Improved dielectric and mechanical properties of Ti3C2Tx MXene/silicone rubber composites achieved by adding a few boron nitride nanoplates

MXenes have attracted great attentions in the fabrication of dielectric polymer composites because of their excellent electrical conductivity. However, the high dielectric loss tangent would suppress the application of such polymer-based composites. Incorporating insulating fillers might be a solution. Herein, Ti₃C₂T_x MXene/silicone rubber (SR) composites incorporated with boron nitride (BN) nanoplates were prepared. The homogeneous distribution of fillers was obtained in the composites, which was also thermally stable up to 400 °C. Dielectric constant of 7.06 (2.54 times of pure SR) and dielectric loss tangent of 0.00131 were achieved when the filling contents of MXene and BN in SR composite were 1.2 wt% and 5 wt%, respectively. The improved dielectric constant can be ascribed to the enhanced interfacial polarization and the formation of conductive network, while the low dielectric loss tangent can be due to the insulating interlayers of BN which could inhibit the transfer of free electrons from conductive fillers to the insulating polymer matrices. BN/MXene/SR composites displayed improved mechanical properties (tensile stress of 671 kPa and elongation at break of 353%) and good flexibility (elastic modulus of 540 kPa) due to the low filling content of fillers. This work is promising for preparing dielectric polymer composites in applications of electronic devices.     

Structural,thermal and dielectric properties of 2D layered Ti3C2Tx (MXene) filled poly (ethylene-co-methyl acrylate) (EMA) nanocomposites

Light-weight and flexible 2D MXene-based polymer materials with low dielectric loss and high dielectric constant have drawn great attention in the power systems and modern electronic field. A series of Ti₃C₂T_x/EMA composites were fabricated via simple solution casting followed by a compression molding method with various mass concentrations of Ti₃C₂T_x (0, 1, 3, 5, 8, 10, 12, and 15 wt%). Morphological and micro structural properties of the prepared composites were studied via X-ray diffraction (XRD) and field-emission scanning electron microscope (FESEM), where the distribution of Ti₃C₂T_x in the Ti₃C₂T_x/EMA composites was confirmed. Thermal behaviors were analyzed by differential scanning calorimetry (DSC) and thermogravimetric analysis (TGA) investigations. The DSC analysis reveals that the % of crystallinity decreases from 11.06 with 1 wt% to 5.68 with 15 wt%, where Ti₃C₂T_x acts as an efficient nucleating agent. TGA data confirm the enhancement of the thermal stability of the composites upon increasing in Ti₃C₂T_x loading. The room temperature electrical and dielectric behavior of the studied composites were examined in the frequency range of 100 Hz–5 MHz. In this work, the 10 wt% of Ti₃C₂T_x loaded poly (ethylene-co-methyl acrylate) composite (EMA) showed higher dielectric permittivity (ε′ = 124.22) with lower dissipation loss (tan δ = 0.051) at 100 Hz among all weight percentages. The behavior of charge carriers in the prepared composites was studied by utilizing the impedance spectroscopy technique. The electrical parameters were calculated from the fitted Nyquist plots with a corresponding circuit model. I–V curves confirmed the conduction mechanisms of the composites. This beneficial enhancement in electrical properties recommends the composite can be utilized in flexible electronic storage devices.     

Broadband electromagnetic absorption of Ti3C2Tx MXene/WS2 composite via constructing two-dimensional heterostructure

Ti₃C₂T_x MXene, an emerging two-dimensional (2D) ceramic material, has rich interfaces and strong conductive networks. Herein, we have successfully built a heterostructure between Ti₃C₂T_x MXene and WS₂ to improve electromagnetic absorption performance. X-ray diffraction and X-ray photoelectron spectroscopy were used to determine the successful synthesis of Ti₃C₂T_x/WS₂ composite. Field emission scanning electron microscopy and transmission electron microscopy images show that WS₂ nanosheets are evenly dispersed on the accordion-like Ti₃C₂T_x MXene. Importantly, Ti₃C₂T_x MXene/WS₂ composite has sufficiently high dielectric loss and impedance matching due to self-adjusting conductivity and 2D heterostructure interfaces. As a result, the Ti₃C₂T_x/WS₂ composite has a minimum reflection loss (RL_min) of −61.06 dB at 13.28 GHz. Besides, it has a broad effective absorption bandwidth (EAB) of 6.5 GHz, with EAB >5.0 GHz covering a wide range of thickness. Such impressive results may provide experience for the application of Ti₃C₂T_x ceramics and 2D materials.     

