Successful tissue engineering strategies in the nervous system must be carefully crafted to interact favorably with the complex biochemical signals of the native environment. To date, all chronic implants incorporating electrical conductivity degrade in performance over time as the foreign body reaction and subsequent fibrous encapsulation isolate them from the host tissue. Our goal is to develop a peptide-based interfacial biomaterial that will non-covalently coat the surface of the conducting polymer polypyrrole, allowing the implant to interact with the nervous system through both electrical and chemical cues. Starting with a candidate peptide sequence discovered through phage display, we used computational simulations of the peptide on polypyrrole to describe the bound peptide structure, explore the mechanism of binding, and suggest new, better binding peptide sequences. After experimentally characterizing the polymer, we created a molecular mechanics model of polypyrrole using quantum mechanics calculations and compared its in silico properties to experimental observables such as density and chain packing. Using replica exchange molecular dynamics, we then modeled the behavior of affinity binding peptides on the surface of polypyrrole in explicit water and saline environments. Relative measurements of the contributions of each amino acid were made using distance measurements and computational alanine scanning. / text

Conductive polymers are promising pseudo capacitive materials as they feature both good conductivity and high capacitance. Formation of composite between conductive polymers and carbon nanotubes is a proven technique in enhancing the material electroactivity. In-situ polymerization of conductive polymers includes polyaniline, polypyrrole and PEDOT: PSS and composite with MWCNT has been successfully achieved. Composites fabricated by using different dopants and their performance were studied. Excellent achieved capacitive performance is due to the combination of pseudo capacitance and double layer capacitance. The MWCNTs content has significant influence on the morphology and structure of the polymerized ECP in the composite. And therefore affects the material conductivity and the charge storage performance. Two electrodes cell performance shows that Ppy/MWCNT composite shows a more promising performance as electrode materials for EC applications in contrast to PANI/MWCNT and PEDOT: PSS/MWCNT composites.

Conductive polymers are promising pseudo capacitive materials as they feature both good conductivity and high capacitance. Formation of composite between conductive polymers and carbon nanotubes is a proven technique in enhancing the material electroactivity. In-situ polymerization of conductive polymers includes polyaniline, polypyrrole and PEDOT: PSS and composite with MWCNT has been successfully achieved. Composites fabricated by using different dopants and their performance were studied. Excellent achieved capacitive performance is due to the combination of pseudo capacitance and double layer capacitance. The MWCNTs content has significant influence on the morphology and structure of the polymerized ECP in the composite. And therefore affects the material conductivity and the charge storage performance. Two electrodes cell performance shows that Ppy/MWCNT composite shows a more promising performance as electrode materials for EC applications in contrast to PANI/MWCNT and PEDOT: PSS/MWCNT composites.

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 electroactive actuation response inherent to conductive polymer trilayer actuators. The main contribution of this investigation was the proposal and development of a new hybrid model that unifies concepts from charge transport and electrochemomechanical models. The output of the proposed model was compared with published data and shown to be accurate to within 10%. Finally, Chapter 6 demonstrated the application of these materials for use as precision mirror positioners in adaptive optical systems.

