rGO Film Research Articles

A reduced graphene oxide-coated conductive surgical silk suture targeting microresistance sensing changes for wound healing

Conventional sutures used in surgical procedures often lack the capability to effectively monitor physical and chemical activities or the microbial environment of surgical wounds due to their inadequate mechanical properties, insufficient electrical accuracy and unstability. Here, we present a straightforward layer-by-layer coating technique that utilizes 3-glycidoxypropyltrimethoxysilane (CA), graphene oxide (GO), and ascorbic acid (AA) to develop conductive silk-based surgical sutures (CA-rGSFS). The CA-rGSFS feature a continuous reduced graphene oxide (rGO) film on their surface, forming robust hydrogen bonds with silk fibroin. The reduction process of rGO is confirmed through Raman analysis, demonstrating an enhanced D peak to G peak ratio. Notably, the CA-rGSFS exhibit exceptional mechanical properties and efficient electron transmission, with a knot-pull tensile strength of 2089.72 ± 1.20 cN and an electrical conductivity of 130.30 ± 11.34 S/m, respectively, meeting the requirements specified by the United States Pharmacopeia (USP) for 2-0 sutures. These novel CA-rGSFS demonstrate the ability to accurately track resistance changes in various fluid environments with rapid response, including saline, intestinal, and gastric fluids. The suture also retains remarkable stretchablility and stability even after enduring 3000 tensile cycles, highlighting their potential for precise surgical site monitoring during the wound healing process.

Droplet bouncing electricity generation on graphene substrate

Abstract Since the discovery of the phenomenon of droplets bouncing on hydrophobic surfaces, researchers have been dedicated to studying the underlying physical mechanisms of this phenomenon. Particularly, in recent years, researchers have focused on the observation that droplet bouncing can generate electrical signals. Inspired by this, we explore the potential applications of electrical signals generated by droplets (water droplets) bouncing in sensors and other relevant fields. In this study, we chose a well-established reduced graphene oxide (rGO) film, typical in the sensor field, as a substrate to investigate the bouncing electricity generation performance of water droplets on it. Three variable factors were considered, including droplet bouncing on rGO substrates with different inclinations, bouncing of droplets of different sizes at the same inclination on rGO substrates, and droplet dropping frequency, to investigate their effects on the electrical signals.

Novel electrochemical synthesis of N-doped ZnO–rGO films for the photoelectrocatalytic degradation of antibiotics

Novel electrochemical synthesis of N-doped ZnO–rGO films for the photoelectrocatalytic degradation of antibiotics

Synergistic effect of rGO decoration on ZnFe2O4 nanorods for low concentration detection of ammonia at room temperature with high selectivity and response

This study introduces an improved sensor for detecting ammonia (NH₃) gas using Zinc Ferrite (ZF) decorated with reduced graphene oxide (rGO) films, prepared through spray pyrolysis and spin coating methods. NH₃, a major pollutant in fertilizer production, poses significant health and environmental risks even at low concentrations. Therefore, detecting NH₃ below exposure limits (25 ppm) is crucial for protecting ecosystems and human health. The prepared optimal rGO concentration and ZF (ZFG1.5) sensor exhibit excellent NH₃ response (45) towards 1 ppm, which is sevenfold better than the ZF film without rGO decoration. This enhancement is attributed to the ZF nanorods on the surface of the rGO, establishing a firm surface interaction with the ZF. This configuration accelerates electron transfer and promotes the adsorption/desorption of gas molecules, further contributing to the improved gas-solid interaction. Besides, the sensor demonstrated excellent repeatability (1.15 %), long-term stability, and high humidity tolerance (coefficient of variation 1.48 %). Additionally, the ZFG1.5 sensor showed a distinct selectivity for NH₃ in a mixed gas environment. The ZFG1.5 sensor is promising for real-time NH₃ monitoring below exposure limits, making it a valuable tool for environmental and health safety.

