Search Results (13)

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

Tantalum carbide MXenes, notably Ta₄C₃T_x and Ta₂CT_x, exhibit distinctive physicochemical properties that distinguish them from the well-studied Ti₃C₂T_x MXene. The combination of exceptional electrochemical properties, efficient photothermal conversion, and tunable surface terminations highlights the versatility of Ta-MXenes. These characteristics render them highly valuable for versatile applications. This minireview summarizes recent progress in tantalum carbide MXenes and their composites, focusing on applications in energy storage, conversion, sensing, and biomedicine. First, synthesis methods for tantalum carbide MXenes are summarized. Subsequently, their key properties are discussed, followed by a systematic review of diverse applications. Finally, this review offers a summary and outlook on the challenges and opportunities in the field of tantalum carbide MXenes research. Full article

Previous studies have demonstrated that underwater low-temperature plasma is effective for synthesizing nanomaterials by generating plasma discharges between metal electrodes submerged in water. This study extends this approach to the one-step synthesis of MXenes containing titanium, molybdenum, and titanium–molybdenum composites through pulsed discharges in carbon tetrachloride, an oxygen-free, non-flammable solvent characterized by a high boiling point and low permittivity. By employing titanium and molybdenum electrodes in various configurations, three MXene samples were synthesized: Ti₂CT_X, Mo₂CT_X, and Mo₂TiC₂T_X. Characterization techniques, including UV-Vis spectroscopy, X-ray diffraction, Raman spectroscopy, scanning electron microscopy, and energy-dispersive X-ray spectroscopy, confirmed the successful synthesis of high-purity MXenes with distinct structural and optical properties. Notably, the bandgap values of the synthesized MXenes were determined as 1.71 eV for Ti₂CT_X, 1.42 eV for Mo₂TiC₂T_X, and 1.07 eV for Mo₂CT_X. The photocatalytic performance of the synthesized MXenes was evaluated, showing a removal efficiency of 65% to 98% for dye mixtures, with methylene blue showing the highest degradation rate. This plasma-assisted method offers a scalable, precursor-free route for the synthesis of MXenes with potential applications in energy storage, environmental remediation, and optoelectronics due to their tunable bandgaps and high catalytic activity. Full article

Ti-based MXenes such as Ti₃C₂T_X and Ti₂CT_X have attracted considerable attention because of their superior electromagnetic interference (EMI) shielding effectiveness compared to other EMI shielding materials, especially for high electromagnetic (EM) wave absorption. In this study, we investigated the microstructural changes produced by heat treatment and their effect on the EMI shielding properties of Ti-based MXenes. Ti₃C₂T_X and Ti₂CT_X films were prepared using vacuum filtration and annealed at temperatures up to 300 °C. The microstructures and chemical bonding properties of these heat-treated Ti₃C₂T_X and Ti₂CT_X films were analyzed, and the EMI shielding effectiveness was measured in the X-band and THz frequency range. The porous Ti₃C₂T_X film showed higher EM absorption than that calculated using the transfer matrix method. On the other hand, the Ti₂CT_X films had a more densely stacked structure and lower EM absorption. As the heat treatment temperature increased, Ti₃C₂T_X developed a more porous structure without significant changes in its chemical bonding. Its EM absorption per unit of thickness increased up to 6 dB/μm, while the reflectance remained constant at less than 1 dB/μm after heat treatment. This suggested that the heat treatment of Ti-based MXenes can increase the porosity of the film by removing residual organics without changing the chemical bonds, thereby increasing electromagnetic shielding through absorption. Full article

The chemoresistive properties of multilayer titanium-containing Ti₂CT_x and Ti₃C₂T_x MXenes, synthesized by etching the corresponding MAX phases with NaF solution in hydrochloric acid, and the composites based on them, obtained by partial oxidation directly in a sensor cell in an air flow at 150 °C, were studied. Significant differences were observed for the initial MXenes, both in microstructure and in the composition of surface functional groups, as well as in gas sensitivity. For single Ti₂CT_x and Ti₃C₂T_x MXenes, significant responses to oxygen and ammonia were observed. For their partial oxidation at a moderate temperature of 150 °C, a high humidity sensitivity (T, RH = 55%) is observed for Ti₂CT_x and a high and selective response to oxygen for Ti₃C₂T_x at 125 °C (RH = 0%). Overall, these titanium-containing MXenes and composites based on them are considered promising as receptor materials for low temperature oxygen sensors. Full article

