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Supercapacitors (SCs) have emerged as attractive energy storage devices due to their rapid charge/discharge rates, long cycle life, and high-power density. However, the development of innovative electrode materials to achieve high-performance remains crucial to meet future requirements in supercapacitor technology. In this work, we have explored the potential of a microwave-engineered NiZrO 3 @GNP composite as a promising electrode material for SCs. A microwave assisted hydrothermal approach was adopted for the fabrication of the NiZrO 3 @GNP nanocomposite. Structural and morphological investigations showed its structural richness and its chemical compositions. When applied as a SC electrode, this innovative combination exhibits battery-like behaviour with higher specific capacity (577.63 C g -1 ) with good cyclic stability, and good performance. We have assembled an asymmetric-type two-electrode SC device and analysed its electrochemical features. This NiZrO 3 @GNP device exhibits the specific capacity of 47 C g -1 with capacitance retention of 70% after 2000 charge-discharge cycles. Further research on optimizing the synthesis process and exploring different device configurations could pave the way for even higher-performance supercapacitors in the future., Competing Interests: All authors declare that they have no conflicts to declare., (This journal is © The Royal Society of Chemistry.)

The polyhedron-structured NiSe 2 @MoSe 2 (NMS) were magnificently produced through hydrothermal method, which makes the active electrode very effective in accessing the redox active sites in the charge/discharge process in supercapacitor applications. Systematic studies of the structural and morphological features of the unique polyhedron NMS were performed. Laser Raman spectra reported the vibrational and rotational modes of NMS. NMS exhibited a maximum 1000 F g -1 (138.8 mA h g -1 ) specific capacitance at 1 A g -1 and attained a capacity retention of 77.67% for 5000 stable cycles at 10 A g -1 using 1 M KOH as an electrolyte. The well assembled asymmetric supercapacitor NMS hydrolyzed for 18 h//AC demonstrated an outstanding electrochemical performance with an improved 305 F g -1 specific capacitance attained at 1 A g -1 with a good cycle life of 87.35% and a capacity retention of over 5000 cycles. Herein, the combined contribution of both the Ni and Mo ions offers a richer redox chemistry, which is beneficial to a higher electrochemical activity. The experimental results indicate that the NMS electrode could be used as a high-performance electrode., Competing Interests: There are no conflicts to declare., (This journal is © The Royal Society of Chemistry.)

Waste water remediation is the ongoing hot research topic that can reduce the water scarcity all over the world. By reducing the pollutants in the waste water drawn from industries and other sources will be more useful for domestic purposes. To reduce the rate of pollutants in water may also help in improving the aquatic environment and decreases other side effects. Efficient and cost effective catalysts were in search for both dye degradation and water remediation treatment applications. NiMoO 4 nanorods were prepared by employing co-precipitation method with different stirrer time (2 h, 4 h and 6 h). The formation of NiMoO 4 was substantiated employing X-ray diffractometer analysis (XRD). Vibrational and rotational property of the samples was analyzed by FT-IR spectra and Raman spectra. The optical property was further confirmed by UV-vis spectral studies. Morphological analysis studies revealed growth of nanorods with 6 h stirrer time. The photocatalytic behavior of the obtained product was carried out under both UV light (364 nm) and visible light irradiation. The samples subjected to visible light environment showed better efficiency on degrading the methylene blue (MB) dye. The efficiency obtained under UV irradiation were 20%, 31%, 33%, 41% and efficiency obtained in visible light irradiation were 27%, 42%, 46%, 55% with respect to bare methylene blue (MB), MB with NiMoO 4 (2 h), MB with NiMoO 4 (4 h), MB with NiMoO 4 (6 h) catalyst added. NiMoO 4 sample with 6 h stirrer time and fine nanorods growth will be the good candidate for future use., (Copyright © 2021 Elsevier Inc. All rights reserved.)

Electrochemical energy storage is a current research area to address energy challenges of the modern world. The Cu 2 FeSnS 4 /PVP/rGO-decorated nanocomposite using PVP as the surface ligand was explored in a simple one-step solvothermal route, for studying their electrochemical behavior by designing asymmetric hybrid supercapacitor devices. The full cell three-electrode arrangements delivered 748 C/g (62.36 mA h/g) at 5 mV/s employing CV and 328 F/g (45.55 mA h/g) at 0.5 A/g employing GCD for the Cu 2 FeSnS 4 /PVP/rGO electrode. The half-cell two-electrode device can endow with 73 W h/kg and 749 W/kg at 1 A/g energy and power density. Furthermore, two Cu 2 FeSnS 4 /PVP/rGO//AC asymmetric devices connected in series for illuminating a commercial red LED more than 1 min were explored. This work focuses the potential use of transition-metal chalcogenide composite and introduces a new material for designing high-performance supercapacitor applications., Competing Interests: The authors declare no competing financial interest., (© 2021 The Authors. Published by American Chemical Society.)

