Nanocrystallites of pure and mixed ternary ferrites, NiFe2O4 (NiF), CuFe2O4 (CuF), CoFe2O4 (CoF), Ni0.5Cu0.5Fe2O4 (CuNiF), Ni0.5Co0.5Fe2O4 (NiCoF), and Cu0.5Co0.5Fe2O4 (CuCoF) were prepared using the auto-combustion method employing urea as a fuel. The obtained materials were investigated by Fourier transform infrared spectroscopy (FTIR), X-ray diffraction (XRD), transmission electron miscroscopy (TEM), scanning electron microscopy (SEM), and BET techniques. The elemental composition of the prepared samples was checked by X-ray fluorescence (XRF) analysis. XRD indicated that the as-synthesized samples exhibit a pure spinel crystal structure. The samples have crystallite sizes ranged from 12 to 47 nm. SEM and TEM analyses showed almost spherical morphology for all ferrite particles. The M–H curves recorded using the VSM (vibrating sample magnetometer) technique showed ferromagnetic hysteresis loop for all the samples investigated. The ferrite samples were tested to be used as a supercapacitor electrode material. It is found that the measured specific capacitance of the ferrite electrodes increases according to CuCoF > NiCoF > CoF > NiCuF > CuF > NiF. The CuCoF sample showed the greatest specific capacitance of 220 F/g at discharging current density l of A/g with, an energy density of 34.72 Wh/kg and power density of 605 W/kg. The magnetic properties were also measured for the obtained nanoparticles.

Lightweight, inexpensive and flexible electrodes are required for flexible technological applications. As polymers are generally low cost, flexible and have low density, they are potential candidates for use as flexible electrodes. However, polymers are not conductive and thus cannot be used as electrodes or current collectors. Polymers have been coated by metals/alloys to make them conductive for use in various applications including electromagnetic shielding and sensors. In this work, a flexible electrode was successfully fabricated by electrodeposition of Cu and Ni on polyester fabric for an energy storage application. The growth of metals was carried out in non-aqueous ionic liquid electrolyte, with the deposition condition of Cu and Ni studied by means of cyclic voltammetry. Non-electrochemical (FTIR, XRD, SEM and EDAX) characterizations of the metal-coated polyester are also presented. Modified flexible electrodes were transferred to an alkaline electrolyte for electrochemical characterization. The specific capacitance of Cu- and Ni-coated polyester reached 33.4 F/g and 50.2 F/g at the same scan rate of 5 mV/s. These results suggest an inexpensive and straightforward method for the fabrication of a flexible electrode for energy storage applications.

Here, a well crystalline 3D flower-like structured MoS2 (~420 nm) has been successfully synthesized on a large scale by a simple hydrothermal technique. The evolution of morphology in the formation process has also been investigated. The crystallinity, purity, and morphology of the sample are characterized by powder X-ray diffraction, Fourier-transform infrared spectroscopy, fieldemission scanning electron microscopy (FESEM), and transmission electron microscopy (TEM) techniques. The FESEM and TEM images reveal that the sample exhibits a uniform 3D flower-like microsphere shape with folded nanosheets, which are stretched out along the edge of the microsphere. The electrochemical performance of the sample has been investigated by cyclic voltammogram, galvanostatic charge–discharge, and electrochemical impedance spectroscopy studies. The results of the electrochemical analysis suggest that the material delivers a maximum specific capacitance (Csp) of 350 F/g at a discharge current density of 0.25 A/g with energy density 17.5 Wh/kg. It also exhibits good capability and excellent cyclic stability (94% capacity retention after 1,000 cycles in 1 A/g) owing to the coupling effect of electrical conductivity with the interesting morphology and larger active surface area. Hence, the sample may be used as a promising electrode material for high-performance energy storage devices.

A supercapacitor electrode featured with a voltage self-stabilizing capability is demonstrated by growing indium tin oxide (ITO) nanowires on Ni foam. The ITO nanowires with a single crystal structure are prepared by using magnetron sputtering technique, and they can act as an active electrode material. Charging–discharging experiments are performed under different current densities, demonstrating a good rate capability. Using properly designing top and bottom double connection circuits, part of the electrode can be used as a resistance switch. An electrode that can function as a supercapacitor and a resistance switch is fabricated. Detailed characteristics confirm that the device not only exhibits high performance as a supercapacitor but also has good characteristics of resistance switching (RS). The specific capacitance is 956 F/g at the scanning rate of 10 mV/s, and the switching ratio as a bipolar resistance switch is as high as 102. The stabilization time of discharging voltage is nearly doubled longer than that without any RS function, revealing the potential application of our devices, which can be used as a supercapacitor with voltage self-stabilizing.

In this work, a three-dimensional (3D) porous hybrid nickel/aluminum layered double hydroxide (Ni/Al-LDH)-carbon cloth (CC), the working electrode without binders or conductive additions for supercapacitor, was successfully synthesized via facile one-step hydrothermal method. The as-obtained Ni/Al-LDH/CC sample exhibited good charge storage performance (the specific capacitance was up to 359 F/g at a current density of 0.3 A/g), as well as superior cycling stability (5.9% capacitance increase after 3000 cycles at 1.0 A/g). Furthermore, an asymmetric supercapacitor, Ni/Al-LDH/CC as positive electrode and activated carbon (AC) as negative electrode (Ni/Al-LDH/CC//AC), achieved a high energy density (20.9 Wh/kg vs. the power density 262.5 W/kg) and good cycle lifetime (83.9% retention of the initial value after 3000 cycle tests at a current density of 0.5 A/g). The unique 3D porous structure and binder-free electrode display great potential in supercapacitors.

