Fabricating Silicon Nanotubes by Electrochemical Exfoliation and Reduction of Layer-Structured CaSiO3 in Molten Salt
Source abstract
Abstract
Silicon nanotubes (SNTs) are very attractive in the fields of energy, catalysis, and sensors, but a facile template- and/or catalyst-free preparation method is still absent. Herein, we study a controllable and cost-effective approach for preparing SNTs by electrochemically reducing layer-structured calcium silicate (CaSiO3) in molten CaCl2/NaCl without any template and catalyst. The underlying mechanism of the SNT formation is uncovered: the layer-structured CaSiO3 is first electrochemically exfoliated into SiOx (0 < x < 2) sheets while releasing CaO into the molten salts, and then the SiOx sheets are electrochemically reduced and simultaneously crimped into SNTs. The diameter (120–312 nm) and wall thickness (∼40 nm) of the SNTs can be tailorable by manipulating the reduction potential between −1.28 and −1.48 V (vs Ag/AgCl). Lastly, the electrolytic SNTs show a high lithium storage capacity of 3737 mAh g–1 at 0.2 A g–1, a high rate capability of 1371 mA h g–1 at 10 A g–1, and stable cycling with a capacity of 974 mAh g–1 after 600 cycles at 1 A g–1. Overall, the template- and catalyst-free electrochemical method provides a straightforward and facile way to prepare SNTs with a brand-new mechanism that can be applied to other tubular structure materials.
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: Advancements in Battery Materials · Semiconductor materials and interfaces · Dielectric properties of ceramics
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
School of Resource and Environmental Sciences, Hubei International Scientific and Technological Cooperation Base of Sustainable Resource and Energy, Wuhan University, Wuhan 430072, P. R. China
Key Laboratory for Ecological Metallurgy of Multimetallic Mineral of Ministry of Education, School of Metallurgy, Northeastern University, Shenyang 110819, P. R. China
Funding
National Natural Science Foundation of China
References (67)
Show source-provided references
1. 10.1038/354056a010.1038/354056a0 ↗
2. 10.1039/C7EE00488E10.1039/C7EE00488E ↗
3. 10.1039/D0EE00477D10.1039/D0EE00477D ↗
4. 10.1016/j.ensm.2020.07.02710.1016/j.ensm.2020.07.027 ↗
5. 10.1016/j.ensm.2016.06.00210.1016/j.ensm.2016.06.002 ↗
6. 10.1002/adma.20070084010.1002/adma.200700840 ↗
7. 10.1038/366324a010.1038/366324a0 ↗
8. 10.1039/C9EE02615K10.1039/C9EE02615K ↗
9. 10.1002/aenm.20170108310.1002/aenm.201701083 ↗
10. 10.1002/adma.20150363310.1002/adma.201503633 ↗
11. 10.1038/s41467-018-02824-w10.1038/s41467-018-02824-w ↗
12. 10.1002/aenm.20200210810.1002/aenm.202002108 ↗
13. 10.1016/j.jechem.2019.04.01410.1016/j.jechem.2019.04.014 ↗
14. 10.1002/ange.20170706410.1002/ange.201707064 ↗
