Organic Electrolyte Research Articles

High‐Current Capable and Non‐Flammable Protic Organic Electrolyte for Rechargeable Zn Batteries

AbstractWiederaufladbare Zinkbatterien (RZBs) gelten aufgrund ihrer zahlreichen Vorteile als potente Konkurrenten für elektrochemische Geräte der nächsten Generation. Dennoch können herkömmliche wässrige Elektrolyte aufgrund der komplexen Reaktionskinetik in wässrigen Systemen durch schnellen Kapazitätsabfall und schlechte Coulomb′sche Effizienz (CE) ernsthafte Gefahren für den langfristigen Batteriebetrieb verursachen. Wir haben hier die neuartige Verwendung des protischen Amid‐Lösungsmittels N‐Methylformamid (NMF) als Zinkbatterie‐Elektrolyt vorgeschlagen, dass eine hohe Dielektrizitätskonstante und einen hohen Flammpunkt besitzt, um gleichzeitig eine schnelle Kinetik und Batteriesicherheit zu fördern. Die dendritenfreie und körnige Zn‐Abscheidung im Zn‐NMF‐Elektrolyten gewährleistet eine ultralange Lebensdauer von 2000 Stunden bei 2.0 mA cm−2/2.0 mAh cm−2, ein hohes CE von 99.57 %, ein breites elektrochemisches Fenster (≈3.43 V vs. Zn2+/Zn) und eine hervorragende Haltbarkeit bis zu 10.0 mAh cm−2. Diese Arbeit wirft ein Licht auf die effiziente Leistung des protischen nichtwässrigen Elektrolyten, der neue Möglichkeiten zur Förderung sicherer und energiedichter RZBs eröffnen wird.

Investigations on the lithium-ion and sodium-ion insertion behavior of amorphous sodium iron carbonophosphate using N-propyl-N-methylpyrrolidinium bis(fluorosulfonyl)imide based ionic liquid electrolyte

In this article, we investigate the electrochemical performance of the amorphous sodium iron carbonophosphate upon transitioning from organic electrolytes (lithium hexafluorophosphate (LiPF6) –ethylene carbonate (EC): diethyl carbonate (DEC) based) to ionic-liquid (N-propyl-N-methylpyrrolidinium bis(fluorosulfonyl)imide; PMP-FSI) based electrolytes. The amorphous sodium iron carbonophosphate is synthesized using microwave-assisted hydrothermal process to obtain the desired phase and microstructure. The nanoparticle morphology, along with the amorphous structure, results in excellent electrochemical properties when tested as cathode for lithium-ion and sodium-ion batteries with organic and ionic-liquid based electrolytes. It is observed that the room-temperature and high-temperature (∼60 °C) cycling performance is superior when ionic-liquids are used instead of organic electrolytes, resulting in nearly fade-free electrochemical cells. Specific capacity retention of ∼97% is reported after 500 cycles with 3 M lithium bis(trifluoromethanesulfonyl)imide (LiTFSI)/PMP-FSI ionic-liquid at a specific current density of 400 mAg−1 (room temperature), in comparison to ∼70% after 500 cycles for 1 M LiPF6 in EC: DEC = 1:1. At high temperatures (∼60 °C), ionic-liquids outperform the conventional organic electrolytes in terms of capacity retention and rate capability. Post-mortem analysis of the electrodes indicates that a dense and ionically conductive protective film, composed of anion-reduced moieties, is responsible for the superior high-temperature performance of amorphous sodium iron carbonophosphate with the ionic-liquids.

Readily Accessible M-Ferrocenyl-Phenyl Sulfonate as Novel Cathodic Electrolyte for Aqueous Organic Redox Flow Batteries

Ferrocene derivatives are amongst the most promising electroactive organic electrolytes. The bottleneck problems of their application in aqueous redox flow batteries are their poor solubility and lower potential as well as the complexity of the modification methods to solve these problems. In this study, a benzenesulfonic acid group is easily introduced into the ferrocene structure by a mature diazotization reaction, and the synthesized sodium m-phenylferrocene sulfonate BASFc is used as the novel cathodic electroactive electrolyte for AORFB. The hydrophilicity and the electron-absorbing effect of the introduced benzenesulfonic group can effectively improve the water solubility and redox potential of ferrocene. Moreover, the introduction of phenyl extends the conjugated structure of ferrocene and increases its structural dimension, which may be conducive to reducing its membrane permeability and improving the structural stability to some extent. The physical structure and the electrochemical properties of BASFc are studied systematically; the feasibility of its application as a cathodic electrolyte in AORFBs is verified by assembling the half-cell and full-cell. The results verify the good electrochemical reaction kinetics of BASFc in acid electrolyte and the corresponding AORFB shows satisfactory efficiency and stability.

