Liu Shuxin, Wang Haibin, Gao Jianfeng, He Jichuan, Yu Guoqiang, Zhou Tianming
Key Laboratory of Inorganic Materials Preparation and Synthesis, Mianyang Normal University, Mianyang, Sichuan 621000, P. R. China.
Yanshan Power Supply Company of China Power Grid, Yanshan, Hebei 061300, P. R. China.
J Nanosci Nanotechnol. 2018 May 1;18(5):3631-3638. doi: 10.1166/jnn.2018.14629.
The Li3PO4 modified LiFePO4/C and Li4P2O7 modified LiFePO4/C cathode materials were synthesized by in-situ synthesis method, respectively. Phase compositions and microstructures of the products were characterized by X-ray powder diffraction (XRD), scanning electronic microscope (SEM). Results indicate that Li3PO4 and Li4P2O7 can sufficiently coat on the LiFePO4 surface and does not alter LiFePO4 crystal structure. The electrochemical behavior of cathode materials was analyzed using galvanostatic measurement and cyclic voltammetry (CV). Compared with Li3PO4, the existence of Li4P2O7 can better improve the electrochemical performance of LiFePO4 cathode materials in specific capability and lithium ion diffusion of cathode materials. The charge-discharge specific capacity and apparent lithium ion diffusion coefficient increase with Li4P2O7 content and maximizes around the Li4P2O7 content is 5 wt%. The results indicated that the Li4P2O7 adding enhances the lithium ion diffusion rate of LiFePO4. However, because of the interface fracture between Li4P2O7 and LiFePO4 particles during charging and discharging process, the cycling performance of Li4P2O7 modified LiFePO4/C cathode materials is very poor.
分别采用原位合成法制备了Li3PO4改性的LiFePO4/C和Li4P2O7改性的LiFePO4/C正极材料。通过X射线粉末衍射(XRD)、扫描电子显微镜(SEM)对产物的相组成和微观结构进行了表征。结果表明,Li3PO4和Li4P2O7能够充分包覆在LiFePO4表面,且不改变LiFePO4的晶体结构。采用恒电流测量和循环伏安法(CV)对正极材料的电化学行为进行了分析。与Li3PO4相比,Li4P2O7的存在能更好地提高LiFePO4正极材料在比容量和锂离子扩散方面的电化学性能。充放电比容量和表观锂离子扩散系数随Li4P2O7含量的增加而增大,在Li4P2O7含量为5 wt%左右时达到最大值。结果表明,Li4P2O7的加入提高了LiFePO4的锂离子扩散速率。然而,由于在充放电过程中Li4P2O7与LiFePO4颗粒之间的界面断裂,Li4P2O7改性LiFePO4/C正极材料的循环性能很差。