Peter C. Innis

High-Performance Multifunctional Graphene Yarns: Toward Wearable All-Carbon Energy Storage Textiles

The successful commercialization of smart wearable garments is hindered by the lack of fully integrated carbon-based energy storage devices into smart wearables. Since electrodes are the active components that determine the performance of energy storage systems, it is important to rationally design and engineer hierarchical architectures atboth the nano- and macroscale that can enjoy all of the necessary requirements for a perfect electrode. Here we demonstrate a large-scale flexible fabrication of highly porous high-performance multifunctional graphene oxide (GO) and rGO fibers and yarns by taking advantage of the intrinsic soft self-assembly behavior of ultralarge graphene oxide liquid crystalline dispersions. The produced yarns, which are the only practical form of these architectures for real-life device applications, were found to be mechanically robust (Youngs modulus in excess of 29 GPa) and exhibited high native electrical conductivity (2508 ± 632 S m(-1)) and exceptionally high specific surface area (2605 m(2) g(-1) before reduction and 2210 m(2) g(-1) after reduction). Furthermore, the highly porous nature of these architectures enabled us to translate the superior electrochemical properties of individual graphene sheets into practical everyday use devices with complex geometrical architectures. The as-prepared final architectures exhibited an open network structure with a continuous ion transport network, resulting in unrivaled charge storage capacity (409 F g(-1) at 1 A g(-1)) and rate capability (56 F g(-1) at 100 A g(-1)) while maintaining their strong flexible nature.

Fibronectin and bovine serum albumin adsorption and conformational dynamics on inherently conducting polymers: A QCM-D study

Quartz crystal microbalance with dissipation monitoring (QCM-D) was employed to characterize the adsorption of the model proteins, bovine serum albumin (BSA) and fibronectin (FN), to polypyrrole doped with dextran sulfate (PPy-DS) as a function of DS loading and surface roughness. BSA adsorption was greater on surfaces of increased roughness and was above what could be explained by the increase in surface area alone. Furthermore, the additional mass adsorbed on the rough films was concomitant with an increase in the rigidity of the protein layer. Analysis of the dynamic viscoelastic properties of the protein adlayer reveal BSA adsorption on the rough films occurs in two phases: (1) arrival and initial adsorption of protein to the polymer surface and (2) postadsorption molecular rearrangement to a more dehydrated and compact conformation that facilitates further recruitment of protein to the polymer interface, likely forming a multilayer. In contrast, FN adsorption was independent of surface roughness. However, films prepared from solutions containing the highest concentration of DS (20 mg/mL) demonstrated both an increase in adsorbed mass and adlayer viscoelasticity. This is attributed to the higher DS loading in the conducting polymer film resulting in presentation of a more hydrated molecular structure indicative of a more unfolded and bioactive conformation. Modulating the redox state of the PPy-DS polymers was shown to modify both the adsorbed mass and viscoelastic nature of FN adlayers. An oxidizing potential increased both the total adsorbed mass and the adlayer viscoelasticity. Our findings demonstrate that modification of polymer physicochemical and redox condition alters the nature of protein-polymer interaction, a process that may be exploited to tailor the bioactivity of protein through which interactions with cells and tissues may be controlled.

Graphene oxide dispersions: tuning rheology to enable fabrication

Here, we show that graphene oxide (GO) dispersions exhibit unique viscoelastic properties, making them a new class of soft materials. The fundamental insights accrued here provide the basis for the development of fabrication protocols for these two-dimensional soft materials, in a diverse array of processing techniques.

TITAN: a conducting polymer based microfluidic pump

The electromechanical actuation properties of polypyrrole have been utilized in the design and development of a low voltage fluid movement system for microfluidic channels. A confined concentric arrangement of polypyrrole actuators is used to induce fluid movement through an inner channel in a single unit. Series connection of these units and appropriate electrical connection/stimulation induces a novel peristaltic action that enables fluids to be pumped in a predetermined direction. Flow rates of up to 2.5 µl min−1 can be achieved against a back pressure of 50 mbar, which is sufficient to enable fluid movement in a glass capillary channel (diameter: 266 µm, length: 12.8 cm). The mechanism of fluid movement enables the use of low voltage devices (1 V) to drive fluid with an average power requirement of 8.7 mW.

Inherently conducting polymer nanostructures.

Inherently conducting polymers (ICPs) have been an area of intense interest over the past 30 years, culminating with the award of the 2000 Nobel Prize in Chemistry to MacDiarmid, Heeger and Shirakawa. More recently the unique properties of these materials (e.g., higher conductivity, more rapid discrete electrochemical switching processes) apparent at the nanodimension have become accessible. Significant breakthroughs in synthesis and fabrication of inherently conducting polymers with nanodimensional control have made this possible. This review aims to discuss some of the synthetic approaches researchers have made in an attempt to probe the nano domain as well as some of the property enhancements afforded to these structures.

