Electrospun Polymer Nanofibers with TiO2@NiCo-LDH as Efficient Polysulfide Barriers for Wide-Temperature-Range Li–S Batteries
Source abstract
Abstract
Herein, we introduce polymer nanofibers of TiO2@NiCo-LDH as interlayers into Li–S batteries. From 0 to 60 °C, the interlayers can deliver high sulfur utilization, an outstanding rate capability, and excellent cycling life. High-temperature excitation makes it easier for the valence band electrons of TiO2 to transition to the conduction band. The electron–hole pairs formed on the surface combine with the ether group of 1,3-dioxolane in the electrolyte, which greatly reduces the decomposition and volatilization rates of the electrolyte, ensuring Li–S batteries with good cycle performance at high temperatures. The capacity can stabilize at 798.6 mAh g–1 after 100 cycles at 60 °C and 1C, and the battery can provide a capacity higher than 323.2 mAh g–1 at 0 °C. Simultaneously, the lithium metal symmetrical battery with a functional separator can be continuously cycled for 1800 and 750 h without a short circuit at the current densities of 0.65 and 1.63 mA cm–2, respectively.
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
Shanghai Key Laboratory of Materials Protection and Advanced Materials Electric Power, Shanghai Engineering Research Center of Energy-Saving in Heat Exchange Systems, Shanghai University of Electric Power, Shanghai 200090, P. R. China
Shanghai Institute of Pollution Control and Ecological Security, Shanghai 200092, P. R. China
Funding
Science and Technology Commission of Shanghai Municipality · National Natural Science Foundation of China · International Joint Laboratory on Resource Chemistry
References (38)
Show source-provided references
1. 10.1038/nmat319110.1038/nmat3191 ↗
2. 10.1002/adfm.20120068910.1002/adfm.201200689 ↗
3. 10.1039/C5RA05481H10.1039/C5RA05481H ↗
4. 10.1039/c2cc33945e10.1039/c2cc33945e ↗
5. 10.1038/s41560-018-0104-510.1038/s41560-018-0104-5 ↗
6. 10.1002/adfm.20180118810.1002/adfm.201801188 ↗
7. Feng W. · J. Phys. Chem. C · 2013 · 115 · 24411
8. 10.1016/j.electacta.2016.03.01810.1016/j.electacta.2016.03.018 ↗
9. 10.1002/adfm.20190105110.1002/adfm.201901051 ↗
10. 10.1039/C8TA08361D10.1039/C8TA08361D ↗
11. 10.1002/anie.20181261110.1002/anie.201812611 ↗
12. 10.1021/acs.nanolett.7b0413110.1021/acs.nanolett.7b04131 ↗
13. 10.1016/j.joule.2018.03.00810.1016/j.joule.2018.03.008 ↗
14. Chen X. · Sci. Adv. · 2019 · 5 · eaau772810.1126/sciadv.aau7728 ↗
15. 10.1002/aenm.20180243110.1002/aenm.201802431 ↗
16. 10.1002/smll.20150313310.1002/smll.201503133 ↗
17. 10.1038/ncomms251310.1038/ncomms2513 ↗
18. 10.1021/cr500062v10.1021/cr500062v ↗
19. 10.1021/ar300179v10.1021/ar300179v ↗
20. 10.1021/ja100102y10.1021/ja100102y ↗
21. 10.1002/anie.20151163210.1002/anie.201511632 ↗
22. 10.1002/adfm.20180142210.1002/adfm.201801422 ↗
23. 10.1002/aenm.20170228810.1002/aenm.201702288 ↗
24. 10.1016/j.joule.2019.01.00310.1016/j.joule.2019.01.003 ↗
25. 10.1002/adma.20190693910.1002/adma.201906939 ↗
26. 10.1002/adma.20150612410.1002/adma.201506124 ↗
27. 10.1002/anie.20150697210.1002/anie.201506972 ↗
28. 10.1002/aenm.20180210710.1002/aenm.201802107 ↗
29. 10.1002/anie.20141017410.1002/anie.201410174 ↗
30. 10.1038/s41467-019-10885-810.1038/s41467-019-10885-8 ↗
31. 10.1016/j.matlet.2019.12665610.1016/j.matlet.2019.126656 ↗
32. 10.1002/anie.20170209910.1002/anie.201702099 ↗
33. 10.1016/j.ensm.2017.04.00310.1016/j.ensm.2017.04.003 ↗
34. 10.1039/C8TA01726C10.1039/C8TA01726C ↗
35. 10.1002/mame.20170012210.1002/mame.201700122 ↗
36. 10.1016/j.ijhydene.2019.09.13410.1016/j.ijhydene.2019.09.134 ↗
37. 10.1038/s41467-019-09211-z10.1038/s41467-019-09211-z ↗
38. 10.1038/nnano.2014.15210.1038/nnano.2014.152 ↗