材料科学
阴极
兴奋剂
插层(化学)
高分辨率透射电子显微镜
X射线吸收精细结构
空位缺陷
钠离子电池
过渡金属
化学工程
透射电子显微镜
光电子学
纳米技术
无机化学
光谱学
结晶学
电化学
电极
物理化学
化学
法拉第效率
催化作用
工程类
物理
量子力学
生物化学
作者
Shi Tao,Wei Zhou,Dajun Wu,Zhicheng Wang,Bin Qian,Wangsheng Chu,A. Marcelli,Li Song
标识
DOI:10.1016/j.jmst.2020.06.055
摘要
Due to the sodium abundance and availability, sodium-ion batteries (SIBs) have the potential to meet the worldwide growing demand of electrical energy storage. P2-type sodium transition-metal layer oxides with a high energy density are considered as the most promising cathode materials for SIBs. We present here a detailed study of the enhanced rate capability and cyclic stability of the Ti-doped Na0.67Ni0.33Mn0.67O2 cathode material. The combined analysis of ex-situ X-ray absorption fine structure (XAFS) spectroscopy, aberration-corrected high resolution transmission electron microscopy (AB-HRTEM) and X-ray diffraction (XRD) show that the strong Ti–O bond in the transition metal layers stabilizes the local structure, destroy the Na+-vacancy ordering and arrest the irreversible multiphase transformation that occurs during the intercalation/deintercalation process. Actually, Na0.67Ni0.33Mn0.52Ti0.15O2 exhibits a reversible capacity of 89.6 mA h g−1 even at 5 C, an excellent cyclability with 88.78 % capacity retention after 200 cycles at 0.5 C. This study provides a better understanding in optimization of the design of high-energy cathode materials based on titanium doped layered oxides for SIBs.
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