Intercalation behaviour of magnesium into natural graphite using organic electrolyte systems

被引:32
作者
God, C. [1 ]
Bitschnau, B. [2 ]
Kapper, K. [1 ]
Lenardt, C. [1 ]
Schmuck, M. [1 ]
Mautner, F. [2 ]
Koller, S. [1 ]
机构
[1] VARTA Micro Innovat GmbH, Stremayrgasse 9, A-8010 Graz, Austria
[2] Graz Univ Technol, Inst Phys & Theoret Chem, Stremayrgasse 9, A-8010 Graz, Austria
关键词
ION BATTERIES; ANODE; MG; CONDUCTIVITY; PERFORMANCE; SOLVATION; ALKALI; METAL;
D O I
10.1039/c6ra28300d
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The focus of this study is on the investigation of electrochemical intercalation and deintercalation behaviour of Mg2+ into natural graphite electrodes in organic electrolyte. We used as a conductive salt magnesium bis(trifluoromethylsulfonyl)imide (Mg(TFSI)(2)) dissolved in N,N-dimethylformamide (DMF) as organic solvent. By utilization of conductivity measurements within a broad temperature range (-20 degrees C to + 60 degrees C), a conductivity maximum is to be found at a concentration of 0.5 M for all temperatures. Thus, in this study all electrochemical investigations dealing with magnesiation of graphite anodes are made with the electrolyte system 0.5 M Mg(TFSI)(2)/DMF. In three electrode cells (Swagelok(C) T-cells) we obtain cathodic and anodic currents, which are highly reversible and last for more than 100 cycles showing a coulombic efficiency above 98%. SEM images reveal a non-destructive intercalation of cationic species into graphite and the formation of a magnesiated graphite intercalation compound is confirmed by ex situ XRD diffraction measurements.
引用
收藏
页码:14168 / 14175
页数:8
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