COMPOSITES SCIENCE AND TECHNOLOGY
·
2018
·
IF 5.16
Huawei Wei,Jidong Dong,Xiaojiao Fang,Wenhui Zheng,Yutong Sun,Yue Qian,Zaixing Jiang,Yudong Huang
MXene , as a new 2-dimensional (2D) material, has excellently potential applications in the field of electrochemistry owing to its high conductivity and fast charge transporting speed. Especially, MXene/polymer composites have attracted widely attentions due to their extensive application in the area of multi-functional materials. Herein, the composites of Ti 3 C 2 T x MXene/polyaniline (PANI) with different PANI contents have been successfully prepared. The microwave absorption mechanism of these materials was investigated. Attributing to the multiple layer structure, the dielectric property of Ti 3 C 2 T x MXene and PANI, and the synergistic effect between the Ti 3 C 2 T x and PANI, the as-prepared composites possessed a specific microwave absorbing behavior. With a proper content of PANI, the MXene/PANI composites in a paraffin matrix exhibited a maximum reflection loss of −56.30 dB at 13.80 GHz with the thickness of 1.8 mm. In addition, the effective absorption bandwidth (>90%) ranged from X-band (8–12.4 GHz) to Ku-band (12.4–18 GHz) with the tunable thickness ranging from 1.5 to 2.6 mm. The results indicate that MXene/PANI composites has great potential to be used in the field of microwave absorption.
研究领域:
材料科学
·
电磁学
·
复合材料
✓ 已验证
产品关联
DOI
高影响因子
ACS Applied Nano Materials
·
2023
·
IF 5.9
Xiaohui Sun,Xueying Zhao,Xuyang Zhang,Guohua Wu,Xianhui Rong,Xiangwei Wang
Ti3C2Tx MXene is a potential microwave absorption material due to its unique physical and chemical properties. However, the impedance mismatch of MXene results in low microwave absorption. In this work, 2D/2D MXene@TiO2 composites were synthesized via a simple hydrothermal oxidation method, TiO2 is derived in situ from MXene without adding any additional Ti precursors. TiO2 with low permittivity can effectively regulate the impedance matching and enhance loss mechanisms. The MXene@TiO2-6 h composite shows a reflection loss (RL) of −58.3 dB at 11.36 GHz with a thickness of 1.75 mm, and the maximum effective absorption bandwidth (EAB) is 4.08 GHz (13.92–18 GHz) at 1.26 mm. Furthermore, the 2D/2D composite can obtain efficient microwave absorption at different frequencies by adjusting the thickness; RL can reach −39.1 dB at 5.04 GHz with a thickness of 3.5 mm. The radar cross section (RCS) of MXene@TiO2-6 h is lower than −19 dB m2 at −60–60°, and the minimum RCS is −56 dB m2 at 15°. This work provides a valuable experience in developing microwave absorption materials.
研究领域:
材料科学
·
电磁学
✓ 已验证
产品关联
DOI
高影响因子
CHEMICAL ENGINEERING JOURNAL
·
2020
·
IF 10.652
Kexuan Hu,Hehe Wang,Xiang Zhang,Hui Huang,Tai Qiu,Yang Wang,Chuanfang (John) Zhang,Limei Pan,Jian Yang
Light weight is one significant pursuit for microwave absorption (MA) materials. Generally, constructing foams with porous structure and low density as the absorber is one efficient way to reduce the absorber content and the quality of MA materials since the porous structure can effectively cause multiple reflections of electromagnetic waves and enhance the MA performance. Herein, we report a new and simple method for fabricating ultralight Ti 3 C 2 T x foams by hydrochloric acid induced self-assembly and freeze-drying, for which the pore structure and MA performance can be effectively regulated by pre-freezing temperature. The decrease of pre-freezing temperature from −20 °C to −196 °C results in a reduced pore size, more homogenous pore structure, a decreased electrical conductivity, a decreased dielectric constant and a significantly enhanced MA performance. 3.3 wt% Ti 3 C 2 T x foams was immersed into molten paraffin to prepare composites for the MA performance tests. Due to the synergy of multiple reflection, conductive loss and polarization relaxation, the Ti 3 C 2 T x foams pre-frozen at −196 °C shows the most superb and impressive MA performance, a minimum reflection loss (RL) of −50.6 dB at the thickness of 1.8 mm and an effective absorption bandwidth (EAB) of 4.2 GHz (13.8–17.6 GHz) at the thickness of 1.4 mm, and the EAB could be adjusted in a range of 11.9 GHz (6.1–18 GHz) by increasing the thickness from 1 mm to 3 mm. This is one of the most lightweight materials with excellent MA performance to our knowledge, which perfectly meet the combined pursuit of light weight, thin thickness, broad bandwidth and strong absorption. This work offers a simple strategy for constructing 3D porous Ti 3 C 2 T x -based foams facing the application such as MA, electromagnetic shielding, environmental governance, energy storage and sensors.
