Ti3C2Tx MXene Research Articles

Stretchable supramolecular hydrogel with instantaneous self-healing for electromagnetic interference shielding control and sensing

Conductive hydrogels possess instantaneous self-healing and adhesive properties have generated great excitement in the fields of sensing and electromagnetic interference (EMI) shielding. In this study, we ingeniously designed hydrogel-based soft materials with high conductivity by using poly(vinyl alcohol) (PVA), positively charged Ti3C2Tx MXene and thioctic acid (TA) as source materials. Through concentration-induced ring-opening polymerization of TA monomers in an aqueous solution of potassium hydroxide (KOH), supramolecular poly(potassium thioctate) (poly(PT)) was obtained. Then, the multifunctional poly(PT)/PVA/p-MXene hydrogel with exceptional stretchability, substrate-adhesion and self-healing capability was achieved through abundant dynamic bonds, including disulfide bonds, hydrogen bonds, coordination bonds and electrostatic interactions. The hydrophobic main chains within poly(PT) provide robust protection against the oxidative degradation of MXene. This hydrogel shows outstanding strain sensing and extraordinary EMI shielding effectiveness (SE) of 48.56 dB caused by the inner structure, conductivity, and water content. Interestingly, the EMI SE can be regulated by reabsorbing moisture from the air, thereby enabling the reuse of dried hydrogel. Furthermore, the EMI SE can be dynamically modulated through controlled deformations, confirming the potential application for electromagnetic waves (EMWs) sensing. This innovative approach not only simplifies the fabrication of multifunctional materials but also expands the applications of adhesive hydrogels with conductivity.

Multifunctional 1D/2D silver nanowires/MXene-based fabric strain sensors for emergency rescue

Abstract Monitoring the vital signs of the injured in accidents is crucial in emergency rescue process. Fabric-based sensing devices show a vast range of potential applications in wearable healthcare monitoring, human motion and thermal management due to their wearable flexibility and high sensitivity. Nevertheless, flexible electronic devices for both precise monitoring of health under low strain and motion under large strain are still a challenge in extremely harsh environment. Therefore, development of sensors with both high sensitivity and wide strain range remains a formidable challenge. Herein, a wearable flexible strain sensor with a one-dimensional/two-dimensional (1D/2D) composite conductive network was developed for healthcare and motion monitoring and thermal management by coating 1D silver nanowires (AgNWs) and 2D Ti3C2Tx MXene composite films on nylon/spandex blended knitted fabric (MANS). The MANS strain sensor can simultaneously achieve high sensitivity (gauge factor for up to 267), a wide range of detection (1–115%), excellent repeatability and cycling stability (1000 cycles). The sensor can be utilized for human health monitoring including heartbeat, pulse detection, breathing and various human motion. Moreover, the MANS sensor also has the electrical heating properties and voltage control temperature between 20-110 °C can achieved at low voltage. In addition, the MANS shows hydrophobicity with water contact angle of 137.1°. The MXene/AgNWs composite conductive layer with high sensitivity under low and large strains, electrical thermal conversion, and hydrophobicity has great potential for precisely monitoring health and motion of the injured in emergency rescue in harsh environment.

Efficient degradation of tetracycline by cobalt ferrite modified alkaline solution nanofibrous Ti3C2Tx MXene activated peroxymonosulfate system: Mechanism analysis and pathway

Magnetic CoFe2O4 nanoparticles have received considerable attention as an activator for peroxymonosulfate (PMS) in the degradation of tetracycline. However, it is still challenging to construct CoFe2O4 composites with good dispersion and highly exposed reactive sites. Herein, the KOH fiber-functionalized MXene matrix decorated by cobalt ferrite nanoparticles (denoted as CoFe2O4@Alk-MXene) was developed by electrostatic self-assembly method. The layered fibrotic structure effectively disperses and fixes cobalt ferrite nanoparticles, increasing the exposure of reactive sites. The as-prepared CoFe2O4@Alk-MXene material exhibited rapid removal of 100% tetracycline hydrochloride (TC-HCl) within 10 minutes by activating PMS, leveraging the excellent conductivity of alkalized MXene and the efficient activation of transition metal atoms. The experimental and theoretical analysis revealed that the electron transfer process of Ti2+/Ti4+, Co2+/Co3+ and Fe3+/Fe2+, as well as the free radical and non-free radical attack behaviors produced by the adsorption of PMS by the composite, are the primary mechanisms for achieving rapid removal of pollutants. A comprehensive degradation mechanism and potential pathways were proposed based on these findings. Overall, CoFe2O4@Alk-MXene/PMS emerges as a promising catalytic system for TC removal.

