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Flexible paper electrodes for supercapacitors were prepared with partially-exfoliated graphite and polypyrrole as the active materials. Graphite was coated on paper with pencil drawing and then electrochemically exfoliated using the cyclic voltammetry (CV) technique to obtain the exfoliated graphite (EG)-coated paper (EG-paper). Polypyrrole (PPy) doped with β-naphthalene sulfonate anions was deposited on EG-paper through in-situ polymerization, leading to the formation of PPy-EG-paper. The as-prepared PPy-EG-paper showed a high electrical conductivity of 10.0 S·cm-1 and could be directly used as supercapacitor electrodes. The PPy-EG-paper electrodes gave a remarkably larger specific capacitance of 2148 F·g-1 at a current density of 0.8 mA.cm-2, compared to PPy-graphite-paper (848 F·g-1). The capacitance value of PPy-EG-paper could be preserved by 80.4% after 1000 charge/discharge cycles. In addition, the PPy-EG-paper electrodes demonstrated a good rate capability and a high energy density of 110.3 Wh·kg-1 at a power density of 121.9W·kg-1. This work will pave the way for the discovery of efficient paper-based electrode materials. [ABSTRACT FROM AUTHOR]

Paper with color changes caused by applied electric voltages was fabricated by combining the electric heating feature of conductive polypyrrole (PPy) and the temperature response color-changing feature of thermochromic ink. Highly conductive PPy was deposited selectively on the graphite-coated side of the paper via electrochemical polymerization. Thermochromic ink was coated on the reverse side with white color. The conductive coatings were tightly covered on the paper due to the hydrogen bonding between the pyrrole rings and the hydroxyl groups of cellulose. The obtained paper could be heated to about 45 °C and change its color significantly under an applied voltage of 4 V. [ABSTRACT FROM AUTHOR]

Flexible poly(3,4-ethylenedioxythiophene):poly(styrenesulfonate)/polypyrrole/paper (PEDOT:PSS/PPy/paper) thermoelectric (TE) nanocomposite films were prepared by a two-step method: first, PPy/paper nanocomposite films were prepared by an in situ chemical polymerization process, and second, PEDOT:PSS/PPy/paper TE composite films were fabricated by coating the as-prepared PPy/paper nanocomposite films using a dimethyl sulfoxide-doped PEDOT:PSS solution. Both the electrical conductivity and the Seebeck coefficient of the PEDOT:PSS/PPy/paper TE nanocomposite films were greatly enhanced from 0.06 S/cm to ~0.365 S/cm, and from 5.44 μV/K to ~16.0 μV/K at ~300 K, respectively, when compared to the PPy/paper TE nanocomposite films. The thermal conductivity of the PEDOT:PSS/PPy/paper composite film (0.1522 Wm-1K-1 at ~300 K) was, however, only slightly higher than that of the PPy/paper composite film (0.1142 Wm-1K-1 at ~300 K). As a result, the ZT value of the PEDOT:PSS/PPy/paper composite film (~1.85 × 10-5 at ~300 K) was significantly enhanced when compared to that of the PPy/paper composite film (~4.73 × 10-7 at ~300 K). The as-prepared nanocomposite films have great potential for application in flexible TE devices. [ABSTRACT FROM AUTHOR]

Wood and cellulose derivatives, in both fibrous and water-soluble macromolecular form, are emerging as outstanding candidates for organic electronics applications due to their large-scale availability, low cost, and easy processability. Paper and wood fibre-based derivatives are considered to be materials of choice as supports for communication world-wide. The interest in producing inexpensive and universally available conducting polymer/cellulose fibres substrates resides in the possibility of creating new materials that can be used for a broad range of advanced applications. For instance, PPy/cellulose fibres composites can be used for the preparation of energy storage devices thanks to the conjugation of the high specific area of cellulose fibres and the electrochemical properties of PPy. Other possible applications of such composites are in the area of the antistatic materials, sensors, electromagnetic interference shielding materials, smart packaging, and tissues. Concerning the woody polymers, some of them (i.e. cellulose derivatives) also exhibit biocompatibility, as well as film-forming properties and transparency. In combination with the electrical properties of PPy, these features make PPy/macromolecular cellulose composites suitable for applications as displays, lighting, and photovoltaics. Due to their chemical structure, macromolecular wood derivatives have been proposed with success as enhancing conductivity additives in Py polymerisation. The aim of the present review is to provide an overview of PPy chemistry and of the most relevant advances attained in the production of PPy/wood derived materials conducting composites.

