting media. An application of conducting polymers allows to overcome this limitation. If such material is in electrochemical equilibrium with dissolved redox active species, its electrical conductivity depends on the redox potential of these species. Therefore, conductometric measurements with conducting polymers can provide about the same information as classical redox electrodes. The approach was applied for redox titration. Equivalent points obtained by this titration in aqueous and organic electrolytes were identical. Then the approach was applied for determination of bromine number by redox titration in non-conducting organic phase.

  16. 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

  17. Incorporation of Metallic Nanoparticles into Conducting Polymer Actuator Films

    NASA Astrophysics Data System (ADS)

    Costa, Alexsandro Santos; Li, Kwong-Chi; Kilmartin, Paul A.; Travas-Sejdic, Jadranka

    2009-07-01

    Nanocomposites of conducting polymer films (CP) with metal nanoparticles have been prepared. Electropolymerization of pyrrole on stainless steel electrodes was undertaken galvanostatically until the thickness of the polypyrrole (PPy) film reached around 7.5 μm, which is suitable for the future application of these films in micropumps and microvalves. Subsequently platinum nanoparticles were deposited from a solution of a platinum precursor (K2PtCl6) onto the PPy coated stainless steel electrodes by applying a potential of -0.1 V for between 3 and 15 s. The length of the deposition time led to significant differences in the morphology and size of the particles obtained. The actuation of the free standing films was studied by electrochemomechanical deformation measurements (ECMD) on strips of films cycled in NaPF6. Depending upon the test conditions, the strain rate and ultimate strain of films containing Pt nanoparticles could be increased by a factor of 2 or more compared to those of pristine PPy films.

  18. Functionalised inherently conducting polymers as low biofouling materials.

    PubMed

    Zhang, Binbin; Nagle, Alex R; Wallace, Gordon G; Hanks, Timothy W; Molino, Paul J

    2015-01-01

    Diatoms are a major component of microbial biofouling layers that develop on man-made surfaces placed in aquatic environments, resulting in significant economic and environmental impacts. This paper describes surface functionalisation of the inherently conducting polymers (ICPs) polypyrrole (PPy) and polyaniline (PANI) with poly(ethylene glycol) (PEG) and their efficacy as fouling resistant materials. Their ability to resist interactions with the model protein bovine serum albumin (BSA) was tested using a quartz crystal microbalance with dissipation monitoring (QCM-D). The capacity of the ICP-PEG materials to prevent settlement and colonisation of the fouling diatom Amphora coffeaeformis (Cleve) was also assayed. Variations were demonstrated in the dopants used during ICP polymerisation, along with the PEG molecular weight, and the ICP-PEG reaction conditions, all playing a role in guiding the eventual fouling resistant properties of the materials. Optimised ICP-PEG materials resulted in a significant reduction in BSA adsorption, and > 98% reduction in diatom adhesion.

  19. 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.

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

    NASA Astrophysics Data System (ADS)

    Abiddin, Jamal Farghali Bin Zainal; Ahmad, Azizah Hanom

    2015-08-01

    Sodium ion (Na+) 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+ 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 × 10-11 S/cm.The conductivity increases as NaI content increases up to optimum NaIcomposition of 40 wt%, which yields an average conductivity of 2.70 × 10-5 S/cm.

  1. Chitosan-cross-linked osmium polymer composites as an efficient platform for electrochemical biosensors.

    PubMed

    Jirimali, Harishchandra Digambar; Nagarale, Rajaram Krishna; Lee, Jong Myung; Saravanakumar, Durai; Shin, Woonsup

    2013-07-22

    A new family of chitosan-cross-linked osmium polymer composites was prepared and its electrochemical properties were examined. The composites were prepared by quaternization of the poly(4-vinylpyridine) osmium bipyridyl polymer (PVP-Os) which was then cross-linked with chitosan, yielding PVP-Os/chitosan. Films made of the composites showed improved mass and electron transport owing to the porous and hydrophilic structure which is derived from the cross-links between the Os polymer and chitosan. The rate for glucose oxidation was enhanced four times when glucose oxidase (GOx) was immobilized on PVP-Os/chitosan compared immobilization on PVP-Os.

  2. The influence of carbon nanotubes in inkjet printing of conductive polymer suspensions

    NASA Astrophysics Data System (ADS)

    Denneulin, Aurore; Bras, Julien; Blayo, Anne; Khelifi, Bertine; Roussel-Dherbey, Francine; Neuman, Charles

    2009-09-01

    In this study, inkjet printing inks were formulated by combining the processability of the conductive polymer poly(3,4-ethylenedioxythiophene) (PEDOT) to the high conductivity of carbon nanotubes (CNTs). Conductive patterns were deposited on polymer films by piezoelectric inkjet printing. Several settings of printing were explored and analyzed by morphological observations and sheet resistance measurements. Performances of several CNTs were evaluated (single-walled, multi-walled and functionalized CNTs). Patterns can have sheet resistances from 10 537 to 225 Ω/sq between two families of CNTs. Functionalized CNTs with polyethylene glycol functions appeared to be the best candidates for printed electronics. This best combination allows us to obtain sheet resistances as low as 225 Ω/sq which is up to now one of the lowest resistances obtained by inkjet printing. This work also discusses the CNT network performances and emphasizes the degradation of electrical properties linked to the use of surfactants. This study represents an important step for the integration of CNTs in printed electronics applications and offers new opportunities to produce cost-effective electronics.

  3. Synthesis and characterization thin films of conductive polymer (PANI) for optoelectronic device application

    NASA Astrophysics Data System (ADS)

    Jarad, Amer N.; Ibrahim, Kamarulazizi; Ahmed, Nasser M.

    2016-07-01

    In this work we report preparation and investigation of structural and optical properties of polyaniline conducting polymer. By using sol-gel in spin coating technique to synthesize thin films of conducting polymer polyaniline (PANI). Conducting polymer polyaniline was synthesized by the chemical oxidative polymerization of aniline monomers. The thin films were characterized by technique: Hall effect, High Resolution X-ray diffraction (HR-XRD), Fourier transform infrared (FTIR) spectroscopy, Field emission scanning electron microscopy (FE-SEM), and UV-vis spectroscopy. Polyaniline conductive polymer exhibit amorphous nature as confirmed by HR-XRD. The presence of characteristic bonds of polyaniline was observed from FTIR spectroscopy technique. Electrical and optical properties revealed that (p-type) conductivity PANI with room temperature, the conductivity was 6.289×10-5 (Ω.cm)-1, with tow of absorption peak at 426,805 nm has been attributed due to quantized size of polyaniline conducting polymer.

  4. New Secondary Batteries Using Electronically Conductive Polymer Cathodes

    NASA Technical Reports Server (NTRS)

    Martin, Charles R.; White, Ralph E.

    1991-01-01

    A Li/Polypyrrole secondary battery was designed and built, and the effect of controlling the morphology of the polymer on enhancement of counterion diffusion in the polymer phase was explored. The experimental work was done at Colorado State University, while the mathematical modeling of the battery was done at Texas A and M University. Manuscripts and publications resulting from the project are listed.

  5. Method for synthesizing peptides with saccharide linked enzyme polymer conjugates

    DOEpatents

    Callstrom, M.R.; Bednarski, M.D.; Gruber, P.R.

    1997-06-17

    A method is disclosed for synthesizing peptides using water soluble enzyme polymer conjugates. The method comprises catalyzing the peptide synthesis with enzyme which has been covalently bonded to a polymer through at least three linkers which linkers have three or more hydroxyl groups. The enzyme is conjugated at lysines or arginines. 19 figs.

  6. Method for synthesizing peptides with saccharide linked enzyme polymer conjugates

    DOEpatents

    Callstrom, Matthew R.; Bednarski, Mark D.; Gruber, Patrick R.

    1997-01-01

    A method is disclosed for synthesizing peptides using water soluble enzyme polymer conjugates. The method comprises catalyzing the peptide synthesis with enzyme which has been covalently bonded to a polymer through at least three linkers which linkers have three or more hydroxyl groups. The enzyme is conjugated at lysines or arginines.

  7. Pattern-definable and low cost fabrication of nanopatterned conducting polymer film on flexible substrates.

    PubMed

    Lee, Jihye; Choi, Dae-Geun; Altun, Ali Ozhan; Kim, Ki-Don; Choi, Jun-Hyuk; Lee, Eung-Sug; Jeong, Jun-Ho

    2010-09-01

    This study reports the pattern definable and low cost fabrication of nanopatterned conducting polymer film on flexible substrates. Noble nanopatterned polymer hard template was fabricated by using nanoimprint lithography (NIL) and used for electropolymerization of conducting polymer. Conducting polymer was electrochemically deposited on the template and transferred over to flexible substrates. Eventually conducting polymer films with various nanopatterns were fabricated on flexible substrates. High pattern definability was achieved by nanoimprinted polymer template, which was molded from lithographically fabricated stamp. Low cost fabrication was accomplished due to low cost NIL, reusable polymer templates, and low material consumption of electrodeposition. The electrodeposited films were transferred using double sided tape. Because the templates are made of flexible polymer, the transfer bonding method applied in this study is adaptable to both wafers and flexible polymer substrates. The fabricated nanopatterned conducting polymer film can be applied to gas sensors, super capacitors, super wetting films, and neuron interfaces due to its characteristic of high surface to volume. For an illustrative application, the gas sensing properties of films were tested. The result showed enhanced sensing characteristic with nanopatterned film, which are attributed to the high surface to volume ratio of nanopatterned films.

  8. Performance of conducting polymer electrodes for stimulating neuroprosthetics

    NASA Astrophysics Data System (ADS)

    Green, R. A.; Matteucci, P. B.; Hassarati, R. T.; Giraud, B.; Dodds, C. W. D.; Chen, S.; Byrnes-Preston, P. J.; Suaning, G. J.; Poole-Warren, L. A.; Lovell, N. H.

    2013-02-01

    Objective. Recent interest in the use of conducting polymers (CPs) for neural stimulation electrodes has been growing; however, concerns remain regarding the stability of coatings under stimulation conditions. These studies examine the factors of the CP and implant environment that affect coating stability. The CP poly(ethylene dioxythiophene) (PEDOT) is examined in comparison to platinum (Pt), to demonstrate the potential performance of these coatings in neuroprosthetic applications. Approach. PEDOT is coated on Pt microelectrode arrays and assessed in vitro for charge injection limit and long-term stability under stimulation in biologically relevant electrolytes. Physical and electrical stability of coatings following ethylene oxide (ETO) sterilization is established and efficacy of PEDOT as a visual prosthesis bioelectrode is assessed in the feline model. Main results. It was demonstrated that PEDOT reduced the potential excursion at a Pt electrode interface by 72% in biologically relevant solutions. The charge injection limit of PEDOT for material stability was found to be on average 30× larger than Pt when tested in physiological saline and 20× larger than Pt when tested in protein supplemented media. Additionally stability of the coating was confirmed electrically and morphologically following ETO processing. It was demonstrated that PEDOT-coated electrodes had lower potential excursions in vivo and electrically evoked potentials (EEPs) could be detected within the visual cortex. Significance. These studies demonstrate that PEDOT can be produced as a stable electrode coating which can be sterilized and perform effectively and safely in neuroprosthetic applications. Furthermore these findings address the necessity for characterizing in vitro properties of electrodes in biologically relevant milieu which mimic the in vivo environment more closely.

  9. Conducting polymer nanostructures for photocatalysis under visible light

    NASA Astrophysics Data System (ADS)

    Ghosh, Srabanti; Kouamé, Natalie A.; Ramos, Laurence; Remita, Samy; Dazzi, Alexandre; Deniset-Besseau, Ariane; Beaunier, Patricia; Goubard, Fabrice; Aubert, Pierre-Henri; Remita, Hynd

    2015-05-01

    Visible-light-responsive photocatalysts can directly harvest energy from solar light, offering a desirable way to solve energy and environment issues. Here, we show that one-dimensional poly(diphenylbutadiyne) nanostructures synthesized by photopolymerization using a soft templating approach have high photocatalytic activity under visible light without the assistance of sacrificial reagents or precious metal co-catalysts. These polymer nanostructures are very stable even after repeated cycling. Transmission electron microscopy and nanoscale infrared characterizations reveal that the morphology and structure of the polymer nanostructures remain unchanged after many photocatalytic cycles. These stable and cheap polymer nanofibres are easy to process and can be reused without appreciable loss of activity. Our findings may help the development of semiconducting-based polymers for applications in self-cleaning surfaces, hydrogen generation and photovoltaics.

  10. Screen printable flexible conductive nanocomposite polymer with applications to wearable sensors

    NASA Astrophysics Data System (ADS)

    Chung, D.; Khosla, A.; Gray, B. L.

    2014-04-01

    We have developed a conductive nanocomposite polymer that possesses both good conductivity and flexibility, and screen printed it onto fabric to realize wearable flexible electrodes and electronic routing. The conductive polymer consists of dispersed silver nanoparticles (90~210nm) in a screen printable plastisol polymer. The conductive polymer is conductive for weight-percentages above approximately 61 wt-% of Ag nanoparticles, and has a resistivity of 2.12×10-6 ohm·m at 70 wt-% of Ag nanoparticles. To test the screen printed conductive polymer's flexibility and its effect on conductivity, we measured the resistivity of the Ag-doped composite polymer at different bending angles (-90˚ ~ 90˚) with a 10° step angle at different wt-% of silver particles, and compared the results. We also tested washability of the screen printed conductive polymer as applied to fabric for long-term use in wearable sensors systems. We also used the screen printed Ag composite polymer to realize an example wearable system. Flexible wearable dry electrocardiogram (ECG) electrodes were developed and ECG signal was measured via the electrodes. The sensing ECG electrodes (3mm diameter circle) were chloridized to form Ag/AgCl electrodes. We measured an ECG signal using a simple right-leg driven ECG circuit and observed normal ECG signals even without application of electrolyte gel.

  11. Hydrogel-mediated direct patterning of conducting polymer films with multiple surface chemistries.

    PubMed

    Park, SooHyun; Yang, Guang; Madduri, Nrutya; Abidian, Mohammad Reza; Majd, Sheereen

    2014-05-01

    A new methodology for selective electropolymerization of conducting polymer films using wet hydrogel stamps is presented. The ability of this simple method to generate patterned films of conducting polymers with multiple surface chemistries in a one-step process and to incorporate fragile biomolecules in these films is demonstrated.

  12. A review of properties and potential aerospace applications of electrically conducting polymers

    NASA Technical Reports Server (NTRS)

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

    1990-01-01

    An overview of current research in conducting polymers is presented. Emphasis is placed on development of materials useful for aeronautic and space applications. Research on organic conducting polymers began in the early 1970s with the discovery of polyacetylene. Since then, many polymers which share structural characteristics with polyacetylene have been prepared which conduct electricity, especially when they are doped with suitable agents. Problems with environmental instability, difficult processing, poor mechanical properties and high cost have slowed the development of conducting polymers. However, practical use of these materials is imminent, based on recent refinements in understanding how polymers conduct, more systematic approaches to the development of new materials, and significant improvements in both the processing and properties.

  13. Redox-active charge carriers of conducting polymers as a tuner of conductivity and its potential window.

    PubMed

    Park, Han-Saem; Ko, Seo-Jin; Park, Jeong-Seok; Kim, Jin Young; Song, Hyun-Kon

    2013-01-01

    Electric conductivity of conducting polymers has been steadily enhanced towards a level worthy of being called its alias, "synthetic metal". PEDOT:PSS (poly(3,4-ethylenedioxythiophene) doped with poly(styrene sulfonate)), as a representative conducting polymer, recently reached around 3,000 S cm(-1), the value to open the possibility to replace transparent conductive oxides. The leading strategy to drive the conductivity increase is solvent annealing in which aqueous solution of PEDOT:PSS is treated with an assistant solvent such as DMSO (dimethyl sulfoxide). In addition to the conductivity enhancement, we found that the potential range in which PEDOT:PSS is conductive is tuned wider into a negative potential direction by the DMSO-annealing. Also, the increase in a redox-active fraction of charge carriers is proposed to be responsible for the enhancement of conductivity in the solvent annealing process. PMID:23949091

  14. Redox-active charge carriers of conducting polymers as a tuner of conductivity and its potential window

    PubMed Central

    Park, Han-Saem; Ko, Seo-Jin; Park, Jeong-Seok; Kim, Jin Young; Song, Hyun-Kon

    2013-01-01

    Electric conductivity of conducting polymers has been steadily enhanced towards a level worthy of being called its alias, “synthetic metal”. PEDOT:PSS (poly(3,4-ethylenedioxythiophene) doped with poly(styrene sulfonate)), as a representative conducting polymer, recently reached around 3,000 S cm−1, the value to open the possibility to replace transparent conductive oxides. The leading strategy to drive the conductivity increase is solvent annealing in which aqueous solution of PEDOT:PSS is treated with an assistant solvent such as DMSO (dimethyl sulfoxide). In addition to the conductivity enhancement, we found that the potential range in which PEDOT:PSS is conductive is tuned wider into a negative potential direction by the DMSO-annealing. Also, the increase in a redox-active fraction of charge carriers is proposed to be responsible for the enhancement of conductivity in the solvent annealing process. PMID:23949091

  15. Application of nano-structured conducting polymers to humidity sensing

    NASA Astrophysics Data System (ADS)

    Park, Pilyeon

    Nanostructures, such as nanowires, nanocolumns, and nanotubes, have attracted a lot of attention because of their huge potential impact on a variety of applications. For sensor applications, nanostructures provide high surface area to volume ratios. The high surface area to volume ratio allows more reaction areas between target species and detection materials and also improves the detection sensitivity and response time. The main goal of this research was to exploit the advantages and develop innovative methods to accomplish the synthesis of nanowires and nano-coulmn conducting polymers used in humidity detection. To accomplish this, two fabrication methods are used. The first one utilizes the geometric confinement effect of a temporary nanochannel template to orient, precisely position, and assemble Polyaniline (PANI) nanowires as they are synthesized. The other approach is to simply spin-coat a polymer onto a substrate, and then oxygen plasma etch to generate a nano-columned Polyethylenedioxythiophene (PEDOT) thin film. 200 nm silicon oxide coated wafers with embedded platinum electrodes are used as a substrate for both fabrication methods. The biggest advantage of this first method is that it is simple, requires a single-step, i.e., synthesizing and positioning procedures are carried out simultaneously. The second method is potentially manufacturable and economic yet environmentally safe. These two methods do not produce extra nano-building materials to discard or create a health hazard. Both PANI nanowires and nano-columned PEDOT films have been tested for humidity detection using a system designed and built for this research to monitor response (current changes) to moisture, To explain the surface to volume ratio effect, 200 nm PANI nanowires and 10 microm PANI wires were directly compared for detecting moisture, and it was shown that the PANI nanowire had a better sensitivity. It was found difficult to monitor the behaviors of the PEDOT reaction to varying

  16. Conductive polymers derived from iron, ruthenium, and osmium metalloporphyrins: The shish-kebab approach

    PubMed Central

    Collman, James P.; McDevitt, John T.; Yee, Gordon T.; Leidner, Charles R.; McCullough, Laughlin G.; Little, William A.; Torrance, Jerry B.

    1986-01-01

    The synthesis and characterization of pyrazine-bridged polymers of iron(II/III), ruthenium(II/III), and osmium(II/III) octaethylporphyrin (dubbed “shish-kebab” polymers) are presented. Optical and dc conductivity measurements reveal that the ruthenium and osmium polymers, when partially oxidized, are highly conductive. Electrochemical and ESR results are presented that indicate the existence of an interesting metal-centered conduction pathway. Unlike most of the previously reported porphyrinic molecular metals in which the conduction electrons are macrocyclic-based, electron transport in these materials proceeds exclusively along the metal-pyrazine backbone. PMID:16593717

  17. Methods of enhancing conductivity of a polymer-ceramic composite electrolyte

    DOEpatents

    Kumar, Binod

    2003-12-02

    Methods for enhancing conductivity of polymer-ceramic composite electrolytes are provided which include forming a polymer-ceramic composite electrolyte film by a melt casting technique and uniaxially stretching the film from about 5 to 15% in length. The polymer-ceramic composite electrolyte is also preferably annealed after stretching such that it has a room temperature conductivity of from 10.sup.-4 S cm.sup.-1 to 10.sup.-3 S cm.sup.-1. The polymer-ceramic composite electrolyte formed by the methods of the present invention may be used in lithium rechargeable batteries.

  18. Methods of enhancing conductivity of a polymer-ceramic composite electrolyte

    NASA Technical Reports Server (NTRS)

    Kumar, Binod (Inventor)

    2003-01-01

    Methods for enhancing conductivity of polymer-ceramic composite electrolytes are provided which include forming a polymer-ceramic composite electrolyte film by a melt casting technique and uniaxially stretching the film from about 5 to 15% in length. The polymer-ceramic composite electrolyte is also preferably annealed after stretching such that it has a room temperature conductivity of from 10.sup.-4 S cm.sup.-1 to 10.sup.-3 S cm.sup.-1. The polymer-ceramic composite electrolyte formed by the methods of the present invention may be used in lithium rechargeable batteries.

  19. Characterization of proton conducting blend polymer electrolyte using PVA-PAN doped with NH4SCN

    NASA Astrophysics Data System (ADS)

    Premalatha, M.; Mathavan, T.; Selvasekarapandian, S.; Genova, F. Kingslin Mary; Umamaheswari, R.

    2016-05-01

    Polymer electrolytes with proton conductivity based on blend polymer using polyvinyl alcohol (PVA) and poly acrylo nitrile (PAN) doped with ammonium thiocyanate have been prepared by solution casting method using DMF as solvent. The complex formation between the blend polymer and the salt has been confirmed by FTIR Spectroscopy. The amorphous nature of the blend polymer electrolytes have been confirmed by XRD analysis. The highest conductivity at 303 K has been found to be 3.25 × 10-3 S cm-1 for 20 mol % NH4SCN doped 92.5PVA:7.5PAN system. The increase in conductivity of the doped blend polymer electrolytes with increasing temperature suggests the Arrhenius type thermally activated process. The activation energy is found to be low (0.066 eV) for the highest conductivity sample.

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

    DOE PAGESBeta

    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 thatmore » 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.« less

  1. High-modulus, high-conductivity nanostructured polymer electrolyte membranes via polymerization-induced phase separation.

    PubMed

    Schulze, Morgan W; McIntosh, Lucas D; Hillmyer, Marc A; Lodge, Timothy P

    2014-01-01

    The primary challenge in solid-state polymer electrolyte membranes (PEMs) is to enhance properties, such as modulus, toughness, and high temperature stability, without sacrificing ionic conductivity. We report a remarkably facile one-pot synthetic strategy based on polymerization-induced phase separation (PIPS) to generate nanostructured PEMs that exhibit an unprecedented combination of high modulus and ionic conductivity. Simple heating of a poly(ethylene oxide) macromolecular chain transfer agent dissolved in a mixture of ionic liquid, styrene and divinylbenzene, leads to a bicontinuous PEM comprising interpenetrating nanodomains of highly cross-linked polystyrene and poly(ethylene oxide)/ionic liquid. Ionic conductivities higher than the 1 mS/cm benchmark were achieved in samples with an elastic modulus approaching 1 GPa at room temperature. Crucially, these samples are robust solids above 100 °C, where the conductivity is significantly higher. This strategy holds tremendous potential to advance lithium-ion battery technology by enabling the use of lithium metal anodes or to serve as membranes in high-temperature fuel cells.

  2. Degradability of an Acrylate-Linked, Fluorotelomer Polymer in Soil

    EPA Science Inventory

    Fluorotelomer polymers are used in a broad array of products in modern societies worldwide and, if they degrade at significant rates, potentially are a significant source of perfluorooctanoic acid (PFOA) and related compounds to the environment. To evaluate this possibility, we i...

  3. Preparation of metallic cation conducting polymers based on sterically hindered phenols containing polymeric systems

    DOEpatents

    Skotheim, Terje A.; Okamoto, Yoshiyuki; Lee, Hung S.

    1989-01-01

    The present invention relates to ion-conducting solvent-free polymeric systems characterized as being cationic single ion conductors. The solvent-free polymer electrolytes comprise a flexible polymer backbone to which is attached a metal salt, such as a lithium, sodium or potassium salt, of a sterically hindered phenol. The solid polymer electrolyte may be prepared either by (1) attaching the hindered phenol directly to a flexible polymeric backbone, followed by neutralization of the phenolic OH's or (2) reacting the hindered phenol with a polymer precursor which is then polymerized to form a flexible polymer having phenolic OH's which are subsequently neutralized. Preferably the hindered phenol-modified polymeric backbone contains a polyether segment. The ionic conductivity of these solvent-free polymer electrolytes has been measured to be in the range of 10.sup.-4 to 10.sup.-7 S cm.sup.-1 at room temperature.

  4. Preparation of metallic cation conducting polymers based on sterically hindered phenols containing polymeric systems

    DOEpatents

    Skotheim, T.A.; Okamoto, Yoshiyuki; Lee, H.S.

    1989-11-21

    The present invention relates to ion-conducting solvent-free polymeric systems characterized as being cationic single ion conductors. The solvent-free polymer electrolytes comprise a flexible polymer backbone to which is attached a metal salt, such as a lithium, sodium or potassium salt, of a sterically hindered phenol. The solid polymer electrolyte may be prepared either by (1) attaching the hindered phenol directly to a flexible polymeric backbone, followed by neutralization of the phenolic OH's or (2) reacting the hindered phenol with a polymer precursor which is then polymerized to form a flexible polymer having phenolic OH's which are subsequently neutralized. Preferably the hindered phenol-modified polymeric backbone contains a polyether segment. The ionic conductivity of these solvent-free polymer electrolytes has been measured to be in the range of 10[sup [minus]4] to 10[sup [minus]7] S cm[sup [minus]1] at room temperature.

  5. Conducting polymers as driving electrodes for Polymer-Dispersed Liquid-Crystals display devices: on the electro-optical efficiency.

    PubMed

    Roussel, F; Chan-Yu-King, R; Buisine, J-M

    2003-07-01

    Intrinsically conducting polymer (ICP) thin films are used as driving electrodes for Polymer-Dispersed Liquid-Crystals (PDLC) display devices. In order to investigate the electro-optical efficiency of these organic electrodes, three different kinds of conducting polymers, i.e. polyaniline doped with 10-camphorsulfonic acid (PANI(HCSA)), polypyrrole doped with dodecylbenzenesulfonic acid (PPY(DBSA)), and polyethylenedioxythiophene doped with polystyrenesulfonate (PEDOT(PSS)), were prepared or purchased, and coated either on glass or plastic substrates. Optical absorption studies in the UV-Vis range of the conducting polymer-coated substrates were first performed showing the presence of conducting species for the three types of polymers. The electrical characteristics of the resulting films were measured with the four-probes technique. PANI(HCSA) exhibits a higher conductivity sigma approximately 122 S x cm(-1) (RS=1.2x10(3) Omega x (-1)) compared to PPY(DBSA) sigma approximately 2.6 S x cm(-1) (RS=150.7x10(3) Omega x (-1)), and PEDOT(PSS) sigma approximately 1.6 S x cm(-1) (RS=637.3x10(3) Omega x (-1)). It is also shown that for a given conducting polymer, its electrical conductivity decreases when a plastic substrate is used. These observations have been related to significant morphological changes observed by scanning electron microscopy (SEM). A mixture of Norland Optical Adhesive 65 and nematic liquid-crystal E7 in the weight ratio (35:65) was used as precursor of the PDLC material. Better electro-optical responses (transmission properties, drive voltages and switching times) of PDLC films were obtained for devices prepared with (PPY(DBSA))-based electrodes. The electro-optical performances of the PDLC display devices also depend on the nature of the ICP substrate used. PMID:15011049

  6. Conducting polymers as driving electrodes for Polymer-Dispersed Liquid-Crystals display devices: On the electro-optical efficiency

    NASA Astrophysics Data System (ADS)

    Roussel, F.; Chan-Yu-King, R.; Buisine, J.-M.

    2003-07-01

    Intrinsically conducting polymer (ICP) thin films are used as driving electrodes for Polymer-Dispersed Liquid-Crystals (PDLC) display devices. In order to investigate the electro-optical efficiency of these organic electrodes, three different kinds of conducting polymers, i.e. polyaniline doped with 10-camphorsulfonic acid (PANI(HCSA)), polypyrrole doped with dodecylbenzenesulfonic acid (PPY(DBSA)), and polyethylenedioxythiophene doped with polystyrenesulfonate (PEDOT(PSS)), were prepared or purchased, and coated either on glass or plastic substrates. Optical absorption studies in the UV-Vis range of the conducting polymer-coated substrates were first performed showing the presence of conducting species for the three types of polymers. The electrical characteristics of the resulting films were measured with the four-probes technique. PANI(HCSA) exhibits a higher conductivity σsim 122\\un{S\\cdot cm^{-1}} (R_S=1.2 ; 10^3; Ω\\cdotBox^{ -1}) compared to PPY(DBSA) σsim 2.6\\un{S\\cdot cm^{-1}} (R_S=150.7 ;10^3;Ω\\cdotBox^{-1}), and PEDOT(PSS) σsim 1.6\\un{S\\cdot cm^{-1}} (R_S=637.3 ; 10^3; Ω\\cdotBox^{-1}). It is also shown that for a given conducting polymer, its electrical conductivity decreases when a plastic substrate is used. These observations have been related to significant morphological changes observed by scanning electron microscopy (SEM). A mixture of Norland Optical Adhesive 65 and nematic liquid-crystal E7 in the weight ratio (\\chem{35:65}) was used as precursor of the PDLC material. Better electro-optical responses (transmission properties, drive voltages and switching times) of PDLC films were obtained for devices prepared with (PPY(DBSA))-based electrodes. The electro-optical performances of the PDLC display devices also depend on the nature of the ICP substrate used.

  7. Cell patterning via linker-free protein functionalization of an organic conducting polymer (polypyrrole) electrode.

    PubMed

    Bax, Daniel V; Tipa, Roxana S; Kondyurin, Alexey; Higgins, Michael J; Tsoutas, Kostadinos; Gelmi, Amy; Wallace, Gordon G; McKenzie, David R; Weiss, Anthony S; Bilek, Marcela M M

    2012-07-01

    The interaction of proteins and cells with polymers is critical to their use in scientific and medical applications. In this study, plasma immersion ion implantation (PIII) was used to modify the surface of the conducting polymer, polypyrrole, which possesses electrical properties. PIII treatment enabled persistent, covalent binding of the cell adhesive protein, tropoelastin, without employing chemical linking molecules. In contrast tropoelastin was readily eluted from the untreated surface. Through this differential persistence of binding, surface bound tropoelastin supported cell adhesion and spreading on the PIII treated but not the untreated polypyrrole surface. The application of a steel shadow mask during PIII treatment allowed for spatial definition of tropoelastin exclusively to PIII treated regions. The general applicability of this approach to other extracellular matrix proteins was illustrated using collagen I, which displayed similar results to tropoelastin but required extended washing conditions. This approach allowed fine patterning of cell adhesion and spreading to tropoelastin and collagen, specifically on PIII treated polypyrrole regions. We therefore present a methodology to alter the functionality of polypyrrole surfaces, generating surfaces that can spatially control cellular interactions through protein functionalization with the potential for electrical stimulation.

  8. Tuning the thermal conductivity of solar cell polymers through side chain engineering.

    PubMed

    Guo, Zhi; Lee, Doyun; Liu, Yi; Sun, Fangyuan; Sliwinski, Anna; Gao, Haifeng; Burns, Peter C; Huang, Libai; Luo, Tengfei

    2014-05-01

    Thermal transport is critical to the performance and reliability of polymer-based energy devices, ranging from solar cells to thermoelectrics. This work shows that the thermal conductivity of a low band gap conjugated polymer, poly(4,8-bis-alkyloxybenzo[1,2-b:4,5-b']dithiophene-2,6-diyl-alt-(alkylthieno[3,4-b]thiophene-2-carboxylate)-2,6-diyl) (PBDTTT), for photovoltaic applications can be actively tuned through side chain engineering. Compared to the original polymer modified with short branched side chains, the engineered polymer using all linear and long side chains shows a 160% increase in thermal conductivity. The thermal conductivity of the polymer exhibits a good correlation with the side chain lengths as well as the crystallinity of the polymer characterized using small-angle X-ray scattering (SAXS) experiments. Molecular dynamics simulations and atomic force microscopy are used to further probe the molecular level local order of different polymers. It is found that the linear side chain modified polymer can facilitate the formation of more ordered structures, as compared to the branched side chain modified ones. The effective medium theory modelling also reveals that the long linear side chain enables a larger heat carrier propagation length and the crystalline phase in the bulk polymer increases the overall thermal conductivity. It is concluded that both the length of the side chains and the induced polymer crystallization are important for thermal transport. These results offer important guidance for actively tuning the thermal conductivity of conjugated polymers through molecular level design.

  9. Dip-pen nanopatterning of photosensitive conducting polymer using a monomer ink

    NASA Astrophysics Data System (ADS)

    Su, Ming; Aslam, Mohammed; Fu, Lei; Wu, Nianqiang; Dravid, Vinayak P.

    2004-05-01

    Controlled patterning of conducting polymers at a micro- or nanoscale is the first step towards the fabrication of miniaturized functional devices. Here, we introduce an approach for the nanopatterning of conducting polymers using an improved monomer "ink" in dip-pen nanolithography (DPN). The nominal monomer "ink" is converted, in situ, to its conducting solid-state polymeric form after patterned. Proof-of-concept experiments have been performed with acid-promoted polymerization of pyrrole in a less reactive environment (tetrahydrofuran). The ratios of reactants are optimized to give an appropriate rate to match the operation of DPN. A similar synthesis process for the same polymer in its bulk form shows a high conductance and crystalline structure. The miniaturized conducting polymer sensors with light detection ability are fabricated by DPN using the improved ink formula, and exhibit excellent response, recovery, and sensitivity parameters.

  10. ROMP-based thermosetting polymers from modified castor oil with various cross-linking agents

    NASA Astrophysics Data System (ADS)

    Ding, Rui

    Polymers derived from bio-renewable resources are finding an increase in global demand. In addition, polymers with distinctive functionalities are required in certain advanced fields, such as aerospace and civil engineering. In an attempt to meet both these needs, the goal of this work aims to develop a range of bio-based thermosetting matrix polymers for potential applications in multifunctional composites. Ring-opening metathesis polymerization (ROMP), which recently has been explored as a powerful method in polymer chemistry, was employed as a unique pathway to polymerize agricultural oil-based reactants. Specifically, a novel norbornyl-functionalized castor oil alcohol (NCA) was investigated to polymerize different cross-linking agents using ROMP. The effects of incorporating dicyclopentadiene (DCPD) and a norbornene-based crosslinker (CL) were systematically evaluated with respect to curing behavior and thermal mechanical properties of the polymers. Isothermal differential scanning calorimetry (DSC) was used to investigate the conversion during cure. Dynamic DSC scans at multiple heating rates revealed conversion-dependent activation energy by Ozawa-Flynn-Wall analysis. The glass transition temperature, storage modulus, and loss modulus for NCA/DCPD and NCA/CL copolymers with different cross-linking agent loading were compared using dynamic mechanical analysis. Cross-link density was examined to explain the very different dynamic mechanical behavior. Mechanical stress-strain curves were developed through tensile test, and thermal stability of the cross-linked polymers was evaluated by thermogravimetric analysis to further investigate the structure-property relationships in these systems.

  11. Investigation of ITO free transparent conducting polymer based electrode

    NASA Astrophysics Data System (ADS)

    Sharma, Vikas; Sapna, Sachdev, Kanupriya

    2016-05-01

    The last few decades have seen a significant improvement in organic semiconductor technology related to solar cell, light emitting diode and display panels. The material and structure of the transparent electrode is one of the major concerns for superior performance of devices such as OPV, OLED, touch screen and LCD display. Commonly used ITO is now restricted due to scarcity of indium, its poor mechanical properties and rigidity, and mismatch of energy levels with the active layer. Nowadays DMD (dielectric-metal-dielectric) structure is one of the prominent candidates as alternatives to ITO based electrode. We have used solution based spin coated polymer layer as the dielectric layer with silver thin film embedded in between to make a polymer-metal-polymer (PMP) structure for TCE applications. The PMP structure shows low resistivity (2.3 x 10-4Ω-cm), high carrier concentration (2.9 x 1021 cm-3) and moderate transparency. The multilayer PMP structure is characterized with XRD, AFM and Hall measurement to prove its suitability for opto-electronic device applications.

  12. Regiochemistry of Poly(3-Hexylthiophene): Synthesis and Investigation of a Conducting Polymer

    ERIC Educational Resources Information Center

    Pappenfus, Ted M.; Hermanson, David L.; Kohl, Stuart G.; Melby, Jacob H.; Thoma, Laura M.; Carpenter, Nancy E.; Filho, Demetrio A. da Silva; Bredas, Jean-Luc

    2010-01-01

    A series of experiments for undergraduate laboratory courses (e.g., organic, polymer, inorganic) have been developed. These experiments focus on understanding the regiochemistry of the conducting polymer poly(3-hexylthiophene) (P3HT). The substitution patterns in P3HTs control their conformational features, which, in turn, dictates the [pi]…

  13. An Integrated Laboratory Approach toward the Preparation of Conductive Poly(phenylene vinylene) Polymers

    ERIC Educational Resources Information Center

    Knoerzer, Timm A.; Balaich, Gary J.; Miller, Hannah A.; Iacono, Scott T.

