In Situ Construction of CeO2-Incorporated Hybrid Covalent Organic Frameworks for Highly Efficient Lithium–Sulfur Batteries
Source abstract
Abstract
Lithium–sulfur (Li-S) batteries with high energy density, environmental friendliness, and low cost have still suffered from the short cycle life due to the shuttle effect of the dissoluble polysulfide intermediates. In this work, a hybrid host comprising ceric dioxide (CeO2) and covalent organic frameworks (COFs) was developed for the sulfur cathode. The hybrid host of CeO2/COFs manifests strong interaction with the polysulfide. Moreover, the polar interface of CeO2 and the highly 2D ordered structure of COFs endow good electrochemically catalytic activity, which accelerates the redox reaction and restrains the shuttle effect. Owing to the chemical and physical adsorption surface, the hybrid host of CeO2/COFs demonstrates a high initial capacity (1384 mAh g–1) and low decay rate (0.1%) at 0.5C. Collectively, the in situ hybrid strategy has high potential in elevating the performance of Li-S batteries.
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: Advanced Battery Materials and Technologies · Advancements in Battery Materials · Advanced battery technologies research
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
School of Materials Science and Hydrogen Energy, Foshan University, Foshan 528000, P. R. China
Institute of Polymer Optoelectronic Materials & Devices, State Key Laboratory of Luminescent Materials & Devices, South China University of Technology, Guangzhou 510640, PR China
School of Chemistry and Chemical Engineering, South China University of Technology, Guangzhou 510640, PR China
Funding
National Natural Science Foundation of China · Natural Science Foundation of Guangdong Province · Foshan Fourth People's Hospital
References (62)
Show source-provided references
1. 10.1016/j.jpowsour.2009.11.04810.1016/j.jpowsour.2009.11.048 ↗
2. 10.1126/science.121274110.1126/science.1212741 ↗
3. 10.1039/c1ee01388b10.1039/c1ee01388b ↗
4. 10.1038/nature1147510.1038/nature11475 ↗
5. 10.1021/ja309143810.1021/ja3091438 ↗
6. 10.1149/1.150307610.1149/1.1503076 ↗
7. 10.1039/b925751a10.1039/b925751a ↗
8. 10.1038/nmat319110.1038/nmat3191 ↗
9. 10.1039/c2cs35256g10.1039/c2cs35256g ↗
10. 10.1021/cr500062v10.1021/cr500062v ↗
11. 10.1002/adma.20140511510.1002/adma.201405115 ↗
12. 10.1039/C5CS00410A10.1039/C5CS00410A ↗
13. 10.1038/nmat246010.1038/nmat2460 ↗
14. 10.1016/j.electacta.2011.03.00510.1016/j.electacta.2011.03.005 ↗
15. 10.1002/anie.20110063710.1002/anie.201100637 ↗
16. 10.1039/C2CC16726C10.1039/C2CC16726C ↗
17. 10.1016/j.nanoen.2012.10.00310.1016/j.nanoen.2012.10.003 ↗
18. 10.1039/c3ta13541a10.1039/c3ta13541a ↗
19. 10.1016/j.carbon.2013.12.06510.1016/j.carbon.2013.12.065 ↗
20. 10.1021/nl202297p10.1021/nl202297p ↗
21. 10.1039/c2cc17925c10.1039/c2cc17925c ↗
22. 10.1021/ja308170k10.1021/ja308170k ↗
23. 10.1002/adfm.20120068910.1002/adfm.201200689 ↗
24. 10.1016/j.nanoen.2013.12.01310.1016/j.nanoen.2013.12.013 ↗
25. 10.1002/aenm.20120001710.1002/aenm.201200017 ↗
26. 10.1002/adma.20110339210.1002/adma.201103392 ↗
27. 10.1039/c2ee03495f10.1039/c2ee03495f ↗
28. 10.1039/c3cc41518j10.1039/c3cc41518j ↗
29. 10.1039/C4TA00523F10.1039/C4TA00523F ↗
30. 10.1002/aenm.20160125010.1002/aenm.201601250 ↗
31. 10.1039/C6TA00483K10.1039/C6TA00483K ↗
32. 10.1002/chem.20130168910.1002/chem.201301689 ↗
33. 10.1039/c3cc38009b10.1039/c3cc38009b ↗
34. 10.1002/sus2.410.1002/sus2.4 ↗
35. Jiang Y. · Energy Environ. Mater. · 2022 · 0 · 1
36. 10.1007/s42765-021-00088-610.1007/s42765-021-00088-6 ↗
37. 10.1038/ncomms232710.1038/ncomms2327 ↗
38. 10.1016/j.joule.2017.06.00310.1016/j.joule.2017.06.003 ↗
39. 10.1038/ncomms575910.1038/ncomms5759 ↗
40. 10.1016/j.jallcom.2017.09.25210.1016/j.jallcom.2017.09.252 ↗
41. 10.1016/j.electacta.2018.01.06610.1016/j.electacta.2018.01.066 ↗
42. 10.1039/c1ee01399h10.1039/c1ee01399h ↗
43. 10.1021/acsnano.8b0546610.1021/acsnano.8b05466 ↗
44. 10.1021/acsami.8b0292010.1021/acsami.8b02920 ↗
45. 10.1002/aenm.20170233710.1002/aenm.201702337 ↗
46. 10.1039/C6EE01662F10.1039/C6EE01662F ↗
47. 10.1021/acs.nanolett.5b0416610.1021/acs.nanolett.5b04166 ↗
48. 10.1002/adma.20160340110.1002/adma.201603401 ↗
49. 10.1016/j.joule.2018.12.01810.1016/j.joule.2018.12.018 ↗
50. 10.1002/adma.20160681710.1002/adma.201606817 ↗
51. 10.1016/j.joule.2017.12.00310.1016/j.joule.2017.12.003 ↗
52. 10.1002/adma.20160175910.1002/adma.201601759 ↗
53. 10.1039/C5CC03413B10.1039/C5CC03413B ↗
54. 10.1021/acsnano.1c0558510.1021/acsnano.1c05585 ↗
55. 10.1016/j.energy.2020.11737210.1016/j.energy.2020.117372 ↗
56. 10.1016/j.jpowsour.2012.04.08010.1016/j.jpowsour.2012.04.080 ↗
57. 10.1002/adma.20170058710.1002/adma.201700587 ↗
58. 10.1021/ja305220610.1021/ja3052206 ↗
59. 10.1039/c2cp40727b10.1039/c2cp40727b ↗
60. 10.1002/aenm.20200084510.1002/aenm.202000845 ↗
61. 10.1016/j.chempr.2022.01.01110.1016/j.chempr.2022.01.011 ↗
62. 10.1016/j.ensm.2022.03.01810.1016/j.ensm.2022.03.018 ↗