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Ti3C2TX
ANALYTICAL CHEMISTRY · 2022 · IF 8.008

Superhydrophobic Functionalized Ti3C2Tx MXene-Based Skin-Attachable and Wearable Electrochemical pH Sensor for Real-Time Sweat Detection

Lijuan Chen,Fan Chen,Gang Liu,Haoliang Lin,Yu Bao,Dongxue Han,Wei Wang,Yingming Ma,Baohua Zhang,Li Niu

Sweat pH is a critical indicator for evaluating human health. With the extensive attention on the wearable and flexible biosensing devices, the technology for the monitoring of human sweat can be realized. In this study, a sensitive, miniaturized, and flexible electrochemical sweat pH sensor was developed for the continuous and real-time monitoring of the hydrogen-ion concentration in human sweat. A flexible electrode was fabricated on the poly(ethylene terephthalate) (PET) substrate by a simple and low-cost screen-printing technology, which was based on the integration of fluoroalkyl silane-functionalized Ti3C2Tx (F–Ti3C2Tx) and the polyaniline (PANI) membrane technology instead of the traditional ion-sensitive membrane. The surface functionalization strategy for Ti3C2Tx with perfluorodecyltrichlorosilane can provide environmental stability. Functionalized Ti3C2Tx (F–Ti3C2Tx) was doped with PANI to obtain improved responsiveness, sensitivity, and reversibility. The constructed microsize, portable, and wearable F–Ti3C2Tx/PANI pH sensor aimed to real-time monitor the pH value of human sweat during exercise. On-body sweat pH monitoring for females and males, respectively, exhibited high accuracy and continuous stability compared with ex situ analyses. This study thus offers a facile and practical solution for developing a highly reliable MXene-based mini-type pH sensor to realize the online monitoring of human sweat pH.

CAS / MDL: 25233-30-1
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CHEMICAL ENGINEERING JOURNAL · 2022 · IF 16.744

Ti3C2Tx@CNF nanohybrid improving the corrosion resistance of waterborne epoxy coating under 15 MPa alternating hydrostatic pressure

Yangmin Wu,Wenjie Zhao,Sheng Liu,Liping Wang

Cellulose nanofiber was grafted on Ti 3 C 2 T x (Ti 3 C 2 T x @CNF) and then Ti 3 C 2 Tx@CNF nanohybrid acted as nanofiller to endow epoxy coating superior barrier property. Electrochemical tests and corrosion products revealed that incorporation of Ti 3 C 2 T x @CNF into epoxy could significantly improve its anti-corrosion performance. Even immersion in marine alternating hydrostatic pressure (AHP) environment for 240 h, the impedance modulus of composite coating was one order of magnitude higher as compared with controlled samples. Besides, cross-sectional structure confirmed that Ti 3 C 2 T x @CNF remarkable improve the compactness of coating and thus conferring active adhesion strength with twice higher than that of pure epoxy after 240 h immersion in AHP.

CAS / MDL: 67-68-5
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JOURNAL OF COLLOID AND INTERFACE SCIENCE · 2022 · IF 9.965

Adhesive and high-sensitivity modified Ti3C2TX (MXene)-based organohydrogels with wide work temperature range for wearable sensors

Jing Wang,Tianyi Dai,Yuchen Zhou,Amel Mohamed,Guoliang Yuan,Hongbing Jia

Hydrogel-based wearable sensors have gained great interest on account of their huge application in human-machine interfaces, electronic skin, and healthcare monitoring. However, there are still challenges in designing hydrogel-based sensors with high stability in a wide temperature range, superior adhesion, and excellent sensitivity. Herein, sensors based on oxidized sodium alginate (OSA)/polyacrylamide (PAm)/polydopamine-Ti 3 C 2 T X (PMXene) /glycerol/water (Gly/H 2 O) organohydrogels were designed. The organohydrogels exhibited excellent mechanical properties (elongation at break of 1037%, tensile strength of 0.17 MPa), predominant self-healing ability (self-healing efficiency of 91%), as well as high sensing stability in a wide temperature range (from −20 to 60   °C). The introduction of PDA (polydopamine) and viscous glycerin (Gly) provide organohydrogels with superior adhesion. Organohydrogels sensors demonstrated high sensitivity (Gauge Factor, GF = 2.2) due to the combination of ionic and electron conduction. Sensors could stably detect human movement under different strain levels at high and low temperatures, providing a new solution for wearable sensors in extreme conditions.

