A self-healing Sn anode with an ultra-long cycle life for sodium-ion batteries
- Authors
- Kim, Changhyeon; Kim, Icpyo; Kim, Huihun; Sadan, Milan K.; Yeo, Hyewon; Cho, Gyubong; Ahn, Jaepyoung; Ahn, Jouhyeon; Ahn, Hyojun
- Issue Date
- 7-Dec-2018
- Publisher
- ROYAL SOC CHEMISTRY
- Citation
- JOURNAL OF MATERIALS CHEMISTRY A, v.6, no.45, pp.22809 - 22818
- Indexed
- SCIE
SCOPUS
- Journal Title
- JOURNAL OF MATERIALS CHEMISTRY A
- Volume
- 6
- Number
- 45
- Start Page
- 22809
- End Page
- 22818
- URI
- https://scholarworks.bwise.kr/gnu/handle/sw.gnu/10957
- DOI
- 10.1039/c8ta09544b
- ISSN
- 2050-7488
- Abstract
- For a next-generation sodium battery to replace lithium ion batteries, it is essential to develop an anode with a long cycle life and high rate. Sn is considered to be an ideal candidate for the anode of sodium ion batteries. Here, we report a Sn anode that exhibits ultra-long-term cycle stability with a high capacity of 554 mA h g(-1) at 10C-rate for 5000 cycles. The optimized cell configuration consists of 1,2-dimethoxyethane as the electrolyte, a double separator including a nanoporous membrane, and a Sn anode with MWCNT as a conductive additive. Its capacity retention reaches up to 99.8% and its coulombic efficiency is near 100% for 5000 cycles. Surprisingly, we have discovered that the Sn powder exhibits a self-healing phenomenon during cycling. Sn is initially pulverized into a nanometer-sized powder, and then forms a three-dimensional porous coral-like structure in which ligament-shaped micrometer-sized Sn particles are connected with a low coordination number by room temperature sintering. The coral-like structure is mechanically stable towards volume change and electrically connected. The self-healing structure and mechanism provide a direction for the design of other electrodes with alloying mechanisms.
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