Wanjing Yu

CNT-Decorated Na3V2(PO4)3 Microspheres as a High-Rate and Cycle-Stable Cathode Material for Sodium Ion Batteries

A novel cathode material, carbon nanotube (CNT)-decorated Na3V2(PO4)3 (NVP) microspheres, was designed and synthesized via spray-drying and carbothermal reduction methods. The microspheres were covered and embedded by CNTs, the surfaces of which were also covered by amorphous carbon layers. Thus, a carbon network composed of CNTs and amorphous carbon layers formed in the materials. The polarization of a 10 wt % CNT-decorated NVP (NVP/C10) electrode was much less compared with that of the electrode with pristine NVP without CNTs. The capacity of the NVP/C10 electrode only decreased from 103.2 to 76.2 mAh g-1 when the current rates increased from 0.2 to 60 C. Even when cycled at a rate of 20 C, the initial discharge capacity of the NVP/C10 electrode was as high as 91.2 mAh g-1, and the discharge capacity was 76.9 mAh g-1 after 150 cycles. The charge-transfer resistance and ohmic resistance became smaller because of CNT decorating. Meanwhile, the addition of CNTs can tune the size of the NVP particles and increase the contact area between NVP and the electrolyte. Consequently, the resulted NVP had a larger sodium ion diffusion coefficient than that of the pristine NVP.

Reduced Graphene Oxide Decorated Na3V2(PO4)3 Microspheres as Cathode Material With Advanced Sodium Storage Performance

Reduced graphene oxide (rGO) sheet decorated Na3V2(PO4)3 (NVP) microspheres were successfully synthesized by spray-drying method. The NVP microspheres were embedded by rGO sheets, and the surface of the particles were coated by rGO sheets and amorphous carbon. Thus, the carbon conductive network consisted of rGO sheets and amorphous carbon generated in the cathode material. NVP microspheres decorated with different content of rGO (about 0, 4, 8, and 12 wt%) were investigated in this study. The electrochemical performance of NVP exhibited a significant enhancement after rGO introduction. The electrode containing about 8 wt% rGO (NVP/G8) showed the best rate and cycle performance. NVP/G8 electrode exhibited the discharge capacity of 64.0 mAh g−1 at 70°C, and achieved high capacity retention of 95.5% after cycling at 10°C for 100 cycles. The polarization of the electrode was inhibited by the introduction of rGO sheets. Meanwhile, compared with the pristine NVP electrode, NVP/G8 electrode exhibited small resistance and high diffusion coefficient of sodium ions.

Comparative Investigation of 0.5Li2MnO3·0.5LiNi0.5Co0.2Mn0.3O2 Cathode Materials Synthesized by Using Different Lithium Sources

Lithium-rich manganese-based cathode materials has been attracted enormous interests as one of the most promising candidates of cathode materials for next-generation lithium ion batteries because of its high theoretic capacity and low cost. In this study, 0.5Li2MnO3·0.5LiNi0.5Co0.2Mn0.3O2 materials are synthesized through a solid-state reaction by using different lithium sources, and the synthesis process and the reaction mechanism are investigated in detail. The morphology, structure, and electrochemical performances of the material synthesized by using LiOH·H2O, Li2CO3, and CH3COOLi·2H2O have been analyzed by using Thermo gravimetric analysis (TGA), X-ray diffraction (XRD), Scanning electron microscope (SEM), Transmission electron microscope (TEM), X-ray photoelectron spectroscopy (XPS), and electrochemical measurements. The 0.5Li2MnO3·0.5LiNi0.5Co0.2Mn0.3O2 material prepared by using LiOH·H2O displays uniform morphology with nano particle and stable layer structure so that it suppresses the first cycle irreversible reaction and structure transfer, and it delivers the best electrochemical performance. The results indicate that LiOH·H2O is the best choice for the synthesis of the 0.5Li2MnO3·0.5LiNi0.5Co0.2Mn0.3O2 material.