Constructing MXene-based mixed-dimensional structure with multiple interfaces to optimize dielectric-magnetic synergistic effect for effective electromagnetic wave absorption.

Exploring efficient microwave absorbing materials (MAMs) which could convert electromagnetic (EM) energy into thermal energy represents an approbatory vision to reducing EM radiation and interference. Designing of mixed-dimensional structure with multiple interfaces represents the available target to investigate an ideal MAMs, which maximizes the superiority of mixed-dimensional structure in electromagnetic wave absorption (EMWA). Herein, we take full advantage of multiple interfaces engineering of MXene for optimizing the impedance matching to improve EMWA, MXene-based mixed-dimensional structure was designed by incorporating three-dimensional Fe3C@Carbon layers coated zero-dimensional Fe3O4 nanoparticles (NPs) supported two-dimensional MXene nanosheets (MXene/Fe3O4@Fe3C@Carbon, MFC). The Fe3O4@Fe3C@C with Core@shell structure arrests the essentially self-restacked of MXene and provides various attenuation mechanisms for the incident electromagnetic waves (EMWs). By regulating the carbonization temperature, the MFC exhibits enhanced EMWA property which is attributed to the characteristic structure and optimized dielectric-magnetic synergy effect. The minimum reflection loss (RLmin) value of MFC can reach to -64.3 dB with a matching thickness of 1.73 mm. Otherwise, the maximum effective absorption bandwidth (EAB) (RLmin < -10 dB) reaches 6.42 GHz at only 1.5 mm. Thus, our study refers a novel-fire enlighten to develop excellent mixed-dimensional microwave absorbent based on MXene.

Efficient solar-driven: Photothermal catalytic reduction of atmospheric CO2 at the gas-solid interface by CuTCPP/MXene/TiO2.

Directly capturing atmospheric CO2 and converting it into valuable fuel through photothermal synergy is an effective way to mitigate the greenhouse effect. This study developed a gas-solid interface photothermal catalytic system for atmospheric CO2 reduction, utilizing the innovative photothermal catalyst (Cu porphyrin) CuTCPP/MXene/TiO2. The catalyst demonstrated a photothermal catalytic performance of 124 µmol·g-1·h-1 for CO and 106 µmol·g-1·h-1 for CH4, significantly outperforming individual components. Density functional theory (DFT) results indicate that the enhanced catalytic performance is attributed to the internal electric field between the components, which significantly enhances carrier utilization. The introduction of CuTCPP reduces free energy of the photothermal catalytic reaction. Additionally, the local surface plasmon resonance (LSPR) effect and high-speed electron transfer properties of MXene further boost the catalytic reaction rate. This well-designed catalyst and catalytic system offer a simple method for capturing atmospheric CO2 and converting it in-situ through photothermal catalysis.

Encapsulation of Se into Cu-decorated MXene nanosheets with superior electrochemical performance for advanced Na-Se batteries.

Sodium-selenium (Na-Se) batteries are promising energy storage systems with high energy density, high safety, and low cost. However, the huge volume change of selenium, the dissolution shuttle of polyselenides, and low selenium loading need to be solved. Herein, Cu nanoparticles decorated MXene nanosheets composite (MXene/Cu) are synthesized by etching Ti3AlC2 using a molten salt etching strategy. The Se-loaded MXene/Cu (Se@MXene/Cu) electrode delivers superior electrochemical performance even with a high Se loading of ∼74.3 wt%, owing to the synergistic effect of the two-dimensional (2D) confined structure and catalytic role of the unique MXene/Cu host. Specifically, the obtained electrode provides a reversible capacity of 587.3 mAh/g at 0.2 A/g, a discharge capacity as high as 511.3 mAh/g at a high rate of 50 A/g, and still maintains a capacity of 471.9 mAh/g even after 5000 cycles based on the mass of Se@MXene/Cu. With such excellent electrochemical kinetic properties, this study highlights the importance of designing various MXene-based composites with synergistic effects of 2D confined structure and Cu catalytic center for the development of high-performance alkali metal-chalcogen battery systems.

