Low-cost Materials Research Articles

Picosecond pulsed laser scribing of Cd2SnO4-based CdTe thin-film solar cells on flexible glass

CdTe photovoltaic modules are the most commercially successful thin-film solar cells. In particular, flexible CdTe modules are a promising development in photovoltaic architecture. Cd2SnO4 (CTO) is a low-cost transparent conductive material with excellent optical and electrical properties. Although laser scribing is commonly used to produce cell interconnects in the manufacturing of thin-film PV modules, the laser scribing process window for CTO-based CdTe cells is narrow, and more research is needed on direct laser scribing of flexible CdTe solar cells. In this study, the picosecond pulsed laser scribing of CdTe solar cells with CTO front electrodes and flexible glass substrates was investigated using lasers with the wavelengths of 355 and 532 nm. The flexible cells were suctioned onto a working platform, and a direct ablation method was adopted. The damage and removal thresholds of the CTO, CdTe, and Ni layers were studied and the effects of the spot spacing, multilayer conditions, and laser polarization state were investigated. A method for determining the scribing parameters was proposed. Very smooth scribing grooves were obtained using the optimized laser scribing process. The series and shunt resistances of the cells after laser scribing showed no significant differences compared to those of the control cells.

The Development of a Flexible Humidity Sensor Using MWCNT/PVA Thin Films.

The exponential demand for real-time monitoring applications has altered the course of sensor development, from sensor electronics miniaturization, e.g., resorting to printing techniques, to low-cost, flexible and functional wearable materials. Humidity sensing has been used in the prevention and diagnosis of medical conditions, as well as in the assessment of physical comfort. This paper presents a resistive flexible humidity sensor composed of silver interdigitated electrodes (IDTs) screen printed onto polyimide film and an active layer of multiwall carbon nanotubes (MWCNT) dispersed in a water-soluble polymer, polyvinyl alcohol (PVA). Different MWCNT/PVA sensor sizes and MWCNT percentages are tested to study their effect on the initial electrical resistance (Ri) values and sensor response at different humidity percentages. The results show that the Ri values decrease with the increase in % MWCNT. The sensor size did not influence the sensor response, while the % MWCNT affected the sensor behavior upon relative humidity (RH) increments. The 1% MWCNT/PVA sensor showed the best response, reaching a relative electrical resistance, ΔR/R0, of 509% at 99% RH. Comparable with other reported sensors, the produced MWCNT/PVA flexible sensor is simpler, greener and shows a good sensitivity to humidity, being easily incorporated in wearable monitoring applications, from sports to medical fields.

Probing the effect of Se doping in S cathode for high performance Mg-S batteries

Magnesium-sulfur (Mg-S) batteries present an attractive option as a new type of energy storage device given their high energy density, safety and the use of low-cost original materials. However, magnesium polysulfide (MgPS) is susceptible to dissolution and shuttling, and the insulating nature of sulfur and MgS leads to high overpotentials and low columbic efficiencies. The selenium-sulfur system is noted to offer enhanced electronic conductivity and improved sulfur utilization. In this study, S K-edge X-ray absorption near-edge structure (XANES) spectra demonstrate that Se doping mitigates irreversibility in Mg-S batteries. Mg-K spectra demonstrate that Se dopants induce local negative charges on S, strengthening the Mg-S bond compared to that of pure sulfur, thereby promoting Mg/Mg2+ redox reactions. Operando Raman spectroscopy was also used to reveal Mg-S0.9Se0.1/C battery redox mechanisms. Hence, kinetically favored S0.9Se0.1/C cathodes deliver an initial capacity of ∼1350 mAh·g−1 at 0.2C. Furthermore, separators modified with layered MoS2 entrap polysulfides, thereby postponing cell death. Thus, Mg-S battery with a S0.9Se0.1/C cathode and a MoS2@polypropylene (PP) separator exhibit a reversible capacity of ∼200 mAh·g−1 at 0.2C after 250 cycles, with a low fade rate of 4 mAh·g−1/cycle. This study delineates the overall impact of Se doped cathodes on Mg-S batteries. Moreover, the MoS2 modified separator provides a route to chemically immobilize MgPS and accelerate sulfur redox reactions, consequently enabling high capacities and sustained cycling.

