Dendrite-Free Sn Anode with High Reversibility for Aqueous Batteries Enabled by “Water-in-Salt” Electrolyte
Source abstract
Abstract
Metallic tin (Sn) has always been considered as an anode candidate for nonaqueous lithium-ion batteries (LIBs). Nevertheless, there were hardly any attempts to use Sn as an anode material in aqueous batteries. Although Sn possesses relatively high specific capacity (451.54 mAh/g, two-electron transfer reaction), mild electrode potential (−0.1375 V vs the standard hydrogen electrode, Sn2+ + 2e– = Sn), high hydrogen overpotential, and environmental friendliness, it also suffers from bad reversibility and low Coulombic efficiency (CE) in common aqueous electrolytes. In this work, a dendrite-free Sn anode with highly improved reversibility in an aqueous electrolyte was realized using a type of “water-in-salt” electrolyte (1 m Sn(OTf)2 + 20 m LiTFSI). The results of Fourier transform infrared (FTIR) spectra and density functional theory (DFT) calculations have verified the significant impact of highly concentrated LiTFSI salt on Sn2+ hydrolysis, which is the key factor in improving the reversibility of the Sn anode and suppressing the dendrite formation. A Sn/LiFePO4 cell applying this electrolyte was acquired with a discharge plateau at around 0.6 V. In the cyclability test, the Sn anode exhibited a stable discharge capacity of more than 107 mAh/g with a Coulombic efficiency (CE) of 95% for 35 cycles (0.2C rate).
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: Advanced battery technologies research · Advancements in Battery Materials · Advanced Battery Materials and Technologies
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
College of Chemistry and Molecular Sciences, Hubei Key Lab of Electrochemical Power Sources, Wuhan University, Wuhan 430072, China
Funding
Ministry of Education of the People's Republic of China · Ministry of Science and Technology of the People's Republic of China · Wuhan University · National Natural Science Foundation of China
References (35)
Show source-provided references
1. 10.1016/0022-0728(92)80574-N10.1016/0022-0728(92)80574-N ↗
2. 10.1007/BF0054388810.1007/BF00543888 ↗
3. 10.1016/1044-5803(94)00060-X10.1016/1044-5803(94)00060-X ↗
4. 10.1016/S1369-7021(13)70012-910.1016/S1369-7021(13)70012-9 ↗
5. 10.1002/adma.20070136410.1002/adma.200701364 ↗
6. 10.1021/ja034552410.1021/ja0345524 ↗
7. 10.1021/cm048137210.1021/cm0481372 ↗
8. 10.1016/j.jpowsour.2016.04.10510.1016/j.jpowsour.2016.04.105 ↗
9. 10.1002/aenm.20160094310.1002/aenm.201600943 ↗
10. 10.1021/acs.accounts.5b0011410.1021/acs.accounts.5b00114 ↗
11. 10.1149/1.345514810.1149/1.3455148 ↗
12. 10.1016/j.electacta.2011.01.01710.1016/j.electacta.2011.01.017 ↗
13. 10.1021/ie102267x10.1021/ie102267x ↗
14. 10.1007/s10854-007-9385-310.1007/s10854-007-9385-3 ↗
15. 10.1179/1743294414Y.000000042710.1179/1743294414Y.0000000427 ↗
16. 10.1023/A:102050372606810.1023/A:1020503726068 ↗
17. 10.1016/j.ijhydene.2006.08.04310.1016/j.ijhydene.2006.08.043 ↗
18. 10.1016/0273-2300(84)90006-010.1016/0273-2300(84)90006-0 ↗
19. 10.1002/adfm.20070063810.1002/adfm.200700638 ↗
20. 10.1002/aenm.20120006510.1002/aenm.201200065 ↗
21. 10.1126/science.aab159510.1126/science.aab1595 ↗
22. 10.1038/s41563-018-0063-z10.1038/s41563-018-0063-z ↗
23. 10.1126/science.105951410.1126/science.1059514 ↗
24. 10.1139/v66-25510.1139/v66-255 ↗
25. 10.1021/ja039248p10.1021/ja039248p ↗
26. 10.1038/nnano.2017.1610.1038/nnano.2017.16 ↗
27. 10.1002/adma.20150612410.1002/adma.201506124 ↗
28. 10.1016/0013-4686(82)85068-810.1016/0013-4686(82)85068-8 ↗
29. 10.1039/C5TA06366C10.1039/C5TA06366C ↗
30. 10.1007/s10853-015-9323-310.1007/s10853-015-9323-3 ↗
31. 10.1007/s10800-009-9963-610.1007/s10800-009-9963-6 ↗
32. 10.1016/j.electacta.2004.03.03910.1016/j.electacta.2004.03.039 ↗
33. 10.1016/j.electacta.2005.02.13710.1016/j.electacta.2005.02.137 ↗
34. 10.1149/2.0901609jes10.1149/2.0901609jes ↗
35. 10.1016/j.electacta.2018.05.13610.1016/j.electacta.2018.05.136 ↗