Interface engineering based NiCoMoO4/Ti3C2Tx MXene heterostructure for high-performance flexible supercapacitors.

The advancement of interface engineering has demonstrated remarkable efficacy in overcoming the primary impediment associated with sluggish reaction kinetics in supercapacitor electrodes. In this investigation, we employed a facile co-precipitation method to synthesize NiCoMoO4/MXene heterostructures utilizing Ti3C2Tx MXene nanosheets as carriers. This heterostructure inhibits the restacking of MXene nanosheets and simultaneously enhances the exposure of electrochemically active sites in NiCoMoO4 nanorods, thereby mitigating the reduction in specific capacitance resulting from volumetric fluctuations. The NiCoMoO4/MXene electrode, possessing pseudo-capacitance properties, demonstrates an impressive level of specific capacitance, exceptional performance across various charging rates, and consistent behavior throughout repeated cycles. By optimizing the mass ratio, this electrode achieves a specific capacity of 1900 F/g under a current density of 1 A/g. Even after enduring 10,000 cycles at a significantly higher current density of 5 A/g, it still maintains an impressive retention rate of 94.73 %. Our density functional theory (DFT) calculations indicate that the enhanced electrochemical performance can be attributed to the improved electronic coupling within the NiCoMoO4/MXene heterostructure. The integration of NiCoMoO4/MXene cathode and activated carbon (AC) anode with an alkaline gel electrolyte containing potassium ferricyanide in flexible quasi-solid-state supercapacitors (FSSCs) results in exceptional electrochemical performance and flexibility. These FSSCs demonstrate a maximum energy density of 72.89 Wh kg-1 at a power density of 850 W kg-1, while maintaining an impressive power output of 16,780 W kg-1 with an energy density of 37.28 Wh kg-1. Based on these outstanding properties, it is evident that the NiCoMoO4/MXene heterojunction possesses significant advantages as electrode material for supercapacitors, and the fabricated FSSCs devices pave a new pathway for flexible electronic devices.

LiFe0.3Mn0.7PO4-on-MXene heterostructures as highly reversible cathode materials for Lithium-ion batteries.

Two-dimensional (2D) heterostructure materials, incorporating the collective strengths and synergetic properties of individual building blocks, have attracted great interest as a novel paradigm in electrode materials science. The family of 2D transition metal carbides and nitrides (e.g., MXenes) has become an appealing platform for fabricating functional materials with strong application performance. Herein, a 2D LiFe0.3Mn0.7PO4 (LFMP)-on-MXene heterostructure composite is prepared through an electrostatic self-assembly procedure. The functional groups on the surface of MXenes possess highly electronegative properties that facilitate the incorporation of LFMPs into MXenes to construct heterostructure composites. The special heterostructure of nanosized-LiFe0.3Mn0.7PO4 and MXene provides rapid Li+ and electron transport in the cathodes. This LiFe0.3Mn0.7PO4-3.0 wt% MXene composite can exhibit an excellent rate capability of 98.3 mAh g-1 at 50C and a very stable cycling performance with a capacity retention of 94.3 % at 5C after 1000 cycles. Furthermore, NaFe0.3Mn0.7PO4-3.0 wt% MXene with stable cyclability can be obtained by an electrochemical conversion method with LiFe0.3Mn0.7PO4-3.0 wt% MXene. Ex-situ XRD suggests that LiFe0.3Mn0.7PO4-on-MXene achieves a highly reversible structural evolution with a solid solution phase transformation (LFMP→LixFe0.3Mn0.7PO4 (LxFMP), LxFMP→LFMP) and a two-phase reaction (LxFMP←→Fe0.3Mn0.7PO4 (FMP)). This work provides a new direction for the use of MXenes to fabricate 2D heterostructures for lithium-ion batteries.

Interfacial coupling of Ce-CoSe2 nanoneedle arrays with MXene for efficient overall water splitting.

