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Electrochemical characterization of nano V, Ti doped MnO2 in primary lithium manganese dioxide batteries with high rate

机译:锂锰二氧化锰初生电池中纳米钒钛掺杂MnO2的电化学表征。

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摘要

The nano-sized gamma-MnO2 precursor is synthesized using a room temperature, liquid-phase reaction route with the assistance of ultrasonic waves. The MnO2 precursor as an electrode material in lithium manganese dioxide primary batteries displays a low capacity of 140mAh g(-1) (45.5% for the theoretical capacity of MnO2) at 20mA g(-1). Therefore, the doped MnO2 with cationic V or/and Ti are prepared at high temperature. After the heat treatment, the gamma phase precursor powder gradually converts into the beta-MnO2 and exhibits a higher specific surface area with a larger pore volume and pore size, providing significantly more electrochemically active sites for the redox reaction. The doped MnO2 matrix has advantage of the ideal lattice parameters and the higher conductivity, resulting in an enhancement of the Li+ diffusion kinetics in the tunnel structure. Especially for co-doped MnO2 with V and Ti, the modified material shows an outstanding electrochemical capacity of 190mAh g(-1) (61.7% for the theoretical capacity) at 20mA g(-1) and 169mAh g(-1) for a higher power output of 100mA g(-1).
机译:纳米级γ-MnO2前体是在室温,液相反应路线下借助超声波合成的。 MnO2前体作为锂二氧化锰一次电池的电极材料在20mA g(-1)下显示140mAh g(-1)的低容量(MnO2理论容量的45.5%)。因此,在高温下制备了具有阳离子V或/和Ti的掺杂MnO 2。热处理后,γ相前体粉末逐渐转变为β-MnO2,并具有较高的比表面积和较大的孔体积和孔径,为氧化还原反应提供了更多的电化学活性位。掺杂的MnO2基体具有理想的晶格参数和较高的电导率的优点,从而增强了隧道结构中Li +扩散动力学。特别是对于V和Ti共掺杂的MnO2,改性材料在20mA g(-1)和169mAh g(-1)的条件下显示出出色的电化学容量,为190mAh g(-1)(理论容量的61.7%)。 100mA g(-1)的更高功率输出。

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