4.6 Article

Performance modulation through selective, homogenous surface doping of lanthanum strontium ferrite electrodes revealed by in situ PLD impedance measurements

期刊

JOURNAL OF MATERIALS CHEMISTRY A
卷 10, 期 6, 页码 2973-2986

出版社

ROYAL SOC CHEMISTRY
DOI: 10.1039/d1ta08634k

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资金

  1. Austrian Sciene Fund (FWF) [P31165 - N37, P31654]
  2. European Research Council (ERC) under the European Union's Horizon 2020 research and innovation programme [755 744]
  3. K1-COMET center CEST (Centre for Electrochemical Surface Technology, Wiener Neustadt) - Austrian Research Promotion Agency (FFG) [865 864]
  4. Austrian Science Fund (FWF) [P31654] Funding Source: Austrian Science Fund (FWF)

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The addition of minor amounts of Pt into LSF thin film electrodes has been found to improve their oxygen exchange performance, with even a 5 nm layer of Pt doped LSF showing a 2.5-fold increase in polarization resistance. In situ impedance measurements were conducted to compare the p(O-2) and temperature dependent impedance properties of pure and Pt doped LSF, leading to the conclusion that Pt4+ introduces additional active sites.
Accelerating the oxygen reduction kinetics of solid oxide fuel cell (SOFC) cathodes is crucial to improve their efficiency and thus to provide the basis for an economically feasible application of intermediate temperature SOFCs. In this work, minor amounts of Pt were doped into lanthanum strontium ferrite (LSF) thin film electrodes to modulate the material's oxygen exchange performance. Surprisingly, Pt was found to be incorporated on the B-site of the perovskite electrode as non metallic Pt4+. The polarization resistance of LSF thin film electrodes with and without additional Pt surface doping was compared directly after film growth employing in situ electrochemical impedance spectroscopy inside a PLD chamber (i-PLD). This technique enables observation of the polarization resistance of pristine electrodes unaltered by degradation or any external contamination of the electrode surface. Moreover, growth of multi-layers of materials with different compositions on the very same single crystalline electrolyte substrate combined with in situ impedance measurements allow excellent comparability of different materials. Even a 5 nm layer of Pt doped LSF (1.5 at% Pt), i.e. a Pt loading of 80 ng cm(-2), improved the polarization resistance by a factor of about 2.5. In addition, p(O-2) and temperature dependent impedance measurements on both pure and Pt doped LSF were performed in situ and obtained similar activation energies and p(O-2) dependence of the polarization resistance, which allow us to make far reaching mechanistic conclusions indicating that Pt4+ introduces additional active sites.

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