LiMn2O4 Li-ion hybrid supercapacitors processed by nitrogen atmospheric-pressure plasma jet

LiCl–Mn(NO₃)₂·4H₂O pastes were screen-printed on a carbon cloth substrate and furnace-calcined to convert them into LiMn₂O₄. The LiMn₂O₄ electrode was then post-processed using a nitrogen atmospheric-pressure plasma jet (APPJ). APPJ processing created oxygen vacancy defects on the electrode surface. Electrochemical tests of the Li-ion hybrid supercapacitors (Li–HSCs) were performed by cyclic voltammetry (CV) and galvanostatic charging/discharging (GCD) in 1-M Li₂SO₄ aqueous solution. The results indicate that proper APPJ treatment optimizes the Li–HSCs performance, whereas excessive APPJ treatment may cause material damage. After 3-min APPJ treatment at 620 °C, the Li–HSCs exhibited a maximum areal capacitance of 87.96 mF/cm² with capacitance retention of 124.8% after a 1000-cycle CV test.     

Electrochemical behavior of CuO/rGO nanopellets for flexible supercapacitor,non-enzymatic glucose,and H2O2 sensing application

In the present article, graphene oxide (GO) sheets and monoclinic copper oxide (CuO) nanocrystals are connected with each other and result in the formation of CuO/rGO nanopellets, and these nanopellets synthesized using coprecipitation method. The nanopellet structured CuO/rGO composite on carbon cloth, which act as current collector exhibits specific capacitance of 188 F g^?1 at a current density of 0.2 A g^?1 and up to 96.3% capacity retention after 2000 charge-discharge cycles. It shows a maximum energy density of 7.32 Wh kg^?1 and power density of 53 W kg^?1. The glucose sensing characteristics of CuO/rGO nanopellet is investigated on carbon cloth and ITO substrate. It shows glucose sensitivity of 0.805 mA mM^?1 cm^?2 and 0.2982 mA mM^?1 cm^?2 for a bundle like structured CuO/rGO composite on carbon cloth and ITO substrate, respectively. Further H₂O₂ sensing is studied on ITO substrate, which manifests H₂O₂ sensitivity of 84.39 μA mM^?1 cm^?2. The results indicate that nanopellet structured CuO/rGO composite could be a promising electrode material for supercapacitor, glucose, and H₂O₂ sensor.     

Effect of electrolyte on the supercapacitive behaviour of copper oxide/reduced graphene oxide nanocomposite

Cupric oxide/reduced graphene oxide (CuO/rGO) nanocomposites were synthesized through a chemical reduction method using hydrazine hydrate as the reducing agent. The morphology, elemental composition, and bonding network of the CuO/rGOnanocomposites were characterized by scanning electron microscopy (SEM), X-ray diffraction (XRD), Fourier transform infrared (FTIR) spectroscopy, X-ray photoelectron spectroscopy (XPS) and Raman spectroscopy respectively. The XRD results reveal lattice spacing and lattice strain from 3.371 to 3.428 Å and 1.05 × 10⁻³to 5.44 × 10⁻³ respectively, with the increasing ratio of rGO: CuO from 1:1 to 1:5. The cyclic voltammetry (CV), electrochemical impedance spectroscopy (EIS)and galvanostatic charge-discharge (GCD) studyofCuO/rGOas the electrode material showed excellent super-capacitive behavior in H₂SO₄ over Na₂SO₄ electrolytes. Moreover CuO/rGO nanocomposites exhibited better capacitance retention in H₂SO₄(75.69%) compared to Na₂SO₄(12.06%).     

Microwave assisted synthesis of rGO/ZnO composites for non-enzymatic glucose sensing and supercapacitor applications

Zinc oxide (ZnO) and Graphene Oxide (GO) are known to show good electrochemical properties. In this paper, rGO/ZnO nanocomposites have been synthesised using a simple microwave assisted method. The nanocomposites are characterized using XRD, Raman, SEM and TEM. XRD reveals the wurtzite structure of ZnO and TEM shows the heterogeneous nucleation of ZnO nanocrystals anchored onto graphene sheets. The electrochemical properties of the rGO/ZnO nanocomposite enhanced significantly for applications in glucose sensors and supercapacitors. The non-enzymatic glucose sensor of this nanocomposite tested using cyclic voltammetry (CV) and chronoamperometry, exhibits high sensitivity (39.78 mA cm⁻² mM⁻¹) and a lower detection limit of 0.2 nM. The supercapacitor electrode of rGO/ZnO nanocomposite exhibits a significant increase in specific capacitance.     

