材料科学
高分辨率透射电子显微镜
电化学
锂(药物)
扫描电子显微镜
透射电子显微镜
分析化学(期刊)
阴极
化学工程
正交晶系
纳米技术
晶体结构
电极
复合材料
结晶学
化学
内分泌学
工程类
物理化学
医学
色谱法
作者
Yonglian Xiong,Ying Wei,Wenyi Rong,Jin Shang,Kepiao He,Ting Yi,Fan Yongsheng
标识
DOI:10.1149/2162-8777/ac9d64
摘要
The LiMn x Fe 1− x PO 4 /C ( x = 0.5, 0.6, and 0.7) cathode materials for lithium-ion batteries were synthesized by polyethylene glycol (PEG) 400 as the carbon source via a combination of wet ball-milling and high-temperature solid-state reaction. The analysis results of X-ray diffraction (XRD), scanning electron microscopy (SEM), and high-resolution transmission electron microscopy (HRTEM) indicate that the as-prepared LiMn 0.6 Fe 0.4 PO 4 /C sample has a single-phase orthorhombic olivine structure, and the majority of particle sizes range from 100 to 200 nm with a ∼2–3 nm carbon coating layer. The electrochemical measurements demonstrate that the obtained LiMn 0.6 Fe 0.4 PO 4 /C composite possesses preferable Li-ion storage properties, and the discharge capacity of 137.7 mAh g −1 at 1 C rate, which is 83.6% of that at 0.1 C rate. The composite also exhibits outstanding cycling stability, with a capacity retention of 98.2% after 100 cycles at 0.2 C rate. And the differential capacity analysis (dQ/dV) reveals that the dominating degradation of LiMn 0.6 Fe 0.4 PO 4 /C is caused by the Mn 2+ /Mn 3+ redox capacity loss which is located at ∼4.12/3.96 V, whether during the charge or discharge process. Moreover, the LiMn 0.6 Fe 0.4 PO 4 /C sample delivers excellent high-temperature performance (45 °C), with improved reversible capacity and capacity retention of 148.7 mAh g −1 and 99.3% after 80 cycles at 0.5 C rate, respectively.
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