Two-Dimensional Cu2MoS4-Loaded Silicon Nanospheres as an Anode for High-Performance Lithium-Ion Batteries
Source abstract
Abstract
Silicon-based anode materials have a theoretical capacity 10 times that of commercial graphite and have attracted attention. Herein, a creative and effective strategy is elaborated for the synthesis of composite Cu2MoS4/SiNS materials through the self-assembly of silicon nanospheres and a two-dimensional Cu2MoS4 material. The porous silicon dispersed in the two-dimensional layered structure can effectively release the volume expansion and mechanical stress generated, which can also provide further active sites and fast channels for Li+ transmission, and improve the conductivity of the material. As expected, when used as the anode of lithium-ion batteries, the Cu2MoS4/SiNS material exhibited a highly improved electrochemical performance. Benefitting from the unique structural features, the Cu2MoS4/SiNS material showed a discharge specific capacity of 1920 mAh g–1 at 100 mA g–1 and an excellent rate capability of 1330 mAh g–1 at 1.0 A g–1 after 100 cycles. When the current density was further increased to 2.0 A g–1 to test the fast charging performance of the Cu2MoS4/SiNS material, we obtained a specific capacity of 1180 mAh g–1 with 69.2% capacity retention that could still be maintained after 400 cycles. The ultrastable properties and superior capacity of the composite material provide the potential direction for the construction of high-performance lithium-ion batteries.
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
Graduate School of Life Science and Systems Engineering, Kyushu Institute of Technology, 2-4 Hibikino, Wakamatsu, Kitakyushu, Fukuoka 808-0196, Japan
College of Materials and Chemistry, China Jiliang University, Hangzhou 310018, P. R. China
Funding
Ministry of Education, Culture, Sports, Science and Technology · Japan Society for the Promotion of Science · National Natural Science Foundation of China · Iwatani Naoji Foundation
References (57)
Show source-provided references
1. 10.1002/anie.20190208510.1002/anie.201902085 ↗
2. 10.1038/s41586-019-1682-510.1038/s41586-019-1682-5 ↗
3. 10.1016/j.nanoen.2019.05.06210.1016/j.nanoen.2019.05.062 ↗
4. 10.1002/adfm.20090025010.1002/adfm.200900250 ↗
5. 10.1039/C8CS00441B10.1039/C8CS00441B ↗
6. 10.1021/acs.energyfuels.0c0294810.1021/acs.energyfuels.0c02948 ↗
7. 10.1038/s41565-019-0465-310.1038/s41565-019-0465-3 ↗
8. 10.1016/j.jpowsour.2013.09.07210.1016/j.jpowsour.2013.09.072 ↗
9. 10.1002/anie.20190370910.1002/anie.201903709 ↗
10. 10.1021/acsnano.9b0665310.1021/acsnano.9b06653 ↗
11. 10.1021/acs.inorgchem.9b0015810.1021/acs.inorgchem.9b00158 ↗
12. 10.1016/j.electacta.2014.01.15810.1016/j.electacta.2014.01.158 ↗
13. 10.1002/smll.20180245710.1002/smll.201802457 ↗
14. 10.1038/s41563-019-0431-310.1038/s41563-019-0431-3 ↗
15. 10.1021/acsami.6b1208010.1021/acsami.6b12080 ↗
16. 10.1007/s12274-019-2361-410.1007/s12274-019-2361-4 ↗
17. 10.1021/ja208232h10.1021/ja208232h ↗
18. 10.1039/C9EE03857D10.1039/C9EE03857D ↗
19. 10.1039/c4ta00993b10.1039/c4ta00993b ↗
20. 10.1002/aenm.20130088210.1002/aenm.201300882 ↗
21. 10.1039/C9TA12660K10.1039/C9TA12660K ↗
22. 10.1021/acsnano.6b0021810.1021/acsnano.6b00218 ↗
23. 10.1016/j.carbon.2014.10.07810.1016/j.carbon.2014.10.078 ↗
24. 10.1016/j.cej.2018.06.10910.1016/j.cej.2018.06.109 ↗
25. 10.1016/j.nanoen.2015.12.01110.1016/j.nanoen.2015.12.011 ↗
26. 10.1007/s12274-020-2677-010.1007/s12274-020-2677-0 ↗
27. 10.1002/adma.20120160110.1002/adma.201201601 ↗
28. 10.1038/s41560-019-0398-y10.1038/s41560-019-0398-y ↗
29. 10.1038/nenergy.2016.11310.1038/nenergy.2016.113 ↗
30. 10.1016/j.carbon.2018.01.02110.1016/j.carbon.2018.01.021 ↗
31. 10.1039/D0DT00566E10.1039/D0DT00566E ↗
32. 10.1039/C8CC00456K10.1039/C8CC00456K ↗
33. 10.1038/ncomms1290910.1038/ncomms12909 ↗
34. 10.1021/acsenergylett.7b0047610.1021/acsenergylett.7b00476 ↗
35. 10.1039/c2ee22611a10.1039/c2ee22611a ↗
36. 10.1016/j.cej.2017.10.00710.1016/j.cej.2017.10.007 ↗
37. 10.1002/anie.20150011010.1002/anie.201500110 ↗
38. 10.1002/adom.20170076710.1002/adom.201700767 ↗
39. 10.1016/j.jcis.2019.11.06810.1016/j.jcis.2019.11.068 ↗
40. 10.1039/D1TA02753K10.1039/D1TA02753K ↗
41. 10.1016/j.ensm.2016.03.00510.1016/j.ensm.2016.03.005 ↗
42. 10.1039/C9NR05631A10.1039/C9NR05631A ↗
43. 10.1016/j.apsusc.2016.10.17110.1016/j.apsusc.2016.10.171 ↗
44. 10.1016/j.cej.2020.12412510.1016/j.cej.2020.124125 ↗
45. 10.1016/j.electacta.2013.10.14910.1016/j.electacta.2013.10.149 ↗
46. 10.1016/j.jcis.2020.05.06910.1016/j.jcis.2020.05.069 ↗
47. 10.1021/acsnano.0c0197610.1021/acsnano.0c01976 ↗
48. 10.1002/smll.20140075210.1002/smll.201400752 ↗
49. 10.1021/acsnano.7b0118510.1021/acsnano.7b01185 ↗
50. 10.1002/aenm.20190328910.1002/aenm.201903289 ↗
51. 10.1039/C6CP07269K10.1039/C6CP07269K ↗
52. 10.1038/s41467-018-04610-010.1038/s41467-018-04610-0 ↗
53. 10.1002/adma.20170241010.1002/adma.201702410 ↗
54. 10.1016/j.jpowsour.2016.09.06210.1016/j.jpowsour.2016.09.062 ↗
55. 10.1002/adfm.20180775310.1002/adfm.201807753 ↗
56. 10.1039/C6NR07650E10.1039/C6NR07650E ↗
57. 10.1038/s41467-020-19605-z10.1038/s41467-020-19605-z ↗