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氧化铜相变中的环氧乙烷反应。

Ethylene Epoxidation at the Phase Transition of Copper Oxides.

机构信息

Fritz-Haber-Institut, Max-Planck-Gesellschaft , Faradayweg 4-6, 14195 Berlin, Germany.

出版信息

J Am Chem Soc. 2017 Aug 30;139(34):11825-11832. doi: 10.1021/jacs.7b05004. Epub 2017 Aug 15.

Abstract

Catalytic materials tend to be metastable. When a material becomes metastable close to a thermodynamic phase transition it can exhibit unique catalytic behavior. Using in situ photoemission spectroscopy and online product analysis, we have found that close to the CuO-CuO phase transition there is a boost in activity for a kinetically driven reaction, ethylene epoxidation, giving rise to a 20-fold selectivity enhancement relative to the selectivity observed far from the phase transition. By tuning conditions toward low oxygen chemical potential, this metastable state and the resulting enhanced selectivity can be sustained. Using density functional theory, we find that metastable O precursors to the CuO phase can account for the selectivity enhancements near the phase transition.

摘要

催化材料往往处于亚稳状态。当材料在接近热力学相转变时变得亚稳时,它可能表现出独特的催化行为。我们使用原位光发射谱和在线产物分析发现,在接近 CuO-CuO 相转变时,动力学驱动的反应(乙烯环氧化)的活性增强,导致相对于远在相转变之外观察到的选择性提高了 20 倍。通过向低氧化学势条件下调整条件,可以维持这种亚稳状态和由此产生的增强选择性。使用密度泛函理论,我们发现 CuO 相的亚稳 O 前体可以解释相转变附近的选择性增强。

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