Electrode Materials For Supercapacitors Research Articles

Microwave irradiation effect of La2O3-CeO2 nanocomposites as a potential electrode material for asymmetric supercapacitor

Microwave irradiation effect of La2O3-CeO2 nanocomposites as a potential electrode material for asymmetric supercapacitor

Cr-Substituted SrCoO3-δ Perovskite with Abundant Oxygen Vacancies for High-Energy and Durable Low-Temperature Antifreezing Flexible Supercapacitor.

Developing high-performance electrodes for flexible antifreezing energy storage devices has been a significant challenge with the increasing demand for portable components. In this work, Cr-substituted SrCoO3-δ perovskites were first proposed as potential low-temperature supercapacitor electrode materials. The high-valence Cr6+ ([Ne]3s23p6) substitution favors a high-spin state of Co ions with enhanced electronic repulsion effect, ultimately forming a stable cubic structure with high conductivity. Accordingly, the modification strategies of SrCoO3 through the p6 configuration cation substitution have been improved. As a result, the asymmetric SrCo0.95Cr0.05O3-δ@CC//PPy@CC device exhibited a high energy density of 44.90 Wh kg-1 at 902.01 W kg-1 and maintained a 95.8% specific capacitance after 10,000 cycles, demonstrating an ultralong cyclic stability. The dramatically improved electrochemical performance was attributed to the stabilized crystal structure, increased oxygen vacancy, and accelerated oxygen diffusion rate. Furthermore, a quasi-solid-state supercapacitor with ethylene glycol (EG)-modified KOH/PVA organohydrogel electrolyte was developed through an advance in situ-integrated strategy. After bending at 180° for 1000 cycles, only a 9.7% capacity decay was observed. Even under -40 °C, the supercapacitor has a large energy density of 46.94 μWh cm-2. The present work represents the initial investigation into utilizing perovskite materials for antifreezing energy storage device, thereby confirming their potential application as low-temperature electronic components.

High performance Symmetric Supercapacitors based on Au incorporated CrN thin films fabricated by reactive magnetron sputtering

Recently, transition metal nitrides are being investigated extensively as potential supercapacitor material. In the present study, Au incorporated CrN (Au_CrN) thin films have been synthesized using reactive magnetron co-sputtering technique for application as supercapacitor electrode material. Films have been prepared at different Ar to N2 flow rates keeping total deposition pressure constant to achieve the required structural phase in the sample. Electrochemical properties of the deposited materials have been investigated with a three-electrode system in 0.5 M H2SO4 aqueous electrolyte. The CrN thin film deposited under 3:1 Ar: N2 partial pressure or flow rate ratio shows the highest specific capacitance. Upon Au incorporation, the film shows an areal capacitance of 56.8 mFcm−2 at 1.0 mAcm−2discharge current density which is an almost nine-fold enhancement in specific capacitance value compared to pristine CrN sample. Symmetric supercapacitors have also been developed by sandwiching two identical Au_CrN thin film electrodes, which have found to deliver excellent specific capacitance of 86.03 mFcm−2at 1.0 mAcm−2discharge current density with no decline in capacitance value till 20000 cycles. Furthermore, it can deliver a high energy density of 52.02mWhcm−2and a power density of 0.12mWcm−2. The electrochemical properties of the supercapacitors fabricated with the Au_CrN thin film electrodes are found to be better than most of the results reported so far in the literature with CrN electrodes. Results of the present study clearly demonstrate that these Au enhanced CrN films prepared by easily scalable and highly reproducible magnetron sputtering technique have great potential as a high capacitance supercapacitor electrode material.

Dense graphene composite hydrogels as advanced electrode materials for high-performance supercapacitors

In this work, alanine functionalized nanocellulose/graphene composite hydrogels (NCGHalas) were prepared via an easy hydrothermal reaction using alanine, GO, and nanocellulose as reactant. Thanks to this synthesis strategy, NCGHalas exhibited large bulk density, abundant heteroatom functional groups, reasonable porous structure and moderate specific surface area. Based on the above characteristics, the aqueous symmetric supercapacitors (ASSC) assembled by NCGHala25 presented high gravimetric and volumetric specific capacitance of 276.5Fg-1 and 320.8Fcm-3 at 0.3Ag-1, excellent rate performance (77.9% at 10Ag-1), and long working life of 95.4% retention after 10,000 cycles at 10Ag-1. Furthermore, the NCGHala25 based ASSC also exhibited large gravimetric and volumetric specific energy densities of 9.6Whkg-1 and 11.1WhL-1. More importantly, the flexible solid-state supercapacitors (FSSC) fabricated by NCGHala25 and PVA-KOH electrolyte delivered high specific capacitance (178.2Fg-1, 0.3Ag-1), and this value can be maintained for 74.2% even at 10Ag-1.