Actividades Experimentais de Física de Baixo Custo: Um exemplo particular na 10ª Classe do curso de Ciências Físicas e Biológicas

The research focused on experimental activities, in the form of low-cost laboratory practice, with the aim of analyzing the reality of teachers in the teaching-learning process of physics in the 10th grade of the Physical and Biological Sciences course. An experimental study was carried out at the Secondary School Liceu 26 de Abril no. 1677 in the Municipality of Lubango, Huíla Province, Republic of Angola. Questionnaires were used as research tool, allowing a quantitative approach to be reported, using the statistical method in laboratory practice. There was a 100% sample of 6 teachers who teach physics and a 25% sample of 367 students. Once the diagnosis had been made, it was found that the institution in question does not have a laboratory equipped to carry out experimental activities, either with low-cost materials or with recycled materials and, of the few laboratory practices observed, there was no example of a calculation that included analysis of the theory of error for direct or indirect measurement.

Dibenzothiophene S, S-Dioxide-Containing Dipolar Molecules As Efficient Hole-Transport Materials for p-i-n Perovskite Solar Cells.

Organic-inorganic hybrid perovskite solar cells (OIH-PSCs) have developed rapidly in the past decade, and the commercialization of OIH-PSCs demands low-cost hole-transport materials (HTMs) with high performance and stability. The present study synthesized two organic HTMs containing dibenzothiophene S-dioxide as the acceptor unit and triphenylamine as the donor (denoted by TPAF-SO2 and TPA-SO2). In TPAF-SO2, the methoxy group and adjacent fluorine atom were introduced to decrease the highest occupied molecular orbital energy level. In TPA-SO2, the methyl sulfide group is the end group that can passivate the lead ion. TPAF-SO2 and TPA-SO2 exhibit hole-transport mobilities as high as 1.12 × 10-3 and 2.31 × 10-3 cm2 v-1 s-1, respectively, and strongly passivate Pb vacancies. Compared with TPAF-SO2, TPA-SO2 is more suitable for the growth of perovskite crystals. The perovskite grown on the latter has a lower trap density and higher carrier mobility; thus, both the nonradiative recombination and the charge-transport loss are decreased. The OIH-PSC based on TPA-SO2 as the HTM achieved a power conversion efficiency (PCE) as high as 22.08%, whereas the device based on TPAF-SO2 achieved a PCE of only 18.42%. In addition, the unencapsulated device based on TPA-SO2 can maintain 85% of the initial PCE after being stored in N2 for 1200 h, whereas the device based on TPAF-SO2 decayed rapidly to zero in 800 h under the same conditions.

Hybrid rib fabric electromagnetic shielding measurement in X-band

This study involves measurement and evaluation of the electromagnetic shielding effectiveness (EMSE) in the X-band frequency range of rib-knitted fabrics formed from hybrid conductors. Hybrid conductive fabrics were made by knitting copper, silver, and stainless steel conductors together with cotton yarn. The basic theory of EMSE is introduced, and the waveguide measurement setup described. The through-reflect-line calibration setup was used to obtain accurate results. After calibration of the established waveguide measurement setup, hybrid conductive fabrics were tested. The measurements were analyzed and the fabrics compared. The aim is to produce a hybrid fabric that is suitable for general use, has a good EMSE, is easy to produce, and offers low-cost high-frequency solutions. An easy-to-produce and low-cost EMSE material is required, especially in new-generation wearable flexible electronic devices and military applications.

Theorizing the Chair: History, Culture, and Design

In Arthur Danto’s The Seat of the Soul: Three Chairs, the chair is a source of power and authority. This paper explores the aesthetic importance of chairs and their designers and determines why people from various cultures create different designs that all perform the same function: seating. Here, the chair is examined as an artwork and design phenomenon from historical, cultural, stylistic, and aesthetic perspectives. Data were gathered through a comprehensive literature review, reports, archival materials, and museum visits. Descriptive, historical, and analytical methods were used to explore the religious, symbolic, spiritual, artistic, competitive, and academic legacies of the chair. Despite the similarity in function, the chair is more important than a sofa, bed, or bench. It displays one’s status, education, knowledge, and artistic taste. However, practicality, low-cost materials, and money have trumped aesthetics in recent years. The findings may help young chair designers highlight their competitiveness and inventiveness.

Recent Advances in Barium Cobaltite-Based Perovskite Oxides as Cathodes for Intermediate-Temperature Solid Oxide Fuel Cells.

