Capacitance Values Research Articles

Fabrication of cerium vanadate-embedded on carbon based graphene material (rGO) with significant performance for supercapacitor electrode

This work examined the electrochemical properties of CeVO3 nanocomposite that were enhanced with reduced graphene oxide (rGO) and CeVO3 nanoparticles. The CeVO3/rGO fabricated using a typical hydrothermal process that was further characterized via XRD revealed the monoclinic crystalline structure of the CeVO3 nanoparticles. The presence of uniformly distributed particles structured CeVO3 and layer-structured (rGO) reduced graphene oxide in the nanocomposite materials was determined using scanning electron microscopy pictures. We evaluated the electro-chemical efficiency of the nanocrystals for enhanced working electrodes and supercapacitors with cerium vanadate (CeVO3) nanoparticles and the cerium vanadate (CeVO3) embedded on reduced graphene oxide (rGO). The analysis was conducted on 2.0 M aqueous KOH (potassium hydroxide) electrolytic solution and it achieved the capacitance of 355.46 F g−1 (10 mVs−1) was concluded by cyclic voltammetry analysis of the working electrode modified with pure CeVO3 nanomaterial. The addition of rGO improved the value of Cs to 947.30 F g−1 at the same scan speed (10 mVs−1). The CeVO3 nanoparticles and CeVO3/rGO nanocomposite exhibited the capacitance values of 698.54 F g−1 and 1403.35 F g−1 at 1 A g−1 respectively, as determined by GCD analysis. The fabricated with CeVO3 nanoparticles exhibited power density values of 254.1 W kg−1 and energy values of 25.05 W h kg−1. On the other hand, the CeVO3/rGO nanocomposite showed greater energy (Ed) and power (Pd) density of 54.72 W h kg−1 and 264.95 W kg−1, individually. After undergoing 5000th cycles, the material utilizing CeVO3/rGO composite maintained its stability. The electrochemical examination of the synthesized cerium vanadate nanoparticles revealed that the inclusion of rGO resulted in a hybrid capacitive nature and the proposed nanocomposite can be employed as supercapacitors or as electrodes in batteries as well as energy storage and generating device for future use.

Size polydisperse model ionic liquid under confinement: A molecular dynamics study

The performance of an electric double-layer capacitor is strongly influenced by the choice of electrolyte, and the use of ionic liquid (IL) mixtures as an electrolyte has shown great promise. In this study, a model IL made of a mixture of anions and size-polydisperse cations in equal numbers and confined between two electrodes is investigated by means of molecular dynamics simulations. In particular, using the extent of size-polydispersity (characterized by polydispersity index, δ) as a control parameter, we systematically explore its effect on the local structure, charge profile, ion size distribution in the vicinity of electrode surfaces, and differential capacitance. It is observed that the charge density profiles near cathode, i.e., region comprising both Stern and diffused layers, are significantly affected under the variation of δ in addition to the electrode charge density. Ion population, ordering of different-size cations, and its effective size in the vicinity of electrodes under neutral and applied potential conditions are also quantified. An interesting observation is that the effective cation size in the Stern layer decreases with increasing value of δ in the case of moderate to strong electrode surface charge density. This behaviour can be qualitatively understood from the interplay of enthalpic and entropic forces in the system. Finally, a non-monotomic dependence of capacitance on δ is observed with maximum value of capacitance at a rather small value of δ(≈3%) for the model system.

Direct Measurement of the Differential Capacitance of Deep Eutectic Solvents on Platinum and Glassy Carbon Electrodes.

Differential capacitance is a crucial parameter that connects the experimental observation of electrical double-layer behavior with theoretical models. However, the current number of reported differential capacitance values for deep eutectic solvents remains limited, making it challenging to verify or refute existing models. In this study, we systematically investigate the differential capacitance in deep eutectic solvents using chronoamperometry. By comparing metal and glassy carbon electrodes across various liquid combinations and ion concentrations, we observed a range of distinct capacitance characteristics. While some findings align with the existing mean-field model for ionic liquids, others clearly reflect the influence of electrode materials, with certain cases resisting full explanation by current theoretical models. These results underscore the importance of selecting appropriate electrode materials in experimental studies of such electrolytes and highlight the need for further theoretical advancements in understanding this complex liquid system.

