电化学
离子
三元运算
阴极
相(物质)
材料科学
氧气
锂(药物)
分析化学(期刊)
化学
物理化学
电极
内分泌学
程序设计语言
有机化学
医学
色谱法
计算机科学
作者
Binpeng Hou,Jingjin Chen,L. Zhang,Xiaowen Shi,Zi‐Zhong Zhu
标识
DOI:10.1016/j.electacta.2023.143463
摘要
As the cathode material of lithium-ion batteries, Li-rich ternary layered oxides usually suffer from high first cycle irreversible capacity, low rate capability, and structural instability during charge–discharge. Recent studies show that Ni-rich Li1.20Mn0.44Ni0.32Co0.04O2 material has good structural stability. In this paper, the electrochemical performance of Li1.20Mn0.44Ni0.32Co0.04O2 and its oxygen-deficient phase Li1.20Mn0.44Ni0.32Co0.04O1.83 are studied by the first-principles calculations. The results show that, for the pristine phase Li1.20Mn0.44Ni0.32Co0.04O2, the theoretical delithiation capacity is 380 mAh/g and the highest charging voltage platform is 4.99 V. The O ions are found to participate in the charge compensation significantly. Ni ions can only contribute 118 mAh/g of the delithiation capacity, and the remaining charging capacity is contributed by O ions. For the oxygen-deficient phase Li1.20Mn0.44Ni0.32Co0.04O1.83, the highest voltage platform is reduced by 0.21 V, O ions are also found to participate in the charge compensation obviously. Compared to the pristine phase, transition metal (TM) ions in the oxygen-deficient phase exhibit higher chemical activity, while the contribution of O ions to charge compensation is relatively reduced. The oxygen-deficient phase has a slightly higher theoretical capacity (392 mAh/g) than the pristine phase.
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