journal article·2017-06-09

Dendrite-Free Lithium Deposition with Self-Aligned Columnar Structure in a Carbonate–Ether Mixed Electrolyte

HaiLong Yu, JunNian Zhao, LiuBin Ben, YuanJie Zhan, YiDa Wu, XueJie Huang

ACS Energy Letters· Volume 2· Issue 6
Publisher page

Abstract

Batteries with lithium metal anodes are promising because of lithium’s high energy density. However, the growth of Li dendrites on the surface of the Li electrode in a liquid electrolyte during cycling reduces the safety and cycle performance of batteries, hindering their commercial application. In this work, we observe for the first time a smooth and dendrite-free Li deposition with a vertically grown, self-aligned, and highly compact columnar structure formed during cycling in a mixed carbonate–ether electrolyte. The stable microsized (∼10 μm in diameter and ∼20 μm in length) Li deposits are aligned in arrays on the surface of the Li electrode. The columnar Li deposits still exhibit a dendrite-free morphology and a compact structure after 200 cycles at a current density of 1 mA/cm 2 and a 1.5 mAh/cm 2 cycling capacity in a mixed carbonate–ether electrolyte. This work shows an optimiztic outlook for Li batteries with liquid electrolytes.
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

P.R. China Beijing National Laboratory for Condensed Matter Physics, Institute of Physics, Chinese Academy of Sciences, Beijing 100190, China

School of Physical Sciences, University of Chinese Academy of Sciences, Beijing 100190, China

Funding

Ministry of Science and Technology of the People's Republic of China · China Postdoctoral Science Foundation · National Natural Science Foundation of China

References (27)

Show source-provided references
1. 10.1039/C3EE40795K10.1039/C3EE40795K ↗
2. 10.1016/j.rser.2015.10.07010.1016/j.rser.2015.10.070 ↗
3. 10.1073/pnas.151818811310.1073/pnas.1518188113 ↗
4. 10.1002/celc.20150052010.1002/celc.201500520 ↗
5. 10.1039/c3cc49029g10.1039/c3cc49029g ↗
6. 10.1016/j.elecom.2014.11.00210.1016/j.elecom.2014.11.002 ↗
7. 10.1016/j.jpowsour.2013.07.05610.1016/j.jpowsour.2013.07.056 ↗
8. 10.1016/j.jpowsour.2014.08.06210.1016/j.jpowsour.2014.08.062 ↗
9. 10.1246/cl.1995.20910.1246/cl.1995.209 ↗
10. 10.1002/aenm.20150215110.1002/aenm.201502151 ↗
11. 10.1021/acsami.6b0389710.1021/acsami.6b03897 ↗
12. 10.1016/j.jpowsour.2014.03.02910.1016/j.jpowsour.2014.03.029 ↗
13. 10.1038/nnano.2014.15210.1038/nnano.2014.152 ↗
14. 10.1038/nnano.2016.3210.1038/nnano.2016.32 ↗
15. 10.1038/nmat404110.1038/nmat4041 ↗
16. 10.1021/nl503125u10.1021/nl503125u ↗
17. 10.1021/acs.nanolett.6b0158110.1021/acs.nanolett.6b01581 ↗
18. 10.1021/jp412775410.1021/jp4127754 ↗
19. 10.1021/ja312241y10.1021/ja312241y ↗
20. 10.1021/nl503911710.1021/nl5039117 ↗
21. 10.1002/aenm.20160081110.1002/aenm.201600811 ↗
22. 10.1016/j.nanoen.2015.04.00910.1016/j.nanoen.2015.04.009 ↗
23. 10.1016/j.jpowsour.2006.10.06510.1016/j.jpowsour.2006.10.065 ↗
24. 10.1016/j.jpowsour.2015.01.03010.1016/j.jpowsour.2015.01.030 ↗
25. 10.1002/adma.20160618710.1002/adma.201606187 ↗
26. 10.1016/S0378-7753(00)00431-610.1016/S0378-7753(00)00431-6 ↗
27. 10.1021/acsami.6b0440610.1021/acsami.6b04406 ↗