Search Results (151)

In this work, a strategy for synergistic regulation of the Ti₃C₂T_x surface structure and redox activity of the electrolyte has been proposed. The surface modification of MXene was achieved via KOH treatment. Meanwhile, to cooperate with the surface-modified MXene electrode materials, Fe³⁺/Fe²⁺ was introduced into its common H₂SO₄ electrolyte to operate as a redox-active electrolyte for the first time. The results indicate that alkali treatment not only effectively reduces the amount of fluorine-terminal groups on the MXene surface but also forms in situ TiO₂ nanowires on its surface, thereby forming a unique hierarchical structure for facilitating the electrochemical reaction. Further utilization of the Fe²⁺/Fe³⁺ redox-active electrolyte introduced additional pseudocapacitive reactions at the electrode/electrolyte interface, significantly enhancing the capacitive performance of the system. This synergistic effect of both the hierarchical 1D TiO₂/MXene composite electrode materials and the redox-active electrolyte resulted in a substantial increase in specific capacitance from 78.17 F g⁻¹ to 655.54 F g⁻¹ at a current density of 10 Ag⁻¹. The reaction kinetics of the electrochemical systems were studied, along with their energy storage mechanism. It is revealed that there is a transition of the energy storage mechanism from being dominated almost solely by diffusion control to collaborative diffusion and surface reactions in the synergistic electrode/electrolyte system, and the corresponding equivalent circuit has evolved from the single-interface model to a dual-interface model. This work has demonstrated that the proposed synergistic strategy can effectively enhance the capacitive performance of the MXene energy storage system and can be applied to other electrochemical systems. Full article

To improve the durability of terahertz (THz) electromagnetic shielding materials in atomic oxygen environments relevant to low Earth orbit (LEO), two MXene/para-aramid nanofiber (ANF) composite architectures were designed, including a uniformly blended structure and a sandwich configuration. Ti₃C₂T_x MXene was used as the conductive phase, while ANF served as a protective matrix. Oxygen plasma treatment was employed to simulate atomic oxygen exposure. The results show that the plasma resistance of blended films strongly depends on MXene content. Increasing the MXene fraction enhances conductive network redundancy and reduces conductivity degradation. In contrast, the sandwich-structured film exhibits superior structural stability. The outer ANF layers effectively limit direct plasma–MXene interaction and undergo surface carbonization during plasma exposure, forming an additional diffusion barrier. As a result, the sandwich film maintains stable THz shielding performance, with the average shielding effectiveness increasing from 42.6 dB to 44.9 dB after plasma treatment. These results indicate that structural regulation of the internal conductive network, which limits plasma penetration, is essential for maintaining stable MXene-based THz shielding performance under oxidative plasma conditions. Full article

The key transformation of 2D Ti₃C₂ MXene nanosheets into 0D Ti₃C₂ MXene quantum dots (Ti₃C₂ QDs) restructures the landscape of surface-active sites and tunable band gaps, enabling visiblelight-driven photocatalytic activity. Interestingly, the evolution of these fascinating Ti₃C₂ QDs retains ordered structural characteristics like the parent 2D Ti₃C₂ MXene nanosheets with controlled surface chemistry even after the facile hydrothermal process. In particular, evidence of tailoring of Ti₃C₂ QDs smaller than 10 nm reinforces the charge carrier separation and suppresses recombination under the strong association of quantum confinement and edge effects. Thus, the physical effects of Ti₃C₂ QDs effectively control the limitations of semiconductors, such as charge carrier recombination, slow charge carrier separation, and transportation in the resultant photocatalyst, for the implementation of promising toxic matter degradation and clean H₂ production. Special considerations are given to the regulation of charge carrier generation and separation for stable photocatalytic performance, such as appropriate band gap formation, localized surface plasmonic behavior, and Schottky barrier formation at the semiconductor interface. Specifically, pure Ti₃C₂ QDs with a size smaller than 10 nm exhibit a band gap of 2.16 eV, which has been found to be a powerful way to enable semiconductor-like photoresponse behavior. Overall, the above features make Ti₃C₂ QDs the preferred choice for facilitating effective charge carrier dynamics for the optimization of chemical stability in optoelectronic applications. The paper concludes with challenges and future perspectives to guide the 0D Ti₃C₂ QDs practical applicability in light-driven and sustainable environmental applications. Full article