Solid oxide fuel cells (SOFCs) are considered as advanced energy conversion technologies due to the high efficiency, fuel flexibility, and all-solid structure. Nevertheless, their widespread applications are strongly hindered by the high operational temperatures, limited material selection choices, inferior long-term stability, and relatively high costs. Therefore, reducing operational temperatures of SOFCs to intermediate-temperature (IT, 500-800°C) range can remarkably promote the practical applications by enabling the use of low-cost materials and enhancing the cell stability. Nevertheless, the conventional cathodes for high-temperature SOFCs display inferior electrocatalytic activity for oxygen reduction reaction (ORR) at reduced temperatures. Barium cobaltite (BaCoO3-δ)-based perovskite oxides are regarded as promising cathodes for IT-SOFCs because of the high free lattice volume and large oxygen vacancy content. However, BaCoO3-δ-based perovskite oxides suffer from poor structural stability, inferior thermal compatibility, and insufficient ionic conductivity. Herein, an in-time review about the recent advances in BaCoO3-δ-based cathodes for IT-SOFCs is presented by emphasizing the material design strategies including functional/selectively doping, deficiency control, and (nano)composite construction to enhance the ORR activity/durability and thermal compatibility. Finally, the currently existed challenges and future research trends are presented. This review will provide valuable insights for the development of BaCoO3-δ-based electrocatalysts for various energy conversion/storage technologies.

Determination of the Hydraulic Conductivity Behavior of Seaweed Added Zeolite-Bentonite Mixtures in the Presence of Temperature with Empirical Relationships

The temperature factor is of great importance in areas that directly affect the environment and engineering parameters of liners, such as solid waste storage areas. It is known that the temperature value increases as a result of the degradation of waste in these areas, and temperature changes affect the engineering properties of the soils. Properties vary depending on the soil type, and additives that can be used to improve the engineering properties of soils come to the fore. One of the most important criteria is that the additive to be used is sustainable and environmentally friendly. Zostera marina, with its terminological name, or dried seaweed an aquatic plant and is a sustainable, low-cost material used in thermal insulation. In this study, dried seaweed additive was added to zeolite-bentonite mixtures and compression parameters were determined under room temperature and 40°C. Hydraulic conductivity values of seaweed-added mixtures were determined with the help of volumetric compression coefficient (mv) and consolidation coefficient (cv) parameters and empirical relationships obtained as a result of consolidation tests. Its potential to be used as a buffer material in the presence of temperature in solid waste storage areas evaluated. The tests results showed that the seaweed additive decreased the hydraulic conductivity values of zeolite-bentonite mixtures at room temperature and under 40°C.

Insight into Carrier and Phonon Transports of PbSnS2 Crystals.

The simultaneous optimization of n-type and p-type thermoelectric materials is advantageous to the practical application of the device. As an emerging thermoelectric material, PbSnS2 exhibits highly competitive thermoelectric properties due to its unique carrier and phonon transport characteristics. To promote the utilization of this low-cost thermoelectric material, p-type PbSnS2 crystals are synthesized and optimized through Na doping and Se alloying. The resulting thermoelectric transport properties differ significantly from those reported for n-type crystals, prompting us to compare and analyze both n-type (Cl-doped) and p-type (Na-doped) PbSnS2 crystals from various perspectives. Cl doping is subject to weaker "Fermi pinning" and lower impurity ionization energy compared with Na doping, leading to higher doping efficiency. The different optimal performance directions in n-type and p-type crystals can be attributed to the distinct charge density distributions near the conduction band minimum (CBM) and the valence band maximum (VBM). Additionally, both n-type and p-type crystals exhibit ultralow lattice thermal conductivity due to the low symmetry of their twisted NaCl structure combined with the strong anharmonicity. This comprehensive analysis of PbSnS2 crystals provides a solid foundation for further performance optimization and device assembly, while also sheds light on the investigation of layered thermoelectric materials.