Design and fabrication of Reduced Graphene Oxide (RGO) incorporated NiCo2S4 hybrid composites as electrode materials for high performance supercapacitors

One of the most promising bimetallic sulphides for use in energy-storage systems is NiCo2S4, but further research is required to give it a high reversibility and electrochemical reaction capacity. In this study, we show the rational materials design of an ideal NiCo2S4 nanoparticle as a NiCo2S4/RGO nanocomposite, embedded in a reduced graphene oxide (RGO) matrix. NiCo2S4 nanoparticles, which ranged in size from 20 to 25 nm and were firmly fixed on the surface of RGO sheets, made up the produced composite. As predicted, the produced nanocomposite displayed a high specific surface area, a mesoporous structure, and high conductivity, resulting in a large electroactive area and rapid electron and ion motion. Additionally, we present the advancements in material science, showcasing the NiCo2S4/RGO nanocomposite electrode, which has a long cycle life of 5000 cycles, a high capacitance retention of 85.6%, and an exceptional specific capacitance of 1505 Fg-1 at 1 Ag-1. A high active-material loading asymmetric supercapacitor serves as an example of the real-world use. The NiCo2S4/RGO nanocomposite exhibits an exceptional 48 Whkg-1 energy density at a power density of 985 Whkg-1, while maintaining a high power density of 7227 Wkg-1 density of 25 Whkg-1. The exceptional stability and electrochemical efficiency of the NiCo2S4/RGO nanocomposite validate that our methodical materials science and technology optimisation in the areas of active substance synthesis, electrode expansion, and device design/fabrication will help advance the development of high-performance supercapacitors in future years.

Metal-organic frameworks and composites on their basis: structure, synthesis methods, electrochemical properties and application prospects (a review)

Various types of metal-organic frameworks (MOF) and their structural parameters have been reviewed and their classification has been presented. Most widely used synthesis methods and approaches for MOF and composites on their basis have been discussed. MOF structure is a regular 3D lattice formed by organic linkers and metallic clusters. It has been shown for an example of literary data on MOF synthesis and structural studies that the types of bonds and metals can strongly affect the spatial structure and dimensions of MOF crystals: they can have nano-, micro- and meso-dimensions, be dense or porous, bulk or layered. This variety of structural parameters determines the wide range of their properties and potential applications. Prospects and methods of controlling the shapes of the crystals, their size and spatial bonds between organic components and metal ions have been reviewed. Major attention has been paid to zeolite-like frameworks (ZIF) as the most promising ones from the viewpoint of structure, synthesis and electrochemical current source applications. Discussion has touched on possible modifications and methods of controlling the properties of those MOFs and composites on their basis and introduction of impurities, including those having magnetic properties. Possible synthesis options of complex composites through controlled MOF pyrolysis have been presented, for either small-batch or scalable processes. The effect of heat treatment conditions on the final properties and electrochemical applications of those materials has been demonstrated. ZIF-67 structured MOF doping with one more metal has been presented as variant of modifying the properties of MOF and composites on their basis. For example, the Authors have implemented cobalt MOF synthesis wherein cobalt is partially substituted for manganese at the synthesis stage. Furthermore, a simple water solution co-deposition synthesis technique has been modified with ultrasonication thus reducing the time consumption of the process. Electrochemical studies have shown that the unit electrochemical capacity of pyrolyzed MOF electrodes with partial cobalt substitution for manganese is appreciably higher as compared to the manganese-free materials. The unit capacity and energy density increase with manganese content in the MOF. MOF manganese doping delivers a considerable improvement in the electrochemical parameters of the electrode materials for hybrid supercapacitors on their basis (from 100 to 298 F/g at 0.25 A/g current density). The results suggest that cobalt substitution for manganese is an effective method of improving the electrochemical parameters of MOFs. It has been demonstrated that the development of new approaches to the design of MOF based composite materials and the study of the physicochemical regularities of their interaction with various carriers is an important task.

