“…Moreover, the arc diameter of the cell using MEA-7800 represents charge transfer resistance R ct [18], which is also bigger than that of MEA-0 and MEA-7800 Renewed. The R U and R ct can be obtained through simulation with R U (R 1 Q 1 ) (R ct Q dl ) equivalent circuit [19] and listed in Table 1. As shown in Table 1, both R U and R ct of MEA-7800 (Fig.…”
“…Moreover, the arc diameter of the cell using MEA-7800 represents charge transfer resistance R ct [18], which is also bigger than that of MEA-0 and MEA-7800 Renewed. The R U and R ct can be obtained through simulation with R U (R 1 Q 1 ) (R ct Q dl ) equivalent circuit [19] and listed in Table 1. As shown in Table 1, both R U and R ct of MEA-7800 (Fig.…”
“…It is well know Ru rapidly dissolves to soluble RuO 4 above 1.4 V RHE 39 and that Ru that can be stabilized in Ru-Ir mixtures to yield a more active catalyst than Ir alone. [8][9][10][11][12][13][14] For the following discussion, let it be assumed that the Ir overlayer has particle-like morphology, and particle size equivalent increases with Ir loading. If Ru mixes well with the Ir overlayer, and as a result yields a bigger particle size equivalent for the discontinuous OER catalyst layer, Ru should have a positive effect on durability.…”
Section: F858mentioning
confidence: 99%
“…Figure 1 shows the deposition scheme. It should be stated that the Ir and/or Ru on Pt catalyst material was not deposited as films, as Figure 1 may seem to suggest, but more akin to nanoparticles because of the high roughness factor (10)(11)(12)(13)(14)(15) 21 of NSTF.…”
mentioning
confidence: 99%
“…Ru is thus often mixed with Ir to balance the activity, stability and cost properties of an OER-in-acid catalyst. [8][9][10][11][12][13][14] Therefore the addition of Ru to Ir is performed in this study with the hope of finding similarly durable catalysts with lower Ir loadings. Further motivation to include Ru in this study is the strong possibility that the NSTF support has a stabilizing effect on Ru.…”
Various amounts of Ir (<20 μg cm −2 ) and Ru (up to 12 μg cm −2 ) on a consistent base Pt loading of 85 μg cm −2 , were sputter deposited on a nanostructured thin film catalyst support to mimic a hydrogen fuel cell's cathode catalyst. The nanostructured support was grown on glassy carbon disks designed for a rotating disk electrode, which was used to simulate what happens to a fuel cell cathode during repeated start-up, operation, and shut-down. The testing protocol subjected the catalyst to a minimum potential of 0.65 V RHE and a maximum between 1.53 and 1.8 V RHE . The upper potential was achieved with a galvanostatic hold which is an alternative way to simulate potential transients on the cathode caused by start-up and shut-down. Increasing Ir loading improved the durability of both oxygen reduction reaction (ORR) and oxygen evolution reaction (OER) activity. When combined with Ir, Ru provided no benefit to OER durability except at an Ir loading of 10 μg cm −2 . Ru addition (no Ir present) improved the ORR durability compared to pure Pt. ORR durability was not influenced by Ru addition to Ir-containing samples. In general, ORR durability showed no dependence on Ru loading for all the Ru containing samples and ORR activity was decreased by OER catalyst addition, though more so for Ir than Ru.
“…Fig.3 shows the effects of 0.05 mol L À1 sodium sulfate in anode poisoning for different cathode catalysts. The cell voltages increase by about 0.730 V. Although RuO 2 hydrogen evolution catalyst is insensitive to poisoning by metal ions and suppresses metal ion UPD [16,24], it does not improve the cell performance when sodium ion poisoning. The possible reason is that sodium ion has very negative Nernst potential and can not be reduced at the cathode or precipitate as hydroxides.…”
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