Carbon Electrode Materials Research Articles

Increasing Specific Capacitance by Optimization of the Thickness of Carbon Electrodes

AbstractIncreasing energy density without sacrificing the lifetime, power and cyclability of electrochemical capacitors is a very important goal. However, most efforts are directed toward the improvement of active charge‐storing materials, while the design of devices and minimization of the weight/volume of the passive component have received less attention. We propose here a mathematical model of a carbon supercapacitor in organic electrolyte, which establishes a relationship between the specific capacitance of a device, the thickness of its electrodes, and the weight of its passive components (case, external current leads, current collectors, etc.). The model was built based on experimentally obtained dependences and has been validated using experiments with electrodes made of two porous carbon materials. Regardless of the pore size distribution in the specified range of electrode thicknesses, the functional dependence of the electrode's specific capacitance on the thickness is well described within the linear approximation. The developed model enables optimization of the electrode thickness, thus maximizing specific energy density for a chosen carbon electrode material.

Fabrication of Ni-foam-assisted graphene@MnO2-doped carbon fabric electrodes from waste cotton fabrics for supercapacitors

Fabrication of Ni-foam-assisted graphene@MnO2-doped carbon fabric electrodes from waste cotton fabrics for supercapacitors

Biomass‐Derived Carbon Materials for Smart Electronics: Insights from Wood Pitch‐based Microsupercapacitors

AbstractWood pitch, derived from dry distillation of wood, is a promising carbon electrode material. A novel strategy is presented for fabricating honeycomb‐like porous carbon nanosheets using a template‐free approach. Wood pitch is pre‐treated with H₂O₂ to introduce oxygen‐containing functional groups selectively at the edges of polycyclic aromatic hydrocarbons, enhancing hydrophilicity and reactivity. Adding rosin groups to the oxidized wood pitch molecules helps to regulate intermolecular spacing and prevent excessive aggregation, facilitating subsequent KOH intercalation activation and the formation of a porous structure. The resulting rosin‐modified wood pitch‐based carbon material (RWPC‐0.2) features a high specific surface area (3521.5 m2 g−1). With a current density of 1 A g−1, the device has a specific capacitance of 376 F g−1. After 5000 cycles at 10 A g−1, it still has 83.8% of its initial specific capacitance. Using direct ink writing (DIW) technology in combination with poly(3,4‐ethylenedioxythiophene): polystyrene sulfonate/RWPC‐0.2 (PEDOT: PSS/RWPC‐0.2) as the electrode ink, microelectrodes are fabricated and microsupercapacitors are constructed with high areal capacitance (460 mF cm−2), excellent rate performance, and good cycling stability. This study offers new insights for developing printed micro‐energy storage devices based on wood pitch‐derived carbon materials and opens new possibilities for the application of biomass materials in smart electronics.

Trichosanthes cucumerina derived activated carbon: the potential electrode material for high energy symmetric supercapacitor

High surface area porous activated carbons obtained from sustainable biomass are excellent functional materials for energy storage applications. This is the first report on snake gourd (Trichosanthes cucumerina) pericarp as a raw material of activated carbon and supercapacitor electrode material. Herein, a simple KOH activation and carbonisation method is used. The obtained SGC900 sample has a surface area of 1841 m2/g and an average pore volume of 0.52 cm3/g. SGC900 based supercapacitor exhibits good electrochemical storage capacity in 1 M H2SO4with a specific capacitance of 206 F/g at 1 A/g. The symmetric device delivered an energy density of 11 Wh/kg at a power density of 1.6 kW/kg. It provides a series resistance (Rs) of 1.2 Ω and a charge transfer resistance Rct of 1.9 Ω. Furthermore, the device retains 95% of capacitance over 5000 cycles. This work presents an easy and feasible approach for producing value‐added activated carbon from sustainable biomass, potentially used in high‐performance energy storage.

Sensitive detection of persulfate by a novel self-powered electrochemical sensor with carbon cloth electrodes modified with tin-doped cobalt tetroxide.

