Simple and scalable synthesis of CuS as an ultrafast and long-cycling anode for sodium ion batteries
- Authors
- Kim, Huihun; Sadan, Milan K.; Kim, Changhyeon; Choe, Seon-Hwa; Cho, Kwon-Koo; Kim, Ki-Won; Ahn, Jou-Hyeon; Ahn, Hyo-Jun
- Issue Date
- 21-Jul-2019
- Publisher
- ROYAL SOC CHEMISTRY
- Citation
- JOURNAL OF MATERIALS CHEMISTRY A, v.7, no.27, pp 16239 - 16248
- Pages
- 10
- Indexed
- SCI
SCIE
SCOPUS
- Journal Title
- JOURNAL OF MATERIALS CHEMISTRY A
- Volume
- 7
- Number
- 27
- Start Page
- 16239
- End Page
- 16248
- URI
- https://scholarworks.gnu.ac.kr/handle/sw.gnu/8947
- DOI
- 10.1039/c9ta04640b
- ISSN
- 2050-7488
2050-7496
- Abstract
- During the development of sodium ion batteries (SIBs), a long cycle life, high capacity, and high rate are required for the anode materials. In this study, CuS is synthesized by heating S on a Cu current collector at 80 degrees C for 5 h, which is a simple and scalable process. The CuS exhibits excellent cycle stability of 517 mA h g(-1) at 5 A g(-1) after 2000 cycles, with 99.2% retention and a coulombic efficiency of almost 100%. CuS also exhibits an ultrahigh rate capability up to 100 A g(-1) with a 268 mA h g(-1). The CuS electrode is suitable for mass production and displays excellent electrochemical performance; therefore, it is a promising anode for SIBs. Moreover, ex situ scanning electron microscopes are applied to investigate their structural changes. During cycling, the shape of the electrode changes to multiundulating, and then to a flat plate covered with nanometer-sized particles, which can be induced by cracking, pulverization, and agglomeration. Through agglomeration, the CuS recovers from the electric isolation caused by pulverization. This self-healing characteristic could represent a new way of obtaining a long cycle life for anodes with volume changes.
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