Galvanostatic Charge-discharge Measurements Research Articles

Facile synthesis, enhanced annealing-structural investigation and supercapacitive potentials of NiFe2O4 spinel nanopowder

Herein, we examined and optimized the influence of annealing temperature on microstructural and electrochemical charge storage properties of spinel NiFe2O4 nanopowder synthesized from a simple one-pot sol-gel route. Microstructural techniques encompassing Raman spectroscopy, scanning electron microscopy, transmission electron microscopy, x-ray diffractometry, and Fourier transform infra-red spectroscopy indicate the resulting powder are composed of spinel NiFe2O4 nanoparticle with metal oxygen vibration, crystal properties and lattice strain, all dependent on annealing temperature. Electrochemical charge storage performance of the electrode fabricated from the synthesized material were investigated with the aid of cyclic voltammetry, galvanostatic charge-discharge and electrochemical impedance spectroscopy measurements. The obtained results showed that the charge storage performance and rate capability of NiFe2O4 electrode is dependent on the annealing temperature. The study also showed that the electrode from the material annealed at 400 °C demonstrated optimum electrochemical charge storage performance having exhibited optimum specific capacitance and capacity values of 1128 Fg−1 and 58 mAh g−1 at 5 mVs−1 scan rate and 0.5 Ag−1 current density, respectively. The electrode EIS fitted equivalent circuit values were also found dependent on annealing temperature indicating the charge transfer process and rate capability of spinel NiFe2O4 nano-powder can be tailored by simply varying the annealing temperature. The study demonstrates cheap route by which spinel NiFe2O4 powder can be prepared. It also unveils the effect annealing temperature on the microstructural build-up and electrochemical charge storage performance of the material.

Synergistic effect of interlayered doping and surface modification to improve the performance of Li-rich manganese-based cathode materials

Li-rich manganese-based oxides (LRMOs) with high energy density have been intensively studied, but their practical use as cathode materials for lithium-ion batteries is still impeded by the shortcomings such as low initial coulombic efficiency, voltage decay and poor rate capability. To address these issues, element Nb is selected to bulk dope and simultaneously surface modify the hierarchical Li1.20Mn0.54Co0.13Ni0.13O2 spheres in this work. Synergistic effect of Nb doping and surface modification on the crystalline structure and electrochemical performance of the resultant LRMOs is characterized in detail. The results suggest that Nb5+ ions are doped into the interlayer sites within the crystals while the LiMn2O4 and LiNb3O8 double layers are coated on the primary nanoparticles. The galvanostatic charge-discharge measurements reveal that the optimal LRMO-Nb2 sample can deliver the capacities of 286 and 167 mAh g−1 at the rates of 0.1 C and 5 C, respectively, and retains a capacity of 191 mAh g−1 at 1 C rate after 200 cycles. Ex-situ XRD patterns prove that the layered structure is strongly pillared by the interlayer-doped Nb5+ during the delithiation/lithiation processes. Especially, some lithium vacancies formed around Nb5+ ions can accelerate the diffusion of Li+ ions, which was proved by DFT calculations and experimental results. Our research demonstrates that cooperating of the interlayered doping of Nb5+ with surface coating of LiNb3O8 layer can improve rate capability and cyclability of the resultant LRMOs significantly.

Activated carbon synthesized from Jack wood biochar for high performing biomass derived composite double layer supercapacitors

