Search Results (918)

A warm-up is a critical procedure in sports science for enhancing muscular performance and optimizing subsequent athletic activities. However, the physiological and athletic performance effects of a warm-up are often transient, diminishing rapidly during the period of inactivity after the warm-up, which is known as the warm-up transition phase. In this study, a multi-functional thermoregulation wearable composite film of graphene–MXene–bacterial cellulose/polyethylene glycol (G-M-BC/PEG) was developed by integrating MXene (a two-dimensional material with good photothermal conversion performance) and graphene into a bacterial cellulose aerogel framework, subsequently impregnated with polyethylene glycol (PEG-2000). The film showed stable structure, efficient solar photothermal conversion and storage (SPCS), and improved mechanical properties. Under 1 sun irradiation, the optimized G-M-BC/PEG wearable film showed excellent SPCS performance, sustaining a temperature plateau of 38–40 °C for 10 min after the xenon lamp was switched off under 1 sun irradiation, with a leakage rate of only 5.32% after five cycles. By constructing a biomimetic sports human body model, the composite aerogel was shown to significantly elevate muscle surface temperature and effectively mitigate heat loss during the transition phase. In the warm-up effectiveness and sports performance tests, the wearable film improved 200 m sprint performance by 0.8% ± 0.4% (p = 0.039). It also maintained subjective thermal sensation during the warm-up transition phase, with no significant decline at 5 or 10 min after the warm-up and a significant decrease only at 15 min (p = 0.02), while thermal comfort remained stable, suggesting improved neuromuscular readiness. This research provided a novel strategy for the fabrication of advanced aerogel-based wearable devices aimed at precision thermal management and athletic performance optimization. Full article

MXene, as a suitable and alternative 2D nanofiller incorporated into a proton exchange membrane (PEM), has recently received considerable attention because of desired mechanical stability, promising conductivity, and active surface functional groups. However, agglomeration or sedimentation in PEMs, as well as the water retention capacity under low humidity of MXene, are limiting factors in the field of PEMs. In this paper, modified MXene and TiO₂ nanoparticles used as functional nanofillers were incorporated into sulfonated poly (ether ether ketone) (SPEEK) to prepare novel SPEEK-based composite PEMs. The effects of the nanofiller contents on self-humidifying and protonic conductivity of the composite PEMs were also investigated under different temperatures. When the contents of functionalized MXene and modified TiO₂ are 5 wt.%, proton conductivity, water uptake and methanol permeability of the composite PEMs can be up to 0.143 S/cm, 60% and 2.27 × 10⁻⁷ cm²/s, respectively, which represent increases of about 192%, about 38% and a decrease of 47%, respectively, compared with that of primary SPEEK PEM. Under the synergistic action of functionalized MXene providing a higher number of exchangeable proton sites, modified TiO₂ with inherent hydrophilicity enhancing water retention and Pt providing catalytic sites for the H₂/O₂ reaction to generate water in situ, the self-humidifying capability and proton conductivity of the composite PEMs were improved significantly. Full article

As a prospective two-dimensional conductive filler, titanium carbide (MXene) can remarkably boost the dielectric constant (ε) of polymer composites at low loadings. Nevertheless, the accompanied large dielectric loss (tan δ) and leakage current greatly limit their practical applications in dielectric-related fields. To tackle this dilemma, an organic polydopamine (PDA) shell was coated on an MXene surface via a self-polymerization method, and the dielectric properties of PDA-modified MXene/poly(vinylidene fluoride) (PVDF) were explored. The findings show that, in comparison to unmodified MXene/PVDF, MXene@PDA/PVDF retains a high ε and improved breakdown strength (E_b). It further realizes a notable decrease in both tan δ and electrical conductivity. The introduced PDA interlayer serves to effectively separate adjacent MXene nanosheets, which inhibits the development of conductive paths and introduces charge traps to restrict carrier migration, thus reducing tan δ. Further, the interlayer not only improves the interfacial compatibility, but also mitigates strong dielectric mismatch between MXene and PVDF, which facilitates the homogeneous redistribution of the local electric field, contributing to enhanced E_b. Theoretical fitting and simulation studies unlock the profound polarization mechanisms and charge migration modulated by the PDA interlayer. The resulting Mxene@PDA/PVDF exhibits concurrently elevated ε (35.68) and enhanced E_b (12.94 kV/mm), as well as low tan δ (0.34) at 10³ Hz and 7 wt% filler loading, which is not achievable in neat MXene/PVDF. This work demonstrates that core–shell interfacial engineering offers an effective strategy for designing flexible polymer dielectrics with superior dielectric performances, showcasing potential applications in energy storage, advanced power systems and flexible electronics. Full article

