An All-Solid-State Sodium–Sulfur Battery Using a Sulfur/Carbonized Polyacrylonitrile Composite Cathode
Source abstract
Abstract
An all-solid-state sodium–sulfur (Na–S) battery using a S/CPAN (carbonized polyacrylonitrile) composite cathode and poly(ethylene oxide) (PEO) electrolyte was prepared and tested at 60 °C. The S/CPAN composites was synthesized by heating a mixture of S and PAN at 600 °C. The solid polymer electrolytes consisted of PEO, NaFSI, and different amounts nano-TiO2. Moreover, the PEO–NaFSI–1% TiO2 electrolyte was chosen to be the electrolyte in all-solid-state Na–S battery due to its high ionic conductivity (4.89 × 10–4 S cm–2 at 60 °C) as well as outstanding electrochemical and thermal stability. The specific capacity of the S/CPAN composite cathode material can be 252 mAh g–1 (713 mAh g–1sulfur) at the second cycle, and it still remains 251 mAh g–1 (710 mAh g–1sulfur) after 100 cycles with a Coulombic efficiency near 100%.
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: Advanced Battery Materials and Technologies · Thermal Expansion and Ionic Conductivity · Advanced battery technologies research
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
Department of Chemistry and Shanghai Key Laboratory of Molecular Catalysis and Innovative Materials, Institute of New Energy, Collaborative Innovation Center of Chemistry for Energy Materials Shanghai, Fudan University, Shanghai 200433, China
Funding
Ministry of Science and Technology of the People's Republic of China · National Natural Science Foundation of China
References (39)
Show source-provided references
1. 10.1038/s41467-017-01202-210.1038/s41467-017-01202-2 ↗
2. 10.1002/celc.20160022110.1002/celc.201600221 ↗
3. 10.1038/ncomms1172210.1038/ncomms11722 ↗
4. 10.1126/sciadv.150103810.1126/sciadv.1501038 ↗
5. 10.1002/anie.20180500810.1002/anie.201805008 ↗
6. 10.1002/smll.20140325710.1002/smll.201403257 ↗
7. 10.1002/anie.20171155210.1002/anie.201711552 ↗
8. 10.1016/j.electacta.2018.06.02610.1016/j.electacta.2018.06.026 ↗
9. 10.1016/j.elecom.2006.08.02910.1016/j.elecom.2006.08.029 ↗
10. 10.1002/adfm.20120047310.1002/adfm.201200473 ↗
11. 10.1002/aenm.20160282910.1002/aenm.201602829 ↗
12. 10.1016/j.ensm.2018.05.00810.1016/j.ensm.2018.05.008 ↗
13. 10.1021/acs.nanolett.6b0517210.1021/acs.nanolett.6b05172 ↗
14. 10.1021/acsami.8b0385010.1021/acsami.8b03850 ↗
15. 10.1021/jacs.6b0868510.1021/jacs.6b08685 ↗
16. 10.1002/aenm.20140022610.1002/aenm.201400226 ↗
17. 10.1038/s41467-018-06144-x10.1038/s41467-018-06144-x ↗
18. 10.1016/j.nanoen.2016.12.01810.1016/j.nanoen.2016.12.018 ↗
19. 10.1039/C6TA04529D10.1039/C6TA04529D ↗
20. 10.1039/c3ta10241f10.1039/c3ta10241f ↗
21. 10.1021/acscentsci.5b0032810.1021/acscentsci.5b00328 ↗
22. 10.1007/s10008-008-0505-710.1007/s10008-008-0505-7 ↗
23. 10.1016/j.ssi.2011.01.01010.1016/j.ssi.2011.01.010 ↗
24. 10.1016/j.jpowsour.2006.11.08310.1016/j.jpowsour.2006.11.083 ↗
25. 10.3389/fenrg.2013.0001010.3389/fenrg.2013.00010 ↗
26. 10.1021/nl402513x10.1021/nl402513x ↗
27. 10.1021/jacs.5b0811310.1021/jacs.5b08113 ↗
28. 10.1039/c2ee03495f10.1039/c2ee03495f ↗
29. 10.3390/en707458810.3390/en7074588 ↗
30. 10.1016/j.electacta.2018.10.00510.1016/j.electacta.2018.10.005 ↗
31. 10.1016/j.ssi.2018.02.03010.1016/j.ssi.2018.02.030 ↗
32. 10.1039/C7RA02603J10.1039/C7RA02603J ↗
33. 10.1007/s10008-018-3891-510.1007/s10008-018-3891-5 ↗
34. 10.1002/advs.20170099610.1002/advs.201700996 ↗
35. 10.1016/j.jpowsour.2015.09.12010.1016/j.jpowsour.2015.09.120 ↗
36. 10.1016/j.jpowsour.2018.06.05610.1016/j.jpowsour.2018.06.056 ↗
37. 10.1021/cm202467u10.1021/cm202467u ↗
38. 10.1021/acsnano.7b0885610.1021/acsnano.7b08856 ↗
39. 10.1149/1.216460710.1149/1.2164607 ↗