Ti3C2Tx Film Research Articles

Thermoelectric Modulation of Neat Ti3C2Tx MXenes by Finely Regulating the Stacking of Nanosheets

Emerging two-dimensional MXenes have been extensively studied in a wide range of fields thanks to their superior electrical and hydrophilic attributes as well as excellent chemical stability and mechanical flexibility. Among them, the ultrahigh electrical conductivity (σ) and tunable band structures of benchmark Ti3C2Tx MXene demonstrate its good potential as thermoelectric (TE) materials. However, both the large variation of σ reported in the literature and the intrinsically low Seebeck coefficient (S) hinder the practical applications. Herein, this study has for the first time systematically investigated the TE properties of neat Ti3C2Tx films, which are finely modulated by exploiting different dispersing solvents, controlling nanosheet sizes and constructing composites. First, deionized water is found to be superior for obtaining closely packed MXene sheets relative to other polar solvents. Second, a simultaneous increase in both S and σ is realized via elevating centrifugal speed on MXene aqueous suspensions to obtain small-sized nanosheets, thus yielding an ultrahigh power factor up to ~ 156μWm-1K-2. Third, S is significantly enhanced yet accompanied by a reduction in σ when constructing MXene-based nanocomposites, the latter of which is originated from the damage to the intimate stackings of MXene nanosheets. Together, a correlation between the TE properties of neat Ti3C2Tx films and the stacking of nanosheets is elucidated, which would stimulate further exploration of MXene TEs.

(Invited) Mechanical Suppression of Electron Transfer in Subnanometer Confinement between MXene Layers

Ion adsorption and electron transfer are the primary charge storage mechanisms in porous electrodes. Desolvation/solvation of ions in subnanometer confinement may alter the balance between those two processes. For 2D materials like MXenes, there is a continuous change in interlayer spacing as ions are transported and stored between the layers. However, little is known about the effect of the mechanical constraint (pressure) on electrochemistry in confinement. In this work, the ion transportation process in between mechanically constrained MXene layers is monitored by combining in-situ UV-vis spectroscopy, in-situ optical spectroscopy, and in-situ XRD characterization. Compared with spray-coated Ti3C2Tx films, physically constrained Ti3C2Tx film with a constant interlayer spacing exhibited exceptional capabilities in suppressing redox reactions. Notably, this property of faradaic suppression under mechanical strain led to the application of MXene-based electrochemical cells as high-pressure electrochemical sensors.

Laser exfoliated 2D MXene for supercapacitor applications

Laser exfoliated 2D MXene for supercapacitor applications

Significantly enhanced electrochemical performance of Al-Ti3C2Tx MXene synthesized from Al-Ti3AlC2 MAX phase

Significantly enhanced electrochemical performance of Al-Ti3C2Tx MXene synthesized from Al-Ti3AlC2 MAX phase

Unveiling the potential: Asymmetric supercapacitors with conductive polymers/Ti3C2Tx/Ni3S4 electrodes deliver high energy densities

Unveiling the potential: Asymmetric supercapacitors with conductive polymers/Ti3C2Tx/Ni3S4 electrodes deliver high energy densities

Flexible Ti3C2Tx-Polyurethane Electrodes for Versatile Wearable Applications.

With the development of science and technology, wearable electronics are increasingly widely used in medical, environmental monitoring, and other fields. Thus, the demand for flexible electrodes is increasing. The two-dimensional material Ti3C2Tx has attracted much attention in the manufacture of flexible electrodes due to its excellent mechanical and electrical properties. However, the brittleness of pure Ti3C2Tx films has become a major obstacle for their use as flexible electrodes in wearable devices. Therefore, solving the brittleness problem of flexible electrodes based on Ti3C2Tx while maintaining the excellent performance of Ti3C2Tx has become an urgent problem. To solve this problem, Ti3C2Tx was compounded with waterborne polyurethane (WPU), and a Ti3C2Tx-WPU composite film with a hierarchical structure was constructed by evaporation-assisted self-assembly. The Ti3C2Tx-WPU composite film not only retains the excellent electrical conductivity of Ti3C2Tx (100 S m-1) but also has flexibility (20 MJ m-3). Furthermore, the Ti3C2Tx-WPU composite film is applied to functional devices such as contact pressure sensors and non-contact proximity sensors. Finally, the Ti3C2Tx-WPU composite film wearable device demonstrates its practical application potential in the field of wearable devices.

