Recent advances in MXene (Ti3C2Tx) fibers, prepared from electrically conductive and mechanically strong MXene nanosheets, address the increasing demand of emerging yet promising electrode materials for the development of textile-based devices and beyond. However, to reveal the full potential of MXene fibers, reaching a balance between electrical conductivity and mechanical property is still the fundamental challenge, mainly due to the difficulties to further compact the loose MXene nanosheets. In this work, we demonstrate a continuous and controllable route to fabricate ultra-compact MXene fibers with an in-situ generated protective layer via the synergy of interfacial interactions and thermal drawing-induced stresses. The resulting ultra-compact MXene fibers with high orientation and low porosity exhibit not only excellent tensile strength and ultra-high toughness, but also high electrical conductivity. Then, we construct meter-scale MXene textiles using these ultra-compact fibers to achieve high-performance electromagnetic interference shielding and personal thermal management, accompanied by the high mechanical durability and stability even after multiple washing cycles. The demonstrated generic strategy can be applied to a broad range of nanostructured materials to construct functional fibers for large-scale applications in both space and daily lives.

No abstract

The biofouling of ureteral stents and subsequent urinary tract infections mainly come from the adsorption and adhesion of proteins and microorganisms and their ensuing proliferation. Although general polycationic surfaces in implants have good antibacterial activities, they suffer from limited durability due to severe protein and bacterial adsorption. Here, a biodegradable and anti‐biofilm fiber‐membrane structured ureteral stent (FMBUS) with synergetic contact‐killing antibacterial activity and antiprotein adsorption is described. The stent is prepared by generating hyperbranched poly(amide‐amine)‐grafted polydopamine microparticles (≈300 nm) on the surface of fibers by in situ polymerization and Schiff base reactions. The biomimetic surface endows the FMBUS with a positive charge (+21.36 mV) and superhydrophilicity (water contact angle: 0°). As a result, the stents fulfilled the following functions: i) reduced attachment of host protein due to superhydrophilicity (Lysozyme: 92.1%; human serum albumin: 39.4%); ii) high bactericidal activities against contact pathogenic bacteria (contact‐killing rate: 99.9999% for both E. coli and S. aureus; antiadhesion rate: 99.2% for E. coli and 99.9999% for S. aureus); iii) biocompatibility in vitro (relative growth rate of L929: >90% on day 3) and in vivo; and iv) gradient biodegradability to avoid a second surgery of stent extraction 1–2 weeks after implantation.

No abstract

Current metal nanomaterials for developing nanofunctional textiles are mostly based on metal nanoparticles (NPs) that show aqueous instability, a tendency to aggregate, and low chemical affinity to biomass textiles, leading to low nano-metal uptake during finishing, significant declines in function, and nano-pollution. Herein, we demonstrate a strategy to transform metal (Ag, Au, and Pt) NPs into homogenous hyperbranched poly(amide-amine) (HBPAA)-encapsulated NPs showing high water solubility, oxidative resistance, and affinity to biomass materials upon surface capping with HBPAA. The proposed method represents a universal, simple, clean, and efficient self-assembly technology to produce monolayered Ag–Au–Pt ternary-coated biomass textiles. The combination of Ag, Au, and Pt NPs yields a positive potential of approximately +37.12 mV depending on the metal concentration and could simultaneously self-assemble onto natural fibers, including cotton, silk, and wool, through the one-step impregnation of textiles. Increasing the temperature and concentration of the mixture favors the self-assembly process. A mixture of 30–110 mg/L Ag, Au, and Pt NPs could nearly completely anchor onto cotton, silk, and wool textiles after impregnation at 100 °C for 1 h without chemical assistance, thereby indicating the possibility of clean production. As-prepared functional cotton, silk, and wool possessed similarly high antibacterial activities, and a mixture containing over 1500 mg/g NPs inhibited 99% of the Escherichia coli and Staphylococcus aureus in the sample textiles. The developed coating technology is simple, clean, controllable, and broadly applicable; thus, it could be potentially applied in functional textiles.