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Stretchable electrodes are critical to the development of advanced technologies such as human–machine interaction, flexible sensing, and wearable power supply, making them of significant research value. However, the current preparation methods for high‐performance stretchable electrodes are complex and inefficient, posing challenges for their large‐scale application in the realm of flexible wearables. To address this need, a straightforward and efficient embedding strategy is reported for fabricating stretchable silver nanowire/thermoplastic elastomer composite electrodes (referred to as Strem‐AT) utilizing the viscoelasticity and outstanding mechanical properties of polymer elastomers to achieve outstanding extensibility, conductivity, and a smooth surface. These electrodes exhibit excellent tensile behavior, low surface roughness, and stable electrical properties, enabling their successful integration into stretchable sensors and intrinsically stretchable organic photovoltaic cells (IS‐OPV). When applied to human skin joints for motion detection, the sensor demonstrates remarkable stretchability and stable signal output. Importantly, the all‐polymer IS‐OPV exhibits a top‐notch power conversion efficiency (PCE) of >12.5% and a PCE80% strain exceeding 50%. Furthermore, even after subjecting high‐strain stretching at 50% for 1000 cycles, the IS‐OPV can retain 76% of the initial PCE. This study presents a multifunctional stretchable electrode with high repeatability and easy‐to‐scale fabrication in wearable sensors and photovoltaics. [ABSTRACT FROM AUTHOR]

Intrinsically stretchable organic photovoltaic cells (OPVs) have garnered significant attention as crucial devices for powering next‐generation wearable electronics. Despite the rapid power conversion efficiency gains in champion OPVs, their brittle stretchability has failed to meet the demands of the Internet of Things era, severely hindering further development and practical applications. In this regard, a new dual‐donor polymer blending strategy is demonstrated for constructing intrinsically stretchable OPVs by designing a novel high‐molecular–weight conjugated polymer PM6‐HD. This PM6 derivative featuring long alkyl chains can reach a sufficiently high molecular weight and thus exhibits a high fracture strain exceeding 90%, which is ≈12 times higher than the benchmark PM6. Synergistic optimization of mechanical properties and photovoltaic performance in polymer:small molecule and all‐polymer systems constructed from the physical blends of PM6 and PM6‐HD is achieved. Crucially, the resulting intrinsically stretchable OPV demonstrates excellent stretchability and stability, with a record PCE80% strain of 50.3% and the efficiency retention of above 80% even after 1000 cycles of cyclic stretching at high strains. This work contributes to the advancement of intrinsically stretchable OPV technology and opens up new possibilities for its integration into wearable electronic devices. [ABSTRACT FROM AUTHOR]

Composite materials with multi-layer structure were prepared by combining polyurethane film and waste polyphenylene sulfide filters by hot melting, which could be used as sound-absorbing materials to contribute to the noise control and reutilization of industrial waste. The structure, mechanical property, pore size distribution and stability of waste polyphenylene sulfide filters were investigated and could directly affect the quality of recycled products. The effects of layer numbers, layering sequence and polyurethane film thickness on sound absorption and insulation properties were also analyzed using an impedance tube absorption test system. The results showed that multi-layer materials had a better sound absorption effect than single-layer polyphenylene sulfide filters at low frequency. The sound absorption coefficients of the single-layer sample was only 0.081 at 1000 Hz, while the sound absorption coefficients of the five-layer sample could reach 0.26. The sound absorption properties of multi-layer materials were slightly affected by layering sequence, but polyurethane film thickness had a significant effect on sound absorption properties. The α of the SUS1 and USU1 samples were 0.151 and 0.170, while the α of the SUS3 and USU3 samples were only 0.076 and 0.056, respectively. Meanwhile, the sound insulation properties of multi-layer materials could be significantly influenced by the polyurethane film position. The sound transmission loss of the SUSUSU3 sample was just 32.83 dB, whereas that of the USUSU3 sample could reach 47.94 dB. Moreover, when polyurethane film was located on the sound facing side of multi-layer materials, the increase in polyurethane film thickness could cause the average sound reduction index of the USUSU sample to increase from 28.76 dB to 47.94 dB. [ABSTRACT FROM AUTHOR]

