Room-temperature cycling of metal fluoride electrodes: Liquid electrolytes for high-energy fluoride ion cells

Author:

Davis Victoria K.1ORCID,Bates Christopher M.2ORCID,Omichi Kaoru3ORCID,Savoie Brett M.2ORCID,Momčilović Nebojša2,Xu Qingmin3ORCID,Wolf William J.2,Webb Michael A.2ORCID,Billings Keith J.1ORCID,Chou Nam Hawn3ORCID,Alayoglu Selim4,McKenney Ryan K.3,Darolles Isabelle M.2,Nair Nanditha G.2ORCID,Hightower Adrian2ORCID,Rosenberg Daniel4ORCID,Ahmed Musahid4ORCID,Brooks Christopher J.3ORCID,Miller Thomas F.2ORCID,Grubbs Robert H.2ORCID,Jones Simon C.1ORCID

Affiliation:

1. Electrochemical Technologies Group, Jet Propulsion Laboratory, California Institute of Technology, Pasadena, CA 91109, USA.

2. Division of Chemistry and Chemical Engineering, California Institute of Technology, Pasadena, CA 91125, USA.

3. Honda Research Institute Inc., 1381 Kinnear Road, Suite 116, Columbus, OH 43212, USA.

4. Chemical Sciences Division, Lawrence Berkeley National Laboratory, Berkeley, CA 94720, USA.

Abstract

Working toward fluoride batteries Owing to the low atomic weight of fluorine, rechargeable fluoride-based batteries could offer very high energy density. However, current batteries need to operate at high temperatures that are required for the molten salt electrolytes. Davis et al. push toward batteries that can operate at room temperature, through two advances. One is the development of a room-temperature liquid electrolyte based on a stable tetraalkylammonium salt–fluorinated ether combination. The second is a copper–lanthanum trifluoride core-shell cathode material that demonstrates reversible partial fluorination and defluorination reactions. Science , this issue p. 1144

Funder

National Science Foundation

U.S. Department of Energy

Resnick Sustainability Institute for Science, Energy and Sustainability, California Institute of Technology

Publisher

American Association for the Advancement of Science (AAAS)

Subject

Multidisciplinary

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