In Situ Lithiation-Delithiation of Mechanically Robust Cu-Si Core-Shell Nanolattices in a Scanning Electron Microscope

被引:47
|
作者
Xia, Xiaoxing [1 ]
Di Leo, Claudio V. [2 ]
Gu, X. Wendy [1 ,3 ]
Greer, Julia R. [1 ]
机构
[1] CALTECH, Div Engn & Appl Sci, 1200 East Calif Blvd, Pasadena, CA 91125 USA
[2] Georgia Inst Technol, Sch Aerosp Engn, 270 Ferst Dr, Atlanta, GA 30332 USA
[3] Univ Calif Berkeley, Dept Chem, 419 Latimer Hall, Berkeley, CA 94720 USA
来源
ACS ENERGY LETTERS | 2016年 / 1卷 / 03期
关键词
LITHIUM-ION BATTERIES; THIN-FILM ELECTRODES; AMORPHOUS-SILICON; HIGH-PERFORMANCE; DEPENDENT FRACTURE; ANODES; ENERGY; MECHANISMS; DEPOSITION; NANOWIRES;
D O I
10.1021/acsenergylett.6b00256
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Nanoarchitected Cu-Si core-shell lattices were fabricated via two-photon lithography and tested as mechanically robust Li-ion battery electrodes which accommodate similar to 250% Si volume expansion during lithiation. The superior mechanical performance of the nanolattice electrodes is directly observed using an in situ scanning electron microscope, which allows volume expansion and morphological changes to be imaged at multiple length scales, from single lattice beam to the architecture level, during electrochemical testing. Finite element modeling of lithiation-induced volume expansion in a core-shell structure reveals that geometry and plasticity mechanisms play a critical role in preventing damage in the nanolattice electrodes. The two-photon lithography-based fabrication method combined with computational modeling and in situ characterization capabilities would potentially enable the rational design and fast discovery of mechanically robust and kinetically agile electrode materials that independently optimize geometry, feature size, porosity, surface area, and chemical composition, as well as other functional devices in which mechanical and transport phenomena are important.
引用
收藏
页码:492 / 499
页数:8
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