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An ethyl bromofluoroacetate redox mediator enables a robust LiF-rich solid electrolyte interphase for advanced lithium-oxygen batteries
The high charging overpotential and poor stability of the lithium anode severely restrict the development of non-aqueous Li-O 2 batteries. Herein, to overcome both intractable challenges, ethyl bromofluoroacetate (EBFA) is introduced into Li-O 2 batteries as an innovative bifunctional redox mediator...
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Published in: | Journal of materials chemistry. A, Materials for energy and sustainability Materials for energy and sustainability, 2023-08, Vol.11 (32), p.17257-17262 |
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Main Authors: | , , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | The high charging overpotential and poor stability of the lithium anode severely restrict the development of non-aqueous Li-O
2
batteries. Herein, to overcome both intractable challenges, ethyl bromofluoroacetate (EBFA) is introduced into Li-O
2
batteries as an innovative bifunctional redox mediator (RM). Through a particular electrochemical pretreatment method in an argon-filled atmosphere, EBFA reacts on the surface of the lithium anode, leading to the dissociation of Br
−
and F
−
from EBFA molecules. The generated Br
−
acts as the effective component of the RM, considerably reducing the charging overpotential of the Li-O
2
battery. At the same time, a robust LiF-rich solid electrolyte interphase (SEI) is
in situ
formed on the surface of the lithium anode. The formed SEI film, with high lithium-ion conductivity and outstanding stability, significantly protects the lithium anode from the growth of lithium dendrites. Hence, the addition of EBFA in a TEGDME-based non-aqueous electrolyte solution enables a stable Li-O
2
coin battery operation up to 265 cycles.
An ethyl bromofluoroacetate redox mediator has been introduced into lithium-oxygen batteries to achieve high performance in long-term cycling by reducing the charging overpotential and simultaneously forming a LiF-rich SEI film. |
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ISSN: | 2050-7488 2050-7496 |
DOI: | 10.1039/d3ta03451h |