Search Results (22)

The rational design of electrode materials with tailored composition and architecture is crucial for advancing high-capability electrochemical energy storage systems. This study reports that gadolinium-modified NiFe₂O₄ nanosheet electrodes were effectively synthesized on nickel foam via a hydrothermal approach followed by thermal treatment. A series of compositions (NiFe, NiFe–Gd1, NiFe–Gd2, and NiFe–Gd3) were prepared to systematically examine the effect of Gd incorporation on structural features and electrochemical properties. X-ray diffraction (XRD) analysis confirmed the formation of the cubic spinel NiFe₂O₄ phase without detectable secondary phases, indicating that the crystal structure remains intact after Gd introduction. X-ray photoelectron spectroscopy (XPS) further verified the presence of Ni²⁺, Fe³⁺, and Gd³⁺ species within the lattice environment. Morphological analysis using field-emission scanning electron microscopy (FESEM) revealed a nanosheet-based architecture, where the optimized NiFe–Gd2 electrode exhibited a porous and interconnected nanosheet framework with abundant exposed edges. This structural configuration improves electrolyte penetration and facilitates efficient ion transport during charge storage processes. Electrochemical measurements demonstrated that the NiFe–Gd2 electrode delivers an areal capacitance of 5235 mF cm⁻² at 10 mA cm⁻², along with improved reaction kinetics and low internal resistance. An asymmetric supercapacitor assembled using NiFe–Gd2 as the positive electrode and activated carbon as the negative electrode operated stably within a 0–1.5 V potential window, achieving an energy density of 0.136 mWh cm⁻² and a power density of 3.14 mW cm⁻², while retaining 86.55% of its initial capacitance after 7000 cycles. These results highlight the potential of rare-earth engineering as a viable strategy for designing advanced spinel ferrite electrodes and pave the way for the development of high-performance, durable, and scalable supercapacitor systems for practical energy storage applications. Full article

The increasing density of wireless and wearable electronic devices necessitates the development of lightweight, flexible, and absorption-dominated electromagnetic interference (EMI) shielding materials. In this study, electrospun poly(vinylidene fluoride) (PVDF) composite mats reinforced with carbon nanotubes (CNTs) and graphene nanosheets at low filler loadings (1–3 wt.%) were fabricated and systematically investigated for X-band (8.0–12.5 GHz) EMI shielding performance. Raman, FTIR, and thermal analyses confirm enhanced electroactive β-phase formation and improved thermal stability upon nanofiller incorporation. The formation of interconnected conductive networks within the electrospun fibrous architecture leads to a significant increase in electrical conductivity from 10⁻⁷ S·cm⁻¹ for pure PVDF to 10⁻² S·cm⁻¹ and 10⁻¹ S·cm⁻¹ for CNT/PVDF and Graphene/PVDF composites, respectively, at 3 wt.% loading. Consequently, the total EMI shielding effectiveness (SE_T) increases from 2.5 dB for pure PVDF to 40 dB for CNT/PVDF and 42 dB for graphene/PVDF composites at 3 wt.%. The shielding effectiveness arising from absorption (SE_A) dominates the overall EMI shielding performance, contributing more than 85% of the total shielding effectiveness (SE_T), which clearly indicates an absorption-controlled shielding mechanism. The combination of high absorption-dominated EMI shielding, low filler content, and mechanical flexibility highlights these electrospun CNT/PVDF and graphene/PVDF composites as promising candidates for next-generation flexible, wearable, and biomedical EMI shielding applications. Full article

Transition-metal dichalcogenides have emerged as promising non-noble-metal electrocatalysts for efficient hydrogen production through the hydrogen evolution reaction (HER). In this work, we fabricated the graphitic carbon nitride-decorated cobalt diselenide (gC₃N₄-CoSe₂) nanocomposites via the facile hydrothermal method. The prepared gC₃N₄-CoSe₂ nanocomposites displayed an interconnected and aggregated morphology of gC₃N₄-decorated CoSe₂ nanoparticles with offering large surface area of 82 m²/g. The gC₃N₄-CoSe₂ nanocomposites exhibited excellent HER activity with a low overpotential (141 mV) and tiny Tafel slope (62 mV/dec) with excellent durability for 100 h at 10 mA/cm² in an alkaline electrolyte. These outstanding HER performances of gC₃N₄-CoSe₂ can be ascribed to the synergistic interaction between the electrochemically active porous CoSe₂ nanoparticles and the highly conductive gC₃N₄ nanosheets. These results indicate that the gC₃N₄-CoSe₂ nanocomposites hold promising and efficient HER electrocatalysts for sustainable green hydrogen production. Full article