15. 10.1016/j.ensm.2019.06.02410.1016/j.ensm.2019.06.024 ↗
16. 10.1039/C8TA06370B10.1039/C8TA06370B ↗
17. 10.1016/j.ensm.2018.03.02510.1016/j.ensm.2018.03.025 ↗
18. 10.1021/acsami.0c1274710.1021/acsami.0c12747 ↗
19. 10.1021/acs.chemrev.9b0032610.1021/acs.chemrev.9b00326 ↗
20. 10.1021/nn201716710.1021/nn2017167 ↗
21. 10.1002/aenm.20170071510.1002/aenm.201700715 ↗
22. 10.1038/nnano.2007.41110.1038/nnano.2007.411 ↗
23. 10.1021/cr500177a10.1021/cr500177a ↗
24. 10.1038/nmat90010.1038/nmat900 ↗
25. 10.1002/anie.20035278610.1002/anie.200352786 ↗
26. Yang J. Y. · Chin. J. Inorg. Chem. · 2009 · 25 · 756
27. 10.1002/anie.20160265310.1002/anie.201602653 ↗
28. 10.1038/nnano.2012.3510.1038/nnano.2012.35 ↗
29. 10.1103/PhysRevB.61.999410.1103/PhysRevB.61.9994 ↗
30. 10.1016/S0009-2614(02)01820-110.1016/S0009-2614(02)01820-1 ↗
31. 10.1021/nl902058c10.1021/nl902058c ↗
32. 10.1002/adma.20120160110.1002/adma.201201601 ↗
33. 10.1002/aenm.20130088210.1002/aenm.201300882 ↗
34. 10.1039/C3RA45439H10.1039/C3RA45439H ↗
35. 10.1038/nnano.2012.3510.1038/nnano.2012.35 ↗
36. 10.1039/c3cc41913d10.1039/c3cc41913d ↗
37. 10.1002/adma.20130539410.1002/adma.201305394 ↗
38. 10.1039/C5TA00961H10.1039/C5TA00961H ↗
39. 10.1021/acs.nanolett.5b0284210.1021/acs.nanolett.5b02842 ↗
40. 10.1021/acsami.6b0638710.1021/acsami.6b06387 ↗
41. 10.1039/c2ra20698f10.1039/c2ra20698f ↗
42. 10.1039/c3ta11823a10.1039/c3ta11823a ↗
43. 10.1021/acs.iecr.9b0443010.1021/acs.iecr.9b04430 ↗
44. 10.1002/smll.20050027610.1002/smll.200500276 ↗
45. Hulliger J. · Adv. Mater. · 2002 · 14 · 118510.1002/1521-4095(20020903)14:17<1185::AID-ADMA1185>3.0.CO;2-8 ↗
46. 10.1088/0957-4484/23/30/30560210.1088/0957-4484/23/30/305602 ↗
47. 10.1021/acsami.6b0977510.1021/acsami.6b09775 ↗
48. 10.1039/C3NR06418B10.1039/C3NR06418B ↗
49. 10.1103/PhysRevB.61.1682710.1103/PhysRevB.61.16827 ↗
50. 10.1021/acs.chemrev.9b0042810.1021/acs.chemrev.9b00428 ↗
51. 10.1002/1521-4095(20020903)14:17<1219::AID-ADMA1219>3.0.CO;2-T10.1002/1521-4095(20020903)14:17<1219::AID-ADMA1219>3.0.CO;2-T ↗
52. 10.1002/adma.20030489810.1002/adma.200304898 ↗
53. 10.1002/adma.20040138110.1002/adma.200401381 ↗
54. 10.1002/adfm.20100119010.1002/adfm.201001190 ↗
55. 10.1002/adma.20120160110.1002/adma.201201601 ↗
56. 10.1002/pssa.20133046810.1002/pssa.201330468 ↗
57. 10.1021/acsami.5b0570510.1021/acsami.5b05705 ↗
58. 10.1002/adem.20160021310.1002/adem.201600213 ↗
59. 10.1016/j.jpowsour.2015.04.12710.1016/j.jpowsour.2015.04.127 ↗
60. 10.1002/adfm.20150295910.1002/adfm.201502959 ↗
61. 10.1149/1.240986210.1149/1.2409862 ↗
62. 10.1063/1.514264310.1063/1.5142643 ↗
63. 10.1021/jp404155y10.1021/jp404155y ↗
64. 10.1021/acsnano.8b0652810.1021/acsnano.8b06528 ↗
65. 10.1021/acsnano.7b0118510.1021/acsnano.7b01185 ↗
66. 10.1021/am402930b10.1021/am402930b ↗
67. 10.1039/c3nr05354g10.1039/c3nr05354g ↗