Owing to its high theoretical sodium-storage capacity of approximately 1000 mAh g⁻¹ and cost-efficient characteristics, Fe₂VO₄ has emerged as a highly attractive anode material for sodium-ion batteries (SIBs). In this work, MXene-incorporated Fe₂VO₄ composites were successfully synthesized. Comprehensive electrochemical characterization demonstrates that MXene incorporation significantly enhances the electronic conductivity and sodium-ion diffusion kinetics of Fe₂VO₄, while effectively mitigating volume expansion during cycling. The synthetic substantially improves its cycling stability and rate capability. When the MXene loading ratio is optimized at 5 wt%, the composite exhibits outstanding cyclic durability, with a remarkable reversible specific capacity of 323.3 mAh g⁻¹ maintained after 200 cycles at a current density of 0.1 A g⁻¹. Furthermore, the composite demonstrates outstanding rate performance, with a specific capacity of 164.5 mAh g⁻¹ achieved at a current density of 2 A g⁻¹. The synergistic integration of Fe₂VO₄ and MXene not only constructs a three-dimensional electrically conductive framework for efficient charge transport but also reinforces strong structural stability against cycling-induced degradation. This work proposes a versatile engineering strategy that can be adapted for other conversion-type electrode materials in the context of advanced energy storage technologies. Full article

Aqueous supercapacitors are a class of crucial high-power, long-life, safe and reliable energy storage devices, with their performance fundamentally dependent on electrode materials. Two-dimensional (2D) vanadium-based MXenes, possessing rich multivalent redox activity and tunable layered structures, have emerged as one of highly promising electrode candidates, exhibiting significantly superior specific capacitance and pseudocapacitive properties compared to conventional Ti₃C₂T_z. To overcome inherent limitations in conductivity and structural stability, this review summarizes strategies for regulating composition and microstructure through transition metal solid solution and medium-/high-entropy design. These approaches synergistically optimize electron conduction, expand ion migration pathways, and suppress electrode degradation, thereby comprehensively enhancing rate performance, cycle life, and energy density. This review systematically reveals the composition–structure–performance relationships, providing critical design insights and theoretical foundations for developing next-generation high-performance, long-life aqueous MXene-based supercapacitors. Full article

Two-dimensional (2D) materials, particularly MXenes and transition metal dichalcogenides (TMDs), have attracted intense interest as supercapacitor electrodes due to their high surface area and tunable electronic structure. However, large discrepancies persist between the quantum capacitance values predicted by density functional theory (DFT) calculations and experimentally measured gravimetric capacitances. In this review, we critically analyze DFT methodologies, surface models, normalization strategies, and electrochemical characterization protocols, and compile an extensive dataset of reported MXene and TMD systems to quantify the degree of experimental–theoretical agreement. We show that MXenes typically achieve less than 20% of their predicted capacitance because of restacking, surface terminations, and limited ion accessibility, whereas TMDs exhibit substantially better correspondence, often approaching or exceeding 70% of theoretical values. These results indicate that the theoretical capacitance predicted by DFT is primarily determined by the electronic structure of the material, which defines the upper limit of charge storage, whereas the experimentally achieved capacitance is largely controlled by morphological factors, surface chemistry, and electrode architecture that limit ion accessibility. Full article

