Nano Research

, Volume 2, Issue 9, pp 713–721 | Cite as

Magnesium microspheres and nanospheres: Morphology-controlled synthesis and application in Mg/MnO2 batteries

  • Chunsheng Li
  • Fangyi Cheng
  • Weiqiang Ji
  • Zhanliang Tao
  • Jun ChenEmail author
Open Access
Research Article


In this paper, we report on the morphology-controlled synthesis of magnesium micro/nanospheres and their electrochemical performance as the anode of primary Mg/MnO2 batteries. Mg micro/nanoscale materials with controllable shapes have been prepared via a conventional vapor-transport method under an inert atmosphere by adjusting the deposition temperatures. Extensive analysis techniques including SEM, XRD, TEM/HRTEM, and Brunauer-Emmett-Teller (BET) were carried out to characterize the as-obtained samples. The results show that the Mg samples are microspheres or micro/nanospheres with specific surface areas of 0.61–1.92 m2/g. The electrochemical properties of the as-prepared Mg and commercial Mg powders were further studied in terms of their linear sweep voltammograms, impedance spectra, and discharge capability. By comparing the performance of different inhibitors in electrolytes, it was found that NaNO2 (2.6 mol/L) as an inhibitor in the Mg(NO3)2 (2.6 mol/L) electrolyte affords a Mg electrode with high current density and low corrosion rate. In particular, the Mg sample consisting of microspheres with a diameter of 1.5–3.0 μm and nanospheres with a diameter of 50–150 nm exhibited superior electrode properties including negative initial potential (−1.08 V), high current density (163 mA/cm2), low apparent activation energy (5.1 kJ/mol), and high discharge specific capacity (784 mAh/g). The mixture of Mg nanospheres and microspheres is promising for application in primary Mg/MnO2 batteries because of the sufficient contact with the electrolyte and greatly reduced charge transfer impedance and polarization.


Magnesium micro/nanospheres vapor-transport method primary Mg/MnO2 batteries 

Supplementary material

12274_2009_9075_MOESM1_ESM.pdf (420 kb)
Supplementary material, approximately 340 KB.


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Copyright information

© Tsinghua University Press and Springer Berlin Heidelberg 2009

Authors and Affiliations

  • Chunsheng Li
    • 1
  • Fangyi Cheng
    • 1
  • Weiqiang Ji
    • 1
  • Zhanliang Tao
    • 1
  • Jun Chen
    • 1
    Email author
  1. 1.Institute of New Energy Material Chemistry and Engineering Research Center of Energy Storage and Conversion (Ministry of Education)Nankai UniversityTianjinChina

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