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Enhanced Carbon Dioxide Electroreduction to Carbon Monoxide over Defect-Rich Plasma-Activated Silver Catalysts

机译:在富含缺陷的等离子体活化银催化剂上增强二氧化碳对一氧化碳的电还原

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摘要

Efficient, stable catalysts with high selectivity for a single product are essential if electroreduction of CO is to become a viable route to the synthesis of industrial feedstocks and fuels. A plasma oxidation pre-treatment of silver foil enhances the number of low-coordinated catalytically active sites, which dramatically lowers the overpotential and increases the activity of CO electroreduction to CO. At −0.6 V versus RHE more than 90% Faradaic efficiency towards CO was achieved on a pre-oxidized silver foil. While transmission electron microscopy (TEM) and operando X-ray absorption spectroscopy showed that oxygen species can survive in the bulk of the catalyst during the reaction, quasi in situ X-ray photoelectron spectroscopy showed that the surface is metallic under reaction conditions. DFT calculations reveal that the defect-rich surface of the plasma-oxidized silver foils in the presence of local electric fields drastically decrease the overpotential of CO electroreduction.
机译:如果要使CO的电还原成为合成工业原料和燃料的可行途径,则对单一产品具有高选择性的高效,稳定的催化剂至关重要。银箔的等离子体氧化预处理可增加低配位催化活性位的数量,从而显着降低过电势并增加CO还原成CO的活性。在-0.6 V相对RHE时,法拉第对CO的效率超过90%,在预氧化的银箔上实现。透射电子显微镜(TEM)和操作X射线吸收光谱法表明,在反应过程中氧可以在大部分催化剂中幸存,而准原位X射线光电子光谱法则表明在反应条件下表面是金属的。 DFT计算表明,在存在局部电场的情况下,等离子氧化银箔的富缺陷表面会大大降低CO电解的过电势。

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