Catalytic materials are central to the advancement of hydrogen generation technologies, playing a pivotal role in enabling sustainable, carbon-neutral energy systems. Hydrogen can be produced via electrochemical water splitting, thermochemical reforming, or photocatalysis—each imposing unique performance requirements on catalysts in terms of activity, selectivity, stability, and efficiency. While traditional noble metals (e.g., platinum, ruthenium, iridium) provide benchmark catalytic activity, their widespread use is hindered by scarcity, high cost, and limited long-term durability. Consequently, researchers have increasingly focused on earth-abundant alternatives such as transition metals (Ni, Co, Fe, Mo), alloys, metal oxides, carbides, sulfides, nitrides, and carbon-based systems. Among these, two-dimensional materials, particularly the MXene family, have attracted significant attention due to their metallic conductivity, layered structure, and tunable surface chemistry. These features enable rapid charge transfer and abundant active sites, making MXenes and related nanostructured catalysts promising for both the Hydrogen Evolution Reaction (HER) and Oxygen Evolution Reaction (OER) across a wide range of electrochemical conditions. Parallel efforts have integrated novel semiconductors, plasmonic nanomaterials, and hybrid heterostructures to improve the efficiency of solar-to-hydrogen energy conversion. This paper reviews the main types of catalytic materials used in hydrogen production, explains their design strategies and structure–performance relationships, and discusses key engineering challenges such as integrating renewable energy sources, scaling up manufacturing, and ensuring long-term durability in real-world systems. Future research goals are also highlighted, including the development of affordable non-noble catalysts, enhancing catalyst stability through surface and defect engineering, and coupling hydrogen production with circular economy principles, all of which are essential to making hydrogen generation more efficient, scalable, and cost-effective as the world transitions to clean and sustainable energy. Full article

The global population explosion and accelerated industrialization have led to an increasing shortage of fossil fuels and environmental contamination, underscoring the urgent need to develop innovative energy storage technologies to improve energy utilization efficiency. As pivotal components in thermal energy storage (TES) systems, phase change materials (PCMs) enable spatiotemporal matching between thermal energy supply and demand through latent heat absorption and release during phase transitions. Organic PCMs are considered ideal candidates for thermal energy storage due to their high energy storage density, stable phase transition temperature, low supercooling, and negligible phase separation. However, inherent drawbacks such as low thermal conductivity, liquid leakage, limited light absorption, and lack of functionality have hindered their widespread application in advanced thermal management systems. Herein, we systematically summarize cutting-edge functionalization strategies for PCMs, progressing from conventional methods like thermal conductive particle blending and microencapsulation to the emerging design of 3D porous thermally conductive skeletons, including metal foams, boron nitride aerogels, carbon-based aerogels, and MXene aerogels. These frameworks not only enhance thermal transport via continuous conductive pathways and impart shape stability through capillary encapsulation but also, when integrated with photo-thermal, electro-thermal, and magneto-thermal conversion properties, enable broad applications in solar photo-thermal/photo-thermo-electric conversion, thermal management of electronics and batteries, building efficiency, and wearable thermal regulation. The review further addresses current challenges and future directions, highlighting scalable 3D framework fabrication, the shift to active thermal management, and innovative applications beyond conventional domains. By establishing a microstructure–property–application correlation, this work provides valuable insights for developing next-generation high-performance multifunctional phase change composites. Full article

In this study, the structural and electrochemical performance of Nb₂CT_x MXene-based composite electrodes modified with activated carbon (AC) derived from food waste was systematically investigated for supercapacitor applications. Three composites with Nb₂CT_x:AC mass ratios of 90:10 (MXAC1), 80:20 (MXAC2), and 70:30 (MXAC3) were prepared and comparatively evaluated. SEM/EDS, XRD, HR-TEM, XPS, and BET analyses revealed that, in the MXAC2 composite, activated carbon was homogeneously distributed between the MXene layers, effectively suppressing restacking and promoting the formation of a hierarchical micro/mesoporous structure. XPS results confirmed the preservation of the Nb–C framework and the enrichment of surface functional groups (–O, –OH, and –F). BET analysis demonstrated that MXAC2 possesses an optimized pore architecture that facilitates efficient ion diffusion. Electrochemical measurements revealed that the MXAC2 electrode exhibited the highest specific capacitance at all scan rates and current densities. At 5 mV·s⁻¹, MXAC2 achieved a specific capacitance of 651.84 F·g⁻¹ and maintained a substantial capacitance even at a high current density of 4 A·g⁻¹. EIS analysis confirmed the very low charge transfer resistance (0.023 Ω) and enhanced capacitive behavior for MXAC2. Additionally, MXAC2 has high cycle stability, demonstrating 82.15% capacitive retention and 92.45% coulombic efficiency after 10000 cycles. These results indicate that food waste-derived AC-optimized Nb₂CT_x MXene composite materials are a strong candidate for sustainable and high-performance supercapacitor electrodes. Full article