Ordered mesoporous carbons (OMCs) are appealing alternatives to conventional porous activated carbon applied to electronic energy storage and conversion devices. Nitrogen-doped OMC (NOMC) was prepared with a soft-template strategy directly using task-specific ionic liquid with dicyanamide anion as the nitrogen dopant, and utilized as supercapacitors for the first time. Compared with pristine OMC, NOMC showed excellent electrochemical capacitive behavior in 6 M KOH electrolyte. NOMC possessed a high specific capacitance of 427 F/g at a current density of 1 A/g and exhibited a stable cycle life (almost 98% retained at a current density of 5 A/g after 2000 cycles). The outstanding capacitive performance of NOMC was ascribed to the synergetic effects of its bimodal mesoporous structure, large specific surface area (1919 m2/g), and nitrogen doping (3.52 wt%), which help to accelerate the ion diffusion, increase the surface charge storage, and intensify pseudo-capacitive reactions.

The differential capacitance of electric double-layer capacitors is studied by developing a generalized model of the self-consistent Gaussian field theory. This model includes many-body effects of particles near the interface such as ionic sizes, the order of water alignment and electrostatic correlations, and thus can present more accurate predictions of the electric double-layer structure and hence the capacitance than traditional continuum theories. Analytical simplification of the model and efficient numerical method are introduced, in particular, the approximation of the self-Green's function which describes the self energy of a mobile ion. We show that, when the applied voltage on interfaces is small the dielectric effect of the electrode materials plays an important role. For large voltage, this effect is screened, but the dielectric saturation due to the alignment of the nearby water is shown to be essential. For 2:1 electrolytes, abnormal enhancement on the capacitance due to the dielectric electrode is observed, which is due to the interplay of the image charge effect and Born solvation energy in the self energy of ions.

Battery-powered wireless sensor networks have been extensively deployed in condition monitoring and structural health monitoring systems, but the performance of wireless sensors are limited by battery capacity and difficulty of application in rotating machines. In this paper, a variety of commercial wireless charging solutions and coil-shaft configurations for magnetic coupling are compared, having in mind of the application of continuously charging wireless sensors on rotating machines. For the co-axial configuration of the transmitter coil and the receiver coil, a Qi standard compliant wireless charging kit and a custom charging circuit are successfully applied to charge wireless sensors on small rotating test rigs. In order to harvest and store intermittent energy input from the wireless power source, a prototype receiver circuit using a supercapacitor and low-dropout regulator is designed and validated. Based on the prototype circuit, the radial configuration of single transmitter coil and multiple receiver coils is demonstrated for wireless power transfer to the sensor nodes on the drivetrain of a small wind turbine test rig.

Developing high energy density supercapacitors is of great importance to the transportation, consumer electronics, and micro-grid energy storage sectors. Recently, the development of high voltage organic electrolyte based supercapacitor devices has been gaining much attention. Among them, there is an on-going intense interest in investigating high capacity lithium ion storage anode materials in hybrid supercapacitors. However, developing high capacity cathode materials for high voltage organic electrolyte supercapacitor devices is rarely investigated. The low electrical double layer capacitances of carbon cathode electrodes, which are widely used in current supercapacitor devices, are often the limiting bottleneck. In this contribution, we investigated the electrochemical energy storage behavior of a polyaniline (PANI)-single wall carbon nanotube (SWCNT) composite material in an organic electrolyte as a supercapacitor cathode. The PANI-SWCNT composite exhibits a high specific capacitance of 503 F/g, of which 58.8% of the total capacitance is attributed to the pseudocapacitive and electrical double layer energy storage. The cycling stability of the PANI-SWCNT composite could be further improved by polydopamine (PDA) modification. The PDA with strong adhesion properties is able to prevent mechanical degradation. The PDA modified PANI-SWCNT shows excellent stability with only 5% degradation after 2000 cycles.

A ternary Nickel foam (NF)–graphene/MnO2/polyaniline (PANI) nanocomposite has been synthesized using green chemistry approach (in situ polymerization). All reactants were dispersed homogeneously in precursor solution in the form of ions and molecules. PANI and MnO2 molecules on the NF–graphene contact each other and are arranged alternately in the composite. Alternative arrangement of PANI and MnO2 nanoparticles separates them and prevents the aggregation of PANI and MnO2 to decrease the particle size of the composite on the surface of NF–graphene. The intermolecule contact improves the conductivity of the composite. The composite showed excellent specific capacitance of 1081 F/g at a scan rate of 1 mV/s and specific capacitance of 815 F/g at a current density of 3 A/g, having excellent cycling stability. Current study provides an alternative pathway to improve the rate capability and cycling stability of nanostructured electrodes, by offering a great promise for their applications in supercapacitors.

We describe the synthesis and fabrication of a graphene oxide (GO) and single-walled carbon nanotube (SWCNT) composite ink (GO–SWCNT ink) for electrochemically stable supercapacitors. Atomic force microscopy and scanning electron microscopy studies demonstrate that the obtained GO flakes are single layer with size distribution from 100 nm to 20 μm. SWCNTs are dispersed using a GO aqueous solution (2 mg/mL) with sonication support to achieve a SWCNT concentration of 12 mg/mL, the highest reported value so far without surfactant assistance. Raman spectroscopy studies indicate that the full-width at half-maximum of the G band increases with the mixing of SWCNT and GO indicating that electronic structure changes via π–π interactions of GO sheets and SWCNTs. Paper-based electrodes of supercapacitor were conveniently fabricated with GO–SWCNT composite ink via a dip casting method. By using different concentrations of SWCNT in the ink, the paper electrodes provide different capacitance values. The highest value of specific capacitance reaches 295 F/g at a current density of 0.5 A/g with a GO/SWCNT weight ratio of 1:5. The cycling stability for the GO–SWCNT paper electrode supercapacitors indicates capacitance retention of 85% over 60,000 cycles.