Advanced Ti3C2Tx MXene-modified cement nanocomposites toward high efficiency electromagnetic functional materials for green buildings

The proliferation of electronic devices and wireless communication is leading to serious electromagnetic (EM) interference. In this work, Ti₃C₂/cement composites were developed as high efficiency EM functional materials by introducing exfoliated Ti₃C₂T_x MXene with cement for green buildings with EM shielding function. In the composites, few-layered Ti₃C₂ MXene were dispersed homogeneously throughout the cement matrix. The EM properties of the composites were studied as a function of the MXene content. With increasing MXene content, real and imaginary part of permittivity was significantly improved owing to the polarization and electrical conduction caused by the MXene phase. Composites with 15 wt.% MXene showed good EM absorbing properties with a maximum effective absorbing bandwidth of 2.67 GHz. Strong EM shielding can be achieved when MXene content increased to 25 wt.%. The EM shielding effectiveness of such composites was higher than 22.0 dB, and the dominating shielding mechanism was EM absorption. This work finds new materials for the development of advanced green buildings with EM shielding function.     

Core@shell and sandwich-like Ti3C2Tx@Ni particles with enhanced electromagnetic interference shielding performance

Novel and highly effective electromagnetic interference (EMI) shielding materials are desirable to attenuate unwanted electromagnetic radiation or interference produced by electrical communication devices. Here, functional Ti₃C₂T_x@Ni particles with a core@shell and sandwich like structure were fabricated using the facile electroless plating technique. The core@shell structured Ti₃C₂T_x@Ni consists of a Ti₃C₂T_x core and a Ni shell. In the core, thin Ni layers are sandwiched in between Ti₃C₂T_x flakes. EMI shielding effectiveness (SE) values of Ti₃C₂T_x@Ni/wax composites increased with increasing Ti₃C₂T_x@Ni content. The average EMI SE value of 60 wt% Ti₃C₂T_x@Ni/wax composite was 43.12 dB, increased by 73% as compared with 24.93 dB for the same content of pristine Ti₃C₂T_x in wax in the frequency range 2–18 GHz. An average EMI SE of 74.14 dB was achieved in the 80 wt% Ti₃C₂T_x@Ni/wax. The enhanced EMI shielding performance should be ascribed to the synergic effect of the absorption loss of the Ti₃C₂T_x core and the magnetic loss of the Ni shell and the inner Ni layers.     

Effects of multiwall carbon nanotubes on dielectric and mechanical properties of CaCu3Ti4O12 composite

This work reports the synthesis of calcium copper titanate (CaCu₃Ti₄O₁₂)/multiwall carbon nanotubes (MWCNT) composites using ultrasonic technique followed by sintering in a high vacuum furnace. The effect of MWCNT content (0.05, 0.1, 0.15, and 0.2 wt%) on the structural, dielectric, and mechanical properties of CaCu₃Ti₄O₁₂ (abbreviated as CCTO) were investigated by TEM, XRD, FTIR, FESEM-EDAX, dielectric measurement, as well as tensile strength and flexural strength tests. XRD patterns revealed that the MWCNT loading did not affect the phase structure; however, the average crystallite size (D) was reduced from 60.88 nm to 40.79 nm. The samples had porous structures and the porosity reduced from 45.57% to 40.73% with MWCNT loading. The dielectric and mechanical properties of CCTO were enhanced with an increase in MWCNT loading. An important observation was that the CCTO mixed with 0.2 wt% MWCNT exhibited the highest dielectric permittivity (ε_r = 27,768) and the lowest dielectric loss (tan δ = 0.52) at 1 kHz. With the addition of 0.2 wt% MWCNT, the values of load, tensile, and flexural strength increased to 10.38 kN, 101.88 MPa, and 275.07 MPa, respectively, due to improvement in densification. These outcomes have values for the fabrication of CCTO and the optimization of its performance for electronic devices such as capacitors and antennas.     

