跳到主要导航 跳到搜索 跳到主要内容

Covalent-Organic-Framework-Based Li–CO2 Batteries

  • Xing Li
  • , Hui Wang
  • , Zhongxin Chen
  • , Hai Sen Xu
  • , Wei Yu
  • , Cuibo Liu
  • , Xiaowei Wang
  • , Kun Zhang
  • , Keyu Xie
  • , Kian Ping Loh
  • National University of Singapore
  • Northwestern Polytechnical University Xian

科研成果: 期刊稿件文章同行评审

182 引用 (Scopus)

摘要

Covalent organic frameworks (COFs) are an emerging class of porous crystalline materials constructed from designer molecular building blocks that are linked and extended periodically via covalent bonds. Their high stability, open channels, and ease of functionalization suggest that they can function as a useful cathode material in reversible lithium batteries. Here, a COF constructed from hydrazone/hydrazide-containing molecular units, which shows good CO2 sequestration properties, is reported. The COF is hybridized to Ru-nanoparticle-coated carbon nanotubes, and the composite is found to function as highly efficient cathode in a Li–CO2 battery. The robust 1D channels in the COF serve as CO2 and lithium-ion-diffusion channels and improve the kinetics of electrochemical reactions. The COF-based Li–CO2 battery exhibits an ultrahigh capacity of 27 348 mAh g−1 at a current density of 200 mA g−1, and a low cut-off overpotential of 1.24 V within a limiting capacity of 1000 mAh g−1. The rate performance of the battery is improved considerably with the use of the COF at the cathode, where the battery shows a slow decay of discharge voltage from a current density of 0.1 to 4 A g−1. The COF-based battery runs for 200 cycles when discharged/charged at a high current density of 1 A g−1.

源语言英语
文章编号1905879
期刊Advanced Materials
31
48
DOI
出版状态已出版 - 1 11月 2019

学术指纹

探究 'Covalent-Organic-Framework-Based Li–CO2 Batteries' 的科研主题。它们共同构成独一无二的学术指纹。

引用此