High rate capability and ultra‐long cycling life: Electrochemical synthesis of PEDOT based electrode material doped with AMPS and its supercapacitor application

AbstractPoly(3,4‐ethylene dioxythiophene) (PEDOT) is a conducting polymer that can be used in flexible bioelectronic devices. The electrode/electrolyte interface interaction is one of the most important factors in improving the electrochemical performance of energy storage materials, and these polymers are often combined with a negatively charged poly(styrene sulfonate) (PSS) chain to improve their interaction with alkali metal cations such as sodium and potassium. In this work, we performed a one‐step electrochemical synthesis of PEDOT on carbon fabric using the molecule 2‐acrylamido‐2‐methyl‐1‐propane sulfonic acid (AMPS) to create highly effective materials for supercapacitor electrodes. The electrode had a significant increase in capacitance value, measured 16.4 times higher than that of the PEDOT electrode. The 2‐electrode system exhibited a specific capacitance value of 495.2 F g−1 at a scan rate of 5 mV s−1. It exhibited a high operating voltage of 2.3 V in aqueous electrolyte system. It showed a significant energy density of 109.0 Wh kg−1 when operating at 6.1 kW kg−1 power density and 85.2 Wh kg−1 when operating at 30.6 kW kg−1 power density. Recent findings reveal that the capacitance retention performance value of the device increased significantly to 113.9% after 25,000 cycles in 3.0 M NaCl aqueous electrolyte, demonstrating its outstanding long‐term durability. Thus, the creation of the synthesized supercapacitor electrode is a significant advance in the study of conducting polymers, which often have a limited lifetime in real‐world electronic applications.

Impact of passivation on GaS nanoflakes: A study on stability, electronic, spectroscopy, and photocatalytic properties

This study uses first-principle calculations to investigate the properties of pristine and passivated gallium sulfide nanoflakes. Passivation significantly enhances stability, with fluorinated nanoflakes being the most stable and pristine nanoflakes the least stable, having formation energies of −0.058 eV/atom and −0.009 eV/atom, respectively. The pristine and passivated nanoflakes show semiconducting band gap, which lies in a visible region. Hydrogenated nanoflakes exhibit the largest band gap of 3.62 eV, making them highly suitable for photocatalysis, while fluorine and chlorine passivation result in band gaps of 3.16 eV and 3.01 eV. Scanning tunneling microscopy reveals distinct topographical features for each passivated nanoflake, affecting their electronic properties, including negative differential conductance, making it suitable for advanced switching devices and sensors. The quantum capacitance value of 815 µF/cm2 for chlorinated nanoflakes suggests that passivated nanoflakes could be beneficial for supercapacitor applications. Spectroscopic studies show that passivation changes the infrared spectrum and moves absorption spectra from the ultraviolet to the visible range. The hydrogenated nanoflakes are found ideal for water splitting, and adjusting the pH can further optimize its photocatalytic performance. These findings highlight the potential of passivated nanoflakes in photovoltaics, biomedical imaging, photocatalysis, and advanced technological devices.

Tailoring novel glycerol-potassium iodide deep eutectic solvents: A comprehensive investigation of physical, structural, and electrochemical properties