Traditional water-based flame-retardant finishing causes serious pollution due to the use of a large number of chemicals, and color change is easily generated since the flame-retardant finishing takes place after the cotton dyeing. An eco-friendly flame-retardant finishing of dyed cotton was explored using 9,10-dihydro-9-oxa-10-phosphaphenanthrene-10-oxide (DOPO), 2,2′-oxybis-(5,5-dimethyl-1,3,2,-dioxaphosphorinane-2,2′-disulfide) (5060), SiO2, DOPO/SiO2 (1:1), 5060/SiO2 (1:1) and DOPO/5060 (1:1) in supercritical CO2. The effects of finishing time and pressure as well as temperature on the flame-retarding properties of the cotton were discussed. As expected, samples with the higher weight gain rates exhibit a lower after-flame time as well as after-glow time. In different flame-retardant systems, cotton fabric finished with DOPO presents the lowest after-flame time of 20.6 s and after-glow time of 0 s at 130°C, 22 MPa and 120 min due to its biphenyl ring and O=P-O bond. Moreover, tiny fluctuations of L *, a *, b * and K / S values occurred from 32.10 to 34.24, 5.78 to 6.05, –37.89 to –37.64 and 10.59 to 10.81 when the cotton samples were treated with DOPO, 5060, SiO2, DOPO/SiO2 (1:1), 5060/SiO2 (1:1) and DOPO/5060 (1:1), proving that no significant negative role in the color property of the samples occurs after supercritical CO2 finishing. [ABSTRACT FROM AUTHOR]

Adopting magnetron sputtering continuous automatic production line equipment for industrial production, polyester fabrics as the substrates were coated with nano-Ag/TiO2 composite films prepared by direct current sputtering method and direct current/radio frequency reactive sputtering method, respectively. The microstructure of Ag/TiO2 composite films deposited on the surface of the fabrics was dense and uniform. Structural colors were generated on the surface of the fabrics coated with the composite films and the coloring mechanism was consistent with the single-layer film interference principle. The color fastness, mechanical properties, comfortable properties were not significantly changed and had better antistatic property, anti-ultraviolet property, and antibacterial property compared with the original polyester fabrics. Therefore, the multi-functional and structurally colored fabrics can be prepared by magnetron sputtering technology, and can achieve industrial production, and have wide application prospects in apparel, home textile, and so on. [ABSTRACT FROM AUTHOR]

The flexible nitrogen (N) doped TiO2/C nanofibrous film (NTCf) was fabricated by a combination of electrospinning and annealing treatment. The BET surface area of the NTCf increases, reaches largest value, and then decreases slightly with increasing of N. And the NTCf-20 has a maximum BET surface area of 175.60 m2·g−1. These are beneficial to the absorption of dye by the photocatalyst. At the same time, the N doping could increase the light absorption of TiO2 and is favorable to the charges transfer of the carbon nanofibers, resulting in improving the photocatalytic activity of NTCf under visible light. As a result, all the NTCf showed excellent photocatalytic performance. Moreover, with the increase of N concentration, the photocatalytic activity of the NTCf increased, reaching the largest value before decreasing. And the highest photocatalytic degradation efficiency of Rhodamine B (RhB) was about 99.1% for 1 h by using NTCf-20. After that, the NTCf film was stuck on organza fabric to form a photocatalytic fabric by hot pressing. And the photocatalytic fabric with degradation efficiency of 98.5% was easily separated from the dye solution and possessed excellent reusability. It has huge potential application in pollutant disposal in flowing water. [ABSTRACT FROM AUTHOR]

Environmental hormones such as bisphenol A have attracted enormous attention due to their potential threat to humans and environment. Herein, we synthesized a BC/MIL-53 (Al)-F127 composite membrane by the vacuum filtration method with a mesostructure metal–organic framework MIL-53 (Al)-F127 and bacterial cellulose as the substrate. The BC/MIL-53 (Al)-F127 composite membrane exhibited efficient adsorption of bisphenol A in aqueous solution. The results exhibited that 94% of bisphenol A could be adsorbed in approximately 120 min, and the equilibrium sorption amounts of bisphenol A reached approximately 8.3 mg/g. Meanwhile, the mechanism of adsorption was explored. The optimum pH and temperature for the adsorption of bisphenol A were 6 and 40°C, respectively. The removal efficiency of bisphenol A was maintained at 90% after five repeated cycles, indicating the advantage to separate freely without a complex filtration system. The results of adsorption indicated that the BC/MIL-53 (Al)-F127 membrane has great potential in the aspect of the sewage treatment as a prospective sorbent. [ABSTRACT FROM AUTHOR]