journal article·2025-10-15Open access

Ionic Liquid Electrolyte Suppresses Deep Sodiation in Nb4P2S21/Mo2CTx Enabling Transition from Mixed-Voltage to Pure High-Voltage Operation for Sodium-Ion Battery Cathodes

Heng Li, Lei Zheng, Zhongquan Liao, Vlastimil Mazánek, Qiliang Wei, Tomáš Hartman, Saeed Ashtiani, Bing Wu, Zdenek Sofer

ACS Applied Materials & Interfaces· Volume 17· Issue 41

Abstract

High Resolution Image Download MS PowerPoint Slide Elemental sulfur has garnered significant attention due to its low cost and high theoretical capacity; however, its reliance on ether electrolytes leads to the formation of soluble polysulfides, thereby limiting its application. Sulfur-rich transition metal polysulfides demonstrate potential as sulfur-equivalent cathodes to replace conventional sulfur in alkali metal–sulfur batteries; however, adequate research in this area remains unrevealed. In this study, we investigate the Nb 4 P 2 S 21 in carbonate, ether, and ionic liquid electrolytes for sodium-ion battery testing. The material exhibits a high discharge capacity exceeding 1000 mAh/g and a prolonged discharge plateau at low potentials in both ether and carbonate electrolytes, same with other high-capacity phosphorus sulfide anodes via conversion reactions. When switching to the NaTFSI/[Emim]TFSI ionic liquid electrolyte, 96.3% of the initial discharge capacity in the 0–3 V range is retained above 0.8 V, with the suppression of low-voltage redox activity. This shift is attributed to the cointercalation of Na + and Emim + ions, preventing the materials from deep sodiation at lower voltage range. The incorporation of Mo 2 CT x MXene into the material further reduces electrochemical polarization and enhances cycle stability. During 100 cycles, a self-activation phenomenon occurs, resulting in a maximum capacity of 384 mAh/g, while the median voltage remains above 1.5 V, predominantly governed by a pair of reversible redox peaks. X-ray photoelectron spectroscopy (XPS) and high-resolution transmission electron microscopy (HRTEM) analyses of postcycled material confirm the structural and compositional stability of the material during cycling. This study advances the understanding of sulfur-rich materials in sodium-ion batteries across various electrolytes, particularly ionic liquids.
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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

Department of Inorganic Chemistry, University of Chemistry and Technology Prague, Technická 5, 166 28 Prague, Czech Republic

Fraunhofer Institute for Ceramic Technologies and Systems (IKTS), Maria-Reiche-Strasse 2, 01109 Dresden, Germany

Institute of Micro/Nano Materials and Devices

Ningbo University of Technology

Funding

Ministerstvo ?kolstv?, Ml?de?e a Telov?chovy · Vysok? ?kola Chemicko-technologick? v Praze · HORIZON EUROPE Digital, Industry and Space

References (41)

Show source-provided references
1. 10.1016/j.cej.2017.11.03910.1016/j.cej.2017.11.039 ↗
2. 10.1002/anie.20240361810.1002/anie.202403618 ↗
3. 10.1038/ncomms1172210.1038/ncomms11722 ↗
4. 10.1002/anie.20110063710.1002/anie.201100637 ↗
5. 10.1016/j.ensm.2017.05.00110.1016/j.ensm.2017.05.001 ↗
6. 10.2109/jcersj2.2117710.2109/jcersj2.21177 ↗
7. 10.1002/aenm.20230096210.1002/aenm.202300962 ↗
8. 10.1073/pnas.171191711410.1073/pnas.1711917114 ↗
9. 10.1016/j.ica.2020.11987510.1016/j.ica.2020.119875 ↗
10. 10.1149/2.0091407eel10.1149/2.0091407eel ↗
11. 10.1021/jacs.7b0390910.1021/jacs.7b03909 ↗
12. 10.2109/jcersj2.1529910.2109/jcersj2.15299 ↗
13. 10.1149/1.213301210.1149/1.2133012 ↗
14. 10.1149/1.209555410.1149/1.2095554 ↗
15. 10.1021/acs.chemmater.8b0498710.1021/acs.chemmater.8b04987 ↗
16. 10.1016/j.materresbull.2009.05.01810.1016/j.materresbull.2009.05.018 ↗
17. 10.1002/cnma.20190052610.1002/cnma.201900526 ↗
18. 10.1021/jp400153m10.1021/jp400153m ↗
19. 10.1016/j.ensm.2023.10306210.1016/j.ensm.2023.103062 ↗
20. 10.1021/jp408037e10.1021/jp408037e ↗
21. 10.1002/jcc.2122410.1002/jcc.21224 ↗
22. 10.1016/0263-7855(96)00018-510.1016/0263-7855(96)00018-5 ↗
23. 10.1021/jp036213310.1021/jp0362133 ↗
24. 10.1007/s00214-012-1129-710.1007/s00214-012-1129-7 ↗
25. Hockney R. W. · 202110.1201/9780367806934 ↗
26. 10.1006/jcph.1995.103910.1006/jcph.1995.1039 ↗
27. 10.1016/j.flatc.2018.11.00310.1016/j.flatc.2018.11.003 ↗
28. 10.1021/acsaem.0c0216810.1021/acsaem.0c02168 ↗
29. 10.1039/D4NA01060D10.1039/D4NA01060D ↗
30. 10.1002/smll.20240833010.1002/smll.202408330 ↗
31. 10.1016/j.apsusc.2022.15309510.1016/j.apsusc.2022.153095 ↗
32. 10.1002/celc.20190117110.1002/celc.201901171 ↗
33. 10.1007/s11581-018-2644-x10.1007/s11581-018-2644-x ↗
34. 10.1002/celc.20180158310.1002/celc.201801583 ↗
35. 10.1039/D3TA06196E10.1039/D3TA06196E ↗
36. 10.1002/aenm.20150011710.1002/aenm.201500117 ↗
37. 10.1002/aenm.20180334610.1002/aenm.201803346 ↗
38. 10.1002/adfm.20200047310.1002/adfm.202000473 ↗
39. 10.1038/ncomms754410.1038/ncomms7544 ↗
40. 10.1021/ja068192710.1021/ja0681927 ↗
41. 10.1039/C9CC06083A10.1039/C9CC06083A ↗