A novel Deep Eutectic Solvent (DES) can be formed between glycerol (Gly) and potassium iodide (KI). This study presents a comprehensive physicochemical characterization of these designed DES. The DES compositions, DES-Gly-KI and DES-Gly-KI-EtOH, consist of a hydrogen bond donor (Gly), a hydrogen bond acceptor (KI), and a viscosity-reducing solvent (ethanol (EtOH)). Experimental methodologies, including UV–VIS spectroscopy, mass spectrometry, Fourier transform infrared spectroscopy, and rheological studies such as density and viscosity, are employed to elucidate molecular interactions and structural characteristics. Karl Fischer titration is also conducted to analyze the moisture content in this prepared DES systems. The electrochemical performance of supercapacitors is also analyzed using cyclic voltammetry and electrochemical impedance spectroscopy. The specific capacitance values are found to be 10.32 F/g and 19.18 F/g for DES-Gly-KI and DES-Gly-KI-EtOH-5, respectively. The findings contribute in understanding DES behaviour, reveal distinctive physicochemical attributes, offering valuable insights into crafting and optimizing novel DESs, which is customized to meet distinct industrial requirements.

Passivation of the positive electrode during the discharge of Li-O2 and O2-assisted Li-CO2 batteries: A comparative study

The effect of passivation of the positive electrode by solid products under discharge is assessed for the first time as one of the factors determining the discharge characteristics of Li-O2 (LOB) and oxygen-assisted Li-CO2 (LCOB) batteries. In order to estimate the passivation, the electrode surface coverage θ by the reaction product (Li2O2 or Li2CO3) is determined on the basis of a decrease in the double-layer capacitance value in the course of the discharge. It is shown that for a given amount of electricity, the electrode surface coverage by Li2CO3 in LCOB is 1.5–2 times that of the coverage by Li2O2 under discharge in LOB. Furthermore, for each of the batteries, achievement of the maximum discharge capacity does not result in the full electrode surface blocking by the discharge products. LCOB manifests higher discharge characteristics than LOB under the kinetic reaction control (in the 100–500 mA g−1 current density range), owing to the accelerated conversion of intermediates and slower solid reaction product deposition on a larger electrode surface area. As the current density increases from 500 to 2000 mA g−1, the discharge capacity of LOB and LCOB decreases, which is mainly due to the effect of diffusion limitations. Moreover, while in the case of LOB the parameter θ decreases, in the case of LCOB it is practically independent of the current density in the studied range. The latter effect may be due to increased passivating properties of Li2CO3 deposits formed under high current density. The results of the work allow considering θ as a new criterion for estimation of the discharge depth and for predicting the characteristics of LCOB and LOB.

Charge storage mechanism and pseudocapacitance performance of NiO and Ce-doped NiO synthesized via modified combustion technique

Supercapacitors, as promising energy storage devices, have gained significant attention due to their ability to deliver high power and efficient charge storage mechanisms. In this work, we report the synthesis and electrochemical characterization of pristine NiO and Ni1-xCexO (x = 0.01, 0.02, 0.03) nanoparticles using a single-step auto ignition combustion method. Preliminary investigations indicate that Ni1-xCexO (x = 0.02) nanoparticles (2 % Ce doping) exhibit superior specific capacitance compared to other compositions. Therefore, we focused on structural, morphological, and vibrational studies on pristine and 2 % Ce-doped NiO. XPS and BET techniques were explored to assess the electronic state and porosity of the samples. Subsequent electrochemical performance evaluations included Cyclic Voltammetry (CV) at various scan rates, Galvanostatic Charge-Discharge (GCD), and Electrochemical Impedance Spectroscopic (EIS) techniques. From CV at a scan rate of 5 mVs−1, specific capacitance values of 419 Fg-1 and 604 Fg-1 were obtained for pristine and 2 % Ce-doped NiO, respectively. GCD studies revealed a specific capacitance of 381 Fg-1 for 2 % Ce-doped NiO at a current density of 1 Ag-1 and demonstrated capacitance retention of 95.1 % over 3000 GCD cycles for a current density of 4 Ag-1. The symmetric two-electrode supercapacitor cell demonstrates exceptional electrochemical performance, exhibiting a high specific capacitance of 122 Fg-1, an impressive energy density of 8.17 WhKg−1, a power density of 700 WKg-1 at 1 Ag-1, and a remarkable 88 % capacitance retention after 5000 GCD cycles. DFT calculations suggest that Ce doping significantly alters pristine NiO's electronic and structural features due to lattice strain. Our work highlights the enhanced electrochemical performance of 2 % Ce-doped NiO and its potential as a good-quality supercapacitor material.