Development of photo-anodes based on strontium doped zinc oxide-reduced graphene oxide nanocomposites for improving performance of dye-sensitized solar cells

The goal of this study was to create highly efficient dye-sensitized solar cells (DSSCs) using strontium doped zinc oxide-reduced graphene oxide (Sr-doped ZnO/rGO) nanocomposites. As photo-anodes of DSSCs, ZnO, ZnO/rGO (with weight percent rGO in composites: 0, 0.01, 0.1, 0.5, and 1 wt%) and Sr-doped ZnO/rGO (with Zn_1-xSr_xO nanoparticle stoichiometry: x = 0, 0.02, 0.04, 0.06 and 0.08) nanocomposites were designed and characterized. AFM, FESEM, XRD, EDS, XPS, PL, and FTIR analyses were used to investigate the morphology and structure properties of prepared nanocomposites. UV–vis spectroscopy and photo-electrochemical measurements were used to investigate the efficiency of prepared photo-anodes. The efficiency (η) and short-circuit photocurrent density (JSC) of DSSCs based on Zn_0.92Sr_0.08O/rGO nanocomposite were 7.98 % and 18.4 mA cm⁻², respectively. The results showed that doping Sr on ZnO/rGO nanocomposites resulted in a wide bandgap energy and increased the values of η, J_SC, IPCE, and photo-anode electron transportability. These findings suggest that Sr-doped ZnO/rGO nanocomposites can provide a novel approach for increasing photo-electrochemical activity in ZnO-based DSSCs.     

Hydrothermally synthesized microrods and microballs of NiCo2O4 for supercapacitor application

The microrods and microballs of NiCo₂O₄ are successfully synthesized by the hydrothermal method. The effect of ammonium hydroxide and ammonium fluoride on the surface microstructure is observed. The prepared microrods and microballs of NiCo₂O₄ are analyzed by various analytical tools like powder X-ray diffraction (PXRD), scanning electron microscopy (SEM), with energy dispersive X-ray spectroscopy (EDS), and X-ray photoelectron spectroscopy (XPS). The electrochemical properties are studied by using cyclic voltammetry (CV), galvanostatic charge discharge (GCD), and electrochemical impedance spectroscopy (EIS), using the workstation Biologic SP-200. The maximum specific capacitance of the NiCo₂O₄ microrods electrode is 1671 F/g. The areal specific capacitance of the NiCo₂O₄ microrods electrode is 284 mF/g. The energy density and power density of microrods of NiCo₂O₄ electrode are 19 Wh/Kg and 282 W/kg, respectively. The equivalent series resistance (Rs) is 0.62 Ω for NiCo₂O₄ microrods.     

Usefulness of a composite electrode with a carbon surface modified by electrosynthesized polypyrrole for supercapacitor applications

Thin polypyrrole (PPy) films (thickness = 5–10 nm) were electrochemically deposited in situ on a carbon paste (97% of graphite plus 3% of Teflon) by means of cyclic voltammetry (CV), from an acetonitrile solution of pyrrole (0.2 M) and NaClO₄ (0.1 M). The obtained PPy/graphite composite electrode was investigated by CV and chronopotentiometry in 0.3 M NaClO₄ aqueous electrolytic solution. The capacitance of a composite electrode, calculated by CV, was about 10 F g⁻¹. The capacitance value of the composite electrode was approximately nine times larger than that of pure graphite. The massic charge and discharge capacity (Q) values, calculated by chronopotentiometry, were considerably higher for the composite electrode—by more than 60 times—than for the pure graphite electrode. Electrochemical impedance spectroscopy (EIS) measurements, performed under stationary conditions, led to an interfacial capacitance value intermediate between that of pure graphite and that of the composite electrode.     