Self-assembled from monometallic-organic framework to bimetallic-organic framework materials with promoted supercapacitor performance

Designing new metal–organic frameworks (MOFs) materials with definite structure and introducing heterometallic atom is an effective strategy to develop new electrocatalytic and energy storage materials. Herein, one new 3D close-packed type manganese metal–organic frameworks, namely [Mn2(BPTC)(DMSO)2.5] (Mn-MOF) have been constructed from a rigid biphenylic acid with a rigid biphenyl-3,3′,5,5′-tetracarboxylic acid (H4BPTC) ligand under a solvothermal condition. Besides, adopting the metal doping strategy, a series of bimetallic MnM’-MOF (M’=Co, Ni and Cu) crystalline materials has been successfully grown on nickel foam (NF) and were used for supercapacitor electrode material. By contrast, the MnNi-MOF/NF shows a specific capacitance of 3391.7 mF cm−2 at 1 mA‧cm−2 in 1.0 M KOH, which is 1.6 times that of Mn-MOF/NF electrode. It also displays excellent cycle stability to keep 92.6 % of the initial capacity after GCD 20000 cycles. Finally, a hybrid supercapacitor (HSC) made from on the MnNi-MOF electrode and activated carbon (AC) could deliver an energy density of 0.224 mWh cm−2 at a power density of 1.04 mW cm−2, and a high cycle-to-cycle stability with 90.1 % of the primary capacitance over 20,000 cycles. This work not only confirms the potential supercapacitor properties of as-synthesized new Mn-MOF, but also effectively improves the specific capacity and device stability of pure Mn-MOF by introducing different transition metal ions.

Research Progress in the Preparation of Transition Metal Sulfide Materials and Their Supercapacitor Performance

Transition metal sulfides are widely used in supercapacitor electrode materials and exhibit excellent performance because of their rich variety, low price, and high theoretical specific capacity. At present, the main methods to prepare transition metal sulfides include the hydrothermal method and the electrochemical method. In order to further improve their electrochemical performance, two aspects can be addressed. Firstly, by controllable synthesis of nanomaterials, porous structures and large surface areas can be achieved, thereby improving ion transport efficiency. Secondly, by combining transition metal sulfides with other energy storage materials, such as carbon materials and metal oxides, the synergy between different materials can be fully utilized. However, future research still needs to address some challenges. In order to guide further in-depth research, it is necessary to combine the current research-derived knowledge and propose a direction for future development of transition metal sulfide electrode materials.

High-performance supercapacitor electrode materials from composite of bamboo tar pitch activated carbon and tannic acid carbon quantum dots

A novel composite electrode material comprising bamboo tar pitch-based activated carbon (BTPAC) and tannic acid-derived carbon quantum dots (TACDs) was prepared. The integration of TACDs into the composite BTPAC-60/TACD not only preserved the high conductivity characteristic of BTPAC but also enhanced its hydrophilicity, pore structure, and specific surface area. Electrochemical evaluations revealed that BTPAC-60/TACD delivers a specific capacitance of 677.7 F/g at 0.5 A/g in a three-electrode system, and 281.8 F/g at 1 A/g in a two-electrode setup. Impressively, it achieves an energy density of 56.4 Wh/kg at a power density of 600 W/kg and maintains 95.7 % of its capacitance after 10,000 cycles. This research not only capitalizes on the high-value application of bamboo tar pitch but also provides a new perspective for the development of high-performance supercapacitor electrodes.

Bimetallic MOF derived Ni[sbnd]Mn phosphide for high-performance supercapacitor electrode material

Nickel‑manganese bimetallic phosphides are prepared by phosphidization of MOF-derived bimetallic hydroxides. The bimetallic phosphides exhibit crystalline Ni2P phase, show high specific surface area, and are composed of nanosheets. When supported on carbon cloth (CC) and used as the electrode material in 4 M KOH, the (Ni0.93Mn0.07)2P-18/CC shows a specific capacitance of 851.1C g−1 at 1 A g−1 and maintains 84.87 % capacity after 5000 cycles. The origin of the high specific capacity is investigated, and electron interaction between Mn and Ni sites, the high specific surface area, and the facile ion transport leads to the high specific capacity and stability. The constructed (Ni0.93Mn0.07)2P-18//AC asymmetric supercapacitor has an energy density of 59.83 Wh kg−1 at a power density of 750 W kg−1 and a capacity retention of 95.5 % after 5000 cycles.

