Abstract
AbstractPower sources with strong mechanical properties and high‐energy density are highly desirable for the next‐generation flexible electronics. However, the challenge arises from the current electrode structure design, which is unable to bring both satisfactory mechanical and electrochemical properties with high active materials content and mass. Herein, we reported novel flexible, high‐strength, and mechanically stable TiO2‐based film electrodes for advanced sodium‐ion batteries, achieving an ultrahigh strength (up to ≈60 MPa) and commercial‐level areal capacity (4.5 mAh cm−2). Highly‐dispersed TiO2 and interlaced carbon nanotube (CNT) networks are embedded in the sheet‐liked cellulose to form porous, high‐conductive, and high‐active TiO2‐C nanosheets that is basic building subunits of TiO2‐C films, allowing the films with structural robustness and origami‐level flexibility. This strategy reconciles the contradiction between mechanical properties and active material content in flexible electrodes, and the fabricated electrode with a high TiO2 content of >65% can be bent more than 11 000 times without breaking. Meanwhile, good capacity and excellent cycle stability (0.02‰ capacity‐decay rate over 9000 cycles) of TiO2‐C film under a higher active content (75%) has well satisfied the demands of flexible energy storage devices for electrochemical performances. This TiO2‐C subunit assembly methodology demonstrates enormous potential in high‐strength/toughness flexible electrode construction for flexible electronics.image
Talk to us
Join us for a 30 min session where you can share your feedback and ask us any queries you have
Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.