Although Ti 3 C 2 T x MXene/fabric composites have shown promise as flexible pressure sensors, the effects of MXene composition and structure on piezoresistive properties and the effects of the textile structure on sensitivity have not been systematically studied. Herein, impregnation at room temperature was used as a cost-effective and scalable method to prepare composite materials using different fabrics [plain-woven fabric, twill-woven fabric, weft plain-knitted fabric, jersey cross-tuck fabric, and nonwoven fabric (NWF)] and MXene nanosheets (Ti 3 C 2 T x , Ti 2 CT x , Ti 3 CNT x , Mo 2 CT x , Nb 2 CT x , and Mo 2 TiC 2 T x ). The MXene nanosheets adhered to the fabric surface through hydrogen bonding, resulting in a conductive network structure. The Ti 3 C 2 T x @NWF composite was found to be the optimal flexible pressure sensor, demonstrating high sensitivity (6.31 kPa −1 ), a wide sensing range (up to 150 kPa), fast response/recovery times (300 ms/260 ms), and excellent durability (2000 cycles). Furthermore, the sensor was successfully used to monitor full-scale human motion, including pulse, and a 4 × 4 pixel flexible sensor array was shown to accurately locate pressure and recognize the pressure magnitude. These findings provide a basis for the rational design of MXene/textile composites as wearable pressure sensors for medical diagnosis, human−computer interactions, and electronic skin applications.

To obtain supercapacitors for wearable electronic devices, highly conductive stretchable electrode substrates with excellent tensile recovery are required. However, the simultaneous realization of the above mentioned characteristics is difficult. In this study, tough stainless‐steel fibers (SSFs) are employed as the substrates for knitting into stainless‐steel meshes (SSMs), for the fabrication of textile electrodes with typical 2D‐interconnected networks. The obtained knitted networks can transform the angular elasticity of SSFs into the stretchability of the textile electrodes. The electrodes based on the SSM substrates can be obtained via the in situ growth of NiCo2S4 nanosheets covered by CoS2 nanowires, which exhibit a high specific capacity, high rate capability, and excellent cycling stability. Moreover, the first stretchable solid‐state hybrid supercapacitors based on SSM display excellent performances with respect to a high energy density (60.2 Wh kg−1 at 800 W kg−1), remarkable tensile recovery (≤40% elongation), and high stability (≈76.4% capacity retention at 30% strain for 1000 stretching cycles). The highly stretchable supercapacitor is sewn on the elbow of a garment to drive a light‐emitting diode, and it maintains a high performance with respect to the repetitive process of bending and straightening, thus demonstrating the high applicability of the designed SSMs to wearable electronics.

Stretchable supercapacitors have received widespread attention due to their potential applications in wearable electronics and health monitoring. Stretchable supercapacitors not only possess advantages such as high power density, long cycle life, safety, and low cost of conventional supercapacitors but also have excellent flexibility and stretchability, which make them well integrated with other wearable systems. In this review, various strategies to fabricate stretchable supercapacitors are focused. The preparation methods for stretchable electrodes/devices in the literature are carefully classified and analyzed. Three strategies for preparing stretchable electrodes/devices are summarized in detail—the design of elastic polymer substrates, stretchable electrode structures, and composite electrodes combined with elastic polymers and stretchable structures. Meanwhile, the interface problem of electrodes/devices in the stretching process is studied in depth. The research progress of multifunctional stretchable supercapacitors is also introduced. Finally, challenges and possible solutions that still need to be addressed in the future development of stretchable supercapacitors are highlighted and prospected. This review comprehensively discusses the latest research progress in the field of stretchable supercapacitors and systematically elucidates the electrochemical and mechanical properties of these devices, hoping to improve the roadmap for scientists and engineers to develop supercapacitors with high electrochemical performance and good stretchability.

Abstract:Interface issues urgently need to be addressed in high-performance fiber reinforced composites. In this study, different periods of O 2 plasma treatment are proposed to modify twist-free polyimide (PI) filaments to improve hydrophilicity and mechanical and interfacial properties. Feeding O 2 produces chemically active particles to modify the filament surface via chemical reactions and physical etching. According to the X-ray photoelectron spectroscopy (XPS) results, the PI filaments exhibit an 87.16% increase in O/C atomic ratio and a 135.71% increase in the C-O functional group after 180 s O 2 plasma treatment. The atomic force microscope (AFM) results show that the root mean square roughness (Rq) of the treated PI filaments increases by 105.34%, from 38.41 to 78.87 nm. Owing to the increased surface oxygenic functional groups and roughness after O 2 plasma treatment, the contact angle between treated PI filaments and water reduces drastically from the pristine state of 105.08 • to 56.15 • . The O 2 plasma treated PI filaments also demonstrate better mechanical properties than the pristine PI filaments. Moreover, after O 2 plasma treatment, the adhesion between PI filaments and poly(amic acid) (PAA) is enhanced, and the tensile strength of the polyimide/poly(amic acid) (PI/PAA) self-reinforced composites increases from 136 to 234 MPa, even causing the failure mode of the composite changes from adhesive failure to partly cohesive failure.

Biomaterials-centered infection or implant-associated infection plays critical roles in all areas of medicine with implantable devices. The widespread over use of antibiotics has caused severe bacterial resistance and even super bugs. Therefore, the development of anti-infection implantable devices with non-antibiotic-based new antimicrobial agents is indeed a priority for all of us. In this study, antimicrobial composite meshes were fabricated with broad-spectrum antimicrobial peptides (AMPs). Macroporous polypropylene meshes with poly-caprolactone electrospun nanosheets were utilized as a substrate to load AMPs and gellan gum presented as a media to gel with AMPs. Different amounts of AMPs were loaded onto gellan gum to determine the appropriate dose. The surface morphologies, Fourier-transform infrared spectroscopy spectra, in vitro release profiles, mechanical performances, in vitro antimicrobial properties, and cytocompatibility of composite scaffolds were evaluated. Results showed that AMPs were loaded into the meshes successfully, the in vitro release of AMPs in phosphatebuffered saline was prolonged, and less than 60% peptides were released in 10 days. The mechanical properties of composite meshes were also within the scope of several commercial surgical meshes. Composite meshes with the AMP loading amount of over 3 mg/cm 2 showed inhibition against both Gram-negative and Gram-positive bacteria effectively, while they presented no toxicity to mammalian cells even at a loading amount of 10 mg/cm 2 . These results demonstrate a new simple and practicable method to offer antimicrobial properties to medical devices for hernia repair.