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Investigations under real operating conditions of the electrochemical promotion by O2 temperature programmed desorption measurements

机译:O2 程序升温脱附测量在电化学促进实际操作条件下的研究

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The origin of the electrochemical promotion of catalysis (EPOC) was investigated via oxygen temperature-programmed desorption (O2-TPD) from a polycrystalline Pt film interfaced with YSZ. TPD experiments were carried out under operating conditions similar to those used for catalytic activity measurements. This study has clearly shown that an anodic current generates the migration of “backspillover” ionic oxygen species from YSZ toward the Pt surface. These ionic species act as promoters and enable the formation of weakly adsorbed oxygen species coming from the gas phase which are more reactive and thus responsible for the activity enhancement. The effect of polarization is to carry or to remove the promoting ionic species on the Pt surface. Therefore, electrochemical promotion of catalysis can be considered as an electrically controlled metal support interaction, where the support is an O2? conducting solid electrolyte.
机译:通过氧温度程序解吸(O2 -TPD)从与YSZ接触的多晶Pt膜中研究了电化学促进催化作用(EPOC)的起源。 TPD实验是在类似于催化活性测量的操作条件下进行的。这项研究清楚地表明,阳极电流会导致“后溢”离子氧从YSZ向Pt表面迁移。这些离子物质起促进剂的作用,并使得能够形成来自气相的弱吸附氧物质,这些氧原子更具反应性,因此有助于提高活性。极化作用是在Pt表面携带或去除促进性离子物质。因此,催化的电化学促进可以认为是电控制的金属载体相互作用,其中载体是O 2传导固体电解质。

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