To overcome the inherent limitations of 2D MXenes in photocatalysis, namely severe nanosheet restacking and rapid charge recombination, this study reports a synergistic dual-modification strategy. By integrating microwave-assisted in situ growth of carbon nanotubes (CNTs) with the hydrothermal incorporation of multivalent cobalt (Co) species, a 3D hierarchical Co-Ti₃C₂/CNT composite was successfully fabricated. Structural characterization reveals that the in situ grown CNTs act as robust spatial spacers and conductive highways, effectively preventing Ti₃C₂ agglomeration while providing a continuous electron-transfer network. The introduction of Co significantly enriches the surface with redox-active sites and facilitates the formation of an interfacial Schottky junction. Under visible-light irradiation, the optimized Co_10%-Ti₃C₂/CNT composite achieved a superior methylene blue degradation efficiency of 90.3% within 120 min. Mechanistic insights, supported by EPR and electrochemical analyses, confirm that the Schottky barrier at the semiconductor-metal interface acts as a potent electron trap, significantly suppressing e⁻/h⁺ recombination and accelerating surface-mediated radical generation (•OH, •O₂⁻). This work provides a sophisticated template for designing high-performance, dimensionally stable MXene-based heterostructures for advanced environmental remediation. Full article

This study explores the influence of MXene solution as an interfacial liquid on the output performance of a Cu/n-Si-based direct current triboelectric nanogenerator (DC-TENG) system. The ${\mathrm{Ti}}_3{\mathrm{AlC}}_2$ MAX phase was successfully transformed into ${\mathrm{Ti}}_3{\mathrm{C}}_2{\mathrm{T}}_{\mathrm{x}}$ MXene through selective etching and was confirmed by scanning electron microscopy with energy-dispersive spectroscopy (SEM/EDS) and X-ray diffraction (XRD) analyses, which revealed an increase in d-spacing from 8.99 to 9.58 Å and a transition from dense layered grains to delaminated, sheet-like structures. Electrochemical impedance spectroscopy (EIS) demonstrated a pronounced reduction in impedance with the introduction of MXene solution, indicating enhanced interfacial conductivity and charge transfer capability. The presence of MXene in deionized (DI) water led to the formation of an electrical double layer (EDL) at the Cu/n-Si interface, contributing to additional interfacial capacitance and more efficient charge relaxation dynamics. As a result, the DC-TENG output was significantly enhanced with the incorporation of MXene into the system, exhibiting a markedly higher current compared to the dry contact condition. Moreover, the MXene solution helped suppress charge decay compared to dry interfaces, highlighting its role as an effective liquid medium for stabilizing surface charge and improving interfacial electron transport in DC-TENG systems. Full article

MXenes, with a high surface area, abundant active sites, and excellent ion transport properties, have demonstrated excellent electrochemical performance. However, systematic comparisons of the structural evolution process and electrochemical performance for MXene are lacking. In this study, multilayer MXene (M-Ti₃C₂T_x) was successfully fabricated by in situ etching. During the subsequent centrifugation process, the thicker and heavier multilayer sheets settled due to their faster sedimentation rate, while the lighter, surface-functionalized monolayer sheets remained colloidally stable in the supernatant due to solvation and electrostatic repulsion, thereby achieving separation and obtaining delaminated MXene (D-Ti₃C₂T_x). Structural analysis indicates that the removal of the aluminum layer synergizes with the exfoliation of the nanosheets, significantly increasing the interlayer spacing and making the sheet structure more pronounced, and the pore structure is more abundant. Especially, in three-electrode and two-electrode systems at an identical mass loading of 5 mg on carbon paper, D-Ti₃C₂T_x delivered a higher specific capacitance, more pronounced pseudocapacitive behavior, and a superior rate capability compared to Ti₃AlC₂ and M-Ti₃C₂T_x. Such excellent electrochemical performance of D-Ti₃C₂T_x is due to the shortened ion diffusion path in the delaminated structure, which enables rapid ion migration, an extremely large specific surface area, and a mesoporous structure that provides abundant active sites. This study underscores the significant potential of D-Ti₃C₂T_x in emerging energy storage systems and offers insights into guiding MAX phase synthesis during its preparation. Full article

This study uses a bismuth ferrite (BiFeO₃) and MXene (Ti₃C₂Tx) to design a surface plasmon resonance (SPR) biosensor for the sensitivity enhancement at a 633 nm wavelength. Here, MXene serves as a biorecognition element (BRE) layer to ensure stable and reliable biomolecule adsorption. The MXene is a family of two-dimensional (2D) materials with metallic-like conductivity, a large surface area that can attach biomolecules, and improve biocompatibility. The addition of a conductive 2D MXene layer and a high-index BiFeO₃ dielectric layer greatly improves light–matter interaction and evanescent field penetration at the sensing interface. Strong plasmonic coupling is indicated by the reflectance analysis, which shows a distinct and consistent shift in the resonance angle as analyte RI increases. This study examined the sensitivity at optimized Ag and BiFeO₃ layer thickness. At an Ag of 39 nm and BiFeO₃ of 3 nm thickness, the maximal sensitivity of 340.68°/RIU with a remarkable figure of merit (FoM) of 47.38/RIU is obtained. The overall detection accuracy (DA) and FoM are significantly improved by the large sensitivity enhancement, despite a slight increase in full width at half maximum (FWHM). Furthermore, the penetration depth (PD) of 198.50 nm (at RI:1.330) and 199.52 nm (at RI:1.335) is attained with the proposed structure. Due to its high sensitivity, reusability, and reproducibility, the SPR biosensor has the potential to be used in biochemical, environmental, and medical detection. Full article

