材料科学
尖晶石
锂(药物)
相(物质)
化学工程
扩散
电化学
相变
锂离子电池
电极
刚玉
结晶
纳米技术
电池(电)
复合材料
热力学
物理化学
冶金
内分泌学
工程类
功率(物理)
有机化学
化学
物理
医学
作者
Zhaoxin Guo,Haoran Jiang,Xin‐Yuan Sun,Xinbo Li,Zhedong Liu,Jingchao Zhang,Jiawei Luo,Jinfeng Zhang,Xian‐Sen Tao,Jianxu Ding,Xiaopeng Han,Rui Liu,Yanan Chen,Wenbin Hu
标识
DOI:10.1002/aenm.202302484
摘要
Abstract Defect engineering is demonstrated to be an important factor in enhancing the electrochemical performance of lithium‐ion batteries by improving structural stability and ion diffusion. However, conventional synthetic methods have long and complicated processes, making it challenging to effectively and easily introduce defects into electrode materials. In this work, a high‐temperature shock technique (HTS) with an ultrafast heating and cooling process that can quickly introduce twin boundaries (TBs) into phase‐pure spinel LiMn 2 O 4 in seconds is reported. Various ex situ techniques reveal the crystallization mechanism of LiMn 2 O 4 during ultrafast synthesis. LiMn 2 O 4 with TBs exhibits a higher rate performance than that obtained from the traditional method. Additionally, alien elements can be evenly incorporated into LiMn 2 O 4 in seconds, resulting in excellent cycling performance. For instance, 2% Ni‐doped LiMn 2 O 4 shows an initial capacity of 121 mAh g −1 and retention of 86.5% after 500 cycles at 1 C.
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