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Towards a high-rate and long-life LiVPO_4F/C cathode material for lithium ion batteries by potassium and zirconium co-doping

机译:通过钾和锆的共掺杂获得一种用于锂离子电池的高速率,长寿命的LiVPO_4F / C正极材料

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摘要

As a high-potential and high-stability cathode material, LiVPO4F/C is modified by K+ and Zr4+ co-doping to significantly improve its high-rate and long-life performance. K+ assisted by Zr4+ slightly enlarges the unit cell volume to expand Li+ migration pathway. K+ substituting Li+ can also achieve pillar effect to increase the structural stability. Hall effect reveals that Zr4+ substituting V3+ is a donor doping, leading to the transformation of conductive type from p-type to n-type and a great increase of carrier density by 10(6) times. Therefore, the electronic conductivity (1.1 x 10(-2)S cm(-1)) increases by a factor of similar to 10(4). The charge transfer resistance decreases to 82.81 Omega and the Li+ diffusion coefficient (9.83 x 10(-13) cm(2) s(-1)) increases to 7 times that of sin doped LiVPO4F/C. The discharge capacities of Li0.99K0.01V0.995Zr0.005PO4F/C at 0.1C and 1C are 143.3 mA h g(-1) and 135.5 mA h g(-1), respectively. The capacity retention at the charge/discharge rate of 10C is as high as 80.0% after 2000 cycles with an initial capacity of 108.1 mA h g(-1). Even at the discharge rate of 60C (charging at 1C), the capacity reaches 105.7 mA h g(-1).
机译:LiVPO4F / C作为一种高电势,高稳定性的阴极材料,通过K +和Zr4 +共掺杂进行改性,以显着提高其高倍率和长寿命性能。 Zr4 +辅助的K +会略微增大单位细胞体积,从而扩展Li +迁移途径。取代Li +的K +还可以实现立柱效应,从而增加结构稳定性。霍尔效应表明,取代V3 +的Zr4 +是施主掺杂,导致导电类型从p型转变为n型,并且载流子密度大大提高了10(6)倍。因此,电子电导率(1.1 x 10(-2)S cm(-1))的增加幅度类似于10(4)。电荷转移电阻降低到82.81Ω,Li +扩散系数(9.83 x 10(-13)cm(2)s(-1))增加到正弦掺杂LiVPO4F / C的7倍。 Li0.99K0.01V0.995Zr0.005PO4F / C在0.1C和1C的放电容量分别为143.3 mA h g(-1)和135.5 mA h g(-1)。 2000次循环后,初始充电容量为108.1 mA h g(-1),充电/放电速率为10C时的容量保持率高达80.0%。即使以60C的放电速率(以1C充电),容量也达到105.7 mA h g(-1)。

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