    2014-01-01

    Poly(phenylene vinylene) (PPV) represents an important class of conjugated, conducting polymers that have been readily exploited in the preparation of organic electronic materials. In this experiment, students prepare a PPV polymer via a facile multistep synthetic sequence with robust spectroscopic evaluation of synthetic intermediates and the…

  14. Dopant-Enabled Supramolecular Approach for Controlled Synthesis of Nanostructured Conductive Polymer Hydrogels.

    PubMed

    Wang, Yaqun; Shi, Ye; Pan, Lijia; Ding, Yu; Zhao, Yu; Li, Yun; Shi, Yi; Yu, Guihua

    2015-11-11

    Conducting polymer hydrogels emerge as a novel class of polymeric materials that show great potential in many energy, environmental, and biomedical devices. We describe here for the first time a general supramolecular approach toward controlled in situ synthesis of one-dimensional nanostructured conductive hydrogels (polypyrrole (PPy) as a model system) using a rational dopant counterion, which is a disc-shaped liquid crystal molecular copper phthalocyanine-3,4',4″,4‴-tetrasulfonic acid tetrasodium salt (CuPcTs). The dopant molecule CuPcTs cross-linked the PPy chains to form a three-dimensional network that gelated into a hydrogel. The PPy hydrogel could be synthesized in bulk quantities with uniform morphology of self-assembled interconnected nanofibers. The tetra-functional dopant favors a supramolecular self-assembly mechanism to form one-dimensional PPy nanostructures. Furthermore, the enhanced interchain charge transport of CuPcTs doped PPy resulted in greatly enhanced conductivity and pseudocapacitance compared with pristine PPy. PMID:26505784

  15. The synthesis of conducting polymers for corrosion prevention

    NASA Technical Reports Server (NTRS)

    Mattson, Guy C.

    1988-01-01

    The formation of an electrically conducting form of polyaniline by the oxidative polymerization of aniline was studied. Optimum yield and conductivities were obtained by treating aniline in 2 molar hydrochloric acid at 0 to 5 C with ammonium persulfate in 1.15 mole ratio. The yield was 37.6 percent of theory and the conductivity of the product was 10.5 S/cm. This material was formulated into epoxy and acrylic coatings which were also electrically conductive.

  16. 3D fabrication of all-polymer conductive microstructures by two photon polymerization.

    PubMed

    Kurselis, Kestutis; Kiyan, Roman; Bagratashvili, Victor N; Popov, Vladimir K; Chichkov, Boris N

    2013-12-16

    A technique to fabricate electrically conductive all-polymer 3D microstructures is reported. Superior conductivity, high spatial resolution and three-dimensionality are achieved by successive application of two-photon polymerization and in situ oxidative polymerization to a bi-component formulation, containing a photosensitive host matrix and an intrinsically conductive polymer precursor. By using polyethylene glycol diacrylate (PEG-DA) and 3,4-ethylenedioxythiophene (EDOT), the conductivity of 0.04 S/cm is reached, which is the highest value for the two-photon polymerized all-polymer microstructures to date. The measured electrical conductivity dependency on the EDOT concentration indicates percolation phenomenon and a three-dimensional nature of the conductive pathways. Tunable conductivity, biocompatibility, and environmental stability are the characteristics offered by PEG-DA/EDOT blends which can be employed in biomedicine, MEMS, microfluidics, and sensorics.

  17. Porous polymer electrolytes with high ionic conductivity and good mechanical property for rechargeable batteries

    NASA Astrophysics Data System (ADS)

    Liang, Bo; Jiang, Qingbai; Tang, Siqi; Li, Shengliang; Chen, Xu

    2016-03-01

    Porous polymer electrolytes (PPEs) are attractive for developing lithium-ion batteries because of the combined advantages of liquid and solid polymer electrolytes. In the present study, a new porous polymer membrane doped with phytic acid (PA) is prepared, which is used as a crosslinker in polymer electrolyte matrix and can also plasticize porous polymer electrolyte membranes, changing them into soft tough flexible materials. A PEO-PMMA-LiClO4-x wt.% PA (x = weight of PA/weight of polymer, PEO: poly(ethylene oxide); PMMA: poly(methyl methacrylate)) polymer membrane is prepared by a simple evaporation method. The effects of the ratio of PA to PEO-PMMA on the properties of the porous membrane, including morphology, porous structure, and mechanical property, are systematically studied. PA improves the porous structure and mechanical properties of polymer membrane. The maximum tensile strength and elongation of the porous polymer membranes are 20.71 MPa and 45.7% at 15 wt.% PA, respectively. Moreover, the PPEs with 15 wt.% PA has a conductivity of 1.59 × 10-5 S/cm at 20 °C, a good electrochemical window (>5 V), and a low interfacial resistance. The results demonstrate the compatibility of the mechanical properties and conductivity of the PPEs, indicating that PPEs have good application prospects for lithium-ion batteries.

  18. Eliminating Piezoresistivity in Flexible Conducting Polymers for Accurate Temperature Sensing under Dynamic Mechanical Deformations.

    PubMed

    Sezen, Melda; Register, Jeffrey T; Yao, Yao; Glisic, Branko; Loo, Yueh-Lin

    2016-06-01

    The polarity and the magnitude of polyaniline's gauge factor are tuned through structural modification. Combining conducting polymers with gauge factors of opposite polarities yields an accurate temperature sensor, even when deployed under dynamic strains. PMID:27061270

  19. Cotton Fabric Coated with Conducting Polymers and its Application in Monitoring of Carnivorous Plant Response.

    PubMed

    Bajgar, Václav; Penhaker, Marek; Martinková, Lenka; Pavlovič, Andrej; Bober, Patrycja; Trchová, Miroslava; Stejskal, Jaroslav

    2016-04-08

    The paper describes the electrical plant response to mechanical stimulation monitored with the help of conducting polymers deposited on cotton fabric. Cotton fabric was coated with conducting polymers, polyaniline or polypyrrole, in situ during the oxidation of respective monomers in aqueous medium. Thus, modified fabrics were again coated with polypyrrole or polyaniline, respectively, in order to investigate any synergetic effect between both polymers with respect to conductivity and its stability during repeated dry cleaning. The coating was confirmed by infrared spectroscopy. The resulting fabrics have been used as electrodes to collect the electrical response to the stimulation of a Venus flytrap plant. This is a paradigm of the use of conducting polymers in monitoring of plant neurobiology.

  20. Cotton Fabric Coated with Conducting Polymers and its Application in Monitoring of Carnivorous Plant Response

    PubMed Central

    Bajgar, Václav; Penhaker, Marek; Martinková, Lenka; Pavlovič, Andrej; Bober, Patrycja; Trchová, Miroslava; Stejskal, Jaroslav

    2016-01-01

    The paper describes the electrical plant response to mechanical stimulation monitored with the help of conducting polymers deposited on cotton fabric. Cotton fabric was coated with conducting polymers, polyaniline or polypyrrole, in situ during the oxidation of respective monomers in aqueous medium. Thus, modified fabrics were again coated with polypyrrole or polyaniline, respectively, in order to investigate any synergetic effect between both polymers with respect to conductivity and its stability during repeated dry cleaning. The coating was confirmed by infrared spectroscopy. The resulting fabrics have been used as electrodes to collect the electrical response to the stimulation of a Venus flytrap plant. This is a paradigm of the use of conducting polymers in monitoring of plant neurobiology. PMID:27070612

  1. BIOAFFINITY SENSORS BASED ON CONDUCTING POLYMERS: A SHORT REVIEW. (R825323)

    EPA Science Inventory

    The development of new electrode materials has expanded the range and classes of detectable compounds using electroanalytical methods. Conducting electroactive polymers (CEPs) have been demonstrated to have remarkable sensing applications through their ability to be reversibly ox...

  2. Feasible Study for Multi-photon Stereolithography Method of Electro Conductive Polymer Actuator with Complex Shape

    NASA Astrophysics Data System (ADS)

    Sone, Junji; Asami, Akihisa; Yamada, Katsumi; Chen, Jun

    Recently, a soft actuator was developed using an electro-conducting polymer and an ionic conducting polymer. Moreover, stereolithography that uses a femtosecond laser was researched as a method of multiphoton-sensitized polymerization. In this study, we tried a more stable and more rapid stereolithography method for fabricating an electro-conducting polymer using a protein material. From the results of this study, we found that the method was 10 times faster when an aqueous solid that included an electro-conducting polymer, a catalyst, and gelatine was used. In addition, it was stable in that the temperature of the aqueous solid was controlled at 10 degree. We built a 3D shape using the newly developed method, and we will apply this method to a complex actuator.

  3. Graft Copolymers with Conducting Polymer Backbones: A Versatile Route to Functional Materials.

    PubMed

    Strover, Lisa T; Malmström, Jenny; Travas-Sejdic, Jadranka

    2016-02-01

    Graft copolymers with a conducting polymer backbone are a promising class of materials for diverse applications including, but not limited to, organic electronics, stimuli-responsive surfaces, sensors, and biomedical devices. These materials take advantage of the unique electrochemical and optoelectronic properties of conducting polymers, complemented by chemical and/or physical properties of the grafted sidechains. In this Personal Account, we discuss our work in designing functional surfaces based on graft copolymers with a conducting polymer backbone, in the context of broader developments in the field. We review the synthetic approaches available for the rational design of conducting-polymer-based graft copolymers, and examine the types of functional surfaces and soluble materials that may be engineered using these techniques.

  4. Cotton Fabric Coated with Conducting Polymers and its Application in Monitoring of Carnivorous Plant Response.

    PubMed

    Bajgar, Václav; Penhaker, Marek; Martinková, Lenka; Pavlovič, Andrej; Bober, Patrycja; Trchová, Miroslava; Stejskal, Jaroslav

    2016-01-01

    The paper describes the electrical plant response to mechanical stimulation monitored with the help of conducting polymers deposited on cotton fabric. Cotton fabric was coated with conducting polymers, polyaniline or polypyrrole, in situ during the oxidation of respective monomers in aqueous medium. Thus, modified fabrics were again coated with polypyrrole or polyaniline, respectively, in order to investigate any synergetic effect between both polymers with respect to conductivity and its stability during repeated dry cleaning. The coating was confirmed by infrared spectroscopy. The resulting fabrics have been used as electrodes to collect the electrical response to the stimulation of a Venus flytrap plant. This is a paradigm of the use of conducting polymers in monitoring of plant neurobiology. PMID:27070612

  5. Spiro-linked hyperbranched architecture in electrophosphorescent conjugated polymers for tailoring triplet energy back transfer.

    PubMed

    Shao, Shiyang; Ma, Zhihua; Ding, Junqiao; Wang, Lixiang; Jing, Xiabin; Wang, Fosong

    2012-04-17

    A spiro-linked hyperbranched architecture has been incorporated into electrophosphorescent conjugated polymers for the first time, aiming at simultaneously tailoring the intra- and intermolecular triplet energy back transfer from the phosphorescent guest to the conjugated polymer host. Based on a prototype with this unique structure, slower decay of triplet excitons, and 5-8 fold enhancement of device efficiencies are obtained compared with the conventional blending counterpart.

  6. Conducting polymers as ion transport and solid electrolyte materials

    NASA Astrophysics Data System (ADS)

    Larmat Gonzalez, Fernando Enrique

    1997-12-01

    The structure-property relationships in a series of poly (1,4-bis(2-heterocycle)-p-phenylenes) (PBHPs) and poly (3,12-bis(2-heterocycle)-p-dialkylfluorenes) (PBHDFs) as well as the use of polypyrrole (PPy) as solid electrolyte for tantalum capacitors have been investigated. PBHPs, where the heterocycle is thiophene or pyrrole, and PBHDFs, where the heterocycle is thiophene or ethylenedioxythiophene (EDOT), were synthesized electrochemically and their electrochemical properties studied using cyclic voltammetry. The ion transport characteristics of the polymers were investigated using the electrochemical quartz microbalance (EQCM) while the electronic properties of the polymers were studied using optoelectrochemical and in situ electron paramagnetic resonance (EPR)/electrochemical techniques. The electrochemical and electronic properties of PBHPs and PBHDFs have been found to be highly dependent on the nature of the heterocycle and on the pendant side groups substituents. Alkoxy substitution on the phenylene rings results in a marked decrease in the monomer and polymer oxidation potentials and a decrease in the electronic band gap. Substitution with long-chain alkoxy groups results in the formation of stable paramagnetic charge carriers at intermediate doping levels. Also, metallic-like character was observed at high doping levels. The presence of electron-rich heterocycles (e.g., pyrrol, EDOT) as terminal electropolymerizable units on the multi-ring conjugated monomers leads to stabilization of the cation-radical intermediates allowing the electropolymerization to be carried out at low potentials. The ion transport behavior of these polymers under electrochemical switching was found to be anion dominant. PPy as solid electrolyte for tantalum capacitors was prepared using a combination of chemical and electrochemical methods, antraquinone-2-sulfonate (AQSsp-) was used as the dopant ion. The redox properties of PPy were studied by cyclic voltammetry while

  7. 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.

  8. Efficient Gene Delivery of Primary Human Cells Using Peptide Linked Polyethylenimine Polymer Hybrid

    PubMed Central

    Dey, Devaveena; Inayathullah, Mohammed; Lee, Andrew S; Limiuex, Melbes; Zhang, Xuexiang; Wu, Yi; Nag, Divya; De Almeida, Patricia Eliza; Han, Leng; Rajadas, Jayakumar; Wu, Joseph C

    2011-01-01

    Polyethylenimine (PEI) based polymers are efficient agents for cell transfection. However, their use has been hampered due to high cell death associated with transfection thereby resulting in low efficiency of gene delivery within the cells. To circumvent the problem of cellular toxicity, metal binding peptides were linked to PEI. Eight peptide-PEI derivatives were synthesized to improve cell survival and transfection efficiency. TAT linked PEI was used as a control polymer. Peptides linked with PEI amines formed nano gels as shown by electron microscopy and atomic force microscopic measurements. Polymers were characterized by spectroscopic methods and their ability to form complexes with plasmids was tested using electrophoretic studies. These modifications improved polymer biocompatibility as well as cell survival markedly when compared to PEI alone. A subset of the modified peptide-polymers also showed significantly higher transfection efficiency in primary human cells with respect to the widely used transfection agent, lipofectamine. Study of the underlying mechanism of the observed phenomena revealed lower levels of ‘reactive oxygen species’ (ROS) in presence of the peptide-polymers when compared to PEI alone. This was further corroborated with global gene expression analysis which showed upregulation of multiple genes and pathways involved in regulating intracellular oxidative stress. PMID:21477858

  9. Electrochemical patterning of the surface of insulators with electrically conductive polymers

    SciTech Connect

    Zheng, X.Y.; Ding, Y.; Bottomley, L.A.

    1995-12-01

    The great potential of {pi}-conjugated polymers, especially polyacetylene, polyarylenes, and poly(arylenevinylene)s, as components in optical displays, sensors, rechargeable batteries, electromagnetic interference shielding, and microelectronics is well recognized. This paper presents a protocol for patterning the surface of insulators with electrically conductive polymers. The pattern is formed on a gold electrode surface via electro-oxidation of heteroarene monomers. An adhesion layer is used to bond the surface of the conducting polymer pattern to the surface of an insulator. The pattern is then developed by etching away the gold. The approach is illustrated with polypyrrole and is applicable to a wide range of substituted polyheteroarenes and insulating substrates.

  10. Highly Electrically Conductive Nanocomposites Based on PolymerInfused Graphene Sponges

    PubMed Central

    Li, Yuanqing; Samad, Yarjan Abdul; Polychronopoulou, Kyriaki; Alhassan, Saeed M.; Liao, Kin

    2014-01-01

    Conductive polymer composites require a threedimensional 3D network to impart electrical conductivity. A general method that is applicable to most polymers for achieving a desirable graphene 3D network is still a challenge. We have developed a facile technique to fabricate highly electrical conductive composite using vacuumassisted infusion of epoxy into graphene sponge GS scaffold. Macroscopic GSs were synthesized from graphene oxide solution by a hydrothermal method combined with freeze drying. The GSepoxy composites prepared display consistent isotropic electrical conductivity around 1Sm, and it is found to be close to that of the pristine GS. Compared with neat epoxy, GSepoxy has a 12ordersofmagnitude increase in electrical conductivity, attributed to the compactly interconnected graphene network constructed in the polymer matrix. This method can be extended to other materials to fabricate highly conductive composites for practical applications such as electronic devices, sensors, actuators, and electromagnetic shielding. PMID:24722145

  11. Conductive network formation of carbon nanotubes in elastic polymer microfibers and its effect on the electrical conductance: Experiment and simulation

    NASA Astrophysics Data System (ADS)

    Cho, Hyun Woo; Kim, Sang Won; Kim, Jeongmin; Kim, Un Jeong; Im, Kyuhyun; Park, Jong-Jin; Sung, Bong June

    2016-05-01

    We investigate how the electrical conductance of microfibers (made of polymers and conductive nanofillers) decreases upon uniaxial deformation by performing both experiments and simulations. Even though various elastic conductors have been developed due to promising applications for deformable electronic devices, the mechanism at a molecular level for electrical conductance change has remained elusive. Previous studies proposed that the decrease in electrical conductance would result from changes in either distances or contact numbers between conductive fillers. In this work, we prepare microfibers of single walled carbon nanotubes (SWCNTs)/polyvinyl alcohol composites and investigate the electrical conductance and the orientation of SWCNTs upon uniaxial deformation. We also perform extensive Monte Carlo simulations, which reproduce experimental results for the relative decrease in conductance and the SWCNTs orientation. We investigate the electrical networks of SWCNTs in microfibers and find that the decrease in the electrical conductance upon uniaxial deformation should be attributed to a subtle change in the topological structure of the electrical network.

  12. Making Glasses Conduct: Electrochemical Doping of Redox-Active Polymer Thin Films

    NASA Astrophysics Data System (ADS)

    Boudouris, Bryan

    Optoelectronically-active macromolecules have been established as promising materials in myriad organic electronic applications (e.g., organic field-effect transistors (OFETs) and organic photovoltaic (OPV) devices). To date, however, the majority of the work surrounding these materials has focused on materials with a great deal of conjugation along their macromolecular backbones and with varying degrees of crystalline structure. Here, we describe an emerging class of macromolecular charge conductors, radical polymers, that: (1) do not contain conjugation and (2) are completely amorphous glasses. Radical polymers contain non-conjugated macromolecular backbones and stable radical sites along the side chains of the electronically-active materials. In contrast to conjugated polymer systems, these materials conduct charge in the solid state through oxidation-reduction (redox) reactions along these pendant groups. Specifically, we demonstrate that controlling the chemical functionality of the pendant groups and the molecular mobility of the macromolecular backbones significantly impacts the charge transport ability of the pristine (i.e., not doped) radical polymers species. Through proper control of these crucial parameters, we show that radical polymers can have electrical conductivity and charge mobility values on par with commonly-used conjugated polymers. Importantly, we also highlight the ability to dope radical polymers with redox-active small molecule species. This doping, in turn, increases the electrical conductivity of the glassy radical polymer thin films in a manner akin to what is observed in traditional conjugated polymer systems. In this way, we establish a means by which to fabricate optically-transparent and colorless thin film glasses capable of conducting charge in a rather rapid manner. We anticipate that these fundamental insights will prove crucial in developing new transparent conducting layers for future electronic applications.

  13. Field effect type devices based on highly doped conducting polymer

    NASA Astrophysics Data System (ADS)

    Waldmann, O.; Park, J. H.; Hsu, F. C.; Chiou, N. R.; Kim, Y. R.; Epstein, A. J.

    2003-03-01

    Field-effect type devices based on the highly doped polymer poly(3,4-ethylenedioxythiophene)/polystyrene sulfonic acid (PEDOT/PSS) show a reversible change of the source-drain current by several orders of magnitude upon application of appropriate gate voltages. However, the underlying physical mechanism of their operation is little understood so far. A field-effect like operation, dopant ion diffusion, or electrochemical process has been conjectured. In this work, we investigated devices fabricated on glass substrates with polyvinyl phenol and aluminum as dielectric layer and gate, respectively. We applied a saw tooth shaped voltage profile to the gate electrode and a very small source-drain voltage while measuring gate and source-drain currents. These measurements resemble capacitance-voltage measurements used to study the field-effect in inorganic devices as well as cyclic voltammetry used in electrochemical work. Conclusions concerning the operation principle will be discussed. Supported in part by ONR.

  14. Click Cross-Linking-Improved Waterborne Polymers for Environment-Friendly Coatings and Adhesives.

    PubMed

    Hu, Jianqing; Peng, Kaimei; Guo, Jinshan; Shan, Dingying; Kim, Gloria B; Li, Qiyao; Gerhard, Ethan; Zhu, Liang; Tu, Weiping; Lv, Weizhong; Hickner, Michael A; Yang, Jian

    2016-07-13

    Waterborne polymers, including waterborne polyurethanes (WPU), polyester dispersions (PED), and polyacrylate emulsions (PAE), are employed as environmentally friendly water-based coatings and adhesives. An efficient, fast, stable, and safe cross-linking strategy is always desirable to impart waterborne polymers with improved mechanical properties and water/solvent/thermal and abrasion resistance. For the first time, click chemistry was introduced into waterborne polymer systems as a cross-linking strategy. Click cross-linking rendered waterborne polymer films with significantly improved tensile strength, hardness, adhesion strength, and water/solvent resistance compared to traditional waterborne polymer films. For example, click cross-linked WPU (WPU-click) has dramatically improved the mechanical strength (tensile strength increased from 0.43 to 6.47 MPa, and Young's modulus increased from 3 to 40 MPa), hardness (increased from 59 to 73.1 MPa), and water resistance (water absorption percentage dropped from 200% to less than 20%); click cross-linked PED (PED-click) film also possessed more than 3 times higher tensile strength (∼28 MPa) than that of normal PED (∼8 MPa). The adhesion strength of click cross-linked PAE (PAE-click) to polypropylene (PP) was also improved (from 3 to 5.5 MPa). In addition, extra click groups can be preserved after click cross-linking for further functionalization of the waterborne polymeric coatings/adhesives. In this work, we have demonstrated that click modification could serve as a convenient and powerful approach to significantly improve the performance of a variety of traditional coatings and adhesives. PMID:27326894

  15. Characteristics and Mechanisms in Ion-Conducting Polymer Films as Chemical Sensors

    SciTech Connect

    HUGHES,ROBERT C.; YELTON,WILLIAM G.; PFEIFER,KENT B.; PATEL,SANJAY V.

    2000-07-12

    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 published work on SPE films used as chemical sensors. The authors have found that thin films of polymers like polyethylene oxide (PEO) are very sensitive to low concentrations of volatile organic compounds (VOCs) such as common solvents. Evidence of a new sensing mechanism involving the percolation of ions through narrow channels of amorphous polymer is presented. They present impedance spectroscopy of PEO films in the frequency range 0.0001 Hz to 1 MHz for different concentrations of VOCs and relative humidity. They find that the measurement frequency is important for distinguishing ionic conductivity from the double layer capacitance and the parasitic capacitance.

  16. Elucidating Interactions and Conductivity of Newly Synthesised Low Bandgap Polymer with Protic and Aprotic Ionic Liquids

    PubMed Central

    Attri, Pankaj; Lee, Seung-Hyun; Hwang, Sun Woo; Kim, Joong I. L.; Lee, Sang Woo; Kwon, Gi-Chung; Choi, Eun Ha; Kim, In Tae

    2013-01-01

    In this paper, we have examined the conductivity and interaction studies of ammonium and imidazolium based ionic liquids (ILs) with the newly synthesised low bandgap polymer (Poly(2-heptadecyl-4-vinylthieno[3,4-d]thiazole) (PHVTT)). Use of low bandgap polymers is the most suitable way to harvest a broader spectrum of solar radiations for solar cells. But, still there is lack of most efficient low bandgap polymer. In order to solve this problem, we have synthesised a new low bandgap polymer and investigated its interaction with the ILs to enhance its conductivity. ILs may undergo almost unlimited structural variations; these structural variations have attracted extensive attention in polymer studies. The aim of present work is to illustrate the state of art progress of implementing the interaction of ILs (protic and aprotic ILs) with newly synthesised low bandgap polymer. In addition to this, our UV-Vis spectroscopy, confocal Raman spectroscopy and FT-IR spectroscopy results have revealed that all studied ILs (tributylmethylammonium methyl sulfate ([N1444][MeSO4] from ammonium family) and 1-methylimidazolium chloride ([Mim]Cl, and 1-butyl-3-methylimidazolium chloride ([Bmim]Cl from imidazolium family) have potential to interact with polymer. Our semi empirical calculation with help of Hyperchem 7 shows that protic IL ([Mim]Cl) interacts strongly with the low bandgap polymer through the H-bonding. Further, protic ILs shows enhanced conductivity than aprotic ILs in association with low bandgap polymer. This study provides the combined effect of low bandgap polymer and ILs that may generate many theoretical and experimental opportunities. PMID:23874829

  17. Conductive polymers for controlled release and treatment of central nervous system injury

    NASA Astrophysics Data System (ADS)

    Saigal, Rajiv

    As one of the most devastating forms of neurotrauma, spinal cord injury remains a challenging clinical problem. The difficulties in treatment could potentially be resolved by better technologies for therapeutic delivery. In order to develop new approaches to treating central nervous system injury, this dissertation focused on using electrically-conductive polymers, controlled drug release, and stem cell transplantation. We first sought to enhance the therapeutic potential of neural stem cells by electrically increasing their production of neurotrophic factors (NTFs), important molecules for neuronal cell survival, differentiation, synaptic development, plasticity, and growth. We fabricated a new cell culture device for growing neural stem cells on a biocompatible, conductive polymer. Electrical stimulation via the polymer led to upregulation of NTF production by neural stem cells. This approach has the potential to enhance stem cell function while avoiding the pitfalls of genetic manipulation, possibly making stem cells more viable as a clinical therapy. Seeing the therapeutic potential of conductive polymers, we extended our studies to an in vivo model of spinal cord injury (SCI). Using a novel fabrication and extraction technique, a conductive polymer was fabricated to fit to the characteristic pathology that follows contusive SCI. Assessed via quantitative analysis of MR images, the conductive polymer significantly reduced compression of the injured spinal cord. Further characterizing astroglial and neuronal response of injured host tissue, we found significant neuronal sparing as a result of this treatment. The in vivo studies also demonstrated improved locomotor recovery mediated by a conductive polymer scaffold over a non-conductive control. We next sought to take advantage of conductive polymers for local, electronically-controlled release of drugs. Seeking to overcome reported limitations in drug delivery via polypyrrole, we first embedded drugs in poly

  18. Microcontact printing for patterning carbon nanotube/polymer composite films with electrical conductivity.

    PubMed

    Ogihara, Hitoshi; Kibayashi, Hiro; Saji, Tetsuo

    2012-09-26

    Patterned carbon nanotube (CNT)/acrylic resin composite films were prepared using microcontact printing (μCP). To prepare ink for μCP, CNTs were dispersed into propylene glycol monomethyl ether acetate (PGMEA) solution in which acrylic resin and a commercially available dispersant (Disperbyk-2001) dissolved. The resulting ink were spin-coated onto poly(dimethylsiloxane) (PDMS) stamps. By drying solvent components from the ink, CNT/polymer composite films were prepared over PDMS stamps. Contact between the stamps and glass substrates provided CNT/polymer composite patternings on the substrates. The transfer behavior of the CNT/polymer composite films depended on the thermal-treatment temperature during μCP; thermal treatment at temperatures near the glass-transition temperature (T(g)) of the acrylic resin was effective to form uniform patternings on substrates. Moreover, contact area between polymer and substrates also affect the transfer behavior. The CNT/polymer composite films showed high electrical conductivity, despite the nonconductivity of polymer components, because CNTs in the films were interconnected. The electrical conductivity of the composite films increased as CNT content in the film became higher; as a result, the composite patternings showed almost as high electrical conductivity as previously reported CNT/polymer bulk composites.

  19. Microcontact printing for patterning carbon nanotube/polymer composite films with electrical conductivity.

    PubMed

    Ogihara, Hitoshi; Kibayashi, Hiro; Saji, Tetsuo

    2012-09-26

    Patterned carbon nanotube (CNT)/acrylic resin composite films were prepared using microcontact printing (μCP). To prepare ink for μCP, CNTs were dispersed into propylene glycol monomethyl ether acetate (PGMEA) solution in which acrylic resin and a commercially available dispersant (Disperbyk-2001) dissolved. The resulting ink were spin-coated onto poly(dimethylsiloxane) (PDMS) stamps. By drying solvent components from the ink, CNT/polymer composite films were prepared over PDMS stamps. Contact between the stamps and glass substrates provided CNT/polymer composite patternings on the substrates. The transfer behavior of the CNT/polymer composite films depended on the thermal-treatment temperature during μCP; thermal treatment at temperatures near the glass-transition temperature (T(g)) of the acrylic resin was effective to form uniform patternings on substrates. Moreover, contact area between polymer and substrates also affect the transfer behavior. The CNT/polymer composite films showed high electrical conductivity, despite the nonconductivity of polymer components, because CNTs in the films were interconnected. The electrical conductivity of the composite films increased as CNT content in the film became higher; as a result, the composite patternings showed almost as high electrical conductivity as previously reported CNT/polymer bulk composites. PMID:22900673

  20. Exploring novel silicon-containing polymers---From preceramic polymers to conducting polymers with nonlinear optical properties

    SciTech Connect

    Pang, Yi.

    1991-10-07

    Several new types of silicon-containing preceramic polymers, i.e., poly(diorganosilacetylene) and poly(diorganosilvinylene) have been synthesized with molecular weights from 10,000 to 120,000. These polymers could be thermally converted to SiC with a moderate to high char yields. Ready solubility and good processability made these types of polymers attractive in their applications to ceramics. The thermal polymerization of diethynyldiphenyl-silane, which was reported in 1968 to afford poly(diphenylsilyldiacetylene) via dehydrogenation, was reinvestigated. Spectroscopic studies showed that the polymer had a structure of polyacetylene type not diacetylene. Diphenyldiethynylgermane and a series of diorganodiethynylsilances were synthesized. These could be polymerized in the presence of MoCl{sub 5} or WCl{sub 6} to afford a soluble, violet material with Mw as high as 108,000. 100 refs., 56 figs., 16 tabs.

  1. Electron-donor dopant, method of improving conductivity of polymers by doping therewith, and a polymer so treated

    SciTech Connect

    Liepins, R.; Aldissi, M.

    1988-07-05

    The electrically conductive material is described comprising a polymer with a conjugated backbone selected from the group consisting of polyacetylene, polypyrrone, and polyphenylquinoxaline, the polymer being electron-donor doped to a controlled degree with an agent derived from an electride dopant or a dopant derived from an alkalide both of which contain a trapping agent being selected from the group consisting of: a crown ether, 1,4,7,10,13,16-hexaoxacyclooctadecane, cryptand, methyl ether cyclodextrin, spherand, methyl ether calixarene, podand, and an octopus molecule, the agent being made in the presence of lithium.

  2. Electrical Characterization and Morphological Studies of Conducting Polymer Nanofibers

    NASA Technical Reports Server (NTRS)

    Pinto, N. J.; Zhou, Y. X.; Freitag, M.; Johnson, A. T.; MacDiarmid, A. G.; Mueller, C. H.; Theofylaktos, N.; Robinson, D. C.; Miranda, F. A.

    2003-01-01

    Doped polyaniline blended with poly(ethylene oxide) has been electrospun in air to give fibers with diameters in the range 3 nm 200 nm. These fibers were captured on wafers of degenerately doped Si/SiO2 by placing the wafer in the path of the fiber jet formed during the electrospinning process. Individual fibers were contacted using shadow mask evaporation and were also captured on prepatterned wafers. Fibers having diameters greater than 100 nm show a slight increase in the conductivity as compared to the bulk film, while fibers with diameters less than 30 nm had lower conductivity than the bulk. Data on Scanning Conductance Microscopy along the length of individual fibers will be presented. For fibers where the diameter was not uniform, we found that below a certain diameter ( approx.15 nm) the fiber was less conducting as compared to thicker diameter fibers. Dependence of the fiber conductivity on a gate bias is underway and these results will also be presented.

  3. Investigating the Inter-Tube Conduction Mechanism in Polycarbonate Nanocomposites Prepared with Conductive Polymer-Coated Carbon Nanotubes

    NASA Astrophysics Data System (ADS)

    Ventura, Isaac Aguilar; Zhou, Jian; Lubineau, Gilles

    2015-12-01

    A well-known strategy to improve the electrical conductivity of polymers is to dope them with high-aspect-ratio and conductive nanoparticles such as carbon nanotubes (CNTs). However, these nanocomposites also exhibit undesirable properties such as damage-sensitive and history-dependent conductivity because their macroscopic electrical conductivity is largely determined by the tunneling effect at the tube/tube interface. To reduce these issues, new nanocomposites have been developed with CNTs that have been coated with a conductive layer of poly(3,4-ethylenedioxythiophene)poly(styrenesulfonate) (PEDOT/PSS). It has been posited that the insulating region between the CNTs is replaced by a conductive polymer bridge; this has not been proven up to now. We propose here to investigate in-depth how the macroscopic conductivity of these materials is changing when (1) varying the frequency of the electrical loading (impedance spectroscopy), (2) varying the mechanical hydrostatic pressure, and (3) varying the voltage of the electrical loading. The response is systematically compared to the one of conventional carbon nanotube/polycarbonate (CNT/PC) nanocomposites so we can clarify how efficiently the tunneling effect is suppressed from these composites. The objective is to elucidate further the mechanism for conduction in such material formulations.

  4. Investigating the Inter-Tube Conduction Mechanism in Polycarbonate Nanocomposites Prepared with Conductive Polymer-Coated Carbon Nanotubes.

    PubMed

    Ventura, Isaac Aguilar; Zhou, Jian; Lubineau, Gilles

    2015-12-01

    A well-known strategy to improve the electrical conductivity of polymers is to dope them with high-aspect-ratio and conductive nanoparticles such as carbon nanotubes (CNTs). However, these nanocomposites also exhibit undesirable properties such as damage-sensitive and history-dependent conductivity because their macroscopic electrical conductivity is largely determined by the tunneling effect at the tube/tube interface. To reduce these issues, new nanocomposites have been developed with CNTs that have been coated with a conductive layer of poly(3,4-ethylenedioxythiophene)poly(styrenesulfonate) (PEDOT/PSS). It has been posited that the insulating region between the CNTs is replaced by a conductive polymer bridge; this has not been proven up to now. We propose here to investigate in-depth how the macroscopic conductivity of these materials is changing when (1) varying the frequency of the electrical loading (impedance spectroscopy), (2) varying the mechanical hydrostatic pressure, and (3) varying the voltage of the electrical loading. The response is systematically compared to the one of conventional carbon nanotube/polycarbonate (CNT/PC) nanocomposites so we can clarify how efficiently the tunneling effect is suppressed from these composites. The objective is to elucidate further the mechanism for conduction in such material formulations.

  5. Probing Rubber Cross-Linking Generation of Industrial Polymer Networks at Nanometer Scale.

    PubMed

    Gabrielle, Brice; Gomez, Emmanuel; Korb, Jean-Pierre

    2016-06-23

    We present improved analyses of rheometric torque measurements as well as (1)H double-quantum (DQ) nuclear magnetic resonance (NMR) buildup data on polymer networks of industrial compounds. This latter DQ NMR analysis allows finding the distribution of an orientation order parameter (Dres) resulting from the noncomplete averaging of proton dipole-dipole couplings within the cross-linked polymer chains. We investigate the influence of the formulation (filler and vulcanization systems) as well as the process (curing temperature) ending to the final polymer network. We show that DQ NMR follows the generation of the polymer network during the vulcanization process from a heterogeneous network to a very homogeneous one. The time variations of microscopic Dres and macroscopic rheometric torques present power-law behaviors above a threshold time scale with characteristic exponents of the percolation theory. We observe also a very good linear correlation between the kinetics of Dres and rheometric data routinely performed in industry. All these observations confirm the description of the polymer network generation as a critical phenomenon. On the basis of all these results, we believe that DQ NMR could become a valuable tool for investigating in situ the cross-linking of industrial polymer networks at the nanometer scale. PMID:27254797

  6. Probing Rubber Cross-Linking Generation of Industrial Polymer Networks at Nanometer Scale.

    PubMed

    Gabrielle, Brice; Gomez, Emmanuel; Korb, Jean-Pierre

    2016-06-23

    We present improved analyses of rheometric torque measurements as well as (1)H double-quantum (DQ) nuclear magnetic resonance (NMR) buildup data on polymer networks of industrial compounds. This latter DQ NMR analysis allows finding the distribution of an orientation order parameter (Dres) resulting from the noncomplete averaging of proton dipole-dipole couplings within the cross-linked polymer chains. We investigate the influence of the formulation (filler and vulcanization systems) as well as the process (curing temperature) ending to the final polymer network. We show that DQ NMR follows the generation of the polymer network during the vulcanization process from a heterogeneous network to a very homogeneous one. The time variations of microscopic Dres and macroscopic rheometric torques present power-law behaviors above a threshold time scale with characteristic exponents of the percolation theory. We observe also a very good linear correlation between the kinetics of Dres and rheometric data routinely performed in industry. All these observations confirm the description of the polymer network generation as a critical phenomenon. On the basis of all these results, we believe that DQ NMR could become a valuable tool for investigating in situ the cross-linking of industrial polymer networks at the nanometer scale.

  7. 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.

