Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
1290616 | Journal of Power Sources | 2008 | 9 Pages |
The structure of lead deposits (approximately 1 mm thick) formed in conditions likely to be met at the negative electrode during the charge/discharge cycling of a soluble lead-acid flow battery is examined. The quality of the lead deposit could be improved by appropriate additives and the preferred additive was shown to be the hexadecyltrimethylammonium cation, C16H33(CH3)3N+, at a concentration of 5 mM. In the presence of this additive, thick layers with acceptable uniformity could be formed over a range of current densities (20–80 mA cm−2) and solution compositions. While electrolyte compositions with lead(II) concentrations in the range 0.1–1.5 M and methanesulfonic acid concentrations in the range 0–2.4 M have been investigated, the best quality deposits are formed at lower concentrations of both species. Surprisingly, the acid concentration was more important than the lead(II) concentration; hence a possible initial electrolyte composition is 1.2 M Pb(II) + 5 mM C16H33(CH3)3N+ without added acid.