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Selective Doping to Controllably Tailor Maximum Unit-Cell-Volume Change of Intercalating Li + -Storage Materials: A Case Study of γ Phase Li 3 VO 4 .

Jianbin DengChangpeng LvTian JiangSiyuan MaXuehua LiuChunfu Lin
Published in: Advanced science (Weinheim, Baden-Wurttemberg, Germany) (2022)
Capacity decay of an intercalating Li + -storage material is mainly due to the its particle microcracks from stress-causing volume change. To extend its cycle life, its unit-cell-volume change has to be minimized as much as possible. Here, based on a γ-Li 3 VO 4 model material, the authors explore selective doping as a general strategy to controllably tailor its maximum unit-cell-volume change, then clarify the relationship between its crystal-structure openness and maximum unit-cell-volume change, and finally demonstrate the superiority of "zero-strain" materials within 25-60 °C (especially at 60 °C). With increasing the large-sized Ge 4+ dopant, the unit-cell volume of γ-Li 3+ x Ge x V 1- x O 4 becomes larger and its crystal structure becomes looser, resulting in the decrease of its maximum unit-cell-volume change. In contrast, the doping with small-sized Si 4+ shows a reverse trend. The tailoring reveals that γ-Li 3.09 Ge 0.09 V 0.91 O 4 owns the smallest maximum unit-cell-volume change of 0.016% in the research field of intercalating Li + -storage materials. Consequently, γ-Li 3.09 Ge 0.09 V 0.91 O 4 nanowires exhibit excellent cycling stability at 25/60 °C with 94.8%/111.5% capacity-retention percentages after 1800/1500 cycles at 2 A g -1 . This material further shows large reversible capacities, proper working potentials, and high rate capability at both temperatures, fully demonstrating its great application potential in long-life lithium-ion batteries.
Keyphrases
  • single cell
  • cell therapy
  • crystal structure
  • ion batteries
  • magnetic resonance
  • magnetic resonance imaging
  • gold nanoparticles
  • high intensity