Enhancing the energy storage capabilities of supercapacitors (SCs) while preserving their electrochemical performance is crucial for their widespread application. Our research focuses on developing Sb-modified tin oxide (ATO) nanoparticles via a scalable hydrothermal process, offering substantial potential in this domain. The tetragonal nanoparticle structure provides abundant active sites and a highly porous pathway, facilitating rapid and efficient energy storage. Additionally, tin's varied oxidation states significantly enhance redox capacitance. Electrochemical measurements demonstrate ATO's promise as an advanced SC electrode, achieving a peak specific capacitance of 332 F/g at 3 mA/cm2, with robust redox capacitance confirmed through kinetic analysis. Moreover, the ATO electrode exhibits exceptional capacitance retention over 2000 cycles. This study establishes ATO as a leading candidate for future energy storage applications, underscoring its pivotal role in advancing energy storage technologies.

Transition metal/porous carbon composite is good electrode candidate since porous carbon provides high surface porosity which promotes the access of electrolyte ions, and transition metal enables redox reactions to improve specific capacitance and energy density. In this study, iron/carbon nanofiber (CNF) composite electrodes were prepared by grafting ferrocenecarboxaldehyde to the CNFs which were fabricated by electrospinning and thermal treatment of polyacrylonitrile (PAN). The presence of iron on the CNF surface was confirmed by SEM/EDS, ICP-MS and XPS. Electrochemical performance was evaluated using a three-electrode cell with 1 M Na2SO4 as an electrolyte. Iron-grafted CNFs exhibited a high specific capacitance of 358 F g− 1 and an energy density of 49.7 Wh kg− 1 at 0.5 A g− 1, which is significantly higher than those for untreated CNFs (68 F g− 1 and 9.4 Wh kg− 1). This demonstrates that this iron/CNF composite is promising candidate for supercapacitor electrode with outstanding energy storage performance.

The high value-added utilization of traditional coal resources is one of the important ways to achieve the strategic goals of carbon peaking and carbon neutrality. Simultaneously, coal-based carbon materials, noted for their cost-effectiveness, superior conductivity, and inherent stability, are emerging as promising candidates for next-generation capacitor technologies. This research presents a series of coal-derived porous carbon by pyrolysis using low rank lignite as raw material and KOH as activator, which are employed in symmetrical supercapacitors filled with liquid electrolytes. The physicochemical properties of the as-prepared electrode materials are characterized by means of scanning electron microscopy, X-ray diffraction, Raman spectroscopy, and their supercapacitive performance are evaluated through cyclic voltammetry and galvanostatic charge–discharge tests. The coal-based porous carbon electrode prepared at an activation temperature of 800 °C (KOH-800) exhibits a specific capacitance of 142.2 F g− 1 at a current density of 1 A g− 1, and retaining 80% of its capacitance (114.0 F g− 1) even at 10 A g− 1. The fabricated liquid supercapacitor displays a power density of 999.8 W kg− 1 and an energy density of 19.4 Wh kg− 1 at a current density of 1 A g− 1. Undergoing 10,000 cycles at 2 A g− 1, the supercapacitor maintains nearperfect capacitance retention and coulombic efficiency close to 100%, demonstrating its excellent durability and stability for supercapacitor applications.

Aqueous zinc–iodine batteries (AZIBs) are gaining attention for their ability to store and convert electrical energy. Nevertheless, their performance is hindered by the continual migration of polyiodides towards the zinc anodes, leading to undesirable side reactions, diminished coulombic efficiency, and compromised cycling stability. Traditional carbon materials have proven inadequate in resolving these challenges, mainly due to their limited iodine capacity and weak binding forces. Herein, we explore the use of porous carbon nanosheets (PCNSs) synthesized via the “Pharaoh’s Serpent” reaction as cathode electrodes in AZIBs without pre-load iodine. The PCNSs, characterized by their nanosheet structure and expansive specific surface area, not only facilitate a shorter diffusion path for rapid electrolyte infiltration but also provide numerous sites for ion adsorption and capacitive storage, markedly improving the efficacy of electrochemical reactions and ion migration rates. Utilizing the synthesized PCNSs as the cathode electrode in AZIBs, a specific capacity of 296 mAh g− 1 was achieved at 0.3 A g− 1. Even when the current density increased to 30 A g− 1, a specific capacity of 144 mAh g− 1 was still attained, with a capacity retention ratio of up to 48.6%, which is competitive with that of supercapacitors. In addition, the AZIBs demonstrated impressive cycling stability, retaining 103% of their capacity after 10,000 cycles, and a notable energy density of 266.4 Wh kg− 1 based on the cathode material. These findings significantly broaden the application of carbon materials in AZIBs research, emphasizing their potential in advancing AZIB technology.