Designing highly effective, low-cost bifunctional electrocatalysts without noble metals for overall water splitting remains a significant challenge. In this work, interfacial coupling of Ce-doped CoSe2 nanoneedle arrays with MXene (Ce-CoSe2/MXene) is developed via the facile hydrothermal and selenization methods. The extensive specific surface area and favorable hydrophilicity of Ti3AlC2, combined with the optimized electronic structure and abundant active sites from Ce-doping and selenization, contribute to the exceptional bifunctional electrocatalytic performance of the Ce-CoSe2/MXene electrode. Specifically, this heterostructure achieves a low hydrogen evolution reaction (HER) overpotential of 34 mV at 10 mA cm-2, an oxygen evolution reaction (OER) overpotential of 279 mV at 100 mA cm-2, and an overall water splitting (OWS) potential as low as 1.45 V at 10 mA cm-2. In-situ Raman spectroscopy reveals that surface reconstruction would improve catalytic activity and stability. Theoretical calculations indicate that the Ce-CoSe2/MXene can improve the adsorption of intermediates and facilitate HER/OER process by lowering the kinetic barrier, thereby enhancing electrocatalytic activity. This research marks a substantial advancement in the development of low-cost, efficient electrocatalysts for overall water splitting.

Inkjet-printed flexible V2CTx film electrodes with excellent photoelectric properties and high capacities for energy storage device.

Energy storage devices are progressively advancing in the light-weight, flexible, and wearable direction. Ti3C2Tx flexible film electrodes fabricated via a non-contact, cost-effective, high-efficiency, and large-scale inkjet printing technology were capable of satisfying these demands in our previous report. However, other MXenes that can be employed in flexible energy storage devices remain undiscovered. Herein, flexible V2CTx film electrodes (with the low formula weight vs Ti3C2Tx film electrodes) with both high capacities and excellent photoelectric properties were first fabricated. The area capacitances of V2CTx film electrodes reached 531.3-5787.0 µF⋅cm-2 at 5 mV⋅s-1, corresponding to the figure of merits (FoMs) of 0.07-0.15. Noteworthy, V2CTx film electrode exhibited excellent cyclic stability with the capacitance retention of 83 % after 7,000 consecutive charge-discharge cycles. Furthermore, flexible all solid-state symmetric V2CTx supercapacitor was assembled with the area capacitance of 23.4 µF⋅cm-2 at 5 mV⋅s-1. Inkjet printing technology reaches the combination of excellent photoelectric properties and high capacities of flexible V2CTx film electrodes, which provides a new strategy for manufacturing MXene film electrodes, broadening the application prospect of flexible energy storage devices.

A disposable ultrasensitive immunosensor based on MXene/NH2-CNT modified screen-printed electrode for the detection of ovarian cancer antigen CA125.

Cancer antigen 125 (CA125) is the gold standard biomarker for clinical diagnosis of ovarian cancer, with a threshold value of 35 U/mL in serum. In this paper, a disposable ultrasensitive immunosensor based on Ti3C2Tx-MXene/amino-functionalized carbon nanotube (NH2-CNT) modified screen-printed carbon electrode (SPCE) was constructed for the detection of the ovarian cancer antigen CA125. By optimizing the mass ratio of Ti3C2Tx to NH2-CNT, Ti3C2Tx/NH2-CNT composite with excellent electrochemical properties was prepared, which is beneficial for amplifying the initial electrochemical signal. The positively charged NH2-CNT effectively alleviated the stacking problem of Ti3C2Tx, and its amino group also facilitated the covalent immobilization of the capture antibody. Meanwhile, chitosan (CS) with excellent film-forming ability was also used to successfully enhance the adsorption of electrode material, thus improving the stability of the sensor. In addition, CS could further enhance the current signal. The prepared immunosensor exhibited excellent performance in CA125 detection with a wide linear range from 1 mU/mL to 500 U/mL, and good selectivity, reproducibility and lomg-term stability. Furthermore, the immunosensor showed satisfactory results for the detection of CA125 in clinical serum samples, which is promising for the clinical screening, early diagnosis and prognostic examination of ovarian cancer.

Highly active Ti3C2Tx MXene nanoribbons@AuPt bimetallic nanozyme constructed in a "two birds with one stone" manner for colorimetric sensing of dipterex.

