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Shaped Pd-Ni-Pt Core-Sandwich-Shell Nanoparticles: Influence of Ni Sandwich Layers on Catalytic Electrooxidations

机译:成形的Pd-Ni-Pt核-三明治壳纳米颗粒:镍三明治层对催化电氧化的影响

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摘要

Shape-controlled metal nanoparticles (NPs) interfacing Pt and nonprecious metals (M) are highly active energy conversion electrocatalysts; however, there are still few routes to shaped M-Pt core-shell NPs and fewer studies on the geometric effects of shape and strain on catalysis by such structures. Here, well-defined cubic multilayered Pd-Ni-Pt sandwich NPs are synthesized as a model platform to study the effects of the nonprecious metal below the shaped Pt surface. The combination of shaped Pd substrates and mild reduction conditions directs the Ni and Pt overgrowth in an oriented, layer-bylayer fashion. Exposing a majority of Pt(100) facets, the catalytic performance in formic acid and methanol electro-oxidations (FOR and MOR) is assessed for two different Ni layer thicknesses and two different particle sizes of the ternary sandwich NPs. The strain imparted to the Pt shell layer by the introduction of the Ni sandwich layer (Ni-Pt lattice mismatch of ~11%) results in higher specific initial activities compared to core-shell Pd-Pt bimetallic NPs in alkaline MOR. The trends in activity are the same for FOR and MOR electrocatalysis in acidic electrolyte. However, restructuring in acidic conditions suggests a more complex catalytic behavior from changes in composition. Notably, we also show that cubic quaternary Au-Pd-Ni-Pt multishelled NPs, and Pd-Ni-Pt nanooctahedra can be generated by the method, the latter of which hold promise as potentially highly active oxygen reduction catalysts.
机译:与Pt和非贵金属(M)接触的形状可控的金属纳米颗粒(NPs)是高活性的能量转化电催化剂。然而,形成M-Pt核-壳NP的途径仍然很少,而且关于形状和应变对这种结构催化的几何效应的研究也很少。在这里,定义明确的立方多层Pd-Ni-Pt夹层NPs作为模型平台被用来研究非贵金属在成形Pt表面之下的影响。成形的Pd衬底和适度的还原条件的结合以定向的逐层方式引导Ni和Pt的过度生长。暴露了大部分Pt(100)面,针对两种不同的Ni层厚度和两种不同的三元夹层NPs粒径,评估了甲酸和甲醇电氧化(FOR和MOR)的催化性能。与碱性MOR中的核壳Pd-Pt双金属NPs相比,通过引入Ni夹心层而赋予Pt壳层的应变(Ni-Pt晶格失配率为11%)导致更高的比初始活性。酸性电解质中FOR和MOR电催化的活性趋势相同。但是,在酸性条件下进行重组表明,由于组成的变化,催化行为更加复杂。值得注意的是,我们还表明,通过该方法可以生成立方季铵Au-Pd-Ni-Pt多壳NP和Pd-Ni-Pt纳米八面体,后者有望成为潜在的高活性氧还原催化剂。

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