Evaluation of carbon composite materials for the negative electrode in the zinc-cerium redox flow cell

被引:48
作者
Nikiforidis, Georgios [1 ]
Berlouis, Leonard [1 ]
Hall, David [2 ]
Hodgson, David [2 ]
机构
[1] Univ Strathclyde, Dept Pure & Appl Chem, WestCHEM, Glasgow G1 1XL, Lanark, Scotland
[2] Plurion Ltd, Glenrothes KY6 2TF, Fife, Scotland
关键词
Redox flow batteries; Zinc-cerium; Carbon substrates; Methane sulfonic acid; BATTERY;
D O I
10.1016/j.jpowsour.2011.01.036
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
An investigation into the suitability of three carbon composites as substrates for the negative electrode in the zinc-cerium redox flow cell has been carried out. The composite electrodes examined comprised the use of polyvinylidene fluoride (PVDF) and high density polyethylene (HDPE) as binders for the carbon and the third was a graphite foil electrode of similar to 1 mm thickness. The zinc deposition process was carried out in a methane sulfonic acid (MSA) electrolyte at 60 degrees C and nucleation studies revealed the growth of the deposits to be instantaneous in this medium. Galvanostatic charge/discharge cycles were performed in order to test the performance of these composite materials under a variety of operating conditions. For all the materials, the highest charge/discharge coulombic efficiencies (similar to 95%) were found for the highest discharge current densities (200 mA cm(-2)) employed in the study but this falls as the charge period is increased. The effect of solution flow velocity is however less clear. Prolonged zinc charging-discharging cycling on the composite materials revealed that whereas the PVDF-based electrode exhibited no loss in efficiency with cycling (>250), a drastic reduction was observed for the HOPE-based and graphite foil electrodes beyond 70 cycles and this was accompanied by the physical deterioration in the electrode surface. (C) 2011 Elsevier B.V. All rights reserved.
引用
收藏
页码:497 / 503
页数:7
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