Improving Electrodeposition of Mg through an Open Circuit Potential Hold

被引:21
作者
Esbenshade, Jennifer L. [1 ]
Barile, Christopher J. [1 ]
Fister, Timothy T. [2 ]
Bassett, Kimberly L. [1 ]
Fenter, Paul [2 ]
Nuzzo, Ralph G. [1 ]
Gewirth, Andrew A. [1 ]
机构
[1] Univ Illinois, Dept Chem, Urbana, IL 61801 USA
[2] Argonne Natl Lab, Chem Sci & Engn Div, Argonne, IL 60439 USA
基金
美国国家科学基金会;
关键词
RECHARGEABLE MAGNESIUM BATTERIES; ELECTROLYTE-SOLUTIONS; SECONDARY BATTERIES; DEPOSITION; DISSOLUTION; CHLORIDE; ELECTROCHEMISTRY; CHALLENGE; SPECTROSCOPY; TECHNOLOGY;
D O I
10.1021/acs.jpcc.5b07825
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
We used in situ X-ray diffraction, XPS, SEM, and electrochemical methods to interrogate the mechanism of Mg electrodeposition from PhMgCl/AlCl3 (APC) and EtMgCl electrolytes. An open circuit potential (OCP) pause following Mg deposition led to retained enhancement of Mg deposition and stripping kinetics along with lowered overpotentials for both. In situ X-ray diffraction demonstrated that the OCP pause led to a more polycrystalline deposit relative to that without the pause, while SEM presented micrographs that showed smaller deposits with an OCP hold. The improvement is attributed to an "enhancement layer" that formed on the electrode during the OCP hold. Analysis of XPS data suggests that the "enhancement layer" consists of Mg and Cl retained on the electrode surface, possibly following electrode depassivation.
引用
收藏
页码:23366 / 23372
页数:7
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