LAUSR.org creates dashboard-style pages of related content for over 1.5 million academic articles. Sign Up to like articles & get recommendations!

Enhanced reversibility of the electrochemical Li conversion reaction with MgH2–TiH2 nanocomposites

Photo from wikipedia

Abstract Nanostructured metallic hydrides are promising anode active materials for the next generations of Li-ion batteries due to their high capacities, adapted working potential and low polarisation. In the present… Click to show full abstract

Abstract Nanostructured metallic hydrides are promising anode active materials for the next generations of Li-ion batteries due to their high capacities, adapted working potential and low polarisation. In the present study, nanocomposites made of y MgH 2 and (1 −  y )TiH 2 with molar composition y  = 0.2, 0.5 and 0.8 were prepared by mechanical milling of elemental metal powders under hydrogen pressure. Microstructural analysis by X-ray Diffraction (XRD) and Transmission Electron Microscopy (TEM) shows the co-existence of the two hydrides at the nanoscale with average crystallite sizes comprised between 4 and 11 nm. Galvanostatic and cyclic voltammetry experiments have been performed to investigate the reversibility of the conversion reaction between both hydrides and lithium. All nanocomposites can be fully lithiated for the first discharge, but the reversibility of the reaction strongly depends on the composition. No reformation of any hydride occurs for the TiH 2 -rich composite ( y  = 0.2), TiH 2 is only partially reformed for the equimolar composite ( y  = 0.5) and both MgH 2 and TiH 2 hydrides are recovered at different extents for the Mg-rich one ( y  = 0.8). A high reversibility (almost 80%) of TiH 2 is attained in the latter composite with a promising capacity retention (70% over ten cycles) by cycling within a restricted potential window.

Keywords: reversibility; conversion reaction; reversibility electrochemical; enhanced reversibility; reaction

Journal Title: International Journal of Hydrogen Energy
Year Published: 2017

Link to full text (if available)


Share on Social Media:                               Sign Up to like & get
recommendations!

Related content

More Information              News              Social Media              Video              Recommended



                Click one of the above tabs to view related content.