Synergistic Adsorption‐Diffusion‐Catalytic Effect Boosting Polysulfides Conversion by Rational Isotype Heterojunction Design for Highly Reversible Lithium–Sulfur Batteries
Source abstract
Abstract
Abstract Sluggish reaction kinetics and ceaseless shuttle effect greatly restrict the actual performance of lithium–sulfur (Li–S) batteries. Herein, a rationally designed WO 3 /SnO 2 isotype heterojunction is proposed as the surface modification on commercial separator to catalyze the redox conversion of the polysulfides. Experimental investigation, theoretical calculation, and in situ analysis cooperatively reveal that the “sesame ball”‐like WO 3 /SnO 2 spontaneously generates an internal electric field across the heterointerface, which offers moderate adsorption but rapid diffusion and accelerated conversion towards polysulfides. Meanwhile, the rich heterointerface acting as profitable nucleation sites guides the 3D growth of sulfide and thus impedes the inactivation of catalytic surface. As a consequence, the polysulfides shuttling is greatly restrained and highly reversible Li–S chemistry is constructed. Impressively, the unique heterojunction design endows a long‐term cycling capability up to 1000 cycles at 2C, illustrating its highly efficient and long‐lived catalysis capability.
Source: crossref · Quality: baseline
Research context
OpenAlex topics: Advanced Battery Materials and Technologies · Advancements in Battery Materials · Conducting polymers and applications
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
School of Materials Science and Engineering Xi'an University of Science and Technology Xi'an 710054 China
School of Metallurgical Engineering Xi'an University of Architecture and Technology Xi'an 710055 China
Institute of Flexible Electronics (IFE) Northwestern Polytechnical University Xi'an 710129 China
Funding
National Natural Science Foundation of China
References (48)
Show source-provided references
1. 10.1021/acsenergylett.5c0033110.1021/acsenergylett.5c00331 ↗
2. 10.1038/s41467-024-46418-110.1038/s41467-024-46418-1 ↗
3. 10.1002/advs.20210387910.1002/advs.202103879 ↗
4. 10.1039/D2TA09266B10.1039/D2TA09266B ↗
5. 10.1002/eem2.1242010.1002/eem2.12420 ↗
6. 10.20517/energymater.2023.10910.20517/energymater.2023.109 ↗
7. 10.1002/advs.20170027010.1002/advs.201700270 ↗
8. 10.1002/adma.20210100610.1002/adma.202101006 ↗
9. 10.1038/s41467-021-24976-y10.1038/s41467-021-24976-y ↗
10. 10.1038/s41929-022-00804-410.1038/s41929-022-00804-4 ↗
11. 10.1016/j.ensm.2022.11.03710.1016/j.ensm.2022.11.037 ↗
12. 10.1021/acsnano.3c0526910.1021/acsnano.3c05269 ↗
13. 10.1016/j.jechem.2020.06.00910.1016/j.jechem.2020.06.009 ↗
14. 10.1002/smll.20220265410.1002/smll.202202654 ↗
15. 10.4028/www.scientific.net/AMR.1070-1072.47110.4028/www.scientific.net/AMR.1070-1072.471 ↗
16. 10.1039/C8TA11646F10.1039/C8TA11646F ↗
17. 10.1016/j.jcis.2022.10.00610.1016/j.jcis.2022.10.006 ↗
18. 10.1039/C5CS00064E10.1039/C5CS00064E ↗
19. 10.1002/adfm.20230657810.1002/adfm.202306578 ↗
20. 10.1016/j.ensm.2023.03.00410.1016/j.ensm.2023.03.004 ↗
21. 10.1016/j.cej.2022.13729410.1016/j.cej.2022.137294 ↗
22. 10.1016/j.carbon.2024.11979010.1016/j.carbon.2024.119790 ↗
23. 10.1002/aenm.20200009110.1002/aenm.202000091 ↗
24. 10.1021/acsnano.2c0281010.1021/acsnano.2c02810 ↗
25. 10.1002/aenm.20180220710.1002/aenm.201802207 ↗
26. 10.1016/S2095-4956(15)60297-210.1016/S2095-4956(15)60297-2 ↗
27. 10.1002/adma.20170013610.1002/adma.201700136 ↗
28. 10.1002/adfm.20240026210.1002/adfm.202400262 ↗
29. 10.1002/smll.20231228810.1002/smll.202312288 ↗
30. 10.1039/D4SC02420F10.1039/D4SC02420F ↗
31. 10.1002/anie.20241762410.1002/anie.202417624 ↗
32. 10.1016/j.ensm.2025.10400910.1016/j.ensm.2025.104009 ↗
33. 10.1021/acscatal.9b0073210.1021/acscatal.9b00732 ↗
34. 10.1021/acsami.3c1530010.1021/acsami.3c15300 ↗
35. 10.1038/ncomms1120310.1038/ncomms11203 ↗
36. 10.1038/s41565-020-00797-w10.1038/s41565-020-00797-w ↗
37. 10.1021/acsnano.1c0125010.1021/acsnano.1c01250 ↗
38. 10.1002/smll.20230154510.1002/smll.202301545 ↗
39. 10.1002/adfm.20230943710.1002/adfm.202309437 ↗
40. 10.1016/j.nanoen.2024.10985910.1016/j.nanoen.2024.109859 ↗
41. 10.1002/adfm.20240930310.1002/adfm.202409303 ↗
42. 10.1016/j.ensm.2023.10292510.1016/j.ensm.2023.102925 ↗
43. 10.1002/aenm.20200123510.1002/aenm.202001235 ↗
44. 10.1002/anie.20190933910.1002/anie.201909339 ↗
45. 10.1002/anie.20241505310.1002/anie.202415053 ↗
46. 10.1002/sstr.20210017010.1002/sstr.202100170 ↗
47. 10.1021/acsnano.4c1170110.1021/acsnano.4c11701 ↗
48. 10.1016/j.cej.2022.14097210.1016/j.cej.2022.140972 ↗