The bimetallic nanoparticles have received significant attention in the field of colorimetric sensing, while the majority of the previous methods for synthesizing such nanoparticles typically require the use of reducers and involve highly harsh synthesis conditions. In this work, the AuPt bimetallic nanoparticles (AuPtNPs) decorated Ti3C2TxNR nanohybrid (Ti3C2TxNR@AuPt) was firstly synthesized in a "two birds with one stone" manner. Innovatively, during the synthesis process, Ti3C2TxNR served as both reducing agent and supporting agent to prevent aggregation of bimetallic nanoparticles. Due to the good synergistic effect of AuPtNPs and the strong metal-support interaction between AuPtNPs and Ti3C2TxNR, the as-prepared Ti3C2TxNR@AuPt exhibited boosted peroxidase (POD)-like activity. In advantage of the exceptional POD-like activity, a cost-effective and sensitive colorimetric sensing platform was fabricated for dipterex detection with a broad linearity of 1.0 ng mL-1-1.0 µg mL-1 and a low detection limit (0.479 ng mL-1). The detection of dipterex in insecticide samples also yielded favorable recoveries. Moreover, this approach provided a convenient and effective strategy to design and develop novel nanozymes via a "two birds with one stone" strategy.

Magneto-Dielectric Synergy and Multiscale Hierarchical Structure Design Enable Flexible Multipurpose Microwave Absorption and Infrared Stealth Compatibility.

Developing advanced stealth devices to cope with radar-infrared (IR) fusion detection and diverse application scenarios is increasingly demanded, which faces significant challenges due to conflicting microwave and IR cloaking mechanisms and functional integration limitations. Here, we propose a multiscale hierarchical structure design, integrating wrinkled MXene IR shielding layer and flexible Fe3O4@C/PDMS microwave absorption layer. The top wrinkled MXene layer induces the intensive diffuse reflection effect, shielding IR radiation signals while allowing microwave to pass through. Meanwhile, the permeable microwaves are assimilated into the bottom Fe3O4@C/PDMS layer via strong magneto-electric synergy. Through theoretical and experimental optimization, the assembled stealth devices realize a near-perfect stealth capability in both X-band (8-12 GHz) and long-wave infrared (8-14 µm) wavelength ranges. Specifically, it delivers a radar cross-section reduction of - 20 dB m2, a large apparent temperature modulation range (ΔT = 70 °C), and a low average IR emissivity of 0.35. Additionally, the optimal device demonstrates exceptional curved surface conformability, self-cleaning capability (contact angle ≈ 129°), and abrasion resistance (recovery time ≈ 5 s). This design strategy promotes the development of multispectral stealth technology and reinforces its applicability and durability in complex and hostile environments.

3D Network Spacer-Embedded Flexible Iontronic Pressure Sensor Array with High Sensitivity over a Broad Sensing Range.

Microstructure construction is a common strategy for enhancing the sensitivity of flexible pressure sensors, but it typically requires complex manufacturing techniques. In this study, we develop a flexible iontronic pressure sensor (FIPS) by embedding an isolated three-dimensional network spacer (3DNS) between an ionic gel and a flexible Ti3C2Tx MXene electrode, thereby avoiding complex microstructure construction techniques. By leveraging substantial deformation of the 3DNS and the high capacitance density resulting from the electrical double layer effect, the sensor exhibits high sensitivity (87.4 kPa-1) over a broad high-pressure range (400-1000 kPa) while maintaining linearity (R2 = 0.998). Additionally, the FIPS demonstrates a rapid response time of 46 ms, a low limit of detection at 50 Pa, and excellent stability over 10 000 cycles under a high pressure of 600 kPa. As practical demonstrations, the FIPS can effectively monitor human motion such as elbow bending and assist a robotic gripper in accurately sensing gripping tasks. Moreover, a real-time, adaptive 7 × 7 sensing array system is built and can recognize both numeric and alphabetic characters. Our design philosophy can be extended for fabricating pressure sensors with high sensing performance without involving complex techniques, facilitating the applications of flexible sensors in human motion monitoring, robotic tactile sensing, and human-machine interaction.

Impact of Asymmetric Microstructure on Ion Transport in Ti3C2Tx Membranes.

