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Ti3C2TX
Small Science · 2022 ·Vol. 2 ·期 7 ·2200018 · IF 0

Gradient Multilayer Design of Ti3C2Tx MXene Nanocomposite for Strong and Broadband Microwave Absorption

Yajun Zhang,Long Pan,Peigen Zhang,ZhengMing Sun

High-performance electromagnetic (EM) absorbing materials are in urgent need due to severe EM pollution caused by fast development of communication technology and electronic devices. Gradient structure benefits EM absorbing performance. However, the relevant study is very limited, and the relationship between component layers and overall performance is unclear. Herein, a gradient structure containing impedance matching layer, lossy layer, and reflective layer is built via repeated casting-drying method using Ti 3 C 2 T x MXene and polyvinyl alcohol. With optimized gradient structure, the minimum reflection loss (RL) reaches −74.8 dB with effective absorbing bandwidth (EAB) covering the whole X-band. The good absorbing performance is ascribed to the good impedance matching, which is derived from the stepwisely increased permittivity of each layer. Moreover, it is found that RL reaches the lowest value when lossy layer permittivity is close to the average permittivity of impedance matching layer and reflective layer. In addition, the decrease of lossy layer permittivity causes the decrease of total thickness of the gradient structure. This work demonstrates the effectiveness of gradient structure toward strong and broadband microwave absorption and provides rules for designing proper gradient structures to satisfy different requirements.

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COLLOIDS AND SURFACES A-PHYSICOCHEMICAL AND ENGINEERING ASPECTS · 2022 · IF 5.518

L-lysine functionalized Ti3C2Tx coated polyurethane sponge for high-throughput oil–water separation

Zhen-Hui Liu,Qing-Ming Wang,Qiu-Feng Lü,Junxiong Wu

Creating an efficient method that can provide simple, practical and high-throughput separation of oil–water mixtures has proved extremely challenging. Two-dimensional layered Ti 3 C 2 T x MXene material with excellent hydrophilicity has attracted substantial attention for oil–water separation. However, conventional Ti 3 C 2 T x separation membranes are susceptible to contamination by oil due to its relatively high adhesion to oil, hindering its practical applications in high-efficiency oil–water separation. To make Ti 3 C 2 T x have underwater superoleophobicity and low oil adhesion, the surface of Ti 3 C 2 T x can be modified by introducing hydrophilic groups. Herein, L-lysine functionalized Ti 3 C 2 T x (Ti 3 C 2 T x -Ly) was firstly prepared by decorating L-lysine on Ti 3 C 2 T x through electrostatic interaction and hydrogen bonding . A facile dip-coating method is then used to coat polyurethane (PU) sponge with Ti 3 C 2 T x -Ly, obtaining a superhydrophilic/underwater superoleophobic Ti 3 C 2 T x -Ly @PU sponge. Owing to the excellent underwater superoleophobicity resulting from hydrophilic groups (–OH、–NH 3 ) on the surface of Ti 3 C 2 T x -Ly nanosheets and the enlarged interlayer spacing of Ti 3 C 2 T x , the Ti 3 C 2 T x -Ly @PU sponges demonstrated outstanding separation performance for a series of oil–water mixtures. Specifically, the Ti 3 C 2 T x -Ly @PU sponge exhibits low oil adhesion and superhydrophilic (WCA = 0°)/submerged superoleophobic (UOCA > 155°) properties. The Ti 3 C 2 T x -Ly @PU sponges displayed the best separation performance for cyclohexane/water mixture, and the maximum permeation flux is up to 221892 L m –2 h –1 , accompanied by a remarkable separation efficiency of higher than 99.2% after 100 cycles. The permeation flux has exceeded most of the previous reported multifunctional separation membranes. In addition, the Ti 3 C 2 T x -Ly @PU sponge also showed excellent separation performance for high-density oil dichloromethane/water with a separation efficiency over 99.4%. Of note, the Ti 3 C 2 Tx-Ly @PU sponge features excellent chemical stability to corrosive media, such as acidic, alkaline, and high salt solutions, possessing great potential for real-world applications. Furthermore, the as-prepared Ti 3 C 2 T x -Ly @PU sponge exhibits rapid and efficient separation of oil-water mixtures through a fully gravity-driven process, which makes it a good candidate for industrial oil-contaminated water treatment and oil spill clean-up, and also provides new insights into the design and development of functional Ti 3 C 2 T x through L-lysine modification. Therefore, this work reports a facile and promising way to fabricate scalable superhydrophilic/underwater superoleophobic sponge material for highly efficient oil–water separation.

