Ultra-thin order–disorder CeO2 nanobelts as the non-carbon support of the PtCu catalyst towards methanol oxidation and oxygen reduction reactions†

Han Zhi, Boda Dong, Xingxing Guo and Feng Xu
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Abstract

The use of carbon supports in direct methanol fuel cells easily leads to the shedding and poisoning of the Pt catalyst and hence the decrease of catalytic activity. Non-carbon materials have been studied to enhance the metal–support interaction and the catalytic performance. Herein, we explored ultra-thin CeO2 nanobelts (2D-CeO2) with the order–disorder structure as the support of the PtCu catalyst. PtCu/2D-CeO2 shows the highest current density of 37.24 mA cm−2 toward the methanol oxidation reaction (MOR), and a limiting current density of 4.82 mA cm−2 towards the oxygen reduction reaction. The order–disorder structure of 2D-CeO2 generates a high volume of oxygen vacancies and strong metal–support interaction. The Pt0 proportion of PtCu/2D-CeO2 is much higher than that of PtCu/C which increases the active sites. The d-band center of PtCu is lowered which facilitates the adsorption and dissociation of reactants, thereby dramatically boosting the electro-catalytic performance.

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超薄有序异序 CeO2 纳米颗粒作为 PtCu 催化剂的非碳载体,用于甲醇氧化和氧还原反应†。
在直接甲醇燃料电池中使用碳载体容易导致铂催化剂脱落和中毒,从而降低催化活性。为了增强金属与支撑物之间的相互作用并提高催化性能,人们对非碳材料进行了研究。在此,我们探索了具有有序-无序结构的超薄 CeO2 纳米颗粒(2D-CeO2)作为铂铜催化剂的载体。PtCu/2D-CeO2 在甲醇氧化反应(MOR)中的最高电流密度为 37.24 mA cm-2,在氧还原反应中的极限电流密度为 4.82 mA cm-2。二维-CeO2 的有序-无序结构产生了大量的氧空位和强烈的金属-支撑相互作用。PtCu/2D-CeO2 的 Pt0 比例远高于 PtCu/C,从而增加了活性位点。PtCu 的 d 带中心降低,有利于反应物的吸附和解离,从而显著提高了电催化性能。
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