Decoration of carbon cloth by manganese oxides for flexible asymmetric supercapacitors

Here we describe the production of carbon cloth coated with MnO₂ nanosheets or MnOOH nanorods through a normal temperature reaction or a hydrothermal approach, respectively. Of note, the electrochemical performance of MnO₂-coated carbon cloth was better (429.2 F g⁻¹) than that of MnOOH-coated carbon cloth. When the MnO₂-coated carbon cloth is introduced as the positive electrode and the Fe₂O₃-coated carbon cloth as the negative electrode, a flexible asymmetric supercapacitor was obtained with an energy density of 22.8 Wh kg⁻¹ and a power density of 159.4 W kg⁻¹. Therefore, such a hierarchical MnO₂-coated carbon cloth nanocomposite is a promising high-performance electrode for flexible supercapacitors.     

NiFe-NiFe2O4/rGO composites: Controlled preparation and superior lithium storage properties

Binary transition-metal oxides with spinel structure have great potential as advanced anode materials for lithium-ion batteries (LIBs). Herein, NiFe-NiFe₂O₄/ reduced graphene oxide (rGO) composites are obtained via a facile cyanometallic framework precursor strategy to improve the lithium storage performance of NiFe₂O₄. In the composites, NiFe-NiFe₂O₄ nanoparticles with adjustable mass ratios of NiFe₂O₄ to NiFe alloy are homogeneously deposited on rGO sheets. As anode material for LIBs, the optimized NiFe-NiFe₂O₄/rGO composite displays remarkably enhanced lithium storage performance with an initial specific capacity as high as 1362 mAh g⁻¹ at 0.1 A g⁻¹ and a decent capacity retention of ca. 80% after 130 cycles. Besides, the composite delivers a reversible capacity of 550 mAh g⁻¹ at 1 A g⁻¹ after 300 cycles. During the charge–discharge cycles, the aggregation of the NiFe-NiFe₂O₄ nanoparticles and the structural collapse of the electrode can be well alleviated by rGO sheets. Moreover, the conductivity of the electrode can be significantly improved by the well-conductive NiFe alloy and rGO sheets. All these contribute to the improved lithium storage performance of NiFe-NiFe₂O₄/rGO composites.     

Bifunctional ternary manganese oxide/vanadium oxide/reduced graphene oxide as electrochromic asymmetric supercapacitor

A bifunctional ternary manganese oxide/vanadium oxide/reduced graphene oxide (MnO₂/V₂O₅/rGO) was developed for asymmetric electrochromic supercapacitor (EC-SC) application. The elemental mapping revealed uniformly distributed MnO₂, V₂O₅ and rGO, depicting homogenous synthesis of the hybrid composite. The phase composition, vibration modes and valance state of the ternary composite were analyzed via X-ray diffraction (XRD), Raman spectroscopy and X-ray photoelectron spectroscopy (XPS) analysis, respectively. Interestingly, the as-prepared MnO₂/V₂O₅/rGO composite disclosed tremendous C_sp of 1403.5 F/g, which was higher compared to MnO₂/V₂O₅ (801.1 F/g), V₂O₅ (613.1 F/g), MnO₂ (126.7 F/g) and rGO (60.7 F/g). MnO₂/V₂O₅/rGO that appeared in dark green switched its visual color to orange at the charged state, confirming the electrochromic property. The bifunctional manganese oxide/vanadium oxide/reduced graphene oxide//copper-based metal-organic framework/reduced graphene oxide (MnO₂/V₂O₅/rGO//MrGO) asymmetrical EC-SC device revealed outstanding cycling stability (90.3% charge retention over 5000 cycles), tremendous specific capacitance (652.7 F/g) and maximum specific energy (60.4 Wh/kg). MnO₂/V₂O₅/rGO//MrGO asymmetrical EC-SC device demonstrated reversible color changes from dark green to orange at the discharged and charged states, respectively. The significantly great electrochromic and supercapacitive performance revealed that MnO₂/V₂O₅/rGO//MrGO is an outstanding electroactive candidate for the next generation of electrochromic supercapacitors.     