Novel Ti3C2Tx MXene/epoxy intumescent fire-retardant coatings for ancient wooden architectures

Most of the ancient buildings are made of inflammable wooden structures, which have serious potential safety hazards. Applying fire-retardant coating is one of the simplest and most effective means of fire prevention in ancient wooden buildings. In this work, we have demonstrated that the Ti₃C₂T_x transition metal carbide/carbonitride (MXene) was applied as the synergetic agent, waterborne epoxy resin as the film-forming agent, ammonium polyphosphate, dipentaerythritol, and melamine (P-C-N system) as the intumescent fire-retardant system to prepare Ti₃C₂T_x/epoxy intumescent fire-retardant coating (TEIFC). The results showed that MXene has significantly improved the fire-retardant performance of the coating. By incorporating 3 wt% Ti₃C₂T_x (TEIFC-3, with 62 wt% P-C-N system), the coating displayed UL-94 V-0 rating with the limiting oxygen index value of 38%. In addition, the combination of Ti₃C₂T_x and P-C-N system enhanced the Shore hardness of the coating to 95 SHD (TEIFC-3). Furthermore, TEIFC-3 presented high thermal stability with the T_HRI of 177.0°C and T_dmax of 380.5°C. This work provides a novel strategy for the design and preparation of intumescent fire-retardant coating, which will greatly broaden the industrial applications of MXene-based polymer composites in the field of fire prevention of ancient buildings.     

Electrochemical storage mechanism of interstratification-assembled Ti3C2Tx MXene/NiCo-LDHs electrode in alkaline,acid and neutral electrolytes

Different kinds of two-dimensional hybrid electrodes have high theoretical capacitance and energy density. However, the origin of the electrochemical storage mechanism still remains elusive in alkaline, acid and neutral electrolytes. Herein, the interstratification-assembled Ti₃C₂T_x MXene/NiCo-LDHs electrodes were successfully prepared and studied in different electrolytes by in-situ Raman spectroscopy. The results show that H₂O molecules in neutral electrolyte combine with –OH at the end of Ti₃C₂T_x MXene during charging, and debonding occurs during discharge. Similarly, this reaction also occurs in the discharge process with NiCo-LDHs and provides smaller pseudocapacitance characteristics. Although this pseudocapacitance reaction also occurs in acidic and alkaline electrolytes, however, the difference is that the hydrogen ions will promote the electrochemical performance of Ti₃C₂T_x MXene and has a certain corrosion consumption effect on NiCo-LDHs, but generally improve the electrochemical performance of Ti₃C₂T_x MXene/NiCo-LDHs. Interestingly, the OH^? in alkaline electrolyte can promote the electrochemical performance of NiCo-LDHs, and produce a new electrochemical reaction with –F between the layers of Ti₃C₂T_x MXene, which greatly improves the overall electrochemical performance of this hybrid electrodes. As a result, Ti₃C₂T_x MXene/NiCo-LDHs electrodes have the best electrochemical performance in alkaline electrolyte with capacitance of 283 F g^?1, energy density of 14.2 Wh kg^?1 and power density of 3007.1 W kg^?1. This work lays a foundation for the preparation of high-performance two-dimensional hybrid electrochemical energy storage devices.     