In this study, the electrochemical properties of bioderived activated carbon-based electrodes for supercapacitors formed using a sintered ceramic binder were investigated. Activated carbon derived from Jack wood tree (Artocarpus heterophyllus) with variable amounts of TiO2 nanoparticles as a binder, were used as electrodes in order to get good, activated carbon films on FTO substrates. No other binders were used in this study since most conventional binders devastate the electrical conductivity in the films. Furthermore, TiO2 has higher temperature tolerance compared to polymeric binders thus the electrode prepared can be used in wider applications. A series of electrochemical double-layer capacitors were fabricated and characterized by cyclic voltammetry and galvanostatic charge-discharge measurements. The supercapacitors prepared showed double-layer capacitive behavior. The electrodes that contain 90 % activated carbon and 10 % TiO2 show optimum performance along with an impressive specific capacitance of 147 F g−1 at 2 mV s−1 scan rate. This supercapacitor exhibits a power density of 68.5 W kg−1 while the energy density is 8.02 Wh kg−1. When the power density is as high as 1186.51 W kg−1 the energy density drops to 5.71 Wh kg−1. According to cyclic voltammetry measurements taken for 1000 cycles, the supercapacitor shows excellent cycle stability without any traces of capacitance drop.

Multiwalled-Carbon-Nanotube-Modified Li2ZnTi3O8 as Anode with Improved Cycling Stability and Rate Capability for Lithium-Ion Batteries

Due to its better electronic conductivity and larger lithium intercalation capacity, a multiwalled-carbon-nanotube (MWCNT)-modified Li2ZnTi3O8 (LZTO) has significant potential for use as an anode material for Li-ion batteries. The rapid and affordable ball-mill-aided solid state approach is used to synthesize LZTO with MWCNT-modified Li2ZnTi3O8 (LZTO@MWCNTs). Electrochemical performance tests of the anode material were carried out using cyclic voltammetry (CV), galvanostatic charge-discharge measurement, and electrochemical impedance spectroscopy (EIS). The CV experiments reveal that the LZTO@MWCNT electrode has a lower anodic and cathodic peak potential difference (0.184 V) than the LZTO electrode (0.211 V) and LZTO@MWCNT electrode has better electrochemical reversibility than that of pristine electrode after five cycles utilizing the same procedure. LZTO@ MWCNTs anode material has a higher charge-discharge capacity than LZTO anode material at 0.1–5 C rates. After 100 cycles, the initial discharge capacities of LZTO@MWCNT electrode are 227 and 142 mAh g−1 at the 1C–5C rate, respectively, whereas the initial discharge capacities of LZTO electrode are only144 and 28 mAh g−1 in the same condition. The charge transfer and SEI resistance of the LZTO anode are 19.31 and 62.74 ohms, respectively, after 30 cycles at 1C, according to the EIS data. Additionally, the values for the LZTO@MWCNTs anode are 7.93 and 12.06 ohms for charge transfer and SEI resistance, respectively.

Sr and Fe substituted LaCoO3 nano perovskites: Electrochemical energy storage and sensing applications

Perovskite-type LaCoO3 (LCO), La0.8Sr0.2CoO3 (LSCO), and La0.8Sr0.2Co0.9Fe0.1O3 (LSCFO) were prepared though a sol gel assisted hydrothermal method for supercapacitors and electrochemical sensors for heavy metal ions detection applications. Rhombohedral crystal structure was confirmed using experimental and DFT based computational XRD pattern. LCO, LSCO and LSCFO based modified carbon paste electrodes were prepared for cyclic voltammetry, electrochemical impedance spectra and galvanostatic charge discharge measurements. Among all electrodes, LSCFO results with 715.5 Fg−1 specific capacitance with 97 % retention after 1500 cycles. Cyclic voltammetry measurements for the sensing and detection of heavy metal ions (chromium and mercury) were carried out using all three electrodes and observed that LSCFO showed better response comparatively to that of other two electrodes, thus can be claimed as a potential mixed metal oxide nanomaterial for the fabrication of electrodes for storage of energy and sensor applications.