Supercapacitive properties of composite electrodes consisting of polyaniline, carbon nanotube, and RuO2

Three types of composite supercapacitor electrodes were prepared; electroactive polyaniline (PANI), PANI/multi-walled carbon nanotube (CNT), and PANI/CNT/RuO₂. Specifically, the PANI and PANI/CNT were prepared by polymerization, and PANI/CNT/RuO₂ was prepared by electrochemical deposition of RuO₂ on the PANI/CNT matrix. Cyclic voltammetry between −0.2 and 0.8 V (vs. Ag/AgCl) at various scan rates was performed to investigate the supercapacitive properties in an electrolyte solution of 1.0 M H₂SO₄. The PANI/CNT/RuO₂ electrode showed the highest specific capacitance at all scan rates (e.g., 441 and 392 F g⁻¹ at 100 and 1,000 mV s⁻¹, respectively). In contrast, the PANI/CNT electrode demonstrated the best capacitance retention (66%) after 10⁴ cycles. Additional analysis including morphology and complex impedance spectroscopy suggested that with small loading of RuO₂, an increase in capacitance was observed, but dissolution and/or detachment of RuO₂ species from the electrode might occur during cycling to reduce the cycle performance.     

High-performance supercapacitor of manganese oxide/reduced graphene oxide nanocomposite coated on flexible carbon fiber paper

Although supercapacitors have higher power density than batteries, they are still limited by low energy density and low capacity retention. Here we report a high-performance supercapacitor electrode of manganese oxide/reduced graphene oxide nanocomposite coated on flexible carbon fiber paper (MnO₂–rGO/CFP). MnO₂–rGO nanocomposite was produced using a colloidal mixing of rGO nanosheets and 1.8 ± 0.2 nm MnO₂ nanoparticles. MnO₂–rGO nanocomposite was coated on CFP using a spray-coating technique. MnO₂–rGO/CFP exhibited ultrahigh specific capacitance and stability. The specific capacitance of MnO₂–rGO/CFP determined by a galvanostatic charge–discharge method at 0.1 A g⁻¹ is about 393 F g⁻¹, which is 1.6-, 2.2-, 2.5-, and 7.4-fold higher than those of MnO₂–GO/CFP, MnO₂/CFP, rGO/CFP, and GO/CFP, respectively. The capacity retention of MnO₂–rGO/CFP is over 98.5% of the original capacitance after 2000 cycles. This electrode has comparatively 6%, 11%, 13%, and 18% higher stability than MnO₂–GO/CFP, MnO₂/CFP, rGO/CFP, and GO/CFP, respectively. It is believed that the ultrahigh performance of MnO₂–rGO/CFP is possibly due to high conductivity of rGO, high active surface area of tiny MnO₂, and high porosity between each MnO₂–rGO nanosheet coated on porous CFP. An as-fabricated all-solid-state prototype MnO₂–rGO/CFP supercapacitor (2 × 14 cm) can spin up a 3 V motor for about 6 min.     

Solvothermal synthesis of SnO2/graphene nanocomposites for supercapacitor application

A facile solvent-based synthesis route based on the oxidation–reduction reaction between graphene oxide (GO) and SnCl₂·2H₂O has been developed to synthesize SnO₂/graphene (SnO₂/G) nanocomposites. The reduction of GO and the in situ formation of SnO₂ nanoparticles were achieved in one step. Characterization by X-ray diffraction (XRD), ultraviolet-visible (UV–vis) absorption spectroscopy, Raman spectroscopy, and field emission scanning electron microscopy (FESEM) confirmed the feasibility of using the solvothermally treated reaction system to simultaneously reduce GO and form SnO₂ nanoparticles with an average particle size of 10 nm. The electrochemical performance of SnO₂/graphene showed an excellent specific capacitance of 363.3 F/g, which was five-fold higher than that of the as-synthesized graphene (68.4 F/g). The contributing factors were the synergistic effects of the excellent conductivity of graphene and the nanosized SnO₂ particles.     

