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Na+ Preintercalated Bilayered V2O5 Cathode Materials for Na-Ion Batteries

  • Qiang Fu
  • , Björn Schwarz
  • , Angelina Sarapulova
  • , Xianlin Luo
  • , Julian Hansen
  • , Zhen Meng
  • , Volodymyr Baran
  • , Alexander Missyul
  • , Edmund Welter
  • , Weibo Hua
  • , Michael Knapp
  • , Helmut Ehrenberg
  • , Sonia Dsoke
  • Karlsruhe Institute of Technology
  • German Electron Synchrotron
  • CELLS-ALBA Synchrotron

科研成果: 期刊稿件文章同行评审

4 引用 (Scopus)

摘要

Na+ preintercalated bilayered vanadium oxide (NVOnH) with a large interlayer spacing of ∼11.1 Å is synthesized via a hydrothermal method. As proven by mass spectrometry and magnetization measurements, NVOnH is “oxygen-rich”. NVOnH undergoes notable structural evolution and thermal instability during heating due to crystal water and O2 release and decomposition. NVOnH and dehydrated NVOnH (NVO) deliver capacities of over 250 and 220 mAh g-1, respectively, despite their fast capacity decay in the first 20 cycles and low capacity retention after 100 cycles. Moreover, the reaction mechanism and reversibility of NVOnH and NVO during Na+-ion (de)insertion are investigated via in operando techniques. NVOnH experiences a two-phase and solid-solution reaction during discharge and charge processes, while NVO undergoes a different phase evolution (NVO starting with charging: two-phase reaction for the first charging and only solid solution for the following cycle; NVO starting with discharging: only a solid-solution reaction). In operando X-ray absorption spectroscopy demonstrates the variation of the oxidation state and the local structural environment of the V ion during Na+ (de)insertion.

源语言英语
页(从-至)10176-10185
页数10
期刊Chemistry of Materials
36
20
DOI
出版状态已出版 - 22 10月 2024

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