Prefabrication of a Lithium Fluoride Interfacial Layer to Enable Dendrite-Free Lithium Deposition

Lithium metal is one of the most attractive anode materials for rechargeable batteries. However, its high reactivity with electrolytes, huge volume change, and dendrite growth upon charge or discharge lead to a low CE and the cycle instability of batteries. Due to the low surface diffusion resistance, LiF is conducive to guiding Li+ deposition rapidly and is an ideal component for the surface coating of lithium metal. In the current study, a fluorinated layer was prepared on a lithium metal anode surface by means of chemical vapor deposition (CVD). In the carbonate-based electrolyte, smooth Li deposits were observed for these LiF-coated lithium anodes after cycling, providing excellent electrochemical stability for the lithium metal anode in the liquid organic electrolyte. The CE of Li|Cu batteries increases from 83% for pristine Li to 92% for LiF-coated ones. Moreover, LiF-Li|LFP exhibits a decent rate and cycling performance. After 120 cycles, the capacity retention of 99% at 1C is obtained, and the specific capacity is maintained above 149 mAh/g. Our investigation provides a simple and low-cost method to improve the performance of rechargeable Li-metal batteries.

Insight into the Desolvation of Quaternary Ammonium Cation with Acetonitrile as a Solvent in Hydroxyl-Flat Pores: A First-Principles Calculation.

Supercapacitors have a wide range of applications in high-technology fields. The desolvation of organic electrolyte cations affects the capacity size and conductivity of supercapacitors. However, few relevant studies have been published in this field. In this experiment, the adsorption behavior of porous carbon was simulated with first-principles calculations using a graphene bilayer with a layer spacing of 4-10 Å as a hydroxyl-flat pore model. The reaction energies of quaternary ammonium cations, acetonitrile, and quaternary ammonium cationic complexes were calculated in a graphene bilayer with different interlayer spacings, and the desolvation behavior of TEA+ and SBP+ ions was described. The critical size for the complete desolvation of [TEA(AN)]+ was 4.7 Å, and the partial desolvation size ranged from 4.7 to 4.8 Å. The critical size for the complete desolvation of [SBP(AN)]+ was 5.2 Å, and the partial desolvation size ranged from 5.2 to 5.5 Å. As the ionic radius of the quaternary ammonium cation decreased, the desolvation size showed a positive trend. A density of states (DOS) analysis of the desolvated quaternary ammonium cations embedded in the hydroxyl-flat pore structure showed that the conductivity of the hydroxyl-flat pore was enhanced after gaining electrons. The results of this paper provide some help in selecting organic electrolytes to improve the capacity and conductivity of supercapacitors.

Polymer electrolyte design strategies for high-performance and safe lithium-ion batteries: Recent developments and future prospects

Although lithium-ion batteries have gained widespread use in high-performance and mobile industries, concerns about their safety due to the low boiling point of their organic liquid electrolyte have posed challenges to their further development. In response, solid polymer electrolytes have emerged as a promising alternative, characterized by low flammability, flexibility, and high safety relative to liquid electrolytes. However, commercialization has been hindered by limitations in Li-ion conductivity and mechanical properties. Recent research efforts have focused on addressing these limitations to improve the performance and safety of polymer-based Li-ion batteries. This review discusses the utilization of polymer materials to enhance battery safety and overcome previous challenges, with a particular emphasis on the design of robust artificial interfaces to increase battery stability. Furthermore, we discuss the prospects for the future of polymer-based battery industries.

Alginate-Xylan Biopolymer as a Multifunctional Binder for 5 V High-Voltage LNMO Electrodes.

LiNi0.5Mn1.5O4 (LNMO) with a spinel structure is one of the most promising cathode materials choices for Li-ion batteries (LIBs). However, at a high operating voltages, the decomposition of organic electrolytes and the dissolution of transition metals, especially Mn(II) ions, cause unsatisfactory cycle stability. The initial application of a sodium alginate (SA)-xylan biopolymer as an aqueous binder aims to address the aforementioned problems. The SX28-LNMO electrode has a sizable discharge capacity, exceptional rate capability, and long-term cyclability with a capacity retention of 99.8% after 450 cycles at 1C and a remarkable rate capability of 121 mAh g-1 even at 10C. A more thorough investigation illustrated that SX28 binder provides a substantial adhesion property and generates a uniform (CEI) layer on the LNMO surface, suppressing electrolytes' oxidative decomposition upon cycling and improving LIB performances. This work highlights the potential of hemicellulose as an aqueous binder for 5.0 V high-voltage cathodes.

