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@ARTICLE{Weinrich:906938,
author = {Weinrich, Henning and Pleie, Jan and Schmid, Bernhard and
Tempel, Hermann and Kungl, Hans and Eichel, Rüdiger-A.},
title = {{I}n {S}itu {H}ydrogen {E}volution {M}onitoring {D}uring
the {E}lectrochemical {F}ormation and {C}ycling of
{P}ressed‐{P}late {C}arbonyl {I}ron {E}lectrodes in
{A}lkaline {E}lectrolyte},
journal = {Batteries $\&$ Supercaps},
volume = {5},
issn = {2566-6223},
address = {Weinheim},
publisher = {Wiley-VCH},
reportid = {FZJ-2022-01763},
pages = {e202100415},
year = {2022},
abstract = {The hydrogen evolution reaction (HER) on iron is a
parasitic side reaction for the reduction of iron
(hydr)oxide in alkaline electrolyte, which lowers the
Coulombic efficiency of iron-based batteries. Tackling this
issue, here we investigate the HER on iron electrodes by
in situ gas chromatography, allowing for a quantitative
correlation of the applied electrode potential and the
resulting hydrogen evolution. As a result, it is shown that
the HER follows a distinctive profile corresponding to the
electrode potential and changes depending on the state of
the iron electrode formation. Moreover, it is shown that the
charging efficiency of the iron electrode can be increased
by an alteration of the charging procedure, i. e., a more
negative cut-off potential for the discharge and a potential
limitation for the recharge. In this study, a charging
efficiency of $96.7 \%$ is achieved, using an optimized
charging procedure for a formed carbonyl iron electrode
containing $8.5 wt.\%$ of Bi2S3.},
cin = {IEK-9},
ddc = {620},
cid = {I:(DE-Juel1)IEK-9-20110218},
pnm = {1223 - Batteries in Application (POF4-122)},
pid = {G:(DE-HGF)POF4-1223},
typ = {PUB:(DE-HGF)16},
UT = {WOS:000761131000001},
doi = {10.1002/batt.202100415},
url = {https://juser.fz-juelich.de/record/906938},
}