Poly(vinylidene fluoride) (PVDF) fibers with diameters ranging from 70 to 400 nm are produced by electrospinning and the effect of fiber size on the ferroelectric β-crystalline phase is determined. Domain switching and associated ferro-/piezo-electric properties of the electrospun PVDF fibers were also determined. The fibers showed well-defined ferroelectric and piezoelectric properties.

Chemical reduction of graphite oxide (GO) to produce graphene nanosheets often results in irreversible agglomeration and precipitation. Herein, stable well-dispersed graphene sheets in solvents were obtained by simultaneous functionalization and reduction of GO under alkaline conditions, in the presence of sodium borohydride and imidazolium ionic liquids (Imi-ILs) containing two vinyl-benzyl groups. In this case, positively charged imidazolium groups of Imi-ILs underwent ion-exchange with negatively charged GO sheets and were linked to their edges, while Imi-ILs were non-covalently attached onto the large surfaces of graphene through π–π and/or cation–π stacking interactions. The vinyl-benzyl reactive sites were then copolymerized in situ with methyl methacrylate to fabricate graphene/poly(methyl methacrylate) (PMMA) composites. Functionalized graphene sheets were uniformly dispersed in the PMMA matrix and contributed to large increases in storage modulus (+58.3%) and glass transition temperature (+19.2 °C) at 2.08 vol.% loading. High electrical conductivity was also achieved at graphene loading levels beyond 1 vol.% (ca. 2.55 Sm⁻¹) with a low percolation threshold (0.25 vol.%) for the composites. Hence, a general methodology which facilitates the development of a multifunctional advanced material has been successfully established. This can be extended to other vinyl polymer-based composites containing graphene.

Porous carbons derived from bimetallic metal–organic frameworks exhibit tunable properties by controlling the ratio of metal ions (Zn and Co) in the precursors. With the optimal ratio of Zn/Co = 3 in the precursors, the porous carbons possess a superior electrosorption capacity of 45.6 mg g⁻¹.

SUMMARY: Spider dragline silk has enormous potential for the development of biomimetic fibers that combine strength and elasticity in low density polymers. These applications necessitate understanding how silk reacts to different environmental conditions. For instance, spider dragline silk`supercontracts' in high humidity. During supercontraction, unrestrained dragline silk contracts up to 50% of its original length and restrained fibers generate substantial stress. Here we characterize the response of dragline silk to changes in humidity before, during and after supercontraction. Our findings demonstrate that dragline silk exhibits two qualitatively different responses to humidity. First, silk undergoes a previously unknown cyclic relaxation–contraction response to wetting and drying. The direction and magnitude of this cyclic response is identical both before and after supercontraction. By contrast, supercontraction is a `permanent' tensioning of restrained silk in response to high humidity. Here, water induces stress,rather than relaxation and the uptake of water molecules results in a permanent change in molecular composition of the silk, as demonstrated by thermogravimetric analysis (TGA). Even after drying, silk mass increased by∼1% after supercontraction. By contrast, the cyclic response to humidity involves a reversible uptake of water. Dried, post-supercontraction silk also differs mechanically from virgin silk. Post-supercontraction silk exhibits reduced stiffness and stress at yield, as well as changes in dynamic energy storage and dissipation. In addition to advancing understanding supercontraction, our findings open up new applications for synthetic silk analogs. For example, dragline silk emerges as a model for a biomimetic muscle, the contraction of which is precisely controlled by humidity alone.