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INTERNATIONAL JOURNAL OF HYDROGEN ENERGY · 2022 · IF 7.139

Quasi zero-dimensional MoS2 quantum dots decorated 2D Ti3C2Tx MXene as advanced electrocatalysts for hydrogen evolution reaction

Long Chen,Junmei Liang,Qicheng Zhang,Xuewen Hu,Wenchao Peng,Yang Li,Fengbao Zhang,Xiaobin Fan

Developing advanced noble-metal-free electrocatalysts for the hydrogen evolution reaction (HER) is still a great challenge. Herein, a novel HER catalyst with quasi zero-dimensional (0D) MoS 2 quantum dots (QDs) supported on two-dimensional (2D) Ti 3 C 2 T x MXene nanosheets is facilely synthesized. The MoS 2 QDs/Ti 3 C 2 T x nanohybrid retains the unique layer structure, and the MoS 2 QDs are in situ formed and distributed uniformly. The obtained MoS 2 QDs/Ti 3 C 2 T x catalyst exhibits superior electrocatalytic activity due to its excellent conductivity, abundant of active sites exposed and a high percentage of 1T metallic phase (∼76%) of MoS 2 QDs. Remarkably, an early HER overpotential of 220 mV at 10 mA cm −2 and a small Tafel slope of 72 mV dec −1 of MoS 2 QDs/Ti 3 C 2 T x are achieved in 0.5 M H 2 SO 4 solution. In addition, the exchange current density of MoS 2 QDs/Ti 3 C 2 T x is ∼5 times larger compared with pure MoS 2 , thus demonstrating an accelerated charge transfer during the electrocatalytic process.

CAS / MDL: 15060-55-6 68-12-2
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Catalysis Science & Technology · 2022 ·Vol. 12 ·期 6 ·1788-1798 · IF 6.177

H-Spill storage to maximize the catalytic performances of Pd-based bimetals@Ti3C2Tx MXenes in selective semihydrogenations

Jing Zhao,Yanzhuo Zhang,Hucheng Zhang,Haiyan Wang,Jianji Wang

Hydrogen spillover is an important theme for hydrogen storage and H-involving catalytic reactions. This work shows that catalytic reactivity and selectivity can be revealed by differentiating the energetic characteristics of spilled H species. With the assistance of Ti, F and C in MXenes, Pd1.8Ni@Ti3C2Tx presents a high capacity for spillover hydrogen storage at ambient temperatures, and the rich oxygenated groups act as the main carriers of hydrogen spillover around metal nanoparticles. Thermodynamic analysis reveals that the catalytic performances are energetically dominated by the adsorption enthalpies of the active spilled H species rather than the amount of spillover hydrogen, and can be tuned by alloying and surface modification. The ideas are verified from the excellent catalysis, chemoselectivity and stereoselectivity of Pd1.8Ni@Ti3C2Tx in semihydrogenations. The strategy of maximizing catalytic performances is applicable to other Pd-based bimetals@Ti3C2Tx, such as Pd2.6Co@Ti3C2Tx and Pd1.5Fe@Ti3C2Tx, and provides new energetics perspectives to understand the catalytic mechanism in spillover-involving chemical procedures.