Aqueous zinc-ion batteries (AZIBs) have attracted considerable attention due to their intrinsic safety, low cost, and environmental friendliness. However, drastic volume expansion, sluggish reaction kinetics, and the insufficient structural stability of electrode materials still remain key challenges. In this work, a cascade structure-guided electron transport strategy was used to construct a vanadium nitride@carbon nanosheet/carbon nanofiber (VN@CNS/CNF) composite as a high-performance cathode for AZIBs. In this rationally engineered architecture, carbon-coated VN nanoparticles are uniformly anchored on a conductive carbon nanofiber network, forming a multidimensional interconnected structure that enables fast electron/ion transport and robust mechanical stability. The carbon shell effectively alleviates volume expansion and prevents VN nanoparticle agglomeration, while the continuous carbon fiber backbone reduces charge transfer resistance and enhances reaction kinetics. Benefiting from this synergistic structural design, the VN@CNS/CNF electrode delivers a high specific capacity of 564 mAh g⁻¹ at 0.1 A g⁻¹, maintains 99% capacity retention after 50 cycles, and retains 280 mAh g⁻¹ even at 8 A g⁻¹ after prolonged cycling. This study provides a new structural engineering strategy for vanadium nitride-based electrodes and provides strategic guidance for the development of fast-charging, durable aqueous zinc-ion batteries. Full article

For future clean and renewable energy technology, designing highly efficient and robust electrocatalysts is of great importance. Particularly, creating efficient bifunctional electrocatalysts capable of effectively catalyzing both hydrogen- and oxygen-evolution reactions (HERs and OERs) is vital for overall water electrolysis. In this study, we employ 2D molybdenum disulfide (MoS₂) nanosheets and pyrolytically fabricated 2D graphitic carbon nitride (gC₃N₄) nanosheets to create 2D gC₃N₄-decorated 2D MoS₂ (2D–2D gC₃N₄–MoS₂) nanocomposites using a facile sonochemical method. The 2D–2D gC₃N₄–MoS₂ nanocomposites show an interconnected and agglomerated structure of 2D gC₃N₄ nanosheets decorated on 2D MoS₂ nanosheets. For water electrolysis, the gC₃N₄–MoS₂ nanocomposites exhibit low overpotentials (OER: 225 mV, HER: 156 mV), small Tafel slope values (OER: 49 mV/dec, HER: 101 mV/dec), and excellent durability (up to 100 h for both OER and HER) at 10 mA/cm² in 1 M KOH. Furthermore, the gC₃N₄–MoS₂ nanocomposites show excellent overall water electrolysis performance with a low full-cell voltage (1.52 V at 10 mA/cm²) and outstanding long-term cell stability. The superb bifunctional activities of the gC₃N₄–MoS₂ nanocomposites are attributed to the synergistic effects of 2D gC₃N₄ (i.e., low charge-transfer resistance) and 2D MoS₂ (i.e., a large electrochemically active surface area). These findings suggest that the 2D–2D gC₃N₄–MoS₂ nanocomposites could serve as excellent bifunctional catalysts for overall water electrolysis. Full article

The development of lightweight composites with superior mechanical properties and electromagnetic interference (EMI) shielding performance is essential for various structural and functional applications. This study investigates the effect of hybrid nanocarbon (graphene nanosheet (GNS) and carbon nanotube (CNT)) reinforcements on the properties of magnesium (Mg) matrix composites. Specifically, the GNS-CNT hybrid, which forms a three-dimensional interconnected network structure, was analyzed and compared to composites reinforced with only GNSs or CNTs. The objective was to determine the benefits of hybrid reinforcements on the mechanical strength and EMI shielding capability of the composites. The results indicated that the GNS-CNT/Mg composite, at a nanocarbon content of 0.5 wt.% and a GNS-CNT ratio of 1:2, achieved optimal performance, with a 55% increase in tensile strength and an EMI shielding effectiveness of 70 dB. The observed enhancements can be attributed to several key mechanisms: effective load transfer, which promotes tensile twinning, along with improved impedance matching and multiple internal reflections within the GNS-CNT network, which enhance absorption loss. These significant improvements position the composite as a promising candidate for advanced applications requiring high strength, toughness, and efficient electromagnetic shielding, providing valuable insights into the design of high-performance lightweight materials. Full article