Graphene aerogel based positive electrode for lithium ion batteries

In this study, a composite of LiNi0.8Mn0.1Co0.1O2 nanoparticles (nNMC-811) supported by three-dimensional (3D) graphene aerogel (GA) was prepared to increase the practical energy density and performance capability of high nickel cathodes. The porous LiNi0.8Mn0.1Co0.1O2 nanoparticle/graphene aerogel (nNMC-811/GA) composite is composed of nNMC-811 and graphene that act as a bridge for electron transfer and acceleration of lithium ion diffusion. nNMC-811 and nNMC-811/GA cathodes characterization data with techniques including X-ray diffraction (XRD), Raman spectroscopy, Fourier transform infrared spectra (FT-IR) and X-ray photoelectron spectroscopy (XPS) are discussed. Both Field Emission Scanning Electron Microscopy (FE-SEM) and Transmission Electron Microscopy (TEM) made clear observations of the uniform distribution of the cathode active powders over the 3D graphene aerogel structure. The electrochemical performance of the nNMC-811 and nNMC-811/GA cathodes was evaluated by the galvanostatic charge-discharge measurement between 2.5 V and 4.5 V at room temperature using a computer-controlled battery tester. In addition, variable speed capacity ratios (C-rate), electrochemical impedance spectroscopy (EIS) and cyclic voltammetry (CV) analyzes were also performed. nNMC-811/GA hybrid composite structure delivers a specific capacity of 183.15 mAhg−1 at C/2 after the 500th cycle. It is understood from the FE-SEM images taken after the cycle that there is no deterioration in the structure. According to results, it was observed that the 3D porous structure of the nNMC-811/GA composite facilitated the mobility of Li+ ions, and the excellent electrochemical performances of the cathodes were improved due to the increasing defects as well as the electrical conductivity of GA.

Tracing the impact of CO2 on the electrochemical and charge–discharge behavior for Al–Mg alloy in KOH and LiOH electrolytes for battery applications

For the first time, it has been found that the electrochemical performance of the Al–Mg alloy as an anode in alkaline batteries has been markedly enhanced in the presence of CO2 and LiOH as an electrolyte. This work compares the electrochemical performance of an Al–Mg alloy used as an anode in Al-air batteries in KOH and LiOH solutions, both with and without CO2. Potentiodynamic polarization (Tafel), charging-discharging (galvanostatic) experiments, and electrochemical impedance spectroscopy (EIS) are used. X-ray diffraction spectroscopy (XRD) and a scanning electron microscope (SEM) outfitted with an energetic-dispersive X-ray spectroscope (EDX) were utilized for the investigation of the products on the corroded surface of the electrode. Findings revealed that the examined electrode’s density of corrosion current (icorr.) density in pure LiOH is significantly lower than in pure KOH (1 M). Nevertheless, in the two CO2-containing solutions investigated, icorr. significantly decreased. The corrosion rate of the examined alloy in the two studied basic solutions with and without CO2 drops in the following order: KOH > LiOH > KOH + CO2 > LiOH + CO2. The obtained results from galvanostatic charge–discharge measurements showed excellent performance of the battery in both LiOH and KOH containing CO2. The electrochemical findings and the XRD, SEM, and EDX results illustrations are in good accordance.

Variation of electrochemical performance of Li2ZrCl6 halide solid electrolyte with Mn substitution for all-solid-state batteries

All-solid-state batteries (ASSLBs) have gained attention as a next-generation battery technology. Halide solid electrolytes may be a candidate material for next-generation batteries due to their high stability in combination with cathode-active materials and good deformability. However, the halide solid electrolyte exhibits low ionic conductivity compared to other solid electrolytes, such as oxide and sulfide solid electrolytes. In this study, in order to improve the ionic conductivity, a strategy is presented to increase the ionic conductivity by changing the Li + concentration and metal charge by doping Mn2+ in the trigonal Li2ZrCl6. Mn-doped Li2ZrCl6 is synthesized by high-energy ball-milling. Structural analysis is conducted by powder X-ray diffraction, 7Li-Nuclear magnetic resonance, Raman spectroscopy and X-ray photoelectron spectroscopy. Electrochemical performance is evaluated using electrochemical impedance spectroscopy, cyclic voltammetry and galvanostatic charge-discharge measurement. Each value of ionic conductivity in the bare and optimized compositions is 0.4 mS cm−1 and 0.8 mS cm−1, respectively. The activation energy of Li2ZrCl6 and 5 mol% Mn doped Li2ZrCl6 is 0.342 and 0.326 eV. Galvanostatic charge-discharge is conducted to confirm cycling performance. The initial discharge capacity for Li2ZrCl6 and 5 mol% Mn-doped Li2ZrCl6 are 171.6 and 185.6 mAh g−1, respectively.