Ultrathin 2D-2D MXene-LDH Interlayer with High Polysulfide Adsorption Ability for Advanced Li-S Batteries.

Lithium-sulfur (Li-S) batteries are considered as promising energy storage systems due to the high energy density of 2600 W h kg-1. However, the practical application of Li-S batteries is hindered by the inadequate conductivity of sulfur and Li2S, as well as the shuttle effect caused by polysulfides during the charge-discharge process. Introducing a conductive interlayer between the cathode and the separator to physically resist polysulfides represents an effective and straightforward approach to mitigate the shuttle effect in Li-S batteries. In this paper, an ultrathin (<1 μm) 2D-2D MXene-LDH interlayer with high polysulfide adsorption ability was introduced to Li-S batteries. The synergistic effect between MXene and layered double hydroxide greatly improved the adsorption effect of the interlayers: the conductive Ti3C2Tx MXene chemically adsorbs polysulfides and promotes their fast transfer, and the NiCo-LDH alleviates the restack of MXene and facilitates Li+ diffusion. After inserting the MXene-LDH interlayer, the Li-S batteries exhibit an enhanced specific capacity of 1137.6 mA h g-1 at 0.1 C and retain 622.6 mA h g-1 after 100 cycles. The ultrathin 2D-2D interlayer offers a feasible way for the development of highly efficient and lightweight interlayers in Li-S batteries.

Pushing Theoretical Potassium Storage Limits of MXenes through Introducing New Carbon Active Sites.

Surface-driven capacitive storage enhances rate performance and cyclability, thereby improving the efficacy of high-power electrode materials and fast-charging batteries. Conventional defect engineering, widely-employed capacitive storage optimization strategy, primarily focuses on the influence of defects themselves on capacitive behaviors. However, the role of local environment surrounding defects, which significantly affects surface properties, remains largely unexplored for lack of suitable material platform and has long been neglected. As proof-of-concept, typical Ti3C2Tx MXenes are chosen as model materials owing to metallic conductivity and tunable surface properties, satisfying the requirements for capacitive-type electrodes. Using density functional theory (DFT) calculations, the potential of MXenes with modulated local atomic environment is anticipated and introducing new carbon sites found near pores can activate electrochemically inert surface, attaining record theoretical potassium storage capacities of MXenes (291 mAh g-1). This supposition is realized through atomic tailoring via chemical scissor within sublayers, exposing new sp3-hybridized carbon active sites. The resulting MXenes demonstrate unprecedented rate performance and cycling stability. Notably, MXenes with higher carbon exposure exhibit a record-breaking capacity over 200 mAh g-1 and sustain a capacity retention higher than 80% after 20 months. These findings underscore the effectiveness of regulating defects' neighboring environment and illuminate future high-performance electrode design.

Fracture Mechanisms and Crack Propagation in Monolayer Ti3C2Tx under Nanoindentation: The Influence of Surface Terminations and Vacancy Defects.

