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MXene
ACS Applied Materials & Interfaces · 2023 · IF 9.5

Dual-Stage Surficial Microstructure to Enhance the Sensitivity of MXene Pressure Sensors for Human Physiological Signal Acquisition

Jie Yang,Liyuan Liu,Di Zhang,Hongli Zhang,Jianhua Ma,Jiaojiao Zheng,Chen Wang

Accompanying the rapid growth of wearable electronics, flexible pressure sensors have received great interest due to their promising application in health monitoring, human-machine interfaces, and intelligent robotics. The high sensitivity over a wide responsive range, integrated with excellent repeatability, is a crucial requirement for the fabrication of reliable pressure sensors for various wearable scenes. In this work, we developed a highly sensitive and long-life flexible pressure sensor by constructing surficial microarrayed architecture polydimethylsiloxane (PDMS) film as a substrate and Ti3C2TX MXene/bacterial cellulose (BC) hybrid as an active sensing layer. The specific surficial morphology of PDMS couples with nanointercalated structure of Ti3C2Tx MXene/BC can effectively improve the sensitivity through controlling the stress distribution and layer spacing under different levels of pressure loading. In addition, abundant spontaneous hydrogen bonds between BC and Ti3C2Tx MXene nanosheets endow the MXene coating with highly adhesive strength on the PDMS surface; hence, the cyclic stability of the pressure sensor is greatly boosted. As a result, the obtained MXene/BC/PDMS (MBP) pressure sensor delivers high sensitivity (528.87 kPa–1), fast response/recovery time (45 ms/29 ms), low detection limit (0.6 Pa), and outstanding repeatability of up to 8000 cycles. Those excellent sensing properties of the MBP sensor allow it to serve as a reliable wearable device to monitor full-range human physiological motions, and it is expected to be applied in next-generation portable electronics, such as E-skins, smart healthcare, and the Internet of Things technology.

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ADVANCED FUNCTIONAL MATERIALS · 2023 ·Vol. 33 ·期 44 ·2307609 · IF 19

Wearable Integrated Self-Powered Electroluminescence Display Device Based on All-In-One MXene Electrode for Information Encryption

Siyu Zhang,Yan Zhu,Yifan Xia,Kangting Liu,Shuhan Li,Biao Yang,Mingyuan Li,Xinrong Zhi,Xin Wang

Anti-counterfeiting and visual optical information encryption/decryption technology have attracted widespread attention in the field of information security. Luminescent encryption technologies still face a huge challenge in external high voltage power supply, complex architecture, and expensive decryption equipment, which hinder their broad applications. Herein, a wearable integrated self-powered electroluminescent (EL) display device (W-ELD) that consists of MXene/Silicone-based triboelectric nanogenerator (MS-TENG) and EL device based on a shared MXene electrode is developed for patterned display and information encryption. The W-ELD features an all-in-one MXene electrode with excellent flexibility and high conductivity of 0.6 kΩ sq −1 , which is shared by both MS-TENG and EL devices. The MS-TENG demonstrates excellent output performances (output power of 0.9 Wm −2 ) and high stability and durability (10 4 cycles), which can directly light up the flexible patterned EL device. More importantly, when dripping conductive electrolyte solution, the W-ELD based on “中國”-patterned MXene electrode can precisely reveal the encryption information through self-powered EL emission for real-time visualized information interaction. Consequently, the all-in-one MXene electrode-based W-ELD that integrates both MS-TENG and EL device demonstrates exceptional patterned EL-based information encryption features, which offers a potential prospect in wearable self-powered optoelectronic devices, flexible displays, and encryption technology.

CAS / MDL: 7647-14-5
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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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APPLIED SURFACE SCIENCE · 2023 · IF 6.7

Au nanoparticles decorated flower-like SnS2/Ti3C2 MXene microcomposite for high performance NO2 sensing at room temperature

Wenlei Zhang,Weiheng Wang,Yunfan Wang,Lei Sun,Yongjiao Sun,Jie Hu

The continuous discharging of nitrogen dioxide (NO 2 ) significantly damaged global environment and human health. In this study, SnS 2 microflowers/Ti 3 C 2 MXene heterostructure was modified by Au nanoparticles (AuNPs) for the detection of NO 2 at room temperature. The microcomposite decorated with 6 wt% AuNPs exhibited excellent sensing properties including response value of 5.34 to 1 ppm NO 2 , which was almost 5 times higher than that of undecorated one. The limit of detection lowered from 500 ppb to 5 ppb with the addition of AuNPs. Besides, the AuNPs decorated SnS 2 /MXene microcomposite revealed good selectivity, fatigue resistance, as well as potential application towards flexible sensing. The NO 2 gas sensing mechanism of AuNPs decorated with SnS 2 /Ti 3 C 2 MXene microcomposite was discussed through density functional theory calculation on adsorption behavior and transferred charges in detail. This work may provide an important pathway for the future development of NO 2 sensors at room temperature.