CAS / MDL: 7664-39-3 56-87-1
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Journal of Environmental Chemical Engineering · 2021 · IF 5.909

Synthesis of TiO2/Ti3C2Tx/AgI Z-scheme photocatalyst for tetracycline hydrochloride photocatalytic degradation

Fang-Di Wu,Jyh-Cherng Chen,Jia-Peng Hu

A ternary composite photocatalyst with high catalytic activity (TiO 2 /Ti 3 C 2 T x /AgI) was synthesized using the simple solvothermal and coprecipitation methods. The structure, morphology, photoelectric properties, and photocatalytic activity of the prepared materials were studied using various characterization techniques. The composite catalysts TiO 2 /Ti 3 C 2 T x /AgI with different proportions of TiO 2 /Ti 3 C 2 T x to AgI of 10%, 20%, 50%, 70%, and 90% were prepared by varying the amounts of AgNO 3 and KI. Compared to AgI and TiO 2 /Ti 3 C 2 T x , TiO 2 /Ti 3 C 2 T x /AgI demonstrated a superior photocatalytic degradation activity for tetracycline hydrochloride (TCH) under simulated sunlight. The degradation rate of TCH with 70% TiO 2 /Ti 3 C 2 T x /AgI composite photocatalyst reached 97%. The photoluminescence (PL) emission spectra showed that the recombination of photogenerated electrons of 70% TiO 2 /Ti 3 C 2 T x /AgI was effectively inhibited after the formation of AgI, TiO 2 , and Ti 3 C 2 T x heterojunctions . The electrochemical impedance spectroscopy (EIS) indicated that a rapid interfacial charge transfer of the 70% TiO 2 /Ti 3 C 2 T x /AgI composite to the electron acceptors (Ti 3 C 2 T x ). Ti 3 C 2 T x had high conductivity and can effectively accelerate the transfer and separation of photogenerated carriers as a charge medium. Therefore, the enhancement of photocatalytic activity of TiO 2 /Ti 3 C 2 T x /AgI can be attributed to the Z-scheme heterojunction with non-metal Ti 3 C 2 T x as the solid medium. In addition, the trapping agent experiment showed that superoxide radicals, singlet oxygen, and holes were the main active substances in the photocatalytic degradation of TCH by the TiO 2 /Ti 3 C 2 T x /AgI composite.

CAS / MDL: 13463-67-7
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ACS Nano · 2021 · IF 15.881

High-Density Anisotropy Magnetism Enhanced Microwave Absorption Performance in Ti3C2Tx MXene@Ni Microspheres

Caiyue Wen,Xiao Li,Ruixuan Zhang,Chunyang Xu,Wenbin You,Zhengwang Liu,Biao Zhao,Renchao Che

Two-dimensional materials, especially the newly emerging MXene, have attracted numerous interests in the fields of energy conversion/storage and electromagnetic shielding/absorption. However, the inherently inevitable aggregation and absence of magnetic loss of MXene considerably limit its electromagnetic absorption application. The introduction of magnetic component and favorable structural engineering are the alternatives to improve the microwave absorption (MA) performance. Herein, we report a spheroidization strategy to assemble double-shell MXene@Ni microspheres, where the commonly lamellar MXene are reshaped into three-dimensional microspheres that provide the substrate for oriented growth of Ni nanospikes. Whereas this structural feature offers massive accessible active surfaces that effectively promote the dielectric loss ability, the introduction of magnetic Ni nanospikes enables the additional magnetic loss capacity. Benefiting from these merits, the synthesized 3D MXene@Ni microspheres exhibit superior MA performance with the minimum reflection loss value of −59.6 dB at an ultrathin thickness (∼1.5 mm) and effective absorption bandwidth of 4.48 GHz. Moreover, the electron holography results reveal that the high-density anisotropy magnetism plays an important role in the improvement of MA performance, which provides an insight for the design of MXene-based materials as high-efficient microwave absorbers.