Hybrid Powder‐Based Additive Manufacturing of Laser‐Induced Graphene 3D Architectures with Tunable Porous Microstructures from Waste Sources of Black Liquor and White Pollution

AbstractMacroscopic 3D‐controllable graphene (3D‐CG) architectures not only retain the intrinsic properties of graphene sheets but also exhibit structural advantages for pollutant adsorption and energy storage. This paper proposes a novel hybrid powder‐based additive manufacturing method to fabricate 3D biomass‐derived laser‐induced graphene (3D B‐LIG) structures with customizable geometries and microporous features. This method utilizes two waste sources as feedstock precursors for sustainable graphene production: “black liquor” (sodium lignosulfonate, NaLS) and “white pollution” (polypropylene, PP). Employing a computer‐aided design process, this method allows for the synchronous creation of various freeform macrostructures, with either identical or variable sections. To optimize the formability and processing efficiency of 3D B‐LIG, systematic studies have been conducted. These studies establish the relationship between processing parameters and the resulting structures by controlling the laser parameters and the mixing ratio of NaLS and PP. By leveraging tunable microporous structures with a maximized specific surface area of 485.3 m2 g−1, 3D B‐LIG demonstrates exceptional performance in pollutant adsorption (with a maximum adsorption capacity of 283.3 mg g−1 for methylene blue) and energy storage (with a gravimetric specific capacitance value of 194.9 F g−1).

Superior performance of asymmetric supercapacitor based on Cu doped bismuth ferrite electrode

Electrochemical energy storage devices, like supercapacitors and batteries, are needed to meet the constantly increasing demands of portable energy devices. Many types of supercapacitor electrodes were synthesized and reported which include carbon-based materials, polymers, oxides and perovskites. In this work, we report on the fabrication of Cu doped bismuth ferrite (Cu-BiFeO3, Cu-BFO) nanoparticles via sol-gel procedure. In most of the doping cases the costly rare earth elements like La, Nd, Sm, Ce and Yb are used to replace Bi. Electrodes of Bi1-xCuxFeO3 where x have the values 0.0, 0.025, 0.05, 0.075, 0.1 and 0.15 were deposited on graphitic sheets. Optimum Cu doping value was found to be at x = 0.05. Cu2+ ions doping in place of Bi3+ ions will reveal the roles of oxygen vacancies, as determined from XPS. The estimated values of specific capacitance was found to be 732 F/g at 0.5 A/g for the electrode at x = 0.05 in three electrode system. 5%Cu-BFO//Carbon black asymmetric supercapacitor (ASC) device can be charged and discharged reversibly at cell voltage of 0.0 up to 1.5 V when using a 0.5 M Na2SO4 aqueous electrolyte. This configuration allows the ASC device to deliver a great energy density of 37.25 Wh/kg at a power density of 752 W/kg. The ASC device demonstrates excellent cycling stability, retaining 88.64 % of its initial specific capacitance after 5000 cycles. Increasing the Cu content up to 15 % causes instability in the crystal structure of BFO resulting on phase segregation into Bi2Fe4O9 along with BFO and deterioration in the electrode overall performance. XPS showed that replacement of Cu2+ in place of Bi3+ disturbs the neutrality and the chemical environment of the compound. Hence to achieve neutrality and ionic balance, oxygen vacancies increase and the Fe2+/Fe3+ ratio increases as well. Both oxygen vacancies and the change in the Fe ions ratio reduce electrochemical impedance and give rise to charge density. The homogenous distribution of the pores at x = 0.05 contributed greatly to its fast electrolyte ion diffusion that improved the observed capacitive properties. One has to mention here, that despite doping that contains ions with different ionic size and/or different oxidation state is unfavorable, to some extent, due to the changes they produce in the electronic structure and the chemical environment, nevertheless it is sometimes beneficial in creating new parameters in the structure that promote specific application like in the case of the current work, oxygen vacancies, increase in surface area and the mixed state valency.

