阴极
材料科学
电化学
氧化物
结构稳定性
容量损失
储能
相变
离子
化学工程
电极
化学
冶金
热力学
物理化学
结构工程
功率(物理)
有机化学
工程类
物理
作者
Lan Wang,Mei‐Yan Sun,Liang Deng,Yin‐Qi Zheng,Xinyu Li,Yunshan Jiang,Lei Zhao,Zhen‐Bo Wang
标识
DOI:10.1016/j.est.2023.110299
摘要
Due to high safety and cost-effective resources, sodium-ion batteries show great prospect in large-scale energy storage systems. Owing to wide structural framework and high theoretical capacity, Na-based layered oxide with prismatic P2-type structure is an ideal cathode candidate for sodium-ion batteries. However, Na-based layered compounds always suffer from detrimental multiple phase transitions during cycle period, resulting in structure deterioration and rapid capacity decay. Herein, stable P2-Na0.67Ni0.33Mn0.67-xTixO2 cathodes are constructed through substituting Mn with Ti. In-situ XRD demonstrates that Ti substitution effectively successfully suppresses the undesired phase transition of P2-O2, and in turn appears a stable Z-symbiotic intermediate phase with minimal volume change. Hence, designed P2-Na0.67Ni0.33Mn0.37Ti0.3O2 cathode shows better structural stability and long-term cycling reliability, yielding a high reversible capacity of 123 mAh g−1 and a high capacity retention of 89 % after 100 cycles at 0.2C. More importantly, a high working voltage of 3.5 V and a boosted energy density of 400 Wh kg−1 is achieved in the NNMTO-3 || HC full cell, which further strengthens the competence of Ti-substituted Na-based layered oxide cathodes. This work provides a feasible design insight for long-life, high-voltage sodium-ion batteries, which can be applied to construct more stable layered compounds and further improves their electrochemical properties.
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