High Volumetric Capacity FeS2/SPAN Composite with Promoted Kinetics for Li–S Battery
Source abstract
Abstract
Sulfurized polyacrylonitrile (SPAN) exhibits a unique solid-phase conversion mechanism in carbonate electrolytes during electrochemical reactions, which avoids the dissolution of polysulfides and self-discharge. However, the limited sulfur content, unsatisfactory redox kinetics, and low volumetric energy density restrict the development of SPAN. Herein, FeS 2 nanodots and carbon nanotubes are proposed to composite with SPAN to achieve better dynamic performance and higher volumetric capacity at higher sulfur content. The as-prepared FeS 2 /SPAN composite is designed using spray granulation to obtain interspersed and interlaced secondary particles with abundant ion/electron transport channels, which ensures a more stable cathode interface and exhibits excellent rate performance. As a result, the FeS 2 /SPAN composite cathode presents a high specific capacity of 683.56 mAh g –1 after 140 cycles at 0.5 C, corresponding to a 91.90% retention, and achieves a volumetric capacity of 716.19 Ah L –1 at 0.2 C with a high areal mass loading of 6.1 mg cm –2 . The outstanding electrochemical performance exhibited at both high sulfur content and mass loading provides a new approach for designing higher energy density sulfur-based cathode materials in the future.
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: Advanced Battery Materials and Technologies · Advancements in Battery Materials · Supercapacitor Materials and Fabrication
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
Department of Chemical Engineering
Shanghai Jiao Tong University
State Key Laboratory of Chemistry and Utilization of Carbon-Based Energy Resources; College of Chemistry
Xinjiang University
Shanghai Jiao Tong University Sichuan Research Institute
Funding
National Key Research and Development Program of China · Natural Science Foundation of Xinjiang Uygur Autonomous Region · National Natural Science Foundation of China
References (49)
Show source-provided references
1. 10.1002/aenm.20150011810.1002/aenm.201500118 ↗
2. 10.1002/adma.20160682310.1002/adma.201606823 ↗
3. 10.1002/eem2.1225710.1002/eem2.12257 ↗
4. 10.1002/adma.20210516310.1002/adma.202105163 ↗
5. 10.1149/2.0041701jes10.1149/2.0041701jes ↗
6. 10.1039/C9NR05670J10.1039/C9NR05670J ↗
7. 10.1039/C4TA00742E10.1039/C4TA00742E ↗
8. 10.1021/acsami.5b0888710.1021/acsami.5b08887 ↗
9. 10.1007/s11664-022-09699-010.1007/s11664-022-09699-0 ↗
10. 10.1016/j.matt.2021.01.01210.1016/j.matt.2021.01.012 ↗
11. 10.1002/adma.20230352010.1002/adma.202303520 ↗
12. 10.1002/1521-4095(20020705)14:13/14<963::AID-ADMA963>3.0.CO;2-P10.1002/1521-4095(20020705)14:13/14<963::AID-ADMA963>3.0.CO;2-P ↗
13. 10.1002/adma.20140256910.1002/adma.201402569 ↗
14. 10.1016/j.electacta.2012.04.00510.1016/j.electacta.2012.04.005 ↗
15. 10.1166/jnn.2018.1569210.1166/jnn.2018.15692 ↗
16. 10.1039/c1jm00047k10.1039/c1jm00047k ↗
17. 10.1016/j.cej.2024.15685710.1016/j.cej.2024.156857 ↗
18. 10.1016/j.energy.2021.12116010.1016/j.energy.2021.121160 ↗
19. 10.1002/adfm.20190292910.1002/adfm.201902929 ↗
20. 10.1016/j.jpowsour.2014.02.07810.1016/j.jpowsour.2014.02.078 ↗
21. 10.1016/j.jpowsour.2018.11.09410.1016/j.jpowsour.2018.11.094 ↗
22. 10.1007/s12274-022-5327-x10.1007/s12274-022-5327-x ↗
23. 10.1021/acsami.0c0765810.1021/acsami.0c07658 ↗
24. 10.1021/acsmaterialslett.3c0045010.1021/acsmaterialslett.3c00450 ↗
25. 10.1021/acsami.1c0600410.1021/acsami.1c06004 ↗
26. 10.1016/j.jelechem.2023.11746510.1016/j.jelechem.2023.117465 ↗
27. 10.1016/j.ensm.2018.11.00110.1016/j.ensm.2018.11.001 ↗
28. 10.1021/acsenergylett.2c0231310.1021/acsenergylett.2c02313 ↗
29. 10.1016/j.ensm.2017.06.01210.1016/j.ensm.2017.06.012 ↗
30. 10.1002/chem.20230345110.1002/chem.202303451 ↗
31. 10.1002/ente.20240042110.1002/ente.202400421 ↗
32. 10.1016/j.jpowsour.2018.01.05710.1016/j.jpowsour.2018.01.057 ↗
33. 10.1016/j.jpowsour.2024.23524010.1016/j.jpowsour.2024.235240 ↗
34. 10.1021/acs.inorgchem.9b0101710.1021/acs.inorgchem.9b01017 ↗
35. 10.1002/aenm.20180182310.1002/aenm.201801823 ↗
36. 10.1016/j.actamat.2022.11763210.1016/j.actamat.2022.117632 ↗
37. 10.1149/1.209642610.1149/1.2096426 ↗
38. 10.1021/acsanm.2c0088110.1021/acsanm.2c00881 ↗
39. 10.1002/aenm.20160049510.1002/aenm.201600495 ↗
40. 10.1016/j.jallcom.2022.16708810.1016/j.jallcom.2022.167088 ↗
41. 10.1016/j.cej.2022.13743310.1016/j.cej.2022.137433 ↗
42. 10.1149/2.0041606jes10.1149/2.0041606jes ↗
43. 10.1016/j.jpowsour.2014.03.01110.1016/j.jpowsour.2014.03.011 ↗
44. 10.1002/adfm.20220547110.1002/adfm.202205471 ↗
45. 10.1016/j.joule.2023.10.00310.1016/j.joule.2023.10.003 ↗
46. 10.1016/0927-0256(96)00008-010.1016/0927-0256(96)00008-0 ↗
47. 10.1103/PhysRevB.54.1116910.1103/PhysRevB.54.11169 ↗
48. 10.1103/PhysRevB.59.175810.1103/PhysRevB.59.1758 ↗
49. 10.1103/PhysRevLett.78.139610.1103/PhysRevLett.78.1396 ↗