Improved-quality graphene films via the synergism of large nanosheet aligning and nanotube bridging for flexible supercapacitors

Scalable production of reduced graphene oxide (rGO) films with high mechanical-electrical properties is desirable as these films are candidates for wearable electronics devices and energy storage applications. Removing structural incompleteness such as wrinkles or voids in the graphene films, which are generated from the assembly process, would greatly optimize their mechanical properties. However, the densely stacked graphene sheets in the films degrade their ionic kinetics and thus limit their development. Here, a horizontal-longitudinal-structure modulating strategy is demonstrated to produce enhanced mechanical, conductive, and capacitive graphene films. Typically, two-dimensional large graphene sheets (LGS) induce regular stacking of graphene oxide (GO) during the assembly process to reduce wrinkles, while one-dimensional single-walled carbon nanotubes (SWCNT) bridge with graphene sheets to strengthen the multidirectional intercalation and reduce GO layer restacking. The simultaneous incorporation of LGS and SWCNT synergistically creates a fine microstructure by improving the alignment of graphene sheets, increasing continuous conductive pathways to facilitate electron transport, and enlarging interlayer spacing to promote electrolyte ion diffusion. As a result, the obtained graphene films are flat and exhibit signally reinforced mechanical properties, electrical conductivity (38727 S m-1), as well as specific capacitance (232 F g-1) as supercapacitor electrodes compared to those of original rGO films. Moreover, owing to the comprehensive improved properties, a flexible gel supercapacitor assembled by the graphene film-based electrodes shows high energy density, good flexibility, and excellent cycling stability (93.8% capacitance retention after 10 000 cycles). This work provides a general strategy to manufacture robust graphene structural materials for energy storage applications in flexible and wearable electronics.

Hierarchical Incorporation of Reduced Graphene Oxide into Anisotropic Cellulose Nanofiber Foams Improves Their Thermal Insulation.

Anisotropic cellulose nanofiber (CNF) foams represent the state-of-the-art in renewable insulation. These foams consist of large (diameter >10 μm) uniaxially aligned macropores with mesoporous pore-walls and aligned CNF. The foams show anisotropic thermal conduction, where heat transports more efficiently in the axial direction (along the aligned CNF and macropores) than in the radial direction (perpendicular to the aligned CNF and macropores). Here we explore the impact on axial and radial thermal conductivity upon depositing a thin film of reduced graphene oxide (rGO) on the macropore walls in anisotropic CNF foams. To obtain rGO films on the foam walls we developed liquid-phase self-assembly to deposit rGO in a layer-by-layer fashion. Using electron and ion microscopy, we thoroughly characterized the resulting rGO-CNF foams and confirmed the successful deposition of rGO. These hierarchical rGO-CNF foams show lower radial thermal conductivity (λr) across a wide range of relative humidity compared to CNF control foams. Our work therefore demonstrates a potential method for improved thermal insulation in anisotropic CNF foams and introduces versatile self-assembly for postmodification of such foams.

A comparative study on humidity response of graphene oxide with reduced graphene oxide and its multifunctional applications

In this paper, we present a comparative study of Graphene Oxide (GO) and chemically reduced Graphene Oxide (rGO) based resistive type humidity sensors fabricated on Ti/Au Inter-Digital Electrodes (IDEs) coated SiO2 substrates. The sensing performance, including sensitivity, response/recovery time, and hysteresis has been evaluated for both sensors. The GO film exhibited quick response (0.3 s) and high sensitivity (104.7 kΩ/%RH) with remarkable repeatability and negligible hysteresis as compared to rGO film sensor. The excellent humidity sensing properties of GO are attributed to the presence of abundant oxygen-containing polar functional groups on GO relative to rGO. To demonstrate the multifunctional applications of developed GO based sensor, we have also demonstrated its use as respiratory monitoring, non-contact proximity detector, and speech event detector through the detection of humidity perturbations. The work suggests GO sensitive material has high potential for the development of wearable and integrated health monitoring platforms and non-contact sensing devices.

Alumina fiber/reduced graphene oxide composite films for high-temperature heating and sensing

Reduced graphene oxide (rGO) and its composite films have aroused intense interest in electrical heating and temperature sensing fields, but the working temperature is usually limited because the internal layer-stacked structure is breakable at high temperature. In order to promote structure stability, a series of Al2O3 fiber/rGO composite films were developed. It is found that gaseous products mainly including CO2 and CO during thermal reduction contribute to pores, bulges and intervals in rGO films, while appropriate Al2O3 fiber has an adhesion effect on rGO sheets and tightens them together, in which case defects can hardly form and the layered structure is significantly compacted. Therefore, the degree of stacking order and tensile strength tend to increase, resulting in the improvement of structure stability and decrease of electrical resistivity. However, excess Al2O3 fiber makes the formation of debris and cracks, causing the deterioration of conductivity and mechanical properties. With 20 wt% Al2O3 fiber, the composite films can bear higher heating voltage than pure rGO films and stabilize at 634.65 °C under 36 V, which also keep a good linearity between resistance and temperature from 25 to 600 °C, exhibiting a considerable temperature coefficient of resistance (TCR) with −1.70×10−3 /°C at room temperature.

