Realizing a single-phase reaction and K+/vacancy disordering in P2-K0.56Na0.11Li0.12Ni0.22Mn0.66O2 by lithium substitution for potassium-ion batteries

  • Yongwei Tang
  • , Haojie Dong
  • , Mengting Liu
  • , Guang Xu Wei
  • , Jin Hong Li
  • , Wenjie Tang
  • , Yifeng Liu
  • , Xu Zhu
  • , Yi Hu Feng
  • , Qiang Liu
  • , Da Wei Wang
  • , Yao Xiao
  • , Peng Fei Wang
  • , Bing Xiao

Research output: Contribution to journalArticlepeer-review

3 Scopus citations

Abstract

Rechargeable potassium-ion batteries (PIBs) have shown great potential as an alternative to lithium-ion batteries (LIBs) owing to the abundant and available potassium reserves. However, their applications are hindered by unsatisfactory cycling stability of cathode materials. Herein, through electrochemical ion-exchange of the Na0.85Li0.12Ni0.22Mn0.66O2 compound, we reported P2-K0.56Na0.11Li0.12Ni0.22Mn0.66O2 (P2-KNaLNM) as a potential high-performance cathode for PIBs. The presence of Li plays a key role in suppressing the K+/vacancy ordering within transition metal slabs. Therefore, P2-KNaLNM underwent a simple single-phase reaction during intercalation/extraction of K+ ions. Consequently, P2-KNaLNM delivers a reversible capacity of 90.2 mA h g−1 and good capacity retention of 89.6% over 150 cycles at 0.2C between 1.5 and 4.6 V (vs. K+/K). Furthermore, a satisfactory capacity retention of 91.5% after 300 cycles is achieved at 0.5C because of the excellent K+ kinetics during the charge and discharge process. This work provides a feasible way to develop a promising cathode candidate for PIBs.

Original languageEnglish
Pages (from-to)14360-14366
Number of pages7
JournalJournal of Materials Chemistry A
Volume12
Issue number24
DOIs
StatePublished - 30 May 2024

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