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Electrochemical Property Investigation of Cobalt Doped LiFePO_4/C during Charge-Discharge by an In-situ X-Ray Near Edge Structure Technique

机译:原位X射线近边缘结构技术在充电放电期间钴掺杂LiFepo_4 / C的电化学性能研究

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LiFePO_4/C and LiFe_(0.9)Co_(0.1)PO_4/C materials were synthesized via a solid state method. 10% cobalt was chosen as a doping element in the Fe-site of LiFePO_4/C to increase its electronic conductivity. The crystal structure and particle morphology of this material were studied using X-ray diffraction (XRD) and scanning electron microscopy (SEM) techniques, respectively. The electrochemical mechanism observed during cycling of a LiFe_(0.9)Co_(0.1)PO_4/C electrode was investigated using in-situ time resolved X-ray absorption near edge structure (in-situ XANES). The experimental results showed that the electrochemical mechanism of LiFe_(0.9)Co_(0.1)PO_4/C mainly took place with the Fe~(2+)/Fe~(3+) redox couple. The Co~(2+)/Co~(3+) couple redox was not active during cycling. The Co doped sample had an improved crystal structure, resulting in a higher energy density than LiFePO_4/C.
机译:通过固态方法合成LiFepo_4 / C和Life_(0.9)CO_(0.1)PO_4 / C材料。选择10%钴作为LiFepo_4 / C的Fe-Site中的掺杂元件,以提高其电子电导率。使用X射线衍射(XRD)和扫描电子显微镜(SEM)技术研究该材料的晶体结构和颗粒形态。使用在边缘结构附近(原位XANES)附近的原位时间来研究期间观察到寿命的循环(0.9)CO_(0.1)PO_4 / C电极的电化学机制。实验结果表明,使用Fe〜(2 +)/ Fe〜(3+)氧化还原耦合主要发生寿命(0.9)CO_(0.1)PO_4 / C的电化学机制。 CO〜(2 +)/ CO〜(3+)循环在循环期间没有活跃。 CO掺杂的样品具有改进的晶体结构,导致比LiFePO_4 / C更高的能量密度。

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