Two-dimensional (2D) materials exhibit electronic and collective excitation properties that are highly sensitive to surface chemistry and thickness, requiring surface-sensitive characterization at low electron energies. Here, we investigate graphene, hexagonal boron nitride (h-BN), molybdenum disulfide (MoS₂), and titanium carbide (Ti₃C₂) MXene using an advanced home-built scanning low-energy electron microscopy system combined with time-of-flight electron spectroscopy (SLEEM/ToF). The system uniquely records electron energy-loss spectra (EELS) from transmitted electrons rather than from the reflected electrons used in conventional SLEEM. Compared with high-energy EELS, our low-energy ToF-EELS approach offers enhanced surface sensitivity and reduced beam-induced damage, enabling direct probing of π and π + σ plasmon excitations. Additionally, complementary techniques, including scanning transmission electron microscopy (STEM), Raman spectroscopy, and X-ray photoelectron spectroscopy (XPS), were employed to characterize structural and chemical properties. EELS were acquired for all investigated 2D materials at electron landing energies of 500–1500 eV, and in the 5–50 eV range for selected materials, including graphene and MoS₂. Analysis of these spectra enabled determination of the average plasmon positions across the measured energy range for all studied materials. Furthermore, a quantitative determination of the inelastic mean free path (IMFP) was achieved for graphene in the 10–50 eV range, yielding a value of 1.9 ± 0.2 nm. These results demonstrate the potential of SLEEM–ToF for surface-sensitive analysis of 2D materials. Full article

Two-dimensional Ti₃C₂O₂ MXene has emerged as a promising electrode material for non-enzymatic glucose sensing due to its metallic conductivity and biocompatibility. However, the atomic-scale sensing mechanism remains unclear. This DFT study uses the PBE functional with the D3(BJ) dispersion correction to elucidate glucose–MXene interactions under idealized vacuum conditions. Pristine Ti₃C₂O₂ shows metallic behavior with a density of states of about 8.2 states per electron volt at the Fermi level, dominated by Ti 3d states. β-d-glucose adsorbs onto the surface through hydrogen bonding, with an adsorption energy of −0.82 eV at a separation distance of 2.8 angstroms. Bader analysis indicates a transfer of about 0.15 electrons from MXene to glucose, resulting in a Fermi level shift of about −0.15 eV and an 18% reduction in the density of states at the Fermi level. These changes correspond to an estimated sensitivity of approximately 0.6 μA mM⁻¹ cm⁻² and a detection limit of about 17 µM, consistent with reported experimental performance of MXene-based sensors. Comparative adsorption calculations for common sweat interferents yield −0.45 eV for lactate and −0.25 eV for urea, indicating weaker interfacial affinity than glucose; these values reflect thermodynamic binding strength and possible surface occupation rather than definitive electrochemical selectivity, which additionally depends on redox potential, electron-transfer kinetics, and operating bias. We acknowledge three main limitations: first, the model considers only pure oxygen termination rather than mixed oxygen, hydroxyl, and fluorine terminations; second, the calculations are performed under vacuum rather than in aqueous conditions; third, the study is based on static zero kelvin structures rather than finite temperature dynamics. Despite these idealizations, the results provide baseline mechanistic insights to support rational design of MXene-based glucose sensors. 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

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

The application of MXene–polymer composites to wearable and implantable medical devices requires the development of hydrophilic and biocompatible MXene–polymer hydrogel composites with high electromechanical response, flexibility, and durability. Here, we formulate low weight percentage MXene–hydrogel copolymer inks enabling the direct light processing (DLP) of Ti₃C₂T_x MXene–polyvinyl alcohol (PVA)–polyacrylic acid (PAA)–hydrogel composites. The low wt% MXene–PVA–PAA composites demonstrate high biocompatibility, mechanical flexibility, high sensitivity and high precision for sensing acute bending angles. The sub-millidegree angle resolution of these electromechanical sensors demonstrates their suitability for applications such as the highly precise tracking of joint movements. In addition, the synthesized MXene membranes show promise for applications in osmotic energy conversion, with a harvested electric power density of 6.79 Wm⁻². Full article

