Enabling materials to undergo reversible dynamic transformations akin to the behaviors of living organisms represents a critical challenge in the field of material assembly. The pursuit of such capabilities using conventional materials has largely been met with limited success. Herein, the discovery of reversible constrained dissociation and reconfiguration in MXene films, offering an effective solution to overcome this obstacle is reported. Specifically, MXene films permit rapid intercalation of water molecules between their distinctive layers, resulting in a significant expansion and exhibiting confined dissociation within constrained spaces. Meanwhile, the process of capillary compression driven by water evaporation reinstates the dissociated MXene film to its original compact state. Further, the adhesive properties emerging from the confined disassociation of MXene films can spontaneously induce fusion between separate films. Utilizing this attribute, complex structures of MXene films can be effortlessly foamed and interlayer porosity precisely controlled, using only water as the inducer. Additionally, a parallel phenomenon has been identified in graphene oxide films. This work not only provides fresh insights into the microscopic mechanisms of 2D materials such as MXene but also paves a transformative path for their macroscopic assembly applications in the future.
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http://dx.doi.org/10.1002/advs.202309171 | DOI Listing |
Int J Biol Macromol
January 2025
School of Engineering and Materials Science, Queen Mary University of London, London E1 4NS, United Kingdom. Electronic address:
The fabrication of eco-friendly and high-performance composite materials has gained significant attention for multifunctional applications. Polyvinyl alcohol (PVA)/starch composite films containing varying amounts of TiCT MXene (2.5-10 wt%) were produced using a simple casting method.
View Article and Find Full Text PDFLangmuir
January 2025
Key Laboratory of Optoelectronic Devices and Systems of Ministry of Education and Guangdong Province, College of Physics and Optoelectronic Engineering, Shenzhen University, Shenzhen 518060, P.R. China.
MXenes have attracted tremendous attention in electromagnetic interference shielding, energy storage, and gas and humidity detections because of their ultralarge surface area and abundant functional groups. However, their poor stability against hydration and oxidation makes them challenging for long-term storage and applications. Herein, we proposed and demonstrated a TiCT MXene composite-based humidity sensor, of which the stability is pronouncedly enhanced by introducing an O adsorption competitor of extracted bentonite (EB).
View Article and Find Full Text PDFMicromachines (Basel)
December 2024
College of Materials and Metallurgy, Guizhou University, Guiyang 550025, China.
This study introduces the development of a W-M electrochromic film, characterized by a "coral"-like TiO@WO heterostructure, synthesized via a hydrothermal process leveraging the inherent instability of MXene. The film showcases exceptional electrochromic performance, with a coloring response time of 2.8 s, a bleaching response time of 4.
View Article and Find Full Text PDFJ Mol Graph Model
January 2025
School of Materials Science and Engineering, Yancheng Institute of Technology, Yancheng, 224051, China. Electronic address:
MXenes quantum dots (QDs), including NbC, NbCO, and NbCF, are emerging materials with exceptional structural, electronic, and optical properties, making them highly suitable for biomedical applications. This study investigates the structural optimization, stability, electronic properties, and drug-loading potential of these QDs using fluorouracil (Flu) as a model drug. Structural analyses show that the functionalization of NbC with O and F atoms enhances stability, with binding energies (BEs) of 7.
View Article and Find Full Text PDFInt J Biol Macromol
December 2024
Department of Plastic and Cosmetic Surgery, Treatment Center of Burn and Trauma, Affiliated Hospital of Jiangnan University, Wuxi 214122, China. Electronic address:
The conversion of mechanical energy into electrical energy by triboelectric nanogenerators (TENG) has attracted attention in recent years, particularly in the field of wearable sensor. In this work, TEMPO-oxidized cellulose nanofibers (TOCNF) with carboxylate groups were compounded with MXene to serve as both the negative friction layer and the electrode in assembling a TENG with nylon. The synergistic effect between TOCNF and MXene was analyzed to disclose its influence on the performance of the as-prepared TENG.
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