Sodium Carbazolide and Derivatives as Solid-State Electrolytes for Sodium-Ion Batteries.

Replacing widely used organic liquid electrolytes with solid-state electrolytes (SSEs) could effectively solve the safety issues in sodium-ion batteries. Efforts on seeking novel solid-state electrolytes have been continued for decades. However, issues about SSEs still exist, such as low ionic conductivity at ambient temperature, difficulty in manufacturing, low electrochemical stability, poor compatibility with electrodes, etc. Here, sodium carbazolide (Na-CZ) and its THF-coordinated derivatives are rationally fabricated as Na+ conductors, and two of their crystal structures are successfully solved. Among these materials, THF-coordinated complexes exhibit fast Na+ conductivities, i.e., 1.20×10-4 S cm-1 and 1.95×10-3 S cm-1 at 90 °C for Na-CZ-1THF and Na-CZ-2THF, respectively, which are among the top Na+ conductors under the same condition. Furthermore, stable Na plating/stripping is observed even over 400 h cycling, showing outstanding interfacial stability and compatibility against Na electrode. More advantages such as ease of synthesis, low-cost, and cold pressing for molding can be obtained. In situ NMR results revealed that the evaporation of THF may play an essential role in the Na+ migration, where the movement of THF creates defects/vacancies and facilitates the migration of Na+ .

Sodium Carbazolide and Derivatives as Solid‐State Electrolytes for Sodium‐Ion Batteries

AbstractReplacing widely used organic liquid electrolytes with solid‐state electrolytes (SSEs) could effectively solve the safety issues in sodium‐ion batteries. Efforts on seeking novel solid‐state electrolytes have been continued for decades. However, issues about SSEs still exist, such as low ionic conductivity at ambient temperature, difficulty in manufacturing, low electrochemical stability, poor compatibility with electrodes, etc. Here, sodium carbazolide (Na‐CZ) and its THF‐coordinated derivatives are rationally fabricated as Na+ conductors, and two of their crystal structures are successfully solved. Among these materials, THF‐coordinated complexes exhibit fast Na+ conductivities, i.e., 1.20×10−4 S cm−1 and 1.95×10−3 S cm−1 at 90 °C for Na‐CZ‐1THF and Na‐CZ‐2THF, respectively, which are among the top Na+ conductors under the same condition. Furthermore, stable Na plating/stripping is observed even over 400 h cycling, showing outstanding interfacial stability and compatibility against Na electrode. More advantages such as ease of synthesis, low‐cost, and cold pressing for molding can be obtained. In situ NMR results revealed that the evaporation of THF may play an essential role in the Na+ migration, where the movement of THF creates defects/vacancies and facilitates the migration of Na+.

A Multifunctional Organic Electrolyte Additive for Aqueous Zinc Ion Batteries Based on Polyaniline Cathode.

The practical applications of aqueous zinc ion batteries are hindered by the formation of dendrites on the anode, the narrow electrochemical window of electrolyte, and the instability of the cathode. To address all these challenges simultaneously, a multi-functional electrolyte additive of 1-phenylethylamine hydrochloride (PEA) is developed for aqueous zinc ion batteries based on polyaniline (PANI) cathode. Experiments and theoretical calculations confirm that the PEA additive can regulate the solvation sheath of Zn2+ and form a protective layer on the surface of the Zn metal anode. This broadens the electrochemical stability window of the aqueous electrolyte and enables uniform deposition of Zn. On the cathode side, the Cl- anions from PEA enter the PANI chain during charge and release fewer water molecules surrounding the oxidized PANI, thus suppressing harmful side reactions. When used in a Zn||PANI battery, this cathode/anode compatible electrolyte exhibits excellent rate performance and long cycle life, making it highly attractive for practical applications.

Study on the Application of Nitrogen-Doped Holey Graphene in Supercapacitors with Organic Electrolyte.