MXene-based microwave absorbers have received extensive attention owing to their high electrical conductivity, abundant interfacial polarization sites, and tunable surface terminations. However, the structure–property relationship of MXene composites remains highly nonlinear, and the design of high-efficiency absorbers still relies heavily on trial-and-error experiments. Herein, multidimensional magnetic components, including zero-dimensional (0D) Fe₃O₄ nanoparticles, one-dimensional (1D) Fe₃O₄/Co₃O₄ nanowires, and two-dimensional (2D) Fe₃O₄-based heterostructures, were rationally integrated with Fe/MXene and Fe/Co/MXene nanosheets to engineer synergistic dielectric and magnetic losses. Comprehensive electromagnetic characterization and loss mechanism analysis reveal that the structural dimensionality strongly impacts impedance matching and attenuation capability. To further enable predictive and data-driven optimization, a machine learning framework was established to correlate the microstructure, component ratio, thickness, and electromagnetic parameters with the microwave absorption performance (e.g., minimum reflection loss (RL_min), effective absorption bandwidth (EAB)). The optimized multidimensional composite achieves an RL_min of −56.4 dB at 10.2 GHz with an EAB of 8.4 GHz (9.6–18.0 GHz) at a thin matching thickness of 1.8 mm. The machine learning model demonstrates excellent accuracy (R² = 0.947) and enables the inverse design of absorber geometries to target specific operational frequencies. This work provides a generalizable paradigm for the intelligent design of MXene-based microwave absorbers and opens up broader opportunities for the AI-accelerated discovery of advanced electromagnetic functional materials. Full article

Poly(vinyl alcohol) (PVA)/montmorillonite (MMT)/Ti₃C₂T_x (MXene) nanocomposite membranes (PVA/MMT/MXene) were developed and evaluated in terms of their mechanical properties, mesoporosity, and adsorption performance toward Pb²⁺ ions and methylene blue (MB). The incorporation of MMT and MXene resulted in a strong synergistic reinforcement, increasing the ultimate tensile strength from 10 to 20 MPa, the Young’s modulus from 14.7 to 29.5 MPa, and reducing the swelling ratio from 2.0 to 1.1 g·g⁻¹. BJH porosimetry revealed a refined and interconnected mesoporous structure, with the cumulative pore volume increasing from 0.134 to 0.448 cm³·g⁻¹. In adsorption experiments (mono-solute systems, 25 °C), the ternary membrane achieved high uptake capacities of 55 mg·g⁻¹ for Pb²⁺ and 80 mg·g⁻¹ for MB, outperforming binary PVA/MMT and neat PVA. Statistical–physics modeling provided microscopic descriptors consistent with the experimental isotherms: Pb²⁺ adsorption follows a monolayer regime (n ≈ 1), whereas MB exhibits multilayer behavior (n > 1) with a higher site density (Nm ≈ 1.6 mmol·g⁻¹). These results demonstrate that the hybrid 2D–2D architecture of MMT and MXene significantly enhances the structural robustness, pore accessibility, and adsorption efficiency of PVA-based membranes, highlighting their potential for efficient removal of metal ions and dyes from aqueous media. Full article