CAS / MDL: 80-62-6 9003-39-8
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Surfaces and Interfaces · 2023 · IF 6.2

3D hydroxylated Ti3C2Tx MXene nanonet architecture supported Pt catalysts for efficient hydrogen evolution

Caiqin Wang,Tingting Zhou,Cheng Qian,Lili Chen,Liyuan Hao,Shumeng Fu,Bingguo Feng,Xiaofei Yang

Ti 3 C 2 T x MXene nanonets (MNNs) with 3D fibrous architecture were obtained from Ti 3 C 2 T x MXene nanoplates (MNPs) via surface modifying of alkalization in concentrated KOH solution, which was further combined with carbon nanotube and used as catalyst supports for Pt nanoparticles. By controlling the treatment time of alkalization, the lamellar surface of MNPs was getting into fibration in different extent. The catalytic performances toward hydrogen evolution reaction (HER) of a series of Pt-loaded MNNs catalysts were investigated, in which 1 %Pt-MNNs-9 composite catalyst presented the best hydrogen evolution performance. In detail, 1 %Pt-MNNs-9 with 1 wt.% of Pt loading exhibits an overpotential of 60 mV at 10 mA·cm −2 , which is much lower than 1 % Pt-MNPs (274 mV). It also keeps stable performance for long term stability. The enhanced catalytic activity is probably due to the fact that, Ti 3 C 2 T x MNNs with 3D architecture not only possesses abundant sites to anchor Pt nanoaprticles, but also facilitates the mass and charge transfer, which are significantly beneficial to catalytic reaction. The 3D architecture MXene fibers are expected to have widespread applications including but not limited to energy storage/conversion, and catalytic fields.

CAS / MDL: 308068-56-6 16941-12-1
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Environmental Science-Nano · 2021 ·Vol. 8 ·期 5 ·1446-1455 · IF 8.131

The photothermal synergy effect of pure Ti3C2Tx in antibacterial reaction and its mechanism

Rumeng Zhang,Chao Li,Wei Liu,Yingping Huang,Bo Wang,Kemeng Xiao,Po Keung Wong,Liqun Ye

As an efficient green water disinfection technology, photothermal synergy sterilization has been paid more attention in recent years with its immeasurable advantages. The development of photocatalysts for efficient sterilization is currently an urgent need. In this manuscript, pure Ti3C2Tx is first studied as a photothermal synergy sterilization material and shows an excellent sterilization effect. The sterilization rate of Escherichia coli (E. coli) reaches 99.9% under visible infrared (vis-IR) light for 40 minutes. The peeling of the Al layer from Ti3AlC2 is the fundamental reason for improving the photothermal conversion ability, and photogenerated free radicals have also proved to be improved. The dilution spreading plate method, enzyme activity test, and leakage of cell contents confirmed the complete death of bacteria. Two aspects, photogenerated free radicals and photothermal synergy, were carried to illuminate the mechanism.

CAS / MDL: 7664-39-3
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JOURNAL OF COLLOID AND INTERFACE SCIENCE · 2021 · IF 8.128

Heterostructure engineering of ultrathin SnS2/Ti3C2Tx nanosheets for high-performance potassium-ion batteries

Huiqiao Liu,Yanan He,Hang Zhang,Shaodan Wang,Kangzhe Cao,Yong Jiang,Xiaogang Liu,Qiang-Shan Jing

Layered metal sulfides are considered as promising candidates for potassium ion batteries (KIBs) owing to the unique interlayer passages for ion diffusion. However, the insufficient electronic conductivity, inevitable volume expansion, and sulfur loss hinder the promotion of K-ion storage performance. Herein, few-layered Ti 3 C 2 T x nanosheets were selected as the multi-functional substrate for cooperating few-layered SnS 2 nanosheets, constructing SnS 2 /Ti 3 C 2 T x hetero-structural nanosheets (HNs) with the thickness as thin as about 5 nm. In this configuration, the formed Ti-S bonds provide robust interaction between SnS 2 and Ti 3 C 2 T x nanosheets, which hinders the agglomeration of SnS 2 and the restack of Ti 3 C 2 T x , endowing the hybrid material with robust nanostructure. Thus, the shortcomings of the SnS 2 anode are muchly relieved. In this way, the as-prepared SnS 2 /Ti 3 C 2 T x HNs electrode delivers reversible capacities of 462.1 mAh g −1 at 0.1 A g −1 and 166.1 mAh g −1 at 2.0 A g −1 , respectively, and a capacity of 85.5 mAh g −1 is remained even after 460 cycles at 2.0 A g −1 . These results are superior to those of the counterpart electrode, confirming aggressive promotion of K-ion storage performance of SnS 2 anode brought by the cooperation of Ti 3 C 2 T x , and presenting a reliable strategy to improve the electrochemical performance of sulfide anodes.

