Electrochemical performance of polyaniline nanofibres and polyaniline/multi-walled carbon nanotube composite as an electrode material for aqueous redox supercapacitors

Polyaniline (PANI) nanofibres are synthesized by interfacial polymerization and their electrochemical performance is evaluated in an aqueous redox supercapacitor constituted as a two-electrode cell. The initial specific capacitance of the cell is 554 F g−1 at a constant current of 1.0 A g−1, but this value rapidly decreases on continuous cycling. In order to improve the cycleability of the supercapacitor, a composite of polyaniline with multi-walled carbon nanotubes (CNTs) is synthesized by in situ chemical polymerization. Its capacitive behaviour is evaluated in a similar cell configuration. A high initial specific capacitance of 606 F g−1 is obtained with good retention on cycling. In both supercapacitors, the effect of charging potential on cycling performances is investigated.

Transition metal nitrides as electrode materials for supercapacitors

This data comprises a collection of Scanning Electron Microscope (SEM) images of transition metal nitrates. Research was conducted to assess the size and morphology of particles

Gamma-irradiated carbon nanotube yarn as substrate for high-performance fiber supercapacitors

As an electrical double layer capacitor, dry-spun carbon nanotube yarn possesses relatively low specific capacitance. This can be significantly increased as a result of the pseudocapacitance of functional groups on the carbon nanotubes developed by oxidation using a gamma irradiation treatment in the presence of air. When coated with high-performance polyaniline nanowires, the gamma-irradiated carbon nanotube yarn acts as a high-strength reinforcement and a high-efficiency current collector in two-ply yarn supercapacitors for transporting charges generated along the long electrodes. The resulting supercapacitors demonstrate excellent electrochemical performance, cycle stability, and resistance to folding-unfolding that are required in wearable electronic textiles.

Core-spun carbon nanotube yarn supercapacitors for wearable electronic textiles

Linear (fiber or yarn) supercapacitors have demonstrated remarkable cyclic electrochemical performance as power source for wearable electronic textiles. The challenges are, first, to scale up the linear supercapacitors to a length that is suitable for textile manufacturing while their electrochemical performance is maintained or preferably further improved and, second, to develop practical, continuous production technology for these linear supercapacitors. Here, we present a core/sheath structured carbon nanotube yarn architecture and a method for one-step continuous spinning of the core/sheath yarn that can be made into long linear supercapacitors. In the core/sheath structured yarn, the carbon nanotubes form a thin surface layer around a highly conductive metal filament core, which serves as current collector so that charges produced on the active materials along the length of the supercapacitor are transported efficiently, resulting in significant improvement in electrochemical performance and scale up of the supercapacitor length. The long, strong, and flexible threadlike supercapacitor is suitable for production of large-size fabrics for wearable electronic applications.

Titanium dioxide nanotube films for electrochemical supercapacitors: Biocompatibility and operation in an electrolyte based on a physiological fluid

Growing interest in developing devices that can be implantable or wearable requires the identification of suitable materials for the components of these devices. Electrochemical supercapacitors are not the exception in this trend, and identifying electrode materials that can be not only suitable for the capacitive device but also biocompatible at the same time is important. In addition, it would be advantageous if physiological fluids could be used instead of more conventional (and often corrosive) electrolytes for implantable or wearable supercapacitors. In this study, we assess the biocompatibility of films of anodized TiO2 nanotubes subjected to the subsequent annealing in Ar atmosphere and evaluate their capacitive performance in a physiological liquid. A biocompatibility test tracking cell proliferation on TiO2 nanotube electrodes and electrochemical tests in 0.01 M phosphate-buffered saline solution are discussed. It is expected that the study will stimulate further developments in this area.