Synthesis of reduced graphene oxide/tungsten trioxide nanocomposite electrode for high electrochemical performance

A facile and well-controllable reduced graphene oxide/tungsten trioxide (rGO/WO₃) nanocomposite electrode was successfully synthesized via an electrostatic assembly route at 350 rpm for 24 h. In this study, hexagonal-phase WO₃ (h-WO₃) nanofiber was well distributed on rGO sheets by applying optimal processing parameters. The as-synthesized rGO/WO₃ nanocomposite electrode was compared with pure h-WO₃ electrode. A maximum specific capacitance of 85.7 F g⁻¹ at a current density of 0.7 A g⁻¹ was obtained for the rGO/WO₃ nanocomposite electrode, which showed better electrochemical performance than the WO₃ electrode. The incorporation of WO₃ into rGO could prevent the restacking of rGO and provide favourable surface adsorption sites for intercalation/de-intercalation reactions. The impedance studies demonstrated that the rGO/WO₃ nanocomposite electrode exhibited lower resistance because of the superior conductivity of rGO that improved ion diffusion into the electrode. To evaluate the contribution of WO₃ to the rGO/WO₃ nanocomposite, the influence of mass loading of WO₃ on the capacitance was investigated.     

Hierarchical 3D starfish-like Ni3S4–NiS on reduced graphene oxide for high-performance supercapacitors

In this research, Ni₃S₄–NiS with starfish morphology was synthesized with a simple hydrothermal method and then hybridized with reduced graphene oxide (rGO) as a material for high-performance supercapacitors. The crystal structure and morphology of the as-prepared materials were studied by X-ray diffraction spectroscopy and electron microscopy. Uniform distribution of Ni₃S₄–NiS on rGO was observed from electron microscopy images. The results showed that Ni₃S₄–NiS/rGO with a specific capacitance of 1578 Fg^-1 and discharge time of 603 s at the current density of 0.5 Ag^-1 has more capacity and stability relative to Ni₃S₄–NiS. The cyclic stability after 5000 cycles showed that the Ni₃S₄–NiS/rGO electrode is stable, and 91% of its corresponding initial capacitance retained at the end of 5000 cycles. The good results in capacitance and stability of this electrode can be regarded as an improvement for the development of highly efficient and economic supercapacitors for portable electronic devices.     

Electrochemical energy storage performance of heterostructured SnO2@MnO2 nanoflakes

In this work, we report synthesis of SnO₂@MnO₂ nanoflakes grown on nickel foam through a facile two-step hydrothermal route. The as-obtained products are characterized by series of techniques such as scanning electron microscopy (SEM), X-ray diffraction spectroscopy (XRD), transmission electron microscopy (TEM) and X-ray photoelectron spectroscopy (XPS). The as-obtained SnO₂@MnO₂ nanoflakes are directly used as supercapacitor electrode materials. The results show that the electrode possesses a high discharge areal capacitance of 1231.6 mF cm⁻² at 1 mA cm⁻² and benign cycling stability with 67.2% of initial areal capacitance retention when the current density is 10 mA cm⁻² after 6000 cycles. Moreover, the heterostructured electrode shows 41.1% retention of the initial capacitance when the current densities change from 1 to 10 mA cm⁻², which reveals good rate capability. SnO₂@MnO₂ nanoflakes products which possess excellent electrochemical properties might be used as potential electrode materials for supercapacitor applications.     

Synthesis of rGO/nanoclay/PVK nanocomposites,electrochemical performances of supercapacitors

ABSTRACT

In this study, graphene oxide (GO) was chemically reacted with sodium borohydride (NaBH₄) to form reduced graphene oxide (rGO). rGO, Montmorillonite nanoclay, and polyvinylcarbazole (PVK) were used to form a ternary nanocomposite via chemical reaction. These nanocomposite qualities were described via scanning electron microscopy (SEM), energy-dispersive X-ray analysis (EDX), Fourier transform infrared spectroscopy-attenuated transmission reflectance (FTIR-ATR). In addition, these materials were used in supercapacitor device as an active material to test electrochemical performances via cyclic voltammetry (CV), galvanostatic charge–discharge (GCD), and electrochemical impedance spectroscopy (EIS). The rGO/nanoclay/PVK nanocomposite shows significantly improved specific capacitance (C_sp = 168.64 Fg^?1) compared to that of rGO (C_sp = 63.26 Fg^?1) at the scan rate of 10 mVs^?1 by CV method. The enhanced capacitance results in high power density (P = 5522.6 Wkg^?1) and energy density (E = 28.84 Whkg^?1) capabilities of the rGO/nanoclay/PVK nanocomposite material. The addition of nanoclay and PVK increased the specific capacitance of rGO material due to a dopant effect for supercapacitor studies. Ragone plots were drawn to observe energy and power density of supercapacitor devices. The C_sp of rGO/nanoclay/PVK nanocomposite has only 86.4% of initial capacitance for charge/discharge performances obtained by CV method for 5000 cycles.     

