Carbon-Coated Yttria Hollow Spheres as Both Sulfur Immobilizer and Catalyst of Polysulfides Conversion in Lithium–Sulfur Batteries
Source abstract
Abstract
Li–S battery has tremendous application prospect on account of the high theoretical specific capacity and large energy density, while its large-scale application is impeded by the severe shuttle effect and the slow electrochemical kinetics of polysulfides conversion. Herein, the Lewis acidic yttria hollow spheres (YHS) are rationally designed as both sulfur immobilizer and catalyst of polysulfides conversion for the advanced Li–S batteries. It can be known that the Lewis acidic yttria can effectively capture the Lewis basic polysulfides and thus mitigate the shuttle effect of Li–S battery; besides, yttria shows the enhanced catalytic effect for the kinetics of interconversion reaction from polysulfides to Li2S. As a result, either as a sulfur host or as the separator coating, yttria plays a vital part in realizing the high specific discharge capacity and good cycle stability for Li–S battery. In particular, Li–S battery with YHS@C/S cathode and YHS/CNT-0.6- modified separator (2.1 mg cm–2 active material loading) shows a good specific discharge capacity of 912.5 mAh g–1 at 0.5C. Even after 200 steady cycles, the discharge specific capacity can keep as 842.3 mAh g–1, and the capacity decay rate is only 0.038% per cycle. When active material areal loading is increased to 4.24 mg cm–2, it still maintains a considerable areal capacity of 3.79 mAh cm–2. In consequence, the synergy of polysulfides confinement and catalytic conversion reaction provides a meaningful exploration for achieving the high performance of Li–S batteries.
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: Advanced Battery Materials and Technologies · Advancements in Battery Materials · Thermal Expansion and Ionic Conductivity
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
National Base for International Science & Technology Cooperation, National Local Joint Engineering Laboratory for Key Materials of New Energy Storage Battery, Hunan Province Key Laboratory of Electrochemical Energy Storage & Conversion, School of Chemistry, Xiangtan University, Xiangtan 411105, China
Chemistry & Chemical Engineering School, Xinxiang College, Henan 453003, China
Funding
Ministry of Science and Technology of the People's Republic of China
References (51)
Show source-provided references
1. 10.1002/aenm.20180347810.1002/aenm.201803478 ↗
2. 10.1002/adfm.20180882510.1002/adfm.201808825 ↗
3. 10.1002/aenm.20180347710.1002/aenm.201803477 ↗
4. 10.1002/adfm.20180672410.1002/adfm.201806724 ↗
5. 10.1002/adfm.20170741110.1002/adfm.201707411 ↗
6. 10.1021/cr500062v10.1021/cr500062v ↗
7. 10.1002/adfm.20160666310.1002/adfm.201606663 ↗
8. 10.1016/j.jallcom.2019.03.03510.1016/j.jallcom.2019.03.035 ↗
9. 10.1002/ange.20181206210.1002/ange.201812062 ↗
10. 10.1002/smtd.20190034410.1002/smtd.201900344 ↗
11. 10.1002/adfm.20190173010.1002/adfm.201901730 ↗
12. 10.1002/adfm.20170753610.1002/adfm.201707536 ↗
13. 10.1021/acssuschemeng.8b0027310.1021/acssuschemeng.8b00273 ↗
14. 10.1016/j.cej.2017.11.03910.1016/j.cej.2017.11.039 ↗
15. 10.1002/smll.20180478610.1002/smll.201804786 ↗
16. 10.1002/smll.20180313410.1002/smll.201803134 ↗
17. 10.1002/adma.20180086310.1002/adma.201800863 ↗
18. 10.1016/j.electacta.2019.06.14510.1016/j.electacta.2019.06.145 ↗
19. 10.1039/C9TA05347F10.1039/C9TA05347F ↗
20. 10.1002/chem.20180315310.1002/chem.201803153 ↗
21. 10.1002/adfm.20190105110.1002/adfm.201901051 ↗
22. 10.1039/C7NR09216D10.1039/C7NR09216D ↗
23. 10.1021/acsami.9b0587410.1021/acsami.9b05874 ↗
24. 10.1039/C8TA07220E10.1039/C8TA07220E ↗
25. 10.1002/adfm.20160226410.1002/adfm.201602264 ↗
26. 10.1021/jacs.8b0041110.1021/jacs.8b00411 ↗
27. 10.1016/j.ccr.2019.03.01110.1016/j.ccr.2019.03.011 ↗
28. 10.1021/jacs.8b1024610.1021/jacs.8b10246 ↗
29. 10.1021/acsnano.7b0322710.1021/acsnano.7b03227 ↗
30. 10.1002/adfm.20190384210.1002/adfm.201903842 ↗
31. 10.1016/j.nanoen.2019.03.06410.1016/j.nanoen.2019.03.064 ↗
32. 10.1016/j.ceramint.2018.11.03010.1016/j.ceramint.2018.11.030 ↗
33. 10.1039/C7NJ02714A10.1039/C7NJ02714A ↗
34. 10.1016/j.jelechem.2017.04.06010.1016/j.jelechem.2017.04.060 ↗
35. 10.1016/j.electacta.2017.04.15610.1016/j.electacta.2017.04.156 ↗
36. 10.1016/j.electacta.2016.01.00910.1016/j.electacta.2016.01.009 ↗
37. 10.1007/s10008-017-3649-510.1007/s10008-017-3649-5 ↗
38. 10.1016/j.ensm.2018.12.02410.1016/j.ensm.2018.12.024 ↗
39. 10.1039/C6EE02364A10.1039/C6EE02364A ↗
40. 10.1021/acssuschemeng.8b0415710.1021/acssuschemeng.8b04157 ↗
41. 10.1016/j.jallcom.2018.01.02610.1016/j.jallcom.2018.01.026 ↗
42. 10.1016/j.jallcom.2011.03.07510.1016/j.jallcom.2011.03.075 ↗
43. 10.1002/smll.20140232010.1002/smll.201402320 ↗
44. 10.1002/aenm.20150253910.1002/aenm.201502539 ↗
45. 10.1016/j.ensm.2019.04.03810.1016/j.ensm.2019.04.038 ↗
46. 10.1038/ncomms575910.1038/ncomms5759 ↗
47. 10.1016/j.tsf.2011.04.11910.1016/j.tsf.2011.04.119 ↗
48. 10.1016/j.ensm.2019.02.03010.1016/j.ensm.2019.02.030 ↗
49. 10.1002/ente.20180100110.1002/ente.201801001 ↗
50. 10.1002/aenm.20190095310.1002/aenm.201900953 ↗
51. 10.1002/adma.20170521910.1002/adma.201705219 ↗