Solvation sheath reorganization enables divalent metal batteries with fast interfacial charge transfer kinetics

Author:

Hou Singyuk1ORCID,Ji Xiao1ORCID,Gaskell Karen2ORCID,Wang Peng-fei1ORCID,Wang Luning2ORCID,Xu Jijian1ORCID,Sun Ruimin1ORCID,Borodin Oleg3ORCID,Wang Chunsheng1ORCID

Affiliation:

1. Department of Chemical and Biomolecular Engineering, University of Maryland, College Park, MD 20740, USA.

2. Department of Chemistry and Biochemistry, University of Maryland, College Park, MD 20742, USA.

3. Battery Science Branch, Sensors and Electron Devices Directorate, US Army Combat Capabilities Development Command Army Research Laboratory, Adelphi, MD 20783, USA.

Abstract

Efficient, rechargeable Mg and Ca batteries Divalent rechargeable metal batteries such as those based on magnesium and calcium are of interest because of the abundance of these elements and their lower tendency to form dendrites, but practical demonstrations are lacking. Hou et al . used methoxyethyl amine chelants in which the ligands attach to the metal atom in more than one place, modulating the solvation structure of the metal ions to enable a facile charge-transfer reaction (see the Perspective by Zuo and Yin). In full battery cells, these components lead to high efficiency and energy density. Theoretical calculations were used to understand the solvation structures. —MSL

Publisher

American Association for the Advancement of Science (AAAS)

Subject

Multidisciplinary

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