journal article·2020-01-15

Achieving Slope-Reigned Na-Ion Storage in Carbon Nanofibers by Constructing Defect-Rich Texture by a Cu-Activation Strategy

Xu Guo, Yunyan Xue, Hongfu Zhou, Yunxuan Weng, Jisheng Zhou

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Abstract

Hard carbons have shown promising application potential as anode materials for sodium-ion batteries (SIBs), but adjusting the texture of hard carbons to manipulate their electrochemical behaviors remains a great challenge. In this work, a Cu-activation strategy is developed to control the defects of hard carbon nanofibers to achieve slope-reigned Na-ion storage behaviors. This method can effectively create defect-rich carbon texture by employing a small amount of Cu(NO3)2 as an activator but cannot induce an increase in the surface area. With the addition of the Cu activator, carbon nanofibers with increasing defects are synthesized by electrospinning and subsequent annealing. When carbon nanofibers are used as anodes for SIBs, their reversible capacity is increased with the increase of defects. Simultaneously, slope capacity gradually increases, while low-voltage plateau capacity reduces. Especially, the reversible capacity of Cu-activated nanofibers with more defects can be increased to 315 mA h g–1 with almost no plateau capacity compared with 203 mA h g–1 of inactivated nanofibers with a plateau capacity of 26%. Noticeably, the initial Coulombic efficiency (70%) of the activated nanofibers is just slightly lower than that (72%) of inactivated ones. The Cu-activated nanofibers also demonstrate superb rate performance and long cycle lifetime. Therefore, this work shows a new pathway for the design of defect-rich hard carbons with superior Na-ion storage performance.
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Research context

OpenAlex topics: Advancements in Battery Materials · Supercapacitor Materials and Fabrication · Advanced Battery Technologies Research

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

Affiliations

State Key Laboratory of Chemical Resource Engineering, Beijing Key Laboratory of Electrochemical Process and Technology for Materials, Beijing University of Chemical Technology, Beijing 100029, P. R. China

School of Materials and Mechanical Engineering, Beijing Technology and Business University, Beijing 100048, P. R. China

Funding

National Natural Science Foundation of China · Beijing Key Laboratory of Quality Evaluation Technology for Hygiene and Safety of Plastics, Beijing Technology and Business University

References (61)

Show source-provided references
1. 10.1002/adfm.20120069110.1002/adfm.201200691 ↗
2. 10.1002/anie.20141037610.1002/anie.201410376 ↗
3. 10.1002/aenm.20160094310.1002/aenm.201600943 ↗
4. 10.1039/C5TA03181H10.1039/C5TA03181H ↗
5. 10.1002/aenm.20160289810.1002/aenm.201602898 ↗
6. 10.1016/j.jallcom.2017.10.09410.1016/j.jallcom.2017.10.094 ↗
7. 10.1039/C8TA01265B10.1039/C8TA01265B ↗
8. 10.1039/C8TA02773K10.1039/C8TA02773K ↗
9. 10.1021/nl502860610.1021/nl5028606 ↗
10. 10.1002/aenm.20120016610.1002/aenm.201200166 ↗
11. 10.1149/2.0091514jes10.1149/2.0091514jes ↗
12. 10.1021/acs.nanolett.5b0196910.1021/acs.nanolett.5b01969 ↗
13. 10.1021/nn404640c10.1021/nn404640c ↗
14. 10.1021/nl301695710.1021/nl3016957 ↗
15. 10.1002/aenm.20170040310.1002/aenm.201700403 ↗
16. 10.1002/aenm.20190135110.1002/aenm.201901351 ↗
17. 10.1002/aenm.20150187410.1002/aenm.201501874 ↗
18. 10.1039/C6TA00950F10.1039/C6TA00950F ↗
19. 10.1021/acs.chemmater.6b0547410.1021/acs.chemmater.6b05474 ↗
20. 10.1002/aenm.20170040310.1002/aenm.201700403 ↗
21. 10.1002/adma.20150230310.1002/adma.201502303 ↗
22. 10.1016/j.jechem.2016.04.01610.1016/j.jechem.2016.04.016 ↗
23. 10.1016/j.jpowsour.2016.04.01310.1016/j.jpowsour.2016.04.013 ↗
24. 10.1149/2.0151514jes10.1149/2.0151514jes ↗
25. 10.1021/acs.chemmater.8b0064510.1021/acs.chemmater.8b00645 ↗
26. 10.1002/ange.20190000510.1002/ange.201900005 ↗
27. 10.1039/C0EE00277A10.1039/C0EE00277A ↗
28. 10.1039/C3NR05374A10.1039/C3NR05374A ↗
29. 10.1039/C4TA02068E10.1039/C4TA02068E ↗
30. 10.1016/S0008-6223(01)00268-810.1016/S0008-6223(01)00268-8 ↗
31. 10.1002/aenm.20170111010.1002/aenm.201701110 ↗
32. 10.1021/acsnano.6b0660810.1021/acsnano.6b06608 ↗
33. 10.1002/adma.20150162210.1002/adma.201501622 ↗
34. 10.1039/C5TA07223A10.1039/C5TA07223A ↗
35. 10.1016/S0008-6223(99)00215-810.1016/S0008-6223(99)00215-8 ↗
36. 10.1039/C0JM02126A10.1039/C0JM02126A ↗
37. 10.1016/j.scriptamat.2004.03.02810.1016/j.scriptamat.2004.03.028 ↗
38. 10.1021/ma051786u10.1021/ma051786u ↗
39. 10.1016/j.colsurfa.2010.06.00510.1016/j.colsurfa.2010.06.005 ↗
40. 10.1021/jp306952d10.1021/jp306952d ↗
41. 10.1016/S0378-7753(99)00122-610.1016/S0378-7753(99)00122-6 ↗
42. 10.1016/j.jpowsour.2017.05.01110.1016/j.jpowsour.2017.05.011 ↗
43. 10.1016/j.ssc.2007.03.05210.1016/j.ssc.2007.03.052 ↗
44. 10.1002/anie.20150217310.1002/anie.201502173 ↗
45. 10.1039/c2ee22085g10.1039/c2ee22085g ↗
46. 10.1021/jp301644e10.1021/jp301644e ↗
47. 10.1016/j.nanoen.2013.12.01110.1016/j.nanoen.2013.12.011 ↗
48. 10.1039/C6TA04244A10.1039/C6TA04244A ↗
49. 10.1088/0953-8984/9/1/00410.1088/0953-8984/9/1/004 ↗
50. 10.1016/j.ijhydene.2016.08.05810.1016/j.ijhydene.2016.08.058 ↗
51. 10.1021/nl901040v10.1021/nl901040v ↗
52. 10.1002/aenm.20150221710.1002/aenm.201502217 ↗
53. 10.1016/j.isci.2018.07.02010.1016/j.isci.2018.07.020 ↗
54. 10.1016/j.carbon.2019.08.00310.1016/j.carbon.2019.08.003 ↗
55. 10.1002/cssc.20180187910.1002/cssc.201801879 ↗
56. 10.1016/j.ensm.2015.12.00410.1016/j.ensm.2015.12.004 ↗
57. 10.1016/j.jpowsour.2015.05.11610.1016/j.jpowsour.2015.05.116 ↗
58. 10.1021/acs.nanolett.5b0418710.1021/acs.nanolett.5b04187 ↗
59. 10.1016/j.ensm.2018.02.01210.1016/j.ensm.2018.02.012 ↗
60. 10.1016/j.electacta.2010.12.10810.1016/j.electacta.2010.12.108 ↗
61. 10.1039/C7TA05621D10.1039/C7TA05621D ↗