Monolayer MXenes are a novel class of two-dimensional transition metal carbides/nitrides with fascinating physicochemical properties. Despite recent advances in the study of MXenes' mechanical properties, a comprehensive understanding of the fundamental physical mechanisms that affect fracture due to surface terminations and vacancy defects in MXenes under nanoindentation remains largely unexplored. Here, we address this gap using molecular dynamics simulations and nanoindentation theory to investigate the effects of surface terminations and vacancy defects on the fracture behavior of Ti3C2Tx MXenes. By inducing the rupture of monolayer MXenes through nanoindentation, we find that bare Ti3C2 exhibits brittle fracture behavior. The presence of surface terminations and vacancy defects reduces the load-carrying capacity and flexibility of MXenes. Interestingly, surface terminations increase the stiffness of the structure, while vacancy defects have the opposite effect. We also find that high concentrations of surface oxidation impart ductile fracture characteristics to MXenes and increase the maximum crack length at failure. Additionally, defects exceeding the critical concentration can effectively prevent brittle crack propagation by causing frequent crack deflection and blunting crack tips. Combining these findings, we propose a new strategy to synergistically enhance the fracture toughness of MXenes through high concentrations of surface oxidation and vacancy defects exceeding the critical concentration without significantly affecting strength and stiffness, thereby avoiding catastrophic failure in MXene monolayers due to brittle fracture. This work provides fundamental insights into the mechanical properties and fracture mechanisms of monolayer MXenes.

Folic acid-assisted in situ solvothermal synthesis of Ni-MOF/MXene composite for high-performance supercapacitors

The synthesis of Ni-based metal-organic framework (MOF) and Ti3C2Tx MXene nanosheets is achieved via a straightforward solvothermal method, resulting in the formation of Ni-MOF/MXene composite material. This study introduces an innovative strategy that employs the biomolecule folic acid for the solvothermal synthesis of Ni-MOF/MXene nanosheets, intending to achieve high-performance supercapacitors. This approach effectively prevents the oxidation and restacking of MXene nanosheets and ensures the uniform dispersion of Ni-MOF on the surface of MXene nanosheets. The Ni-MOF/MXene composite exhibits an outstanding specific capacitance of 716.19 F/g at 1 A/g current density. Furthermore, an asymmetric supercapacitor device was assembled using activated carbon and Ni-MOF/MXene composite as negative and positive electrodes, respectively. The asymmetric device exhibited an impressive energy density of 23.28 Wh/kg at a power density of 2.841 KW/kg, along with good cyclic stability. These results establish an excellent potential of the Ni-MOF/MXene composite material as a candidate for next-generation energy devices.

Boosting Zinc‐Ion Storage Capability in Longitudinally Aligned MXene Arrays with Microchannel Architecture

AbstractFlexible Zn2+ ion hybrid capacitors (ZHCs) will play a crucial role in developing next‐generation wearable products, which demand portability, durability, and environmental adaptability. To further meet these requirements, Ti3C2Tx MXene with exceptional conductivity and robust mechanical properties can be utilized as cathodes, except for challenges such as the dense stacking of Ti3C2Tx nanosheets. In this study, a novel MXene cathode architecture has been developed with the facilitation of an ice template, which creates longitudinally aligned Ti3C2Tx arrays with microchannels. The introduction of hydrochloric acid to the Ti3C2Tx slurry induces a crumpled morphology, increasing active sites and enhancing ion transport with expanded interlayer spacing. Interestingly, experimental results and COMSOL simulations verify that the cathode structure also has effective impacts on the Zn anode with a weakened ion concentration gradient and suppressed dendrite formation. Consequently, the ZHCs exhibit enhanced electrochemical performance with excellent rate performance and long‐term cycling stability (enduring over 50 000 cycles at 5 A g−1) and further deliver a reliable low‐temperature operation by applying an anti‐freezing electrolyte. Moreover, flexible ZHCs assembled with gel electrolytes demonstrate excellent flexibility, improved rate performance, and mechanical stability, making them well‐suited for flexible electronics that power flexible LED panels.

Guided Heterostructure Growth of CoFe LDH on Ti3C2Tx MXene for Durably High Oxygen Evolution Activity.

