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Prototype systems for rechargeable magnesium batteries

Abstract

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 reaction1,2,3. Second, the choice of cathode materials has been limited by the difficulty of intercalating Mg ions in many hosts4. Following previous studies of the electrochemistry of Mg electrodes in various non-aqueous solutions1,5, and of a variety of intercalation electrodes6,7, we have now developed rechargeable Mg battery systems that show promise for applications. The systems comprise electrolyte solutions based on Mg organohaloaluminate salts, and MgxMo3S4 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.

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Figure 1: Comparison of cyclic voltammograms of electrolyte solutions in which magnesium can be deposited reversibly.
Figure 2: Results of typical galvanostatic EQCM experiments of Mg deposition–dissolution cycles with gold/quartz electrodes13.
Figure 3: Typical electrochemical behaviour and the basic structure of the MgxMo3S4 cathodes, 0 < x <1, corresponding to a maximal charge capacity of 122 mA h g-1.
Figure 4: Performance of rechargeable Mg–MgxMo3S4 coin-cell batteries during cycling at constant currents (0.2–0.3 mA cm-2).

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References

  1. Lu, Z., Schechter, A., Moshkovich, M. & Aurbach, D. On the electroanalytical behavior of magnesium in a polar aprotic electrolyte solution. J. Electroanal. Chem. 466, 203 –217 (1999).

    Article  CAS  Google Scholar 

  2. Gendler, J. D. & Pletcher, D. Studies using microelectrodes of the Mg(++)/Mg couple in tetrahydrofurane and propylene carbonate. J. Electroanal. Chem. 199, 93– 100 (1986).

    Article  Google Scholar 

  3. Brown, O. R. & McIntyre, R. The magnesium and magnesium amalgam electrodes in aprotic organic solvents. A kinetic study. Electrochim. Acta 30, 627–633 ( 1985).

    Article  CAS  Google Scholar 

  4. Novak, P., Tuhof, R. & Haas, O. Magnesium insertion electrodes of rechargeable nonaqueous batteries. A competitive alternative to lithium? Electrochim. Acta 45, 351–367 (1999).

    Article  CAS  Google Scholar 

  5. Aurbach, D., Moshkovich, M., Schechter, A. & Turgeman, R. The study of magnesium deposition and dissolution processes in ethereal Grignard salt solution using simultaneous EQCM-EIS and in situ FTIR spectroscopic measurements. Electrochem. Solid State Lett. 3, 31–34 (2000).

    Article  CAS  Google Scholar 

  6. Aurbach, D. et al. Common electroanalytical behavior of Li intercalation processes into graphite and transition metal oxides. J. Electrochem. Soc. 145, 3024–3034 ( 1998).

    Article  CAS  Google Scholar 

  7. Aurbach, D. et al. New insights into the interactions between electrode materials and electrolyte solutions for advanced nonaqueous batteries. J. Power Sources 81–82, 95–111 (1999).

    Article  Google Scholar 

  8. Connor, J. H., Reid, W. E. & Wood, G. B. Electrodeposition of metals from organic solutions: electrodeposition of magnesium and magnesium alloys. J. Electrochem. Soc. 104, 38–41 ( 1957).

    Article  CAS  Google Scholar 

  9. Liebenow, C. Reversibility of electrochemical magnesium deposition from Grignard salt solutions. J. Appl. Chem. 27, 221– 225 (1997).

    CAS  Google Scholar 

  10. Gregory, T., Hoffman, R. & Winterton, R. Nonaqueous electrochemistry of magnesium. Application to energy storage. J. Electrochem. Soc. 137, 775–780 (1990).

    Article  CAS  Google Scholar 

  11. Blomgren, J. in Nonaqueous Electrochemistry Ch. 2 (ed. Aurbach, D.) 53– 79 (Dekker, New York, 1999).

    Google Scholar 

  12. Aurbach, D. & Moshkovich, M. The study of Li deposition-dissolution processes in a few selected electrolyte solutions by electrochemical quartz crystal microbalance (EQCM). J. Electrochem. Soc. 145 , 2629–2639 (1998).

    Article  CAS  Google Scholar 

  13. Aurbach, D., Goren, E. & Chusid, O. The application of in situ FTIR spectroscopy to the study of surface films formed on lithium and noble metal at low potentials in Li battery electrolytes. J. Electrochem. Soc. 138, L6–L9 (1991).

    Article  Google Scholar 

  14. Aurbach, D., Weissman, I., Schechter, A. & Cohen, H. XPS studies of Li surfaces prepared in several important electrolyte solutions. A comparison with previous studies by FTIR spectroscopy. Langmuir 12, 3991–4007 ( 1996).

    Article  CAS  Google Scholar 

  15. Cohen, Y. & Aurbach, D. The use of a special work station for in situ measurements of highly reactive electrochemical systems by atomic force and scanning tunneling microscopes (AFM, STM). Rev. Sci. Instrum. 70, 4668–4675 (1999).

    Article  ADS  CAS  Google Scholar 

  16. Yvon, K. in Current Topics in Material Science Vol. 3 (ed. Kaldis, E.) 53–129 (North-Holland, Amsterdam, 1979).

    Google Scholar 

  17. Chevrel, R., Sergent, M. & Prigent, J. Sur le nouvelles phases sulfurèes ternaires du Molybdène. J. Solid State Chem. 3, 515–519 (1971).

    Article  ADS  CAS  Google Scholar 

  18. Ritter, C., Gocke, E., Fischer, C. & Schollhorn, R. Neutron diffraction study of the crystal structure of lithium intercalated Chevrel phases. Mater. Res. Bull. 27, 1217–1225 (1992).

    Article  CAS  Google Scholar 

  19. Linden, D. in Handbook of Batteries 2nd edn Ch. 23 (ed. Linden, D.) 23.3– 23.22 (McGraw Hill, New York, 1994).

    Google Scholar 

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Acknowledgements

This work was partially supported by Advance Technology Upgrading (ATU) Ltd, Israel.

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Aurbach, D., Lu, Z., Schechter, A. et al. Prototype systems for rechargeable magnesium batteries. Nature 407, 724–727 (2000). https://doi.org/10.1038/35037553

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