CHEMICAL ENGINEERING JOURNAL
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2024
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IF 13.3
Jingxuan Cui,Jiao Wu,Aihu Feng,Yang Yu,Le Mi,Yun Yu
As a novel material with low infrared emissivity, Ti 3 C 2 T x MXene is promising in infrared stealth. However, the problem that MXene is easily oxidized poses a great challenge to its practical applications. In this paper, a tannic acid (TA) enhanced MXene oxidation stability composite film with low infrared emissivity is reported. TA effectively diminishes the pore size within the MXene film and leads to a tight and orderly arrangement of nanosheets, maintaining the low emissivity properties of Ti 3 C 2 T x MXene itself. In addition, TA reacts preferentially with H 2 O/O 2 entering the film to consume the oxidizing source, while also being able to form coordination with Ti atoms for protection against oxidation, resulting in the composite film exhibiting excellent oxidation resistance. Remarkably, there is no formation of TiO 2 and the emissivity only rises from 0.16 to 0.18 after 72 h in the humid heat environment. Even after prolonged exposure to 20-day humid heat, it still maintains exceptional infrared emissivity (0.24) and stealth performance (reducing the radiant temperature of the object from 94 °C to 47.4 °C, △T = 46.6 °C). In contrast, the original Ti 3 C 2 T x MXene film has lost its infrared stealth performance after 10-day humid heat (△T = 5.3 °C) with an infrared emissivity of 0.76. This paper provides a new strategy to solve the problem of MXene performance stability in humid and oxidizing environments.
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MICROCHIMICA ACTA
·
2024
·Vol. 191
·期 8
·1-10
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IF 5.3
Feng Lei,Chen Junji,Yang Min,Wang Juan,Yin Shougen,Zhang Deliang,Qin Wenjing,Song Jibin
Ti 3 C 2 T x MXene/Cu x O composites were prepared by acid etching combined with electrochemical technique. The abundant active sites on the surface of MXene greatly increase the loading of Cu x O nanoparticles, and the synergistic effect between the different components of the composite can accelerate the oxidation reaction of glucose. The results indicate that at the working potential of 0.55 V (vs. Ag/AgCl), the glucose sensor based on Ti 3 C 2 T x MXene/Cu x O composite presents large linear concentration ranges from 1 µM to 4.655 mM (sensitivity of 361 µA mM −1 cm −2 ) and from 5.155 mM to 16.155 mM (sensitivity of 133 µA mM −1 cm −2 ). The limit of detection is 0.065 µM. In addition, the sensor effectively avoids the oxidative interference of common interfering species such as ascorbic acid, dopamine and uric acid. The sensor has good reproducibility, stability and acceptable recoveries for the detection of glucose in human sweat sample (97.5-103.3%) with RSD values less than 4%. Based on these excellent properties it has great potential for the detection of glucose in real samples. Graphical abstract
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Advanced Composites and Hybrid Materials
·
2024
·Vol. 7
·期 2
·1-15
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IF 23.2
Bi Xiaoyu,Shi Yang,Ge Shengbo,Xu Ben Bin,Li Xia,He Ximin,Huang Runzhou
Reduced graphene oxide (rGO) and MXene have garnered significant attention due to their exceptional pseudocapacitance and electrical conductivity that are viable in energy storage applications. Nevertheless, the challenge of self-restacking between the 2D material surfaces and the tendency of MXene to oxidise has posed obstacles to their further utilisation. This prompted researchers to use cellulose nanofibre (CNF) as a prospective “bridge” to connect the two materials. This approach has been shown to prevent MXene from oxidising while facilitating GO conversion into rGO via reduction. Consequently, 3D macroporous Ti 3 C 2 T x MXene/cellulose nanofibres/reduced graphene oxide (MCG) aerogels have been successfully prepared. A breakthrough in solving the self-stacking problem and creating a sensibly designed 3D macroporous electrode structure has yielded excellent electrochemical capabilities for MCG aerogel electrodes. Specifically at 1.0 mW cm −2 power density, these electrodes have demonstrated an outstanding performance in 5000 cycles with 79.4% retention rate, favourable areal specific capacitance of 671 mF cm −2 and unparalleled energy density of 60.9 mWh cm −2 . Overall, this study offers significant perspectives on the possible uses of 2D materials, especially in terms of adjusting their structure and functionality.
