Controllable assembly of continuous hollow graphene fibers with robust mechanical performance and multifunctionalities.

Macroscopic conformation of individual graphene sheets serves as the backbone of translating their intrinsic merits towards multifunctional practical applications. However, controllable and continuous assemblies of graphene-based nanomaterials to create stable macroscopic structural components are always in face of great challenge. We have developed a scalable converging-flow assisted wet-spinning methodology for continuously fabricating hollow graphene fibers (HGFs, the newest variation of solid graphene fibers) with high quality. The degradable silk thread is selectively utilized as the continuous hollow structure former that holds the coaxially stacked graphene sheets aligned through the converging-flow modulating process. For the first time, we have created the longest freestanding HGF in length of 2.1 m. The continuous HGFs are in an average diameter of 180µm and with 4-8µm adjustable wall thicknesses. The optimal HGF demonstrates an average tensile strength of 300 MPa and modulus of 2.49 GPa (comparable to typical solid graphene fibers, but the highest among the reported HGFs in literature) and an exceptional failure elongation of 10.8%. Additionally, our continuous HGFs exhibit spontaneous resistive response to thermal and strain stimuli (in form of large deformations and human motions), offering great potential for developing multifunctional sensors. We envision that this work demonstrates an effective and well-controlled macroscopic assembly methodology for the scaled-up mass production of HGFs.

Degradable photo-crosslinked starch-based films with excellent shape memory property.

With the increasingly serious plastic pollution, people's demand for the multi-functional biodegradable plastics is becoming more and more urgent. Inspired by the crosslinked shape memory polymers, the crosslinked starch films were synthesized by inducing the decomposition of benzophenone into free radical and depriving hydrogen on starch macromolecules under UV irradiation, in order to gain a high shape memory performance. The results showed that a three-dimensional crosslinking network between starch macromolecule chains was formed. Compared with the uncrosslinked starch films, the photo-crosslinked films not only had higher mechanical property (tensile strength increased by 154%), but also had better water resistance (water contact angle from 60° to 87°) due to the reduction of free hydroxyl groups. In addition, the stable covalent bonds serving as netpoints endow photo-crosslinked films with great improvement in shape memory property, with nearly 180° bending recovery. More importantly, the maximum shape memory fixity ratio (Rf) and shape memory recovery ratio (Rr) under stretch deformation were 96.5% and 99.8%, respectively. And the Rf and Rr could reach 94.6% and 79.8% even at higher strain. In all, the excellent shape memory performance and good degradability crosslinked starch films, which have great potential application in disposable heat-shrinkable packaging materials.