Consolidation or densification of low-dimensional MXene materials into membranes can result in the formation of asymmetric membrane structures. Nanostructural (short-range) and microstructural (long-range) heterogeneity can influence mass transport and separation mechanisms. Short-range structural dynamics include the presence of water confined between the 2D layers, while long-range structural properties include the formation of defects, micropores, and mesopores. Herein, it is demonstrated that structural heterogeneity in Ti3C2Tx membranes fabricated via vacuum-assisted filtration significantly affects ion transport. Higher ion permeabilities are achieved when the dense "bottom" side of the membrane, rather than the porous "top" side, faces the feed solution. Characterization of the membrane reveals distinct differences in flake alignment, surface roughness, and porosity across the membrane. The directional dependence on permeability suggests that one region of the membrane experiences stronger internal concentration polarization, potentially suppressing permeability through the porous side of the membrane.

Recent Advances in MXene-Based Aerogels for Electromagnetic Wave Absorption.

Developing lightweight, high-performance electromagnetic wave (EMW) absorbing materials those can absorb the adverse electromagnetic radiation or waves are of great significance. Transition metal carbides and/or nitrides (MXenes) are a novel type of 2D nanosheets associated with a large aspect ratio, abundant polar functional groups, adjustable conductivity, and remarkable mechanical properties. This contributes to the high-efficiency assembly of MXene-based aerogels possessing the ultra-low density, large specific surface area, tunable conductivity, and unique 3D porous microstructure, which is beneficial for promoting the EMW absorption. Therefore, MXene-based aerogels for EMW absorption have attracted widespread attention. This review provides an overview of the research progress on MXene-based aerogels for EMW absorption, focusing on the recent advances in component and structure design strategies, and summarizes the main strategies for constructing EMW absorbing MXene-based aerogels. In addition, based on EMW absorption mechanisms and structure regulation strategies, the preparation methods and properties of MXene-based aerogels with varieties of components and pore structures are detailed to advance understanding the relationships of composition-structure-performance. Furthermore, the future development and challenges faced by MXene-based aerogels for EMW absorption are summarized and prospected.

Engineering of Interface Barrier in Hybrid MXene/GaN Heterostructures for Schottky Diode Applications.

The Fermi level position at the interface of a heterostructure is a critical factor for device functionality, strongly influenced by surface-related phenomena. In this study, contactless electroreflectance (CER) was utilized for the first time to investigate the built-in electric field in MXene/GaN structures with the goal of understanding the carrier transfer across the MXene/GaN interface. Five MXenes with high work functions were examined: Cr2C, Mo2C, V2C, V4C3, and Ti3C2. The physicochemical properties of the MXene/GaN structures were analyzed by using X-ray and UV photoelectron spectroscopies. It was shown that upon the coverage of the GaN surface by all investigated MXenes, a shift in the position of the surface Fermi level occurs, consequently raising the interface barrier. Additionally, the physicochemical stability of MXenes on the GaN surface was studied after annealing the structures at 750 °C. Our findings indicate that the annealing process increases the barrier height and the ionization energies of all studied structures. Furthermore, it has been shown that removing excess MXene material from the surface did not significantly impact the built-in electric field, emphasizing the robust physicochemical stability of the MXenes on the GaN surface. To validate the potential of engineering of MXene/GaN interface barrier, Schottky diodes with MXenes exhibiting the highest barrier height (Mo2C and V2C) were demonstrated.

Polydopamine-modified 3D flower-like ZnMoO4 integrated MXene-based label-free electrochemical immunosensor for the food-borne pathogen Listeria monocytogenes detection in milk and seafood.