A highly conductive porous graphene electrode prepared via in situ reduction of graphene oxide using Cu nanoparticles for the fabrication of high performance supercapacitors

Herein, a new graphene/Cu nanoparticle composite was prepared via the in situ reduction of GO in the presence of Cu nanoparticles which was then utilized as a sacrificing template for the formation of flexible and porous graphene capacitor electrodes by the dissolution of the intercalated Cu nanoparticle in a mixed solution of FeCl3 and HCl. The porous RGO electrode was characterized by atomic force microscopy (AFM), Fourier transform infrared (FTIR) spectroscopy, X-ray diffraction (XRD), Raman spectroscopy, X-ray photoelectron spectroscopy (XPS) and thermogravimetric analysis (TGA). The as-prepared graphene/Cu nanoparticle composite and the pure graphene film after removal of Cu nanoparticles possessed high conductivity of 3.1 × 10³ S m^-1 and 436 S m^-1 respectively. The porous RGO can be used as the electrode for the fabrication of supercapacitors with high gravimetric specific capacitances up to 146 F g^-1, good rate capability and satisfactory electrochemical stability. This environmentally friendly and efficient approach to fabricating porous graphene nanostructures could have enormous potential applications in the field of energy storage and nanotechnology.

Stable deep doping of vapor-phase polymerized poly(3,4-ethylenedioxythiophene)/ionic liquid supercapacitors

Liquid-solution polymerization and vapor-phase polymerization (VPP) have been used to manufacture a series of chloride- and tosylate-doped poly(3,4-ethylenedioxythiophene) (PEDOT) carbon paper electrodes. The electrochemistry, specific capacitance, and specific charge were determined for single electrodes in 1-ethyl-3-methylimidazolium dicyanamide (emim dca) ionic liquid electrolyte. VPP-PEDOT exhibits outstanding properties with a specific capacitance higher than 300 F g(-1) , the highest value reported for a PEDOT-based conducting polymer, and doping levels as high as 0.7 charges per monomer were achieved. Furthermore, symmetric PEDOT supercapacitor cells with the emim dca electrolyte exhibited a high specific capacitance (76.4 F g(-1) ) and high specific energy (19.8 Wh kg(-1) ). A Ragone plot shows that the VPP-PEDOT cells combine the high specific power of conventional ("pure") capacitors with the high specific energy of batteries, a highly sought-after target for energy storage.

Facile fabrication of supercapacitors with high rate capability using graphene/nickel foam electrode

High-performance reduced graphene oxide/nickel foam (rGO/NF) composite electrodes for high-performance supercapacitors were prepared by flame-induced reduction of dry graphene oxide (GO) coated on nickel foam. Flame reduction of GO is a facile, feasible and cost-effective reduction technique, which is conducted without the need of any reductant. Most importantly, the rGO obtained by flame reduction showed a typical disordered cross-linking network and randomly distributed pores, which provide accessible routes for fast transportation of ions. It was demonstrated that the rGO/NF electrode with embedded current collector (NF) exhibited better electrochemical performance than conventional rGO film counterparts, including a high gravimetric specific capacitance of 228.6 F g-1 at a current density of 1 A g-1, excellent rate capability (over 81% retention at 32 A g-1) and high cycling stability with only 5.3% capacitance decay over 10,000 cycles of cyclic voltammetry at a ultrahigh scan rate of 1000 mV s-1. This facile method for the fabrication of rGO/NF electrodes could envision enormous potential for high performance energy storage devices.

Ionic liquids in electrochemical devices and processes : managing interfacial electrochemistry

Many ionic liquids offer a range of properties that make them attractive to the field of electrochemistry; indeed it was electrochemical research and applications that ushered in the modern era of interest in ionic liquids. In parallel with this, a variety of electrochemical devices including solar cells, high energy density batteries, fuel cells, and supercapacitors have become of intense interest as part of various proposed solutions to improve sustainability of energy supply in our societies. Much of our work over the last ten years has been motivated by such applications. Here we summarize the role of ionic liquids in these devices and the insights that the research provides for the broader field of interest of these fascinating liquids.

Zwitterionic additives for electrochemical devices

Zwitterionic electrolytes such as N-methyl-N-(n-butanesulfonate) pyrrolidinium are added to electrolyte compositions such as polyelectrolytes, ionic liquid electrolytes and molecular solvent electrolytes (for example, lithium hexafluorophosphate) to improve conductivity of the ion species, such as lithium, in the electrolyte. This has application to lithium based energy storage devices such as batteries and supercapacitors.

