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Part of the book series: Springer Theses ((Springer Theses))

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Abstract

The main part of this thesis is divided into several thematic sections. Firstly, the setting up of our PEM-WE testing cell is described (Sect. 3.1) and the way of catalyst loading determination is explained (Sect. 3.2).

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Notes

  1. 1.

    18.2 MΩ cm at 25 ℃ obtained from Merck Direct Q 3 UV purificator.

  2. 2.

    The experimental and measuring conditions of PEM-URFC in FC mode are summed up later in text, in Sect. 3.4.1.

  3. 3.

    Standard gravimetric methods are not ideal due to the very low mass increment after the thin film deposition.

  4. 4.

    All of the PEIS measurements mentioned from this point onward were done keeping the same parameters.

  5. 5.

    When referring to break-in procedure later in the text, we will always mean constant voltage of 1.7 V for duration of 8.5 h.

  6. 6.

    Applying 100 mA steps with 15 s stabilization period. From Sect. 3.3.4 onwards the stepped galvanostatic mode was due to the instrumental reasons (random occurrences of sharp high voltage spikes) replaced by finer stepped potentiostatic mode (applying 5 mV steps with 10 s stabilization period).

  7. 7.

    Certain formulations and figures within Sect. 3.3.4 are taken from already published paper written by Kúš et al. [14].

  8. 8.

    Note that even if not mentioned in text, EDX analysis was routinely carried out on all future samples to confirm homogeneous distribution of elements within.

  9. 9.

    Lower loadings than 0.1 mg cm−2 resulted in undesired discontinuous layers and were not further investigated.

  10. 10.

    This is relevant for simulation of switching on and off of the PEM-WE cell.

  11. 11.

    It is fair to expect that O 1s signal is from iridium oxide and not from the Ti foil since no Ti 2p peaks are visible in the XPS spectra (both before and after the aging procedure).

  12. 12.

    According the literature, the information depths for our SRPES and XPS energies for TiC are approximately 1 nm and 2 nm, respectively [17].

  13. 13.

    The same loading and composition of TiC-based support that was also hot-pressed on anode side of the PEM and then sputtered over by Ir thin film.

  14. 14.

    Certain formulations and figures within Sect. 3.4 are taken from the submitted paper written by Kúš et al. [21].

  15. 15.

    These parameters are kept the same for later measurements of PEM-URFC in FC mode.

  16. 16.

    More details on PEM-FC testing setup can be found in [25].

  17. 17.

    It was the very same sample which was measured in Fig. 53, i.e. 10 nm Pt–Ir on Ti foil.

  18. 18.

    HOPG is a highly pure and ordered form of synthetic graphite with well aligned individual laterally oriented crystallites.

  19. 19.

    Again, miniature leak-free Ag/AgCl (3.4 M KCl) electrode was used as reference; Pt wire as counter electrode.

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Kúš, P. (2019). Results. In: Thin-Film Catalysts for Proton Exchange Membrane Water Electrolyzers and Unitized Regenerative Fuel Cells. Springer Theses. Springer, Cham. https://doi.org/10.1007/978-3-030-20859-2_3

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