In this work, we report a facile and tunable electrodeposition approach for engineering polyacrylic acid (PAA)-modified Co₃O₄ electrodes on nickel foam for high-performance asymmetric pouch-type supercapacitors. By systematically varying the PAA concentration (0.5 wt %, 1 wt %, and 1.5 wt %), we demonstrate that the CO-1 sample (1 wt % PAA) exhibited the most optimized structure and electrochemical behavior. The CO-1 electrode delivered a remarkable areal capacitance of 3467 mF/cm² at 30 mA/cm², attributed to its interconnected nanosheet morphology, enhanced ion diffusion, and reversible Co²⁺/Co³⁺/Co⁴⁺ redox transitions. Electrochemical impedance spectroscopy confirmed low internal resistance (0.4267 Ω), while kinetic analysis revealed a dominant diffusion-controlled charge storage contribution of 91.7%. To evaluate practical applicability, an asymmetric pouch-type supercapacitor device was assembled using CO-1 as the positive electrode and activated carbon as the negative electrode. The device operated efficiently within a 1.6 V window, achieving an impressive areal capacitance of 157 mF/cm², an energy density of 0.056 mWh/cm², a power density of 1.9 mW/cm², and excellent cycling stability. This study underscores the critical role of polymer-assisted growth in tailoring electrode architecture and provides a promising route for integrating cost-effective and scalable supercapacitor devices into next-generation energy storage technologies. Full article

The demand for high-performance supercapacitors has driven extensive research into novel electrode materials with superior electrochemical properties. This study explores the supercapacitive behavior of quaternary CuNiCoZnO (CNCZO) films engineered into a three-dimensional (3D) flower-like morphology and developed on versatile substrates, including carbon cloth, stainless steel mesh, and nickel foam. The unique structural design, comprising interconnected nanosheets, enhances the electroactive surface area, facilitates ion diffusion, and improves charge storage capability. The synergistic effect of the multi-metallic composition contributes to remarkable electrochemical characteristics, including high specific capacitance, excellent rate capability, and outstanding cycling stability. Furthermore, the influence of different substrates on the electrochemical performance is systematically investigated to optimize material–substrate interactions. Electrochemical evaluations reveal outstanding specific capacitance values of 2318.5 F/g, 1993.7 F/g, and 2741.3 F/g at 2 mA/cm² for CNCZO electrodes on stainless steel mesh, carbon cloth, and nickel foam, respectively, with capacitance retention of 77.3%, 95.7%, and 86.1% over 5000 cycles. Furthermore, a symmetric device of CNCZO@Ni exhibits a peak specific capacitance of 67.7 F/g at a current density of 4 mA/cm², a power density of 717.4 W/kg, and an energy density of 25.6 Wh/kg, maintaining 84.5% stability over 5000 cycles. The straightforward synthesis of CNCZO on multiple substrates presents a promising route for the development of flexible, high-performance energy storage devices. Full article

This work explores the role of cetyltrimethylammonium bromide (CTAB) as a morphology-directing agent in the hydrothermal synthesis of NiFe₂O₄ electrodes for high-performance supercapacitor applications. By fine-tuning CTAB concentrations (0.5%, 1%, and 1.5%), a tunable nanosheet morphology was achieved, with the NiFe-1 sample exhibiting uniformly interconnected nanosheets that enhanced ion diffusion, charge transport, and surface redox activity. Structural and surface analyses confirmed the formation of single-phase cubic NiFe₂O₄ and the presence of Ni²⁺ and Fe³⁺ oxidation states. Electrochemical characterization in a 2 M KOH electrolyte revealed that the NiFe-1 electrode achieved an areal capacitance of 8.21 F/cm² at 20 mA/cm², with an energy density of 0.34 mWh/cm² and a power density of 5.5 mW/cm². The electrode retained 79.61% of its capacitance after 10,000 cycles, demonstrating excellent stability. An asymmetric pouch-type supercapacitor device (APSD), assembled using NiFe-1 and activated carbon, exhibited an areal capacitance of 1.215 F/cm² and delivered an energy density of 0.285 mWh/cm² at a power density of 6.5 mW/cm² across a wide 0–1.8 V voltage window. These results confirm that CTAB-assisted nanostructuring significantly improves the electrochemical performance of NiFe₂O₄ electrodes, offering a scalable and effective approach for next-generation energy storage applications. Full article