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 5mV⋅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 5mV⋅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.

Wafer-Scale Transfer of MXene Films with Enhanced Device Performance via 2D Liquid Intercalation.

Wafer-scale transfer processes of 2D materials significantly expand their application space in scalable microelectronic devices with excellent and tunable properties through van der Waals (vdW) stacking. Unlike many 2D materials, wafer-scale transfer of MXene films for vdW contact engineering has not yet been reported. With their rich surface chemistry and tunable properties, the transfer of MXenes can enable enormous possibilities in electronic devices using interface engineering. Taking advantage of the MXene hydrophilic surface, a straightforward, green, and fast process for the transfer of MXene films at the wafer scale (4-inch) is developed. Uniform vdW stacking of several types of large-area heterojunctions including MXene/MXene (Ti3C2Tx, Nb2CTx, and V2CTx), MXene/MoS2, and MXene/Au is further demonstrated. Multilayer support is applied to minimize damage or deformation in the transfer process of patterned Ti3C2Tx film. It allows us to fabricate thin film transistors and manipulate the MXene/MoS2 interface through the intercalation of various 2D liquids. Particularly noteworthy is the significant enhancement of the interfacial carrier transfer efficiency by ≈2 orders of magnitude using hydrogen iodide (HI) intercalation. This finding indicates a wide range of possibilities for interface engineering by transferring MXene films and employing liquid-assisted interfacial intercalation.

Ti3C2Tx Electromagnetic Shielding Performance: Investigating Environmental Influences and Structural Changes

AbstractMXenes, a promising family of 2D transition metal carbides/nitrides, are renowned for their exceptional electronic conductivity and mechanical stability, establishing them as highly desirable candidates for advanced electromagnetic interference (EMI) shielding material. Despite these advantages, challenges persist in optimizing MXene synthesis methods and improving their oxidation resistance. Surface defects on MXenes significantly impact their electronic properties, impeding charge transport and catalyzing the oxidation process. In this study, a novel synthesis protocol derived from the conventional, minimally invasive layer delamination (MILD) method, is presented. Two additional steps are introduced aiming at enhancing process yield, addressing a crucial issue as conventional methods often yield high‐quality individual MXene flakes but struggle to generate sufficient quantities for bulk material production. This approach successfully yields Ti3C2Tx films with excellent conductivity (3973.72 ±121.31 Scm−1) and an average EMI shielding effectiveness (SE) of 56.09 ± 1.60 dB within the 1.5 to 10 GHz frequency range at 35% relative humidity (RH). Furthermore, this investigation delves into the long‐term oxidation stability of these films under varying RH conditions. These findings underscore the effectiveness of this innovative synthesis approach in elevating both the conductivity and EMI shielding capabilities of MXene materials. This advancement represents a significant step toward harnessing MXenes for practical applications requiring robust EMI shielding solutions. Additionally, insights into long‐term stability offer critical considerations for implementing MXenes in real‐world environments.

Surface functional group regulation of Ti3C2Tx based on atmospheric pressure cold plasma

AbstractThe modulation of surface properties of Ti3C2Tx plays a crucial role in its diverse applications across various fields. However, a straightforward and reliable technique for controlling its surface functional groups remains elusive. In this study, we achieved controlled modification of Ti3C2Tx surface functional groups using atmospheric‐pressure cold plasma. We evaluated the plasma generation characteristics and found that the gas parameters could influence the discharge power and lead to different gas temperatures with the same voltage. Spectral analysis confirmed the presence of numerous reactive species in the plasma, facilitating the breaking and recombination of chemical bonds of functional groups on the Ti3C2Tx surface. The interaction between the plasma jet and Ti3C2Tx film revealed that the semiconductor properties of the Ti3C2Tx film limit the plasma diffusion area, while N2 doping and increased gas flow rates respectively reduce and enlarge the coverage area of cold plasma. A brief one‐minute cold plasma treatment induced a slight etching effect on the Ti3C2Tx film surface, effectively altering the ‐O and ‐F functional groups. However, it is noteworthy that excessive cold plasma treatment in the air may result in partial oxidation of Ti3C2Tx, necessitating the use of custom gas environments in further applications. This research provides valuable insights into surface modification techniques for Ti3C2Tx with potential implications in a wide range of applications.