研究领域:
材料科学
·
电磁学
✓ 已验证
DOI
高影响因子
COMPOSITES PART A-APPLIED SCIENCE AND MANUFACTURING
·
2020
·
IF 6.444
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.
研究领域:
材料科学
·
电子工程
✓ 已验证
产品关联
DOI
高影响因子
Advanced Materials Interfaces
·
2022
·Vol. 9
·期 24
·2201165
·
IF 6.389
Xiaohan Xu,La Li,Weijia Liu,Zhongming Chen,Di Chen,Guozhen Shen
Thermally chargeable supercapacitors (TCSCs) are emerging and promising devices that could convert thermal energy spontaneously existing in nature into electricity and then store energy for further utilization. Herein, this work reports on the freestanding 3D Ti 3 C 2 T x MXene-based TCSC, where lithium bis(trifluoromethanesulfonyl)imide (LiTFSI), poly(ethylene oxide) (PEO), and polyvinylidene fluoride-hexafluoropropylene (PVDF-HFP) serve as gel electrolyte. Different from the semiconductor-based thermoelectric materials, the fabricated Ti 3 C 2 T x TCSC exhibits a high Seebeck coefficient of 78.4 mV K −1 . Moreover, when applying a temperature difference (ΔT) of 5.8 K between the cold and hot sides, the Ti 3 C 2 T x TCSC devices provide a stable high voltage of 400.6 mV. The charging/discharging cycles of the Ti 3 C 2 T x TCSC devices upon periodic Δ T of 3.3 and 5.8 K demonstrate their excellent stability. To realize the practical application, the four Ti 3 C 2 T x TCSCs devices connected in series are charged by supplying a Δ T of 5.8 K and used to power a digital timer, demonstrating the possibility and application of the TCSCs in self-powered integrated electronics.
研究领域:
材料科学
·
能源技术
✓ 已验证
产品关联
DOI
高影响因子
ACS Applied Nano Materials
·
2025
·
IF 5.5
Lu Tang,Kechen Zhou,Huiyu Su,Jiahong Tang,Qirui Wu,Lingfei Luo,Xiang Guo,Dawen Zeng
Detecting nitrogen dioxide (NO2) at room temperature (RT) is crucial for advancing environmental monitoring technologies, enabling efficient and practical air quality assessment. Two-dimensional (2D) MXene nanomaterials, recognized for their large specific surface area (SSA), abundant functional groups, and tunable electrical properties, have attracted considerable attention as promising candidates for room temperature gas-sensing applications. However, despite their potential, challenges, such as low gas adsorption efficiency, limited sensitivity, and poor selectivity, hinder their broader application and development, highlighting the need for further research. Here, we introduce a zero-dimensional (0D)/2D heterojunction gas-sensitive structure by synthesizing SnS2 quantum dot (QD)-sensitized Ti3C2Tx MXene nanocomposites via a hydrothermal method. The carefully designed gas sensor exhibits a significantly enhanced response value (RV) of 5.83% for 10 ppm of NO2 and a low detection limit of 500 ppb at RT, achieving an RV that is 5.8 times higher than that of pure Ti3C2Tx. Additionally, the sensor demonstrates high sensitivity (0.76 ppm–1 in the 0.5–5 ppm range), excellent selectivity, and outstanding stability, with a performance degradation of only 3.2% over 4 weeks. The exceptional performance arises from the synergistic effects of the quantum confinement properties of SnS2 QDs and the superior conductivity of Ti3C2Tx, which together provide abundant active sites for gas adsorption and facilitate efficient charge transfer pathways. Furthermore, the formation of the heterojunction modulates the resistance, enhancing room temperature sensing capabilities. The synthesized nanomaterials offer significant potential for advancing the design of heterostructures that integrate 0D QDs with 2D nanomaterials, paving the way for highly efficient NO2 detection at RT. Moreover, maintaining an optimal operating temperature further enhances the accuracy and reliability of real-time NO2 monitoring systems.
