journal article·2017-01-18

Mechanism of Capacity Fade in Sodium Storage and the Strategies of Improvement for FeS2 Anode

Kongyao Chen, Wuxing Zhang, Lihong Xue, Weilun Chen, Xinghua Xiang, Min Wan, Yunhui Huang

Publisher page

Abstract

Pyrite FeS2 has attracted extensive interest as anode material for sodium-ion batteries due to its high capacity, low cost, and abundant resource. However, the micron-sized FeS2 usually suffers from poor cyclability, which stems from structure collapse, exfoliation of active materials, and sulfur dissolution. Here, we use a synergistic approach to enhance the sodium storage performance of the micron-sized FeS2 through voltage control (0.5-3 V), binder choice, and graphene coating. The FeS2 electrode with the synergistic approach exhibits high specific capacity (524 mA h g-1), long cycle life (87.8% capacity retention after 800 cycles), and excellent rate capability (323 mA h g-1 at 5 A g-1). The results prove that a synergistic approach can be applied in the micron-sized sulfides to achieve high electrochemical performance.
Source: europepmc · Quality: candidate unverified · Source record ↗

Research context

OpenAlex topics: Advancements in Battery Materials · Advanced Battery Materials and Technologies · Extraction and Separation Processes

SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.

Affiliations

State Key Laboratory of Material Processing and Die & Mold Technology, School of Materials Science and Engineering, Huazhong University of Science and Technology, Wuhan, Hubei 430074, China

Funding

Ministry of Science and Technology of the People's Republic of China · National Natural Science Foundation of China

References (32)

Show source-provided references
1. 10.1002/aenm.20140120510.1002/aenm.201401205 ↗
2. 10.1021/acsami.5b0659010.1021/acsami.5b06590 ↗
3. 10.1039/c2nr31822a10.1039/c2nr31822a ↗
4. 10.1002/adma.20130631410.1002/adma.201306314 ↗
5. 10.1016/j.nanoen.2015.12.02810.1016/j.nanoen.2015.12.028 ↗
6. 10.1021/nn503582c10.1021/nn503582c ↗
7. 10.1021/acsami.5b0638510.1021/acsami.5b06385 ↗
8. 10.1002/chem.20150457910.1002/chem.201504579 ↗
9. 10.1038/ncomms840210.1038/ncomms8402 ↗
10. 10.1002/adma.20140149610.1002/adma.201401496 ↗
11. 10.1002/adfm.20140093410.1002/adfm.201400934 ↗
12. 10.1039/c2jm35227c10.1039/c2jm35227c ↗
13. 10.1166/jnn.2012.466010.1166/jnn.2012.4660 ↗
14. 10.1016/j.jpowsour.2014.03.01110.1016/j.jpowsour.2014.03.011 ↗
15. 10.1016/j.jpowsour.2007.11.01710.1016/j.jpowsour.2007.11.017 ↗
16. 10.1002/anie.20160746910.1002/anie.201607469 ↗
17. 10.1038/ncomms968910.1038/ncomms9689 ↗
18. 10.1016/j.jallcom.2006.02.11310.1016/j.jallcom.2006.02.113 ↗
19. 10.1016/j.jpowsour.2007.06.09310.1016/j.jpowsour.2007.06.093 ↗
20. 10.1038/ncomms392210.1038/ncomms3922 ↗
21. 10.1039/C5NR00398A10.1039/C5NR00398A ↗
22. 10.1039/C4EE03759F10.1039/C4EE03759F ↗
23. 10.1021/acsnano.5b0470010.1021/acsnano.5b04700 ↗
24. 10.1016/j.jpowsour.2013.08.12310.1016/j.jpowsour.2013.08.123 ↗
25. 10.1039/C5TA00623F10.1039/C5TA00623F ↗
26. 10.1016/j.elecom.2015.02.00610.1016/j.elecom.2015.02.006 ↗
27. 10.1002/adfm.20150046910.1002/adfm.201500469 ↗
28. 10.1038/nmat246010.1038/nmat2460 ↗
29. 10.1039/C4CP04939J10.1039/C4CP04939J ↗
30. 10.1016/j.electacta.2015.06.03910.1016/j.electacta.2015.06.039 ↗
31. 10.1038/ncomms216310.1038/ncomms2163 ↗
32. 10.1038/ncomms985010.1038/ncomms9850 ↗