journal article·2026-06-29

Dual‐Metal MOF‐Derived Carbon Fibers Achieve Efficient Polysulfide Anchoring and Conversion Simultaneously in Li‐S Batteries

Si‐Qi Wang, Yu‐Xuan Li, Ben Li, Xin Li, Ye Zhang, Han Zhao, Ge‐Xi Guo, Rui Zhang, De‐Quan Liu, Xi‐Wen Du

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Abstract

ABSTRACT Lithium‐sulfur (Li‐S) batteries are regarded as strong contenders for next‐generation high‐energy‐density energy storage systems. However, the practical application of Li‐S batteries is severely hampered by the notorious polysulfide shuttle effect and sluggish redox kinetics. Herein, we designed and synthesized CoS 2 ‐ZnS‐modified carbon nanofiber networks (CoS 2 ‐ZnS@CNF) using bimetallic metal–organic frameworks (MOFs) as precursors for Li‐S batteries. This integrates the synergistic catalytic activity of bimetallic sulfides with the structural benefits of a conductive carbon nanofiber network to improve the electrochemical performance of the battery. Experimental results demonstrate that the CoS 2 ‐ZnS nanoparticles are uniformly anchored on the carbon nanofibers. These strong chemisorptions of polysulfides and accelerated conversion kinetics through synergistic bimetallic catalysis. This inhibits polysulfide dissolution and diffusion in the electrolyte, alleviating the shuttle effect. Furthermore, the three‐dimensional porous CNF framework provides sufficient space for the physical adsorption of polysulfides. Simultaneously, its continuous conductive framework constructs efficient electron transport pathways, significantly enhancing the conductivity of the electrode material. Electrochemical tests show that the battery with the CoS 2 ‐ZnS@CNF maintains a high discharge specific capacity of 788.5 mAh g −1 after 500 cycles at 0.5 A g −1 . Even under a high sulfur loading of 5.8 mg cm −2 , the battery exhibits an initial discharge capacity of 1042.6 mAh g −1 .
Source: crossref · Quality: baseline

Research context

OpenAlex topics: Advanced Battery Materials and Technologies · Advancements in Battery Materials · Advanced battery technologies research

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Affiliations

School of Materials Science and Engineering Tianjin University Tianjin China

School of Materials and Energy Lanzhou University Lanzhou China

Funding

National Natural Science Foundation of China

References (62)