Bioremediation of textile wastewater using Bacillus cereus isolated from refinery site: Comparative analysis of free and immobilized cells systems

The textile industries consume a considerable amount of freshwater and discharge untreated or semi-treated pollutants to the environment. Azo dyes, generally employed in textile manufacturing industries, have a hazardous impact on the ecosystem. Incomplete treatment of wastewater containing azo dyes discharges into the aquatic system, which has recalcitrant and toxic properties. Hence, the need for cost-effective and high-performing technologies is essential. In this direction, bacterial degradation is considered an economically viable and efficient technique for the treatment of Active blue (AB) dye. Polyurethane foam (PUF) is a low-cost and hydrophilic material with a microporous structure, which offers an excellent surface-to-volume ratio. Hence, PUF was preferred for the immobilization of isolated bacterial species. For this, a dye-degrading gram-positive bacteria namely Bacillus cereus GS2 IIT (BHU) was isolated from the petroleum sludge. A comparative analysis between free and immobilized cell systems was carried out by varying the process parameters, i.e., batch time, pH, temperature, glucose concentration, and initial AB dye concentration. The corresponding optimum conditions were found to be 6.0 days, 6.5, 30 °C, 1.0 g/L, and 50 mg/L, respectively. The immobilized cell system exceeds the dye removal efficiency (RE) by 10. 7 % compared to the free cell system. The packed bed bioreactor could be able to deliver 98.56 % of dye removal at an inlet loading rate of 30 mg/L d and 50 mg/L of initial dye concentration.

Fabrication of SnSe nanostructures visible light photodetectors

Tin selenide (SnSe), a potential low-cost material for technological use, possesses good optical, electrical, and optoelectronic properties. In the present study, thermally evaporated SnSe thin films with vertically grown nanosheet morphology are used to fabricate photoconductor-type photodetectors for visible light detection. The as-deposited films at room temperature (RT) are annealed in a vacuum from 100 to 250 °C and are investigated by EDX, XRD, Raman, FE-SEM, and UV–visible spectroscopy. The morphology and crystallinity of films that had been annealed at 200 °C were better, with (111) plane being the preferred orientation. From the optical transmittance measurements, the absorption coefficient and optical bandgap (Eg) of the deposited films were determined. Here, photo-sensing parameters of the detectors fabricated by depositing Ag contact and tested systematically using a 532 nm laser source of varied power intensities (1–5 mW/cm2) are reported. The photodetector’s performances were evaluated, and the fabricated film annealed at 200 °C had a responsivity of 25 × 10−2 AW−1, a peak EQE of 83 %, and an elevated detectivity of 30 × 108 Jones. The response speed of the fabricated photodetector was reasonably good with τr = 3.8 s and τf = 4.4 s under 5 V bias. The research showed the potential SnSe thin films might be used in the field of detecting visible light.

Wet-Spinning Carbon Nanotube/Shape Memory Polymer Composite Fibers with High Actuation Stress and Predesigned Shape Change.

Actuators based on shape memory polymers and composites incorporating nanomaterial additives have been extensively studied; achieving both high output stress and precise shape change by low-cost, scalable methods is a long-term-desired yet challenging task. Here, conventional polymers (polyurea) and carbon nanotube (CNT) fillers are combined to fabricate reinforced composite fibers with exceptional actuation performance, by a wet-spinning method amenable for continuous production. It is found that a thermal-induced shrinkage step could obtain densified strong fibers, and the presence of CNTs effectively promotes the tensile orientation of polymer molecular chains, leading to much improved mechanical properties. Consequently, the CNT/ polyurea composite fibers exhibit stresses as high as 33MPa within 0.36 s during thermal actuation, and stresses up to 22MPa upon electrical stimulation enabled by the built-in conductive CNT networks. Utilizing the flexible thin fibers, various shape change behavior are also demonstrated including the conversion between different structures/curvatures, and recovery of predefined simple patterns. This high-performance composite fibers, capable of both thermal and electrical actuation and produced by low-cost materials and fabrication process, may find many potential applications in wearable devices, robotics, and biomedical areas.

Sustainable control of microplastics in wastewater using the electrochemically enhanced living membrane bioreactor

