Metal–Organic Frameworks as Electrolyte Additives To Enable Ultrastable Plating/Stripping of Li Anode with Dendrite Inhibition
Source abstract
Abstract
Suppressing the extrusion of Li dendrites and alleviating the volume expansion of Li anode during long-term cycling are of great significance to achieve highly reversible Li metal batteries of high energy density potential. However, the exploration of facile and effective solutions to smoothen anode surface is still a big challenge. Here, we propose a solid additive strategy by blending tailored metal–organic framework (MOF) grains with typical carbonate electrolyte to enable an ultrastable plating/stripping cycling of Li anode for at least 1400 h with evident inhibition of anode roughening and voltage polarization. Zr-based MOF (UiO-66) additive enables the smallest nucleation and plateau overpotentials (∼80 mV) during Li plating especially under high current density (2 mA/cm2) and large areal capacity (4 mAh/cm2). The kinetic and cyclic advantages of Li anode modulated by UiO-66 not only benefit from its intrinsic features (high surface area/porosity and thermal/electrochemical stability) but also from the reinforced solid electrolyte interface with low resistance, which consists of concentrated LiF and robust Zr–O–C moieties. Li–Li4Ti5O12 cell based on MOF additive can achieve a high reversibility for at least 900 cycles.
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
State Key Laboratory of High Performance Ceramics and Superfine Microstructure, Shanghai Institute of Ceramics, Chinese Academy of Sciences, 1295 Ding Xi Road, Shanghai 200050, China
School of Materials Science and Engineering, Xiangtan University, Xiangtan 411105, China
Funding
Ministry of Science and Technology of the People's Republic of China · National Natural Science Foundation of China · Chinese Academy of Sciences
References (41)
Show source-provided references
1. 10.1021/ja309143810.1021/ja3091438 ↗
2. 10.1016/j.ensm.2018.02.01710.1016/j.ensm.2018.02.017 ↗
3. 10.1038/nnano.2017.1610.1038/nnano.2017.16 ↗
4. 10.1038/s41524-018-0079-610.1038/s41524-018-0079-6 ↗
5. 10.1039/C6EE02326F10.1039/C6EE02326F ↗
6. 10.1021/acs.chemrev.7b0011510.1021/acs.chemrev.7b00115 ↗
7. 10.1021/acsenergylett.6b0065010.1021/acsenergylett.6b00650 ↗
8. 10.1039/C3EE40795K10.1039/C3EE40795K ↗
9. 10.1002/anie.20171270210.1002/anie.201712702 ↗
10. 10.1073/pnas.151818811310.1073/pnas.1518188113 ↗
11. 10.1021/jacs.6b1008810.1021/jacs.6b10088 ↗
12. 10.1038/nmat482110.1038/nmat4821 ↗
13. 10.1002/adma.20170762910.1002/adma.201707629 ↗
14. 10.1002/adfm.20160598910.1002/adfm.201605989 ↗
15. 10.1002/anie.20170775410.1002/anie.201707754 ↗
16. 10.1038/nenergy.2017.11910.1038/nenergy.2017.119 ↗
17. 10.1021/acsami.8b0098910.1021/acsami.8b00989 ↗
18. 10.1038/nmat404110.1038/nmat4041 ↗
19. 10.1002/aenm.20170073210.1002/aenm.201700732 ↗
20. 10.1016/j.nanoen.2017.04.05610.1016/j.nanoen.2017.04.056 ↗
21. 10.1021/acsami.7b0047810.1021/acsami.7b00478 ↗
22. 10.1002/adma.20160113310.1002/adma.201601133 ↗
23. 10.1002/anie.20161091410.1002/anie.201610914 ↗
24. 10.1016/S1387-1811(02)00405-510.1016/S1387-1811(02)00405-5 ↗
25. 10.1021/cm103644b10.1021/cm103644b ↗
26. 10.1021/ja805795310.1021/ja8057953 ↗
27. 10.1126/science.283.5405.114810.1126/science.283.5405.1148 ↗
28. 10.1021/acs.nanolett.6b0475510.1021/acs.nanolett.6b04755 ↗
29. 10.1149/1.274655010.1149/1.2746550 ↗
30. 10.1016/j.elecom.2005.12.00210.1016/j.elecom.2005.12.002 ↗
31. 10.1149/2.100310jes10.1149/2.100310jes ↗
32. 10.1038/ncomms1510610.1038/ncomms15106 ↗
33. 10.1021/ic50205a02410.1021/ic50205a024 ↗
34. 10.1006/jcat.1996.021710.1006/jcat.1996.0217 ↗
35. 10.1016/j.ssi.2012.02.03610.1016/j.ssi.2012.02.036 ↗
36. 10.1002/adma.20180557410.1002/adma.201805574 ↗
37. 10.1016/j.ensm.2017.11.00310.1016/j.ensm.2017.11.003 ↗
38. 10.1016/j.joule.2018.07.01010.1016/j.joule.2018.07.010 ↗
39. 10.1126/science.aap878710.1126/science.aap8787 ↗
40. 10.1126/sciadv.170130110.1126/sciadv.1701301 ↗
41. 10.1002/adfm.20170583810.1002/adfm.201705838 ↗