Anisotropic, free-standing anodic films with aligned anatase-bronze TiO2-integrated graphene for high-capacity lithium-ion batteries

The composition modification and structure manipulation of carbon-based battery electrodes is becoming an increasingly urgent need for safer, more reliable, and effective electric vehicles. Herein, we fabricate a free-standing hybrid anatase-bronze TiO2-grafted reduced graphene oxide (TiO2-rGO) through a one-pot solvothermal procedure. The TiO2-rGO composite was transformed into a film with an anisotropic alignment and assembled as an anode into lithium-ion batteries (LIBs) to enhance its performance. Our previously developed “Pulse Freezing” process, with modifications including: (1) dimensional and structural optimization for larger and faster film production and (2) optimal microfluidic condition for vertical porous alignment, is utilized for assembling this nanocomposite anodic film. During the microfluidic assembly process, we achieved the desirable flowrate, flow patterns, and alignments of the integrated TiO2-rGO layers while forming porous microstructures through freeze drying. The porous and aligned TiO2-integrated rGO film exhibits a significantly enhanced specific capacity of 400 mAh/g at 0.2 A/g, which is a drastic increase compared to traditional TiO2 and carbon black electrodes possessing <50 mAh/g capacity, attributed to the anisotropic alignment and porous microstructure of rGO in combination with TiO2 grafting. The developed TiO2-rGO composite film provides a promising application of Ti-based electrodes in LIBs for commercial battery industries.

Capillary Force-Induced Graphene Spontaneous Transfer and Encapsulation of Silver Nanowires for Highly-Stable Transparent Electrodes.

Silver nanowires (NWs) (AgNWs) have emerged as the most promising conductive materials in flexible optoelectronic devices owing to their excellent photoelectric properties and mechanical flexibility. It is widely acknowledged that the practical application of AgNW networks faces challenges, such as high surface roughness, poor substrate adhesion, and limited stability. Encapsulating AgNW networks with graphene has been recognized as a viable strategy to tackle these issues. However, conventional methods like self-assembly reduction-oxidation or chemical vapor deposition often yield graphene protective layers with inherent defects. Here, we propose a novel one-step hot-pressing method containing ethanol solution that combines the spontaneous transfer and encapsulation process of rGO films onto the surface of the AgNWs network, enabling the preparation of flexible rGO/AgNWs/PET (reduced graphene oxide/silver NWs/polyethylene terephthalate) electrodes. The composite electrode exhibits outstanding photoelectric properties (T ≈ 88%, R ≈ 6 Ω sq-1) and possesses a smooth surface, primarily attributed to the capillary force generated by ethanol evaporation, ensuring the integrity of the rGO delamination process on the original substrate. The capillary force simultaneously promotes the tight encapsulation of rGO and AgNWs, as well as the welding of the AgNWs junction, thereby enhancing the mechanical stability (20,000 bending cycles and 100 cycles of taping tests), thermal stability (∼30 °C and ∼25% humidity for 150 days), and environmental adaptability (100 days of chemical attack) of the electrode. The electrode's practical feasibility has been validated by its exceptional flexibility and cycle stability (95 and 98% retention after 5000 bending cycles and 12,000 s long-term cycles) in flexible electrochromic devices.

Construction of Fire Safe Thermoplastic Polyurethane/Reduced Graphene Oxide Hierarchical Composites with Electromagnetic Interference Shielding.

Incorporating outstanding flame retardancy and electromagnetic interference shielding effectiveness (EMI SE) into polymers is a pressing requirement for practical utilization. In this study, we first employed the principles of microencapsulation and electrostatic interaction-driven self-assembly to encapsulate polyethyleneimine (PEI) molecules and Ti3C2Tx nanosheets on the surface of ammonium polyphosphate (APP), forming a double-layer-encapsulated structure of ammonium polyphosphate (APP@PEI@Ti3C2Tx). Subsequently, flame-retardant thermoplastic polyurethane (TPU) composites were fabricated by melting the flame-retardant agent with TPU. Afterwards, by using air-assisted thermocompression technology, we combined a reduced graphene oxide (rGO) film with flame-retardant TPU composites to fabricate hierarchical TPU/APP@PEI@Ti3C2Tx/rGO composites. We systematically studied the combustion behavior, flame retardancy, and smoke-suppression performance of these composite materials, as well as the flame-retardant mechanism of the expansion system. The results indicated a significant improvement in the interface interaction between APP@PEI@Ti3C2Tx and the TPU matrix. Compared to pure TPU, the TPU/10APP@PEI@1TC composite exhibited reductions of 84.1%, 43.2%, 62.4%, and 85.2% in peak heat release rate, total heat release, total smoke release, and total carbon dioxide yield, respectively. The averaged EMI SE of hierarchical TPU/5APP@PEI@1TC/rGO also reached 15.53 dB in the X-band.