MXenes are high-performance pseudocapacitive materials known for their excellent conductivity, large surface area and fast redox reactions occurring at the surface. Despite these advantages, their practical application is hindered by the tendency of MXene nanosheets to aggregate and restack, which significantly compromises cycling stability. In this work, post-delamination metal-ion intercalation was employed to successfully expand the interlayer spacing of Ti₃C₂ while simultaneously optimizing its surface functional groups. Benefiting from the enlarged interlayer spacing and improved surface chemistry, the Mn-intercalated MXene (Mn–MXene) delivers a high specific capacitance of 285 F g⁻¹ at a scan rate of 10 mV s⁻¹ in 1 M H₂SO₄ electrolyte, which represents a 26% enhancement compared with pristine Ti₃C₂. Notably, Mn–MXene exhibits nearly 100% capacitance retention after 3000 cycles. Full article

The future growth of alkali metal-based batteries requires an understanding of how ion size affects the exchange mechanisms. In this work, we present a direct, comparative electrochemical study of MXene-based electrodes mechanism vs. lithium (Li⁺), sodium (Na⁺), and potassium (K⁺) ions using the same electrochemical conditions. This controlled method enables an extensive investigation of the size-dependent interactions between the MXene structure and alkali metal ions. X-ray photoelectron spectroscopy and Raman analysis of TMAOH-treated Ti₃C₂T_x MXene electrodes show that delamination and cycling alter vibrational modes and the surface chemistry. Voltage profile study reveals diverse storage behaviors: Li⁺ has a prominent intercalation plateau, Na⁺ shows intermediate properties, and K⁺ displays sloping profiles, indicating surface-dominated adsorption. The significant correlation between ionic radius and electrochemical reversibility is shown by long-term cycling data over 300 cycles, which show greater capacity retention and stability for Li⁺ and progressively lower performance for Na⁺ and K⁺. These findings provide new mechanistic insights into MXene–ion interactions and build the foundation for developing MXene-based materials for specific alkali-ion chemistries in next-generation energy storage devices. Full article

Magnetic metals are of considerable importance for stealth technology and electromagnetic pollution control. However, they suffer from inherent limitations, such as the Snoek limit and narrow absorption bandwidth, which restrict their applications in complex scenarios. To address these challenges, this review systematically summarizes the recent advances of magnetic metal-based microwave-absorbing materials (MAMs), focusing on four core directions: alloy design, composite engineering, structural regulation, and preparation technology. The intensity and frequency bands of absorption in alloys are dictated by the material’s composition as well as its structural attributes. Moreover, composite systems incorporating carbon materials, MXenes, oxides, ceramics, and conductive polymers are discussed, where the synergistic design of components optimizes impedance matching and loss mechanisms. Key structural design strategies include core-shell structures, interface engineering, self-assembled hierarchical structures, and macroscopic structural design. These structures achieve the synergistic improvement of thin, lightweight, broadband, and strong absorption performance by enhancing interface polarization, multiple scattering, and resonance effects, while endowing materials with excellent environmental stability. Notably, metamaterial-based designs can further achieve an ultrawide bandwidth spanning 0.3–18 GHz. Additionally, preparation processes are crucial for regulating the microstructure and activating loss mechanisms. This review aims to offer theoretical and practical insights for developing high-performance, multifunctional magnetic MAMs. Full article

In the post-Moore’s Law era, conventional Von Neumann architectures face critical limitations, such as the “memory wall” and excessive power consumption, particularly when processing unstructured data. Neuromorphic computing, inspired by the human brain, offers a promising solution through parallel processing and adaptive learning. Among the candidates for artificial synapses, memristors based on two-dimensional MXenes (specifically Ti₃C₂T_x) have attracted significant attention due to their unique layered structure, high metallic conductivity, and tunable physicochemical properties. This review provides a comprehensive analysis of MXene-based memristors, from material synthesis to system-level applications. We examine how different synthesis strategies, including etching methods, directly influence device performance and elucidate the underlying resistive switching mechanisms driven by ion migration, valence change, and interfacial processes. Furthermore, the review demonstrates the efficacy of MXenes in emulating biological synaptic functions—such as spike-timing-dependent plasticity (STDP) and long-term potentiation/depression (LTP/LTD)—and their application in tasks like handwritten digit recognition. Finally, we highlight emerging frontiers in flexible electronics and in-sensor computing, offering insights into the future trajectory of integrated sensing, memory, and computation. Full article