journal article·2018-07-11

Enabling High-Energy-Density Cathode for Lithium–Sulfur Batteries

Dongping Lu, Qiuyan Li, Jian Liu, Jianming Zheng, Yuxing Wang, Seth Ferrara, Jie Xiao, Ji-Guang Zhang, Jun Liu

ACS Applied Materials & Interfaces· Volume 10· Issue 27
Publisher page

Abstract

High-energy lithium–sulfur (Li–S) battery is built on high loading and dense sulfur electrodes. Unfortunately, these electrodes usually suffer from a low sulfur utilization rate and limited cycle life due to the gap in scientific knowledge between the fundamental research and the application at relevant scales. In this work, effects of electrode porosity on the electrode energy density, cell cycling stability, Li anode interface, and electrolyte/sulfur ratio were investigated on the basis of high-loading sulfur electrodes. Using electrodes with sulfur loading of 4 mg cm–2 and thickness at ∼60 μm, a high energy density of over 1300 Wh L–1 has been obtained at electrode level, which provides a decent basis for high-energy Li–S cell development. In addition, Li–S cells with the high-loading and dense electrodes demonstrate promising cycling stability (∼80% capacity retention for 200 cycles). These significant improvements are contributed by the synergistic effects of dense sulfur cathode, improved electrode wetting, and suppressed quick growth of the interphase layer on Li-metal anode. This study sheds light on rational design of sulfur cathode for balanced cell energy density and cycling life.
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

Electrochemical Materials & Systems Group, Energy and Environment Directorate, Pacific Northwest National Laboratory (PNNL), Richland, Washington 99354, United States

Funding

Vehicle Technologies Program

References (36)

Show source-provided references
1. 10.1038/nmat319110.1038/nmat3191 ↗
2. 10.1039/C5CS00410A10.1039/C5CS00410A ↗
3. 10.1038/nmat246010.1038/nmat2460 ↗
4. 10.1002/adfm.20130263110.1002/adfm.201302631 ↗
5. 10.1149/2.013310jes10.1149/2.013310jes ↗
6. 10.1039/c2cs35256g10.1039/c2cs35256g ↗
7. 10.1016/j.jpowsour.2012.12.10210.1016/j.jpowsour.2012.12.102 ↗
8. 10.1039/C5CC05171A10.1039/C5CC05171A ↗
9. 10.1002/anie.20151183010.1002/anie.201511830 ↗
10. 10.1149/2.039208jes10.1149/2.039208jes ↗
11. 10.1016/j.elecom.2006.09.01310.1016/j.elecom.2006.09.013 ↗
12. 10.1002/adfm.20120184710.1002/adfm.201201847 ↗
13. 10.1016/j.jpowsour.2011.12.06110.1016/j.jpowsour.2011.12.061 ↗
14. 10.1016/j.jpowsour.2012.06.10010.1016/j.jpowsour.2012.06.100 ↗
15. 10.1038/ncomms401510.1038/ncomms4015 ↗
16. 10.1149/1.180639410.1149/1.1806394 ↗
17. 10.1021/acs.nanolett.5b0052110.1021/acs.nanolett.5b00521 ↗
18. 10.1021/acsami.6b0890410.1021/acsami.6b08904 ↗
19. 10.1002/aenm.20150007210.1002/aenm.201500072 ↗
20. 10.1002/adfm.20170754310.1002/adfm.201707543 ↗
21. 10.1002/anie.20130476210.1002/anie.201304762 ↗
22. 10.1002/aenm.20150110210.1002/aenm.201501102 ↗
23. 10.1002/aenm.20140198610.1002/aenm.201401986 ↗
24. 10.1002/aenm.20140229010.1002/aenm.201402290 ↗
25. 10.1016/j.jpowsour.2014.04.01810.1016/j.jpowsour.2014.04.018 ↗
26. 10.1016/j.jpowsour.2012.03.06210.1016/j.jpowsour.2012.03.062 ↗
27. 10.1016/j.jpowsour.2014.03.08810.1016/j.jpowsour.2014.03.088 ↗
28. 10.1002/adma.20140568910.1002/adma.201405689 ↗
29. 10.1039/C4TA00742E10.1039/C4TA00742E ↗
30. 10.1002/adma.20110327410.1002/adma.201103274 ↗
31. 10.1002/adfm.20150426210.1002/adfm.201504262 ↗
32. 10.1021/acs.chemmater.5b0253310.1021/acs.chemmater.5b02533 ↗
33. 10.1021/acsenergylett.6b0019410.1021/acsenergylett.6b00194 ↗
34. 10.1038/ncomms843610.1038/ncomms8436 ↗
35. 10.1016/j.jpowsour.2016.07.05610.1016/j.jpowsour.2016.07.056 ↗
36. 10.1021/jacs.6b1235810.1021/jacs.6b12358 ↗