The accurate and rapid detection of persulfate concentration is important for environmental decontamination and human health protection. In this work, a novel self-powered electrochemical sensor for the sensitive monitoring of persulfate was developed, which utilized cobalt tetroxide (Co3O4@CC) or tin-doped cobalt tetroxide (SnxCo3-xO4@CC) cathode as the sensing element and anode with electrogenic microorganisms as the power supplier. The Co3O4@CC and SnxCo3-xO4@CC electrodes were fabricated by in situ growing nanostructured Co3O4 or SnxCo3-xO4 catalysts on carbon cloth. Electrochemical tests revealed that these electrodes exhibited excellent catalytic reduction performance toward persulfate because of the synergistic catalysis by Co3O4 and electrode electrons, well-exposed Co2+/Co3+ catalytic sites, and high electron transfer efficiency. Tin doping could enhance the catalytic persulfate reduction by improving the conductivity and electron transfer of the Co3O4 catalyst. The electrode prepared at a hydrothermal temperature of 90°C and a tin dosage of 0.286g·cm-2 achieved the highest persulfate reduction activity under pH 7. The sensing properties of the self-powered sensors toward persulfate were explored in detail. Results showed that under the optimal external load of 300 Ω, the proposed sensor could display a broad detection range of 0 to 1500μmol L-1 K2S2O8 with sensitivities of 1.13 and 0.12 μA μmol-1 L, a detection limit of 1.11μmol L-1 (S/N = 3), and a fast response time within 30s. The sensors also presented satisfactory reproducibility and selectivity during the detection of persulfate. The proposed sensor will provide a new approach for sensitive, on-site, and real-time monitoring of persulfate for a wide range of applications.

Effect of Triton X-100 surfactant concentration on the wettability of polyethylene-based separators used in supercapacitors

Polyethylene-based separators are generally unsuitable for aqueous supercapacitors due to their poor wettability with the electrolyte, which impedes ion transport. However, incorporating Triton X-100 (2-[4-(2,4,4-trimethylpentan-2-yl)phenoxy]ethanol) into the aqueous sulfuric acid (H2SO4) electrolyte improves the wettability of polyethylene and facilitates ionic movement through its pores. In this study, Triton X-100 was added to 1.0 M H2SO4 at various concentrations (0.122%–1.210% V/V) to evaluate its impact on supercapacitor performance. Supercapacitors were assembled using activated carbon-filled carbon cloth electrodes, each of the above electrolytes and polyethylene sheet separators. Scanning electron microscopy revealed that the carbon cloth exhibited a uniform fiber distribution and high surface area for activated carbon integration. The polyethylene separator displayed a porous structure with an average pore size of 165 ± 35 nm. Triton X-100 significantly reduced the water contact angle from 101.5° (without surfactant) to 30.2° (with 1.21% V/V Triton X-100), enhancing polyethylene’s wettability. This change from hydrophobic to hydrophilic characteristics enabled the formation of an electrical double layer at the separator/electrolyte interface, improving ionic transport. However, higher Triton X-100 concentrations increased the electrolyte's viscosity, which impeded ion movement. The highest specific capacitance of 55.3 F/g (at a scan rate of 0.005 V s−1) was achieved with 0.488% V/V Triton X-100. The specific capacitance varied with surfactant concentration in a complex manner, influenced by micelle formation and precipitation. These findings were corroborated by cyclic voltammetry and AC impedance spectroscopy.

Enhanced construction of 3D carbon skeleton through molten salt coupling activation effect for high efficiency capacitive deionization of lead (II) ions removal in wastewater

Efficiently eliminating of highly toxic ultra-dilute lead ions (Pb2+) from wastewater is a challenging task. Capacitive deionization (CDI) technology, based on the electrochemical capacitance mechanism, has emerged as a pivotal approach to address this challenge. In this work, a KNO3-mediated molten salt-coupled activation strategy was proposed to prepare nitrogen-doped hierarchical porous biomass carbon electrode material (3DCF-650-0.2) with a three-dimensional carbon skeleton, which was integrated into a symmetrical CDI device for Pb2+ removal. The 3DCF-650-0.2 electrode exhibited a high specific capacitance of 330.3 F g-1 at a current density of 1 A g-1, with a capacity retention rate of 98.45% after 10,000 cycles at 10 A g-1. Furthermore, the electrochemical adsorption capacity of the CDI device for Pb2+ reached 72.86 mg g-1 (1.2 V, 50 mg L-1), and the CDI device retained a high adsorption capacity of 91.14% after twenty adsorption/desorption cycles. These excellent adsorption properties are attributed to the in-situ activation and gas foaming of KNO3, which favors the production of reasonable pore structure (electric double-layer capacitance) and an appropriate pyrrolic nitrogen doping amount (selective adsorption) in the carbon materials. This work provides insight into the mechanism of the molten salt-coupled activation strategy, offering new ideas for the targeted design of high-performance CDI biomass carbon materials.

