Cu-Ti thin films were fabricated using a combinatorial sputtering system to realize highly sensitive surface acoustic wave (SAW) devices. The Cu-Ti sample library was grown with various chemical compositions and electrical resistivity, providing important information for selecting the most suitable materials for SAW devices. Considering that acoustic waves generated from piezoelectric materials are significantly affected by the resistivity and density of interdigital transducer (IDT) electrodes, three types of Cu-Ti thin films with different Cu contents were fabricated. The thickness of the Cu-Ti thin films used in the SAW-IDT electrode was fixed at 150 nm. As the Cu content of the Cu-Ti films was increased from 31.2 to 71.3 at%, the resistivity decreased from 10.5 to 5.8 × 10-5 ohm-cm, and the density increased from 5.5 to 7.3 g/cm3, respectively. A SAW device composed of Cu-Ti IDT electrodes resonated at exactly 143 MHz without frequency shifts, but the full width at half maximum (FWHM) values of the resonant frequency gradually increased as the Cu content increased. This means that although the increase in Cu content in the Cu-Ti thin film helps to improve the electrical properties of the IDT electrode, the increased density of the IDT electrode deteriorates the acoustic performance of SAW devices.

Porous carbon nanofiber (CNF) electrodes for supercapacitors were prepared by using polyacrylonitrile (PAN) and cucurbituril (CB), which is a macrocyclic compound comprising glycoluril units containing hollow cores. Mixture of PAN and CB in dimethyl sulfoxide was electrospun, and thermally treated to produce CNF electrodes. Their thermal stability, surface morphology, carbon microstructures, and surface porosity were investigated. Electrochemical properties were measured using three-electrode with synthesized CNFs without further treatment as a working electrode and 1 M Na2SO4 as an electrolyte. CNFs derived from PAN and CB exhibited a high specific capacitance of 183.5 F g− 1 and an energy density of 25.4 Wh kg− 1 at 0.5 A g− 1 with stable cyclic stability during 1000 cycles, which is significantly higher than those for CNFs derived from PAN only. This demonstrated that the introduction of CB successfully improved the energy storage performance of CNF electrodes.

Synthesis of extremely competent materials is of great interest in addressing the energy storage concerns. Manganese oxide nanowires ( MnO2 NWs) are prepared in situ with multiwall carbon nanotubes (MWCNT) and graphene oxide (GO) using a simple and effective hydrothermal method. Powder XRD, Raman and XPS analysis are utilized to examine the structural characteristics and chemical state of composites. The initial specific discharge capacity of pure MnO2 NWs, MnO2 NWs/ MWCNT and MnO2 NWs/rGO composites are 1225, 1589 and 1685 mAh/g, respectively. The MnO2 NWs/MWCNT and MnO2 NWs/rGO composites showed stable behavior with a specific capacity of 957 and 1108 mAh/g, respectively, after 60 cycles. Moreover, MnO2 NWs/rGO composite sustained a specific capacity of 784 mAh/g, even after 250 cycles at a current density of 1 A/g showing outstanding cycling stability.

We have prepared MIL-101/graphene oxide (GO) composites with various mixing molar ratio of Fe-containing metal– organic frameworks (MOFs) against GO. When synthesizing MOFs, it was possible to synthesize uniform crystal powders using hydrothermal method. MIL-101 consists of a terephthalic acid (TPA) ligand, with the central metal composed of Fe, which was the working electrode material for supercapacitors. Field emission scanning electron microscopy, X-ray diffraction, Fourier transform infrared spectroscopy, and X-ray photoelectron spectroscopy analysis had been done to ascertain microstructures and morphologies of the composites. Cyclic voltammetry, electrochemical impedance spectroscopy, and galvanostatic charge–discharge measurements were performed to analyze the electrochemical properties of the composite electrodes in 6 M KOH electrolyte. By controlling the metal ligand mole ratio against GO, we prepared a changed MOF structure and a different composite morphology, which could be studied as one of the promising optimized electrode materials for supercapacitors.

Energy storage systems should address issues such as power fluctuations and rapid charge-discharge; to meet this requirement, CoFe2O4 (CFO) spinel nanoparticles with a suitable electrical conductivity and various redox states are synthesized and used as electrode materials for supercapacitors. In particular, CFO electrodes combined with carbon nanofibers (CNFs) can provide long-term cycling stability by fabricating binder-free three-dimensional electrodes. In this study, CFO-decorated CNFs are prepared by electrospinning and a low-cost hydrothermal method. The effects of heat treatment, such as the activation of CNFs (ACNFs) and calcination of CFO-decorated CNFs (C-CFO/ACNFs), are investigated. The C-CFO/ACNF electrode exhibits a high specific capacitance of 142.9 F/g at a scan rate of 5 mV/s and superior rate capability of 77.6% capacitance retention at a high scan rate of 500 mV/s. This electrode also achieves the lowest charge transfer resistance of 0.0063 Ω and excellent cycling stability (93.5% retention after 5,000 cycles) because of the improved ion conductivity by pathway formation and structural stability. The results of our work are expected to open a new route for manufacturing hybrid capacitor electrodes containing the C-CFO/ACNF electrode that can be easily prepared with a low-cost and simple process with enhanced electrochemical performance.

