Ternary metal fluorides as high-energy cathodes with low cycling hysteresis
Transition metal fluorides are an appealing alternative to conventional intercalation compounds for use as cathodes in next-generation lithium batteries due to their extremely high capacity (3–4 times greater than the current state-of-the-art). However, issues related to reversibility, energy effici...
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Published in | Nature communications Vol. 6; no. 1; p. 6668 |
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Main Authors | , , , , , , , , |
Format | Journal Article |
Language | English |
Published |
London
Nature Publishing Group UK
26.03.2015
Nature Publishing Group Nature Pub. Group |
Subjects | |
Online Access | Get full text |
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Summary: | Transition metal fluorides are an appealing alternative to conventional intercalation compounds for use as cathodes in next-generation lithium batteries due to their extremely high capacity (3–4 times greater than the current state-of-the-art). However, issues related to reversibility, energy efficiency and kinetics prevent their practical application. Here we report on the synthesis, structural and electrochemical properties of ternary metal fluorides (M
1
y
M
2
1-
y
F
x
: M
1
, M
2
=Fe, Cu), which may overcome these issues. By substituting Cu into the Fe lattice, forming the solid–solution Cu
y
Fe
1-
y
F
2
, reversible Cu and Fe redox reactions are achieved with surprisingly small hysteresis (<150 mV). This finding indicates that cation substitution may provide a new avenue for tailoring key electrochemical properties of conversion electrodes. Although the reversible capacity of Cu conversion fades rapidly, likely due to Cu
+
dissolution, the low hysteresis and high energy suggest that a Cu-based fluoride cathode remains an intriguing candidate for rechargeable lithium batteries.
Transition metal fluorides have high theoretical specific capacities as cathodes for lithium ion batteries, but low working potentials and poor energy efficiency limit their practical applications. Here, the authors report a group of ternary metal fluorides, which may overcome these problems. |
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Bibliography: | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 SC0012704; SC0001060; SC0001294; AC02- 98CH10886 BNL-111520-2015-JA USDOE Office of Science (SC), Basic Energy Sciences (BES) Present address: Department of Materials Science and Engineering, Massachusetts Institute of Technology, Cambridge, Massachusetts 02139, USA Present address: Nuclear Fuel Cycle Process Development Group, Korea Atomic Energy Research Institute, Daejeon 305-353, Republic of Korea |
ISSN: | 2041-1723 2041-1723 |
DOI: | 10.1038/ncomms7668 |