Heterostructures of layered double hydroxides (LDHs) and MXenes have shown great promise for oxygen evolution reaction (OER) catalysts, owing to their complementary physical properties. Coupling LDHs with MXenes can potentially enhance their conductivity, stability, and OER activity. In this work, a scalable and straightforward in situ guided growth of CoFeLDH on Ti3C2Tx is introduced, where the surface chemistry of Ti3C2Tx dominates the resulting heterostructures, allowing tunable crystal domain sizes of LDHs. Combined simulation results of Monte Carlo and density functional theory (DFT) validate this guided growth mechanism. Through this way, the optimized heterostructures allow the highest OER activity of the overpotential = 301mV and Tafel slope = 43mV dec-1 at 10mA cm-2, and a considerably durable stability of 0.1% decay over 200h use, remarkably outperforming all reported LDHs-MXenes materials. DFT calculations indicate that the charge transfer in heterostructures can decrease the rate-limiting energy barrier for OER, facilitating OER activity. The combined experimental and theoretical efforts identify the participation role of MXene in heterostructures for OER reactions, providing insights into designing advanced heterostructures for robust OER electrocatalysis.

Tandem Effect Promotes MXene‐Supported Dual‐Site Janus Nanoparticles for High‐Efficiency Nitrate Reduction to Ammonia and Energy Output through Zn‐Nitrate Battery

AbstractElectrocatalytic nitrate reduction reaction (NO3RR) can convert nitrate contaminants into ammonia with higher added value. However, due to the NO3RR involving complex multi‐electron reactions, there is an urgent need to develop efficient electrocatalysts. Herein, CoCu Janus nanoparticles loaded on Ti3C2Tx MXene (CoCu‐Ti3C2Tx) is synthesized via the combination of molten salt etching and galvanic replacement strategy. The tandem catalysis of CoCu Janus NPs can maintain the balance between nitrogenous intermediates and active hydrogen (Hads). CoCu‐Ti3C2Tx exhibits a high NH3 yield of 8.08 mg h−1 mgcat.−1 and a satisfactory Faradaic efficiency of 93.6% at −0.7 V versus reversible hydrogen electrode (RHE). The Zn‐NO3− battery assembled with CoCu‐Ti3C2Tx shows an excellent power density of 10.33 mW cm−2, an NH3 yield of 1.52 mg h−1 mgcat.−1 and a Faradaic efficiency of 95.3% at 10 mA cm−2, which enables the simultaneous elimination of nitrate pollutants, ammonia production, and energy supply. Moreover, a series of verification experiments and density functional theory calculation are combined to reveal the reaction path and tandem catalytic mechanism. This work not only provides a new inspiration for the design of tandem catalysts but also promotes the development of Zn‐nitrate battery.

Influence of MXene Interlayer Spacing on the Interaction with Microwave Radiation

AbstractThe origin of MXene's excellent electromagnetic shielding performance is not fully understood. MXene films, despite being inhomogeneous at the nanometer scale, are often treated as if they are compared to bulk conductors. It is reasonable to wonder if the treatment of MXene as a homogeneous material remains valid at very small film thickness and if it depends on the interlayer spacing. The goal of the present work is to test if the homogeneous material model is applicable to nanometer‐thin Ti3C2Tx MXene films and, if so, to investigate how the model parameters may depend on variations in MXene interlayer spacings. MXene films containing flakes with interlayer spacing between 1.9 and 5.5 Å have been prepared using various intercalating agents. It is shown that modeling the films as being homogeneous agrees with experimental tests in the microwave frequency range. Microwave conductivity and dielectric constant parameters are estimated for the homogeneous film model by fitting measured results. The direct current (DC) conductivity matches the estimated microwave conductivity on the order of magnitude. A highly effective dielectric constant provides a good fit for the lower conductivity MXene films. Optical absorption agrees with the homogeneous material model of thin films as well.