Wastewater treatment plant (WWTP) discharges are major contributors to the release of microplastics (MPs) into the environment. This research work aimed to assess the performance of the novel living membrane bioreactor (LMBR), which utilizes a biological layer as a membrane filter for the removal of polyethylene (PE) MPs from wastewater. The impact of an intermittently applied low current density (0.5 mA/cm2) on the reduction of MPs in the electrochemically enhanced LMBR (e-LMBR) has also been examined. The reactors were also compared to a conventional membrane bioreactor (MBR) and an electro-MBR (e-MBR). 1H nuclear magnetic resonance spectroscopy (1H NMR) was implemented for the MPs detection and quantification in terms of mass per volume of sample.The LMBR and MBR achieved comparable mean PE MPs reduction at 95% and 96%, respectively. The MPs mass reduction in the e-LMBR slightly decreased by 2% compared to that achieved in the LMBR. This potentially indicated the partial breakdown of the MPs due to electrochemical processes. Decreasing and inconsistent NH4-N and PO4-P removal efficiencies were observed over time due to the addition of PE MPs in the MBR and LMBR. In contrast, the integration of electric field in the e-MBR and e-LMBR resulted in consistently high values of conventional contaminant removals of COD (99.72–99.77 %), NH4-N (97.96–98.67%), and PO4-P (98.44–100.00%), despite the MPs accumulation.Integrating electrochemical processes in the e-LMBR led to the development of a stable living membrane (LM) layer, as manifested in the consistently low effluent turbidity 0.49 ± 0.33 NTU. Despite the increasing MPs concentration in the mixed liquor, applying electrochemical processes reduced the fouling rates in the e-LMBR. The e-LMBR achieved comparable efficiencies in contaminant reductions as those observed in the e-MBR, while using a low-cost membrane material.

Recycling of water treatment plant sludge for copper adsorption from aqueous solutions

Recent studies have explored various adsorbent materials that are low-cost, available in quantity, and effective for heavy metal removal, one of them is the Water Treatment Plant (WTP) sludge. The study aimed to investigate the potential of recycling Water Treatment Plant sludge into an adsorbent for Cu (II) removal. The sludge adsorbent was carbonized by using a furnace at 600°C for 2 hours. This study was conducted in batch. The adsorbent effectiveness was analyzed by varying the dosage, contact time, and activation of the sludge adsorbent on Cu (II) removal. The adsorption isotherm was analyzed using the Langmuir and Ferundlich models, and the kinetic study used pseudo-first-order and pseudo-second-order model. The results showed the removal efficiency of Cu (II) for both activated and non-activated sludge adsorbents reached 98.6–99.9%. The addition of dosage did not affect the increase in Cu (II) adsorption capacity. Activation of the adsorbent increased the adsorption capacity of Cu (II) with the equilibrium time at 60–90 min, shorter than the non-activated adsorbent at 90–120 min. The adsorption isotherm model for both adsorbent types fitted well to the Langmuir model, indicating the adsorption process occurs in a single layer on a homogeneous surface. The adsorption kinetics followed pseudo-second-order with a high correlation coefficient. Water treatment sludge, an industrial by-product, has the potential to be an effective and low-cost adsorbent material for Cu removal.

Fabrication of MnSnO2 intercalated TA-rGO modified sensor for selective electrochemical detection of chloramphenicol in real samples

Chloramphenicol (CAP), a potent antibiotic capable of inhibiting protein synthesis, presents significant challenges related to long-term dosing and its persistent leaching into the environment, raising concerns about environmental contamination and resistance development. To address this issue, we developed a reliable, low-cost, and biocompatible nanocomposite material comprising tannic acid (TA)-reduced graphene oxide (rGO) intercalated into manganese-doped tin oxide nanoparticles (MnSnO₂ NPs). The structural formation and catalytic activity of the MnSnO₂ NPs/TA-rGO nanocomposite were characterized using field emission-scanning electron microscopy (FE-SEM), high-resolution transmission electron microscopy (HR-TEM), X-ray diffraction (XRD), Fourier-transform infrared spectroscopy (FT-IR), Raman spectroscopy, X-ray photoelectron spectroscopy (XPS), and electrochemical techniques. This material exhibits robust interfacial interactions and synergistic effects, resulting in an admirable electrocatalytic reduction response for CAP sensing. The presence of co-interference molecules improved the selectivity performance of the MnSnO2 NPs/TA-rGO-modified glassy carbon electrode. The fabricated exhibited a two linear determination range (0.011–103.43 μmol L−1 and 103.43–1924.16 μmol L−1), with a detection limit (LOD) is 6.7 nmol L−1 and limit of quantification (LOQ) is 12.3 nmol L−1. Furthermore, this sensor demonstrated good sensitivity, admirable reproducibility, repeatability, and storage stability. Finally, the practicability of the fabricated MnSnO2 NPs/TA-rGO glassy carbon electrode sensor was evaluated by analyzing the CAP content in milk, honey, eye drops, biofluids (human serum and urine), and river water, and satisfactory recovery rates of 95.4 %–100.3 % were noted.

