介电谱
材料科学
电化学
锂(药物)
阴极
扫描电子显微镜
热液循环
兴奋剂
纳米结构
分析化学(期刊)
锂离子电池
化学工程
电池(电)
纳米技术
化学
电极
物理化学
复合材料
医学
功率(物理)
物理
光电子学
色谱法
量子力学
工程类
内分泌学
作者
Dung V. Trinh,Nguyễn Thị Tuyết,Đặng Thị Minh Huệ,Dũng Đặng,Hang T. T. Le,Huynh T. N. Le,Hoang Vinh Tran,Chinh Dang Huynh
标识
DOI:10.1038/s41598-021-91881-1
摘要
Abstract Nanostructured cathode materials based on Mn-doped olivine LiMn x Fe 1−x PO 4 ( x = 0, 0.1, 0.2, and 0.3) were successfully synthesized via a hydrothermal route. The field-emission scanning electron microscopy (SEM) and energy-dispersive X-ray spectroscopy (EDS) analyzed results indicated that the synthesized LiMn x Fe 1−x PO 4 ( x = 0, 0.1, 0.2, and 0.3) samples possessed a sphere-like nanostructure and a relatively homogeneous size distribution in the range of 100–200 nm. Electrochemical experiments and analysis showed that the Mn doping increased the redox potential and boosted the capacity. While the undoped olivine (LiFePO 4 ) had a capacity of 169 mAh g −1 with a slight reduction (10%) in the initial capacity after 50 cycles (150 mAh g −1 ), the Mn-doped olivine samples (LiMn x Fe 1−x PO 4 ) demonstrated reliable cycling tests with negligible capacity loss, reaching 151, 147, and 157 mAh g −1 for x = 0.1, 0.2, and 0.3, respectively. The results from electrochemical impedance spectroscopy (EIS) accompanied by the galvanostatic intermittent titration technique (GITT) have resulted that the Mn substitution for Fe promoted the charge transfer process and hence the rapid Li transport. These findings indicate that the LiMn x Fe 1−x PO 4 nanostructures are promising cathode materials for lithium ion battery applications.
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