journal article·2021-09

Expanded Graphite Inserted by Few Red Phosphorus for Improved Sodium Storage at Room Temperature and Low Temperatures

Li‐Feng Zhou, He Gong, Li‐Ying Liu, Yi‐Song Wang, Tao Du

ChemNanoMat· Volume 7· Issue 9
Publisher page

Abstract

Abstract Sodium‐ion batteries are experiencing a rapid development as one of the most promising candidates to replace lithium‐ion batteries. Carbonaceous materials attract widespread attention because of the successful commercialization. Among them, expanded graphite with a long‐range‐ordered layered structure and a high specific surface area gain further exploration and modification as potential materials. Expanded graphite inserted by few red phosphorus was prepared by oxidation/reduction process and vapor deposition process and exhibited a high reversible specific capacity of 418 mAh g−1 at a current density of 100 mA g−1 and 296 mAh g−1 with the retention of 83.3% after 1000 cycles at the current density of 500 mA g−1 at room temperature. At −10 °C, a reversible capacity of 228 mAh g−1 with a retention of nearly 100% after 100 cycles was obtained. At a low temperature of −50 °C, a specific capacity of more than 50 mAh g−1 remains, indicating actual availability under extreme cold conditions.
Source: crossref · Quality: baseline

Research context

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

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

Affiliations

School of Metallurgy Northeastern University Shenyang 110004 P. R. China

Funding

National Natural Science Foundation of China · Fundamental Research Funds for the Central Universities

References (53)

Show source-provided references
1.
2. 10.1002/adma.20090332810.1002/adma.200903328 ↗
3. 10.1038/3510464410.1038/35104644 ↗
4. 10.1021/cr500192f10.1021/cr500192f ↗
5. Cao Z. · Adv. Energy Mater. · 2020 · 10
6. 10.1007/s12598-020-01492-410.1007/s12598-020-01492-4 ↗
7. Ma J. · J. Phys. D · 2021 · 54
8. 10.1002/asia.20200141410.1002/asia.202001414 ↗
9.
10. 10.1002/aenm.20110069110.1002/aenm.201100691 ↗
11. 10.1021/acsami.9b2273610.1021/acsami.9b22736 ↗
12. 10.1039/C8TA09751H10.1039/C8TA09751H ↗
13.
14. 10.1039/c3ta12389h10.1039/c3ta12389h ↗
15. 10.1038/s41467-018-04190-z10.1038/s41467-018-04190-z ↗
16.
17. 10.1149/2.0091514jes10.1149/2.0091514jes ↗
18. 10.1039/C4TA05451B10.1039/C4TA05451B ↗
19. 10.1021/nl301695710.1021/nl3016957 ↗
20.
21. 10.1149/1.137956510.1149/1.1379565 ↗
22. 10.1016/j.jallcom.2018.10.18010.1016/j.jallcom.2018.10.180 ↗
23.
24. 10.1002/aenm.20180334210.1002/aenm.201803342 ↗
25. 10.1021/acsami.1c0592810.1021/acsami.1c05928 ↗
26. 10.1039/C9TA02244A10.1039/C9TA02244A ↗
27. 10.1016/j.carbon.2021.02.06710.1016/j.carbon.2021.02.067 ↗
28. 10.1002/aenm.20180321510.1002/aenm.201803215 ↗
29. 10.1038/ncomms503310.1038/ncomms5033 ↗
30. 10.1002/adfm.20120069110.1002/adfm.201200691 ↗
31. Wang F. · Adv. Energy Mater. · 2014 · 4 · 6
32.
33. 10.1016/j.carbpol.2014.01.07010.1016/j.carbpol.2014.01.070 ↗
34. 10.1002/chem.20140477910.1002/chem.201404779 ↗
35. 10.1016/j.carbon.2005.06.01410.1016/j.carbon.2005.06.014 ↗
36.
37. 10.1016/j.carbon.2017.01.10110.1016/j.carbon.2017.01.101 ↗
38. 10.1021/acs.nanolett.5b0418710.1021/acs.nanolett.5b04187 ↗
39. 10.1002/smll.20150227810.1002/smll.201502278 ↗
40. 10.1016/j.carbon.2018.06.03510.1016/j.carbon.2018.06.035 ↗
41. 10.1039/C5TA00727E10.1039/C5TA00727E ↗
42. 10.1002/advs.20170088010.1002/advs.201700880 ↗
43. 10.1002/adma.20140590410.1002/adma.201405904 ↗
44. 10.1016/j.nanoen.2017.12.01210.1016/j.nanoen.2017.12.012 ↗
45. 10.1002/aenm.20180035310.1002/aenm.201800353 ↗
46.
47. 10.1016/j.jpowsour.2016.06.05510.1016/j.jpowsour.2016.06.055 ↗
48. Q. Ni H. Jiang S. Sandstrom Y. Bai X. J. A. F. M. Ji 2020 30 202003511
49.
50. 10.1039/c3nr04406h10.1039/c3nr04406h ↗
51. 10.1002/adfm.20150469510.1002/adfm.201504695 ↗
52. 10.1016/j.electacta.2019.06.02710.1016/j.electacta.2019.06.027 ↗
53. 10.1016/j.carbon.2013.07.05510.1016/j.carbon.2013.07.055 ↗