Moisture-Stable CsSnBr2Cl Halide Perovskite: Electrochemical Insights in Aqueous Environments.

In this investigation, moisture-stable CsSnBr2Cl nanoparticles were synthesized by incorporating Cl into CsSnBr3 halide perovskite using the hot injection method. Various analyses including XRD, XPS, UV-vis absorbance, photoluminescence, and Mott-Schottky have confirmed that the structural properties, chemical states, optical properties, and electronic band structure of CsSnBr2Cl nanoparticles remain intact even after 75 days of water immersion, thereby conclusively demonstrating their moisture stability. In a three-electrode system, the comparative electrochemical performance of pristine CsSnBr3 nanoparticles and moisture-stable Cl-incorporated CsSnBr2Cl nanoparticles was evaluated in various aqueous electrolytes, including HCl, Na2SO4, and KOH. The results indicate that the CsSnBr2Cl electrode material exhibits superior electrochemical properties, such as a larger integrated cyclic voltammetry (CV) area, a wider potential window, longer charge-discharge times, and lower impedance parameters compared to the pristine CsSnBr3 nanoparticles. The electrochemical performance of CsSnBr2Cl nanoparticles was evaluated for potential applications in batteries, supercapacitors, fuel cells, and water splitting, with a focus on reaction kinetics, charge storage mechanisms, and impedance parameters. The electrochemical properties of the nanoparticles were assessed using a three-electrode configuration across various 0.5 M aqueous electrolytes (HCl, Na2SO4, and KOH). In HCl, the nanoparticles demonstrated impressive charge storage capability, achieving a capacitance of 474 F g-1 at 1 A g-1, affirming their suitability for energy storage devices. In Na2SO4(aq.), the nanoparticles exhibited excellent stability for supercapacitors, operating up to 1.6 V without significant oxygen evolution. Notably, in KOH, they demonstrated potential as effective water-splitting electrodes. The practical applicability of the nanoparticles was evaluated using a symmetric two-electrode configuration with HCl and Na2SO4 electrolytes. The capacitance values were 117 F g-1 in HCl and 70 F g-1 in Na2SO4 at 1 A g-1. Notably, after 5000 GCD cycles in HCl(aq.), the nanoparticles retained 93% of their capacitance and maintained 91% Coulombic efficiency. They also demonstrated stable operation across a temperature range of 3 to 60 °C, achieving an energy density of 5.83 W h kg-1 at a power density of 600 W kg-1. This study emphasizes the considerable potential of CsSnBr2Cl nanoparticles in advancing electrochemical energy storage technologies and sets a solid foundation for future research and development in metal halide perovskites.

Synergistic Enhancements of Zn-ZIF with Nano Zinc Oxide for Hydrogen adsorption, energy storage, and photocatalytic technologies

Creating the porous Zinc-Zeolitic Imidazolate Framework (Zn-ZIF) using a solvothermal technique addresses the need for advanced materials with distinctive properties and cost-effectiveness in modern applications. The PXRD, SEM, UV-DRS, TEM, and TGA/DTG are used to characterize different concentrations of Zn-ZIF. Zn-ZIF's crystalline structure and phase purity have been verified by PXRD. Using diffuse reflectance spectra, the Kubelka-Monk function determined the band gaps of the Zn-ZIF samples, and scanning electron microscopy revealed a more porous structure. At 77 K and 1 bar, the Zn-ZIF solution with a 2:1 ratio had the highest hydrogen storage capacity (1.71 wt%). The electrochemical behavior of several Zn-ZIF electrodes in a 6 M KOH electrolyte was evaluated by cyclic voltammetry (CV) and electrochemical impedance spectroscopy (EIS) experiments. The Zn-ZIF electrode with a 2:1 ratio exhibits a low charge transfer resistance and a high proton diffusion coefficient (D) of 1.687 × 10−4 cm2 s−1. The characteristics of the 2:1 synthesized Zn-ZIF electrode as a supercapacitor were investigated. Our analysis of the generated Zn-ZIF material's specific capacitance values after 2000 cycles revealed an impressive retention rate of nearly 89 %, with values of 296.6 Fg-1. In addition, we examined the photocatalytic activities of the as-synthesized material by exposing it to ultraviolet light and seeing how it degraded organic dyes such as Cango-Red (CR) dye. With a photocatalytic efficacy of 95.06 % for CR dye, Zn-ZIF (2:1 ratio) is the most effective. These findings should provide new knowledge for researchers interested in developing novel Zn-ZIF materials for photocatalytic, energy storage, and hydrogen storage applications.

