Enhancing the electrochemical performance of lithium-rich manganese-based layered oxides through the phosphorus–vanadium coating of single-crystalline particles
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引用次数: 0
Abstract
Lithium-rich manganese-based cathode materials are considered next-generation cathode materials for high-energy-density lithium-ion batteries. However, their practical application is limited by continuous voltage decay, poor cycle stability, and inferior rate performance. In this study, single-crystalline Li1.2Ni0.13Co0.13Mn0.54O2 (LNCMO) with different coating levels of Li3V2(PO4)3 was synthesized using the sol–gel method, moreover, a spinel phase and oxygen vacancies were induced between the bulk material and coating layer during the coating process. This modification strategy can effectively suppress voltage decay, improve the rate performance, and reduce side reactions between the active materials and electrolytes during cycling. These results showed that the Li+ ion diffusion coefficient of the LNCMO electrode modified with 3 wt% phosphorus–vanadium is 52 times that of the original sample. The 3 wt% phosphorus–vanadium modified LNCMO delivers a capacity of 201.4 mA h g−1 at 1C rate and retains 176.4 mA h g−1 (87.7% retention) after 100 cycles at 1C, while the pristine material only displayed 72.2% retention under identical conditions. Furthermore, the average discharge midpoint voltage decay of pristine LNCMO (2.4 mV per cycle) decreased to 1.9 mV per cycle. These results provide insights into the future application of lithium-rich manganese-based materials.
富锂锰基正极材料被认为是高能量密度锂离子电池的下一代正极材料。然而,它们的实际应用受到持续电压衰减、周期稳定性差和较差的速率性能的限制。本研究采用溶胶-凝胶法制备了不同Li3V2(PO4)3包覆水平的Li1.2Ni0.13Co0.13Mn0.54O2 (LNCMO)单晶,包覆过程中在本体材料与包覆层之间产生尖晶石相和氧空位。这种改性策略可以有效地抑制电压衰减,提高倍率性能,减少循环过程中活性材料与电解质之间的副反应。结果表明,经3 wt%磷钒修饰的LNCMO电极的Li+离子扩散系数是原样品的52倍。3 wt%磷钒改性LNCMO在1C条件下的容量为201.4 mA h g - 1,在1C条件下循环100次后仍保持176.4 mA h g - 1(保留率87.7%),而原始材料在相同条件下仅显示72.2%的保留率。此外,原始LNCMO的平均放电中点电压衰减从2.4 mV /循环下降到1.9 mV /循环。这些结果为富锂锰基材料的未来应用提供了见解。
期刊介绍:
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