RESUMO
Fiber-based supercapacitors (FSCs) exhibit desirable application potential and development prospects in wearable energy storage devices because of their flexibility and wearability. However, the low capacity in the unit volume and insufficient fiber strength hinder their further development in practical application. Herein, the MnO2 nanomaterials with regulatable crystalline structure were synthesized by one-step hydrothermal strategy. The formation of the MnO2 crystalline structure involved the "crimp-phase transition" process. Among them, the 2 × 2 tunnel type α-MnO2 nanowires exhibited excellent electrochemical capacitance (43.8 F g-1), high rate performance (61%, 0.25 to 6 A g-1), and remarkable cyclic stability (99%), which can be attributed to their good symmetry in space and high shared vertices proportion. On this basis, the α-MnO2 nanowires were coblended with GO to construct MnO2/rGO hybrid fibers by scalable continuous wet spinning and in situ acid reduction. Noteworthily, in MnO2/rGO hybrid fibers, the doping amount of MnO2 nanowires as high as 50 wt % could be achieved, while the strength reached 11.73 MPa, which can be ascribed to the superior surface morphology of MnO2 nanowires and the unique cement wall structure of hybrid fibers. Finally, the obtained hybrid fiber electrodes were assembled into symmetrical FSCs. Notably, the FSCs delivered remarkable volume specific capacitance (129.5 F cm-3) and impressive energy density (18 mWh cm-3) at 1.75 A cm-3. In addition, the assembled all-solid-state FSCs indicated excellent deformability and application potential. This work offers some insight for promoting the continuous preparation of fiber electrodes, the development of FSCs, and practical application in wearable energy textile.
RESUMO
Toward the goal of preventing microbial infections in hospitals or other healthcare institutions, here we developed a self-disinfecting textile with synergistic photodynamic/photothermal antibacterial property. Porphyrinic Metal-organic frameworks (PCN-224) and Ag nanoparticles (NPs) were in situ grown on knitted cotton textile (KCT) successively to achieve rapid photodynamic antibacterial and durable bacteriostatic effect. Light-driven singlet oxygen (1O2) generated from PCN-224 and heat generated from Ag could function synergistically to realize rapid bacterial inactivation. Interestingly, 1O2 could promote Ag NPs to be degraded to release more Ag+ ions, achieving durable bacteriostatic effect. Antibacterial assay demonstrated 6 and 4.49 log unit inactivation toward two typical bacterial strains (E. coli and S. aureus) under Xe arc lamp in 30 min, respectively. Even after ten washes, the textile still maintained 6 log unit bacterial inactivation. Mechanism study proved light-driven 1O2 and heat are main factors causing bacterial inactivation, they could work synergistically to enhance bacterial inactivation efficiency. Photothermal study revealed that the textile could reach to 69 â under visible light and 79.1 â under 780-nm light-laser, which showed much potential in photothermal material applications. Taken together, our findings demonstrated a synergistic self-disinfecting cotton textile that exhibited constructive significance for preventing microbial infections and transmissions.