八面体
阴极
材料科学
离子
结构稳定性
钠离子电池
过渡金属
X射线吸收光谱法
同步加速器
替代(逻辑)
相变
结晶学
化学工程
电化学
化学
电极
晶体结构
吸收光谱法
物理化学
热力学
工程类
法拉第效率
物理
催化作用
有机化学
核物理学
结构工程
量子力学
程序设计语言
生物化学
计算机科学
作者
Huanqing Liu,Xu Gao,Jun Chen,Jinqiang Gao,Haoji Wang,Yu Mei,Huan Liu,Wentao Deng,Guoqiang Zou,Hongshuai Hou,Xiaobo Ji
标识
DOI:10.1016/j.jechem.2022.09.010
摘要
P2-type Mn-based layered oxides are viewed as promising cathode materials for sodium ion battery by virtue of their high theoretical capacity. Considering that pure Na2/3MnO2 suffers from poor cycling performances, Cu-substitution strategy is proposed to effectively alleviate this issue. However, the structural evolution mechanism of the Cu-containing samples still remains unclear. Herein, we propose that Cu-Substitution P2-type Na0.66Mn1-xCuxO2 with enlarged lattice parameters are conducive to improving the interlayer structure stability through mitigating TMO2 slabs distortion. Proved by synchrotron XAS spectra and ex/in situ XRD, the expansion/contraction of MnO6 octahedron is dramatically reduced with the increased Cu content, showing the facilitated Na ion diffusion. Furthermore, when the ratio of Cu to Mn reaches 1:4, the phase transition from P2 to P'2 type at the end of discharge can be suppressed, resulting in the improved interlayer skeleton stability. The Cu-containing samples with stable interlayer structure exhibit high capacity retention and outstanding rate performances (a capacity of 79.9 mAh g−1 at 5 C). This Cu-substitution strategy provides a promising approach to designing highly stable cathodes.
科研通智能强力驱动
Strongly Powered by AbleSci AI