Graphene aerogels have gained widespread recognition in recent years as electrode materials for supercapacitors, primarily attributed to their excellent stability and impressive specific capacitance. However, further enhancing their specific capacitance is a formidable task. One viable strategy to overcome this hurdle is to composite them with metal oxides. In doing so, the metal oxides boost the specific capacitance of graphene aerogels, while the latter addresses the stability issues inherent in metal oxides. This article reviews recent research on Ni, Co, and Mn oxide–graphene composite aerogels in supercapacitors, summarizing their preparation processes, performance and energy storage mechanism. While existing studies have demonstrated the feasibility of metal oxide–graphene composite aerogels as supercapacitor electrodes, several challenges remain, necessitating deeper exploration by researchers in this field.

Fiber supercapacitors have attracted significant interest as potential textile energy storage devices due to their remarkable flexibility and rapid charge/discharge capabilities. This study describes the fabrication of a composite fiber supercapacitor (FSC) electrode through a multi-shell architecture, featuring layers of carbon nanotube (CNT) conductive shells and MnO2 nanoparticle active shells. The number of layers was adjusted to assess their impact on FSC energy storage performance. Increasing the number of shells reduced electrode resistance and enhanced pseudocapacitive characteristics. Compared to the MnS@1 electrode, the MnS@5 electrode exhibited a high areal capacitance of 301.2 mF/cm2, a 411% increase, but showed a higher charge transfer resistance (RCT) of 701.6 Ω. This is attributed to reduced ion diffusion and charge transfer ability resulting from the thicker multi-shell configuration. These results indicate that fine-tuning the quantity of shells is crucial for achieving an optimal balance between energy storage efficiency and stability.

Supercapacitors, renowned for their high power density and rapid charge-discharge rates, are limited by their low energy density. This limitation has prompted the need for advanced electrode materials. The present study investigated reduced graphene oxide (rGO) in two distinct structures, as a film and as an aerogel, for use as supercapacitor electrodes. The rGO film, prepared by vacuum filtration and thermal reduction, exhibited a compact, lamellar structure, while the aerogel, synthesized through hydrothermal treatment, was a highly porous three-dimensional network. Electrochemical analyses demonstrated the aerogel’s superior performance, as shown by a specific capacitance of 121.2 F/g at 5 mV/s, with 94% capacitance retention after 10,000 cycles. These findings emphasize the importance of structural design in optimizing ion accessibility and charge transfer. They also demonstrate the potential of rGO aerogels for increasing the energy storage efficiency of advanced supercapacitor systems.

Graphene-based solar cells and supercapacitors integrated into photosupercapacitors represent a pioneering advancement. These devices leverage the exceptional properties of graphene, such as high conductivity and large surface area, to enhance both solar energy conversion and energy storage. The integration of these technologies into photosupercapacitors creates a multifunctional device capable of harnessing solar energy and storing it efficiently. This innovative approach holds promise for sustainable and versatile energy solutions, marking a significant step towards developing efficient and compact energy storage systems. This integration addresses the intermittent nature of solar power generation by providing a continuous and reliable power supply through energy storage. Supercapacitors are one such energy device with a high-power density and excellent specific capacitance which is integrated will a dye-sensitized solar cell (DSSC) comprising a single system of photosupercapacitor. A novel electrode material of NiO/CuO/Co3O4/rGO was synthesized which serves as the Pt-free counter electrode of DSSC and working or storage electrode of supercapacitor later was used as the intermediate electrode and storage electrode of a photosupercapacitor. The integrated photosupercapacitor device had a photovoltage of 0.81 V with arealspecific capacitance, energy and power density of 190.12 mF cm− 2, 17.325 μW h cm− 2 and 0.162 mW cm− 2, respectively. The device self-discharged in 385 s with an overall conversion efficiency of 2.17%, resulting in a self-charged energy device.