Impact of Li-ions and CO2 on the electrochemical efficiency of Al and Al-4%Sn in KOH electrolyte for alkaline batteries application

This study investigates the electrochemical behavior of aluminum (Al) and aluminum‑tin (Al-Sn) alloy as anodes in aluminum-air (Al-air) batteries in a potassium hydroxide (KOH) electrolyte with varying concentrations of lithium hydroxide (LiOH), in both the presence and absence of carbon dioxide gas (CO2). Experimental techniques such as potentiodynamic polarization (Tafel behavior), galvanostatic charging-discharging processes, and electrochemical impedance spectroscopy (EIS) were employed. Characterization techniques including X-ray diffraction spectroscopy (XRD), X-ray photoelectron spectroscopy (XPS), and scanning electron microscopy (SEM) with energy-dispersive X-ray spectroscopy (EDX) were utilized to analyze the surface products of each electrode. The findings indicate a significant decrease in the corrosion current density (icorr.) for both two electrodes with increasing LiOH concentration, however, Al-Sn exhibits lower values than those of commercial Al. Moreover, the presence of Li-ions revealed an interesting phenomenon of Al, where icorr. gradually decreased with temperature rise. Also, in the presence of CO2, icorr. significantly decreased for both two electrodes, particularly Al-Sn, indicating complete repression of the corrosion process on the surface. The corrosion rate of the studied electrodes in basic solutions, with and without CO2, follows the order: KOH > KOH + LiOH > KOH + LiOH + CO2. Galvanostatic charge-discharge measurements demonstrated higher capacity, improved electrochemical performance, and excellent charge-discharge behavior in the presence of LiOH. The electrochemical findings align well with the results from XRD, SEM, and EDX analysis.

The effect of B – site cation on the supercapacitive properties of LaBO3 (B = Cr, Mn, Fe and Co) porous perovskites

Perovskite oxides have attracted great attention as favorable electrode materials for supercapacitors due to their sole structure, intrinsic oxygen vacancy and compositional flexibility. However, a facile synthetic route which is simple and economical is a challenging issue related to the synthesis of such complex functional oxides. We present a facile and ultrafast way to synthesize LaBO3 (B = Cr, Mn, Fe and Co) perovskite nanocrystallites using glycine-nitrate autocombustion followed by annealing. The structure, phase purity, thermal stability, morphology and surface features of thus synthesized perovskite oxides were analyzed by X-ray diffraction, Fourier transform infrared spectroscopy, Field emission scanning electron microscopy, High resolution transmission electron microscopy, X-ray photoelectron spectroscopy, and Brunauer-Emmet-Teller measurements. The role of B – site cation on the electrochemical performance has been investigated by cyclic voltammetry, galvanostatic charge discharge measurements and electrochemical impedance spectroscopy. Electrochemical measurements showed that, among the synthesized materials, LaBO3 nanoparticles with smallest transition metal cation at its B – site, that is LaCoO3 delivered highest value of specific capacitance (750 F/g) and the value of specific capacitance decreases in the order LaCoO3 ˃ LaMnO3 ˃ LaCrO3 ˃ LaFeO3. Therefore, B – site transition metal cation holds the key to regulate perovskite's properties which are essential prerequisites for supercapacitors. An asymmetric device fabricated using LaCoO3 and activated carbon as the positive and negative electrode respectively acted in broad potential window (1.7 V) and delivered an energy density of 22.2 Wh/kg at a power density of 997.7 W/kg and two supercapacitors connected in series could power a red light emitting diode efficiently.