α-Bi2O3 tubular rods coated on Bi2O2CO3 nanosheets for high-performance asymmetric supercapacitor applications

Mixed phases of bismuth oxide nanostructures as an active electrode material in supercapacitor applications have recently gained huge research interest. In this study, the layered Bi2O2CO3 nanosheets and the secondary phase of α-Bi2O3 tubular rods named Bi2O2CO3/α-Bi2O3 heterostructure have been synthesized and utilized for supercapacitor applications. The crystal nature and microstructure of the Bi2O2CO3/α-Bi2O3 heterostructure were initially confirmed by powder X-ray diffraction (p-XRD), Raman, UV-Vis diffuse reflectance spectroscopy (UV-DRS, absorbance), scanning electron microscopy (SEM), and transmission electron microscopy (TEM) studies. X-ray photoelectron spectroscopy (XPS) measurements have investigated the oxidation states and chemical binding energies. Regarding the electrochemical performances, the Bi2O2CO3/α-Bi2O3 heterostructure as electro-active material delivered a maximum specific capacitance (Cs) value of 635 F g−1 at the given current density value of 1 A g−1 in a conventional three-electrode mode. A coin cell type electrode has been fabricated using Bi2O2CO3/α-Bi2O3 heterostructure, resulting in an asymmetric supercapacitor device cell (ASC), which has a Cs of 112 F g− 1 (at 1 A g− 1) and a power density and energy density values of 515 W kg−1 and 22.5 Wh kg−1 respectively. The two supercapacitor electrodes in sequence effectively ignite the red-light-emitting diode (LED). Moreover, in the ASC type Bi2O2CO3 /α-Bi2O3 heterostructure, the specific capacitance value was slightly reduced to 12.3 % by 2000 cycles, showing favourable cyclic performance and stability during the electrochemical process. Based on the above-mentioned characterization, the appropriate electrochemical performances of Bi2O2CO3/α-Bi2O3 tubular rod heterostructures make them a promising candidate for future energy storage devices.

Induction Coil Design Considerations for High-Frequency Domestic Cooktops

The use of wide band gap (WBG) semiconductor switches in power converters is increasing day by day due to their superior chemical and physical properties, such as electrical field strength, drift speed, and thermal conductivity. These new-generation power switches offer advantages over traditional induction cooker systems, such as fast and environmentally friendly heating. The size of passive components can be reduced, and the decreasing inductance value of induction coils and capacitors with low ESR (equivalent series resistance) values contributes to total efficiency. Other design parameters, such as passive components with lower values, heatsinks with low volumes, cooling fans with low power, and induction coils with fewer turns, can offset the cost of WBG power devices. High-frequency operation can also be effective in heating non-ferromagnetic materials like aluminum and copper, making them suitable for heating these types of pans without complex induction coil and power converter designs. However, the use of these new generation power switches necessitates a re-examination of induction coil design. High switching frequency leads to a high resonance frequency in the power converter, which requires lower-value passive components compared to conventional cookers. The most important component is the induction coil, which requires fewer turns and magnetic cores. This study examines the induction heating equivalent circuit, discusses the general structure and design parameters of the induction coil, and performs FEM (finite element method) analyses using Ansys Maxwell. The results show that the induction coil inductance value in new-generation cookers decreases by 80% compared to traditional cookers, and the number of windings and magnetic cores decreases by 50%. These analyses, performed for high-power applications, are also performed for low-power applications. While the inductance value of the induction coil is 90 μH at low frequencies, it is reduced to the range of 5 μH to 20 μH at high frequencies. The number of windings is reduced by half or a quarter. The new-generation cooker system experimentally verifies the coil design based on the parameters derived from the analysis.