Show source-provided references
1. 10.1002/adfm.20180118810.1002/adfm.201801188 ↗
2. 10.1007/s12598‐024‐02708‐710.1007/s12598‐024‐02708‐7 ↗
3. 10.1016/j.ensm.2020.01.00210.1016/j.ensm.2020.01.002 ↗
4. 10.1021/jacs.3c0110210.1021/jacs.3c01102 ↗
5. 10.1002/aenm.200289310.1002/aenm.2002893 ↗
6. 10.1021/acsnano.3c0839510.1021/acsnano.3c08395 ↗
7. 10.1002/adfm.20242201310.1002/adfm.202422013 ↗
8. 10.1002/aenm.20190107510.1002/aenm.201901075 ↗
9. 10.1016/j.mattod.2019.09.01810.1016/j.mattod.2019.09.018 ↗
10. 10.1002/adma.20140511510.1002/adma.201405115 ↗
11. 10.1016/j.joule.2019.01.00310.1016/j.joule.2019.01.003 ↗
12. Strongly Anchoring Polysulfides by Hierarchical Fe3O4/C3N4 Nanostructures for Advanced Lithium–Sulfur Batteries10.1007/s40820-020-00475-5 ↗
13. 10.1016/j.jechem.2020.08.03910.1016/j.jechem.2020.08.039 ↗
14. 10.1016/j.cej.2025.16909610.1016/j.cej.2025.169096 ↗
15. 10.1016/j.ccr.2024.21587710.1016/j.ccr.2024.215877 ↗
16. 10.1016/j.esci.2022.10008810.1016/j.esci.2022.100088 ↗
17. 10.1021/acs.nanolett.7b0442510.1021/acs.nanolett.7b04425 ↗
18. 10.1016/j.ces.2023.11923610.1016/j.ces.2023.119236 ↗
19. 10.1016/j.carbon.2017.08.06210.1016/j.carbon.2017.08.062 ↗
20. 10.1007/s12274‐023‐5512‐610.1007/s12274‐023‐5512‐6 ↗
21. 10.1126/science.119216010.1126/science.1192160 ↗
22. 10.1021/acsaem.2c0058510.1021/acsaem.2c00585 ↗
23. 10.1016/j.jechem.2024.03.05210.1016/j.jechem.2024.03.052 ↗
24. 10.1021/acs.jpcc.3c0731310.1021/acs.jpcc.3c07313 ↗
25. 10.1021/acsmaterialslett.2c0026610.1021/acsmaterialslett.2c00266 ↗
26. 10.1002/advs.20210345610.1002/advs.202103456 ↗
27. 10.1016/j.ensm.2022.02.01010.1016/j.ensm.2022.02.010 ↗
28. 10.1016/j.cej.2022.13729410.1016/j.cej.2022.137294 ↗
29. 10.1016/j.ensm.2022.11.03710.1016/j.ensm.2022.11.037 ↗
30. 10.1021/acsnano.9b0923110.1021/acsnano.9b09231 ↗
31. 10.1002/advs.20210345610.1002/advs.202103456 ↗
32. 10.1021/acsnano.7b0194510.1021/acsnano.7b01945 ↗
33. 10.1016/j.ensm.2022.12.01410.1016/j.ensm.2022.12.014 ↗
34. 10.1016/j.matt.2020.01.00110.1016/j.matt.2020.01.001 ↗
35. 10.1016/j.apsusc.2022.15262010.1016/j.apsusc.2022.152620 ↗
36. 10.1002/smll.20230006510.1002/smll.202300065 ↗
37. 10.1021/acs.nanolett.5c0105210.1021/acs.nanolett.5c01052 ↗
38. 10.1002/aenm.20240064810.1002/aenm.202400648 ↗
39. 10.1016/j.cej.2025.16214710.1016/j.cej.2025.162147 ↗
40. 10.1039/C7EE01047H10.1039/C7EE01047H ↗
41. 10.1016/j.cej.2024.15152610.1016/j.cej.2024.151526 ↗
42. 10.1016/j.cej.2024.15554110.1016/j.cej.2024.155541 ↗
43. 10.1021/acsnano.5c1168810.1021/acsnano.5c11688 ↗
44. 10.1021/acsnano.5c1091310.1021/acsnano.5c10913 ↗
45. 10.1021/acsnano.2c0281010.1021/acsnano.2c02810 ↗
46. 10.1002/anie.20251714510.1002/anie.202517145 ↗
47. 10.1002/adfm.20242178010.1002/adfm.202421780 ↗
48. 10.1002/adfm.20221420610.1002/adfm.202214206 ↗
49. 10.1021/acsnano.3c0526910.1021/acsnano.3c05269 ↗
50. 10.1016/j.jmst.2024.02.01410.1016/j.jmst.2024.02.014 ↗
51. 10.1002/smll.20230319210.1002/smll.202303192 ↗
52. 10.1002/smll.20240641510.1002/smll.202406415 ↗
53. 10.1021/acssuschemeng.5c0737010.1021/acssuschemeng.5c07370 ↗
54. 10.1002/aenm.20230045210.1002/aenm.202300452 ↗
55. 10.1002/anie.20181279710.1002/anie.201812797 ↗
56. 10.1103/PhysRevB.54.1116910.1103/PhysRevB.54.11169 ↗
57. 10.1016/0927‐0256(96)00008‐010.1016/0927‐0256(96)00008‐0 ↗
58. 10.1103/PhysRevLett.77.386510.1103/PhysRevLett.77.3865 ↗
59. 10.1063/1.47293310.1063/1.472933 ↗
60. 10.1103/PhysRevB.50.1795310.1103/PhysRevB.50.17953 ↗
61. 10.1063/1.338234410.1063/1.3382344 ↗
62. 10.1103/PhysRevB.13.518810.1103/PhysRevB.13.5188 ↗