Carbonaceous-based metal-free catalysts are promising aspirants for effective electrocatalytic hydrogen generation. Herein, we synthesized mesoporous-activated carbon nanosheets (ELC) from biomass eucalyptus leaves through KOH activation. The microstructure, structural, and textural characteristics of the prepared materials were characterized by FE-SEM, Raman, XRD, and BET measurements. The high temperature (700 °C) KOH-activated ELC nanosheets exhibited an interconnected nanosheet morphology with a large specific surface area (1436 m²/g) and high mesoporosity. The ELC-700 catalyst exhibited an excellent electrocatalytic HER performance with a low overpotential (39 mV at 10 mA/cm²), excellent durability, and a Trivial Tafel slope (36 mV/dec) in 0.5 M H₂SO₄ electrolyte. These findings indicate a new approach for developing excellent biomass-derived electrocatalysts for substantially efficient green hydrogen production. Full article

Designing efficient electrode materials is necessary for supercapacitors but remains highly challenging. Herein, cobalt sulfide with crystalline/amorphous heterophase (denoted as Co(Al)S) derived from an Al metal–organic framework was constructed by ion exchange/acid etching and subsequent sulfidation strategy. It was found that rational sulfidation by adjusting the sulfur source concentration to a suitable level was favorable to form a 3D nanosheet-interconnected network architecture with a large specific surface area, which promoted ion/electron transport and charge separation. Benefiting from the features of the unique network structure and heterophase accompanied by aluminum, nitrogen and carbon coordinated in amorphous phase, the optimal Co(Al)S₍₁₀₎ exhibited a high specific capacity (1791.8 C g⁻¹ at 1 A g⁻¹), an outstanding rate capability and an excellent cycling stability. Furthermore, the as-assembled Co(Al)S//AC device afforded an energy density of 72.3 Wh kg⁻¹ at a power density of 750 W kg⁻¹, verifying that the Co(Al)S was a promising material for energy storage devices. The developed scheme is expected to promote the application of MOF-derived electrode materials in electrochemical energy storage and conversion fields. Full article

The design of a reasonable heterostructure electrode to achieve enhanced areal performance for supercapacitors remains a great challenge. Here, we constructed hierarchical porous NiCoP/NiO nanocomposites anchored on Ni foam with tunable electronic and structural properties, as well as robust interfacial interaction. In NiCoP/NiO, the interconnected NiO nanosheets serve as a carrier with enriched anchoring sites to confine the NiCoP and improve its stability. Meanwhile, the ultrathin NiCoP nanosheets with bimetallic centers are connected with porous NiO nanosheets to form a reliable heterojunction, enhancing the electrochemical reaction kinetics. Taking advantage of the synergistic contribution of bimetallic centers, phosphides and unique structure, the NiCoP/NiO delivers a high areal specific capacitance (1860 mF cm⁻² at 5 mA cm⁻²), good rate performance of 78.5% at six times the increased current density, and remarkable durability (11.0% decrease after 10,000 cycles). Furthermore, the assembled hybrid supercapacitor NiCoP/NiO//porous-activated carbon (PAC) delivers a high areal energy density of 173.7 μWh cm⁻² (116.4 μWh cm⁻²) at 1.6 mW cm⁻² (32 mW cm⁻²). The results indicate that the design of the heterostructure interface with strong chemical interface and tunable electronic structure is an effective and promising approach to boost the electrochemical performance for advanced supercapacitors. Full article

