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Mechanical Stirring Synthesis of 1D Electrode Materials and Designing of Pyramid/Inverted Pyramid Interlocking for Highly Flexible and Foldable Li-Ion Batteries with High Mass Loading.

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Flexible and foldable Li-ion batteries (LIBs) are presently attracting immense research interest for their potential use in wearable electronics but are still limited to electrodes with very small mass loading,… Click to show full abstract

Flexible and foldable Li-ion batteries (LIBs) are presently attracting immense research interest for their potential use in wearable electronics but are still limited to electrodes with very small mass loading, low bending/folding endurance, and poor electrochemical stability during repeated bending and folding movements. Moreover, one-dimensional (1D) structured electrode materials have shown excellent electrochemical performance but are still restricted by the high cost and complicated fabrication process. Here, we present a very simple yet novel approach for fabricating extra-long Li4Ti5O12 (LTO) and LiCoO2 (LCO) nanofiber precursors by directly stirring the reagents in an atmospheric vessel. In addition, we present multilayer pyramid/inverted pyramid interlocking inside the LTO and LCO nanofiber films as well as between films and current collectors, which can create strengthened interfacial bonding like a zipper and tangentially disperse the strains generated during folding through the pyramidal planes and edges, leading to the realization of thick-film electrodes with outstanding electrochemical stability during folding movements. The foldable LIBs that are assembled with LTO and LCO nanofiber electrodes at a practical level of mass loading (14.9-19.4 mg cm-2) can maintain 102% of the initial capacity after 15 000 times of fully folding (180°) motions.

Keywords: mass loading; electrode materials; mass; foldable ion; flexible foldable; ion batteries

Journal Title: ACS applied materials & interfaces
Year Published: 2021

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