dc.contributor.author
Schneider, Jonathan
dc.date.accessioned
2023-10-11T09:49:38Z
dc.date.available
2023-10-11T09:49:38Z
dc.identifier.uri
https://refubium.fu-berlin.de/handle/fub188/39906
dc.identifier.uri
http://dx.doi.org/10.17169/refubium-39628
dc.description.abstract
Vanadium redox-flow batteries (VRFBs) are emerging as promising systems
for large-scale energy storage. Yet, certain key aspects require for substantial
improvements in order to achieve broad commercial success of this technology.
In that respect, further development of electrode materials in terms of increased
and durable electrocatalytic activity is of essence, especially in the negative
half cell. Myriads of approaches for surface modification of the predominantly
employed macroporous carbons have thus been proposed so far. However, upon
thorough review of pre-existing literature, it became evident that meaningfully
benchmarking and quantifying the effects of those procedures with regard to
resulting performance enhancement is anything but a straightforward task. The
emphasis of this thesis was therefore put on establishing methodical approaches
for reliable and unambiguous quantification of electrode kinetics by properly
utilizing electrochemical techniques, predominantly electrochemical impedance
spectroscopy (EIS), and exploiting their full capabilities.
In an exemplary study on bismuth-modified carbon felt electrodes it was demonstrated how applying proper normalization to ex-situ impedance data enables
thorough characterization and standardized comparison of electrocatalytic effects induced by incorporation of metal (oxide) particles or any other type
of supposedly activating treatment. Intrinsic catalytic activity of Bi for the
V(II)/V(III) redox reaction has been verified and stability of modified electrodes
was assessed for the first time. By eliminating the often misleading impact
of electrode wetting, reproducibility of obtained results was greatly enhanced
compared to other approaches commonly pursued in the open literature.
Subsequently, the innovative concept of distribution of relaxation times (DRT)
analysis was introduced to the field of in-situ examination of VRFB cells. Loss
processes during operation of the battery have been unraveled before proving
the feasibility of DRT-based monitoring of electrode ageing. Gained insights
underline the importance of keeping future research focused on the negative
half cell electrode, at least in terms of electrocatalysis and degradation.
Further investigations explored how synergistic use of additional techniques
may complement the experimental capabilities of EIS to determine electrode
characteristics in the most comprehensive way. This involved unequivocal separation of respective current contributions from V(III) -reduction and parasitic
hydrogen evolution reaction (HER) at planar model electrodes during rotating
ring-disc electrode (RRDE) and alternating current cyclic voltammetry (ACCV)
measurements as well as visualization of bismuth dissolution and redeposition
in an operating VRFB by utilization of X-ray-based imaging procedures.
en
dc.format.extent
XI, 140 Seiten
dc.rights.uri
http://www.fu-berlin.de/sites/refubium/rechtliches/Nutzungsbedingungen
dc.subject
impedance spectroscopy
en
dc.subject
electrode degradation
en
dc.subject.ddc
500 Naturwissenschaften und Mathematik::540 Chemie::541 Physikalische Chemie
dc.title
Electrochemical impedance spectroscopy for the study of catalysis and electrode degradation in vanadium redox-flow batteries
dc.contributor.gender
male
dc.contributor.firstReferee
Roth, Christina
dc.contributor.furtherReferee
Paulus, Beate
dc.date.accepted
2023-03-31
dc.identifier.urn
urn:nbn:de:kobv:188-refubium-39906-9
refubium.affiliation
Biologie, Chemie, Pharmazie
dcterms.accessRights.dnb
free
dcterms.accessRights.openaire
open access