锂(药物)
离子
降水
无机化学
材料科学
化学
物理化学
有机化学
物理
医学
内分泌学
气象学
作者
Xiaoyan Jiang,Lanyan Li,Xianyou Wang,Zhigao Luo
标识
DOI:10.1002/cphc.202300930
摘要
Abstract The intrinsically low electronic conductivity and slow ion diffusion kinetics limit further development of olivine LiFe x Mn 1‐x PO 4 cathode materials. In this paper, with the aim of improving the performance of such materials and alleviating the Jahn‐Taller effect of Mn 3+ ion, a bimetallic oxalate precursor with gradient distribution of elemental concentration followed with an efficient process is applied to synthesize LiFe 0.5 Mn 0.5 PO 4 nanocomposite. The results shown that with certain structural modulation of the precursor, the discharge capacity of synthesized LiFe 0.5 Mn 0.5 PO 4 increased from 149 mAh g −1 to 156 mAh g −1 at 0.1 C, the cycling capacity was also remarkably improved. the Fe 0.5 Mn 0.5 C 2 O 4 ⋅ 2H 2 O‐1 precursor with gradient distribution of elemental concentration effectively restricts the reaction between electrode material and electrolyte, thereby alleviates the dissolution of Mn 3+ ion, reduces the decay of capacity and improves the stability of the material.
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