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ACS Applied Materials & Interfaces
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2024
·
IF 8.3
Leikai Zhao,Rui Zhang,Guixin Yang,Yuhang Wang,Shili Gai,Xin Zhao,Mengmeng Huang,Piaoping Yang
Foreseen as foundational in forthcoming oncology interventions are multimodal therapeutic systems. Nevertheless, the tumor microenvironment (TME), marked by heightened glucose levels, hypoxia, and scant concentrations of endogenous hydrogen peroxide could potentially impair their effectiveness. In this research, two-dimensional (2D) Ti3C2 MXene nanosheets are engineered with CeO2 nanozymes and glucose oxidase (GOD), optimizing them for TME, specifically targeting cancer therapy. Following our therapeutic design, CeO2 nanozymes, embodying both peroxidase-like and catalase-like characteristics, enable transformation of H2O2 into hydroxyl radicals for catalytic therapy while also producing oxygen to mitigate hypoxia. Concurrently, GOD metabolizes glucose, thereby augmenting H2O2 levels and disrupting the intracellular energy supply. When subjected to a near-infrared laser, 2D Ti3C2 MXene accomplishes photothermal therapy (PTT) and photodynamic therapy (PDT), additionally amplifying cascade catalytic treatment via thermal enhancement. Empirical evidence demonstrates robust tumor suppression both in vitro and in vivo by the CeO2/Ti3C2-PEG-GOD nanocomposite. Consequently, this integrated approach, which combines PTT/PDT and enzymatic catalysis, could offer a valuable blueprint for the development of advanced oncology therapies.
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COMPOSITES PART A-APPLIED SCIENCE AND MANUFACTURING
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2025
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IF 8.9
Miaomiao Ma,Yuhong Qi,Qi’an Chen,Zhanping Zhang
Biofouling of underwater equipment caused by marine organisms is a major problem in the marine industry. Although hydrogel exhibits excellent antifouling properties, its mechanical performance greatly limits its practical application. In this work, a suitable marine antifouling hydrogel (PSM) was designed utilizing a polyethylene glycol–modified MXene (Ti 3 C 2 T x -PEG) toughening mechanism and a silica loaded with nitrogen-doped carbon dots (SiO 2 @N-CDs) reinforcement strategy to enhance the durability of the hydrogel. The PSM hydrogel exhibited a fracture strength of up to 1.62 MPa, elongation of 1734 %, and toughness of 17.7 MJ/m 3 . Furthermore, the PSM hydrogel exhibited excellent photothermal antibacterial properties, with antibacterial rates against E. coli and S. aureus reaching 100%. After 180 days of immersion in seawater, the PSM hydrogel morphology remained stable. Because of its long-term durability and effective antifouling properties, our PSM hydrogel can be developed for use in marine ship coatings.
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MOLECULES
·
2024
·Vol. 29
·期 10
·2383
·
IF 4.2
Zhi Yang,Lu Yang,Yucun Liu,Lei Chen
Surface-enhanced Raman scattering (SERS) is a promising technique for sensitive detection. The design and optimization of plasma-enhanced structures for SERS applications is an interesting challenge. In this study, we found that the SERS activity of MXene (Ti3C2Tx) can be improved by adding Au nanoparticles (NPs) in a simple photoreduction process. Fluoride-salt-etched MXene was deposited by drop-casting on a glass slide, and Au NPs were formed by the photocatalytic growth of gold(III) chloride trihydrate solutions under ultraviolet (UV) irradiation. The Au–MXene substrate formed by Au NPs anchored on the Ti3C2Txsheet produced significant SERS through the synergistic effect of chemical and electromagnetic mechanisms. The structure and size of the Au-decorated MXene depended on the reaction time. When the MXene films were irradiated with a large number of UV photons, the size of the Au NPs increased. Hot spots were formed in the nanoscale gaps between the Au NPs, and the abundant surface functional groups of the MXene effectively adsorbed and interacted with the probe molecules. Simultaneously, as a SERS substrate, the proposed Au–MXene composite exhibited a wider linear range of 10−4–10−9mol/L for detecting carbendazim. In addition, the enhancement factor of the optimized SERS substrate Au–MXene was 1.39 × 106, and its relative standard deviation was less than 13%. This study provides a new concept for extending experimental strategies to further improve the performance of SERS.