We present a facile low-cost method to produce nitrogen-doped holey graphene (N-HGE) and its application to supercapacitors. A composite of N-HGE and activated carbon (AC) was used as the electrode active material in organic-electrolyte supercapacitors, and the performances were evaluated. Melamine was mixed into graphite oxide (GO) as the N source, and an ultra-rapid heating method was used to create numerous holes during the reduction process of GO. X-ray photoelectron spectra confirmed the successful doping with 2.9-4.5 at.% of nitrogen on all samples. Scanning electron micrographs and Raman spectra revealed that a higher heating rate resulted in more holes and defects on the reduced graphene sheets. An extra annealing step at 1000 °C for 1 h was carried out to further eliminate residual oxygen functional groups, which are undesirable in the organic electrolyte system. Compared to the low-heating-rate counterpart (N-GE-15), N-HGE boosted the specific capacity of the supercapacitor by 42 and 22% at current densities of 0.5 and 20 A/g, respectively. The effects of annealing time (0.5, 1, and 2 h) at 1000 °C were also studied. Longer annealing time resulted in higher capacitance values at all current densities due to the minimized oxygen content. Volumetric specific capacitances of 49 and 24 F/cm3 were achieved at current densities of 0.5 and 20 A/g, respectively. For the high-power-density operation at 31,000 W/kg (or 10,000 W/L), an energy density as high as 11 Wh/kg (or 3.5 Wh/L) was achieved. The results indicated that N-HGE not only improved the conductivity of the composite supercapacitors but also accelerated ion transport by way of shortened diffusion paths through the numerous holes all over the graphene sheets.

Reciprocal effects of NOM and solution electrolyte ions on aggregation of ferrihydrite nanoparticles

The effects of natural organic matter (NOM) types and electrolyte ions are crucial to the aggregation of ferrihydrite nanoparticles (Fh NPs) in the environment. Dynamic light scattering (DLS) was employed for the aggregation kinetics of Fh NPs (10 mg/L as Fe) in the present study. The critical coagulation concentration (CCC) values of Fh NPs aggregation in NaCl were obtained in the presence of 15 mg C/L NOM as SRHA (857.4 mM) > PPHA (752.3 mM) > SRFA > (420.1 mM) > ESHA (141.0 mM) > NOM-free (125.3 mM), indicating Fh NPs aggregation was inhibited as the above order. Comparatively in CaCl2, the CCC values were measured in ESHA (0.9 mM), PPHA (2.7 mM), SRFA (3.6 mM), SRHA (5.9 mM), NOM-free (76.6 mM), implying NPs aggregation was enhanced following the order of ESHA > PPHA > SRFA > SRHA. To investigate the dominant mechanisms, the aggregation of Fh NPs was comprehensively studied under the effects of NOM types, concentrations (0–15 mg C/L) and electrolyte ions (NaCl/CaCl2 beyond CCC). In NaCl/CaCl2, the low concentration of NOM (<7.5 mg C/L) could accelerate NPs aggregation mainly due to patch-charge attraction. When NOM concentration was high (> 7.5 mg C/L), the inhibition effect on NPs aggregation occurred in NaCl due to steric repulsion, whereas the enhancement effect in CaCl2 of aggregation was dominated by the bridging effect. The results indicated that the effects of NOM types, concentration and electrolyte ions should be carefully considered for the environmental behavior of NPs.

Origin of dendrite-free lithium deposition in concentrated electrolytes

The electrolyte solvation structure and the solid-electrolyte interphase (SEI) formation are critical to dictate the morphology of lithium deposition in organic electrolytes. However, the link between the electrolyte solvation structure and SEI composition and its implications on lithium morphology evolution are poorly understood. Herein, we use a single-salt and single-solvent model electrolyte system to systematically study the correlation between the electrolyte solvation structure, SEI formation process and lithium deposition morphology. The mechanism of lithium deposition is thoroughly investigated using cryo-electron microscopy characterizations and computational simulations. It is observed that, in the high concentration electrolytes, concentrated Li+ and anion-dominated solvation structure initiate the uniform Li nucleation kinetically and favor the decomposition of anions rather than solvents, resulting in inorganic-rich amorphous SEI with high interface energy, which thermodynamically facilitates the formation of granular Li. On the contrary, solvent-dominated solvation structure in the low concentration electrolytes tends to exacerbate the solvolysis process, forming organic-rich mosaic SEI with low interface energy, which leads to aggregated whisker-like nucleation and growth. These results are helpful to tackle the long-standing question on the origin of lithium dendrite formation and guide the rational design of high-performance electrolytes for advanced lithium metal batteries.

