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Triboelectric nanogenerators (TENGs) are foreseen as a leading candidate to harvest mechanical energy from ambient sources such as human body movements. However, wearable TENGs, which are used for this purpose, require adequate wearability for long durations, in addition to sufficient electrical outputs. So far, it has been difficult to achieve this through the predominantly plastic-based wearable TENGs constructed using conventional nanogenerator fabrication methods. This Article evaluates the use of textile materials and scalable fabrication techniques to develop TENGs targeting balanced electrical and wearable properties. The fabrication process is conducted using yarn-coating, dip-coating, and screen-printing techniques, which are common textile manufacturing methods, and converted into fabrics using flat-bed knitting, resulting in TENGs with improved wearable and electrical performances. The electrical properties (open circuit voltage ( V oc ), short circuit current ( I sc ), and short circuit charge ( Q sc )) and wearable properties (air permeability, stretch and recovery, and moisture management) of these structures are evaluated, during which the yarn-coated TENG resulted in maximum electrical outputs recording V oc ≈ 35 V, I sc ≈ 60 nA, and Q sc ≈ 12 nC, under mild excitations. In terms of wearability, the yarn-coated TENG again performed exceptionally during the majority of tests providing the best moisture management, air permeability (101 cm 3 /cm 2 /s), and stretch (∼75%), thus proving its suitability for wearable TENG applications., Competing Interests: The authors declare no competing financial interest., (© 2022 American Chemical Society.)

Cellulose nanocrystals (CNC)/poly(ethylene oxide) (PEO) composite fibers were successfully produced in situ by injection into a hydrophobic solvent. Using a similar principle, a single step manufacturing method of injectable composites was developed by injection of a CNC solution into a hydrophobic resin. Molecular orientation and deformation of the fibers and composites were obtained using Raman spectroscopy. CNCs were found to be highly aligned along the fiber's axes, as confirmed by 2-fold symmetry of polar plots and second and fourth order orientation parameters. A shift in the position of a characteristic Raman band, initially located at ∼1095 cm -1 , corresponding to vibrations of the cellulose backbone polymer chains was followed under tensile deformation. Using this shift, it was possible to estimate the fiber modulus as being ∼33 GPa, which is remarkably high. Stress transfer between the hydrophobic resin and the injected CNC fibers was quantified in this new type of composite using a modified shear-lag theory showing that appreciable reinforcement occurs. Our approach presents a new way to introduce highly loaded CNC fibers in situ into a composite structure.

Design strategies from nature provide vital clues for the development of synthetic materials with tunable mechanical properties. Employing the concept of hierarchy and controlled percolation, a new class of polymer nanocomposites containing a montmorillonite (MMT)-reinforced electrospun poly(vinyl alcohol) (PVA) filler embedded within a polymeric matrix of either poly(vinyl acetate) (PVAc) or ethylene oxide-epichlorohydrin copolymer (EO-EPI) were developed to achieve a tunable mechanical response upon exposure to specific stimuli. Mechanical response and switching times upon hydration were shown to be dependent on the weight-fraction of MMT in the PVA electrospun fibers and type of composite matrix. PVA/MMT.PVAc composite films retained excellent two-way switchability for all MMT fractions; however, the switching time upon hydration was decreased dramatically as the MMT content was increased due to the highly hydrophilic nature of MMT. Additionally, for the first time, significant two-way switchability of PVA/MMT.EO-EPI composites was achieved for higher weight fractions (12 wt %) of MMT. An extensive investigation into the effects of fiber diameter, crystallinity, and MMT content revealed that inherent rigidity of MMT platelets plays an important role in controlling the mechanical response of these hierarchical electrospun composites.

One of the key design components of nature is the utilization of hierarchical arrangements to fabricate materials with outstanding mechanical properties. Employing the concept of hierarchy, a new class of segmented polyurethane/ureas (PUUs) was synthesized containing either a peptidic, triblock soft segment, or an amorphous, nonpeptidic homoblock block soft segment with either an amorphous or a crystalline hard segment to investigate the effects of bioinspired, multiple levels of organization on thermal and mechanical properties. The peptidic soft segment was composed of poly(benzyl-l-glutamate)-block-poly(dimethylsiloxane)-block-poly(benzyl-l-glutamate) (PBLG-b-PDMS-b-PBLG), restricted to the β-sheet conformation by limiting the peptide segment length to <10 residues, whereas the amorphous soft segment was poly(dimethylsiloxane) (PDMS). The hard segment consisted of either 1,6-hexamethylene diisocyanate (crystalline) or isophorone diisocyanate (amorphous) and chain extended with 1,4-butanediol. Thermal and morphological characterization indicated microphase separation in these hierarchically assembled PUUs; furthermore, inclusion of the peptidic segment significantly increased the average long spacing between domains, whereas the peptide domain retained its β-sheet conformation regardless of the hard segment chemistry. Mechanical analysis revealed an enhanced dynamic modulus for the peptidic polymers over a broader temperature range as compared with the nonpeptidic PUUs as well as an over three-fold increase in tensile modulus. However, the elongation-at-break was dramatically reduced, which was attributed to a shift from a flexible, continuous domain morphology to a rigid, continuous matrix in which the peptide, in conjunction with the hard segment, acts as a stiff reinforcing element.

Stimuli-responsive materials are desired for a wide range of applications. Here, we report the design and fabrication of all-organic, stimuli-responsive polymer composites using electrospun nanofibers as the filler. The incorporation of 4 wt % of filler into the polymer matrix increased the tensile storage modulus by 2 orders of magnitude. Upon exposure to water, the filler fibers plasticize and no longer provide mechanical reinforcement. The tensile storage modulus subsequently diminishes 2 orders of magnitude to the value of the neat matrix polymer.