CAS / MDL: 6132-04-3
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ACS Applied Nano Materials · 2023 · IF 5.9

Flexible and Stretchable Poly(styrene-butadiene-styrene)/MXene Nanosheet Composite and Coaxial Fibers for Wearable Strain Sensors

Jieyu Huang,Qufu Wei,Min Zhao

Fiber-based strain sensors have become a vital part for wearable electronics owing to their lightweight, flexibility, and easy processing. A poly(styrene-butadiene-styrene) (SBS)/MXene composite and coaxial fiber-based strain sensors were produced through a continuous, facile, and scalable wet-spinning approach, which exhibited both high stretchability and sensitivity. Electromechanical properties displayed that SBS/MXene composite fibers showed extremely high sensitivity (1.63 × 104), low strain detection (0.5%), and outstanding durability and reliability, which laid a foundation for detecting human motion including subtle activities, such as breathing and wrist pulse, and large-scale activities, such as bending of limb joints. The strain-sensing performance was further investigated by SBS/MXene coaxial fibers with SBS/MXene as sheath and SBS as core, presenting high sensitivity (4.69 × 103) and repeatability. SBS/MXene composite and coaxial fiber sensors demonstrated the potential application in wearable electronics with human motion detection.

CAS / MDL: 7789-24-4
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Journal of Energy Storage · 2023 · IF 9.4

MXene/d-Mannitol aerogel phase change material composites for medium-temperature energy storage and solar-thermal conversion

Yu Bai,Shuangfeng Wang

Accelerate the development of medium-temperature phase change materials (PCMs) with high enthalpy of phase change and light absorption capability is very important for medium-temperature energy storage and solar thermal utilization. However, low energy conversion capacity and easy leakage limit the practical application of PCMs. To improve these properties of materials, a MXene/DM aerogel composite phase change material was prepared by self-assembly followed by freeze-drying of d -mannitol (DM) and MXene nanosheets using a simple solution blending method. The MXene/DM containing 20 wt% MXene has a high enthalpy (H m ) of phase change (202.7 J/g) with phase change temperature (T m ) of 153.3 °C, and still has good shape stability at 170 °C without leakage. In addition, MXene/DM has strong absorption ability in UV–Vis-NIR regions, with significant solar-thermal conversion efficiency of 88.1 %. The results indicate that the MXene/DM aerogel have comprehensive performance and have promising applications in medium-temperature thermal storage and photothermal conversion.

CAS / MDL: 7789-24-4 69-65-8
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JOURNAL OF ALLOYS AND COMPOUNDS · 2023 · IF 6.2

Ti3C2 MXene-induced interface charge transferred in Z-scheme heterojunction for efficient photocatalytic removal of nitric oxide

Shuang Zhao,Dongyun Chen,Najun Li,Qingfeng Xu,Hua Li,Jianmei Lu

Currently, NO pollution is an urgent challenge for us to face, and photocatalytic degradation has been recognized as one of the most promising methods to reduce it. As a representative photocatalyst , g-C 3 N 4 has attracted researchers because of its low cost and excellent performance. In this work, a new triphasic Z-scheme heterostructure was built, TiO 2 /Ti 3 C 2 MXene/g-C 3 N 4 , to improve the visible-light irradiation-induced NO removal efficiency of g-C 3 N 4 . In this Z-scheme heterostructure, Ti 3 C 2 MXene could form a directional electron transfer thoroughfare between g-C 3 N 4 and TiO 2 to accelerate the electronic transmission rate, meanwhile, due to the specificity of the band structure, electrons on conduction band of g-C 3 N 4 and holes on valence band of TiO 2 can be well separated and react with the adsorbed species to achieve good photocatalytic performance. Because of the triphasic heterostructure formed by TiO 2 , Ti 3 C 2 MXene and g-C 3 N 4 , the efficiency of this compound for visible-light irradiation-induced NO removal improves from 32% to 56%. This work provides a new strategy to improve NO removal efficiency and shows a broader application prospect of photocatalysts with a triphasic structure.

CAS / MDL: 57-13-6
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ACS Applied Energy Materials · 2023 · IF 6.4

2D Ti3C2Tx MXene-Supported Graphitic Carbon-Nitride-Decorated Co3O4 Nanoparticles as Efficient Catalysts for Oxygen Evolution Reaction

Xi Li,Youping Guo,Yiran Li,Renchun Fu

Transition metal cobalt oxide (Co3O4) with a typical spinel structure is considered a promising electrocatalyst for oxygen evolution reaction (OER). However, its OER catalytic performance is unsatisfactory owing to its limited activity. In this study, we demonstrate that using graphitic carbon nitride (g-C3N4) loaded Co3O4 nanoparticles and then anchoring them onto 2D Ti3C2Tx MXene with a layered structure can significantly enhance the OER catalytic performance. This performance may be due to the well-layered structure of g-C3N4, thereby enabling it to provide more attachment sites for Co3O4 nanoparticles, reducing their agglomeration properties and exposing more active sites to promote OER catalytic performance. When anchoring Co3O4@g-C3N4 on Ti3C2Tx MXene, solid-state interfacial interactions can adjust the structure of electrons and promote the rate of interfacial charge transfer, which enhances the conductivity of the catalyst and further promotes its OER catalytic performance. The overpotential required for TCN is 247 mV at a current density of 10 mA cm–2, which is significantly lower than that of pure Ti3C2Tx MXene (600 mV) and Co3O4@g-C3N4 (387 mV), in addition to exhibiting excellent electrochemical stability.

