Breaking the lithium storage limit via independent bilayer units within 2D layer materials

被引:11
作者
Lu, Ming [1 ,2 ,3 ,4 ]
Zhang, Bingsen [4 ]
Zhang, Wei [1 ,2 ,3 ]
Zheng, Weitao [1 ,2 ,3 ]
机构
[1] Jilin Univ, Sch Mat Sci & Engn, Key Lab Automobile Mat, MOE, Changchun 130012, Jilin, Peoples R China
[2] Jilin Univ, Electron Microscopy Ctr, Changchun 130012, Jilin, Peoples R China
[3] Jilin Univ, Int Ctr Future Sci, Changchun 130012, Jilin, Peoples R China
[4] Chinese Acad Sci, Shenyang Natl Lab Mat Sci, Inst Met Res, Shenyang 110016, Liaoning, Peoples R China
来源
JOURNAL OF ENERGY CHEMISTRY | 2020年 / 41卷
关键词
Low-voltage TEM; Bilayer graphene; Close-packed; LiC6; TITANIUM CARBIDE MXENE; INTERCALATION;
D O I
10.1016/j.jechem.2019.03.019
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
The study of Kühne et al. has identified lithium intercalation into independent bilayer graphene sheets by in-situ low-voltage (80 kV) TEM combined with both spherical and chromatic aberration correction. The breakthrough lies in a multi-layered close-packed Li superdense phase found in the bilayer graphenes. Based on this superdense phase, a larger expected lithium storage amount, which far exceeds that in the LiC6, was obtained. Bilayer graphene sheets, as the smallest units for the lithiation process, obtained a free expandable space without resistance from the adjacent graphene layers. If the bilayer unit was reproduced as a basic module of electrode materials, a designed architecture with countless independent bilayer units can be assembled to store more Li. Also, the bilayer graphene units can also obtain a higher ionic and electronic conductivity, owing to the decreased Coulomic repulsion and steric hindrance. The bilayer structure represents a new understanding of the nanocrystallization of two-dimensional materials.
引用
收藏
页码:1 / 2
页数:2
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