3D isotropic MXene films enabling minimized polarization for enhanced sodium-ion storage performance

3D isotropic MXene films enabling minimized polarization for enhanced sodium-ion storage performance

One-step synthesizing Ti3C2Tx doped with slight amount of Ni2+ to enhance the electrochemical stability

One-step synthesizing Ti3C2Tx doped with slight amount of Ni2+ to enhance the electrochemical stability

Pristine Ti3C2Tx MXene Enables Flexible and Transparent Electrochemical Sensors.

In the era of the internet of things, there exists a pressing need for technologies that meet the stringent demands of wearable, self-powered, and seamlessly integrated devices. Current approaches to developing MXene-based electrochemical sensors involve either rigid or opaque components, limiting their use in niche applications. This study investigates the potential of pristine Ti3C2Tx electrodes for flexible and transparent electrochemical sensing, achieved through an exploration of how material characteristics (flake size, flake orientation, film geometry, and uniformity) impact the electrochemical activity of the outer sphere redox probe ruthenium hexamine using cyclic voltammetry. The optimized electrode made of stacked large Ti3C2Tx flakes demonstrated excellent reproducibility and resistance to bending conditions, suggesting their use for reliable, robust, and flexible sensors. Reducing electrode thickness resulted in an amplified faradaic-to-capacitance signal, which is advantageous for this application. This led to the deposition of transparent thin Ti3C2Tx films, which maintained their best performance up to 73% transparency. These findings underscore its promise for high-performance, tailored sensors, marking a significant stride in advancing MXene utilization in next-generation electrochemical sensing technologies. The results encourage the analytical electrochemistry field to take advantage of the unique properties that pristine Ti3C2Tx electrodes can provide in sensing through more parametric studies.

Human-friendly flexible solid-state biodegradable supercapacitor based on Ti3C2Tx MXene film without adhesive structure

Human-friendly flexible solid-state biodegradable supercapacitor based on Ti3C2Tx MXene film without adhesive structure

Laser-assisted exfoliation of Ti3C2Tx.

As an emerging two-dimensional material, MXene has shown a wide range of applications, which has triggered the demand for efficient exfoliation of nanoflakes with large size and specific surface area. Here, we took advantage of the efficient photo-thermal conversion of Ti3C2Tx and employed 532 nm continuous wave laser irradiation to assist the traditional ultrasonic exfoliation, with no need for complex equipment and an expensive femtosecond or picosecond laser. This approach greatly improves the exfoliation efficiency, increases the size, uniformity and specific surface area of the Ti3C2Tx nanoflakes, and reduces energy consumption as well. The electrical conductivity of Ti3C2Tx film is also significantly enhanced (from 3135 to 7433 S m-1). It is demonstrated that the laser promotes the formation of Ti-OH and enhances the solubility of Ti3C2Tx in water, facilitating the exfoliation and preventing oxidation as a result.

Molten salt-shielded synthesis of Ti3AlC2 as a precursor for large-scale preparation of Ti3C2Tx MXene binder-free film electrode supercapacitors.