High-voltage aqueous supercapacitors enabled by polysiloxane passivation coating-modified carbon cloth electrode

The voltage window plays a crucial role in determining the energy density of supercapacitors. The limited energy density of carbon-based supercapacitors poses a significant challenge to their widespread adoption. Here, we propose a novel approach to modify carbon cloth by implementing a polysiloxane (PSiO) passivation coating. This forms an ion-conductive and electron-insulating thin film on the surface, effectively impeding electron conduction from electrode surface to electrode/electrolyte interface and suppressing electrolyte electrolysis. Consequently, an expanded voltage window is realized, thereby enhancing the energy density of aqueous carbon-based supercapacitors. The carbon cloth electrode modified with the PSiO passivation coating (CC-A-KH560) exhibits exceptional electrochemical performance, with a significantly increased 78.6 % widened applicable potential range compared to the activated carbon cloth electrode (CC-A). In a two-electrode configuration, the voltage window is broadened from 0.8 V for CC-A to 1.4 V for CC-A-KH560, and the energy density based on CC-A-KH560 is 8 times that based on CC-A. The good stability and durability are also obtained for the firm C–O–Si bonds during PSiO modification. More importantly, this design provides a generic solution of PSiO passivation coating-modified carbon electrode, applicable for diversified silicane couple agents, to realize a high-voltage energy storage performance for aqueous supercapacitors.

Facile Synthesis of Colocasia esculenta Peels‐Derived Activated Carbon for High‐Performance Supercapacitor

ABSTRACTBiomass and biowaste resources can be used to create self‐doped carbon with a distinctive microstructure. Using an economical and environmentally friendly method to create heteroatom‐doped carbon electrode materials with excellent electrochemical performance has attracted much attention in the energy storage industry. A novel facile two‐step, low‐cost, and eco‐friendly synthesis method for Colocasia esculenta peels has been developed to manufacture activated carbon (CEPAC) and used as an electrode material for supercapacitor application. The CEPAC 1:1 displayed a high specific surface area of 910 m2/g with oxygen‐heteroatom polar sites in the carbon network. A specific capacitance of 525.3 F/g was recorded in the three‐electrode system using a 3 M KOH solution. The assembled symmetric cell delivered an impressive specific capacitance of 98.7 F/g at 1 A/g while maintaining 98.4% of the initially recorded capacitance after 10 000 charge–discharge cycles. These results present a promising low‐cost and simple processing route for synthesizing electrode materials with superior surface properties for high‐performance supercapacitors.

Bipolar Membrane Capacitive Deionization for the Selective Capture of Lithium Ions from Brines and Conversion to Lithium Hydroxide

Meeting the increasing demand for lithium in vehicle electrification and renewable energy storage requires innovations in lithium-ion (Li+) separations. Traditional solar evaporation methods for lithium recovery are slow and consume tremendous volumes of water and secondary chemicals (acids and bases). This study introduces a bipolar membrane capacitive deionization (BPM-CDI) unit for direct lithium extraction and LiOH production without the external addition of acids and bases. Utilizing de-lithiated lithium-iron-phosphate (LFP) coated carbon cloth electrodes, the BPM-CDI unit demonstrates selective Li+ capture over competing ions. Molecular dynamics simulations and H-cell experiments elucidate pH inversion mechanisms during Li+ release, yielding LiOH. The BPM-CDI platform efficiently removes Li+ from synthetic brines featuring 8x higher Mg2+ concentrations (200 ppm Mg2+) and 26x higher Na+ concentrations (682 ppm Na+), achieving a LiOH concentration of 124 ppm (36 ppm Li+) after 8 cycles of recirculation. Post-mortem analysis confirms electrode integrity and stability. BPM-CDI integrated with selective electrodes is a promising electrochemical separation-reactor platform for lithium recovery while producing LiOH.

Synthesis of rice husk derived porous carbon as low-cost and high-performance electrode material for supercapacitors