Listeria monocytogenes is a gram-positive bacterium that causes listeriosis in humans. This contaminates the ready-to-eat food products and compromises their safety. Thus, detecting its presence in food samples with high sensitivity and reliability is necessary. Herein, we propose a label-free electrochemical immunosensor based on a mussel-inspired polydopamine-modified zinc molybdate/MXene (PDA@ZnMoO4/MXene) composite for effective and rapid detection of L. monocytogenes in food products. Spectrophotometry approaches were employed to examine the resulting composites. Voltammetry and impedimetry techniques were used to confirm the step-by-step assembly of the immunosensor and its sensitive detection of L. monocytogenes in various food products, such as milk and smoked seafood. The results demonstrated the practicality of the constructed immunosensor, with an appreciable linearity of 10-107 CFU/ml and a reasonably low detection limit (LOD, 12 CFU/ml). Moreover, the immunosensor exhibited excellent selectivity for microbial cocktails and acceptable repeatability, reproducibility, and storage stability. Thus, we believe that the proposed sensitive, reliable, and label-free immunosensor based on the PDA surface modification technique for detecting L. monocytogenes can be extended to monitor various food-borne pathogens to ensure food safety.

Synergistic Effect of GO and MXene Enables Ultrasensitive, Reversible, and Self-Powered Fire Warning of a GO/MXene/Chitosan Aerogel.

Graphene oxide (GO)-based fire alarm materials have garnered extensive attention because the thermal reduction of GO to reduced GO (RGO) enables rapid fire warning. However, they suffer from poor flame retardancy, irreversible fire warning, and dependence on an external power supply. Herein, a GO/MXene/chitosan aerogel with a low density of 0.018 g cm-3 and good compressibility has been developed. The experimental results demonstrate that (i) MXene effectively reduces the peak and mean heat release rate of GO, while RGO nanosheets compensate for the structural instability of MXene in the flame due to thermal oxidation into TiO2; as such, long-lasting fire warning (>120 s) has been achieved; (ii) the reducibility and conductivity of MXene contribute to the ultrasensitive response of GO, with a fire response time of 1 s; and (iii) notably, the thermoelectric effect of MXene enables the reversible and self-powered fire warning of the GO/MXene/CS aerogel without an external power supply. Compared to pure MXene/CS aerogel, the presence of GO improves the sensitivity and stability of self-powered fire warning, owing to the formation of the highly conductive RGO nanosheets. The results of this work highlight the cooperation between GO and MXene in realizing ultrasensitive, long-lasting, reversible, and self-powered fire warning.

Functionalized MXene (Ti3C2TX) Loaded with Ag Nanoparticles as a Raman Scattering Substrate for Rapid Furfural Detection in Baijiu.

Furfural is an essential compound that contributes to the distinctive flavor of sauce-flavored Baijiu. However, traditional detection methods are hindered by lengthy and complex sample preparation procedures, as well as the need for expensive equipment. Therefore, there is an urgent need for a new approach that allows rapid detection. In this study, we developed a novel surface-enhanced Raman spectroscopy (SERS) substrate by constructing MXene (Ti3C2TX) @Ag nanoparticles (Ag NPs) through an electrostatic attraction method. The MXene (Ti3C2TX) @Ag NPs were successfully fabricated, with adsorbed NaCl-treated Ag NPs uniformly absorbed on the surface of MXene (Ti3C2TX), creating high-density distributed SERS "hot spots". The prepared substrate demonstrated excellent sensitivity, uniformity, repeatability, and long-term stability, with a low detectable concentration of 10-9 M for R6G (Rhodamine 6G) and an enhancement factor of up to 7.08 × 105. When applied for the in situ SERS detection of furfural in Baijiu, the detection limit was as low as 0.5 mg/L. Overall, the proposed method offers rapid, low-cost, and sensitive quantitative analysis, which is significant not only for detecting furfural in Baijiu but also for identifying hazardous substances and distinguishing between authentic and counterfeit Baijiu products.

Proton conductive 2D MXene-derived potassium titanate nanoribbons fabricated electrochemical platform for trace detection of enrofloxacin.