  8. Molecule-to-metal bonds: electrografting polymers on conducting surfaces.

    PubMed

    Palacin, Serge; Bureau, Christophe; Charlier, Julienne; Deniau, Guy; Mouanda, Brigitte; Viel, Pascal

    2004-10-18

    Electrografting is a powerful and versatile technique for modifying and decorating conducting surfaces with organic matter. Mainly based on the electro-induced polymerization of dissolved electro-active monomers on metallic or semiconducting surfaces, it finds applications in various fields including biocompatibility, protection against corrosion, lubrication, soldering, functionalization, adhesion, and template chemistry. Starting from experimental observations, this Review highlights the mechanism of the formation of covalent metal-carbon bonds by electro-induced processes, together with major applications such as derivatization of conducting surfaces with biomolecules that can be used in biosensing, lubrication of low-level electrical contacts, reversible trapping of ionic waste on reactive electrografted surfaces as an alternative to ion-exchange resins, and localized modification of conducting surfaces, a one-step process providing submicrometer grafted areas and which is used in microelectronics.

  9. Role of Chain Morphology and Stiffness in Thermal Conductivity of Amorphous Polymers.

    PubMed

    Zhang, Teng; Luo, Tengfei

    2016-02-01

    Designing thermally conductive polymer is of scientific interest and practical importance for applications like thermal interface materials, electronics packing, and plastic heat exchangers. In this work, we study the fundamental relationship between the molecular morphology and thermal conductivity in bulk amorphous polymers. We use polyethylene as a model system and performed systematic parametric study in molecular dynamics simulations. We find that the thermal conductivity is a strong function of the radius of gyration of the molecular chains, which is further correlated to persistence length, an intrinsic property of the molecule that characterizes molecular stiffness. Larger persistence length can lead to more extended chain morphology and thus higher thermal conductivity. Further thermal conductivity decomposition analysis shows that thermal transport through covalent bonds dominates the effective thermal conductivity over other contributions from nonbonded interactions (van der Waals) and translation of molecules disregarding the morphology. As a result, the more extended chains due to larger persistence length provide longer spatial paths for heat to transfer efficiently and thus lead to higher thermal conductivity. In addition, rigid rod-like polymers with very large persistence length tend to spontaneously crystallize and form orientated chains, leading to a thermal conductivity increase by more than 1 order of magnitude. Our results will provide important insights into the design of thermally conductive amorphous polymers. PMID:26751002

  10. Role of Chain Morphology and Stiffness in Thermal Conductivity of Amorphous Polymers.

    PubMed

    Zhang, Teng; Luo, Tengfei

    2016-02-01

    Designing thermally conductive polymer is of scientific interest and practical importance for applications like thermal interface materials, electronics packing, and plastic heat exchangers. In this work, we study the fundamental relationship between the molecular morphology and thermal conductivity in bulk amorphous polymers. We use polyethylene as a model system and performed systematic parametric study in molecular dynamics simulations. We find that the thermal conductivity is a strong function of the radius of gyration of the molecular chains, which is further correlated to persistence length, an intrinsic property of the molecule that characterizes molecular stiffness. Larger persistence length can lead to more extended chain morphology and thus higher thermal conductivity. Further thermal conductivity decomposition analysis shows that thermal transport through covalent bonds dominates the effective thermal conductivity over other contributions from nonbonded interactions (van der Waals) and translation of molecules disregarding the morphology. As a result, the more extended chains due to larger persistence length provide longer spatial paths for heat to transfer efficiently and thus lead to higher thermal conductivity. In addition, rigid rod-like polymers with very large persistence length tend to spontaneously crystallize and form orientated chains, leading to a thermal conductivity increase by more than 1 order of magnitude. Our results will provide important insights into the design of thermally conductive amorphous polymers.

  11. Coffee bean arabinogalactans: acidic polymers covalently linked to protein.

    PubMed

    Redgwell, Robert J; Curti, Delphine; Fischer, Monica; Nicolas, Pierre; Fay, Laurent B

    2002-02-11

    The arabinogalactan content of green coffee beans (Coffea arabica var. Yellow Caturra) was released by a combination of chemical extraction and enzymatic hydrolysis of the mannan-cellulose component of the wall. Several arabinogalactan fractions were isolated, purified by gel-permeation and ion-exchange chromatography and characterised by compositional and linkage analysis. The AG fractions contained between 6 and 8% glucuronic acid, and gave a positive test for the beta-glucosyl-Yariv reagent, a stain specific for arabinogalactan-proteins. The protein component accounted for between 0.5 and 2.0% of the AGPs and contained between 7 and 12% hydroxyproline. The AG moieties displayed considerable heterogeneity with regard to their degree of arabinosylation and the extent and composition of their side-chains. They possessed a MW average of 650 kDa which ranged between 150 and 2000 kDa. An investigation of the structural features of the major AG fraction, released following enzymatic hydrolysis of the mannan-cellulose polymers, allowed a partial structure of coffee arabinogalactan to be proposed.

  12. Printed organic conductive polymers thermocouples in textile and smart clothing applications.

    PubMed

    Seeberg, Trine M; Røyset, Arne; Jahren, Susannah; Strisland, Frode

    2011-01-01

    This work reports on an experimental investigation of the potential of using selected commercially available organic conductive polymers as active ingredients in thermocouples printed on textiles. Poly(3, 4-ethylenedioxythiophene): poly(4 styrenesulfonate) (PEDOT:PSS) and polyaniline (PANI) were screen printed onto woven cotton textile. The influence of multiple thermocycles between 235 K (-38 °C) and 350 K (+77 °C) on resistivity and thermoelectric properties was examined. The Seebeck coefficients of PEDOT:PSS and PANI were found to be about +18 μV/K and +15 uV/K, respectively, when "metal-polymer" thermocouples were realized by combining the polymer with copper. When "polymer-polymer" thermocouples were formed by combining PEDOT:PSS and PANI, a thermoelectric voltage of about +10 μV/K was observed. A challenge recognized in the experiments is that the generated voltage exhibited drift and fluctuations. PMID:22255039

  13. Tailoring Thermal Conductivity of Single-stranded Carbon-chain Polymers through Atomic Mass Modification

    PubMed Central

    Liao, Quanwen; Zeng, Lingping; Liu, Zhichun; Liu, Wei

    2016-01-01

    Tailoring the thermal conductivity of polymers is central to enlarge their applications in the thermal management of flexible integrated circuits. Progress has been made over the past decade by fabricating materials with various nanostructures, but a clear relationship between various functional groups and thermal properties of polymers remains to be established. Here, we numerically study the thermal conductivity of single-stranded carbon-chain polymers with multiple substituents of hydrogen atoms through atomic mass modification. We find that their thermal conductivity can be tuned by atomic mass modifications as revealed through molecular dynamics simulations. The simulation results suggest that heavy homogeneous substituents do not assist heat transport and trace amounts of heavy substituents can in fact hinder heat transport substantially. Our analysis indicates that carbon chain has the biggest contribution (over 80%) to the thermal conduction in single-stranded carbon-chain polymers. We further demonstrate that atomic mass modifications influence the phonon bands of bonding carbon atoms, and the discrepancies of phonon bands between carbon atoms are responsible for the remarkable drops in thermal conductivity and large thermal resistances in carbon chains. Our study provides fundamental insight into how to tailor the thermal conductivity of polymers through variable substituents. PMID:27713563

  14. Development, characterization and applications of electrodes modified with conductive polymers, ionic liquids and proteins

    NASA Astrophysics Data System (ADS)

    Tang, Yijun

    My research involves both fundamental studies and applications of the electrodes whose surfaces are chemically modified. Conductive polymers are one of the major materials that are used to modify electrode surfaces. The thorough understanding of the behavior of conductive polymers in ionic liquids is interesting and important as the ionic liquids are becoming promising solvents. With poly(vinyl ferrocene) as the model conductive polymer, electrochemical studies were performed in various ionic liquid electrolytes. A theoretical square model and dynamic equilibrium were proposed to describe the interaction between conductive polymers and ionic liquids when the electrons transferred between the electrode and electrolyte. These findings were applied to enable and accelerate the structure relaxation of conductive polymers so that the conductive polymers were capable of delivering peptides efficiently. Incorporation of metallic nanoparticles to the conductive polymer matrix entitled new properties to the conductive polymer, increasing conductivity and providing catalytic abilities. This modification on electrode surface might bring potential uses in gas sensing, energy storage, energy conversion, etc. Conductive polymer coated electrodes produced unique double layer in ionic liquids and a fundamental study of quantum charging help to understand the double layer properties. I also studied the application of surface modified electrodes in chemo- and biosensing. A nonregeneration protocol was created to save the cost and the time in analyzing interfacial binding activities and to prevent the potential of deterioration caused to biological ligands by the conventional regeneration. In the study of carbohydrate/protein interactions, a "click" chemical reaction was first used in constructing a carbohydrate-based biosensor, which was capable of detecting and analyzing proteins specifically and accurately. In another biosensor design, the hydrogen bonding between the template and

  15. Direct Patterning of Organic Functional Polymers through Conventional Photolithography and Noninvasive Cross-Link Agents.

    PubMed

    Squillaci, Marco A; Qiu, Feng; Aliprandi, Alessandro; Zhang, Fan; Feng, Xinliang; Samorì, Paolo

    2016-07-01

    A new technique for direct patterning of functional organic polymers using commercial photolithography setups with a minimal loss of the materials' performances is reported. This result is achieved through novel cross-link agents made by boron- and fluorine-containing heterocycles that can react between themselves upon UV- and white-light exposure.

  16. Cross-linking carbon nanotubes by glycidyl azide polymer via click chemistry.

    PubMed

    Wei, Zhong; Du, Liang; Wang, Lin

    2012-01-01

    Functionalization and cross linking of carbon nanotubes was necessary to fabricate nanotube composites with good interfacial properties and mechanical performance. Glycidyl azide polymer was used as cross-linker of carbon nanotubes via a simple clickable one step reaction initiated by decomposition of azide groups. Both heating and UV irradiation were used to carry out the reaction. FTIR and Raman spectra confirmed the decomposition of azide groups and the anchoring of glycidyl azide polymer onto the surface of carbon nanotubes. Thermal gravity analysis showed that the polymer anchored onto carbon nanotubes was about 10% of the total mass in the solid product, but the efficiency of the reaction was low. The result of tensile test using bulky paper infiltrated with 10% GAP showed that cross linking could bring forth a higher strength, about 4 times higher than the not cross linked. The success of cross linking carbon nanotubes by glycidyl azide polymer paves a new way to fabrication of ultra strong carbon nanotube composites.

  17. Cross-Linked Nanoporous Materials from Reactive and Multifunctional Block Polymers

    SciTech Connect

    Seo, Myungeun; Amendt, Mark A.; Hillmyer, Marc A.

    2012-10-10

    Polylactide-b-poly(styrene-co-2-hydroxyethylmethacrylate) (PLA-b-P(S-co-HEMA)) and polylactide-b-poly(styrene-co-2-hydroxyethylacrylate) (PLA-b-P(S-co-HEA)) were synthesized by combination of ring-opening polymerization and reversible addition-fragmentation chain transfer polymerization. {sup 1}H nuclear magnetic resonance spectroscopy and size exclusion chromatography data indicated that the polymerizations were controlled and that hydroxyl groups were successfully incorporated into the block polymers. The polymers were reacted with 4,4{prime}-methylenebis(phenyl isocyanate) (MDI) to form the corresponding cross-linked materials. The materials were annealed at 150 C to complete the coupling reaction. Robust nanoporous materials were obtained from the cross-linked polymers by treatment with aqueous base to hydrolyze the PLA phase. Small-angle X-ray scattering study combined with scanning electron microscopy showed that MDI-cross-linked PLA-b-P(S-co-HEMA)/PLA-b-P(S-co-HEA) can adopt lamellar, hexagonally perforated lamellar, and hexagonally packed cylindrical morphologies after annealing. In particular, the HPL morphology was found to evolve from lamellae due to increase in volume fraction of PS phase as MDI reacted with hydroxyl groups. The reaction also kinetically trapped the morphology by cross-linking. Bicontinuous morphologies were also observed when dibutyltin dilaurate was added to accelerate reaction between the polymer and MDI.

  18. Polymers and Cross-Linking: A CORE Experiment to Help Students Think on the Submicroscopic Level

    ERIC Educational Resources Information Center

    Bruce, Mitchell R. M.; Bruce, Alice E.; Avargil, Shirly; Amar, Francois G.; Wemyss, Thomas M.; Flood, Virginia J.

    2016-01-01

    The Polymers and Cross-Linking experiment is presented via a new three phase learning cycle: CORE (Chemical Observations, Representations, Experimentation), which is designed to model productive chemical inquiry and to promote a deeper understanding about the chemistry operating at the submicroscopic level. The experiment is built on two familiar…

  19. 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

  20. Impact of molecular orientation on thermal conduction in linear-chain polymer films

    SciTech Connect

    Kurabayashi, K.; Goodson, K.E.

    1999-07-01

    Polymer films are serving as passive regions in fast logic circuits and as active regions in organic optoelectronic devices, such as light-emitting diodes. Recent data illustrated the strong anisotropy in the thermal conductivity of polyimide films of thickness near one micrometer, with the in-plane value larger by a factor of approximately five. This manuscript extends previous theoretical work on heat conduction in stretched bulk polymers to model the conductivity anisotropy in linear-chain polymer films. Predictions are based on the standard deviation of the angle of molecular orientation with respect to the film in-plane direction, which can be investigated using birefringence data, and the expected conductivity anisotropy in a material with perfectly-aligned strands. The modeling and previous data indicate that the anisotropy factor could increase to a value larger than 10 for polyimide films much thinner than 1 micrometer.

  1. Kinetic factors determining conducting filament formation in solid polymer electrolyte based planar devices.

    PubMed

    Krishnan, Karthik; Aono, Masakazu; Tsuruoka, Tohru

    2016-08-01

    Resistive switching characteristics and conducting filament formation dynamics in solid polymer electrolyte (SPE) based planar-type atomic switches, with opposing active Ag and inert Pt electrodes, have been investigated by optimizing the device configuration and experimental parameters such as the gap distance between the electrodes, the salt inclusion in the polymer matrix, and the compliance current applied in current-voltage measurements. The high ionic conductivities of SPE enabled us to make scanning electron microscopy observations of the filament formation processes in the sub-micrometer to micrometer ranges. It was found that switching behaviour and filament growth morphology depend strongly on several kinetic factors, such as the redox reaction rate at the electrode-polymer interfaces, ion mobility in the polymer matrix, electric field strength, and the reduction sites for precipitation. Different filament formations, resulting from unidirectional and dendritic growth behaviours, can be controlled by tuning specified parameters, which in turn improves the stability and performance of SPE-based devices.

  2. Mixed ionic and electronic conductivity in polymers. Progress report, January 1, 1990--December 31, 1990

    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.

  3. Potential of D-Octaarginine-Linked Polymers as an in Vitro Transfection Tool for Biomolecules.

    PubMed

    Mohri, Kohta; Morimoto, Naoki; Maruyama, Megumi; Nakamoto, Norimasa; Hayashi, Emi; Nagata, Kengo; Miyata, Kohei; Ochiai, Kyohei; Hiwatari, Ken-ichiro; Tsubaki, Kazufumi; Tobita, Etsuo; Ishimaru, Yuki; Maeda, Sadaaki; Sakuma, Shinji

    2015-08-19

    We have been investigating the potential use of cell-penetrating peptide-linked polymers as a novel penetration enhancer. Since previous in vivo studies demonstrated that poly(N-vinylacetamide-co-acrylic acid) bearing D-octaarginine, a typical cell-penetrating peptide, enhanced membrane permeation of biomolecules, its potential as an in vitro transfection tool was evaluated in this study. A plasmid DNA encoding green fluorescent protein (pGFP-C1), β-galactosidase, and bovine serum albumin (BSA) were used as model biomolecules. Anionic pGFP-C1 interacted electrostatically with cationic d-octaarginine-linked polymers. When the ratio of mass concentration of polymers to that of pGFP-C1 reached 2.5, complexes whose size and zeta potential were approximately 200 nm and 15 mV, respectively, were obtained. GFP expression was observed in cells incubated with complexes prepared under conditions in which the polymer/pDNA concentration ratio exceeded 2.5. The expression level elevated with an increase in the concentration ratio, but physicochemical properties of the complexes remained unchanged. Results suggested that free polymers contributed to pGFP-C1 internalization. Another cell study demonstrated that β-galactosidase premixed with polymers was taken up into cells in its active tetrameric form. Similar electrostatic interaction-driven complex formation was observed for BSA charged negatively in neutral solution. However, it appeared that the internalization processes of BSA differed from those of pGFP-C1. A mass concentration-dependent increase in internalized BSA was observed, irrespective of the polymer/protein concentration ratio. Due to frail interactions, polymers that were released from the complexes and subsequently immobilized on cell membranes might also contribute to membrane permeation of BSA.

  4. New secondary batteries utilizing electronically conductive polymer cathodes

    NASA Technical Reports Server (NTRS)

    Martin, Charles R.; White, Ralph E.

    1987-01-01

    The objectives are to optimize the transport rates in electronically conductive polypyrrole films by controlling the morphology of the film and to assess the utility of these films as cathodes in a lithium/polypyrrole secondary battery. During this research period, a better understanding was gained of the fundamental electrochemical switching processes within the polypyrrole film. Three publications were submitted based on the work completed.

  5. Thermal Conductivity of Polymer/Nano-filler Blends

    NASA Technical Reports Server (NTRS)

    Ghose, Sayata; Watson, Kent A.; Delozier, Donovan M.; Working, Dennis C.; Connell, John W.; Smith, Joseph G.; Sun, Y. P.; Lin, Y.

    2006-01-01

    To improve the thermal conductivity of an ethylene vinyl acetate copolymer, Elvax 260 was compounded with three carbon based nano-fillers. Multiwalled carbon nanotubes (MWCNT), vapor grown carbon nanofibers (CNF) and expanded graphite (EG) were investigated. In an attempt to improve compatibility between the Elvax and nanofillers, MWCNTs and EGs were modified through non covalent and covalent attachment of alkyl groups. Ribbons were extruded to form samples in which the nanofillers were aligned, and samples were also fabricated by compression molding in which the nano-fillers were randomly oriented. The thermal properties were evaluated by DSC and TGA, and mechanical properties of the aligned samples were determined by tensile testing. The degree of dispersion and alignment of the nanoparticles were investigated using high-resolution scanning electron microscopy. Thermal conductivity measurements were performed using a Nanoflash technique. The thermal conductivity of the samples was measured in both the direction of alignment as well as perpendicular to that direction. The results of this study will be presented.

  6. Mixed-ionic and electronic conductivity in polymers. Annual technical progress report

    SciTech Connect

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

    1991-12-31

    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.

  7. Application for continuation of mixed ionic and electronic conductivity in polymers

    SciTech Connect

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

    1990-01-01

    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.

  8. Investigation of the electronic properties and morphology of conducting polymer electrodes for engineering applications

    SciTech Connect

    Landeros, J. Jr.; Pizzo, P.; Cantow, M.; Uribe, F.

    1995-02-01

    We evaluate the performance of the conducting polymers, polyaniline (PAni) and poly-3-(4-fluorophenyl)-thiophene (PFPT), as the active material in electrochemical capacitors. Using scanning electron microscopy and cyclic voltammetry, the morphology and charge/discharge characteristics of the as-grown polymers were studied under different electrochemical conditions. When electropolymerized at high current densities in aqueous acid solution, PAni exhibits a morphology consisting of a network of interwoven fibrils. It was shown that layers of this PAni network can be electropolymerized onto a thin-planar metal substrate resulting in a decrease in cathodic and anodic peak separations, improving charge/discharge reversibility. A continuous PAni network will make possible a decreases in the total weight of the electrodes with respect to those electrodes grown onto a fibrous carbon substrate of high surface area and high porosity. The effect of different growth electrolytes on the charge/discharge process was also characterized. Hydrochloric acid electrolyte provided an optimum polymer deposition, with respect to morphology and capacitive performance. PFPT films were grown from a solution in a non-aqueous solution. High growth current densities affected the performance of PFPT polymer films in a positive manner. A growth rate of 20 mA/cm{sup 2} not only provided an increase in charge storage, but in the amount of polymer deposited when compared to equivalent amounts deposited at 1 mA/cm{sup 2}. The morphology of the deposited conducting polymer is shown to be one of the most important characteristics in the attempt to achieve an ideal electrochemical capacitor electrode. The polymer morphology directly affects the charge/discharge process because of the strong interaction between ionic conductivity in the electrolyte and the electronic conductivity of the polymer. Cyclic-dependent degradation of the PFPT films was observed.

  9. Destruction and recovery of a nanorod conductive network in polymer nanocomposites via molecular dynamics simulation.

    PubMed

    Gao, Yangyang; Cao, Dapeng; Wu, Youping; Liu, Jun; Zhang, Liqun

    2016-03-28

    By adopting coarse-grained molecular dynamics simulation, we investigate the effects of end-functionalization and shear flow on the destruction and recovery of a nanorod conductive network in a functionalized polymer matrix. We find that the end-functionalization of polymeric chains can enhance the electrical conductivity of nanorod filled polymer nanocomposites, indicated by the decrease of the percolation threshold. However, there exists an optimal end-functionalization extent to reach the maximum electrical conductivity. In the case of steady shear flow, both homogeneous conductive probability and directional conductive probability perpendicular to the shear direction decrease with the shear rate, while the directional conductive probability parallel to the shear direction increases. Importantly, we develop a semi-empirical equation to describe the change of the homogeneous conductive probability as a function of the shear rate. Meanwhile, we obtain an empirical formula describing the relationship between the anisotropy of the conductive probability and the orientation of the nanorods. In addition, the conductivity stability increases with increasing nanorod volume fraction. During the recovery process of the nanorod conductive network, it can be fitted well by the model combining classical percolation theory and a time-dependent nanorod aggregation kinetic equation. The fitted recovery rate is similar for different nanorod volume fractions. In summary, this work provides some rational rules for fabricating polymer nanocomposites with excellent performance of electrical conductivity. PMID:26895557

  10. Destruction and recovery of a nanorod conductive network in polymer nanocomposites via molecular dynamics simulation.

    PubMed

    Gao, Yangyang; Cao, Dapeng; Wu, Youping; Liu, Jun; Zhang, Liqun

    2016-03-28

    By adopting coarse-grained molecular dynamics simulation, we investigate the effects of end-functionalization and shear flow on the destruction and recovery of a nanorod conductive network in a functionalized polymer matrix. We find that the end-functionalization of polymeric chains can enhance the electrical conductivity of nanorod filled polymer nanocomposites, indicated by the decrease of the percolation threshold. However, there exists an optimal end-functionalization extent to reach the maximum electrical conductivity. In the case of steady shear flow, both homogeneous conductive probability and directional conductive probability perpendicular to the shear direction decrease with the shear rate, while the directional conductive probability parallel to the shear direction increases. Importantly, we develop a semi-empirical equation to describe the change of the homogeneous conductive probability as a function of the shear rate. Meanwhile, we obtain an empirical formula describing the relationship between the anisotropy of the conductive probability and the orientation of the nanorods. In addition, the conductivity stability increases with increasing nanorod volume fraction. During the recovery process of the nanorod conductive network, it can be fitted well by the model combining classical percolation theory and a time-dependent nanorod aggregation kinetic equation. The fitted recovery rate is similar for different nanorod volume fractions. In summary, this work provides some rational rules for fabricating polymer nanocomposites with excellent performance of electrical conductivity.

  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 optimize the transport rates in electronically conductive polypyrrole films by controlling the morphology of the film and to assess the utility of these films as cathodes in a lithium/polypyrrole secondary battery. During this research period, progress has been made in improving the charge transport rate of the supermolecular-engineered polypyrrole electrode by eliminating the polypyrrole baselayer that hampered earlier work. Also, the fibril density of the polypyrrole electrode was increased, providing more electroactive sites per unit area.

  12. Effect of low energy oxygen ion beam irradiation on ionic conductivity of solid polymer electrolyte

    SciTech Connect

    Manjunatha, H. Kumaraswamy, G. N.; Damle, R.

    2014-04-24

    Over the past three decades, solid polymer electrolytes (SPEs) have drawn significant attention of researchers due to their prospective commercial applications in high energy-density batteries, electrochemical sensors and super-capacitors. The optimum conductivity required for such applications is about 10{sup −2} – 10{sup −4} S/cm, which is hard to achieve in these systems. It is known that the increase in the concentration of salt in the host polymer results in a continuous increase in the ionic conductivity. However, there is a critical concentration of the salt beyond which the conductivity decreases due to formation of ion pairs with no net charge. In the present study, an attempt is made to identify the concentration at which ion pair formation occurs in PEO: RbBr. We have attempted to modify microstructure of the host polymer matrix by low energy ion (Oxygen ion, O{sup +1} with energy 100 keV) irradiation. Ionic conductivity measurements in these systems were carried out using Impedance Spectroscopy before and after irradiation to different fluencies of the oxygen ion. It is observed that the conductivity increases by one order in magnitude. The increase in ionic conductivity may be attributed to the enhanced segmental motion of the polymer chains. The study reveals the importance of ion irradiation as an effective tool to enhance conductivity in SPEs.

  13. Effect of low energy oxygen ion beam irradiation on ionic conductivity of solid polymer electrolyte

    NASA Astrophysics Data System (ADS)

    Manjunatha, H.; Kumaraswamy, G. N.; Damle, R.

    2014-04-01

    Over the past three decades, solid polymer electrolytes (SPEs) have drawn significant attention of researchers due to their prospective commercial applications in high energy-density batteries, electrochemical sensors and super-capacitors. The optimum conductivity required for such applications is about 10-2 - 10-4 S/cm, which is hard to achieve in these systems. It is known that the increase in the concentration of salt in the host polymer results in a continuous increase in the ionic conductivity. However, there is a critical concentration of the salt beyond which the conductivity decreases due to formation of ion pairs with no net charge. In the present study, an attempt is made to identify the concentration at which ion pair formation occurs in PEO: RbBr. We have attempted to modify microstructure of the host polymer matrix by low energy ion (Oxygen ion, O+1 with energy 100 keV) irradiation. Ionic conductivity measurements in these systems were carried out using Impedance Spectroscopy before and after irradiation to different fluencies of the oxygen ion. It is observed that the conductivity increases by one order in magnitude. The increase in ionic conductivity may be attributed to the enhanced segmental motion of the polymer chains. The study reveals the importance of ion irradiation as an effective tool to enhance conductivity in SPEs.

  14. Electron-donor dopant, method of improving conductivity of polymers by doping therewith, and a polymer so treated

    DOEpatents

    Liepins, R.; Aldissi, M.

    1984-07-27

    Polymers with conjugated backbones, both polyacetylene and polyaromatic heterocyclic types, are doped with electron-donor agents to increase their electrical conductivity. The electron-donor agents are either electride dopants made in the presence of lithium or dopants derived from alkalides made in the presence of lithium. The dopants also contain a metal such as cesium and a trapping agent such as a crown ether.

  15. Electron-donor dopant, method of improving conductivity of polymers by doping therewith, and a polymer so treated

    DOEpatents

    Liepins, Raimond; Aldissi, Mahmoud

    1988-01-01

    Polymers with conjugated backbones, both polyacetylene and polyaromatic heterocyclic types, are doped with electron-donor agents to increase their electrical conductivity. The electron-donor agents are either electride dopants made in the presence of lithium or dopants derived from alkalides made in the presence of lithium. The dopants also contain a metal such as cesium and a trapping agent such as a crown ether.

  16. Highly Transparent Conducting Polymer Top Contacts for Future III-Nitride Based Single Photon Emitters

    NASA Astrophysics Data System (ADS)

    Riess, Sally; Mikulics, Martin; Winden, Andreas; Adam, Roman; Marso, Michel; Grützmacher, Detlev; Hardtdegen, Hilde

    2013-08-01

    In this paper we report on a simple conductive polymer based contacting technology for III-nitride based nanostructures with respect to the electrical operation within the telecommunication wavelength range. Singularly addressable InN/GaN pyramidal nanostructures were selectively grown by metalorganic vapour phase epitaxy (MOVPE) and subsequently integrated into a high-frequency device layout for future ultrafast electro-optical operation. The employment of the p-conducting polymer poly(3,4-ethylenedioxythiophene)-poly(styrene sulfonate) (PEDOT:PSS) is found to increase the light transmittance up to 89% at a wavelength of 1550 nm compared to 72% in the case of a conventional Ni/Au thin layer top contact. DC measurements using a quasi operation mode for 1000 h reveal no degradation and only a moderate increase of the dark currents. Thus, conducting polymer technology shows tremendous potential for future highly efficient and reliable room temperature operation of nitride based single photon emitters (SPEs).

  17. Conducting polymers as electron glasses: surface charge domains and slow relaxation

    PubMed Central

    Ortuño, Miguel; Escasain, Elisa; Lopez-Elvira, Elena; Somoza, Andres M.; Colchero, Jaime; Palacios-Lidon, Elisa

    2016-01-01

    The surface potential of conducting polymers has been studied with scanning Kelvin probe microscopy. The results show that this technique can become an excellent tool to really ‘see’ interesting surface charge interaction effects at the nanoscale. The electron glass model, which assumes that charges are localized by the disorder and that interactions between them are relevant, is employed to understand the complex behavior of conducting polymers. At equilibrium, we find surface potential domains with a typical lateral size of 50 nm, basically uncorrelated with the topography and strongly fluctuating in time. These fluctuations are about three times larger than thermal energy. The charge dynamics is characterized by an exponentially broad time distribution. When the conducting polymers are excited with light the surface potential relaxes logarithmically with time, as usually observed in electron glasses. In addition, the relaxation for different illumination times can be scaled within the full aging model. PMID:26911652

  18. Individually addressed large-scale patterning of conducting polymers by localized electric fields

    NASA Astrophysics Data System (ADS)

    Su, Ming; Fu, Lei; Wu, Nianqiang; Aslam, Mohammed; Dravid, Vinayak P.

    2004-02-01

    A scaleable and site-specific patterning approach with individual addressability is demonstrated via an electropolymerization process within the gap of electrodes. The method can pattern conducting polymer structures by applying a bias between desired electrodes in a monomer vapor. The reaction is proposed to happen in a thin water film condensed inside the electrode gap at ambient environment. It is possible to pattern different conducting polymers on the same substrate by exposing to different monomers. Proof-of-concept experiments on pyrrole and thiophene have shown the generality of this simple and robust method, which enables the real-time monitoring of the resistance and deposition of the conducting polymers. Finally, chemical sensing of the patterned polypyrrole structures to ethanol vapor and ammonia gas are presented.

  19. Cross-linked poly (vinyl alcohol)/sulfosuccinic acid polymer as an electrolyte/electrode material for H2-O2 proton exchange membrane fuel cells

    NASA Astrophysics Data System (ADS)

    Ebenezer, D.; Deshpande, Abhijit P.; Haridoss, Prathap

    2016-02-01

    Proton exchange membrane fuel cell (PEMFC) performance with a cross-linked poly (vinyl alcohol)/sulfosuccinic acid (PVA/SSA) polymer is compared with Nafion® N-115 polymer. In this study, PVA/SSA (≈5 wt. % SSA) polymer membranes are synthesized by a solution casting technique. These cross-linked PVA/SSA polymers and Nafion are used as electrolytes and ionomers in catalyst layers, to fabricate different membrane electrode assemblies (MEAs) for PEMFCs. Properties of each MEA are evaluated using scanning electron microscopy, contact angle measurements, impedance spectroscopy and hydrogen pumping technique. I-V characteristics of each cell are evaluated in a H2-O2 fuel cell testing fixture under different operating conditions. PVA/SSA ionomer causes only an additional ≈4% loss in the anode performance compared to Nafion ionomer. The maximum power density obtained from PVA/SSA based cells range from 99 to 117.4 mW cm-2 with current density range of 247 to 293.4 mA cm-2. Ionic conductivity of PVA/SSA based cells is more sensitive to state of hydration of MEA, while maximum power density obtained is less sensitive to state of hydration of MEA. Maximum power density of cross-linked PVA/SSA membrane based cell is about 35% that of Nafion® N-115 based cell. From these results, cross-linked PVA/SSA polymer is identified as potential candidate for PEMFCs.

  20. Use of conducting polymers to facilitate neurite branching in schizophrenia-related neuronal development.

    PubMed

    Stewart, Elise M; Wu, Zhixiang; Huang, Xu Feng; Kapsa, Robert M I; Wallace, Gordon G

    2016-07-19

    Schizophrenia (SCZ) is a debilitating mental disorder which results in high healthcare and loss of productivity costs to society. This disease remains poorly understood, however there is increasing evidence suggesting a role for oxidative damage in the disease etiology. We aimed to examine the effect of the conducting polymer polypyrrole on the growth and morphology of both wildtype and neuregulin-1 knock out (NRG-1 +/-) explant cells. Polypyrrole is an organic conducting polymer known to be cytocompatible and capable of acting as a platform for effective stimulation of neurons. Here we demonstrate for the first time the ability of this material to mediate processes occurring in disease affected neurons: schizophrenic model cortical neurons. Prefrontal cortical cells were grown on conducting polymer scaffolds of specific composition and showed significantly increased neurite branching and outgrowth length on the polymers compared to controls. Concurrently, a more significant enhancement was seen in both parameters in the NRG-1 +/- model cells. This finding implies that conducting polymers such as polypyrrole may be utilised to overcome neuro-functional deficits associated with neurological disease in humans. PMID:27376413

  1. Conductivity behavior of very thin gold films ruptured by mass transport in photosensitive polymer film

    SciTech Connect

    Linde, Felix; Sekhar Yadavalli, Nataraja; Santer, Svetlana

    2013-12-16

    We report on conductivity behavior of very thin gold layer deposited on a photosensitive polymer film. Under irradiation with light interference pattern, the azobenzene containing photosensitive polymer film undergoes deformation at which topography follows a distribution of intensity, resulting in the formation of a surface relief grating. This process is accompanied by a change in the shape of the polymer surface from flat to sinusoidal together with a corresponding increase in surface area. The gold layer placed above deforms along with the polymer and ruptures at a strain of 4%. The rupturing is spatially well defined, occurring at the topographic maxima and minima resulting in periodic cracks across the whole irradiated area. We have shown that this periodic micro-rupturing of a thin metal film has no significant impact on the electrical conductivity of the films. We suggest a model to explain this phenomenon and support this by additional experiments where the conductivity is measured in a process when a single nanoscopic scratch is formed with an AFM tip. Our results indicate that in flexible electronic materials consisting of a polymer support and an integrated metal circuit, nano- and micro cracks do not alter significantly the behavior of the conductivity unless the metal is disrupted completely.

  2. Ion beam irradiation as a tool to improve the ionic conductivity in solid polymer electrolyte systems

    NASA Astrophysics Data System (ADS)

    Manjunatha, H.; Damle, R.; Kumaraswamy, G. N.

    2016-05-01

    Solid polymer electrolytes (SPEs) have potential applications in solid state electronic and energy devices. The optimum conductivity of SPEs required for such applications is about 10-1 - 10-3 Scm-1, which is hard to achieve in these systems. It is observed that ionic conductivity of SPEs continuously increase with increasing concentration of inorganic salt in the host polymer. However, there is a critical concentration of the salt beyond which the conductivity of SPEs decreases due to the formation of ion pairs. In the present study, solid polymer thin films based on poly (ethylene oxide) (PEO) complexed with NaBr salt with different concentrations have been prepared and the concentration at which ion pair formation occurs in PEOxNaBr is identified. The microstructure of the SPE with highest ionic conductivity is modified by irradiating it with low energy O+1 ion (100 keV) of different fluencies. It is observed that the ionic conductivity of irradiated SPEs increases by one order in magnitude. The increase in ionic conductivity may be attributed to the enhanced segmental motion of the polymer chains due to radiation induced micro structural modification.

  3. Thermoelectric Behavior of Conducting Polymers Hybridized with Inorganic Nanoparticles

    NASA Astrophysics Data System (ADS)

    Son, Woohyun; Lee, Seung Hwan; Park, Hongkwan; Choi, Hyang Hee; Kim, Jung Hyun

    2016-06-01

    We introduce a simple and facile method for fabrication of a poly(3,4-ethylenedioxythiophene):poly(styrene sulfonate) (PEDOT:PSS)/germanium nanoparticle (Ge NP) composite film with enhanced thermoelectric conversion efficiency. The Ge NP were prepared by mechanical grinding and mixed with solution-phase PEDOT:PSS. The film processability of the composite was excellent and the overall process did not involve complicated synthetic procedures. The thermoelectric power factor of the composite film was optimized to 31.20 μW m-1 K-2 by controlling the composition. The composite film had an exceptionally low thermal conductivity of 0.417 W m-1 K-1 and the thermoelectric figure of merit ( ZT) was maximized at 0.0223 at room temperature. The mechanism for the improvement of the thermoelectric conversion efficiency was investigated by introducing energy models based on interfacial scattering of charge carriers and phonons. We expect that this robust method could lead to a facile route for design of organic-inorganic composite-based thermoelectric materials.

  4. Microfluidic enhanced conductive polymer microspheres for sensor applications

    NASA Astrophysics Data System (ADS)

    Snyder, Jessica; Lu, Donglai; Shen, Amy

    2010-11-01

    Methods and devices were developed to produce monodispersed, conducting, responsive polyaniline (PANI) particles for drug delivery and sensor applications. Liquid droplets are produced containing a dispersed phase carried through the device by the continuous phase. The two phases are immiscible. Each phase can be either oil or water based. The aniline monomer is contained within the dispersed phase while the oxidizing agent, ammonium persulfate (APS) is contained within the aqueous phase. The production of either solid (aniline, APS in dispersed phase) or shell particles (aniline in dispersed phase, APS in continuous phase) is possible. Droplets are formed by controlling the viscous and capillary forces at the interface. Droplet size is controlled by phase flow rates, the interfacial tension and viscosity ratio between the phases and the inlet geometry. PANI particles are produce via oxidative polymerization. The polymerization is pH dependent and the time of polymerization is monitored by the distance the droplets travel in the channel. The morphology and electrochemical characteristics of the particles resulting from these methods are studied.