Knitted Strain Sensor Textiles of Highly Conductive All-Polymeric Fibers

A scaled-up fiber wet-spinning production of electrically conductive and highly stretchable PU/PEDOT:PSS fibers is demonstrated for the first time. The PU/PEDOT:PSS fibers possess the mechanical properties appropriate for knitting various textile structures. The knitted textiles exhibit strain sensing properties that were dependent upon the number of PU/PEDOT:PSS fibers used in knitting. The knitted textiles show sensitivity (as measured by the gauge factor) that increases with the number of PU/PEDOT:PSS fibers deployed. A highly stable sensor response was observed when four PU/PEDOT:PSS fibers were co-knitted with a commercial Spandex yarn. The knitted textile sensor can distinguish different magnitudes of applied strain with cyclically repeatable sensor responses at applied strains of up to 160%. When used in conjunction with a commercial wireless transmitter, the knitted textile responded well to the magnitude of bending deformations, demonstrating potential for remote strain sensing applications. The feasibility of an all-polymeric knitted textile wearable strain sensor was demonstrated in a knee sleeve prototype with application in personal training and rehabilitation following injury.

Putting function into fashion: Organic conducting polymer fibres and textiles

Textiles have traditionally been employed over the centuries with great utility in areas as diverse as fashion through to technical textiles. In all these instances the textile itself has been a structural element that once fabricated has limited utility beyond the intended structural and aesthetic application. In recent years there has been a shift towards the incorporation of electronic systems into textile structures. The new paradigm for textiles is the development of systems that not only provide the more traditional aspects of textiles but expands upon this to provide a unique capability to transmit and store information and energy. More importantly these next generation materials will be capable of responding to external stimuli, modifying features of the textile in a direct response to its working environment. A potential route to truly functional electronic textiles is through the application of conducting polymers.

Conducting polymer electrochemistry in ionic liquids

Applications of polymers like polypyrrole and polythiophene often require interaction with an electrolyte consisting of solvent and dissolved salt. Ionic Liquids (ILs) are pure salts, fluid at room temperature, that form charged electrolytes. Pure l-Bu-3-Me-Imidazolium PF 6 (BMI PF 6 ). a hydrophobic IL that has a wide potential window, was used to investigate the electrochemistry of polypyrrole. Enhanced electrochemical stability of polypyrrole was obtained on repetitive redox cycling with respect to the equivalent propylene carbonate electrolyte with tetrabutylammonium hexaflurophosphate (TBA PF 6 ) electrolyte.

Wholly printed polypyrrole nanoparticle-based biosensors on flexible substrate

Printing has been widely used in the sensor industry for its speed, low cost and production scalability. In this work we present a wholly-printed polypyrrole (PPy) based biosensor produced by inkjet printing bioinks composed of dispersions of PPy nanoparticles and enzymes onto screen-printed carbon electrodes. Two enzymes, horseradish peroxidase (HRP) or glucose oxidase (GoD) were incorporated into the PPy nanoparticle dispersions to impart biosensing functionality and selectivity into the conducting polymer ink. Further functionality was also introduced by deposition of a permselective ethyl cellulose (EC) membrane using inkjet printing. Cyclic voltammetry (CV) and chrono-amperometry were used to characterize the response of the PPy biosensors to H2O2 and glucose. Results demonstrated the possibility of PPy based biosensor fabrication using the rapid and low cost technique of inkjet printing. The detection range of H2O2 was found to be 10 μM-10 mM and for glucose was 1-5 mM.

EPR characterisation of platinum nanoparticle functionalised CNT hybrid materials

The use of nanostructured carbon materials as electrodes for energy storage and conversion is an expanding area of research in recent years. Herein, platinum nanoparticles have been deposited onto both multi-walled and single-walled carbon nanotubes (CNTs) via a microwave assisted polyol reduction method. This interaction has been probed with electron paramagnetic resonance (EPR) and Raman spectroscopies to elucidate the charge/electron transfer interactions between the Pt nanoparticles and the CNTs. Observed shifts in the g factors of the CNTs are indicative of such an electronic interaction, strongly suggesting the covalent attachment of the nanoparticles to the carboxylic groups on the CNTs, formed during the microwave-assisted reduction process. The Pt decorated CNTs show a dramatic increase in electrochemical behaviour in terms of high reversible capacity and relatively stable cycle performance compared to unmodified CNTs increasing their applicability in energy storage devices. For instance, significant increases in the electrochemical double layer capacitance are observed for the CNT-NP composite electrode.