One-pot synthesis of low-cost CuS/Vulcan carbon composites applied as electrode materials for supercapacitors

One-pot synthesis of low-cost CuS/Vulcan carbon composites applied as electrode materials for supercapacitors

Synthesis of surfactant-assisted nickel ferrite nanoparticles (NFNPs@surfactant) to amplify their application as an advanced electrode material for high-performance supercapacitors.

Nickel ferrite nanoparticles (NFNPs) were synthesized in an alkaline medium (pH ∼ 11) using a wet chemical co-precipitation technique. To probe the effect of surfactants on the surface morphology, particle size and size distribution of nanoparticles; two surfactants, namely, cetyl trimethyl ammonium bromide (CTAB) and sodium dodecyl sulphate (SDS), were applied. The native and surfactant-assisted nickel ferrite NPs were characterized using Fourier transform infrared (FTIR) spectroscopy, X-ray diffraction (XRD), scanning electron microscopy (SEM), atomic force microscopy (AFM), dynamic light scattering (DLS) and transmission electron microscopy (TEM). The addition of surfactants (CTAB/SDS) effectively controlled the secondary growth of nickel ferrite particles and reduced their size, as examined by XRD, AFM, DLS, SEM and TEM. Characterization technique results affirmed that CTAB is a more optimistic surfactant to control the clustering, dispersion and particle size (∼22 nm) of NFNPs. To identify the impact of ferrite particle size on charge storage devices, their electrochemical properties were studied by using cyclic voltammetry (CV), galvanic charge-discharge (GCD) and electrochemical impedance spectroscopy (EIS) in 1 M KOH electrolyte through three-electrode assembly. NiFe2O4@CTAB showed a specific capacity of 267.1 C g-1, specific capacitance of 593.6 F g-1 and energy density of 16.69 W h kg-1, which was far better than the performances of other synthesized native NFNPs and NiFe2O4@SDS having larger surface areas.

Study and characterization of BaFe12O19/PVDF composites as electrode materials for supercapacitors

Supercapacitors are an interesting energy storage technology to be studied. This research uses mesoporous BaFe12O19 particles and synthesized Polyvinylidene fluoride (PVDF) polymers as materials to obtain high performance supercapacitors. Composites were synthesized by facile one-step method using BaFe12O19 which was prepared through co-precipitation chemical method with a calcination process at 200 °C along with PVDF with variations in sample composition of BaFe12O19, BaFe12O19 20%, BaFe12O19 30%, BaFe12O19 40%, and BaFe12O19 60%. And finally the fabrication of supercapacitor electrodes is carried out. The result of the synthesized material is distributed grains with the average particle size of each sample ranging from 180 to 185 nm. Then it has the highest peak in crystals with a miller index (114). Furthermore, it has the main functional group, Ba–O with a wave number of 1632 cm−1. Furthermore, the best supercapacitor electrode is BaFe12O19/PVDF 60% which produces an area of 0.51 mVA where the greater the surface area, the higher the capacitance obtained. Then at BaFe12O19/PVDF 60% has the highest power density value at 12.36 Wh/kg and the highest power density value at 299.14 Wh/kg. It is expected that the results obtained can be a reference for further electrode material research.

MXene/Nitrogen-Doped Carbon Nanosheet Scaffold Electrode toward High-Performance Solid-State Zinc Ion Supercapacitor.

While MXene is widely used as an electrode material for supercapacitor, the intrinsic limitation of stacking caused by the interlayer van der Waals forces has yet to be overcome. In this work, a strategy is proposed to fabricate a composite scaffold electrode (MCN) by intercalating MXene with highly nitrogen-doped carbon nanosheets (CN). The 2D structured CN, thermally converted and pickling from Zn-hexamine (Zn-HMT), serves as a spacer that effectively prevents the stacking of MXene and contributes to a hierarchically scaffolded structure, which is conducive to ion movement; meanwhile, the high nitrogen-doping of CN tunes the electronic structure of MCN to facilitate charge transfer and providing additional pseudocapacitance. As a result, the MCN50 composite electrode achieves a high specific capacitance of 418.4 Fg-1 at 1 Ag-1. The assembled symmetric supercapacitor delivers a corresponding power density of 1658.9 Wkg-1 and an energy density of 30.8 Whkg-1. The all-solid-state zinc ion supercapacitor demonstrates a superior energy density of 68.4 Whkg-1 and a power density of 403.5 Wkg-1 and shows a high capacitance retention of 93% after 8000 charge-discharge cycles. This study sheds a new light on the design and development of novel MXene-based composite electrodes for high performance all-solid-state zinc ion supercapacitor.