CAS / MDL: 196506-01-1
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ACS Applied Materials & Interfaces · 2020 · IF 8.758

Multiresponsive MXene (Ti3C2Tx)-Decorated Textiles for Wearable Thermal Management and Human Motion Monitoring

Chang Ma,Qi Yuan,Haishun Du,Ming-Guo Ma,Chuanling Si,Pengbo Wan

Over the past few years, wearable electronics and smart textiles have seen tremendous growth in both academia and industries. However, it is still a challenge to prepare robust, flexible, wearable, and multiresponsive textile electronics. A newly blooming two-dimensional (2D) transition-metal carbide/nitride (MXene) is regarded as an ideal active material to build multifunctional electronics due to its intriguing properties. Herein, a hydrophobic and multifunctional textile composite (Si-MAP) was prepared by decoration of conductive MXene nanosheets onto air-laid paper, followed by wrapping with poly(dimethylsiloxane) (PDMS). These obtained smart textiles exhibited excellent electronic/photonic/mechanical triresponsive properties: Si-MAPs could reach high equilibrium temperatures (104.9 and 118.7 °C) under quite low power illumination (1.25 W cm–2) and working voltage (4 V). The Si-MAP pressure sensor exhibited high sensitivity and rapid response time (30–40 ms), which can capture a wide range of human movements. Moreover, the thin PDMS layer not only rendered the textile composites hydrophobic but also improved the stability and adaptation for daily use. Remarkably, the hydrophobic Si-MAPs have maintained the advantages of breathability and washability, which make them suitable for wearing. Thus, this smart Si-MAP textile provides a reference for the study of the next generation of light, portable, and wearable textile-based electronic devices.

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INORGANIC CHEMISTRY · 2020 · IF 4.825

Self-assembled GeOX/Ti3C2TX Composites as Promising Anode Materials for Lithium Ion Batteries

Sheng-chao Song,Ding-chuan Zuo,Chang-sheng An,Xia-hui Zhang,Jin-hui Li,Zhen-jiang He,Yun-jiao Li,Jun-chao Zheng

High-capacity germanium-based anode materials are alternative materials for outstanding electrochemical performance lithium-ion batteries (LIBs), but severe volume variation and pulverization problems during charging–discharging processes can seriously affect their electrochemical performance. In addressing this challenge, a simple strategy was used to prepare the self-assembled GeOX/Ti3C2TX composite in which the GeOX nanoparticles can grow directly on Ti3C2TX layers. Nanoscale GeOX uniformly renucleates on the surface and interlayers of Ti3C2TX, forming the stable multiphase structure, which guarantees its excellent electrochemical performance. Electrochemical evaluation has shown that the rate capability and reversibility of GeOX/Ti3C2TX are both greatly improved, which delivers a reversible discharge specific capacity of above 1400 mAh g–1 (at 100 mA g–1) and a reversible specific capacity of 900 mAh g–1 after 50 cycles while it still maintains a stable specific capacity of 725 mAh g–1 at 5000 mA g–1. Furthermore, the composite exhibits an exceptionally superior rate capability, making it a good electrochemical performance anode for LIBs.

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COMPOSITES PART A-APPLIED SCIENCE AND MANUFACTURING · 2020 · IF 6.444

UV-light modulated Ti3C2Tx MXene/g-C3N4 heterojunction film for electromagnetic interference shielding

Qianfan Zhou,Kunpeng Qian,Jianhui Fang,Miao Miao,Shaomei Cao,Xin Feng

With the mushrooming of smart electronic devices, ultrathin Ti 3 C 2 T x MXene based EMI shielding materials with long term durability have aroused much interest. Herein, 2D Ti 3 C 2 T x /g-C 3 N 4 heterojunction films were firstly assembled using cellulose nanofibrils (CNF) as green binder via a solution-based pressured-filtration process. The heterojunction film with Ti 3 C 2 T x /g-C 3 N 4 mass ratio of 5:1 (28.20 µm in thick) exhibited distinguished performance with EMI shielding effectiveness of 42.99 dB in X-band and high tensile strength of 23.85 MPa. Specially, the generation of photo-electrons from g-C 3 N 4 nanosheets reduced TiO 2 into lower valence states under 365 nm UV light-irritation, resulting in lower loss on electrical conductivity as well as EMI shielding performance compared to their unilluminated counterparts. The reduction on TiO 2 offered by the g-C 3 N 4 enables the heterojunction film to be considered as a promising alternative EMI shielding material for future potential applications, because it can run long time just need UV light modulation.