In this work, to obtain textile triboelectric layers for wearable flexible triboelectric nanogenerators (TENGs), we used two modes of growing nanostructured zinc oxide (ZnO) arrays on a carbon fabric (CF) using the automatic Successive Ionic Layer Adsorption and Reaction (SILAR) method. To produce a CF/ZnO_nr triboelectric textile with an array of intergrown short ZnO nanorods, we used a pre-coating of carbon fibers with ZnO seed layers. When the ZnO layer was fabricated by automatic SILAR on bare carbon fabric, we obtained the CF/ZnO_ns textile with an array of interconnected ZnO nanosheets 50–100 nm thick. As a proof of concept, we developed and tested two prototypes of flexible vertical contact–separation mode CF/ZnO_nr/PET/ITO and CF/ZnO_ns/PET/ITO TENGs, in which a gap was involuntarily formed between the smooth PET layer and the woven carbon textile coated with nanostructured ZnO films. In pressing tests with a force of ~5 N (pressure ~33 kPa), the CF/ZnO_ns/PET/ITO TENG created a higher open-circuit voltage up to 30 V and a higher maximum surface charge density of 1.3 μC/m². In the successive press–release tests, this TENG showed an output voltage of 3.6 V, a current density of 1.47 μA/cm², and a power density of 1.8 µW/cm², confirming its effectiveness. Full article

The development of Li-CO₂/O₂ battery with high energy density and long-term stability is urgently needed to fulfill the carbon neutralization and pollution-free environment targets. The biomass-derived heteroatom-doped carbon catalyst with the combination of high-efficiency catalytic activity and sustainable supply is a promising cathode catalyst in Li-CO₂/O₂ battery. Specifically, the unique morphology and mesopore structure can promote the transfer of CO₂, O₂, and Li⁺. Abundant channel pores can provide discharge products accommodation to the largest extent. Nitrogen dopant, the commonly recognized active sites in carbon, can improve the electron conductivity and accelerate the sluggish kinetic reaction. Therefore, utilizing the louts leaves as the precursor, we successfully prepare the cellular-like nitrogen-doped activated carbon nanosheets (N-CNs) through the appropriate pyrolysis carbonization method. The as-synthesized carbon nanosheets display a three-dimensional interconnecting pore structure and abundant N-dopant actives, which dramatically improve the electrochemical catalytic activity of N-CNs. The Li-CO₂/O₂ battery with the N-CNs cathode delivers a high discharge capacity of 9825 mAh g⁻¹, low overpotential of 1.21 V, and stable cycling performance of 95 cycles. Thus, we carry out a facile method for N-doped carbon nanosheets preparation derived from the cheap natural biomass, which can be the effective cathode catalyst for environmental-friendly Li-CO₂/O₂ battery. Full article

Exploring high-efficiency, low-cost, and long-life bifunctional self-supporting electrocatalysts is of great significance for the practical application of advanced rechargeable Zn-air batteries (ZABs), especially flexible solid-state ZABs. Herein, ultrathin CoFe-layered double hydroxide (CoFe-LDH) nanosheets are strongly coupled on the surface of leaf-like bimetallic metal-organic frameworks (MOFs)-derived hybrid carbon (Co@NC) nanoflake nanoarrays supported by carbon cloth (CC) via a facile and scalable method for rechargeable and flexible ZABs. This interfacial engineering for CoFe-LDHs on Co@NC improves the electronic conductivity of CoFe-LDH nanosheets as well as achieves the balance of oxygen evolution reduction (OER) and oxygen reduction reaction (ORR) activity. The unique three-dimensional (3D) open interconnected hierarchical structure facilitates the transport of substances during the electrochemical process while ensuring adequate exposure of OER/ORR active centers. When applied as an additive-free air cathode in rechargeable liquid ZABs, CC/Co@NC/CoFe-LDH-700 demonstrates high open-circuit potential of 1.47 V, maximum power density of 129.3 mW cm⁻², and satisfactory specific capacity of 710.7 mAh g⁻¹_Zn. Further, the flexible all-solid-state ZAB assembled by CC/Co@NC/CoFe-LDH-700 displays gratifying mechanical flexibility and stable cycling performance over 40 h. More significantly, the series-connected flexible ZAB is further verified as a chain power supply for LED strips and performs well throughout the bending process, showing great application prospects in portable and wearable electronics. This work sheds new light on the design of high-performance self-supporting non-precious metal bifunctional electrocatalysts for OER/ORR and air cathodes for rechargeable ZABs. Full article