Numerous studies have addressed the commercial viability of lithium–air batteries (LABs). However, the high reactivity of Li with air moisture and CO2 has hindered the broad applicability of LABs. In this study, lithium-protective hybrid lithium–air batteries (HLABs) were fabricated with Super P (SP) and composites of fluorinated carbon ( CFx), MoS2, and WS2 as the cathodes. Subsequently, their potential use as a power source for the next generation of defense technologies was investigated. It was observed that a single cell HLAB with the SP-CFx composite cathode exhibited a specific capacity of 893 mAhg− 1 cathode. In comparison, a Tomcell with the SP cathode demonstrated a specific capacity of 465 mAhg− 1 cathode when discharged. The cells with SP-MoS2 and SP-WS2 cathode yielded specific capacities of 357 and 386 mAhg− 1 cathode, respectively. The improved performance of the SP-CFx cell can be attributed to synergistic effects of lithium–air cell and lithium battery reactions between CFx and SP. To assess all functionalities of the SP-CFx HLAB, lithium-protective HLABs were fabricated and discharged in air. To operate the lithium–air battery in air, pure lithium metal was sealed with solid electrodes (lithium-ion conducting glass–ceramics (LICGC)) and a buffer electrolyte (1 M LiFTSI in TEGDME) was applied. The SP-CFx cell was discharged for 25 days in air, greatly exceeding the 72 h requirement for the next-generation soldier power systems. These results demonstrate significant potential for HLABs to be used as a pioneering power source in nextgeneration energy-independent tactical defense units.

Electrochemical properties and performance of composites performed by incorporating metal oxide or metal hydroxide on carbon materials based on graphene and carbon nanotube (CNT) were analyzed. From the surface analysis by field emission scanning electron microscopy and field emission transmission electron microscopy, it was confirmed that graphene, CNT and metal materials are well dispersed in the ternary composites. In addition, structural and elemental analyses of the composite were conducted. The electrochemical characteristics of the ternary composites were analyzed by cyclic voltammetry, galvanostatic charge-discharge tests, and electrochemical impedance spectroscopy in 6 M KOH, or 1 M Na2SO4 electrolyte solution. The highest specific capacitance was 1622 F g–1 obtained for NiCo-containing graphene with NiCo ratio of 2 to 1 (GNiCo 2:1) and the GNS/single-walled carbon nanotubes/Ni(OH)2 (20 wt%) composite had the maximum specific capacitance of 1149 F g–1. The specific capacitance and rate-capability of the CNT/MnO2/reduced graphene oxide (RGO) composites were improved as compared to the MnO2/RGO composites without CNTs. The MnO2/RGO composite containing 20 wt% CNT with reference to RGO exhibited the best specific capacitance of 208.9 F g–1 at a current density of 0.5 A g–1 and 77.2% capacitance retention at a current density of 10 A g–1.

In this study, an electro-catalyst of Pt nanoparticles supported by polypyrrole-functionalized graphene (Pt/PPy-reduced graphene oxide [RGO]) is reported. The Pt nanoparticles are deposited on the PPy-RGO composite by chemical reduction of H2PtCl6 using NaBH4. The presence of graphene (RGO) caused higher activity. This might have been due to increased electro-chemically accessible surface areas, increased electronic conductivity, and easier charge-transfer at polymer-electrolyte interfaces, allowing higher dispersion and utilization of the deposited Pt nano-particles. Microstructure, morphology and crystallinity of the synthesized materials were investigated using X-ray diffraction and transmission electron microscopy. The results showed successful deposition of Pt nano-particles, with crystallite size of about 2.7 nm, on the PPy-RGO support film. Catalytic activity for methanol electro-oxidation in fuel cells was investigated using cyclic voltammetry. The fundamental electrochemical test results indicated that the electro-catalytic activity, for methanol oxidation, of the Pt/PPy-RGO combination was much better than for commercial catalyst.

Gold have been used as an electrode materials having a good mechanical flexibility as well as electrical conductivity, however the stretchability of the gold on a flexible substrate is poor because of its small elastic modulus. To overcome this mechanical inferiority, the reinforcing gold is necessary for the stretchable electronics. Among the reinforcing materials having a large elastic modulus, carbon nanotube (CNT) is the best candidate due to its good electrical conductivity and nanoscale diameter. Therefore, similarly to ferroconcrete technology, here we demonstrated gold electrodes mechanically reinforced by inserting fabrics of CNTs into their bodies. Flexibility and stretchability of the electrodes were determined for various densities of CNT fabrics. The roles of CNTs in resisting electrical disconnection of gold electrodes from the mechanical stress were confirmed using field emission scanning electron microscope and optical microscope. The best mechanical stability was achieved at a density of CNT fabrics manufactured by 1.5 ml spraying. The concept of the mechanical reinforced metal electrode by CNT is the first trial for the high stretchable conductive materials, and can be applied as electrodes materials in various flexible and stretchable electronic devices such as transistor, diode, sensor and solar cell and so on.