尖晶石
材料科学
电化学
阴极
氧化钠
应变工程
离子
氧化物
化学工程
异质结
相变
纳米技术
电极
光电子学
物理化学
化学
有机化学
硅
工程类
冶金
物理
量子力学
作者
Haiyan Hu,Yan‐Fang Zhu,Yao Xiao,Shi Li,Jing Wang,Zhiqiang Hao,Jiahua Zhao,Shulei Chou
标识
DOI:10.1002/aenm.202201511
摘要
Abstract Sodium‐ion oxide cathodes with triphase heterostructures have attracted intensive attention, since the sodium‐storage performance can be enhanced by utilizing the synergistic effect of different phases. However, the composite structures generally suffer from multiple irreversible phase transitions and high lattice strain because of interlayer‐gliding during the charge/discharge process. Here, the concept of strain engineering via manipulating the local chemistry of heterostructured oxide cathode is proposed to regulate the relevant physical and chemical properties, resulting in highly reversible structural evolution (P2/P3/spinel → P2/P3″/spinel) and low intrinsic stress in the potential window of 1.5–4.0 V. Also, the simple structural evolution at a relatively high cut‐off potential of 4.3 V can be detected by in situ X‐ray diffraction and other electrochemical characterization techniques during Na + extraction/insertion. Meanwhile, the electrode exhibits a high reversible capacity (169.4 mAh g −1 at 0.2 C) and excellent rate performance from 1.5 to 4.3 V. Overall, this study reveals the mechanisms of regulating local chemistry to realize strain engineering of the cathode materials and paves the way for the further improvement of high‐performance sodium‐ion batteries.
科研通智能强力驱动
Strongly Powered by AbleSci AI