研究领域:
材料科学
·
环境科学
✓ 已验证
产品关联
DOI
高影响因子
Surfaces and Interfaces
·
2023
·
IF 6.2
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.
研究领域:
材料科学
·
催化化学
·
能源转换
✓ 已验证
产品关联
DOI
高影响因子
APPLIED CATALYSIS B-ENVIRONMENTAL
·
2022
·
IF 24.319
Daoyuan Zu,Haoran Song,Changping Li,Yuwei Wang,Rong Du,Rui Zhou,Wei Zhang,Shiting Pan,Yang Cai,Yongming Shen,Zhifeng Yang
Self-catalyzed decomplexation of Cu-ethylene diamine tetraacetic acid complex (Cu-EDTA) and recovery of Cu without addition of extraneous transition metals were achieved in Ti 3 C 2 T x MXene/peroxymonosulfate (Ti 3 C 2 T x /PMS) process. Free radical quenching experiments and electron spin resonance (ESR) measurements demonstrated that both hydroxyl radical (HO • ) and sulfate radical (SO 4 •- ) contributed to the degradation of Cu-EDTA. Activation of PMS by Ti 3 C 2 T x initiated Cu-EDTA decomplexation and released free Cu ions . Then, the formation of Ti-O-Cu bonds between Cu ions and Ti 3 C 2 T x accelerated the electron transfer from Ti 3 C 2 T x to Cu(Ⅱ) and triggered Cu(Ⅱ)/Cu(Ⅰ) cycle, which further enhanced PMS activation and led to the self-catalyzed decomplexation of Cu-EDTA. Simultaneous recovery of Cu was achieved due to the excellent absorption performance of negative charged Ti 3 C 2 T x towards Cu ions. This study revealed the self-catalyzed decomplexation mechanism of Cu-EDTA in the Ti 3 C 2 T x /PMS process and provided a feasible strategy for heavy metal complexes treatment.
研究领域:
环境科学
·
材料科学
✓ 已验证
产品关联
DOI
高影响因子
CERAMICS INTERNATIONAL
·
2024
·
IF 5.1
Jingyu Song,Yongqian Shen,Guibin Zhang,Mingxuan Sun,Mengyao Han,Xueyan Du
While two-dimensional lamellar materials, specifically Ti 3 C 2 T x MXenes, have shown great promise as wave-absorbing materials, the precise design of interlayer spacing poses a persistent challenge. In this study, Ti 3 C 2 T x MXene layers with adjustable interlayer spacings were crafted using a straightforward molecular welding technique. Through the incorporation of Ni nanoparticles onto the Ti 3 C 2 T x MXene layers using a combination of simple mechanical stirring and carbonation reactions, we successfully developed Ti 3 C 2 T x MXene/Ni/C composites featuring a distinct lamellar structure. A uniform dispersion of Ni nanoparticles on the surface of the Ti 3 C 2 T x MXene nanosheets was found with some of the nanoparticles intercalated into the layers. The Ti 3 C 2 T x MXene/Ni/C composites exhibited a maximum reflection loss (RL) value of −42.3 dB at 12.3 GHz, accompanied by an impressive effective absorption bandwidth (EAB) of 5.6 GHz. This outstanding absorption performance could be attributed to various factors, including the dielectric loss of the Ti 3 C 2 T x MXene lamellae, reflections and scattering of multiphase heterostructures, the magnetic loss of the Ni nanoparticles, and their synergistic attenuation. Furthermore, Ni nanoparticles with high electrical conductivity induced vortex currents under the alternating influence of electromagnetic waves (EMWs), resulting in a substantial depletion. This study introduces an innovative approach for synthesizing Ti 3 C 2 T x MXene/Ni/C composites with tunable interlayer spacing, showing their potential for applications in microwave absorption (MA).
