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