Multi-phase heterostructures of flower-like Ni(NiO) decorated on two-dimensional Ti3C2Tx/TiO2 for high-performance microwave absorption properties

Three-dimensional flower-like Ni(NiO) decorated on two-dimensional Ti₃C₂T_x/TiO₂ composites were successfully synthesized by an in situ solvothermal reaction, and the electromagnetic (EM) wave absorption performance of the hybrids were explored at 2.00–18.00 GHz. The as-prepared Ni(NiO)/Ti₃C₂T_x/TiO₂ composites include flower-like Ni(NiO) with uniform distribution on the surface of Ti₃C₂T_x MXenes and part of them get into the space between interlayers. The Ni(NiO)/Ti₃C₂T_x/TiO₂ composites exhibit a maximum reflection loss (RL) value of ?41.74 dB at 14.96 GHz with the absorber thickness of merely 1.3 mm and the effective absorption bandwidth (EAB) reaches 3.20 GHz. The outstanding electromagnetic wave absorbing performance can be attributed to the dielectric loss of Ti₃C₂T_x MXenes and multi-phase heterostructures, the magnetic loss of Ni(NiO) and their synergistic loss mechanism. Moreover, the zigzag path formed by flower-like Ni(NiO) also has a great consumption effect on electromagnetic waves by incurring the eddy current under the affect of alternating EM waves. The laminated structure of Ti₃C₂T_x MXenes also dissipates microwaves by offering the space for multiple reflections and scattering. This paper furnished a novel modus for synthesizing original EM wave absorption materials and making the balance among thickness, broad bandwidth, oxidation resistance and light weight, which makes Ni(NiO)/Ti₃C₂T_x/TiO₂ composites a hopeful material for microwave absorption (MA).     

2D/2D SnO2 nanosheets/Ti3C2Tx MXene nanocomposites for detection of triethylamine at low temperature

Highly active two-dimensional (2D) nanocomposites have been widely concerned in the field of gas sensors because of their unique advantages and synergistic effects. 2D/2D SnO₂ nanosheets/Ti₃C₂T_x MXene nanocomposites were synthesized by using layered Ti₃C₂T_x MXene and uniform SnO₂ nanosheets by hydrothermal method. Characterization results show that the SnO₂ nanosheets are well dispersed and vertically anchored on the layered Ti₃C₂T_x MXene surface, forming heterogeneous interfaces. Based on the gas-adsorption capabilities and synergistic effects of electronic properties, SnO₂ nanosheets/Ti₃C₂T_x MXene nanocomposites show high triethylamine (TEA) gas-sensing performance at low temperature (140 °C). The sensor responses of the nanocomposites and pure SnO₂ nanosheets to 50 ppm of TEA are 33.9 and 3.4, respectively. An enhancement mechanism for SnO₂ nanosheets/Ti₃C₂T_x MXene nanocomposites is proposed for highly sensitive and selective detection of TEA at low temperature. The combination strategy of two-dimensional metal oxide semiconductor and multilayer MXene provides a new way for the development of cryogenic gas sensors in the future.     

In2O3 nanocubes/Ti3C2Tx MXene composites for enhanced methanol gas sensing properties at room temperature

Highly active two-dimensional (2D) nanocomposites, integrating the unique merits of individual components and synergistic effects of composites, have been recently receiving attention for gas sensing. In this work, In₂O₃ nanocubes/Ti₃C₂T_x MXene nanocomposites were synthesized using In₂O₃ nanocubes and layered Ti₃C₂T_x MXene via a facile hydrothermal self-assembly method. Characterization results indicated that the In₂O₃ nanocubes with sizes approximately 20–130 nm in width were well dispersed on the surface of layered Ti₃C₂T_x MXene to form numerous heterostructure interfaces. Based on the synergistic effects of electronic properties and gas-adsorption capabilities, In₂O₃ nanocubes/Ti₃C₂Tx MXene nanocomposites exhibited high response (29.6%–5 ppm) and prominent selectivity to methanol at room temperature. Meanwhile, the low detection concentration could be reduced to ppm-level, the response/recovery times are shortened to 6.5/3.5 s, excellent linearity and outstanding repeatability. The strategy of compositing layered MXene with metal oxide semiconductor provides a novel pathway for the future development of room temperature gas sensors.     

