首页> 外文期刊>The journal of physical chemistry, C. Nanomaterials and interfaces >Enhanced Oxygen Reduction Reaction Activity and Characterization of Pt-Pd/C Bimetallic Fuel Cell Catalysts with Pt-Enriched Surfaces in Acid Media
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Enhanced Oxygen Reduction Reaction Activity and Characterization of Pt-Pd/C Bimetallic Fuel Cell Catalysts with Pt-Enriched Surfaces in Acid Media

机译:在酸性介质中具有富Pt表面的Pt-Pd / C双金属燃料电池催化剂的增氧还原反应活性和表征

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Three types of bimetallic Pt—Pd nanoparticles with different core—shell structures besides Pt and Pd nanoparticles were synthesized by coreduction and sequential reduction methods in ethylene glycol. The synthesized nanoparticles were supported on carbon to prepare five different electrocatalysts Pt/C, Pd/C, PdPt alloy/C, Pd(core)-Pt(shell)/C, and Pt(core)— Pd(shell)/C for oxygen reduction reaction (ORR) in fuel cells. The nanoparticles and supported catalysts were characterized by means of transmission electron microscopy (TEM), Fourier transform infrared spectroscopy (FT-IR), X-ray powder diffraction (XRD), extended X-ray absorption fine structure (EXAFS), and cyclic voltammetry (CV). It was proposed by these characterizations that the PdPt alloy/C, Pd(core)— Pt(shell)/C, and Pt(core)-Pd(shell)/C catalysts constituted Pd4Pt1(core)-Pt(two-layers shell), Pd (core)— PdjPt^three-layers)— Pt (three-layers shell), and Pt(core)—Pt2Pd1(two-layers)~Pd (microcrystal shell), respectively. The Pt surface-enriched catalysts were more stable than the Pd surface-enriched catalysts in long-term CV scanning in acid electrolyte. The Pt/C, PdPt alloy/C, and Pd(core)— Pt(shell)/C catalysts with Pt-enriched surfaces showed much higher ORR specific activity than the Pd/C and Pt(core)— Pd(shell)/C catalysts with Pd-enriched surfaces. The Pt surface-enriched bimetal catalysts with core—shell structures showed the higher Pt-based mass activity than the Pt monometal catalyst. The PdPt catalysts with Pd/ Pt = 2 and 4 in an atomic ratio were also prepared by the coreduction method. The Pt-enriched surfaces formed also with these samples, but the ORR specific activity and (Pd + Pt)-based mass activity decreased with increasing Pd/Pt ratios (l, 2, and 4). The present study provided core—shell catalysts with better ORR activity, which may be useful for understanding key issues to develop next-generation fuel-cell cathode catalysts.
机译:通过乙二醇的共感应和顺序还原法合成了除Pt和Pd纳米粒子外的三种不同核壳结构的双金属Pt-Pd纳米粒子。将合成的纳米颗粒负载在碳上以制备五种不同的电催化剂Pt / C,Pd / C,PdPt合金/ C,Pd(核)-Pt(壳)/ C和Pt(核)-Pd(壳)/ C燃料电池中的氧还原反应(ORR)。通过透射电子显微镜(TEM),傅立叶变换红外光谱(FT-IR),X射线粉末衍射(XRD),扩展X射线吸收精细结构(EXAFS)和循环伏安法对纳米颗粒和负载型催化剂进行了表征(简历)。由这些特征提出,PdPt合金/ C,Pd(核)-Pt(壳)/ C和Pt(核)-Pd(壳)/ C催化剂构成了Pd4Pt1(核)-Pt(两层壳) ),Pd(核心)-PdjPt ^ 3层)-Pt(三层壳)和Pt(核心)-Pt2Pd1(两层)〜Pd(微晶壳)。在酸性电解液中进行长期CV扫描时,Pt表面富集的催化剂比Pd表面富集的催化剂更稳定。具有富Pt表面的Pt / C,PdPt合金/ C和Pd(核)-Pt(壳)/ C催化剂显示出比Pd / C和Pt(核)-Pd(壳)/具有富Pd表面的C催化剂。具有核-壳结构的Pt表面富集的双金属催化剂显示出比Pt单金属催化剂更高的Pt基质量活性。还通过共芯法制备了原子比为Pd / Pt = 2和4的PdPt催化剂。这些样品也形成了富含Pt的表面,但是ORR比活性和(Pd + Pt)基质量活性随Pd / Pt比值的增加而降低(1、2和4)。本研究为核壳催化剂提供了更好的ORR活性,这可能有助于理解开发下一代燃料电池阴极催化剂的关键问题。

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