<p>Co-free lithium-rich manganese-based oxides (LRMOs), which offer energy densities over 1000 Wh·kg<sup>−1</sup> and low raw material cost, are attractive cathode candidates for next generation high-energy density lithium-ion batteries (LIBs). Nonetheless, their practical application is hindered by their high initial irreversible capacity, capacity and voltage decay, and voltage hysteresis. Herein, a novel iron phosphide modification strategy is presented, where Fe<sub>3</sub>P is incorporated into the bulk phase of the Li<sub>1.2</sub>Ni<sub>0.2</sub>Mn<sub>0.6</sub>O<sub>2</sub> (LNMO) cathode material during its fabrication process of high-temperature calcination of the precursor after spray drying. This regulation stabilizes the crystal lattice of LNMO, promotes the formation of a robust cathode–electrolyte interphase, and mitigates decomposition of the electrolyte, thereby significantly enhancing the cycling stability and rate capability. Consequently, the modified LNMO achieves a capacity of 179 mAh·g<sup>−1</sup> (98% capacity retention) after 450 cycles at 1C (1C = 200 mA·g<sup>−1</sup>), and 82% capacity retention after 1000 cycles at 5C. The regulatory strategy is facile and straightforward contributes superior electrochemical performance for LNMO cathode materials, which has potential for wide-ranging applications.</p>

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Iron phosphide stabilization strategy enables long-cycling Co-free lithium-rich manganese-based cathode materials

  • Bufan Cheng,
  • Yiran Cai,
  • Guanxi Lin,
  • Zhiyuan Lu,
  • Ziming Fang,
  • Ruizi Wang,
  • Xin Zhang,
  • Wenping Sun,
  • Mingxia Gao,
  • Hongge Pan

摘要

Co-free lithium-rich manganese-based oxides (LRMOs), which offer energy densities over 1000 Wh·kg−1 and low raw material cost, are attractive cathode candidates for next generation high-energy density lithium-ion batteries (LIBs). Nonetheless, their practical application is hindered by their high initial irreversible capacity, capacity and voltage decay, and voltage hysteresis. Herein, a novel iron phosphide modification strategy is presented, where Fe3P is incorporated into the bulk phase of the Li1.2Ni0.2Mn0.6O2 (LNMO) cathode material during its fabrication process of high-temperature calcination of the precursor after spray drying. This regulation stabilizes the crystal lattice of LNMO, promotes the formation of a robust cathode–electrolyte interphase, and mitigates decomposition of the electrolyte, thereby significantly enhancing the cycling stability and rate capability. Consequently, the modified LNMO achieves a capacity of 179 mAh·g−1 (98% capacity retention) after 450 cycles at 1C (1C = 200 mA·g−1), and 82% capacity retention after 1000 cycles at 5C. The regulatory strategy is facile and straightforward contributes superior electrochemical performance for LNMO cathode materials, which has potential for wide-ranging applications.