Electrochemically Induced Metallization of NaCl: Use of the Main Component of Salt as a Cost-Effective Electrode Material for Sodium-Ion Batteries
Source abstract
Abstract
Sodium chloride (NaCl), a typical stoichiometric ionic compound, breaks all of the basic rules of chemistry at high pressures and can form new metallic compounds with different stoichiometries of NaxCl at x > 1. However, the electrochemical phase transition of NaCl from an insulating state to a metallic state without pressurization has not been achieved to date. In this study, we first demonstrate that nonmetallic NaCl can be transformed to a metallic compound through an electrochemical activation process. Subsequently, the activated NaCl electrode was shown to intercalate/deintercalate sodium ions into the structure, with a discharge capacity of 267 mAh/g by reversibly accommodating 0.6 Na ions. We believe that this method may represent a new approach for designing inexpensive electrode materials using the main component of table and sea salt for sodium-ion batteries. In addition, these results will contribute to the development of low-cost and sustainable rechargeable batteries that can be operated at a room temperature.
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: Advancements in Battery Materials · Advanced Battery Materials and Technologies · Advanced Battery Technologies Research
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
Center for Energy Storage Research, Korea Institute of Science and technology, Hwarang-ro 14-gil 5, Seongbuk-gu, Seoul 02792, Republic of Korea
Division of Energy and Environment Technology, KIST School, Korea University of Science and Technology, Seoul 02792, Republic of Korea
Department of Materials Science and Engineering, Korea University, Seoul 02841, Republic of Korea
Funding
National Research Foundation of Korea · Korea Institute of Science and Technology
References (29)
Show source-provided references
1. 10.1063/1.37159610.1063/1.371596 ↗
2. 10.1126/science.124498910.1126/science.1244989 ↗
3. 10.1039/C5CP06026E10.1039/C5CP06026E ↗
4. 10.1021/j100019a06210.1021/j100019a062 ↗
5. 10.1016/j.physleta.2016.02.03610.1016/j.physleta.2016.02.036 ↗
6. 10.1103/PhysRevB.42.275210.1103/PhysRevB.42.2752 ↗
7. 10.1063/1.165575210.1063/1.1655752 ↗
8. 10.1103/PhysRevB.46.1054710.1103/PhysRevB.46.10547 ↗
9. 10.1103/PhysRevLett.67.72710.1103/PhysRevLett.67.727 ↗
10. 10.1088/0953-8984/17/6/02110.1088/0953-8984/17/6/021 ↗
11. 10.1063/1.47183710.1063/1.471837 ↗
12. 10.1149/2.0151514jes10.1149/2.0151514jes ↗
13. 10.1038/nmat292010.1038/nmat2920 ↗
14. 10.1149/2.023302jes10.1149/2.023302jes ↗
15. 10.1016/j.cossms.2012.04.00210.1016/j.cossms.2012.04.002 ↗
16. 10.1016/j.elecom.2012.08.02810.1016/j.elecom.2012.08.028 ↗
17. 10.1038/nmat330910.1038/nmat3309 ↗
18. 10.1038/s41467-017-00157-810.1038/s41467-017-00157-8 ↗
19. 10.1002/adfm.20110085410.1002/adfm.201100854 ↗
20. 10.1002/cssc.20150128210.1002/cssc.201501282 ↗
21. 10.1021/am200973k10.1021/am200973k ↗
22. 10.1039/c3ee41379a10.1039/c3ee41379a ↗
23. 10.1149/2.0071509jes10.1149/2.0071509jes ↗
24. 10.1142/S021798491450062610.1142/S0217984914500626 ↗
25. 10.1016/j.physleta.2016.02.03610.1016/j.physleta.2016.02.036 ↗
26. 10.1017/S143192769898002310.1017/S1431927698980023 ↗
27. 10.1016/j.jpowsour.2014.09.03710.1016/j.jpowsour.2014.09.037 ↗
28. 10.5194/acp-15-3379-201510.5194/acp-15-3379-2015 ↗
29. 10.1016/0039-6028(87)90207-X10.1016/0039-6028(87)90207-X ↗