In Situ Formed LiZn Alloy Skeleton for Stable Lithium Anodes
Source abstract
Abstract
Lithium metal is the most promising anode for developing high-energy density rechargeable batteries because of its ultrahigh theoretical capacity and extremely low reduction potential. However, the formation of dendritic lithium and the huge volume change of the anode during the charge/discharge process severely hinder the practical application of the lithium anode. Obtaining high-performance, simple methods that can simultaneously modify the interface and restrict the volume change of the Li anode are highly required. Herein, the lithiophilic Zn nanoparticles are introduced into molten lithium directly to obtain a composite anode filled with in situ formed LiZn alloy rods. These micrometer-sized alloy rods can serve as a skeleton to provide a large number of lithium deposition sites as well as volume suppression for lithium deposition. Benefiting from these two aspects, the composite anode exhibits superior electrochemical performance by means of lowering the overpotential and prolonging the cycle life of symmetrical cells. Furthermore, the full cell paired with this composite anode and LiFePO4 cathode also demonstrates a better capacity retention than its counterpart with raw Li anode.
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
State Key Laboratory of Material Processing and Die & Mould Technology, School of Materials Science and Engineering, Huazhong University of Science and Technology (HUST), Wuhan, Hubei 430074, P.R. China
Key Laboratory of Advanced Energy Materials Chemistry (Ministry of Education), Nankai University, Tianjin 300071, China
Funding
Ministry of Science and Technology of the People's Republic of China · National Natural Science Foundation of China
References (37)
Show source-provided references
1. 10.1038/451652a10.1038/451652a ↗
2. 10.1021/cm901452z10.1021/cm901452z ↗
3. 10.1038/3510464410.1038/35104644 ↗
4. 10.1039/C3EE40795K10.1039/C3EE40795K ↗
5. 10.1002/adma.20170000710.1002/adma.201700007 ↗
6. 10.1016/S0378-7753(00)00431-610.1016/S0378-7753(00)00431-6 ↗
7. 10.1038/nenergy.2016.11410.1038/nenergy.2016.114 ↗
8. 10.1021/acs.chemrev.7b0011510.1021/acs.chemrev.7b00115 ↗
9. 10.1002/admi.20170109710.1002/admi.201701097 ↗
10. 10.1002/advs.20160044510.1002/advs.201600445 ↗
11. 10.1021/jp002526b10.1021/jp002526b ↗
12. 10.1002/adfm.20170034810.1002/adfm.201700348 ↗
13. 10.1002/aenm.20190353410.1002/aenm.201903534 ↗
14. 10.1002/adma.20190182010.1002/adma.201901820 ↗
15. 10.1002/adma.20190131010.1002/adma.201901310 ↗
16. 10.1021/acsami.7b1511710.1021/acsami.7b15117 ↗
17. 10.1038/ncomms251310.1038/ncomms2513 ↗
18. 10.1002/anie.20171080610.1002/anie.201710806 ↗
19. 10.1038/nenergy.2017.11910.1038/nenergy.2017.119 ↗
20. 10.1002/adma.20160553110.1002/adma.201605531 ↗
21. 10.1002/adma.20160375510.1002/adma.201603755 ↗
22. 10.1021/acs.nanolett.8b0018310.1021/acs.nanolett.8b00183 ↗
23. 10.1002/aenm.20180243010.1002/aenm.201802430 ↗
24. 10.1021/acsnano.7b0208510.1021/acsnano.7b02085 ↗
25. 10.1002/adma.20160140910.1002/adma.201601409 ↗
26. 10.1021/acs.nanolett.6b0158110.1021/acs.nanolett.6b01581 ↗
27. 10.1007/s12274-016-1219-210.1007/s12274-016-1219-2 ↗
28. 10.1002/adma.20170038910.1002/adma.201700389 ↗
29. 10.1021/jacs.7b0176310.1021/jacs.7b01763 ↗
30. 10.1038/nnano.2016.3210.1038/nnano.2016.32 ↗
31. 10.1002/aenm.20170350510.1002/aenm.201703505 ↗
32. 10.1073/pnas.161887111410.1073/pnas.1618871114 ↗
33. 10.1038/nenergy.2016.1010.1038/nenergy.2016.10 ↗
34. 10.1021/acsami.7b0457710.1021/acsami.7b04577 ↗
35. 10.1016/j.nanoen.2017.07.02310.1016/j.nanoen.2017.07.023 ↗
36. 10.1021/acsami.8b2142010.1021/acsami.8b21420 ↗
37. 10.1002/adfm.20180875610.1002/adfm.201808756 ↗