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The mechanism of highly selective PROX reaction of CO deduced from the dynamics of intermediates: Oxidation of CO via HCOO with OH

机译:由中间体动力学推导的CO的高选择性PROX反应机理:通过HCOO与OH氧化CO

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Introduction Oxidation of CO on our developed FeOx/Pt/TiO2 catalyst was markedly enhanced by H2O, and the enhancement by H2O and D2O showed an isotope effect. The selective oxidation of CO enhanced by H2O is difficult to explain by the traditional competitive reaction mechanism of CO (a) and H(a) with O(a). The dynamics of the intermediates studied by in-situ DRIFT-IR spectroscopy proved that the oxidation of CO occurs via HCOO intermediate with OH, which is responsible for the highly selective low temperature preferential oxidation (PROX) reaction of CO on the FeOx/Pt/TiO2 catalyst.
机译:简介在我们开发的FeOx / Pt / TiO2催化剂上,CO的氧化显着增强了H2O,而H2O和D2O的增强表现出了同位素效应。传统的CO(a)和H(a)与O(a)的竞争反应机理很难解释H2O增强的CO的选择性氧化。原位DRIFT-IR光谱研究的中间体动力学表明,CO的氧化是通过HCOO中间体与OH发生的,这是CO在FeOx / Pt /上的高选择性低温优先氧化(PROX)反应的原因。 TiO2催化剂。

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