Energy storage is one of the leading problems being faced globally, due to the population explosion in recent times. The conventional energy sources that are available are on the verge of extinction, hence researchers are keen on developing a storage system that will face the upcoming energy needs. Supercapacitors, also known as ultracapacitors or electrochemical capacitors, are advanced energy storage devices characterised by high power density and rapid charge–discharge cycles. Unlike traditional batteries, supercapacitors store energy through electrostatic separation, offering quick energy release and prolonged operational life. They hold exceptional performance in various applications, from portable electronics to electric vehicles, where their ability to deliver bursts of energy efficiently complements or replaces conventional energy storage solutions. Ongoing research focuses on enhancing energy density and overall efficiency, positioning supercapacitors as pivotal components in the evolving landscape of energy storage technologies. A novel electrode material of NiO/CuO/Co3O4/rGO was synthesized which when used as a supercapacitor, the highest value of CS is 873.14 F/g which is achieved for a current density of 1 A/g under with an energy density of 190 Wh/kg and the highest power density of 2.5 kW/kg along with 87.3% retention after 5000 GCD cycles under 1 M KOH.

Porous carbon nanofiber (CNF) electrodes for supercapacitors were prepared by using polyacrylonitrile (PAN) and cucurbituril (CB), which is a macrocyclic compound comprising glycoluril units containing hollow cores. Mixture of PAN and CB in dimethyl sulfoxide was electrospun, and thermally treated to produce CNF electrodes. Their thermal stability, surface morphology, carbon microstructures, and surface porosity were investigated. Electrochemical properties were measured using three-electrode with synthesized CNFs without further treatment as a working electrode and 1 M Na2SO4 as an electrolyte. CNFs derived from PAN and CB exhibited a high specific capacitance of 183.5 F g− 1 and an energy density of 25.4 Wh kg− 1 at 0.5 A g− 1 with stable cyclic stability during 1000 cycles, which is significantly higher than those for CNFs derived from PAN only. This demonstrated that the introduction of CB successfully improved the energy storage performance of CNF electrodes.

Large-area porous carbon is easily produced for supercapacitors from polyvinylidene chloride (PVDC) and polyvinylidene fluoride (PVDF) precursors, composed of carbon backbone and attached heteroatoms. The released heteroatoms during pyrolysis leave the porous carbon. This study explored the activation of both precursors using chemical agents (ZnO, Mg(OH)2, and KOH) to develop carbon with multiple micropores and mesopores. The activation process and relevant precursors were studied to implement synthesized porous carbon as an electrode in supercapacitors. During the activation of PVDC-resin, ZnO served both as templates and activating agents, while Mg(OH)2 served only as a template, and KOH served as an activating agent. For activation of PVDF, ZnO acted as a template and activating agent, whereas Mg(OH)2 and KOH impeded activation owing to side reactions. Therefore, with the above chemical agents, PVDC-resin was converted to carbon with a higher surface area than PVDF. The porous carbon produced using PVDC-resin with KOH had the highest specific capacitance of 137 F g− 1 and rate performance of 79% at 50 mV s− 1 (vs. 5 mV s− 1) owing to the successful creation of micropores and mesopores. This study identifies optimal conditions for synthesizing porous carbon using polymer precursors and chemical agents for supercapacitors.

Carbon-based materials, particularly graphite, have been extensively studied for their potential in fabricating flexible conductive fabrics with high electrical conductivity, which are attractive for wearable electronics. In this study, we investigated the effects of polar solvents, graphite concentration, and temperature on the electrical properties of conductive cotton fabrics. Our results show that the type of polar solvent and graphite concentration strongly influence the electrical conductivity of the fabrics. By controlling the graphite concentration, a wide range of conductive cotton fabrics with different conductivity values can be produced. Additionally, temperature resistance studies revealed that the fabrics exhibit both semiconductor and metallic behavior in the temperature range from room temperature to 160 °C. These interesting properties make the conductive cotton fabrics suitable for use as electrical components in circuits with resistive and inductive loads. Furthermore, we fabricated a supercapacitor with electrodes based on dispersed graphite and an electrolyte of sodium chloride salt dissolved in deionized water. Our findings suggest that conductive cotton fabrics have great potential for use in high-performance wearable electronics and energy storage devices.

Hierarchically porous carbon foam composites with highly dispersed Fe2O3 nanoparticles confined in the foam pores, facilely fabricated by hydrolysis-driven emulsion polymerization strategy. The as-generated acidic conditions of Fe3+ hydrolysis could catalyze the polymerization of phenolic resin, and the carbon-based composite materials containing iron oxides were obtained in situ. The structural characterization results show that HCF@Fe2O3 NPs-2 electrode has the largest specific surface area (549 m2/ g) and pore volume (0.46 cm3/ g). Electrochemical results indicates that typical HCF@Fe2O3 NPs-2 electrode displays good capacitive properties. including high specific capacitance (225 F/g at 0.2 A/g current density). Excellent magnification performance (capacity retention rate 80% as current density increases from 0.2 to 10 A/g). At the same time, HCF@SnO2 NPs was successfully synthesized by replacing hydrolyzed tin tetrachloride with ferric chloride. This study provides a new idea for the preparation of metal oxide–carbon matrix composites, and also highlights the potential of such carbon foams in application of energy storage.