  5. A review study of (bio)sensor systems based on conducting polymers.

    PubMed

    Ates, Murat

    2013-05-01

    This review article concentrates on the electrochemical biosensor systems with conducting polymers. The area of electro-active polymers confined to different electrode surfaces has attracted great attention. Polymer modified carbon substrate electrodes can be designed through polymer screening to provide tremendous improvements in sensitivity, selectivity, stability and reproducibility of the electrode response to detect a variety of analytes. The electro-active films have been used to entrap different enzymes and/or proteins at the electrode surface, but without obvious loss of their bioactivity for the development of biosensors. Electropolymerization is a well-known technique used to immobilize biomaterials to the modified electrode surface. Polymers might be covalently bonding to enzymes or proteins; therefore, thickness, permeation and charge transport characteristics of the polymeric films can be easily and precisely controlled by modulating the electrochemical parameters for various electrochemical techniques, such as chronoamperometry, chronopotentiometry, cyclic voltammetry, and differential pulse voltammetry. This review article is divided into three main parts as given in the table of contents related to the immobilization process of some important conducting polymers, polypyrrole, polythiophene, poly(3,4-ethylenedioxythiophene), polycarbazole, polyaniline, polyphenol, poly(o-phenylenediamine), polyacetylene, polyfuran and their derivatives. A total of 216 references are cited in this review article. The literature reviewed covers a 7 year period beginning from 2005.

  6. Graft copolymerization onto polybutadiene: Cross-linking and thermal degradation of vinyl polymers and copolymers

    NASA Astrophysics Data System (ADS)

    Jiang, Dayue (David)

    This work consists of three parts. In Part I, the graft copolymerization of methyl methacrylate, methyl acrylate, methacylic acid and acrylic acid onto polybutadiene and its copolymers by benzoyl peroxide, BPO, or 2, 2'azobis(2-methylpropionitrile), AIBN, initiation were explored. The results show that these monomers can be grafted onto butadiene region of butadiene-containing polymers. The extent of both graft copolymerization and homopolymerization are dependent on the time and temperature of the reaction and the concentration of all of the reactants. One must specify the monomer, initiator and solvent for the efficient graft copolymerization. The methyl methacrylate adds directly to the radical sites which are formed on the backbone by the interaction of the polymer and the primary radical form the initiator, while for the other three monomers, the graft copolymerization occurs by addition of macro-radical to the double bonds. In Part II, the cross-linking of polybutadiene, butadiene-styrene copolymers, and polystyrene by irradiation, thermal and chemical processes, and Friedel-Crafts chemistry and the effect of cross-linking on the thermal stability were investigated. The proof of cross-linking of the polymer comes from the insolubility of the product after the cross-linking reaction and is characterized by gel content and swelling ratio. The results show that the thermal stability of the polymer can be improved by cross-linking. In Part III, the thermal degradation of three vinyl polymers, poly(vinylsulfonic acid) and its sodium salt and poly(vinylphosphonic acid) were studied by combination technique: TGA/FTIR. The results show that TGA/FTIR combined with analysis of residues provides an excellent opportunity to understand the degradation pathway of the compounds. The observation of foaming indicates that the char which is formed contains carbon as well as the inorganic salts which have been observed. The carbon is in a partially graphitized form. The salts

  7. Water harvesting using a conducting polymer: A study by molecular dynamics simulation

    SciTech Connect

    Ostwal, Mayur M.; Sahimi, Muhammad; Tsotsis, Theodore T.

    2009-06-15

    The results of extensive molecular simulations of adsorption and diffusion of water vapor in polyaniline, made conducting by doping it with HCl or HBr over a broad range of temperatures, are reported. The atomistic model of the polymers was generated using energy minimization, equilibrium molecular dynamics simulations, and two different force fields. The computed sorption isotherms are in excellent agreement with the experimental data. The computed activation energies for the diffusion of water molecules in the polymers also compare well with what has been reported in the literature. The results demonstrate the potential of conducting polyaniline for water harvesting from air.

  8. Conducting polymers and corrosion: Part 2 -- Polyaniline on aluminum alloys

    SciTech Connect

    Tallman, D.E.; Pae, Y.; Bierwagen, G.P.

    2000-04-01

    The electrochemical behavior of conducting polyaniline coatings on various aluminum alloys subjected to immersion in dilute Harrison solution (0.35% ammonium sulfate [(NH{sub 4}){sub 2}SO{sub 4}], 0.05% sodium chloride [NaCl]) was studied. Electrochemical impedance spectroscopy revealed that the charge-transfer resistance (R{sub ct}) of polyaniline-coated alloys increased as a function of immersion time. Polyaniline-coated platinum did not exhibit a significant increase in impedance under similar conditions, indicating that an active metal in contact with the polyaniline is required for the observed increase in R{sub ct}. A similar pattern of increasing R{sub ct} was observed for Alodine (Product A)-treated Al 7075T-6 (UNS A97075) alloys. Mean current and mean potential values obtained from electrochemical noise measurements also suggest a substantial electrochemical interaction between the polyaniline and the aluminum alloy during the early stages of immersion. Polarization experiments and open-circuit potential measurements revealed an ennobling of aluminum alloys to higher potential in the presence of polyaniline coatings. The corrosion protection afforded by a polyaniline/epoxy two-coat system on Al 2024T-3 (UNS A92024) alloy also was evaluated using impedance spectroscopy and compared with that for a single coat of epoxy on untreated and Product A-treated Al2024T-3 alloy. The Product A treatment and the polyaniline coating were found to increase the lifetime of the epoxy topcoat, although these two-coating systems exhibited rather different variations in low-frequency impedance with immersion time. A mechanism consistent with these observations was suggested.

  9. π-Conjugated Microporous Polymer Films: Designed Synthesis, Conducting Properties, and Photoenergy Conversions

    PubMed Central

    Gu, Cheng; Huang, Ning; Chen, Youchun; Qin, Leiqiang; Xu, Hong; Zhang, Shitong; Li, Fenghong; Ma, Yuguang; Jiang, Donglin

    2015-01-01

    Conjugated microporous polymers are a unique class of polymers that combine extended π-conjugation with inherent porosity. However, these polymers are synthesized through solution-phase reactions to yield insoluble and unprocessable solids, which preclude not only the evaluation of their conducting properties but also the fabrication of thin films for device implementation. Here, we report a strategy for the synthesis of thin films of π-conjugated microporous polymers by designing thiophene-based electropolymerization at the solution–electrode interface. High-quality films are prepared on a large area of various electrodes, the film thickness is controllable, and the films are used for device fabrication. These films are outstanding hole conductors and, upon incorporation of fullerenes into the pores, function as highly efficient photoactive layers for energy conversions. Our film strategy may boost the applications in photocatalysis, energy storage, and optoelectronics. PMID:26418672

  10. Light-scattering thermal cross-linking material using morphology of nanoparticle free polymer blends

    NASA Astrophysics Data System (ADS)

    Takei, Satoshi

    2015-03-01

    A newly light-scattering thermal cross-linking material based on self-assembly for forming the morphology of nanoparticle free polymer blends was reported. The material design concept to use light-scattering thermal cross-linking material with high uniformity of light on display panel from LED for high quality such as brightness and evenness, mechanical properties, and gas and water barrier properties. The high light scattering rate of 8 % at 350-450 nm of wavelength, fast cure film at 140 ºC and 120 s, and thermal stability at 190 ºC in bake condition for high productivity were indicated in the light-scattering thermal cross-linking material using the nanoparticle free polymers with carboxylic acid functional groups. These novel system using morphology of nanoparticle free polymer blends in light-scattering package material for a LCD using LED was a valuable approach to the design of material formulations for newly light-scattering thermal cross-linking material.

  11. Highly conductive polymer electrolyte membranes modified with polyethylene glycol-bis-carbamate

    NASA Astrophysics Data System (ADS)

    Fu, Guopeng; Dempsey, Janel; Kyu, Thein

    By virtue of its non-flammability and chemical stability, polyethylene glycol (PEG) networks have shown potential application in all solid-state polymer electrolyte membranes (PEM). However, room temperature ionic conductivity of these PEG based PEMs is inherently low. Plasticization of these PEMs is needed to improve the ionic conductivity. It was demonstrated by this group that small-molecule plasticizers such as succinonitrile, ethylene carbonate, or urea-carbamate can boost ionic conductivity of solid-state polymer electrolyte membranes. Polyethylene glycol bis-carbamate (PEGBC) was synthesized via condensation reaction of polyethylene glycol diamine and ethylene carbonate. The PEGBC modified PEM has shown higher ionic conductivity relative to the unmodified PEM. Moreover, PEGBC modified PEM has a better thermal stability relative to ethylene carbonate based liquid electrolyte with enhanced ionic conductivity. Supported by NSF-DMR 1161070, 1502543 and REU 1359321.

  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. Electrochemical Deposition of Nanostructured Conducting Polymer Coatings on Neural Prosthetic Devices

    NASA Astrophysics Data System (ADS)

    Yang, Junyan; Martin, David

    2003-03-01

    Micromachined neural prosthetic devices facilitate the functional stimulation of and recording from the central nervous system (CNS). These devices have been fabricated to consist of silicon shanks that have gold or iridium sites along their surface. Our goal is to improve the biocompatibility and long-term performance of the neural prosthetic probes when they are implanted chronically in the brain. In our most recent efforts we have established that electrochemical polymerization can be used to deposit fuzzy coatings of conducting polymers specifically on the electrode sites. For neural prosthetic devices that are intended for long term implantation, we need to develop surfaces that provide intimate contact and promote efficient signal transport at the interface of the microelectrode array and brain tissue. We have developed methods to rapidly and reliably fabricate nanostructured conducting polymer coatings on the electrode probes using templated and surfactant-mediated techniques. Conducting polymer nanomushrooms and nanohairs of polypyrrole (PPy) were electrochemically polymerized onto the functional sites of neural probes by using either nanoporous block copolymers thin films, "track-etched" polycarbonate films or anodic aluminium oxide membranes as templates. Nanofibers of conducting polymers have also been successfully obtained by polymerizations in the presence of surfactants. The influence of current density, monomer concentration, surfactant concentration, and deposition charge on the thickness and morphology of the nanostructured conducting polymer coatings has been studied by optical, scanned probe, scanning electron and transmission electron microscopy. As compared with the normal nodular morphology of polypyrrole, the nanostructured morphologies grown from the neural electrode result in fuzzy coatings with extremely high surface area. The electrical properties of the polymer coatings were studied by Impedance Spectroscopy (IS) and Cyclic Voltammetry

  14. All-Polymer Electrolytic Tilt Sensor with Conductive Poly(dimethylsiloxane) Electrodes

    NASA Astrophysics Data System (ADS)

    Lee, June Kyoo; Choi, Ju Chan; Kong, Seong Ho

    2013-06-01

    In this study, an all-polymer electrolytic tilt sensor with conductive and corrosion-resistant poly(dimethylsiloxane) (PDMS) electrodes was designed and its performances were characterized. A PDMS cavity in the sensor for holding an electrolyte was fabricated by soft lithography using an ultraviolet-sensitive polymer. A conductive PDMS composite (gPDMS) with graphite powder was used for the electrode to measure the inclination angle of the electrolyte. A gPDMS composite with a graphite concentration above 40 wt % was able to function as a conductive polymer. The fabricated all-polymer tilt sensor exhibited a detectable inclination range of ± 60° and showed a relatively linear output signal compared with those exhibited by conventional micromachined tilt sensors with axis asymmetrical cavities. The maximum hysteresis of the output signal was approximately 0.1 V\\text{rms when the sensor repeatedly tilted and leveled off. In addition to the fundamental characterization of the sensor, various characteristics of the all-polymer tilt sensor, such as time-dependent and electrolyte-volume-dependent variations in the output signal, were investigated in this study. While the performance of the proposed sensor was comparable to that of conventional silicon-micromachined tilt sensors, the sensor could be produced at a fraction of the cost required to fabricate the conventional sensors.

  15. Ti3C2Tx Filler Effect on the Proton Conduction Property of Polymer Electrolyte Membrane.

    PubMed

    Liu, Yahua; Zhang, Jiakui; Zhang, Xiang; Li, Yifan; Wang, Jingtao

    2016-08-10

    Conductive polymer electrolyte membranes are increasingly attractive for a wide range of applications in hydrogen-relevant devices, for instance hydrogen fuel cells. In this study, two-dimensional Ti3C2Tx, a typical representative of the recently developed MXene family, is synthesized and employed as a universal filler for its features of large specific surface area, high aspect ratio, and sufficient terminated -OH groups. The Ti3C2Tx is incorporated into polymer matrix to explore its function on membrane microstructure and proton conduction property. Both phase-separated (acidic Nafion and sulfonated poly(ether ether ketone)) and non-phase-separated (basic chitosan) polymers are utilized as membrane matrixes. The microstructures, physicochemical properties, and proton conduction properties of the membranes are extensively investigated. It is demonstrated that Ti3C2Tx generates significant promotion effect on proton conduction of the composite membrane by facilitating both vehicle-type and Grotthuss-type proton transfer, yielding several times increased proton conductivity for every polymer-based composite membrane under various conditions, and the composite membrane achieves elevated hydrogen fuel cell performance. The stable Ti3C2Tx also reinforces the thermal and mechanical stabilities of these composite membranes. Since the MXene family includes more than 70 members, this exploration is expected to open up new perspectives for expanding their applications, especially as membrane modifiers and proton conductors. PMID:27430190

  16. Ti3C2Tx Filler Effect on the Proton Conduction Property of Polymer Electrolyte Membrane.

    PubMed

    Liu, Yahua; Zhang, Jiakui; Zhang, Xiang; Li, Yifan; Wang, Jingtao

    2016-08-10

    Conductive polymer electrolyte membranes are increasingly attractive for a wide range of applications in hydrogen-relevant devices, for instance hydrogen fuel cells. In this study, two-dimensional Ti3C2Tx, a typical representative of the recently developed MXene family, is synthesized and employed as a universal filler for its features of large specific surface area, high aspect ratio, and sufficient terminated -OH groups. The Ti3C2Tx is incorporated into polymer matrix to explore its function on membrane microstructure and proton conduction property. Both phase-separated (acidic Nafion and sulfonated poly(ether ether ketone)) and non-phase-separated (basic chitosan) polymers are utilized as membrane matrixes. The microstructures, physicochemical properties, and proton conduction properties of the membranes are extensively investigated. It is demonstrated that Ti3C2Tx generates significant promotion effect on proton conduction of the composite membrane by facilitating both vehicle-type and Grotthuss-type proton transfer, yielding several times increased proton conductivity for every polymer-based composite membrane under various conditions, and the composite membrane achieves elevated hydrogen fuel cell performance. The stable Ti3C2Tx also reinforces the thermal and mechanical stabilities of these composite membranes. Since the MXene family includes more than 70 members, this exploration is expected to open up new perspectives for expanding their applications, especially as membrane modifiers and proton conductors.

  17. Development and Characterization of Healable Carbon Fiber Composites with a Reversibly Cross Linked Polymer

    SciTech Connect

    Ghezzo, Fabrizia; Smith, David R.; Starr, Tatiana N.; Perram, Timothy; Starr, Anthony F.; Darlington, Thomas K.; Baldwin, Richard K.; Oldenburg, Steven J.

    2010-10-18

    Carbon fiber reinforced polymer (CFRP) laminates with remendable cross-linked polymeric matrices were fabricated using a modified resin transfer mold (RTM) technique. The healable composite resin, bis-maleimide tetrafuran (2MEP4F), was synthesized by mixing two monomers, furan (4F) and maleimide (2MEP), at elevated temperatures. The fast kinetic rate of the reaction of polymer constituents requires a fast injection of the healable resin into the carbon fiber preform. The polymer viscosity as a function of time and temperature was experimentally quantified in order to optimize the fabrication of the composite material and to guarantee a uniform flow of the resin through the reinforcement. The method was validated by characterizing the thermo-mechanical properties of the polymerized 2MEP4F. Additionally, the thermo-mechanical properties of the remendable CFRP material were studied.

  18. Developments in the Field of Conducting and Non-conducting Polymer Based Potentiometric Membrane Sensors for Ions Over the Past Decade

    PubMed Central

    Faridbod, Farnoush; Ganjali, Mohammad Reza; Dinarvand, Rassoul; Norouzi, Parviz

    2008-01-01

    Many research studies have been conducted on the use of conjugated polymers in the construction of chemical sensors including potentiometric, conductometric and amperometric sensors or biosensors over the last decade. The induction of conductivity on conjugated polymers by treating them with suitable oxidizing agents won Heeger, MacDiarmid and Shirakawa the 2000 Nobel Prize in Chemistry. Common conjugated polymers are poly(acetylene)s, poly(pyrrole)s, poly(thiophene)s, poly(terthiophene)s, poly(aniline)s, poly(fluorine)s, poly(3-alkylthiophene)s, polytetrathiafulvalenes, poly-napthalenes, poly(p-phenylene sulfide), poly(p-phenylenevinylene)s, poly(3,4-ethylene-dioxythiophene), polyparaphenylene, polyazulene, polyparaphenylene sulfide, poly-carbazole and polydiaminonaphthalene. More than 60 sensors for inorganic cations and anions with different characteristics based on conducting polymers have been reported. There have also been reports on the application of non-conducting polymers (nCPs), i.e. PVC, in the construction of potentiometric membrane sensors for determination of more than 60 inorganic cations and anions. However, the leakage of ionophores from the membranes based on these polymers leads to relatively lower life times. In this article, we try to give an overview of Solid-Contact ISE (SCISE), Single-Piece ISE (SPISE), Conducting Polymer (CP)-Based, and also non-conducting polymer PVC-based ISEs for various ions which their difference is in the way of the polymer used with selective\\ membrane. In SCISEs and SPISEs, the plasticized PVC containing the ionophore and ionic additives govern the selectivity behavior of the electrode and the conducting polymer is responsible of ion-to-electron transducer. However, in CPISEs, the conducting polymer layer is doped with a suitable ionophore which enhances the ion selectivity of the CP while its redox response has to be suppressed.

  19. Hierarchical patterning of multifunctional conducting polymer nanoparticles as a bionic platform for topographic contact guidance.

    PubMed

    Ho, Dominic; Zou, Jianli; Chen, Xianjue; Munshi, Alaa; Smith, Nicole M; Agarwal, Vipul; Hodgetts, Stuart I; Plant, Giles W; Bakker, Anthony J; Harvey, Alan R; Luzinov, Igor; Iyer, K Swaminathan

    2015-02-24

    The use of programmed electrical signals to influence biological events has been a widely accepted clinical methodology for neurostimulation. An optimal biocompatible platform for neural activation efficiently transfers electrical signals across the electrode-cell interface and also incorporates large-area neural guidance conduits. Inherently conducting polymers (ICPs) have emerged as frontrunners as soft biocompatible alternatives to traditionally used metal electrodes, which are highly invasive and elicit tissue damage over long-term implantation. However, fabrication techniques for the ICPs suffer a major bottleneck, which limits their usability and medical translation. Herein, we report that these limitations can be overcome using colloidal chemistry to fabricate multimodal conducting polymer nanoparticles. Furthermore, we demonstrate that these polymer nanoparticles can be precisely assembled into large-area linear conduits using surface chemistry. Finally, we validate that this platform can act as guidance conduits for neurostimulation, whereby the presence of electrical current induces remarkable dendritic axonal sprouting of cells.

  20. Conducting polymer and its composite materials based electrochemical sensor for Nicotinamide Adenine Dinucleotide (NADH).

    PubMed

    Omar, Fatin Saiha; Duraisamy, Navaneethan; Ramesh, K; Ramesh, S

    2016-05-15

    Nicotinamide Adenine Dinucleotide (NADH) is an important coenzyme in the human body that participates in many metabolic reactions. The impact of abnormal concentrations of NADH significantly causes different diseases in human body. Electrochemical detection of NADH using bare electrode is a challenging task especially in the presence of main electroactive interferences such as ascorbic acid (AA), uric acid (UA) and dopamine (DA). Modified electrodes have been widely explored to overcome the problems of poor sensitivity and selectivity occurred from bare electrodes. This review gives an overview on the progress of using conducting polymers, polyelectrolyte and its composites (co-polymer, carbonaceous, metal, metal oxide and clay) based modified electrodes for the sensing of NADH. In addition, developments on the fabrication of numerous conducting polymer composites based modified electrodes are clearly described.

  1. Large enhancement in neurite outgrowth on a cell membrane-mimicking conducting polymer.

    PubMed

    Zhu, Bo; Luo, Shyh-Chyang; Zhao, Haichao; Lin, Hsing-An; Sekine, Jun; Nakao, Aiko; Chen, Chi; Yamashita, Yoshiro; Yu, Hsiao-Hua

    2014-01-01

    Although electrically stimulated neurite outgrowth on bioelectronic devices is a promising means of nerve regeneration, immunogenic scar formation can insulate electrodes from targeted cells and tissues, thereby reducing the lifetime of the device. Ideally, an electrode material capable of electrically interfacing with neurons selectively and efficiently would be integrated without being recognized by the immune system and minimize its response. Here we develop a cell membrane-mimicking conducting polymer possessing several attractive features. This polymer displays high resistance towards nonspecific enzyme/cell binding and recognizes targeted cells specifically to allow intimate electrical communication over long periods of time. Its low electrical impedance relays electrical signals efficiently. This material is capable to integrate biochemical and electrical stimulation to promote neural cellular behaviour. Neurite outgrowth is enhanced greatly on this new conducting polymer; in addition, electrically stimulated secretion of proteins from primary Schwann cells can also occur on it. PMID:25060339

  2. Thermal conductivity of polymer composites with the geometrical characteristics of graphene nanoplatelets

    PubMed Central

    Kim, Hyun Su; Bae, Hyun Sung; Yu, Jaesang; Kim, Seong Yun

    2016-01-01

    One of the most important physical factors related to the thermal conductivity of composites filled with graphene nanoplatelets (GNPs) is the dimensions of the GNPs, that is, their lateral size and thickness. In this study, we reveal the relationship between the thermal conductivity of polymer composites and the realistic size of GNP fillers within the polymer composites (measured using three-dimensional (3D) non-destructive micro X-ray CT analysis) while minimizing the effects of the physical parameters other than size. A larger lateral size and thickness of the GNPs increased the likelihood of the matrix-bonded interface being reduced, resulting in an effective improvement in the thermal conductivity and in the heat dissipation ability of the composites. The thermal conductivity was improved by up to 121% according to the filler size; the highest bulk and in-plane thermal conductivity values of the composites filled with 20 wt% GNPs were 1.8 and 7.3 W/m·K, respectively. The bulk and in-plane thermal conductivity values increased by 650 and 2,942%, respectively, when compared to the thermal conductivity values of the polymer matrix employed (0.24 W/m·K). PMID:27220415

  3. Thermal conductivity of polymer composites with the geometrical characteristics of graphene nanoplatelets.

    PubMed

    Kim, Hyun Su; Bae, Hyun Sung; Yu, Jaesang; Kim, Seong Yun

    2016-05-25

    One of the most important physical factors related to the thermal conductivity of composites filled with graphene nanoplatelets (GNPs) is the dimensions of the GNPs, that is, their lateral size and thickness. In this study, we reveal the relationship between the thermal conductivity of polymer composites and the realistic size of GNP fillers within the polymer composites (measured using three-dimensional (3D) non-destructive micro X-ray CT analysis) while minimizing the effects of the physical parameters other than size. A larger lateral size and thickness of the GNPs increased the likelihood of the matrix-bonded interface being reduced, resulting in an effective improvement in the thermal conductivity and in the heat dissipation ability of the composites. The thermal conductivity was improved by up to 121% according to the filler size; the highest bulk and in-plane thermal conductivity values of the composites filled with 20 wt% GNPs were 1.8 and 7.3 W/m·K, respectively. The bulk and in-plane thermal conductivity values increased by 650 and 2,942%, respectively, when compared to the thermal conductivity values of the polymer matrix employed (0.24 W/m·K).

  4. MeV ion beam interaction with polymer films containing cross-linking agents

    SciTech Connect

    Evelyn, A. L.

    1999-06-10

    Polymer films containing cross linking enhancers were irradiated with MeV alpha particles to determine the effects of MeV ion beam interaction on these materials. The contributed effects from the electronic and nuclear stopping powers were separated by irradiating stacked thin films of polyvinyl chloride (PVC), polystyrene (PS) and polyethersulfone (PES). This layered system allowed most of the effects of the electronic energy deposited to be experienced by the first layers and the last layers to receive most of the effects of the nuclear stopping power. RGA, Raman microprobe analysis, RBS and FTIR measured changes in the chemical structures of the irradiated films. The characterization resolved the effects of the stopping powers on the PVC, PS and PES and the results were compared with those from previously studied polymers that did not contain any cross linking agents.

  5. Gold Nanorod Linking to Control Plasmonic Properties in Solution and Polymer Nanocomposites

    PubMed Central

    2015-01-01

    A novel, solution-based method is presented to prepare bifunctional gold nanorods (B-NRs), assemble B-NRs end-to-end in various solvents, and disperse linked B-NRs in a polymer matrix. The B-NRs have poly(ethylene glycol) grafted along its long axis and cysteine adsorbed to its ends. By controlling cysteine coverage, bifunctional ligands or polymer can be end-grafted to the AuNRs. Here, two dithiol ligands (C6DT and C9DT) are used to link the B-NRs in organic solvents. With increasing incubation time, the nanorod chain length increases linearly as the longitudinal surface plasmon resonance shifts toward lower adsorption wavelengths (i.e., red shift). Analogous to step-growth polymerization, the polydispersity in chain length also increases. Upon adding poly(ethylene glycol) or poly(methyl methacrylate) to chloroform solution with linked B-NR, the nanorod chains are shown to retain end-to-end linking upon spin-casting into PEO or PMMA films. Using quartz crystal microbalance with dissipation (QCM-D), the mechanism of nanorod linking is investigated on planar gold surfaces. At submonolayer coverage of cysteine, C6DT molecules can insert between cysteines and reach an areal density of 3.4 molecules per nm2. To mimic the linking of Au NRs, this planar surface is exposed to cysteine-coated Au nanoparticles, which graft at 7 NPs per μm2. This solution-based method to prepare, assemble, and disperse Au nanorods is applicable to other nanorod systems (e.g., CdSe) and presents a new strategy to assemble anisotropic particles in organic solvents and polymer coatings. PMID:24483622

  6. Gold nanorod linking to control plasmonic properties in solution and polymer nanocomposites.

    PubMed

    Ferrier, Robert C; Lee, Hyun-Su; Hore, Michael J A; Caporizzo, Matthew; Eckmann, David M; Composto, Russell J

    2014-02-25

    A novel, solution-based method is presented to prepare bifunctional gold nanorods (B-NRs), assemble B-NRs end-to-end in various solvents, and disperse linked B-NRs in a polymer matrix. The B-NRs have poly(ethylene glycol) grafted along its long axis and cysteine adsorbed to its ends. By controlling cysteine coverage, bifunctional ligands or polymer can be end-grafted to the AuNRs. Here, two dithiol ligands (C6DT and C9DT) are used to link the B-NRs in organic solvents. With increasing incubation time, the nanorod chain length increases linearly as the longitudinal surface plasmon resonance shifts toward lower adsorption wavelengths (i.e., red shift). Analogous to step-growth polymerization, the polydispersity in chain length also increases. Upon adding poly(ethylene glycol) or poly(methyl methacrylate) to chloroform solution with linked B-NR, the nanorod chains are shown to retain end-to-end linking upon spin-casting into PEO or PMMA films. Using quartz crystal microbalance with dissipation (QCM-D), the mechanism of nanorod linking is investigated on planar gold surfaces. At submonolayer coverage of cysteine, C6DT molecules can insert between cysteines and reach an areal density of 3.4 molecules per nm(2). To mimic the linking of Au NRs, this planar surface is exposed to cysteine-coated Au nanoparticles, which graft at 7 NPs per μm(2). This solution-based method to prepare, assemble, and disperse Au nanorods is applicable to other nanorod systems (e.g., CdSe) and presents a new strategy to assemble anisotropic particles in organic solvents and polymer coatings. PMID:24483622

  7. Hopping conduction in 3,4-cycloalkylpolypyrrole perchlorates: A model study of conductivity in polymers:

    NASA Astrophysics Data System (ADS)

    Ezquerra, T. A.; Rühe, J.; Wegner, G.

    1988-02-01

    The conductivity of 3,4-cycloalkyl-substituted polypyrrole perchlorates has been analyzed using hopping theory. The localization length of the charge carriers was found to be 0.8 nm, the actual conductivity at constant temperature being exponentially dependent on the minimum distance, R, between adjacent chains. R can be reasonably estimated from molecular models and was systematically varied between 0.38 nm (unsubstituted polypyrrole) and 1.38 nm (decamethylene chain attached in 3,4-position). The conduction is activated in the temperature range 150-300 K, the activation energy varying systematically from 0.012 to 0.066 eV on increasing R from 0.38 to 1.38 nm.

  8. Meniscus confined fabrication of multidimensional conducting polymer nanostructures with scanning electrochemical cell microscopy (SECCM).

    PubMed

    McKelvey, Kim; O'Connell, Michael A; Unwin, Patrick R

    2013-04-14

    Scanning electrochemical cell microscopy (SECCM) is demonstrated as a new approach for the construction of extended multi-dimensional conducting polymer (polyaniline) nanostructures, making use of a mobile dual-channel theta pipette cell to control and monitor the location, rate and extent of electropolymerisation.

  9. Photomodulation spectroscopy of photocarrier dynamics, electronic defects and morphology of conducting polymers

    SciTech Connect

    Vardeny, Z.V.

    1993-01-01

    A variety of techniques were used: CW photomodulation, photomodulation in femtosecond and picosecond time ranges, CW resonant Raman scattering, transient photoinduced Raman scattering, electro-absorption, degenerate four-wave mixing, spin dependent photomodulation, and absorption detected magnetic resonance. The following conducting polymers were studied: polyacetylene, polythiophene, polydiacetylene 4-BCMU, polydiethynylsilanes, polysilane embedded in a-Si:H matrix, and fullerenes.

  10. THE ELECTROCHEMISTRY OF ANTIBODY-MODIFIED CONDUCTING POLYMER ELECTRODES. (R825323)

    EPA Science Inventory

    Abstract

    The modification of conducting polymer electrodes with antibodies (i.e. proteins) by means of electrochemical polymerization is a simple step that can be used to develop an immunological sensor. However, the electrochemical processes involved leading to the ge...

  11. A Fiber Supercapacitor with High Energy Density Based on Hollow Graphene/Conducting Polymer Fiber Electrode.

    PubMed

    Qu, Guoxing; Cheng, Jianli; Li, Xiaodong; Yuan, Demao; Chen, Peining; Chen, Xuli; Wang, Bin; Peng, Huisheng

    2016-05-01

    A hollow graphene/conducting polymer composite fiber is created with high mechanical and electronic properties and used to fabricate novel fiber-shaped supercapacitors that display high energy densities and long life stability. The fiber supercapacitors can be woven into flexible powering textiles that are particularly promising for portable and wearable electronic devices.

  12. Conductivity enhancement and resistance changes in polymer films filled with reduced graphene oxide

    NASA Astrophysics Data System (ADS)

    Okhay, O.; Krishna, R.; Salimian, M.; Titus, E.; Gracio, J.; Guerra, L. M.; Ventura, J.

    2013-02-01

    The electrical properties of polymer composites based on polycarbonate (PC) and panipol CXM (CX), filled with reduced graphene oxide (rGO), were investigated. The composite preparation conditions allowed good dispersion of rGO in the polymer matrix. We show here that when used as a nanofiller in polymers, rGO offers an appreciable improvement of the electrical current in 3 orders of magnitude (from 10-10 A to 10-7 A at 10 V), as observed in current-voltage (I-V) data for both PC and CX polymers with rGO. The suggested mechanism for the observed switching effects is the migration of oxygen groups aided by both the electrical field and Joule heating. Moreover, some reset- and set- like changes similar to resistive switching were observed in the I-V data of PC and CX-based films upon the addition of rGO. Clockwise (resembling a memristive system type II) and counter-clockwise (resembling a memristive system type I) directions were detected in the I-V data of the analyzed films. According to the obtained results, rGO can be a good filler for PC and CX polymer-based films for application in electronic and photonic areas, due to the significant improvement of the electrical conductivity of these polymers.

  13. Removal of parabens from aqueous solution using β-cyclodextrin cross-linked polymer.

    PubMed

    Chin, Yuk Ping; Mohamad, Sharifah; Abas, Mhd Radzi Bin

    2010-01-01

    The removal of four parabens, methyl-, ethyl-, propyl-, and benzyl-paraben, by β-cyclodextrin (β-CD) polymer from aqueous solution was studied. Different β-CD polymers were prepared by using two cross-linkers, i.e., hexamethylene diisocyanate (HMDI) and toluene-2,6-diisocyanate (TDI), with various molar ratios of cross-linker. β-CD-HMDI polymer with molar ratio of 1:7 and β-CD-TDI polymer with ratio 1:4 gave the highest adsorption of parabens among the β-CD-HMDI and β-CD-TDI series, and were subsequently used for further studies. The adsorption capacity of β-CD-HMDI is 0.0305, 0.0376, 0.1854 and 0.3026 mmol/g for methyl-, ethyl-, propyl-, and benzyl-paraben, respectively. β-CD-TDI have higher adsorption capacities compared with β-CD-HMDI, the adsorption capacity are 0.1019, 0.1286, 0.2551, and 0.3699 mmol/g methyl-, ethyl-, propyl-, and benzyl-paraben respectively. The parameters studied were adsorption capacity, water retention, and reusability. Role of both cross-linker in adsorption, hydrophobicity of polymers, and adsorption capacity of different parabens were compared and discussed. All experiments were conducted in batch adsorption technique. These polymers were applied to real samples and showed positive results. PMID:20957106

  14. Removal of Parabens from Aqueous Solution Using β-Cyclodextrin Cross-Linked Polymer

    PubMed Central

    Chin, Yuk Ping; Mohamad, Sharifah; Abas, Mhd Radzi Bin

    2010-01-01

    The removal of four parabens, methyl-, ethyl-, propyl-, and benzyl-paraben, by β-cyclodextrin (β-CD) polymer from aqueous solution was studied. Different β-CD polymers were prepared by using two cross-linkers, i.e., hexamethylene diisocyanate (HMDI) and toluene-2,6-diisocyanate (TDI), with various molar ratios of cross-linker. β-CD-HMDI polymer with molar ratio of 1:7 and β-CD-TDI polymer with ratio 1:4 gave the highest adsorption of parabens among the β-CD-HMDI and β-CD-TDI series, and were subsequently used for further studies. The adsorption capacity of β-CD-HMDI is 0.0305, 0.0376, 0.1854 and 0.3026 mmol/g for methyl-, ethyl-, propyl-, and benzyl-paraben, respectively. β-CD-TDI have higher adsorption capacities compared with β-CD-HMDI, the adsorption capacity are 0.1019, 0.1286, 0.2551, and 0.3699 mmol/g methyl-, ethyl-, propyl-, and benzyl-paraben respectively. The parameters studied were adsorption capacity, water retention, and reusability. Role of both cross-linker in adsorption, hydrophobicity of polymers, and adsorption capacity of different parabens were compared and discussed. All experiments were conducted in batch adsorption technique. These polymers were applied to real samples and showed positive results. PMID:20957106

  15. Surface modification of neural prosthetic devices by conducting polymers and biopolymers

    NASA Astrophysics Data System (ADS)

    Cui, Xinyan

    Micromachined neural prosthetic devices facilitate the functional stimulation of and recording from the peripheral and central nervous systems. The microelectrode sites on the neural probes are the actual interface to communicate with neurons. The surfaces of the devices should provide intimate interfacial contact between electrodes and neurons, facilitate the charge transport from ionically conductive tissue to electronically conductive electrode and induce selected neurons or neuron processes to attach onto the microelectrode. Traditional metal electrode materials do not fulfill these functions. Biocompatible conducting polymers were therefore used to modify the surface of the microelectrodes. An electrochemical polymerization approach was developed to directly deposit conductive polymers, such as polypyrrole and poly (3,4-ethylenedioxythiophene) (PEDOT), together with biopolymers, such as protein polymers and bioactive peptides, onto the microelectrode sites. It was found that the deposition of conducting polymer significantly lowered the electrode impedance which is beneficial to neural signal transport. The electronic properties of the conductive polymers were found to be influenced by the film morphology, which could be tailored by controlling the polymerization conditions. The incorporation of biopolymers was confirmed by microfocused Fourier-Transformed infrared (FTIR) spectroscopy. Rat glia and human neuroblastoma cells were shown to preferentially attach and grow on the coated electrode site area of the neural probes. The chemical stability of conducting polymer/biomolecule coatings was studied using FTIR, impedance spectroscopy and cyclic voltammetry. The biomolecules were stable in the film after seven weeks of soaking in deionized water, while polypyrrole underwent some subtle changes in chemical structure. PEDOT was proven to be a more stable material under potential cycling and provided even lower impedance. The adhesion between the coating and

  16. Ordered structures in proton conducting membranes from supramolecular liquid crystal polymers.

    PubMed

    Every, Hayley A; Mendes, Eduardo; Picken, Stephen J

    2006-11-30

    Highly sulfonated forms of poly(p-phenylene terephthalamide) (PPTA) have been prepared in three different molecular configurations; sulfonated diamine form (S-PPTA), sulfonated terephthalic acid form (S-invert-PPTA), and the bi-sulfonated form (S2-PPTA). All three polymers are water soluble to a certain degree and films were cast from solution for S-PPTA and S-invert-PPTA. S-PPTA films absorb less water than S-invert-PPTA (under controlled humidity conditions) and consequently, the conductivity for this polymer is also slightly lower. Although the conductivities are comparable to Nafion (of the order of 10(-2) to 10(-1) Scm(-1)), proton mobility is more restricted. X-ray diffraction showed that the rigid molecules are aligned in opposite directions for the two polymer films, being homeotropic in S-PPTA films and planar for S-invert-PPTA. SEM analysis demonstrated layering in the same direction as the alignment of the polymer chains. The variation in the polymer alignment is most likely the result of the differences in the solution properties and the film forming process. It is possible, however, that this alignment could be exploited to enhance proton transport and thus these films are of interest for fuel cell membranes. PMID:17125333

  17. Application of conductive polymers in biocathode of microbial fuel cells and microbial community.

    PubMed

    Li, Chao; Ding, Lili; Cui, Hao; Zhang, Libin; Xu, Ke; Ren, Hongqiang

    2012-07-01

    Four kinds of conductive polymers, polyaniline (PANI) and its co-polymers poly (aniline-co-o-aminophenol) (PANOA), poly (aniline-co-2, 4-diaminophenol) (PANDAP) and poly (aniline-1, 8-diaminonaphthalene) (PANDAN) were applied to modify carbon felts as the aerobic abiotic cathodes and biocathodes in microbial fuel cells (MFC). Compare to unmodified, all the four polymers can significantly improve the power densities for both abiotic cathodes (increased by 300%) and biocathodes (increased by 180%). The co-polymers with different functional groups introduction had further special advantages in MFC performance: PANOA and PANDAP with -OH showed less sensitivity to DO and pH change in cathode; PANDAP and PANDAN with -NH(3) provided better attachment condition for biofilm which endowed them higher power output. With the help of conductive polymer coats, the cathode biofilm became thicker, and according to biodiversity analysis, the predominated phyla changed from β-Proteobacteria (unmodified) to α, γ-Proteobacteria (modified), which may be responsible for the superiority of the modified MFCs.