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JOURNAL OF MATERIALS SCIENCE · 2022 ·Vol. 57 ·期 5 ·3348-3359 · IF 4.682

Mechanical, thermal stability, and flame retardancy performance of transparent wood composite improved with delaminated Ti3C2Tx (MXene) nanosheets

Zhang Liren,Jiang Yingqiu,Zhou Lingyue,Jiang Zhihong,Li Lu,Che Wenbo,Yu Youming

Abstract Transparent wood (TW) is a promising optical material, which provides a potential choice for windows applications. As a polymer composite material, the mechanical, thermal stability, and flame retardant of TW are crucial properties in practical applications. In this study, the delaminated Ti 3 C 2 T x (MXene) were dispersed into polyvinyl alcohol (PVA) and then infiltrated into delignified wood to prepare MXene-reinforced transparent wood (TW-MXene). The MXene addition leads to an interlocking mechanism between MXene fillers with a polymer matrix (e.g., PVA, cellulose scaffold), thereby improving the tensile strength of TW. Besides, the dynamic mechanical analysis also proved that the tensile strength of TW-MXene is significantly higher than pure transparent wood with changing the temperature at −50 to 150 °C. The TW added with 1 wt% MXene maintained a lower thermal conductivity of 0.31 W m −1  K −1 , and it showed better UV resistance than TW. Besides, the thermal decomposition rate of TW-MXene composite slows down, and its weight loss rate decreases with the addition of MXene. Furthermore, the presence of 1 wt% MXene endowed TW with 9.3 and 22.0% reductions for PHRR and THR, respectively. This strategy provides an insight into the development of high-performance transparent wood composites with the potential to be used in building fields. Graphical abstract

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Journal of Materials Chemistry C · 2023 ·Vol. 11 ·期 35 ·12057-12067 · IF 6.4

Anchoring magnetic ZIF-67 on Ti3C2Tx MXene to form composite films with high electromagnetic interference shielding performance

Zhenping Ma,Lei Zhang,Xianzhen Wang,Guang Xiao,Yongbao Feng,Wei Wang,Konghu Tian,Dewei Liang,Yagang Yao,Qiulong Li

With the rapid advancements of portable and wearable devices, high-efficiency electromagnetic interference (EMI) shielding materials are highly required to eliminate radiated electromagnetic pollution. Ti3C2Tx MXene has shown great application potential as an EMI SE material due to its good conductivity. However, a single-loss mechanism has many limitations. Herein, to enrich the electromagnetic-wave-loss ways, MXene@ZIF-67/multiwalled carbon nanotubes (MWCNTs) composite films were successfully prepared by vacuum-assisted filtration, combined with the introduction of magnetic ZIF-67 anchored on MXene by an electrostatic self-assembly method. The MXene@ZIF-67/MWCNTs composite film (MZ2M8) achieved the best EMI shielding performance of 63.6 dB at 32 μm thickness, and the contribution ratio of the scattering parameters for absorption to reflection, i.e., SEA to SET, was 66.94%, thus achieving high absorption loss. Due to the high aspect ratio of the MWCNTs and the densely stacked “brick–mortar” layered structure, the composite film also exhibited excellent flexibility and mechanical performance, in which MZ8M2 could deliver a high tensile strength of 115.2 MPa, ensuring practical applications in different environments. Moreover, the thermal conductivity of MZ2M8 reached 3.367 W m−1 K−1, realizing the synergistic effect of high shielding efficiency and heat-dissipation performance, and avoiding the phenomenon of heat accumulation caused by the conversion of electromagnetic waves into heat energy.

CAS / MDL: 10026-22-9 693-98-1
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Nano Research · 2023 · IF 9.9

Electroactive and antibacterial wound dressings based on Ti3C2Tx MXene/poly(ε-caprolactone)/gelatin coaxial electrospun nanofibrous membranes

Xu Shixin,Du Chen,Zhang Miaomiao,Wang Ruoying,Feng Wei,Wang Chengwei,Liu Qinsong,Zhao Wen