At present, a new class of 2D nanomaterials, MXenes, is of great scientific and applied interest, and their application prospects are very broad, including as effective doping components for receptor materials of MOS sensors. In this work we have studied the influence on the gas-sensitive properties of nanocrystalline zinc oxide synthesized by atmospheric pressure solvothermal synthesis, with the addition of 1–5% of multilayer two-dimensional titanium carbide Ti₂CT_x, obtained by etching Ti₂AlC with NaF solution in hydrochloric acid. It was found that all the obtained materials have high sensitivity and selectivity with respect to 4–20 ppm NO₂ at a detection temperature of 200 °C. It is shown that the selectivity towards this compound is best for the sample containing the highest amount of Ti₂CT_x dopant. It has been found that as the MXene content increases, there is an increase in nitrogen dioxide (4 ppm) from 1.6 (ZnO) to 20.5 (ZnO-5 mol% Ti₂CT_x). reactions which the responses to nitrogen dioxide increase. This may be due to the increase in the specific surface area of the receptor layers, the presence of MXene surface functional groups, as well as the formation of the Schottky barrier at the interface between the phases of the components. Full article

The titanium carbide MXenes currently attract an extreme amount of interest from the material science community due to their promising functional properties arising from the two-dimensionality of these layered structures. In particular, the interaction between MXene and gaseous molecules, even at the physisorption level, yields a substantial shift in electrical parameters, which makes it possible to design gas sensors working at RT as a prerequisite to low-powered detection units. Herein, we consider to review such sensors, primarily based on Ti₃C₂T_x and Ti₂CT_x crystals as the most studied ones to date, delivering a chemiresistive type of signal. We analyze the ways reported in the literature to modify these 2D nanomaterials for (i) detecting various analyte gases, (ii) improving stability and sensitivity, (iii) reducing response/recovery times, and (iv) advancing a sensitivity to atmospheric humidity. The most powerful approach based on designing hetero-layers of MXenes with other crystals is discussed with regard to employing semiconductor metal oxides and chalcogenides, noble metal nanoparticles, carbon materials (graphene and nanotubes), and polymeric components. The current concepts on the detection mechanisms of MXenes and their hetero-composites are considered, and the background reasons for improving gas-sensing functionality in the hetero-composite when compared with pristine MXenes are classified. We formulate state-of-the-art advances and challenges in the field while proposing some possible solutions, in particular via employing a multisensor array paradigm. Full article

Transition metal carbonitrides (MXenes) are promising catalysts due to their special structures. Recently, many studies have shown that MXenes have a catalytic effect on the thermal decomposition of ammonium perchlorate (AP). However, the catalytic effects have not been extensively investigated. Therefore, it is important to illustrate the catalytic mechanisms of pure MXene in AP thermal decomposition. Herein, the catalytic properties of Ti₂CT_x for ammonium perchlorate (AP) thermal decomposition were investigated by numerous catalytic experiments. The results showed that the high-temperature decomposition (HTD) decreased by 83 °C, and the decomposition heat of AP mixed with Ti₂CT_x increased by 1897.3 J/g. Moreover, the mass spectrum (MS) data showed that the NH₃, H₂O, O₂, N₂O, NO, HCl, and NO₂ were formed. In addition, according to the X-ray diffraction (XRD), Raman spectrum, high-resolution transmission electron microscopy (HRTEM), selected area electron diffraction (SAED), and X-ray photoelectron spectra (XPS) results, the Ti₂CT_x nanosheets can adsorb the gaseous products and react with them in-situ, generating anatase-TiO₂ and carbon layers. The Ti₂CT_x, as-resulted anatase-TiO₂, and carbon can synergize and further catalyze the thermal decomposition of AP when both electron and proton transfers are accelerated during AP decomposition. Full article

The oxidation process was studied for the synthesized low-layer Ti₂CT_x MXene deposited on a special Al₂O₃/Pt sensor substrate using in situ Raman spectroscopy. It is noted that on the ceramic parts of the substrate (Al₂O₃), the beginning of oxidation (appearance of anatase mod phase) is observed already at 316 °C, in comparison with platinum, for which the appearance of anatase is noted only at 372 °C. At the temperature 447 °C, the initial MXene film is completely oxidized to TiO₂. Using scanning electron microscopy and atomic force microscopy, the microstructure and dispersity of the obtained MXene film were studied. It was found that the obtained films exhibit chemoresistive responses to the detection of a wide group of gases, H₂, CO, NH₃, C₆H₆, C₃H₆O, CH₄, C₂H₅OH and O₂, at room temperature and RH = 50%. The highest sensitivity is observed for NH₃. The partial oxidation of the Ti₂CT_x MXene was shown to favorably affect the gas-sensitive properties. Full article

