journal article·2022-10-05

Less is More: Trace Amount of a Cyclic Sulfate Electrolyte Additive Enable Ultra-Stable Graphite Anode for High-Performance Potassium-Ion Batteries

Minghan Zhou, Yuqin Fan, Yang Gao, Zhaohui Ma, Zhaoen Liu, Wenxiang Wang, Hussein A. Younus, Zhengjian Chen, Xiwen Wang, Shiguo Zhang

ACS Applied Materials & Interfaces· Volume 14· Issue 39
Publisher page

Abstract

Graphite can be successfully used as an anode for potassium-ion batteries (PIBs), while its conversion to KC8 leads to huge volume expansion, destruction of solid electrolyte interphase (SEI), and thus poor cycling stability. Incorporating additives into electrolytes is an economical and effective way to construct robust SEI for high-performance PIBs. Herein, we developed a series of sulfur-containing additives for PIB graphite anodes, and the impacts of their molecular structure and contents on the SEI are also systematically investigated. Compared with butylene sulfites and 1,3-propane sultone, the 1,3,2-dioxathiolane 2,2-dioxide (DTD) additive endows the graphite electrode (GE) with a higher reversible capacity, and better cycling stability in both the dilute potassium bis(fluorosulfonyl)imide (KFSI)- and potassium hexafluorophosphate (KPF6)-based carbonate electrolyte, as a result of a thinner and sulfate-enriched SEI. Moreover, the addition of a trace amount (0.2 wt %) DTD to the electrolyte can effectively protect the GE running over 800 cycles at 1 C. Excessive additives in the electrolyte will induce continuous SEI growth and render a rapid capacity fading of the GE. This strategy using the electrolyte additive paves the way for the design of novel PIB electrolytes and thus provides a great opportunity for commercial PIBs.
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

College of Materials Science and Engineering, Hunan University, Changsha 410082, P. R. China

BTR New Material Group Co., Ltd., Shenzhen 518106, P. R. China

Chemistry Department, Faculty of Science, Fayoum University, Fayoum 63514, Egypt

Biomaterials Research Center, Zhuhai Institute of Advanced Technology Chinese Academy of Sciences, Zhuhai 519003, P. R. China

Funding

Natural Science Foundation of?Hunan Province · Central University Basic Research Fund of China · National Natural Science Foundation of China · Key Research and Development Program of Ningxia · Songshan Lake Materials Laboratory · Key Laboratory Research Fund of Guangxi · Zhuhai Science and Technology Department Project

References (48)

Show source-provided references
1. 10.1021/acs.chemrev.9b0046310.1021/acs.chemrev.9b00463 ↗
2. 10.1021/acs.chemmater.7b0176410.1021/acs.chemmater.7b01764 ↗
3. 10.1351/pac19855708112910.1351/pac198557081129 ↗
4. 10.1149/2.0211702jes10.1149/2.0211702jes ↗
5. 10.1002/ange.20180920310.1002/ange.201809203 ↗
6. 10.1021/acs.nanolett.5b0366710.1021/acs.nanolett.5b03667 ↗
7. 10.1021/jacs.5b0680910.1021/jacs.5b06809 ↗
8. 10.1016/j.elecom.2015.09.00210.1016/j.elecom.2015.09.002 ↗
9. 10.1021/acsami.6b0676710.1021/acsami.6b06767 ↗
10. 10.1002/adfm.20160224810.1002/adfm.201602248 ↗
11. 10.1039/d0ee01638a10.1039/d0ee01638a ↗
12. 10.1002/adma.20200374110.1002/adma.202003741 ↗
13. 10.1039/c8cc04433c10.1039/c8cc04433c ↗
14. 10.1002/anie.20190425810.1002/anie.201904258 ↗
15. 10.1002/aenm.20190261810.1002/aenm.201902618 ↗
16. 10.1002/anie.20191317410.1002/anie.201913174 ↗
17. 10.1021/cr500003w10.1021/cr500003w ↗
18. 10.1021/acsenergylett.1c0123810.1021/acsenergylett.1c01238 ↗
19. 10.1016/j.ensm.2021.08.01310.1016/j.ensm.2021.08.013 ↗
20. 10.1021/acsami.0c0956210.1021/acsami.0c09562 ↗
21. 10.1021/acsami.1c1517410.1021/acsami.1c15174 ↗
22. 10.1002/adfm.20200193410.1002/adfm.202001934 ↗
23. 10.1021/acsenergylett.0c0140110.1021/acsenergylett.0c01401 ↗
24. 10.1016/j.electacta.2014.01.02310.1016/j.electacta.2014.01.023 ↗
25. 10.1149/1.217046210.1149/1.2170462 ↗
26. 10.1016/j.jpowsour.2007.05.07810.1016/j.jpowsour.2007.05.078 ↗
27. 10.1016/j.jpowsour.2008.08.07710.1016/j.jpowsour.2008.08.077 ↗
28. 10.1149/1.351470510.1149/1.3514705 ↗
29. 10.1021/acsenergylett.1c0242510.1021/acsenergylett.1c02425 ↗
30. 10.1021/acs.jpcc.0c0302010.1021/acs.jpcc.0c03020 ↗
31. 10.1039/d1ee01789f10.1039/d1ee01789f ↗
32. 10.1002/smll.20180180610.1002/smll.201801806 ↗
33. 10.1149/2.0331811jes10.1149/2.0331811jes ↗
34. 10.1021/jp509731y10.1021/jp509731y ↗
35. 10.1142/s179360472051041810.1142/s1793604720510418 ↗
36. 10.1021/acs.jpcc.5b0007210.1021/acs.jpcc.5b00072 ↗
37. 10.1039/c2ra20200j10.1039/c2ra20200j ↗
38. 10.1021/acs.jpcc.8b1200010.1021/acs.jpcc.8b12000 ↗
39. 10.1039/b905162g10.1039/b905162g ↗
40. 10.1002/adfm.20180713710.1002/adfm.201807137 ↗
41. 10.1016/j.jpowsour.2020.22846210.1016/j.jpowsour.2020.228462 ↗
42. 10.1002/aenm.20170328810.1002/aenm.201703288 ↗
43. 10.1039/c6ee03185d10.1039/c6ee03185d ↗
44. 10.1002/aenm.20200364010.1002/aenm.202003640 ↗
45. 10.1002/aenm.20210085610.1002/aenm.202100856 ↗
46. 10.1002/adma.20200631310.1002/adma.202006313 ↗
47. 10.1002/advs.20200363910.1002/advs.202003639 ↗
48. 10.1002/anie.20220829110.1002/anie.202208291 ↗