ZWITTERIONIC ADDITIVES FOR ELECTROCHEMICAL DEVICES

Zwitterionic electrolytes such as N-methyl-N-(n-butanesulfonate) pyrrolidinium are added to electrolyte compositions such as polyelectrolytes, ionic liquid electrolytes and molecular solvent electrolytes (for example, lithium hexafluorophosphate) to improve conductivity of the ion species, such as lithium, in the electrolyte. This has application to lithium based energy storage devices such as batteries and supercapacitors.

Structure and capacitive properties of porous nanocrystalline VN produced by NH3 reduction of V2O5

Vanadium nitride (VN) is currently one of the most promising materials for electrodes of supercapacitors. The structure and electrochemical properties of VN synthesized by temperature-programmed NH₃ reduction of V₂O₅ are analyzed in this paper. Vanadium nitride produced via this route has distinctive structural characteristics. VN mimics the shape of the initial V₂O₅ precursor indicating a pronounced direct attachment of nitride grains. The particles have domains of grains with a preferential orientation (texture). The large volume of pores in VN is represented by the range of 15−110 nm. VN demonstrates capacitive properties in three different types of aqueous electrolytes, 1 M KOH, 1 M H₂SO₄, and 3 M NaCl. The material has an acceptable rate capability in all electrolytes, showing about 80% of its maximal capacitance at a current load of 1 A/g in galvanostatic charging/discharging experiments. The capacitance of 186 F/g is observed in 1 M KOH electrolyte at 1 A/g. The previously reported negative effect of material loading on the capacitance is significantly suppressed. The observed electrochemical characteristics related to the application of this material in supercapacitors can be correlated with the crystalline structure of the nitride and the composition of its surface layer.

Ilmenite FeTiO3 nanoflowers and their pseudocapacitance

Pronounced and stable pseudocapacitance has been found in flowerlike FeTiO3 nanostructures that were synthesized from ball-milled ilmenite (natural mineral) under mild hydrothermal conditions. Each nanoflower is composed of many thin petals with a thickness of 5–20 nm and a width of 100–200 nm. The formation of these flowerlike nanostructures is attributed to a dissolution–precipitation mechanism involving an intermediate sodium-containing phase. Electrochemical properties of the obtained FeTiO3 nanostructures are evaluated in aqueous electrolytes. The capacitance of 122 ± 14.5 F/g is measured in 1 M KOH aqueous electrolyte at the current rate of 500 mA/g, and 50 ± 6 F/g is retained at 5 A/g. The material has good long-term cycling stability. According to our data, FeTiO3 nanostructures show functionality as an electrode material for supercapacitors.

Nanorods of vanadium compounds: synthesis, characterisation, and application in electrochemical energy storage

The synthesis and characterisation of nanorods of vanadium pentoxide, V(2)O(5), vanadium trioxide, V(2)O(3), vanadium dioxide, VO(2)(B), and vanadium nitride, VN, are presented, and their application in electrochemical supercapacitors and lithium-ion batteries is outlined. Specifically, a novel method for the preparation of V(2)O(5) nanorods is discussed. It involves ball milling as a first step and controlled annealing as a second step. Nanorods of V(2)O(5) can be converted into those of other vanadium-related phases by simple chemical reduction treatments. Such chemical transformations are pseudomorphic and often topotactic, that is, the resulting nanorods belong to a different chemical phase but tend to retain the original morphology and preferential crystal orientation dictated by parent V(2)O(5) crystals.

The corresponding properties of nanorods for their prospective application in electrochemical energy storage (lithium-ion batteries and electrochemical supercapacitors) are discussed. The synthesised V(2)O(5) nanorods possess a stable cyclic behaviour when they are used in a cathode of a lithium-ion battery and are suitable for use in an anode. VN nanorods synthesised by NH(3) reduction of V(2)O(5) were found to possess pseudocapacitive properties in aqueous electrolytes.