Ti3C2Tx-coated diatom frustules-derived porous SiO2 composites with high EMI shielding and mechanical properties

Effective electromagnetic interference (EMI) shielding materials have garnered substantial interest for their efficacy in attenuating electromagnetic wave energy, ensuring data confidentiality, ensuring the operational stability of fragile electronic systems. To begin, artificially cultured diatom frustules (DF)-derived porous silica (DFPS) skeletons were constructed as templates in this study. Porous ceramics hot-pressed at 800 °C displayed a high compressive strength with a high specific surface area due to their three-dimensional (3D) multilayered and porous structures. Then, mechanically robust Ti₃C₂T_x/DFPS composites with exceptional EMI shielding performance were fabricated by immersing porous DF-based ceramics into Ti₃C₂T_x solutions and annealing in an argon environment to increase the materials’ shielding efficiency (SE). The EMI SE of composites hot-pressed at 800 °C achieved the maximum EMI SE of 43.2 dB in the X-band and a compressive strength of 67.5 MPa, establishing a hitherto unreported balance of mechanical characteristics and shielding performance. Prolonged transmission paths, multiple dissipation, scattering and reflection of electromagnetic energy were achieved using a well-maintained hierarchical porous silica framework decorated with MXene, with adsorption caused by surface MXene serving as the primary shielding mechanism for the composites. Due to their superior overall performance, MXene/DFPS EMI shielding composites have a bright future in the aircraft sector as delicate electronic device components.     

Improvement of gas sensing property for two-dimensional Ti3C2Tx treated with oxygen plasma by microwave energy excitation

Two-dimensional layered Ti₃C₂T_x MXene was prepared through hydrothermal etching method with LiF and hydrochloric (HCl) acid. Ti₃C₂T_x was further treated with oxygen plasma activated by microwave energy to obtain the activated Ti₃C₂T_x at different temperatures ranging from 350 °C to 550 °C. The gas-sensing properties of raw Ti₃C₂T_x and Ti₃C₂T_x activated with oxygen microwave plasma were tested toward different volatile organic compounds gases. The results indicated that Ti₃C₂T_x activated at 500 °C exhibited excellent gas-sensing properties at room temperature (25 °C) to 100 ppm ethanol with a value of 22.47, which is attributed to the enhancement of the amount of oxygen functional groups and defects on the MXene Ti₃C₂T_x film, and in turn to lead to more oxygen molecules adsorption and desorption reaction in the active defect sites. The enhancement of ethanol-sensing performance demonstrated that the activated Ti₃C₂T_x possess great potential in gas sensing.     

Multilayer Ti3C2Tx: From microwave absorption to electromagnetic interference shielding

Ti₃C₂T_x MXene has attracted extensive attention in the field of electromagnetic (EM) protection over recent years. Multilayer Ti₃C₂T_x (M-Ti₃C₂T_x), as an intermediate product of MXene ultra-thin structure, has potential advantages in the field of EM protection. Herein, the M-Ti₃C₂T_x was obtained by HCl/LiF etching Ti₃AlC₂. The microwave absorption (MA) and electromagnetic interference (EMI) shielding performance of Ti₃AlC₂ and M-Ti₃C₂T_x were compared. The mechanism research of MA and EMI shielding indicates that the construction of local conductive network plays a leading role in the EM wave attenuation. The sample with 30% M-Ti₃C₂T_x display RL_min of ?50.26 dB, and corresponding bandwidth of 4.64 GHz at the thickness of 1.7 mm. Especially, the metastructure based on the EM parameters of M-Ti₃C₂T_x/wax exhibits ultra-wide bandwidth (15.54 GHz). Our research will provide a basis for the design of MXene-based EM protection performance.     

