dc.contributor.author |
SundarRajan, A. |
|
dc.contributor.author |
Ravikumar, M. |
|
dc.contributor.author |
Priolkar, K.R. |
|
dc.contributor.author |
Sampath, S. |
|
dc.contributor.author |
Shukla, A.K. |
|
dc.date.accessioned |
2015-09-29T06:49:27Z |
|
dc.date.available |
2015-09-29T06:49:27Z |
|
dc.date.issued |
2015 |
|
dc.identifier.citation |
Electrochemical Energy Technology. 1(1); 2015; 2-9. |
en_US |
dc.identifier.uri |
http://dx.doi.org/10.2478/eetech-2014-0002 |
|
dc.identifier.uri |
http://irgu.unigoa.ac.in/drs/handle/unigoa/4091 |
|
dc.description.abstract |
Nickel-iron and iron-air batteries are attractive for large-scale-electrical-energy storage because iron is abundant, low-cost and non-toxic. However, these batteries suffer from poor charge acceptance due to hydrogen evolution during charging. In this study, we have demonstrated iron electrodes prepared from carbonyl iron powder (CIP) that are capable of delivering a specific discharge capacity of about 400 mAh g-1 at a current density of 100 mA g-1 with a faradaic efficiency of about 80 percent. The specific capacity of the electrodes increases gradually during formation cycles and reaches a maximum in the 180th cycle. The slow increase in the specific capacity is attributed to the low surface area and limited porosity of the pristine CIP. Evolution of charge potential profiles is investigated to understand the extent of charge acceptance during formation cycles. In situ XRD pattern for the electrodes subsequent to 300 charge/discharge cycles confirms the presence of Fe with Fe(OH)2 as dominant phase. |
en_US |
dc.subject |
Physics |
en_US |
dc.title |
Carbonyl-iron electrodes for rechargeable-iron batteries |
en_US |
dc.type |
Journal article |
en_US |