Prototype systems for rechargeable magnesium batteries

The thermodynamic properties of magnesium make it a natural choice for use as an anode material in rechargeable batteries, because it may provide a considerably higher energy density than the commonly used lead–acid and nickel–cadmium systems. Moreover, in contrast to lead and cadmium, magnesium is inexpensive, environmentally friendly and safe to handle. But the development of Mg batteries has been hindered by two problems. First, owing to the chemical activity of Mg, only solutions that neither donate nor accept protons are suitable as electrolytes; but most of these solutions allow the growth of passivating surface films, which inhibit any electrochemical reaction. Second, the choice of cathode materials has been limited by the difficulty of intercalating Mg ions in many hosts. Following previous studies of the electrochemistry of Mg electrodes in various non-aqueous solutions, and of a variety of intercalation electrodes, we have now developed rechargeable Mg battery systems that show promise for applications. The systems comprise electrolyte solutions based on Mg organohaloaluminate salts, and MgxMo 3S4 cathodes, into which Mg ions can be intercalated reversibly, and with relatively fast kinetics. We expect that further improvements in the energy density will make these batteries a viable alternative to existing systems.

[1]  D. Aurbach,et al.  On the electrochemical behavior of magnesium electrodes in polar aprotic electrolyte solutions , 1999 .

[2]  C. Liebenow Reversibility of electrochemical magnesium deposition from Grignard solutions , 2013 .

[3]  D. Aurbach,et al.  New insights into the interactions between electrode materials and electrolyte solutions for advanced nonaqueous batteries , 1999 .

[4]  Petr Novák,et al.  Magnesium Insertion Electrodes for Rechargeable Nonaqueous Batteries — A Competitive Alternative to Lithium? , 1999 .

[5]  T. Gregory,et al.  Nonaqueous Electrochemistry of Magnesium Applications to Energy Storage , 1990 .

[6]  O. Brown,et al.  The magnesium and magnesium amalgam electrodes in aprotic organic solvents a kinetic study , 1985 .

[7]  D. Aurbach,et al.  Common Electroanalytical Behavior of Li Intercalation Processes into Graphite and Transition Metal Oxides , 1998 .

[8]  D. Aurbach,et al.  A Study of Lithium Deposition‐Dissolution Processes in a Few Selected Electrolyte Solutions by Electrochemical Quartz Crystal Microbalance , 1998 .

[9]  C. Ritter,et al.  Neutron diffraction study on the crystal structure of lithium intercalated Chevrel phases , 1992 .

[10]  D. Aurbach,et al.  The use of a special work station for in situ measurements of highly reactive electrochemical systems by atomic force and scanning tunneling microscopes , 1999 .

[11]  D. Pletcher,et al.  Studies using microelectrodes of the Mg(II)/Mg couple in tetrahydrofuran and propylene carbonate , 1986 .

[12]  The Application of In Situ FTIR Spectroscopy to the Study of Surface Films Formed on Lithium and Noble Metals at Low Potentials in Li Battery Electrolytes , 1991 .

[13]  D. Aurbach,et al.  Magnesium Deposition and Dissolution Processes in Ethereal Grignard Salt Solutions Using Simultaneous EQCM‐EIS and In Situ FTIR Spectroscopy , 1999 .

[14]  M. Sergent,et al.  Sur de nouvelles phases séléniées ternaires du molybdène , 1971 .

[15]  D. Aurbach,et al.  X-ray photoelectron spectroscopy studies of lithium surfaces prepared in several important electrolyte solutions. A comparison with previous studies by Fourier transform infrared spectroscopy , 1996 .

[16]  G. B. Wood,et al.  Electrodeposition of Metals from Organic Solutions V . Electrodeposition of Magnesium and Magnesium Alloys , 1957 .

[17]  D. Linden Handbook Of Batteries , 2001 .