  18. Investigation and Characterization of Conductive DEAP Polymer Materials with Nickel Nanocomposites

    NASA Astrophysics Data System (ADS)

    Wrisley, Seaver

    Dielectric ElectroActive Polymers, or DEAPs, are devices with coupled electrical and mechanical responses that resemble stretchable parallel plate capacitors, that can act as actuators, sensors, or electrical generators. Currently, the electrode layers on the top and bottom are generally conductive carbon grease, which is dirty and also causes curing issues for certain polymers. This thesis explores several polymers and conductive fillers to identify a conductive nanocomposite material, to replace the grease electrode with a solid material and eliminate issues associated with grease electrodes. It then characterizes the mechanical and electric properties and how they change during cyclic loading, while augmenting an equibiaxial tensile testing machine and advancing the knowledge of equibiaxial characterization. The most promising polymer/filler combination was found to be EcoFlex30, a platinum cure silicone rubber, containing seven volume percent of nickel nanostrands and three volume percent of 0.1 mm length nickel-coated carbon fiber. Using two conductive fillers of different sizes resulted in much higher conductivity than a single filler alone, and an enormous piezoresistive effect. This material gave weak conductivity at no load, increasing several orders of magnitude as strained and well surpassing the benchmark of 1.2 S/m set by conductive carbon grease. Elastomer materials were found to have conductivities as high as 275 S/m under peak strain, and changing the nickel-coated carbon fiber length allowed for strains over 120%. Equibiaxial stress-strain curves were also analyzed for energy lost through hysteresis, in order to compare to published results for DEAPs used as Dielectric Energy Generators. Results and recommendations are presented for using and further improving the materials for applications of DEAPs used as energy harvesters and capacitive sensors, using the material alone as a piezoresistive sensor, and improving the equibiaxial characterization

  19. A Single Molecular Diels-Alder Crosslinker for Achieving Recyclable Cross-Linked Polymers.

    PubMed

    Chen, Shengli; Wang, Fenfen; Peng, Yongjin; Chen, Tiehong; Wu, Qiang; Sun, Pingchuan

    2015-09-01

    A triol-functional crosslinker combining the thermoreversible properties of Diels-Alder (DA) adducts in one molecule is designed, synthesized, and used as an ideal substitute of a traditional crosslinker to prepare thermal recyclable cross-linked polyurethanes with excellent mechanical properties and recyclability in a very simple and efficient way. The recycle property of these materials achieved by the DA/retro-DA reaction at a suitable temperature is verified by differential scanning calorimetry and in situ variable temperature solid-state NMR experiments during the cyclic heating and cooling processes. The thermal recyclability and remending ability of the bulk polyurethanes is demonstrated by three polymer processing methods, including hot-press molding, injection molding, and solution casting. It is notable that all the recycled cross-linked polymers display nearly invariable elongation/stress at break compared to the as-synthesized samples. Further end-group functionalization of this single molecular DA crosslinker provides the potential in preparing a wide range of recyclable cross-linked polymers.

  20. A Single Molecular Diels-Alder Crosslinker for Achieving Recyclable Cross-Linked Polymers.

    PubMed

    Chen, Shengli; Wang, Fenfen; Peng, Yongjin; Chen, Tiehong; Wu, Qiang; Sun, Pingchuan

    2015-09-01

    A triol-functional crosslinker combining the thermoreversible properties of Diels-Alder (DA) adducts in one molecule is designed, synthesized, and used as an ideal substitute of a traditional crosslinker to prepare thermal recyclable cross-linked polyurethanes with excellent mechanical properties and recyclability in a very simple and efficient way. The recycle property of these materials achieved by the DA/retro-DA reaction at a suitable temperature is verified by differential scanning calorimetry and in situ variable temperature solid-state NMR experiments during the cyclic heating and cooling processes. The thermal recyclability and remending ability of the bulk polyurethanes is demonstrated by three polymer processing methods, including hot-press molding, injection molding, and solution casting. It is notable that all the recycled cross-linked polymers display nearly invariable elongation/stress at break compared to the as-synthesized samples. Further end-group functionalization of this single molecular DA crosslinker provides the potential in preparing a wide range of recyclable cross-linked polymers. PMID:26248230

  1. Light-harvesting cross-linked polymers for efficient heterogeneous photocatalysis.

    PubMed

    Wang, Cheng; Xie, Zhigang; deKrafft, Kathryn E; Lin, Wenbin

    2012-04-01

    Nonporous, phosphorescent cross-linked polymers (Ru-CP and Ir-CP) were synthesized via Pd-catalyzed Sonogashira cross-coupling reactions between tetra(p-ethynylphenyl)methane and dibrominated Ru(bpy)(3)(2+) or Ir(ppy)(2)(bpy)(+), respectively. The resultant particulate cross-linked polymer (CP) materials have very high catalyst loadings (76.3 wt % for Ru-CP and 71.6 wt % for Ir-CP), and are nonporous with negligibly small surface areas (2.9 m(2)/g for Ru-CP and 2.7 m(2)/g for Ir-CP). Despite their nonporous nature, the insoluble CP materials serve as highly active and recyclable heterogeneous photocatalysts for a range of organic transformations such as aza-Henry reaction, aerobic amine coupling, and dehalogenation of benzyl bromoacetate. An efficient light-harvesting mechanism, which involves collection of photons by exciting the (3)MLCT states of the phosphors and migration of the excited states to the particle surface, is proposed to account for the very high catalytic activities of these nonporous CPs. Steady-state and time-resolved emission data, as well as the reduced catalytic activity of Os(bpy)(3)(2+)-doped Ru-CPs supports efficient excited state migration for the CP frameworks. This work uncovers a new strategy in designing highly efficient photocatalysts based on light-harvesting cross-linked polymers.

  2. Ion transport study in polymer-nanocomposite films by dielectric spectroscopy and conductivity scaling

    NASA Astrophysics Data System (ADS)

    Tripathi, Namrata; Thakur, Awalendra K.; Shukla, Archana; Marx, David T.

    2015-07-01

    The dielectric and conductivity response of polymer nanocomposite electrolytes (films of PMMA4LiClO4 dispersed with nano-CeO2 powder) have been investigated. The dielectric behavior was analyzed via the dielectric permittivity (ε‧) and dissipation factor (tan δ) of the samples. The analysis has shown the presence of space charge polarization at lower frequencies. The real part of ac conductivity spectra of materials obeys the Jonscher power law. Parameters such as dc conductivity, hopping rate, activation energies and the concentration of charge carriers were determined from conductivity data using the Almond West formalism. It is observed that the higher ionic conductivity at higher temperature is due to increased thermally-activated hopping rates accompanied by a significant increase in carrier concentration. The contribution of carrier concentration to the total conductivity is also confirmed from activation energy of migration conduction and from Summerfield scaling. The ac conductivity results are also well correlated with TEM results.

  3. Emerging synthetic strategies for core cross-linked star (CCS) polymers and applications as interfacial stabilizers: bridging linear polymers and nanoparticles.

    PubMed

    Chen, Qijing; Cao, Xueteng; Xu, Yuanyuan; An, Zesheng

    2013-10-01

    Core cross-linked star (CCS) polymers become increasingly important in polymer science and are evaluated in many value-added applications. However, limitations exist to varied degrees for different synthetic methods. It is clear that improvement in synthetic efficiency is fundamental in driving this field moving even further. Here, the most recent advances are highlighted in synthetic strategies, including cross-linking with cross-linkers of low solubility, polymerization-induced self-assembly in aqueous-based heterogeneous media, and cross-linking via dynamic covalent bonds. The understanding of CCS polymers is also further refined to advocate their role as an intermediate between linear polymers and polymeric nanoparticles, and their use as interfacial stabilizers is rationalized within this context.

  4. Fabrication of conductive polymer nanofibers through SWNT supramolecular functionalization and aqueous solution processing

    NASA Astrophysics Data System (ADS)

    Naeem, Fahim; Prestayko, Rachel; Saem, Sokunthearath; Nowicki, Lauren; Imit, Mokhtar; Adronov, Alex; Moran-Mirabal, Jose M.

    2015-10-01

    Polymeric thin films and nanostructured composites with excellent electrical properties are required for the development of advanced optoelectronic devices, flexible electronics, wearable sensors, and tissue engineering scaffolds. Because most polymers available for fabrication are insulating, one of the biggest challenges remains the preparation of inexpensive polymer composites with good electrical conductivity. Among the nanomaterials used to enhance composite performance, single walled carbon nanotubes (SWNTs) are ideal due to their unique physical and electrical properties. Yet, a barrier to their widespread application is that they do not readily disperse in solvents traditionally used for polymer processing. In this study, we employed supramolecular functionalization of SWNTs with a conjugated polyelectrolyte as a simple approach to produce stable aqueous nanotube suspensions, that could be effortlessly blended with the polymer poly(ethyleneoxide) (PEO). The homogeneous SWNT:PEO mixtures were used to fabricate conductive thin films and nanofibers with improved conductivities through drop casting and electrospinning. The physical characterization of electrospun nanofibers through Raman spectroscopy and SEM revealed that the SWNTs were uniformly incorporated throughout the composites. The electrical characterization of SWNT:PEO thin films allowed us to assess their conductivity and establish a percolation threshold of 0.1 wt% SWNT. Similarly, measurement of the nanofiber conductivity showed that the electrospinning process improved the contact between nanotube complexes, resulting in conductivities in the S m-1 range with much lower weight loading of SWNTs than their thin film counterparts. The methods reported for the fabrication of conductive nanofibers are simple, inexpensive, and enable SWNT processing in aqueous solutions, and offer great potential for nanofiber use in applications involving flexible electronics, sensing devices, and tissue engineering

  5. Fabrication of conductive polymer nanofibers through SWNT supramolecular functionalization and aqueous solution processing.

    PubMed

    Naeem, Fahim; Prestayko, Rachel; Saem, Sokunthearath; Nowicki, Lauren; Imit, Mokhtar; Adronov, Alex; Moran-Mirabal, Jose M

    2015-10-01

    Polymeric thin films and nanostructured composites with excellent electrical properties are required for the development of advanced optoelectronic devices, flexible electronics, wearable sensors, and tissue engineering scaffolds. Because most polymers available for fabrication are insulating, one of the biggest challenges remains the preparation of inexpensive polymer composites with good electrical conductivity. Among the nanomaterials used to enhance composite performance, single walled carbon nanotubes (SWNTs) are ideal due to their unique physical and electrical properties. Yet, a barrier to their widespread application is that they do not readily disperse in solvents traditionally used for polymer processing. In this study, we employed supramolecular functionalization of SWNTs with a conjugated polyelectrolyte as a simple approach to produce stable aqueous nanotube suspensions, that could be effortlessly blended with the polymer poly(ethyleneoxide) (PEO). The homogeneous SWNT:PEO mixtures were used to fabricate conductive thin films and nanofibers with improved conductivities through drop casting and electrospinning. The physical characterization of electrospun nanofibers through Raman spectroscopy and SEM revealed that the SWNTs were uniformly incorporated throughout the composites. The electrical characterization of SWNT:PEO thin films allowed us to assess their conductivity and establish a percolation threshold of 0.1 wt% SWNT. Similarly, measurement of the nanofiber conductivity showed that the electrospinning process improved the contact between nanotube complexes, resulting in conductivities in the S m(-1) range with much lower weight loading of SWNTs than their thin film counterparts. The methods reported for the fabrication of conductive nanofibers are simple, inexpensive, and enable SWNT processing in aqueous solutions, and offer great potential for nanofiber use in applications involving flexible electronics, sensing devices, and tissue engineering

  6. Kinetic factors determining conducting filament formation in solid polymer electrolyte based planar devices

    NASA Astrophysics Data System (ADS)

    Krishnan, Karthik; Aono, Masakazu; Tsuruoka, Tohru

    2016-07-01

    Resistive switching characteristics and conducting filament formation dynamics in solid polymer electrolyte (SPE) based planar-type atomic switches, with opposing active Ag and inert Pt electrodes, have been investigated by optimizing the device configuration and experimental parameters such as the gap distance between the electrodes, the salt inclusion in the polymer matrix, and the compliance current applied in current-voltage measurements. The high ionic conductivities of SPE enabled us to make scanning electron microscopy observations of the filament formation processes in the sub-micrometer to micrometer ranges. It was found that switching behaviour and filament growth morphology depend strongly on several kinetic factors, such as the redox reaction rate at the electrode-polymer interfaces, ion mobility in the polymer matrix, electric field strength, and the reduction sites for precipitation. Different filament formations, resulting from unidirectional and dendritic growth behaviours, can be controlled by tuning specified parameters, which in turn improves the stability and performance of SPE-based devices.Resistive switching characteristics and conducting filament formation dynamics in solid polymer electrolyte (SPE) based planar-type atomic switches, with opposing active Ag and inert Pt electrodes, have been investigated by optimizing the device configuration and experimental parameters such as the gap distance between the electrodes, the salt inclusion in the polymer matrix, and the compliance current applied in current-voltage measurements. The high ionic conductivities of SPE enabled us to make scanning electron microscopy observations of the filament formation processes in the sub-micrometer to micrometer ranges. It was found that switching behaviour and filament growth morphology depend strongly on several kinetic factors, such as the redox reaction rate at the electrode-polymer interfaces, ion mobility in the polymer matrix, electric field strength

  7. Growth of self-assembled copper nanostructure on conducting polymer by electrodeposition

    NASA Astrophysics Data System (ADS)

    Sarkar, D. K.; Zhou, X. J.; Tannous, A.; Louie, M.; Leung, K. T.

    2003-02-01

    In the present work, self-assembled nanostructures of copper are grown by electrodeposition on a thin conducting polymer (polypyrrole) film electropolymerized on a gold electrode. The shapes, sizes and the densities of the nanostructures are found to depend on the thickness of the polypyrrole thin film, which provides an easy means to control the morphology of these nanostructures. In particular, for the same applied potential on the gold electrode, smaller nanocrystals with a higher density are observed on thinner polymer films while bigger nanocrystals at a lower density are found on thicker films.

  8. Enhancement of Li+ ion conductivity in solid polymer electrolytes using surface tailored porous silica nanofillers

    NASA Astrophysics Data System (ADS)

    Mohanta, Jagdeep; Singh, Udai P.; Panda, Subhendu K.; Si, Satyabrata

    2016-09-01

    The current study represents the design and synthesis of polyethylene oxide (PEO)-based solid polymer electrolytes by solvent casting approach using surface tailored porous silica as nanofillers. The surface tailoring of porous silica nanostructure is achieved through silanization chemistry using 3-glycidyloxypropyl trimethoxysilane in which silane part get anchored to the silica surface whereas epoxy group get stellated from the silica surface. Surface tailoring of silica with epoxy group increases the room temperature electrochemical performances of the resulting polymer electrolytes. Ammonical hydrolysis of organosilicate precursor is used for both silica preparation and their surface tailoring. The composite solid polymer electrolyte films are prepared by solution mixing of PEO with lithium salt in presence of silica nanofillers and cast into film by solvent drying, which are then characterized by impedance measurement for conductivity study and wide angle x-ray diffraction for change in polymer crystallinity. Room temperature impedance measurement reveals Li+ ion conductivity in the order of 10‑4 S cm‑1, which is correlated to the decrease in PEO crystallinity. The enhancement of conductivity is further observed to be dependent on the amount of silica as well as on their surface characteristics.

  9. Control of conducting polymer actuators without physical feedback: simulated feedback control approach with particle swarm optimization

    NASA Astrophysics Data System (ADS)

    Xiang, Xingcan; Mutlu, Rahim; Alici, Gursel; Li, Weihua

    2014-03-01

    Conducting polymer actuators have shown significant potential in articulating micro instruments, manipulation devices, and robotics. However, implementing a feedback control strategy to enhance their positioning ability and accuracy in any application requires a feedback sensor, which is extremely large in size compared to the size of the actuators. Therefore, this paper proposes a new sensorless control scheme without the use of a position feedback sensor. With the help of the system identification technique and particle swarm optimization, the control scheme, which we call the simulated feedback control system, showed a satisfactory command tracking performance for the conducting polymer actuator’s step and dynamic displacement responses, especially under a disturbance, without needing a physical feedback loop, but using a simulated feedback loop. The primary contribution of this study is to propose and experimentally evaluate the simulated feedback control scheme for a class of the conducting polymer actuators known as tri-layer polymer actuators, which can operate both in dry and wet media. This control approach can also be extended to other smart actuators or systems, for which the feedback control based on external sensing is impractical.

  10. Thermoreversible Morphology and Conductivity of a Conjugated Polymer Network Embedded in Block Copolymer Self-Assemblies

    DOE PAGESBeta

    Han, Youngkyu; Carrillo, Jan-Michael Y.; Zhang, Zhe; Li, Yunchao; Hong, Kunlun; Sumpter, Bobby G.; Ohl, Michael; Paranthaman, Mariappan Parans; Smith, Gregory S.; Do, Changwoo

    2016-07-19

    Self-assembly of block copolymers provides numerous opportunities to create functional materials, utilizing self-assembled microdomains with a variety of morphology and periodic architectures as templates for functional nanofillers. Here new progress is reported toward the fabrication of thermally responsive and electrically conductive polymeric self-assemblies made from a water-soluble poly(thiophene) derivative with short poly(ethylene oxide) side chains and Pluronic L62 block copolymer solution in water. The structural and electrical properties of conjugated polymer-embedded self-assembled architectures are investigated by combining small-angle neutron and X-ray scattering, coarse-grained molecular dynamics simulations, and impedance spectroscopy. The L62 solution template organizes the conjugated polymers by stably incorporatingmore » them into the hydrophilic domains thus inhibiting aggregation. The changing morphology of L62 during the micellarto- lamellar phase transition defines the embedded conjugated polymer network. As a result, the conductivity is strongly coupled to the structural change of the templating L62 phase and exhibits thermally reversible behavior with no signs of quenching of the conductivity at high temperature. In conclusion, this study shows promise for enabling more flexibility in processing and utilizing water-soluble conjugated polymers in aqueous solutions for self-assembly based fabrication of stimuli-responsive nanostructures and sensory materials.« less

  11. Electrochromic conductive polymer fuses for hybrid organic/inorganic semiconductor memories

    NASA Astrophysics Data System (ADS)

    Möller, Sven; Forrest, Stephen R.; Perlov, Craig; Jackson, Warren; Taussig, Carl

    2003-12-01

    We demonstrate a nonvolatile, write-once-read-many-times (WORM) memory device employing a hybrid organic/inorganic semiconductor architecture consisting of thin film p-i-n silicon diode on a stainless steel substrate integrated in series with a conductive polymer fuse. The nonlinearity of the silicon diodes enables a passive matrix memory architecture, while the conductive polyethylenedioxythiophene:polystyrene sulfonic acid polymer serves as a reliable switch with fuse-like behavior for data storage. The polymer can be switched at ˜2 μs, resulting in a permanent decrease of conductivity of the memory pixel by up to a factor of 103. The switching mechanism is primarily due to a current and thermally dependent redox reaction in the polymer, limited by the double injection of both holes and electrons. The switched device performance does not degrade after many thousand read cycles in ambient at room temperature. Our results suggest that low cost, organic/inorganic WORM memories are feasible for light weight, high density, robust, and fast archival storage applications.

  12. Enhancement of Li+ ion conductivity in solid polymer electrolytes using surface tailored porous silica nanofillers

    NASA Astrophysics Data System (ADS)

    Mohanta, Jagdeep; Singh, Udai P.; Panda, Subhendu K.; Si, Satyabrata

    2016-09-01

    The current study represents the design and synthesis of polyethylene oxide (PEO)-based solid polymer electrolytes by solvent casting approach using surface tailored porous silica as nanofillers. The surface tailoring of porous silica nanostructure is achieved through silanization chemistry using 3-glycidyloxypropyl trimethoxysilane in which silane part get anchored to the silica surface whereas epoxy group get stellated from the silica surface. Surface tailoring of silica with epoxy group increases the room temperature electrochemical performances of the resulting polymer electrolytes. Ammonical hydrolysis of organosilicate precursor is used for both silica preparation and their surface tailoring. The composite solid polymer electrolyte films are prepared by solution mixing of PEO with lithium salt in presence of silica nanofillers and cast into film by solvent drying, which are then characterized by impedance measurement for conductivity study and wide angle x-ray diffraction for change in polymer crystallinity. Room temperature impedance measurement reveals Li+ ion conductivity in the order of 10-4 S cm-1, which is correlated to the decrease in PEO crystallinity. The enhancement of conductivity is further observed to be dependent on the amount of silica as well as on their surface characteristics.

  13. Exploiting the Different Polarity in Piezoresistive Characteristics of Conducting Polymers for Strain Gauge Applications

    NASA Astrophysics Data System (ADS)

    Sezen, Melda; Register, Jeffrey T.; Yao, Yao; Glisic, Branko; Loo, Yueh-Lin

    2015-03-01

    Piezoresistivity defines the change in resistance of a material in response to mechanical stress. We exploited the effects of structural modifications on the piezoresistive properties of conducting polymers, poly(2-acrylamido-2-methyl-1-propanesulfonic acid) doped polyaniline, PANI-PAAMPSA, and poly(3,4-ethylenedioxythiophene):poly(styrenesulfonate), PEDOT:PSS, for strain gauge applications. Under tensile deformation, the resistances of as-cast PANI-PAAMPSA and PEDOT:PSS increase due to increased separation between the electrostatically stabilized conducting polymer particles. Upon solvent annealing in dichloroacetic acid, DCA, PANI-PAAMPSA's resistance decreases whereas PEDOT:PSS's resistance still increases with tension. While DCA treatment reduces the electrostatic interactions between PANI and PAAMPSA, it only removes the PSS overlayer in PEDOT:PSS. The change in the polarity of PANI-PAAMPSA's piezoresistivity is attributed to the unlocking of the globular structure of the as-synthesized conducting polymer complex with DCA-treatment, which then enables strain-induced crystallization on deformation. By tuning the piezoresistive characteristics of the polymers through structural modification, we can design strain gauge circuits for monitoring the conditions of civil structures.

  14. Cross-linked polymers: Chemistry, properties, and applications; Proceedings of the Symposium, Denver, CO, Apr. 5-10, 1987

    SciTech Connect

    Dickie, R.A.; Labana, S.S.; Bauer, R.S.

    1988-01-01

    This symposium presents papers on the molecular architecture, degradation properties, and mechanical properties of cross-linked polymers, together with examples of high-performance polymer networks. Consideration is given to the effects of intramolecular reaction on network formation and properties, the effects of branching and cross-linking on polymer properties of star-branched Nylon 6, the effect of ionizing radiation on an epoxy structural adhesive, the performance characteristics of the fluorescence optrode cure sensor, the deformation kinetics of cross-linked polymers, and the fatigue behavior of acrylic interpenetrating polymer networks. Other papers are on thermal stress development in thick epoxy coatings, semiinterpenetrating networks based on triazine thermoset and N-alkylamide thermoplastics, liquid crystalline oligoester diols as thermoset coating binders, and the characterization of bisbenzocyclobutene high-temperature resin and bisbenzocyclobutene blended with a compatible bismaleimide resin.

  15. Detection of Secondhand Cigarette Smoke via Nicotine Using Conductive Polymer Films

    PubMed Central

    2013-01-01

    Introduction: The 2006 U.S. Surgeon General’s Report found that there is no safe level of exposure to secondhand smoke (SHS). Many smokers attempt to protect others from exposure to SHS; however, it is difficult to assess effectiveness of these behavior changes. There is a need for personal monitoring devices that provide real-time SHS exposure data; at present, there is no device that measures ambient nicotine levels in real time. The development of such a sensor is the objective of this research. Methods: A nicotine sensing film comprising the conductive polymer polyaniline was linked with a reporting layer, recording changes in chemiresistance due to adsorption of nicotine. Experiments were carried out in a microprocessor-controlled smoking chamber using sidestream smoke from standard reference cigarettes; up to 10 cigarettes were smoked simultaneously. The exposure chamber was calibrated for total suspended particle, carbon monoxide, and nicotine concentrations. Results: We found significant real-time increases in the resistance of films upon exposure to SHS. The sensors were shown to be sensitive to the number of cigarettes consumed and ambient nicotine and demonstrated reasonable recovery between measurements. The sensors have sufficient sensitivity to detect off-gassing of nicotine or “thirdhand smoke.” Conclusions: A sensing element has been developed that can reliably detect secondhand and thirdhand tobacco smoke in real time through the adsorption of ambient nicotine vapor. The device was calibrated to the number of smoked cigarettes and to nicotine concentration. Development of integrated personal sensors to record exposure to SHS using this technology is currently underway. PMID:23482719

  16. Inorganic backbone ionomers: Design and dielectric response of single-ion conducting polymers

    NASA Astrophysics Data System (ADS)

    Bartels, Joshua

    Ion-conducting polymers were studied primarily through the use of dielectric spectroscopy. The conclusions drawn from ion conduction models of the dielectric data are corroborated by additional independent experiments, including x-ray scattering, calorimetry, prism coupling, and DFT calculations. The broad concern of this dissertation is to understand and clarify a path forward in ion conducting polymer research. This is achieved by considering low-Tg ionomers and the advantages imparted by siloxane and phosphazene backbones. The most successful dielectric spectroscopy model for the materials studied is the electrode polarization model (EP), whereas other models, such as the Dyre random barrier model, fail to describe the experimental results. Seven nonionic ether oxygen (EO) containing polymers were studied in order to observe the effect that backbone chemistry has on dipole motion. Conventional carboncarbon backbone EO-containing polymers show no distinct advantage over similar EO-pendant polysiloxane or polyphosphazene systems. The mobility and effective backbone Tg imparted by the inorganic backbones are comparable. A short EO pendant results in a lower static dielectric constant due to restricted motion of dipoles close to the chain. The flexibility and chemical versatility of inorganic backbone polymers motivates further study of two ionomer systems. A polypohosphazene iodide conducting system was characterized by dielectric spectroscopy and x-ray scattering. Two end "tail" functionalization of the ammonium ion were used, a tail with two EOs and an alkyl tail of six carbons. This functional group plays an important role in ion dynamics and can wrap around the ion and self-solvate when EOs are present. The iodide-ammonium ionomers are observed to have unusually large high-frequency dielectric constants due to atomic polarization of ions. The strength of the atomic polarization scales with ion content. The aggregation state of ions is able to be determined from

  17. Conductive polymer-mediated 2D and 3D arrays of Mn3O4 nanoblocks and mesoporous conductive polymers as their replicas

    NASA Astrophysics Data System (ADS)

    Nakagawa, Yoshitaka; Kageyama, Hiroyuki; Matsumoto, Riho; Oaki, Yuya; Imai, Hiroaki

    2015-11-01

    Orientation-controlled 2D and 3D microarrays of Mn3O4 nanocuboids that were mediated by a conductive polymer were fabricated by evaporation-induced self-assembly of the oxide nanoblocks and subsequent polymerization of pyrrole in the interparticle spaces. Free-standing mesoporous polypyrroles (PPy) having chain- and square-grid-like nanovoid arrays were obtained as replicas of the composite assemblies by dissolving the oxide nanoblocks. The PPy-mediated manganese oxide arrays exhibited stable electrochemical performance as an ultrathin anode of a lithium-ion secondary battery.Orientation-controlled 2D and 3D microarrays of Mn3O4 nanocuboids that were mediated by a conductive polymer were fabricated by evaporation-induced self-assembly of the oxide nanoblocks and subsequent polymerization of pyrrole in the interparticle spaces. Free-standing mesoporous polypyrroles (PPy) having chain- and square-grid-like nanovoid arrays were obtained as replicas of the composite assemblies by dissolving the oxide nanoblocks. The PPy-mediated manganese oxide arrays exhibited stable electrochemical performance as an ultrathin anode of a lithium-ion secondary battery. Electronic supplementary information (ESI) available. See DOI: 10.1039/c5nr05912g

  18. Counter electrodes from conducting polymer intercalated graphene for dye-sensitized solar cells

    NASA Astrophysics Data System (ADS)

    Li, Ru; Tang, Qunwei; Yu, Liangmin; Yan, Xuefeng; Zhang, Zhiming; Yang, Peizhi

    2016-03-01

    Creation of cost-effective and platinum-free counter electrodes (CEs) is persistent for developing advanced dye-sensitized solar cells (DSSCs). We present here the fabrication of conducting polymers such as polyaniline (PANi), polypyrole (PPy), or poly(3,4-ethylenedioxythiophene) (PEDOT) intercalated reduced graphene oxide (rGO) CEs on flexible Ti foil or polyethylene-terephthalate substrate for liquid-junction DSSC applications. The ration architecture integrates the high electron-conducting ability of graphene and good electrocatalytic activity of a conducting polymer into a single CE material. The preliminary results demonstrate that the resultant CEs follow an order of rGO/PPy > rGO/PANi > rGO/PEDOT > rGO. A maximal cell efficiency of 6.23% is determined on the optimized solar cell device, yielding 104.9% enhancement in comparison to rGO based device.

  19. Conducting Polymer Coated Graphene Oxide Electrode for Rechargeable Lithium-Sulfur Batteries.

    PubMed

    Lee, Hee-Yoon; Jung, Yongju; Kim, Seok

    2016-03-01

    Poly(diallyldimethylammonium chloride) (PDDA)/graphene oxide-sulfur composites were prepared by a chemical oxidation method. For the PDDA-GO composites, conducting polymers (PDDA) were coated on the surface of GO sheets. PDDA-GO composites could be expected to increase electrical conductivity and protect restacking of graphene sheets. And then, sulfur particles were dispersed into the PDDA-GO composites by mixing in the CS2 solvent. It is expected the PDDA-GO/S composites show the limited release of polysulfides due to the fact that it can provide high surface area, because conducting polymer can be used as spacer between graphene sheets. Electrochemical performances of prepared composites were characterized by cyclic voltammetry (CV). The PDDA-GO/S composites showed a high discharge capacity of 1102 mAh g(-1) at the first cycle and a good cycle retention of 60% after 100 cycles. PMID:27455691

  20. Electrochemical deposition of conducting polymer coatings on magnesium surfaces in ionic liquid

    PubMed Central

    Luo, Xiliang; Cui, Xinyan Tracy

    2012-01-01

    A conducting polymer based smart coating for magnesium (Mg) implants that can both improve the corrosion resistance of Mg and release drug in a controllable way is reported. As the ionic liquid is a highly conductive and stable solvent with a very wide electrochemical window, the conducting polymer coatings can be directly electrodeposited on the active metal Mg in ionic liquid at mild conditions, and Mg is considerably stable during the electrodeposition. The electrodeposited Poly(3,4-ethylenedioxythiophene) (PEDOT) coatings on Mg are uniform and can significantly improve the corrosion resistance of Mg. In addition, the PEDOT coatings can load the anti-inflammatory drug dexamethasone during the electrodeposition which can be subsequently released upon electric stimulation. PMID:20832505

  1. Conducting Polymer Coated Graphene Oxide Electrode for Rechargeable Lithium-Sulfur Batteries.

    PubMed

    Lee, Hee-Yoon; Jung, Yongju; Kim, Seok

    2016-03-01

    Poly(diallyldimethylammonium chloride) (PDDA)/graphene oxide-sulfur composites were prepared by a chemical oxidation method. For the PDDA-GO composites, conducting polymers (PDDA) were coated on the surface of GO sheets. PDDA-GO composites could be expected to increase electrical conductivity and protect restacking of graphene sheets. And then, sulfur particles were dispersed into the PDDA-GO composites by mixing in the CS2 solvent. It is expected the PDDA-GO/S composites show the limited release of polysulfides due to the fact that it can provide high surface area, because conducting polymer can be used as spacer between graphene sheets. Electrochemical performances of prepared composites were characterized by cyclic voltammetry (CV). The PDDA-GO/S composites showed a high discharge capacity of 1102 mAh g(-1) at the first cycle and a good cycle retention of 60% after 100 cycles.

  2. Highly conductive carbon nanotube buckypapers with improved doping stability via conjugational cross-linking

    NASA Astrophysics Data System (ADS)

    Chen, I.-Wen Peter; Liang, Richard; Zhao, Haibo; Wang, Ben; Zhang, Chuck

    2011-12-01

    Carbon nanotube (CNT) sheets or buckypapers have demonstrated promising electrical conductivity and mechanical performance. However, their electrical conductivity is still far below the requirements for engineering applications, such as using as a substitute for copper mesh, which is currently used in composite aircraft structures for lightning strike protection. In this study, different CNT buckypapers were stretched to increase their alignment, and then subjected to conjugational cross-linking via chemical functionalization. The conjugationally cross-linked buckypapers (CCL-BPs) demonstrated higher electrical conductivity of up to 6200 S cm - 1, which is more than one order increase compared to the pristine buckypapers. The CCL-BPs also showed excellent doping stability in over 300 h in atmosphere and were resistant to degradation at elevated temperatures. The tensile strength of the stretched CCL-BPs reached 220 MPa, which is about three times that of pristine buckypapers. We attribute these property improvements to the effective and stable conjugational cross-links of CNTs, which can simultaneously improve the electrical conductivity, doping stability and mechanical properties. Specifically, the electrical conductivity increase resulted from improving the CNT alignment and inter-tube electron transport capability. The conjugational cross-links provide effective 3D conductive paths to increase the mobility of electrons among individual nanotubes. The stable covalent bonding also enhances the thermal stability and load transfer. The significant electrical and mechanical property improvement renders buckypaper a multifunctional material for various applications, such as conducting composites, battery electrodes, capacitors, etc.

  3. Polymer single crystal-decorated superhydrophobic buckypaper with controlled wetting and conductivity.

    PubMed

    Laird, Eric D; Wang, Wenda; Cheng, Shan; Li, Bing; Presser, Volker; Dyatkin, Boris; Gogotsi, Yury; Li, Christopher Y

    2012-02-28

    Herein we report fabrication of uniform, free-standing nanohybrid buckypaper with high carbon nanotube (CNT) contents (13-70%) using polymer single crystal-decorated CNTs as the precursor. Polyethylene single crystals were periodically grown on CNT surfaces, forming a nanohybrid shish kebab (NHSK) structure. Vacuum filtering a NHSK suspension led to polymer single crystal-decorated buckypaper (named as NHSK paper) with a wide range of CNT contents and uniform CNT dispersion. Porosity, surface roughness, and conductivity of NHSK paper can be controlled by tuning the polymer single crystal size. Because of the hierarchical roughness created by intra- and inter-NHSK nanostructure, NHSK paper with controlled kebab size exhibits both superhydrophobicity and high surface water adhesion, which mimics the rose petal effect. We anticipate that this unique NHSK paper can find applications in sensors, electrochemical devices, and coatings.

  4. Electrocatalytic Transformation of Carbon Dioxide into Low Carbon Compounds on Conducting Polymers Derived from Multimetallic Porphyrins.

    PubMed

    Dreyse, Paulina; Honores, Jessica; Quezada, Diego; Isaacs, Mauricio

    2015-11-01

    The electrochemical reduction of carbon dioxide is studied herein by using conducting polymers based on metallotetraruthenated porphyrins (MTRPs). The polymers on glassy carbon electrodes were obtained by electropolymerization processes of the monomeric MTRP. The linear sweep voltammetry technique resulted in polymeric films that showed electrocatalytic activity toward carbon dioxide reduction with an onset potential of -0.70 V. The reduction products obtained were hydrogen, formic acid, formaldehyde, and methanol, with a tendency for a high production of methanol with a maximum value of turnover frequency equal to 15.07 when using a zinc(II) polymeric surface. Studies of the morphology (AFM) and electrochemical impedance spectroscopy results provide an adequate background to explain that the electrochemical reduction is governed by the roughness of the polymer, for which the possible mechanism involves a series of one-electron reduction reactions.