Inkjet‐Printed Flexible and Transparent Ti3C2Tx/TiO2 Composite Films: A Strategy for Photoelectrically Controllable Photocatalytic Degradation

The 2D Ti3C2Tx MXene has a large specific surface area, abundant functional groups, and low work function, which has potential in the field of photocatalytic materials. However, the manufacturing of controllable films with high photocatalytic properties and desirable transmittance is a challenging task. Herein, low‐cost, large‐scale, and rapid preparation of Ti3C2Tx/TiO2 flexible composite films have been successfully prepared by inkjet printing technology, which can be applied in complex and special environments, as well as in photoelectrically controllable places for photocatalytic performance. With the increase of the anatase TiO2, the transmittance of Ti3C2Tx/TiO2 films increases from 55.37% to 73.27% at 780 nm, corresponding to the square resistance of 1.112–206.496 kΩ sq−1 and the figure of merit of 0.48–0.005. When the amount of anatase TiO2 is 15%, the film has the best photocatalytic effect on methylene blue (MB) dye, reaching 68.94%. After five cycles of testing, the degradation efficiency of MB dye decreases by only 5.68%, showing that the film has good cycling stability. This work provides a new research direction for photoelectrically controllable photocatalytic degradation in complex and special environments.

All-printed MXene/WS2-based flexible humidity sensor for multi-scenario applications

As non-contact sensing, non-invasive medical diagnostics and environmental humidity monitoring technologies advance, the demand for high-performance humidity sensors is becoming increasingly apparent. Ti3C2Tx MXene is an attractive humidity-sensitive candidate due to its excellent chemical activity and hydrophilic surface. However, achieving fast responsiveness and high sensitivity of dynamic changes in humidity is still challenging. Herein, this work introduced a WS2-modified Ti3C2Tx MXene composite material as humidity sensing material with superior sensing performance. Then sodium carboxymethyl cellulose solution was added to the Ti3C2Tx MXene/WS2 composite material to adjust viscosity of the composite material, enabling the formulation of printable humidity-sensitive ink. Utilizing screen-printing technology, a mass-producible humidity sensor (CMXW2) was successfully fabricated. Experimental results show that the sensor has short response and recovery times of 4.65 s/1.33 s in the relative humidity of 11–97 % with a high humidity response of 1707 % and excellent mechanical properties. The efficacy of the humidity sensor for skin moisture monitoring, real-time respiration monitoring, and non-contact switch was also evaluated. The successful demonstration of multi-scenario applications using the CMXW2 humidity sensor opens up new possibilities and applications in the fields of smart healthcare and non-contact sensing.

MXene-based kirigami designs: showcasing reconfigurable frequency selectivity in microwave regime

Today’s wireless environments, soft robotics, and space applications demand delicate design of devices with tunable performances and simple fabrication processes. Here we show strain-based adjustability of RF/microwave performance by applying frequency-selective patterns of conductive Ti3C2Tx MXene coatings on low-cost acetate substrates under ambient conditions. The tailored performances were achieved by applying frequency-selective patterns of thin Ti3C2Tx MXene coatings with high electrical conductivity as a replacement to metal on low-cost flexible acetate substrates under ambient conditions. Under quasi-axial stress, the Kirigami design enables displacements of individual resonant cells, changing the overall electromagnetic performance of a surface (i.e., array) within a simulated wireless channel. Two flexible Kirigami-inspired prototypes were implemented and tested within the S, C, and X (2-4 GHz, 4-8 GHz, and 8-12 GHz) microwave frequency bands. The resonant surface, having ~1/4 of the size of a standard A4 paper, was able to steer a beam of scattered waves from each resonator by ~25°. Under a strain of 22%, the resonant frequency of the wired co-planar resonator was shifted by 400 MHz, while the reflection coefficient changed by 158%. Deforming the geometry impacted the spectral response of the components across three arbitrary frequencies in the 4-10 GHz frequency range. With this proof of concept, we anticipate implementing thin films of MXenes on technologically relevant substrates, achieving multi-functionality through cost-effective and straightforward manufacturing.