Nanodiamond particles/reduced graphene oxide composites as efficient supercapacitor electrodes

The paper reports on the preparation of reduced graphene oxide (rGO) modified with nanodiamond particles composites by a simple solution phase and their use as efficient electrode in electrochemical supercapacitors. The technique relies on heating aqueous solutions of graphene oxide (GO) and nanodiamond particles (NDs) at different ratios at 100 °C for 48 h. The morphological properties, chemical composition and electrochemical behavior of the resulting rGO/NDs nanocomposites were investigated using UV/vis spectrometry, Fourier transform infrared (FTIR) spectroscopy, Raman spectroscopy, transmission electron microscopy (TEM) and electrochemical means. The electrochemical performance, including the capacitive behavior of the rGO/NDs composites were investigated by cyclic voltammetry and galvanostatic charge/discharge curves at 1 and 2 A g⁻¹ in 1 M H₂SO₄. The rGO/ND matrix with 10/1 ratio displayed the best performance with a specific capacitance of 186 ± 10 F g⁻¹ and excellent cycling stability.     

A highly selective carbon paste electrode enhanced by Cu-encapsulated poly(amidoamine) for the simultaneous detection of organic and inorganic contaminants

In this study, a copper/poly(amidoamine)/multi-walled carbon nanotube/reduced graphene oxide (Cu/PAMAM/MWCNT/rGO) complex was synthesized for fabricating an electrochemical sensor to simultaneously detect nitrate and nitrite ions as inorganic contaminants, and 4-chlorophenol (4-CP) and 1,2,5,8 tetrahydroxy anthraquinone (THA) as organic pollutants. The prepared Cu/PAMAM/MWCNT/rGO electrode was characterized using scanning electron microscopy (SEM), Fourier-transform infrared (FT-IR), X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS), and electrochemical impedance spectroscopy (EIS). Cyclic voltammetry (CV) was performed to investigate the influence of the pH of the solution, concentration of anions, and scan rate on the analytical performance of the electrodes. The simultaneous determination of nitrite/nitrate ions using a Cu/PAMAM/MWCNT/rGO electrode showed sensitivities of 8.030 × 10⁻³ and 5.370 × 10⁻³ μA μM⁻¹ mm⁻², and limits of detection (LODs) of 0.081 and 0.115 μM, respectively. For the simultaneous determination of 4-CP/THA, the sensitivities of the modified electrode were 0.0105 and 9.399 × 10⁻³ μA μM⁻¹ mm⁻², and detection limits were 0.062 and 0.070 μM respectively.     

Unique hierarchical mesoporous LaCrO3 perovskite oxides for highly efficient electrochemical energy storage applications

Following sol-gel route, hierarchical mesoporous nanostructures of lanthanum chromates (LaCrO₃) perovskite oxides are successfully synthesized for supercapacitor applications. The structural behaviors of nano perovskite oxides are investigated using X-rays diffraction, low and high resolution scanning and transmission electron microscopes, photoelectron X-ray spectroscopy, and Brunauer-Emmett-Teller (BET). The as-prepared LaCrO₃ powders is mingled with activated carbon and subsequently glazed on a flexible carbon cloth current collector (LCO@CC). The electrochemical capabilities of LCO@CC based electrode, such as: cyclic voltammetry, galvanostatic charge:discharge and electrochemical impedance spectroscopy are investigated in neutral M LiCl aqueous solutions. Moreover, the fabricated LCO@CC electrode achieves maximum capacitance of 1268 F/g at 2 A/g and retains excellent cyclic ability of 91.5% after 5000 charge:discharge cycles. The efficient electrochemical performances of carbon cloth decorated LaCrO₃ electrode are credited to dynamic charge storage mechanism by fast redox reaction of electrolyte-electrode interactions with extremely low charge transfer resistance.