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Journal of Materials Chemistry A
·
2024
·
IF 10.7
Ruyue Su,Jingyi Chen,Xueqin Zhang,Wenqing Wang,Rujie He,Ying Li
Terahertz (THz) electromagnetic interference (EMI) shielding materials with superior performance are urgently needed with the development of THz electronic devices. Herein, a photocured Ti3C2Tx MXene/SiOC ceramic (MSiOC) composite with a sandwich-like structure was prepared using a photosensitive resin as a precursor. In addition, the EMI shielding properties of the MSiOC composite with a low mass loading of the MXene were greatly improved. The influence of the content of Ti3C2Tx MXenes on the EMI shielding properties of the MSiOC composite was studied, and its EMI shielding mechanism was further elucidated. The resultant MSiOC composite exhibited an average shielding effectiveness (SET) of 24.5 dB in the frequency range of 0.2–1.6 THz at a MXene mass loading of only 0.3 wt%, which was remarkably improved by 53% compared to pure SiOC. In addition, the MSiOC composite with a broad high-absorptivity frequency band showed an absorption-dominated THz EMI shielding mechanism. This result proved that the synergistic effect of the MXene and SiOC was responsible for the high attenuation capability of MSiOC for THz waves. Finally, MSiOC with customized structures was easily fabricated via vat photopolymerization 3D printing, followed by a pyrolysis process. The smallest feature size of these structures was about 140 μm. Moreover, the flexible photocured green part could be secondary molded, which improved the structural controllability of the composite. Our work provides insights into the rational design of MXene-based composites for new-generation THz EMI shielding materials.
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JOURNAL OF MATERIALS SCIENCE & TECHNOLOGY
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2024
·
IF 11.2
Hao Xu,Shuai Liu,Zhiang Li,Fan Ding,Ting Wang,Ting Liu,Weimin Wang,Kaikai Song,Jie Liu,Lina Hu
Succinonitrile has shown significant promise for application in polymer electrolytes for solid-state lithium metal batteries due to its high ionic conductivity at low-temperature. However, the use of Succinonitrile is limited due to its corrosion of Li metal. Herein, we report a solid polymer electrolyte with high ionic conductivity (2.17 × 10 −3 S cm −1 , 35 °C) enhanced by Ti 3 C 2 T x . Corrosion of the Li anode is prevented due to the Succinonitrile molecules being efficiently anchored by Ti 3 C 2 T x . Meanwhile, the coordination environment of Li + is weakened due to the introduction of competitive coordination induction effects into the polymer electrolyte, resulting in efficient Li + conduction. Furthermore, the mechanical properties of the electrolyte are enhanced by modulating the ratio of Ti 3 C 2 T x to suppress the growth of Li dendrites. Therefore, Li||Li symmetric batteries deliver stable cycling up to 8000 h at 28 °C. LiFePO 4 ||Li full batteries exhibit excellent cycling stability of 151.7 mAh g −1 with a capacity retention of 99.3% after 300 cycles. This work not only presents a new idea to suppress the corrosion of the Li anode by Succinonitrile but also provides a simple, feasible, and scalable strategy for high-performance Li metal batteries.
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Materials Today Communications
·
2025
·
IF 4.5
Yuntong Wen,Hao Bian,Yongpeng Ran,Yonghao Xie,Minmin You,Huimin Wen,Liyun Shi,Jingquan Liu,Zude Lin
The 2D Ti 3 C 2 T x MXene anchored with magnetic particles has garnered significant attention due to its superior electromagnetic shielding performance and low reflection coefficient. However, current research on MXene-anchored magnetic particles faces several challenges, including complex fabrication processes, difficulty in controlling compositional ratios, the predominant use of spherical magnetic particles. In this work, by employing surfactants, FeCo alloy and Ni flakes were uniformly anchored onto MXene, the preparation process of the composite is simple and facilitates better control over the ratios of individual samples. Due to the unique structure formed by the intercalation of FeCo alloy and Ni flakes within the MXene layers, M-FC-N-35 exhibits an average electromagnetic shielding effectiveness of 61.2 dB within the Ku-band and maintains a reflection coefficient as low as 0.69. Additionally, the M-FC-N-35 composite was applied to the surface of the temperature sensor casing. It was found that under an electromagnetic field strength of 200 V/m and within a frequency range of 6–18 GHz, the temperature measurement deviation was reduced to 9.35 % of that of the sensor without the shielding material, demonstrating high electromagnetic interference resistance. This work provides guidance for simplifying the fabrication process of MXene composites with magnetic metals and enriching the system of electromagnetic shielding materials.
