Anisotropic Amorphization and Phase Transition in Na2Ti3O7 Anode Caused by Electron Beam Irradiation

被引:4
|
作者
Cheng, Lixun [1 ]
Shen, Yaoling [2 ]
Nan, Pengfei [1 ]
Wu, Chuanqiang [1 ]
Tai, Yilin [1 ]
Luo, Xiaonan [3 ]
Zhang, Yongsheng [4 ]
Ge, Binghui [1 ]
机构
[1] Anhui Univ, Inst Phys Sci & Informat Technol, Informat Mat & Intelligent Sensing Lab Anhui Prov, Hefei 230601, Peoples R China
[2] Chinese Acad Sci, Inst Solid State Phys, Key Lab Mat Phys, Hefei 230031, Peoples R China
[3] 2, Xingang Rd, Zhangwan Town, Ningde 352000, Fujian, Peoples R China
[4] Qufu Normal Univ, Adv Res Inst Multidisciplinary Sci, Qufu 273165, Shandong, Peoples R China
基金
中国国家自然科学基金;
关键词
anisotropic amorphization; electron beam irradiation; in situ; phase transition; transmission electron microscopy; METAL-ORGANIC FRAMEWORKS; ION; CONTRAST; STEM;
D O I
10.1002/smll.202305655
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Na2Ti3O7 is considered one of the most promising anode materials for sodium ion batteries due to its superior safety, environmental friendliness, and low manufacturing cost. However, its structural stability and reaction mechanism still have not been fully explored. As the electron beam irradiation introduces a similar impact on the Na2Ti3O7 anode as the extraction of Na+ ions during the battery discharge process, the microstructure evolution of the materials is investigated by advanced electron microscopy techniques at the atomic scale. Anisotropic amorphization is successfully observed. Through the integrated differential phase contrast-scanning transmission electron microscopy technique and density functional theory calculation, a phase transition pathway involving a new phase, Na2Ti24O49, is proposed with the reduction of Na atoms. Additionally, it is found that the amorphization is dominated by the surface energy and electron dose rate. These findings will deepen the understanding of structural stability and deintercalation mechanism of the Na2Ti3O7 anode, providing new insight into exploring the failure mechanism of electrode materials.
引用
收藏
页数:7
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