  5. Persistence of slow dynamics in Tb(OETAP)2 single molecule magnets embedded in conducting polymers

    NASA Astrophysics Data System (ADS)

    Orlando, T.; Filibian, M.; Sanna, S.; Giménez-Agullo, N.; Sáenz de Pipaón, C.; Ballester, P.; Galán-Mascarós, J. R.; Carretta, P.

    2016-09-01

    The spin dynamics of Tb(OETAP)2 single ion magnets was investigated by means of muon spin relaxation (μSR) both in the bulk material as well as when the molecule is embedded into PEDOT:PSS polymer conductor. The spin fluctuation time is characterized by a high temperature activated trend, with an energy barrier around 320 K, and by a low temperature tunneling regime. When the single ion magnet is embedded into the polymer the energy barrier only slightly decreases and the fluctuation time remains of the same order of magnitude, even at low temperature. This finding shows that these single molecule magnets preserve their characteristics which, if combined with those of the conducting polymer, result in a hybrid material of potential interest for organic spintronics.

  6. Electrically Conductive, Optically Transparent Polymer/Carbon Nanotube Composites and Process for Preparation Thereof

    NASA Technical Reports Server (NTRS)

    Connell, John W. (Inventor); Smith, 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.

  7. Electrically Conductive, Optically Transparent Polymer/Carbon Nanotube Composites and Process for Preparation Thereof

    NASA Technical Reports Server (NTRS)

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

    2009-01-01

    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 hy selection of the polymer matrix and CNT to fabricate articles that possess high optical transparency and antistatic behavior.

  8. Electrically conductive, optically transparent polymer/carbon nanotube composites and process for preparation thereof

    NASA Technical Reports Server (NTRS)

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

    2009-01-01

    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.

  9. High Yield Sample Preconcentration Using a Highly Ion-conductive Charge-selective Polymer

    PubMed Central

    Chun, Honggu; Chung, Taek Dong; Ramsey, J. Michael

    2011-01-01

    The development and analysis of a microfluidic sample preconcentration system using a highly ion-conductive charge-selective polymer (poly-AMPS) is reported. The preconcentration is based on the phenomenon of concentration polarization which develops at the boundaries of the poly-AMPS with buffer solutions. A negatively charged polymer, poly-AMPS, positioned between two microchannels efficiently extracts cations through its large cross section, resulting in efficient anion sample preconcentration. The present work includes the development of a robust polymer that is stable over a wide range of buffers with varying chemical compositions. The sample preconcentration effect remains linear to over 3 mM (0.15 pmol) and 500 μM (15 fmol) for fluorescein and TRITC-tagged albumin solutions, respectively. The system can potentially be used for concentrating proteins on microfluidic devices with subsequent analysis for proteomic applications. PMID:20575520

  10. Cross-linked supramolecular polymer metallogels constructed via a self-sorting strategy and their multiple stimulus-response behaviors.

    PubMed

    Wang, Xu-Qing; Wang, Wei; Yin, Guang-Qiang; Wang, Yu-Xuan; Zhang, Chang-Wei; Shi, Jia-Meng; Yu, Yihua; Yang, Hai-Bo

    2015-12-01

    Novel cross-linked supramolecular polymer metallogels were successfully constructed from four components via a self-sorting strategy, and feature interesting multiple stimulus-response behaviors under various external stimuli, including halide, base, and competitive guests.

  11. Cross-linked supramolecular polymer metallogels constructed via a self-sorting strategy and their multiple stimulus-response behaviors.

    PubMed

    Wang, Xu-Qing; Wang, Wei; Yin, Guang-Qiang; Wang, Yu-Xuan; Zhang, Chang-Wei; Shi, Jia-Meng; Yu, Yihua; Yang, Hai-Bo

    2015-12-01

    Novel cross-linked supramolecular polymer metallogels were successfully constructed from four components via a self-sorting strategy, and feature interesting multiple stimulus-response behaviors under various external stimuli, including halide, base, and competitive guests. PMID:26436148

  12. Increase in Electrical Conductivity of MOF to Billion-Fold upon Filling the Nanochannels with Conducting Polymer.

    PubMed

    Dhara, Barun; Nagarkar, Sanjog S; Kumar, Jitender; Kumar, Vikash; Jha, Plawan Kumar; Ghosh, Sujit K; Nair, Sunil; Ballav, Nirmalya

    2016-08-01

    Redox-active pyrrole (Py) monomers were intercalated into 1D nanochannels of [Cd(NDC)0.5(PCA)]·Gx (H2NDC = 2,6-napthalenedicarboxylic acid, HPCA = 4-pyridinecarboxylic acid, G = guest molecules) (1) - a fluorescent 3D MOF (λem = 385 nm). Subsequent activation of 1⊃Py upon immersing into iodine (I2) solution resulted in an increment of the bulk electrical conductivity by ∼9 orders of magnitude. The unusual increase in conductivity was attributed to the formation of highly oriented and conducting polypyrrole (PPy) chains inside 1D nanochannels and specific host-guest interaction in 1⊃PPy thereof. The Hall-effect measurements suggested 1⊃PPy to be an n-type semiconductor material with remarkably high-carrier density (η) of ∼1.5 × 10(17) cm(-3) and mobility (μ) of ∼8.15 cm(2) V(-1) s(-1). The fluorescence property of 1 was almost retained in 1⊃PPy with concomitant exciplex-type emission at higher wavelength (λem = 520 nm). The here-presented results on [MOF⊃Conducting Polymer] systems in general will serve as a prototype experiment toward rational design for the development of highly conductive yet fluorescent MOF-based materials for various optoelectronic applications. PMID:27404432

  13. Protection of Conductive and Non-conductive Advanced Polymer-based Paints from Highly Aggressive Oxidative Environments

    NASA Technical Reports Server (NTRS)

    Gudimenko, Y.; Ng, R.; Iskanderova, Z.; Kleiman, J.; Grigorevsky, A.; Kiseleva, L.; Finckenor, M.; Edwards, D.

    2005-01-01

    Research has been continued to further improve the space durability of conductive and non-conductive polymer-based paints and of conductive thermal control paints for space applications. Efforts have been made to enhance the space durability and stability of functional Characteristics in ground-based space environment imitating conditions, using specially developed surface modification treatment. The results of surface modification of new conductive paints, including the ground-based testing in aggressive oxidative environments, such as atomic oxygen/UV and oxygen plasma, and performance evaluation are presented. Functional properties and performance characteristics, such as thermal optical properties (differential solar absorptance and thermal emittance representing the thermal optical performance of thermal control paints) and surface resistivity characteristics of pristine, surface modified, and tested materials were verified. Extensive surface analysis studies have been performed using complementary surface analyses including SEM/EDS and XPS. Test results revealed that the successfully treated materials exhibit reduced mass loss and no surface morphology change, thus indicating good protection from the severe oxidative environment. It was demonstrated that the developed surface modification treatment could be applied successfully to charge dissipative and conductive paints.

  14. Increase in Electrical Conductivity of MOF to Billion-Fold upon Filling the Nanochannels with Conducting Polymer.

    PubMed

    Dhara, Barun; Nagarkar, Sanjog S; Kumar, Jitender; Kumar, Vikash; Jha, Plawan Kumar; Ghosh, Sujit K; Nair, Sunil; Ballav, Nirmalya

    2016-08-01

    Redox-active pyrrole (Py) monomers were intercalated into 1D nanochannels of [Cd(NDC)0.5(PCA)]·Gx (H2NDC = 2,6-napthalenedicarboxylic acid, HPCA = 4-pyridinecarboxylic acid, G = guest molecules) (1) - a fluorescent 3D MOF (λem = 385 nm). Subsequent activation of 1⊃Py upon immersing into iodine (I2) solution resulted in an increment of the bulk electrical conductivity by ∼9 orders of magnitude. The unusual increase in conductivity was attributed to the formation of highly oriented and conducting polypyrrole (PPy) chains inside 1D nanochannels and specific host-guest interaction in 1⊃PPy thereof. The Hall-effect measurements suggested 1⊃PPy to be an n-type semiconductor material with remarkably high-carrier density (η) of ∼1.5 × 10(17) cm(-3) and mobility (μ) of ∼8.15 cm(2) V(-1) s(-1). The fluorescence property of 1 was almost retained in 1⊃PPy with concomitant exciplex-type emission at higher wavelength (λem = 520 nm). The here-presented results on [MOF⊃Conducting Polymer] systems in general will serve as a prototype experiment toward rational design for the development of highly conductive yet fluorescent MOF-based materials for various optoelectronic applications.

  15. Electronic conduction and microstructure in polymer composites filled with carbonaceous particles

    NASA Astrophysics Data System (ADS)

    Mdarhri, A.; Brosseau, C.; Zaghrioui, M.; El Aboudi, I.

    2012-08-01

    Physical and physico-chemical properties of polymer filled with carbon black (CB) particles, namely, the microstructure dependence of these properties, are not only interesting on their own but are particularly important for electronic applications as they can impose limits on the sensitivity of a device. With this purpose, we report on an experimental study of the structural and electrical properties of semi-crystalline ethylene-co-butyl acrylate polymer filled with conductive CB nano-particles. We found that the value of the direct current conductivity exhibits a jump of 12 orders of magnitude over a small change in CB concentration and is due to a percolation-like behavior. To assess the temperature evolution of supercolative samples, we present measurements of the conductivity as function of temperature. Above the glass transition temperature of the polymer, the CB network restricts the motions of the polymer chains. This behavior was ascribed to the change in CB mesostructure in the polymer matrix as probed by scanning electron microscopy and atomic force microscopy as well as to the difference in the thermal expansion between the two phases. In addition to the observed conductivity increase, the effect of adding CB particles in the polymer matrix is to increase the thermal stability as is probed by thermogravimetric analysis tests. The room temperature alternating current conductivity, studied over the frequency range from 100 Hz to 15 MHz, is interpreted as arising mainly from inter-aggregate polarization effects. By considering carefully the CB content of the alternating current conductivity, we found that our experimental data agree well with the Sheng's model of fluctuation-induced tunnelling of charge carriers over nanometric gaps between adjacent CB aggregates. For studying the filler content dependence of the effective permittivity, several mixing laws and effective medium theories have been used. The observed discrepancies between our experimental

  16. Cross-linked sulfonated aromatic ionomers via SO2 bridges: Conductivity properties

    NASA Astrophysics Data System (ADS)

    Di Vona, M. L.; Pasquini, L.; Narducci, R.; Pelzer, K.; Donnadio, A.; Casciola, M.; Knauth, P.

    2013-12-01

    The proton conductivity of SPEEK membranes in situ cross-linked by thermal treatment at 180 °C for various times was investigated by impedance spectroscopy. The conductivity measurements were made on fully humidified membranes between 25 and 65 °C and on membranes exposed to different relative humidity between 80 and 140 °C. The Ionic Exchange Capacity (IEC) was determined by acid-base titration and the water uptake by gravimetry. The proton conductivity was determined as function of temperature, IEC, degree of cross-linking and hydration number. A curve of proton conductivity vs. hydration number allows predicting that in order to reach a value of 0.1 S/cm at 100 °C a hydration number above 20 is necessary. The measured conductivity at this temperature is 0.16 S/cm for a hydration number of 60.

  17. DNA-programmed modular assembly of cyclic and linear nanoarrays for the synthesis of two-dimensional conducting polymers.

    PubMed

    Chen, Wen; Schuster, Gary B

    2012-01-18

    Nanometer-scale arrays of conducting polymers were prepared on scaffolds of self-assembling DNA modules. A series of DNA oligomers was prepared, each containing six 2,5-bis(2-thienyl)pyrrole (SNS) monomer units linked covalently to N4 atoms of alternating cytosines placed between leading and trailing 12-nucleobase recognition sequences. These DNA modules were encoded so the recognition sequences would uniquely associate through Watson-Crick assembly to form closed-cycle or linear arrays of aligned SNS monomers. The melting behavior and electrophoretic migration of these assemblies showed cooperative formation of multicomponent arrays containing two to five DNA modules (i.e., 12-30 SNS monomers). The treatment of these arrays with horseradish peroxidase and H(2)O(2) resulted in oxidative polymerization of the SNS monomers with concomitant ligation of the DNA modules. The resulting cyclic and linear arrays exhibited chemical and optical properties typical of conducting thiophene-like polymers, with a red-end absorption beyond 1250 nm. AFM images of the cyclic array containing 18 SNS units revealed highly regular 10 nm diameter objects. PMID:22242713

  18. TITANIUM DIOXIDE TRIADS FOR IMPROVED CHARGE-SEPARATION USING CONDUCTIVE POLYMERS

    SciTech Connect

    Cochran, T.M.; Gaylor, T.N.; de la Garza, L.; Rajh, T.

    2009-01-01

    Dye-sensitized solar cells are potentially one of the best solutions to solar energy conversion because of the low cost of required materials and production processes. Titanium dioxide (TiO2) nanoparticulate fi lms are the basis for one of these types of cells, providing large surface area for dye-sensitizer adsorption. Because TiO2 nanoparticulate fi lms develop defects caused by oxygen defi ciency, deep reactive electron traps are formed. With the addition of an enediol ligand, these electron traps are deliberately removed, enhancing the conduction of electrons within the fi lm. In this project, TiO2 nanoparticulate fi lms made by a layer-by-layer dip coating method were modifi ed with 3,4-dihydroxyphenylacetic acid (DOPAC). DOPAC binds to the titanium atoms on the surface of the nanoparticles, restoring their octahedral geometry. This restructuring of the surface shifts the spectral properties of the TiO2 to the visible spectrum and improves the separation of charges which is observed using photoelectrochemistry. Furthermore, DOPAC enables the electronic attachment of other molecules to the surface of TiO2 fi lms, such as the conductive polymer polyaniline base. This conductive polymer provides an extended separation of charges which increases photocurrent production by forming a triad with the TiO2 semiconductor through the 3,4-dihydroxyphenylacetic acid linker. The photocurrent increases due to the donor properties of the conductive polymer thereby decreasing charge pair recombination.

  19. Molecular junctions of self-assembled monolayers with conducting polymer contacts.

    PubMed

    Neuhausen, Alexander B; Hosseini, Ali; Sulpizio, Joseph A; Chidsey, Christopher E D; Goldhaber-Gordon, David

    2012-11-27

    We present a method to fabricate individually addressable junctions of self-assembled monolayers (SAMs) that builds on previous studies which have shown that soft conductive polymer top contacts virtually eliminate shorts through the SAMs. We demonstrate devices with nanoscale lateral dimensions, representing an order of magnitude reduction in device area, with high yield and relatively low device-to-device variation, improving several features of previous soft contact devices. The devices are formed in pores in an inorganic dielectric layer with features defined by e-beam lithography and dry etching. We replace the aqueous PEDOT:PSS conductive polymer used in prior devices with Aedotron P, a low-viscosity, amphiphilic polymer, allowing incorporation of self-assembled monolayers with either hydrophobic or hydrophilic termination with the same junction geometry and materials. We demonstrate the adaptability of this new design by presenting transport measurements on SAMs composed of alkanethiols with methyl, thiol, carboxyl, and azide terminations. We establish that the observed room-temperature tunnel barrier is primarily a function of monolayer thickness, independent of the terminal group's hydrophilicity. Finally, we investigate the temperature dependence of transport and show that the low-temperature behavior is based on the energy distribution of sites from which carriers can tunnel between the polymer and gold contacts, as described by a model of variable-range hopping transport in a disordered conductor.

  20. Molecular junctions of self-assembled monolayers with conducting polymer contacts.

    PubMed

    Neuhausen, Alexander B; Hosseini, Ali; Sulpizio, Joseph A; Chidsey, Christopher E D; Goldhaber-Gordon, David

    2012-11-27

    We present a method to fabricate individually addressable junctions of self-assembled monolayers (SAMs) that builds on previous studies which have shown that soft conductive polymer top contacts virtually eliminate shorts through the SAMs. We demonstrate devices with nanoscale lateral dimensions, representing an order of magnitude reduction in device area, with high yield and relatively low device-to-device variation, improving several features of previous soft contact devices. The devices are formed in pores in an inorganic dielectric layer with features defined by e-beam lithography and dry etching. We replace the aqueous PEDOT:PSS conductive polymer used in prior devices with Aedotron P, a low-viscosity, amphiphilic polymer, allowing incorporation of self-assembled monolayers with either hydrophobic or hydrophilic termination with the same junction geometry and materials. We demonstrate the adaptability of this new design by presenting transport measurements on SAMs composed of alkanethiols with methyl, thiol, carboxyl, and azide terminations. We establish that the observed room-temperature tunnel barrier is primarily a function of monolayer thickness, independent of the terminal group's hydrophilicity. Finally, we investigate the temperature dependence of transport and show that the low-temperature behavior is based on the energy distribution of sites from which carriers can tunnel between the polymer and gold contacts, as described by a model of variable-range hopping transport in a disordered conductor. PMID:23035989

  1. Low power, lightweight vapor sensing using arrays of conducting polymer composite chemically-sensitive resistors

    NASA Technical Reports Server (NTRS)

    Ryan, M. A.; Lewis, N. S.

    2001-01-01

    Arrays of broadly responsive vapor detectors can be used to detect, identify, and quantify vapors and vapor mixtures. One implementation of this strategy involves the use of arrays of chemically-sensitive resistors made from conducting polymer composites. Sorption of an analyte into the polymer composite detector leads to swelling of the film material. The swelling is in turn transduced into a change in electrical resistance because the detector films consist of polymers filled with conducting particles such as carbon black. The differential sorption, and thus differential swelling, of an analyte into each polymer composite in the array produces a unique pattern for each different analyte of interest, Pattern recognition algorithms are then used to analyze the multivariate data arising from the responses of such a detector array. Chiral detector films can provide differential detection of the presence of certain chiral organic vapor analytes. Aspects of the spaceflight qualification and deployment of such a detector array, along with its performance for certain analytes of interest in manned life support applications, are reviewed and summarized in this article.

  2. Characterization and modeling of piezo-resistive properties of carbon nanotube-based conductive polymer composites

    NASA Astrophysics Data System (ADS)

    Pham, Giang Truong

    Electrically conductive polymers (ECPs), offering capabilities such as electrostatic discharge protection and electromagnetic interference shielding, have been the subject of intensive research and development both in academia and industry. The emergence of new conductive nano-fillers in recent decades, particularly carbon nanotubes (CNTs), further fuels more enthusiasm. Thanks to CNTs' excellent mechanical, thermal, and electrical/electronic properties, CNT-filled polymers possess not only conductive properties, but a range of other properties desirable for multi-functional and high performance applications. In order to fully exploit the benefits of CNT-based conductive polymers (CNT-ECPs), researchers have conducted diverse studies primarily to characterize the electrical conductivity of the composites. A crucial area that is less studied is the piezoresistive behaviors of CNT-ECPs, that is, the change in material conductive properties due to an applied stress or strain. Given broad usage of ECPs, it would be reasonable to assume that ECP products commonly operate under certain stress or strain conditions. For instance, an electrostatic discharge (ESD)-protected conductive coating for spacecraft would be affected by strain induced by mechanical or aerodynamic loads. A more systematic understanding of the materials' piezoresistivity, therefore, is instrumental in ensuring satisfactory conductive performance of those material applications. Additionally, knowledge of conductive characteristics of the CNT-ECPs against stress/strain can open the door to newer material applications, e.g., strain gage or multifunctional conductive coating with strain-sensing capability. This research aims to achieve a more fundamental understanding of the mechanism of piezoresistive property of CNT-ECPs, and to develop a model that permits quantifying the structure-property relationships of CNT-ECPs' piezoresistivity. In this research, expanded experimental studies with various

  3. Nanofluidic Diodes with Dynamic Rectification Properties Stemming from Reversible Electrochemical Conversions in Conducting Polymers.

    PubMed

    Pérez-Mitta, Gonzalo; Marmisollé, Waldemar A; Trautmann, Christina; Toimil-Molares, María Eugenia; Azzaroni, Omar

    2015-12-16

    The use of solid state nanochannels as nanofluidic diodes is currently a topic of large interest in nanotechnology. Particularly, there is a focus in the development of nanochannels with surface functionalities that make them responsive to multiple environmental variables. Here, we present for the first time the construction of electrochemical potential- and pH-responsive nanofluidic diodes using a novel approach based on a controlled electrochemical polymerization of aniline on gold-coated polycarbonate asymmetric nanochannels. The polyaniline-modified nanochannels showed three different levels of reversible ionic rectification corresponding to the degrees of oxidation of the conducting polymer. Our results demonstrate that this strategy enables an accurate and reversible control of the rectification properties due to the well-defined and predictable electrochemical conversion of charged species generated on the pore walls. We envision that these results will create novel avenues to fabricate electrochemically modulated nanofluidic diodes using conducting polymers integrated into single conical nanopores.

  4. Conducting Polymer-Based Nanohybrid Transducers: A Potential Route to High Sensitivity and Selectivity Sensors

    PubMed Central

    Park, Seon Joo; Kwon, Oh Seok; Lee, Ji Eun; Jang, Jyongsik; Yoon, Hyeonseok

    2014-01-01

    The development of novel sensing materials provides good opportunities to realize previously unachievable sensor performance. In this review, conducting polymer-based nanohybrids are highlighted as innovative transducers for high-performance chemical and biological sensing devices. Synthetic strategies of the nanohybrids are categorized into four groups: (1) impregnation, followed by reduction; (2) concurrent redox reactions; (3) electrochemical deposition; (4) seeding approach. Nanocale hybridization of conducting polymers with inorganic components can lead to improved sorption, catalytic reaction and/or transport behavior of the material systems. The nanohybrids have thus been used to detect nerve agents, toxic gases, volatile organic compounds, glucose, dopamine, and DNA. Given further advances in nanohybrids synthesis, it is expected that sensor technology will also evolve, especially in terms of sensitivity and selectivity. PMID:24561406

  5. Current-dependent anisotropic conductivity of locally assembled silver nanoparticles in hybrid polymer films.

    PubMed

    Goel, Pooja; Vinokur, Rostislav; Weichold, Oliver

    2010-12-15

    The electrical behaviour of hybrid poly(ethylene terephthalate) films containing localised, percolating networks of silver nanoparticles separated by pure polymer is studied. The films resemble an array of parallel wires in the submicron range and, thus, exhibit anisotropic conductivity. In the high-conductivity direction at low amplitudes, the films show Ohmic behaviour, while at moderate voltage, non-linearity and a decreasing resistance is observed. The samples were found to heat up during the measurements and the deviation from Ohm's law coincides with the Tg of the polymer. Microstructural analysis of the samples revealed an irreversible agglomeration of the particles at moderate voltages leading to the formation of filaments with higher metallic character than the random particle network.

  6. Li Ion Conducting Polymer Gel Electrolytes Based on Ionic Liquid/PVDF-HFP Blends

    PubMed Central

    Ye, Hui; Huang, Jian; Xu, Jun John; Khalfan, Amish; Greenbaum, Steve G.

    2009-01-01

    Ionic liquids thermodynamically compatible with Li metal are very promising for applications to rechargeable lithium batteries. 1-methyl-3-propylpyrrolidinium bis(trifluoromethanesulfonyl)imide (P13TFSI) is screened out as a particularly promising ionic liquid in this study. Dimensionally stable, elastic, flexible, nonvolatile polymer gel electrolytes (PGEs) with high electrochemical stabilities, high ionic conductivities and other desirable properties have been synthesized by dissolving Li imide salt (LiTFSI) in P13TFSI ionic liquid and then mixing the electrolyte solution with poly(vinylidene-co-hexafluoropropylene) (PVDF-HFP) copolymer. Adding small amounts of ethylene carbonate to the polymer gel electrolytes dramatically improves the ionic conductivity, net Li ion transport concentration, and Li ion transport kinetics of these electrolytes. They are thus favorable and offer good prospects in the application to rechargeable Li batteries including open systems like Li/air batteries, as well as more “conventional” rechargeable lithium and lithium ion batteries. PMID:20354587

  7. Investigations on the Mechanical Properties of Conducting Polymer Coating-Substrate Structures and Their Influencing Factors

    PubMed Central

    Wang, Xi-Shu; Tang, Hua-Ping; Li, Xu-Dong; Hua, Xin

    2009-01-01

    This review covers recent advances and work on the microstructure features, mechanical properties and cracking processes of conducting polymer film/coating- substrate structures under different testing conditions. An attempt is made to characterize and quantify the relationships between mechanical properties and microstructure features. In addition, the film cracking mechanism on the micro scale and some influencing factors that play a significant role in the service of the film-substrate structure are presented. These investigations cover the conducting polymer film/coating nucleation process, microstructure-fracture characterization, translation of brittle-ductile fractures, and cracking processes near the largest inherent macromolecule defects under thermal-mechanical loadings, and were carried out using in situ scanning electron microscopy (SEM) observations, as a novel method for evaluation of interface strength and critical failure stress. PMID:20054470

  8. Radiation-induced reduction-polymerization route for the synthesis of PEDOT conducting polymers

    NASA Astrophysics Data System (ADS)

    Cui, Zhenpeng; Coletta, Cecilia; Rebois, Rolando; Baiz, Sarah; Gervais, Matthieu; Goubard, Fabrice; Aubert, Pierre-Henri; Dazzi, Alexandre; Remita, Samy

    2016-02-01

    Synthesis of conducting poly(3,4-ethylenedioxythiophene), PEDOT, is achieved through an original reduction-polymerization route: γ-radiolysis of aqueous solutions containing EDOT monomers under N2 atmosphere. According to UV-vis absorption spectrophotometry and ATR-FTIR spectroscopy, reduction of EDOT is initiated by hydrated electrons produced by water radiolysis and leads to PEDOT polymers through coupling reactions. The morphology of PEDOT is characterized by Cryo- TEM microscopy in aqueous solution and by SEM after deposition. In an original way, high resolution AFM microscopy, coupled with infrared nanospectroscopy, is used to probe the local chemical composition of PEDOT nanostructures. The results demonstrate that spherical self-assembled PEDOT nanostructures are formed. TGA analysis and four point probe measurements demonstrate that thermal stability and electrical conductivity of PEDOT polymers obtained by the present original reduction-polymerization method are close to those of PEDOT we previously prepared by radiolysis according to an oxidation-polymerization route.

  9. A physical interpretation of impedance at conducting polymer/electrolyte junctions

    SciTech Connect

    Stavrinidou, Eleni; Sessolo, Michele; Sanaur, Sébastien; Malliaras, George G.; Winther-Jensen, Bjorn

    2014-01-15

    We monitor the process of dedoping in a planar junction between an electrolyte and a conducting polymer using electrochemical impedance spectroscopy performed during moving front measurements. The impedance spectra are consistent with an equivalent circuit of a time varying resistor in parallel with a capacitor. We show that the resistor corresponds to ion transport in the dedoped region of the film, and can be quantitatively described using ion density and drift mobility obtained from the moving front measurements. The capacitor, on the other hand, does not depend on time and is associated with charge separation at the moving front. This work offers a physical description of the impedance of conducting polymer/electrolyte interfaces based on materials parameters.

  10. Entangled polymer dynamics in equilibrium and flow modeled through slip links.

    PubMed

    Schieber, Jay D; Andreev, Marat

    2014-01-01

    The idea that the dynamics of concentrated, high-molecular weight polymers are largely governed by entanglements is now widely accepted and typically understood through the tube model. Here we review alternative approaches, slip-link models, that share some similarities to and offer some advantages over tube models. Although slip links were proposed at the same time as tubes, only recently have detailed, quantitative mathematical models arisen based on this picture. In this review, we focus on these models, with most discussion limited to mathematically well-defined objects that conform to state-of-the-art beyond-equilibrium thermodynamics. These models are connected to each other through successive coarse graining, using nonequilibrium thermodynamics along the way, and with a minimal parameter set. In particular, the most detailed level of description has four parameters, three of which can be determined directly from atomistic simulations. Once the remaining parameter is determined for any system, all parameters for all members of the hierarchy are determined. We show how, using this hierarchy of slip-link models combined with atomistic simulations, we can make predictions about the nonlinear rheology of monodisperse homopolymer melts, polydisperse melts, or blends of different architectures. Mathematical details are given elsewhere, so these are limited here, and physical ideas are emphasized. We conclude with an outlook on remaining challenges that might be tackled successfully using this approach, including complex flow fields and polymer blends. PMID:24655135

  11. Interfacial friction and adhesion of cross-linked polymer thin films swollen with linear chains.

    PubMed

    Zhang, Qing; Archer, Lynden A

    2007-07-01

    The preparation and interfacial properties of a new type of tethered, thin-film lubricant coating are presented. These coatings are composed of three components: a dense self-assembled monolayer (SAM) underlayer that presents reactive vinyl groups at its surface; a cross-linked polydimethylsiloxane (PDMS) overlayer that is covalently tethered to the SAM; and free, mobile linear PDMS chains dispersed in the network. We investigate the influence of the molecular weight (Ms) and concentration of the free PDMS chains on the structure and equilibrium swelling properties of the cross-linked films. Using a bead-probe lateral force microscopy measurement technique, we also quantify the interfacial friction and adhesion characteristics of surfaces functionalized with these coatings. We find that both the volume fraction and the molecular weight of free PDMS molecules in the coatings influence their interfacial friction and adhesion properties. For example, the addition of short PDMS chains in dry, cross-linked PDMS thin films yields tethered surface coatings with ultralow friction coefficients (mu = 5.2 x 10(-3)). An analysis based on classical lubrication theory suggests that the reduction in friction force produced by free polymer is a consequence of the gradual separation of asperities on opposing surfaces and the consequent substitution of solid-solid friction by viscous drag of the free polymer chains in the network.

  12. Free-Standing, Nanopatterned Janus Membranes of Conducting Polymer-Virus Nanoparticle Arrays.

    PubMed

    Tiu, Brylee David B; Tiu, Sicily B; Wen, Amy M; Lam, Patricia; Steinmetz, Nicole F; Advincula, Rigoberto C

    2016-06-21

    Nanostructured mesoscale materials find wide-ranging applications in medicine and energy. Top-down manufacturing schemes are limited by the smallest dimension accessible; therefore, we set out to study a bottom-up approach mimicking biological systems, which self-assemble into systems that orchestrate complex energy conversion functionalities. Inspired by nature, we turned toward protein-based nanoparticle structures formed by plant viruses, specifically the cowpea mosaic virus (CPMV). We report the formation of hierarchical CPMV nanoparticle assemblies on colloidal-patterned, conducting polymer arrays using a protocol combining colloidal lithography, electrochemical polymerization, and electrostatic adsorption. In this approach, a hexagonally close-packed array of polystyrene microspheres was assembled on a conductive electrode to function as the sacrificial colloidal template. A thin layer of conducting polypyrrole material was electrodeposited within the interstices of the colloidal microspheres and monitored in situ using electrochemical quartz crystal microbalance with dissipation (EC-QCM-D). Etching the template revealed an inverse opaline conducting polymer pattern capable of forming strong electrostatic interactions with CPMV and therefore enabling immobilization of CPMV on the surface. The CPMV-polymer films were characterized by atomic force microscopy (AFM) and X-ray photoelectron spectroscopy (XPS). Furthermore, molecular probe diffusion experiments revealed selective ion transport properties as a function of the presence of the CPMV nanoparticles on the surface. Lastly, by utilizing its electromechanical behavior, the polymer/protein membrane was electrochemically released as a free-standing film, which can potentially be used for developing high surface area cargo delivery systems, stimuli-responsive plasmonic devices, and chemical and biological sensors. PMID:27244119

  13. How the type of input function affects the dynamic response of conducting polymer actuators

    NASA Astrophysics Data System (ADS)

    Xiang, Xingcan; Alici, Gursel; Mutlu, Rahim; Li, Weihua

    2014-10-01

    There has been a growing interest in smart actuators typified by conducting polymer actuators, especially in their (i) fabrication, modeling and control with minimum external data and (ii) applications in bio-inspired devices, robotics and mechatronics. Their control is a challenging research problem due to the complex and nonlinear properties of these actuators, which cannot be predicted accurately. Based on an input-shaping technique, we propose a new method to improve the conducting polymer actuators’ command-following ability, while minimizing their electric power consumption. We applied four input functions with smooth characteristics to a trilayer conducting polymer actuator to experimentally evaluate its command-following ability under an open-loop control strategy and a simulated feedback control strategy, and, more importantly, to quantify how the type of input function affects the dynamic response of this class of actuators. We have found that the four smooth inputs consume less electrical power than sharp inputs such as a step input with discontinuous higher-order derivatives. We also obtained an improved transient response performance from the smooth inputs, especially under the simulated feedback control strategy, which we have proposed previously [X Xiang, R Mutlu, G Alici, and W Li, 2014 “Control of conducting polymer actuators without physical feedback: simulated feedback control approach with particle swarm optimization’, Journal of Smart Materials and Structure, 23]. The idea of using a smooth input command, which results in lower power consumption and better control performance, can be extended to other smart actuators. Consuming less electrical energy or power will have a direct effect on enhancing the operational life of these actuators.

  14. What conductive polymers have taught us about the meaning of education: education before innovation

    NASA Astrophysics Data System (ADS)

    Hiroki, Kazuaki

    2014-03-01

    There are many scientists and engineers who made a great discovery or a breakthrough invention. What is common to them? It is that they had a chance to experience a deep impression of science and technology in their childhood. Science shows and experiment classes are extremely effective methods to help students learn the excitement of Chemistry. In this paper, I discuss the importance of education in chemistry by presenting an illustration about the development and implementation of experiment classes on conductive polymers.

  15. Impedance study of tea with added taste compounds using conducting polymer and metal electrodes.

    PubMed

    Dhiman, Mopsy; Kapur, Pawan; Ganguli, Abhijit; Singla, Madan Lal

    2012-09-01

    In this study the sensing capabilities of a combination of metals and conducting polymer sensing/working electrodes for tea liquor prepared by addition of different compounds using an impedance mode in frequency range 1 Hz-100 KHz at 0.1 V potential has been carried out. Classification of six different tea liquor samples made by dissolving various compounds (black tea liquor + raw milk from milkman), (black tea liquor + sweetened clove syrup), (black tea liquor + sweetened ginger syrup), (black tea liquor + sweetened cardamom syrup), (black tea liquor + sweet chocolate syrup) and (black tea liquor + vanilla flavoured milk without sugar) using six different working electrodes in a multi electrode setup has been studied using impedance and further its PCA has been carried out. Working electrodes of Platinum (Pt), Gold (Au), Silver (Ag), Glassy Carbon (GC) and conducting polymer electrodes of Polyaniline (PANI) and Polypyrrole (PPY) grown on an ITO surface potentiostatically have been deployed in a three electrode set up. The impedance response of these tea liquor samples using number of working electrodes shows a decrease in the real and imaginary impedance values presented on nyquist plots depending upon the nature of the electrode and amount of dissolved salts present in compounds added to tea liquor/solution. The different sensing surfaces allowed a high cross-selectivity in response to the same analyte. From Principal Component Analysis (PCA) plots it was possible to classify tea liquor in 3-4 classes using conducting polymer electrodes; however tea liquors were well separated from the PCA plots employing the impedance data of both conducting polymer and metal electrodes. PMID:23035436

  16. Electro-generated conducting polypyrrole polymers and applications in photoelectrochemical cells

    SciTech Connect

    Noufi, R.N.

    1983-01-01

    A major problem in the development of photoelectrochemical cells for solar energy conversion and storage is the susceptibility of small bandgap semiconductor materials to photodegradation. This problem could be overcome, in principle, by protecting the semiconductor electrode surface with electrically conducting polymer film. This film, acting as a barrier to ion/solvent transport, would inhibit photodegradation of the electrode surface while permitting electron exchange with the electrode. Recent studies on the electrogenerated polypyrrole and its applications in photoelectrochemical cells are presented.

  17. Structural properties of end-linked polymer networks: Monte Carlo simulation and neutron scattering studies

    NASA Astrophysics Data System (ADS)

    Gilra, Nisha

    2000-12-01

    In this work, computational and experimental approaches were taken to elucidate the structural behavior of end- linked polymer networks. Monte Carlo simulations with the bond fluctuation model were used to study the formation and structure of 10-, 20-, and 50-mer networks cured with various ratios of cross-link sites to chain ends, r. The simulations confirmed experimental results that optimum r values for structural properties are found at non- stoichiometric ratios, increase with increasing precursor polymer chain length, and increase with side reaction. The same structural properties were determined for 50-mer networks formed in the presence of a series of concentrations of 50-mer unreactive linear chain diluent. A slight maximum in the fraction of elastic material was observed at a small degree of dilution and was explained in terms of entanglement effects. The conformational behavior of a small fraction of 50-mer linear probe chains was studied in various polymer network mesh sizes, where mesh size is the number of monomers between cross- links. The radius of gyration, R g, of the probe chains decreased by less than 6% for all mesh sizes studied. Uniaxial network deformation was studied using constant pressure simulations. A new methodology to perform volume change moves was developed. The equation of state of 10- mer athermal network system was determined and found to be similar to the corresponding athermal linear polymer equation of state at high volume fractions, but approached a region of negative pressures at low volume fractions. The chain segment orientational correlation was determined for probe free chains trapped in isotropic and deformed networks. Increased correlation was observed at small distances, whereas no orientational preference was evident at larger distances. The study of probe free chains trapped in polymer networks was also performed using small-angle neutron scattering. The conformational behavior of 70K poly(dimethylsiloxane) (PDMS

  18. Thermal Conductivity of Polymer-Based Composites with Magnetic Aligned Hexagonal Boron Nitride Platelets.

    PubMed

    Yuan, Chao; Duan, Bin; Li, Lan; Xie, Bin; Huang, Mengyu; Luo, Xiaobing

    2015-06-17

    Hexagonal boron nitride (hBN) platelets are widely used as the reinforcing fillers for enhancing the thermal conductivity of polymer-based composites. Since hBN platelets have high aspect ratio and show a highly anisotropic thermal property, the thermal conductivity of the hBNs-filled composites should be strongly associated with the platelets' orientation. However, the orientation effect has been explored less frequently due to the technical difficulties in precontrol of the platelets' orientation in the polymer matrix. In this paper, we report the use of magnetic fields to assemble the platelets into various microstructures and to study the thermal conductivities of the designed composites. The experimental results showed that thermal conductivities are dramatically different among these composites. For instance, the thermal conductivities of the composites with platelets oriented parallel and perpendicular to the heat flux direction are respectively 44.5% higher and 37.9% lower than that of unaligned composites at the volume fraction of 9.14%. The results were also analyzed by a theoretical model. The model suggests that the orientation of the hBN platelets is the main reason for the variance in the thermal conductivity.

