材料科学
上部结构
电化学
阴极
氧化物
离子
超晶格
过渡金属
储能
氧化还原
容量损失
化学工程
电极
纳米技术
光电子学
热力学
物理化学
催化作用
冶金
物理
工程类
功率(物理)
化学
量子力学
生物化学
作者
Libing Yao,Peichao Zou,Chunyang Wang,Jiahao Jiang,Lu Ma,Sha Tan,Kevin A. Beyer,Feng Xu,Enyuan Hu,Huolin L. Xin
标识
DOI:10.1002/aenm.202201989
摘要
Abstract Layered transition metal oxides are appealing cathodes for sodium‐ion batteries due to their overall advantages in energy density and cost. But their stabilities are usually compromised by the complicated phase transition and the oxygen redox, particularly when operating at high voltages, leading to poor structural stability and substantial capacity loss. Here an integrated strategy combing the high‐entropy design with the superlattice‐stabilization to extend the cycle life and enhance the rate capability of layered cathodes is reported. It is shown that the as‐prepared high‐entropy Na 2/3 Li 1/6 Fe 1/6 Co 1/6 Ni 1/6 Mn 1/3 O 2 cathode enables a superlattice structure with Li/transition metal ordering and delivers excellent electrochemical performance that is not affected by the presence of phase transition and oxygen redox. It achieves a high reversible capacity (171.2 mAh g −1 at 0.1 C), a high energy density (531 Wh kg −1 ), extended cycling stability (89.3% capacity retention at 1 C for 90 cycles and 63.7% capacity retention at 5 C after 300 cycles), and excellent fast‐charging capability (78 mAh g −1 at 10 C). This strategy would inspire more rational designs that can be leveraged to improve the reliability of layered cathodes for secondary‐ion batteries.
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