Dielectric Characteristics of UV‐Curable CaCu3Ti4O12 Composite Thick Film Capacitors on Cu Foils

Dielectric composite thick films containing a high dielectric constant CaCu₃Ti₄O₁₂ (CCTO) filler in a UV‐cured polymer matrix were investigated as flexible planar capacitors on Cu foils. Dielectric performance depended on the volume fraction and size of CCTO particles dispersed in the cured polymer matrix. As a result, the thick films containing 33.3 vol.% CCTO with an average particle size of 0.47 μm exhibited a dielectric constant of ~80 and a dielectric loss of ~0.06 at 10 kHz. The effective medium theory model incorporating a morphology fitting parameter has been proven to be most close to the experimental values.     

Enhanced dielectric response of ternary polymeric composite films via interfacial bonding between V2C MXene and wide-bandgap ZnS

Increasing the dielectric constant of polymer/sulfide ceramic composites by using wide-bandgap semiconducting sulfide ceramic fillers like ZnS is difficult because of their low interface polarization. To increase the dielectric constant, in this study, ternary polymer-based composite films were designed and fabricated using a hybrid filler consisting of shell-like ZnS particles and core-like V₂C MXene particles. First, V₂C MXene with a multi-layered structure was synthesized from the simplest raw materials followed by the in-situ hydrothermal growth of ZnS particles around the V₂C particles. Then, binary polymer/ZnS and ternary polymer/V₂C–ZnS composites were fabricated, and their dielectric, conductive, and electrical breakdown properties were investigated. Finally, the effect of interfacial bonding between the V₂C and ZnS phases was investigated by density functional theory calculations, and the contribution of V₂C/ZnS interfacial bonding to the higher dielectric constant of the ternary composites than that of the binary composites was explained. The ternary composites exhibited balanced electrical properties suitable for energy storage applications. The ternary composite with 10 wt% hybrid filler loading exhibited a high dielectric constant of ~52, a low dielectric loss of ~0.11 at 100 Hz, and a high electrical breakdown strength of ~202 MV m⁻¹. This study paves the way for the facile fabrication of high-performance composite dielectrics for application in advanced capacitors.     

In-situ growth of bamboo-shaped carbon nanotubes and helical carbon nanofibers on Ti3C2Tx MXene at ultra-low temperature for enhanced electromagnetic wave absorption properties

The potential of two-dimensional layered MXenes in electromagnetic wave (EMW) absorption needs further development. Herein, we carried out the in situ growth of carbon nanotubes (CNTs) on the surface of Ti₃C₂T_x MXene at ultra-low temperature via chemical vapor deposition. The obtained CNTs exhibited a bamboo-like structure and were accompanied by helical carbon nanofibers. The ultra-low temperature solved the problem that the high temperature required in the traditional CNT growth process would destroy the structural integrity of MXene. The lush CNT forest cross-linked the MXene layers, transforming the two-dimensional layered structure into a three-dimensional conductive network, providing abundant conductive channels for carriers, optimizing the impedance matching of the CNT/MXene hybrid, and resulting in a significant dielectric loss. The as-prepared CNT/MXene hybrid exhibited a minimal reflection loss of ?52.56 dB (99.9994% EMW absorption) in the X-band. This work proposes a new idea to enhance the EMW absorption properties of Ti₃C₂T_x MXene and fabricate high-performance MXene-based EMW absorbers.     