Flexible paper electrodes for supercapacitors were prepared with partially-exfoliated graphite and polypyrrole as the active materials. Graphite was coated on paper with pencil drawing and then electrochemically exfoliated using the cyclic voltammetry (CV) technique to obtain the exfoliated graphite (EG)-coated paper (EG-paper). Polypyrrole (PPy) doped with β-naphthalene sulfonate anions was deposited on EG-paper through in-situ polymerization, leading to the formation of PPy-EG-paper. The as-prepared PPy-EG-paper showed a high electrical conductivity of 10.0 S·cm−1 and could be directly used as supercapacitor electrodes. The PPy-EG-paper electrodes gave a remarkably larger specific capacitance of 2148 F∙g−1 at a current density of 0.8 mA∙cm−2, compared to PPy-graphite-paper (848 F∙g−1). The capacitance value of PPy-EG-paper could be preserved by 80.4% after 1000 charge/discharge cycles. In addition, the PPy-EG-paper electrodes demonstrated a good rate capability and a high energy density of 110.3 Wh∙kg−1 at a power density of 121.9 W∙kg−1. This work will pave the way for the discovery of efficient paper-based electrode materials.

A solid-state powerful supercapacitor (SC) is fabricated with a substrate of Xerox paper. Its current collector based on a foldable electronic circuit is developed by simply pencil drawing. Thin graphite sheets on paper provide effective channels for electron transmission with a low resistance of 95 Ω sq. The conductive organic material of polypyrrole coated on thin graphite sheets acts as the electrode material of the device. The as-fabricated SC exhibits a high specific capacitance of 52.9 F cm at a scan rate of 1 mV s. An energy storage unit fabricated by three full-charged series SCs can drive a commercial light-emitting diode robustly. This work demonstrated a simple, versatile and cost-effective method for paper-based devices. [ABSTRACT FROM AUTHOR]

Conducting polymers have been considered for use as cathode materials in rechargeable lithium-ion batteries (LIBs) since 1981 but problems with poor cycling stability, rapid self-discharge, and low energy and power densities have so far limited their applicability. Herein it is shown that nanostructured freestanding conducting polymer composites [e.g., polypyrrole (PPy) and polyaniline (PANI)] can be used to circumvent these shortcomings. Freestanding and binder-free PPy and cellulose-based composites can straightforwardly be used as versatile organic cathode materials for LIBs. The composite, reinforced with chopped carbon filaments (CCFs), exhibited a large active mass loading of approximately 10 mg cm−2, an areal capacity of 1.0 mAh cm−2 (corresponding to 102 mAh g−1), and stable cycling. With an active mass loading of 4.4 mg cm−2, a capacity of 0.22 mAh cm−2 (corresponding to 58 mAh g−1) was found for current densities of 5 A g−1 yielding discharge times of approximately 40 seconds, and a capacity retention of 91 % over 100 cycles was obtained at 0.2 A g−1. The present method constitutes a straightforward approach for the manufacturing of high-performance freestanding electroactive conducting-polymer-based paper-like electrodes for use in inexpensive and sustainable, high-performance organic LIBs. [ABSTRACT FROM AUTHOR]