Realizing fast plating/stripping of high-performance Zn metal anode with a low Zn loading

Zn metal batteries and capacitors (ZMBs/ZMCs) are gaining significant attention due to their low cost, high safety, and high theoretical capacity. However, the low utilization of Zn metal decreases the coulombic efficiency. Here, we present a novel approach to enhance the conductivity of host materials by utilizing a 3D conductive structural network of copper mesh. The 3D copper mesh serves as a high-conductive matrix and additionally coating it with Zn serves as a Zn source. Finally, a flexible reduced graphene oxide (rGO) was deposited on the Zn-coated copper mesh as an anode protective layer. The conductive copper mesh renders a fast plating/stripping of Zn and enables more contact of Zn with the electrolyte. The flexible rGO film deposited on Zn-coated copper mesh alleviates the local charge accumulation and inhibits corrosion. As a result, the Zn-coated copper mesh anode modified with rGO (RCZ) exhibited a longer lifespan of 200 h than the Zn-coated planar copper foil anode which cycled only for 30 h. The RCZ||AC full capacitor obtained high capacity retention of 97.9% after 9000 times cycling. The RCZ anode integrates the merits of 3D structure matrix and rGO realizing a dual-functionalized Zn metal anode. The conductive matrix strategy sheds light on other metal batteries.

Laser-induced 2D/0D graphene-nanoceria freestanding paper-based films for on-site hydrogen peroxide monitoring in no-touch disinfection treatments

A one-shot CO2 laser-based strategy to generate conductive reduced graphene oxide (rGO) decorated with nanoceria (nCe) is proposed. The 2D/0D rGO-nCe films, integrated as catalytic sensing layers in paper-based sensors, were employed for on-site monitoring of indoor fogging treatments against Listeria monocytogenes (Lm), a ubiquitous pathogenic bacterium. The rGO-nCe laser-assisted synthesis was optimized to preserve the rGO film morphological and electron-transfer features and simultaneously integrate catalytic nCe. The films were characterized by microscopical (SEM), spectroscopical (EDX, Raman, and FTIR), and electrochemical techniques. The most performing film was integrated into a nitrocellulose substrate, and the complete sensor was assembled via a combination of xurography and stencil printing. The rGO-nCe sensor's catalytic activity was proved toward the detection of H2O2, obtaining sensitive determination (LOD = 0.3 µM) and an extended linear range (0.5–1500 µM). Eventually, the rGO-nCe sensor was challenged for the real-time continuous monitoring of hydrogen peroxide aerosol during no-touch fogging treatment conducted following the EU’s recommendation for biocidal product use. Treatment effectiveness was proved toward three Lm strains characterized by different origins, i.e., type strain ATCC 7644, clinical strain 338, and food strain 641/6II. The sensor allows for discrimination and quantification treatments at different environmental biocidal amounts and fogging times, and correlates with the microbiological inhibition, promoting the proposed sensor as a useful tool to modulate and monitor no-touch treatments.Graphical

Improving strength and toughness of graphene film through metal ion bridging

The fangs, jaws, and mandibles of marine invertebrates such as Chiton and Glycera show excellent mechanical properties, which are mostly contributed to the interactions between metal (Fe, Cu, Zn, etc.) and oxygen-containing functional groups in proteins. Inspired by these load-bearing skeletal biomaterials, we improved tensile strength and toughness of graphene films through bridging graphene oxide (GO) nanosheets by metal ions. By optimizing the metal coordination form and density of cross-linking network. We revealed the relationship between mechanical properties and the unique spatial geometry of the GO nanosheets bridged by different valence metal ions. The results demonstrated that the divalent metal ions form tetrahedral geometry with carboxylate groups on the edges of the GO nanosheets, and the bond energy is relatively low, which is helpful for improving the toughness of resultant graphene films. While the trivalent metal ions are easily to form octahedral geometry with the GO nanosheets with higher bond energy, which is better for enhancing the tensile strength of graphene films. After reduction, the reduced GO (rGO) film bridged by divalent metal ions shows 43% improvement in toughness, while the rGO film bridged by trivalent metal ions shows 64% improvement in tensile strength. Our work reveals the mechanism of metal coordination bond energy and spatial geometry to improve the mechanical properties of graphene films, which lays a theoretical foundation for improving the tensile strength and toughness of resultant graphene films, and provides an avenue for fabricating high-performance graphene films and other two-dimensional nanocomposites.