Synthesis,characterization and antifungal property of Ti3C2Tx MXene nanosheets

Although the antibacterial properties of MXene nanosheets containing Ti₃C₂T_x are known, their antifungal properties have not been well studied. Herein, we present for the first time a report on the antifungal properties of Ti₃C₂T_x MXene. The Ti₃C₂T_x MXene was obtained by first exfoliating MAX phase of Ti₃AlC₂ with concentrated hydrofluoric acid, then the Ti₃C₂T_x was intercalated and deliminated by ethanol treatment and ultrasonication process. The delaminated Ti₃C₂T_x MXene nanosheets (d-Ti₃C₂Tx) were characterized using field emission scanning electron microscopy (FE-SEM), energy dispersive X-ray (EDX), X-ray diffraction spectroscopy (XRD), and Raman spectroscopy. It was found that Ti₃C₂T_x MXene was characterized by lamellar structure alternating with layers of Ti, Al and C. The EDX results revealed that the delaminated Ti₃C₂T_x MXene nanosheets were composed of Ti, C, Si, O, F, and a trace amount of Al. The XRD and Raman spectra further indicated the elimination of Al and the formation of two-dimensional Ti₃C₂T_x MXene nanosheets. The antifungal activity of the delaminated Ti₃C₂T_x MXene was determined against Trichoderma reesei using the modified agar disc method. Observation using inverted phase contrastmicroscopy revealed inhibited fungus growth with the absence of hyphae around the discs treated wtih MXene. The surrounding of the control groups without an inclusion of MXene was found with large number of hyphae and spores. In addition, the spores of the fungi treated with the samples containing d-Ti₃C₂T_x MXene nanosheets did not germinate even after 11 days of culture. The results demonstrated disruption to the hemispheric structural formation of fungi colony, inhibition of hyphae growth and cell damage for fungi grown on the d-Ti₃C₂T_x MXene nanosheets. These new findings suggest that d-Ti₃C₂T_x MXene nanosheets developed in this work could be a promising anti-fungi material.     

Ti3C2Tx aerogel with 1D unidirectional channels for high mass loading supercapacitor electrodes

As one of the typical MXenes materials, 2D Ti₃C₂T_x has attracted extensive attention in the field of energy storage. However, due to the restacking problem of Ti₃C₂T_x nanosheets, the electrochemical performance of Ti₃C₂T_x is unsatisfactory. In this paper, a scheme is proposed to obtain 3D aerogel with 1D channels by directional freeze drying of Ti₃C₂T_x. With the help of the unidirectional channels, the 3D Ti₃C₂T_x/Sodium alginate (SA) aerogel can effectively solve the stacking problem of Ti₃C₂T_x nanosheets, and it also accelerates the diffusion of ions. The Ti₃C₂T_x/SA-5 electrode can still reach the mass capacitance of 284.5 F g^?1 and the areal capacitance of 4030.4 mF cm^?2 at 2 mV s^?1 when the loading is 14.2 mg cm^?2 in 1 M H₂SO₄ electrolyte. In addition, the electrode showed good cycling performance without capacitor degradation after 20,000 cycles at 50 mV s^?1. These results suggest that by using the strategy of building special 3D structure of 2D MXene with 1D unidirectional channels, high performance supercapacitor electrodes with high mass loading can be realized.     

The multiple synthesis of 2D layered Ti3C2Tx/Ag/MWCNTs/Ag composites with enhanced electrochemical properties

MXene, a novel two-dimensional material composed of alternating transition metal carbon/nitrogen, has the advantages of large specific surface area, many active sites, and short ion transport paths, and has shown great potential in the field of capacitors in the beginning. However, the unique two-dimensional structure is prone to collapse and accumulation, which inhibits the electron migration rate and ion penetration, resulting in poor energy storage capacity. In this paper, Ti₃C₂T_x/Ag/MWCNTs/Ag composites with good capacitive properties were successfully prepared by Ti₃C₂T_x which directly reduces silver nitrate solution and further introduces nanoscale MWCNTs. Ag NPs are introduced twice to grow and distribute uniformly on the surface and between the layers of Ti₃C₂T_x to play a supporting role. The introduction of MWCNTs in the intermediate process can enter the interlayer and act as spacers together with Ag NPs to prevent the collapse and stacking of Ti₃C₂T_x and improve its surface utilization. However, the preparation process unavoidably leads to partial oxidation of Ti₃C₂T_x, which deteriorates its electrochemical properties. Owing to the synergy between Ti₃C₂T_x, Ag NPs and MWCNTs, the Ti₃C₂T_x/Ag/MWCNTs/Ag composites show good electrical conductivity, low internal resistance (0.67 Ω) and extreme high capacitance contribution (97%) in electrochemical tests.