4.8 Article

The Interplay of Al and Mg Speciation in Advanced Mg Battery Electrolyte Solutions

期刊

JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
卷 138, 期 1, 页码 328-337

出版社

AMER CHEMICAL SOC
DOI: 10.1021/jacs.5b10987

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资金

  1. Joint Center for Energy Storage Research, an Energy Innovation Hub - U.S. Department of Energy, Office of Science, Basic Energy Sciences
  2. U.S. Department of Energy [DE-AC02-06CH11357]
  3. St. Elmo Brady Future Faculty Fellowship
  4. National Science Foundation Graduate Research Fellowship [NSF DGE-1144245]

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Mg batteries are an attractive alternative to Li-based energy storage due to the possibility of higher volumetric capacities with the added advantage of using sustainable materials. A promising emerging electrolyte for Mg batteries is the magnesium aluminum chloride complex (MACC) which shows high Mg electrodeposition and stripping efficiencies and relatively high anodic stabilities. As prepared, MACC is inactive with respect to Mg deposition; however, efficient Mg electrodeposition can be achieved following an electrolytic conditioning process. Through the use of Raman spectroscopy, surface enhanced Raman spectroscopy, Al-27 and Cl-35 nuclear magnetic resonance spectroscopy, and pair distribution function analysis, we explore the active vs inactive complexes in the MACC electrolyte and demonstrate the codependence of Al and Mg speciation. These techniques report on significant changes occurring in the bulk speciation of the conditioned electrolyte relative to the as-prepared solution. Analysis shows that the active Mg complex in conditioned MACC is very likely the [Mg-2(mu-Cl)(3)center dot 6THF](+) complex that is observed in the solid state structure. Additionally, conditioning creates free Cl- in the electrolyte solution, and we suggest the free Cl- adsorbs at the electrode surface to enhance Mg electrodeposition.

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