The electrochemical performances of high surface area mesocellular anatase TiO2 foam anode for lithium–ion battery

Porous anatase TiO2 with mesocellular foam structure (MCF−TiO2) was facilely prepared through hard-templating using mesocellular foam carbon (MCF−C), which had been prepared through hard-templating using mesocellular silica foam (MCF). During the dual hard-templating processes, the MCF−TiO2 well preserved the original three-dimensional (3D) mesocellular nanostructure of MCF. The wall of MCF−TiO2 was composed of very tiny anatase TiO2 nanocrystals (NCs). The TiO2 NCs were of less than 20 nm dimension. The surface area of MCF−TiO2 was 144 m2 g−1, and the MCF−TiO2 also contained large void spaces. The high surface area 3D nanostructured anatase MCF−TiO2 with large void spaces was ideal for Li+ transport and charge transfer reactions when MCF−TiO2 was applied to the anode material of the lithium–ion battery (LIB). Galvanostatic charge–discharge measurement and cyclic voltammetry confirmed that the MCF−TiO2 was an efficient anode material. The specific capacity after 50 cycles at a current rate of 0.1C reached 187 mAh g−1; it also showed stable recycling performances due to the robust high surface area 3D nanostructure.

High‐Strength Self‐Healable Supercapacitor Based on Supramolecular Polymer Hydrogel with Upper Critical Solubility Temperature

AbstractHere, poly(N‐acryloylglycinamide‐co‐vinyltriazole) p(NAGA‐co‐VTZ) supramolecular polymer hydrogel doped with carbonized and activated polypyrrole nanotubes as a high‐strength self‐healable material is presented for supercapacitors. Initially, the p(NAGA‐co‐VTZ) hydrogel films are synthesized by photopolymerization of N‐acryloylglycinamide and 1‐vinyl‐1,2,4‐triazole without the use of any cross‐linkers. The hydrogels demonstrated remarkable self‐healing ability via hydrogen bonding at temperatures above upper critical solubility temperature, excellent mechanical properties (0.86 MPa), large stretchability (1300%) and cut resistance. Subsequently, carbonized and ethanol/KOH‐activated polypyrrole nanotubes (acNTs) are prepared as the active material for electrochemical double‐layer capacitors (EDLC). Then, a symmetric self‐healable supercapacitor employing p(NAGA‐co‐VTZ) hydrogel, acNTs and aqueous 3 m KCl solution is assembled. Cyclic voltammetry and galvanostatic charge–discharge measurements show that the prepared device gives a specific capacitance of 282.62 F g−1 at 0.2 A g−1 and a high areal capacitance of 316.86 mF cm−2 at a scan rate of 10 mV s−1. Importantly, the supercapacitor operates over a wide voltage window (0–1.2 V) and provides excellent cyclic performance with capacitance retention of 97% after 10 000 cycles and 94% after self‐healing. In summary, the developed self‐healable supercapacitor exhibits considerable potential as a high‐performance energy storage device.

Electrochemical capacitance and hydrogen adsorption behavior of activated carbon derived from cattail fiber

AbstractIn this paper, we have reported the synthesis of activated carbon (AC) from biomass cattail fiber through hydrothermal carbonization, followed by chemical activation, and its electrochemical capacitance and hydrogen storage properties. The AC exhibits a Brunauer‐Emmett‐Teller (BET) surface area (SBET) of 1597.5 m2g−1, determined from the low‐pressure N2 adsorption isotherm at 77 K using a BET‐multipoint plot. The AC sample shows a reversible hydrogen adsorption capacity of 0.25 wt.% H2 (1.25 mmol H2 g−1) at 293 K and 74 atm. The capacitance performance of AC was investigated with various conductive additives such as carbon nanotubes (CNTs), carbon black (CB), and reduced graphene‐oxide (rGO). From galvanostatic charge discharge (GCD) and cyclic voltammetry (CV) measurements, the as‐derived AC with polymer binder exhibits a specific capacitance (Cs) of 245.2 F g−1 at 0.2 A g−1 and 158.1 F g−1 at 5 mV s−1. Among the investigated conductive additives, AC with CNTs in KOH electrolyte exhibit highest Cs of 326 F g−1 at 0.2 A g−1 and 173 F g−1 at 5 mV s−1. Furthermore, the symmetrical two‐electrode device fabricated using AC with CNTs (as a conductive additive) in 1 M aq. Na2SO4 electrolyte shows a Cs of 97.2 F g−1 at 0.1 A g−1. The energy and power densities of the two‐electrode device were observed to be 28 kW kg−1 and 2.64 Wh kg−1, respectively.

