电化学
阴极
材料科学
收缩率
扩散
电导率
化学工程
复合数
动力学
离子电导率
兴奋剂
分析化学(期刊)
复合材料
化学
电极
热力学
物理化学
电解质
色谱法
光电子学
量子力学
物理
工程类
作者
Jun Cheng,Yanjun Chen,Yanzhong Wang,Chao Wang,Zhenfeng He,Dan Li,Li Guo
标识
DOI:10.1016/j.jpowsour.2020.228632
摘要
Na3V2(PO4)3(NVP) is a promising cathode material. However, the poor intrinsic conductivity and sever volumetric shrinkage constrain the applications of NVP. Herein, we propose a remarkable Si/Zr co-doped Na3V2-xZrx(PO4)3-x(SiO4)x/C composite. The optimized co-doped sample exhibits superior rate and cycling performance resulting from the improved ionic conductivity. The synergetic effects of Si/Zr co-doping on the crystal structural stability and Na+ migration capability are significant, leading to superior electrochemical performance for the co-doped composites. Moreover, the Na3V2-xZrx(PO4)3-x(SiO4)x/C possess an extra high voltage plateau at 3.7 V, corresponding to the V4+/V5+ reaction. The optimized Na3V1.97Zr0.03(PO4)2.97(SiO4)0.03/C reveals an initial capacity of 109.6 mA h g−1 at 0.1 C. It performs a capacity retention of 87.7% at 6 C after 500 cycles. At a higher density of 12 C, the initial capacity is 95.7 mA h g−1, and it retains a value of 68.3 mA h g−1 after 2000 cycles, corresponding to a low decay of 0.014% per cycle. Due to the high potential platform and superior capacity value, it delivers an energy density of 403.5 Wh kg−1, surpassing the theoretical one (397.8 Wh kg−1). The kinetic behavior is explored by GITT, and the lowest diffusion coefficients appeared at 3.4 V and 3.7 V conforms to the electrochemical tests.
科研通智能强力驱动
Strongly Powered by AbleSci AI