CAS / MDL: 7789-24-4
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ENERGY & FUELS · 2023 · IF 5.3

Surface Engineering with Interfacial Poly(glutamic acid)/MXene/Aramid Nanofibers Protective Layer for Dendrite-Free Zinc Anodes

Weikang Yuan,Liuliu Zhu,Yujun Zheng,Wenyao Guo,Yulin Min,Jinchen Fan

Aqueous zinc-ion batteries (AZIBs) use zinc metal as anodes are expected to be used for large-scale energy storage due to their good safety, low cost, environmental friendliness, etc. However, the zinc dendrite growth and associated side reactions seriously cause low Coulomb efficiency and reduce the cycle life of AZIBs, finally hampering further practical application. Herein, the γ-poly(glutamic acid) (γ-PGA)/aramid nanofibers (ANFs)/MXene (PAM) protection layer was designed toward a dendrite-free Zn metal anode. The PAM layer with a three-dimensional (3D) network formed by strong hydrogen bonding interactions effectively inhibits the growth of zinc dendrites, corrosion of the electrolyte, and hydrogen precipitation due to the reduced nucleation overpotential, which facilitates uniform galvanization/de-zincification. At a current density of 0.1 mA·cm–2 and 0.1 mAh·cm–2, the cycle life of PAM@Zn//PAM@Zn symmetric cell could extend to 3500 h. Meanwhile, the PAM@Zn//V2O5 full cell could also exhibit a capacity retention of 82.49% after 1500 cycles at 1 C. This strategy of designing a polymer-based composite protection layer by integrating the advantages of different materials opens up more possibilities for the development of a dendrite-free Zn anode.

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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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LANGMUIR · 2023 · IF 3.9

Efficient Construction of MXene/V2O5 Nanocomposites for Optimizing the Combustion of Ammonium Perchlorate-Based Composite Solid Propellants

Baoyun Ye,Hongyi Chen,Chang Liu,Chongwei An,Jingyu Wang,Yong Zhang

The combustion performance of composite solid propellants (CSPs) significantly affects their application in the field of military and civil aircraft. Ammonium perchlorate/hydroxyl-terminated polybutadiene (AP/HTPB) composite propellants are one of the common CSPs, and their combustion performance is mainly affected by AP thermal decomposition. In this work, a simple strategy was put forward to effectively construct MXene-supported vanadium pentoxide nanocomposites (MXene/V2O5, MXV). MXene provided a good loading interface for V2O5 nanoparticles, which made MXV obtain a large specific surface area and simultaneously improved the catalytic performance of MXV for AP thermal decomposition. The catalytic experiment results showed that the decomposition temperature of AP mixed with MXV (MXV-4, 2.0 wt %) was 83.4 °C lower than that of pure AP. Moreover, the ignition delay of the AP/HTPB propellant was significantly reduced by 80.4% after adding MXV-4. The burning rate of the propellant was also increased by 202% under the catalytic action of MXV-4. Based on the above results, MXV-4 was expected to be an additive for optimizing the burning process of AP-based composite solid propellants.

CAS / MDL: 7789-24-4
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Crystals · 2023 ·Vol. 13 ·期 7 ·1005 · IF 2.7

Surface Groups and Dielectric Properties of Ti3C2Tx MXene Nanosheets after NH3·H2O Solvothermal Treatment under Different Temperatures

Zhiwei Liu,Guanlong Li,Yan Zhao,Xiangbao Chen

The rapid development of electronic technology has brought convenience and efficiency to the lives of modern people, while emphasizing the need for novel materials with designability and excellent dielectric properties at the same time. In this work, Ti3C2TxMXene nanosheets (MNSs) underwent NH3·H2O solvothermal treatment at temperatures of 40 °C, 60 °C, 80 °C, 100 °C, 120 °C, 140 °C, 160 °C, and 180 °C. The changes in the surface groups and dielectric properties after the solvothermal treatment were studied. The solvothermal treatment increased the proportion of surface -OH groups, which was beneficial to the permittivity of the MNSs. However, as the treating temperature increased, the amount of -OH on the surface of the MNSs showed a reducing trend, according to XPS spectra. As the treating temperature rose from 40 °C to 80 °C, the real part of the permittivity of MNS sample showed a significant decrease, eventually remaining approximately stable in the 80 °C to 180 °C samples. The results of electromagnetic characterization were in line with the group proportion, as determined via the XPS O1s spectra, supporting the previous conclusion that the -OH group played an important role in the permittivity.Keywords:NH3·H2O solvothermal;end groups;dielectric property;2D nanosheets

CAS / MDL: 7789-24-4
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