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Optimization of the membrane electrode assembly for an alkaline water electrolyser based on the catalyst-coated membrane

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    SYSNO ASEP0557382
    Document TypeJ - Journal Article
    R&D Document TypeJournal Article
    Subsidiary JČlánek ve WOS
    TitleOptimization of the membrane electrode assembly for an alkaline water electrolyser based on the catalyst-coated membrane
    Author(s) Plevová, M. (CZ)
    Hnát, J. (CZ)
    Žitka, Jan (UMCH-V) RID
    Pavlovec, Lukáš (UMCH-V) RID
    Otmar, Miroslav (UMCH-V) RID, ORCID
    Bouzek, K. (CZ)
    Article number231476
    Source TitleJournal of Power Sources. - : Elsevier - ISSN 0378-7753
    Roč. 539, 15 August (2022)
    Number of pages10 s.
    Languageeng - English
    CountryCH - Switzerland
    Keywordsmembrane electrode ; alkaline water electrolyser ; catalyst-coated membrane
    Subject RIVCD - Macromolecular Chemistry
    OECD categoryPolymer science
    Method of publishingOpen access
    Institutional supportUMCH-V - RVO:61389013
    UT WOS000833529800001
    EID SCOPUS85130172266
    DOI10.1016/j.jpowsour.2022.231476
    AnnotationThis study deals with the preparation and characterisation of catalyst-coated membranes for an alkaline water electrolysis process. For this purpose, a chloromethylated anion-selective block copolymer of styrene-ethylene-butylene-styrene with 1,4-diazabicyclo[2.2.2]octane functional groups was used both as an alkaline polymer electrolyte membrane and as an ionomer binder. Non-PGM catalysts (platinum group metals), specifically NiCo2O4 and NiFe2O4, were used on the anode and cathode side of the membrane, respectively. Air-brush deposition or computer-controlled ultrasonic dispersion of the catalytic ink were used to deposit the catalyst layers. The influence of the composition of the catalyst layer on its stability and the resulting electrolysis cell performance was investigated under typical membrane alkaline water electrolysis conditions (1–15 wt.% KOH, 45 °C). The optimal catalyst-to-binder ratio in the catalyst layer was identified as 93/7 using a catalyst loading of 2.5 mg cm-2 on each side of the membrane. The membrane electrode assembly prepared under optimal conditions showed high stability over 140 h at a current density of 250 mA cm-2. At this current load, the cell exhibited a voltage of 2.025 ± 0.010 V. The increase in cell voltage observed during the stability test did not exceed 1 μV h-1.
    WorkplaceInstitute of Macromolecular Chemistry
    ContactEva Čechová, cechova@imc.cas.cz ; Tel.: 296 809 358
    Year of Publishing2023
    Electronic addresshttps://www.sciencedirect.com/science/article/pii/S0378775322004839
Number of the records: 1  

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