Endogenous electric fields (EFs) are capable of regulating the behaviors of skin cells in wound healing. However, majority of current dressings are primarily engaged in the passive repair of defective tissue, as they lack the ability to actively respond to physiological electrical signals. In this work, a series of nanofibrous membranes (NFMs) were fabricated by coaxial electrospinning, combining the good mechanical properties of poly(ε-caprolactone) (PCL), the bioactivity of gelatin and the electroactivity of Ti 3 C 2 T x MXene, as electroactive and antibacterial dressings for cutaneous wound healing. The obtained NFMs exhibited suitable mechanical properties and hydrophilicity, excellent electroactivity, antibacterial activity, and biocompatibility. Especially, Ti 3 C 2 T x MXene/PCL/gelatin-6 (MPG-6, 6 wt.% of Ti 3 C 2 T x MXene in sheath spinning liquids) showed the optimal conductivity and antibacterial activity. Excitingly, this scaffold significantly promoted the adhesion, proliferation, and migration of NIH 3T3 cells under the electrical stimulation (ES). The in vivo evaluation in a full-thickness wounds defect model demonstrated that the MPG-6 films significantly accelerated wound closure, increased granulation tissue formation, increased collagen deposition, and promoted wound vascularization. In summary, the versatile scaffold is expected to be an ideal candidate as wound dressings due to its ability to promote the transmission of physiological electrical signals and thus improved the therapeutic outcomes of wound regeneration.

CAS / MDL: 920-66-1
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ADVANCED FUNCTIONAL MATERIALS · 2023 ·Vol. 33 ·期 37 ·2300700 · IF 19

Buried Interface Modulation via Preferential Crystallization in All-Inorganic Perovskite Solar Cells: The Case of Multifunctional Ti3C2Tx

Mengqi Wang,Wenwen Wu,Yulin Liu,Songyang Yuan,Dehua Tian,Cuili Zhang,Zhipeng Ma,Jiahuan Deng,Jianhui Chen,Zaizhu Lou,Wenzhe Li,Jiandong Fan

Despite inorganic CsPbI 3− x Br x perovskite solar cells (PSCs) being promising in thermal stability, the perovskite degradation and severe nonradiative recombination at the interface hamper their further development. Herein, the typical MXene material, that is, Ti 3 C 2 T x , is employed to be the buried interface prior to the perovskite absorber layer in the device, which multi-functionalizes the as-prepared electron-transfer layers by means of both fascinating preferential crystallization of perovskite and/or accelerating the charge extraction with respect to an ideal energy-level alignment and suppressed trap states. Accordingly, the power conversion efficiency of the modified PSC device is substantially enhanced by as high as 19.56% in comparison to their counterparts with only the pristine CsPbI 3− x Br x active layer. More importantly, MXene modification is favorable to improve the wettability of perovskite precursor solution with enhanced grain size and crystallinity, thereby increasing the UV long-term stability of solar cells. This work provides a new paradigm toward alleviating the severe nonradiative recombination at the interface in the device whilst enhancing the long-term stability via the preferential crystallization process.

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INTERNATIONAL JOURNAL OF HYDROGEN ENERGY · 2021 · IF 5.816

In situ oxidation of ultrathin Ti3C2Tx MXene modified with crystalline g-C3N4 nanosheets for photocatalytic H2 evolution

Jingjun Liu,Haiping Zhou,Jiajie Fan,Quanjun Xiang

With photoconductor being transferred and separated, interface contact plays a crucial role in developing composites photocatalyst . In the present work, 2D crystalline g-C 3 N 4 (called as CCN) with 2D TiO 2 nanosheets (called as TO) obtained in situ oxidized single-layered Ti 3 C 2 T x MXene is designed by an electrostatic self-assembly technology. This CCN/TO nanosheets system with a few TiO 2 nanosheets distributed to the surface is not only prolonging lifetime of photoelectron but also stimulating photogenerated carriers transferred in contact interface. The electron transfer mechanism of CCN/TO is further proved by Pt photo-deposition method. Therein, the optimal CCN-TO-0.6 exhibits excellent performance of H 2 generation compared with single photocatalyst of CCN. The result shows that the crystalline g-C 3 N 4 photocatalysts introduced TiO 2 with interfacial effect favorably reduce H + to H 2 and enhance photocatalytic activity .

