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Highly elastic polyrotaxane binders for mechanically stable lithium hosts in lithium‐metal batteries

  • Yoo, Dong‐Joo Institute of Chemical Processes, Seoul National University, Republic of Korea
  • Elabd, Ahmed Department of Chemistry, University of Fribourg, Switzerland
  • Choi, Sunghun Institute of Chemical Processes, Seoul National University, Republic of Korea
  • Cho, Yunshik Institute of Chemical Processes, Seoul National University, Republic of Korea
  • Kim, Jaemin Institute of Chemical Processes, Seoul National University, Republic of Korea
  • Lee, Seung Jong Institute of Chemical Processes, Seoul National University, Republic of Korea
  • Choi, Seung Ho Institute of Chemical Processes, Seoul National University, Republic of Korea
  • Kwon, Tae‐woo Institute of Chemical Processes, Seoul National University, Republic of Korea
  • Char, Kookheon Institute of Chemical Processes, Seoul National University, Republic of Korea
  • Kim, Ki Jae Institute of Chemical Processes, Seoul National University, Republic of Korea
  • Coskun, Ali Department of Chemistry, University of Fribourg, Switzerland
  • Choi, Jang Wook Institute of Chemical Processes, Seoul National University, Republic of Korea
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    2019
Published in:
  • Advanced Materials. - 2019, vol. 31, no. 29, p. 1901645
English Despite their unparalleled theoretical capacity, lithium‐metal anodes suffer from well‐ known indiscriminate dendrite growth and parasitic surface reactions. Conductive scaffolds with lithium uptake capacity are recently highlighted as promising lithium hosts, and carbon nanotubes (CNTs) are an ideal candidate for this purpose because of their capability of percolating a conductive network. However, CNT networks are prone to rupture easily due to a large tensile stress generated during lithium uptake– release cycles. Herein, CNT networks integrated with a polyrotaxane‐incorporated poly(acrylic acid) (PRPAA) binder via supramolecular interactions are reported, in which the ring‐sliding motion of the polyrotaxanes endows extraordinary stretchability and elasticity to the entire binder network. In comparison to a control sample with inelastic binder (i.e., poly(vinyl alcohol)), the CNT network with PRPAA binder can endure a large stress during repeated lithium uptake–release cycles, thereby enhancing the mechanical integrity of the corresponding electrode over battery cycling. As a result, the PRPAA‐incorporated CNT network exhibits substantially improved cyclability in lithium–copper asymmetric cells and full cells paired with olivine‐LiFePO4, indicating that high elasticity enabled by mechanically interlocked molecules such as polyrotaxanes can be a useful concept in advancing lithium‐metal batteries.
Faculty
Faculté des sciences et de médecine
Department
Département de Chimie
Language
  • English
Classification
Chemistry
License
License undefined
Identifiers
Persistent URL
https://folia.unifr.ch/unifr/documents/308078
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