A multifunctional fire-retardant gel electrolyte to enable Li-S batteries with higher Li-ion conductivity and effectively inhibited shuttling of polysulfides

A main huddle against the practical application of lithium-sulfur battery lies in serious safety concerns due to liquid organic electrolyte, shuttling of polysulfides and formation of lithium dendrites. Herein, we have devised an asymmetric and structurally stable gel electrolyte system to enable high ionic conductivity, flame-retardancy, and effective blockage of shuttling. Such a multi-functional gel electrolyte utilizes an electro-spun network of interwoven nano-fibers of poly vinylidene fluoride-co-hexafluoropropylene (PVDF-HFP) as structural scaffolds, with SiO2-polyvinyl alcohol (SiO2@PVA) suspension being loaded at one surface by blade coating. Such asymmetrically coated PVDF-HFP membranes are highly wettable that is essential to thorough gelling, with its well-connected porous channels to enable outstanding ionic conductivity above the limit by conventional Celgard separator, to accommodate huge volumetric changes over redox reactions, to shield polysulfides and fend off lithium dendrites. Ultimately, application of the gel electrolyte to a model Li-S cell with cathode containing 90% S delivered high initial capacity of 1439 mA h g−1 at 0.1C and a remarkable cycling stability over 300 cycles at 1C. The current gel electrolyte is expected to provide a valuable means for developing safe low-cost and durable Li–S batteries of practical importance.

A Space‐Confined Polymerization Templated by Ice Enables Large‐Scale Synthesis of Two‐Dimensional Polymer Sheets

AbstractDespite significant progress in the preparation and characterization of two‐dimensional (2D) materials, the synthesis of 2D organic materials remains challenging. Here, we report a novel space‐confined polymerization method that enables the large‐scale synthesis of 2D sheets of a functional conjugated polymer, namely, poly(3,4‐ethylenedioxythiophene) (PEDOT). A key step in this method is the confinement of monomer to the boundaries of ice crystals using micelles. This spatial confinement directs the polymerization to form 2D PEDOT sheets with high crystallinity and controlled morphology. Supercapacitors prepared from the 2D PEDOT sheets exhibit outstanding performance metrics. In aqueous electrolyte, a high areal specific capacitance of 898 mF cm−2 at 0.2 mA cm−2 along with an excellent rate capability is achieved (e.g., capacitance retention of 67.6 % at a 50‐fold higher current). Moreover, the 2D PEDOT‐based supercapacitors exhibit outstanding cycling stability (capacitance retention of 98.5 % after 30,000 cycles). Device performance is further improved when an organic electrolyte is used.

Cyclotetrabenzil Derivatives for Electrochemical Lithium‐Ion Storage

AbstractOrganic electrode materials could revolutionize batteries because of their high energy densities, the use of Earth‐abundant elements, and structural diversity which allows fine‐tuning of electrochemical properties. However, small organic molecules and intermediates formed during their redox cycling in lithium‐ion batteries (LIBs) have high solubility in organic electrolytes, leading to rapid decay of cycling performance. We report the use of three cyclotetrabenzil octaketone macrocycles as cathode materials for LIBs. The rigid and insoluble naphthalene‐based cyclotetrabenzil reversibly accepts eight electrons in a two‐step process with a specific capacity of 279 mAh g−1 and a stable cycling performance with ≈65 % capacity retention after 135 cycles. DFT calculations indicate that its reduction increases both ring strain and ring rigidity, as demonstrated by computed high distortion energies, repulsive regions in NCI plots, and close [C⋅⋅⋅C] contacts between the naphthalenes. This work highlights the importance of shape‐persistency and ring strain in the design of redox‐active macrocycles that maintain very low solubility in various redox states.

Cyclotetrabenzil Derivatives for Electrochemical Lithium-Ion Storage.

Organic electrode materials could revolutionize batteries because of their high energy densities, the use of Earth-abundant elements, and structural diversity which allows fine-tuning of electrochemical properties. However, small organic molecules and intermediates formed during their redox cycling in lithium-ion batteries (LIBs) have high solubility in organic electrolytes, leading to rapid decay of cycling performance. We report the use of three cyclotetrabenzil octaketone macrocycles as cathode materials for LIBs. The rigid and insoluble naphthalene-based cyclotetrabenzil reversibly accepts eight electrons in a two-step process with a specific capacity of 279 mAh g-1 and a stable cycling performance with ≈65 % capacity retention after 135 cycles. DFT calculations indicate that its reduction increases both ring strain and ring rigidity, as demonstrated by computed high distortion energies, repulsive regions in NCI plots, and close [C⋅⋅⋅C] contacts between the naphthalenes. This work highlights the importance of shape-persistency and ring strain in the design of redox-active macrocycles that maintain very low solubility in various redox states.

