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Pd-shaped nanoparticles modified by gold ad-atoms: effects on surface structure and activity towards glucose electrooxidation

机译:金原子修饰的钯状纳米颗粒:对表面结构和葡萄糖电氧化活性的影响

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Palladium nanoparticles (Pd-NPs) with controlled distributions of sizes and shapes (nanospheres - Pd-NS-, nanocubes -Pd-NC-, and nanooctahedrons -Pd-NO-) are synthesized by wet chemistry methods and characterized by TEM/HRTEM. The surfaces of Pd-NPs are modified by spontaneous adsorption of gold and characterized by cyclic voltammetry in acidic medium. It is shown that the modification of Pd-NPs by dipping in HAuCl4 solutions of different concentrations allows controlling the surface coverage by gold. It is also shown that the modification of Pd-NPs surfaces involves first the formation of PdAu surface alloys. For higher coverages, both PdAu surface alloys and pure Au structures are formed. The activity towards the glucose electrooxidation reaction is determined by linear scan voltammetry (LSV). Higher activity is observed on pure Pd-NC presenting extended (100) surfaces than on Pd-NO with mainly (111) surface orientation and on Pd-NS without preferential surface orientation, both these latter Pd-NPs displaying almost the same activity. The modification of the surface by spontaneous adsorption of gold greatly improves the activity of all Pd-NPs. However, Au-modified Pd-NC materials remain the most active catalysts. PdAu surface alloys seem to be involved in the improvement of the catalytic activity at low potentials, although the role of pure gold structures on Pd-NPs towards the enhancement of the catalytic activity cannot be excluded for high gold coverage. The study allows a better understanding of the material structure/electrocatalytic behavior relationship.
机译:通过湿化学方法合成尺寸和形状(纳米球-Pd-NS-,纳米立方体-Pd-NC-和纳米八面体-Pd-NO-)具有受控大小和形状分布的钯纳米粒子(Pd-NPs),并通过TEM / HRTEM对其进行表征。 Pd-NPs的表面通过金的自发吸附而改性,并通过在酸性介质中的循环伏安法进行表征。结果表明,通过浸入不同浓度的HAuCl4溶液来修饰Pd-NPs可以控制金的表面覆盖。还显示出Pd-NPs表面的改性首先涉及PdAu表面合金的形成。为了获得更高的覆盖率,可以同时形成PdAu表面合金和纯金结构。通过线性扫描伏安法(LSV)测定对葡萄糖电氧化反应的活性。在具有延伸的(100)表面的纯Pd-NC上观察到的活性高于在主要具有(111)表面取向的Pd-NO和没有优先表面取向的Pd-NS上的活性,后两个Pd-NP都显示出几乎相同的活性。通过自发吸附金对表面进行的改性大大提高了所有Pd-NP的活性。但是,Au改性的Pd-NC材料仍然是最具活性的催化剂。尽管不能排除高金覆盖率下Pd-NPs上纯金结构对增强催化活性的作用,但PdAu表面合金似乎在低电位下参与了催化活性的改善。该研究可以更好地了解材料结构/电催化行为之间的关系。

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