journal article·2024-09-13

Chemically Active Sulfonate Additive with Transition Metal and Oxygen Dual-Site Deactivation for High-Voltage LiCoO2

Haoyi Yang, Yajun Zhao, Tian Qin, Hongyi Pan, Shuhang Feng, Quan Li, Xuelong Wang, Xiqian Yu, Hong Li

ACS Energy Letters· Volume 9· Issue 9
Publisher page

Abstract

Modulating a solid electrolyte interphase (SEI) through additives represents a crucial approach for stable operation of cathode materials. Traditional perspectives focus on the electrochemical decomposition of the additive itself while underestimating the reactivity and catalytic ability from cathode surfaces. Inspired by the sulfur-containing species causing catalyst poisoning, the catalytic effects of LiCoO 2 (LCO) for the sulfur-based molecule (−SO x ) additives have been investigated. We elucidate the mechanism of additives by assessing multiple interactions with the LCO surface, which are primarily characterized by chemical ring-opening reactions. Furthermore, decreasing the saturated carbon in molecules can enhance its reactivity, while the −SO x groups deactivate both the lattice oxygen and transition metal center through dual-site bond formation. Benefiting from the chemically passivated surface, the sulfonate additive enables LCO cycling at a high temperature and a high voltage of 4.65 V. This provides new insights into the mechanisms for stabilizing the cathode interface and molecular design for additives.
Source: openalex_inverted_index · Quality: baseline

Research context

OpenAlex topics: Advancements in Battery Materials · Advanced Battery Materials and Technologies · Advanced Battery Technologies Research

SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.

Affiliations

Beijing Frontier Research Center on Clean Energy, Institute of Physics, Chinese Academy of Sciences, Beijing 100190, People’s Republic of China

Center of Materials Science and Optoelectronics Engineering, University of Chinese Academy of Sciences, Beijing 100190, People’s Republic of China

Funding

National Key Research and Development Program of China · National Natural Science Foundation of China

References (46)

Show source-provided references
1. 10.1016/j.jpowsour.2020.22806210.1016/j.jpowsour.2020.228062 ↗
2. 10.1021/acs.jpclett.5b0172710.1021/acs.jpclett.5b01727 ↗
3. 10.1002/admi.20210207810.1002/admi.202102078 ↗
4. 10.1007/s40820-022-00917-210.1007/s40820-022-00917-2 ↗
5. 10.1021/jacs.0c0636310.1021/jacs.0c06363 ↗
6. 10.1021/acscatal.3c0245510.1021/acscatal.3c02455 ↗
7. 10.1039/C9EE02543J10.1039/C9EE02543J ↗
8. 10.1021/acsami.1c2281210.1021/acsami.1c22812 ↗
9. 10.1021/acs.jpcc.0c0755010.1021/acs.jpcc.0c07550 ↗
10. 10.1021/acsenergylett.2c0143310.1021/acsenergylett.2c01433 ↗
11. 10.1021/acsenergylett.3c0050410.1021/acsenergylett.3c00504 ↗
12. 10.1021/acsenergylett.2c0031610.1021/acsenergylett.2c00316 ↗
13. 10.1021/acsenergylett.3c0253410.1021/acsenergylett.3c02534 ↗
14. 10.1007/s12598-022-02101-210.1007/s12598-022-02101-2 ↗
15. 10.1002/aenm.20220427210.1002/aenm.202204272 ↗
16. 10.1038/s41570-023-00557-z10.1038/s41570-023-00557-z ↗
17. 10.1021/acsenergylett.3c0032410.1021/acsenergylett.3c00324 ↗
18. 10.1002/anie.20231560810.1002/anie.202315608 ↗
19. 10.1021/acs.chemmater.9b0076710.1021/acs.chemmater.9b00767 ↗
20. 10.1007/s11783-016-0832-310.1007/s11783-016-0832-3 ↗
21. 10.1021/jacs.0c0968310.1021/jacs.0c09683 ↗
22. 10.1002/1096-9918(200008)30:1<65::AID-SIA782>3.0.CO;2-R10.1002/1096-9918(200008)30:1<65::AID-SIA782>3.0.CO;2-R ↗
23. 10.1002/inf2.1223510.1002/inf2.12235 ↗
24. 10.1021/acsaem.8b0029510.1021/acsaem.8b00295 ↗
25. 10.1149/2.0331811jes10.1149/2.0331811jes ↗
26. 10.1016/j.jpowsour.2021.22959610.1016/j.jpowsour.2021.229596 ↗
27. 10.1021/acsami.9b1179510.1021/acsami.9b11795 ↗
28. 10.1002/adfm.20221215010.1002/adfm.202212150 ↗
29. 10.1002/anie.20230888810.1002/anie.202308888 ↗
30. 10.1063/1.513144710.1063/1.5131447 ↗
31. 10.1021/acs.jpcc.9b0209610.1021/acs.jpcc.9b02096 ↗
32. 10.1149/2.049404jes10.1149/2.049404jes ↗
33. 10.1038/s41598-019-49568-110.1038/s41598-019-49568-1 ↗
34. 10.1149/2.074311jes10.1149/2.074311jes ↗
35. 10.1021/acsenergylett.9b0082210.1021/acsenergylett.9b00822 ↗
36. 10.1002/aenm.20230432110.1002/aenm.202304321 ↗
37. 10.1039/D4EE01831A10.1039/D4EE01831A ↗
38. 10.1021/acsenergylett.3c0278910.1021/acsenergylett.3c02789 ↗
39. 10.1002/cphc.20230016210.1002/cphc.202300162 ↗
40. 10.1039/D0CS00535E10.1039/D0CS00535E ↗
41. 10.1016/S0040-4020(00)00494-410.1016/S0040-4020(00)00494-4 ↗
42. 10.1002/anie.20221513110.1002/anie.202215131 ↗
43. 10.1016/S0040-4020(01)90041-910.1016/S0040-4020(01)90041-9 ↗
44. 10.1021/acs.jpcc.8b0171310.1021/acs.jpcc.8b01713 ↗
45. 10.1002/admi.20180165010.1002/admi.201801650 ↗
46. 10.1002/anie.20200852810.1002/anie.202008528 ↗