GO-modified flexible polymer nanocomposites fabricated via 3D stereolithography

Graphene oxide (GO) induced enhancement of elastomer properties showed a great deal of potential in recent years, but it is still limited by the barrier of the complicated synthesis processes. Stereolithography (SLA), used in fabrication of thermosets and very recently in “flexible” polymers with elastomeric properties, presents itself as simple and user-friendly method for integration of GO into elastomers. In this work, it was first time demonstrated that GO loadings can be incorporated into commercial flexible photopolymer resins to successfully fabricate GO/elastomer nanocomposites via readily accessible, consumer-oriented SLA printer. The material properties of the resulting polymer was characterized and tested. The mechanical strength, stiffness, and the elongation of the resulting polymer decreased with the addition of GO. The thermal properties were also adversely affected upon the increase in the GO content based on differential scanning calorimetry and thermogravimetric analysis results. It was proposed that the GO agglomerates within the 3D printed composites, can result in significant change in both mechanical and thermal properties of the resulting nanocomposites. This study demonstrated the possibility for the development of the GO/elastomer nanocomposites after the optimization of the GO/“flexible” photoreactive resin formulation for SLA with suitable annealing process of the composite in future

Supplementary Information Files for 'GO-modified flexible polymer nanocomposites fabricated via 3D stereolithography'

Supplementary Information Files for 'GO-modified flexible polymer nanocomposites fabricated via 3D stereolithography'Abstract:Graphene oxide (GO) induced enhancement of elastomer properties showed a great deal of potential in recent years, but it is still limited by the barrier of the complicated synthesis processes. Stereolithography (SLA), used in fabrication of thermosets and very recently in “flexible” polymers with elastomeric properties, presents itself as simple and user-friendly method for integration of GO into elastomers. In this work, it was first time demonstrated that GO loadings can be incorporated into commercial flexible photopolymer resins to successfully fabricate GO/elastomer nanocomposites via readily accessible, consumer-oriented SLA printer. The material properties of the resulting polymer was characterized and tested. The mechanical strength, stiffness, and the elongation of the resulting polymer decreased with the addition of GO. The thermal properties were also adversely affected upon the increase in the GO content based on differential scanning calorimetry and thermogravimetric analysis results. It was proposed that the GO agglomerates within the 3D printed composites, can result in significant change in both mechanical and thermal properties of the resulting nanocomposites. This study demonstrated the possibility for the development of the GO/elastomer nanocomposites after the optimization of the GO/“flexible” photoreactive resin formulation for SLA with suitable annealing process of the composite in future.</div

High-energy SWCNT cathode for aqueous Al-ion battery boosted by multi-ion intercalation chemistry

The aqueous Al-ion battery has achieved great progress in recent years. It now shows comparable performance to that of even non-aqueous Al-ion batteries. However, it also shows relatively low energy output and there is limited general understanding of the mechanism behind this restriction to its practical application. Thus, the development of a high-performance cathode material is in great demand. Herein, a high-capacity single-walled carbon nanotube (SWCNT) is developed as a cathode for the water-in-salt electrolyte-based aqueous Al-ion battery, which provides an ultra-high specific capacity of 790 mAh g–1 (based on the mass of SWCNT) at a high current density of 5 A g–1 even after 1000 cycles. Moreover, the SWCNT/Al battery shows a complicated multi-ion intercalation mechanism, where AlCl4–, Cl–, Al3+, and H+ can function at the same time, improving the battery output. Beyond recently revealed H+ and metal ion co-intercalation, the Cl-assisted intercalation of Al3+ ions mechanism is also studied by experimental characterization and modeling for the first time, which significantly boosts the Al3+ storage capacity. This multi-ion intercalation mechanism combines the high-voltage anion deintercalation and the high-capacity cation intercalation, and thus, benefits the development and application of high-energy Al-ion batteries in the future