Synthesis of Ultrathin Si Nanosheets from Natural Clays for Lithium-Ion Battery Anodes
Source abstract
Abstract
Two-dimensional Si nanosheets have been studied as a promising candidate for lithium-ion battery anode materials. However, Si nanosheets reported so far showed poor cycling performances and required further improvements. In this work, we utilize inexpensive natural clays for preparing high quality Si nanosheets via a one-step simultaneous molten salt-induced exfoliation and chemical reduction process. This approach produces high purity mesoporous Si nanosheets in high yield. As a control experiment, two-step process (pre-exfoliated silicate sheets and subsequent chemical reduction) cannot sustain their original two-dimensional structure. In contrast, one-step method results in a production of 5 nm-thick highly porous Si nanosheets. Carbon-coated Si nanosheet anodes exhibit a high reversible capacity of 865 mAh g(-1) at 1.0 A g(-1) with an outstanding capacity retention of 92.3% after 500 cycles. It also delivers high rate capability, corresponding to a capacity of 60% at 20 A g(-1) compared to that of 2.0 A g(-1). Furthermore, the Si nanosheet electrodes show volume expansion of only 42% after 200 cycles.
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: Advancements in Battery Materials · Extraction and Separation Processes · Supercapacitor Materials and Fabrication
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
Department of Energy Engineering, School of Energy and Chemical Engineering, Ulsan National Institute of Science and Technology (UNIST), Ulsan 689-798, South Korea
Funding
Korea Evaluation Institute of Industrial Technology
References (38)
Show source-provided references
1. 10.1016/j.nantod.2012.08.00410.1016/j.nantod.2012.08.004 ↗
2. 10.1149/1.159691710.1149/1.1596917 ↗
3. 10.1039/b919877f10.1039/b919877f ↗
4. 10.1016/j.jpowsour.2006.09.08410.1016/j.jpowsour.2006.09.084 ↗
5. 10.1039/C0EE00281J10.1039/C0EE00281J ↗
6. 10.1016/j.nanoen.2012.04.00110.1016/j.nanoen.2012.04.001 ↗
7. 10.1002/anie.20070250510.1002/anie.200702505 ↗
8. 10.1038/nmat136810.1038/nmat1368 ↗
9. 10.1038/ncomms460510.1038/ncomms4605 ↗
10. 10.1002/aenm.20130049610.1002/aenm.201300496 ↗
11. 10.1021/nl501500g10.1021/nl501500g ↗
12. 10.1038/srep0222210.1038/srep02222 ↗
13. 10.1039/c2cc31712e10.1039/c2cc31712e ↗
14. 10.1002/adma.20120398110.1002/adma.201203981 ↗
15. 10.1039/c3ta11714f10.1039/c3ta11714f ↗
16. 10.1038/nnano.2007.41110.1038/nnano.2007.411 ↗
17. 10.1021/nl902058c10.1021/nl902058c ↗
18. 10.1038/nnano.2012.3510.1038/nnano.2012.35 ↗
19. 10.1021/cm202891p10.1021/cm202891p ↗
20. 10.1039/c3nr05354g10.1039/c3nr05354g ↗
21. 10.1021/nn103385p10.1021/nn103385p ↗
22. 10.1021/nn501683f10.1021/nn501683f ↗
23. 10.1021/ja100919d10.1021/ja100919d ↗
24. 10.1021/ja908827z10.1021/ja908827z ↗
25. 10.1346/CCMN.1995.043021310.1346/CCMN.1995.0430213 ↗
26. 10.1038/174799a010.1038/174799a0 ↗
27. 10.1016/j.nanoen.2013.12.00210.1016/j.nanoen.2013.12.002 ↗
28. 10.1039/c2cc17083c10.1039/c2cc17083c ↗
29. 10.1002/aenm.20140062210.1002/aenm.201400622 ↗
30. 10.1039/c3cp54507e10.1039/c3cp54507e ↗
31. 10.1103/PhysRev.56.97810.1103/PhysRev.56.978 ↗
32. 10.1103/PhysRevB.61.1682710.1103/PhysRevB.61.16827 ↗
33. 10.1021/jp404155y10.1021/jp404155y ↗
34. 10.1038/ncomms421710.1038/ncomms4217 ↗
35. 10.1149/1.240211210.1149/1.2402112 ↗
36. 10.1016/j.jpowsour.2008.12.04710.1016/j.jpowsour.2008.12.047 ↗
37. 10.1016/j.jpowsour.2009.06.03310.1016/j.jpowsour.2009.06.033 ↗
38. 10.1021/nn201716710.1021/nn2017167 ↗