Porous carbon electrode materials derived from agricultural by-products of food processing have attracted widespread interest. Rice husk (RH) is a promising raw material owing to its abundance and low price. In this study, a supercapacitor electrode was prepared by using recycled RH and secondarily activated with ZnCl2 to enhance its electrochemical energy storage performance. RH carbonized at the optimum temperature (i.e., 800 °C) was activated to synthesize RH-800-X (X = 1, 2, 3, 4, or 5, representing the mass ratio of ZnCl2 to RH-800). Sample RH-800-3 exhibited the highest specific surface area (1348.29 m2 g−1) and mesoporous pore volume (0.8375 cm3 g−1) among the samples. In a three-electrode system, the prepared electrodes delivered a high specific capacitance (242 F g−1 at 0.3 A g−1 in 6 M KOH solution). Furthermore, the capacitance retention of RH-800-3 remained at 99.9 % after 17,000 charge/discharge cycles. The results demonstrate the excellent capacitive behavior and superior electrochemical performance of RH-800-3. In addition, symmetrical capacitors prepared using RH-800-3 have an energy density of up to 101 Wh kg−1 at a power density of 900 W kg−1. Therefore, this study presents a simple and effective method for preparing a high-performance electrode material from biomass-derived porous carbon (i.e., recycled RH) and offers a new perspective for the efficient utilization of waste biomass resources.

Ag@CuS/CC electrode promoting antibiotics removal in DBD system: Mechanism analysis and practical application

In this study, rice-granular CuS nanoparticles are grown in situ on carbon cloth (CC) using a hydrothermal method and Ag is then loaded on the CuS/CC via ultrasonic-assisted reduction. The electrodes combined with a dielectric barrier discharge (DBD) system can improve the plasma discharge efficiency and have good oxidation properties for tetracycline, amoxicillin and sulfamethoxazole. The removal rate is further improved after adding Cr(VI). The active substances, H2O2 and O3, are consumed during the process of antibiotic degradation. Trapping agent experiments indicate that h+, ∙OH and O2∙− play a crucial oxidation role in the reaction, with O2∙− being identified as the primary active substance. The pollutant degradation can be further accelerated by capturing e− and ·H for the reduction of Cr(VI). By calculating the adsorption energies of H2O and O2 on the surface of Ag@CuS, it is also concluded that O2 is easily adsorbed and preferentially generates O2∙−. The residual intermediates in the samples after the degradation of tetracycline, amoxicillin and sulfamethoxazole are determined and their degradation pathways also explored. The Ag@CuS/CC-DBD system has application potential in actual wastewater treatment as it can not only reduce the chemical oxygen demand but also improve the biodegradability of wastewater.

Exploration of cobalt-based spinel oxide nanocatalysts MCo2O4 (M = Mn, Fe, Co, Ni, Cu, Zn) for glucose electrochemical sensing: NiCo2O4 exhibits largest Faradaic current

In traditional glucose sensing, glucose undergoes an enzyme-catalyzed oxidation reaction (GOR) on the electrode, causing electron transfer and generating a Faradaic current, which allows for quantitative glucose concentration analysis by measuring the current. Replacing enzymes with transition metal-based catalysts for glucose electrochemical sensing is a promising approach. As an extension of the study of spinel oxide Co3O4 for glucose electrochemical sensing, a series of cobalt-based spinel oxide nanocatalysts, MCo2O4 (M = Mn, Fe, Co, Ni, Cu, Zn), were prepared and studied. Their electrocatalytic oxidation activities for 3 mM glucose in 0.1 M KOH electrolyte solution (pH = 13) at potentials of 0.5 ∼ 0.6 V (vs Hg/HgO) are in the order: NiCo2O4 > CuCo2O4 > MnCo2O4 > Co3O4 > FeCo2O4 > ZnCo2O4, the Faradic current by NiCo2O4 is more than three times that of Co3O4. When NiCo2O4 is loaded onto a carbon cloth electrode for glucose electrochemical sensing, it exhibits high linear sensitivity and stability. Furthermore, theoretical calculations revealed that the high electrocatalytic oxidation activity of NiCo2O4 for glucose is due to its effective reduction of the Gibbs free energy barrier for the desorption of intermediates to form glucose oxidation product. Finally, it is proposed that the electrocatalytic oxidation activities of MCo2O4 (M = Mn, Fe, Co, Ni, Cu, and Zn) towards glucose exhibit a “volcano plot” relationship with their d-band centers. This offers valuable guidance into using the d-band center as a descriptor to screen effective glucose electrocatalysts for glucose sensing and potentially other applications.

Biomass Hydrogel Electrolytes toward Green and Durable Supercapacitors: Enhancing Flame Retardancy, Low-Temperature Self-Healing, Self-Adhesion, and Long-Term Cycling Stability.