A Space-Confined Polymerization Templated by Ice Enables Large-Scale Synthesis of Two-Dimensional Polymer Sheets.

Despite significant progress in the preparation and characterization of many two-dimensional (2D) materials, the synthesis of 2D organic materials remains challenging. Here, we report a novel space-confined polymerization method that enables the large-scale synthesis of 2D sheets of a functional conjugated polymer, namely, poly(3,4-ethylenedioxythiophene) (PEDOT). A key step in this method is the confinement of monomer to the boundaries of ice crystals using micelles. This spatial confinement directs the polymerization to form 2D PEDOT sheets with high crystallinity and controlled morphology. Supercapacitors prepared from the 2D PEDOT sheets exhibit outstanding performance metrics. In aqueous electrolyte, a high areal specific capacitance of 898 mF cm-2 at 0.2 mA cm-2 along with an excellent rate capability is achieved (e.g., capacitance retention of 67.6% at a 50-fold higher current). Moreover, the 2D PEDOT-based supercapacitors exhibit outstanding cycling stability (capacitance retention of 98.5% after 30,000 cycles). Device performance is further improved when an organic electrolyte is used.

Water-Assisted Ion Conduction in Solid-State Charge-Transfer Complex Electrolytes for Lithium Batteries

Current research on solid-state organic electrolytes mainly focuses on polymer electrolytes where ion transport is facilitated by chain segmental motion. A limited number of prior reports suggest that solid-state electrolytes based on organic charge-transfer (CT) complexes can have surprisingly high ionic conductivity. Here, we report that processing and environmental conditions drastically impact charge transport properties of CT complex electrolytes based on tetrathiafulvalene-tetracyanoquinodimethane (TTF-TCNQ) mixed with lithium bis(trifluoromethanesulfonyl)imide (LiTFSI). Thermal annealing and water vapor treatment decreases electronic conductivity and increases ionic conductivity. The electrolyte with a 1-1-2-0.45 molar ratio of TTF-TCNQ-LiTFSI-H2O has an ionic conductivity of 2 × 10–3 S/cm at 25 °C with order 104 times lower electronic conductivity. In this system where ion conduction is decoupled from the mobility of the organic phase, thermal annealing helps reduce CT connectivity and expose more surfaces to interact with LiTFSI, and water promotes the dissociation of LiTFSI.

The Performance of Chitosan-based Activated Carbon for Supercapacitor Applications towards Sustainable Energy Technologies

In sustainable technologies, the application of supercapacitors (SC) for energy conversion and storage systems is rapidly increasing. Supercapacitors are widely employed in applications that require fast charge and discharge phases, such as in the automobile industry, where they are utilized in energy storage. Chitosan (CS) is a natural polymer material utilized in supercapacitor fabrication. Interest in supercapacitors is due to their high-energy capacity, storage for a shorter period, and longer lifetime. In this research, the fabrication of symmetric supercapacitors with activated carbon (AC) electrodes has been investigated in order to analyze their performance characteristics. AC is derived from CS biomass, which has remarkable biodegradability. It has been chemically activated using ZnCl <sub xmlns:mml="http://www.w3.org/1998/Math/MathML" xmlns:xlink="http://www.w3.org/1999/xlink">2</sub> as the activating agent. CS has been activated inside a furnace at 500, 600, and 700°C in an inert N <sub xmlns:mml="http://www.w3.org/1998/Math/MathML" xmlns:xlink="http://www.w3.org/1999/xlink">2</sub> atmosphere. A 1M aqueous potassium hydroxide (KOH) solution is used as the electrolyte. The test using electrolytes (KOH) revealed that the electrode's specific capacitance was 74.7 Fg <sup xmlns:mml="http://www.w3.org/1998/Math/MathML" xmlns:xlink="http://www.w3.org/1999/xlink">-1</sup> , the highest value discovered. However, using organic electrolytes would have produced better results that can be used as a guide for future advancements. The influence of activation temperature on the porous characteristics of prepared AC was investigated utilizing surface area and pore size analyses. The morphological characteristics of synthesized AC were analyzed through scanning electron microscopy (SEM) and Energy Dispersive X-Ray Analysis (EDX). Symmetric SC electrodes fabricated is analyzed in a two-electrode system applying standard electrochemical characterization methods using the potentiostat. Symmetric SC electrodes fabricated are analyzed in a two-electrode system applying standard electrochemical characterization methods using the potentiostat.