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Lattice-governed electrochemical catalysis: Pd-Rh nanoboxes synthesized via control of metal migration

机译:晶格控制的电化学催化:通过控制金属迁移合成的Pd-Rh纳米盒

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摘要

Developing the synthesis of more sophisticated nanostructuresncomprising more than one late transition metal broadens the librarynof materials available in the quest to find suitable heterogeneousncatalysts. The synthesis of well-defined multi-metal nanoparticlesncontaining Rh element remains a challenge because of the element’snpropensity toward random island and dendrite growth. Herein wenreport a wet chemistry method to synthesize the Pd-Rhnheterogeneous nanoboxes and to fine tune their structures at atomicnlevel. The structures of the nanoboxes were characterized by electronnmicroscopy and a metal migration mechanism for their formationnwas proposed. The surfaces of nanoboxes were examined bynelectrochemical catalysis. We reveal that both lattice strain from thennanoscale separation of metal phases and element composition of ourncomplex nanostructures govern the catalytic behavior.
机译:发展包含多于一种晚过渡金属的更复杂的纳米结构的合成,拓宽了可用于寻找合适的多相催化剂的材料库。明确定义的含Rh元素的多金属纳米颗粒的合成仍然是一个挑战,因为该元素倾向于随机岛和枝晶生长。在此,我们报道了一种湿化学方法,用于合成Pd-Rhn多相纳米盒,并在原子级微调其结构。通过电子显微镜对纳米盒的结构进行了表征,并提出了形成金属盒的金属迁移机理。纳米盒的表面通过电化学催化进行了检测。我们揭示了金属相的纳米尺度分离的晶格应变和我们复杂的纳米结构的元素组成决定了催化行为。

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