Pistachio Waste-Derived Activated Carbon Materials for Sustainable Energy Storage: Supercapacitor Applications

This study explores the potential of utilizing pistachio waste which is of low-cost and eco-friendly precursor for the synthesis of activated carbon for supercapacitor applications. Pistachio shells, a common agricultural waste product, were subjected to a controlled pyrolysis process followed by the activation to produce activated carbon materials. The resulting activated carbon was characterized by using various analytical techniques, including scanning electron microscopy (SEM), Raman spectroscopy, X-ray Photoelectron spectroscopy (XPS), X-ray diffraction (XRD), and electrochemical testing. The electrochemical performance of the pistachio waste-derived activated carbon was evaluated through cyclic voltammetry (CV) and galvanostatic charge-discharge (GCD) measurements. The pistachio waste-derived activated carbon exhibits excellent capacitive behaviour, with a high specific capacitance and good cycling stability. The use of agricultural waste-derived activated carbon not only addresses the environmental concerns but also contributes to the development of green energy storage solutions.

Exploring the potential of polyaniline-calcium titanate (PANI-CaTiO3) nanocomposites in supercapacitors: Synthesis and electrochemical investigation

This work presents the simple approach for the synthesis of CaTiO3 incorporated polyaniline nanocomposites (PANI- CaTiO3) by facile in-situ oxidative polymerization route, to be used as electrode materials for supercapacitors (SCs). The developed samples were evaluated using several analytical methods viz. X-ray diffraction (XRD), thermogravimetric analysis (TGA), Fourier transform infrared (FTIR) spectroscopy, Raman spectroscopy, field emission scanning electron microscopy (FESEM), and Brunauer-Emmett-Teller analysis (BET). The electrochemical performance of the prepared nanocomposites for energy storage application was evaluated by cyclic voltammetry (CV), galvanostatic charge-discharge (GCD), and electrochemical impedance spectroscopy (EIS) in 3 M of KOH as an electrolyte. In comparison to pristine PANI, which demonstrated a specific capacitance of 257 Fg−1, and pure CaTiO3, which exhibited a specific capacitance of 142 Fg−1, the results of cyclic voltammetry (CV) for PANI-35 % CaTiO3 nanocomposites revealed a higher specific capacitance of 966 Fg−1 at 10 mV/s sweep rate. The highest energy density and power density for the PANI-35 % CaTiO3 nanocomposites were shown by galvanostatic charge-discharge (GCD) measurements to be 58.14 Whkg−1 and 3.2 kWkg−1, respectively, at a higher specific capacitance value of 984.21 Fg−1 at 6.86 Ag−1 current density. Additionally, the straight line in low frequency Nyquist plots was linked to the low electrolyte diffusion (Warburg) resistance within the electrode and ions diffusion into the electrode surface, confirming the CV results. Moreover, this study proposes an innovative research concept for the fabrication of electrode materials specifically designed for supercapacitors.