  19. Proton conducting membrane for fuel cells

    DOEpatents

    Colombo, Daniel G.; Krumpelt, Michael; Myers, Deborah J.; Kopasz, John P.

    2007-03-27

    An ion conducting membrane comprising dendrimeric polymers covalently linked into a network structure. The dendrimeric polymers have acid functional terminal groups and may be covalently linked via linking compounds, cross-coupling reactions, or copolymerization reactions. The ion conducting membranes may be produced by various methods and used in fuel cells.

  20. Proton conducting membrane for fuel cells

    DOEpatents

    Colombo, Daniel G.; Krumpelt, Michael; Myers, Deborah J.; Kopasz, John P.

    2005-12-20

    An ion conducting membrane comprising dendrimeric polymers covalently linked into a network structure. The dendrimeric polymers have acid functional terminal groups and may be covalently linked via linking compounds, cross-coupling reactions, or copolymerization reactions. The ion conducting membranes may be produced by various methods and used in fuel cells.

  1. Ionic conductivity and transport properties of poly(vinylidene fluoride-co-hexafluoropropylene)-based solid polymer electrolytes

    NASA Astrophysics Data System (ADS)

    Abreha, Merhawi; Subrahmanyam, A. R.; Siva Kumar, J.

    2016-08-01

    Polymer electrolytes containing poly(vinylidene fluoride-co-hexafluoropropylene) (PVdF-HFP) and various concentrations of lithium triflate were prepared to determine the optimal polymer-salt composition for maximum ionic conductivity. Complex formation was ascertained from X-ray diffraction (XRD), Fourier transform infrared spectroscopy (FTIR), scanning electron microscopy (SEM) and differential scanning calorimetry (DSC) studies. The conductivity measurements reveal that the ionic conductivity of the polymer electrolytes containing various salt concentrations increases with temperature and obeys the Arrhenius rule. It is found that the electrolyte containing 25 wt.% of lithium triflate exhibits the highest room temperature conductivity. Moreover, Ionic transference measurements show predominance of ionic motion.

  2. Electroanalysis of NADH Using Conducting and Redox Active Polymer/Carbon Nanotubes Modified Electrodes-A Review

    PubMed Central

    Kumar, S. Ashok; Chen, Shen-Ming

    2008-01-01

    Past few decades, conducting and redox active polymers play a critical role in the development of transducers for biosensing. It has been evidenced by increasing numerous reports on conducting and redox active polymers incorporated electrodes for assay of biomolcules. This review highlights the potential uses of electrogenerated polymer modified electrodes and polymer/carbon nanotubes composite modified electrodes for electroanalysis of reduced form of nicotinamide adenine dinuceltoide (NADH). In addition, carbon electrodes modified with organic and inorganic materials as modifier have been discussed in detail for the quantification of NADH based on mediator or mediator-less methods.

  3. A pulsed electron beam synthesis of PEDOT conducting polymers by using sulfate radicals as oxidizing species

    NASA Astrophysics Data System (ADS)

    Coletta, Cecilia; Cui, Zhenpeng; Dazzi, Alexandre; Guigner, Jean-Michel; Néron, Stéphane; Marignier, Jean-Louis; Remita, Samy

    2016-09-01

    In this study, an original radiolytic method, based on pulsed electron beam irradiation, is used for the synthesis of conducting PEDOT in an aqueous solution containing EDOT monomers in the presence of potassium persulfate, K2S2O8, at 0 °C. At this low temperature, EDOT monomers are not chemically oxidized by S2O82- anions, initiating PEDOT polymerization, but are rather oxidized by sulfate radicals, SO4•-, which are radiolytically generated by the reaction of solvated electrons, produced by water radiolysis, with persulfate anions. Successfully, as demonstrated by UV-vis absorption spectrophotometry and ATR-FTIR spectroscopy, irradiating the aqueous solution, by using a series of accumulated electron pulses, enables complete EDOT oxidation and quantitative in situ PEDOT polymerization through a step-by-step oxidation mechanism. The morphology of PEDOT polymers, mixed with unreacted K2S2O8 salt, is characterized by Cryo-TEM microscopy in aqueous solution and by SEM after deposition. Successfully, in the absence of any washing step, high resolution AFM microscopy, coupled with infrared nanospectroscopy, is used to discriminate between the organic polymers and the inorganic salt and to probe the local chemical composition of PEDOT nanostructures. The results demonstrate that PEDOT polymers form globular self-assembled nanostructures which preferentially adsorb onto unreacted K2S2O8 solid nanoplates. The present results first demonstrate the efficiency of sulfate radicals as oxidizing species for the preparation of nanostructured PEDOT polymers and second highlight the promising potentiality of electron accelerators in the field of conducting polymers synthesis.

  4. Computational exploration of polymer nanocomposite mechanical property modification via cross-linking topology

    SciTech Connect

    Lacevic, N; Gee, R; Saab, A; Maxwell, R

    2008-04-24

    Molecular dynamics simulations have been performed in order to study the effects of nanoscale filler cross-linking topologies and loading levels on the mechanical properties of a model elastomeric nanocomposite. The model system considered here is constructed from octa-functional polyhedral oligomeric silsesquioxane (POSS) dispersed in a poly(dimethylsiloxane) (PDMS) matrix. Shear moduli, G, have been computed for pure and for filled and unfilled PDMS as a function of cross-linking density, POSS fill loading level, and polymer network topology. The results reported here show that G increases as the cross-linking (covalent bonds formed between the POSS and the PDMS network) density increases. Further, G is found to have a strong dependence on cross-linking topology. The increase in shear modulus, G, for POSS filled PDMS is significantly higher than that for unfilled PDMS cross-linked with standard molecular species, suggesting an enhanced reinforcement mechanism for POSS. In contrast, in blended systems (POSS/PDMS mixture with no cross-linking) G was not observed to significantly increase with POSS loading. Finally, we find intriguing differences in the structural arrangement of bond strains between the cross-linked and the blended systems. In the unfilled PDMS the distribution of highly strained bonds appears to be random, while in the POSS filled system, the strained bonds form a net-like distribution that spans the network. Such a distribution may form a structural network 'holding' the composite together and resulting in increases in G compared to an unfilled, cross-linked system. These results are of importance for engineering of new POSS-based multifunctional materials with tailor-made mechanical properties.

  5. Computational exploration of polymer nanocomposite mechanical property modification via cross-linking topology.

    PubMed

    Lacevic, Naida; Gee, Richard H; Saab, Andrew; Maxwell, Robert

    2008-09-28

    Molecular dynamics simulations have been performed in order to study the effects of nanoscale filler cross-linking topologies and loading levels on the mechanical properties of a model elastomeric nanocomposite. The model system considered here is constructed from octafunctional polyhedral oligomeric silsesquioxane (POSS) dispersed in a poly(dimethylsiloxane) (PDMS) matrix. Shear moduli, G, have been computed for pure and for filled and unfilled PDMS as a function of cross-linking density, POSS fill loading level, and polymer network topology. The results reported here show that G increases as the cross-linking (covalent bonds formed between the POSS and the PDMS network) density increases. Further, G is found to have a strong dependence on cross-linking topology. The increase in shear modulus, G, for POSS filled PDMS is significantly higher than that for unfilled PDMS cross-linked with standard molecular species, suggesting an enhanced reinforcement mechanism for POSS. In contrast, in blended systems (POSS/PDMS mixture with no cross-linking) G was not observed to significantly increase with POSS loading. Finally, we find intriguing differences in the structural arrangement of bond strains between the cross-linked and the blended systems. In the unfilled PDMS the distribution of highly strained bonds appears to be random, while in the POSS filled system, the strained bonds form a netlike distribution that spans the network. Such a distribution may form a structural network "holding" the composite together and resulting in increases in G compared to an unfilled, cross-linked system. These results are of importance for engineering of new POSS-based multifunctional materials with tailor-made mechanical properties. PMID:19045061

  6. Studies of interactions between conducting polymer and organic vapors, applications to chemical sensing

    SciTech Connect

    Josowicz, M.; Topart, P.; Cabala, R.

    1993-05-01

    In order to understand the physicochemical mechanism involved in the organic semiconductor charge-transfer processes occurring upon doping of the films with vapor molecules different experimental approaches much be taken. The effect of vapor diffusion into the electrochemically deposited poly(pyrrole), PP and poly(N-vinylcarbazole), PNVCz, films was investigated by monitoring the mass change of the exposed polymer, absorbance changes in the absorption spectra, and the work function change due to the modulation of the Fermi level in the material. An important step in that investigation was to establish the link between the distribution of the active dopant within the surface and the bulk of the material (1).

  7. Integrated reactive ion etching to pattern cross-linked hydrophilic polymer structures for protein immobilization

    NASA Astrophysics Data System (ADS)

    Bhatnagar, Parijat; Strickland, Aaron D.; Kim, Il; Malliaras, George G.; Batt, Carl A.

    2007-04-01

    Patterning of cross-linked hydrophilic polymer features using reactive ion etching (RIE) capable of covalently immobilizing proteins has been achieved. Projection photolithography was used to pattern photoresist to create micromolds. Vapor phase molecular self-assembly of polymerizable monolayer in molds allowed covalent binding of hydrogel on surface during free-radical polymerization. Excess hydrogel blanket film was consumed with oxygen RIE resulting into hydrogel pattern of 1μm size aligned to prefabricated silicon oxide structures. Proteins were finally coupled through their primary amine groups selectively to acid functionalized hydrogel features through stable amide linkages using 1-ethyl-3-[3-dimethylaminopropyl]carbodiimide hydrochloride and N-hydroxysulfosuccinimide.

  8. Ionic conductivity and dielectric permittivity of polymer electrolyte plasticized with polyethylene glycol

    NASA Astrophysics Data System (ADS)

    Das, S.; Ghosh, A.

    2016-05-01

    We have studied ionic conductivity and dielectric permittivity of PEO-LiClO4 solid polymer electrolyte plasticized with polyethylene glycol (PEG). The temperature dependence of the ionic conductivity has been well interpreted using Vogel-Tamman-Fulcher equation. The maximum dielectric constant is observed for 30 wt. % of PEG content. To get further insights into the ion dynamics, the complex dielectric permittivity has been studied with Havriliak-Negami function. The variation of relaxation time with inverse temperature obtained from HN formalism follows VTF nature.

  9. Ion-Electron-Conducting Polymer Composites: Promising Electromagnetic Interference Shielding Material.

    PubMed

    Vyas, Manoj Kumar; Chandra, Amita

    2016-07-20

    Polymer nanocomposites consisting of poly(vinylidenefluoride-co-hexafluoropropylene) PVdF-HFP, inorganic salt (LiBF4), organic salt (EMIMBF4), multiwalled carbon nanotubes (MWCNTs), and Fe3O4 nanoparticles were prepared as electromagnetic shield material. Improvement in conductivity and dielectric property due to the introduction of EMIMBF4, LiBF4, and MWCNTs was confirmed by complex impedance spectroscopy. The highest conductivity obtained is ∼1.86 mS/cm. This is attributed to the high ionic conductivity of the ionic liquids and the formation of a connecting network by the MWCNTs facilitating electron conduction. The total electromagnetic interference (EMI) shielding effectiveness has a major contribution to it due to absorption. Although the total shielding effectiveness in the Ku band (12.4-18 GHz) of pure ion-conducting system was found to be ∼19 dB and that for the polymer composites which are mixed (ion + electron) conductors is ∼46 dB, the contributions due to absorption are ∼16 and ∼42 dB, respectively. PMID:27351810

  10. Advanced two-photon photolithography for patterning of transparent, electrically conductive ionic liquid-polymer nanostructures

    NASA Astrophysics Data System (ADS)

    Bakhtina, Natalia A.; MacKinnon, Neil; Korvink, Jan G.

    2016-04-01

    A key challenge in micro- and nanotechnology is the direct patterning of functional structures. For example, it is highly desirable to possess the ability to create three-dimensional (3D), conductive, and optically transparent structures. Efforts in this direction have, to date, yielded less than optimal results since the polymer composites had low optical transparency over the visible range, were only slightly conductive, or incompatible with high resolution structuring. We have previously presented the novel cross-linkable, conductive, highly transparent composite material based on a photoresist (IP-L 780, OrmoComp, or SU-8) and the ionic liquid 1-butyl-3-methylimidazolium dicyanamide. Material patterning by conventional and two-photon photolithography has been demonstrated as proof-of-concept. Aiming to increase the resolution and to extend the spectrum of exciting applications we continued our research into identifying new ionic liquid - polymer composites. In this paper, we report the precise 3D single-step structuring of optically transparent and electrically conductive ionic liquid - polymer nanostructures with the highest spatial resolution (down to 150 nm) achieved to date. This was achieved via the development of novel cross-linkable composite based on the photoresist IP-G 780 and the ionic liquid 1-butyl-3-methylimidazolium dicyanamide. The successful combination of the developed material with the advanced direct laser writing technique enabled the time- and cost-saving direct manufacturing of transparent, electrically conductive components. We believe that the excellent characteristics of the structured material will open a wider range of exciting applications.

  11. Development of novel semi-conducting ortho-carborane based polymer films: Enhanced electronic and chemical properties

    NASA Astrophysics Data System (ADS)

    Pasquale, Frank L.

    A novel class of semi-conducting ortho-carborane (B 10C2H12) based polymer films with enhanced electronic and chemical properties has been developed. The novel films are formed from electron-beam cross-linking of condensed B10C2H 12 and B10C2H12 co-condensed with aromatic linking units (Y) (Y=1,4-diaminobenzene (DAB), benzene (BNZ) and pyridine (PY)) at 110 K. The bonding and electronic properties of the novel films were investigated using X-ray photoelectron spectroscopy (XPS), UV photoelectron spectroscopy (UPS) and Mulliken charge analysis using density functional theory (DFT). These films exhibit site-specific cross-linking with bonding, in the pure B10C2HX films, occurring at B sites non-adjacent to C in the B10C2H12 icosahedra. The B10C2H12:Y films exhibit the same phenomena, with cross-linking that creates bonds primarily between B sites non-adjacent to C in the B10C2H12 icosahedra to C sites in the Y linking units. These novel B10C2HX: Y linked films exhibit significantly different electron structure when compared to pure B10C2HX films as seen in the UPS spectra. The valence band maxima (VBM) shift from - 4.3 eV below the Fermi level for pure B10C2HX to -2.6, -2.2, and -1.7 for B10C2HX:BNZ, B10C 2HX:PY, and B10C2HX:DAB, respectively. The top of the valence band is composed of states derived primarily from the Y linking units, suggesting that the bottom of the conduction band is composed of states primarily from B10C2H12. Consequently these B10C2HX:Y films may exhibit longer electron-hole separation lifetimes as compared to pure B10C 2HX films. This research should lead to an enhancement of boron carbide based neutron detectors, and is of potential significance for microelectronics, spintronics and photo-catalysis.

  12. Observation of Quantized and Partial Quantized Conductance in Polymer-Suspended Graphene Nanoplatelets

    NASA Astrophysics Data System (ADS)

    Kang, Yuhong; Ruan, Hang; Claus, Richard O.; Heremans, Jean; Orlowski, Marius

    2016-04-01

    Quantized conductance is observed at zero magnetic field and room temperature in metal-insulator-metal structures with graphene submicron-sized nanoplatelets embedded in a 3-hexylthiophene (P3HT) polymer layer. In devices with medium concentration of graphene platelets, integer multiples of G o = 2 e 2/ h (=12.91 kΩ-1), and in some devices partially quantized including a series of with ( n/7) × G o, steps are observed. Such an organic memory device exhibits reliable memory operation with an on/off ratio of more than 10. We attribute the quantized conductance to the existence of a 1-D electron waveguide along the conductive path. The partial quantized conductance results likely from imperfect transmission coefficient due to impedance mismatch of the first waveguide modes.

  13. Proton Conducting Polymer Electrolytes: Polyethylene Oxide +(NH4)2SO4 System

    NASA Astrophysics Data System (ADS)

    Maurya, K. K.; Hashmi, S. A.; Chandra, S.

    1992-05-01

    A new proton-conducting polymer electrolyte polyethylene oxide (PEO)+(NH4)2SO4 has been reported. The proton transport in solution-cast films of PEO complexed with (NH4)2SO4 has been established using optical microscopy, XRD, DTA, IR, coulometry, transient ionic current and electrical conductivity studies. The highest electrical conductivity has been found to be 9.3× 10-7 S\\cdotcm-1 for the NH4+/EO ratio equal to 0.0416. The transference number and mobility of protonic movement have been found to be tH+≃0.61 and μH+≃2.9× 10-7 cm2/volt-sec, respectively. The movement of anions (possibly HSO4-) also contribute to the overall conductivity.

  14. Fast ultrahigh-density writing of low-conductivity patterns on semiconducting polymers.

    PubMed

    Farina, Marco; Ye, Tengling; Lanzani, Guglielmo; di Donato, Andrea; Venanzoni, Giuseppe; Mencarelli, Davide; Pietrangelo, Tiziana; Morini, Antonio; Keivanidis, Panagiotis E

    2013-01-01

    The exceptional interest in improving the limitations of data storage, molecular electronics and optoelectronics has promoted the development of an ever increasing number of techniques used to pattern polymers at micro and nanoscale. Most of them rely on atomic force microscopy to thermally or electrostatically induce mass transport, thereby creating topographic features. Here we show that the mechanical interaction between the tip of the atomic force microscope and the surface of π-conjugated polymeric films produces a local increase of molecular disorder, inducing a localized lowering of the semiconductor conductivity, not associated to detectable modifications in the surface topography. This phenomenon allows for the swift production of low-conductivity patterns on the film surface at a speed exceeding 20 μm s⁻¹; paths have a resolution in the order of the tip size (20 nm) and are detected by a conducting-atomic force microscopy tip in the conductivity maps.

  15. Pressure-induced amorphization of a dense coordination polymer and its impact on proton conductivity

    SciTech Connect

    Umeyama, Daiki; Hagi, Keisuke; Ogiwara, Naoki; Horike, Satoshi E-mail: kitagawa@icems.kyoto-u.ac.jp; Tassel, Cedric; Kageyama, Hiroshi; Higo, Yuji; Kitagawa, Susumu E-mail: kitagawa@icems.kyoto-u.ac.jp

    2014-12-01

    The proton conductivity of a dense coordination polymer (CP) was investigated under high-pressure conditions. Impedance measurements under high pressures revealed that the proton conductivity of the CP decreased more than 1000-fold at pressures of 3–7 GPa and that the activation energy for proton conduction almost doubled compared with that at ambient pressure. A synchrotron X-ray study under high pressure identified the amorphization process of the CP during compression, which rationally explains the decrease in conductivity and increase in activation energy. This phenomenon is categorized as reversible pressure-induced amorphization of a dense CP and is regarded as a demonstration of the coupling of the mechanical and electrical properties of a CP.

  16. Disulphide cross linked pullulan based cationic polymer for improved gene delivery and efflux pump inhibition.

    PubMed

    S, Priya S; R, Rekha M

    2016-10-01

    Multidrug resistance is a hurdle to successful cancer chemotherapy. Over expression of P-glycoprotein (P-gp) is a prime contributing factor for drug resistance. In this study, a disulphide cross-linked pullulan-based cationic polymer (PPSS) was synthesized to act simultaneously as gene delivery vehicle and efflux pump inhibitor. The PPSS nanoplexes were of size <200nm with the zeta potential of +15 to +20mV. The cytotoxicity studies using C6 and L929 cells showed that PPSS polymers are non-toxic even at high polymer concentrations. The PPSS/pDNA nanoplex showed superior uptake in confocal microscopy with 97% uptake by flow cytometry. The efficacy of efflux pump inhibition by the PPSS nanoplex was established by the enhanced intracellular retention of DOX. The enhanced cell death by p53/PPSS/DOX nanoplexes was attributed to the synergistic effect of P-gp inhibition and p53 transfection efficiency. Therefore, this multifunctional polymeric system may have significant promise for therapeutic application against cancer drug resistance. PMID:27459414

  17. The change in dielectric constant, AC conductivity and optical band gaps of polymer electrolyte film: Gamma irradiation

    SciTech Connect

    Raghu, S. Subramanya, K. Sharanappa, C. Mini, V. Archana, K. Sanjeev, Ganesh Devendrappa, H.

    2014-04-24

    The effects of gamma (γ) irradiation on dielectric and optical properties of polymer electrolyte film were investigated. The dielectric constant and ac conductivity increases with γ dose. Also optical band gap decreased from 4.23 to 3.78ev after irradiation. A large dependence of the polymer properties on the irradiation dose was noticed. This suggests that there is a possibility of improving polymer electrolyte properties on gamma irradiation.

  18. Electro-active Polymer Actuator Based on Sulfonated Polyimide with Highly Conductive Silver Electrodes Via Self-metallization.

    PubMed

    Song, Jiangxuan; Jeon, Jin-Han; Oh, Il-Kwon; Park, K C

    2011-10-01

    We report here a facile synthesis of high performance electro-active polymer actuator based on a sulfonated polyimide with well-defined silver electrodes via self-metallization. The proposed method greatly reduces fabrication time and cost, and obviates a cation exchange process required in the fabrication of ionic polymer-metal composite actuators. Also, the self-metallized silver electrodes exhibit outstanding metal-polymer adhesion with high conductivity, resulting in substantially larger tip displacements compared with Nafion-based actuators.

  19. Microtexturing of the conductive PEDOT:PSS polymer for superhydrophobic organic electrochemical transistors.

    PubMed

    Gentile, Francesco; Coppedè, Nicola; Tarabella, Giuseppe; Villani, Marco; Calestani, Davide; Candeloro, Patrizio; Iannotta, Salvatore; Di Fabrizio, Enzo

    2014-01-01

    Superhydrophobic surfaces are bioinspired, nanotechnology artifacts, which feature a reduced friction coefficient, whereby they can be used for a number of very practical applications including, on the medical side, the manipulation of biological solutions. In this work, we integrated superhydrophobic patterns with the conducting polymer PEDOT:PSS, one of the most used polymers in organic electronics because highly sensitive to ionized species in solution. In doing so, we combined geometry and materials science to obtain an advanced device where, on account of the superhydrophobicity of the system, the solutions of interest can be manipulated and, on account of the conductive PEDOT:PSS polymer, the charged molecules dispersed inside can be quantitatively measured. This original substrate preparation allowed to perform electrochemical measurements on ionized species in solution with decreasing concentration down to 10(-7) molar. Moreover, it was demonstrated the ability of the device of realizing specific, combined time and space resolved analysis of the sample. Collectively, these results demonstrate how a tight, interweaving integration of different disciplines can provide realistic tools for the detection of pathologies. The scheme here introduced offers breakthrough capabilities that are expected to radically improve both the pace and the productivity of biomedical research, creating an access revolution. PMID:24579079

  20. Single Lithium-Ion Conducting Polymer Electrolytes Based on a Super-Delocalized Polyanion.

    PubMed

    Ma, Qiang; Zhang, Heng; Zhou, Chongwang; Zheng, Liping; Cheng, Pengfei; Nie, Jin; Feng, Wenfang; Hu, Yong-Sheng; Li, Hong; Huang, Xuejie; Chen, Liquan; Armand, Michel; Zhou, Zhibin

    2016-02-12

    A novel single lithium-ion (Li-ion) conducting polymer electrolyte is presented that is composed of the lithium salt of a polyanion, poly[(4-styrenesulfonyl)(trifluoromethyl(S-trifluoromethylsulfonylimino)sulfonyl)imide] (PSsTFSI(-)), and high-molecular-weight poly(ethylene oxide) (PEO). The neat LiPSsTFSI ionomer displays a low glass-transition temperature (44.3 °C; that is, strongly plasticizing effect). The complex of LiPSsTFSI/PEO exhibits a high Li-ion transference number (tLi (+) =0.91) and is thermally stable up to 300 °C. Meanwhile, it exhibits a Li-ion conductivity as high as 1.35×10(-4)  S cm(-1) at 90 °C, which is comparable to that for the classic ambipolar LiTFSI/PEO SPEs at the same temperature. These outstanding properties of the LiPSsTFSI/PEO blended polymer electrolyte would make it promising as solid polymer electrolytes for Li batteries.

  1. Microtexturing of the conductive PEDOT:PSS polymer for superhydrophobic organic electrochemical transistors.

    PubMed

    Gentile, Francesco; Coppedè, Nicola; Tarabella, Giuseppe; Villani, Marco; Calestani, Davide; Candeloro, Patrizio; Iannotta, Salvatore; Di Fabrizio, Enzo

    2014-01-01

    Superhydrophobic surfaces are bioinspired, nanotechnology artifacts, which feature a reduced friction coefficient, whereby they can be used for a number of very practical applications including, on the medical side, the manipulation of biological solutions. In this work, we integrated superhydrophobic patterns with the conducting polymer PEDOT:PSS, one of the most used polymers in organic electronics because highly sensitive to ionized species in solution. In doing so, we combined geometry and materials science to obtain an advanced device where, on account of the superhydrophobicity of the system, the solutions of interest can be manipulated and, on account of the conductive PEDOT:PSS polymer, the charged molecules dispersed inside can be quantitatively measured. This original substrate preparation allowed to perform electrochemical measurements on ionized species in solution with decreasing concentration down to 10(-7) molar. Moreover, it was demonstrated the ability of the device of realizing specific, combined time and space resolved analysis of the sample. Collectively, these results demonstrate how a tight, interweaving integration of different disciplines can provide realistic tools for the detection of pathologies. The scheme here introduced offers breakthrough capabilities that are expected to radically improve both the pace and the productivity of biomedical research, creating an access revolution.

  2. Single Lithium-Ion Conducting Polymer Electrolytes Based on a Super-Delocalized Polyanion.

    PubMed

    Ma, Qiang; Zhang, Heng; Zhou, Chongwang; Zheng, Liping; Cheng, Pengfei; Nie, Jin; Feng, Wenfang; Hu, Yong-Sheng; Li, Hong; Huang, Xuejie; Chen, Liquan; Armand, Michel; Zhou, Zhibin

    2016-02-12

    A novel single lithium-ion (Li-ion) conducting polymer electrolyte is presented that is composed of the lithium salt of a polyanion, poly[(4-styrenesulfonyl)(trifluoromethyl(S-trifluoromethylsulfonylimino)sulfonyl)imide] (PSsTFSI(-)), and high-molecular-weight poly(ethylene oxide) (PEO). The neat LiPSsTFSI ionomer displays a low glass-transition temperature (44.3 °C; that is, strongly plasticizing effect). The complex of LiPSsTFSI/PEO exhibits a high Li-ion transference number (tLi (+) =0.91) and is thermally stable up to 300 °C. Meanwhile, it exhibits a Li-ion conductivity as high as 1.35×10(-4)  S cm(-1) at 90 °C, which is comparable to that for the classic ambipolar LiTFSI/PEO SPEs at the same temperature. These outstanding properties of the LiPSsTFSI/PEO blended polymer electrolyte would make it promising as solid polymer electrolytes for Li batteries. PMID:26840215

  3. Light-triggered conducting properties of a random carbon nanotubes network in a photochromic polymer matrix

    NASA Astrophysics Data System (ADS)

    Castagna, R.; Sciascia, C.; Srimath Kandada, A. R.; Meneghetti, M.; Lanzani, G.; Bertarelli, C.

    2011-10-01

    Photochromic materials reversibly change their colour due to a photochemical reaction that takes place when the material is irradiated with photons of suitable energy. This peculiar feature has been extensively exploited to develop smart sunglasses, filters and inks. With a proper molecular design it is possible to enable modulation not only of colour but also of other properties such as refractive index, dipole moment, nonlinear optical properties or conductivity by a photoswitching of the molecular structure. The approach herein developed consists in modifying, upon irradiation, the properties of a molecular component coupled with the photochromic molecule. In particular, the switching features of photochromic systems are matched with the intriguing peculiar properties of carbon nanotubes (CNTs). A photochromic polyester has been properly synthesised to be used as switching polymer matrix coupled with a network of CNTs. Irradiation of the polymer/CNTs blend results into a light-triggered conductance switching. The reversible electrocyclization of the polymer under UV-vis illumination results into a modification of the inter-tube charge mobility, and accordingly, of the overall resistance of the blend. Solution techniques allow us to obtain blended films with sheet resistance modulation larger than 150%, good thermal stability and fatigue resistance at room conditions, in an easier, faster and scalable way as respect to the single-molecule approach.ÿ

  4. Electrochemical Li insertion into conductive polymer/V{sub 2}O{sub 5} nanocomposites

    SciTech Connect

    Leroux, F.; Goward, G.; Power, W.P.; Nazar, L.F.

    1997-11-01

    Electrochemical insertion of Li into a series of nanocomposites comprised of alternating V{sub 2}O{sub 5} sheets and conductive polymer layers [polypyrrole (PPY) and polyaniline (PANI)] was examined and compared to the pristine V{sub 2}O{sub 5} material in terms of reversibility, Li site occupancy, and Li diffusion coefficients, and to the materials after oxidation treatment. The electrochemical characteristics are very sensitive to the nature of the polymer, its content, and location. The presence of surface polymer hinders Li insertion in these materials (by comparison to materials without surface polymer) and appears to result in the partial entrapment of Li ions. For modified [PANI]{sub 0.4}V{sub 2}O{sub 5}, polymer incorporation results in better reversibility and increased Li capacity in the nanocomposite. [PPY]{sub 0.40}V{sub 2}O{sub 5} displays a greater first discharge capacity than the respective PANI material, but is not as cyclable as in O{sub 2}-[PANI]{sub 0.40}V{sub 2}O{sub 5}. O{sub 2}-treatment results in the reformation of a high-potential Li site that is lost during the reductive intercalative polymerization. Li chemical diffusion coefficients are greater for the O{sub 2}-[PANI]V{sub 2}O{sub 5} nanocomposite than the xerogel by one order of magnitude, resulting in better performance at high current densities. Most important, the electrochemical response of these nanocomposites is greater than the sum of the two components (inorganic and organic), underlining the synergy of these hybrid materials.

  5. Conducting polymer nanocomposites loaded with nanotubes and fibers for electrical and thermal applications

    NASA Astrophysics Data System (ADS)

    Chiguma, Jasper

    The design, fabrication and measurement of electrical and thermal properties of polymers loaded with nanotubes and fibers are the foci of the work presented in this dissertation. The resulting products of blending polymers with nanomaterials are called nanocomposites and are already finding applications in many areas of human endeavour. Among some of the most recent envisioned applications of nanocomposites is in electronic devices as thermal interface materials (TIMs). This potential application as TIMs, has been made more real by the realization that carbon nanotubes, could potentially transfer their high electrical, thermal and mechanical properties to polymers in the nanocomposites. In Chapter 1, the events leading to the discovery of carbon nanotubes are reviewed followed by an elaborate discussion of their structure and properties. The discussion of the structure and properties of carbon nanotubes help in understanding the envisaged applications. Chapter 2 focuses on the fabrication of insulating polymer nanocomposites, their electrical and mechanical properties. Poly (methyl methacrylate) (PMMA) and a polyimide formed by reacting pyromellitic dianhydride (PMDA) and 4, 4'-oxydianiline (ODA) (PMDA-ODA) nanocomposites with carbon nanotubes were prepared by in-situ polymerization. Poly (1-methyl-4-pentene) (TPX), Polycarbonate (PC), Poly (vinyl chloride) (PVC), Poly (acrylonitrile-butadiene-styrene) (ABS), the alloys ABS-PC, ABS-PVC, and ABS-PC-PVC nanocomposites were prepared from the respective polymers and carbon nanotubes and their mechanical and electrical properties measured. Chapter 3 covers the nanocomposites that were prepared by the in-situ polymerization of the conducting polymers Polyaniline (PANi), Polypyrrole (PPy) and Poly (3, 4-ethylenedioxythiophene) (PEDOT) by in-situ polymerization. These are evaluated for electrical conductivity. The use of surfactants in facilitating carbon nanotube dispersion is discussed and applied in the preparation of

  6. Removal of anionic azo dyes from aqueous solution by functional ionic liquid cross-linked polymer.

    PubMed

    Gao, Hejun; Kan, Taotao; Zhao, Siyuan; Qian, Yixia; Cheng, Xiyuan; Wu, Wenli; Wang, Xiaodong; Zheng, Liqiang

    2013-10-15

    A novel functional ionic liquid based cross-linked polymer (PDVB-IL) was synthesized from 1-aminoethyl-3-vinylimidazolium chloride and divinylbenzene for use as an adsorbent. The physicochemical properties of PDVB-IL were investigated by Fourier transform infrared spectroscopy, scanning electron microscopy and thermogravimetric analysis. The adsorptive capacity was investigated using anionic azo dyes of orange II, sunset yellow FCF, and amaranth as adsorbates. The maximum adsorption capacity could reach 925.09, 734.62, and 547.17 mg/g for orange II, sunset yellow FCF and amaranth at 25°C, respectively, which are much better than most of the other adsorbents reported earlier. The effect of pH value was investigated in the range of 1-8. The result shows that a low pH value is found to favor the adsorption of those anionic azo dyes. The adsorption kinetics and isotherms are well fitted by a pseudo second-order model and Langmuir model, respectively. The adsorption process is found to be dominated by physisorption. The introduction of functional ionic liquid moieties into cross-linked poly(divinylbenzene) polymer constitutes a new and efficient kind of adsorbent.

  7. Polymerization of the conducting polymer poly(3,4-ethylenedioxythiophene) (PEDOT) around living neural cells

    PubMed Central

    Richardson-Burns, Sarah M.; Hendricks, Jeffrey L.; Foster, Brian; Povlich, Laura K.; Kim, Dong-Hwan; Martin, David C.

    2007-01-01

    In this paper we describe interactions between neural cells and the conducting polymer poly(3,4-ethylenedioxythiophene (PEDOT) toward development of electrically conductive biomaterials intended for direct, functional contact with electrically-active tissues such as the nervous system, heart, and skeletal muscle. We introduce a process for polymerizing PEDOT around living cells and describe a neural cell-templated conducting polymer coating for microelectrodes and a hybrid conducting polymer-live neural cell electrode. We found that neural cells could be exposed to working concentrations (0.01 M) of the EDOT monomer for as long as 72 hours while maintaining 80% cell viability. PEDOT could be electrochemically deposited around neurons cultured on electrodes using 0.5-1 μA/mm2 galvanostatic current. PEDOT polymerized on the electrode and surrounded the cells, covering cell processes. The polymerization was impeded in regions where cells were well-adhered to the substrate. The cells could be removed from the PEDOT matrix to generate a neural cell-templated biomimetic conductive substrate with cell-shaped features that were cell-attracting. Live cells embedded within the conductive polymer matrix remained viable for at least 120 hours following polymerization. Dying cells primarily underwent apoptotic cell death. PEDOT, PEDOT+live neurons, and neuron-templated PEDOT coatings on electrodes significantly enhanced the electrical properties as compared to the bare electrode as indicated by decreased electrical impedance of 1-1.5 orders of magnitude at 0.01-1 kHz and significantly increased charge transfer capacity. PEDOT coatings showed a decrease of the phase angle of the impedance from roughly 80 degrees for the bare electrode to 5-35 degrees at frequencies >0.1 kHz. Equivalent circuit modeling indicated that PEDOT-coated electrodes were best described by R(C(RT)) circuit. We found that an RC parallel circuit must be added to the model for PEDOT+live neuron and neuron

  8. High rate lithium-sulfur battery enabled by sandwiched single ion conducting polymer electrolyte

    PubMed Central

    Sun, Yubao; Li, Gai; Lai, Yuanchu; Zeng, Danli; Cheng, Hansong

    2016-01-01

    Lithium-sulfur batteries are highly promising for electric energy storage with high energy density, abundant resources and low cost. However, the battery technologies have often suffered from a short cycle life and poor rate stability arising from the well-known “polysulfide shuttle” effect. Here, we report a novel cell design by sandwiching a sp3 boron based single ion conducting polymer electrolyte film between two carbon films to fabricate a composite separator for lithium-sulfur batteries. The dense negative charges uniformly distributed in the electrolyte membrane inherently prohibit transport of polysulfide anions formed in the cathode inside the polymer matrix and effectively blocks polysulfide shuttling. A battery assembled with the composite separator exhibits a remarkably long cycle life at high charge/discharge rates. PMID:26898772

  9. Computational design of mixers and pumps for microfluidic systems, based on electrochemically-active conducting polymers.