Herein, we report a novel, low-temperature solvothermal method to grow 3D-Bi2O3 flower-like microspheres on Ti substrates as a binder-free negative electrode for supercapacitor applications. The Bi2O3/Ti electrode showed an areal capacitance of 1.65 F cm-2 at 4 mA cm-2. Moreover, the 3D-NiCo2O4||3D-Bi2O3 hybrid device delivered high energy and power densities of 31.17 μW h cm-2 and 7500 μW cm-2, respectively. The more optimal energy storage performance based on the strong adhesion of the current collector and self-assembled three-dimensional nanostructures permits efficient electron and ion transportation.

Comparative investigation of the electrochemical oxygen evolution reaction (OER) activity for clean energy production was performed by fabricating three different electrodes, namely, NiSe 2 , CoSe 2 , and CoNiSe 2 , synthesized by hydrothermal treatment. Cubic, orthorhombic, and hexagonal structures of NiSe 2 , CoSe 2 , and CoNiSe 2 were confirmed by X-ray diffraction (XRD) and also by other characterization studies. Perfect nanospheres, combination of distorted nanospheres and tiny nanoparticles, and sharp-edge nanostructures of NiSe 2 , CoSe 2 , and CoNiSe 2 were explored by surface morphological images. Higher OER activity of the binary CoNiSe 2 electrode was achieved as 188 mA/g current density with a comparatively low overpotential of 234 mV along with higher conductivity and low charge transfer resistance when compared to its unary NiSe 2 and CoSe 2 electrodes. A low Tafel slope value of 82 mV/dec was also achieved for the same binary CoNiSe 2 electrode in a half-cell configuration. The overall 100% retention achieved for all of the fabricated electrodes in a stability test of OER activity suggested that the excellent optimum condition was obtained during the synthesis. This could definitely be a revelation in the synthesis of novel binary combinations of affordable metal selenides for clean energy production., Competing Interests: The authors declare no competing financial interest., (Copyright © 2020 American Chemical Society.)

In this study, a general and effective phosphorization strategy is demonstrated to enhance the super capacitor performance of Ni, Cu, and Mn transition metals. The composites such as Ni₃(PO₄)₂, Cu₃(PO₄)₂ and Mn₃(PO₄)₂ were achieved by employing hydrothermal method mixing with ethylene glycol. These composite nanostructures were characterized by standard sophisticated techniques such as XRD, RAMAN, FTIR, UV, PL and SEM studies. X-ray diffraction (XRD) studies revealed the monoclinic crystallographic structure of the materials. The optical and vibrational properties of the product are characterized by photoluminescence and FTIR studies. These prepared materials have shown desired electrochemical stability. The above characterization indicates the functional groups and materials nature. The electrochemical properties of synthesized phosphate materials are analyzed by cyclic voltammetry (CV), electrochemical impedance spectroscopy (EIS) and galvanostatic charging and discharging studies (GCD). The Cu₃(PO₄)₂ electrode showed a remarkable specific capacitance of 232.025 F g -1 at a scan rate of 20 mV/s, which is expected to have a promising electrode for super capacitor applications. The GCD study of synthesized Cu₃(PO₄)₂ nanostructure has also been tested for 1000 cycles at 10 A/g current density to evaluate the cyclic stability of the electrode and retains 94% of initial specific capacitance.

A copper sulfide nanoflakes-decorated carbon nanofragments-modified glassy carbon electrode (CuS-CNF/GCE) was fabricated for the electrocatalytic differentiation and determination of hydroquinone (HQ) and catechol (CC). The physicochemical properties of the CuS-CNF were characterized by scanning electron microscopy, transmission electron microscopy, X-ray diffraction, X-ray photoelectron spectroscopy and Raman spectroscopy. The electrocatalytic determination of HQ and CC over the CuS-CNF/GCE was evaluated by cyclic voltammetry and differential pulse voltammetry. An excellent detection limit and sensitivity of the CuS-CNF/GCE are obtained (0.293 µM and 0.259 µM) with a sensitivity of 184 nA µM -1 cm -2 and 208 nA µM -1 cm -2 (S/N=3) for HQ and CC, respectively. In addition, the CuS-CNF/GCE shows a selective identification of HQ and CC over potential interfering metal ions (Zn 2+ , Na + , K + , NO 3- , SO 4 2- , Cl - ) and organic compounds (ascorbic acid, glucose), and a satisfactory recovery is also obtained in the spiked water samples. These results suggest that the CuS-CNF/GCE can be used as an efficient electrochemical sensor for the simultaneous determination of co-existing environmental pollutants such as HQ and CC in water environments with high selectivity and acceptable reproducibility.