Bimetallic ions modified 2‐methylimidazolium functionalized polypyrrole/graphene oxide for the improved supercapacitor

AbstractThin films with two‐dimensional (2D) nanostructures possess good environmental stability, thinner thickness and large surface area, which are widely used as a promising modified electrode material in the field of energy storage, supercapacitors, electrochemical sensors and biosensors. Herein, unique bimetallic ions modified polypyrrole/graphene oxide (PPy/GO) nanosheets, including Co2+‐Zr4+/(2‐MeIm)x@PPy/GO and Co2+‐Run+/(2‐MeIm)x@PPy/GO (n = 0, 4), are prepared by using 2‐methylimidazolium (2‐MeIm) as the linkers between PPy/GO and metal ions. The obtained electrodes constructed by Co2+‐Run+/(2‐MeIm)x@PPy/GO (n = 0, 4) and Co2+‐Zr4+/(2‐MeIm)x@PPy/GO exhibit improved capacitor electrochemical properties due to the reversible redox reaction, the large specific surface area and the high theoretical specific capacitance value of the metal ions compared to the unmodified PPy/GO. Especially, the specific capacitance value of Co2+‐Run+/(2‐MeIm)x@PPy/GO (n = 0, 4) electrode reaches 321.78 F g−1 at a current density of 1 A g−1 and the capacitance retention rate is achieved to 100% in the long cycle charge/discharge test after 10 000 cycles (10 A g−1). It will provide a practical experience for the design and preparation of supercapacitors based on bimetallic ions modified PPy/GO.

Co-precipitation Synthesis and Characterization Studies of Manganese Oxide Doped with Nickel for High-Performance Energy Storage Supercapacitor Application

The advancement in nanotechnology research has facilitated the development of eco-friendly methods for the synthesis of nanoparticles. In this work, nickel (Ni)-doped manganese oxide was synthesized using the co-precipitation method. The prepared Ni-doped manganese oxide products have been characterized by X-ray powder diffraction, scanning electron microscopy (SEM), transmission electron microscope (TEM), and energy dispersive X-ray spectroscopy (EDS). The preliminary electrochemical characteristics include charge-discharge cycling, which improves the conductivity and capacitance of the high-performance aqueous asymmetrical supercapacitor. The CV analysis of the Ni-doped manganese oxide electrode demonstrated a distinctive pseudocapacitive behavior in 1 M KOH solution. The nickel (Ni) doped electrode has a higher specific capacitance value than the pure manganese oxide electrode, with a value of 2225.07 F×g-1 at a scan rate of 5 mV×s-1. Keywords: Supercapacitor, Co-precipitation method, Nanotechnology, Synthesized, Electrochemical

Sandwich-structured electrospun polyvinylidene difluoride sensor for structural health monitoring of glass fiber reinforced polymer composites

Stress monitoring and interlaminar failure detection attract much attention in glass fiber reinforced polymer (GFRP) structural health monitoring area. However, due to limitations of sensing or electrode materials, existing embedding sensors cannot be designed to have both of the abilities without sacrificing mechanical properties. This work fabricated a sandwich-structured sensor, which is composed of three layers of electrospun polyvinylidene difluoride membranes. The upper and lower electrodes are flexible membranes that ensure stable signal collection in the rigid GFRP material system. The sensor can quantitatively monitor the stress based on piezoelectric effect, and interlaminar crack propagation based on parallel plate capacitors. The voltage and capacitance values have a linear relationship with the stress level and crack length (R-square of the functions is 0.999 and 0.933), respectively. Due to the porous microstructure of electrospun membranes, polymer matric can well infiltrate the polyvinylidene difluoride nanofibers while preparing the sensor embedded GFRP. Thus, the perfect bonding of the sensor within GFRP ensures the effective sensing abilities until sample failure and negligible effect (< -7%) on the mechanical properties of GFRP.