To address the bottleneck of insufficient broadband sound insulation performance of traditional sound insulation materials at the subwavelength scale, this paper designs a composite subwavelength sound insulation unit (size: 20 mm × 20 mm × 5 mm) composed of Ti₃C₂T_x MXene, and PZT-5H piezoelectric ceramics, and porous aluminum alloy. Based on the electromagnetic-structural-acoustic multi-physics field coupling theory, the regulation laws of external electric field intensity and effect of MXene layer number on sound insulation performance are systematically investigated via numerical simulation, and the sound insulation enhancement mechanism dominated by dielectric tunability is clarified. The results show that the dielectric constant of MXene increases monotonically with the external electric field intensity, and the optimal regulation sensitivity is achieved when the layer number N = 3; when the electric field intensity increases from 0 V to 500 V, the equivalent density of the system increases from 1.25 g/cm³ to 1.87 g/cm³, the acoustic impedance increases from 3.42 × 10⁶ Pa·s/m³ to 5.13 × 10⁶ Pa·s/m³, the average transmission loss TL in the 200–600 Hz frequency band is increased by 2 dB compared with the state without electric field, and the sound pressure on the transmission side is reduced by 3.56% at 400 Hz; the vibration displacement of PZT decreases from 0.0055 mm to nearly 0 mm with the increase in electric field, and the electric field energy density increases from 0 J/m³ to 7.47056 × 10³ J/m³, verifying the core mechanism of converting electromagnetic energy into structural damping through dielectric loss. This study supplements parameter sensitivity analysis and literature benchmark comparison to compensate for the lack of experimental data, confirming the stability and rationality of the simulation results. The established cross-field coupling framework of “dielectric regulation–density optimization–impedance matching–sound insulation enhancement” fills the theoretical gap of the coupling mechanism of MXene in the field of subwavelength sound insulation, and provides new theoretical and technical pathways for the design of broadband active sound insulation materials in the 200–1000 Hz frequency range. Full article

The global decarbonisation strategy has accelerated the shift toward renewable energy and electric transport, demanding advanced electrochemical energy storage systems. Conventional anodes such as graphite and silicon composites face challenges in conductivity, stability and cycling performance. MXenes, a class of two-dimensional (2D) materials, offer promising alternatives owing to their metallic conductivity, tunable surface chemistry and high theoretical capacity. Here, we synthesise and characterise Mo₂TiC₂T_x and V₂CT_x (T = O, OH, F and/or Cl) MXenes for lithium-ion battery anodes and supercapacitors. Unlike Ti₃C₂T_x, which stores charge via intercalation and surface redox reactions, Mo₂TiC₂T_x and V₂CT_x exhibit conversion-type mechanisms. We also identify novel V₂C–VO_x heterostructures, achieving a specific capacitance of 532.4 F g⁻¹ at 2 mV s⁻¹ and an initial capacity of 493.3 mAh g⁻¹ at 50 mA g⁻¹ in lithium half-cells, with a low decay rate of 0.071% per cycle over 200 cycles. Pristine Mo₂TiC₂T_x shows 391.7 mAh g⁻¹ at 50 mA g⁻¹, decaying by 0.109% per cycle. These results experimentally validate theoretical predictions, revealing how MXene structure and transition metal chemistry govern electrochemical behaviour, thus guiding electrode design for next-generation batteries and supercapacitors. Full article

Lithium–sulfur (Li-S) batteries are renowned for their high theoretical energy density and low cost, yet their practical implementation is hampered by the polysulfide shuttle effect and sluggish redox kinetics. Herein, a sol–gel strategy is proposed to engineer a multifunctional MXene/Fe₃O₄ composite as an efficient mediator for the cathode interlayer. The synthesized composite features Fe₃O₄ nanospheres uniformly anchored on the highly conductive Ti₃C₂T_x MXene lamellae, forming a unique 0D/2D conductive network. This structure not only provides abundant polar sites for strong chemical adsorption of polysulfides but also significantly enhances charge transfer, thereby accelerating the conversion kinetics. As a result, the Li-S battery based on the MXene/Fe₃O₄ interlayer delivers a high initial discharge capacity of 1367.1 mAh g⁻¹ at 0.2 C and maintains a stable capacity of 1103.4 mAh g⁻¹ after 100 cycles, demonstrating an exceptionally low capacity decay rate of only 0.19% per cycle. Even at a high rate of 1 C, a remarkable capacity of 1066.1 mAh g⁻¹ is retained. Electrochemical analyses confirm the dual role of the composite in effectively suppressing the shuttle effect and catalyzing the polysulfide conversion. This sol–gel engineering approach offers valuable insight into the design of high-performance mediators for advanced Li-S batteries. Full article