研究领域:
材料科学
·
电磁学
✓ 已验证
产品关联
DOI
高影响因子
Carbohydrate Polymer Technologies and Applications
·
2022
·
IF 0
Kun Hou,Hu Zhou,Ke Zhu,Chunye Xie,Simin Liu,Yingxiang He,Xingyi Zhu,Ming Wu,Tiefan Huang
Oily wastewater seriously endangers human health. Ti 3 C 2 T x MXene has attracted extensive attention as a building block for separating membranes because of its unique two-dimensional structure and excellent hydrophilicity. In this study, we constructed a superwetting Ti 3 C 2 T x MXene membrane intercalated with sodium alginate. The hydrophilic sodium alginate not only enlarged the nanochannel of the MXene membrane but also decorated the membrane surface and endowed the membrane with excellent surface superwetting properties. The underwater oil contact angle (OCA) was about 151°, indicating an extremely low adhesion between oil and membrane surface. The membrane could also separate a series of oil-water emulsions with high separation efficiency and flux. Due to its excellent underwater superoleophobicity, the membrane demonstrated outstanding antifouling property. Excellent separation performance was maintained even after separation cycles. This work provides insights into the rational use of MXene-based membranes design and demonstrates its potential in the field of membrane separation.
研究领域:
材料科学
·
环境工程
✓ 已验证
产品关联
DOI
ACS Nano
·
2019
·
IF 13.903
Xifan Chen,Yuanzhi Zhu,Miao Zhang,Jinyi Sui,Wenchao Peng,Yang Li,GuoLiang Zhang,Fengbao Zhang,Xiaobin Fan
MXenes, a family of two-dimensional (2D) transition-metal carbide and nitride materials, are supposed to be promising pseudocapacitive materials because of their high electronic conductivity and hydrophilic surfaces. MXenes, prepared by removing the “A” elements of their corresponding MAX phases by hydrofluoric acid (HF) or LiF–HCl etching, possess abundant terminal groups like −F, −OH, and −O groups. It has been proven that the MXenes with fewer −F terminal groups and more −O groups showed a higher pseudocapacitor performance. In organic reactions, −OH and −X (X = halogen) groups could turn to ether groups in strong nucleophilic reagent. Inspired by that, herein, we report an n-butyllithium-treated method to turn the −F and −OH terminal groups to −O groups on the Ti3C2Tx MXenes. Two types of Ti3C2Tx MXenes prepared by either HF or LiF–HCl etching were systematically investigated, and a comparison with the traditional KOH/NaOH/LiOH-treated method was also carried out. It is found that most of the −F terminal groups on the Ti3C2Tx MXenes can be successfully removed by n-butyllithium, and abundant −O terminal groups were formed. The n-butyllithium-treated Ti3C2Tx MXenes show promising applications in high-performance pseudocapacitors. A record high capacitance of 523 F g–1 at 2 mV s–1 was obtained for the n-butyllithium-treated Ti3C2Tx MXenes, and 96% capacity can remain even after 10 000 cycles.
研究领域:
材料科学
·
电化学
·
能源存储
✓ 已验证
产品关联
DOI
PubMed
高影响因子
JOURNAL OF MEMBRANE SCIENCE
·
2025
·
IF 9
Junzhi Li,Yanan Li,Haiyu Luo,Lili Tang,Nan Xu,Wenlan Ji,Shihao Zhang,Pei Nian,Yibin Wei
Construction of well-confined sub-nanochannels for molecular-sieving in organic solvent environment remains a challenge for organic solvent nanofiltration (OSN) membranes in precise fluid separation. Herein, cyclodextrin (CD) cross-linked 2D Ti 3 C 2 T x MXene membranes with laminar nanostructure containing unique sub-nanoscale mass transfer channels for unprecedented OSN performance is reported. Density-functional theory (DFT) calculation and experimental results confirm that CD monomers (α-, β-, γ-) with 3D intrinsic cavity structures are anchored with Ti 3 C 2 T x MXene nanosheets forming a stable polyester cross-linking network via an interfacial molecular engineering using trimesoyl chloride (TMC). The prepared membranes exhibit ultrahigh OSN performance with excellent stability in organic solvents. The optimal membrane can effectively reject dyes such as methylene blue (99.8%), rhodamine B (98.0%), and Congo Red (100%), while having high ethanol permeability ranging from 22.58 to 85.31 L/(m 2 h bar). Remarkably, the membrane structure remained intact after 4 weeks immersion in ethanol and acetone. This work provides a facile and reliable strategy to construct a high-performance 2D material-based OSN membrane with well-confined mass transfer channels.
研究领域:
材料科学
·
化学工程
✓ 已验证
产品关联
DOI
高影响因子