Using anodic oxidation for boosting supercapacitive performance of thermally-oxidized cobalt coatings with various morphologies

Metal oxide electrodes for supercapacitors are commonly synthesized through the hydrothermal method. Despite the simplicity and cost-effectiveness of electrodeposition for producing electrode materials, there is a scarcity of literature on electrodeposited electrodes. Previous studies have utilized nitrate-based solutions and subsequent heat-treatment to fabricate these materials without additional treatments to enhance their performance. This research explores the creation of cobalt coatings with varying morphologies (pyramidal, ridge-shaped, powdery, and rough nodular) using electrodeposition from sulfate-based solutions by adjusting deposition parameters. The cobalt coatings were then heat-treated at 550˚C for 3 h to convert them to cobalt oxide, a promising material for supercapacitor electrodes. The study investigates the impact of initial morphology on the structure, phases formed, and supercapacitive properties of the heat-treated coatings. Analysis of XRD and FTIR data indicated that the primary phase post-heat treatment was Co3O4, alongside some CoO. Cyclic voltammetry (CV) measurements in 1 M KOH solution revealed that the powdery coating exhibited the highest specific capacitance of 796±21 mF cm−2 (∼110 F g−1) at a scanning rate of 2 mV s−1, surpassing the heat-treated pyramidal coating by approximately tenfold. These CV findings were corroborated by galvanostatic charge-discharge (GCD) and electrochemical impedance spectroscopy (EIS) analyses. Furthermore, the heat-treated coatings underwent anodic oxidation in a 3 M KCl solution for 5 minutes to assess the impact of this lesser-known process on their capacitive behavior. Following anodic oxidation, the ridge-shaped and pyramidal coatings displayed significantly enhanced specific capacitance due to the formation of fine pores and surface modifications. Specifically, the specific capacitance of the ridge-shaped coating surged from 103±4 mF cm−2 (∼11 F g−1) to 1832±64 mF cm−2 (∼201 F g−1) at a scanning rate of 2 mV s−1 after anodic oxidation. Although the rough nodular coating also experienced an increase in specific capacitance, the morphology and electrochemical characteristics of the powdery coating remained relatively stable throughout the study.

Samarium-doped vanadium pentoxide nanorods anchored reduced graphene oxide nanocomposite as a bi-functional electrode material for supercapacitor and direct methanol oxidation fuel cell applications

In this work, we demonstrate a novel, facile synthesis of reduced graphene oxide nanosheets decorated samarium-doped vanadium pentoxide (RGO/Sm:V2O5) nanocomposite material and explore its application toward supercapacitor and direct methanol oxidation process. As-fabricated material and electrode were well-characterized to evaluate its surface morphology and functionalities. Results indicate a maximum capacitance value of 544 F/g for RGO/Sm:V2O5 modified electrode than the 2% Sm:V2O5 (346 F/g) and V2O5 (133 F/g) modified electrodes. In addition, an excellent Rct value (3.2 Ω) was achieved for the RGO-loaded Sm:V2O5 electrode than the 2% Sm:V2O5 electrode (4.7Ω). The RGO/Sm:V2O5 electrode also shows higher cyclic efficiency (98 %) at the 1000th cycle than the non-RGO loaded Sm:V2O5 electrodes. Furthermore, the fabricated electrodes were also examined for the direct methanol oxidation performances, and the results indicate a higher current density value of 181 mA/cm2 for RGO/Sm:V2O5 electrode than 2% Sm:V2O5 electrode (139 mA/cm2). The excellent electrochemical performance of the RGO/Sm: V2O5 electrode is mainly due to the presence of RGO nanosheet in the synthesized nanocomposite material. Therefore, as-prepared material can be applied as an excellent alternative electrode material for energy storage and conversion systems.

β-Ni(OH)2 nanoparticles@activated sugarcane bagasse carbon nanocomposites as an advanced hybrid electrode material for asymmetric supercapacitors

β-Ni(OH)2 nanoparticles (NPs)@activated sugarcane bagasse carbon (ASBC) nanocomposites (N@ASBC NCps) with different Ni loadings were synthesized using a hydrothermal process. The products were characterized using techniques such as X-ray diffraction (XRD), field emission scanning and transmission electron microscopy (FE-SEM and TEM), Raman spectroscopy, and Fourier transform infrared spectroscopy (FT-IR). Electrochemical performance of the products was studied. Interestingly, the maximum specific capacitance of 1213.32 F/g at 1 A/g could be achieved in a 3N@ASBC NCps positive electrode. Concurrently, the ASBC negative electrode revealed a high specific capacitance of 233.34 F/g at 1 A/g. Additionally, the fabricated asymmetric supercapacitor (ASC), ASC-ASBC//3N@ASBC NCps, had a specific capacitance (Csc) of 34.03 F/g at 1 A/g with a specific energy density (Ed) and specific power density (Pd) of 9.93 Wh/kg and 181.26 W/kg, respectively. Moreover, the device could maintain 69.47% of its capacity after a 5000-cycle test.

