Ternary metal fluorides as high-energy cathodes with low cycling hysteresis

Feng Wang(Brookhaven National Laboratory), Sung‐Wook Kim(Brookhaven National Laboratory), Dong‐Hwa Seo(Seoul National University), Kisuk Kang(Seoul National University), Liping Wang(Brookhaven National Laboratory), Dong Su(Brookhaven National Laboratory), John J. Vajo(HRL Laboratories (United States)), John Wang(HRL Laboratories (United States)), Jason Graetz(HRL Laboratories (United States))
Nature Communications
March 26, 2015
Cited by 182Open Access
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Abstract

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)yM(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.


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