In recent years, supercapacitors have attracted extensive attention due to their advantages such as fast charge and discharge rate, high power density and long cycle life. Because of its unique porous structure and excellent electrochemical properties, heteroatom-doped porous carbon (HPC) is deemed as a promising electrode material for supercapacitors. However, it is a great challenge to synthesize electrode materials with large surface area, ultra-high porosity and good electrochemical performance. In this work, two-dimensional conjugated microporous polymers (CMPs) containing ketones were synthesized by a simple one-step coupling reaction and used as carbon precursors. A series of samples (CMP-Ts) were prepared with the procedures of coupling reaction and carbonization. The optimized carbon material has high specific surface area (up to 2229.85 m2 g− 1), porous structure, high specific capacitance (375 F g− 1 at 0.5 A g− 1), and good cycling stability (capacitance retention of 98.8% after 1000 cycles at 5 A g− 1). Further, the supercapacitor has an energy density of 28.8 Wh kg− 1 at a power density of 5000 W kg− 1. This work lays a foundation for the preparation of carbon materials using microporous polymer as a precursor system, provides a new way of thinking, and demonstrates a great potential of high-performance supercapacitors.

In this study, we synthesized pH-controlled resorcinol-formaldehyde (RF) gels through the polymerization of two starting materials: resorcinol and formaldehyde. The prepared RF gels were dried using an acetone substitution method, and they were subsequently carbonized under nitrogen atmosphere to obtain carbon xerogels (CX_Y) prepared at different pH (Y). The carbon xerogels were utilized as active materials for coin-type organic supercapacitor electrodes to investigate the influence of pH on the electrochemical properties of the carbon xerogels. The carbon xerogels prepared at lower pH (CX_9.5 and CX_10) exhibited sufficient particle growth, with a three-dimensional network of particles during the RF gel formation, resulting in the development of abundant mesopores. Conversely, the carbon xerogels prepared at higher pH (CX_11 and CX_12) retained densely packed structures of small particles, leading to pore collapse and low specific surface areas. Consequently, CX_9.5 and CX_10 showed high specific surface areas, and provided ample adsorption sites for the formation of electric double layers with electrolyte ions. Moreover, the three-dimensional particle network in CX_9.5 and CX_10 significantly enhanced electrical conductivity. The presence of well-developed mesopores in these materials further facilitated the effective transport of electrolyte ions, contributing to their superior performance as organic supercapacitor electrodes. This study confirmed that pH-controlled carbon xerogels are one of the promising active materials for organic supercapacitor electrodes. Furthermore, we concluded that pH during RF gel formation is a crucial factor determining the electrode performance of the carbon xerogels, highlighting the need for precise pH control to obtain high-performance carbon xerogel electrodes.

본 연구는 에너지 저장 응용을 위한 PVI-PGMA/LiTFSI 고분자 막 전해질 및 CxNy-C 유연 전극의 합성 및 특성 에 관한 연구이다. 이중 기능을 갖는 PVI-PGMA 공중합체는 우수한 이온 전도성을 나타내었으며, PVI-GMA73/LiTFSI200 막 전해질은 1.0 × 10-3 S cm-1의 최고 전도도를 달성하였다. CxNy-C 전극의 전기화학적 성능을 체계적으로 분석하였으며, C3N2-C는 나노와이어와 다면체로 구성된 높은 연결성을 갖는 하이브리드 구조와 이중 Co/Ni 산화물을 포함하여 풍부한 산 화환원 활성 부위와 이온 확산을 용이하게 하는 특징으로 인해 958 F g-1의 최고용량 및 최소한의 전하 전달 저항(Rct)을 달성 하였다. 흑연 탄소 껍질의 존재는 충전-방전 동안 높은 전기화학적 안정성에 기여하였다. 이러한 결과들은 고성능 에너지 저 장 장치인 슈퍼커패시터 및 리튬 이온 전지와 같은 첨단 에너지 저장 장비에 PVI-PGMA/LiTFSI 고분자 막 전해질과 CxNy-C 전극을 활용하는 잠재력을 보여주었으며, 지속 가능하고 고성능의 에너지 저장 기술을 더욱 발전시키는 길을 열어가 고 있다.