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        <identifier>oai:figshare.com:article/33289713</identifier>
        <datestamp>2026-09-25T16:18:13Z</datestamp>
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          <dc:title>&lt;b&gt;Corrosion Behavior of CeOx-Pd/C HOR Catalyst in Alkaline Electrolyte&lt;/b&gt;</dc:title>
          <dc:creator>Ramesh Kumar Singh (20362386)</dc:creator>
          <dc:creator>Eduardo B. Ferreira (24803953)</dc:creator>
          <dc:creator>Bryan J. Allen (24803957)</dc:creator>
          <dc:creator>Andres O. Godoy (24803977)</dc:creator>
          <dc:creator>Ana C. Alba-Rubio (24803997)</dc:creator>
          <dc:creator>Jasna Jankovic (6899759)</dc:creator>
          <dc:creator>Gregory Jerkiewicz (1659334)</dc:creator>
          <dc:creator>Dario R Dekel (20859466)</dc:creator>
          <dc:subject>Electrochemistry</dc:subject>
          <dc:subject>Nanomaterials</dc:subject>
          <dc:subject>Electroanalytical chemistry</dc:subject>
          <dc:subject>Corrosion, Pd/C and CeOx-Pd/C, aqueous alkaline electrolyte, potentiodynamic polarization</dc:subject>
          <dc:description>&lt;p dir="ltr"&gt;This contribution investigates the corrosion behavior (stability) of CeO&lt;sub&gt;x&lt;/sub&gt;-Pd/C and Pd/C catalysts in 0.10 M aqueous KOH solution saturated with reactive (H&lt;sub&gt;2&lt;/sub&gt; or O&lt;sub&gt;2&lt;/sub&gt;) or neutral (N&lt;sub&gt;2&lt;/sub&gt;) gases using potentiodynamic polarization (PDP). These catalysts are characterized by advanced electron microscopy, and the results demonstrate a uniform distribution of Pd and CeO&lt;sub&gt;x&lt;/sub&gt;-Pd nanoparticles on the carbon support. For comparative analysis, the corrosion parameters, namely the corrosion current and corrosion potential, &lt;i&gt;I&lt;/i&gt;&lt;sub&gt;corr&lt;/sub&gt; and &lt;i&gt;E&lt;/i&gt;&lt;sub&gt;corr&lt;/sub&gt;, are determined in the presence of N&lt;sub&gt;2&lt;/sub&gt;(g) and O&lt;sub&gt;2&lt;/sub&gt;(g) for the CeO&lt;sub&gt;x&lt;/sub&gt;-Pd/C and Pd/C catalysts. An order of magnitude higher&lt;i&gt; I&lt;/i&gt;&lt;sub&gt;corr&lt;/sub&gt; is obtained in the presence of O&lt;sub&gt;2&lt;/sub&gt;(g) as compared to N&lt;sub&gt;2&lt;/sub&gt;(g) in PDP anodic scans. Additionally, lower &lt;i&gt;I&lt;/i&gt;&lt;sub&gt;corr&lt;/sub&gt; values are observed for the CeO&lt;sub&gt;x&lt;/sub&gt;-Pd/C catalysts in anodic scans in the presence of both N&lt;sub&gt;2&lt;/sub&gt;(diss) and O&lt;sub&gt;2&lt;/sub&gt;(diss) as compared to the monometallic Pd/C, thus further highlighting its stability as a promising alkaline hydrogen oxidation reaction catalyst. Determination of &lt;i&gt;I&lt;/i&gt;&lt;sub&gt;corr&lt;/sub&gt; and &lt;i&gt;E&lt;/i&gt;&lt;sub&gt;corr&lt;/sub&gt; in the presence of H&lt;sub&gt;2&lt;/sub&gt;(diss) is challenging due to the significantly high hydrogen oxidation current. Interestingly, cyclic voltammograms recorded before and after the PDP measurements in the three gaseous environments show that the CeO&lt;sub&gt;x&lt;/sub&gt;-Pd/C catalysts demonstrate better stability than Pd/C.&lt;/p&gt;</dc:description>
          <dc:date>2026-09-25T16:18:13Z</dc:date>
          <dc:type>Dataset</dc:type>
          <dc:type>Dataset</dc:type>
          <dc:identifier>10.6084/m9.figshare.33289713.v1</dc:identifier>
          <dc:relation>https://figshare.com/articles/dataset/_b_Corrosion_Behavior_of_CeOx-Pd_C_HOR_Catalyst_in_Alkaline_Electrolyte_b_/33289713</dc:relation>
          <dc:rights>CC BY 4.0</dc:rights>
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