Wire type supercapacitors with high energy and power densities have generated considerable interest in wearable applications. Herein, we report a novel NiCo 2 S 4 -decorated 3D, porous Ni film@Ni wire electrode for high performance supercapacitor application. In this work, a facile method is introduced to fabricate a 3D, porous Ni film deposited on a Ni wire as a flexible electrode, followed by decoration with NiCo 2 S 4 as an electroactive material. The fabricated NiCo 2 S 4 -decorated 3D, porous Ni film@Ni wire electrode displays a superior performance with an areal and volumetric capacitance of 1.228 F cm -2 and 199.74 F cm -3 , respectively, at a current density of 0.2 mA cm -1 with a maximum volumetric energy and power density (E V : 6.935 mW h cm -3 ; P V : 1.019 W cm -3 ). Finally, the solid state asymmetric wire type supercapacitor is fabricated using the fabricated NiCo 2 S 4 -decorated 3D, porous Ni film@Ni wire as a positive electrode and N-doped reduced graphene oxide (N-rGO) as a negative electrode and this exhibits good areal and volumetric capacitances of C A : 0.12 F cm -2 and C V : 19.57 F cm -2 with a higher rate capability (92%). This asymmetric wire type supercapacitor demonstrates a low leakage current and self-discharge with a maximum volumetric energy (E V : 5.33 mW h cm -3 ) and power (P V : 855.69 mW cm -3 ) density.

Bi 2 O 3 rods/RGO composite has been synthesized by a simple precipitation and calcination method. The crystallnity, structural, and morphological features were studied by X-ray diffraction (XRD), field-emission scanning electron microscopy (FE-SEM), and high resolution transmission electron microscopy (HR-TEM) techniques. The supercapacitor behavior was studied using cyclic voltammetry, galvanostatic charge discharge and impedance analysis, respectively. The Bi 2 O 3 rods/RGO nanocomposite exhibits a maximum specific capacitance of 1041Fg -1 at a current density of 2Ag -1 . The photocatalytic activity of Bi 2 O 3 rods/RGO composite was evaluated by photocatalytic degradation of methylene blue (MB) dye under visible-light irradiation. The enhancement of photocatalytic properties of Bi 2 O 3 rods/RGO composite attributed to the synergistic effect between Bi 2 O 3 rods and graphene sheets which effectively prevents recombination of the photogenerated electron-hole pairs in Bi 2 O 3 rods. The present study provides a new approach in improving the performance of Bi 2 O 3 rods/RGO composite in energy and environmental applications., (Copyright © 2017 Elsevier Inc. All rights reserved.)

A lightweight, flexible, cost-effective, and robust, single-electrode-based Smart Seat-Triboelectric Nanogenerator (SS-TENG) is introduced as a promising eco-friendly approach for harvesting energy from the living environment, for use in integrated self-powered systems. An effective method for harvesting biomechanical energy from human motion such as walking, running, and sitting, utilizing widely adaptable everyday contact materials (newspaper, denim, polyethylene covers, and bus cards) is demonstrated. The working mechanism of the SS-TENG is based on the generation and transfer of triboelectric charge carriers between the active layer and user-friendly contact materials. The performance of SS-TENG (52 V and 5.2 μA for a multiunit SS-TENG) is systematically studied and demonstrated in a range of applications including a self-powered passenger seat number indicator and a STOP-indicator using LEDs, using a simple logical circuit. Harvested energy is used as a direct power source to drive 60 blue and green commercially available LEDs and a monochrome LCD. This feasibility study confirms that triboelectric nanogenerators are a suitable technology for energy harvesting from human motion during transportation, which could be used to operate a variety of wireless devices, GPS systems, electronic devices, and other sensors during travel.

A new paradigm in cancer theranostics is enabled by safe multifunctional nanoplatform that can be applied for therapeutic functions together with imaging capabilities. Herein, we develop a multifunctional nanocomposite consisting of Graphene Oxide-Iron Oxide -Doxorubicin (GO-IO-DOX) as a theranostic cancer platform. The smart magnetic nanoplatform acts both as a hyperthermic agent that delivers heat when an alternating magnetic field is applied and a chemotherapeutic agent in a cancer environment by providing a pH-dependent drug release to administer a synergistic anticancer treatment with an enhanced T2 contrast for MRI. The novel GO-IO-DOX nanocomposites were tested in vitro and were observed to exhibit an enhanced tumoricidal effect through both hyperthermia and cancer cell-specific DOX release along with an excellent MRI performance, enabling a versatile theranostic platform for cancer. Moreover the localized antitumor effects of GO-IO-DOX increased substantially as a result of the drug sensitization through repeated application of hyperthermia.

