Spatially heterogeneous carbon-fiber papers as surface dendrite-free current collectors for lithium deposition

被引:161
作者
Ji, Xiulei [1 ]
Liu, De-Yu [1 ]
Prendiville, Daniel G. [1 ]
Zhang, Yichi [1 ]
Liu, Xiaonao [1 ]
Stucky, Galen D. [1 ]
机构
[1] Univ Calif Santa Barbara, Dept Chem & Biochem, Santa Barbara, CA 93106 USA
基金
美国国家科学基金会; 加拿大自然科学与工程研究理事会;
关键词
Lithium dendrite; Current collector; Line-of-sight deposition; Spatial heterogeneity; Insulating; NONAQUEOUS ELECTROLYTE; LI-AIR; METAL; BATTERIES; ION; MORPHOLOGY; GRAPHITE; ANODE; FILM;
D O I
10.1016/j.nantod.2011.11.002
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Despite the high energy density, the lithium metal electrode has been plagued for decades with a dendrite growth problem that can result in a battery thermal runaway. Here, we introduce anisotropic spatially heterogeneous three dimensional (3D) current collectors that prevent lithium deposition on the insulating electrolyte-facing surface and accommodate lithium deposition inside the spacious voids. The anisotropic spatial heterogeneity was introduced by a line-of-sight deposition of a thin SiO2 layer onto a carbon-fiber paper. The deposited SiO2 was later converted into SiC by a magnesiothermic reaction. The SiO2 and SiC decorated 3D current collectors were confirmed dendrite-free by ex situ SEM observation after a deep lithium deposition of 28.8 C cm(-2) at a high current density of 4 mA cm(-2). A high lithium cycling efficiency of 94% was achieved over deep deposition (14.4 C cm(-2)) and stripping cycles in a carbonate based organic electrolyte, demonstrating the superiority of the novel current collector for dendrite control and lithium cycling. This strategy opens new avenues to address the dendrite problem by rationally designed current collectors and for the creation of a high energy density electrode. (C) 2011 Elsevier Ltd. All rights reserved.
引用
收藏
页码:10 / 20
页数:11
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