Efficient Sodium-Ion Storage Using MoS2@rGO Nanocomposite Anode: Exploring Na-Ion Diffusion in Metallic Phase

Sodium-ion batteries (SIBs) are gaining attention as a better and more economical option than lithium-ion batteries, owing to the abundance and low cost of sodium in comparison to lithium. The anode component of rechargeable batteries plays a vital role in obtaining superior energy and power density. Consequently, the investigation of novel materials for SIBs with enhanced performance is imperative. Transition metal chalcogenides (TMDs) are found to be promising contenders for this purpose, particularly MoS2 due to their two-dimensional open framework, structural tunability, and high theoretical specific capacity as an anode material in sodium ion storage. In this regard, we conducted a facile strategy to synthesize MoS2 and aluminium-doped MoS2 incorporated into reduced graphene oxide (rGO) using the hydrothermal method. The structural and morphological properties of the samples have been explored through X-ray diffraction (XRD), Raman spectroscopy, field-emission scanning electron microscopy (SEM), and high-resolution transmission electron microscopy (HRTEM) measurements which revealed that the addition of aluminium increased the interlayer spacing of the (002) plane of MoS2 nanosheets and stabilized it in metallic 1T phase. The enhanced interlayer distance and improved conductivity of the electrode material displayed a significantly higher initial discharge specific capacity of around 750 mAhg−1 which is stabilized around 380 mAhg−1 at the current rate of 50 mAg−1 after 10 cycles as investigated through galvanostatic charge-discharge measurement. The long cycling test for 200 cycles revealed the capacity retention of ~65% and ~55 % at the current density of 100 and 300 mAg-1, respectively. The kinetic behavior of the Na-ion is studied employing cyclic voltammetry (CV), galvanostatic intermittent titration technique (GITT), and electrochemical impedance spectroscopy (EIS), and the diffusion coefficient of Na-ion in the bulk of the electrode was found to be in the range of 10-10 to 10-12 cm2s-1. Additionally, in-situ EIS analysis demonstrates the electrode's electrochemical kinetics at different charge-discharge states by showing variations in charge transfer resistance. Ex-situ XRD and X-ray photoemission spectroscopy (XPS) demonstrated the coexistence of 1T and 2H phases, and field-emission SEM validated the stable morphology after cycling. Keywords: Sodium-ion batteries, Transition metal chalcogenides (TMDs), Anode material, MoS2

Electrochemical Analysis of Charge Overpotentials in Non-Aqueous Lithium and Sodium Oxygen Batteries

Aprotic metal-oxygen batteries, especially Li-O2 and Na-O2 batteries, could afford theoretical specific energies of more than 500 Wh/kg. However, while not compromising on rechargeability, the practical realization of the theoretically possible high specific energies has been elusive. A better understanding of the differences and similarities between Li–O2 and Na–O2 battery systems in terms of charge-discharge mechanisms and parasitic chemistry will be meaningful in solving these challenges. Here, we explore the differences between the two systems using a combination of galvanostatic charge-discharge measurements, Differential Electrochemical Mass spectrometry (DEMS), and Potentiostatic Electrochemical Impedance Spectroscopy (PEIS) analysis. The discharge profiles of these battery chemistries are similar in terms of overpotential and have been widely studied. But the origins of the differences in charge overpotentials are not clear. Using in-situ pressure decay measurements during discharge, we calculated the number of electrons/oxygen (e-/O2) to be 2.02 and 1.01 for Li-O2 and Na-O2 cells, respectively. Further, DEMS analysis during charge has shown that the ideal 2 e-/O2 is attained only during the initial phases of charging for Li-O2 cells. However, for Na-O2, the ideal 1 e-/O2 is achieved during a signification portion of the galvanostatic charge step. We corroborate these findings with PEIS and distribution of relaxation times (DRT) analysis to develop a mechanistic view of the processes that lead to poor coulombic and oxygen evolution efficiencies in metal-oxygen cells. Based on DRT analysis, we identify a lower time constant process that is common to both Li-O2 and Na-O2 cells. Interestingly, we observed that voltage polarization is preceded by the observation of this lower time constant peak. In the case of Li-O2 cells, this lower time constant process was observed at the end of discharge and throughout the recharge process, while for the Na-O2 cells, this was only observed after about 70% of recharge. We discuss the possible origins of this low time-constant process and its implications for recharging metal-oxygen batteries. We will also discuss the role of singlet oxygen, if any, in the recharge efficiencies of these two aprotic metal-oxygen batteries. Our results imply that the identification of the origins of this lower time constant process and possible suppression of this process will be key for rechargeable metal-oxygen batteries.

