Pore structure regulation of hard carbon: Towards fast and high‐capacity sodium‐ion storage

Le Yang, Mingxiang Hu, Hongwei Zhang, Wen Yang*, Ruitao Lv

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

68 Citations (Scopus)

Abstract

Hard carbon is regarded as one of the most promising anode material for sodium-ion batteries in virtue of the low cost and stable framework. However, the correlation between pore structures of hard carbon and sodium-ion storage is still ambiguous. In this work, based on precise control of pore-size distribution, the capacity, ion diffusion, and initial Coulombic efficiency were improved. Meanwhile, the relationship between pore structure and capacity was investigated. Our result indicates that the micropores hinder ion diffusion and hardly ever accommodate Na+ ions, while mesopores facilitate Na+ ion intercalation. Hard carbon with negligible micropores and abundant mesopores delivers a maximum capacity of 283.7 mAh g−1 at 20 mA g−1, which is 83% higher than that of micropore-rich one. Even after 320 cycles at 200 mA g−1, the capacity still remains 189.4 mAh g−1.

Original languageEnglish
Pages (from-to)257-264
Number of pages8
JournalJournal of Colloid and Interface Science
Volume566
DOIs
Publication statusPublished - 15 Apr 2020

Keywords

  • Anode
  • Hard carbon
  • Mesopore
  • Micropore
  • Pore-structure evolution
  • Sodium-ion battery

Fingerprint

Dive into the research topics of 'Pore structure regulation of hard carbon: Towards fast and high‐capacity sodium‐ion storage'. Together they form a unique fingerprint.

Cite this