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Synthesis and electrochemical performance of Na_(0.7)Fe_(0.7)Mn_(0.3)O_2 as a cathode material for Na-ion battery

机译:Na_(0.7)Fe_(0.7)Mn_(0.3)O_2作为Na离子电池正极材料的合成及电化学性能

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摘要

A new technique was employed to synthesize Na_(0.7)Fe_(0.7)Mn_(0.3)O_2 precursor by adding citric acid to an aqueous solution of sodium, iron, and manganese salts. The rhombohedral Na_(0.7)Fe_(0.7)Mn_(0.3)O_2 was obtained by calcining the precursor in air. The precursor and its calcined products were characterized by X-ray powder diffraction and scanning electron microscopy. The results showed that a high-crystallized Na_(0.7)Fe_(0.7)Mn_(0.3)O_2 with a rhombohedral structure was obtained when the precursor was calcined over 600 °C in air for 8 h. The product obtained at 800 °C delivered a discharge capacity of about 130 mA h g~(-1) at the specific current of 13 mA g~(-1) in the 1st cycle between 1.5 V and 4.3 V.
机译:通过向钠,铁和锰盐的水溶液中添加柠檬酸,采用一种新技术来合成Na_(0.7)Fe_(0.7)Mn_(0.3)O_2前体。通过在空气中煅烧得到菱形的Na_(0.7)Fe_(0.7)Mn_(0.3)O_2。通过X射线粉末衍射和扫描电子显微镜对前体及其煅烧产物进行表征。结果表明,将前驱体在600°C的空气中煅烧8 h,可得到具有菱形结构的高结晶Na_(0.7)Fe_(0.7)Mn_(0.3)O_2。在800 V的温度下获得的产物在1.5 V至4.3 V的第一个循环中以13 mA g〜(-1)的比电流提供了约130 mA h g〜(-1)的放电容量。

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