A hydrogel-based moist-electric generator with superior energy output and environmental adaptability

Harvesting energy from ubiquitous moisture has emerged as a promising way to collect energy irrespective of location and time. However, the electrical output of moist-electric generators (MEGs) is currently insufficient for practical applications. In this study, a highly efficient electricity-generating film was constructed by combining silicon dioxide (SiO2) nanofibers, sodium alginate (SA) and reduced graphene oxide (rGO) matrix impregnated with calcium chloride. The resulting SA–SiO2–rGO (SSG) film demonstrates a strong moisture-adsorption ability of 1.6 g/g at 80 % RH and 30 °C, and a relatively high ionic conductivity of 1.46 S m-1. The SSG film's strong moisture-adsorption capacity allows rapid ion dissociation, and its excellent electrical conductivity enhances ion migration. Thus, a single centimeter-sized device generates an open-circuit voltage (Voc) of up to ∼0.6 V and a short-circuit current (Isc) of ∼2.24 mA (0.14 mA cm−2). This short-circuit current is more than 10 times those of most reported MEGs. Moreover, an SSG-film-based MEG maintains a voltage output of ∼0.6 V over rather wide ranges of temperature (0–40 °C) and relative humidity (20 %–80 %), demonstrating superior environmental adaptability. In summary, this study provides fresh insights into the design of high-performance composite materials for efficient moist-electric energy conversion.

Xylan derived carbon sphere/graphene composite film with low resistance for supercapacitor electrode

Reduced graphene oxide (rGO) films suffer from low capacitance for inner unreduced oxygen functional groups, restacking of sheets and high contact resistance. Herein, carbon spheres derived from renewable xylan were added to graphene oxide with large sheet area to fabricate film by gelation and filtration, followed by in situ reduction for high-performance flexible supercapacitor. rGO film with transverse size about 13 μm showed a good specific capacitance of 967 mF/cm2 at a scanning rate of 5 mV/s and increased to 1786 mF/cm2 by in situ reducing its inner part, which generally remained oxidized due to outer hindering from hydrophobic graphene. Then, by hydrothermal carbonization of xylan and activation with KOH, activated carbon sphere (aXCS) was prepared, which had a diameter of 150–200 nm and a specific capacitance of 270 F/g. The aXCS acted as spacer and connector to avoid restacking of graphene sheets and decrease interlayer contact resistance, resulting 94% increase in capacitance performance from rGO film to aXCS/rGO film. Therefore, combined in situ reduction and enhancement through compositing aXCS, the final film (aXCS/rGO-AA) showed a boosted specific capacitance of 755 mF/cm2 at 1 mA/cm2 in double electrode system, power density of 22.5–2250 mW/cm2, and energy density of 11.88–25.2 mWh/cm2. Meanwhile, aXCS/rGO-AA had outstanding cycling stability that its specific capacitance maintained 108.7% after 10,000 cycles of charge–discharge, showing promising potential in wearable and portable electronics.Graphical abstract

Environmentally Friendly Water-Based Reduced Graphene Oxide/Cellulose Nanofiber Ink for Supercapacitor Electrode Applications.

The agglomeration of reduced graphene oxide (rGO) in water makes the development of rGO inks for supercapacitor printing challenging. Cellulose nanofiber (CNF), a biodegradable and renewable nanomaterial, can act as a nanospacer, preventing the agglomeration and restacking of rGO flakes. In this work, rGO/CNF films were fabricated using an environmentally friendly water-based rGO/CNF ink. In the absence of an additional binder/surfactant, the rGO/CNF films demonstrated remarkably enhanced hydrophilicity while retaining good electrical conductivity. The concentration of CNF was varied to observe the variation in the electrochemical performance. At a current density of 1 mA/cm2, the rGO/CNF-15 film exhibited a maximum areal capacitance of 98.61 mF/cm2, closely matching that of pure rGO films. Because of its excellent electrical performance, ease of manufacturing, and environmental friendliness, this water-based rGO/CNF ink may have promising applications in the printing of supercapacitor electrodes.