Hydrogels have shown promise as quasi-solid-state electrolytes for flexible supercapacitors but face challenges such as poor self-repair, unstable electrode adhesion, limited temperature range, and flammability. Herein, an all-round green hydrogel electrolyte (silk nanofibers (SNFs)/peach gum polysaccharide (PGP)/borax/glycerol (SPBG)-ZnSO4) addresses these issues through dynamic cross-linking of peach gum polysaccharide and silk nanofibers with borax, integrating varieties of key property including high water retention, broad temperature tolerance (-20 to 90 °C), excellent self-adhesion (60.7 kPa for carbon cloth electrodes), satisfactory flame retardancy (limited oxygen index of 51%), low-temperature self-healing (-20 °C), and good ionic conductivity (7.68 mS cm-1). The resulting supercapacitor exhibits excellent cycling stability with 98.2% capacitance retention after 40,000 long cycles at 25 °C. The specific capacitance retention remains above 90% even after 15,000 cycles at high/low temperatures (50 °C/-20 °C). Furthermore, the flexible supercapacitor demonstrates stable performance under mechanical stimuli (180° bending and perforation), highlighting the potential of biomass hydrogels in flexible energy storage devices.

Supercapacitive behaviors of N/S co-doped biomass porous carbon-based supercapacitors in “water-in-salt” electrolyte

The design of carbon electrode materials and electrolytes is distinct significance for improving the energy density of supercapacitors. Herein, N/S co-doped biomass porous carbon materials based on sustainable resource were prepared by in-situ expansion, heteroatom doping, and subsequent KOH activation strategy by using camellia seed shell as carbon source and ammonium persulfate as dopant and expander. The as-prepared N/S co-doped biomass porous carbon (N/S-CSAC-650) possesses the characteristics of high specific surface area, large pore volume, and suitable heteroatom content. The N/S-CSAC-650 electrode achieves a high specific capacitance of 335.9 F g−1 in the 3 M KOH electrolyte at 0.5 A g−1. The constructed symmetric supercapacitor demonstrates excellent cyclic stability and shows a high retention rate of 98.4 % after 30,000 charge and discharge processes at 2 A g−1. Especially, the energy density of supercapacitors is usually constrained by the narrow electrochemical stability window (ESW) of dilute aqueous solution (1.23 V), in order to effectively widen the ESW of water, herein the “water-in-salt” (WIS) electrolyte strategy is put forward and the ESW of water was extended to 2.94 V by using a 25 M KAc WIS electrolyte. The operating voltage window of the symmetric supercapacitor assembled by 25 M KAc WIS electrolyte and N/S-CSAC-650 electrodes can reach 2.0 V, and a high energy density of 48.86 Wh kg−1 is realized.

Oxygen atom activated ZIF-67/carbon cloth in plasma system for CO2 reduction

ZIF-67 was grown in situ on carbon cloth (CC) using a simple one-step method. The prepared ZIF-67/CC electrodes exhibited excellent CO2 reduction reaction (CO2RR) performance in a dielectric barrier discharge plasma reactor. The highest concentrations of produced formic acid and formaldehyde were 9.16 and 0.068 mmol L−1 at a reaction time of 1 h, respectively. The high performance is related to the unique high aspect ratio structure and pad-like cavity of ZIF-67, which results not only in an increase in the specific surface area for CO2 adsorption but also in the hydrophobicity of the electrode. Unexpectedly, the superoxide radical (·O2−) greatly affects the reduction performance of the electrode. In addition, the ZIF-67/CC electrode maintained good CO2RR performance in the presence of different pollutants, and the production of formic acid and formaldehyde increased to 10.81 and 0.11 mmol L−1 at 1 h with the addition of 10 mg L−1 phenol. This research provides new directions in the field of plasma catalysis.

Ultrasound-assisted fungal self-growth and heteroatom doping for the preparation of high-performance lignocellulose-based supercapacitor electrodes

Biomass materials are widely used as supercapacitor electrode materials due to their cost-effectiveness and eco-friendliness. In this work, ultrasound-assisted impregnation was employed for the thorough mixing of the liquid medium, and fungal treatment was conducted on the three main components of lignocellulose to prepare a fungi-modified heteroatom-doped lignocellulose-based carbon material (LCF-NP). The effects of heteroatom doping, the content of the three main components, and fungal modification on the electrochemical performance of lignocellulose-based carbon materials was investigated. The results revealed the synergistic effect of heteroatom doping and fungal treatment on the electrochemical performance. Compared with its counterpart free of fungal treatment, LCF-NP has a more reasonable pore structure and exhibits excellent electrochemical performance. LCF-NP porous carbon material has the highest specific surface area (792 m2/g), large pore volume (0.523 cm3/g), and ideal specific capacitance (1940 mF/cm2) under the conditions of 1.0 M Na2SO4 electrolyte and current density of 0.5 mA/cm2. After 10,000 cycles, there is almost no loss of capacitance. These results indicate that the joint utilization of heteroatom doping and fungal treatment has a promising application prospect in pore structure regulation and electrochemical performance improvement. This study provides a new strategy for the preparation of lignocellulose-based carbon electrode materials.

