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首页> 外文期刊>Applied Catalysis, B. Environmental: An International Journal Devoted to Catalytic Science and Its Applications >Core-shell Pt modified Pd/C as an active and durable electrocatalyst for the oxygen reduction reaction in PEMFCs
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Core-shell Pt modified Pd/C as an active and durable electrocatalyst for the oxygen reduction reaction in PEMFCs

机译:核-壳Pt修饰的Pd / C作为PEMFC中氧还原反应的活性持久电催化剂

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摘要

A series of Pt modified Pd/C catalysts (Pt/Pd/C) with different Pt/Pd molar ratio (Pt:Pd = 1:4.1:2 and 1:1) are synthesized by a chemical reduction method for oxygen reduction reaction (ORR). X-ray diffraction (XRD), transmission electron microscope (TEM) and cyclic voltammetry (CV) measurements confirm that Pt is deposited on the Pd nanoparticles and the Pt/Pd/C catalysts have a Pd_(COre)@Pt_(shell) structure. In the half cell testing, the catalytic ORR activity of Pt1 /Pd2/C and Pt1 /Pd4/C are superior to commercial Pt/C Moreover, the electrochemical durability to potential cycling of Pt1 /Pd2/C and Pt1 /Pd1 /C catalysts is better than Pt/C catalysts. The improved durability is believed to be associated with the dissolution of Pd and the corresponding structure transformation from core-shell structure to Pt-Pd alloy with Pt rich surface. The structure change is confirmed by TEM, CV, XRD and X-ray photoelectron spectroscopy (XPS). In addition, the electrochemical active surface area (ECSA) loss and polarization behavior in the single cell testing also suggest that the Pt/Pd/C show a much better durability than Pt/C catalysts. Similarly, the dissolution of Pd is observed by CV and scanning electron microscope-energy dispersive X-ray spectra (SEM-EDX). The Pt/Pd/C electrocatalysts have high ORR activity and this high activity can be further improved during potential cycling, that is, the activity and durability can be obtained simultaneously. This Pd_(COre)@Pt_(Shell) structure allows for the development of highly active and durable ORR electrocatalysts, with potential for the application in proton exchange membrane fuel cells (PEMFCs).
机译:通过化学还原法进行氧还原反应合成了一系列不同的Pt / Pd摩尔比(Pt:Pd = 1:4.1:2和1:1)的Pt改性Pd / C催化剂(Pt / Pd / C)( ORR)。 X射线衍射(XRD),透射电子显微镜(TEM)和循环伏安法(CV)测量证实Pt沉积在Pd纳米颗粒上且Pt / Pd / C催化剂具有Pd_(COre)@Pt_(shell)结构。在半电池测试中,Pt1 / Pd2 / C和Pt1 / Pd4 / C的催化ORR活性优于商用Pt / C。此外,Pt1 / Pd2 / C和Pt1 / Pd1 / C催化剂对潜在循环的电化学耐久性比Pt / C催化剂好。据信,提高的耐久性与Pd的溶解以及相应的结构从核-壳结构到具有富Pt表面的Pt-Pd合金的转化有关。通过TEM,CV,XRD和X射线光电子能谱(XPS)确认了结构变化。此外,单电池测试中的电化学活性表面积(ECSA)损失和极化行为也表明Pt / Pd / C的耐久性比Pt / C催化剂好得多。同样,通过CV和扫描电子显微镜-能量色散X射线光谱(SEM-EDX)观察到Pd的溶解。 Pt / Pd / C电催化剂具有高的ORR活性,并且在电位循环期间可以进一步提高该高活性,即,可以同时获得活性和耐久性。这种Pd_(COre)@Pt_(Shell)结构允许开发高活性和持久性的ORR电催化剂,并有可能应用于质子交换膜燃料电池(PEMFC)。

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