4.6 Article

Room Temperature Magnesium Electrodeposition from Glyme-Coordinated Ammonium Amide Electrolytes

Journal

JOURNAL OF THE ELECTROCHEMICAL SOCIETY
Volume 162, Issue 8, Pages D389-D396

Publisher

ELECTROCHEMICAL SOC INC
DOI: 10.1149/2.0731508jes

Keywords

-

Funding

  1. Core Research for Evolutional Science and Technology (CREST) program of Japan Science and Technology Agency (JST)
  2. Japan Society for Promotion of Science (JSPS) [25249106, 15K18253]
  3. Kyoto University Global Frontier Project for Young Professionals (John-Mung Advanced Program)

Ask authors/readers for more resources

We prepared less volatile and halide-free electrolytes for room temperature non-dendritic magnesium (Mg) electrodeposition by mixing a Mg2+-amide-containing ionic liquid (IL) with equimolar glyme (Mg2++IL : glyme = 1:1). Raman spectroscopy suggested that in the equimolar mixture most glyme molecules are coordinated to Mg2+ cations and/or IL cations, which is also supported by a single crystal X-ray diffraction study. The glyme-coordinated IL electrolytes showed sizable redox currents (order of mA cm(-2)), while aging deterioration of electrochemical properties was observed for the triglyme mixture due to partial bath decomposition. The tetraglyme-coordinated IL electrolyte enabled flat electrodeposition of Mg with a metallic luster and showed with very high anodic stability (ca. +4 V vs. Mg) because of decrease in uncoordinated glymes, which can be used for high-voltage Mg ion batteries. (C) The Author( s) 2015. Published by ECS.

Authors

I am an author on this paper
Click your name to claim this paper and add it to your profile.

Reviews

Primary Rating

4.6
Not enough ratings

Secondary Ratings

Novelty
-
Significance
-
Scientific rigor
-
Rate this paper

Recommended

No Data Available
No Data Available