Destructive-Treatment-Free Rapid Polymer-Assisted Metal Deposition for Versatile Electronic Textiles.

Highly conductive, durable, and breathable metal-coated textiles are critical building block materials for future wearable electronics. In order to enhance the metal adhesion on the textile surface, existing solution-based approaches to preparing these materials require time-consuming presynthesis and/or premodification processes, typically in the order of tens of minutes to hours, on textiles prior to metal plating. Herein, we report a UV-induced rapid polymer-assisted metal deposition (r-PAMD) that offers a destructive-treatment-free process to deposit highly conductive metals on a wide variety of textile materials, including cotton, polyester, nylon, Kevlar, glass fiber, and carbon cloth. In comparison to the state of the arts, r-PAMD significantly shortens the modification time to several minutes and is compatible with the roll-to-roll fabrication manner. Moreover, the deposited metals show outstanding adhesion, which withstands rigorous flexing, abrasion, and machine washing tests. We demonstrate that these metal-coated textiles are suitable for applications in two vastly different fields, being wearable and washable sensors, and lithium batteries.

Bioinspired Photo-Cross-Linking of Stretched Solid Silks for Enhanced Strength.

In this study, solid fibroin fibers (FFs) were directly cross-linked by employing a ruthenium-mediated redox pair under visible light at room temperature for the first time. The chemical cross-link through dityrosine connection was confirmed by Fourier-transform infrared (FTIR) spectroscopy, fluorescence spectra, and a solubility test. The resultant cross-link density of fibers was calculated based on their swelling ratio evaluation in LiBr solution. Further applying stretch to the fibers during irradiation increased the fiber strength to higher values. The break stress and Young's modulus of photo-cross-linked 15% stretch FFs reached a 60-90% increase in comparison to the original FFs in dry and wet conditions. This approach constitutes an easy and straightforward strategy for strengthening FFs, which is scalable industrially to enhance FFs in a wide range of applications.

Bacterial cellulose reinforced double-network hydrogels for shape memory strand.

Tough hydrogels with shape memory property are highly desirable for actuators and smart engineering materials. Herein, super-tough polyacrylamide/iota-carrageenan double-network hydrogels were synthesized via a one-pot radical polymerization and strengthened by incorporating bacterial cellulose microclusters, through the intermolecular hydrogen bonds and topological interlock between microclusters and polymer network. Such hydrogels were able to withstand over 200 kPa of tensile stress, or be stretched over 27 times of initial length, and reached a high toughness of ∼2000 kJ/m3. By tension-drying and post-annealing treatments on the strongest hydrogel, dry strands were fabricated to withstand over 100 MPa of tensile stress. Moreover, these strands presented water-stimulated shape memory by a recovery ratio of 84.3 % in 4 min. Based on these characteristics, this super-tough hydrogel may serve as smart textile or actuator for a variety of applications.

Fabrication of 3D PDMS Microchannels of Adjustable Cross-Sections via Versatile Gel Templates.

Flexible gel fibers with high stretchability were synthesized from physically cross-linked agar and covalently cross-linked polyacrylamide networks. Such gel material can withstand the temperature required for thermal curing of polydimethylsiloxane (PDMS), when the water in the gel was partially replaced with ethylene glycol. This gel template supported thermal replica molding of PDMS to produce high quality microchannels. Microchannels with different cross sections and representative 3D structures, including bifurcating junction, helical and weave networks, were smoothly fabricated, based on the versatile manipulation of gel templates. This gel material was confirmed as a flexible and reliable template in fabricating 3D microfluidic channels for potential devices.

Wet Spinning of Silk Fibroin-Based Core-Sheath Fibers.

In order to improve the water absorbency of natural silk and extend its applications in wider areas, silk fibroin (SF)-based fibers were prepared by coaxial wet spinning. Using a custom-made wet spinning device with coaxial spinneret, continuous core-sheath fibers were finally obtained by adjusting the core dope into iota-carrageenan/polyacrylamide hot solution and sheath dope into SF/polyurethane solution. These core-sheath fibers were characterized with respect to morphology, SF secondary structure, mechanical property, and water absorbency. Fibers fabricated from 17 wt % SF/polyurethane solution presented the most regular morphology with homogeneous and circular cross-section. Double-layered hollow structure was observed in these fibers. ß-Sheet conformation was mainly adopted by the SF in fibers as indicated in XRD analysis and FTIR spectra. The fibers demonstrated higher absorbency than the raw silk and fine incorporation of long-lasting glowing pigment, indicating potential applications in water or thermal management textile and phototherapy.

Polyethylenimine coated bacterial cellulose nanofiber membrane and application as adsorbent and catalyst.

Bacterial cellulose (BC) nanofiber membranes were simply aminalized by a flush-coating and post-crosslinking method. Firstly, wet BC membranes were flushed through by an aqueous solution of polyethylenimine (PEI) and glycerol diglycidyl ether (GDE) under vacuum suction, then further heated up to 70 °C to crosslink the resultant coating on the surface of the nanofibers. The PEI coated bacterial cellulose (BC@PEI) nanofiber membrane presented excellent adsorption performance for Cu(2+) and Pb(2+) ions from aqueous solutions. Desorption of these ions was achieved using ethylene diamine tetraacetic acid treatment. This cycle of adsorption and desorption was repeated for several times with good remain adsorption performance (over 90%). Furthermore, the adsorbed Cu(2+) ions can be reduced to copper nanoparticles, and showed excellent catalytic performance for methylene blue reduction in aqueous solution. The catalytic performance can remained after several times of usage.

Super-tough and thermo-healable hydrogel - promising for shape-memory absorbent fiber.

Recoverable hydrogels with high stretch and toughness have been synthesized by a one-step radical polymerization. They consist of covalently crosslinked polyacrylamide (PAAm) and ionically crosslinked carrageenan. Such double network (DN) hydrogels can be stretched beyond 20 times their initial length, and their fracture energy reached a high value of ∼9500 J m-2. By comparing hydrogel tensile properties at different temperatures, the contribution of ionic network to the toughness was quantitatively determined in percentage for the first time. The stretched hydrogels were completely healed by short treatment at a mild temperature. Through drying at stretch, they were also transformed into stiff absorbent fibers that still preserved their shape memory of wet state.