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Rational syntheses of core-shell Fex@Pt nanoparticles for the study of electrocatalytic oxygen reduction reaction

机译:用于电催化氧还原反应研究的核-壳Fex @ Pt纳米粒子的合理合成

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摘要

We report on the syntheses of core-shell Fex@Pt (x = 0.4–1.2) nanoparticles (NPs) with Pt-shell thickness systematically controlled while the overall particle size is constant. The syntheses were achieved via one-pot ultrasound-assisted polyol synthesis (UPS) reactions. Fe1.2@Pt showed a record-breaking high core-element content (55 at%) of core-shell NPs. Based on observations from a series of control experiments, we propose a mechanism of the NPs' formation that enables control of shell thickness in UPS reactions. Fex@Pt NPs showed drastic enhancements in mass and specific activity for oxygen reduction reaction (ORR) and significantly enhanced durability compared to commercial Pt NPs. Fex@Pt with a 1 (monolayer) ML Pt shell showed the highest activity. The ab initio density functional theory calculations on the binding energies of oxygen species on the surfaces of Fex@Pt NPs showed that the 1 ML case is most favourable for the ORR, and in good agreement with the experimental results.
机译:我们报告了核-壳Fex @ Pt(x = 0.4-1.2)纳米粒子(NPs)的合成,其中Pt-壳的厚度受到系统控制,而总粒径恒定。合成是通过一锅超声辅助多元醇合成(UPS)反应完成的。 Fe1.2@Pt显示出核壳NP的高核元素含量(55 at%)破记录。基于一系列控制实验的观察结果,我们提出了NP形成的机制,该机制可以控制UPS反应中的壳厚度。与商用Pt NP相比,Fex @ Pt NPs的质量和氧还原反应(ORR)的比活度显着提高,并且耐久性大大提高。具有1个(单层)ML Pt壳的Fex @ Pt表现出最高的活性。从头算密度泛函理论对Fex @ Pt NPs表面氧原子结合能的计算表明,1 ML情况最适合ORR,与实验结果吻合良好。

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