Wood and cellulose derivatives, in both fibrous and water-soluble macromolecular form, are emerging as outstanding candidates for organic electronics applications due to their large-scale availability, low cost, and easy processability. Paper and wood fibre-based derivatives are considered to be materials of choice as supports for communication world-wide. The interest in producing inexpensive and universally available conducting polymer/cellulose fibres substrates resides in the possibility of creating new materials that can be used for a broad range of advanced applications. For instance, PPy/cellulose fibres composites can be used for the preparation of energy storage devices thanks to the conjugation of the high specific area of cellulose fibres and the electrochemical properties of PPy. Other possible applications of such composites are in the area of the antistatic materials, sensors, electromagnetic interference shielding materials, smart packaging, and tissues. Concerning the woody polymers, some of them (i.e. cellulose derivatives) also exhibit biocompatibility, as well as film-forming properties and transparency. In combination with the electrical properties of PPy, these features make PPy/macromolecular cellulose composites suitable for applications as displays, lighting, and photovoltaics. Due to their chemical structure, macromolecular wood derivatives have been proposed with success as enhancing conductivity additives in Py polymerisation. The aim of the present review is to provide an overview of PPy chemistry and of the most relevant advances attained in the production of PPy/wood derived materials conducting composites. [ABSTRACT FROM AUTHOR]

Abstract: Conducting polymer–fibre composites with polypyrrole cellulose (paper) and protein (wool) fibres have been produced by polymerizing pyrrole with ferric chloride as the oxidant around separated individual cellulose (wood) fibres from bleached Pinus radiata Kraft pulp, and merino wool fibres respectively to generate new composite materials that retain the inherent properties of the polymer and individual fibres. For the polypyrrole–cellulose composite, the polypyrrole consisted of spheres of about 100nm in size fused together to form a continuous coating that fully encapsulates the cellulose fibre and associated finer fibrils. For the polypyrrole–wool composite the polypyrrole formed a similar coating of about 200nm spheres. Electrical conductivities of the composites were substantially increased over those of the precursor fibres. [Copyright &y& Elsevier]

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Abstract: Conducting polymers have generated a great deal of interest because of their physical and chemical properties as well as their potential in industrially useful materials. However, one of the shortcomings of most conducting polymers is that they are often formed as intractable films that are difficult to process [1]. To overcome this problem we have incorporated various conducting polymers into sheets of paper in order to create new composite materials which combine the universal properties of a paper sheet or paper products with the chemical and electrically conducting properties of the conducting polymer. Various composite paper – conducting polymer products have been prepared by polymerizing polypyrrole and polyaniline directly onto the paper sheet using ferric chloride as the oxidant. Electronmicroscopy shows that the polymers comprise spheres of about 50–150 nanometers in size fused together such that they fully encapsulate the individual cellulose fibres in the paper sheet. The open matrix of fibres characteristic of the original paper sheet is maintained and hence provides a much greater specific surface area for the conducting polymer than that of a continuous flat sheet which would be the case if the polymer simply formed a laminar coating on the paper surface. In the case of polyaniline, it was also possible to form a different morphology of the polymer comprising a mix of nano-size spheres, rods and plates using ammonium persulfate as the oxidant. Conductivities of up to 6 Scm−1 have been measured for paper-polypyrrole composites and up to 2x10−3 Scm−1 for paper-polyaniline composites. [Copyright &y& Elsevier]

Here, we prepared planar polypyrrole (PPy) coated paper-based supercapacitors by applying simple laser carving assisted method. The planar structure of the device showed a significant performance improvement (13.9 mF/cm2) compared to the sandwiched structure device (12.3 mF/cm2). In addition, by adjusting the polymerization time of pyrrole, the device capacity can be further increased to 87.4 mF/cm2. We firmly believed that the laser carving assisted method has a significant role in promoting the development of flexible planar electronic devices. • Planar PPy coated paper-based supercapacitors were obtained by laser carving. • The planar device showed a significant performance improvement. • The optimal device capacity can be further increased to 87.4 mF/cm2. Paper-based supercapacitors have attracted more and more attention for high electrochemical performance. However, most of them adopt sandwiched structure. Here, we prepared planar polypyrrole (PPy) coated paper-based supercapacitors by applying simple laser carving assisted method. The planar device showed a significant performance improvement (13.9 mF/cm2) compared to the sandwiched device (12.3 mF/cm2). In addition, by adjusting the polymerization time of pyrrole, the device capacity can be further increased to 87.4 mF/cm2. We firmly believed that the laser carving assisted method has a significant role in promoting the development of flexible planar electronic devices. [ABSTRACT FROM AUTHOR]