Facile synthesis of SSZ-16 nanoaggregates with excellent performance in NH3-SCR reaction

d6r units were proved to be crucial for the synthesis of SSZ-16 zeolite with AFX topology, and FAU zeolite owning plenty of d6r units was chosen as the essential raw material for constructing AFX frameworks. In this work, SSZ-16 zeolite was directly synthesized using colloidal silica and sodium aluminate as the raw materials in short crystallization time of 5 h. The corresponding crystallization process were carefully investigated by various characterizations, demonstrating that the key to this success was the formation of d6r units built up by a large amount of s4r units which were formed with the assistance of the appropriate organic structure directing agent (OSDA) and seeds in the synthetic media. Interestingly, the products of C-SSZ-16 zeolites presented spherical shapes consisted of relatively small particles with size range from 30 to 50 nm. Moreover, after ion-exchanged with Cu ions, the Cu-C-SSZ-16 products showed excellent performance in the selective catalytic reduction of NOx with NH3 (NH3-SCR) and better hydrothermal stability than conventional Cu-SSZ-16-con samples due to slightly higher Si/Al ratio of the Cu-C-SSZ-16. Therefore, remarkable catalytic performance and the use of low-cost raw materials as well as short period of synthesis time make AFX zeolites as potential applicants in NH3-SCR field, from an industrial viewpoint.

Effect of vanadium doping on electrochemical properties of lithium iron manganese phosphate

Abstract The low-cost lithium iron manganese phosphate anode material has a 15% higher energy density than lithium iron phosphate, and it has received wide attention in recent years. However, the poor electronic/ionic conductivity of lithium ferromanganese phosphate leads to poor power performance, which makes it difficult to meet the needs of practical applications. In this study, a V-doped LiMn0.2Fe0.8PO4(LFMP) material is designed and prepared, and every particle is coated by a uniform carbon layer. The V-doped LFMP material shows better rate performance and cycle performance. When the optimal vanadium doping amount is 0.01, the specific discharge capacity of the material is 164.0 mAh/g at 0.1 C.

Preparation and performance study of sludge biomass bamboo charcoal

Abstract The purpose of this study is to explore a new low-cost and high-efficiency biochar adsorption material. The residual sludge as solid waste and fresh bamboo with fast growth and high yield were used as raw materials, modified by the KOH chemical activation method, and pyrolyzed in a tubular furnace with nitrogen atmosphere to obtain sludge biomass bamboo charcoal. In the performance test, the H2S gas adsorption experiment in a fixed bed reactor and the heavy metal adsorption experiment in soil were designed. Using different proportions of biochar, the preparation process of biochar was optimized by adjusting the raw material ratio and activation conditions. The results showed that when dealing with H2S gas, the appropriate amount of sludge can improve the adsorption effect, while the increase of bamboo component will reduce the adsorption rate. In the soil Cr(VI) restoration experiment, it was found that the best restoration effect was achieved after adding 10% biochar and applying it for 28 days, and the restoration rate reached 63.5%.

Enhanced Electrochemical Performance of NiMn Layered Double Hydroxides/Graphene Oxide Composites Synthesized by One-Step Hydrothermal Method for Supercapacitors.

This study aims to enhance the performance of supercapacitors, focusing particularly on optimizing electrode materials. While pure NiMn layered double hydroxides (LDHs) exhibit excellent electrochemical properties, they have limitations in achieving high specific capacitance. Therefore, this paper successfully synthesized composite materials of NiMn LDHs with varying loadings of graphene oxide (GO) using a hydrothermal method. Systematic physicochemical characterization of the synthesized materials, such as powder X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS), field-emission scanning electron microscopy (FE-SEM), and Raman spectroscopy, revealed the influence of GO doping on the microstructure and electrochemical performance of NiMn LDHs. Electrochemical tests demonstrated that the NiMn LDHs/GO electrode material exhibited optimal electrochemical performance with a specific capacitance of 2096 F g-1 at 1 A g-1 current density and 1471 F g-1 at 10 A g-1, when GO doping level was 0.45 wt %. Furthermore, after 1000 cycles of stability testing, the material retained 53.3 % capacitance at 5 A g-1, indicating good cyclic stability. This study not only provides new directions for research on supercapacitor electrode materials but also offers new strategies for developing low-cost and efficient electrode materials.