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JOURNAL OF COLLOID AND INTERFACE SCIENCE
·
2024
·
IF 9.4
Yun Tian,Luowen Xu,Shuo Ning,Changfu Wang,Yun Wang,Hao Jiang,Dingzhong Yuan,Fengtao Yu,Yan Liu
Photocatalysis has emerged as a extremely promising green technology for the treatment of uranium-containing wastewater. This study focuses on the fabrication of Ti 3 C 2 T x /Cd 0.8 Zn 0.2 S composites with Schottky junctions through the in-situ growth of Cd 0.8 Zn 0.2 S on Ti 3 C 2 T x nanosheets, enabling efficient photoreduction of U(VI) without the requirement of sacrificial agents. The results demonstrate that the Ti 3 C 2 T x /Cd 0.8 Zn 0.2 S composites achieve remarkable 99.48 % U(VI) reduction efficiency within 60 min in a 100 ppm uranium solution. Furthermore, the removal rate remains above 90 % after five cycles. The formation of Schottky heterojunctions by Ti 3 C 2 T x and Cd 0.8 Zn 0.2 S leads to the generation of an internal electric field that significantly promotes the rapid separation and transfer of photogenerated carriers, thereby enhancing the photocatalytic reduction efficiency of Ti 3 C 2 T x /Cd 0.8 Zn 0.2 S-3:100 (TC/CZS-3:100). A considerable amount of electrons accumulate on Ti 3 C 2 T x via the Schottky barrier, effectively facilitating the reduction of U(VI) to U(IV). As a co-catalyst, Ti 3 C 2 T x enhances the photocatalytic performance and stability of Cd 0.8 Zn 0.2 S. Moreover, the practical application in the waste liquid of rare earth tailings reveals that the removal rate can be as high as 91.24 %. This research is of significant value in the development of effective photocatalysts for the elimination of uranium from wastewater.
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ACS Applied Nano Materials
·
2025
·
IF 5.5
Feng Ding,Xiong Shuai,Yanyan Chen,Donglan Zhang,Fangwei Qi,Cijun Shuai
Following peripheral nerve injury, a large number of macrophages will be recruited to the nerve defect site to regulate the immune microenvironment and then initiate a series of inflammatory reactions, which is not conducive to nerve repair. Electrical stimulation can not only affect the polarity of macrophages by regulating the immune microenvironment but also promote nerve regeneration by modulating voltage-gated ion channels. However, traditional electrical stimulation relies on power sources, wires, and implanted electrodes, which may pose risks of infection and secondary surgery. Here piezoelectric materials Ti3C2Tx/UiO-66 are synthesized by a hydrothermal method and then blended into PLLA to prepare a self-power nerve scaffold using laser additive manufacturing technology. Under ultrasound stimulation, UiO-66 nanoparticles can generate localized piezoelectric potential, while Ti3C2Tx nanosheets accelerate the charge transfer. The results indicate that a nerve scaffold promotes the current generation, with a current of up to 0.036 μA. The results indicate that electrical stimulation can promote the transformation of macrophages into the M2 antiinflammatory phenotype by inhibiting the Ca2+-CaMKII-NF-κB signaling pathway. Furthermore, the scaffold can upregulate the expression of bone marrow mesenchymal stem cell neural markers Tuj and Map under ultrasound treatment. This work provides insights into wireless electrical stimulation regulating the immune microenvironment to promote nerve repair.
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Journal of Energy Storage
·
2025
·
IF 9.8
Yongjie Huang,Yuqing Chen,Qing Xu,Chunyan Xu,Liying Yang,Ningyi Jiang,Jibin Zhong,Xinghan Zhao,Shougen Yin
Lithium‑sulfur (Li S) batteries are regarded as a potential candidate of next-generation energy storage devices. However, the poor long-term cycling performance arose from shuttle effect remains a challenge. The recent studies have shown that two dimensional (2D) MXenes have great potential in high efficient Li S cells due to strong adsorption ability for lithium polysulfides (LiPSs) and effective catalytic activity for rapid kinetics. Herein, a polypropylene separator modified by a three-dimensional (3D) TiO 2 -Ti 3 C 2 T x MXene@CNTs heterostructure using sulfur templates combined with H 2 O 2 partial oxidation treatment is proposed to alleviate the shuttle effect and improve the overall utilization efficiency of sulfur in Li S batteries. The as-prepared separator effectively enhances the LiPSs trapping ability and significantly reduces the oxidation overpotential of Li 2 S, demonstrating high catalytic efficiency and sufficient conductivity to promote the transformation of LiPS to Li 2 S and thus accelerating the transformation kinetics of Li S batteries. Remarkably, the TiO 2 -MX@CNTs modified separator with 1.3 mg cm −2 sulfur loading enables a stable capacity of 859 mAh g −1 after 300 cycles at 1C with a capacity decay rate of approximately 0.035 % per cycle, suggesting promising potential for practical applications. This work presents a new method to regulate the electrochemical performance of Li S batteries.
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