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Tailoring Au-core Pd-shell Pt-cluster nanoparticles for enhanced electrocatalytic activity

机译:定制Au-core Pd-shell Pt-簇纳米颗粒以增强电催化活性

摘要

We have rationally synthesized and optimized catalytic nanoparticles consisting of a gold core, covered by a palladium shell, onto which platinum clusters are deposited (Au@Pd@Pt NPs). The amount of Pt and Pd used is extremely small, yet they show unusually high activity for electrooxidation of formic acid. The optimized structure has only 2 atomic layers of Pd and a half-monolayer equivalent of Pt (theta(Pt) approximate to 0.5) but a further increase in the loading of Pd or Pt will actually reduce catalytic activity, inferring that a synergistic effect exists between the three different nanostructure components (sphere, shell and islands). A combined electrochemical, surface-enhanced Raman scattering (SERS) and density functional theory (DFT) study of formic acid and CO oxidation reveals that our core-shell-cluster trimetallic nanostructure has some unique electronic and morphological properties, and that it could be the first in a new family of nanocatalysts possessing unusually high chemical reactivity. Our results are immediately applicable to the design of catalysts for direct formic acid fuel cells (DFAFCs).
机译:我们已经合理地合成和优化了由金核组成的催化纳米颗粒,该金核被钯壳覆盖,铂簇沉积在其上(Au @ Pd @ Pt NPs)。 Pt和Pd的使用量极少,但是它们对甲酸的电氧化显示出异常高的活性。优化的结构仅具有2个Pd原子层和等价的Pt半单层(theta(Pt)大约为0.5),但是Pd或Pt负载量的进一步增加实际上会降低催化活性,这表明存在协同作用。在三个不同的纳米结构组件(球形,壳形和岛形)之间。甲酸,CO氧化的电化学,表面增强拉曼散射(SERS)和密度泛函理论(DFT)的组合研究表明,我们的核-壳-簇三金属纳米结构具有某些独特的电子和形态学性质,并且可能是在具有异常高化学反应性的纳米催化剂的新家族中率先我们的结果可立即应用于直接甲酸燃料电池(DFAFC)的催化剂设计。

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