In recent years, due to exceptional properties like broad interlayered spacing and low working potential, MXene-derived titanate nanoribbons have been established as promising electrode materials. Herein, the electrocatalytic activity of MXene-derived potassium titanate nanoribbon was employed to develop a voltammetric sensor for the detection of enrofloxacin. The sensor's significance is to provide a sustainable solution to quantify the presence of enrofloxacin regarding food safety and environmental monitoring. Moreover, to achieve the United Nations' Sustainable Development Goals by preventing antimicrobial resistance to accomplish the One Health approach. Potassium titanate nanoribbons were synthesized using 2D Ti3C2 MXene as an active precursor material, while X-ray diffraction spectroscopy, field emission scanning electron microscopy, high-resolution transmission electron microscopy, selected area electron diffraction pattern, elemental mapping, and energy-dispersive X-ray spectroscopy were used to characterize the crystallinity, surface and layered morphology of synthesized nanoribbons. The Brunauer-Emmett-Teller (BET) technique was applied to calculate the specific surface area of the synthesized materials. The materials underwent electrochemical characterization using cyclic voltammetry (CV), differential pulse voltammetry (DPV), and electrochemical impedance spectroscopy (EIS). Later on, the nanoribbons were fabricated on the surface of a glassy carbon electrode, and the electro-oxidative behaviour of enrofloxacin was studied by CV, DPV, square wave voltammetry (SWV) in 0.1 M phosphate buffer (optimized pH 8). The developed sensor depicts a significantly lower limit of quantification of 0.007 µM (≈2.5 µg/L), and an upper limit of quantification of 18 µM (≈6.5 mg/L) along with a limit of detection (LOD) of 0.00279, 0.00803, 0.00881 µM obtained from CV, DPV, and SWV respectively. Furthermore, the developed electrodes show a reliable selectivity to be examined in real complex matrices, i.e. marine water, river water, agricultural soil, organic fertilizer, milk, honey, and poultry egg.

2D MXene Nanosheets with ROS Scavenging Ability Effectively Delay Osteoarthritis Progression.

MXenes nanosheets with high conductivity, hydrophilicity, and excellent reactive oxygen species (ROS) scavenging ability have shown promise in treating various degenerative diseases correlated with abnormal ROS accumulation. Herein, the therapeutic potential of Ti3C2Tx nanosheets, which is the most widely investigated MXene material, in delaying osteoarthritis (OA) progression is demonstrated. In vitro experiments indicate the strong ROS scavenging capacity of Ti3C2Tx nanosheets and their acceptable biocompatibility. Ti3C2Tx nanosheets effectively protect chondrocytes from cell death induced by oxidative stress. In addition, Ti3C2Tx nanosheets demonstrate a prominent anti-inflammatory effect and the ability to restore homeostasis between anabolic activities and catabolic activities in chondrocytes. Furthermore, RNA sequencing reveals the potential mechanism underlying the Ti3C2Tx nanosheet-mediated therapeutic effect. Finally, the in vivo curative effect of Ti3C2Tx nanosheets is verified using a rat OA model. Histological staining and immunohistochemical analyses indicate that Ti3C2Tx nanosheets effectively ameliorate OA progression. Conclusively, the in vitro and in vivo experiments suggest that Ti3C2Tx nanosheets could be a promising and effective option for OA treatment.

Improvement of Electrical and Thermal Properties of Carbon Nanotube Sheets by Adding Silver Nanowire and Mxene for an Electromagnetic-Interference-Shielding Property Study.

Hybrid carbon nanotube (CNT) sheets were fabricated by mixing CNTs with silver nanowires (AgNWs) and MXene to study their electromagnetic-interference (EMI)-shielding properties. CNT/AgNW and CNT/MXene hybrid sheets were produced by ultrasonic homogenization and vacuum filtration, resulting in free-standing CNT sheets. Three different weight ratios of AgNW and MXene were added to the CNT dispersions to produce hybrid CNT sheets. Microstructure characterization was performed using scanning electron microscopy, and the Wiedemann-Franz law was used to characterize transport properties. The resulting hybrid sheets exhibited improved electrical conductivity, thermal conductivity, and EMI-shielding effectiveness compared to pristine CNT sheets. X-band EMI-shielding effectiveness improved by over 200%, while electrical conductivity improved by more than 1500% in the hybrid sheets due to a higher charge-carrier density and synergistic effects between nanomaterials. The addition of AgNW to CNT sheets resulted in a large improvement in electrical conductivity and EMI shielding; however, this may also result in increased weight and sample thickness. Similarly, the addition of MXene to CNT sheets may result in an increase in weight due to the presence of the denser MXene flakes.