材料科学
阴极
钠
空位缺陷
氧气
化学工程
无机化学
纳米技术
冶金
结晶学
物理化学
有机化学
工程类
化学
作者
Chenxiang Li,Meng Li,Guozhuang Liu,Haoxiang Zhuo,Qian Li,Qian Zhang,Guoyao Pang,Xuan Yang,Liangmo Zhou,Kuan Wang,Dongniu Wang,Biwei Xiao,Dongsheng Geng
标识
DOI:10.1021/acsami.4c07264
摘要
Layered P2-type sodium manganese oxide has emerged as a promising cathode candidate for sodium-ion batteries due to its appealing cost-effectiveness and high discharge voltage. However, its practical capacity within the voltage range of 2.0–4.0 V (vs Na+/Na) is relatively low, and its rate capability is hampered by the adverse charge/vacancy ordering during charge/discharge. In this study, a layered P′2/P3 mixed-phase Na0.8-aMn0.675Ni0.225Li0.1O2–x cathode with high (003) crystal plane intensity was designed by introducing oxygen vacancies to P2-structured materials. Aided by these advantages, the hybrid cathode material demonstrates impressive structural and thermal stability and faster Na-ion diffusion kinetics compared to a regular P2 material. Half-cell shows an initial discharge capacity retention of 101 mA h/g at 12 mA/g and 92.25% retention after 500 cycles at 120 mA/g. In combination with a hard carbon anode, the 0.5 A h pouch cell achieved a prevailing capacity retention of 95.2% after 2600 cycles at 36 mA/g. This work opens new dimensions for layered cathode materials with the aim of achieving superior cyclabilities.
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