    PubMed

    Kannappan, Karthik; Bogle, Gib; Travas-Sejdic, Jadranka; Williams, David E

    2011-03-28

    We present a theoretical description of the propagation of composition waves along a strip of electrochemically-active conducting polymer, upon electrochemical stimulation. We develop an efficient solution of the electro-neutral Nernst-Plank equations in 2-D for electromigration and diffusional transport in the solution based on an extension of the methods of Scharfetter and Gummel [D. L. Scharfetter and H. K. Gummel, IEEE Trans. Electron Devices, 1969, ED16, 64-77.] and of Cohen and Cooley [H. Cohen and J. W. Cooley, Biophys. J., 1965, 5, 145-162.], and demonstrate important effects of the geometry of the cell. Under some circumstances, waves reflecting back from the end of the strip are predicted. We then demonstrate theoretically how such waves, associated as they are with expansion of the polymer, could be employed to enhance mixing or induce pumping in microfluidic systems.

  10. Preparation of conductive gold nanowires in confined environment of gold-filled polymer nanotubes.

    PubMed

    Mitschang, Fabian; Langner, Markus; Vieker, Henning; Beyer, André; Greiner, Andreas

    2015-02-01

    Continuous conductive gold nanofibers are prepared via the "tubes by fiber templates" process. First, poly(l-lactide) (PLLA)-stabilized gold nanoparticles (AuNP) with over 60 wt% gold are synthesized and characterized, including gel permeation chromatography coupled with a diode array detector. Subsequent electrospinning of these AuNP with template PLLA results in composite nanofibers featuring a high gold content of 57 wt%. Highly homogeneous gold nanowires are obtained after chemical vapor deposition of 345 nm of poly(p-xylylene) (PPX) onto the composite fibers followed by pyrolysis of the polymers at 1050 °C. The corresponding heat-induced transition from continuous gold-loaded polymer tubes to smooth gold nanofibers is studied by transmission electron microscopy and helium ion microscopy using both secondary electrons and Rutherford backscattered ions.

  11. Chemical synthesis of water-soluble, chiral conducting-polymer complexes

    DOEpatents

    Wang, Hsing-Lin; McCarthy, Patrick A.; Yang, Sze Cheng

    2003-01-01

    The template-guided synthesis of water-soluble, chiral conducting polymer complexes is described. Synthesis of water-soluble polyaniline complexes is achieved by carefully controlling the experimental parameters such as; acid concentration, ionic strength, monomer/template ratio, total reagent concentration, and order of reagent addition. Chiral (helical) polyaniline complexes can be synthesized by addition of a chiral inducing agent (chiral acid) prior to polymerization, and the polyaniline helix can be controlled by the addition of the (+) or (-) form of the chiral acid. Moreover the quantity of chiral acid and the salt content has a significant impact on the degree of chirality in the final polymer complexes. The polyaniline and the template have been found to be mixed at the molecular level which results in chiral complexes that are robust through repeated doping and dedoping cycles.

  12. Photovoltaic Cells involving Nonconjugated Conductive Polymer, Iodine-doped cis-Polyisoprene (Natural Rubber)

    NASA Astrophysics Data System (ADS)

    Jaju, S.; Thakur, M.

    2014-03-01

    Photovoltaic cells have been fabricated using titanium dioxide/doped cis-polyisoprene/carbon on ITO glass-substrates. Photocurrents and photo-voltages for different intensities of light (from a white light bulb, emission at 300-700 nm) have been measured. Use of the iodine-doped nonconjugated conductive polymer film (absorption ~ 250 to 700 nm) has led to significant enhancement of photocurrent compared to previous reports which included undoped polymer in a different cell-structure. A maximum photocurrent of about 0.20 mA was observed for a light intensity of ~ 5 mW/cm2. The maximum photo-voltage as observed was about 0.70 V for the same light intensity. Natural rubber being inexpensive these cells may provide cheaper alternatives to other reported cell structures.

  13. High rate lithium-sulfur battery enabled by sandwiched single ion conducting polymer electrolyte

    NASA Astrophysics Data System (ADS)

    Sun, Yubao; Li, Gai; Lai, Yuanchu; Zeng, Danli; Cheng, Hansong

    2016-02-01

    Lithium-sulfur batteries are highly promising for electric energy storage with high energy density, abundant resources and low cost. However, the battery technologies have often suffered from a short cycle life and poor rate stability arising from the well-known “polysulfide shuttle” effect. Here, we report a novel cell design by sandwiching a sp3 boron based single ion conducting polymer electrolyte film between two carbon films to fabricate a composite separator for lithium-sulfur batteries. The dense negative charges uniformly distributed in the electrolyte membrane inherently prohibit transport of polysulfide anions formed in the cathode inside the polymer matrix and effectively blocks polysulfide shuttling. A battery assembled with the composite separator exhibits a remarkably long cycle life at high charge/discharge rates.

  14. High rate lithium-sulfur battery enabled by sandwiched single ion conducting polymer electrolyte.

    PubMed

    Sun, Yubao; Li, Gai; Lai, Yuanchu; Zeng, Danli; Cheng, Hansong

    2016-02-22

    Lithium-sulfur batteries are highly promising for electric energy storage with high energy density, abundant resources and low cost. However, the battery technologies have often suffered from a short cycle life and poor rate stability arising from the well-known "polysulfide shuttle" effect. Here, we report a novel cell design by sandwiching a sp(3) boron based single ion conducting polymer electrolyte film between two carbon films to fabricate a composite separator for lithium-sulfur batteries. The dense negative charges uniformly distributed in the electrolyte membrane inherently prohibit transport of polysulfide anions formed in the cathode inside the polymer matrix and effectively blocks polysulfide shuttling. A battery assembled with the composite separator exhibits a remarkably long cycle life at high charge/discharge rates.

  15. Ion conduction and relaxation in PEO-LiTFSI-Al2O3 polymer nanocomposite electrolytes

    NASA Astrophysics Data System (ADS)

    Das, S.; Ghosh, A.

    2015-05-01

    Ion conduction and relaxation in PEO-LiTFSI-Al2O3 polymer nanocomposite electrolytes have been studied for different concentrations of Al2O3 nanoparticles. X-ray diffraction and differential scanning calorimetric studies show that the maximum amorphous phase of PEO is observed for PEO-LiTFSI embedded with 5 wt. % Al2O3. The maximum ionic conductivity ˜3.3 × 10-4 S cm-1 has been obtained for this composition. The transmission electron microscopic image shows a distribution of Al2O3 nanoparticles in all compositions with size of <50 nm. The temperature dependence of the ionic conductivity follows Vogel-Tamman-Fulcher nature, indicating a strong coupling between ionic and polymer chain segmental motions. The scaling of the ac conductivity implies that relaxation dynamics follows a common mechanism for different temperatures and Al2O3 concentrations. The imaginary modulus spectra are asymmetric and skewed toward the high frequency sides of the maxima and analyzed using Havriliak-Negami formalism. The temperature dependence of the relaxation time obtained from modulus spectra also exhibits Vogel-Tamman-Fulcher nature. The values of the stretched exponent obtained from Kohlrausch-Williams-Watts fit to the modulus data are fairly low, suggesting highly non-exponential relaxation for all concentrations of Al2O3 in these electrolytes.

  16. Thermoelectric behavior of conducting polymers: On the possibility of off-diagonal thermoelectricity

    SciTech Connect

    Mateeva, N.; Testardi, L.; Niculescu, H. ||

    1998-12-01

    Non-cubic materials, when structurally aligned, possess sufficient anisotropy to exhibit thermoelectric effects where the electrical and thermal paths can be orthogonal due to off-diagonal thermoelectricity (ODTE). The authors discuss the benefits of this form of thermoelectricity for device applications and describe a search for suitable thermoelectric properties in the air-stable conducting polymers polyaniline and polypyrrole. They find, at 300K for diagonal (ordinary) thermoelectricity (DTE), the general correlation that the logarithm of the electrical conductivity varies linearly with the Seebeck coefficient on doping, but with a proportionality in excess of a prediction from theory. The correlation is unexpected in its universality and unfavorable in its consequences for applications in DTE and ODTE. A standard model suggests that conduction by carriers of both signs occurs in these polymers, which thus leads to reduced thermoelectric efficiency. They also discuss polyacetylene (which is not air-stable), where this ambipolar conduction does not occur, and where properties seem more favorable for thermoelectricity.

  17. A first approach to foot motion monitoring using conductive polymer sensors

    NASA Astrophysics Data System (ADS)

    Castano, L. M.; Winkelmann, A. E.; Flatau, A. B.

    2009-03-01

    A study was conducted of socks fitted with thin flexible conductive polymer sensors for the potential use as a smart sock for monitoring foot motion. The thin flexible sensors consisted of a conductive polymer applied on an elastic textile substrate that exhibited a resistance change when strained. Quasi-static response tests of the basic sensor over a static load range of a few Newtons were conducted and showed a time varying response as observed by previous investigators. Dynamic testing through an electrodynamic shaker shows good dynamic response at a low frequency range, less than 4Hz. Strips of 12 cm x 1 cm of the sensor on fabric showed a reproducible basal resistance on the order of 10KOhms. Other geometries of the continuous sensors and correlation of strain to resistance variation were studied. Similar tests were performed on different textile substrates which vary in composition and microstructure, i.e. woven, knitted, nylon%, polyester%, etc... These sensors were integrated into socks and preliminary results indicate that distinct responses to different foot motion patterns are detected in sensors placed at different joint locations on the foot. Further processing of strain results from smart socks should provide information about the kinematics and dynamics of the human foot.

  18. Electrochemical co-deposition of conductive polymer-silica hybrid thin films.

    PubMed

    Raveh, Moran; Liu, Liang; Mandler, Daniel

    2013-07-14

    Conductive polymers, such as polypyrrole (ppy), have been the subject of numerous studies due to their promising applications in organic solar cells, flexible electronics, electrochromic devices, super capacitors, etc. Yet, their application is still limited as a result of poor processability. Silica has been reported to improve the mechanical strength and adhesion of conductive polymer films. In this work, we propose a controllable electrochemical approach for preparing ppy-silica hybrid thin films from a solution containing both pyrrole and silane monomers. It is known that pyrrole can be electropolymerised using anodic potentials, while silica can be electrodeposited under cathodic potentials. Thus, we studied the formation of ppy-silica hybrid thin films on a stainless steel surface by applying alternating potentials, i.e. cathodic followed by anodic pulses (denoted C + A) or anodic followed by cathodic pulses (denoted A + C). We show that by controlling the deposition potential and time for the cathodic and anodic pulses, the film thickness and composition can be manipulated well as analysed using profilometry and EDX. The element depth profile of the films was characterized using secondary ion mass spectroscopy (SIMS). In essence, for the C + A process, pyrrole diffuses through the cathodically electrodeposited wet silica gel layer and undergoes anodic polymerisation on the substrate, while for the A + C process, silane can be electrodeposited both on top of the anodically electrodeposited conductive ppy films as well as on the stainless steel through the pinholes in the ppy film. This offers a simple approach for tuning the structure of conductive polymer-sol-gel composite films.

  19. 3D networked graphene-ferromagnetic hybrids for fast shape memory polymers with enhanced mechanical stiffness and thermal conductivity.

    PubMed

    Lee, Sang-Heon; Jung, Jung-Hwan; Oh, Il-Kwon

    2014-10-15

    A novel 3D networked graphene-ferromagnetic hybrid can be easily fabricated using one-step microwave irradiation. By incorporating this hybrid material into shape memory polymers, the synergistic effects of fast speed and the enhancement of thermal conductivity and mechanical stiffness can be achieved. This can be broadly applicable to designing magneto-responsive shape memory polymers for multifunction applications.

  20. Conductive Circuit Containing a Polymer Composition Containing Thermally Exfoliated Graphite Oxide and Method of Making the Same

    NASA Technical Reports Server (NTRS)

    Prud'Homme, Robert K. (Inventor); Aksay, Ilhan A. (Inventor)

    2014-01-01

    A conductive circuit containing a polymer composite, which contains at least one polymer and a modified graphite oxide material, containing thermally exfoliated graphite oxide having a surface area of from about 300 m(sup.2)/g to 2600 m(sup.2)/g, and a method of making the same.

  1. Cross-linked branching nanohybrid polymer electrolyte with monodispersed TiO2 nanoparticles for high performance lithium-ion batteries

    NASA Astrophysics Data System (ADS)

    Ma, Cheng; Zhang, Jinfang; Xu, Mingquan; Xia, Qingbing; Liu, Jiatu; Zhao, Shuai; Chen, Libao; Pan, Anqiang; Ivey, Douglas G.; Wei, Weifeng

    2016-06-01

    Nanohybrid polymer electrolytes (NHPE) with ceramic particles have attracted significant attention owing to their improvement in electrochemical performance. However, particle aggregation and weak nanoparticle/polymer matrix interaction restrict their further application in lithium-ion batteries (LIBs). We demonstrate a facile in-situ polymerization/crystallization method to synthesize a homogeneous TiO2-grafted NHPE with a cross-linked branching structure, comprised of ion-conducting poly(ethylene glycol) methyl ether methacrylate (PEGMEM) and non-polar stearyl methacrylate (SMA). This technique is different from existing methods of blending functionalized ceramic particles into the polymer matrix. Highly monodispersed TiO2 nanocrystals enhance the effective interfacial interactions between particles and polymer matrix, which suppress the crystallization of ethylene oxide (EO) groups and facilitate forming continuously interconnected ion-conducting channels. Moreover, an increased dissociation degree of Li salt can also be achieved. The TiO2-grafted NHPE exhibits superior electrochemical properties with an ionic conductivity of 1.1 × 10-4 S cm-1 at 30 °C, a high lithium ion transference number and excellent interfacial compatibility with the lithium electrode. In particular, a lithium-ion battery based on TiO2-grafted NHPE demonstrates good C-rate performance, as well as excellent cycling stability with an initial discharge capacity of 153.5 mAh g-1 and a capacity retention of 96% after 300 cycles at 1 C (80 °C).

  2. Effect of Eutectic Concentration on Conductivity in PEO:LiX Based Solid Polymer Electrolytes

    NASA Astrophysics Data System (ADS)

    Zhan, Pengfei; Ganapatibhotla, Lalitha; Maranas, Janna

    Polyethylene oxide (PEO) and lithium salt based solid polymer electrolytes (SPEs) have been widely proposed as a substitution for the liquid electrolyte in Li-ion batteries. As salt concentration varies, these systems demonstrate rich phase behavior. Conductivity as a function of salt concentration has been measured for decades and various concentration dependences have been observed. A PEO:LiX mixture can have one or two conductivity maximums, while some mixtures with salt of high ionic strength will have higher conductivity as the salt concentration decrease. The factors that affect the conductivity are specific for each sample. The universal factor that affects conductivity is still not clear. In this work, we measured the conductivity of a series of PEO:LiX mixtures and statistical analysis shows conductivity is affected by the concentration difference from the eutectic concentration (Δc). The correlation with Δc is stronger than the correlation with glass transition temperature. We believe that at the eutectic concentration, during the solidification process, unique structures can form which aid conduction. Currently at Dow Chemical.

  3. Compliant glass-polymer hybrid single ion-conducting electrolytes for lithium batteries.

    PubMed

    Villaluenga, Irune; Wujcik, Kevin H; Tong, Wei; Devaux, Didier; Wong, Dominica H C; DeSimone, Joseph M; Balsara, Nitash P

    2016-01-01

    Despite high ionic conductivities, current inorganic solid electrolytes cannot be used in lithium batteries because of a lack of compliance and adhesion to active particles in battery electrodes as they are discharged and charged. We have successfully developed a compliant, nonflammable, hybrid single ion-conducting electrolyte comprising inorganic sulfide glass particles covalently bonded to a perfluoropolyether polymer. The hybrid with 23 wt% perfluoropolyether exhibits low shear modulus relative to neat glass electrolytes, ionic conductivity of 10(-4) S/cm at room temperature, a cation transference number close to unity, and an electrochemical stability window up to 5 V relative to Li(+)/Li. X-ray absorption spectroscopy indicates that the hybrid electrolyte limits lithium polysulfide dissolution and is, thus, ideally suited for Li-S cells. Our work opens a previously unidentified route for developing compliant solid electrolytes that will address the challenges of lithium batteries. PMID:26699512

  4. Compliant glass–polymer hybrid single ion-conducting electrolytes for lithium batteries

    PubMed Central

    Villaluenga, Irune; Wujcik, Kevin H.; Tong, Wei; Devaux, Didier; Wong, Dominica H. C.; DeSimone, Joseph M.; Balsara, Nitash P.

    2016-01-01

    Despite high ionic conductivities, current inorganic solid electrolytes cannot be used in lithium batteries because of a lack of compliance and adhesion to active particles in battery electrodes as they are discharged and charged. We have successfully developed a compliant, nonflammable, hybrid single ion-conducting electrolyte comprising inorganic sulfide glass particles covalently bonded to a perfluoropolyether polymer. The hybrid with 23 wt% perfluoropolyether exhibits low shear modulus relative to neat glass electrolytes, ionic conductivity of 10−4 S/cm at room temperature, a cation transference number close to unity, and an electrochemical stability window up to 5 V relative to Li+/Li. X-ray absorption spectroscopy indicates that the hybrid electrolyte limits lithium polysulfide dissolution and is, thus, ideally suited for Li-S cells. Our work opens a previously unidentified route for developing compliant solid electrolytes that will address the challenges of lithium batteries. PMID:26699512

  5. Discontinuous anchoring transition and photothermal switching in composites of liquid crystals and conducting polymer nanofibers

    NASA Astrophysics Data System (ADS)

    Rasna, M. V.; Zuhail, K. P.; Manda, R.; Paik, P.; Haase, W.; Dhara, Surajit

    2014-05-01

    We prepared nanocomposites of a nematic liquid crystal and nanofibers of a conducting polymer (polyaniline). All the nanocomposites exhibit a discontinuous surface anchoring transition from planar to homeotropic in the nematic phase on a perfluoropolymer coated surface with a thermal hysteresis (≈5.3∘C). We observe a relatively large bistable conductivity and demonstrate a light driven switching of conductivity and dielectric constant in dye doped nanocomposites in the thermal hysteresis (bistable) region. The experimental results have been explained based on the reorientation of the nanofibers driven by the anchoring transition of the nematic liquid crystal. We show a significant enhancement of the bistable temperature range (≈13∘C) by an appropriate choice of compound in the binary system.

  6. Protic Salt Polymer Membranes: High-Temperature Water-Free Proton-Conducting Membranes

    SciTech Connect

    Gervasio, Dominic Francis

    2010-09-30

    This research on proton-containing (protic) salts directly addresses proton conduction at high and low temperatures. This research is unique, because no water is used for proton ionization nor conduction, so the properties of water do not limit proton fuel cells. A protic salt is all that is needed to give rise to ionized proton and to support proton mobility. A protic salt forms when proton transfers from an acid to a base. Protic salts were found to have proton conductivities that are as high as or higher than the best aqueous electrolytes at ambient pressures and comparable temperatures without or with water present. Proton conductivity of the protic salts occurs providing two conditions exist: i) the energy difference is about 0.8 eV between the protic-salt state versus the state in which the acid and base are separated and 2) the chemical constituents rotate freely. The physical state of these proton-conducting salts can be liquid, plastic crystal as well as solid organic and inorganic polymer membranes and their mixtures. Many acids and bases can be used to make a protic salt which allows tailoring of proton conductivity, as well as other properties that affect their use as electrolytes in fuel cells, such as, stability, adsorption on catalysts, environmental impact, etc. During this project, highly proton conducting (~ 0.1S/cm) protic salts were made that are stable under fuel-cell operating conditions and that gave highly efficient fuel cells. The high efficiency is attributed to an improved oxygen electroreduction process on Pt which was found to be virtually reversible in a number of liquid protic salts with low water activity (< 1% water). Solid flexible non-porous composite membranes, made from inorganic polymer (e.g., 10%indium 90%tin pyrophosphate, ITP) and organic polymer (e.g., polyvinyl pyridinium phosphate, PVPP), were found that give conductivity and fuel cell performances similar to phosphoric acid electrolyte with no need for hydration at

  7. Compliant glass-polymer hybrid single ion-conducting electrolytes for lithium batteries.

    PubMed

    Villaluenga, Irune; Wujcik, Kevin H; Tong, Wei; Devaux, Didier; Wong, Dominica H C; DeSimone, Joseph M; Balsara, Nitash P

    2016-01-01

    Despite high ionic conductivities, current inorganic solid electrolytes cannot be used in lithium batteries because of a lack of compliance and adhesion to active particles in battery electrodes as they are discharged and charged. We have successfully developed a compliant, nonflammable, hybrid single ion-conducting electrolyte comprising inorganic sulfide glass particles covalently bonded to a perfluoropolyether polymer. The hybrid with 23 wt% perfluoropolyether exhibits low shear modulus relative to neat glass electrolytes, ionic conductivity of 10(-4) S/cm at room temperature, a cation transference number close to unity, and an electrochemical stability window up to 5 V relative to Li(+)/Li. X-ray absorption spectroscopy indicates that the hybrid electrolyte limits lithium polysulfide dissolution and is, thus, ideally suited for Li-S cells. Our work opens a previously unidentified route for developing compliant solid electrolytes that will address the challenges of lithium batteries.

  8. Ion conductivity and transport by porous coordination polymers and metal-organic frameworks.

    PubMed

    Horike, Satoshi; Umeyama, Daiki; Kitagawa, Susumu

    2013-11-19

    Ion conduction and transport in solids are both interesting and useful and are found in widely distinct materials, from those in battery-related technologies to those in biological systems. Scientists have approached the synthesis of ion-conductive compounds in a variety of ways, in the areas of organic and inorganic chemistry. Recently, based on their ion-conducting behavior, porous coordination polymers (PCPs) and metal-organic frameworks (MOFs) have been recognized for their easy design and the dynamic behavior of the ionic components in the structures. These PCP/MOFs consist of metal ions (or clusters) and organic ligands structured via coordination bonds. They could have highly concentrated mobile ions with dynamic behavior, and their characteristics have inspired the design of a new class of ion conductors and transporters. In this Account, we describe the state-of-the-art of studies of ion conductivity by PCP/MOFs and nonporous coordination polymers (CPs) and offer future perspectives. PCP/MOF structures tend to have high hydrophilicity and guest-accessible voids, and scientists have reported many water-mediated proton (H(+)) conductivities. Chemical modification of organic ligands can change the hydrated H(+) conductivity over a wide range. On the other hand, the designable structures also permit water-free (anhydrous) H(+) conductivity. The incorporation of protic guests such as imidazole and 1,2,4-triazole into the microchannels of PCP/MOFs promotes the dynamic motion of guest molecules, resulting in high H(+) conduction without water. Not only the host-guest systems, but the embedding of protic organic groups on CPs also results in inherent H(+) conductivity. We have observed high H(+) conductivities under anhydrous conditions and in the intermediate temperature region of organic and inorganic conductors. The keys to successful construction are highly mobile ionic species and appropriate intervals of ion-hopping sites in the structures. Lithium (Li

  9. Effect of interface on surface morphology and proton conduction of polymer electrolyte thin films.

    PubMed

    Ohira, Akihiro; Kuroda, Seiichi; Mohamed, Hamdy F M; Tavernier, Bruno

    2013-07-21

    To understand the relationship between surface morphology and proton conduction of polymer electrolyte thin films, perfluorinated ionomer Nafion® thin films were prepared on different substrates such as glassy carbon (GC), hydrophilic-GC (H-GC), and platinum (Pt) as models for the ionomer film within a catalyst layer. Atomic force microscopy coupled with an electrochemical (e-AFM) technique revealed that proton conduction decreased with film thickness; an abrupt decrease in proton conductance was observed when the film thickness was less than ca. 10 nm on GC substrates in addition to a significant change in surface morphology. Furthermore, thin films prepared on H-GC substrates with UV-ozone treatment exhibited higher proton conduction than those on untreated GC substrates. However, Pt substrates exhibited proton conduction comparable to that of GCs for films thicker than 20 nm; a decrease in proton conduction was observed at ∼5 nm thick film but was still much higher than for carbon substrates. These results indicate that the number of active proton-conductive pathways and/or the connectivity of the proton path network changed with film thickness. The surface morphology of thinner films was significantly affected by the film/substrate interface and was fundamentally different from that of the bulk thick membrane.

  10. Carbon Nanotube/Conductive Additive/Space Durable Polymer Nanocomposite Films for Electrostatic Charge Dissipation

    NASA Technical Reports Server (NTRS)

    Smith, Joseph G., Jr.; Watson, Kent A.; Delozier, Donavon M.; Connell, John W.

    2003-01-01

    Thin film membranes of space environmentally stable polymeric materials possessing low color/solar absorptivity (alpha) are of interest for potential applications on Gossamer spacecraft. In addition to these properties, sufficient electrical conductivity is required in order to dissipate electrostatic charge (ESC) build-up brought about by the charged orbital environment. One approach to achieve sufficient electrical conductivity for ESC mitigation is the incorporation of single wall carbon nanotubes (SWNTs). However, when the SWNTs are dispersed throughout the polymer matrix, the nanocomposite films tend to be significantly darker than the pristine material resulting in a higher alpha. The incorporation of conductive additives in combination with a decreased loading level of SWNTs is one approach for improving alpha while retaining conductivity. Taken individually, the low loading level of conductive additives and SWNTs is insufficient in achieving the percolation level necessary for electrical conductivity. When added simultaneously to the film, conductivity is achieved through a synergistic effect. The chemistry, physical, and mechanical properties of the nanocomposite films will be presented.

  11. Experimental and theoretical characterization of implantable neural microelectrodes modified with conducting polymer nanotubes

    PubMed Central

    Abidian, Mohammad Reza; Martin, David C.

    2009-01-01

    Neural prostheses transduce bioelectric signals to electronic signals at the interface between neural tissue and neural microelectrodes. A low impedance electrode-tissue interface is important for the quality of signal during recording as well as quantity of applied charge density during stimulation. However, neural microelectrode sites exhibit high impedance because of their small geometric surface area. Here we analyze nanostructured-conducting polymers that can be used to significantly decrease the impedance of microelectrode typically by about two orders of magnitude and increase the charge transfer capacity of microelectrodes by three orders of magnitude. In this study poly(pyrrole) (PPy) and poly(3, 4- ethylenedioxythiophene) (PEDOT) nanotubes were electrochemically polymerized on the surface of neural microelectrode sites (1250 μm2). An equivalent circuit model comprising a coating capacitance in parallel with a pore resistance and interface impedance in series was developed and fitted to experimental results to characterize the physical and electrical properties of the interface. To confirm that the fitting parameters correlate with physical quantities of interface, theoretical equations were used to calculate the parameter values thereby validating the proposed model. Finally, an apparent diffusion coefficient was calculated for PPy film (29.2 ± 1.1 cm2/s), PPy nanotubes (72.4 ± 3.3 cm2/s), PEDOT film (7.4 ± 2.1 cm2/s), and PEDOT nanotubes (13.0 ± 1.8 cm2/s). The apparent diffusion coefficient of conducting polymer nanotubes was larger than the corresponding conducting polymer films. PMID:18093644

  12. Effect of silver nanoparticles on the DC conductivity in chitosan-silver triflate polymer electrolyte

    NASA Astrophysics Data System (ADS)

    Aziz, Shujahadeen B.; Abidin, Z. H. Z.; Arof, A. K.

    2010-11-01

    A solid polymer electrolyte composed of chitosan and silver triflate (AgCF 3SO 3) has been prepared by the solution cast technique. The formation of polymer-salt complex has been confirmed by X-ray diffraction. The DC electrical conductivity of chitosan-silver triflate electrolyte has been investigated between 303 and 423 K, using electrochemical impedance spectroscopy over the frequency range from 50 Hz to 1000 kHz. The conductivity was found to increase with increase in AgCF 3SO 3 concentration at room temperature. The DC conductivity obeys Arrhenius relationship up to a particular temperature and decreases at higher temperatures due to decrease in silver ions as a result of the formation of silver nanoparticles. The presence of an additional semicircular arc in the Cole-Cole plot obtained above 328 K indicates the existence of grain boundaries, which can be attributed to the silver particles. The presence of silver particles also have been proven by XRD after heating at 333, 363, and 393 K where the (1 1 1) peak of Ag is observed to increase with temperature. The silver particles were shown to be of nanosize using transmission electron microscopy (TEM).

  13. Quantitative Conductive Atomic Force Microscopy on Single-Walled Carbon Nanotube-Based Polymer Composites.

    PubMed

    Bârsan, Oana A; Hoffmann, Günter G; van der Ven, Leendert G J; de With, Gijsbertus

    2016-08-01

    Conductive atomic force microscopy (C-AFM) is a valuable technique for correlating the electrical properties of a material with its topographic features and for identifying and characterizing conductive pathways in polymer composites. However, aspects such as compatibility between tip material and sample, contact force and area between the tip and the sample, tip degradation and environmental conditions render quantifying the results quite challenging. This study aims at finding the suitable conditions for C-AFM to generate reliable, reproducible, and quantitative current maps that can be used to calculate the resistance in each point of a single-walled carbon nanotube (SWCNT) network, nonimpregnated as well as impregnated with a polymer. The results obtained emphasize the technique's limitation at the macroscale as the resistance of these highly conductive samples cannot be distinguished from the tip-sample contact resistance. Quantitative C-AFM measurements on thin composite sections of 150-350 nm enable the separation of sample and tip-sample contact resistance, but also indicate that these sections are not representative for the overall SWCNT network. Nevertheless, the technique was successfully used to characterize the local electrical properties of the composite material, such as sample homogeneity and resistance range of individual SWCNT clusters, at the nano- and microscale. PMID:27404764

  14. Free-Standing Conducting Polymer Films for High-Performance Energy Devices.

    PubMed

    Li, Zaifang; Ma, Guoqiang; Ge, Ru; Qin, Fei; Dong, Xinyun; Meng, Wei; Liu, Tiefeng; Tong, Jinhui; Jiang, Fangyuan; Zhou, Yifeng; Li, Ke; Min, Xue; Huo, Kaifu; Zhou, Yinhua

    2016-01-18

    Thick, uniform, easily processed, highly conductive polymer films are desirable as electrodes for solar cells as well as polymer capacitors. Here, a novel scalable strategy is developed to prepare highly conductive thick poly(3,4-ethylenedioxythiophene):polystyrene sulfonate (HCT-PEDOT:PSS) films with layered structure that display a conductivity of 1400 S cm(-1) and a low sheet resistance of 0.59 ohm sq(-1). Organic solar cells with laminated HCT-PEDOT:PSS exhibit a performance comparable to the reference devices with vacuum-deposited Ag top electrodes. More importantly, the HCT-PEDOT:PSS film delivers a specific capacitance of 120 F g(-1) at a current density of 0.4 A g(-1). All-solid-state flexible symmetric supercapacitors with the HCT-PEDOT:PSS films display a high volumetric energy density of 6.80 mWh cm(-3) at a power density of 100 mW cm(-3) and 3.15 mWh cm(-3) at a very high power density of 16160 mW cm(-3) that outperforms previous reported solid-state supercapacitors based on PEDOT materials.

  15. Application of conductive polymers, scaffolds and electrical stimulation for nerve tissue engineering.

    PubMed

    Ghasemi-Mobarakeh, Laleh; Prabhakaran, Molamma P; Morshed, Mohammad; Nasr-Esfahani, Mohammad Hossein; Baharvand, Hossein; Kiani, Sahar; Al-Deyab, Salem S; Ramakrishna, Seeram

    2011-04-01

    Among the numerous attempts to integrate tissue engineering concepts into strategies to repair nearly all parts of the body, neuronal repair stands out. This is partially due to the complexity of the nervous anatomical system, its functioning and the inefficiency of conventional repair approaches, which are based on single components of either biomaterials or cells alone. Electrical stimulation has been shown to enhance the nerve regeneration process and this consequently makes the use of electrically conductive polymers very attractive for the construction of scaffolds for nerve tissue engineering. In this review, by taking into consideration the electrical properties of nerve cells and the effect of electrical stimulation on nerve cells, we discuss the most commonly utilized conductive polymers, polypyrrole (PPy) and polyaniline (PANI), along with their design and modifications, thus making them suitable scaffolds for nerve tissue engineering. Other electrospun, composite, conductive scaffolds, such as PANI/gelatin and PPy/poly(ε-caprolactone), with or without electrical stimulation, are also discussed. Different procedures of electrical stimulation which have been used in tissue engineering, with examples on their specific applications in tissue engineering, are also discussed.

  16. Mesoscale Origin of the Enhanced Cycling-Stability of the Si-Conductive Polymer Anode for Li-ion Batteries

    PubMed Central

    Gu, Meng; Xiao, Xing-Cheng; Liu, Gao; Thevuthasan, Suntharampillai; Baer, Donald R.; Zhang, Ji-Guang; Liu, Jun; Browning, Nigel D.; Wang, Chong-Min

    2014-01-01

    Electrode used in lithium-ion battery is invariably a composite of multifunctional components. The performance of the electrode is controlled by the interactive function of all components at mesoscale. Fundamental understanding of mesoscale phenomenon sets the basis for innovative designing of new materials. Here we report the achievement and origin of a significant performance enhancement of electrode for lithium ion batteries based on Si nanoparticles wrapped with conductive polymer. This new material is in marked contrast with conventional material, which exhibit fast capacity fade. In-situ TEM unveils that the enhanced cycling stability of the conductive polymer-Si composite is associated with mesoscale concordant function of Si nanoparticles and the conductive polymer. Reversible accommodation of the volume changes of Si by the conductive polymer allows good electrical contact between all the particles during the cycling process. In contrast, the failure of the conventional Si-electrode is probed to be the inadequate electrical contact. PMID:24418812

  17. 2D coherent charge transport in highly ordered conducting polymers doped by solid state diffusion

    NASA Astrophysics Data System (ADS)

    Kang, Keehoon; Watanabe, Shun; Broch, Katharina; Sepe, Alessandro; Brown, Adam; Nasrallah, Iyad; Nikolka, Mark; Fei, Zhuping; Heeney, Martin; Matsumoto, Daisuke; Marumoto, Kazuhiro; Tanaka, Hisaaki; Kuroda, Shin-Ichi; Sirringhaus, Henning

    2016-08-01

    Doping is one of the most important methods to control charge carrier concentration in semiconductors. Ideally, the introduction of dopants should not perturb the ordered microstructure of the semiconducting host. In some systems, such as modulation-doped inorganic semiconductors or molecular charge transfer crystals, this can be achieved by spatially separating the dopants from the charge transport pathways. However, in conducting polymers, dopants tend to be randomly distributed within the conjugated polymer, and as a result the transport properties are strongly affected by the resulting structural and electronic disorder. Here, we show that in the highly ordered lamellar microstructure of a regioregular thiophene-based conjugated polymer, a small-molecule p-type dopant can be incorporated by solid state diffusion into the layers of solubilizing side chains without disrupting the conjugated layers. In contrast to more disordered systems, this allows us to observe coherent, free-electron-like charge transport properties, including a nearly ideal Hall effect in a wide temperature range, a positive magnetoconductance due to weak localization and the Pauli paramagnetic spin susceptibility.

  18. Superhydrophobic SAM Modified Electrodes for Enhanced Current Limiting Properties in Intrinsic Conducting Polymer Surge Protection Devices.

    PubMed

    Jabarullah, Noor H; Verrelli, Emanuele; Mauldin, Clayton; Navarro, Luis A; Golden, Josh H; Madianos, Leonidas M; Kemp, Neil T

    2015-06-01

    Surface interface engineering using superhydrophobic gold electrodes made with 1-dodecanethiol self-assembled monolayer (SAM) has been used to enhance the current limiting properties of novel surge protection devices based on the intrinsic conducting polymer, polyaniline doped with methanesulfonic acid. The resulting devices show significantly enhanced current limiting characteristics, including current saturation, foldback, and negative differential effects. We show how SAM modification changes the morphology of the polymer film directly adjacent to the electrodes, leading to the formation of an interfacial compact thin film that lowers the contact resistance at the Au-polymer interface. We attribute the enhanced current limiting properties of the devices to a combination of lower contact resistance and increased Joule heating within this interface region which during a current surge produces a current blocking resistive barrier due to a thermally induced dedoping effect caused by the rapid diffusion of moisture away from this region. The effect is exacerbated at higher applied voltages as the higher temperature leads to stronger depletion of charge carriers in this region, resulting in a negative differential resistance effect. PMID:25996202

  19. Superhydrophobic SAM Modified Electrodes for Enhanced Current Limiting Properties in Intrinsic Conducting Polymer Surge Protection Devices.

    PubMed

    Jabarullah, Noor H; Verrelli, Emanuele; Mauldin, Clayton; Navarro, Luis A; Golden, Josh H; Madianos, Leonidas M; Kemp, Neil T

    2015-06-01

    Surface interface engineering using superhydrophobic gold electrodes made with 1-dodecanethiol self-assembled monolayer (SAM) has been used to enhance the current limiting properties of novel surge protection devices based on the intrinsic conducting polymer, polyaniline doped with methanesulfonic acid. The resulting devices show significantly enhanced current limiting characteristics, including current saturation, foldback, and negative differential effects. We show how SAM modification changes the morphology of the polymer film directly adjacent to the electrodes, leading to the formation of an interfacial compact thin film that lowers the contact resistance at the Au-polymer interface. We attribute the enhanced current limiting properties of the devices to a combination of lower contact resistance and increased Joule heating within this interface region which during a current surge produces a current blocking resistive barrier due to a thermally induced dedoping effect caused by the rapid diffusion of moisture away from this region. The effect is exacerbated at higher applied voltages as the higher temperature leads to stronger depletion of charge carriers in this region, resulting in a negative differential resistance effect.

  20. Electrical Conductivity Studies on Individual Conjugated Polymer Nanowires: Two-Probe and Four-Probe Results

    PubMed Central

    2010-01-01

    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