阴极
电化学
兴奋剂
离子
动力学
空位缺陷
氧化物
材料科学
钠离子电池
过渡金属
化学工程
分析化学(期刊)
化学
无机化学
电极
结晶学
物理化学
冶金
光电子学
催化作用
色谱法
生物化学
量子力学
物理
工程类
法拉第效率
有机化学
作者
Yong Ren,Qinglei Ge,Yijie Wu,Qin Peng,Jun Qian,Xuli Ding
标识
DOI:10.1016/j.jpcs.2024.112241
摘要
The O3 layered oxides have been extensively investigated as cathode materials for sodium-ion batteries due to their remarkable theoretical capacity. However, the large radius of Na+ lead to complex phase transitions and tortuous diffusion channels during extraction/insertion, which ultimately restricts the Na+ diffusion kinetics and cyclic stability. In this study, we report a Zn and Cu co-doping strategy to the high entropy layer oxide Na [Ni0·2Fe0·2Mn0·4Cu0·15Zn0.05]O2 (HEO-CuZn) using the sol-gel method to prepare the oxides. Here, Zn is used to stabilize the structure of layer between the transition metal and O atoms, which slows down the adverse phase transition. In the fabricated sample, the element Cu provides additional capacity and inhibits excessive oxidation. The prepared HEO-CuZn used as cathode for Na+ ion battery exhibits better electrochemical performance, delivering a high specific capacity of 148 mA h g−1, and 84 % capacity retention after 100 cycles, which is attributed to the expanded Na+ transfer channels, reduced activation energy and interface side reactions, thus enhancing the Na+ diffusion kinetics. Meanwhile, the high entropy strategy stabilizes the overall structure by reducing the John-Teller distortion and suppressing the Na+/vacancy order, and effectively avoids adverse phase transitions such as O′3 and P′3. This study provides a new insight for the advance of the next generation high specific energy sodium-ion battery.
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