MAX phases are the parent materials used for the formation of MXenes, and are generally obtained by etching using the highly corrosive acid HF. To develop a more environmentally friendly approach for the synthesis of MXenes, in this work, titanium aluminum carbide MAX phase (Ti₂AlC) was fabricated and etched using NaOH. Further, magnetic properties were induced during the etching process in a single-step etching process that led to the formation of a magnetic composite. By carefully controlling etching conditions such as etching agent concentration and time, different structures could be produced (denoted as M.Ti₂CT_x). Magnetic nanostructures with unique physico-chemical characteristics, including a large number of binding sites, were utilized to adsorb radionuclide Sr²⁺ and Cs⁺ cations from different matrices, including deionized, tap, and seawater. The produced adsorbents were analyzed using X-ray diffraction (XRD), scanning electron microscopy (SEM), X-ray energy dispersive spectroscopy (EDS), and X-ray photoelectron spectroscopy (XPS). The synthesized materials were found to be very stable in the aqueous phase, compared with corrosive acid-etched MXenes, acquiring a distinctive structure with oxygen-containing functional moieties. Sr²⁺ and Cs⁺ removal efficiencies of M.Ti₂CT_x were assessed via conventional batch adsorption experiments. M.Ti₂CT_x-A_III showed the highest adsorption performance among other M.Ti₂CT_x phases, with maximum adsorption capacities of 376.05 and 142.88 mg/g for Sr²⁺ and Cs⁺, respectively, which are among the highest adsorption capacities reported for comparable adsorbents such as graphene oxide and MXenes. Moreover, in seawater, the removal efficiencies for Sr²⁺ and Cs⁺ were greater than 93% and 31%, respectively. Analysis of the removal mechanism validates the electrostatic interactions between M.Ti₂C-A_III and radionuclides. Full article

Mesenchymal stem cell (MSC)-based therapy and tissue repair necessitate the use of an ideal clinical biomaterial capable of increasing cell proliferation and differentiation. Recently, MXenes 2D nanomaterials have shown remarkable potential for improving the functional properties of MSCs. In the present study, we elucidated the potential of Ti₂CTx MXene as a biomaterial through its primary biological response to human Wharton’s Jelly MSCs (hWJ-MSCs). A Ti₂CTx nanosheet was synthesized and thoroughly characterized using various microscopic and spectroscopic tools. Our findings suggest that Ti₂CTx MXene nanosheet exposure does not alter the morphology of the hWJ-MSCs; however, it causes a dose-dependent (10–200 µg/mL) increase in cell proliferation, and upon using it with conditional media, it also enhanced its tri-lineage differentiation potential, which is a novel finding of our study. A two-fold increase in cell viability was also noticed at the highest tested dose of the nanosheet. The treated hWJ-MSCs showed no sign of cellular stress or toxicity. Taken together, these findings suggest that the Ti₂CTx MXene nanosheet is capable of augmenting the proliferation and differentiation potential of the cells. Full article

Owing to their unique characteristics, two-dimensional (2-D) materials and their complexes have become very attractive in photoelectric applications. Two-dimensional heterojunctions, as novel 2-D complex materials, have drawn much attention in recent years. Herein, we propose a 2-D heterojunction composed of MXene (Ti₂CT_x) materials and graphene oxide (GO), and apply it to an Nd:YAG solid-state laser as a saturable absorber (SA) for passive Q-switching. Our results suggest that a nano-heterojunction between MXene and GO was achieved based on morphological characterization, and the advantages of a broadband response, higher stability in GO, and strong interaction with light waves in MXene could be combined. In the passively Q-switched laser study, the single-pulse energy was measured to be approximately 0.79 µJ when the pump power was 3.72 W, and the corresponding peak power was approximately 7.25 W. In addition, the generation of a stable ultrashort pulse down to 109 ns was demonstrated, which is the narrowest pulse among Q-switched solid-state lasers using a 2-D heterojunction SA. Our work indicates that the MXene–GO nano-heterojunction could operate as a promising SA for ultrafast systems with ultrahigh pulse energy and ultranarrow pulse duration. We believe that this work opens up a new approach to designing 2-D heterojunctions and provides insight into the formation of new 2-D materials with desirable photonic properties. Full article

In this work, we successfully fabricated a transmissive saturable absorber (SA) with Ti₂CT_x MXene using the spin-coating method. By inserting the Ti₂CT_x saturable absorber into the diode-pumped solid-state (DPSS) Nd:YAG laser, a stable passively Q-switched operation was obtained near 1.06 μm. At a pump power of 4.5 W, we obtained the shortest pulse duration of 163 ns with a repetition rate of 260 kHz. The corresponding single pulse energy and peak pulse power were 3.638 μJ and 22.3 W, respectively. The slope efficiency and the optical conversion efficiency of the laser were 21% and 25.5%, respectively. To the best of our knowledge, this is the first time that Ti₂CT_x was used in the passively Q-switched solid-state lasers. This work demonstrates that Ti₂CT_x can be a promising saturable absorber for solid-state laser pulse generation. Full article