Tailoring the Coordination Microenvironment of Polymolybdate within a Metal-Organic Coordination System for Enhanced Capacitive Activity.

The design of a low-cost and efficient electrode material is crucial for electrochemical energy storage. Effectual utilization of polymolybdate as an electrode material for a supercapacitor is promising. Meanwhile, the coordination microenvironments of polymolybdate sho potential effects on its performance. Herein, we designed and synthesized four polymolybdate-based metal-organic complexes using a structure design strategy. Their structures were characterized and analyzed using single crystallographic data. The theoretical calculations revealed that the coordination microenvironments of polymolybdate play a vital role in the hydrogen ions migration. High H adsorption capacity can obviously boost the electrochemical activity. The 1-based glassy carbon electrode showed the highest specific capacitance value of 1739.4 F·g-1 at the current density of 1 A·g-1. Meanwhile, the carbon cloth-based electrode fabricated by complex 1 (1/CC) also displayed a high capacitance performance. A hybrid supercapacitor was assembled using the 1/CC electrodes and showed a high energy density of 29.0 Wh kg-1 at the power density of 0.80 kW kg-1.

Development of a Capacitive Pressure Sensor Based on Nanoporous Anodic Aluminium Oxide

Capacitive pressure sensors make pressure sensing technology more accessible to a wider range of applications and industries, including consumer electronics, automotive, healthcare etc. However, developing a capacitive pressure sensor with brilliant performance using a lowcost technique remains a difficulty. In this work, the development of a capacitive pressure sensor based on nanoporous AAO fabricated by a two-step anodization approach which offers a promising solution for precise pressure measurement is fabricated by a two-step anodization approach. A parallel plate capacitive sensor was fabricated by placing two AAO deposited sheets are placed face to face, with the non-anodized aluminum component at the base functioning as the top and bottom electrodes. A variation in the capacitance value of the as fabricated sensor was observed over an applied pressure range (100 Pa-100 kPa). This change in capacitance can be attributed to the decrease in the distance between the two plates and the non-homogenous distribution of contact stress and strain due to the presence of nanoporous AAO structure. In this pressure range the sensor showed high sensitivity, short response time and excellent repeatability which indicates a promising future of the fabricated sensor in consumer electronics, intelligent robotics etc.

WO3 Nanoparticle/Biomass Derived N‐Doped Activated Carbon Decorated with Polyaniline Nanofibers Ternary Nanocomposite for High‐Performance Symmetric and Asymmetric Supercapacitor

AbstractSupercapacitors have captured the curiosity of researchers due to their extremely high energy storage capacity. Hybrid supercapacitors deliver high specific capacitance values compared to the exciting (electrical double layer capacitor) EDLC and pseudocapacitors. This work presents a simple and scalable synthetic method to design a hybrid ternary composite as electrode material. In this work, the combination of EDLC‐type behaviour material, i. e., sustainable biomass‐derived Nitrogen‐doped activated carbon (NAC) and pseudocapacitive behaviour electrode materials, i. e., metal oxides (tungsten oxide) and conductive polymer (polyaniline) are selected to achieve a high gravimetric capacity. The PANi/WO3/NAC (PWNAC) ternary composite is tested for symmetric and asymmetric supercapacitor (ASC). In a symmetric capacitor, PWNAC acts as both the positive and negative electrode, whereas in ASC, PWNAC acts as the positive electrode and NAC as the negative electrode. It is observed that the ASC shows a better capacitance value than symmetric. ASC operates at a potential range of 1.4 V in 1 M H2SO4 aqueous electrolyte, shows a maximum capacitance of 608.2 F/g at 0.5 A/g, and has long capacitance retention of 98.32 % of its initial capacitance after 2000 charge‐discharge cycles.