CAS / MDL: 108-78-1
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ACS Nano · 2022 · IF 18.027

Inhibition Effect of Ti3C2Tx MXene on Ice Crystals Combined with Laser-Mediated Heating Facilitates High-Performance Cryopreservation

Yuan Cao,Tie Chang,Chao Fang,Yuanyuan Zhang,Huilan Liu,Gang Zhao

The phenomena of ice formation and growth are of great importance for climate science, regenerative medicine, cryobiology, and food science. Hence, how to control ice formation and growth remains a challenge in these fields and attracts great interest from widespread researchers. Herein, the ice regulation ability of the two-dimensional MXene Ti3C2Tx in both the cooling and thawing processes is explored. Molecularly speaking, the ice growth inhibition mechanism of Ti3C2Tx MXene is ascribed to the formation of hydrogen bonds between functional groups of −O–, −OH, and −F distributed on the surface of Ti3C2Tx and ice/water molecules, which was elucidated by the molecular dynamics simulation method. In the cooling process, Ti3C2Tx can decrease the supercooling degree and inhibit the sharp edge morphology of ice crystals. Moreover, taking advantage of the outstanding photothermal conversion property of Ti3C2Tx, rapid ice melting can be achieved, thus reducing the phenomena of devitrification and ice recrystallization. Based on the ice restriction performance of Ti3C2Tx mentioned above, Ti3C2Tx is applied for cryopreservation of stem-cell-laden hydrogel constructs. The results show that Ti3C2Tx can reduce cryodamage to stem cells induced by ice injury in both the cooling and thawing processes and finally increase the cell viability from 38.4% to 80.9%. In addition, Ti3C2Tx also shows synergetic antibacterial activity under laser irradiation, thus realizing sterile cryopreservation of stem cells. Overall, this work explores the ice inhibition performance of Ti3C2Tx, elucidates the physical mechanism, and further achieves application of Ti3C2Tx in the field of cell cryopreservation.

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MOLECULES · 2023 ·Vol. 28 ·期 22 ·7475 · IF 4.6

A Molecularly Imprinted Electrochemical Sensor Based on TiO2@Ti3C2Tx for Highly Sensitive and Selective Detection of Chlortetracycline

Linbo Deng,Jiawei Liu,Haiyan Huang,Changxi Deng,Limin Lu,Linyu Wang,Xiaoqiang Wang

In view of the serious side effects of chlortetracycline (CTC) on the human body, it is particularly important to develop rapid, sensitive, and selective technologies for the detection of CTC in food. In this work, a molecularly imprinted electrochemical sensor with [Fe(CN)6]3−/4−as signal probe was proposed for the highly sensitive and selective detection of CTC. For this purpose, TiO2, which acts as an interlayer scaffold, was uniformly grown on the surface of Ti3C2Txsheets through a simple two-step calcination process using Ti3C2Txas the precursor to effectively avoid the stacking of Ti3C2Txlayers due to hydrogen bonding and van der Waals forces. This endowed TiO2@Ti3C2Txwith large specific surface, abundant functional sites, and rapid mass transfer. Then, polypyrrole molecularly imprinted polymers (MIPs) with outstanding electrical conductivity were modified on the surface of TiO2@Ti3C2Txvia simple electro-polymerization, where the pyrrole was employed as a polymeric monomer and the CTC provided a source of template molecules. This will not only provide specific recognition sites for CTC, but also facilitate electron transport on the electrode surface. The synergistic effects between TiO2@Ti3C2Txand polypyrrole MIPs afforded the TiO2@Ti3C2Tx/MIP-based electrochemical sensor excellent detection properties toward CTC, including ultra-low limits of detection (LOD) (0.027 nM), a wide linear range (0.06–1000 nM), and outstanding stability, reproducibility, selectivity, and feasibility in real samples. The results indicate that this strategy is feasible and will broaden the horizon for highly sensitive and selective detection of CTC.

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