CAS / MDL: 7789-24-4 108-78-1
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POLYMER · 2021 · IF 4.43

Engineering MXenes (Ti3C2Tx) surface with TiO2 for enhancing anti-corrosion performance of coatings

Fengyuan Zhang,Weiqu Liu,Shuo Wang,Hongyi Shi,Chunhua Liu,Liyan Liang,Ke Pi

MXenes (Ti 3 C 2 T x ), an emerging two-dimensional (2D) material, derived from MAX phases, may have outstanding corrosion resistance performance due to its sheet property. However, pristine Ti 3 C 2 T x is inappropriate to be used directly as an anti-corrosion filler, owing to the existence of hydrophilic groups. Herein, few-layered Ti 3 C 2 T x sheets were modified via TiO 2 . Then functional Ti 3 C 2 T x (Ti 3 C 2 &TiO 2 ) was introduced to the waterborne polyurethane (WPU) coating. Finally, the corrosion resistance of the prepared composite coating was studied in detail. The results revealed that containing 0.1 wt%Ti 3 C 2 &TiO 2 composite coating has excellent corrosion resistant performance. After 28 days' immersion, the lowest frequency impedance of WPU/0.1%Ti 3 C 2 &TiO 2 composite coating was 6.64 × 10 7  Ω cm 2 , which was higher than that of WPU coating (3.48 × 10 6  Ω cm 2 ). After 110 days’ immersion, the lowest frequency impedance of WPU/0.1%Ti 3 C 2 &TiO 2 composite coating was 1.75 × 10 6  Ω cm 2 . Furthermore, the results of Tafel curves demonstrated that the corrosion current and corrosion rate of WPU/0.1%Ti 3 C 2 &TiO 2 composite coating were the lowest. That were 2.79 × 10 −9 A/cm 2 and 3.25 × 10 −5  mm/year, respectively. In conclusion, this work extended the great application prospects of functional Ti 3 C 2 T x sheets in the fields of anti-corrosion.

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APPLIED SURFACE SCIENCE · 2021 · IF 6.707

Adjustable electromagnetic response of ultralight 3D Ti3C2Tx composite via control of crystal defects

Ruixiang DENG,Bingbing CHEN,Haogeng LI,Zhong LI,Tao ZHANG,Yun YU,Lixin SONG

Microwave shielding materials and absorbers serve important roles in improving the reliability of smart devices and military equipment. In this work, three-dimensional (3D) Ti 3 C 2 T x /Fe 3 O 4 composites with adjustable electromagnetic responses are studied. Taking advantage of the negatively charged surface of the Ti 3 C 2 T x , the cationic surfactant cetyltrimethylammonium bromide (CTAB) is used to precipitate the delaminated Ti 3 C 2 T x sheets. The volatilization of CTAB during the annealing process inflates the Ti 3 C 2 T x , and leads to the three-dimensional architecture of the composite. The results show that the free-standing 3D Ti 3 C 2 T x /Fe 3 O 4 composite film exhibits a high shielding efficiency of 60 dB in the X band. Owing to the traits of great flexibility, low apparent density, and thin thickness, the 3D Ti 3 C 2 T x /Fe 3 O 4 composite film achieves a high specific shielding efficiency of 3.5 × 10 5 dB/(g·cm −2 ). Furthermore, through the control of crystal defects in one-step annealing treatment, the shielding material can be transformed into a wideband microwave absorber. A high reflection loss up to −57 dB can be realized. And a 2-mm-thick absorber whose reflection loss is better than −10 dB in 11.2 ~ 18 GHz is also achieved. The experimental and first-principal studies on the evolution mechanism reveal that the destruction of the Ti-C bond mainly leads to the degradation of electrical conductivity and the improvement of impedance matching. Introduced crystal defects can help enhance the dielectric loss as well. The synergistic effects of ohmic loss, dielectric loss, and magnetic loss give birth to a broadband absorption of the composite.

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