Synthesis of Ti3C2Tx MXene@Carbon-Enhanced cellulose fiber composite-based photothermal absorber for sustainable water desalination

Desalination is a process that extracts salt and minerals from seawater to produce fresh water. It is critical, particularly for those who live on islands or coastal areas. Solar thermal desalination harnesses solar energy to address some of the challenges of traditional desalination methods. It uses solar power to heat seawater directly, initiating evaporation and leaving the salt behind, and further the vapor is condensed to produce fresh water. This method reduces reliance on fossil fuels, minimizing environmental impact and energy costs. This research unveils the synthesis of a solar evaporator consisting of Ti3C2Tx MXene coated over the carbon-enhanced cellulose fibers (CCF) (hereby termed the Ti3C2Tx MXene@CCF composite), which is the first-time report in the field of solar water desalination in using sustainable solar heat absorber. The Ti3C2Tx MXene@CCF composite achieves an impressive evaporation rate of 3.8 kg m−2 h−1 under 1 sun exposure. The hydrophilic Ti3C2Tx MXene coating on the porous CCF promotes rapid water evaporation. Ti3C2Tx MXene@CCF composite maximizes evaporation rates while maintaining water purity, which is in accordance with the World Health OrganizationFF (WHO) standards.

Mechanisms of mercury removal from water with highly efficient MXene and silver-modified polyethyleneimine cryogel composite filters

Safeguarding aquatic ecosystems and human health requires effective methods for removing pollutants. Mercury (Hg) is a very toxic pollutant with a global presence and is highly mobile and persistent. Here, innovative materials were prepared for separating Hg(II) from water, and the mechanisms underlying the efficient uptake of Hg species have been investigated. The sorbents include silver (Ag) nanoparticles and multilayered Ti3C2Tx MXene, both incorporated into the structure of a three-dimensional polyethyleneimine porous cryogel (PEI) that acts as a scaffold holding and exposing nano active sites involved in the removal of Hg. Specifically, Ag particles were deposited onto MXene phases, and the resulting composite was embedded in the macroporous PEI polymer (PEI/MXene@Ag cryogel). The composite has beneficial properties regarding Hg removal: 99% of Hg was separated from waste within 24 h in batch studies. The maximum removal capacity of Hg reached 875 mg/g from HgCl2, and 761 mg/g and 1280 mg/g from Hg(OAc)2 and Hg(NO3)2 salts by PEI/MXene@Ag. The Hg uptake stems from the composite’s relatively large specific surface area, layered porous channels, and highly dispersed Ag nanoparticles in the multilayered Ti3C2Tx MXene. The matrix in the water samples that were treated with the composite did not hinder the uptake of Hg by PEI/MXene@Ag. The high effectiveness achieved for the removal of Hg, combined with rapid adsorption kinetics, high efficiency, and selectivity, positions it as an efficient solution. Future work should address upscaling its preparation for increasing readiness towards mitigating Hg in surface water.

Robust and Environmentally Friendly MXene-Based Electronic Skin Enabling the Three Essential Functions of Natural Skin: Perception, Protection, and Thermoregulation.

The development of electronic skin (e-skin) emulating the human skin's three essential functions (perception, protection, and thermoregulation) has great potential for human-machine interfaces and intelligent robotics. However, existing studies mainly focus on perception. This study presents a novel, eco-friendly, mechanically robust e-skin replicating human skin's three essential functions. The e-skin is composed of Ti3C2Tx MXene, polypyrrole, and bacterial cellulose nanofibers, where the MXene nanoflakes form the matrix, the bacterial cellulose nanofibers act as the filler, and the polypyrrole serves as a conductive "cross-linker". This design allows customization of the electrical conductivity, microarchitecture, and mechanical properties, integrating sensing (perception), EMI shielding (protection), and thermal management (thermoregulation). The optimal e-skin can effectively sense various motions (including minuscule artery pulses), achieve an EMI shielding efficiency of 63.32 dB at 78 μm thickness, and regulate temperature up to 129 °C in 30 s at 2.4 V, demonstrating its potential for smart robotics in complex scenarios.

