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Formation of Stable Solid–Electrolyte Interphase Layer on Few-Layer Graphene-Coated Silicon Nanoparticles for High-Capacity Li-Ion Battery Anodes

Silicon-based anode materials exhibit higher specific and volumetric capacities than other materials and have therefore received much attention for potential use in lithium-ion batteries. However, the continuous growth of a solid–electrolyte interphase at the surface of silicon is a primary cause of...

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Bibliographic Details
Published in:Journal of physical chemistry. C 2017-11, Vol.121 (47), p.26155-26162
Main Authors: Park, Jong Hwan, Moon, Junhyuk, Han, Sangil, Park, Seongyong, Lim, Ju Wan, Yun, Dong-Jin, Kim, Dong Young, Park, Kwangjin, Son, In Hyuk
Format: Article
Language:English
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Summary:Silicon-based anode materials exhibit higher specific and volumetric capacities than other materials and have therefore received much attention for potential use in lithium-ion batteries. However, the continuous growth of a solid–electrolyte interphase at the surface of silicon is a primary cause of chronic capacity fading of silicon electrodes. In this paper, we report the formation of an electrochemically stable solid–electrolyte interphase layer on the surfaces of the few-layer graphene-coated silicon nanoparticles. During the first lithiation, electrolyte molecules were electrochemically decomposed and deposited on the surface of few-layer graphene, thus forming a stable protective layer. When combined with an ionic liquid electrolyte based on pyrrolidinium and bis­(fluorosulfonyl)­imide, an anode containing 75% few-layer graphene-coated silicon delivered a reversible capacity of 1770 mAh g–1 (1430 mAh/ccelectrode) at a current density of 400 mAh g–1 (2 mAh cm–2) after 200 cycles. Averaged over the first 200 cycles, the half-cell exhibits a capacity loss of only 7.2% with a Coulombic efficiency of 99.4%. The results of our study demonstrate that the few-layer graphene coating may lead to an ideal candidate for the generation of a stable protecting layer for a silicon anode that is otherwise harmed by side reactions with electrolytes during cycling.
ISSN:1932-7447
1932-7455
DOI:10.1021/acs.jpcc.7b05876