One‐Step Laser Synthesis of Copper Nanoparticles and Laser‐Induced Graphene in a Paper Substrate for Non‐Enzymatic Glucose Sensing

AbstractThe synergy resulting from the high conductivity of graphene and catalytic properties of metal nanoparticle has been a resource to improve the activity and functionality of electrochemical sensors. This work focuses on the simultaneous synthesis of copper nanoparticles (CuNPs) and laser‐induced graphene (LIG) derived from paper, through a one‐step laser processing approach. A chromatography paper substrate with drop‐casted copper sulfate is used for the fabrication of this hybrid material, characterized in terms of its morphological, chemical, and conductive properties. Appealing conductive properties are achieved, with sheet resistance of 170 Ω sq−1 being reached, while chemical characterization confirms the simultaneous synthesis of the conductive carbon electrode material and metallic copper nanostructures. Using optimized laser synthesis and patterning conditions, LIG/CuNPs‐based working electrodes are fabricated within a three‐electrode planar cell, and their electrochemical performance is assessed against pristine LIG electrodes, demonstrating good electron transfer kinetics appropriate for electrochemical sensing. The sensor's ability to detect glucose through a non‐enzymatic route is optimized, to assure good sensing performance in standard samples and in artificial sweat complex matrix.

Bimolecular Salt Strategy Enhances Heteroatom Doping and Porosity Optimization of Porous Carbon for Supercapacitors.

The incompatibility between electrolyte ions and electrode pore sizes, coupled with the extensive use of activators and dopants, significantly restricts the fabrication of porous carbon materials. Consequently, developing environmentally sustainable and efficient methodologies that exploit the intrinsic properties and pretreatment of materials to facilitate self-activation and self-doping becomes crucial. In this study, potassium histidine and magnesium histidine molecular salts were synthesized as precursors, enabling specific ion activation and bimetallic template-directed tunable porosity through a one-step carbonization process. Notably, the ratio of bimolecular salts significantly influenced the porous structure of carbon, the properties of heteroatoms, and the electrochemical performance. By optimizing the ratio, the porous carbon materials exhibited high accessibility to electrolyte ions and effective ion/electron transport channels. Consequently, the optimal sample (NOSPC-2) achieved a high specific capacitance of 318 F g-1 at 0.1 A g-1 and a good capacitance retention rate of 98.8% after 50,000 cycles at 5 A g-1. In addition, NOSPC-2 also boasted high energy density and power density, reaching 22 Wh kg-1 and 25 kW kg-1, respectively. This research represents a significant stride in advancing preparation technologies for small molecule derived porous carbon materials, providing valuable insights for the rational design of carbon electrode materials for capacitive energy storage.

Hydrothermal preparation of cotton-based rGO/N-doped porous carbon as electrode materials of supercapacitors

Porous carbon electrode materials are commonly used in supercapacitors due to their inexpensive raw materials, simple processing, and low pollution, aligning with the vision for green energy storage. Consequently, there is a current trend to discover porous carbon electrode materials with superior electrochemical properties. To enhance the pore volume ratio and electrochemical performance of porous carbon materials, this study proposes a hydrothermal method to pretreat the raw materials, facilitating the doping of nitrogen from urea. Moreover, graphene is introduced for its excellent conductivity, which can further improve the electrochemical properties of the material. We found a new one-step reduction Graphene Oxide (rGO)and the doping of nitrogen (N) elements were optimized by hydrothermal method, the wettability and pseudo-capacitance performance of the material are improved, and HTPC-700 shows a very excellent specific capacitance, its specific capacitance reaches 600 F g−1 at a current density of 0.5 A g−1, and it even reaches 260 F g−1 at a current density of 1 A g−1. Meanwhile the power density and energy density are respectively 74 W h kg−1 and 280 W kg−1. It also exhibits a remarkable capacitance retention rate of over 98.7 % after 5000 cycles at a current density of 1 A g−1. Additionally, it demonstrates a rich ant nest-like pore structure and good specific surface area of 2427 m2/g, and a large pore volume of 1.09 cm3/g after carbonization and KOH activation. This study offers a novel doping method and provides a unique perspective for the development of porous carbon electrodes.