Development of a high-sensitivity and fast-response fiber temperature sensor utilizing Ti3C2TX MXene/PDMS composites and Vernier effect

Precisely measuring temperature holds great significance for human daily life and industrial production. A high-sensitivity and fast-response optical fiber temperature sensor based on the vernier effect is proposed. A Fabry-Perot interferometer (FPI) filled with Ti3C2TX MXene and polydimethylsiloxane (PDMS) composites is employed as a sensing probe for the first time, and a cascaded Mach-Zender interferometer (MZI) as a reference unit due to its insensitivity to temperature. The temperature sensitivity of the FPI filled with Ti3C2TX MXene/PDMS composites is 1.63 nm/°C owing to the excellent thermal expansion characteristics of PDMS, and the response time is shortened from 3.021 s to 719 ms compared to that of the FPI filled with pure PDMS attributed to the high thermal conductivity of MXene. The cascading of FPI and MZI with similar free spectral ranges generates the vernier effect. The sensitivity is magnified by 19.44 times, reaching up to 31.62 nm/°C in the range of 36.5 - 37.2 °C, and the response time is 721 ms. Furthermore, experimental results demonstrate the sensor’s good stability, implying its potential applications of the sensor in medical diagnosis, environmental monitoring and biosensing.

An electrochemical sensor based on porous heterojunction hollow NiCo-LDH/Ti3C2Tx MXenes composites for the detection of quercetin in natural plants.

Cubic hollow-structured NiCo-LDH was synthesized using a solvothermal method. Subsequently, clay-like Ti3C2Tx MXenes were electrostatically self-assembled with NiCo layered double hydroxides (NiCo-LDH) to form composites featuring three-dimensional porous heterostructures. The composites were characterized using SEM, TEM, XRD, XPS, and FT-IR spectroscopy. Ti3C2Tx MXenes exhibit excellent electrical conductivity and hydrophilicity, providing abundant binding sites for NiCo-LDH, thereby promoting an increase in ion diffusion channels. The formation of three-dimensional porous heterostructural composites enhances charge transport, significantly improving sensor sensitivity and response speed. Consequently, the sensor demonstrates excellent electrochemical detection capabilityfor quercetin (Qu), with a detection range of 0.1-20 µM and a detection limit of 23 nM. Additionally, it has been applied to the detection of Qu in natural plants such as onion, golden cypress, and chrysanthemum. The recovery ranged from 97.6 to 102.28%.

Enhanced removal of lead ions from wastewaters by electrochemical adsorption using nitrogen-doped Ti3C2Tx MXene

As a two-dimensional material containing transition metal carbides and nitrides, MXene is often used in capacitive deionization for its excellent hydrophilic and pseudocapacitive properties. Nitrogen doping is widely used to improve the adsorption properties of certain materials. However, the effect of nitrogen doping on the electrochemical adsorption properties of MXene remains unclear. In this work, nitrogen-doped Ti3C2Tx MXene was synthesized using a simple hydrothermal method to achieve highly selective and efficient removal of Pb(II) at a constant cell voltage. The concentration of Pb(II) decreased from 4.95 to 0.02 mg L−1 in a 100 mg L−1 NaCl supporting electrolyte after electrosorption. The removal efficiency of Pb(II) reached 99.5%, whereas it was only 15.2% for Na+. The introduction of nitrogen functional groups increased the electrical conductivity and layer spacing of MXene, thereby improving the pseudocapacitive adsorption performance in the presence of Pb(II). The complexation function of the Ti-OH group on nitrogen-doped Ti3C2Tx surface increased and contributed to the selective adsorption of Pb(II). The removal efficiency of Pb(II) increased with increasing solution pH and cell voltage, reaching the maximum value at pH 5.0 and 1.5 V, respectively. The effect of supporting electrolyte type on the removal of Pb(II) was negligible. In addition, the removal efficiency for mixed heavy metal ion solutions, including Cu(II), Ni(II), and Pb(II), exceeded 79.0%. It exhibited the highest removal efficiency for Pb(II) at 97.9%. After five cycles of electrochemical adsorption–desorption, the nitrogen-doped Ti3C2Tx maintained a stable Pb(II) removal efficiency of 97.0%. This work provides a promising material for the electrochemical removal of low-concentration heavy metal ions from wastewaters.