Reductive Treatment of δ-MnO2 with Sodium Borohydride: Method for Increasing the Electrode Material Capacitance

The effect of reductive treatment on the phase composition, morphology, and electrochemical parameters of δ-MnO2 produced by the hydrothermal method from KMnO4 at a temperature of 160°C in the presence of HNO3 was studied. δ-MnO2 processing with 3 M NaBH4 aqueous solution leads to partial reduction of Mn(IV) to Mn(III) and Mn(II). The electrochemical characteristics of the obtained electrode materials were examined by cyclic voltammetry, galvanostatic charge–discharge measurements, and impedance spectroscopy. Reductive treatment increases the specific capacitance of δ-MnO2 in 1 M Na2SO4 up to 204 F g–1 at a current density of 0.1 A g–1, and also reduces diffusion limitations during cycling due to an increase in the specific surface area. The loss of specific capacitance after 2000 charge–discharge cycles does not exceed 2.6%, which confirms the high electrochemical stability of the obtained electrode materials.

Preparation of Zn–Al–Gd-hydrotalcite and performance in zinc-nickel batteries

In this study, Zn–Al-Gd layered double hydroxides (LDHs) were synthesized via a hydrothermal method and investigated as possible negative electrode materials for zinc-nickel batteries. X-ray diffraction analysis and scanning electron microscopy images showed that the as-prepared samples were well crystallized with a hexagonal structure. The electrochemical performance was investigated for Zn–Al-LDHs and Zn–Al-Gd-LDHs with different Zn/Al/Gd molar ratios by cyclic voltammetry, Tafel polarization, electrochemical impedance spectroscopy, galvanostatic charge–discharge measurement, and cycle charge–discharge analysis. The initial discharge capacity reached 416.7 mAh g−1 for the Zn–Al-LDHs electrode and the discharge capacity decreased to 347.3 mAh g−1 after 150 cycles, with a cycle retention rate of 83.34 %. Compared with Zn–Al-LDHs, Zn–Al-Gd-LDHs with different Zn/Al/Gd molar ratios had higher discharge capacities and more stable cycling performance, especially the sample with Zn/Al/Gd = 3:0.8:0.2 (molar ratio). After 150 cycles, the retention rate for the sample with Zn/Al/Gd = 3:0.8:0.2 (molar ratio) was 88.73 %. Zn–Al-Gd-LDHs with a high rate capability can meet the needs of high-storage applications.

E-waste Derived Enhanced Activated Carbon for Supercapacitor Applications

Increase in the usage of electronic appliance and gadgets leads to more e-waste for example printed circuit boards which have a huge impact in the environment that makes toxic. This study gives an idea about how to make an e-waste as a raw material and it is converted into activated carbon using the activation process which reduces the wastage. It is used as an electrode for supercapacitors which suits for energy storage application and it is a cost-effective method. Using X-ray diffraction, scanning electron microscopy techniques and Raman spectroscopy, the electrochemical behaviours were studied. By cyclic voltammetry, galvanostatic charge-discharge measurements and electrochemical impedance spectroscopy techniques, the capacitance behaviour of activated carbon which is obtained by e-waste were calculated. Different scan rate values were performed and the corresponding specific capacitance values were obtained. In that, at the scan rate of 10 mV s−1, the obtained specific capacitance value was found to be 308 Fg−1. Good specific capacitance values were obtained for activated carbon which indicates that activated carbon is a suitable material for the supercapacitor fabrication.