The mounting concern for renewable energies from ecologically conscious alternatives is growing in parallel with the demand for portable energy storage devices, fuelling research in the fields of electrochemical energy storage technologies. The supercapacitor, also known as electrochemical capacitor, is an energy storage device possessing a near infinite life-cycle and high power density recognized to store energy in an electrostatic double-layer, or through a pseudocapacitance mechanism as a result of an applied potential. The power density of supercapacitors far exceeds that of batteries with an ability to charge and discharge stored energy within seconds. Supercapacitors compliment this characteristic very well with a cycle life in excess of 106 cycles of deep discharge within a wide operational temperature range, and generally require no further maintenance upon integration. Conscientious of environmental standards, these devices are also recyclable. Electrochemical capacitors are currently a promising candidate to assist in addressing energy storage concerns, particularly in hybridized energy storage systems where batteries and supercapacitors compliment each other’s strengths; however specific challenges must be addressed to realize their potential. In order to further build upon the range of supercapacitors for future market applications, advancements made in nanomaterial research and design are expected to continue the materials development trend with a goal to improve the energy density through the development of a cost-efficient and correspondingly plentiful material. However, it is important to note that the characteristic power performance and exceptional life-cycle should be preserved alongside these efforts to maintain their niche as a power device, and not simply develop an alternative to the average battery. It is with this clear objective that this thesis presents research on an emerging carbon material derived from an abundant precursor, where the investigations focus on its potential to achieve high energy and power density, stability and integration with other electroactive materials. Activated carbons have been the dominant carbon material used in electric double-layer capacitors since their inception in the early 1970s. Despite a wide range of carbon precursors and activation methods available for the generation of high surface area carbons, difficulties remain in controlling the pore size distribution, pore shape and an interconnected pore structure to achieve a high energy density. These factors have restricted the market growth for supercapacitors in terms of the price per unit of energy storage. Activation procedures and subsequent processes for these materials can also be energy intensive (i.e. high temperatures) or environmentally unfriendly, thus the challenge remains in fabricating an inexpensive high surface-area electroactive material with favourable physical properties from a source available in abundance. Double-layer capacitive materials researched to replace active carbons generally require properties that include: high, accessible surface-area; good electrical conductivity; a pore size distribution that includes mesopore and micropore; structural stability; and possibly functional groups that lend to energy storage through pseudocapacitive mechanisms. Templated, fibrous and aerogel carbons offer an alternative to activated carbons; however the drawbacks to these materials can include difficult preparation procedures or deficient physical properties with respect to those listed above. In recent years nanostructured carbon materials possessing favourable properties have also contributed to the field. Graphene nanoplatelet (GNP) and carbon nanotube (CNT) are nanostructured materials that are being progressively explored for suitable development as supercapacitor electrodes. As carbon lattice structured materials either in the form of a 2-dimensional sheet or rolled into a cylinder both of these materials possess unique properties desirable in for electrode development. In the proceeding report, GNPs are investigated as a primary material for the synthesis of electrodes in both a pure and composite form. Three projects are presented herein that emphasize the suitability of GNP as a singular carbon electrode material as well as a structural substrate for additional electroactive materials. Investigation in these projects focuses on the electrochemical activity of the materials for supercapacitor devices, and elucidation of the physical factors which contribute towards the observed capacitance. An initial study of the GNPs investigates their distinct capacitive ability as an electric double-layer material for thin-film applications. The high electrically conductivity and sheet-like structure of GNPs supported the fabrication of flexible and transparent films with a thickness ranging from 25 to 100 nm. The thinnest film fabricated (25 nm) yielded a high specific capacitance from preliminary evaluation with a notable high energy and power density. Furthermore, fast charging capabilities were observed from the GNP thin film electrodes. The second study examines the use of CNT entanglements dispersed between GNP to increase the active surface area and reduce contact resistances with thin-film electrodes. Through the use MWNT/GNP and SWNT/GNP composites it was determined that tube aspect ratio influences the resulting capacitive performance, with the formation of micropores in SWNT/GNP yielding favourable results as a composite EDLC. The third study utilizes electrically conducting polypyrrole (PPy) deposited onto a GNP film through pulse electrodeposition for use as a supercapacitor electrode. Total pulse deposition times were evaluated in terms of their corresponding improvements to the specific capacitance, where an optimal deposition time was discovered. A significant increase to the total specific capacitance was observed through the integration PPy, with the majority charge storage being developed via psuedocapacitive redox mechanisms. A summary of the studies presented here centers on the development of GNP electrodes for application in high power supercapacitor devices. The potential use for GNP in both pure and composite electrode films is explored for electrochemical activity and capacitive capabilities, with corresponding physical characterization techniques performed to examine influential factors which contribute to the final results. The work emphasizes the suitability of GNP material for future investigations into their application as carbon or carbon composite electrodes in supercapacitor devices.

Living polytetrahydrofuran (PTHF) was terminated with sodium thiophenemethonate to yield a polymer with thiophene groups at one (PTHF1) and both ends (PTHF2). Copolymerizations of PTHF1 and PTHF2 insulating polymers with pyrrole and thiophene were achieved in water-p-toluene sulfonic acid (PTSA) and acetonitrile (AN)-tetrabutylammonium tetrafluoroborate (TBAFB) solvent-electrolyte couples via constant potential electrolysis. Characterization of the samples were performed by Nuclear Magnetic Resonance Spectroscopy (NMR), cyclic voltammetry (CV), Fourier Transform Infrared Spectroscopy (FT-IR), Thermal Analyses (TGA), (DSC) and Scanning Electron Microscopy (SEM). Electrical conductivities were measured by four-probe technique. PTHF1/PTh and PTHF2/PTh films which were deposited on ITO-glass in dichloromethane-TBAFB solvent-electrolyte couple found out to be anodically coloring copolymers that electrochemically switch between an oxidized blue and reduced red state exhibiting electrochromic behavior. Spectroelectrochemical Analysis (SEC) was run in UV-VIS region to reach a better understanding of the band structures of PTHF1/PTh and PTHF2/PTh electrochromic copolymers. Optoelectrochemical analyses were introduced as a new method for the characterization of copolymers.

Thèse (M.Sc.)--Université Laval, 2008. / Bibliogr.: f. [82]-94. Publié aussi en version électronique dans la Collection Mémoires et thèses électroniques.

Techn. University, Diss., 2005--Dresden.

Techn. University, Diss., 2005--Dresden.

Techn. University, Diss., 2005--Dresden.