We demonstrate a flexible piezoelectric nanogenerator (PNG) constructed using a hybrid (or composite) film composed of highly crystalline BaTi(1-x)Zr(x)O3 (x = 0, 0.05, 0.1, 0.15, and 0.2) nanocubes (abbreviated as BTZO) synthesized using a molten-salt process embedded into a poly(vinylidene fluoride) (PVDF) matrix solution via ultrasonication. The potential of a BTZO/PVDF hybrid film is realized in fabricating eco-friendly devices, active sensors, and flexible nanogenerators to interpret its functionality. Our strategy is based on the incorporation of various Zr(4+) doping ratios into the Ti(4+) site of BaTiO3 nanocubes to enhance the performance of the PNG. The flexible nanogenerator (BTZO/PVDF) exhibits a high electrical output up to ∼11.9 V and ∼1.35 μA compared to the nanogenerator (BTO/PVDF) output of 7.99 V and 1.01 μA upon the application of cyclic pushing-releasing frequencies with a constant load (11 N). We also demonstrate another exciting application of the PNG as a self-powered sensor to measure different water velocities at an outlet pipe. The average maximum peak power of the PNG varies from 0.2 to 15.8 nW for water velocities ranging from 31.43 to 125.7 m/s during the water ON condition. This study shows the compositional dependence approach, fabrication of nanostructures for energy harvesting, and self-powered devices in the field of monitoring for remote area applications.

In this work, we have fabricated a piezoelectric-driven self-charging supercapacitor power cell (SCSPC) using MnO2 nanowires as positive and negative electrodes and a polyvinylidene difluoride (PVDF)-ZnO film as a separator (as well as a piezoelectric), which directly converts mechanical energy into electrochemical energy. Such a SCSPC consists of a nanogenerator, a supercapacitor, and a power-management system, which can be directly used as a power source. The self-charging capability of SCSPC was demonstrated by mechanical deformation under human palm impact. The SCSPC can be charged to 110 mV (aluminum foil) in 300 s under palm impact. In addition, the green light-emitting diode glowed using serially connected SCSPC as the power source. This finding opens up the possibility of making self-powered flexible hybrid electronic devices.

We report the gate-tunable photoresponse of a defective graphene over the ultraviolet (UV) and the visible light illumination, where the defect was generated by plasma irradiation. Plasma induced Dirac point shift indicates the p-doping effect. Interestingly the defective-graphene field effect transistor (defective-GFET) showed a negative shift upon UV illumination, whereas the device showed a positive shift under visible light illumination, along with the change in the photocurrent. The defective-GFET device showed a high photoresponsivity of 37 mA W(-1) under visible light, that is ∼3 times higher than that of the pristine graphene device. Photoinduced molecular desorption causes the UV light responsivity to 18 mA W(-1). This study shows that the tunable photodetector with high responsivity is feasible by introducing an artificial defect on graphene surface.

In this study, we developed an innovative, flexible, organic-inorganic hybrid composite nanogenerator, which was used to drive a self-powered microwire-based pH sensor. The hybrid composite nanogenerator was fabricated using ZnO nanowire and piezoelectric polymer poly(vinylidene fluoride), through a simple, inexpensive solution-casting technique. The fabricated hybrid composite nanogenerator delivered a maximum open-circuit voltage of 6.9 V and a short-circuit current of 0.96 μA, with an output power of 6.624 μW under uniaxial compression. This high-performance, electric poling free composite nanogenerator opens up the possibility of industrial-scale fabrication. The hybrid nanogenerator demonstrated its ability to drive five green LEDs simultaneously, without using an energy-storage device. Additionally, we constructed a self-powered pH sensor, using a ZnO microwire powered with our hybrid nanogenerator. The output voltage varied according to changes in the pH level. This study demonstrates the feasibility of using a hybrid nanogenerator as a self-powered device that can be extended for use as a biosensor for environmental monitoring and/or as a smart, wearable, vibration sensor in future applications.

We report the electronic characteristics of an avant-garde graphene-field-effect transistor (G-FETs) based on ZnO microwire as top-gate electrode with self-induced dielectric layer. Surface-adsorbed oxygen is wrapped up the ZnO microwire to provide high electrostatic gate-channel capacitance. This nonconventional device structure yields an on-current of 175 μA, on/off current ratio of 55, and a device mobility exceeding 1630 cm(2)/(V s) for holes and 1240 cm(2)/(V s) for electrons at room temperature. Self-induced gate dielectric process prevents G-FETs from impurity doping and defect formation in graphene lattice and facilitates the lithographic process. Performance degradation of G-FETs can be overcome by this avant-garde device structure.