Exceptional Viscoelastic Properties in Graphene Oxide Films.

Materials that combine high stiffness with effective damping are in high demand across various industries. While polymers excel in damping, they often lack stiffness and thermal stability. Conversely, metals and ceramics boast high mechanical and thermal properties but lack damping. This study demonstrates that graphene oxide (GO) and reduced graphene oxide (rGO) films can achieve exceptional viscoelastic properties across a wide temperature range. Furthermore, it explains the damping mechanisms and structural characteristics that influence the unique viscoelastic behavior of GO and rGO films. Through comprehensive characterizations, this study correlates the structure and spatial variation in local strain (measured with in situ Raman microscopy) of GO and rGO films with their storage and loss moduli. This correlation links these properties to the water loss as a function of the temperature rise. GO and rGO films exhibited a damping coefficient of 0.2-0.4 while maintaining stiffness values of 10-20 GPa in the 30-120 °C range. These high damping values were attributed to intermittent slippage and hydrogen bond density between the constituent sheets. Numerical modeling was conducted to further elucidate the mechanisms responsible for the properties noted in these films. This study enhances our understanding of the viscoelastic properties of GO films and offers a new potential material for applications across various fields.

Autoclave-mediated reduction of graphene oxide for enhanced conductive films

A highly efficient and environmentally friendly method for producing high-quality reduced graphene oxide (rGO) films is explored. It consists of a scalable autoclave process devoid of hazardous reductants. In detail, the reduction of four distinct graphene oxide materials, whose O/C ratio varied from 0.28 to 0.58, through an autoclave-mediated hydrothermal process at 200 °C and 12 bars pressure is carried out. This employs overheated steam as a heat carrier, without any additional solvents or reducing agents. Upon mild annealing (80 °C), the final rGO films result being robust, self-supporting, and electrically conductive. This study investigates the impact of both the initial GO’s oxidation degree and the volume distribution on the efficacy of the hydrothermal process in synthesizing rGO systems. Furthermore, a comparison between films, created through both hydrothermal autoclave-mediated and thermal oven-mediated methods, is conducted, by assessing their electrical, morphological, chemical, and structural properties. Films produced via the autoclave method display notably improved electrical surface resistivity (3.34·102 Ω/sq) compared to the traditional thermal treatments (6.71·105 Ω/sq). These promising results emphasize the potential of this eco-friendly route as a foundation for scalable and sustainable fabrication of valuable graphene-based conductive materials.

Exploring the potential of reduced graphene oxide/polyaniline (rGO@PANI) nanocomposites for high-performance supercapacitor application

This study introduces a facile synthesis method for synthesizing reduced graphene oxide (rGO) nanosheets with surface decoration of polyaniline (PANI). The resultant rGO@PANI nanocomposite (NC) exhibit substantial potential as advanced electrode materials for high-performance supercapacitors. The strategic integration of PANI onto the rGO surface serves dual purposes, effectively mitigating agglomeration of rGO films and augmenting their utility in supercapacitor applications. The PANI coating manifests a highly porous and nanosized morphology, fostering increased surface area and optimized mass transport by reducing diffusion kinetics. The nanosized structure of PANI contributes to the maximization of active sites, thereby bolstering the efficacy of the nanocomposites for diverse applications. The inherent conductive nature of the rGO surface significantly expedites electron transport, thereby amplifying the overall electrochemical performance of the nanocomposites. To systematically evaluate the influence of PANI concentration on the electrode performance, varying concentrations of PANI were incorporated. Notably, an elevated PANI concentration was found to enhance the response owing to the unique morphology of PANI. Remarkably, the 5 % rGO@PANI NC emerged as the most promising candidate, demonstrating exceptional response characteristics with a specific capacitance of 314.2 F/g at a current density of 1 A/g. Furthermore, this catalyst exhibits outstanding long-term stability, retaining approximately 92 % of its capacitance even after enduring 4000 cycles. This research underscores the significance of the synergistic integration of rGO and PANI in the design of high-performance supercapacitors. The elucidation of the underlying mechanisms governing the improved electrochemical properties contributes to the fundamental understanding of nanocomposite behavior, thereby paving the way for the rational design of next-generation energy storage materials.