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Updated: Oct 17, 2025

In Situ Neutron Powder Diffraction Using Custom-made Lithium-ion Batteries
Published on: November 10, 2014
Solvation sheath reorganization enables divalent metal batteries with fast interfacial charge transfer kinetics
Singyuk Hou1, Xiao Ji1, Karen Gaskell2
1Department of Chemical and Biomolecular Engineering, University of Maryland, College Park, MD 20740, USA.
Abstract:
Rechargeable magnesium and calcium metal batteries (RMBs and RCBs) are promising alternatives to lithium-ion batteries because of the high crustal abundance and capacity of magnesium and calcium. Yet, they are plagued by sluggish kinetics and parasitic reactions. We found a family of methoxyethyl-amine chelants that greatly promote interfacial charge transfer kinetics and suppress side reactions on both the cathode and metal anode through solvation sheath reorganization, thus enabling stable and highly reversible cycling of the RMB and RCB full cells with energy densities of 412 and 471 watt-hours per kilogram, respectively. This work provides a versatile electrolyte design strategy for divalent metal batteries.
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