Stable lithium electrodeposition in salt-reinforced electrolytes

Yingying Lu, Zhengyuan Tu, Jonathan Shu, Lynden A. Archer

Research output: Contribution to journalArticlepeer-review

99 Scopus citations

Abstract

© 2015 Elsevier B.V. Development of high-energy lithium-based batteries that are safe remains a challenge due to the non-uniform lithium electrodeposition during repeated charge and discharge cycles. We report on the effectiveness of lithium bromide (LiBr) salt additives in a common liquid electrolyte (i.e. propylene carbonate (PC)) on the stability of lithium electrodeposition. From galvanostatic cycling measurements, we find that the presence of LiBr in PC provides more than 20-fold enhancement in cell lifetime over the control LiTFSI/PC electrolyte. Batteries containing 30 mol% LiBr additive in the electrolytes are able to cycle stably for at least 1.8 months with no observations of cell failure. From galvanostatic polarization measurements, an electrolyte containing 30 mol% LiBr shows a maximum improvement in lifetime. The formation of uneven lithium electrodeposits is significantly suppressed by the Br-containing SEI layers, evidenced by impedance spectra, post-mortem SEM and XPS analyses. The study also concludes that good solubility of halogenated salts is not necessary for achieving the observed improvements in cell lifetime.
Original languageEnglish (US)
Pages (from-to)413-418
Number of pages6
JournalJournal of Power Sources
Volume279
DOIs
StatePublished - Apr 2015
Externally publishedYes

Bibliographical note

KAUST Repository Item: Exported on 2020-10-01
Acknowledged KAUST grant number(s): KUS-C1-018-02
Acknowledgements: This material is based on work supported as part of the Energy Materials Center at Cornell, an Energy Frontier Research Center funded by the US Department of Energy, Office of Science, Office of Basic Energy Sciences under Award Number DESC0001086. This work made use of the electrochemical characterization facilities of the KAUST-CU Center for Energy and Sustainability, which is supported by the King Abdullah University of Science and Technology (KAUST) through Award number KUS-C1-018-02. The Cell Fabrication Facility is fully supported by the DOE Vehicle Technologies Program (VTP) within the core funding of the Applied Battery Research (ABR) for Transportation Program. Electron microscopy facilities made use of the Cornell Center for Materials Research Shared Facilities which are supported through the NSF MRSEC program (DMR-1120296).
This publication acknowledges KAUST support, but has no KAUST affiliated authors.

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