A Dithiin-Linked Covalent Organic Polymer for Ultrahigh Capacity Half-Cell and Symmetric Full-Cell Sodium-Ion Batteries

Shen Xu, Chenchen Wang, Tianyi Song, Huiying Yao, Jie Yang, Xin Wang, Jia Zhu*, Chun-Sing Lee*, Qichun Zhang*

*Corresponding author for this work

Research output: Journal Publications and ReviewsRGC 21 - Publication in refereed journalpeer-review

30 Citations (Scopus)
50 Downloads (CityUHK Scholars)

Abstract

Sodium ion-batteries (SIBs) are considered as a class of promising alternatives to lithium-ion batteries (LIBs) to overcome their drawbacks of limited sources and safety problems. However, the lack of high-performance electrode materials hinders the wide-range commercialization of SIBs. Comparing to inorganic counterparts, organic electrode materials, which are benefitted from flexibly designable structures, low cost, environmental friendliness, and high theoretical gravimetric capacities, should be a prior choice. Here, a covalent organic polymer (COP) based material (denoted as CityU-9) is designed and synthesized by integrating multiple redox motifs (benzoquinone and thioether), improved conductivity (sulfur induction), and intrinsic insolubility (rigid skeleton). The half-cell SIBs exhibit ultrahigh specific capacity of 1009 mAh g−1 and nearly no capacity drop after 650 cycles. The first all-COP symmetric full-cell shows high specific capacity of 90 mAh g−1 and excellent rate capability. This work can extend the selection of redox-active moieties and provide a rational design strategy of high-performance novel organic electrode materials. © 2023 The Authors. Advanced Science published by Wiley-VCH GmbH.
Original languageEnglish
Article number2304497
JournalAdvanced Science
Volume10
Issue number32
Online published25 Sept 2023
DOIs
Publication statusPublished - 14 Nov 2023

Research Keywords

  • covalent organic polymers
  • dithiin linkage
  • Na-ion batteries
  • Na-ion storage mechanism
  • organic electrodes
  • symmetric full-cells

Publisher's Copyright Statement

  • This full text is made available under CC-BY 4.0. https://creativecommons.org/licenses/by/4.0/

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