堆积
电化学
阴极
材料科学
氧化物
双功能
电化学动力学
化学工程
电池(电)
钠离子电池
法拉第效率
无机化学
化学
冶金
有机化学
电极
工程类
功率(物理)
物理
物理化学
量子力学
催化作用
作者
Shi Li,Yao Xiao,Yan‐Fang Zhu,Yongchun Li,Ting Chen,Dong Wang,Yi‐Hua Liu,Hao Liu,Yuan Li,Decheng Li,Gongke Wang,Yuxia Liu,Yang Song,Zhenguo Wu,Benhe Zhong,Xiaodong Guo
标识
DOI:10.1016/j.cej.2021.128719
摘要
As one of the most prospective transitional metal oxide cathode materials for sodium-ion batteries (SIBs), P2-type Na2/3Ni1/3Mn2/3O2 layered oxide generally suffers from sluggish Na+ kinetics and complicated structural evolution. Here, a stable Co-free P2-Na2/3Li1/9Ni2/9Mn2/3O2 cathode material with multilayer oriented stacking nanoplates is reported, which exhibits high hydrostability realized by partial Li element substitution for Ni. A prominent rate capability (71.7% capacity retention at 5 C compared to 0.2 C), an excellent cycling stability (78.7% capacity retention at 2 C after 300 cycles) and a promoted performance even at a higher cutoff potential of 4.4 V were displayed owing to bifunctional strategy of chemical substitution coupled with structure modulation, and the as-synthesized material retains its original structure and electrochemical performance after being aged in water. Moreover, dominant Na+ capacitive storage mechanism, high thermostability and complete solid-solution reaction are explicitly elucidated through quantitative calculation of electrochemical kinetics and in-situ X-ray diffraction technique. These findings reveal the importance of rational chemical substitution and structure modulation strategy, and inspire novel design of high-performance cathode materials for rechargeable SIBs.
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