Non-preoxidation synthesis of MXene integrated flexible carbon film for supercapacitors

Although the flexible carbon film integrated with MXene has been proven to be a new generation of supercapacitor material with good energy storage prospects, the MXene oxidation and the lack of active sites during the preparation of the carbon film can lead to irreversible capacity loss. Herein, a flexible carbon film constructed by MXene-integrated N-doped cavity-interconnected porous carbon nanofibers was prepared by a non-pre-oxidation synthesis strategy combining electrospinning and metal–organic framework derivatization. This flexible carbon film overcomes the oxidation problem of MXene during the stabilization of polyacrylonitrile, and the derived porous structure of cavity interconnection exposes more active sites. Due to its unique structural characteristics and ideal chemical composition, this independent flexible carbon film exhibits significantly enhanced electrochemical performance as an electrode material for supercapacitors. It exhibits an energy density of 26.2 Wh kg−1 at a power density of 500 W kg−1, and a capacitance retention rate of 96.3 % after 10,000 charge–discharge cycles. This study provides a unique strategy for the preparation of high-performance flexible carbon films, and this technology can also be extended to other integrated CNF composites for the design of high-performance supercapacitor electrodes.

Biomass nanoarchitectonics with activated rice husk char for nanoporous carbon as electrode material: Enhancing supercapacitor electrochemical performance

Nanoporous carbon from activated rice husk char was prepared via KOH activation at different ratios of rice husk: KOH, for using as electrode material in supercapacitor. The electrode could exhibit high performance in 6 M KOH aqueous electrolytes, particularly in terms of specific capacitance and power density. The Brunauer-Emmett-Teller (BET) analysis showed a high specific surface area of 2833 m²/g with a mesoporous structure in a sample activated with a 1:3 ratio of rice husk to KOH. In this sample, a high specific capacitance of 195.36 F/g was obtained at a current density of 1 A/g with excellent cycle stability of 99.87 % after continuous charge/discharge test for 10,000 cycles at 10 A/g. Furthermore, the fabricated symmetric coin cell exhibits a power density of 526.88 W/kg and an energy density of 14.77 Wh/kg. The practical application of this cell is demonstrated by its ability to power a 3 V LED light bulb for over 900 s.

Algae Derived Carbon from Hydrothermal Liquefaction as Sustainable Carbon Electrode Material for Supercapacitor

With the worldwide awareness of sustainability, biomass-derived carbon electrode materials for supercapacitors have attracted growing attention. In this research, for the first time, we explored the feasibility of making use of the carbon byproduct from hydrothermal liquefaction (HTL) of microalgae, termed herein as algae-derived carbon (ADC), to prepare sustainable carbon electrode materials for high-performance supercapacitor development. Specifically, we investigated carbon activation with a variety of activating reagents as well as N- and Fe-doping of the obtained ADC with the intention to enhance its electrochemical performance. We characterized the structure of the activated and doped ADCs using scanning electron microscope (SEM), Raman spectroscopy, Fourier transform infrared spectroscopy (FTIR), X-ray photoelectron spectroscopy (XPS), and BET surface area and pore analysis, and correlated the ADCs’ structure with their electrochemical performance as evaluated using cyclic voltammetry (CV), galvanostatic charge/discharge (GCD), impedance, and cycle stability through an assembled symmetric two-electrode cell with 1 M H2SO4 as electrolyte. It was found that the ADC that is activated using KOH (KOH-ADC) showed the best electrochemical performance, and its specific capacitance was 14.1-fold larger with respect to that of the raw ADC and reached 234.5 F/g in the GCD test at a current density of 0.5 A/g. The KOH-ADC also demonstrated excellent capacitance retention (97% after 10,000 cycles at a high current density of 10 A/g) for stable long-term operations. This research pointed out a promising direction to develop sustainable electrode materials for supercapacitors from the carbon byproduct produced after HTL processing of algae.