MXenes are a group of two-dimensional materials that are promising for many applications, including as film electrode supercapacitors. When synthesizing such materials, special attention is paid to the conditions for obtaining the MAX phase, the chemical, morphological and structural features of which determine the functional properties of the final product. In this study, the Ti3AlC2 precursor is proposed to be obtained using a technologically simple and accessible method of synthesis in molten salt. This method allows reducing the reaction temperature and creating an antioxidant atmosphere. Ti3C2Tx MXene electrode films are produced by the easily scalable blade coating method without a binder. The synthesized materials were studied by X-ray phase analysis and scanning electron microscopy. Electrochemical testing of Ti3C2Tx film electrodes was carried out in a three-electrode configuration in aqueous solutions of 1M H2SO4, 6M KOH, 1M LiOH and 1M Na2SO4 electrolytes. The maximum specific capacity value for Ti3C2Tx MXene binder-free film electrode supercapacitors is obtained in 1M H2SO4 electrolyte (480 F g-1 at a scan rate of 1 mV s-1). The simple, low-cost and scalable production technology and promising electrochemical characteristics of the Ti3C2Tx MXene binder-free film electrode make it an excellent candidate for new-generation supercapacitors.

Investigation on high EMI shielding effectiveness and shielding mechanism of spherical Ti3C2Tx microfilm prepared by spray-freezing

Investigation on high EMI shielding effectiveness and shielding mechanism of spherical Ti3C2Tx microfilm prepared by spray-freezing

Diffusion kinetics of ionic charge carriers across Ti3C2Tx MXene-aqueous electrochemical interfaces

Diffusion kinetics of ionic charge carriers across Ti3C2Tx MXene-aqueous electrochemical interfaces

Ultrathin MXene film interaction with electromagnetic radiation in the microwave range

The quick progress in communication technologies demands superior electromagnetic interference (EMI) shielding materials. However, achieving a high shielding effectiveness (SE) with thin films, which is needed for microscale, flexible, and wearable devices, through absorption of EM radiation remains a challenge. 2D titanium carbide MXene, Ti3C2Tx, has been shown to efficiently reflect electromagnetic waves. In this paper, we investigated the electromagnetic shielding of ultrathin printed Ti3C2Tx films and recorded absorption up to 50% for 4 nm-thick films. This behavior is explained by impedance matching. Analysis of the sheet impedance in the X-band frequency range allows us to correlate the EMI shielding mechanism with the electrical conductivity measured within the same range. The average bulk in-plane conductivity for 4 to 40 nm-thick films reaches 106 S/m, while the average relaxation time is estimated at around 2.3 ps. Our figures of merit are similar to those reported for ultrathin metal films, such as gold, showing that an abundant MXene material can replace noble metals. We demonstrate that the MXene conductivity mechanism does not change from direct current to THz. The conventional method of reporting EMI SE is correlated with absolute values of transmitted, reflected, and absorbed power, which allows us to interpret previous results on MXene EMI shielding. Considering the easy deposition of thin MXenes films from solution onto a variety of surfaces, our findings offer an attractive alternative for shielding microscale devices and personal electronics.

An Ultra-Thin MXene Film for Multimodal Sensing of Neuroelectrical Signals with Artifacts Removal.

Neuroelectrical signals transmitted onto the skin tend to decay to an extremely weak level, making them highly susceptible to interference from the environment and body movement. Meanwhile, for comprehensively understanding cognitive nerve conduction, multimodal sensing of neural signals, such as magnetic resonance imaging (MRI) and functional near-infrared spectroscopy (fNIRS), is highly required. Previous metal or polymer conductors cannot either provide a seamless on-skin feature for accurate sensing of neuroelectrical signals or be compatible with multimodal imaging techniques without opto- and magnet- artifacts. Herein, a ≈20nm thick MXene film that is able to simultaneously detect electrophysiological signals and perform imaging by MRI and fNIRS with high fidelity is reported. The ultrathin film is made of crosslinked Ti3 C2 Tx film via poly (3,4-ethylene dioxythiophene): polystyrene sulfonate (PEDOT:PSS), showing a record high electroconductivity and transparency combination (11000Scm-1 @89%). Among them, PEDOT: PSS not only plays a cross-linking role to stabilize MXene film but also shortens the interlayer distance for effective charge transfer and high transparency. Thus, it can achieve a low interfacial impedance with skin or neural surfaces for accurate recording of electrophysiological signals with low motion artifacts. Besides, the high transparency originating from the ultrathin feature leads to good compatibility with fNIRS and MRI without optical and magnetic artifacts, enabling multimodal cognitive neural monitoring during prolonged use.